CN1820034B

CN1820034B - Polyolefin adhesive composition and articles made therefrom

Info

Publication number: CN1820034B
Application number: CN200380106170.8A
Authority: CN
Inventors: 江培军; K·A·纳尔森; C·L·柯里; A·德克梅齐安; J·A·M·卡尼奇; C·L·西姆斯; R·阿巴里; C·A·加西亚-佛朗哥; N·纳蓬斯; M·L·费塞特; L·E·雅各布
Original assignee: ExxonMobil Chemical Patents Inc
Current assignee: ExxonMobil Chemical Patents Inc
Priority date: 2002-10-15
Filing date: 2003-10-15
Publication date: 2010-10-27
Anticipated expiration: 2023-10-15
Also published as: CN100588663C; CN1820034A; CN1705688A

Abstract

Specific embodiments of the present invention are directed to articles comprising a polymer comprising one or more _C3-40 olefins, optionally one or more dienes, and less than 5 mol% ethylene, having a Point T-Peel Force of 1 Newton or greater, a branching index (g') of 0.95 or less, as measured at the Mz of the polymer, and an Mw of 100,000 or less. The present invention also relates to a process for producing an olefin polymer comprising: 1) selecting a first catalyst component that produces a polymer having an Mw of 100,000 or less and a crystallinity of 20% or less; 2) selecting a second catalyst component that produces a polymer having an Mw of 100,000 or less and a crystallinity of 40% or greater; and 3) contacting the catalyst component with one or more _C3-40 olefins in the presence of one or more activators in a reaction zone.

Description

Polyolefin adhesive compositions and by its goods of making

The cross reference of related application

It is right of priority that the application requires the provisional application USSN 60/418,482 with being entitled as of application on October 15th, 2002 " for olefines polymerization multi-component catalyst systems and by the polymkeric substance of its production ".It is right of priority that the application also requires the USSN 60/460,714 with being entitled as of on April 4th, 2003 application " polyolefin adhesive compositions and by its goods of making ".

The application also relates to the US2000000199093P of the right of priority that requires USSN 60/199,093 of the USSN 60/199,093 of on April 21st, 2000 application and 20 applications in April calendar year 2001.The application also relates to the USSN 60/171,715 of application on December 21st, 1999; The USSN 09/745,394 of application on December 21st, 2000; With the USSN09/746 of application on December 21st, 2000,332.The application also relates to WO 01/81493.

Invention field

The present invention relates to comprise C _3-40The tackiness agent of olefin polymer, the some T shape peeling force (Dot T-Peel) of described polymkeric substance is 1 newton or higher; The branch index of under the z-of described polymkeric substance average molecular weight (Mz), measuring (g ') be 0.95 or lower; Weight-average molecular weight (Mw) is 100000 or lower; And intensity is good.

Background of invention

For some application such as tackiness agents, single polymers does not have required performance combination.The various polyolefine that will have certain characteristic usually are blended together to have both the positive attributes of each component.Normally a kind of blend of result demonstrates the mean value of the individual performance of each resin.For example, EP 0 527 589 blend that discloses flexible lower molecular weight amorphous polypropylene and higher molecular weight isotactic polyprophlene obtains physical strength and snappiness isostatic composition.These composition exhibiting go out than the better snappiness of independent isotactic polyprophlene, but other rerum natura is still not enough.The physics blending also has the not enough problem of miscibility.Unless select component according to its consistency, be separated or less component may be to surface transport otherwise may produce.Usually be also referred to as the tight blend composition of two or the multiple polymers that prepare in the series reaction device (be included in the same reactor or) head it off with reactor blend, but the catalyst system that finds under equivalent environment operation to produce different polymkeric substance becomes challenge.

Past is produced reactor blend (being also referred to as tight blend) and other polymer composition of different polymkeric substance always with multi-component catalyst systems.It has been generally acknowledged that reactor blend and other one-pot (one-pot) polymer composition are better than the physical blending thing of similar polymkeric substance.For example, US6,248,832 disclose a kind of polymer composition, select production in the presence of the metallocene catalyst system at one or more Stereoselective metallocene catalyst system and at least a non-upright structure.Resulting polymers has the advantageous property of disclosed physical blending thing among EP of being better than 0 527 589 and the US 5,539,056.

Therefore look on the bright side of things always and send out multi-component catalyst systems to produce new polymer composition in this area.For example, US 5,516, and 848 openly adopt aikyiaiurnirsoxan beta or two kinds of different cyclopentadienyl transition metal compounds of non-coordination anion activatory.Particularly, wherein there is embodiment to disclose for example with methylaluminoxane or four (pentafluorophenyl group) boric acid N, activator activatory (Me such as N-dimethyl puratized agricultural spray ₂Si (Me ₄C ₅) (N-c-C ₁₂H ₂₃) TiCl ₂With racemize-Me ₂Si (H ₄Ind) ZrCl ₂, or Me ₂Si (Me ₄C ₅) (N-c-C ₁₂H ₂₃) TiCl ₂With Me ₂Si (Ind ₂) HfMe ₂Catalyst compound such as (Ind=indenyls) combination has bimodal molecular weight distribution (Mw/Mn), different degree of isotacticity (in

embodiment

2,3 and 4 the product 12 to 52wt% isotaxy PP being arranged) and weight-average molecular weight surpass 100000 polypropylene of (as thermoplastics time some even up to 1200000) with production.Equally, US6,184,327 disclose a kind of thermoplastic elastomer, the branched olefin polymer that includes crystalline state side chain and non-crystalline state main chain, wherein the side chain of 90mol% is isotaxy or syndiotactic polypropylene at least, at least the main chain of 80mol% is an Atactic Polypropelene, by the method production that may further comprise the steps: a) to about 120 ℃ temperature propylene monomer is contacted about 90 with catalyst composition, described catalyst composition comprises can the production isotaxy or the transition metal catalyst compound of the chirality solid rigid of syndiotactic polypropylene; B) in polymerization reactor, make a) product and propylene and nonessential one or more copolymerisable monomer copolymerization with the achirality transition-metal catalyst that can produce Atactic Polypropelene; And c) reclaims branched olefin polymer.Similarly, US6,147,180 disclose the synthetic of a kind of thermoplastic polymer composition, produce the macromonomer of at least 40% ethenyl blocking, make described macromonomer and ethylene copolymer production then by making monomer polymerization earlier.In addition, US6,323,284 also disclose with two kinds of independent catalyst systems and have made alpha-olefin and α, and the method for thermoplastic compounds (mixture of crystalline state and amorphous poly olefin copolymer) is produced in ω-diolefine copolymerization.

Tested equally with multistep processes and produced the novel polymeric compositions.For example, EP 0 366 411 discloses a kind of graftomer of the EPDM of having main chain, has thereon polypropylene graftedly at one or more diene monomers position, produces with two-step approach, and per step is adopted different ziegler-natta catalyst systems.It is said that this graftomer is applicable to the impact property of improving the co-blend polypropylene composition.

Though polymkeric substance described in the above reference all has attractive performance combination, but still need provide other to be fit to the new different performance equilibrated novel composition of various end-uses.Special wish to find a kind of firm but binding property is arranged and can stick with glue the composition of technology and equipment coating.

The embodiment 30 of WO 01/46277 discloses with the propylene of two kinds of Preparation of Catalyst and the multipolymer of hexene.

Can reference about the general information of this area:

1.DeSouza and Casagrande，in 2001 addressed the issue of binary catalyst systems in″ Recent Advances in Olefin Polymerization Using Binary Catalyst Systems，Macromol.Rapid Commun.2001，22，No.16(pages 1293 to 1301)。1299 pages of propylene systems of reporting production " gluing " product.

2. nearest Lieber and Brintzinger in " Propene Polymerization with Catalyst Mixtures Containing Different Ansa-Zirconocenes:Chain Transfer to Alkylaluminum Cocatalysts and Formation of Stereoblock Polymers ", Macromolecules 2000,33, No.25 (pages9192-9199) studies the field mix thing production stereoblock polypropylene with different stereoselective metallocene catalysts.Use metallocene catalyst H ₄C ₂(Flu) ₂ZrCl ₂, racemize-Me ₂Si (2-Me-4-tBu-C ₅H ₂) ₂ZrCl ₂And racemize-Me ₂Si (2-MeInd) ₂ZrCl ₂At MAO (methylaluminoxane) or triisobutyl aluminium (Al (iBu) as promotor ₃)/four (perfluorophenyl boric acid) triphenylcarbenium

(trityl borate) carries out propylene polymerization under existing.Spent mixed catalyst H ₄C ₂(Flu) ₂ZrCl ₂And racemize-Me ₂Si (2-MeInd) ₂ZrCl ₂At MAO or Al (iBu) ₃Carry out propylene polymerization under/trityl borate exists and produce waxy solid, they can be separated into atactic (dissolving in diethyl ether) and isotaxy (insoluble) fraction fully.Arbitrary fraction does not comprise any combination of isotaxy and atactic five unit group patterns, represents that these catalyst mixtures do not form stereoblock polymer.

3.Aggarwal at " Structures and Properties of Block Polymers and Multiphase Polymer Systems:An Overview of Present Status and Future Potential ", S.L.Aggarwal, the various polymkeric substance of being produced have been discussed among the Sixth Biennial Manchester Polymer Symposium (UMIST Manchester, March 1976).

4.“Selectivity in Propene Polymerization with Metallocene Catalysts”Resconi，et al，Chem Rev。2000，100，1253-1345。

Above reference is not all directly spoken of the polyolefin-based tackiness agent that need comprise non-crystalline state and crystalline component.This type of tackiness agent of industrial needs needing to replace the blend of a large amount of tackifier and/or other additive.

Other relevant reference comprises:

1) EP patent: EP 0 619 325 B1, EP 719 802 B1;

2) US patent/open: US 6,207, and 606; 6,258,903; 6,271,323; 6,340,703; 6,297,301; US 2001/0007896 A1; US 6,184, and 327; 6,225,432; 6,342,574; 6,147,180; 6,114,457; 6,143,846; 5,998,547; 5,696,045; 5,350,817;

3) PCT is open: WO 00/37514, WO 01/81493, WO 98/49229, WO98/32784 and WO 01/09200;

4)″Metallocene-Based Branch-Block thermoplastic Elastomers，″Markel，et al.Macromolecules 2000，Volume 33，No.23.pgs.8541-8548。

Summary of the invention

The present invention relates to a kind of tackiness agent, comprise and contain one or more C _3-40The polymkeric substance of alkene, wherein said polymkeric substance has following feature:

A) the some T shape peeling force on kraft paper is 1 newton or higher;

B) branch index of measuring under the Mz of described polymkeric substance (g ') is 0.95 or lower;

C) Mw is 10000 to 100000; With

D) melting heat is 1 to 70J/g.

The invention still further relates to a kind of tackiness agent, comprise and contain one or more C _3-40The polymkeric substance of alkene, wherein said polymkeric substance has following feature:

A) the some T shape peeling force on kraft paper is 1 newton or higher;

B) branch index of measuring under the Mz of described polymkeric substance (g ') is 0.98 or lower;

C) Mw is 10000 to 60000; With

D) melting heat is 1 to 50J/g.

The invention still further relates to a kind of tackiness agent, include the homo-polypropylene of following feature or the multipolymer of propylene and maximum 5mol% ethene:

A) pass through C ¹³The isotaxy continuous length (run length) (isotaxy continuous length " IRL " is defined as the percentage of the percentage of mmmm five unit groups divided by 0.5 * mmmr, five unit groups) that NMR measures is 1 to 30, preferred 3 to 25, more preferably 4 to 20,

B) pass through C ¹³The percentage of the r diad that NMR measures greater than 20%, be preferably 20 to 70% and

C) melting heat be 70J/g or lower, preferred 60J/g or lower, more preferably 1 and 55J/g between, more preferably 4 and 50J/g between.

The accompanying drawing summary

Fig. 1 be the sample of embodiment 12,22 and 49 when cooling off with 10 ℃/min complex viscosity with variation of temperature figure.

The diagram of Fig. 2 for concerning between the branch index g ' of the polymkeric substance produced among the embodiment 4 and 31 and the molecular weight.

Fig. 3 is the heptane Soxhlet extractron insolubles (going up trace) of extraction among the embodiment 4 and the C-13 NMR wave spectrum of hexane room temperature solvend (following trace).

Fig. 4 is the C-13 NMR wave spectrum of aPP/scPP side chain block (branch block) with respect to scPP and aPP control sample.Control sample is once produced with a kind of catalyzer; APP uses the special catalyst synthetic, and scPP stereospecific Catalyst Production.Last trace is the aPP control sample.Middle trace is the scPP control sample, and following trace is embodiment 4.

Fig. 5 illustrates the temperature of the classification sample of extraction among the embodiment 31 and the relation between the complex viscosity.

Figure A6 illustrates the skeleton view that is equipped with the cardboard case of tackiness agent of the present invention on it at least in part.

Figure A7 is that sealing forms the skeleton view that encloses container is schemed the cardboard case of A6 afterwards.

Figure B6 illustrates the floor map of disposable diaper of the present invention.

The synoptic diagram of the disposable diaper of figure B6 when figure B7 illustrates and arranges with the airtight configuration of part.

Figure H6 illustrates the cross-sectional view of representational single face adhesive tape.

Figure H7 illustrates the side-view of the figure H6 adhesive tape of web-like.

Figure H8 illustrates the cross-sectional view of representational double sticky tape.

Figure J6 is the cross-sectional view of label.

Figure K is the DSC trace diagram of the polymkeric substance of embodiment 32 in the table 6.

DESCRIPTION OF THE PREFERRED

For the present invention and claims,, mention when polymkeric substance comprises alkene that the alkene that exists in the polymkeric substance is the alkene of polymerized form for ease of reference.For ease of reference, the amorphous poly propylene is abbreviated as aPP, isotactic polyprophlene is abbreviated as iPP, and syndiotactic polypropylene is abbreviated as sPP, and the hypocrystalline polypropylene is abbreviated as scPP, and the described component of " g-" expression is a grafted.

In another embodiment, the present invention relates to a kind of tackiness agent, comprise and contain one or more C _3-40The preferred propylene of alkene and (in some embodiment) are less than the 15mol% ethene polymkeric substance of (preferably being less than 5mol% ethene), and following feature is arranged:

A) in the some T shape peeling force on the kraft paper between 1 and 10000 newton;

B) Mz/Mn is 2 to 200; With

C) g ' of the Mw of the X shown in following table C and Y (as described in measure under the Mz of polymkeric substance):

Table C

In another embodiment, Mw between 15,000 and 100,000 the time, g '＜(10 then ^-12Mw ²-10 ^-6Mw+1.0178).

In some embodiment, under the Mz of described polymkeric substance, measure g ' and be 0.9 or lower, 0.8 or lower, 0.7 or lower, 0.6 or lower.

In another embodiment, above-mentioned polymkeric substance also has following feature: peak value fusing point (Tm) is between 40 and 250 ℃ or between 60 and 190 ℃ or between about 60 and 150 ℃ or between 80 and 130 ℃.In some embodiment, the peak value fusing point is between 60 and 160 ℃.In other embodiment, the peak value fusing point is between 124-140 ℃.In other embodiment, the peak value fusing point is between 40-130 ℃.

In another embodiment, above-mentioned polymkeric substance also has following feature: viscosity (being also referred to as brookfield viscosity or melt viscosity) (is measured by ASTM D 3236 down at 190 ℃ under 190 ℃; ASTM=American Society for Testing and Materials) be 90000mPas or lower; 80000 or lower 70000 or lower 60000 or lower 50000 or lower 40000 or lower 30000 or lower 20000 or lower 10000 or lower 8000 or lower 5000 or lower 4000 or lower 3000 or lower 1500 or lower or 250 and 6000mPas between or 500 and 5500mPas between or 500 and 3000mPas between or 500 and 1500mPas between, and/or viscosity (to measure by ASTM D 3236 down at 160 ℃) under 160 ℃ be 8000mPas or lower; 7000 or lower 6000 or lower 5000 or lower 4000 or lower 3000 or lower 1500 or lower or 250 and 6000mPas between or 500 and 5500mPas between or 500 and 3000mPas between or 500 and 1500mPas between.In other embodiment, be 200000mPas or lower, depend on application 190 ℃ of following viscosity.In other embodiment, viscosity is 50000mPas or lower, depends on application.

In another embodiment, above-mentioned polymkeric substance also has following feature: melting heat be 70J/g or lower or 60J/g or lower or 50J/g or lower or 40J/g or lower or 30J/g or lower or 20J/g or lower and greater than zero or big 1J/g or greater than 10J/g or 20 and 50J/g between.

In another embodiment, above-mentioned polymkeric substance also has following feature: Xiao A hardness (measuring) by ASTM2240 be 95 or lower, 70 or lower or 60 or lower or 50 or lower or 40 or lower or 30 or lower or 20 or lower.In other embodiment, Xiao A hardness be 5 or higher, 10 or higher or 15 or higher.During some was used as packs, Xiao A hardness was preferably 50-85.In another embodiment, the Xiao A hardness of described polymkeric substance is 20-90.

In another embodiment, the Mz/Mn of polymkeric substance of the present invention is 2 to 200, preferred 2 to 150, preferred 10 to 100.

In another embodiment, above-mentioned polymkeric substance also has following feature: shear adhesion fail temperature (SAFT measures by ASTM 4498) is 200 ℃ or lower or 40 to 150 ℃ or 60 to 130 ℃ or 65 to 110 ℃ or 70-80 ℃.In some embodiment, preferred SAFT is 130-140 ℃.In other embodiments, preferred SAFT is 100-130 ℃.Preferred SAFT is 110-140 ℃ in other embodiments.

In another embodiment, above-mentioned polymkeric substance also has following feature: in the some T shape peeling force on the kraft paper between 1 and 10000 newton or between 3 and 4000 newton or between 5 and 3000 newton or between 10 and 2000 newton or between 15 and 1000 newton.Point T shape peeling force is pressed ASTM D 1876 and is measured, as hereinafter described.

In another embodiment, above-mentioned polymkeric substance also has following feature: be a couple of days to 1 second or 60 seconds or shorter or 30 seconds or shorter or 20 seconds or shorter or 15 seconds or shorter or 10 seconds or shorter or 5 seconds or shorter or 4 seconds or shorter or 3 seconds or shorter or 2 seconds or shorter or 1 second or shorter set time.

In another embodiment, it is 2 to 75 or 4 to 60 or 5 to 50 or 6 to 20 that above-mentioned polymkeric substance also has following feature: Mw/Mn.

In another embodiment, it is 1000000 or lower, preferred 15000 to 1000000 or 20000 to 800000 or 25000 to 350000 that above-mentioned polymkeric substance also has following feature: Mz.

In another embodiment, above-mentioned polymkeric substance can also have following feature: breaking strain (measuring by ASTM D-1708 down at 25 ℃) is 50 to 1000%, preferred 80 to 200%.In some other embodiment, breaking strain is 100 to 500%.

In another embodiment, the fracture tensile strength of polymkeric substance described herein (measuring by ASTM D-1708 down at 25 ℃) is 0.5MPa or higher or 0.75MPa or higher or 1.0MPa or higher or 1.5MPa or higher or 2.0MPa or higher or 2.5MPa or higher or 3.0MPa or higher or 3.5MPa or higher.

In another embodiment, above-mentioned polymkeric substance also has following feature: ctystallizing point (Tc) is between 20 and 110 ℃.In some embodiment, Tc is between 70 to 100 ℃.Tc is between 30 to 80 ℃ in other embodiments.In other embodiments, Tc is between 20 to 50 ℃.

In some embodiment, above-mentioned polymkeric substance also has following feature: the slope in the temperature variant trace of complex viscosity shown in Figure 1 (measuring with ARES dynamic mechanical spectrometer under the speed of cooling of 20% strain and 10 ℃/min under the frequency of 10rad/s, nitrogen atmosphere) in Tc+10 ℃ to Tc+40 ℃ temperature range is-0.1 or lower, preferred-0.15 or lower, more preferably-0.25 or lower.This slope is defined as the derivative of log (complex viscosity) to temperature.

In another embodiment, above-mentioned polymkeric substance have following feature: Tc than low at least 10 ℃ of Tm, preferably lower at least 20 ℃ than Tm, preferably than low at least 30 ℃ of Tm, more preferably than low at least 35 ℃ of Tm.

In another embodiment, more above-mentioned polymkeric substance have following feature: melt index is than (I ₁₀/ I ₂) be 6.5 lower, preferred 6.0 or lower, preferred 5.5 lower, preferred 5.0 or lower, preferred 4.5 or lower, preferably between 1 and 6.0.(I ₁₀And I ₂By ASTM 1238 D, 2.16kg, 190 ℃ of measurements).

In another embodiment, more above-mentioned polymkeric substance have following feature: melt index (pressing ASTM1238 D, 2.16kg, 190 ℃ of measurements) is 25dg/min or higher, preferred 50dg/min or higher, preferred 100dg/min or higher, more preferably 200dg/min or higher, more preferably 500dg/min or higher, more preferably 2000dg/min or higher.

In another embodiment, crystallisation range is 10 to 60 ℃, preferred 20 to 50 ℃, preferred 30 to 45 ℃ in the DSC trace of above-mentioned polymkeric substance.Have in the DSC trace at two or more non-overlapped peak, then the crystallisation range at each peak all is 10 to 60 ℃, preferred 20 to 50 ℃, preferred 30 to 45 ℃ in the DSC trace.

In another embodiment, the molecular weight distribution (Mw/Mn) of the polymkeric substance of producing by the present invention is at least 2, preferably at least 5, preferably at least 10 even more preferably at least 20.

In another embodiment, the polymkeric substance of being produced can have unimodal, the bimodal or multimodal molecular weight of type of polymer to distribute (Mw/Mn), measures by size exclusion chromatography, (SEC).Bimodal or multimodal means the SEC trace to be had more than a peak or flex point.Flex point is that the point that signal changes (for example just being become or on the contrary by negative) appears in the second derivative of curve.

In another embodiment, the activation energy of above-mentioned polymkeric substance is 8 to 15cal/mol.Activation energy is to cause (the supposing that similar Arrhenius concerns) that complex viscosity and the relation of temperature calculate in the zone that viscosity increases with heat effect.

In another embodiment, the cloud point of polymkeric substance that the present invention produces is 200 ℃ or lower, preferred 180 ℃ or lower, preferred 160 ℃ or lower, preferred 120 ℃ or lower, preferred 100 ℃ or lower.Equally, described polymkeric substance preferably has 200 ℃ or lower, preferred 180 ℃ or lower, preferred 160 ℃ or lower, preferred 120 ℃ or lower, preferred 100 ℃ or lower cloud point as any composition of its part.

In another embodiment, above-mentioned polymkeric substance can also have one or more of following feature:

A) the peak value fusing point is between 30 and 190 ℃ or between about 60 and 150 ℃ or between 80 and 130 ℃; And/or

B) (measuring) viscosity down by ASTM D 3236 at 190 ℃ under 190 ℃ is 8000mPas or lower; 5000 or lower 4000 or lower 3000 or lower 1500 or lower or 250 and 6000mPas between or 500 and 5500mPas between or 500 and 3000mPas between or 500 and 1500mPas between, or (at 160 ℃ down by ASTM D 3236 measurements) viscosity is 8000mPas or lower under 160 ℃; 7000 or lower 6000 or lower 5000 or lower 4000 or lower 3000 or lower 1500 or lower or 250 and 6000mPas between or 500 and 5500mPas between or 500 and 3000mPas between or 500 and 1500mPas between; And/or

C) H _f(melting heat) be 70J/g or lower or 60J/g or lower or 50J/g or lower or 40J/g or lower or 30J/g or lower or 20J/g or lower and greater than zero or greater than 1J/g or greater than 10J/g or 10 and 50J/g between; And/or

D) Xiao A hardness (measuring by ASTM 2240) is 90 or lower or 60 or lower or 50 or lower or 40 or lower or 30 or lower or 20 or lower; And/or

E) shear adhesion fail temperature (SAFT measures by ASTM 4498) is 40 to 150 ℃ or 60 to 130 ℃ or 65 to 110 ℃ or 70-80 ℃; And/or

F) some T shape peeling force is between 1 and 10000 newton or between 3 and 4000 newton or between 5 and 3000 newton or between 10 and 2000 newton or between 15 and 1000 newton; And/or

G) be a couple of days to 0.1 second or 60 seconds or shorter or 30 seconds or shorter or 20 seconds or shorter or 15 seconds or shorter or 10 seconds or shorter or 5 seconds or shorter or 4 seconds or shorter or 3 seconds or shorter or 2 seconds or shorter or 1 second or shorter set time; And/or

H) Mw/Mn is greater than 1 to 75 or 2 to 60 or 2 to 50 or 3 to 20; And/or

I) Mz is 500000 or lower, preferred 15000 to 500000 or 20000 to 400000 or 25000 to 350000.

Useful characteristics combination comprises the some T shape peeling force of above-mentioned polymkeric substance between 1 and 10000 newton or between 3 and 4000 newton or between 5 and 3000 newton or between 10 and 2000 newton or between 15 and 1000 newton, and:

1) Mw be 30000 or lower, peak value fusing point between 60 and 190 ℃, melting heat is 1 to 70J/g, measure branch index under the Mz at polymkeric substance (g ') be 0.90 or lower and 190 ℃ of following melt viscosities be 8000mPas or lower; Or

2) Mz be 20000 to 5000000 and SAFT be 60 to 150 ℃; Or

3) Mz/Mn is that 2-200 and set time are 4 seconds or lower; Or

4) H _f(melting heat) is 20 to 50J/g, Mz be 20000 to 500000 and Shore hardness be 50 or lower; Or

5) Mw/Mn is for being 5000mPas or lower greater than 1 to 50,190 ℃ of following viscosity; Or

6) Mw be 50000 or lower, peak value fusing point between 60 and 190 ℃, melting heat is 2 to 70J/g, measure branch index under the Mz at polymkeric substance (g ') be 0.70 or lower and 190 ℃ of following melt viscosities be 8000mPas or lower.

In one preferred embodiment, polymkeric substance of the present invention comprises non-crystalline state, crystalline state and side chain block molecule structure.

In one preferred embodiment, described polymkeric substance comprises at least 50wt% propylene, preferably at least 60% propylene or at least 70% propylene or at least 80% propylene.

In another embodiment, the second-order transition temperature (Tg) of the polymkeric substance of producing is measured by ASTM E1356) be 5 ℃ or lower, preferred 0 ℃ or lower or between 0 ℃ and-40 ℃ or between-5 ℃ and-15 ℃.

In another embodiment, the non-crystalline region content of polymkeric substance of the present invention is at least 50% or at least 60% or at least 70% or even between 50 and 99%.The percentage composition of non-crystalline region deducts the crystallization gon with 100 and determines.The crystallization gon is measured with differential scanning calorimetry by ASTM E 794-85.

In another embodiment, crystallinity of polymer of the present invention is 40% or lower or 30% or lower or 20% or lower even between 10 and 30%.The crystallization gon is measured with differential scanning calorimetry by ASTM E794-85.In another embodiment, the crystallization gon of polymkeric substance described herein is between 5 and 40% or between 10 to 30%.

In another embodiment, the molecular weight distribution (Mw/Mn) of polymkeric substance that the present invention produces is at least 1.5, preferably at least 2, preferably at least 5, preferably at least 10 even at least 20.In another embodiment, Mw/Mn be 20 or lower, 10 or lower even 5 or lower.Molecular weight distribution generally depends on catalyst system therefor and processing condition such as temperature, monomer concentration, catalyst ratio (if using multiple catalyzer) and whether has hydrogen.The consumption of hydrogen can be maximum 2% (weights), but is preferably 50 to 500ppm.

In another embodiment, the polymkeric substance of producing by gel permeation chromatography measurement have at least two kinds greater than 2% (weight), be preferably greater than the molecular weight fraction of 20% (weight), all based on the weight of polymkeric substance.Can on the GPC trace, determine described fraction by two kinds of different modes by observed molecular weight.Example be a peak of GPC trace appear at the 20000Mw place and another peak at the 50000Mw place, wherein the area under the first peak accounts for greater than 2% (weight) of described polymkeric substance and the area under second peak and accounts for 2% (weight) greater than described polymkeric substance.

In another embodiment, polymkeric substance of the present invention have the solvable fraction of hexane room temperature of 20% (weight) or more (based on the weight of starting polymer) and 70% (weight) or still less, preferred 50% (weight) or the Soxhlet boiling heptane insoluble fraction of (based on the weight of polymkeric substance) still less.Soxhlet heptane insoluble fraction means one of gained fraction when solvent extraction technology makes the sample classification one by one.Described classification is carried out in two steps: a step relates to the room temperature solvent extraction, and another step relates to Soxhlet extractron.In the room temperature solvent extraction, make about 1g polymkeric substance be dissolved in 50ml solvent (for example hexane) to isolate the type of polymer of non-crystalline state or very low molecular weight.With mixture stir about 12 hours at room temperature.With vacuum filtration solvable fraction is separated with insolubles.Make insolubles through Soxhlet extractron then.This relates to based on it and just has been higher than solubleness isolating polymer fraction in all kinds of SOLVENTS of room temperature to 110 ℃ at boiling point.Earlier will be from the solvent-extracted insolubles of room temperature hexane and heptane (Soxhlet) equal solvent extracted overnight; Make solvent evaporation reclaim the weight of extract and weighing resistates.Insoluble sample as described in extracting as heptane with the higher solvent of boiling point is then weighed after the solvent evaporation.Gained insolubles and sleeve pipe are air-dry in stink cupboard in the final stage makes most of solvent evaporation, then at the vacuum oven inner drying of nitrogen purging.Calculate the amount of residue insolubles in the sleeve pipe then, as long as the deadweight of known sleeve.

In another embodiment, the polymkeric substance that the present invention produced has 70% (weight) or heptane insoluble fraction still less (based on the weight of starting polymer), and the branch index g ' of this heptane insoluble fraction is 0.9 (preferred 0.7) or lower, measures under the Mz of polymkeric substance.In one preferred embodiment, described composition also has the solvable fraction of hexane of at least 20% (weight), based on the weight of starting polymer.In another embodiment, the polymkeric substance that the present invention produced has the Mz of 70% (weight) or heptane insoluble fraction still less (based on the weight of starting polymer) and this heptane insoluble part between 20000 and 5000000.In one preferred embodiment, described composition also has the solvable fraction of hexane of at least 20% (weight), based on the weight of starting polymer.In another embodiment, the polymkeric substance of being produced has the hexane soluble part of at least 20% (weight), based on the weight of starting polymer.

In another embodiment, described polymkeric substance comprise propylene and 15mol% ethene or still less, preferred 10mol% ethene or still less, more preferably 9mol% ethene or still less, more preferably 8mol% ethene or still less, more preferably 7mol% ethene or still less, more preferably 6mol% ethene or still less, more preferably 5mol% ethene or still less, more preferably 4mol% ethene or still less, more preferably 3mol% ethene or still less, more preferably 2mol% ethene or still less, more preferably 1mol% ethene or still less.

In another embodiment, polymkeric substance of the present invention comprise the ethene that is less than 5mol%, preferably be less than the ethene of 4.5mol%, preferably be less than the ethene of 4.0mol% or be less than the ethene of 3.5mol% or be less than the ethene of 3.0mol% or be less than the ethene of 2.5mol% or be less than the ethene of 2.0mol% or be less than the ethene of 1.5mol% or be less than the ethene of 1.0mol% or be less than the ethene of 0.5mol% or be less than the ethene of 0.25mol% or the ethene of 0mol%.

For ease of reference, also can be described as " semi-crystalline polymer " with the degree of crystallinity of second kind of Catalyst Production at least 20% polymkeric substance, be lower than 5% polymkeric substance with the degree of crystallinity of first kind of catalyst component production and can be described as " amorphous polymer ".

In another embodiment of the present invention, the polymkeric substance of being produced has three regional complex viscosity-hygrograms of feature shown in Figure 1.This complex viscosity is to measure with ARES dynamic mechanical spectrometer under the speed of cooling of 20% strain and 10 ℃/min under the frequency, nitrogen atmosphere at 10rad/s dependence on temperature.Make the sample fusing earlier, be cooled to room temperature then gradually, monitor the increase of complex viscosity simultaneously.More than fusing point (this is typical polymer processing temperature), complex viscosity relatively low (I district) and along with the reduction of temperature increases gradually.In the II district, complex viscosity increased rapidly when temperature descended.The 3rd district (III district) is high complex viscosity district, appears at corresponding under the lesser temps of using (the final application) temperature.In the III district, complex viscosity is high and along with the further decline of temperature changes very little.Such complex viscosity distribution pattern in hot melt adhesive is used, be provided at the following open hour of processing temperature (opening time) long and at a lower temperature set time short desirable combination.

In one preferred embodiment, the polymkeric substance that is less than 1mol% ethene that has that the present invention produces has 2mol% (CH at least ₂) ₂Unit, preferred 4mol%, preferred 6mol%, more preferably 8mol%, more preferably 10mol%, more preferably 12mol%, more preferably 15mol%, more preferably 18mol%, more preferably 5mol% pass through C as hereinafter described ¹³NMR measures.

In another embodiment, the present invention produces have 1 and 10mol% between the polymkeric substance of ethene 2+Xmol% (CH is at least arranged ₂) ₂Unit, preferred 4+Xmol%, preferred 6+Xmol%, more preferably 8+Xmol%, more preferably 10+Xmol%, more preferably 12+Xmol%, more preferably 15+Xmol%, more preferably 18+Xmol%, more preferably 20+Xmol%, wherein X is the mol% of ethene, described (CH ₂) ₂The unit is to pass through C as hereinafter described ¹³NMR measures.

In one preferred embodiment, the polymkeric substance that is less than 1mol% ethene that has that the present invention produces has non-crystalline state component (degree of crystallinity that is defined as described polymer composition is lower than that part of 5%), and this non-crystalline state component comprises 3mol% (CH at least ₂) ₂Unit, preferred 4mol%, preferred 6mol%, more preferably 8mol%, more preferably 10mol%, more preferably 12mol%, more preferably 15mol%, more preferably 18mol%, more preferably 20mol% pass through C as hereinafter described ¹³NMR measures.

In another embodiment, the present invention produces have 1 and 10mol% between the polymkeric substance of ethene non-crystalline state component (degree of crystallinity that is defined as described polymer composition is lower than that part of 20%) is arranged, this non-crystalline state component comprises 3+Xmol% (CH at least ₂) ₂Unit, preferred 4+Xmol%, preferred 6+Xmol%, more preferably 8+Xmol%, more preferably 10+Xmol%, more preferably 12+Xmol%, more preferably 15+Xmol%, more preferably 18+Xmol%, more preferably 20+Xmol%, wherein X is the mol% of ethene, described (CH ₂) ₂The unit is to pass through C as hereinafter described ¹³NMR measures.

Monomer

In one preferred embodiment, described polymkeric substance comprises olefin homo or multipolymer, the 5mol% of being less than ethene is arranged and comprise one or more C _3-40Alpha-olefin.In another preferred embodiment, there is the olefin polymer that is less than 5mol% ethene also to comprise one or more diolefinic monomer, preferred one or more C _4-40Diolefine.

In one preferred embodiment, the polymkeric substance that the present invention produces is alfon or multipolymer.Comonomer is preferably C _4-20Straight chain, side chain or cyclic monomer are C in one embodiment _4-12The straight or branched alpha-olefin, preferred butylene, amylene, hexene, heptene, octene, nonene, decene, dodecylene, 4-methyl-amylene-1,3-methyl-amylene-1 and 3,5,5-trimethylammonium-hexene-1 etc.Can there be 5mol% or ethene still less.

In another embodiment, the polymkeric substance that the present invention produces is one or more straight or branched C that can use stereospecific and non-stereospecific polymerization catalyst _3-30Prochirality alpha-olefin or C _5-30The multipolymer that contains cycloolefin or its combination." prochirality " used herein is beneficial to the monomer that forms isotaxy or syndiotactic polymer when meaning with the stereospecific polymerization catalyst.

Polymerisable olefinic structure division can be straight chain, side chain, contain the mixing of structure or these structures of ring.Preferred linear alpha-olefin comprises C _3-8Alpha-olefin, more preferably propylene, 1-butylene, 1-hexene and 1-octene, even more preferably propylene or 1-butylene.Preferred side chain alpha-olefin comprises 4-methyl-1-pentene, 3-Methyl-1-pentene and 3,5,5-trimethylammonium-1-hexene, 5-ethyl-1-nonene.The monomer that preferably contains aryl comprises maximum 30 carbon atoms.The monomer that contains aryl that is fit to comprises at least one aromatic structure, preferred one to three, and more preferably phenyl, indenyl, fluorenyl or naphthyl structure division.Thereby also comprising at least one polymerisable double bonds described aromatic structure after polymerization, the monomer that contains aryl will become the side chain of main polymer chain.The monomer that contains aryl can further be included but not limited to C by one or more alkyl _1-10Alkyl replaces.In addition, two adjacent substituting groups can be linked to be ring structure.The monomer that preferably contains aryl comprises at least one and is attached to aromatic structure on the polymerisable olefinic structure division.Particularly preferred aromatic monomer comprises vinylbenzene, alpha-methyl styrene, to ring-alkylated styrenes, Vinyl toluene, vinyl naphthalene, allyl benzene and indenes, particularly vinylbenzene, p-methylstyrene, 4-phenyl-1-butylene and allyl benzene.

The monomer that comprises non-aromatics cyclic group also is preferred.These monomers can comprise maximum 30 carbon atoms.The monomer that comprises non-aromatics cyclic group that is fit to preferably has at least one polymerisable ethylenic group, and it is suspended on this ring structure or as the part of this ring structure.Described ring structure also can be further by one or more alkyl (but being not limited to) C for example _1-10Alkyl replaces.The monomer that preferably comprises non-aromatics cyclic group comprises vinyl cyclohexane, vinyl cyclohexene, vinyl norbornene, ethylidene norbornene, cyclopentadiene, cyclopentenes, tetrahydrobenzene, cyclobutene and vinyl diamantane etc.

Be preferred for any hydrocarbon structure (preferred C that diolefinic monomer of the present invention includes at least two unsaturated link(age)s _4-30), wherein at least two unsaturated link(age)s are easily introduced in the polymkeric substance by stereospecific or non-stereospecific catalyzer.More preferably described diolefinic monomer is selected from α, ω-diene monomers (being di-vinyl monomers).More preferably described diolefinic monomer is the straight chain di-vinyl monomers, most preferably contains 4 to 30 carbon atoms.The example of preferred diene comprises divinyl, pentadiene, hexadiene, heptadiene, octadiene, nonadiene, decadiene, 11 carbon diene, 12 carbon diene, oleatridecadiene, 14 carbon diene, 15 carbon diene, 16 carbon diene, 17 carbon diene, 18 carbon diene, 19 carbon diene, 20 carbon diene, 21 carbon diene, 22 carbon diene, two oleatridecadienes, the tetracosa carbon diene, 25 carbon diene, 26 carbon diene, heptacosadiene, 28 carbon diene, 29 carbon diene, 30 carbon diene, particularly preferred diene comprises 1, the 6-heptadiene, 1, the 7-octadiene, 1, the 8-nonadiene, 1, the 9-decadiene, 1,10-11 carbon diene, 1,11-12 carbon diene, 1, the 12-oleatridecadiene, 1,13-14 carbon diene and low molecular weight polybutadiene (Mw is lower than 1000g/mol).Preferred cyclic diene comprises the diolefine that is with or without substituent cyclopentadiene, vinyl norbornene, norbornadiene, ethylidene norbornene, Vinylstyrene, Dicyclopentadiene (DCPD) or contains more senior ring on each ring position.

In one preferred embodiment, one or more diene is produced amount in the polymkeric substance for the highest by 10% (weight), preferred 0.00001 to 1.0% (weight), preferred 0.002 to 0.5% (weight) even more preferably 0.003 to 0.2% (weight), based on the gross weight of composition in the present invention.In some embodiment, add in the polymerization 500ppm or diene still less, preferred 400ppm or still less, preferred 300ppm or still less.In other embodiment, add diene or 100ppm or the more or 150ppm or more of 50ppm at least in the polymerization.

In one preferred embodiment, described olefin polymer is a homo-polypropylene.In another preferred embodiment, described olefin polymer comprises propylene, is less than 5mol% ethene and at least a divinyl comonomer.In another preferred embodiment, described olefin polymer comprises propylene and at least a divinyl comonomer.

In another embodiment, described olefin polymer comprises:

40 to 95mol%, preferred 50 to 90mol%, preferred 60 to 80mol% first monomer,

5 to 40mol%, preferred 10 to 60mol%, more preferably 20 to 40mol% comonomer and

0 to 10mol%, more preferably 0.5 to 5mol%, more preferably 1 to 3mol% the 3rd monomer.

In one preferred embodiment, described first monomer comprises any C _3-8One or more of straight chain, side chain or ring-type alpha-olefin comprises propylene, butylene (and all isomer), amylene (and all isomer), hexene (and all isomer), heptene (and all isomer) and octene (and all isomer).Preferred monomer comprises propylene, 1-butylene, 1-hexene and 1-octene etc.

In one preferred embodiment, described comonomer comprises any C _2-40(condition is when having ethene to one or more of straight chain, side chain or ring-type alpha-olefin, its amount is 5mol% or lower), comprise ethene, propylene, butylene, amylene, hexene, heptene and octene, nonene, decene, undecylene, dodecylene, cetene, vinylbenzene, 3,5,5-trimethylammonium hexene-1,3-methylpentene-1,4-methylpentene-1, norbornylene and cyclopentenes.

In one preferred embodiment, described the 3rd monomer comprises any C _2-40(condition is when having ethene to one or more of straight chain, side chain or ring-type alpha-olefin, its amount is 5mol% or lower), include but not limited to ethene, propylene, butylene, amylene, hexene, heptene and octene, nonene, decene, undecylene, dodecylene, cetene, divinyl, 1,5-hexadiene, 1,6-heptadiene, 1,4-pentadiene, 1,7-octadiene, 1,8-nonadiene, 1,9-decadiene, 1,11-dodecylene, vinylbenzene, 3,5,5-trimethylammonium hexene-1,3-methylpentene-1,4-methylpentene-1 and cyclopentadiene.

Method

Polymkeric substance described herein can be by the method production that may further comprise the steps:

1) be chosen in can produce under the selected reaction conditions Mw be 100000 or lower and melting heat be first kind of catalyst component of 10J/g or lower polymkeric substance;

2) be chosen in can produce under the selected reaction conditions Mw be 100000 or lower and degree of crystallinity be 20% or second kind of catalyst component of higher polymkeric substance; With

3) described catalyst component is contacted in reaction zone with one or more alkene.

1) select to produce Mw be 100000 or lower and melting heat be first kind of catalyst component of 10J/g or lower polymkeric substance;

2) select to produce Mw be 100000 or lower and degree of crystallinity be 20% or second kind of catalyst component of higher polymkeric substance; With

3) described catalyst component is contacted in reaction zone with one or more diene with one or more alkene.

1) select to produce Mw be 100000 or lower and melting heat be 10J/g or lower first kind of catalyst component of macromonomer polymeric polymkeric substance, that can make responding property end;

2) select to produce responding property end, Mw be 100000 or lower and degree of crystallinity be 20% or second kind of catalyst component of higher macromonomer; With

3) described catalyst component is contacted in reaction zone with nonessential diolefine with one or more alkene.

1) select to produce Mw be 50000 or lower and melting heat be 10J/g or lower first kind of catalyst component of macromonomer polymeric polymkeric substance, that can make responding property end;

2) select to produce responding property end, Mw be 30000 or lower and degree of crystallinity be 20% or second kind of catalyst component of higher macromonomer; With

3) described catalyst component is contacted in reaction zone with nonessential other alkene with propylene.

Polymkeric substance described herein can be by the continuation method production that may further comprise the steps:

1) be chosen in can produce under the selected polymerizing condition Mw be 100000 lower, preferred 80000 or lower, preferred 60000 or lower and degree of crystallinity be 5% lower, preferred 3% or lower, more preferably 2% or first kind of catalyst component of lower polymkeric substance;

2) be chosen in can produce under the selected polymerizing condition Mw be 100000 lower, preferred 80000 or lower, preferred 60000 or lower and degree of crystallinity be 30% higher, preferred 50% or higher, more preferably 60% or second kind of catalyst component of higher polymkeric substance; With

3) under selected polymerizing condition, make described catalyst component in the presence of one or more activator with one or more C _3-40Alkene, preferred one or more C _3-12Alkene, preferred C ₃Alkene and one or more C _4-20Comonomer and nonessential one or more diolefine, preferred C _4-20The diene contact;

4) be higher than 100 ℃, preferably be higher than 105 ℃, more preferably be higher than 110 ℃, more preferably be higher than under 115 ℃ the temperature;

5) residence time be 120 minutes or shorter, preferred 50 minutes or shorter, preferred 40 minutes, preferred 30 minutes or shorter, preferred 25 minutes or shorter, more preferably 20 minutes or shorter, more preferably 15 minutes or shorter, more preferably 10 minutes or shorter, more preferably 5 minutes or shorter or between 120 minutes and 60 minutes;

6) wherein the ratio of first kind of catalyzer and second kind of catalyzer is 1: 1 to 50: 1, preferred 1: 1 to 40: 1, more preferably 1: 1 to 1: 30;

7) wherein the activity of catalyst component is 3kg, preferred 50kg at least, more preferably 100kg, more preferably 200kg, more preferably 300kg, more preferably 400kg, the more preferably polymkeric substance of 500kg/g catalyst mixture at least at least at least; Change into polymkeric substance with at least 80%, preferably at least 85%, more preferably at least 90%, more preferably at least 95% of wherein said alkene.

In another embodiment, at least 20% or more conversion of olefines become polymkeric substance, preferred 20% or more, more preferably 60% or more, more preferably 75% or more, more preferably 85% or more, more preferably 95% or more.

In one preferred embodiment, aforesaid method carries out with solution phase, slurry or body phase polymerisation process.

Mean the system of not operation interruptedly (or planning interruptedly not operate) continuously.For example, the continuous processing of production polymkeric substance is to add in one or more reactor continuously reactant and the process of taking out polymeric articles continuously.

In another preferred embodiment, in the aforesaid method concentration of reaction zone internal reaction thing in the described residence time, change 20% or still less, preferred 15% or still less, more preferably 10% or still less.In one preferred embodiment, monomer concentration remained unchanged in the described residence time in the reaction zone.Preferred monomers concentration change 20% or still less, preferred 15% or still less, more preferably 10% or still less, more preferably 5% or still less.

In one preferred embodiment, remain unchanged in internal reaction district inner catalyst component concentrations of the described residence time.Preferred monomers concentration change 20% or still less, preferred 15% or still less, more preferably 10% or still less, more preferably 5% or still less.

In one preferred embodiment, the concentration of activator remains unchanged in described residence time internal reaction district.Preferred monomers concentration change 20% or still less, preferred 15% or still less, more preferably 10% or still less, more preferably 5% or still less.

In another preferred embodiment, there is the third catalyzer (or more kinds of) in the aforesaid method.Described the third catalyzer can be the listed any catalyst component of this paper.Preferred the third catalyzer comprises the catalyzer that can produce wax.Other preferred the third catalyzer can comprise any catalyzer described herein.Can select two or multiple catalyzer produce the macromonomer of different responding property ends, use with making this macromonomer polymeric catalyst combination.Can select two or multiplely can make macromonomer polymeric catalyzer and a kind of catalyzer that can produce the macromonomer of responding property end.Equally also can be chosen in three kinds of catalyzer that produce different polymkeric substance under the same reaction conditions.For example, can select to produce the catalyzer of catalyzer, the catalyzer that produces high crystalline state polymer and the generation amorphous polymer of the polymkeric substance of crystalline state a little, its arbitrary polymer polymerizing that produces the macromonomer of responding property end or make responding property end.Similarly, can select two kinds of catalyzer, a kind of generation crystalline state polymer and the another kind of amorphous polymer that produces, its arbitrary polymer polymerizing that produces the macromonomer of responding property end or make responding property end.Can select a kind of generation catalyzer of catalyzer, the catalyzer that produces wax and the generation amorphous polymer of the polymkeric substance of crystalline state a little equally, its arbitrary polymer polymerizing that produces the macromonomer of responding property end or make responding property end.

Reaction zone means the zone that described activatory catalyzer and monomer can react.

The macromonomer of responding property end meant 12 or more carbon atoms (preferred 20 or more, more preferably 30 or more, more preferably between 12 and 8000 carbon atoms) and vinyl, 1 is arranged, 1-vinylidene, vinylene or other can be grouped to the polymkeric substance of the end group of growing polymer chain.Can make the macromonomer polymerization of responding property end mean the catalyst component that the macromonomer (meaning than typical monomers such as ethene or the big molecule of propylene) that can make responding property end is introduced the growing polymer chain.The chain of ethenyl blocking is generally than vinylene or 1, and the end capped chain reaction of 1-vinylidene is active high.

In one particular, the present invention relates to a kind of polyolefin polymer, is by one or more C ₃Or more high alpha-olefin and/or one or more di-vinyl monomers and nonessential maximum 5mol% ethene copolymerization is produced in same polymerisation medium in the presence of at least a stereospecific catalyst system and at least a other catalyst system.Preferably carry out polymerization simultaneously at two kinds of catalyzer.So the polymkeric substance of producing can comprise amorphous polymer segment and crystalline state polymer segment, and wherein at least some segments link to each other.Described non-crystalline state and crystalline state polymer segment normally one or more alpha-olefin (comprising maximum 5mol% ethene alternatively) and/or one or more have the monomeric multipolymer of at least two ethylenic unsaturated bonds.Thereby these two unsaturated link(age)s be fit to and also be easy to by independently with first or second kind of catalyst system polycoordination introduce the growing polymer chain described diolefine introduced in the polymer segment by two kinds of catalyzer generations in the hybrid catalyst system of the present invention.In one preferred embodiment, these monomers that at least two ethylenic unsaturated bonds are arranged are diolefine, preferred di-vinyl monomers.Thereby the crosslinked of at least a portion of believing described polymer segment mixture is to make two kinds of polymer segments of part introducing of divinyl comonomer produce crosslinked realization in the composition polymerization process between these segments.

In another embodiment, can in single reaction vessel, prepare contain non-crystalline state and semi-crystalline state component polyolefine branched block composition to reach desired performance balance.Especially, but spent mixed catalyst and as propylene situ production aPP-g-scPP branched structure in successive soln formula reactor of preferred feedstock.In one embodiment, can select bridged bis-indenyl the 4th stereospecific Catalyst Production semi-crystalline state PP of family macromonomer.(reference of all elements periodictable is Chemical and Engineering News, 63 (5), 27,1985 periodictables of announcing.) available bridging monocyclopentadienyl heteroatoms the 4th family's catalyzer sets up non-crystalline state PP (aPP) main chain, introduces some semi-crystalline state macromonomers (scPP) simultaneously.It is believed that like this to produce the aPP-g-scPP structure that wherein the type of the described polymkeric substance of " g-" expression is partially grafted at least.By selecting catalyst, polymeric reaction condition and/or adding diolefine properties-correcting agent, can make non-crystalline state and crystalline component be connected some and produce various branched block structures.For introducing effectively in the growing chain, preferably have the macromonomer of vinyl ends.Also can use the end of the chain of other type unsaturated (vinylene and 1,1-vinylidene).Do not wish bound by theory, believe that the branched block multipolymer includes the non-crystalline state main chain of the crystalline state side chain that comes from the scPP macromonomer, believe that described side chain is a polypropylene macromers, can be with the Preparation of Catalyst that is fit to preparation isotaxy or syndiotactic polypropylene under solution polymerization condition.

The preferred reaction method of the polypropylene macromers that the unsaturated content of manufacturing side vinyl is high is described in US6, in 117,962.Catalyzer commonly used is solid rigid, chirality or asymmetrical, bridge metallocenes.Referring to for example US 4,892,851, US 5,017,714, US 5,132, and 281, US 5,296,434, US 5,278, and 264, US 5,304,614, US 5,510, and 502, WO-A-(PCT/US92/10066) WO-A-93/19103, EP-A2-0 577 581, EP-A1-0 578838, and academic documents " The Influence of Aromatic Substituents on the Polymerization Behavior of Bridged Zirconocene Catalysts ", Spaleck, W., et al, Organometallics 1994,13,954-963, " ansa-Zirconocene Polymerization Catalysts with Annelated Ring Ligands-Effects on Catalytic Activity and Polymer Chain Lengths ", Brinzinger, H., et al, Organometallics 1994,13,964-970, and the document of wherein quoting.

In some embodiment, first catalyzer that comprises solid rigid transition-metal catalyst precursor compound that is used for production semi-crystalline state polypropylene macromers of the present invention is selected from two (indenyl) zirconocenes of racemic bridging or hafnocene.In another embodiment, described transition-metal catalyst precursor compound is two (indenyl) zirconocenes or the hafnocene of racemize-dimetylsilyl bridging.In another embodiment, described transition-metal catalyst precursor compound is that racemize-dichloro or dimethylformamide dimethyl base silyl-two (2-methyl-4-phenyl indenyl) close zirconium or hafnium.In another preferred embodiment, described transition-metal catalyst is that two (indenyl) hafnocenes of racemize-dimetylsilyl bridging such as racemize-dimethyl or dichloro-dimethyl silyl two (indenyl) close hafnium.

The macromonomer that it is believed that the mark of branched block and operability that the degree of branching depends on the macromonomer that the unsaturated chain end is arranged and special catalyst is introduced ability.For improving the mode that the aPP-g-scPP branched block is formed, under the processing condition that are beneficial to the macromonomer generation and insert, operate usually.This condition is described in US6, and 117,962 and W.Weng et al., Macromol.Rapid Commun., 2000,21, among the 1103-1107, and wherein further specify by embodiment.

The scPP macromonomer number of also believing ethenyl blocking is high more, and its probability of introducing the aPP main chain is high more, thereby the branched block number is high more.

For further improving the number of the macromonomer that the vinyl chain end is arranged, can in reaction medium, add diolefinic monomer.The blend of the branched block kind that number increases due to the additional coupling that products therefrom is normally caused by isotactic polyprophlene segment, Atactic Polypropelene segment and etidine hydrocarbon linking agent.

In crosslinked two different polymer segments of each two keys introducing that mean usually by diolefinic monomer two polymer segments are linked to each other.So the polymer segment that connects can be identical or different aspect its degree of crystallinity.Also can by two or more diolefine in the polymer segment introduce two other polymer segments make three or more the heteropolymer segment link to each other.

What selection monomer or combination of monomers will be considered is can form crystalline state and amorphous polymer segment under the situation of selection two or multiple different catalysts system.In some embodiment, also require diolefinic monomer (if present) to introduce crystalline state segmental introducing amount and be limited to the amount that does not significantly change its degree of crystallinity.Usually make the amount of diolefine coupling agent minimum to avoid forming gel.

As mentioned above, for improving the number that the aPP-g-scPP branched block is formed, under the processing condition that are beneficial to the macromonomer generation and insert, operate usually.Advantageous conditions comprises:

1. produce the high concentration catalyst of the macromonomer of semi-crystalline state ethenyl blocking; And/or

2. regulate the ratio of Al/ metal; And/or

3. High Operating Temperature; And/or

4. the high catalyst structure of introducing for macromonomer of avidity; And/or

5. the long residence time; And/or

6. the high monomer transformation efficiency insertion of macromonomer (monomer deficiency (monomer starvation) condition strengthen); And/or

7. add the number that properties-correcting agent (diene) improves the macromonomer of ethenyl blocking.

Increase other method that the aPP-g-scPP branched block forms and be and add chain-transfer agent and make vinyl be transferred to the polymer chain end to make described catalyst deactivation simultaneously.This chain-transfer agent includes but not limited to vinylchlorid, vinyl fluoride, bromine ethene.In this method, make reactivation of catalyst by having alkyl aluminum activator such as aikyiaiurnirsoxan beta (being generally methylaluminoxane).

Similarly, can pass through selecting catalyst, interpolation comonomer and change processing condition such as temperature and catalyst ratio (if use) control molecular weight distribution, fusion and crystallization property more than a kind of catalyzer.

Catalyst compound

Implement can to use among the present invention can produce the type of polymer of wanting (be Mw be 100000 or lower and melting heat as 70J/g or lower polymkeric substance or Mw be 100000 lower and degree of crystallinity be 40% or lower polymkeric substance) any catalyst compound.In the description of this paper, transistion metal compound can be described as catalyst precursor, catalyst precursor compound or catalyst compound, and these terms are used interchangeably.Catalyst system is the combination of catalyst precursor and activator.

Catalyst compound and selection

Any catalyst precursor compound that can produce the type of polymer of wanting all can be used for implementing the present invention.Spendable catalyst precursor compound comprises the early transition metal compound (include amino and/or phenol root type part those) of metallocene transition metal compound (comprising one, two or three cyclopentadienyl ligands/atoms metal), non-metallocene, the rear transition metal compound of non-metallocene (include diimine or diimine pyridyl ligands those) and other transistion metal compound in the inventive method.

Usually, be applicable to that bulky ligand metallocene compound of the present invention (catalyst precursor) includes the full sandwich compound of half-sum with one or more bulky ligand of at least one atoms metal bonding.Typical bulky ligand metallocene compound is commonly referred to as one or more bulky ligand and one or more leavings group that comprises with at least one atoms metal bonding.Described bulky ligand generally is combined as representative with one or more open loop, acyclic or condensed ring or member ring systems or its.Preferred described ring of these bulky ligand or member ring systems are made up of the atom that is selected from the periodic table of elements the 13rd to 16 family's atom usually, and described atom is preferably selected from carbon, nitrogen, oxygen, silicon, sulphur, phosphorus, germanium, boron and aluminium or its combination.More preferably described ring or member ring systems are made up of carbon atom, the allyl group part that acts on similar ligand structure such as pentadienyl, cyclooctatetraene two bases, cyclobutadiene base or replace such as but not limited to those cyclopentadienyl ligands or cyclopentadienyl-type ligands structure or other.Can comprise the phenol root that amino (amide), phosphine root (phosphide), imines, phosphinimine, amidine root (amidinate) and ortho position replace with other part that cyclopentadienyl-type ligands works similarly.Described atoms metal is preferably selected from the periodic table of elements the 3rd to 15 family and/or lanthanum or actinium series.Preferred described metal is the transition metal of the 3rd to 12 family, more preferably the 4th, 5 and 6 group 4 transition metals, and most preferably described transition metal is the 4th family.

In one embodiment, be applicable to that catalyst composition of the present invention comprises bulky ligand metallocene catalyst compound shown in one or more following formula:

^AL ^BMQ ^* _n (1)

Wherein M is the atoms metal in the periodic table of elements, can be the periodic table of elements the 3rd to 12 family's metal or group of the lanthanides or actinide metals, and preferred M is the 4th, 5 or 6 group 4 transition metals, and more preferably M is the 4th group 4 transition metal, even more preferably M is zirconium, hafnium or titanium.Described bulky ligand L ^AAnd L ^BBe open loop, acyclic or condensed ring or member ring systems and be any assistant ligand system, comprise that the cyclopentadienyl ligands that do not replace or replace or cyclopentadienyl-type ligands, heteroatoms replace and/or contain heteroatomic cyclopentadienyl-type ligands.The limiting examples of bulky ligand comprises cyclopentadienyl ligands, cyclopenta phenanthryl part, indenyl ligands, the benzindene ylidene ligands, fluorenyl ligand, dibenzo [b, h] fluorenyl ligand, benzo [b] fluorenyl ligand, cyclooctatetraene two ylidene ligands, cyclopenta cyclododecene part, the nitrence ylidene ligands, the azulene part, the pentalene part, phosphinylidyne (phosphoyl) part, phosphinimine (WO99/40125), the pyrryl part, pyrazolyl (pyrozolyl) part, the carbazyl part, with the assorted benzene part of boron etc., comprise its hydrogenated form, for example the tetrahydro indenyl part.In one embodiment, L ^AAnd L ^BCan be can with any other ligand structure of M π-bonding.In another embodiment, L ^AOr L ^BAtom and molecule amount (MW) surpass 60a.m.u., be preferably greater than 65a.m.u..In another embodiment, L ^AAnd L ^BCan comprise one or more heteroatoms, for example nitrogen, silicon, boron, germanium, sulphur and phosphorus are combined to form open loop, acyclic or preferred condensed ring or member ring systems, for example assorted-cyclopentadienyl assistant ligand with carbon atom.Other L ^AAnd L ^BBulky ligand includes but not limited to huge amino, phosphine root, pure root, aryl oxide root (aryloxide), imines root, carboline root (carbolides), borollides, porphyrin, phthalocyanine, corrin and the big ring of other polyazo.Independently, each L ^AAnd L ^BCan be identical or different type and the bulky ligand M bonding.In one embodiment of formula 1, only there is L ^AOr L ^BOne of.

Independently, each L ^AAnd L ^BCan be not replace or be substituted basic R ^*Combination replace.Substituent R ^*Limiting examples comprise the alkyl that is selected from hydrogen or straight or branched, alkenyl, alkynyl, cycloalkyl, aryl, acyl group, aroyl, alkoxyl group, aryloxy, alkylthio, dialkylamino, carbalkoxy, aryloxy carbonyl, carbomoyl, alkyl-or one or more substituting group of dialkyl amido formyl radical, acyloxy, amido, aromatic acylamino or its combination.In one preferred embodiment, substituent R ^*Maximum 50 non-hydrogen atoms, preferred 1 to 30 carbon atom are arranged, also can be by replacements such as halogen or heteroatomss.Alkyl substituent R ^*Limiting examples comprise methyl, ethyl, propyl group, butyl, amyl group, hexyl, cyclopentyl, cyclohexyl, benzyl or phenyl etc., comprise its all isomer, for example the tertiary butyl and sec.-propyl etc.Other alkyl comprises the organic quasi-metal base that methyl fluoride, fluoro ethyl, two fluoro ethyls, iodine propyl group, bromine hexyl, benzyl chloride base and alkyl replace, and comprises trimethyl silyl, trimethylammonium germyl and methyl diethylsilane base etc.; Organic quasi-metal base with brine alkyl replaces comprises three (trifluoromethyl) silyl, methyl-two (difluoromethyl) silyl and brooethyl dimethyl germyl etc.; With dibasic boryl, comprise for example dimethyl boron; Comprise dimethyl amine, dimethyl phosphine, diphenylamine, aminomethyl phenyl phosphine with dibasic phosphorus family element group, the sulfur family element group comprises methoxyl group, oxyethyl group, propoxy-, phenoxy group, methylthio group and ethylmercapto group.Non-hydrogen substituent R ^*Comprise atoms such as carbon, silicon, boron, aluminium, nitrogen, phosphorus, oxygen, tin, sulphur and germanium, comprise that alkene comprises the part of ethenyl blocking such as but not limited to the unsaturated substituting group of olefinic, for example fourth-3-thiazolinyl, third-2-thiazolinyl and oneself-5-thiazolinyl etc.And, at least two R ^*Preferred two the adjacent R bases of base are connected to form 3 to 30 ring structures that are selected from the atom of carbon, nitrogen, oxygen, phosphorus, silicon, germanium, aluminium, boron or its combination.Substituent R ^*Can also be an end and L bonding and form the double-basis of carbon σ-key with metal M.Other part can with metal M bonding, for example at least one leavings group Q ^*In one embodiment, Q ^*It is the variable part of single anion that forms σ-key with M.The oxidation state that depends on metal, the value of n are 0,1 or 2 to make following formula 1 represent neutral bulky ligand metallocene catalyst compound.Q ^*The limiting examples of part comprises weak base such as amine, phosphine, ether, carboxylicesters/salt, diene, the alkyl that 1 to 20 carbon atom is arranged, hydrogen root or halogen etc. or its combination.In another embodiment, two or more Q ^*Constitute the part of condensed ring or member ring systems.Q ^*Other example of part comprises that the front is at R ^*Described those substituting groups comprise cyclobutyl, cyclohexyl, heptyl, tolyl, trifluoromethyl, tetramethylene (two Q ^*), pentamethylene (two Q ^*), methene base (methylidene) (two Q ^*), methoxyl group, oxyethyl group, propoxy-, phenoxy group, two (N-methyl anilide roots), dimethylamine root and dimethylphosphine foundation group etc.

In another embodiment, be applicable to that catalyst composition of the present invention can comprise one or more bulky ligand metallocene catalyst compound, the L of its Chinese style 1 ^AAnd L ^BBy at least one bridging group A ^*Bridging mutually, as shown in Equation 2:

L ^AA ^*L ^BMQ ^* _n (2)

Formula 2 compounds are called the bulky ligand metallocene catalyst compound of bridging.L ^A, L ^B, M, Q ^*With n as mentioned above.Bridging group A ^*Limiting examples comprise the bridging group that contains at least one the 13rd to 16 family's atom, be commonly referred to the divalence structure division, one of at least or its combination such as but not limited to carbon, oxygen, nitrogen, silicon, aluminium, boron, germanium and tin atom.Preferred bridging group A ^*Contain carbon, silicon or germanium atom, most preferably A ^*Contain at least one Siliciumatom or at least one carbon atom.Bridging group A ^*Can also contain substituent R as defined above ^*, comprise halogen and iron.Bridging group A ^*Limiting examples can be expressed as R ' ₂C, R ' ₂CCR ' ₂, R ' ₂Si, R ' ₂SiCR ' ₂, R ' ₂SiSiR ' ₂, R ' ₂Ge, R ' P, R ' N, R ' B, wherein R ' is the sulfur family element or the halogen of alkyl, the brine alkyl of hydrogen root, alkyl, replacement, the brine alkyl of replacement, the organic quasi-metal that alkyl replaces, the organic quasi-metal that brine alkyl replaces, dibasic boron, dibasic phosphorus family element, replacement independently, and perhaps two or more R ' can be connected to form ring or member ring systems.In one embodiment, the bridging bulky ligand metallocene catalyst compound of formula 2 has two or more bridging group A ^*(EP664 301B1).In another embodiment, described bulky ligand metallocene catalyst compound is the bulky ligand L of its Chinese style 1 and 2 ^AAnd L ^BOn R ^*Those that substituting group is replaced by the substituting group of the identical or different quantity on each bulky ligand.In another embodiment, formula 1 and 2 bulky ligand L ^AAnd L ^BDiffer from one another.

Be applicable to that other bulky ligand metallocene catalyst compound of the present invention and catalyst system can comprise US 5,064,802,5,145,819,5,149,819,5,243,001,5,239,022,5,276,208,5,296,434,5,321,106,5,329,031,5,304,614,5,677,401,5,723,398,5,753,578,5,854,363,5,856,547,5,858,903,5,859,158,5,900,517 and 5,939,503, WO 93/08221, WO 93/08199, WO 95/07140, WO 98/11144, WO 98/41530, WO 98/41529, WO 98/46650, WO 99/02540, WO 99/14221, EP-A-0 578 838, EP-A-0 638 595, EP-B-0 513 380, EP-A1-0 816 372, EP-A2-0 839 834, EP-B1-0 632 819, those that describe among EP-B1-0 748821 and the EP-B1-0 757 996 all are incorporated herein for reference.

In another embodiment, be applicable to that catalyst composition of the present invention can comprise the heteroatoms list bulky ligand metallocene catalyst of bridging.The catalyzer of these types and catalyst system are described in for example WO 92/00333, WO 94/07928, WO 91/04257, WO 94/03506, WO 96/00244, WO 97/15602, WO 99/20637 and US 5,057,475,5,096,867,5,055,438,5,198,401,5,227,440 and 5,264,405 and EP-A-0 420 436 in, all be incorporated herein for reference.

In another embodiment, be applicable to that catalyst composition of the present invention comprises bulky ligand metallocene catalyst compound shown in one or more formula 3:

L ^CA ^*J ^*MQ ^* _n (3)

Wherein M is the periodic table of elements the 3rd to 16 family's atoms metal or is selected from group of the lanthanides and the metal of actinium series, and preferred M is the 3rd to 12 group 4 transition metal, and more preferably M is the 4th, 5 or 6 group 4 transition metals, and most preferably M is the 4th group 4 transition metal, the especially titanium of any oxidation state; L ^CFor with the replacement or the unsubstituted bulky ligand of M bonding; J ^*With the M bonding; A ^*With J ^*And L ^CBonding; J ^*Be the heteroatoms assistant ligand; A ^*Be bridging group; Q ^*Be the univalent anion part; With n be integer 0,1 or 2.In the following formula 3, L ^C, A ^*And J ^*Form the condensed member ring systems.In one embodiment, the L of formula 3 ^CAs the front at L ^ADefine.The A of formula 3 ^*, M and Q ^*Such as in the front formula 1 definition.In the formula 3, J ^*Be to contain heteroatomic part, wherein J ^*Be that the periodic table of elements the 15th family's ligancy is that 3 element or the 16th family's ligancy are 2 element.Preferred J ^*Contain nitrogen, phosphorus, oxygen or sulphur atom, nitrogen.In the one embodiment of this invention, described bulky ligand metallocene catalyst compound is the heterocyclic ligand title complex, and wherein said bulky ligand (ring or member ring systems) comprises one or more heteroatoms or its combination.Heteroatomic limiting examples comprises the 13rd to 16 family's element, preferred nitrogen, boron, sulphur, oxygen, aluminium, silicon, phosphorus and tin.The example of these bulky ligand metallocene catalyst compounds is described in WO 96/33202, WO 96/34021, WO 97/17379, WO 98/22486, EP-A1-0874 005 and US 5,637,660,5,539,124,5,554,775,5,756,611,5,233,049,5,744,417 and 5, in 856,258, all be incorporated herein for reference.

In one embodiment, described bulky ligand metallocene compound (catalyst precursor) is based on those title complexs of the bidentate ligand that contains pyridine or quinoline moiety, as describing among the USSN 09/,103 620 of application on June 23rd, 1998 those are incorporated herein for reference.In another embodiment, described bulky ligand metallocene catalyst compound is those that describe among WO 99/01481 and the WO 98/42664, all is incorporated herein for reference.

In another embodiment, described bulky ligand metallocene catalyst compound is the title complex of metal (preferred transition metal), bulky ligand (preferably replacing or unsubstituted π-ligands bound thereto) and one or more assorted allyl group part, as US 5,527,752 and 5,747,406 and EP-B1-0735057 in describe those, all be incorporated herein for reference.

In another embodiment, described bulky ligand metallocene catalyst compound is those that describe among WO99/01481 and the WO 98/42664, all is incorporated herein for reference.

The 6th family's bulky ligand metallocene catalyst system that is suitable for is described in US 5,942, in 462, is incorporated herein for reference.

Other catalyzer that is suitable for comprises WO 99/20665 and US 6,010, and transition metal metaaracyle structure described in the catalyzer of multinuclear metallocene described in 794, EP 0 969 101 A2 is incorporated herein for reference.Other metallocene catalyst comprises the metallocene catalyst (EP 0 970 074 A1) of those that describe among EP 0 950 667 A1, double cross connection, the metallocene (EP 970 963 A2) and the US 6 of bolt system (tethered); 008; those alkylsulfonyl catalyzer of describing in 394 are incorporated herein for reference.

Consider that also above-mentioned bulky ligand metallocene catalyst comprises its structure or optics or enantiomer (meso and racemic isomer for example referring to US 5,852,143, are incorporated herein for reference) and composition thereof in the embodiment.

That also considers above-mentioned bulky ligand metallocene catalyst compound arbitraryly has at least one fluorine root or a fluorine-containing leavings group, described in the USSN 09/,191 916 of application on November 13rd, 1998.

The used metallic compound that contains the 15th family's element prepares by means known in the art in the catalyst composition of the present invention, reaches and wherein draws those disclosed method in the reference as EP 0 893 454 A1, US 5,889,128, all is incorporated herein for reference.The USSN 09/,312 878 of application on May 17th, 1999 discloses gas phase or the slurry phase polymerisation method of utilizing the two amino catalyzer of loading type, also is incorporated herein for reference.

Out of Memory about the metallic compound that contains the 15th family's element sees also Mitsui Chemicals, and EP 0 893 454 A1 of Inc. wherein disclose the transition metal amide that makes olefinic polymerization with the activator combination.

In one embodiment, be used for making the metallic compound that contains the 15th family's element aging before the polymerization.Have at least and noticed once once that such catalyst compound (aging at least 48 hours) was better than the catalyst compound performance that newly makes.

Also consider to use two amino based catalyst precursors.Exemplary compounds comprises WO96/23010, WO 97/48735 and Gibson, et al., those that describe among the Chem.Comm., pp.849-850 (1998), wherein disclose the di-imidogen part that is used for the 8-10 compounds of group, made olefinic polymerization through ion activation.US 5,502,124 and division US 5,504,049 in the polymerisation catalyst system of 5-10 family metal has been described, wherein the active centre is that polyanionic ligand system highly oxidized and by low ligancy keeps stable.Also referring to US5,851,945 the 5th family's organo-metallic catalyst compound and the 5-10 family organo-metallic catalyst that contains tridentate ligand of US 6,294,495.Available ionization promotor activatory the 11st family's catalyst precursor compound that is applicable to alkene and vinyl-based polar molecule has been described among the WO 99/30822.

Other catalyst compound that is suitable for is EP-A2-0 816 384 and US 5,851, and the imino-title complex of the 5th and 6 family's metals is incorporated herein for reference described in 945.In addition, metallocene catalyst also comprises D.H.McConville etc. at Organometallics 1995,14, and the bridging of describing among the 5478-5480 two (virtue is amino) the 4th compounds of group is incorporated herein for reference.In addition, also described two (amino) catalyst compound of bridging among the WO 96/27439, be incorporated herein for reference.Other catalyzer that is suitable for is at US 5,852, is called two (hydroxyaromatic nitrogen ligand) in 146, is incorporated herein for reference.Other catalyzer that contains one or more the 15th family atom that is suitable for comprises those that describe among the WO 98/46651, is incorporated herein for reference.

US 5,318, and 935 have described bridging and non-bridged two amino catalyst compound of the group-4 metal that can be used for olefinic polymerization.D.H.McConville etc. have described the bridging that is used for olefinic polymerization two (virtue is amino) the 4th compounds of group at Organometallics 1995,14 among the 5478-5480.This reference has introduced synthetic method and compound characterizes.D.H.McConville, et al, Macromolecules 1996,29, and the further work of 5241-5243 has been described two (virtue is amino) the 4th compounds of group of bridging, is the polymerizing catalyst that is used for the 1-hexene.Other is applicable to that transistion metal compound of the present invention comprises those that describe among the WO 96/40805.Cationic group-3 or lanthanide series metal olefinic polymerization title complex are disclosed among the common co-pending application USSN 09/408050 of application on September 29th, 1999.Single anion bidentate ligand and two kinds of single anion ligands make those catalyst precursors stable, this available ion promotor activation of the present invention.

Many catalyst precursor compounds that other is suitable for have been described in the document.Comprise to capture part or can be comprised the compound that to capture part and be applicable to the present invention by alkylation.Referring to for example V.C.Gibson, et al; " The Search for New-Generation Olefin Polymerization Catalysts:Life Beyond Metallocenes ", Angew.Chem.Int.Ed., 38,428-447 (1999).

The present invention is also available to be comprised among the catalyzer of phenol root part such as EP 0 874 005 A1 disclosed those catalyzer and implements, and is incorporated herein for reference.

In another embodiment, the transition-metal catalyst of available general type is implemented the present invention.The transition-metal catalyst of general type is those traditional Z-Ns well known in the art, vanadium and Philips's type catalyzer.For example Ziegler-Natta Catalysts and Polymerizations, John Boor, Academic Press, New York, Ziegler-Natta catalyst described in 1979.US 4,115, also described the example of the transition-metal catalyst of general type in 639,4,077,904,4,482,687,4,564,605,4,721,763,4,879,359 and 4,960,741, all are incorporated herein for reference.The transition metal catalyst compound that can be used for general type of the present invention comprises the periodic table of elements the 3rd to 17 family, preferred the 4th to 12 family, more preferably the 4th to 6 group transition metal compound.

The transition-metal catalyst of preferred general type can be represented by the formula: MR _x, wherein M is the 3rd to 17 family, preferred the 4th to 6 family, more preferably group-4 metal, titanium most preferably; R is halogen or-oxyl; With x be the oxidation state of metal M.The limiting examples of R comprises alkoxyl group, phenoxy group, bromide anion, chlorion and fluorion.Wherein M is that the limiting examples of transition-metal catalyst of the general type of titanium comprises TiCl ₄, TiBr ₄, Ti (OC ₂H ₅) ₃Cl, Ti (OC ₂H ₅) Cl ₃, Ti (OC ₄H ₉) ₃Cl, Ti (OC ₃H ₇) ₂Cl ₂, Ti (OC ₂H ₅) ₂Br ₂, TiCl ₃1/3AlCl ₃And Ti (OC ₁₂H ₂₅) Cl ₃

The transition metal catalyst compound that is applicable to the general type based on magnesium/titanium electron donor(ED) title complex of the present invention for example is described among the US 4,302,565 and 4,302,566, is incorporated herein for reference.MgTiCl ₆(ethyl acetate) ₄Derivative is particularly preferred.

UK Patent Application 2,105,355 and US 5,317,036 (being incorporated herein for reference) the vanadium catalyst compound of various general types has been described.The limiting examples of the vanadium catalyst compound of general type comprises three halogenation vanadyl, halogenated alkoxy vanadyl and alkoxyl group vanadyl such as VOCl ₃, VOCl ₂(OBu) (wherein Bu=butyl) and VO (OC ₂H ₅) ₃Four halogenation vanadium and halogenated alkoxy vanadium such as VCl ₄And VCl ₃(OBu); Methyl ethyl diketone and chloracetyl acetonization vanadium and vanadyl such as V (AcAc) ₃And VOCl ₂(AcAc) (wherein (AcAc) is the methyl ethyl diketone root).The vanadium catalyst compound of preferred general type is VOCl ₃, VCl ₄And VOCl ₂-OR, wherein R is alkyl, preferred C _1-10Aliphatic series or aromatic hydrocarbyl such as ethyl, phenyl, sec.-propyl, butyl, propyl group, normal-butyl, isobutyl-, the tertiary butyl, hexyl, cyclohexyl, naphthyl etc. and acetylacetonate vanadium.

The chrome catalysts compound (being commonly referred to Philips's type catalyzer) that is applicable to general type of the present invention comprises CrO ₃, two luxuriant chromium, chromic acid silyl ester, chromyl chloride (CrO ₂Cl ₂), 2 ethyl hexanoic acid chromium and acetylacetonate chromium (Cr (AcAc) ₃) etc.Limiting examples is disclosed in US3, in 709,853,3,709,954,3,231,550,3,242,099 and 4,077,904, all is incorporated herein for reference.

The transition metal catalyst compound and the catalyst system that are applicable to other general type of the present invention are disclosed in US 4,124,532,4,302,565,4,302,566,4,376,062,4,379,758,5,066,737,5,763,723,5,849,655,5,852,144,5,854,164 and 5,869,585 and EP-A2 0 416 815 A2 and EP-A1 0 420 436 in, all be incorporated herein for reference.

Other catalyzer can comprise cationic catalyst such as AlCl ₃, and other cobalt well known in the art, iron, nickel and palladium catalyst.Referring to for example US 3,487,112,4,472,559,4,182,814 and 4,689,437, all be incorporated herein for reference.

Think that also other catalyzer can make up with the catalyst compound that is used for catalyst composition of the present invention.For example referring to US 4,937,299,4,935,474,5,281,679,5,359,015,5,470,811 and 5,719,241, all be incorporated herein for reference.

Think that one or more or catalyst system of above-mentioned catalyst compound can be used in combination with one or more conventional catalyst compound or catalyst system.The limiting examples of mixed catalyst and catalyst system is described in US 4,159, and 965,4,325,837,4,701,432,5,124,418,5,077,255,5,183,867,5,391,660,5,395,810,5,691,264,5,723,399 and 5,767, among on August 1st, the 031 and 1996 disclosed WO 96/23010, all be incorporated herein for reference.

More specifically, being preferred for metallocene catalyst of the present invention can be with one of following general formula (all families of mentioning all are Chemical and Engineering News, 63 (5), the new meter family method of 27, the 1985 described periodic table of elements) expression:

[{[(A-Cp)MX ₁] ⁺} _d]{[B′] ^d-} (4)

[{[(A-Cp)MX ₁L] ⁺} _d]{[B′] ^d-} (5)

Wherein:

(A-Cp) be (Cp), (Cp ^*) or Cp-A '-Cp ^*Cp and Cp ^*" the identical or different cyclopentadienyl rings that replaces; each substituting group S " base be the sulfur family element or the halogen group of alkyl, the brine alkyl of alkyl, replacement, the brine alkyl of replacement, the organic quasi-metal of alkyl replacement, the organic quasi-metal of brine alkyl replacement, dibasic boron, dibasic phosphorus family element, replacement, perhaps Cp and Cp independently by 0 to 5 substituting group S ^*Be cyclopentadienyl rings, wherein any two adjacent S " are connected to form C _4-20Ring obtains saturated or undersaturated many ring cyclopentadienyl ligands; Cp and Cp ^*Also can have by carbon atom in the 15th or 16 family's elements especially S, O, N or P metathetical one or two rings;

A ' is a bridging group;

(C ₅H _5-y-xS " _x) " the cyclopentadienyl rings that replaces by 0 to 5 above-mentioned group S;

X is 0 to 5, represents substitution value;

M is titanium, zirconium or hafnium;

X ₁Be the alkyl of hydrogen foundation, alkyl, replacement, the organic quasi-metal base of alkyl replacement or the organic quasi-metal base that brine alkyl replaces, this group can be randomly with M and L or L ' both or one of covalent bonding or with M, S " or arbitrary or whole covalent bonding of S ', condition is X ₁Not to replace or unsubstituted cyclopentadienyl rings;

(JS ' _Z-1-y) be heteroatom ligand, wherein J is that the periodic table of elements the 15th family's ligancy is that 3 element or the 16th family's ligancy are 2 element; S ' is alkyl, brine alkyl, the brine alkyl of replacement, the organic quasi-metal of alkyl replacement or the organic quasi-metal group that brine alkyl replaces of alkyl, replacement; With z be the ligancy of element J;

Y is 0 or 1;

L is alkene, diolefine or aryne part.L ' is identical with L, can also be amine, phosphine, ether or thioether part or any other neutral Lewis base; L ' can also be second transistion metal compound so that two the metal center M and the M of same type ^*Pass through X ₁And X ' ₁Bridging, wherein M ^*Identical with the implication of M, X ' ₁, X ₂And X ' ₂With X ₁Implication identical, wherein represent with following formula as the dimeric compounds of the precursor of described catalyzer cationic moiety:

Wherein:

W is 0 to 3 integer;

B ' is the precursors reaction gained negatively charged ion Lewis acid activation agent of the cationic moiety of catalyst system described in about 4 dusts or bigger non-nucleophilicity anionic complex or Lewis acid activation agent and the formula 1-4 for chemically stable, molecular diameter.When B ' is the Lewis acid activation agent, X ₁Also can be the alkyl that described Lewis acid activation agent provides; With

D is the integer of the electric charge of representative B '.

Described catalyzer preferably passes through at least two components in conjunction with preparation.In one preferred method, first component be contain at least one will with the cyclopentadienyl derivative of the group 4 metal compounds of second component or its at least a portion such as its cationic moiety bonded part.Second component be comprise with described group 4 metal compounds (first component) in contained at least one part and the cationic ion-exchange compound of non-coordination anion generation irreversible reaction, it be comprise the charged in form metal in a plurality of and center or the coordination of metalloid atom covalence and shield this atom lipophilic group single coordination compound or comprise negatively charged ion such as multiaspect borine, carborane and the metal card borine of a plurality of boron atoms.

Usually, the negatively charged ion that is suitable for second component can be any stable and huge anionic complex that following characterization of molecules is arranged: 1) described negatively charged ion should have the molecular diameter greater than 4 dusts; 2) described negatively charged ion should form stable ammonium salt; 3) negative charge on the described negatively charged ion not delocalization on anionic skeleton structure or be positioned at anionic in-core; 4) described negatively charged ion should be relatively poor relatively nucleophile; With 5) described negatively charged ion should not be strong reduction or oxygenant.The negatively charged ion that satisfies these standards has been described fully, as multinuclear borine, carborane, metal card borine, polyoxy negatively charged ion and anion binding compound in the chemical literature.

The cationic moiety of described second component can comprise Bronsted acid such as proton or protonated Lewis base, perhaps can comprise Lewis acid such as ferrocene

Triphenylcarbenium

Or silver-colored positively charged ion.

In another preferred method, described second component is a Lewis acid complex, at least one part reaction of it and first component, thereby ionic species described in the production 4-6, the part of from first component, capturing now with the second component bonding.Aikyiaiurnirsoxan beta especially methylaluminoxane (product that trimethyl aluminium generates with stoichiometric water reaction in aliphatic series or aromatic hydrocarbon) is particularly preferred Lewis acid second component.Modified alumoxane also is preferred.Aikyiaiurnirsoxan beta is known in this field, and its preparation method is described in US 4,542, in 199,4,544,762,5,015,749 and 5,041,585.US 5,041, and 584, disclose the technology of preparation modified alumoxane among EPA 0 516 476 and the EPA 0 561 476, be incorporated herein for reference.

First and second components in conjunction with the time, the reaction of one of part of second component and first component, thereby produce the ion pair of forming by group-4 metal positively charged ion and above-mentioned negatively charged ion, this negatively charged ion and the group-4 metal cationic-compatible that forms by first component and be coordinate non-with it.The negatively charged ion of second component must be able to be stablized the group-4 metal positively charged ion and play the ability of catalyst action and must be enough variable so that can be replaced by alkene, diolefine or acetylene series unsaturated monomer in polymerization process.Catalyzer of the present invention can be a loading type.US 4,808,561 (1989-02-28 is open), US4,897,455 (1990-01-03 is open), US 5,057,475 (1991-10-15 is open), USSN459,921 (WO 91/09882), CA 1,268,753, US 5,240,894 and WO 94/03506 this type of loaded catalyst and production method thereof are disclosed, be incorporated herein for reference.

Group 4 metal compounds as first component (catalyst precursor) in the preferred metallocene catalyst of preparation the present invention is that titanium, zirconium and hafnium metallocene compound are the cyclopentadienyl derivatives of titanium, zirconium and hafnium.Usually, two luxuriant titaniums, zirconocene and the hafnocene of Shi Heing can be represented with following general formula:

(A-Cp)MX ₁X ₂ (8)

(A-Cp)ML (9)

Wherein:

(A-Cp) be (Cp) (Cp ^*) or Cp-A '-Cp ^*Cp and Cp ^*" the identical or different cyclopentadienyl rings that replaces; each substituting group S " be the sulfur family element or the halogen group of alkyl, the brine alkyl of alkyl, replacement, the brine alkyl of replacement, the organic quasi-metal that alkyl replaces, the organic quasi-metal of brine alkyl replacement, dibasic boron, dibasic phosphorus family element, replacement, perhaps Cp and Cp independently by 0 to 5 substituting group S ^*Be cyclopentadienyl rings, " base is connected to form C to wherein any two adjacent S _4-20Ring obtains saturated or undersaturated many ring cyclopentadienyl ligands;

A ' is a bridging group;

Y is 0 or 1;

(C ₅H _5-y-xS " _x) " the cyclopentadienyl rings that replaces by 0 to 5 above-mentioned substituting group S;

X is 0 to 5, represents substitution value;

L is alkene, diolefine or aryne part.L ' is identical with L, can also be amine, phosphine, ether or thioether part or any other neutral Lewis base; L ' can also be second transistion metal compound so that two the metal center M and the M of same type ^*Pass through X ₁And X ' ₁Bridging, wherein M ^*Identical with the implication of M, X ' ₁With X ₁Implication identical, X ' ₂With X ₂Implication identical, wherein represent with following formula 7 as this dimeric compounds of the precursor of described catalyzer cationic moiety;

W is 0 to 3 integer; With

X ₁And X ₂Be brine alkyl, alkyl-and the organic quasi-metal group of brine alkyl-replacement, the phosphorus family element group of replacement or the sulfur family element group that replaces of alkyl, brine alkyl, the replacement of hydrogen foundation, alkyl, replacement independently; Perhaps X ₁And X ₂Link to each other and form and contain about 3 metallic heterocyclic (metallacycle) to about 20 carbon atoms with the atoms metal bonding; Perhaps X ₁And X ₂Can be alkene, diolefine or aryne part together; Perhaps can provide above-mentioned X to transition metal component when using ₁The Lewis acid activation agent of part is for example during methylaluminoxane, X ₁And X ₂Can be halogen, pure root, aryl oxide root, amino, phosphine root or other univalent anion part, perhaps X independently ₁And X ₂Also can be connected to form the negatively charged ion chelating ligand, condition is X ₁And X ₂Not to replace or unsubstituted cyclopentadienyl rings.

Table A illustrates the typical integral part of the metallocenes of formula 7-10.This tabulation only is used to illustrate and should be interpreted as by any way limiting.The mutual all possible permutation and combination of described component part can form a lot of final components.When open alkyl comprised alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl group, cycloalkynyl radical and aromatic group among the application, this term comprised all isomer.For example, butyl comprises normal-butyl, 2-methyl-propyl, 1-methyl-propyl, the tertiary butyl and cyclobutyl; Amyl group comprises n-pentyl, 1-methyl butyl, 2-methyl butyl, 3-methyl butyl, 1-ethyl propyl, neo-pentyl, cyclopentyl and methyl cyclobutyl; Butenyl comprises E and Z type 1-butylene base, crotyl, 3-butenyl, 1-methyl isophthalic acid-propenyl, 1-methyl-2-propenyl, 2-methyl isophthalic acid-propenyl and 2-methyl-2-propenyl.This comprises group and another group bonding situation, and for example the propyl group cyclopentadienyl comprises n-propyl cyclopentadienyl, sec.-propyl cyclopentadienyl and cyclopropyl rings pentadienyl.Usually, listed part or group comprise all isomeric form in the Table A.For example, the dimethyl cyclopentadienyl comprises 1,2-dimethyl cyclopentadienyl and 1,3-dimethyl cyclopentadienyl; The methyl indenyl comprises 1-methyl indenyl, 2-methyl indenyl, 3-methyl indenyl, 4-methyl indenyl, 5-methyl indenyl, 6-methyl indenyl and 7-methyl indenyl; The methylethyl phenyl comprise neighbour-methylethyl phenyl ,-methylethyl phenyl and right-methylethyl phenyl.The example of catalyst precursor of the present invention adopts following formula, and wherein some component is listed in the Table A.For the composition of described transition metal component being described, the arbitrary combination of listed material among the option table A.For ease of name, for bridging group A ', word " silyl " and " silicylene " are used interchangeably, and represent the double-basis material.For bridging group A ', " ethylidene " means the ethylene key and is different from 1, the 1-ethylidene.Therefore, for bridging group A ', " ethylidene " and " ethylene " is used interchangeably.For the compound that bridging group A ' is arranged, the bridging position on the cyclopentadienyl type ring is thought the 1-position all the time.Therefore, for example " 1-fluorenyl " can exchange with " fluorenyl " and use.

Illustrational formula 8 type compounds are that dimethyl two (cyclopentadienyls) closes that hafnium, dihydro (dihidryde) ethylenebis (tetrahydro indenyl) close zirconium, diethyl two (pentamethyl-) closes zirconium and dichloro-dimethyl silyl (1-indenyl) (cyclopentadienyl) closes titanium etc.Illustrational formula 9 type compounds are two (cyclopentadienyls) (1, the 3-divinyl) closes zirconium, two (cyclopentadienyl) (2,3-dimethyl-1,3-butadiene) close zirconium, two (pentamethyl-cyclopentadienyl) (benzene) close zirconium and two (pentamethyl-cyclopentadienyl) ethene closes titanium etc.Illustrational formula 10 type compounds are that dichloro-dimethyl silyl (tetramethyl-ring pentadienyl) (uncle's fourth amino) closes that zirconium, dimethyl ethylidene (methyl cyclopentadienyl) (phenylamino) close titanium, dihydro aminomethyl phenyl silyl (indenyl) (phenyl phosphino-) closes hafnium and dimethoxy (pentamethyl-cyclopentadienyl) (two uncle's fourth amino) closes hafnium.

The condition that title complex comprises neutral Lewis base ligands such as ether or formation dimeric compounds depends on the metal center spatial volume of part on every side.Me for example ₂Si (Me ₄C ₅) (N-t-Bu) ZrCl ₂In the tertiary butyl Me of ratio is arranged ₂Si (Me ₄C ₅) (NPh) ZrCl ₂.Et ₂The space requirement that phenyl among the O is bigger, thereby last compound does not solid-stately allow the ether coordination at it.Similarly, [Me ₂Si (Me ₃SiC ₅H ₃) (N-t-Bu) ZrCl ₂] ₂The spatial volume of middle trimethyl silyl cyclopentadienyl compares Me ₂Si (Me ₄C ₅) (N-t-Bu) ZrCl ₂The spatial volume of middle tetramethyl-ring pentadienyl is little, and last compound is that a compound then of dimerization is not a dimerization.

Table A

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	The dimethylated methylene silylation	Cyclopentadienyl
The diethyl silicylene	Methyl cyclopentadienyl	The dimethylated methylene silylation	Cyclopentadienyl
The diethyl silicylene	Methyl cyclopentadienyl	The dipropyl silicylene	The dimethyl cyclopentadienyl
The dibutyl silicylene	The trimethylammonium cyclopentadienyl	The dipropyl silicylene	The dimethyl cyclopentadienyl
The dibutyl silicylene	The trimethylammonium cyclopentadienyl	The diamyl silicylene	The tetramethyl-ring pentadienyl
The dihexyl silicylene	Pentamethyl-cyclopentadienyl (no A ')	The diamyl silicylene	The tetramethyl-ring pentadienyl
The dihexyl silicylene	Pentamethyl-cyclopentadienyl (no A ')	The diheptyl silicylene	The ethyl cyclopentadienyl
The dioctyl silicylene	The diethyl cyclopentadienyl	The diheptyl silicylene	The ethyl cyclopentadienyl
The dioctyl silicylene	The diethyl cyclopentadienyl	The dinonyl silicylene	The propyl group cyclopentadienyl
The didecyl silicylene	The dipropyl cyclopentadienyl	The dinonyl silicylene	The propyl group cyclopentadienyl
The didecyl silicylene	The dipropyl cyclopentadienyl	Two (undecyl) silicylene	The butyl cyclopentadienyl
Two (dodecyl) silicylene	The dibutyl cyclopentadienyl	Two (undecyl) silicylene	The butyl cyclopentadienyl
Two (dodecyl) silicylene	The dibutyl cyclopentadienyl	Two (tridecyl) silicylene	The amyl group cyclopentadienyl
Two (tetradecyl) silicylene	The diamyl cyclopentadienyl	Two (tridecyl) silicylene	The amyl group cyclopentadienyl
Two (tetradecyl) silicylene	The diamyl cyclopentadienyl	Two (pentadecyl) silicylene	The hexyl cyclopentadienyl
Two (hexadecyl) silicylene	The dihexyl cyclopentadienyl	Two (pentadecyl) silicylene	The hexyl cyclopentadienyl
Two (hexadecyl) silicylene	The dihexyl cyclopentadienyl	Two (heptadecyl) silicylene	The heptyl cyclopentadienyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	Two (octadecyl) silicylene	The diheptyl cyclopentadienyl
Two (nonadecyl) silicylene	The octyl group cyclopentadienyl	Two (octadecyl) silicylene	The diheptyl cyclopentadienyl
Two (nonadecyl) silicylene	The octyl group cyclopentadienyl	Two (eicosyl) silicylene	The dioctyl cyclopentadienyl
Two (heneicosyl) silicylene	The nonyl cyclopentadienyl	Two (eicosyl) silicylene	The dioctyl cyclopentadienyl
Two (heneicosyl) silicylene	The nonyl cyclopentadienyl	Two (docosyl) silicylene	The dinonyl cyclopentadienyl
Two (tricosyl) silicylene	The decyl cyclopentadienyl	Two (docosyl) silicylene	The dinonyl cyclopentadienyl
Two (tricosyl) silicylene	The decyl cyclopentadienyl	Two (tetracosyl) silicylene	The didecyl cyclopentadienyl
Two (pentacosyl) silicylene	The undecyl cyclopentadienyl	Two (tetracosyl) silicylene	The didecyl cyclopentadienyl
Two (pentacosyl) silicylene	The undecyl cyclopentadienyl	Two (ceryl) silicylene	The dodecyl cyclopentadienyl
Two (heptacosyl) silicylene	The tridecyl cyclopentadienyl	Two (ceryl) silicylene	The dodecyl cyclopentadienyl
Two (heptacosyl) silicylene	The tridecyl cyclopentadienyl	Two (octacosyl) silicylene	The tetradecyl cyclopentadienyl
Two (nonacosyl) silicylene	The pentadecyl cyclopentadienyl	Two (octacosyl) silicylene	The tetradecyl cyclopentadienyl
Two (nonacosyl) silicylene	The pentadecyl cyclopentadienyl	Two (triacontyl) silicylene	The hexadecyl cyclopentadienyl
The dicyclohexyl silicylene	The heptadecyl cyclopentadienyl	Two (triacontyl) silicylene	The hexadecyl cyclopentadienyl
The dicyclohexyl silicylene	The heptadecyl cyclopentadienyl	Two cyclopentyl silicylene	The octadecyl cyclopentadienyl
Two suberyl silicylene	The nonadecyl cyclopentadienyl	Two cyclopentyl silicylene	The octadecyl cyclopentadienyl
Two suberyl silicylene	The nonadecyl cyclopentadienyl	Two ring octyl group silicylene	The eicosyl cyclopentadienyl
Two ring decyl silicylene	The heneicosyl cyclopentadienyl	Two ring octyl group silicylene	The eicosyl cyclopentadienyl
Two ring decyl silicylene	The heneicosyl cyclopentadienyl	Two cyclo-dodecyl silicylene	The docosyl cyclopentadienyl
The dinaphthyl silicylene	The tricosyl cyclopentadienyl	Two cyclo-dodecyl silicylene	The docosyl cyclopentadienyl
The dinaphthyl silicylene	The tricosyl cyclopentadienyl	The phenylbenzene silicylene	The tetracosyl cyclopentadienyl
The xylyl silicylene	The pentacosyl cyclopentadienyl	The phenylbenzene silicylene	The tetracosyl cyclopentadienyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	The dibenzyl silicylene	The ceryl cyclopentadienyl
Two styroyl silicylene	The heptacosyl cyclopentadienyl	The dibenzyl silicylene	The ceryl cyclopentadienyl
Two styroyl silicylene	The heptacosyl cyclopentadienyl	Two (butylbenzene ethyl) silicylene	The octacosyl cyclopentadienyl
The methylethyl silicylene	The nonacosyl cyclopentadienyl	Two (butylbenzene ethyl) silicylene	The octacosyl cyclopentadienyl
The methylethyl silicylene	The nonacosyl cyclopentadienyl	The methyl-propyl silicylene	The triacontyl cyclopentadienyl
The methyl butyl silicylene	The cyclohexyl ring pentadienyl	The methyl-propyl silicylene	The triacontyl cyclopentadienyl
The methyl butyl silicylene	The cyclohexyl ring pentadienyl	Methyl hexyl silicylene	The benzyl ring pentadienyl
The aminomethyl phenyl silicylene	The phenylbenzene cyclopentadienyl	Methyl hexyl silicylene	The benzyl ring pentadienyl
The aminomethyl phenyl silicylene	The phenylbenzene cyclopentadienyl	The ethylphenyl silicylene	The triphenyl cyclopentadienyl
The ethyl propyl silicylene	The tetraphenyl cyclopentadienyl	The ethylphenyl silicylene	The triphenyl cyclopentadienyl
The ethyl propyl silicylene	The tetraphenyl cyclopentadienyl	The ethyl-butyl silicylene	The pentapheneyl cyclopentadienyl
Propyl group phenyl silicylene	The tolyl cyclopentadienyl	The ethyl-butyl silicylene	The pentapheneyl cyclopentadienyl
Propyl group phenyl silicylene	The tolyl cyclopentadienyl	Dimethylated methylene germane base	The benzyl rings pentadienyl
Diethyl methylene germane base	The styroyl cyclopentadienyl	Dimethylated methylene germane base	The benzyl rings pentadienyl
Diethyl methylene germane base	The styroyl cyclopentadienyl	Phenylbenzene methylene germane base	The cyclohexyl methyl cyclopentadienyl
Aminomethyl phenyl methylene germane base	The naphthyl cyclopentadienyl	Phenylbenzene methylene germane base	The cyclohexyl methyl cyclopentadienyl
Aminomethyl phenyl methylene germane base	The naphthyl cyclopentadienyl	Ring tetramethylene silicylene	The aminomethyl phenyl cyclopentadienyl
The cyclopentamethylene silicylene	Methyl tolyl cyclopentadienyl	Ring tetramethylene silicylene	The aminomethyl phenyl cyclopentadienyl
The cyclopentamethylene silicylene	Methyl tolyl cyclopentadienyl	Ring trimethylene silicylene	The methylethyl cyclopentadienyl
The inferior azanyl of cyclohexyl	The methyl-propyl cyclopentadienyl	Ring trimethylene silicylene	The methylethyl cyclopentadienyl
The inferior azanyl of cyclohexyl	The methyl-propyl cyclopentadienyl	The inferior azanyl of butyl	The methyl butyl cyclopentadienyl
The inferior azanyl of methyl	The methyl amyl cyclopentadienyl	The inferior azanyl of butyl	The methyl butyl cyclopentadienyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	The inferior azanyl of phenyl	Methyl hexyl cyclopentadienyl
The inferior azanyl of perfluorophenyl	The methylheptyl cyclopentadienyl	The inferior azanyl of phenyl	Methyl hexyl cyclopentadienyl
The inferior azanyl of perfluorophenyl	The methylheptyl cyclopentadienyl	The inferior phosphine base (methylphosphanediyl) of methyl	The Methyl Octyl cyclopentadienyl
The inferior phosphine base of ethyl	Methyl nonyl cyclopentadienyl	The inferior phosphine base (methylphosphanediyl) of methyl	The Methyl Octyl cyclopentadienyl
The inferior phosphine base of ethyl	Methyl nonyl cyclopentadienyl	The inferior phosphine base of propyl group	Methyl decyl cyclopentadienyl
The inferior phosphine base of butyl	The vinyl cyclopentadienyl	The inferior phosphine base of propyl group	Methyl decyl cyclopentadienyl
The inferior phosphine base of butyl	The vinyl cyclopentadienyl	The inferior phosphine base of cyclohexyl	The propenyl cyclopentadienyl
The inferior phosphine base of phenyl	The butenyl cyclopentadienyl	The inferior phosphine base of cyclohexyl	The propenyl cyclopentadienyl
The inferior phosphine base of phenyl	The butenyl cyclopentadienyl	The methyl borylene	Indenyl
The phenyl borylene	The methyl indenyl	The methyl borylene	Indenyl
The phenyl borylene	The methyl indenyl	Methylene radical	The dimethyl indenyl
The dimethylated methylene base	The trimethylammonium indenyl	Methylene radical	The dimethyl indenyl
The dimethylated methylene base	The trimethylammonium indenyl	The diethyl methylene radical	The methyl-propyl indenyl
The dibutyl methylene radical	The dimethyl propyl indenyl	The diethyl methylene radical	The methyl-propyl indenyl
The dibutyl methylene radical	The dimethyl propyl indenyl	The dipropyl methylene radical	Methyl dipropyl indenyl
The phenylbenzene methylene radical	The methylethyl indenyl	The dipropyl methylene radical	Methyl dipropyl indenyl
The phenylbenzene methylene radical	The methylethyl indenyl	The xylyl methylene radical	The methyl butyl indenyl
Two (butyl phenyl) methylene radical	Ethyl-indenyl	The xylyl methylene radical	The methyl butyl indenyl
Two (butyl phenyl) methylene radical	Ethyl-indenyl	Two (trimethyl silyl phenyl) methylene radical	The propyl group indenyl
Two (triethylsilyl phenyl) methylene radical	The butyl indenyl	Two (trimethyl silyl phenyl) methylene radical	The propyl group indenyl
Two (triethylsilyl phenyl) methylene radical	The butyl indenyl	The dibenzyl methylene radical	The amyl group indenyl
Ring tetramethylene methylene radical	The hexyl indenyl	The dibenzyl methylene radical	The amyl group indenyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	The cyclopentamethylene methylene radical	The heptyl indenyl
Ethylidene	The octyl group indenyl	The cyclopentamethylene methylene radical	The heptyl indenyl
Ethylidene	The octyl group indenyl	The methyl ethylidene	The nonyl indenyl
The dimethyl ethylidene	The decyl indenyl	The methyl ethylidene	The nonyl indenyl
The dimethyl ethylidene	The decyl indenyl	The trimethylammonium ethylidene	Phenyl indenyl
The tetramethyl-ethylidene	(fluorophenyl) indenyl	The trimethylammonium ethylidene	Phenyl indenyl
The tetramethyl-ethylidene	(fluorophenyl) indenyl	Cyclopentylidene	(aminomethyl phenyl) indenyl
Cyclohexylidene	The xenyl indenyl	Cyclopentylidene	(aminomethyl phenyl) indenyl
Cyclohexylidene	The xenyl indenyl	Inferior suberyl	(two (trifluoromethyl) phenyl) indenyl
Inferior ring octyl group	The naphthyl indenyl	Inferior suberyl	(two (trifluoromethyl) phenyl) indenyl
Inferior ring octyl group	The naphthyl indenyl	Propylidene	The phenanthryl indenyl
The methyl propylidene	The benzyl indenyl	Propylidene	The phenanthryl indenyl
The methyl propylidene	The benzyl indenyl	The dimethyl propylidene	The benzo indenyl
The trimethylammonium propylidene	The cyclohexyl indenyl	The dimethyl propylidene	The benzo indenyl
The trimethylammonium propylidene	The cyclohexyl indenyl	The tetramethyl-propylidene	The aminomethyl phenyl indenyl
The pentamethyl-propylidene	The ethylphenyl indenyl	The tetramethyl-propylidene	The aminomethyl phenyl indenyl
The pentamethyl-propylidene	The ethylphenyl indenyl	The hexamethyl propylidene	The propyl group phenyl indenyl
Inferior two silyloxies of tetramethyl-	Methyl naphthyl indenyl	The hexamethyl propylidene	The propyl group phenyl indenyl
Inferior two silyloxies of tetramethyl-	Methyl naphthyl indenyl	Vinylidene	Ethyl naphthyl indenyl
1, the 1-ethylidene	Propyl group naphthyl indenyl	Vinylidene	Ethyl naphthyl indenyl
1, the 1-ethylidene	Propyl group naphthyl indenyl	The divinyl silicylene	(aminomethyl phenyl) indenyl
The diallyl silicylene	(3,5-dimethylphenyl) indenyl	The divinyl silicylene	(aminomethyl phenyl) indenyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	Dibutene base silicylene	(ethylphenyl) indenyl
The methyl ethylene silicylene	(diethyl phenyl) indenyl	Dibutene base silicylene	(ethylphenyl) indenyl
The methyl ethylene silicylene	(diethyl phenyl) indenyl	The methylpropenyl silicylene	(propyl group phenyl) indenyl
Methyl butene base silicylene	(dipropyl phenyl) indenyl	The methylpropenyl silicylene	(propyl group phenyl) indenyl
Methyl butene base silicylene	(dipropyl phenyl) indenyl	The dimetylsilyl methylene radical	The methyl tetrahydro indenyl
Diphenylmethyl silylation methylene radical	The dimethyl tetrahydro indenyl	The dimetylsilyl methylene radical	The methyl tetrahydro indenyl
Diphenylmethyl silylation methylene radical	The dimethyl tetrahydro indenyl	The dimetylsilyl ethylidene	Dimethyl dihydro indenyl
Diphenylmethyl silylation ethylidene	Dimethyl three hydrogen indenyls	The dimetylsilyl ethylidene	Dimethyl dihydro indenyl
Diphenylmethyl silylation ethylidene	Dimethyl three hydrogen indenyls	The dimetylsilyl propylidene	The aminomethyl phenyl tetrahydro indenyl
Diphenylmethyl silylation propylidene	Aminomethyl phenyl dihydro indenyl	The dimetylsilyl propylidene	The aminomethyl phenyl tetrahydro indenyl
Diphenylmethyl silylation propylidene	Aminomethyl phenyl dihydro indenyl	Dimethylated methylene stannane base	Aminomethyl phenyl three hydrogen indenyls
The phenylbenzene stannylene	The ethyl tetrahydro indenyl	Dimethylated methylene stannane base	Aminomethyl phenyl three hydrogen indenyls
The phenylbenzene stannylene	The ethyl tetrahydro indenyl		The propyl group tetrahydro indenyl
	The butyl tetrahydro indenyl		The propyl group tetrahydro indenyl
	The butyl tetrahydro indenyl		The phenyl tetrahydro indenyl
	Fluorenyl		The phenyl tetrahydro indenyl
	Fluorenyl		Methylfluorenyl
	The dimethyl fluorenyl		Methylfluorenyl
	The dimethyl fluorenyl		The trimethylammonium fluorenyl
	The ethyl fluorenyl		The trimethylammonium fluorenyl
	The ethyl fluorenyl		The propyl group fluorenyl
	The butyl fluorenyl		The propyl group fluorenyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	The dibutyl fluorenyl
	The amyl group fluorenyl	The dibutyl fluorenyl
	The amyl group fluorenyl	The hexyl fluorenyl
	The heptyl fluorenyl	The hexyl fluorenyl
	The heptyl fluorenyl	The octyl group fluorenyl
	The nonyl fluorenyl	The octyl group fluorenyl
	The nonyl fluorenyl	The decyl fluorenyl
	The phenyl fluorenyl	The decyl fluorenyl
	The phenyl fluorenyl	The naphthyl fluorenyl
	The benzyl fluorenyl	The naphthyl fluorenyl
	The benzyl fluorenyl	The aminomethyl phenyl fluorenyl
	The ethylphenyl fluorenyl	The aminomethyl phenyl fluorenyl
	The ethylphenyl fluorenyl	Propyl group phenyl fluorenyl
	Methyl naphthyl fluorenyl	Propyl group phenyl fluorenyl
	Methyl naphthyl fluorenyl	Ethyl naphthyl fluorenyl
	Propyl group naphthyl fluorenyl	Ethyl naphthyl fluorenyl
	Propyl group naphthyl fluorenyl	Octahydrofluorenyl
	Tetrahydrofluorenyl	Octahydrofluorenyl
	Tetrahydrofluorenyl	Prestox octahydro dibenzo [b, h] fluorenyl
	Tetramethyl-tetrahydro benzo [b] fluorenyl	Prestox octahydro dibenzo [b, h] fluorenyl
	Tetramethyl-tetrahydro benzo [b] fluorenyl	The diphenyl methyl cyclopentadienyl
	The trimethyl silyl cyclopentadienyl	The diphenyl methyl cyclopentadienyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	The triethylsilyl cyclopentadienyl
	Trimethylammonium germyl cyclopentadienyl	The triethylsilyl cyclopentadienyl
	Trimethylammonium germyl cyclopentadienyl	Trimethylammonium stannyl cyclopentadienyl
	Triethyl first plumbyl cyclopentadienyl	Trimethylammonium stannyl cyclopentadienyl
	Triethyl first plumbyl cyclopentadienyl	The trifluoromethyl cyclopentadienyl
	N, N-dimethylamino cyclopentadienyl	The trifluoromethyl cyclopentadienyl
	N, N-dimethylamino cyclopentadienyl	P, P-dimethylphosphine basic ring pentadienyl
	N, N-diethylin cyclopentadienyl	P, P-dimethylphosphine basic ring pentadienyl
	N, N-diethylin cyclopentadienyl	The methoxyl group cyclopentadienyl
	The oxyethyl group cyclopentadienyl	The methoxyl group cyclopentadienyl
	The oxyethyl group cyclopentadienyl	The trimethylsiloxy cyclopentadienyl
	(N，N-	The trimethylsiloxy cyclopentadienyl
	(N，N-	The methoxyl group indenyl
	The dimethoxy indenyl	The methoxyl group indenyl
	The dimethoxy indenyl	N, N-dimethylamino indenyl
	The trimethylsiloxy indenyl	N, N-dimethylamino indenyl
	The trimethylsiloxy indenyl	Butyl dimethylsilane oxygen base indenyl
	Two (N, N-dimethylamino) indenyl	Butyl dimethylsilane oxygen base indenyl
	Two (N, N-dimethylamino) indenyl	Two (trimethylsiloxy) indenyl
	Two (butyl dimethylsilane oxygen base) indenyl	Two (trimethylsiloxy) indenyl
	Two (butyl dimethylsilane oxygen base) indenyl	The methoxyl group fluorenyl
	The dimethoxy fluorenyl	The methoxyl group fluorenyl

A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)
A′	Cp、Cp ^*, CpR or (C ₅H _5-y-xS″ _x)	N, N-dimethylamino fluorenyl
	The trimethylsiloxy fluorenyl	N, N-dimethylamino fluorenyl
	The trimethylsiloxy fluorenyl	Butyl dimethylsilane oxygen base fluorenyl
	The dimethoxy fluorenyl	Butyl dimethylsilane oxygen base fluorenyl
	The dimethoxy fluorenyl	Two (N, N-dimethylamino) fluorenyl
	Two (trimethylsiloxy) fluorenyl	Two (N, N-dimethylamino) fluorenyl
	Two (trimethylsiloxy) fluorenyl	Two (butyl dimethylsilane oxygen base) fluorenyl

Table A (continuing)

(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M
(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M	Methylamino-	Chlorion	Titanium
Ethylamino	Bromide anion	Zirconium	Methylamino-	Chlorion	Titanium
Ethylamino	Bromide anion	Zirconium	Third amino	Iodide ion	Hafnium
Fourth amino	Fluorion		Third amino	Iodide ion	Hafnium
Fourth amino	Fluorion		Penta amino	Hydride ion	L or L ' (nonessential)
Oneself is amino	Methyl	Ethene	Penta amino	Hydride ion	L or L ' (nonessential)
Oneself is amino	Methyl	Ethene	Heptan amino	Ethyl	Propylene
Hot amino	Propyl group	Butylene	Heptan amino	Ethyl	Propylene
Hot amino	Propyl group	Butylene	The ninth of the ten Heavenly Stems amino	Butyl	Hexene
The last of the ten Heavenly stems amino	Amyl group	Vinylbenzene	The ninth of the ten Heavenly Stems amino	Butyl	Hexene
The last of the ten Heavenly stems amino	Amyl group	Vinylbenzene	Eicosane amino	Hexyl	Hexadiene
Heneicosane amino	Heptyl	Divinyl	Eicosane amino	Hexyl	Hexadiene

(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M
(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M	Docosane amino	Octyl group	Dimethylbutadiene
Tricosane amino	Nonyl	Pentadiene	Docosane amino	Octyl group	Dimethylbutadiene
Tricosane amino	Nonyl	Pentadiene	Tetracosane amino	Decyl	The methyl hexadiene
Pentacosane amino	Undecyl	The dimethyl hexadiene	Tetracosane amino	Decyl	The methyl hexadiene
Pentacosane amino	Undecyl	The dimethyl hexadiene	Hexacosane amino	Dodecyl	Acetylene
Heptacosane amino	Tridecyl	Methylacetylene	Hexacosane amino	Dodecyl	Acetylene
Heptacosane amino	Tridecyl	Methylacetylene	Octacosane amino	Tetradecyl	Ethylacetylene
Nonacosane amino	Pentadecyl	Benzyne	Octacosane amino	Tetradecyl	Ethylacetylene
Nonacosane amino	Pentadecyl	Benzyne	Triacontane amino	Hexadecyl	Cyclopentenes
Phenyl amino	Heptadecyl	Tetrahydrobenzene	Triacontane amino	Hexadecyl	Cyclopentenes
Phenyl amino	Heptadecyl	Tetrahydrobenzene	Tolyl amino	Octadecyl
Styroyl amino	Nonadecyl	L ' (nonessential)	Tolyl amino	Octadecyl
Styroyl amino	Nonadecyl	L ' (nonessential)	Benzylamino	Eicosyl	Diethyl ether
Cyclobutyl amino	Heneicosyl	Dme	Benzylamino	Eicosyl	Diethyl ether
Cyclobutyl amino	Heneicosyl	Dme	Cyclopentyl amino	Docosyl	Trimethylamine 99
Cyclohexyl amino	Tricosyl	Triphenylamine	Cyclopentyl amino	Docosyl	Trimethylamine 99
Cyclohexyl amino	Tricosyl	Triphenylamine	Suberyl amino	Tetracosyl	Triethylamine
Ring octyl group amino	Pentacosyl	Tricyclohexyl phosphine	Suberyl amino	Tetracosyl	Triethylamine
Ring octyl group amino	Pentacosyl	Tricyclohexyl phosphine	Ring nonyl amino	Ceryl	Triphenylphosphine
Ring decyl amino	Heptacosyl	Trimethyl-phosphine	Ring nonyl amino	Ceryl	Triphenylphosphine

(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M
(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M	Cyclo-dodecyl amino	Octacosyl	Tetrahydrofuran (THF)
Adamantyl amino	Nonacosyl	Furans	Cyclo-dodecyl amino	Octacosyl	Tetrahydrofuran (THF)
Adamantyl amino	Nonacosyl	Furans	Norcamphyl amino	Triacontyl	Thiophene
Perfluorophenyl amino	Phenyl	Dimethyl thioether	Norcamphyl amino	Triacontyl	Thiophene
Perfluorophenyl amino	Phenyl	Dimethyl thioether	Fluorophenyl amino	Benzyl	Diphenylsulfide
Difluorophenyl amino	Styroyl		Fluorophenyl amino	Benzyl	Diphenylsulfide
Difluorophenyl amino	Styroyl		Oxygen base (oxo)	Tolyl
Sulfenyl (sulfido)	Methoxyl group		Oxygen base (oxo)	Tolyl
Sulfenyl (sulfido)	Methoxyl group			Oxyethyl group
(JS′ _z-1-y)(y＝0)	Propoxy-			Oxyethyl group
(JS′ _z-1-y)(y＝0)	Propoxy-		Methoxyl group	Butoxy
Oxyethyl group	Dimethylamino		Methoxyl group	Butoxy
Oxyethyl group	Dimethylamino		Phenoxy group	Diethylin
Dimethyl phenoxy	Methylethyl amino		Phenoxy group	Diethylin
Dimethyl phenoxy	Methylethyl amino		The dipropyl phenoxy group	Phenoxy group
Methylthio group	Benzyloxy		The dipropyl phenoxy group	Phenoxy group
Methylthio group	Benzyloxy		Ethylmercapto group	Allyl group
Thiophenyl			Ethylmercapto group	Allyl group
Thiophenyl			The dimethyl benzene sulfenyl
The dipropyl thiophenyl			The dimethyl benzene sulfenyl

(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M
(JS′ _z-1-y)(y＝1)	X ₁Or X ₂	M	X ₁And X ₂Together
	The methene base		X ₁And X ₂Together
	The methene base		Ethidine
	The propylidene base		Ethidine
	The propylidene base		Tetramethylene
	Pentamethylene		Tetramethylene
	Pentamethylene		Hexa-methylene
	The ethylene hydroxyl		Hexa-methylene
	The ethylene hydroxyl		Divinyl
	Dimethyl butadiene		Divinyl
	Dimethyl butadiene		Dimethylbutadiene
	Pentadiene		Dimethylbutadiene
	Pentadiene		Methylpentadiene
	Dimethyl pentadiene		Methylpentadiene
	Dimethyl pentadiene		Hexadiene
	The methyl hexadiene		Hexadiene
	The methyl hexadiene		The dimethyl hexadiene
			The dimethyl hexadiene

Other preferred catalyzer comprises those catalyzer described in the WO 01/48034, is incorporated herein for reference.Particularly preferred catalyst compound comprises the 9th page 38 and walks to that 25 page of 42 row, the 28th page of 5 to 17 row and the 30th page 37 walk to 35 page of 28 capable those disclosed.

The activator of catalyst compound and activation method

Above-mentioned polymerization catalyst precursor compound activating is produced have the compound that can make the empty coordination of alkene coordination, insertion and polymeric position.For patent specification and appended claims, term " promotor " and " activator " are used interchangeably in this article, are defined as any compound of arbitrary activatory that can make above-mentioned catalyst compound by the catalyst compound positively charged ion that makes the neutral catalyst compound change into catalytic activity.Nonrestrictive activator comprises for example promotor of aikyiaiurnirsoxan beta, aluminum alkyls, ionization activator (can be neutrality or ionic) and general type.The metal ligand that preferred activator generally includes aluminium alkoxide compound, modified aluminium-oxygen hydride compounds and captures a reactive σ-bonding makes metal complexes become positively charged ion and provides the non-coordination of charge balance or the ionization negatively charged ion precursor compound of weakly coordinating anion.

Aikyiaiurnirsoxan beta and alkyl aluminum activator

In one embodiment, alumoxane activator is used as activator in catalyst composition of the present invention.Aikyiaiurnirsoxan beta generally is to comprise-Al (R ¹The oligomeric compound of)-O-subunit, wherein R ¹Be alkyl.The example of aikyiaiurnirsoxan beta comprises methylaluminoxane (MAO), modified methylaluminoxane (MMAO), ethyl aikyiaiurnirsoxan beta and isobutyl aluminium alkoxide.Alkylaluminoxane and modification alkylaluminoxane are fit to do catalyst activator, particularly when seizable part be halogen ion, pure root or when amino.Also can use the mixture of different aikyiaiurnirsoxan beta and modified alumoxane.

Described activator compound comprises that Lewis acid activation agent and especially aikyiaiurnirsoxan beta represent with following general formula:

(R ³-Al-O) _p (11)

R ⁴(R ⁵-Al-O) _p-AlR ⁶ ₂ (12)

(M′) ^m+Q′ _m (13)

Aikyiaiurnirsoxan beta generally is the mixture of linear and ring compound.In the general formula of described aikyiaiurnirsoxan beta, R ³, R ⁴, R ⁵And R ⁶Be C independently _1-30Alkyl, for example methyl, ethyl, propyl group, butyl, amyl group, hexyl, heptyl, octyl group, nonyl, decyl, " p " is 1 to about 50 integer.R most preferably ³, R ⁴, R ⁵And R ⁶Be methyl, " p " is at least 4.When preparing aikyiaiurnirsoxan beta with alkyl aluminum halide or alkanol aluminum alkyls, one or more R ^3-6Base can be halogen ion or pure root.M ' is metal or metalloid, and Q ' is part or fluoridized alkyl.

Generally acknowledged aikyiaiurnirsoxan beta is not an one matter.Typical aikyiaiurnirsoxan beta comprises free three replacements or trialkylaluminium, three replacements of constraint or the aikyiaiurnirsoxan beta molecule of trialkylaluminium and different oligomeric degree.Methylaluminoxane most preferably comprises more a spot of trimethyl aluminium.Make trimethyl aluminium and Lewis base reaction or trimethyl aluminium vacuum distilling or the content that can realize trimethyl aluminium by any other means known in the art is lower.Also recognize with transistion metal compound reaction after, some aikyiaiurnirsoxan beta molecule is the anionic form represented with the negatively charged ion among the formula 4-6, so we are referred to as " non-coordination " negatively charged ion.

Further describe referring to US 4,665 208,4,952,540,5,041,584,5,091,352,5,206,199,5,204,419,4,874,734,4,924,018,4,908,463,4,968,827,5,329,032,5,248,801,5,235,081,5,157,137,5,103,031 and EP 0 561 476 A1, EP 0 279 586 B1, EP 0 516 476 A, EP 0 594 218A1 and WO 94/10180.

When activator was aikyiaiurnirsoxan beta (modification or unmodified), some embodiment was selected the maximum activator with respect to 5000 times of molar excess Al/M of catalyst precursor (each metal catalytic position).Activator is 1: 1 mol ratio with the minimum value of the ratio of catalyst precursor.

Aikyiaiurnirsoxan beta can be by the hydrolytic action production of various trialkyl aluminium compounds.MMAO can be by the hydrolytic action production of trimethyl aluminium and more senior trialkylaluminium such as triisobutyl aluminium.MMAO generally more is soluble in aliphatic solvents and more stable in storage process.The preparation method that many aikyiaiurnirsoxan beta and modified alumoxane are arranged, its limiting examples is described in US 4,665,208,4,952,540,5,091,352,5,206,199,5,204,419,4,874,734,4,924,018,4,908,463,4,968,827,5,308,815,5,329,032,5,248,801,5,235,081,5,157,137,5,103,031,5,391,793,5,391,529,5,693,838,5,731,253,5,731,451,5,744,656,5,847,177,5,854,166,5,856,256 and 5,939,346 and EP-A-0561 476, EP-B1-0 279 586, EP-A-0 594 218, EP-B1-0 586 665, among WO94/10180 and the WO99/15534, all be incorporated herein for reference.It may be preferred using visual transparent methylaluminoxane.Muddiness or agglomerative aikyiaiurnirsoxan beta can be filtered produce clear solution or from turbid solution decantation go out transparent aikyiaiurnirsoxan beta.Another kind of aikyiaiurnirsoxan beta is 3A type modified methylaluminoxane (MMAO) promotor (available from Akzo Chemicals, Inc., is encompassed in US5 with trade(brand)name Modified Methylalumoxane type 3A, 041,584 in).

The aluminum alkyls or the organo-aluminium compound that can be used as activator (or scavenging agent) comprise trimethyl aluminium, triethyl aluminum, triisobutyl aluminium, tri-n-hexyl aluminum and tri-n-octylaluminium etc.

The ionization activator

Using ionization or stoichiometric activator (neutrality or ionic) is within the scope of the invention as four (pentafluorophenyl group) boron, three normal-butyl ammoniums, three perfluorophenyl boron metalloid precursors or three perfluor naphthyl boron metalloid precursors, the assorted borine negatively charged ion (WO98/43983) of many halogenations, boric acid (US5 942 459) or its composition.Neutrality or ion activation agent are used separately or are used in combination also within the scope of the invention with aikyiaiurnirsoxan beta or modified alumoxane activator.

The example of neutral stoichiometry activator comprises trisubstituted boron, tellurium, aluminium, gallium and indium or its mixture.These three substituting groups are independently selected from alkyl, thiazolinyl, halogen, substituted alkyl, aryl, aryl halide, alkoxyl group and halogen ion.Preferred these three substituting groups are independently selected from halogen, list or encircle (comprising halogenated) aryl, alkyl and thiazolinyl and composition thereof more, preferably have 1 to 20 carbon atom thiazolinyl, have 1 to 20 carbon atom alkyl, the alkoxyl group of 1 to 20 carbon atom is arranged and the aryl (comprising substituted aryl) of 3 to 20 carbon atoms is arranged.More preferably these three substituting groups are alkyl, phenyl, naphthyl or its mixture that 1 to 4 carbon atom is arranged.Even more preferably these three substituting groups are halogenation (preferred fluorinated) aryl.Most preferably described neutral stoichiometry activator is three perfluorophenyl boron or three perfluor naphthyl boron.

The residual ion that ionic stoichiometry activator compound can comprise active proton or some and described ionizing compound associates but not coordination or only loose with it other positively charged ion of coordinate with it.This compounds etc. is described in EP-A-0 570 982, EP-A-0 520 732, EP-A-0 495 375, EP-B1-0 500 944, EP-A-0 277 003 and EP-A-0 277 004, reaches US 5,153,157,5,198,401,5,066,741,5,206,197,5,241,025,5,384,299 and 5, among the USSN08/285 380 of application on August 3rd, 502,124 and 1994, all be incorporated herein for reference.

Ionic catalyst can be by transistion metal compound and some neutral lewis acid such as B (C ₆F ₆) ₃Prepared in reaction generates negatively charged ion as ([B (C when the hydrolyzable part (X) of described acid and transistion metal compound reacts ₆F ₅) ₃(X)] ^-), the cationic transition metal material that reaction is produced keeps stable.Described catalyzer can and also preferably with the activator component preparation of ionic compound or composition forms.But the present invention also considers to prepare activator with neutral compound.

The compound that is used as activator component in the used ionic catalyst system of preparation the inventive method comprises positively charged ion (Bronsted acid of proton preferably can be provided) and compatible non-coordination anion, this negatively charged ion is big (bulky), can stablize two compounds in conjunction with the time active catalyst kind (the 4th family's positively charged ion) that generates, and enough mutability with by the unsaturated matrix of olefinic, diolefinic and acetylene series or other neutral Lewis base such as displacements such as ether and nitrile.The compatible non-coordination anions of two classes are disclosed among disclosed EPA 277 003 in 1988 and the EPA 277 004: 1) comprise a plurality of and center live metal or metalloid core covalent coordinate and shield the anion binding title complex and 2 of the lipophilic group of this core) comprise the negatively charged ion of a plurality of boron atoms such as carborane, metal card borine (metallacarborane) and borine.

In one preferred embodiment, described stoichiometry activator comprises positively charged ion and anionic group, can be represented by the formula:

(L-H) _d ⁺(A ^d-) (14)

Wherein L is a neutral Lewis base;

H is a hydrogen;

(L-H) ⁺Be Bronsted acid;

A ^D-For the non-coordination anion of d-electric charge is arranged; With

D is 1 to 3 integer.

Described cationic components (L-H) _d ⁺It is protonated or therefrom capture structure division such as alkyl or aryl and form the reducible Lewis acid of transition-metal cation kind to comprise that Bronsted acid contains the transition-metal catalyst precursor of bulky ligand metallocene as described in maybe making as proton or protonated Lewis base.

Described activation positively charged ion (L-H) _d ⁺Can be provide proton to form the Bronsted acid of transition-metal cation can for described transition metal-catalyzed precursor, comprise ammonium, oxygen

, silicon

(silylium) and composition thereof, preferably from methylamine, aniline, dimethylamine, diethylamine, methylphenylamine, pentanoic, Trimethylamine 99, triethylamine, N, accelerine, methyldiphenylamine, pyridine, to bromo-N, accelerine, to nitro-N, the ammonium of accelerine, from triethylphosphine, triphenyl phosphine and diphenyl phosphine

, from ether such as dme, diethyl ether, tetrahydrofuran (THF) and two The oxygen of alkane From sulfonium of thioether such as diethyl thioether and tetramethylene sulfide and composition thereof.Described activation positively charged ion (L-H) _d ⁺Can also be such as silver,

Carbon

Ferrocene

And composition thereof wait structure division, preferred carbon

And ferrocene

Most preferably (L-H) _d ⁺Be triphenylcarbenium

Described anionic group A ^D-Include those of following formula: [M ^K+Q _n] ^D-, wherein k is 1 to 3 integer; N is the integer of 2-6; N-k=d; M is the element that is selected from the periodic table of elements the 13rd family, preferred boron or aluminium; Q is the brine alkyl and the halo alkyl of dialkyl amido, the halogen root of hydrogen root, bridging or not bridging, pure root, aryl oxide root, alkyl, substituted hydrocarbon radical, brine alkyl, replacement independently, and described Q has maximum 20 carbon atoms, and condition is that Q is that the halogen root is once no more than.Preferred Q is the fluoro alkyl of 1 to 20 carbon atom, and more preferably Q is fluorinated aryl, and most preferably Q is five fluoro aryls.The A that is fit to ^D-Example also comprise disclosed two boron compounds among the US5 447 895, be incorporated herein for reference.

Preparation the present invention improve the illustrative of the boron compound that can be used as active cocatalyst in the catalyzer and nonrestrictive example be trisubstituted ammonium salt as:

Tetraphenyl boric acid TMA (TriMethylAmine),

Tetraphenyl boron triethylenetetraminehexaacetic acid ammonium,

Tetraphenyl boric acid 3 third ammoniums,

Tetraphenyl boric acid three positive fourth ammoniums,

Tetraphenyl boric acid three uncle's fourth ammoniums,

Tetraphenyl boric acid N, N-dimethyl puratized agricultural spray,

Tetraphenyl boric acid N, N-diethyl puratized agricultural spray,

Tetraphenyl boric acid N, N-dimethyl-(2,4,6-trimethylammonium puratized agricultural spray),

Tetraphenyl boric acid

Tetraphenyl boric acid triphenylcarbenium

Tetraphenyl boric acid triphenyl

Tetraphenyl boric acid triethyl silicon

Tetraphenyl boric acid diazobenzene,

Four (pentafluorophenyl group) boric acid TMA (TriMethylAmine),

Four (pentafluorophenyl group) boron triethylenetetraminehexaacetic acid ammonium,

Four (pentafluorophenyl group) boric acid, 3 third ammoniums,

Four (pentafluorophenyl group) boric acid, three positive fourth ammoniums,

Four (pentafluorophenyl group) boric acid, three Zhong Ding ammoniums,

Four (pentafluorophenyl group) boric acid N, N-dimethyl puratized agricultural spray,

Four (pentafluorophenyl group) boric acid N, N-diethyl puratized agricultural spray,

Four (pentafluorophenyl group) boric acid N, N-dimethyl-(2,4,6-trimethylammonium puratized agricultural spray),

Four (pentafluorophenyl group) boric acid

Four (pentafluorophenyl group) boric acid triphenylcarbenium

Four (pentafluorophenyl group) boric acid triphenyl

Four (pentafluorophenyl group) boric acid triethyl silicon

Four (pentafluorophenyl group) boric acid diazobenzene,

Four (2,3,4,6-tetrafluoro phenyl) boric acid TMA (TriMethylAmine),

Four (2,3,4,6-tetrafluoro phenyl) boron triethylenetetraminehexaacetic acid ammonium,

Four (2,3,4,6-tetrafluoro phenyl) boric acid 3 third ammoniums,

Four (2,3,4,6-tetrafluoro phenyl) boric acid three positive fourth ammoniums,

Four (2,3,4,6-tetrafluoro phenyl) boric acid dimethyl (tertiary butyl) ammonium,

Four (2,3,4,6-tetrafluoro phenyl) boric acid N, N-dimethyl puratized agricultural spray,

Four (2,3,4,6-tetrafluoro phenyl) boric acid N, N-diethyl puratized agricultural spray,

Four (2,3,4,6-tetrafluoro phenyl) boric acid N, N-dimethyl-(2,4,6-trimethylammonium puratized agricultural spray),

Four (2,3,4,6-tetrafluoro phenyl) boric acid

Four (2,3,4,6-tetrafluoro phenyl) boric acid triphenylcarbenium

Four (2,3,4,6-tetrafluoro phenyl) boric acid triphenyl

Four (2,3,4,6-tetrafluoro phenyl) boric acid triethyl silicon

Four (2,3,4,6-tetrafluoro phenyl) boric acid diazobenzene,

Four (perfluor naphthyl) boric acid TMA (TriMethylAmine),

Four (perfluor naphthyl) boron triethylenetetraminehexaacetic acid ammonium,

Four (perfluor naphthyl) boric acid, 3 third ammoniums,

Four (perfluor naphthyl) boric acid, three positive fourth ammoniums,

Four (perfluor naphthyl) boric acid, three uncle's fourth ammoniums,

Four (perfluor naphthyl) boric acid N, N-dimethyl puratized agricultural spray,

Four (perfluor naphthyl) boric acid N, N-diethyl puratized agricultural spray,

Four (perfluor naphthyl) boric acid N, N-dimethyl-(2,4,6-trimethylammonium puratized agricultural spray),

Four (perfluor naphthyl) boric acid

Four (perfluor naphthyl) boric acid triphenylcarbenium

Four (perfluor naphthyl) boric acid triphenyl

Four (perfluor naphthyl) boric acid triethyl silicon

Four (perfluor naphthyl) boric acid diazobenzene,

Four (perfluorinated biphenyl) boric acid TMA (TriMethylAmine),

Four (perfluorinated biphenyl) boron triethylenetetraminehexaacetic acid ammonium,

Four (perfluorinated biphenyl) boric acid, 3 third ammoniums,

Four (perfluorinated biphenyl) boric acid, three positive fourth ammoniums,

Four (perfluorinated biphenyl) boric acid, three uncle's fourth ammoniums,

Four (perfluorinated biphenyl) boric acid N, N-dimethyl puratized agricultural spray,

Four (perfluorinated biphenyl) boric acid N, N-diethyl puratized agricultural spray,

Four (perfluorinated biphenyl) boric acid N, N-dimethyl-(2,4,6-trimethylammonium puratized agricultural spray),

Four (perfluorinated biphenyl) boric acid

Four (perfluorinated biphenyl) boric acid triphenylcarbenium

Four (perfluorinated biphenyl) boric acid triphenyl

Four (perfluorinated biphenyl) boric acid triethyl silicon

Four (perfluorinated biphenyl) boric acid diazobenzene,

Four (3,5-two (trifluoromethyl) phenyl) boric acid TMA (TriMethylAmine),

Four (3,5-two (trifluoromethyl) phenyl) boron triethylenetetraminehexaacetic acid ammonium,

Four (3,5-two (trifluoromethyl) phenyl) boric acid 3 third ammoniums,

Four (3,5-two (trifluoromethyl) phenyl) boric acid three positive fourth ammoniums,

Four (3,5-two (trifluoromethyl) phenyl) boric acid three uncle's fourth ammoniums,

Four (3,5-two (trifluoromethyl) phenyl) boric acid N, N-dimethyl puratized agricultural spray,

Four (3,5-two (trifluoromethyl) phenyl) boric acid N, N-diethyl puratized agricultural spray,

Four (3,5-two (trifluoromethyl) phenyl) boric acid N, N-dimethyl-(2,4,6-trimethylammonium puratized agricultural spray),

Four (3,5-two (trifluoromethyl) phenyl) boric acid

Four (3,5-two (trifluoromethyl) phenyl) boric acid triphenylcarbenium

Four (3,5-two (trifluoromethyl) phenyl) boric acid triphenyl

Four (3,5-two (trifluoromethyl) phenyl) boric acid triethyl silicon

Four (3,5-two (trifluoromethyl) phenyl) boric acid diazobenzene; With

Dialkyl ammonium salt is as four (pentafluorophenyl group) boric acid di-isopropyl ammonium and four (pentafluorophenyl group) boric acid dicyclohexyl ammonium; Trisubstituted with other

Salt is as four (pentafluorophenyl group) boric acid three (o-tolyls)

, and four (pentafluorophenyl group) boric acid three (2, the 6-3,5-dimethylphenyl)

Most preferably described ionic stoichiometry activator (L-H) _d ⁺(A ^D-) be four (perfluorophenyl) boric acid N, N-dimethyl puratized agricultural spray, four (perfluor naphthyl) boric acid N, N-dimethyl puratized agricultural spray, four (perfluorinated biphenyl) boric acid N, N-dimethyl puratized agricultural spray, four (3,5-two (trifluoromethyl) phenyl) boric acid N, N-dimethyl puratized agricultural spray, four (perfluor naphthyl) boric acid triphenylcarbenium Four (perfluorinated biphenyl) boric acid triphenylcarbenium

Four (3,5-two (trifluoromethyl) phenyl) boric acid triphenylcarbenium

Or four (perfluorophenyl) boric acid triphenylcarbenium

In one embodiment, also the imagination use does not contain active proton but can produce bulky ligand metallocene catalyst positively charged ion and the activation method of the ionization ionic compound of Qi Fei coordination anion, be described among EP-A-0 426 637, EP-A-0 573 403 and the US5 387 568, all be incorporated herein for reference.

Term " non-coordination anion " thus (NCA) mean not with described positively charged ion coordination or only with described positively charged ion a little less than the enough mutabilities of coordination can be by neutral Lewis base metathetical negatively charged ion." compatible " non-coordination anion is not become the neutral negatively charged ion when the initial title complex that forms decomposes.In addition, this negatively charged ion is not transferred to anionic substituting group or fragment that positively charged ion makes it to form neutral four-coordination metallocene compound and from this anionic neutral by product.Be applicable to non-coordination anion of the present invention be compatible, making metallocene cation keep stable and still keep enough volatilities on the meaning with+1 its ionic charge of balance can be by olefinic or acetylene series unsaturated monomer metathetical negatively charged ion in polymerization process.The promotor of these types is made scavenging agent with triisobutyl aluminium or trioctylaluminum sometimes.

The inventive method also can be used cocatalyst compound or the activator compound that is initially neutral lewis acid but generates cationic metal title complex and non-coordination anion or zwitter-ion title complex when reacting with The compounds of this invention.For example, three (pentafluorophenyl group) boron or aluminium are captured alkyl or hydrogen root part and are produced cationic metal title complex of the present invention and stablize non-coordination anion, referring to EP-A-0427 697 and EP-A-0 520 732 explanation about similar the 4th family's metallocene compound.Also referring to method and the compound of EP-A-0 495 375.About forming the zwitter-ion title complex with similar the 4th compounds of group, referring to US 5,624,878,5,486,632 and 5,527,929.

The promotor of general type (activator)

Usually with one or more conventional promotor activation, the promotor of described routine can be represented by the formula conventional transition metal catalyst compound except that the chrome catalysts compound of some general type:

M ³M ⁴ _vX ² _cR ³ _b-c (15)

M wherein ³Metal for the periodic table of elements the 1st to 3 and 12 to 13 families; M ⁴Metal for the periodic table of elements the 1st family; V is 0 to 1 number; Each X ²Be any halogen; C is 0 to 3 number; Each R ²Be monovalence alkyl or hydrogen; B is 1 to 4 number; Wherein b-c is at least 1.Other general type organo-metallic cocatalyst compound that is used for above-mentioned general type transition-metal catalyst has following formula: M ³R ² _k, M wherein ³Be IA, IIA, IIB or IIIA family metal, as lithium, sodium, beryllium, barium, boron, aluminium, zinc, cadmium and gallium; K equals 1,2 or 3, depends on M ³Valency, described valency depends on M usually again ³Affiliated family; Each R ²It can be any monovalence alkyl.

The limiting examples that is fit to the general type organo-metallic cocatalyst compound that uses with above-mentioned general type catalyst compound comprises that lithium methide, butyllithium, dihexyl mercury, dibutyl magnesium, diethyl cadmium, benzyl potassium, zinc ethyl, three n-butylaluminum, diisobutyl ethyl boron, diethyl cadmium, di-n-butyl zinc and three n-pentyl boron, particularly aluminum alkyls are as three hexyl aluminium, triethyl aluminum, trimethyl aluminium and triisobutyl aluminium.The cocatalyst compound of other general type comprises single Organohalogen compounds of group II metal and the list of hydride and the 3rd to 13 family's metal-or two-Organohalogen compounds and hydride.The limiting examples of the cocatalyst compound of this general type comprises bromination diisobutyl aluminum, isobutyl dichloride boron, methylmagnesium-chloride, tonsilon beryllium, bromination ethyl-cadmium, diisobutylaluminium hydride, hydrogenation methyl cadmium, hydrogenation diethyl boron, hydrogenation hexyl beryllium, hydrogenation dipropyl boron, hydrogenation octyl group magnesium, hydrogenation butyl zinc, hydrogenation dichloro boron, hydrogenation dibromo aluminium and hydrogenation bromine cadmium.The organo-metallic cocatalyst compound of general type is known in the art, and the more complete argumentation of these compounds can all be incorporated herein for reference referring to US3 221 002 and 5 093 415.

The additional activation agent

Other activator comprises those described in the WO 98/07515, and as three (2,2 ', 2 "-nine fluorine xenyls) fluoaluminate/ester, the document all is incorporated herein for reference.The present invention also imagines the combination of activator, and for example aikyiaiurnirsoxan beta and ionization activator combination referring to for example EP-B1-0 573 120, WO94/07928 and WO95/14044 and US5 153 157 and 5 453 410, all is incorporated herein for reference.

Other activator that is fit to is disclosed among the WO98/09996 (being incorporated herein for reference), wherein describes with perchlorate, periodate and iodate to comprise that its hydrate makes the activation of bulky ligand metallocene catalyst compound.WO98/30602 and WO98/30603 (being incorporated herein for reference) describe with (2,2 '-phenylbenzene-two (trimethylammonium) silicic acid) lithium 4THF and make the activator of bulky ligand metallocene catalyst compound.WO99/18135 (being incorporated herein for reference) has described the purposes of organic boron-aluminium activator.EP-B1-0 781 299 describes silicon

The compatible negatively charged ion combination with non-coordinate of salt is used.And, also imagination makes described neutral bulky ligand metallocene catalyst compound or precursor become the activation method of the bulky ligand metallocene cation that can make olefinic polymerization with activation method as utilizing conducts such as radiation (referring to EP-B1-0 615 981, being incorporated herein for reference) and electrochemical oxidation.Be used for making other activator of bulky ligand metallocene catalyst compound activatory or method for example to be described in US5 849 852,5 859 653 and 5 869 723 and WO98/32775, WO99/42467 (two (three (pentafluorophenyl group) borine) benzoglyoxalineization two (octadecyl) ammonium methyl), be incorporated herein for reference.

The another kind of formation ionic active cocatalyst that is suitable for comprises the compatible anionic salt with non-coordination of cation oxidant shown in the following formula:

(OX ^e+) _d(A ^d-) _e (16)

OX wherein ^E+For the cation oxidant of e+ electric charge is arranged; E is 1 to 3 integer; A ^-Define with d such as front.The example of cation oxidant comprises: ferrocene

The ferrocene that alkyl replaces

Ag ⁺, or Pb ^{+ 2}A ^D-Preferred embodiment be the front at defined those negatively charged ion of the activator that contains Bronsted acid, four (pentafluorophenyl group) borate especially.

Catalyst compound can make up with one or more above-mentioned activator or activation method within the scope of the present invention.For example, the combination of activator is described among US5 153 157 and 5 453 410, EP-B1-0573 120, WO94/07928 and the WO95/14044.Aikyiaiurnirsoxan beta all discussed by these documents and the ionization activator uses with the bulky ligand metallocene catalyst compound.

When the positively charged ion of non-coordination anion precursor is Bronsted acid such as proton or protonated Lewis base (outside dewatering) or reducible Lewis acid such as ferrocene Or when silver-colored positively charged ion or basic metal or alkaline earth metal cation such as sodium, magnesium or lithium ion, the mol ratio of catalyst precursor and activator can be arbitrary proportion.The combination of above-mentioned activator compound also can be used for activation.For example three (perfluorophenyl) boron can use with methylaluminoxane.

The selection of transition metal catalyst component

Catalyst system of the present invention comprises two or multiple above-mentioned transistion metal compound.It is 40% or higher crystalline state poly-alpha olefins that at least a compound must be able to produce degree of crystallinity, preferred isotactic polyprophlene or syndiotactic polypropylene.It is 20% or lower amorphous poly alpha-olefin that another compound must be able to produce degree of crystallinity, preferred atactic polypropylene(APP).

The transition metal component that is used for the crystalline state polymer fraction is selected from the subclass of the transition metal component of formula 8-9.This preferred ingredient shown in the formula 17:

Wherein A ', M, X ₁And X ₂Define as the front.Substituting group S " _vBe defined as the S among the formula 8-9 independently ", wherein subscript " v " is represented this substituting group carbon atom on the Cp-ring of bonding with it.

The metallocene precursor that is preferred for producing isotaxy feature enhanced poly-alpha olefins is the metallocene precursor of formula 17, wherein S " _vSelect to make metallocene skeleton 1 independently) do not comprise the symmetrical plane and 2 of metal center) the symmetrical C by metal center arranged ₂-axle.This type of title complex such as racemize-Me ₂Si (indenyl) ₂ZrMe ₂And racemize-Me ₂Si (indenyl) ₂HfMe ₂For known in this field, generally produce tacticity than the higher isotactic polymer of low symmetric chiral system.Similarly, be applicable to that the another kind of preferred transistion metal compound that produces isotactic polymer of the present invention is those disclosed monocyclopentadienyl catalyzer among the US 5 026 798, is incorporated herein for reference.The USSN 60/,418 482 of the detailed description application on October 15th, 1 that catalyst compound that is fit to and catalyzer are selected is incorporated herein for reference.Should be specifically noted that the catalyst compound, catalyst system and the catalyzer that are entitled as description in " selection of transition metal catalyst component " part are right.

Similarly, have the metallocene precursor that tacticity control is provided, wherein (A-Cp) is (Cp) (Cp ^*), Cp and Cp ^*All there is the spatial volume that makes that is positioned on the cyclopentadienyl rings to be enough to limit the substituting group of this cyclopentadienyl ligands rotation to satisfy above-mentioned symmetric condition.Preferred this type of chiral racemic metallocene comprises the two (three ring [5.2.1.0 of dimethyl ^2,6] last of the ten Heavenly stems-2, the 5-dialkylene) close zirconium and-hafnium, dimethyl two ((1R)-9,9-dimethyl three ring [6.1.1.0 ^2,6] last of the ten Heavenly stems-2, the 5-dialkylene) close the two (three ring [5.2.1.0 of zirconium, dimethyl ^2,6] last of the ten Heavenly stems-2,5,8-trialkenyl) close zirconium, the two (three ring [5.2.2.0 of dimethyl ^2,6] 11 carbon-2,5, the 8-trialkenyl) close zirconium and-hafnium, and dimethyl two ((1R, 8R)-7,7,9,9-tetramethyl-[6.1.1.0 ^2,6] last of the ten Heavenly stems-2, the 5-dialkylene) close zirconium and-hafnium.

The metallocene precursor that is preferred for producing syndiotaxy feature enhanced poly-alpha olefins also is the metallocene precursor of formula 17, wherein S " to be selected to make two Cp-parts that visibly different spatial volume be arranged independently.For producing syndiotactic polymer, the form of described Cp-substitution in ring group is very important.Therefore, not being both on potential difference used herein or the space will hint Cp and Cp ^*The difference of space characteristics of ring makes it with respect to A bridging group symmetry but different mutually, control to add polymer chain each in succession monomeric unit near approach.Cp and Cp ^*Potential difference between the ring stops approaching monomer arbitrarily near monomer is added in the polymer chain with the syndiotactic configuration.

Being preferable over the metallocene precursor that produces syndiotactic polymer is the metallocene precursor of formula 17, wherein S " select so that 1 so independently) potential difference between two Cp-parts maximum and 2) still have the C that Cp-encircles in the plane of symmetry by metal center and the formula 17 ₁And C _{1 '}Carbon atom.Therefore, this symmetric title complex such as Me is arranged ₂C (η ⁵-C ₅H ₄) (1-fluorenyl) MMe ₂(wherein M=Ti, Zr or Hf) is preferred, produces tacticity usually than the similar but low higher syndiotactic polymer of symmetric system.In addition, in the following formula, the 1-fluorenyl can be by 3,8-di-t-butyl fluorenyl, octahydrofluorenyl or 3,3,6,6,9,9,12, and 12-prestox-4,4,5,5,10,10,11,11-octahydro dibenzo [b, h] fluorenes replaces.Because the ability of this type of catalyst precursor common polymer tacticity out of hand under the pyroreaction condition, institute thinks that the degree of crystallinity of determining material is higher and need preferably be lower than these catalyzer of use under 80 ℃ the temperature than the low reactor temperature.

The preferred catalyst that can produce the lower molecular weight isotactic polyprophlene is those that describe among the US 5 120 867, is incorporated herein for reference.Can in single reaction vessel or in the tandem reactor configuration, use together and can produce the polyacrylic any catalyst mixture of wanting and comprise that loaded catalyst all can be used for the production scene blend in the present invention.Preferred catalyzer comprises cyclopentadienyl transition metal compounds and the derivative thereof that uses with aikyiaiurnirsoxan beta and/or compatible non-coordination anion.

The polyacrylic catalyzer of other preferably production crystalline state is described in Chem.rev.2000,100, among the 1253-1345, be incorporated herein for reference.

The transition metal component that is used for the amorphous polymer fraction is preferably selected from the monocyclopentadienyl transition metal component of formula 10, and wherein y equals 1.This preferred ingredient shown in the formula 18:

Wherein A ', J, S ', X ₁, X ₂, L ', z and w such as front define, M is a titanium.Substituting group S " _vBe defined as with formula 10 in S " identical, wherein subscript " v " is represented this substituting group carbon atom on the cyclopentadienyl rings of bonding with it, and 0,2 or 4 substituting group S can be arranged on the described cyclopentadienyl rings ", condition is that described cyclopentadienyl is symmetrically substituted.Replace symmetrically and mean described cyclopentadienyl rings 2 and 5 and/or 3 and 4 " base replacements by the approximately uniform S of spatial volume." size of base differs in 2 carbon these S usually each other.Therefore 2 and 5 are considered as symmetric by methyl and ethyl replaces or 3 and 4 are replaced by hexyl and octyl group respectively cyclopentadienyl respectively.Similarly, described cyclopentadienyl rings can be at all four positions all by S " base replaces, as long as symmetric every pair of spatial volume similar then think symmetric.In addition, " base can connect into ring to two adjacent S of 3 and 4, as long as this new ring also is symmetrically substituted.

Known this type of catalyst body ties up to introduces C3 and more generation 2 during high alpha-olefin, 1-mistake.When wherein the catalyst precursor of S ' by 3 ° of carbon and nitrogen ligand (J) bonding (when for example S ' be the tertiary butyl or 1-adamantyl) passes through 1 ° of carbon (for example S ' is normal-butyl, methyl or benzyl) or 2 ° of carbon (for example S ' is cyclo-dodecyl, cyclohexyl or sec-butyl) and nitrogen ligand (J) bonding than S ' 2, the 1-mistake still less.In the main polymer chain 2, the 1-mistake produces (CH ₂) ₂The unit has the polymer performance of being beneficial to.The catalyst system that the sign of this base polymer, this base polymer and being used for is produced this base polymer is described in US5 723 560, is incorporated herein for reference.Change processing condition and for example improve this base polymer that temperature of reactor can produce low Mw.

In addition, in fact some catalyzer that produce the syndiotaxy poly-alpha olefins at a lower temperature will be created in the amorphous poly-alpha olefins under the comparatively high temps under higher reaction temperatures.The transition metal component that is used for this amorphous polymer fraction is selected from the subclass of the transition metal component of formula 8-9.Preferred this type of component shown in the formula 19:

Wherein A ', M, X ₁And X ₂Define as the front.Substituting group S " _vAnd S ' " _vBe defined as the S among the formula 8-9 independently ", wherein subscript " v " is represented this substituting group the Cp-ring of bonding or the carbon atom on the Flu-ring (fluorenyl ring) with it.

The metallocene precursor that is preferred for producing the poly-alpha olefins (when being used as catalyzer under higher temperature of reactor condition) that is mainly the non-crystalline state feature is the metallocene precursor of formula 19, wherein S ' " _vSelect like this that independently described metallocene skeleton is had and comprise metal center and section Flu-and the plane of symmetry of Cp-ring.A ' part needn't symmetry-for example dimetylsilyl or aminomethyl phenyl silyl influence the stereochemistry of the polymkeric substance of producing.Substituting group S ' " _vBe defined as with formula 8-9 in S " identical, wherein subscript " v " is represented this substituting group carbon atom on the cyclopentadienyl rings of bonding with it, and 0,2 or 4 substituting group S ' can be arranged on the described cyclopentadienyl rings ", condition is that described cyclopentadienyl is symmetrically substituted.Replace symmetrically and mean described cyclopentadienyl rings 2 and 5 and/or 3 and 4 " base replacements by the approximately uniform S ' of spatial volume." size of base differs in 2 carbon these S ' usually each other.Therefore 2 and 5 are considered as symmetric by methyl and ethyl replaces or 3 and 4 are replaced by hexyl and octyl group respectively cyclopentadienyl respectively.Similarly, described cyclopentadienyl rings can be at all four positions all by S ' " base replaces, as long as symmetric every pair spatial volume similar then think symmetric.In addition, two adjacent S of 3 and 4 ' " base can connect into ring, as long as this new ring also is symmetrically substituted.Because S on the described fluorenyl ring " _vSubstituent position is far away, and these substituting groups needn't be arranged on the fluorenyl ring symmetrically.Thereby described fluorenyl ring can be replaced by 0-7 substituting group, and these substituting groups can be identical or different." base can randomly connect into ring to two or more adjacent S.

In addition, the compound of available formula 20 is produced the amorphous polymer fraction.

In the case, S " _vSelect so independently to make the metallocene skeleton that the plane of symmetry that sections M and A ' be arranged.Substituting group S " _vBe defined as independently with formula 8-9 in S " identical, wherein subscript " v " is represented this substituting group carbon atom on the cyclopentadienyl rings of bonding with it, and 0 to 4 substituting group S can be arranged on the described cyclopentadienyl rings ", condition is that described cyclopentadienyl is symmetrically substituted.Replace symmetrically and mean described cyclopentadienyl rings 2 and 2 ' and/or 3 and 3 ' and/or 4 and 4 ' and/or 5 and 5 ' " base replacement by the approximately uniform S of spatial volume." size of base differs in 2 carbon these S usually each other.Therefore 2 and 2 ' respectively by methyl and ethyl replaces or 3 and 3 ' be considered as symmetric by the cyclopentadienyl of hexyl and octyl group replacement respectively.Similarly, described cyclopentadienyl rings can be at all four positions all by S " base replaces, as long as symmetric every pair of spatial volume similar then think symmetric.In addition, " base can connect into ring to two adjacent S, as long as this new ring also is symmetrically substituted.This type of title complex such as meso-Me ₂Si (indenyl) ₂ZrMe ₂, meso CH ₂CH ₂(indenyl) ₂ZrCl ₂For known in this field, the general generation is applicable to amorphous polymer of the present invention.

When the catalyzer based on two kinds of transistion metal compounds used in a reactor as hybrid catalyst system, these two kinds of transistion metal compounds should be selected like this so that the two is compatible.The known simple screening method of available those of ordinary skills is as passing through ¹H or ¹³C NMR determines which transistion metal compound is compatible.

The identical activator of preferred use is used for described transistion metal compound, but two kinds of different activators such as non-coordination anion activator and aikyiaiurnirsoxan beta use capable of being combined.If one or more transistion metal compound comprises the X that is not hydrogen root, alkyl or substituted hydrocarbon radical ₁Or X ₂Part then should make aikyiaiurnirsoxan beta contact with transistion metal compound before adding non-coordination anion activator.

Two kinds of transistion metal compounds (catalyst precursor) can any ratio use.(A) preferred molar ratio of producing the transistion metal compound of amorphous polymer and the transistion metal compound of (B) producing crystalline state polymer is at (A: B) in the scope of 1: 1000 to 1000: 1 or 1: 100 to 500: 1 or 1: 10 to 200: 1 or 1: 1 to 100: 1 or 1: 1 to 75: 1 or 5: 1 to 50: 1.Selected ratio depends on selected catalyst precursor, activation method and desired the finished product.In one particular, when using two kinds of catalyst precursors (A-" produces the catalyst precursor of amorphous polymer " and B-" produces the catalyzer of crystalline state polymer "), the two with same activator activatory situation under, preferred mol% (based on the molecular weight of catalyst precursor) compares 1-10%B than 0.5-50%B or 50-99%A than 1-25%B or 75-99%A than 0.1-90%B or 25-99%A for 10-99.9%A.

The catalyst precursor compound of combination and activator generally with about 1: 10000 to the combination of about 10: 1 ratio.When using aikyiaiurnirsoxan beta or alkyl aluminum activator, the catalyst precursor of combination and the mol ratio of activator are 1: 5000 to 10: 1 or 1: 1000 to 10: 1 or 1: 500 to 2: 1 or 1: 300 to 1: 1.When using the ionization activator, the catalyst precursor of combination and the mol ratio of activator are 10: 1 to 1: 10,5: 1 to 1: 5,2: 1 to 1: 2 or 1.2: 1 to 1: 1.Can use multiple activator, comprise the mixture that uses aikyiaiurnirsoxan beta or aluminum alkyls and ionization activator.

In another preferred embodiment, there is the third catalyzer (catalyst precursor+activator) in the said process.The third catalyzer can be the arbitrary of the listed catalyst precursor component of this paper.Preferred the third catalyst precursor comprises those that can produce wax.

Three kinds of transistion metal compounds (catalyst precursor) can use by arbitrary proportion.(A) preferred molar ratio of the polyacrylic transistion metal compound of production non-crystalline state and the polyacrylic transistion metal compound of (B) production crystalline state and the transistion metal compound of (C) producing wax is at (A: B: C) in the scope of 1: 1000: 500 to 1000: 1: 1 or 1: 100: 50 to 500: 1: 1 or 1: 10: 10 to 200: 1: 1 or 1: 1: 1 to 100: 1: 50 or 1: 1: 10 to 75: 1: 50 or 5: 1: 1 to 50: 1: 50.Selected ratio depends on selected catalyst precursor, activation method and desired the finished product.

Other preferred Catalyst And Method is described in US 6 376 410 and 6 380 122, is incorporated herein for reference.

In another embodiment, catalyst composition of the present invention comprises solid support material or carrier.For example, can make one or more catalyst component and/or one or more activator be deposited on one or more carrier, contact, vaporize with one or more carrier to one or more carrier, with one or more carrier bonding, introduce within one or more carrier, absorption or absorb to one or more carrier or on.

Described solid support material is the solid support material of any routine.Preferred described solid support material is a porous carrier materials, for example talcum, inorganic oxide and butter.Other solid support material comprises resin type solid support material such as polystyrene, functionalized or crosslinked organic carrier such as polystyrene divinylbenzene polyolefine or aggretion type compound, zeolite, clay or any other organic or inorganic solid support material etc. or its mixture.

Preferred solid support material is an inorganic oxide, comprises those the 2nd, 3,4,5,13 or 14 family metal oxides.Preferred carrier comprises silicon oxide (can be dehydration or not dehydration), fumed silica, aluminum oxide (WO99/60033), silica-alumina and composition thereof.Other carrier that is suitable for comprises magnesium oxide, titanium oxide, zirconium white, magnesium chloride (US5 965 477), montmorillonite (EP-B1-0 511 665), phyllosilicate, zeolite, talcum and clay (US6 034 187) etc.Also can use the binding substances of these solid support materials, for example silicon oxide-chromium, silica-alumina and silicon oxide-titanium oxide etc.Other solid support material can comprise those porous propylene acids polymkeric substance described in EP 0 767 184B1, is incorporated herein for reference.Other solid support material comprises polymer beads described in spherocrystal described in aerogel described in nano composite material described in the WO99/47598, the WO99/48605, the US5 972510 and the WO99/50311, all is incorporated herein for reference.

The surface-area of preferred described solid support material (most preferably inorganic oxide) about 10 to about 700m ²In the scope of/g, pore volume in about scope of 0.1 to about 4.0cc/g, mean particle size about 5 to the scope of about 500 μ m.More preferably the surface-area of described solid support material about 50 to about 500m ²In the scope of/g, pore volume in about scope of 0.5 to about 3.5cc/g, mean particle size about 10 to the scope of about 200 μ m.Most preferably the surface-area of described solid support material about 100 to about 400m ²In the scope of/g, pore volume in about scope of 0.8 to about 3.0cc/g, mean particle size about 5 to the scope of about 100 μ m.The mean pore size of carrier of the present invention typically 10 to

Scope in, preferred 50 to approximately

Most preferably 75 to about

As known in the art, described catalyzer is carried on a kind of inert support together, described catalyzer is placed on two kinds of inert supports independently mix then.In these two kinds of methods, the former is preferred.

In another embodiment, described carrier can comprise the solid support material of one or more type, and these solid support materials can be through different treatment.For example, can use pore volume different or under differing temps two kinds of different silicon oxide of incinerating.Can use silicon oxide and undressed silicon oxide equally through scavenging agent or other additive treating.

Described stereospecific catalyzer can be used for preparing Mw be 100000 or lower and degree of crystallinity be 20% or the bigger macromonomer that preferably has the vinyl end.

As one of special case, the preparation method based on the macromonomer of propylene that the terminal key percentage of a kind of vinyl is high relates to:

A) propylene is contacted to about 140 ℃ temperature about 80 with the catalyst composition of nonessential a small amount of copolymerisable monomer with the activatory transition metal catalyst compound that comprises described solid rigid; With

B) reclaiming number-average molecular weight is about 2000 to about 30000 daltonian isotaxy or syndiotactic polypropylene chains.

Preferred described solution comprises varsol.More preferably described varsol is aliphatic series or aromatics.And, propylene monomer is contacted under 90 to 120 ℃ temperature.More preferably use 95 to 115 ℃ temperature.Propylene monomer is contacted under 100 to 110 ℃ temperature.Reactor pressure generally can be at normal pressure to 345MPa, preferably change to the scope of 182MPa.Described reaction can intermittence or continuous mode operation.The condition that is applicable to slurry-type reaction also be fit to and also be similar to solution condition, described polymerization is carried out in liquid propene under the pressure that is fit to usually.

The right choice criteria of catalyzer as previously described.A kind of catalyzer normally can produce the stereospecific catalyzer of macromonomer of the ethenyl blocking of high number, and another kind of catalyzer normally can be introduced atactic (aspecific) catalyzer of described reactive macromonomer.It is generally acknowledged that the symmetric bulky ligand metallocene catalyst of C2 can produce the isotactic polyprophlene macromonomer of ethenyl blocking.As if the catalyzer that is beneficial to the Beta-methyl cancellation also be beneficial to usually and form the isotactic polyprophlene macromonomer.Racemize-dimethylformamide dimethyl base silyl-two (indenyls) close hafnium, dichloro-dimethyl silyl-two (2-methyl-4-phenyl indenyl) and close zirconium and racemize-dimethyl ethylidene-two (4,7-dimethyl indenyl) to close hafnium be to produce the catalyzer that is used for the high isotactic polyprophlene of the terminal ratio of vinyl chain of the present invention.As if high temperature (common more than 80 ℃) have favourable influence to ethenyl blocking.Similarly, Me ₂Si (Me ₄C ₅) (N-c-C ₁₂H ₂₃) TiMe ₂And Me ₂Si (Me ₄C ₅) (N-c-C ₁₂H ₂₃) TiMe ₂Generation is applicable to amorphous poly propylene of the present invention, and believes that the macromonomer of introducing ethenyl blocking also is created in the Grafting Structure that the scPP side chain is arranged on the non-crystalline state main chain.

In other embodiments, as 1, the 9-decadiene promotes the aPP of ethenyl blocking and the production of scPP macromonomer, helps to improve the number of branched block kind to reaction zone input diolefine.

Polymerization process

Above-mentioned catalyzer and catalyst system are applicable to solution, body, gas phase and slurry polymerization process or its combination, preferred solution phase or body phase polymerisation process.

In one embodiment, one or more has 3 to 30 carbon atoms, preferred 3 to 12 carbon atoms, more preferably monomeric solution, body, slurry or the gas phase polymerization process of 3 to 8 carbon atoms to the present invention relates to polymerization.Preferred monomer comprises one or more or its combination of propylene, butene-1, amylene-1,4-methyl-amylene-1, hexene-1, octene-1, decylene-1,3-methyl-amylene-1 and cycloolefin.Other monomer can comprise vinyl monomer, diolefine such as diene, polyenoid, norbornylene, norbornadiene, vinyl norbornene, ethylidene norbornene monomer.Preferred homopolymer or the multipolymer of producing propylene.In another embodiment, the multipolymer of one or more of production alfon and propylene and above listed monomer.

The present invention can use the reactor of one or more serial or parallel connection.Catalyst component and activator can solution, dry powder or slurries form are carried, this or send in the reactor respectively and next-door neighbour's reactor before online activation, or pre-activation is pumped in the reactor with activatory solution or slurries form then.A kind of preferred operation is two kinds of solution of online activatory.About in reactor, carrying the more information of the method for multiple catalyzer to see also US 6 399 722 and WO0130862A1.Though these reference may be emphasized Gas-phase reactor, described technology is equally applicable to the reactor of other type, comprises continuous stirred tank reactor (CSTR) and slurry loop reactor etc.Carry out polymerization with single reactor or tandem reactor operation format, in the single reactor operation, monomer, comonomer, catalyzer/activator, scavenging agent and nonessential properties-correcting agent add in the single reaction vessel continuously; In tandem reactor operation, in each of two or more reactor that is connected in series, add said components.Catalyst component can add in first reactor of this series.Described catalyst component also can add in two reactors, and a component adds first reactor and another component adds in other reactor.

In one embodiment, add 500ppm or hydrogen still less or 400ppm or still less or 300ppm or still less in the described polymerization.In other embodiment, add hydrogen or 100ppm or the more or 150ppm or more of 50ppm at least in the described polymerization.

Vapour phase polymerization

Generally speaking, at the gas fluidized bed process that is used for producing polymkeric substance, make to comprise one or more monomeric air-flow and in the presence of catalyzer, under reaction conditions, pass through fluidized bed circulation continuously.Described air-flow is discharged from fluidized-bed, and recirculation is returned in the described reactor.Simultaneously, from reactor, take out polymeric articles and add fresh monomer and replace described polymeric monomer.(, all be incorporated herein for reference referring to for example US4543 399,4 588 790,5 028 670,5 317 036,5 352 749,5 405 922,5 436 304,5 453 471,5 462 999,5 616 661 and 5 668 228.)

Slurry phase polymerisation

Slurry polymerization process generally 1 to about 50 normal atmosphere (15-735psi, 103-5068kPa) or the pressure in the higher scope and under 0 temperature to about 120 ℃ of scopes, operating.In slurry polymerization, monomer and comonomer add in the liquid polymeric diluent media with catalyzer, form the suspensoid of solid particulate shaped polymer.Intermittently or continuously from reactor, discharge the suspensoid that comprises thinner, volatile constituent is separated with polymkeric substance, after distillation, loop back reactor alternatively.Used liquid diluent typically is the alkane of 3 to 7 carbon atoms, the alkane of preferred branched in the described polymerisation medium.Used medium should be liquid and relative inertness under polymerizing condition.When using propane medium, described process is preferably in the critical temperature of reaction diluent with operate more than the pressure.Preferred hexane or the Trimethylmethane medium of using.

In one embodiment, be preferred for polymerization technique of the present invention and be called particle shape polymerization or temperature and remain on the following slurry process of temperature that polymkeric substance enters solution.This technology is known in this field, for example is described among the US3 248 179, is incorporated herein for reference.In the described particle shape method preferred temperature about 50 to about 110 ℃ scope.Two kinds of preferred polymerization processes that are used for slurry process be to use annular-pipe reactor those and use those of stirred reactor of a plurality of series, parallel or its combination.The limiting examples of slurry process comprises continuous endless tube or stirring tank method.Other example of slurry process also is described among the US4 613 484, is incorporated herein for reference.

In another embodiment, described slurry process carries out in annular-pipe reactor continuously.Catalyzer is with Trimethylmethane slurries or free-pouring dry powder form injection ring pipe reactor regularly, and reactor itself is full of the slurries of growth polymerization composition granule in isobutane diluent that comprise monomer and comonomer that circulating.Add hydrogen alternatively as molecular weight regulator.(in the embodiment, add 500ppm or hydrogen still less or 400ppm or still less or 300ppm or still less.In other embodiment, add hydrogen or 100ppm or the more or 150ppm or more of 50ppm at least.)

Reactor remains under the temperature of 3620 to 4309kPa pressure and about 60 to about 104 ℃ of scopes, depends on the melting characteristic of the polymkeric substance of wanting.Remove reaction heat by the endless tube wall, because described reactor major part is the bilayer sleeve form.The low pressure flash vessel, rotatory drier and the nitrogen purging tower that make slurries leave reactor at regular intervals or continuously to enter heating successively are to remove isobutane diluent and all unreacted monomer and comonomer.Then gained is not had hydrocarbon (hydrocarbon free) powder compounding and be used for various application.

In another embodiment, the reactor used energy of slurry process of the present invention produces and the inventive method produces greater than 2000lbs polymkeric substance/hr (907kg/hr), more preferably greater than 5000lbs/hr (2268kg/hr), most preferably greater than 10000lbs/hr (4540kg/hr).In another embodiment, the used slurry-phase reactor production of the inventive method greater than 15000lbs polymkeric substance/hr (6804kg/hr), be preferably greater than 25000lbs/hr (11340kg/hr) to about 100000lbs/hr (45500kg/hr).

In another embodiment, in the slurry process of the present invention total reactor pressure 400psig (2758kPa) to 800psig (5516kPa), preferred 450psig (3103kPa) to about 700psig (4827kPa), more preferably 500psig (3448kPa) extremely about 650psig (4482kPa), most preferably from about 525psig (3620kPa) to the scope of 625psig (4309kPa).

Again in another embodiment, in the slurry process of the present invention the concentration of principal monomer in the liquid reactor medium at about 1 to 100% (weight), preferred about 10 to about 80% (weight), more preferably from about 20 to about 70% (weight), most preferably from about 20 to the scope of about 40% (weight).

Be applicable to that other method of the present invention is not exist or be substantially free of method of operating preferred slurries method under the situation of any scavenging agent such as triethyl aluminum, trimethyl aluminium, triisobutyl aluminium and tri-n-hexyl aluminum and diethylaluminum chloride and dibutyl suffering etc.This method is described among WO96/08520 and the US5 712 352, is incorporated herein for reference.

In another embodiment, the described process of operation under the situation of using scavenging agent.Typical scavenging agent comprises trimethyl aluminium, triisobutyl aluminium, tri-n-octylaluminium, tri-n-hexyl aluminum and excessive aikyiaiurnirsoxan beta or modified alumoxane.

Homogeneous phase, body or solution phase are closed

Catalyzer described herein can be advantageously used in the homogeneous phase solution method.Relate generally to the polymerization in flow reactor, carried out, wherein the polymkeric substance that generates and the monomer that infeeds and catalyzer raw material are stirred to reduce or to avoid concentration gradient.The process that is fit to is wherein used solvent with monomer operating more than the fusing point of polymkeric substance and under the high pressure of 1 to 3000bar (10-30000MPa) as thinner or in solution polymerization.

By with reactor jacket or external heat exchanger or built-in spiral coil cooling tube cooling reactor content, vaporization or three's combination of refrigeration, pre-cold feed, liquid medium (thinner, monomer or solvent) make reactor cooling come equilibrium polymerization heat to obtain the temperature control of reactor automatically.Also can use the adiabatic reactor of pre-cold feed.Temperature of reactor depends on catalyst system therefor.In general, temperature of reactor preferably about 30 and about 200 ℃ between, more preferably from about 90 to about 150 ℃, most preferably from about 100 to about 140 ℃ scope, change.Polymerization temperature can change with selection of catalysts.For example, diimine closes nickel catalyzator and can use down at 40 ℃, and two metallocene-titanium catalysts can use under 100 ℃ or higher temperature.In serial operation, second temperature of reactor is preferably than the first temperature of reactor height.In the parallel reactor operation, the temperature of two reactors is independently.Pressure can about 1mmHg to 2500bar (25,000MPa), preferred 0.1 to 1600bar (1-16,000MPa), most preferably change in the scope of 1.0 to 500bar (10-5000MPa).

These methods also can be used in single reaction vessel, parallel connection or tandem reactor configuration.Described liquid phase method comprises ties up to olefinic monomer and above-mentioned catalyst body to contact in suitable thinner or the solvent and makes the described monomer reaction sufficiently long time to produce the polymkeric substance of being wanted.Varsol (aliphatic series and aromatics) is fit to.Paraffinic hydrocarbons such as hexane, pentane, iso-pentane, hexanaphthene and octane are preferred.

Described process can be carried out in a plurality of reactors of continuous stirred tank reactor (CSTR), batch reactor or plug flow reactor or serial or parallel connection.These reactors can be with or without inner cooling or heating, can make monomer feed cool off or not cool off.Open referring to US 5 001 205 about the generality of processing condition.Also referring to WO 96/33227 and WO 97/22639.All documents all are incorporated herein to describe polymerization process, the selection of metallocene and suitable removing compound.

The invention still further relates to a kind of continuation method for preparing tackiness agent, comprising:

1) make monomer, nonessential solvent, catalyzer and activator combination in reactor assembly,

2) from described reactor assembly, take out polymers soln,

3) if there is solvent, from described polymers soln, remove at least 10% solvent,

4) extinguish reaction,

5) make described polymers soln devolatilization form molten polymer,

6) molten polymer combines (in the preferred embodiment with one or more additive (for example the following stated) as described in mixing tank makes in as static mixer, do not add tackifier or add-on be lower than 30% (weight), preferably be lower than 20% (weight), more preferably less than 10% (weight))

7) described polymer conjugates is taken out from described mixing tank and

8) with described polymer conjugates granulation or rotary drum processing;

Wherein step 1) comprises the arbitrary of aforesaid method.

In another embodiment, the present invention relates to a kind of continuation method for preparing tackiness agent, comprising:

2) from described reactor assembly, take out polymers soln,

4) extinguish reaction,

5) make described polymers soln devolatilization form molten polymer,

6) molten polymer combines with one or more additive as described in mixing tank makes in as static mixer,

7) described polymer conjugates is taken out from described mixing tank and

8) with described polymer conjugates granulation or rotary drum processing.

In one particularly preferred embodiment, the present invention relates to a kind of continuation method for preparing tackiness agent, comprising:

1) be chosen in can produce under the selected polymerizing condition Mw be 100000 or lower and degree of crystallinity be 5% or first kind of catalyst component of lower polymkeric substance;

2) be chosen in can produce under the selected polymerizing condition Mw be 100000 or lower and degree of crystallinity be 20% or second kind of catalyst component of higher polymkeric substance;

3) in solvent neutralization reaction district, under selected polymerizing condition, make described catalyst component in the presence of one or more activator with one or more C _3-40Alkene contacts with nonessential one or more diolefine;

4) be higher than under 70 ℃ the temperature;

5) under residence time of (preferred 60 to 120 minutes) up to 120 minutes;

6) wherein the ratio of first kind of catalyzer and second kind of catalyzer is 1: 1 to 50: 1;

7) activity of wherein said catalyst component is 50kg polymkeric substance/g catalyst component at least; Change into polymkeric substance with at least 20% of wherein said alkene;

8) from described reaction zone, take out polymers soln,

9) from described polymers soln, remove at least 10% solvent,

10) extinguish reaction,

11) make described polymers soln devolatilization form molten polymer,

12) molten polymer combines with one or more additive as described in mixing tank makes in as static mixer,

13) described polymer conjugates is taken out from described mixing tank and

14) with described polymer conjugates granulation or rotary drum processing.

4) be higher than under 70 ℃ the temperature;

5) under 120 minutes or shorter residence time;

7) activity of wherein said catalyst component is 50kg polymkeric substance/g catalyst component at least; Change into polymkeric substance with at least 50% of wherein said alkene;

8) from described reaction zone, take out polymers soln,

9) from described polymers soln, remove at least 10% solvent,

10) extinguish reaction,

11) form molten polymer,

Wherein said polymkeric substance comprises one or more C _3-40Alkene and the ethene that is less than 5mol%, and described polymkeric substance has following feature:

A) some T shape peeling force is 1 newton or higher;

B) branch index of measuring under the Mz of described polymkeric substance (g ') is 0.95 or lower; With

C) Mw is 100000 or lower;

13) described polymer conjugates is taken out from described mixing tank and

14) with described polymer conjugates granulation or rotary drum processing.

4) be higher than under 100 ℃ the temperature;

5) under 120 minutes or shorter residence time;

8) from described reaction zone, take out polymers soln,

9) from described polymers soln, remove at least 10% solvent,

10) extinguish reaction,

11) form molten polymer,

Wherein said polymkeric substance comprises one or more C _3-40Alkene (preferred propylene) and be less than the ethene of 5mol%, and described polymkeric substance has following feature:

A) some T shape peeling force is 3 newton or higher; With

B) branch index of measuring under the Mz of described polymkeric substance (g ') is 0.90 or lower; With

C) Mw is 30000 or lower;

D) the peak value fusing point is between 60 and 190 ℃;

E) melting heat is 1 to 70J/g;

F) 190 ℃ of following melt viscosities are 8000mPas or lower; With

13) described polymer conjugates is taken out from described mixing tank and

14) with described polymer conjugates granulation or rotary drum processing.

1) make the combination in reactor assembly of monomer, catalyzer and activator,

2) from described reactor assembly, take out polymkeric substance,

3) extinguish reaction,

4) form molten polymer,

5) described molten polymer is combined with one or more additive and

6) with described polymer conjugates granulation or rotary drum processing.

The preparation of polymkeric substance

The polymkeric substance that this paper produced can directly form tackiness agent as tackiness agent or with other component compounding.

Tackifier can use with polymkeric substance of the present invention.The example of the tackifier that are fit to includes but not limited to aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, and hydrogenated wood rosin glycerol ester.In some embodiment, make tackifier hydrogenation.

In other embodiment, described tackifier are nonpolar.(nonpolarly mean that described tackifier are substantially free of the monomer with polar group.Preferably there is not polar group, if but have then preferred no more than 5wt%, preferred no more than 2wt% even more preferably no more than 0.5wt%.) in some embodiment, the softening temperature of tackifier (ring and ball softening point is measured by ASTM E-28) is 80 to 150 ℃, preferred 100 to 130 ℃.In another embodiment, described resin is a liquid, and ring and ball softening point is between 10 and 70 ℃.

The amount of tackifier (if exist) is generally about 1 to about 80wt% (based on the weight of blend), more preferably 2 to 40wt% even more preferably 3 to 30wt%.

The hydrocarbon resin that is preferably used as tackifier or properties-correcting agent comprises:

1. such as C5/C6 terpine resin, vinylbenzene terpenes, alpha-methyl styrene terpine resin, C9 terpine resin, aromatic modified C5/C6, aromatic modified cyclic resin, aromatic modified resin or resin such as its mixture based on Dicyclopentadiene (DCPD).Other preferred resin comprises those resins of describing among WO91/07472, US5 571 867, US5 171 793 and the US4 078 132.These resins are obtained by one or more the composition cationoid polymerisation that comprises following monomer usually: C5 diolefine (as 1-3 pentadiene, isoprene etc.); C5 alkene (as 2-methyl butene, cyclopentenes etc.); C6 alkene (as hexene); C9 vinyl-arene (as vinylbenzene, alpha-methyl styrene, Vinyl toluene, indenes, methyl indenes etc.); Cycloolefin (as Dicyclopentadiene (DCPD), methyl bicyclic pentadiene etc.); And/or terpenes (as limonene, carene etc.).

2. the dipolymer of Dicyclopentadiene (DCPD) thermopolymerization and/or cyclopentadiene and/or methyl cyclopentadiene or oligopolymer thermopolymerization gained resin carry out thermopolymerization with vinyl-arene (as vinylbenzene, alpha-methyl styrene, Vinyl toluene, indenes, methyl indenes) alternatively.

Can make polymerization when needing and isolate the gained resin hydrogenation afterwards of unreacted material.The example of preferred resin comprises those resins of describing among US4 078 132, WO91/07472, US4 994 516, EP0 046 344A, EP0 082 726A and the US5 171 793.

In another embodiment, the binder composition that comprises polymeric articles of the present invention also comprises linking agent.Preferred cross-linking agents include can with those of the functional group of acid or anhydride radical reaction.Preferred cross-linking agents comprises alcohol, polyvalent alcohol, amine, diamines and/or triamine.The example that is applicable to linking agent of the present invention comprises polyamines such as quadrol, diethylenetriamine, hexamethylene-diamine, diethylaminopropylamine and/or menthanediamine.

In another embodiment, the binder composition that comprises polymeric articles of the present invention also comprises typical additive known in the art such as filler, antioxidant, auxiliary material, tackifier, oil and/or softening agent.Preferred filler comprises titanium dioxide, lime carbonate, barium sulfate, silica, silicon-dioxide, carbon black, sand, granulated glass sphere, mineral aggregate, talcum and clay etc.Preferred anti-oxidants comprises phenol antioxidant such as Irganox 1010, Irganox 1076, all available from Ciba-Geigy.Preferred oil comprises paraffin or naphthenic oil such as Primol 352 or Primol 876, from ExxonMobil Chemical France, S.A.in Paris, France.Preferred plasticizer comprises polybutene, as Parapol 950 and Parapol 1300, from ExxonMobil Chemical Company in Houston Texas.Other preferred additives comprises adhesion agent, anti, pigment, processing aid, UV stablizer, neutralizing agent, lubricant, tensio-active agent and/or nucleator, also can be present in the one layer or more of film.Preferred additives comprises silicon-dioxide, titanium dioxide, polydimethylsiloxane, talcum, dyestuff, wax, calcium stearate, carbon black, low-molecular-weight resin and granulated glass sphere.Preferred tackifier comprise polarity acid, polyaminoamide is (as the Versamid 115 from Henkel, 125,140), ammonia ester class is (as isocyanic ester/hydroxy-end capped polyester system, tackiness agent TN/Mondur Cb-75 (Miles, Inc.)) for example, coupling agent (as silicon ester (from the Z-6020 of Dow Corning)), titanic acid ester (as Kr-44) from Kenrich, reactive acrylate monomer (as sarbox SB-600) from Sartomer, metal acid-salt (as Saret 633) from Sartomer, polyphenylene oxide, oxidized polyolefin, the polyolefine of acid modification, polyolefine with anhydride modification.

In another embodiment, polymkeric substance of the present invention and the antioxidant that is less than 3wt%, the FLOW IMPROVERS that is less than 3wt%, the crystallization auxiliary that is less than the wax of 10wt% and/or is less than 3wt% combine.

Can be that softening agent or other additive are as oil, tensio-active agent, filler with colour batch etc. is arranged with other selectable components of polymeric articles bonded of the present invention.Preferred plasticizer comprises mineral oil, polybutene and phthalic ester etc.Particularly preferred softening agent comprises phthalic ester such as phthalic acid two different undecyl esters (DIUP), diisononyl phthalate (DINP) and dioctyl phthalate (DOP) (DOP) etc.Particularly preferred oil comprises aliphatic naphthenic oil.

Can with other selectable components of polymeric articles bonded of the present invention be low molecular weight product such as wax, oil or low Mn polymkeric substance (low mean Mn be lower than 5000, preferably be lower than 4000, more preferably less than 3000 even more preferably less than 2500).Preferred wax comprises polarity or nonpolar wax, functionalized waxes, Poly Propylene Wax, polyethylene wax and wax modifiers.Preferred wax comprises ESCOMER ^TM101.Preferred functionalized waxes comprises the wax with modifications such as alcohol, acid, ketone and acid anhydrides.Preferred embodiment comprises the wax with methyl ketone, maleic anhydride or toxilic acid modification.Preferred oil comprises aliphatic naphthenic oil or white oil etc.Preferred low Mn polymkeric substance comprises the polymkeric substance of rudimentary alpha-olefin such as propylene, butylene, amylene and hexene etc.Particularly preferred polymkeric substance comprises that Mn is lower than 1000 polybutene.One of this base polymer example can trade(brand)name PARAPOL ^TM950 available from ExxonMobil Chemical Company.PARAPOL ^TMThe 950th, Mn is that 950 and 100 ℃ of following kinematic viscosity are the liquid polybutylene polymer of 220cSt (measuring by ASTMD 445).In some embodiment, polarity and nonpolar wax one are used from same composition.

But in some embodiment, may not need wax, its amount be lower than 5wt%, preferably be lower than 3wt%, more preferably less than 1wt%, more preferably less than 0.5wt%, based on composition weight.

In another embodiment, in the polymkeric substance of the present invention the total amount of the arbitrary combination of above-mentioned additive be lower than 30wt%, preferably be lower than 25wt%, preferably be lower than 20wt%, preferably be lower than 15wt%, preferably be lower than 10wt%, preferably be lower than 5wt%, based on the weight of polymkeric substance and additive.

In another embodiment, the polymkeric substance that the present invention produces can with elastomer (preferred elastomerics comprises all natural and synthetic rubber, comprises those that define among the ASTM D1566).In one preferred embodiment, the compounding of polymers that elastomerics and the present invention are produced forms rubber toughened composition.In one particularly preferred embodiment, described rubber toughened composition is that wherein rubber is discontinuous phase and described polymkeric substance is two (or many) phase systems of external phase.The example of preferred elastomer comprises following one or more: ethylene-propylene rubber(EPR), ethylene-propylene-diene monomer rubber, chloroprene rubber, styrenic block copolymer rubber (comprise that (S is a vinylbenzene for SI, SIS, SB, SBS, SIBS, SEBS and SEPS etc., I is an isoprene, B is a divinyl, EB is ethene-butylene, and EP is an ethylene-propylene)), isoprene-isobutylene rubber, halogen butyl rubber, iso-butylene and to the multipolymer of ring-alkylated styrenes, iso-butylene-to the ring-alkylated styrenes halogenated copolymers.This blend can with above-mentioned tackifier and/or other additive combination.

In another embodiment, the polymkeric substance that the present invention produces can with the impact copolymer compounding.Impact copolymer is defined as the blend of isotaxy PP and elastomerics such as ethylene-propylene rubber(EPR).In one preferred embodiment, this blend is that wherein impact copolymer is a discontinuous phase and described polymkeric substance is two (or many) phase systems of external phase.

In another embodiment, the polymkeric substance that the present invention produces can with the esters polymer compounding.In one preferred embodiment, this blend is that wherein polyester is a discontinuous phase and described polymkeric substance is two (or many) phase systems of external phase.

In one preferred embodiment, the invention described above polymkeric substance and metallocene PE (mPE) or metallocene polypropylene (mPP) combination.MPE and mPP homopolymer or multipolymer usually with single-or two-cyclopentadienyl transition-metal catalyst and aikyiaiurnirsoxan beta and/or non-coordination anion activator be combined in solution, slurry, high pressure or the gas phase and produce.Described catalyzer and activator can be loading type or non-loading type, and described cyclopentadienyl rings can be replacement or unsubstituted.Several commodity with this type of catalyzer/activator combinations produce can be from ExxonMobil Chemical Company in Baytown, and Texas is with trade(brand)name EXCEED ^TM, ACHIEVE ^TMAnd EXACT ^TMBe purchased.About the more information of the production method of this type of mPE homopolymer and multipolymer and catalyzer/activator referring to WO 94/26816; WO 94/03506; EPA 277,003; EPA 277,004; US 5,153, and 157; US 5,198, and 401; US 5,240, and 894; US 5,017, and 714; CA 1,268, and 753; US5,324,800; EPA 129,368; US 5,264, and 405; EPA 520,732; WO 92 00333; US 5,096, and 867; US 5,507, and 475; EPA 426 637; EPA 573 403; EPA 520 732; EPA 495 375; EPA 500 944; EPA 570 982; WO91/09882; WO94/03506 and US 5,055,438.

In another embodiment, olefin polymer of the present invention, preferred homopolymer polypropylene of the present invention or multipolymer, can with another kind of homopolymer and/or multipolymer compounding, include but not limited to homo-polypropylene, maximum 50wt% ethene or C arranged _4-20(density is 0.915 to being lower than 0.935g/cm for the random copolymers of the propylene copolymer of alpha-olefin, isotactic polyprophlene, height isotactic polyprophlene, syndiotactic polypropylene, propylene and ethene and/or butylene and/or hexene, polybutene, ethane-acetic acid ethyenyl ester, new LDPE (film grade) ³), (density is 0.86 to being lower than 0.90g/cm for linear low density polyethylene, ultra-low density polyethylene ³), (density is 0.90 to being lower than 0.915g/cm to very low density polyethylene ³), (density is 0.935 to being lower than 0.945g/cm to medium-density polyethylene ³), (density is 0.945 to 0.98g/cm to high density polyethylene(HDPE) ³), ethane-acetic acid ethyenyl ester, ethylene-methyl acrylate, acrylic copolymer, polymethylmethacrylate maybe can pass through any other polymkeric substance of high-pressure free radical method polymeric, polyvinyl chloride, polybutene-1, the isotaxy polybutene, ABS resin, elastomerics such as ethylene-propylene rubber(EPR) (EPR), sulfuration EPR, EPDM, elastomer block copolymer such as SBS, nylon (polymeric amide), polycarbonate, the PET resin, crosslinked polyethylene, ethylene-vinyl alcohol copolymer (EVOH), the polymkeric substance of aromatic monomer such as polystyrene, poly--1 ester, density is 0.94 to 0.98g/cm ³High molecular weight polyethylene, density be 0.94 to 0.98g/cm ³Low molecular weight polyethylene, general graft copolymer, polyacrylonitrile homopolymer or multipolymer, polyamide thermoplastic, polyacetal, polyvinylidene difluoride (PVDF) and other fluorinated elastomer, polyoxyethylene glycol and polyisobutene.

In one preferred embodiment, the amount of the preferred polypropylene of the present invention of olefin polymer of the present invention in blend is that 10 to 99wt% (based on the weight of polymkeric substance described in the blend), preferred 20 to 95wt% even more preferably at least 30 to 90wt% even more preferably at least 40 to 90wt% even more preferably at least 50 to 90wt% even more preferably at least 60 to 90wt% even more preferably at least 70 are to 90wt%.

Above-mentioned blend can be produced by the following method: make two or multiple polymers be mixed together, make reactors in series connect to produce reactor blend or in same reactor, use multiple Catalyst Production multiple polymers.Described polymkeric substance was mixed before entering forcing machine or in forcing machine, mix.

Above-mentioned polymkeric substance comprises the arbitrary all functionalisable of polymkeric substance that the present invention produces.Functionalized meaning makes polymkeric substance contact with unsaturated acid or anhydride.Preferred unsaturated acid or anhydride comprises any unsaturated organic compound that contains at least one two key and at least one carbonyl.Typical acid comprises carboxylic acid, acid anhydride, ester and salt thereof (metal and non-metal salt).Preferred described organic compound contains that (C=O) the conjugated ethylenic is unsaturated with carbonyl.Example comprises toxilic acid, fumaric acid, vinylformic acid, methacrylic acid, methylene-succinic acid, Ba Dousuan, tiglic acid and styracin and acid anhydride, ester and salt derivative.Particularly preferred functional group comprises toxilic acid and maleic anhydride.Maleic anhydride is particularly preferred.The amount of unsaturated acid or anhydride is preferably about 0.1 to about 10wt%, preferred about 0.5 to about 7wt% even more preferably from about 1 to about 4wt%, based on the weight of hydrocarbon resin and insatiable hunger acid or anhydride.

In one preferred embodiment, described unsaturated acid or anhydride comprises the carboxylic acid or derivatives thereof, is selected from unsaturated carboxylic acid, is selected from ester, olefinically unsaturated carboxylic acid derivatives or its mixture of imide, acid amides, acid anhydride and cyclic acid anhydride.

Blend described herein can form with routine techniques known in the art.For example available one or more static mixer, on-line mixing device, bend pipe, aperture, baffle plate and any combination thereof realize blend.

There are many methods that are used to make the functionalization of polymers that can use with polymkeric substance described herein this area.Include but not limited to selective oxidation, free radical grafting, ozone decomposition and epoxidation etc.

Use

For the present invention and claims thereof, except as otherwise noted, adopt following test.

Tensile strength, fracture tensile strength and extension at break are measured by ASTM D 1708.Extension at break is also referred to as breaking strain or elongation.

Stripping strength-ASTM D-1876 (being also referred to as 180 ° of peel angle peel adhesion, 180 ° of stripping strengths, 180 ° of peel adhesion, T shape stripping strength, T shape peeling force).

Dynamic storage modulus is also referred to as storage modulus, is G '.

Creep resistance ASTM D-2293.

Spin viscosity PSTC 6.

The following mensuration of hot shearing intensity: the 1000g counterweight is suspended on scribble described polymkeric substance or tackiness agent to adhere to the contact area of 12.5mm * 25mm on the 25mm wide strip of MYLAR polyester film of stainless steel plate.Sample placed in 40 ℃ the draft furnace.The time of record till stress rupture takes place.

Probe tack (being also referred to as the Polyken probe tack) ASTM D 2979.

Cement strength-PSTC 7, are also referred to as shearing resistance bounding force or shearing resistance.

Density-25 ℃ following ASTM D792.

Gardner's colour-ASTM D 1544-68.

SAFT is also referred to as thermotolerance.

Tensile strength modulus under 100% elongation and Young's modulus are pressed ASTM E-1876 and are measured.

Brightness is divided by 100 by the reflectance " Y " in the CIE color coordinate of ASTM D 1925 mensuration.

Needle penetration is pressed ASTM D5 and is measured.

Hang from above and be also referred to as creep.

Bond strength is pressed ASTM D3983 and is measured.

The road surface clinging power is pressed ASTM D4541 and is measured.

Polymeric articles of the present invention or its preparaton can directly be applied on the base material or can be sprayed on the base material, make described polymer melted usually.Polymeric articles of the present invention or its preparaton can directly be applied on the base material or can be sprayed on the base material by runner, roller, nozzle, seam shape die head.Spraying is defined as and comprises atomizing as produce long filament that even point type figure, spiral injection strain as Nordson Controlled Fiberization or vibration as carrying out in from the ITW Dynafiber/Omega heads of Nordson or Summit technology and melt blown technology.Melt blown technology is defined as and comprises method described in the US5 145 689 or utilize air-flow to make the filament breakage of extrudate make the long filament of fracture be deposited into any method on the base material then.In general, melt blown technology is to utilize air spinning hotmelt fiber and be delivered to adherent method on the base material.Ratio that can be by changing melt and air at an easy rate the controlling fiber size at the 20-200 micron.Because of tackiness agent melts and sprays the intrinsic stability of coating machine, (preferably not) produces stray fiber hardly.Bonding with dot pattern regular, level and smooth, expansion under UV light.Atomizing is to utilize air to make hotmelt be atomized into minimum point to be delivered to adherent method on the base material then.

End-use

Tackiness agent of the present invention can be used for any bonding to be used, and includes but not limited to that disposable, packing, laminating material, pressure sensitive adhesive, adhesive tape, label, bonding wood, paper are bonding, non-woven fabrics, road sign and reflective coating etc.

In one preferred embodiment, tackiness agent of the present invention can be used for flexible fastening that disposable diaper and sanitary towel infrastructure, disposable goods carry, packs, labels, bookbinding, wood working and other assembling are used.Particularly preferred application comprises: the packing of the laminated and perishable prod of laminated, the surgical drape of laminated, laminated, the surgical gown that filters mask of the stabilization of laminated, the sanitary towel core of laminated, the diaper elasticity flange of the stabilization of the preceding band of the leg elastic of baby diaper, diaper, the trouser legs flange of diaper, diaper infrastructure, diaper cores, the liquid transfer layer of diaper, diaper outer cover, sanitary towel adhesive tape, industrial filtering bonding, industrial filter material.

Above-mentioned binding agent can impose on any base material.Preferred substrate comprises that timber, paper, card board kai, plastics, thermoplastic material, rubber, metal, tinsel (as aluminium foil and tinfoil paper), metalized surface, cloth, non-woven fabrics (particularly polypropylene spunbond fibers or non-woven fabrics), spun-bonded fibre, card board kai, stone, gypsum, glass (comprise the silicon oxide (SiO that is coated with on the film surface by silicon oxide is evaporated to _x) coating), foam, rock, pottery, film, foam of polymers (as polyurethane foam) and scribble base material or its combination of printing ink, dyestuff, pigment, PVDC etc.

Other preferred substrate comprises polyethylene, polypropylene, polyacrylic ester, acrylic acid or the like, polyethylene terephthalate or the above listed any combination that is suitable for the polymkeric substance of blend.

The arbitrary of above-mentioned base material and/or polymkeric substance of the present invention can handle through Corona discharge Treatment, flame treating, electron beam irradiation, gamma-radiation, microwave irradiation or silanization.

When the tackiness agent that the present invention produces was applied between two adherends with certain form, preferred effect in such a way was so that described material is compared with enough forms with the standard binders of standard specifications or like configurations combines.

Polymeric articles of the present invention can with combination of polymers described in the WO 97/33921 or any adhesive application that replaces wherein said polymkeric substance to be used for wherein describing.

Polymeric articles of the present invention also can be used for forming the hook and eye of describing among the WO 02/35956 separately or with other polymkeric substance and/or additive combination.

The polymkeric substance that the present invention produces can with other composition combined preparation binder composition.Described binder composition can comprise wax, as is selected from polar waxes, nonpolar wax, f-t synthetic wax, the f-t synthetic wax of oxidation, the hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers, amorphous wax, carnauba wax, Viscotrol C wax, Microcrystalline Wax, beeswax, carnauba wax, castor wax, spermaceti, vegetable wax, gama wax, Japan wax, ouricury wax, Pseudotsuga menziesii (Mirbel) Franco bark wax, rice bran wax, jojoba wax, fruit of Grecian Laurel wax, montanin wax, peat wax, ceresine, ceresin(e)wax, petroleum wax, paraffin, polyethylene wax, the chloroflo of chemical modification, the amide waxe that replaces, and combination and derivative.Similarly, described binder composition can comprise and is selected from thioesters, phosphoric acid ester, hindered phenol, four (3-(3 ', 5 '-di-t-butyl-4-hydroxyphenyl) methane propionic acid methylene ester), 2,2 '-ethylenebis (4, the 6-DI-tert-butylphenol compounds), 1,1,3-three (2-methyl-4-hydroxyl-5-tert-butyl-phenyl) butane, 1,3,5-trimethylammonium-2,4,6-three (3,5-di-t-butyl-4-acrinyl) benzene, Tyox B, tetramethylolmethane four (β-lauryl sulfo-propionic ester), alkyl-aryl two-and polyphosphate, thiophosphite, and the antioxidant of combination or derivative.

A. pack

In one particular, tackiness agent of the present invention can be used for packing articles.Described packing articles can be fit to do for example cardboard case, container, crate, chamber, Corrugated Box or pallet.More specifically, the container that packing articles of the present invention can be fit to make tobacco product, cereal product, biscuit product, beer packed, frozen product, paper bag, drinking glasses, milk box, juice box, drinking glasses or be used to transport product, this only is several typical application.

Form described packing articles by applied adhesives composition at least a portion of one or more packaging member.Described packaging member can be formed with hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, film, plastic film, laminating material, sheet material or its arbitrary combination by paper, cardboard, container board, shipping tag.On the one hand, described binder composition can be used for making two or more packaging member bonding or bond together, and wherein said packaging member is formed by the material of identical or different type.Therefore, described packaging member can be formed with hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, film, plastic film, laminating material, sheet material or its arbitrary combination by paper, cardboard, container board, shipping tag independently.One or more packaging member also can be used the coating of paper, tinsel, metal, metal alloy, polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer and combination thereof and multipolymer independently.

Described binder composition comprises polymkeric substance of the present invention described herein and will further describe in the back.Available toxilic acid or maleic anhydride make described functionalization of polymers.Other component can be combined to form binder composition with the preparation of described polymkeric substance or described polymkeric substance.

Clear for ease of describing, below with reference to Fig. 6 and 7 typical packing articles is described in more detail.Fig. 6 illustrates the skeleton view of the cardboard case 600 that is equipped with tackiness agent 605 of the present invention on it at least in part.Cardboard case 600 comprises the sidewall 610 that first end links to each other with diapire 615.Cardboard case 600 also comprise respectively be set to or otherwise with shown in four tabs (flap) 620,625,630 and 635 of linking to each other of second end of each sidewall 610.Tackiness agent 605 is arranged on one or more of tabs 620,625,630,635 at least in part, thereby when tabs was amounted to, tackiness agent contact and adhesion tabs formed sealed vessel shown in Figure 7.

Fig. 7 is that sealing forms encloses container 700 skeleton view of cardboard case 600 afterwards.As seen, tabs 620 and 630 folds to bottom surface 615.Tabs 630 and 635 also folds and is supported on adjacent tabs 620 and 630 to bottom surface 615.The tackiness agent 605 that is arranged on the tabs 635 makes tabs 635 adhere to tabs 625, forms encloses container 700.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can be aliphatic hydrocarbon resins for example, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise one or more tackifier of 1 to 60% (weight).More preferably described binder composition comprises 1 to 40% (weight), 1 to 20% (weight) most preferably.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise one or more wax that is less than 30% (weight).More preferably described binder composition can comprise and be less than 15% (weight).

Again on the other hand, described binder composition can comprise and is less than 30% (weight), is less than 20% (weight), is less than 10% (weight) or is less than one or more additive of 5% (weight).Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.Typical softening agent can comprise for example mineral oil, polybutene, phthalic ester and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical oil can comprise aliphatic naphthenic oil, white oil, its combination and derivative thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer (comprising the acrylic acid alkyl ester polymer) of diolefine.

Described binder composition is mixed with solidification value and is-20 to 250 ℃ for-20 to 250 ℃ and open temperature.Described binder composition also should have under 22 ℃ or about room temperature 75 to 100%, preferred 95 to 100% substrate fiber is torn rate.Described binder composition also should have under-20 ℃ or other freezing temp 50 to 100%, preferred 90 to 100% substrate fiber is torn rate.Described binder composition also should have 50 ℃ down 50 to 100%, preferred 95 to 100% substrate fiber tears rate.

It is that 60 ℃ or higher, preferred PAFT are 200 ℃ or lower greater than 1MPa and PAFT that described binder composition also is mixed with under 25 ℃ and 1 radian per second dynamic storage modulus.Described binder composition also should have 70 ℃ or higher SAFT or 200 ℃ or lower SAFT.The viscosity of described binder composition should be 177 ℃ of following 9Pas or lower, preferred 177 ℃ down 0.5 to 2.5Pas.The cloud point of described binder composition should be 275 ℃ or lower, preferred 130 ℃ or lower.

One of representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 25% (weights) and one or more additive of maximum 15% (weights).

Following embodiment further relates to composition described herein or combination.

A. packing articles that comprises binder composition and one or more packaging member, described binder composition comprise and have one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, with Mw be 100000 or lower, wherein said binder composition imposes at least a portion of described one or more packaging member.

The packing articles of B. top A section, wherein said packaging member are selected from paper, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, film, plastic film, laminating material and sheet material.

C. arbitrary section packing articles above, wherein said packing articles is selected from cardboard case, container, crate, chamber, Corrugated Box and pallet.

D. arbitrary section packing articles above, wherein said packing articles is selected from tobacco product, cereal product, biscuit product, beer packed, frozen product, paper bag, drinking glasses, milk box, juice box, drinking glasses and is used to transport the container of product.

E. arbitrary section packing articles above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of composition.

F. arbitrary section packing articles above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

G. arbitrary section packing articles above, wherein said binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

H. arbitrary section packing articles above, wherein said binder composition comprise 30% (weight) or still less or 15% (weight) or one or more wax still less.

I. arbitrary section packing articles above, wherein said binder composition comprises one or more tackifier of 1 to 60% (weight) or 1 to 40% (weight) or 1 to 20% (weight).

J. arbitrary section packing articles above, wherein said binder composition comprise 30% (weight) or still less or 20% (weight) or still less or 10% (weight) or still less or 5% (weight) or still less or 3% (weight) or still less or 1% (weight) or still less or 0.5% (weight) or one or more additive still less.

K. arbitrary section packing articles above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

L. arbitrary section packing articles above, the setting time of wherein said polymkeric substance is 30 minutes or shorter.

M. arbitrary section packing articles above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

N. arbitrary section packing articles above, the substrate fiber rate of tearing of wherein said binder composition are 22 ℃ following 75 to 100%, preferred 95 to 100%.

O. arbitrary section packing articles above, the solidification value of wherein said binder composition is-20 to 250 ℃.

P. packaged goods comprise the goods that are encapsulated at least in part in the top arbitrary section packing articles.

Q. arbitrary section packing articles above, wherein said packaging member are independently with paper, tinsel, metal, metal alloy, polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer and combination thereof and multipolymer coating.

R. the preparation method of a packing articles comprises forming including one or more C _3-40The binder composition of the polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With described binder composition is imposed at least a portion of packaging member.

B. disposable

In one particular, tackiness agent of the present invention can be used for disposable." disposable " used herein means the article of not wanting to prolong use.The typical life of disposable can be in any given time and once uses to the repeatedly use that continues several seconds to a couple of days even several weeks or longer time.Usually make on the first disposable member at least a portion with binder composition and form disposable attached to the second disposable member.Perhaps make on a part another part of disposable member and form disposable attached to this disposable member with binder composition.Disposable member can be by supatex fabric, non-woven webs, non-elastic nonwoven, elastic nonwovens, shrink the laminating material of bonding (necked-bonded), strain the laminating material of bonding (stretch-bonded), spunbond-as to melt and spray-the spunbonded type laminating material, polypropylene spunbond layer, polyethylene layer, composite polyethylene and polypropylene spunbond layer, elastic wire, styrene-isoprene-phenylethene, styrene-butadiene-styrene, styrene-ethylene/propylene-styrene, vinylbenzene-altogether-butadiene-styrene, urethane, Woven fabric, polypropylene, polyester, the back sheet of not saturating body fluid, not saturating body fluid layer, the permeable mass liquid layer, the skin of infiltration body fluid, absorption agent, tissue paper, resilient material, super absorbent polymer, polyolefin film, polyester film, polychloroethylene film, polyvinylidene chlorida film, the polyvinyl acetate film, the flexible fastening adhesive tape, preceding tape backing, timber, paper, barrier film, film laminate, non-woven composite, textile material, weaving material, durable fabrics, absorption agent, the elastica material, elastic webs, tissue paper, film, cladding material, non-woven polyethylene, porous polyethylene, super absorbent polymer, long filament, the multiporous fiber net, fiber, the latch closure material, the spunbonded type non-woven fleece, lining, elastomeric side panels, fixation adhesive tape, elastic tape, regenerated fiber, nylon, the cellulose paper dregs of rice, cellulose villus, the superabsorbent cotton-wool, or it is combined to form.Described disposable member can have any thickness and can change along its cross section, depends on its intended application.Under some situation, described thickness can be at micron to the scope of rice.Preferred thickness at micron to the scope of millimeter.

Typical disposable can comprise diaper, training pants, sanitary towel, pantiliner, incontinence garments either, mattress, surgical gown, surgical drape, mousetrap, hook and eye, clothes, medical clothes, swim suit or its combination.

Described binder composition comprises polymkeric substance of the present invention described herein.Available toxilic acid or maleic anhydride make described functionalization of polymers.Other component can be combined to form binder composition with the preparation of described polymkeric substance or described polymkeric substance.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 70% (weight) or one or more tackifier still less.Preferred described binder composition comprises one or more tackifier of 40% (weight), 20% (weight) or still less most preferably.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise one or more wax of 30% (weight).More preferably described binder composition can comprise one or more wax of 5% (weight).

Again on the other hand, described binder composition can comprise 30% (weight) or one or more additive still less.More preferably described binder composition comprises 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, solvent, nucleator, tensio-active agent, sequestrant, jelling agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.

Typical oil can comprise aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.On the one hand, described binder composition can comprise one or more softening agent of 30% (weight).

Typical antioxidant comprises three (di-t-butyl-to acrinyl)-Three methyl Benzene, alkylation bis-phenol, zinc dibutyl dithiocarbamate, 4,4 '-methylene-bis (2, the 6-DI-tert-butylphenol compounds), four [methylene radical (3,5-di-t-butyl-4-hydroxyl hydrogenated cinnamate) methane], thio-2 acid lauryl stearyl, 3,3 '-thiodipropionate dilauryl, 2,6 ditertiary butyl p cresol and combination thereof or derivative.On the one hand, described binder composition comprises 2% (weight) or one or more antioxidant still less.

Typical stablizer comprises hindered phenol, thiophenol, phosphorated phenol, 1,3,5-trimethylammonium-2,4,6-three (3,5-di-t-butyl-4-acrinyl) benzene, four-3-(3,5-di-t-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester, 3-(3,5-di-t-butyl-4-hydroxyphenyl) propionic acid Octadecane base ester, 4,4 '-methylene-bis (4-methyl-6-tert butyl phenol), 4,4 '-thiobis (6-tert-butyl o cresols), 2, the 6-DI-tert-butylphenol compounds, 6-(4-hydroxyl phenoxy group)-2, two (the positive hot sulfenyls)-1,3 of 4-, the 5-triazine, 2,4,6-three (4-hydroxyl-3,5-di-t-butyl-phenoxy group)-1,3, the 5-triazine, 3,5-di-t-butyl-4-acrinyl phosphonic acids two Octadecane base esters, 3,5-di-tert-butyl-4-hydroxybenzoic acid 2-(positive hot sulfenyl) ethyl ester, six (3,3,5-di-t-butyl-4-hydroxyphenyl) the propionic acid sorbitol ester, and combination or derivative.On the one hand, described binder composition comprises one or more stablizer of 0.1 to 3% (weight).

It is that 30 ℃ or higher, preferred PAFT are 30 to 110 ℃ that described binder composition is mixed with PAFT.Described binder composition also should have 50 ℃ or the highest 200 ℃ higher and preferred SAFT.The brookfield viscosity of described binder composition should be 177 ℃ of following 25000mPas or lower, preferred 177 ℃, and down 50 to 10000mPas, more preferably 177 ℃ down 50 to 7000mPas.The second-order transition temperature of described binder composition should be-65 to 25 ℃.In one preferred embodiment, 0.69MPa, preferred 1.38MPa at least also should be arranged under 25 ℃ at least described binder composition or more preferably the fracture tensile strength of 3.45MPa and 25 ℃ are at least 300,500 or 800% strained elongation of raw footage down at least.In another embodiment, the cloud point of described binder composition is 200 ℃ or lower.

In addition, the binder composition in the disposable should have 90 to 625g/cm or 265 to 625g/cm or 15 to 450g/cm stripping strength (pressing ASTM D 1876 measures).In another embodiment, the stripping strength of described binder composition is 90 to 1000g/cm or 200 to 900g/cm.In addition, described disposable should have 30 to 140kPa, the dynamic shear strength as 45 to 70kPa.

In one preferred embodiment, the stripping strength of described binder composition under 40 ℃ greater than 30 minutes, be preferably greater than 1 hour, be preferably greater than 6 hours.In another embodiment, the static stripping strength of described binder composition is 30 minutes to 24 hours, preferred 12 to 24 hours, preferred 6 to 24 hours under 40 ℃.

In another embodiment, the complex viscosity of described binder composition is 50 pools or lower under the shearing rate of 177 ℃ and 1000rad/s.

In another embodiment, the creep resistance of described binder composition is 70% to 95% under 38 ℃.

In one embodiment, described disposable is that two kinds of dissimilar binder composition diapers are arranged.First kind of binder composition can be flexible fastening type tackiness agent, and second kind of tackiness agent can be the structure-type tackiness agent, is sometimes referred to as core and bottom adhesive.It is favourable that described flexible fastening tackiness agent and construction adhesive all use a kind of binder composition, because use two kinds of tackiness agents to bring problem for diaper production person on the same diaper, must guarantee that correct tackiness agent is used for correct melt jar and imposes on the tram of diaper.Therefore, the tackiness agent that can play two class adhesive effects is unusual ideal.

1. flexible fastening tackiness agent

The flexible fastening tackiness agent makes elastomer bonded on disposable member.The trouser legs and/or the waist of diaper have elastic tape, generally include disposable member as being fixed on the elastic tape on the second disposable member, and it is the part that diaper forms leg opening or waist.Described binder composition is used to make elastic tape to be fixed on the second disposable member, the normally liquid-tight impervious barrier of the described second disposable member.The flexible fastening tackiness agent mainly demonstrates higher creep resistance to guarantee elastic tape and do not move with respect to the second disposable component surface or partly or entirely to unclamp under stress.If elastic tape moves or unclamps, the cooperation that caused loss with make troubles, waste, in straitened circumstances, uncomfortable, and the problem of relevant health and safety.

Especially, can form the elastic region by making the centre have the non-resilient non-woven fabrics of at least one elastic wire be bonded together.In this method, described elastic region is the laminate structures that comprises non-woven fabrics base material, at least one elastic wire and hot-melt adhesive composition, and described binder composition makes non-woven fabrics base material and at least one elastic wire bonding mutually.Described non-woven fabrics base material be selected from shrink adherent laminating material, tension adherent laminating material, spunbond-as to melt and spray-the spunbonded type laminating material, polypropylene spunbond layer and with polypropylene spunbond layer compound polyethylene layer or its combination.Described elastic wire is selected from styrene-isoprene-phenylethene, styrene-butadiene-styrene, styrene-ethylene/propylene-styrene, styrene/ethylene-be total to-butadiene/styrene copolymers, urethane and combination thereof.

The other method that forms the elastic region comprises is bonded together elastic non-woven cloth and non-resilient non-woven fabrics.In this method, hot-melt adhesive composition makes the first non-woven fabrics elastic substrate and second non-woven fabrics base material bonding mutually.The described first no cloth spin elastic substrate be selected from shrink adherent laminating material, tension adherent laminating material, polypropylene spunbond layer, with polypropylene spunbond layer compound polyethylene layer, styrene-isoprene-phenylethene wire rod, styrene-butadiene-styrene wire rod, styrene-ethylene/propylene-styrene wire rod, styrene/ethylene-altogether-butadiene/styrene copolymers wire rod and urethane wire rod.Described second non-woven fabrics base material be selected from shrink adherent laminating material, tension adherent laminating material, spunbond-as to melt and spray-the spunbonded type laminating material, polypropylene spunbond layer, with polypropylene spunbond layer compound polyethylene layer, styrene-isoprene-phenylethene wire rod, styrene-butadiene-styrene wire rod, styrene-ethylene/propylene-styrene wire rod, styrene/ethylene-altogether-butadiene/styrene copolymers wire rod and urethane wire rod.

The flexible fastening tackiness agent should be effectively long-time under high peel stress or shearing force under body temperature, makes described adhesive exhibits go out high-peeling strength and high shear strength.

2. construction adhesive

Construction adhesive is used to construct the core and the bottom of diaper.The structure of diaper partly comprises the disposable member of liquid-tight back sheet form and executes the second disposable member of absorbing material form thereon with binder composition.Alternatively, described structure part can comprise the second disposable member of the absorbing material form on the backing layer that imposes on binder composition.

Fig. 6 and 7 illustrates a kind of synoptic diagram of typical diaper 100.Diaper 100 comprises waistband portion 115, shank 120 and bottom 130.Diaper 100 also comprises by binder composition adhesion sublayer 130 liquid-tight backing 125 thereon.Liquid-tight backing 125 is liquid-tight, prevents diaper 100 seepages.The liquid-tight backing is generally plastics or polyolefin film base material.The plastic basis material that is fit to comprises the film that can film forming material be made by polyethylene, polypropylene, polyester such as polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate and other.

Diaper 100 also comprises the fixation adhesive tape 105 that binder composition 110 is arranged above one or more.Binder composition 110 can be by being fixed on identical the forming of binder composition on the backing 125 with making bottom 130, or by different forming.Fixation adhesive tape 105 (illustrating two) is positioned on the outside surface of liquid-tight backing 125 (not shown), and is relative with a side of bottom 130 backing 125 adhered thereto.When diaper 100 was in closed state, fixation adhesive tape 105 contacted with the described opposite side of liquid-tight backing 125 and makes tackiness agent 110 adhere to the described opposite side of liquid-tight backing 125.

Make waistband portion 115 and shank 120 adhere to liquid-tight backing 125 with the first binder composition (not shown).Because waistband portion 115 and shank 120 generally include elastic tape to be fit to the waist and the leg of wearer, therefore described second binder composition is the flexible fastening tackiness agent.

Bottom 130 comprises multilayer, as adhering to the absorption layer 135 of backing layer 140 with the second binder composition (not shown), described second binder composition can by with identical or different the forming of first binder composition.Preferred described second binder composition is the structure-type tackiness agent.Backing layer 140 allows the absorption layer 135 of fluid by entering absorption fluids.Absorption layer 135 generally includes the combination of the cellulose paper dregs of rice or fine hair, superabsorbent cotton-wool or fine hair and super-absorbent material.This tapetum is made to be wrapped in to make in the tissue paper does not usually almost have the fine hair of inherent physical strength to have mechanical integrity.Typically make fine hair, but also available other material forms high-absorbable fine hair or paper dregs of rice layer by forming the fine cellulose fiber.

Described backing layer 140 is usually included in fabric or the nonwoven layer (not shown) that forms on the tissue ply (not shown).Tissue ply can be the loose fiber cellulose sheet of high porosity or rate of permeation.Fabric or nonwoven layer can be made of hydrophilic or hydrophobic fibre component, the flexible material natural or fluid permeable that synthon, regenerated fiber, polyester, polypropylene, polyethylene, nylon or its mixture are made.

On the one hand, described elastic adhesive composition can comprise the wax of the mineral oil of the tackifier of the described polymkeric substance of at least 50% (weight), maximum 50% (weights), maximum 30% (weights), maximum 10% (weights) and the antioxidant of maximum 2% (weights).On the other hand, described elastic adhesive composition can comprise the wax of the mineral oil of the tackifier of the described polymkeric substance of at least 75% (weight), maximum 50% (weights), maximum 20% (weights), maximum 5% (weights) and the antioxidant of maximum 2% (weights).Again on the other hand, described elastic adhesive composition can comprise the wax of the mineral oil of the tackifier of the described polymkeric substance of at least 80% (weight), maximum 50% (weights), maximum 30% (weights), maximum 10% (weights) and the antioxidant of maximum 2% (weights).

On the one hand, described structural adhesive composition can comprise the wax of the mineral oil of the tackifier of the described polymkeric substance of at least 50% (weight), maximum 50% (weights), maximum 30% (weights), maximum 10% (weights) and the antioxidant of maximum 2% (weights).On the other hand, described structural adhesive composition can comprise the wax of the mineral oil of the tackifier of the described polymkeric substance of 75 to 95% (weights), maximum 50% (weights), maximum 20% (weights), maximum 5% (weights) and the antioxidant of maximum 2% (weights).Again on the other hand, described structural adhesive composition can comprise the wax of the mineral oil of the tackifier of the described polymkeric substance of at least 80% (weight), maximum 50% (weights), maximum 30% (weights), maximum 10% (weights) and the antioxidant of maximum 2% (weights).

A. disposable that comprises binder composition and disposable member, described binder composition comprise and have one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, with Mw be 100000 or lower, wherein said binder composition imposes at least a portion of described disposable member.Described disposable member can be selected from supatex fabric, non-woven webs, non-elastic nonwoven, elastic nonwovens, shrink the adherent laminating material, tension adherent laminating material, spunbond-as to melt and spray-the spunbonded type laminating material, polypropylene spunbond layer, polyethylene layer, composite polyethylene and polypropylene spunbond layer, elastic wire, styrene-isoprene-phenylethene, styrene-butadiene-styrene, styrene-ethylene/propylene-styrene, vinylbenzene-altogether-butadiene-styrene, urethane, Woven fabric, polypropylene, polyester, the back sheet of not saturating body fluid, not saturating body fluid layer, the permeable mass liquid layer, the skin of infiltration body fluid, absorption agent, tissue paper, resilient material, super absorbent polymer, polyolefin film, polyester film, polychloroethylene film, polyvinylidene chlorida film, the polyvinyl acetate film, the flexible fastening adhesive tape, preceding tape backing, timber, paper, barrier film, film laminate, non-woven composite, textile material, weaving material, durable fabrics, absorption agent, elastic wire, elastic webs, tissue paper, film, cladding material, non-woven polyethylene, porous polyethylene, super absorbent polymer, long filament, the multiporous fiber net, fiber, the latch closure material, the spunbonded type nonwoven articles, lining, elastomeric side panels, fixation adhesive tape, elastic tape, regenerated fiber, nylon, the cellulose paper dregs of rice, cellulose villus, the superabsorbent cotton-wool, or its combination.

The disposable of B. top A section is as diaper, training pants, sanitary towel, pantiliner, incontinence garments either, mattress, surgical gown, surgical drape, mousetrap, hook and eye, clothes, medical clothes, swim suit or its combination.

C. arbitrary section disposable wherein makes described disposable member adhere to the second disposable member by described binder composition above.

D. arbitrary section disposable above, wherein said binder composition also comprises one or more tackifier.Described tackifier are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, the hydriding terpene of modification, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.

Described binder composition can also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers, chloroflo, petroleum wax, paraffin, synthetic wax, polyolefin-wax and combination or the derivative that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can also comprise one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, tinting material, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, solvent, nucleator, water, stablizer, sequestrant, jelling agent and combination thereof or derivative.

E. arbitrary section disposable above, wherein said binder composition comprises 30% (weight) or one or more wax, 20% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax, 3% (weight) still less or one or more wax, 2% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

F. arbitrary section disposable above, wherein said binder composition comprises 70% (weight) or one or more tackifier, 60% (weight) still less or one or more tackifier, 50% (weight) still less or one or more tackifier, 40% (weight) still less or one or more tackifier, 30% (weight) still less or one or more tackifier, 20% (weight) still less or one or more tackifier, 10% (weight) still less or one or more tackifier, 5% (weight) still less or one or more tackifier or 1% (weight) still less or one or more tackifier still less.

G. arbitrary section disposable above, wherein said binder composition comprises 30% (weight) or one or more additive, 25% (weight) still less or one or more additive, 20% (weight) still less or one or more additive, 15% (weight) still less or one or more additive, 10% (weight) still less or one or more additive, 5% (weight) still less or one or more additive or 1% (weight) still less or one or more additive still less.

H. arbitrary section disposable above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.The setting time of described polymkeric substance is 30 minutes or shorter, and some T shape peeling force is 3 to 4000N or 3 to 400N or 3 to 40N.

I. arbitrary section disposable above, the viscosity of wherein said binder composition are 177 ℃ and descend 0.05 to 25Pas.The cloud point of described binder composition is 200 ℃ or lower, and second-order transition temperature is-65 to 30 ℃.

J. the preparation method of arbitrary section disposable above comprises forming to comprise to have one or more C _3-40The binder composition of the polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With described binder composition is imposed at least a portion of disposable member.

C. laminating material

In one particular, tackiness agent described herein can be used for laminated product.Laminated product is made of the layer or the thin slice that are bonded together by the tackiness agent that is fit to.The material that thin slice normally obtains with the continuous sheet form easily is as paper or fabric.Described tackiness agent is a synthetic resins, mainly is resol, with solvent application or be immersed in the basic thin slice.After the drying, make several sheet stackings, under heating and pressurizing, make whole the merging form hard sheet or the plate that is suitable for its machinery, electricity, chemistry or aesthetic qualities.Utilize electrical property, shock strength, wear resistance or the chemical resistant properties of thin slice in the industry.Be used for electronic application, electric switch, gear etc.Although they have very important effect, seldom attract attention.

Laminated product can be made of the fortifying fibre net that runs through the synthetic resins material matrix.The performance of fibrous reticulum and resin choice decision laminated product, and on degree, determining very much its production method.Term used herein " laminated product " comprises through being heated and/or pressure forms any multi-layer product of multilayered structure.One laminate layers is that usable resins such as following tackifier are handled and by the sheet material that is heated and pressure merges.Typical layer comprises paper, fabric, pad, felt and analogous material.Described layer is continuous web-like normally, but the facing plate is tangible exception.Laminate layers is by form (paper, fabric etc.) or form classification, can be from the absorptivity organic cellulose to the variation of nonabsorbable unorganic glass.Every layer can be thin film layer, dope layer, layer of fibers, foam layer, substrate layer and/or other layer that is fit to independently.Each of laminating material layer can be formed by identical or different material, (comprises the silicon oxide (SiO that is coated with on the film surface by silicon oxide is evaporated to as timber, plastics, paper, rubber, thermoplastic material, card board kai, metal (comprising metal alloy, matrix material, tinsel such as aluminium and tinfoil paper, metalized surface and dynamic vulcanization alloy), cloth, spun-bonded fibre, stone, gypsum, glass _x) coating), rock, pottery, film, foam, non-woven fabrics (especially comprising polypropylene spunbond fibers) and scribble base material and any combination, blend and the mixture of printing ink, dyestuff, pigment, PVDC etc.In addition, every layer thickness can change with intended application.

On the one hand, described layer can comprise following one or more (making up separately or with binder composition described herein).

1. polyolefine

Preferred polyolefine comprises C ₂-C ₄₀Alkene, preferred C ₂-C ₂₀The homopolymer of alkene or multipolymer, the more preferably multipolymer (for the present invention, ethene is defined as alpha-olefin) of alpha-olefin and another kind of alkene or alpha-olefin.Most preferably described polymkeric substance comprise ceridust, homo-polypropylene, with the propylene of ethene and/or butylene copolymerization, with the ethene of one or more and nonessential diene copolymerization of propylene, butylene or hexene.Preferred embodiment comprises thermoplastic polymer such as ultra-low density polyethylene, very low density polyethylene, linear low density polyethylene, new LDPE (film grade), medium-density polyethylene, high density polyethylene(HDPE), polypropylene, isotactic polyprophlene, the height isotactic polyprophlene, syndiotactic polypropylene, the random copolymers of propylene and ethene and/or butylene and/or hexene, elastomerics such as ethylene-propylene rubber(EPR), the Ethylene Propylene Terpolymer diene monomer rubber, chloroprene rubber, with thermoplastic polymer and elastomeric blend for example thermoplastic elastomer and rubber toughened plastics.

2. polar polymer

Preferred polar polymer comprises the homopolymer and the multipolymer of ester, acid amides, acetic ester, acid anhydride, C ₂-C ₂₀The multipolymer of alkene such as ethene and/or propylene and/or butylene and one or more polar monomer such as acetic ester, acid anhydride, ester, alcohol and/or acrylic monomer.Preferred embodiment comprises polyester, polymeric amide, vinyl-vinyl acetate copolymer and polyvinyl chloride.

3. cationic polymers

The preferred cation polymkeric substance comprises the polymkeric substance or the multipolymer of alkene, α-heteroatoms alkene and/or the styrene monomer of paired replacement.The preferred alkene that replaces in pairs comprises iso-butylene, isopentene, iso-heptene, dissident's alkene, isooctene, isodecyl alkene and different dodecylene.Preferred α-heteroatoms alkene comprises Vinyl Ether and vinylcarbazole.Preferred styrene monomer comprises vinylbenzene, ring-alkylated styrenes, to ring-alkylated styrenes, alpha-methyl styrene, chloro-styrene and bromo-p-methylstyrene.The example of preferred cation polymkeric substance comprise isoprene-isobutylene rubber, with iso-butylene, polystyrene and the poly alpha methylstyrene of p-methylstyrene copolymerization.

In addition, every layer of all available toxilic acid or maleic anhydride are functionalized.

For example, described layer can comprise that one layer or more contains the film of the arbitrary and blend of above-mentioned materials, is with or without binder composition described herein.The thickness of every tunic can change, and depends on to use.For example, the thick film of 1 to 250 μ m is fit to laminated product usually, and that the film that is used to pack is generally 10 to 60 μ m is thick.On the one hand, described laminated product can comprise that one layer or more is used to seal another rete of described laminated product or the film of part.The thickness of sealing ply is generally 0.2 to 50 μ m.The internal surface of film or laminated product and outside surface can all have sealing ply, and perhaps described sealing ply can exist only on internal surface or the outside surface.These films can comprise by routine techniques known in the art extrude, either party's method of co-extrusion, squeezing and coating, lamination, blowing and curtain coating makes.

On the one hand, described laminated product comprises two-layer at least with binder composition combination.Described laminated product preferably includes 2 to 70 layers.On the one hand, described laminated product can comprise 2,3,4 or 5 layers.For example, described laminated product can comprise two-layer, and wherein the first layer is a timber, and the second layer is pellicle (veneer film).

Binder composition described herein can be included in the arbitrary layer of laminated product or impose on the interlayer of laminated product.For example, described binder composition can be used as binder couse or binder layer, as on the contact ply of paper.

Described binder composition comprises polymkeric substance of the present invention described herein.Can make described functionalization of polymers.Other component as tackifier, wax and additive can with as described in polymkeric substance or as described in the preparation of polymkeric substance be combined to form binder composition.

On the one hand, described binder composition comprises one or more tackifier.Described tackifier can be aliphatic hydrocarbon resins for example, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise one or more tackifier of 1 to 80% (weight).More preferably described binder composition comprises one or more tackifier of 2 to 40% (weights), 3 to 30% (weights) most preferably.In addition, described one or more tackifier can also be included in the one layer or more.The described layer that comprises tackifier can be on identical or different degree single shaft or diaxial orientation.

On the other hand, described binder composition comprises one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 5% (weight) or one or more wax or 3% (weight) still less or still less or 1% (weight) or still less or 0.5% (weight) or still less.

Again on the other hand, described binder composition comprise 30% (weight) or still less, 25% (weight) or still less, 20% (weight) or still less, 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, fluorescent agent, He Shui.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.

On the one hand, substrate fiber the tear rate of described binder composition under 22 ℃ is 75% to 100%.Under-35 ℃, the substrate fiber rate of tearing of described binder composition is 75% to 100%, is 75% to 100% under 40 ℃.In one embodiment, the release adhesive fail temperature (PAFT) of described binder composition is 50 ℃ or higher, preferred 60 ℃ or higher, preferred 70 ℃ or higher, preferred 75 ℃ or higher.In another embodiment, the shear adhesion fail temperature of described binder composition is 50 ℃ or higher again.In one embodiment, the viscosity of described binder composition is 177 ℃ following 0.2 to 8Pas or 177 ℃ and descends 0.5 to 2.5Pas.In addition, the second-order transition temperature of described binder composition can be-65 to 30 ℃.In another embodiment, the open hour of described binder composition can be 60 seconds or shorter, preferred 3 seconds or longer.In another embodiment, the cloud point of described binder composition is 200 ℃ or lower, preferred 190 ℃ or lower, preferred 130 ℃ or lower.

The exemplary formulations of described polymkeric substance comprises:

One or more additive such as the filler of one or more tackifier and 10% (weight) of 1.80% (weight) or more described polymkeric substance, 20% (weight).

2.95% (weight) or more described polymkeric substance and 5% (weight) or one or more tackifier still less.

3.92% (weight) or more described polymkeric substance, 5% (weight) or one or more tackifier and 3% (weight) still less or more one or more filler.

Described laminated product can be with arbitrary formation of known in the art or the routine techniques found so far.Some typical technology are described below.

In one of furniture or the processing of facing plate example, described lamination process is by handling, put in order (collating) and suppressing and form.In the first step, described layer is contacted with resin solution by dipping or coating; And dry removing desolvated.The material of handling is cut into sheet material makes it stacked abreast; This is called arrangement.Applying heat and pressure makes described sheet material be merged into permanent adhesive and insoluble monoblock; This step is called pressing or mold pressing.Finishing operations is finished this process.

Perhaps, can obtain laminated product, can carry out in the plane of film single shaft direction or two orthogonal directions then and be orientated by flat film or tubular processing.The one layer or more of described laminated product can be horizontal and/or machine-direction oriented on identical or different degree.This orientation can take place before or after each layer combined.For example, can or be laminated on the oriented polypropylene layer or polyethylene and polypropylene co-extrusion film forming can be orientated then the polyethylene layer squeezing and coating.Similarly, oriented polypropylene can be laminated on the orientation polyethylene or will be orientated polyethylene and be applied on the polypropylene then and further be orientated together alternatively.Typically make described film with the highest by 15, preferred vertical (MD) orientation of the ratio between 5 and 7, with horizontal (TD) orientation of the highest by 15, preferred 7 to 9 ratio.But in another embodiment, laminated product is orientated to same degree at MD and TD direction.

Above-mentioned laminated product can be used as stretching and/or is close to film.The film that stretches/be close to is used for bundling, packing and piling and stacks operation.For making film have cling property or improving cling property, can utilize many known adhesion promoting additives.Also can improve the sliding resistance of film by the known physical method that is called corona discharge.Some polymkeric substance (as ethylene-methyl acrylate copolymer) does not need the antiskid additive, can not have under the situation of tackifier as being close to layer.The film that stretches/be close to can comprise and contains particularly C of any suitable polyolefine or polyolefine such as polyethylene, polypropylene, ethylene-propylene copolymer and ethene and/or propylene and a small amount of other alkene _4-12The smooth layer of the composition of olefin-copolymerization resulting polymers.Particularly preferably be polypropylene and linear low density polyethylene (LLDPE).The polypropylene that is fit to is normally solid-state and isotactic, and the instant heating heptane insolubles is greater than 90%, 0.1 to about 300g/10min the wide melt flow rate (MFR) scope of having an appointment.In addition, smooth layer can comprise one or more anti stick (smooth and/or anti) additive, can add in producing the polyolefine process or sneak into subsequently to improve the smooth property of this layer.Examples of such additives is known in this field, comprises for example silicon oxide, silicate, diatomite, talcum and various lubricant.The consumption of these additives preferably in about scope of 100 to about 20000ppm, more preferably between about 500 to about 10000ppm (weight), based on the weight of smooth layer.When needing, smooth layer can also comprise one or more other additive as mentioned above.

Described laminated product also can be used for for example facing plate, counter top, clothes, window processing and furniture etc.The National Electrical Manufacturers Association (NEMA) discloses about industry and the performance of decorative laminate and the complete information of testing method.For example, laminated product can comprise following laminated product:

The copper facing laminating material.Use one or both sides to be stained with X, XXP, XXXPC, FR-2, FR-3, FR-4, FR-5, FR-6, G-10, G-11, CEM-1 and the CEM-3 level laminating material of Copper Foil, be mainly used in printed-wiring board (PWB) but be not used in multiplication circuit (multiplayer) and use.

Epoxy-glass laminates.Make the woven fiber glass curing of the epoxy resin-impregnated of semicure attitude make each circuit layer of multiplication circuit printed-wiring board (PWB) bonding.

Polyester-glass laminates.GPO-1, GPO-2 and GPO-3 level polyester glass fiber felt veneer sheet are used for machinery and electricity is used.

In one specific examples, laminated product is following to be made:

Binder composition imposed between the first layer and the second layer and the second layer and the 3rd layer between form three stampings layer by layer, wherein said binder composition comprises 95% (weight) polymkeric substance and 5% (weight) tackifier.

In another specific examples, laminated product is following to be made:

Binder composition imposed on form 6 stampings layer by layer between 6 layers every layer, wherein said binder composition comprises 92% (weight) polymkeric substance, 5% (weight) tackifier and the exfoliate clay of 3% (weight).

One imaginary example comprises forming to decorate uses laminated product.Handle the painted alpha-cellulose decorative paper of a volume with melamine-formaldehyde reaction product and prepare panel, the weight of this paper is about 69lb/3000ft ³The gauze that delivery is so made on contrary roll-coater carries out resin impregnation (using binder composition described herein) and reaches 55% resin content by air knife metering resin then.Making gauze then is 6% at baking oven inner drying to the volatile content of treatment unit, therefrom cuts out the sheet length of wanting.The viscosity of preferred described binder composition is 0.05Pas.The multilayer colored solid layer pressing plate of the decorative sheet of the first layer and the decorative sheet that comprises aluminium foil barrier film, melamine process, central layer that vinyl ester is handled and melamine process is merged, and be 1 hour total set time.

A. one kind comprises and binder composition bonded two or multiwalled laminated product, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.Described binder composition can be present between the one layer or more.In one embodiment, described two or multilayer comprise one of at least and be selected from one or more material of timber, plastics, paper, rubber, thermoplastic material, card board kai, metal, tinsel, metalized surface, cloth, non-woven fabrics, spun-bonded fibre, stone, gypsum, glass, rock, pottery, film and foamy.In another embodiment, described laminated product comprises that more than two-layer wherein every layer is independently selected from timber, plastics, paper, rubber, thermoplastic material, card board kai, metal, tinsel, metalized surface, cloth, non-woven fabrics, spun-bonded fibre, stone, gypsum, glass, rock, pottery, film and foam.

The laminated product of B. top A section also comprises one or more tackifier.Described one or more tackifier can be selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, the hydriding terpene of modification, hydrogenated wood rosin glycerol ester, its derivative, and composition.

The laminated product of top A or B section can also comprise one or more wax.Described one or more wax is selected from f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

Described laminated product can also comprise one or more additive.Described additive is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, He Shui.Described one or more oil comprises aliphatic naphthenic oil, white oil, its combination and derivative thereof.Described one or more polymeric additive is selected from the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Described one or more softening agent is selected from mineral oil, polybutene, phthalic ester and combination thereof.Described one or more phthalic ester comprises phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.

The laminated product of C. top B section, wherein said binder composition comprise 5% (weight) or one or more wax still less, one or more tackifier and 30% (weight) of 1 to 90% (weight) or one or more additive still less.

D. arbitrary section laminated product above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.The setting time of described polymkeric substance is 30 minutes or shorter, and some T shape peeling force is 3 to 4000N.

E. arbitrary section laminated product above, the viscosity of wherein said binder composition are 177 ℃ and descend 0.2 to 8Pas.The point T shape peeling force of described binder composition is 3 to 4000N.

F. the diaper that comprises top arbitrary section described laminated product.

G. the preparation method of arbitrary section laminated product comprises that the two-layer at least form layers stampings that combine with binder composition, described binder composition are comprised has one or more C above _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.98 or lower and Mw be 100000 or lower.

D. non-woven fabrics/fiber

In one particular, tackiness agent of the present invention can be used for fiber product.Fiber product is made of the top filamentary material that scribbles binder composition.Described filamentary material can comprise monocomponent fibre, multicomponent fibre or its combination.Available a few fiber material forms fiber product, generally distinguishes based on the fibrous tissue in the fiber product.For example, a fiber material is the isotropy assembly, and wherein each fiber is fully randomly arranged, and does not have preferred orientation in the either direction of three principal space axles.Another example of filamentary material is the weaving yarn, and the fibre orientation of height is arranged with respect to the main shaft of described material.Weaving is produced by the combination process step that is referred to as spinning by staple fibre (finite length) with yarn.After the preliminary fibre orientation, make fiber interweaving form spun yarn prolongation and uniform basically by twisting together.Usually form fabric with yarn, by braiding or knitting.

Described filamentary material can comprise cotton, kapok, coir, flax, hemp, ramie, jute, sisal hemp, abaca, Mierocrystalline cellulose, wool, mohair, cashmere, hair, common goathair, Pilus Cameli, llama hair, Aloysia gratissima alpaca, vigone (vicun) hair, silk, nylon, aromatic poly, Kev draws, Nomex (Nomex nylon), polymeric amide, polyacrylic ester, polyolefine is (as propylene, butene-1, polyethylene, polypropylene and ethane-acetic acid ethyenyl ester), polyester is (as polyethylene terephthalate, polybutylene terephthalate and poly-hydroxy-benzoic acid second diester (poly-ethyleneoxybenzonate)), asbestos, polymeric amide, polycarbonate, polystyrene, thermoplastic elastomer, fluoropolymer, the vinyl based polymer, mineral, acrylic acid or the like, polyvinyl chloride, organic binder bond, glass, metal, aluminum oxide, silicon carbide, boron nitride, norbide, and combination.

Typical fiber product comprises non-woven fabrics, carpet, diaper, swim suit, child's training pants, the adult-incontinence clothes, feminine care products, medical clothes, mattress, surgical drape, the cloth lining, scouring pad, the automotive interior member, clothes, adhesive tape, face shield and respirator, air filter, vacuum bag, oil and chemical leakage absorption agent, thermal insulation, first aid dressing, medical binder, fiberfill, coat, the cotton-wadded quilt stopping composition, the furniture liner, filtration medium, scouring pad, Wiping material, and combination.

" non-woven fabrics " used herein means the textile materials of producing by the means except that weaving.In the non-woven fabrics, fiber directly is processed into plain film shape woven fabric structure through middle one dimension yarn conditions, obtains the bonding fabric by chemical adhesion or mechanical interlock (or the two) then.Nonwoven articles can comprise natural or synthon or its mixture.The material that is used to form nonwoven articles comprises regenerated fiber, polyester, polypropylene, polyethylene and nylon etc.Single fiber is staple fibre or continuous filament yarn normally.Typical fiber can comprise polypropylene fibre, regenerated fiber, trevira, polyethylene fibre, nylon fiber, cellulosic fibre, viscose fiber, the ethylene-propylene copolymer fiber, polyolein fiber, tynex, polycarbonate fibre, styroflex, thermoplastic elastomer fiber, fluoropolymer fibers, vinyl based polymer fiber, carbon fiber, glass fibre, mineral fibre, wool fiber, acrylic fiber, thermovyl, polyurethane fiber, the organic binder bond fiber, and combination.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 80% (weight) or one or more tackifier or 60% (weight) still less or 40% (weight).More preferably described binder composition comprises one or more tackifier of 30% (weight).

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 30% (weight) or still less or 25% (weight) or still less or 20% (weight) or one or more wax still less.More preferably described binder composition comprises 15% (weight) or still less or 10% (weight) or still less or one or more wax of 5% (weight).

Again on the other hand, described binder composition can comprise 90% (weight) or still less or 30% (weight) or still less or 25% (weight) or still less or 20% (weight) or one or more additive still less.More preferably described binder composition comprises 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.

On the one hand, substrate fiber the tear rate of described binder composition under 22 ℃ is 75% to 100%.On the other hand, the PAFT of described binder composition is 60 ℃ or higher, and preferred, the PAFT of described binder composition is 150 ℃ or higher.Again on the other hand, the SAFT of described binder composition is 70 ℃ or higher.Described binder composition can also have under 25 ℃ the fracture tensile strength of 6.89bar at least.On the one hand, the viscosity of described binder composition is to be lower than 9Pas under 177 ℃.The viscosity of preferred described binder composition is 177 ℃ and descends 0.2 to 8Pas.More preferably the viscosity of described binder composition be 177 ℃ down 0.5 to 2.5Pas.On the other hand, the cloud point of described binder composition is 275 ℃ or lower.The cloud point of preferred described binder composition is 190 ℃ or lower.More preferably the cloud point of described binder composition is 130 ℃ or lower.Again on the other hand, the second-order transition temperature of described binder composition is-65 to 30 ℃.

A kind of representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 80% (weights), maximum 30% (weights) and one or more additive of maximum 30% (weights).Another representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 50% (weights), maximum 10% (weights) and one or more additive of maximum 10% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 80% (weights), maximum 10% (weights) and one or more additive of maximum 10% (weights).

Fiber product can be made by any method known in the art, for example comprise that melt-spun, dry-spinning, wet spinning, thermal-setting, heat are loose, twist, interweave, boundling, curl, melt and spray, spunbond, air-laid, bonded carded fibrous web method and cutting.For example, binder composition can be extruded onto one or plurality of fibers on form fiber product or binder composition be applied to and make plurality of fibers (filamentary material) formation fiber product attached to it on the base material.

In one example such as the melt-spun, described method comprises forces molten polymer to make molten polymer solidify the driven roll that arrival is pulled away from fiber spinning jet by the pore in the spinning jet and by freezing air.

In another example, the pine assembling fibrous reticulum that floods each fiber with binder composition forms nonwoven articles, and mildly heating makes the fibrous reticulum drying then.This mildly heating also plays the binder composition solidified effect that makes.Fiber and binder composition are heated to the temperature that is enough to described binder composition is softened but still is lower than the fiber fusing point.Described original fibers net can be by being used to that fiber is made with the form deposition of net or layer or arbitrary routine techniques of arranging.These technology comprise combing, garnetting and air-laid.Also can make each fibrous reticulum of one or more formation by these technology or thin layer overlap joint or lamination form thick-layer to be transformed into heavy weight fabric.In general, fiber is extending simultaneously mutual crossover with a plurality of different directions of principal plane aligned, is intersecting and support formation open-celled structure.

Fibrous reticulum one of at least is anchored on each fiber in several latex bonded operations and forms the self-supporting fibrous reticulum together then.Some known adhesive bonding methods are the intermittence of the binder composition that extends across fibrous reticulum and also extend along fibrous reticulum when needing with general horizontal or diagonal or overall dipping, spraying or the printed web in successive straight line or wavy line or zone.

One of the binder composition representative formula that is applicable to nonwoven articles comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 80% (weights), maximum 30% (weights) and one or more additive of maximum 30% (weights).Another representative formula that is applicable to the binder composition of nonwoven articles comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 50% (weights), maximum 10% (weights) and one or more additive of maximum 5% (weights).

Above-mentioned fiber product can be used as the furniture of clothes, hosiery, swim suit, foundation garment, underwear, medical treatment product, parachute, golf ball, vehicle seat and dress cushion.

Nonwoven articles is applicable to preparation surgical drape, women sanitary articles, incontinence garments either, diaper, training pants, swim suit, medical clothes, coat, cotton-wadded quilt stopping composition, furniture liner, filtration medium, scouring pad, cloth lining, automotive interior member, face shield and respirator, vacuum bag, oil and chemical leakage absorption agent, thermal isolation, first aid dressing, medical binder, Wiping material and other products.The non-woven fabrics of described nonwoven articles or fibrous reticulum can comprise for example diaper, swim suit, child's training pants, the adult-incontinence clothes, feminine care products, medical clothes, mattress, surgical drape, the cloth lining, scouring pad, the automotive interior member, clothes, adhesive tape, face shield and respirator, air filter, vacuum bag, oil and chemical leakage absorption agent, thermal insulation, first aid dressing, medical binder, fiberfill, coat, the cotton-wadded quilt stopping composition, the furniture liner, filtration medium, scouring pad, Wiping material, and combination.

Tufted carpet is generally composite structure, wherein form pile for example the yarn of carpet surface pass base fabric, thereby make every bunch base run through base fabric and can see in the bottom surface of base fabric.Tufted carpet generally has two types.First kind is called " fine hair " (nap) carpet, and wherein the successive yarn passes base fabric and forms yarn coil, thereby forms the substrate of carpet, and the top of coil can reach 1/4 to 3/4 inch long, thereby forms the wearing surface of carpet.Second kind is commonly referred to " long wool " carpet, the base fabric identical with pile carpet can be arranged, but coil top is isolated.The beginning of many U-shape yarns forms the surface of long wool carpet.

Yarn coil passes base fabric and embeds in the base fabric, thereby forms the tufting substrate, is fixed in base fabric and prevents that coil from pulling out from base fabric.Generally applying tackiness agent binder composition as described herein by the back side at unprocessed tufted carpet is bonded in tufted yarn to fix described tufting substrate on the base fabric.Also can apply second layer back lining materials, use with to make yarn adhere to the identical binder composition of base fabric or another kind of binder composition sticking thereon at the unprocessed tufted carpet back side.Use second layer back lining materials that yarn coil is fixed, because yarn coil also sticks on described back lining materials and the base fabric by described binder composition.

Described yarn can be made by the fiber of any kind of tufted carpet that is applicable to known in the art, for example nylon, acrylic resin, wool, cotton and regenerated fiber.Described base fabric or basic backing can be any kinds known in the art, can be woven.For example, described base fabric can be woven jute, woven finedraw polypropylene screen, sack cloth, also can be supatex fabric, for example acupuncture or non-woven polypropylene fiber net.Similarly, second layer back lining materials also can be an any kind known in the art, for example woven jute, woven finedraw (woven slit) polypropylene screen, sack cloth, foam materials such as polyurethane foam or blowing ethene base system film and supatex fabric such as acupuncture, non-woven polypropylene fiber net or polyester and polypropylene blend.

Prepare in this tufted carpet, usually binder composition is applied to basic backing, support the tufting matrix with the latex form.Usually on carpet, apply second layer backing then.Carpet heating is solidified latex to guarantee latex and tufted carpet, and latex and bonding between backing and the second layer backing substantially.As previously described, described binder composition can comprise or not comprise filler.The binder composition that comprises filler can be used for making the face yarn fibers fix in position.The binder composition that does not comprise filler can be used as the main rubberised layer tackiness agent of structure tufted yarn carpet or as the main backing of free-lay carpet.

When being used to make carpet, described binder composition preferably has 1kg or higher, more preferably 3kg or higher, most preferably 5kg or higher tufting bounding force." tufting bounding force " used herein is defined as and takes out the required power of single thread from carpet, measures by ASTM D1335.Even more preferably described binder composition has 15kg or higher tufting bounding force.In addition, described binder composition should have 10 ℃ or lower or more preferably 5 ℃ or lower flexible." flexible " used herein is by making the crooked 180 degree angular measurements of a carpet sample under the temperature that reduces in succession., successfully passes through by sample test if not rupturing.

A kind of typical adhesive prescription that is used for carpet comprises at least a softening agent of at least a wax of at least a tackifying resin of the polymkeric substance described herein of 2 to 98% (weights), maximum 80% (weights), maximum 20% (weights), maximum 30% (weights) and at least a antioxidant of maximum 5% (weights).

The typical adhesive prescription that another kind is used for carpet comprises at least a filler of at least a whipping agent of at least a softening agent of at least a wax of at least a tackifying resin of the polymkeric substance described herein of 2 to 98% (weights), maximum 50% (weights), maximum 10% (weights), maximum 20% (weights), maximum 2% (weights), maximum 90% (weights) and at least a antioxidant of maximum 5% (weights).

A. fiber product that comprises binder composition and one or more filamentary material, described binder composition comprise and have one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.Described filamentary material can be selected from that cotton, hemp, cellulose ester, polyester, wool, hair, Kev are drawn, nylon, Nomex (Nomex nylon), polymeric amide, polyacrylic ester, polyolefine and combination thereof.

The fiber product of B. top A section, wherein said fiber product is a nonwoven articles.Described filamentary material can comprise one or more material that is selected from polypropylene, regenerated fiber, polyester, polyethylene, nylon, Mierocrystalline cellulose, viscose glue, ethylene-propylene copolymer, polyolefine, polymeric amide, polycarbonate, polystyrene, thermoplastic elastomer, fluoropolymer, vinyl based polymer, carbon, glass, mineral, wool, acrylic acid or the like, polyvinyl chloride, urethane, organic binder bond and combination thereof.

The fiber product of C. top B section is as diaper, swim suit, child's training pants, adult-incontinence clothes, feminine care products, medical clothes, mattress, surgical drape, cloth lining, scouring pad, automotive interior member, clothes, adhesive tape, face shield and respirator, air filter, vacuum bag, oil and chemical leakage absorption agent, thermal isolation, first aid dressing, medical binder, fiberfill, coat, cotton-wadded quilt stopping composition, furniture liner, filtration medium, scouring pad, Wiping material or its combination.

The fiber product of D. top A section is as the carpet backing goods.Described carpet backing goods can comprise basic back lining materials, and wherein said filamentary material is fixed on the described basic back lining materials, and described binder composition places at least a portion of described filamentary material.Described carpet backing goods can also comprise the second layer back lining materials that adheres to described binder composition.Described basic back lining materials is selected from woven jute, woven finedraw polypropylene screen, sack cloth, needling material, non-woven polypropylene and combination thereof.

E. arbitrary section fiber product above, wherein said binder composition also comprises one or more tackifier.Described one or more tackifier are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, the hydriding terpene of modification, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described tackiness agent compound can also comprise one or more wax.Described one or more wax is selected from f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can also comprise one or more additive.Described one or more additive is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, whipping agent, polymer compatibilizer, fire retardant and water.

F. arbitrary section fiber product above, wherein said binder composition comprises 30% (weight) or one or more wax, 25% (weight) still less or one or more wax, 20% (weight) still less or one or more wax, 15% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax, 3% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

G. arbitrary section fiber product above, wherein said binder composition comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

H. arbitrary section fiber product above, wherein said binder composition comprises 30% (weight) or one or more additive, 25% (weight) still less or one or more additive, 20% (weight) still less or one or more additive, 15% (weight) still less or one or more additive, 10% (weight) still less or one or more additive, 5% (weight) still less or one or more additive, 3% (weight) still less or one or more additive, 2% (weight) still less or one or more additive or 1% (weight) still less or one or more additive still less.

I. arbitrary section fiber product above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.The setting time of described polymkeric substance is 30 minutes or shorter, and some T shape peeling force is 3 to 4000N.

J. arbitrary section fiber product above, the viscosity of wherein said binder composition is to be lower than 9Pas under 177 ℃.Described binder composition can also have 1kg or higher tufting bounding force.

K. arbitrary section the preparation method of fiber product comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With described binder composition is applied at least a portion of filamentary material.

E. film

In one particular, polymeric constituent described herein can be used for unitary film.Perhaps described polymeric constituent can be imposed at least one external part of unitary film.Unitary film be enough thick with self-supporting and also enough thin with activation be bent, folding or wrinkle and the planeform that do not rupture.The thickness of film depends on to be used and produces, but is generally 125 μ m or littler.Unitary film can be non-oriented, uniaxial orientation or diaxial orientation, by forming at least a portion that polymeric constituent is imposed on film base material.Perhaps can make polymeric constituent and film base material blend change its performance.

Described film base material can comprise paper, tinsel, metal, metal alloy, polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer and combination and multipolymer.

Described unitary film can also comprise other polymeric constituent that is selected from polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer, its combination and multipolymer thereof.

On the one hand, described polymeric constituent comprises one or more tackifier.Described tackifier comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described polymeric constituent can comprise 80% (weight) or one or more tackifier still less.More preferably described polymeric constituent comprises 60% (weight) or still less or 40% (weight) or one or more tackifier still less, most preferably 20% (weight) or one or more tackifier still less.

On the other hand, described polymeric constituent comprises one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described polymeric constituent can comprise 30% (weight) or one or more wax or 3% (weight) still less or still less.

Again on the other hand, described polymeric constituent comprises 30% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.

One of described polymeric constituent representative formula comprises one or more C _3-40Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.Another representative formula of described polymeric constituent comprises one or more C _3-5Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 90000 or lower.Another representative formula again of described polymeric constituent comprises one or more C _3-6Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 90000 or lower.

Another representative formula again of described polymeric constituent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described polymeric constituent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described polymeric constituent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 25% (weights) and one or more additive of maximum 15% (weights).

It is 60 ℃ or higher that described polymeric constituent is mixed with release adhesive fail temperature (PAFT).Described polymeric constituent also should have 70 ℃ or higher shear adhesion fail temperature.It is 177 ℃ of following 15Pas or lower that described polymeric constituent also is mixed with viscosity.In addition, described polymeric constituent should have-65 to 30 ℃ second-order transition temperature.More preferably the second-order transition temperature of described polymeric constituent is 0 to 20 ℃, most preferably 10 to 20 ℃.

Described unitary film can be with any suitable technology production.One of film technique example is the curtain coating technology, as the cooling roller casting method.The curtain coating technology generally comprises composition extruded by flat die with molten state and makes composition cools form film then.As specific examples, the casting films production line that is purchased of available pilot scale is prepared as follows casting films.Make polymkeric substance pelletizing fusion, select the melt viscosity coupling of melt temperature and resin.Make this laminar flow be distributed to the width of wanting by pure road film extrusion die.Make material extending to final thickness then.Vacuum available chamber or air knife will be followed closely on main cooling roller from the melt that die openings is discharged.The resulting polymers film is collected on the wrapping machine.Can monitor thickness by the thickness monitor instrument, and available trimming machine finishing film limit.When needing, available one or more nonessential treater carries out surface treatment to film.This cooling roller casting method and device are for known in this field, be described in for example " The Wiley Encyclopedia of Packaging Technology ", Second Edition, A.L.Brody and K.S.Marsh, Ed., John Wiley and Sons, Inc. is among the New York (1997).Though with the cooling roller casting method is an example, also can adopt other casting method.

Another example of film technique is the blown film technology.The blown film technology generally comprises to be extruded with molten state composition by annular die head, make composition blowing and cooling form tubular blown film then, and axially the rip cutting reconciliation is folded to form flat film then.As specific examples, can be prepared as follows blown film.Polymer composition is imported the loading hopper of forcing machine.Be extruded into film and make the film cooling by die head by blow air to the film surface.Film is pulled out from die head, form tubular membrane usually, make it to cool off, fold, and alternatively through auxiliary process such as rip cutting, processing, sealing or the printing of needs.But finished films coiled volume is used for aftertreatment, perhaps can infeed other machine and make described film be transformed into the goods of wanting.Be applicable to that according to an embodiment of the present invention film forming specific inflation film process and unit describe are in US5 569 693.Certainly, other is blow molded into embrane method and also can adopts.

Another example of film technique is a coating technique.For example, the solution that will comprise the composition of described binder polymer is applied on the stripping film.After the coating, make the film drying, peel off described coating from stripping film and obtain bonding film with warm air.Certainly, also can adopt other coating technique.

Described unitary film can be used for various application.In general, described unitary film be suitably for various materials provide gluing backing and make first with second bonding.For example, described unitary film can be used for structural member such as shaving board etc. so that bonding decoration laminating material on it.Another example is that described unitary film can be used for decoration element such as wallpaper, coverture or panel, or ground cover material such as ceramic tile, Vinylite, rostone or building stones, so that these article are fitted on another side or the bracing member.

A. unitary film that comprises polymeric constituent and film base material, described polymeric constituent comprises one or more C _3-40Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.

The unitary film of B. top A section also comprises one or more other polymeric constituent that is selected from polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer, its combination and multipolymer thereof.

C. arbitrary section unitary film above, wherein said film base material is selected from paper, tinsel, metal, metal alloy, polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer and combination and multipolymer.

D. arbitrary section unitary film above, wherein said unitary film also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of composition.

E. arbitrary section unitary film above, wherein said polymeric constituent also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

F. arbitrary section unitary film above, wherein said polymeric constituent also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

G. arbitrary section unitary film above, wherein said polymeric constituent comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

H. arbitrary section unitary film above, wherein said polymeric constituent comprises 75% (weight) or one or more wax, 70% (weight) still less or one or more wax, 60% (weight) still less or one or more wax, 50% (weight) still less or one or more wax, 40% (weight) still less or one or more wax, 30% (weight) still less or one or more wax, 20% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

I. arbitrary section unitary film above, wherein said polymeric constituent comprises 60% (weight) or one or more additive, 50% (weight) still less or one or more additive, 40% (weight) still less or one or more additive, 30% (weight) still less or one or more additive, 20% (weight) still less or one or more additive, 10% (weight) still less or one or more additive, 5% (weight) still less or one or more additive, 3% (weight) still less or one or more additive or 1% (weight) still less or one or more additive still less.

J. arbitrary section unitary film above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

K. arbitrary section unitary film above, the setting time of wherein said polymkeric substance is 30 minutes or shorter.

L. arbitrary section unitary film above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

N.52. arbitrary section unitary film above, the viscosity of wherein said polymeric constituent is 177 ℃ of following 15Pas or lower.

M. arbitrary section unitary film above, the second-order transition temperature of wherein said polymeric constituent is-65 to 30 ℃.

N. arbitrary section unitary film above, the second-order transition temperature of wherein said polymeric constituent is 0 to 20 ℃.

O. arbitrary section unitary film above, the second-order transition temperature of wherein said polymeric constituent is 10 to 20 ℃.

P. the preparation method of arbitrary section unitary film comprises the formation polymeric constituent above, and described polymeric constituent includes one or more C _3-40Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.98 or lower and Mw be 100000 or lower; With described polymeric constituent is applied at least a portion of film base material.

F. hotmelt

In one particular, tackiness agent of the present invention can be used for hot-melt adhesive composition.Hotmelt exists with solid form at ambient temperature and can become viscous liquid by thermal conversion.Hotmelt imposes on the base material with the fusion form usually.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 60% (weight) or one or more tackifier still less.More preferably described binder composition comprises one or more tackifier of 40% (weight), 20% (weight) or still less most preferably.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 75% (weight) or one or more wax still less.More preferably described binder composition comprises 15% (weight) or one or more wax still less.

Again on the other hand, described binder composition can comprise 60% (weight) or still less, 30% (weight) or still less, 20% (weight) or still less, 15% (weight) or still less, 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, solvent, nucleator, tensio-active agent, sequestrant, jelling agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.

Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.

On the one hand, substrate fiber the tear rate of described hot-melt adhesive composition under room temperature (about 25 ℃) is 75% to 100%.The more preferably described hot-melt adhesive composition substrate fiber rate of tearing at room temperature is 95% to 100%.Under freezing temp (-20 ℃ approximately), the substrate fiber rate of tearing of described hot-melt adhesive composition is 50% to 100% or more preferably 95% to 100%.

On the other hand, the release adhesive fail temperature (PAFT) of described hot-melt adhesive composition is 200 ℃ or lower, and shear adhesion fail temperature (SAFT) is 200 ℃ or lower.On the other hand, the fracture tensile strength of described hot-melt adhesive composition under 25 ℃ is 20bar or higher or 27bar or higher or 34bar or higher or 55bar or higher.In addition, the elongation of described hot-melt adhesive composition under 25 ℃ or higher temperature can be 200% strain of raw footage.

Again on the other hand, the solidification value of described hot-melt adhesive composition is-20 to 250 ℃, and open temperature is-20 to 250 ℃.In addition, on the other hand, the cloud point of described hot-melt adhesive composition is 275 ℃ or lower or 120 ℃ or lower.More preferably the cloud point of described hot-melt adhesive composition is 100 ℃ or lower.

Hot-melt adhesive composition described herein can prepare with ordinary method well known in the art.For example, make blend under heating up under low or the high shear mixing such as described polymkeric substance, tackifier and needed nonessential composition such as softening agent oil, wax, liquid resin tackifier form the fluid melt.Mixing temperature depends on concrete adhesive formula, and generally about 130 to about 200 ℃ scope, about 150 to about 160 ℃ is typically to be fit to scope.

A kind of representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 25% (weights) and one or more additive of maximum 15% (weights).

A. hot-melt adhesive composition that comprises binder composition, described binder composition comprise and have one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, with Mw be 100000 or lower, wherein said binder composition is configured to and will imposes on the base material with the fusion form.

B. arbitrary section hot-melt adhesive composition above, wherein said binder composition also comprises one or more tackifier.Described one or more tackifier are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, modified hydrogenated terpenes, hydrogenated wood rosin glycerol ester, its derivative, and composition.

C. arbitrary section hot-melt adhesive composition above, wherein said binder composition also comprises one or more wax.Described one or more wax is selected from f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

D. arbitrary section hot-melt adhesive composition also comprises one or more additive above.The optional self-plasticization agent of described one or more additive, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, water and combination thereof.

E. arbitrary section hot-melt adhesive composition above, wherein said binder composition comprises 75% (weight) or one or more wax, 70% (weight) still less or one or more wax, 60% (weight) still less or one or more wax, 50% (weight) still less or one or more wax, 40% (weight) still less or one or more wax, 30% (weight) still less or one or more wax, 20% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

F. arbitrary section hot-melt adhesive composition above, wherein said binder composition comprises 60% (weight) or one or more additive still less, 50% (weight) or one or more additive still less, 40% (weight) or one or more additive still less, 30% (weight) or one or more additive still less, 20% (weight) or one or more additive still less, 10% (weight) or one or more additive still less, 5% (weight) or one or more additive still less, 3% (weight) or one or more additive still less, or 1% (weight) or one or more additive still less.

G. arbitrary section hot-melt adhesive composition above, wherein said binder composition comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

H. arbitrary section hot-melt adhesive composition above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

I. arbitrary section hot-melt adhesive composition above, the setting time of wherein said polymkeric substance is 30 minutes or shorter.

J. arbitrary section hot-melt adhesive composition above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

K. arbitrary section the preparation method of hot-melt adhesive composition comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.98 or lower and Mw be 100000 or lower; Impose on the base material with described binder composition heating and with molten state.

G. pressure sensitive adhesive

In one particular, binder composition described herein can be used for contact adhesive composition." contact adhesive composition " used herein be or down can form effective adherent binder composition about room temperature (about 25 ℃) gently depressing abundant wetting base material.Term used herein " effectively bonding " changes with base material, means bonding and corresponding balance cohesive strength.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 70% (weight) or one or more tackifier still less.More preferably described binder composition comprises 40% (weight) or one or more tackifier still less, 20% (weight) or still less most preferably.On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 40% (weight) or one or more wax still less.

Again on the other hand, described binder composition can comprise 40% (weight) or still less, 30% (weight) or still less, 25% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.

It is 0.001 to 1MPa that one preferred aspect, described contact adhesive composition are mixed with dynamic storage modulus, and second-order transition temperature is-65 to 30 ℃.Again on the other hand, the viscosity of described contact adhesive composition is 200Pas or lower down at 150 ℃.

A kind of representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 95% (weights), maximum 40% (weights) and one or more additive of maximum 15% (weights).Another representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 95% (weights), maximum 40% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 40% (weights) and one or more additive of maximum 40% (weights).

Contact adhesive composition can variety of way well known by persons skilled in the art be made, and is melt blended described in the first US4 152 189, is incorporated herein for reference.

A. contact adhesive composition that comprises binder composition, described binder composition comprise and have one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, Mw is 100000 or lower, dynamic storage modulus is 0.001 to 1MPa, and second-order transition temperature (Tg) is-65 to 30 ℃.

The contact adhesive composition of B. top A section, wherein said binder composition also comprises one or more tackifier.

C. arbitrary section contact adhesive composition above, the wherein said binder composition of stating also comprises and is selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, modified hydrogenated terpenes, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

D. arbitrary section contact adhesive composition above, wherein said binder composition also comprises one or more wax.

E. arbitrary section contact adhesive composition above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

F. arbitrary section contact adhesive composition also comprises one or more additive above.

G. arbitrary section contact adhesive composition above, wherein said binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

H. arbitrary section contact adhesive composition above, wherein said binder composition comprises 40% (weight) or one or more wax, 30% (weight) still less or one or more wax, 25% (weight) still less or one or more wax, 20% (weight) still less or one or more wax, 15% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

I. arbitrary section contact adhesive composition above, wherein said binder composition comprises 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

J. arbitrary section contact adhesive composition above, wherein said binder composition comprises 40% (weight) or one or more additive, 30% (weight) still less or one or more additive, 25% (weight) still less or one or more additive, 5% (weight) still less or one or more additive or 1% (weight) still less or one or more additive still less.

K. arbitrary section contact adhesive composition above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

L. arbitrary section contact adhesive composition above, the setting time of wherein said polymkeric substance is 30 minutes or shorter.

M. arbitrary section contact adhesive composition above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

H. adhesive tape

In one particular, tackiness agent of the present invention can be used for adhesive tape.Adhesive tape generally is configured to two or more base material is bonded together.Adhesive tape comprises the binder composition that is applied on the backing spare.The optional autohemagglutination compound of described backing spare film, polyester film, polyolefine thin film, polyurethane film, polyvinyl chloride foam, polyethylene, non-woven urethane, non-woven polyester, fabric, lining (face stock), paper, synthesized polymer material, plastics, polyolefin polymer such as polyethylene and polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, kraft paper, polymkeric substance, laminating material, latex dipping paper, tinsel, building stones (litho stock), light material, styrenic foams, the polystyrene foam of foaming, Woven fabric, supatex fabric, cloth, crepe paper, thermoplastic elastomer, and combination.The thickness of typical case's backing spare changes to the number cm range at 1 micron.Particularly preferred backing spare comprises oriented polypropylene, Biaially oriented polypropylene and polyvinyl chloride.Oriented polypropylene, Biaially oriented polypropylene and polyvinyl chloride film are particularly preferred backing spares.

Described adhesive tape can be the single or double adhesive tape, and promptly adhesive material is applied to the one side or the tow sides of back lining materials.Fig. 6 illustrates the cross-sectional view of typical single face adhesive tape.Adhesive tape 100 comprises the binder composition 110 and the release liner 115 on the relative two sides that is applied to backing spare 105.Fig. 6 illustrates the cross-sectional view of typical double sticky tape.Double sticky tape 300 comprises first binder composition 315 and second binder composition 310 on the relative two sides that is applied to backing spare 305.One of at least comprise binder composition described herein in first binder composition 305 or second binder composition 315, for example one of binder composition or both comprise binder composition of the present invention.

Adhesive tape can be configured to multiple base material is adhered to mutually, as first base material and second base material are adhered to, and perhaps adhesive tape can be configured to and adhere to single base material.First base material and second base material can be same materials, and perhaps described base material can be formed by differing materials.One of two base materials or two can comprise plastics, polyolefine, stainless steel, paper, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, skin, film, plastic film, laminating material, cloth, container, instruments, medical devices, glass and sheet material.

Adhesive tape can volume, sheet, pad or other form provide, and depends on service requirements, not inadvertently is bonded on the surface beyond the predetermined base material with the binder composition that prevents to adhere to backing spare.For example, the binder composition that is affixed on the back lining materials can be attached on the release liner before the use.Release liner is attached on the adhesive tape with the bond strength that keeps binder composition usually and is configured to stripping tape from it.The general release liner that uses when providing adhesive tape with the form of sheet or volume.Release liner comprises release coating such as silicon usually.The adhesive tape that provides with web-like can use or tears with hand with tape dispenser.The adhesive tape that provides with the liner form can be included in two binder compositions between the peeling liner, and at least one peeling liner scribbles release coating composition.

Fig. 7 illustrates the side-view of Fig. 6 adhesive tape of rolling.Tape roll 200 comprises adhesive tape 100, and adhesive tape wherein twines the one side of posting release liner 215 of posting the described adhesive tape of binder composition one side 220 contacts that makes described adhesive tape like this.

Described binder composition is applied on back lining materials at least a portion at least simultaneously.In general, described binder composition or under room temperature, can form effectively bonding gently depressing abundant wetting base material.Term used herein " effectively bonding " means bonding (with the adhesion failure of base material) and interior poly-(inner adhesion failure) intensity balance, and this application according to adhesive tape is optimized.For example, the binder composition in the band that can remove photoresist can have compares relatively low bond strength with cohesive strength, thereby can remove adhesive tape and do not stay remnants (for example tackiness agent) on base material.On the contrary, efficient adhesive tape for example is used to the bonding and cohesive strength of the adhesive tape that transports and pack can be all high, causes base material or backing spare destruction.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can be for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 70% (weight) or one or more tackifier still less.More preferably described binder composition comprises 40% (weight) or one or more tackifier still less.Most preferably described binder composition comprises 20% (weight) or one or more tackifier still less.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 40% (weight) or one or more wax still less.

Again on the other hand, described binder composition can comprise 40% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, compatilizer and biocide.Described binder composition can comprise 30% (weight) or one or more oil still less.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Described binder composition can comprise 40% (weight) or one or more softening agent still less.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Described binder composition can also comprise one or more filler, 6% (weight) or one or more linking agent still less and the combination thereof of 5% (weight) or one or more antioxidant, 30% (weight) still less.

Described binder composition be mixed with viscosity under 160 ℃ less than 200000cps, second-order transition temperature is-65 to 30 ℃.When base material comprised glass, the peel adhesion of 180 ° of peel angles of described binder composition was 90 to 1800g/cm; When base material comprised stainless steel, the peel adhesion of 180 ° of peel angles of described binder composition was 100 to 2000g/cm.

In addition, to be mixed with spin viscosity be 0.5 to 30cm to described binder composition.When base material comprises stainless steel, the hot shearing intensity of described binder composition should be 40 ℃ following 1 minute or longer, preferred 10 minutes or longer, and cement strength is 1 minute or longer under 12.5 * 25.0cm and 1kg load.The peak value tan δ of described binder composition is-65 to 30 ℃, and probe tack is 1 to 1000g.Described binder composition also should have 25 ℃ following 1 * 10 ⁴To 1 * 10 ⁷The shearing modulus of dynes/cm.Described binder composition also should have 175 ℃ of melt viscosities of 1000 to 250000mPas down.

Adhesive tape can be made by any conventional technique known in the art, is included in the hot melt or the solvent application release liner of back lining materials, then at the another side hot melt or the described binder composition of solvent application of this back lining materials.Perhaps can be with three layers of coextrusion simultaneously.

Above-mentioned adhesive tape can be used for for example mark, cementation, protection, seals and covers.In addition, available adhesive tape adheres to each other two base materials.For example available adhesive tape is bonded together the tabs of back lining materials.Adhesive tape also can be used for medical applications such as bandage.

A. adhesive tape that is used to adhere to base material comprises binder composition and the backing spare of at least two opposite faces is arranged, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mo l% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, Mw is 100000 or lower, and wherein said binder composition is applied at least a portion of described backing spare.

B. arbitrary section the adhesive tape that is used to adhere to base material above, wherein said base material is selected from plastics, polyolefine, stainless steel, paper, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, skin, film, plastic film, laminating material, cloth, container, instruments, medical devices, glass and sheet material.

C. arbitrary section the adhesive tape that is used to adhere to base material above, wherein said backing spare is selected from polymeric film, polyester film, polyolefine thin film, polyurethane film, polyvinyl chloride foam, polyethylene, non-woven urethane, non-woven polyester, knit goods, lining, paper, synthesized polymer material, plastics, polyolefin polymer such as polyethylene and polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, kraft paper, polymkeric substance, laminating material, latex dipping paper, tinsel, building stones, light material, styrenic foams, laminated foam, the polystyrene foam of foaming, Woven fabric, supatex fabric, cloth, crepe paper, thermoplastic material, and combination.

D. arbitrary section the adhesive tape that is used to adhere to base material above, wherein said binder composition are applied at least a portion of one of described two opposite faces or wherein said binder composition is applied on the part on two sides of described two opposite faces.

E. arbitrary section the adhesive tape that is used to adhere to base material also comprises the release liner that places described binder composition opposite above.Described binder composition strippingly contacts described release liner.

F. arbitrary section the adhesive tape that is used to adhere to base material above, wherein said binder composition also comprises one or more tackifier.Described tackifier are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, modified hydrogenated terpenes, hydrogenated wood rosin glycerol ester, its derivative, and composition.

G. arbitrary section the adhesive tape that is used to adhere to base material wherein also comprises one or more wax above.Described one or more wax is selected from f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

H. arbitrary section the adhesive tape that is used to adhere to base material wherein also comprises one or more additive above.Described one or more additive is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, thickening material, rheology modifier, filler, antiblocking additive, polymeric additive, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, compatilizer and biocide.

I. arbitrary section the adhesive tape that is used to adhere to base material above, wherein said binder composition comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

J. arbitrary section the adhesive tape that is used to adhere to base material above, wherein said binder composition comprises 75% (weight) or one or more wax, 70% (weight) still less or one or more wax, 60% (weight) still less or one or more wax, 50% (weight) still less or one or more wax, 40% (weight) still less or one or more wax, 30% (weight) still less or one or more wax, 20% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

K. arbitrary section the adhesive tape that is used to adhere to base material above, wherein said binder composition comprises 60% (weight) or one or more additive still less, 50% (weight) or one or more additive still less, 40% (weight) or one or more additive still less, 30% (weight) or one or more additive still less, 20% (weight) or one or more additive still less, 10% (weight) or one or more additive still less, 5% (weight) or one or more additive still less, 3% (weight) or one or more additive still less, 1% (weight) or one or more additive still less, or 0.25% (weight) or one or more additive still less.

L. arbitrary section the adhesive tape that is used to adhere to base material above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.The setting time of described polymkeric substance is 30 minutes or shorter, and some T shape peeling force is 3 to 4000N.

M. arbitrary section the preparation method of adhesive tape comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; On at least a portion of the backing spare that described binder composition is applied at least two opposite faces.

I. wood working

In one particular, tackiness agent described herein can be used for the wood working process.The wood working process relates to and applies binder composition form the wood working goods at least a portion of structural member.Described structural member can comprise various materials, includes but not limited to timber or glued board or plastics or facing plate.For example, structural member can also comprise plank, timber, fiberboard, plasterboard, plaster board, wallboard, glued board, PVC, melamine, polyester, impregnated paper and asbestos cement plate (sheetrock).The wood working process can be used for forming for example indoor furniture, outdoor furniture, ornament, filler rod, door, frame, window, factory's woodwork and thin wooden furniture (cabinetry).

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can be for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 80% (weight) or still less or 60% (weight) or still less or 2 to 40% (weights) or 3 to 30% (weights) or one or more tackifier still less.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 30% (weight) or still less or 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or still less or 3% (weight) or still less or 1% (weight) or still less or 0.5% (weight) or one or more wax still less.

Again on the other hand, described binder composition can comprise 60% (weight) or still less or 50% (weight) or still less or 40% (weight) or still less or 30% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, adhesion promotor, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.

Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.Typical antioxidant comprises alkylphenol, hindered phenol and amphyl, as tertiary butylated hydroquinone, butylated hydroxyanisol, many butyl bis-phenol, Yoshinox BHT (BHT), alkylation quinhydrones, 2,6-ditertbutylparacresol, 2,5-two uncle's aryl quinhydrones, Octadecane base-3-(3,5-di-t-butyl-4-hydroxyphenyl) etc.

Typical filler comprises silicon oxide, diatomite, lime carbonate, ferric oxide, hydrogenated castor oil, fumed silica, precipitated chalk, the fumed silica of hydrophobic treatment, hydrophobic precipitated lime carbonate, talcum, zinc oxide, polyvinyl chloride powder, mycocide, graphite, carbon black, pitch, carbon packing (carbon filler), clay, mica, fiber, titanium dioxide, Cadmium Sulfide, asbestos, wood powder, the polyethylene powder, chopped fibres, bubble shape thing, bead, thixotrope, wilkinite, calcium sulfate, calcium oxide, magnesium oxide, and combination or derivative.Exemplary surfactants comprises the organopolysiloxane that contains vinyl or contain sulfydryl, polydimethylsiloxanemacromer macromer and the combination or the derivative of ethenyl blocking.

Typical adhesion promotor comprises silane, titanic acid ester, organosilane (organosylane), acrylic acid or the like, acid, acid anhydride, Resins, epoxy, stiffening agent, polymeric amide, methyl acrylate, epoxide, resol, polyisobutene, aminoalkyl, the mercapto alkyl, epoxy alkyl, the urea alkyl, carboxyl, the functional silane of acrylate and isocyanuric acid ester, mercaptopropyl trimethoxysilane, epoxypropoxy (glycidoxpropyl) Trimethoxy silane, aminopropyl triethoxysilane, the aminoethyl aminopropyl trimethoxysilane, the urea propyl trimethoxy silicane, two-γ-trimethoxysilyl-third ureas, 1,3,5-three-γ-trimethoxy-silylpropyl isocyanuric acid ester, two-γ-the trimethoxy-silylpropyl maleic acid ester, fumarate and gamma-methyl allyl acyloxypropyl trimethoxysilane, aminopropyl triethoxysilane, and combination and derivative.Typical linking agent comprises oxime linking agent, organoalkoxysilane, epoxy alkyl organoalkoxysilane, amido silane, aminosilane, alkene oxygen base (enoxy) silane, tetraethoxysilane, methyltrimethoxy silane, vinyltrimethoxy silane, glycidoxy-propyltrimethoxy silane, vinyl three iso-propenyloxysilanes, methyl three iso-propenyloxysilanes, methyl three hexamethylene aminosilanes, methyl three Zhong Ding aminosilanes, polyisocyanates and combination or derivative.Typical organic solvent comprises aliphatic solvents, alicyclic solvents, mineral turpentine, aromatic solvent, hexane, hexanaphthene, benzene,toluene,xylene and combination thereof or derivative.

On the one hand, to be mixed with viscosity be 10 to 150Pas to described binder composition.On the other hand, the plateau region shearing modulus of described binder composition is 1 * 10 under 25 ℃ and 1 radian per second ⁶To 1 * 10 ⁸Dynes/cm.On the other hand, the second-order transition temperature of described binder composition is-65 to 30 ℃.Again on the other hand, the open hour of described binder composition are 5 minutes or longer.The open hour of preferred described binder composition are 10 minutes or longer.More preferably the open hour of described binder composition are 20 minutes or longer.On the other hand, the setting time of described binder composition is 1 minute or shorter.The setting time of preferred described binder composition is 5 minutes or shorter.More preferably the setting time of described binder composition is 10 minutes or shorter.

A. wood working goods comprise binder composition and structural member, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, Mw is 100000 or lower, and wherein said binder composition is applied at least a portion of described structural member.

The wood working goods of B. top A section, wherein said structural member comprise timber or glued board or plastics or facing plate.

C. arbitrary section wood working goods above, wherein said structural member is selected from plank, timber, fiberboard, plasterboard, plaster board, wallboard, glued board, PVC, melamine, polyester, impregnated paper and asbestos cement plate.

D. arbitrary section wood working goods above, wherein said wood working goods are selected from indoor furniture, outdoor furniture, ornament, filler rod, door, frame, window, factory's woodwork and thin wooden furniture.

E. arbitrary section wood working goods above, the wherein said binder composition of stating also comprises and is selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

F. arbitrary section wood working goods above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

G. arbitrary section wood working goods above, wherein said binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

H. arbitrary section wood working goods above, wherein said binder composition comprise 30% (weight) or still less or 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or still less or 3% (weight) or still less or 1% (weight) or still less or 0.5% (weight) or one or more wax still less.

I. arbitrary section wood working goods above, wherein said binder composition comprise 80% (weight) or still less or 60% (weight) or still less or 2 to 40% (weights) or 3 to 30% (weights) or one or more tackifier still less.

J. arbitrary section wood working goods above, wherein said binder composition comprise 60% (weight) or still less or 50% (weight) or still less or 40% (weight) or still less or 30% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.

K. arbitrary section wood working goods above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

L. arbitrary section wood working goods above, the setting time of wherein said polymkeric substance is 30 minutes or shorter.

M. arbitrary section wood working goods above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

N. arbitrary section wood working goods above, the viscosity of wherein said binder composition are 10 to 150Pas.

O. arbitrary section wood working goods above, the setting time of wherein said binder composition are 1 minute or shorter or 5 minutes or shorter or 10 minutes or shorter.

P. arbitrary section the preparation method of wood working goods comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; On at least a portion of the structural member that described binder composition is applied at least two opposite faces.

J. label

In one particular, binder composition described herein can be used for label.In general, label is will only make himself to adhere to base material.Therefore, label is not will be as construction package.Thereby standard can have higher intrinsic strength and lower bond strength.

Label comprises the layer of adhesive composition that is applied on the backing spare, and described binder composition opposite has peelable.The peeling liner of label will adhere to label till described label is attached on its target substrate.Label backing spare is that the label field is known.Any suitable backing spare all can be used for the present invention.Backing spare can comprise polymeric film, polyester film, polyolefine thin film, polyurethane film, polyvinyl chloride foam, polyethylene, non-woven urethane, non-woven polyester, knit goods, paper, synthesized polymer material, plastics, polyolefine, polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, kraft paper, polymkeric substance, laminating material, latex dipping paper, tinsel, building stones, light material, styrenic foams, laminated foam, the polystyrene foam of foaming, Woven fabric, supatex fabric, cloth, crepe paper, thermoplastic material, and polyethylene and polyacrylic mixture.

The base material that is fit to can comprise for example plastics, polyolefine, stainless steel, paper, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, skin, film, plastic film, laminating material, cloth, container, instruments, medical devices, glass and sheet material.

Adhesive tape can be volume, sheet or other form, depends on concrete service requirements, not inadvertently adheres to other surface to prevent it.As previously described, label can be laminated to and prevent its accidental other surface that adheres on the peeling liner.The peeling off of label is lined with release coating such as organosilicon makes peeling liner be easy to remove from label.Peeling liner is the sheet material that scribbles release liner that is used for label.Estimate that peeling liner reproducibly provides appropriateness and separability described tackiness agent, described tackiness agent is not had harmful effect and ageing-resistant so that rippability is relative predictable in time.

For ease of clearly describing, typical label is described in more detail in conjunction with Fig. 6.Fig. 6 is the cross-sectional view of label 100.Label 100 comprises backing spare 105, binder composition 110 and peeling liner 115.Binder composition 110 is applied on the backing spare 105, and peeling liner 115 imposes on the binder composition 110.Perhaps, binder composition 110 is applied on the peeling liner 115, then backing spare 105 is imposed on the binder composition 110.Remove peeling liner 115 from binder composition 110 before being affixed on base material.

In general, the binder composition that is used to form label or under room temperature, can form effectively bonding gently depressing abundant wetting base material.Effectively bonding generalized bonding (with the adhesion failure of base material) and interior poly-(inner adhesion failure) intensity of comprising.Be optimized bonding and balance cohesive strength according to this application.For example, thus can go that the lower and cohesive strength of labeling requirement bond strength is higher can be removed label and do not stay remnants on base material.On the other hand, efficient labeling requirement is bonding all high with cohesive strength.Under some situation, this efficient label has high bonding and cohesive strength like this that base material or backing spare are destroyed.The adhesive therefor composition should have the desired stretchiness of its intended application, elasticity and intensity (comprising tensile strength) in the label.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 70% (weight) or still less or 40% (weight) or still less or 20% (weight) or one or more tackifier still less.

Again on the other hand, described binder composition can comprise one or more additive.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, adhesion promotor, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.

Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.On the one hand, described binder composition comprises 40% (weight) or one or more softening agent still less.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.In another embodiment, described binder composition comprises 5% (weight) or one or more antioxidant still less.Typical antioxidant comprises alkylphenol, hindered phenol and amphyl, as tertiary butylated hydroquinone, butylated hydroxyanisol, many butyl bis-phenol, Yoshinox BHT (BHT), alkylation quinhydrones, 2,6-ditertbutylparacresol, 2,5-two uncle's aryl quinhydrones, Octadecane base-3-(3,5-di-t-butyl-4-hydroxyphenyl) etc.

On the other hand, described binder composition comprises 30% (weight) or one or more filler still less.Typical filler comprises silicon oxide, diatomite, lime carbonate, ferric oxide, hydrogenated castor oil, fumed silica, precipitated chalk, the fumed silica of hydrophobic treatment, hydrophobic precipitated lime carbonate, talcum, zinc oxide, polyvinyl chloride powder, mycocide, graphite, carbon black, pitch, carbon packing, clay, mica, fiber, titanium dioxide, Cadmium Sulfide, asbestos, wood powder, the polyethylene powder, chopped fibres, bubble shape thing, bead, thixotrope, wilkinite, calcium sulfate, calcium oxide, magnesium oxide, and combination or derivative.Exemplary surfactants comprises the organopolysiloxane that contains vinyl or contain sulfydryl, polydimethylsiloxanemacromer macromer and the combination or the derivative of ethenyl blocking.

Typical adhesion promotor comprises silane, titanic acid ester, organosilane, acrylic acid or the like, acid, acid anhydride, Resins, epoxy, stiffening agent, polymeric amide, methyl acrylate, epoxide, resol, polyisobutene, aminoalkyl, the mercapto alkyl, epoxy alkyl, the urea alkyl, carboxyl, the functional silane of acrylate and isocyanuric acid ester, mercaptopropyl trimethoxysilane, glycidoxy-propyltrimethoxy silane, aminopropyl triethoxysilane, the aminoethyl aminopropyl trimethoxysilane, the urea propyl trimethoxy silicane, two-γ-trimethoxysilyl-third ureas, 1,3,5-three-γ-trimethoxy-silylpropyl isocyanuric acid ester, two-γ-the trimethoxy-silylpropyl maleic acid ester, fumarate and gamma-methyl allyl acyloxypropyl trimethoxysilane, aminopropyl triethoxysilane, and combination and derivative.Typical linking agent comprises oxime linking agent, organoalkoxysilane, epoxy alkyl organoalkoxysilane, amido silane, aminosilane, alkene TMOS, tetraethoxysilane, methyltrimethoxy silane, vinyltrimethoxy silane, glycidoxy-propyltrimethoxy silane, vinyl three iso-propenyloxysilanes, methyl three iso-propenyloxysilanes, methyl three hexamethylene aminosilanes, methyl three Zhong Ding aminosilanes, polyisocyanates and combination or derivative.Typical organic solvent comprises aliphatic solvents, alicyclic solvents, mineral turpentine, aromatic solvent, hexane, hexanaphthene, benzene,toluene,xylene and combination thereof or derivative.

The binder composition that is used for label as well known to those skilled in the art has following performance: (1) aggressive tack and permanent adhesive, (2) adhere to being no more than under the finger pressure, and (3) are enough to adhere on the base material and (4) enough cohesive strengths.The material of having found to be used for effectively label is to be mixed with to have required visco-elasticity to reach the equilibrated binder composition of desired viscosity, peel adhesion and anti-shearing cement strength.Therefore best binder composition has about 5 * 10 ⁵To 1 * 10 ⁵Shearing modulus in the dynes/cm scope, its second-order transition temperature is-10 to 10 ℃.

Usually by the peeling force decision, peeling force is to peel off 1 inch needed power of sample bar with the right angle from stainless steel substrate adhered thereto to the character of tackiness agent (be permanent adhesives or can remove tackiness agent).Permanent adhesives has 3 pounds or bigger peeling force usually, and peeling force is commonly referred to less than about 2 pounds tackiness agent and can removes tackiness agent.More generally, when considering to comprise that backing spare, binder composition and label will paste the whole system of base material thereon, permanent adhesives is wherein whole coatings will prevent to remove label under the situation of the structural integrity of not damaging label or base material a tackiness agent.On the contrary, can remove label is not influence the structural integrity of label or base material and the peelable and label of usefulness again.

Therefore, on the one hand, the second-order transition temperature of described binder composition is-65 to 30 ℃, preferred-65 to 20 ℃.On the other hand, the plateau region shearing modulus of described binder composition is 1 * 10 under 25 ℃ ⁴To 1 * 10 ⁷Dynes/cm.On the other hand, when base material comprised glass, the stripping strength of 180 ° of peel angles of described binder composition was 1 to 1800g/cm.Preferably, when base material comprised polyethylene film, the peel adhesion of 180 ° of peel angles of described binder composition was 1 to 1800g/cm.On the other hand, the spin viscosity of described binder composition is 0.1 to 30cm.Again on the other hand, when base material comprised glass, the loops viscosity of described binder composition (loop tack) was 1 to 10N/cm.Preferably, when base material comprised polyethylene film, the loops viscosity of described binder composition was 1 to 10N/cm.Again on the other hand, when base material comprised stainless steel, the hot shearing intensity of described binder composition should be under 40 ℃ greater than 40 minutes.Again on the other hand, when base material comprised stainless steel, described binder composition cement strength under 12.5 * 25.0mm and 1kg load was preferably greater than 30 minutes greater than 1 minute.On the other hand, the peak value tan δ of described binder composition is-20 to 10 ℃.Again on the other hand, the Polyken probe tack of described binder composition is 1 to 900g.In another embodiment, the brookfield viscosity of described binder composition should be 177 ℃ of following 50000mPas or lower.

Label can be made by routine techniques known in the art.For example, in the typical label configurations, can remove peeling liner, make it to contact with backing spare with described binder composition coating.Perhaps, binder composition is applied on the backing spare, then peeling liner is attached on the binder composition.Whole or most of at least areas of label scribble binder composition.Before label is affixed on base material, remove peeling liner from binder composition, and binder composition is stayed on the backing spare still.Removing peeling liner makes label can adhere to base material.Peeling liner is protected binder composition between transportation and shelf lives.

A. a label that is used to adhere to base material comprises binder composition, backing spare and peeling liner, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, Mw is 100000 or lower, wherein makes described peeling liner adhere to described backing spare with described binder composition.

The label of B. top A section, wherein said backing spare are selected from plastics, polyolefine, stainless steel, paper, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, skin, film, plastic film, laminating material, cloth, container, instruments, medical devices, glass and sheet material.

C. arbitrary section label above, wherein said backing spare is selected from polymeric film, polyester film, polyolefine thin film, polyurethane film, polyvinyl chloride foam, polyethylene, non-woven urethane, non-woven polyester, knit goods, paper, synthesized polymer material, plastics, polyolefine, polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, kraft paper, polymkeric substance, laminating material, latex dipping paper, tinsel, building stones, light material, styrenic foams, laminated foam, the polystyrene foam of foaming, Woven fabric, supatex fabric, cloth, crepe paper, thermoplastic material, and polyethylene and polyacrylic mixture.

D. two opposite faces that arbitrary section label above, wherein said backing spare and peel off and be lined with two opposite faces, described binder composition are applied to described backing spare one of at least or two opposite faces of described peeling liner one of at least on.

E. arbitrary section label above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of composition.

F. arbitrary section label above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

G. arbitrary section label above, wherein said binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, thickening material, rheology modifier, filler, antiblocking additive, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, compatilizer and biocide.

H. arbitrary section label above, wherein said binder composition comprises 40% (weight) or one or more wax still less.

I. arbitrary section label above, wherein said binder composition comprise 70% (weight) or still less or 40% (weight) or still less or 20% (weight) or one or more tackifier still less.

J. arbitrary section label above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

K. arbitrary section label above, the setting time of wherein said polymkeric substance is 30 minutes or shorter.

L. arbitrary section label above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

M. arbitrary section label above, the viscosity of wherein said binder composition is 177 ℃ of following 90Pas.

N. arbitrary section label above, when wherein base material comprised glass, the loops viscosity of described binder composition was 1 to 10N/cm.

O. arbitrary section label above, when wherein base material comprises stainless steel, described binder composition under 25.4 * 25.4cm and 2kg load cement strength greater than 30 minutes.

P. arbitrary section the preparation method of label comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With at least a portion of the peeling liner that described binder composition is applied at least two opposite faces or have at least a portion of backing spare of two opposite faces.

K. bookbinding

In one particular, tackiness agent of the present invention can be used for bookbinding.For simplicity, will describe the production method of the book that adhesive is arranged with " bookbinding " speech, wherein binder composition is applied at least a portion of described adhesive.But embodiment described herein is not limited to only be fit to the binder composition of bonding book.Term used herein " book " comprises other goods that contain useful binder composition adherent page or leaf, as paperbound, soft cover books, working instructions, magazine, catalogue, trade journal and numbering directory etc.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and composition.Described binder composition can comprise 80% (weight) or still less or 60% (weight) or one or more tackifier still less.Again on the other hand, described binder composition comprises 45% (weight) or still less or 20% (weight) or one or more tackifier still less.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 30% (weight) or still less or 20% (weight) or one or more wax still less.

Again on the other hand, described binder composition can comprise 55% (weight) or still less or 40% (weight) or one or more additive still less.Preferred described binder composition comprises 30% (weight) or one or more additive still less, and most preferably described binder composition comprises 10% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.

The key property of bookbinding adhesive composition comprises that page power of taking out, the flat property opened, page flexibility, cold cracking, Yi Kaixing and spine are flexible.Take out page power and mean the required power of extraction one page from the book of bookbinding.Take out page power and depend on the surface treatment of the tackiness agent and the style of calligraphy.The flat property opened means smooth degree opened and kept by book at given page or leaf characteristic (spine up or down).The flat property opened depends on the characteristic and the consumption thereof of tackiness agent.Page flexibility is the infiltration in the style of calligraphy of adhesive properties, tackiness agent and the surface-treated complex function of the style of calligraphy.Cold cracking means and opens spine rimose temperature when contacting between book so that book cover fast.Cold cracking depends on tackiness agent and consumption thereof.Easily the property opened means the resistance that book produces when opening first.Easily the property opened depends on the characteristic and the consumption of tackiness agent.The flexible book that means of spine is not had spine folding line or corrugated ability by repeated open.Spine is flexible to be the function of binder performance and binder dosage.

It is 75% to 100% that described binder composition can be mixed with 22 ℃ of following substrate fiber rates of tearing.It is 95% to 100% that preferred described binder composition is mixed with 22 ℃ of following substrate fiber rates of tearing.On the other hand, the PAFT of described binder composition is 60 ℃ or higher, and preferred, the PAFT of described binder composition is 200 ℃ or lower.Again on the other hand, the SAFT of described binder composition is 70 ℃ or higher.The SAFT of preferred described binder composition is 200 ℃ or lower.Again on the other hand, the fracture tensile strength of described hot-melt adhesive composition under 25 ℃ is 27.5 to 82bar.The fracture tensile strength of preferred described hot-melt adhesive composition under 25 ℃ is 27.5 to 65bar.The fracture tensile strength of more preferably described hot-melt adhesive composition under 25 ℃ is 27.5 to 40bar.Again on the other hand, the elongation of described binder composition under 25 ℃ is 100% to 1000% strain of raw footage.The elongation of preferred described binder composition under 25 ℃ is 100% to 750% strain of raw footage.The elongation of more preferably described binder composition under 25 ℃ is 100% to 600% strain of raw footage.

The fracture tensile strength of described binder composition can be 1.5 or lower with the ratio of extension at break.The tensile strength of preferred described binder composition is 1.25 or lower with the ratio of elongation.More preferably the tensile strength of described binder composition is 0.9 or lower with the ratio of elongation.On the one hand, described binder composition viscosity be 177 ℃ of following 2.5Pas or lower.Preferred described binder composition viscosity be 177 ℃ of following 10Pas or lower.Again on the other hand, the second-order transition temperature of described binder composition is-65 to 30 ℃.Again on the other hand, the Young's modulus of described binder composition is 65 to 690bar.Again on the other hand, the some T shape peeling force of described binder composition is 3 to 4000N.The point T shape peeling force of preferred described binder composition is 5 to 3000N.More preferably the some T shape peeling force of described binder composition is 15 to 1000N.

A kind of representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 60% (weights), maximum 20% (weights) and one or more additive of maximum 15% (weights).Another representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 20% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 5% (weights) and one or more additive of maximum 5% (weights).

In the tradition bookbinding, in many different steps, use tackiness agent.In the step that is called " glued (gluing off) ", except that line or wire, also the page bonding is in the same place with involution with tackiness agent.In the step that is called " lining ", make strongthener such as cloth or paper be fixed in for example bonding piece of spine with tackiness agent.

In the step that is called " dress skin (casing-in) ", make the front cover of book be fixed in spine with tackiness agent.In the perfect binding, only page is bonded together and the fixing front cover of book with tackiness agent.If only use tackiness agent structure book one time, then be called " single stage method ".When adopting twice tackiness agent, be called " two-step approach ".In two-step approach, the tackiness agent that uses is bonded together page for the first time.This tackiness agent is called primer.The tackiness agent that uses is used to make the front cover of book to be fixed in spine for the second time.This tackiness agent is called face glue.

A. bookbinding goods comprise binder composition and adhesive, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, Mw is 100000 or lower, and wherein said binder composition is applied at least a portion of described adhesive.

The bookbinding goods of B. top A section, wherein said bookbinding goods are selected from hardcover, periodical, textbook, handbook, magazine, moccasin textbook, paperbound, magazine and catalogue.

C. arbitrary section bookbinding goods above, wherein said adhesive comprises paper or thick material paper (heavy stock paper).

D. arbitrary section bookbinding goods above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, modified hydrogenated terpenes, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of composition.

E. arbitrary section bookbinding goods above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

F. arbitrary section bookbinding goods above, wherein said binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

G. arbitrary section bookbinding goods above, wherein said binder composition comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

H. arbitrary section bookbinding goods above, wherein said binder composition comprises 75% (weight) or one or more wax, 70% (weight) still less or one or more wax, 60% (weight) still less or one or more wax, 50% (weight) still less or one or more wax, 40% (weight) still less or one or more wax, 30% (weight) still less or one or more wax, 20% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

I. arbitrary section bookbinding goods above, wherein said binder composition comprises 60% (weight) or one or more additive, 50% (weight) still less or one or more additive, 40% (weight) still less or one or more additive, 30% (weight) still less or one or more additive, 20% (weight) still less or one or more additive, 10% (weight) still less or one or more additive, 5% (weight) still less or one or more additive, 3% (weight) still less or one or more additive or 1% (weight) still less or one or more additive still less.

J. arbitrary section bookbinding goods above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

K. arbitrary section bookbinding goods above, the setting time of wherein said polymkeric substance is 30 minutes or shorter.

L. arbitrary section bookbinding goods above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

M. arbitrary section bookbinding goods above, the tensile strength of wherein said binder composition is 1.5 or lower with the ratio of elongation.

N. arbitrary section bookbinding goods above, the tensile strength of wherein said binder composition is 1.25 or lower with the ratio of elongation.

O. arbitrary section bookbinding goods above, the tensile strength of wherein said binder composition is 0.9 or lower with the ratio of elongation.

P. arbitrary section the preparation method of bookbinding goods comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With described binder composition is applied at least a portion of adhesive.

L. road sign

In one particular, binder composition described herein can be used for road marking compositions.Road marking compositions generally comprises binder composition and one or more filler that is applied to one or more base material.Described one or more base material can comprise pitch, concrete, metal, brick, paving stone, pottery, polymeric material, cinder brick, soft motion ground, ground, playground, runway, synthetic rubber surrogate (tartan substitutes), concrete, metal, pitch, pitch earth, brick, paving stone, ceramic tile, steel plate, timber, pottery, polymeric material, glass, concrete blocks, porcelain, stone, plank, shaving board, wooden auto parts, cinder brick, beaujolais, and combination.

Road marking compositions comprises that one or more filler is to improve weathering resistance, visibility meter, opacifying power, wear resistance, adhesivity and/or the reflectivity of road marking compositions.In addition, also can add some fillers with total rheological of improving the thermoplasticity road sign, prevent the road sign segregation, be the cost that frictional force and/or reduction road marking compositions are provided between binder composition and its base material that will be coated with.The filler that can be used for this comprises sand, pigment, granulated glass sphere, the polymer-based carbon bead, lime carbonate, crushed marble, gather materials, rhombspar, talcum, granulated glass sphere, prismatic tamper, the reflection from lens body, the calcite spar, silica sand, graphite, floating dust, cement flour, clay, feldspar, nepheline, fumed silica, aluminum oxide, magnesium oxide, zinc oxide, barium sulfate, pure aluminium silicate, Calucium Silicate powder, titanate, chalk, the reflective mineral filler, the increment filler, bead, calcium sulfate, calcium metasilicate, silica powder, the calcining flint powder, mica, the calcium silicate glass fiber, dyestuff, grouan, gypsum, slaked lime, aluminum oxide, diatomite, tamper, properties-correcting agent, white lead, lithopone, chrome yellow, cadmium yellow, resin particle, polymer gel, polymkeric substance, stupalith, glass cullet, stone, corundum, aluminium hydroxide, silicon oxide, glass envelope, and zinc neodecanoate.Typical pigment comprises titanium dioxide, zinc oxide, magnesium oxide, lead chromate and composition thereof.The type of pigment and content are selected according to the concrete purposes of road sign, and those skilled in the art can determine at an easy rate.In addition, can in road marking compositions, add one or more filler and give color, opacity or pattern to road marking compositions.

The key characteristic of road marking compositions is the visibility meter under all envrionment conditionss.Thereby road marking compositions can comprise one or more reflective filler.In road marking compositions, introduce one or more reflective filler and in rainy day and dark, make road sign visibility meter maximum by the light of reflection car light.Can comprise a certain amount of one or more reflective filler in the road marking compositions is enough to improve by the reflective visibility meter of composition that makes.The reflective filler that is fit to includes but not limited to be used in granulated glass sphere, polymer beads, sand, silicon oxide compounds, stupalith and/or the road marking compositions of being everlasting any other reflective filler of this purpose.Bead is preferred reflective filler, includes but not limited to polymer-based carbon bead or granulated glass sphere.Granulated glass sphere is most preferred.The cohesive strength of bead reply refrigerative tackiness agent does not have negative impact, must form bonding by force between tackiness agent and bead.Basic demand is to keep stable under the heat that applied in preparation, mixing and the use of road sign of bead.Keep stable at least when preferred described bead stands more than 200 ℃ hot about 20 minutes.

The bead of being made by polymkeric substance should be able to tolerate applied pressure in the normal traffic and not break or broken.In addition, reflective filler should be evenly distributed in the tackiness agent so that performance is consistent and make the reflective of road sign permanently effective.The stylish reflective filler in upper strata that the uniform distribution of reflective filler makes traffic wear and wind erosion remove road sign is exposed to the surface.The add-on increase of reflective filler also helps the long-term reflective that keeps satisfaction when improving the road sign reflectivity in the road marking compositions.If the amount of reflective filler is few in the road marking compositions, cause the reflecting power variation when then the reflective filler that scatters in the composition being reduced because of tire wear, and if the add-on of reflective filler is too many, the intensity of road marking compositions is reduced.

When being used for road marking compositions, filler the intensity that makes road sign improve and also keep road sign thickness constant aspect be effective; But the filler that used volume can cause producing the fragility road sign.Therefore, road marking compositions comprises one or more filler of 20 to 90% (weights).On the one hand, described one or more filler comprises 50% (weight) or still less or one or more bead of 10 to 40% (weights) or 15 to 30% (weights).Again on the other hand, described one or more filler comprises 20% (weight) or still less or one or more pigment of 2 to 15% (weights) or 3 to 10% (weights).

On the one hand, described road marking compositions comprises the tackiness agent of 10 to 80% (weights).Described binder composition comprises polymkeric substance of the present invention described herein.Available toxilic acid or maleic anhydride make described functionalization of polymers.Other component can be combined to form binder composition with the preparation of described polymkeric substance or described polymkeric substance.

On the one hand, described tackiness agent can comprise one or more tackifier.Tackifier for example comprise aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, modified hydrogenated terpenes, hydrogenated wood rosin glycerol ester, its derivative, and composition.On the one hand, described tackiness agent comprises the tackifier of 80% (weight).

On the other hand, described tackiness agent comprises one or more wax, and typical wax comprises that f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers, the maleic anhydride grafted of polar waxes, nonpolar wax, f-t synthetic wax, oxidation have side to hang the polyethylene of acid functional group part, paraffin, Microcrystalline Wax and combination thereof.On the one hand, described tackiness agent comprises 30% (weight) or one or more wax still less.

Again on the other hand, described tackiness agent comprises one or more additive.Typical additive comprises softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, extender, hindered phenol, phosphoric acid ester/salt, antiblocking additive, lubricant, photostabilizer, UV light absorber, dispersion agent, thickening material, alkali, wetting agent, fire retardant, linking agent, solidifying agent, covering agent, He Shui.Typical oil comprises aliphatic oil, naphthenic oil, white oil, soya-bean oil, its combination and derivative thereof.On the one hand, described tackiness agent comprises one or more polymeric additive of 40% (weight).Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.On the one hand, described tackiness agent comprises 20% (weight) or one or more softening agent still less.Typical softening agent comprises mineral oil, polybutene, phthalic ester, hydrocarbon ils, soya-bean oil, phthalic ester, elastomerics, olefin oligomer, vegetables oil, cyclohexane dimethanol bisbenzoate and combination thereof.Typical phthalic ester comprises phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.On the other hand, described tackiness agent comprises 5% (weight) or one or more stablizer still less.Again on the other hand, described tackiness agent comprises 1% (weight) or one or more antioxidant still less.The example of the covering agent that is fit to includes but not limited to titanium dioxide, diatomite and barium sulfate.

Described tackiness agent can also comprise one or more properties-correcting agent and not reduce softening temperature simultaneously to strengthen the wetting of one or more filler and reduction melt viscosity.The properties-correcting agent that is applicable to road marking compositions of the present invention includes but not limited to acid; Metal oxide such as zinc oxide, white lead, lithopone, sublimed lead, magnesium oxide, thermotolerance chrome yellow, cadmium yellow, ferric oxide and titanium dioxide; Acid anhydride such as polyisobutylene succinic anhydride (PIBSA); And combination and derivative.

In some embodiment, described tackiness agent comprises also that Mw is 100000 to 250000, preferred 250000 to 500000 multipolymer.

In another embodiment of road marking compositions, two or the different polymkeric substance of various molecular weights make road marking compositions have excellent weather resistance and other rheological benefit.Particularly, can make one or more high-molecular weight polymer and polydispersity polymer combination in one or more.In addition, can make polydispersity polymer and the combination of one or more low-molecular weight polymer in one or more.Can make the combination of one or more high-molecular weight polymer and one or more low-molecular weight polymer.In another embodiment, can make height, in and low-molecular weight polymer all combine.The weight average molecular weight range of polymkeric substance is as follows: high-molecular weight polymer is 250000 to 500000; Middle polydispersity polymer is 100000 to 250000; Low-molecular weight polymer is 50000 to 100000.In one preferred embodiment, it is that 100000 to 250000 first multipolymer and Mw are 250000 to 500000 second multipolymer that described tackiness agent also comprises Mw.

A kind of representative formula of described tackiness agent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 99% (weights), maximum 20% (weights) and one or more filler of maximum 90% (weights).The another kind of representative formula of described tackiness agent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 80% (weights), maximum 15% (weights) and one or more additive of maximum 75% (weights).The another kind of again representative formula of described tackiness agent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 40% (weights), maximum 20% (weights) and one or more additive of maximum 70% (weights).The another kind of again representative formula of described tackiness agent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 10% (weight), maximum 60% (weights), maximum 20% (weights) and one or more additive of maximum 60% (weights).The another kind of again representative formula of described tackiness agent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 5% (weight), maximum 80% (weights), maximum 5% (weights) and one or more additive of maximum 10% (weights).The another kind of again representative formula of described tackiness agent comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 10% (weight), maximum 30% (weights), maximum 10% (weights) and one or more additive of maximum 50% (weights).

On the one hand, described tackiness agent be mixed with viscosity be 177 ℃ down 0.05 to 0.5Pas.On the other hand, the second-order transition temperature of described tackiness agent is-65 to 30 ℃.Again on the other hand, described tackiness agent is praised grace viscosity less than 120 seconds under 190 ℃.Again on the other hand, the praise grace viscosity of described tackiness agent under 190 ℃ is 35 to 180 seconds.Again on the other hand, the some T shape peeling force of described tackiness agent is 3 to 4000N.The point T shape peeling force of preferred described tackiness agent is 5 to 3000N.More preferably the some T shape peeling force of described tackiness agent is 15 to 1000N.On the other hand, the bounding force on described tackiness agent and road surface is 1.0N/mm ²Or it is bigger.The bounding force on preferred described tackiness agent and road surface is 1.2N/mm ²Or it is bigger.The bounding force on more preferably described tackiness agent and road surface is 1.3N/mm ²Or it is bigger.The bounding force on most preferably described tackiness agent and road surface is 1.5N/mm ²Or it is bigger.Bounding force with the road surface used herein is measured by ExxonMobil test method E-22.On the other hand, the softening temperature of described tackiness agent is 90 ℃ or higher.The softening temperature of preferred described tackiness agent is 95 ℃ or higher.More preferably the softening temperature of described tackiness agent is 98 ℃ or higher.Most preferably the softening temperature of described tackiness agent is 100 ℃ or higher.On the other hand, the acupuncture degree of described tackiness agent is 5 to 120s/10mm.Again on the other hand, the brightness of described tackiness agent is 70 or higher.The brightness of preferred described tackiness agent is 75 or higher.More preferably the brightness of described tackiness agent is 76 or higher or 78 or higher.Again on the other hand, the melt viscosity of described tackiness agent be 177 ℃ down 0.4 to 30Pas.

Described road marking compositions can be applied to the surface that is moved through such as road surface to convey a message.Road marking compositions also is applicable to various coating, sign and japanning are used, and include but not limited to traffic signals, runway marking, crossing, buildings advertisement and sign, cycle track, the tennis court, the sign of synthetic rubber surrogate, stop line, the travel route sign, traffic character, the traffic adhesive tape, soft motion ground sign, the playground sign, the shipping safety sign, the oil rig safety notice, the traffic safety reflective coating, the boundary line, road sign, the embossing road sign, pipeline, electric pole, highway barrier, concrete blocks, curb, the walkway, the parking lot, abutment, wooden passage, wooden roadblock, ceramic surface, brick, the japanning road sign, with the japanning signal surface.

Road marking compositions usually by scraper plate case (screed box), extrude or spraying technology coating.Scraper plate case coating method is usually used in the higher road marking compositions of viscosity, extrudes to be usually used in moderately viscous road marking compositions, and spraying is usually used in the lower road marking compositions of viscosity.Can make said composition be fit to be coated with at the road marking compositions that wide use temperature scope is particularly used in 150 to 250 ℃ by different methods.The composition that can be coated with under 150 to 170 ℃ low use temperature makes it to be fit to by the coating of squeezing and coating technology, and the composition that can be coated with under 200 to 250 ℃ higher use temperature makes it to be fit to be coated with by spraying technology.

When it heated more than fusing point, road marking compositions fusion or be melted became liquid or fluid state by solid.When following, road marking compositions becomes solid-state again the fused composition cools to its fusing point.Road marking compositions of the present invention usually like this uses: make the composition fusion and melting material is applied on the base material to about 250 ℃ temperature 175.

In the use, be under the situation of molten state at tackiness agent one or more filler is introduced in tackiness agent.Then the gained road marking compositions is applied on the base material,, road marking compositions is solidified with postcooling.Perhaps, earlier tackiness agent is applied on the base material with molten state.Before adhesive cools and tackiness agent when being in molten state, granulated glass sphere is attached on the tackiness agent.Tackiness agent curing makes granulated glass sphere adhere to base material then, forms road sign.Two kinds of method combinations are a kind of optional methods of road sign.Bead can be introduced in the tackiness agent and still be under the situation of molten state spread-coating at road marking compositions on road marking compositions.This method guarantees that the reflective satisfactory of road sign rises to the road sign surface until the traffic wear and the bead that causes introducing of eroding.

Road marking compositions should not experience the over-drastic slump or stir and smash, and this relates to spread-coating and the described composition of rotation when being applied to base material.Over-drastic collapses or stirs and smash the line or the shape that can cause the gained road sign that irregular and profile differences are arranged.Use temperature (application temperature is lower usually) should be regulated or additive should be in composition, added to prevent slump or to stir and smash.Change application temperature and should consider that also the viscosity of road marking compositions easily is applied on the base material composition, cause that described tackiness agent is applied to base material and become more difficult or impossible because make road marking compositions be cooled to too low temperature.

A. road marking compositions comprises tackiness agent and one or more filler, and described tackiness agent comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, Mw is 100000 or lower.

The road marking compositions of B. top A section, wherein said road marking compositions are used to be selected from one or more base material of pitch, concrete, metal, brick, paving stone, pottery, polymeric material, cinder brick, soft motion ground, ground, playground, runway, synthetic rubber surrogate, concrete, metal, pitch, pitch earth, brick, paving stone, ceramic tile, steel plate, timber, pottery, polymeric material, glass, concrete blocks, porcelain, stone, plank, shaving board, wooden auto parts, cinder brick and beaujolais.

C. it is 100000 to 250000 multipolymer that arbitrary section road marking compositions above, wherein said tackiness agent also comprise Mw.

D. it is 250000 to 500000 multipolymer that arbitrary section road marking compositions above, wherein said tackiness agent also comprise Mw.

E. it is that 100000 to 250000 first multipolymer and Mw are 250000 to 500000 second multipolymer that arbitrary section road marking compositions above, wherein said tackiness agent also comprise Mw.

F. arbitrary section road marking compositions above, wherein said tackiness agent also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene base resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, the hydriding terpene of modification, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

G. arbitrary section road marking compositions above, wherein said tackiness agent also comprise the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers, the maleic anhydride grafted that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation has side to hang one or more wax of the polyethylene of acid functional group part, paraffin, Microcrystalline Wax and combination thereof.

H. arbitrary section road marking compositions above, wherein said tackiness agent also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, extender, hindered phenol, phosphoric acid ester, antiblocking additive, lubricant, photostabilizer, UV light absorber, dispersion agent, thickening material, alkali, wetting agent, fire retardant, linking agent, solidifying agent, covering agent, water and combination thereof.

I. arbitrary section road marking compositions above, wherein said tackiness agent also comprise and are selected from sand, pigment, granulated glass sphere, the polymer-based carbon bead, lime carbonate, crushed marble, (aggregate) gathers materials, rhombspar, talcum, granulated glass sphere, prismatic tamper, the reflection from lens body, the calcite spar, silica sand, graphite, floating dust, cement flour, clay, feldspar, nepheline, fumed silica, aluminum oxide, magnesium oxide, zinc oxide, barium sulfate, pure aluminium silicate, Calucium Silicate powder, titanate, chalk, the reflective mineral filler, the increment filler, bead, calcium sulfate, calcium metasilicate, silica powder, the calcining flint powder, mica, the calcium silicate glass fiber, dyestuff, grouan, gypsum, slaked lime, aluminum oxide, diatomite, tamper, properties-correcting agent, white lead, lithopone, chrome yellow, cadmium yellow, resin particle, polymer gel, polymkeric substance, stupalith, glass cullet, stone, corundum, aluminium hydroxide, silicon oxide, glass envelope, zinc neodecanoate, and one or more filler of combination.

J. arbitrary section road marking compositions above, wherein said tackiness agent comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

K. arbitrary section road marking compositions above, wherein said tackiness agent comprises 75% (weight) or one or more wax, 70% (weight) still less or one or more wax, 60% (weight) still less or one or more wax, 50% (weight) still less or one or more wax, 40% (weight) still less or one or more wax, 30% (weight) still less or one or more wax, 20% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

L. arbitrary section road marking compositions above, wherein said tackiness agent comprises 90% (weight) or filler still less, 80% (weight) or filler still less, 70% (weight) or filler still less, 60% (weight) or filler still less, 50% (weight) or one or more filler, 40% (weight) still less or one or more filler, 30% (weight) still less or one or more filler, 20% (weight) still less or one or more filler, 10% (weight) still less or one or more filler or 5% (weight) still less or one or more filler still less.

N. arbitrary section road marking compositions above, wherein said tackiness agent comprises 90% (weight) or one or more softening agent, 80% (weight) still less or one or more softening agent, 70% (weight) still less or one or more softening agent, 60% (weight) still less or one or more softening agent, 50% (weight) still less or one or more softening agent, 40% (weight) still less or one or more softening agent, 30% (weight) still less or one or more softening agent, 20% (weight) still less or one or more softening agent or 10% (weight) still less or one or more softening agent still less.

O. arbitrary section road marking compositions above, wherein said one or more filler comprises 50% (weight) or one or more bead still less.

P. arbitrary section road marking compositions above, wherein said one or more filler comprises one or more bead of 10 to 40% (weights).

Q. arbitrary section road marking compositions above, wherein said one or more filler comprises one or more bead of 15 to 30% (weights).

R. arbitrary section road marking compositions above, wherein said one or more filler comprises 20% (weight) or one or more pigment still less.

S. arbitrary section road marking compositions above, wherein said one or more filler comprises one or more pigment of 2 to 15% (weights).

T. arbitrary section road marking compositions above, wherein said one or more filler comprises one or more pigment of 3 to 10% (weights).

U. arbitrary section road marking compositions above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

V. arbitrary section road marking compositions above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

W. arbitrary section road marking compositions above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

X. arbitrary section road marking compositions above, the bounding force on wherein said tackiness agent and road surface is 1.0N/mm ²Or it is bigger.

Y. arbitrary section road marking compositions above, the brightness of wherein said tackiness agent is 70 or higher.

Z. the preparation method of arbitrary section road marking compositions above comprises making one or more filler and mixed with polymers form road marking compositions that described polymkeric substance has one or more C _3-40Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.

M. sealing agent

In one particular, binder composition described herein can be used for encapsulant composition.Thereby the purposes of sealing agent is to keep sealing to repair this base material between the two sides of single base material, perhaps sets up between a pair of base material and the maintenance sealing.Described base material can comprise concrete, roof Material, marble, anodized aluminum, brick, mortar, grouan, Wingdale, porcelain, glass, painted surface, timber, polyvinyl chloride, polyacrylic ester, polycarbonate, polystyrene, fabric, packing ring, plastics, stone, masonry materials, pipeline, flexible pipe, metal, distribution, sled, polyethylene, polypropylene, polyester, acrylic resin, PVDC, paper, ethane-acetic acid ethyenyl ester, automobile, buildings, aircraft, dashboard, the deck, skeleton, the road surface, rear deflector door, door-plate, wheel house, panel, fireproof brickwork, the flange at edge, ground, vehicle body, and floor pan.For example, encapsulant composition can be used for repairing the pipeline or the rimose windshield of leakage.Sealing agent also forms the elastic joint of carrying and prevents that air, water and dirt from passing through between two or more.

Thereby encapsulant composition not only is used for joint filling on repair operation adhesive substrate surface, and can be used for making first base material and another base material bonding.Especially automotive industry is the main users that is used for the sealing agent of this purposes.Automobile is by several member assemblings, and the stress levels that must tolerate according to concrete parts and these parts links together by different way.For example, sectional door panels, four is opened in plate (quarter panel), rear deflector door and the roof and is used sealing agent.Welding or also use encapsulant composition at its seam crossing with bolted other automobile assembling.Other example that flange, floor pan and the vehicle body at wheel house, vibroshock (shock lower), panel, fireproof brickwork, edge, ground is to use the automobile of sealing agent to use.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and combination.Described binder composition can comprise 80% (weight) or still less or 60% (weight) or one or more tackifier still less.Preferred described binder composition comprises 40% (weight) or still less or 20% (weight) or one or more tackifier still less.

Again on the other hand, described binder composition can comprise 95% (weight) or still less or 50% (weight) or still less or 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.In one embodiment, described binder composition comprises 50% (weight) or one or more polymeric additive still less.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.Described composition can comprise 95% (weight) or still less or 70% (weight) or still less or 35% (weight) or still less or 20% (weight) or still less or 10% (weight) or one or more softening agent still less.On the other hand, described binder composition comprises one or more antioxidant of 0.01 to 10% or one or more antioxidant of 0.05 to 5% (weight) or 0.1 to 2.5% (weight) or 0.1 to 2% (weight).Described antioxidant can comprise alkylphenol, hindered phenol and amphyl, as tertiary butylated hydroquinone, butylated hydroxyanisol, many butyl bis-phenol, Yoshinox BHT (BHT), alkylation quinhydrones, 2,6-ditertbutylparacresol, 2,5-two uncle's aryl quinhydrones, Octadecane base-3-(3,5-di-t-butyl-4-hydroxyphenyl) etc.On the one hand, described binder composition comprises 5% (weight) or one or more linking agent still less.Again on the other hand, described binder composition comprises 50% (weight) or one or more filler still less.

Typical filler comprises silicon oxide, diatomite, lime carbonate, ferric oxide, hydrogenated castor oil, fumed silica, precipitated chalk, the fumed silica of hydrophobic treatment, hydrophobic precipitated lime carbonate, talcum, zinc oxide, polyvinyl chloride powder, mycocide, graphite, carbon black, pitch, carbon packing, clay, mica, fiber, titanium dioxide, Cadmium Sulfide, asbestos, wood powder, the polyethylene powder, chopped fibres, glass envelope, granulated glass sphere, thixotrope, wilkinite, calcium sulfate, calcium oxide, magnesium oxide, and combination or derivative.Again on the other hand, described binder composition comprises 15% (weight) or one or more tensio-active agent still less.Exemplary surfactants comprises the organopolysiloxane that contains vinyl or contain sulfydryl, polydimethylsiloxanemacromer macromer and the combination or the derivative of ethenyl blocking.

Again on the other hand, described binder composition comprises 15% (weight) or still less or 2.5% (weight) or one or more adhesion promotor still less.Typical adhesion promotor comprises silane, titanic acid ester, organosilane, acrylic acid or the like, acid, acid anhydride, Resins, epoxy, stiffening agent, polymeric amide, methyl acrylate, epoxide, resol, polyisobutene, aminoalkyl, the mercapto alkyl, epoxy alkyl, the urea alkyl, carboxyl, the functional silane of acrylate and isocyanuric acid ester, mercaptopropyl trimethoxysilane, glycidoxy-propyltrimethoxy silane, aminopropyl triethoxysilane, the aminoethyl aminopropyl trimethoxysilane, the urea propyl trimethoxy silicane, two-γ-trimethoxysilyl-third ureas, 1,3,5-three-γ-trimethoxy-silylpropyl isocyanuric acid ester, two-γ-the trimethoxy-silylpropyl maleic acid ester, fumarate and gamma-methyl allyl acyloxypropyl trimethoxysilane, aminopropyl triethoxysilane, and combination and derivative.

On the one hand, described binder composition comprises 75% (weight) or one or more toughener or 30% (weight) still less or still less.Typical linking agent comprises oxime linking agent, organoalkoxysilane, epoxy alkyl organoalkoxysilane, amido silane, aminosilane, vinyl silanes, tetraethoxysilane, methyltrimethoxy silane, vinyltrimethoxy silane, glycidoxy-propyltrimethoxy silane, vinyl three iso-propenyloxysilanes, methyl three iso-propenyloxysilanes, methyl three hexamethylene aminosilanes, methyl three Zhong Ding aminosilanes, polyisocyanates and combination or derivative.Typical organic solvent comprises aliphatic solvents, alicyclic solvents, mineral turpentine, aromatic solvent, hexane, hexanaphthene, benzene,toluene,xylene and combination thereof or derivative.

Typical chainextender comprise aminosilane, amido silane, acetoxysilane and aminooxy silane, methyl ethylene two-N-methyl kharophen silane, methyl hydrogen diacetoxy silane, dimethyl is two-diethyl hydroxylamino silane, dimethyl is two-Zhong Ding aminosilane, polyisocyanates and combination or derivative.

During as caulking joint glue, sealing agent should comprise linking agent and preferred one or more following additive: adhesion promotor, toughener, chainextender and softening agent.Can also use in the encapsulant composition antioxidant with prevent sealing agent store and final use in oxidation and thermal destruction under the temperature that adopted and the environment.

A kind of representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 80% (weights), maximum 30% (weights) and one or more additive of maximum 80% (weights).Another representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 80% (weights), maximum 30% (weights) and one or more additive of maximum 50% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 80% (weights), maximum 25% (weights) and one or more additive of maximum 15% (weights).

In another embodiment, binder composition of the present invention is used for the very important sealing agent of steam breathability and uses.For example, encapsulant composition can be used for the extremely low window of requirement steam breathability and uses with sealing agent.Can reach 0.07g/100in ²/ 24hr or lower transmitance.

No matter its purposes how, encapsulant composition is a kind of pointing.Therefore, when forming sealing, encapsulant composition should have enough low elasticity so that encapsulant composition can flow in its base material that will use and be full of the slit and still be full of this slit after sealant cures makes described base material sealing.In its uncured state, encapsulant composition should keep viscosity and have enough low viscosity suitably wetting to guarantee base material.

Basically be not clamminess when preferably touching in case encapsulant composition has solidified.During curing, sealing agent should have is enough to tolerate the weather resistance that the user exposes in normal weathering and several application.Sealing agent mainly should stop oxygen, water and air effectively.Solidified sealing agent reply mechanical stress has resistance to cracking and anti-contracility as the bulging of the base material that heats up down, so that sealing agent does not drop down stream or mobile as time goes by.Particularly under the situation of glass baseplate, heavily stressedly may cause glass breakage.Though sealing agent should be enough firm to keep its total shape and size, also must be enough pliable and tough so that reply basically when stretching.Thereby the mixture that is used as sealing agent requires high bond strength and high elongation rate and low tensile modulus balance.The composition of high bond strength generally provides effective seal, because bond strength is high more, the required power of taking-up base material is big more from mixture.The elongation of this mixture relates to composition basic ability of replying its former configuration behind specified elongation degree.Provide very favorable self-healing properties requirement elongation height.Be that sealing agent should be out of shape the stress that is applied on the base material hermetic unit to adapt to.

On the one hand, to be mixed with 100% elongation tensile strength modulus be 0.003 to 0.06bar under 20 ℃ for described binder composition or binder blend.100% elongation tensile strength modulus of preferred described mixture is 0.05 to 0.5bar under 20 ℃.More preferably 100% of described mixture elongation tensile strength modulus is 0.05 to 0.02bar under 20 ℃.Even more preferably 100% elongation tensile strength modulus of described mixture is being that 0.0007 to 0.01bar or 100% elongation tensile strength modulus is 0.05 to 0.0095bar under 20 ℃ under 20 ℃.On the other hand, the elongation at break of described mixture is 190% or higher under 20 ℃.The elongation at break of preferred described mixture is 200% or higher under 20 ℃.More preferably the elongation at break of described mixture is 250% or higher under 20 ℃.Even more preferably the elongation at break of described mixture is 300% or higher under 20 ℃.Most preferably the elongation at break of described mixture under 20 ℃ be 350% or higher or elongation at break under 20 ℃ be 500% higher or elongation at break under 20 ℃ be 600% or higher or elongation at break under 20 ℃ be 700% higher or elongation at break under 20 ℃ be 800% or higher or elongation at break be 1100% or higher under 20 ℃.

On the other hand, the viscosity of described mixture is 177 ℃ of following 9Pas or lower.Preferred described mixture viscosity be 177 ℃ down 0.2 to 8Pas.More preferably described mixture viscosity be 177 ℃ down 0.5 to 2.5Pas.Again on the other hand, the second-order transition temperature of described mixture is-65 to 30 ℃.Again on the other hand, the some T shape peeling force of described mixture is 3 to 4000N.The point T shape peeling force of preferred described mixture is 5 to 3000N.More preferably the some T shape peeling force of described mixture is 15 to 1000N.On the other hand, to drop down stream (sag) after 70 ℃ of following 1 weeks be 7.5cm or lower to described mixture.Preferred described mixture drops down stream and is 2.5cm or lower after 70 ℃ of following 1 weeks.More preferably described mixture drops down stream and is 1cm or lower after 70 ℃ of following 1 weeks.Most preferably described mixture drops down stream and is 0.5cm or lower after 70 ℃ of following 1 weeks.

On the other hand, the Xiao A hardness of described mixture is 3 to 45.The Xiao A hardness of preferred described mixture is 8 to 35.More preferably described mixture Xiao A hardness is 10 to 25.Again on the other hand, the tensile strength of described mixture is 0.0095 to 0.2bar.The tensile strength of preferred described mixture is 0.025 to 0.15bar.More preferably the tensile strength of described mixture is 0.028 to 0.095bar.Again on the other hand, the stress relaxation rate of described mixture is 75% or lower under 25 ℃.The stress relaxation rate of preferred described mixture is 25% or lower under 25 ℃.On the other hand, the acupuncture degree of described mixture is 8 to 66dmm under 25 ℃.

Again on the other hand, described mixture is 0.01bar or higher in shear adhesion power on glass.Preferred described mixture is 0.02bar or higher in shear adhesion power on glass.More preferably described mixture is 0.04bar or higher in shear adhesion power on glass.Most preferably described mixture is that 0.14bar or higher or described mixture are that 0.24bar or higher or described mixture are 0.34bar or higher in shear adhesion power on glass in shear adhesion power on glass in shear adhesion power on glass.

Again on the other hand, the fusing point of described mixture is 200 ℃ or lower.On the other hand, described mixture is 10pli or higher with respect to 180 ° of stripping strengths of glass.Preferred described mixture is 20pli or higher with respect to 180 ° of stripping strengths of glass.More preferably described mixture is 30pli or higher with respect to 180 ° of stripping strengths of glass.

The sealing agent that is used to repair base material generally with the form of sheet impose on the zone of extending above base material otch, indenture or cut with coverings basically and form on every side at it that some are overlapping.Solidify with the contact area between sealing agent and described surface by heating and cooling to envrionment temperature then.Not necessarily when being exposed to airborne moisture, make sealant cures by envrionment conditions.Described encapsulant composition is exposed to that said composition is cured when not being clamminess when touching after ambient air, heat or the moisture.

Require encapsulant composition to show fast set time, represent that encapsulant composition solidifies required time set time on base material.Grinding, boring, the loading and unloading that set time, short composition can experience adherent part with it may to pollute with the part of cohesive material connection, subsequent operations such as pack.

A. encapsulant composition that comprises mixture, described mixture comprise and have one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, Mw is 100000 or lower; Wherein said mixture imposes at least a portion of sealed substrate surface.

The encapsulant composition of B. top A section, wherein said base material is selected from concrete, roof Material, marble, anodized aluminum, brick, mortar, grouan, Wingdale, porcelain, glass, painted surface, timber, polyvinyl chloride, polyacrylic ester, polycarbonate, polystyrene, fabric, packing ring, plastics, stone, masonry materials, pipeline, flexible pipe, metal, distribution, sled, polyethylene, polypropylene, polyester, acrylic resin, PVDC, paper, ethane-acetic acid ethyenyl ester, automobile, buildings, aircraft, dashboard, the deck, skeleton, the road surface, rear deflector door, door-plate, wheel house, panel, fireproof brickwork, the flange at edge, ground, vehicle body, and floor pan.

C. arbitrary section encapsulant composition above, wherein said mixture also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, the hydriding terpene of modification, the Hydrogenated aliphatic rosin ester, its derivative, and one or more tackifier of combination.

D. arbitrary section encapsulant composition above, wherein said mixture also comprise and are selected from polar waxes, nonpolar wax, f-t synthetic wax, the f-t synthetic wax of oxidation, the hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers, amorphous wax, carnauba wax, Viscotrol C wax, Microcrystalline Wax, beeswax, carnauba wax, castor wax, spermaceti, vegetable wax, gama wax, Japan wax, ouricury wax, Pseudotsuga menziesii (Mirbel) Franco bark wax, rice bran wax, jojoba wax, fruit of Grecian Laurel wax, montanin wax, peat wax, ceresine, ceresin(e)wax, petroleum wax, paraffin, polyethylene wax, the chloroflo of chemical modification, the amide waxe that replaces, and one or more wax of combination and derivative.

E. arbitrary section encapsulant composition above, wherein said mixture also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, water, linking agent, thixotropic agent, tensio-active agent, adhesion promotor, toughener, chainextender, ultra-violet stabilizer, tinting material, organic solvent, stablizer, siccative, wetting agent, nucleator, promotor, solidifying agent and combination thereof or derivative.

F. arbitrary section encapsulant composition above, wherein said mixture comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

G. arbitrary section encapsulant composition above, wherein said mixture comprises 30% (weight) or one or more wax, 20% (weight) still less or one or more wax, 10% (weight) still less or one or more wax, 5% (weight) still less or one or more wax or 1% (weight) still less or one or more wax still less.

H. arbitrary section encapsulant composition above, wherein said mixture comprises 95% (weight) or one or more additive still less, 90% (weight) or one or more additive still less, 80% (weight) or one or more additive still less, 70% (weight) or one or more additive still less, 60% (weight) or one or more additive still less, 50% (weight) or one or more additive still less, 40% (weight) or one or more additive still less, 30% (weight) or one or more additive still less, 20% (weight) or one or more additive still less, 10% (weight) or one or more additive still less, 5% (weight) or one or more additive still less, 3% (weight) or one or more additive still less, or 1% (weight) or one or more additive still less.

I. arbitrary section encapsulant composition above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

J. arbitrary section encapsulant composition above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

K. arbitrary section encapsulant composition above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

L. arbitrary section encapsulant composition above, wherein said mixture drop down stream and are 7.5cm or lower after 70 ℃ of following 1 weeks.

M. arbitrary section encapsulant composition above, the fusing point of wherein said mixture is 200 ℃ or lower.

N. arbitrary section encapsulant composition above, wherein said mixture is 10pli or higher with respect to 180 ° of stripping strengths of glass.

O. the preparation method of arbitrary section encapsulant composition above comprises forming comprising mixture of polymers that described polymkeric substance has one or more C _3-40Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; On at least a portion that described mixture is imposed on the substrate surface of wanting sealed.

N. paving compositions

In the one special embodiment, binder composition described herein can be used for paving compositions.Paving compositions generally includes pitch, gathers materials and binder composition.That term used herein " pitch " liquefies when meaning under the room temperature and to be heated for solid-state or semi-solid state gradually and wherein main component be the arbitrary of naturally occurring bitum many materials of obtaining as residue in the refining of petroleum.Kirk-Othmer, Encyclopedia of Chemical Technology, Vol.3, Third Ed. (1978) pp.284-327, John Wiley ﹠amp; Sons has further defined pitch among the New York.Another argumentation is published in " A Brief Introduction to Asphalt and some of its Uses ", Manual Series No.5 (MS-5), and The Asphalt Institute, 7th Ed., September is in 1974.

Typical naturally occurring bituminous matter comprises pitch, asphalite, destructive distillation overhead product, still bed material (bottom stock) and other destructive distillation residue of rock asphalt for example or refining of petroleum such as pyrogenous asphalt, petroleum pitch, coal-tar pitch and composition thereof.The feature of this type of material is that usually penetration value is 0-300 or higher (ASTM D-5-51), preferred about 40-300, softening temperature in about 32 to 120 ℃ of scopes (ASTM D-36-26), preferably between 38 to 65 ℃.

Available asphalt source comprises at present commercially available many.For example, can use known rock asphalt and the petroleum pitch that is used for roof and pavement applications.Described rock asphalt comprises for example asphalite such as stellar coal, grahamite and manjak; Lake pitch such as Trinidad asphalt; And rock asphalt.Petroleum pitch comprises the unfilled bitumen that crude distillation obtains (not blowing and unoxidized basically), be blown into oxidized bitumen that oxygen-containing gas produces under the situation that has or do not exist catalyzer in unfilled bitumen, obtain during the separate bitumen material from bitumeniferous petroleum fractions with propane or other solvent solvent extraction pitch and fluxed asphalt (mixture of unfilled bitumen and V.M.. naphtha solvent).Described pitch can also comprise petroleum tar and asphalt cement.Oil gas tar, refined tar, the V.M.. naphtha fraction that obtains as by product when petroleum tar comprises by the petroleum fractions process gas mixed the cut back tar that obtains and remove the tar-bitumen that the timesharing of volatilization level obtains as residue from this tar with this tar.The arbitrary of these class pitches is used singly or in combination.For example, unfilled bitumen is applicable to pavement applications, and oxidation and oxidized bitumen are applicable to rooftop applications.

Paving compositions of the present invention is particularly useful for making asphalt coating composition.These comprise and contain paving the way and sectional repair or mend in the hole used of the pitch Ru Lu, bridge, airfield runway and the walkway that gather materials.Paving compositions of the present invention can be under fluid or molten state mixes with gathering materials.Usually make paving compositions and preheating, pre-dried gathering materials mix the uniform mixture that the even coating of formation is gathered materials.Can under time that is enough to drive away all free water contents basically and temperature condition, heat before mixing and gather materials.In the mixing process, paving compositions usually about 100 to about 160 ℃ temperature.Be cooled to before the temperature that loses its workability at resulting composition, for example can be laid on the roadbed, then compacting and make it to solidify.After the curing, the gained paving compositions comprises by bituminous cement matrix adherent and gathers materials.

" gather materials " solid particulate of planning to include the certain size scope of term used herein comprises that particulate such as sand are to thicker particle such as rubble, gravel or slag relatively.Usually, used gathering materials be mainly inorganic materials in the preparation paving compositions, for example crushed rocks, stone and (under some situation) sand.The size of gathering materials depends in part on the end-use of specific paving compositions.For example, bigger gathering materials is generally used for laying road surface new or surfacing, and the composition that mends a split has less the gathering materials of mean particle size usually.Certainly, described gathering materials particularly ground or when pulverizing, may be very irregular.Typically gathering materials comprises inorganic materials, comprises sand, gravel and rubble etc.; Some organic materials comprises retread material and thermoplastic material; And one or more inorganic and mixture organic materials.Other inorganic and organic materials (though not illustrating here) that known suitable work gathers materials also can be used for the present composition.

Paving compositions of the present invention also can be used for preparing the modified version seal coating.Seal coating is generally used with heated bitumen, fluxed asphalt or emulsified bitumen form.Generally from truck, spray fusion or fluid asphalt, on pitch, place and gather materials, will gather materials then to roll or be pressed into and finish this operation in the pitch.

Can handle by routine techniques after paving compositions of the present invention is made and make it under the condition of for example building the road, to keep fluid or molten state.For example, available suitable volatile solvent or distillate glallzing are made fluxed asphalt with pitch.Fluxed asphalt is directly mixed and as the paving compositions use of fluid form (can at ambient temperature) with gathering materials.Be to make asphalt emulsification with another routine techniques that makes the pitch fluidisation before mixing and form paving compositions that gathers materials by known technology.The advantage of this fluidization process be with gather materials mix after, can use as paving compositions at ambient temperature.

The gordian technique of producing paving compositions is to guarantee the end-use of the chemical compatibility and the paving compositions of asphalt cement.About chemical compatibility, exist factor such as undesired salt in must considering to gather materials to reduce the possibility of bituminous pavement road composition fracture.

In addition, also require in the paving compositions contained gather materials and asphalt cement bonding better with guarantee bituminous composition thoroughly " wetting " and also before the bituminous pavement road composition is placed on the road surface and afterwards these materials mix well.In addition, also must consider the rerum natura of gathering materials, promptly under high traffic flow and/or fully loaded transportation condition that expectation can run into, can select to be fit to estimate the mixture of use pattern.

Therefore, described paving compositions comprises the tackiness agent that contains polymkeric substance of the present invention described herein.Available toxilic acid or maleic anhydride make described functionalization of polymers.Other component can be combined to form binder composition with the preparation of described polymkeric substance or described polymkeric substance.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and combination.Described binder composition can comprise 80% (weight) or still less or 60% (weight) or still less or 40% (weight) or still less or 30% (weight) or still less or 20% (weight) or one or more tackifier still less.

Again on the other hand, described binder composition can comprise 70% (weight) or still less or one or more additive of 30 to 60% (weights).Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, He Shui.Typical filler comprises carbon black, broken ore, mine tailing, cinder, slag, lime-ash, broken tire, clay and glass.The size of this filler is smaller than gathering materials usually, introduces this filler usually and reduces in the concrete road surface pave with maximum dose and form the space.

Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical antioxidant comprises alkylphenol, hindered phenol and amphyl, as tertiary butylated hydroquinone, butylated hydroxyanisol, many butyl bis-phenol, Yoshinox BHT (BHT), alkylation quinhydrones, 2,6-ditertbutylparacresol, 2,5-two uncle's aryl quinhydrones, Octadecane base-3-(3,5-di-t-butyl-4-hydroxyphenyl) etc.

On the one hand, to be mixed with PAFT be 60 ℃ or higher to described binder composition.On the other hand, the SAFT of described binder composition is 70 ℃ or higher.On the other hand, the solidification value of described binder composition is-20 to 250 ℃.Again on the other hand, the open temperature of described binder composition is-20 to 250 ℃.

Described paving compositions comprises 95% (weight) or still less or the gathering materials of 90 to 96% (weights) usually.On the one hand, described paving compositions comprises the pitch of 80 to 99% (weights).On the other hand, described paving compositions comprises the gathering materials of binder composition, at least 40% (weight) of at least 20% (weight), the pitch of at least 20% (weight) and other additive of maximum 10% (weights).

A. a paving compositions comprises pitch, gathers materials and binder composition, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.

The paving compositions of B. top A section, wherein said pitch are one or more rock asphalt, petroleum pitch or its arbitrary combination.

C. arbitrary section paving compositions above, wherein said rock asphalt comprises asphalite, stellar coal, grahamite, manjak, lake pitch, Trinidad asphalt or rock asphalt.

D. arbitrary section paving compositions above, wherein said gathering materials is selected from clay, stone, sand, rock, gravel and slag.

E. arbitrary section paving compositions above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

F. arbitrary section paving compositions above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

G. arbitrary section paving compositions above, wherein said binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

H. arbitrary section paving compositions above, wherein said filler is selected from carbon black, broken ore, mine tailing, cinder, slag, lime-ash, broken tire, clay and glass.

I. arbitrary section paving compositions above, wherein said binder composition comprise 30% (weight) or still less or 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or still less or 3% (weight) or still less or 1% (weight) or still less or 0.5% (weight) or one or more wax still less.

J. arbitrary section paving compositions above, wherein said binder composition comprise 80% (weight) or still less or 60% (weight) or still less or 40% (weight) or still less or 30% (weight) or still less or 20% (weight) or one or more tackifier still less.

K. arbitrary section paving compositions above, wherein said binder composition comprise 70% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or one or more additive of 30 to 60% (weights).

L. arbitrary section paving compositions above, wherein said paving compositions comprise 95% (weight) or still less or the gathering materials of 90 to 96% (weights).

M. arbitrary section paving compositions above, wherein said paving compositions comprises the pitch of 80 to 99% (weights).

N. arbitrary section paving compositions above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

O. arbitrary section paving compositions above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

P. arbitrary section paving compositions above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

Q. arbitrary section the preparation method of paving compositions comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With described binder composition is applied at least a portion of asphalt mixture.

O. glue rod

In one particular, binder composition described herein can be used for the glue rod.The glue rod is sold in a variety of forms, and one of them is a hotmelt glue rod.Hotmelt glue rod is designed for binder spray usually.Binder spray is fit to be held in operator's the hand, and the melt chamber of accepting the glue stick end and making it to melt by the heat that infeeds is arranged.Hotmelt glue rod is pressed into melt chamber can make hotmelt glue rod melt gradually.Along with hotmelt glue rod infeeds melt chamber and fusing therein, the fused tackiness agent flows out from the nozzle of binder spray.Thereby, hotmelt glue rod is heated to the use temperature that enough glue is imposed on base material with the fusion form.Described base material can comprise paper, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, film, plastic film, laminating material, sheet material, timber, plastics, polystyrene, nylon, polycarbonate, polypropylene, styrenic porous plastics, porous substrate, polyvinyl chloride, wall, polyester or its combination.

The use temperature of regulating hotmelt glue rod provide enough low adhesive melt viscosity with guarantee base material wetting well and provide suitable open hour behind gluing, base material is placed on the appropriate location.Described binder composition be cooled to about room temperature or following after to become basically sticking be ideal.The tackiness agent that is used for hotmelt glue rod also should be able to be bonded in multiple base material.

Another kind of glue rod is a pressure sensitive adhesive glue rod.Pressure sensitive adhesive glue rod is the commercially available product that comprises cased a collection of solid binder.Usually, removable lid is with shell seal, and outer casing bottom has opening.This opening with pressure sensitive adhesive glue rod the axle vertical plane in.Can remove lid when wanting to use pressure sensitive adhesive glue rod.

Pressure sensitive adhesive glue rod is used for base material and does not need heating, but tackiness agent is adhered on the base material.Similarly, can when exerting pressure, make base material adhere to another base material subsequently, because the glue that is applied by the glue rod at room temperature is clamminess.

For pressure sensitive adhesive, at least a component of described binder composition is liquid at ambient temperature.Described liquid ingredient makes pressure sensitive adhesive glue rod have pressure-sensitive or surface glue viscosity at ambient temperature.Usually in binder composition, add polymeric additive, tackifier and/or softening agent the glue rod is clamminess and also when contact its part stay on the base material.

The glue rod can be made up of the mixture of binder polymer, tackifier and wax.Make fusing point, use temperature, open hour, bond strength, weather resistance and the thermotolerance just compromise of binder composition according to the amount of using the change component.Wish to have when meeting with stresses good bonding not have the binder composition of inefficacy, this measured by bond strength and adhesion failure time.The bond strength and the adhesion failure time of preferred glue stick compositions are all high.The adhesion failure time, the long snappiness of glue rod that makes improved.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and combination.Described binder composition can comprise 65% (weight) or one or more tackifier still less.Preferred described binder composition comprises one or more tackifier of 20 to 40% (weights) or 5 to 20% (weights).

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 40% (weight) or one or more wax still less.Preferred described binder composition comprises 30% (weight) or still less or 20% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more wax still less.

Again on the other hand, described binder composition can comprise 30% (weight) or one or more additive still less.Preferred described binder composition comprises 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, tinting material, spices, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.For example described binder composition can comprise 3% (weight) or still less or 1.5% (weight) or still less or one or more antioxidant of 0.1 to 1.5% (weight) or 0.25 to 1% (weight).Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.Described binder composition can comprise 30% (weight) or still less or one or more softening agent of 5 to 20% (weights) or 1 to 12% (weight) or 5 to 10% (weights).Described binder composition can also comprise 3% (weight) or one or more pigment or 1% (weight) still less or still less.Again on the other hand, described binder composition comprises 3% (weight) or one or more filler still less.Again on the other hand, described binder composition comprises one or more inorganic salt of 5 to 30% (weights).Again on the other hand, described binder composition comprises 1% (weight) or one or more biocide still less.

The another kind of again representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 25% (weights) and one or more additive of maximum 15% (weights).

The glue rod should show enough thermotolerances.The normal thermotolerance scope of conventional hot-melt is 52 to 68 ℃.Satisfy the open market demand, thermotolerance should be not less than 52 ℃.The glue rod should be not softening at ambient temperature, and this softening temperature by binder composition is measured.Viscosity that in addition should be such when the glue rod melts in binder spray and rheological so that be easy to extrude glue when needing and do not need a large amount of hydrostomias during the plastic squeeze.The glue rod should have relatively low softening temperature and melt viscosity.When melt viscosity increased, degree of wetting generally descended.Melt viscosity is too high to cause being difficult to apply an amount of binder composition on base material before the glue cooling and becomes too sticking so that can't be effectively bonding with base material.Glue become too sticking or too hard so that can't operate before to make binder composition and base material form the satisfied bonding available time be the open hour.

Hot melt rubber stick should be designed to fine threading binder spray and finely therefrom distribute, and this requires the glue rod enough to make it firmly to be pushed into and enough glue by binder spray and under the use temperature that requires to keep adhesive properties with hot melt adhesive well in use simultaneously.Show enough hardness, the Xiao A hardness of glue rod under 25 ℃ should be 35 or higher.The hardness of glue rod is easy to regulate by the melt index of tackifier or wax content or used polymeric constituent.In addition, substrate fiber the tear rate of glue rod under 25 ℃ is 75% to 100%.Substrate fiber the tear rate of preferred described binder composition under 25 ℃ is 95% to 100%.On the other hand, the PAFT of described binder composition is 60 ℃ or higher.The PAFT of preferred described binder composition is 200 ℃ or lower.Again on the other hand, the SAFT of described binder composition is 70 ℃ or higher.The SAFT of preferred described binder composition is 200 ℃ or lower.On the other hand, the viscosity of described binder composition be 177 ℃ down 1 to 50Pas.The viscosity of preferred described binder composition is 177 ℃ and descends 0.8 to 13Pas.Again on the other hand, the softening temperature of described binder composition is 70 to 100 ℃.The softening temperature of preferred described binder composition is 80 to 90 ℃.More preferably the softening temperature of described binder composition is 70 to 80 ℃.On the other hand, the use temperature of described binder composition is 190 ℃ or lower.Again on the other hand, the use temperature of described binder composition is 138 ℃ or lower or 121 ℃ or lower.On the one hand, the bond strength of described binder composition on beech is 6 to 8N/mm ²The bond strength of preferred described binder composition on beech is 4N/mm ²Or it is higher.The bond strength of more preferably described binder composition on beech is 5N/mm ²Or it is higher.Again on the other hand, the bond strength of described binder composition on the oak material is 5N/mm ²Or it is higher.Again on the other hand, the some T shape peeling force of described binder composition is 3 to 4000N.The point T shape peeling force of preferred described binder composition is 5 to 3000N.More preferably the some T shape peeling force of described binder composition is 15 to 1000N.

Usually in melt jar or reactor, processing the glue rod under about 177 ℃ temperature.The melt index of material and fusing point require this temperature in the binder composition.Binder composition of the present invention can prepare with blending technology well known in the art, for example processing is then by known standard granulation process in forcing machine, and the tubular die that perhaps binder composition can be extruded into rod or be cast into specified dimension is with the hand-held binder spray of packing into.Can in mould, make glue rod age overnight before using, form at least some degree of crystallinity.

A. glue rod that uses with the binder spray that comprises the slender member that comprises binder composition, described binder composition comprise and have one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.

The glue rod of B. top A section, wherein exert pressure or when heating described glue rod on base material, produce binder deposition.

C. arbitrary section glue rod above, wherein said base material is selected from paper, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, Plastic Resin, metal, metal alloy, tinsel, film, plastic film, laminating material, sheet material, timber, plastics, polystyrene, nylon, polycarbonate, polypropylene, styrenic porous plastics, porous substrate, polyvinyl chloride, wall and polyester.

D. arbitrary section glue rod above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, modified hydrogenated terpenes, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

E. arbitrary section glue rod above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

F. arbitrary section glue rod above, wherein said binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, water, tinting material, nucleator and solvent.

G. arbitrary section glue rod above, wherein said binder composition comprises 40% (weight) or one or more wax still less.

H. arbitrary section glue rod above, wherein said binder composition comprises 30% (weight) or one or more wax still less.

I. arbitrary section glue rod above, wherein said binder composition comprises 20% (weight) or one or more wax still less.

J. arbitrary section glue rod above, wherein said binder composition comprises 60% (weight) or one or more tackifier still less.

K. arbitrary section glue rod above, wherein said binder composition comprises one or more tackifier of 20 to 30% (weights).

L. arbitrary section glue rod above, wherein said binder composition comprises 30% (weight) or one or more additive still less.

M. arbitrary section glue rod above, wherein said binder composition comprises 25% (weight) or one or more additive still less.

N. arbitrary section glue rod above, wherein said binder composition comprises 20% (weight) or one or more additive still less.

O. arbitrary section glue rod above, wherein said binder composition comprises 10% (weight) or one or more additive still less.

P. arbitrary section glue rod above, wherein said binder composition comprises 5% (weight) or one or more additive still less.

Q. arbitrary section glue rod above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

R. arbitrary section glue rod above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

S. arbitrary section glue rod above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

T. arbitrary section glue rod above, wherein said binder composition use temperature is 190 ℃ or lower.

U. arbitrary section glue rod above, wherein said binder composition use temperature is 138 ℃ or lower.

V. arbitrary section glue rod above, wherein said binder composition use temperature is 121 ℃ or lower.

W. arbitrary section glue rod above, wherein said binder composition is 35 or higher at 25 ℃ of following Xiao A hardness.

X. use the method for top arbitrary section glue rod with the fusion form, comprise the binder composition that comprises polymkeric substance is made the glue rod, described polymkeric substance has one or more C _3-40Alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; Described glue rod is heated to use temperature and described binder composition is imposed at least a portion of base material.

P. pipeline wraps up

In one particular, tackiness agent of the present invention can be used for pipeline parcel goods.Pipeline parcel goods or pipeline parcel can be used for making pressurized vessel, industrial container, umformer, pipeline, accessory, jar, vessel and container insulation or mending-leakage.In addition, pipeline parcel goods also can comprise on plane, ring joint and other mechanical part on all kinds of surfaces and using.Pipeline parcel goods described herein can be used in all types of industries such as building, structure, construction, food, beverage, mining, petrochemical industry, oil, gas and the water treatment.

Pipeline parcel goods generally form by coating adhesive composition at least a portion of parcel member.Described parcel member can comprise for example poly-uncle's butylene of fiberglass, fiber, Woven fabric, supatex fabric, fabric, cloth, polyethylene, polypropylene, acrylic rubber, EPDM, paracril, nylon, epichlorohydrin elastomer, polysulphide, acrylic elastomer or isoprene-isobutylene rubber.Pipeline parcel goods can be made by for example timber, cement, concrete, supatex fabric, Woven fabric, aluminium, stainless steel, brass, nickel, glass, glazed ceramics, unglazed pottery, ceramic tile, polyvinyl chloride, polyethylene terephthalate, gypsum, plaster, bituminous coating, roofing felt, synthetic polymer membranes and polyurathamc insulating material.Described parcel member can have any thickness.The exemplary package member that for example is used for civilian structure industry can have the minimum thickness of 1.27mm.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and combination.Described binder composition can comprise 80% (weight) or still less or 40% (weight) or still less or 60% (weight) or still less or 30% (weight) or still less or 20% (weight) or one or more tackifier still less.

Again on the other hand, described binder composition can comprise 70% (weight) or still less or one or more additive of 30 to 60% (weights).Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, adhesion promotor, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.

Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.Typical antioxidant can comprise alkylphenol, hindered phenol and amphyl, as tertiary butylated hydroquinone, butylated hydroxyanisol, many butyl bis-phenol, Yoshinox BHT (BHT), alkylation quinhydrones, 2,6-ditertbutylparacresol, 2,5-two uncle's aryl quinhydrones, Octadecane base-3-(3,5-di-t-butyl-4-hydroxyphenyl) etc.

Typical filler comprises silicon oxide, diatomite, lime carbonate, ferric oxide, hydrogenated castor oil, fumed silica, precipitated chalk, the fumed silica of hydrophobic treatment, hydrophobic precipitated lime carbonate, talcum, zinc oxide, polyvinyl chloride powder, mycocide, graphite, carbon black, pitch, carbon packing, clay, mica, fiber, titanium dioxide, Cadmium Sulfide, asbestos, wood powder, the polyethylene powder, chopped fibres, bubble shape thing, bead, thixotrope, wilkinite, calcium sulfate, calcium oxide, magnesium oxide, and combination or derivative.Exemplary surfactants comprises the organopolysiloxane that contains vinyl or contain sulfydryl, polydimethylsiloxanemacromer macromer and the combination or the derivative of ethenyl blocking.

It is 60 ℃ or higher that described binder composition can be mixed with PAFT.On the one hand, the SAFT of described binder composition is 70 ℃ or higher.On the other hand, the fracture tensile strength of described binder composition under 23 ℃ is 0.7 to 1.5bar.On the other hand, the elongation of described binder composition under 23 ℃ is 50% strain of raw footage or higher.On the other hand, the solidification value of described binder composition is-20 to 250 ℃.The open temperature of preferred described binder composition is-20 to 250 ℃.On the other hand, the cloud point of described binder composition is 275 ℃ or lower.The cloud point of preferred described binder composition is 190 ℃ or lower.More preferably the cloud point of described binder composition is 130 ℃ or lower.Again on the other hand, the second-order transition temperature of described binder composition is 0 ℃ or lower.

A. pipeline parcel goods comprise binder composition and parcel member, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, with Mw be 100000 or lower, wherein said binder composition place at least in part on the described parcel member or within.

B. arbitrary section pipeline parcel goods above, wherein said parcel member is selected from fiberglass, fiber, Woven fabric, supatex fabric, fabric, cloth, polyethylene, polypropylene, acrylic rubber, EPDM, paracril, nylon, epichlorohydrin elastomer, polysulphide, acrylic elastomer and isoprene-isobutylene rubber.

C. arbitrary section pipeline parcel goods above, wherein said pipeline parcel goods are selected from pipeline, accessory, jar, vessel and container.

D. arbitrary section pipeline parcel goods above, wherein said pipeline parcel goods are made by the material that is selected from timber, cement, concrete, supatex fabric, Woven fabric, aluminium, stainless steel, brass, nickel, glass, glazed ceramics, unglazed pottery, ceramic tile, polyvinyl chloride, polyethylene terephthalate, gypsum, plaster, bituminous coating, roofing felt, synthetic polymer membranes and polyurathamc isolator.

E. arbitrary section pipeline parcel goods above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

F. arbitrary section pipeline parcel goods above, wherein said binder composition also comprises one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

G. arbitrary section pipeline parcel goods above, described binder composition also comprises one or more additive that is selected from carbon black, silica gel, clay, aluminum oxide, metal oxide, softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

H. arbitrary section pipeline parcel goods above, wherein said binder composition comprise 30% (weight) or still less, 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or still less or 3% (weight) or still less or 1% (weight) or still less or 0.5% (weight) or one or more wax still less.

I. arbitrary section pipeline parcel goods above, wherein said binder composition comprise 80% (weight) or still less or 60% (weight) or still less or 40% (weight) or still less or 30% (weight) or still less or 20% (weight) or one or more tackifier still less.

J. arbitrary section pipeline parcel goods above, wherein said binder composition comprise 70% (weight) or still less or one or more additive of 30 to 60% (weights).

K. arbitrary section pipeline parcel goods above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

L. arbitrary section pipeline parcel goods above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

M. arbitrary section pipeline parcel goods above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

N. the preparation method of arbitrary section pipeline parcel goods comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; On at least a portion that described binder composition is applied to the parcel member.

Q. shatter proof glass

In one particular, tackiness agent described herein can be used for shatter proof glass.Two kinds of shatter proof glasses are arranged, lamination and tempering shatter proof glass.Laminated safety glass generally reduces the conduction of high-frequency sound and stops 97% uv-radiation.Thereby the tempering shatter proof glass is to make the glass sclerosis improve the monolithic glass of intensity by rapid heating and refrigerative tempering.

" shatter proof glass " used herein is the goods that transparent panel (pane) arranged.A vital role of shatter proof glass be wherein the adhesive therefor composition be not subjected to influence of temperature change and also under the situation of glass breakage described binder composition cling sheet glass.In addition, described binder composition absorption is applied to the shear-stress on the shatter proof glass because of the speed of expansion difference (when for example shatter proof glass comprises first glass coating and second layer of polycarbonate) of glass ingredient.Shatter proof glass generally comprises multilayer material, binder layer be applied to the outside of one deck or be applied to two or multilayer between make it bonding mutually.Form transparent panel by coating adhesive composition on one or more transparent panel, described binder composition can form film on one or more transparent panel.Described one or more transparent panel can be made by polyvinyl butyral acetal, urethane, vinyl-acetic ester, polyethylene, polypropylene, polycarbonate, glass, silicate glass or its combination.

Again on the other hand, described binder composition can comprise 30% (weight) or still less or 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, adhesion promotor, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.

On the one hand, to be mixed with the substrate fiber rate of tearing be 75% to 100% under 22 ℃ to described binder composition.It is 75% to 100% under-35 to 22 ℃ that the substrate fiber of preferred described binder composition is torn rate.More preferably the substrate fiber of the described binder composition rate of tearing is 75% to 100% under 22 to 40 ℃.On the other hand, the PAFT of described binder composition is 60 ℃ or higher.On the other hand, the SAFT of described binder composition is 70 ℃ or higher.Again on the other hand, the viscosity of described binder composition is 177 ℃ of following 9Pas or lower.The viscosity of preferred described binder composition is 177 ℃ and descends 0.5 to 2.5Pas.Again on the other hand, the cloud point of described binder composition is 275 ℃ or lower.The cloud point of preferred described binder composition is 190 ℃ or lower.More preferably the cloud point of described binder composition is 130 ℃ or lower.Most preferably the cloud point of described binder composition is 100 ℃ or lower.On the other hand, the second-order transition temperature of described binder composition is-65 to 30 ℃.The second-order transition temperature of preferred described binder composition is 0 to 20 ℃.More preferably the second-order transition temperature of described binder composition is 10 to 20 ℃.

A kind of representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula of described binder composition comprises one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 30% (weights) and one or more additive of maximum 15% (weights).Another representative formula again of described binder composition comprises that one or more wax of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 25% (weights) and one or more additive of maximum 15% (weights) comprise antioxidant.

Above-mentioned transparent panel can be used as for example splinter-proof glass, sound control glass and shatter proof glass.Shatter proof glass also can be used for sound insulation.In another example, shatter proof glass is to make 3 layer silicate sheet glass (every layer of 6mm is thick) adhere to the thick sheet of polyvinyl butyral of 0.76mm with binder composition to form as the splinter-proof glass panel.Described binder composition can be binder composition described herein or be used to make two-layer adherent other binder composition.On passenger's face of described glass, make polycarbonate plate be bonded in the splinter-proof glass panel by thermoplastic urethane layers.The film that has binder composition of the present invention to form on the outside surface of splinter-proof glass panel.

In another example, transparent panel can be used as laminated safety glass such as vehicle glass.Be the preparation laminated safety glass, two or multi-disc glass between place skim flexible plastic film such as polyvinyl butyral acetal (PVB).Plastic film is the glass fix in position during glass breakage, helps to alleviate the injury that glass causes of dispersing.This film also can stretch, and glass is still sticking thereon.Laminated safety glass also is used for thermometer, cuts the thing plate, greenhouse window, shower enclosure and office partitions.

A. goods that transparent panel is arranged comprise one or more transparent panel and are applied to binder composition at least a portion of described one or more panel, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.

The goods of B. top A section, wherein said one or more transparent panel comprises polyvinyl butyral acetal, urethane, vinyl-acetic ester, polyethylene, polypropylene, polycarbonate, glass, silicate glass or its combination.

C. arbitrary section goods above, wherein said goods are selected from splinter-proof glass, sound control glass and shatter proof glass.

D. arbitrary section goods above, wherein said binder composition forms film on described one or more transparent panel.

E. arbitrary section goods above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

F. arbitrary section goods above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

G. arbitrary section goods above, described binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

H. arbitrary section goods above, wherein said binder composition comprise 30% (weight) or still less, 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or still less or 3% (weight) or still less or 1% (weight) or still less or 0.5% (weight) or one or more wax still less.

I. arbitrary section goods above, wherein said binder composition comprise 80% (weight) or still less or 60% (weight) or still less or 40% (weight) or still less or 20% (weight) or one or more tackifier still less.

J. arbitrary section goods above, wherein said binder composition comprise 30% (weight) or still less, 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.

K. arbitrary section goods above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

L. arbitrary section goods above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

M. arbitrary section goods above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

N. arbitrary section goods above, the viscosity of wherein said binder composition is lower than 9Pas under 177 ℃.

O., the preparation method that the goods of transparent panel are arranged comprises the formation binder composition, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With described binder composition is applied at least a portion of transparent panel.

R. roofing board

In one particular, tackiness agent of the present invention can be used for roofing board.Roofing board is generally formed by roofing element and the tackiness agent that makes roofing element stick at the roof.Described roofing element is generally formed by metal sheet such as copper, the stainless steel that is coated with slicker solder, zinc, aluminium or its alloy.

Thereby the major criterion of roofing board comprise resistance to crushing, the melt temperature when the roofing board stacking package loads and transports lower can be under without the situation of heating installation selfsealings and connect good bond between the face, higher wind resistance and good low-temperature stability are arranged.Other important consideration item comprises that anti-photo-oxidation is good; Particularly tackiness agent was exposed to sunlight can keeps tackiness after two hour.

In addition, described binder composition should show " ooze and move " property so that more firm bonding and better wind resistance to be provided under 32 to 37 ℃ low temperature." ooze and move " used herein means in the contact surface that binder composition partly flows into roof Material.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and combination.Described binder composition can comprise 95% (weight) or one or more tackifier still less.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

Again on the other hand, described binder composition can comprise 50% (weight) or one or more additive still less.Described one or more additive can comprise for example softening agent, oil, stablizer, antioxidant, pigment, dyestuff, antiblocking additive, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, fluorescent agent, compatilizer, biocide, He Shui.Typical oil can comprise for example aliphatic naphthenic oil, white oil and combination thereof.Described phthalic ester can comprise phthalic acid two different undecyl esters (DIUP), phthalic acid diisononyl esters (DINP), dioctyl phthalate (DOP) (DOP), its combination, or derivatives thereof.Typical polymeric additive comprises the multipolymer of equal poly-alpha olefins, alpha-olefin, binary and terpolymer, elastomerics, polyester, segmented copolymer (comprising two blocks and triblock copolymer), esters polymer, acrylic acid alkyl ester polymer and the acrylic ester polymer of diolefine.Typical softening agent can comprise mineral oil, polybutene, phthalic ester and combination thereof.

Again on the other hand, described binder composition comprises one or more bituminous material such as the pitch of 80% (weight).On the one hand, described tackiness agent can also comprise fire retardant.The example of the fire retardant that is fit to comprises Secondary ammonium phosphate, ammonium polyphosphate, phosphoric acid tribromo peopentyl ester; Halogenated fire-retardants is as the chlorodiphenyl that is used in combination with metal oxide and halogenation cyclopentadiene, halogenated polymer; The condensation product, 2 of the mixture of halogen and phosphorus fire retardant such as amine and tricresyl phosphate (2, the 3-dibromopropyl) ester, the condensation product of mixture, two (propyloic) phosphine oxide and the monochloromethyl benzene of 3-dibromo-propanol and tricresyl phosphate (2, the 3-dibromopropyl) ester; The mixture of metal carboxylate and phosphoric acid β-halogen ethyl ester; Salt with inorganic combustion inhibitor such as halogen-containing antimony oxide sol and Sb (V) ester.

It is 90 ℃ or higher that described binder composition can be mixed with SAFT.On the other hand, to be mixed with the fracture tensile strength under 25 ℃ be 6.5bar or higher to described binder composition.The elongation of described binder composition under 25 ℃ is 5% strain of raw footage or higher.In addition, the viscosity of described binder composition can be at 177 ℃ following 0.2 to 10Pas.Again on the other hand, the second-order transition temperature of described binder composition is-65 to 30 ℃.Again on the other hand, the softening temperature of described binder composition is 80 to 200 ℃.

A kind of representative formula of described binder composition comprises one or more bituminous material of one or more tackifier of the polymkeric substance of the present invention of at least 35% (weight), maximum 80% (weights), maximum 80% (weights) and one or more additive of maximum 50% (weights).Another representative formula of described binder composition comprises one or more bituminous material of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 40% (weights) and one or more additive of maximum 50% (weights).Another representative formula again of described binder composition comprises one or more bituminous material of one or more tackifier of the polymkeric substance of the present invention of at least 50% (weight), maximum 60% (weights), maximum 25% (weights) and one or more additive of maximum 35% (weights).

Described binder composition can adhesive tape or the droplet form (for example under in succession plate or bar generation crossover or partly overlapping situation at the lower surface or the upper surface of roof Material) is applied to roofing element such as roofing board or continuously or on the roof sheet material of rolling along the zone that will contact with second roofing element with droplet or other configuration.Can be used for sealing side line plate or plate equally.Described binder composition can also the hot melts form be used to assemble the roof.

Be preparation gluing roofing board, roofing element is being equipped with above the spreadometer of adhesive material or below by.Described spreadometer can be one group of print wheel or can be on the described material surface that will be connected with another member with sealing with the droplet of consistent size or be connected band gummed forcing machine.Described binder composition be fixed on want after the zone water, air cooling or make the binder composition quenching with any suitable quenching medium contact cooling.

Generally will be behind gluing gummed material such as roofing element by the size cutting, but cut roofing board in advance or plate is sent into the spreadometer gluing also within the scope of the present invention then.

A. roofing board comprises binder composition and the roofing element of first side and second side is arranged, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the point T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower, with Mw be 100000 or lower, wherein said binder composition puts at least a portion of described second side.

The roofing board of B. top A section, wherein said roofing element are selected from copper, steel, zinc, aluminium, its combination and alloy thereof.

C. arbitrary section roofing board above, wherein said first side comprises one or more material that is selected from roof pitch, fabric, gathers materials and makes up.

D. arbitrary section roofing board above, wherein said second side comprises one or more material that is selected from rubber, fiberglass, aromatic poly, carbon, polyester, nylon, pitch and metal sheet.

E. arbitrary section roofing board above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, modification polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene, the modification terpenes, hydroabietic acid, modified hydrogenated terpenes, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

F. arbitrary section roofing board above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

G. arbitrary section roofing board above, described binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, fire retardant, filler and water.

H. arbitrary section roofing board above, wherein said binder composition also comprises one or more bituminous material.

I. arbitrary section roofing board above, wherein said binder composition comprises 80% (weight) or one or more bituminous material still less.

J. arbitrary section roofing board above, wherein said binder composition comprises 95% (weight) or one or more tackifier still less.

K. arbitrary section roofing board above, wherein said binder composition comprises 50% (weight) or one or more additive still less.

L. arbitrary section roofing board above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

M. arbitrary section roofing board above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

N. arbitrary section roofing board above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

O. arbitrary section roofing board above, the viscosity of wherein said binder composition are 177 ℃ and descend 0.2 to 10Pas.

P. arbitrary section roofing board above, the softening temperature of wherein said binder composition is 80 to 200 ℃.

Q. arbitrary section roofing board above, wherein said binder composition comprises 80% (weight) or one or more tackifier still less, 70% (weight) or one or more tackifier still less, 60% (weight) or one or more tackifier still less, 50% (weight) or one or more tackifier still less, 40% (weight) or one or more tackifier still less, 30% (weight) or one or more tackifier still less, 20% (weight) or one or more tackifier still less, 10% (weight) or one or more tackifier still less, 5% (weight) or one or more tackifier still less, or 1% (weight) or one or more tackifier still less.

R. arbitrary section roofing board above, wherein said binder composition comprises 50% (weight) or one or more wax, 40% (weight) still less or one or more pitch still less or other bituminous material, 30% (weight) or one or more pitch still less or other bituminous material, 20% (weight) or one or more pitch still less or other bituminous material, 10% (weight) or one or more pitch still less or other bituminous material or 5% (weight) or one or more pitch still less or other bituminous material.

S. arbitrary section roofing board above, wherein said binder composition comprises 60% (weight) or one or more additives, 50% (weight) still less or one or more additive, 40% (weight) still less or one or more additive, 30% (weight) still less or one or more additive, 20% (weight) still less or one or more additive, 10% (weight) still less or one or more additive, 5% (weight) still less or one or more additive, 3% (weight) still less or one or more additive or 1% (weight) still less or one or more additive still less.

T. arbitrary section the preparation method of roofing board comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; On at least a portion of the bottom side that described binder composition is applied to the roofing element that comprises flat basically panel.

S. reflectance coating

In one particular, tackiness agent of the present invention can be used for reflective article.Form reflective article by making the part of base material have reflectivity at substrate surface coating reflecting material.Described reflecting material can comprise any material well known by persons skilled in the art.For example, described reflecting material can comprise prism and granulated glass sphere.Described substrate surface can comprise the road surface, cycle track, traffic sign, soft motion ground, ground, playground, ship, runway, crossing, buildings, the tennis court, traffic route, the synthetic rubber surrogate, oil rig, the tunnel, concrete, metal, pitch, pitch earth, brick, paving stone, ceramic tile, steel plate, timber, pottery, polymeric material, glass, abutment, the traffic roadblock, fence, pipeline, electric pole, guardrail, concrete blocks, curb, the parking lot, porcelain, stone, plank, shaving board, wooden auto parts, cinder brick, glass port, traffic cylinder (traffic drum), traffic cone, beaujolais, liquid-crystal display, lamp, duplicating machine, the electronics backboard, scattering whiteness standard substance, and lamp for photography.

The coating adhesive composition adheres on the base material reflecting material at least a portion of reflecting material.Described binder composition comprises polymkeric substance of the present invention described herein.Available toxilic acid or maleic anhydride make described functionalization of polymers.Other component can be combined to form binder composition with the preparation of described polymkeric substance or described polymkeric substance.

On the one hand, described binder composition can comprise one or more tackifier.Described tackifier can comprise for example aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and combination.Described binder composition can comprise 99% (weight) or one or more tackifier still less.

On the other hand, described binder composition can comprise one or more wax, as f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof of polar waxes, nonpolar wax, f-t synthetic wax, oxidation.Described binder composition can comprise 30% (weight) or one or more wax still less.

On the one hand, described binder composition is mixed with solidification value and is-20 to 250 ℃.Again on the other hand, the open temperature of described binder composition is-20 to 250 ℃.On the one hand, the viscosity of described binder composition is 177 ℃ of following 9Pas or lower.The viscosity of preferred described binder composition is 177 ℃ and descends 0.2 to 8Pas.More preferably the viscosity of described binder composition be 177 ℃ down 0.5 to 2.5Pas.On the other hand, the cloud point of described binder composition is 275 ℃ or lower.Again on the other hand, the density of described binder composition is 25 ℃ of following 0.99g/cm ³Or it is lower.Again on the other hand, the second-order transition temperature of described binder composition is-65 to 30 ℃.Again on the other hand, the brightness of described binder composition is 70 or higher.The brightness of preferred described binder composition is 75 or higher.

A. a reflective article comprises the reflecting material and the binder composition that are applied at least in part on the substrate surface, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower.

The reflective article of B. top A section, wherein said reflecting material is selected from prism and granulated glass sphere.

C. arbitrary section reflective article above, wherein said substrate surface is selected from the road surface, cycle track, traffic sign, soft motion ground, ground, playground, ship, runway, crossing, buildings, the tennis court, traffic route, the synthetic rubber surrogate, oil rig, the tunnel, concrete, metal, pitch, pitch earth, brick, paving stone, ceramic tile, steel plate, timber, pottery, polymeric material, glass, abutment, the traffic roadblock, fence, pipeline, electric pole, guardrail, concrete blocks, curb, the parking lot, porcelain, stone, plank, shaving board, wooden auto parts, cinder brick, glass port, the traffic cylinder, traffic cone, beaujolais, liquid-crystal display, lamp, duplicating machine, the electronics backboard, scattering whiteness standard substance, and lamp for photography.

D. arbitrary section reflective article above, wherein said binder composition also comprise and are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, the polycyclopentadiene resin, rosin, rosin ester, wood rosin, the wood rosin ester, starex, the starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, the Hydrogenated aliphatic resin, the Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid, hydrogenated wood rosin glycerol ester, its derivative, and one or more tackifier of combination.

E. arbitrary section reflective article above, wherein said binder composition also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers and the combination thereof that are selected from polar waxes, nonpolar wax, f-t synthetic wax, oxidation.

F. arbitrary section reflective article above, described binder composition also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

G. arbitrary section reflective article above, wherein said binder composition comprises 30% (weight) or one or more wax still less.

H. arbitrary section reflective article above, wherein said binder composition comprises 99% (weight) or one or more tackifier still less.

I. arbitrary section reflective article above, wherein said binder composition comprise 30% (weight) or still less, 25% (weight) or still less or 20% (weight) or still less or 15% (weight) or still less or 10% (weight) or still less or 5% (weight) or one or more additive still less.

J. arbitrary section reflective article above, the melt viscosity of wherein said polymkeric substance is 190 ℃ of following 90000mPas or lower.

K. arbitrary section reflective article above, be 30 minutes or shorter the set time of wherein said polymkeric substance.

L. arbitrary section reflective article above, the some T shape peeling force of wherein said polymkeric substance are 3 to 4000N.

M. arbitrary section reflective article above, the viscosity of wherein said binder composition is 9Pas or lower down at 177 ℃.

N. arbitrary section reflective article above, the brightness of wherein said binder composition are 70 or higher or 75 or higher.

O. arbitrary section the preparation method of reflective article comprises the formation binder composition above, and described binder composition comprises and has one or more C _3-40The polymkeric substance of alkene and 0 to 5mol% ethene, the some T shape peeling force of wherein said polymkeric substance is 1 newton or higher, the branch index of under the Mz of described polymkeric substance, measuring (g ') be 0.95 or lower and Mw be 100000 or lower; With described binder composition is applied at least a portion of reflecting material.

Characterize and test

Molecular weight (number-average molecular weight (Mn), weight-average molecular weight (Mw) and z-average molecular weight (Mz)) is measured with the Waters150 size exclusion chromatography (SEC) that differential refraction rate detector (DRI), online low angle light scattering (LALLS) detector and viscometer (VIS) are housed.The details of detector calibration has been described [Volume 34 for reference: T.Sun, P.Brant, R.R.Chance and W.W.Graessley, Macromolecules, Number19,6812-6820, (2001)] in other document; Following note is the concise and to the point description to its assembly.

Have three Polymer Laboratories PLgel 10mm Mixed-B posts, nominal flow rate 0.5cm ³The SEC that volume 300 microlitres are injected in/min and nominal is common to two kinds of detector configurations.Various transfer lines, pillar and differential refractometer (the DRI detector is mainly used in and measures elute soln concentration) are put into the baking oven of 135 ℃ of maintenances.

The LALLS detector is the two angular light light scattering photometers (Precision Detector Inc.) of 2040 types.Its fluid chamber that is positioned on the SEC baking oven uses 690nm diode laser light source and collects the scattered light at 15 and 90 ° of two angle places.Only 15 ° of work outpuies are used for these experiments.Its signal is sent into data gathering plate (National Instruments), and this collecting board is collected reading with 16/second speed.Four minimum readings are average, then a scaling signal is sent into the SEC-LALLS-VIS computer.The LALLS detector is arranged on after the SEC post, but before viscometer.

Viscosity is counted high temperature 150R type (Viscotek Corporation).It is made of four kapillaries and two pressure transmitters of arranging with the comparison bridge configuration.Sensor measurement is along the total pressure drop of detector, and another measures differential pressure between the bridge both sides.Calculate the specific viscosity of the solution that flows through viscometer by its work output.Viscometer is positioned at after the LALLS detector in the SEC baking oven, but before the DRI detector.

The solvent that is used for SEC experiment be equipped with 1,2 by adding as the 6g Yoshinox BHT (BHT) of antioxidant, and 4 litre flasks of 4-trichlorobenzene (TCB) (Aldrich SILVER REAGENT) are also waited for BHT to dissolve and prepared.Then this TCB mixture is filtered through 0.7 μ m glass prefilter, filter by 0.1 μ m polytetrafluoroethylene filter then.Between high-pressure pump and SEC post, there is another online 0.7 micron glass prefilter/0.22 micron polytetrafluoroethylene filter assembly.Then (Phenomenex, ModelDG-4000) degassing enters SEC then with online degasser with TCB.

Prepare polymers soln by the following method: the exsiccant polymkeric substance is dropped in the Glass Containers, adds the TCB of aequum, with this mixture 160

C heated the while continuously stirring down about 2 hours.All amounts are carried out gravimetric analysis.Be used to represent that the TCB density (mass/volume) of polymer concentration at room temperature is 1.463g/ml, 135

C is 1.324g/ml down.The injection concentration scope is 1.0 to 2.0mg/ml, and wherein low concentration is used for the higher molecular weight sample.

Before each sample of operation, DRI detector and syringe are purged.Then the flow velocity in the instrument is increased to 0.5ml/min, before injecting the 1st sample, DR I was stablized 8-9 hour.Argon ion laser was opened 1 to 1.5 hour, promptly before the operation sample by with idle mode running laser apparatus 20-30 minute, switch to full power with light adjusting pattern then.

Branch index is measured with the SEC (SEC-VIS) that in-line viscometer is housed, and the g ' under each molecular weight in the record SEC trace.This branch index g ' is defined as;

g′＝η _b/η ₁

η wherein _bBe the limiting viscosity of branched polymer, η ₁Be identical viscosity-average molecular weight (M with this branched polymer _v) the limiting viscosity of linear polymer.η ₁=KM _v ^α, wherein K and α are the observed value of linear polymer, and Ying Zaiyu is used for obtaining on the identical SEC-DRI-LS-VIS instrument that branch index measures.For the polypropylene specimen for preparing among the present invention, use K=0.0002288 and α=0.705.The SEC-DRI-LS-VIS method does not need to carry out polymolecularity proofreaies and correct, because limiting viscosity and molecular weight are measured under elution volume separately, can think that it comprises narrow dispersed polymeres.The linear polymer of the standard substance of choosing as a comparison should have identical viscosity-average molecular weight and co-monomer content.Contain Carbon-13NMR method confirmation (Rev.Macromol.Chem.Phys., the C29 (2﹠amp of the linear feature of C2 to C10 polymer of monomers by Randall; 3), p.285-297).

C11 and above-mentioned monomeric linear feature confirm by the gpc analysis that uses the MALLS detector.For example, for propylene copolymer, NMR should not show the degree of branching (even comonomer is a butylene, then should not have the side chain greater than 2 carbon atoms) greater than comonomer.For alfon, GPC should not show the side chain greater than a carbon atom.When comonomer wherein is that C9 or higher polymkeric substance are when needing linear standard, can be with reference to T.Sun, P.Brant, R.R.Chance, and W.W.Graessley, Macromolecules, Volume 34, Number 19,6812-6820, the scheme of relevant those polymer determination standards in (2001).For syndiotactic polymer, this standard should have and can measure by correlated syndiotaxy, measures by Carbon 13 NMR.

In another embodiment, the polymkeric substance that the present invention produces has molecular weight distribution (Mw/Mn) at least 2, and preferably at least 5, preferably at least 10, further more preferably at least 20.

In another embodiment, unimodal, the bimodal or multimodal molecular weight that the polymkeric substance of production can have polymer material distributes (Mw/Mn), measures by size exclusion chromatography (SEC).Bimodal or the multi-modal SEC of being meant trace have more than one peak or flex point.Flex point is that the second derivative signal of wherein curve changes the point of (for example just becoming or on the contrary from negative).

Peak value fusing point (Tm), peak crystallization temperature (Tc), melting heat and degree of crystallinity are according to the following program determination of ASTM E794-85.Difference formula scanning calorimetric (DSC) data obtain with 2920 type machines of TA Instruments company.The sample of weighing for about 7-10mg is sealed in the aluminium sample disc.The DSC data are record by the following method; At first sample is cooled to-50 ℃, then it is heated to 200 ℃ gradually with 10 ℃/min of speed.This sample was kept 5 minutes down at 200 ℃, apply cooling-heating cycle for the second time then.Write down first and second times the cycling hot process.Measure this area under a curve and be used to measure melting heat and degree of crystallinity.Percent crvstallinity is calculated with formula [area below the curve (J/g)/B (J/g)] * 100, and wherein B is the melting heat of the homopolymer of principal monomer component.These B values are from Polymer Handbook, and the 4th edition, John Wiley and Sons publishes, and obtains among the New York 1999.Numerical value 189J/g (B) is as the melting heat of 100% crystalline polypropylene.For the polymkeric substance that shows a plurality of fusings or peak crystallization, as the peak value fusing point, the highest peak crystallization is as peak crystallization temperature with the highest melting hump.

Second-order transition temperature (Tg) is measured by 2920 type machines of ASTM E 1356 usefulness TA Instruments companies.

To be used for ¹³C NMR spectrographic polymer samples is dissolved in d ₂In-the sym.-tetrachloroethane, and with 75 or the NMR spectrograph of 100MHz at 125 ℃ of record samples down.The polymkeric substance resonance peak relates to mmmm=21.8ppm.The calculating that relates in the polymer characterization that is undertaken by NMR is followed F.A.Bovey at " Polymer Conformation and Configuration ", Academic Press, New York 1969 and J.Randall exist " Polymer Sequence Determination; Carbon-13 NMR Method ", Academic Press, New York, the work in 1977.The length sequences per-cent of two methylene radical, % (CH ₂) ₂, according to following calculating: multiply by 100 again divided by the integration of the length sequences of a methylene radical between the 45-49ppm and the summation of the methine carbon atom integration between the 14-18ppm at the methine carbon atom integration between the 14-18ppm (equaling the length sequences number of two methylene radical on the concentration).This is the minimum of computation of methylene base unit weight contained in the sequence to two or more methylene radical, because get rid of greater than the methylene sequences of two methylene radical.This explanation is based on H.N.Cheng and J.A.Ewen, Makromol.Chem.1989,190,1931.

The ethylene content of polymkeric substance can followingly be determined.At temperature about 150 ℃ or the thin uniform thin film of relative superiority or inferiority compacting more, then it is placed on Perkin Elmer PE 1760 infrared spectrometers.The record sample is from 600cm ^-1To 4000cm ^-1Full spectrum, and calculate vinyl monomer wt% content: ethene wt%=82.585-111.987X+30.045X according to following formula ², wherein X is 1155cm ^-1The peak height and the 722cm at place ^-1Place or 732cm ^-1The ratio of the peak height (choosing peak higher among both) at place.The also available this method of the concentration of other monomer in polymkeric substance is calculated.

Adhesive test

The performance of the temperature that rises with 10 (5.5 ℃)/15min is born in SAFT (D4498 of modification) measurement bonding place under the constant force of drawing back the bonding place with shear mode.The bonding place forms (1 inch x3 inch (2.5cmx7.6cm) (on kraft paper) in a manner described.Will be in baking oven at room temperature at the sample vertical hanging of its bottom-loaded 500g load.Temperature when the record weight falls (when idol has sample to reach to be higher than baking oven to hold on the fair temperature (＞265 (129 ℃)), stop, and with other sample average under this final temperature).

Be defined as that compacting adhesive substrate structure enough fixedly secures together set time so that cause substrate fiber to be torn separately the time, therefore should be bonding enough by force down to the time that can remove compacting.Also can be bonding by further cooling off enhancing, yet, no longer need compacting.Measure these set times in the following way; The fluxing point of tackiness agent placed be fixed on the folder base material that lies on the flat surface.On adhesive spots, place folder intermediate plate (file folder tab) (1 inch x3 inch) after 3 seconds (2.5cmx7.6cm)) and use the compacting of 500g weight.This weight was stopped about 0.5 to about 10 seconds.The structure that so forms is drawn back, to such an extent as to check the enough good bondability that the generation substrate fiber is torn.Record produces this good bonding required shortest time as set time.Calibrate this method with standard substance.

After making structure, it is carried out various damages with the assessment bonding effect.When to the adhesion failure of paper base material, quantitatively a plain mode of bonding effect is that estimation is retained in the adhesive spots area in the paper fiber when along the cement line structure deteriorate.This assessment is called substrate fiber tears per-cent.An example of good fiber is, when with sample-12 ℃ of conditionings 15 hours and attempt to destroy when bonding down, will have the 80-100% substrate fiber to tear estimated value.To tear may be the signal of bounding force forfeiture to 0% substrate fiber under these conditions.

Xiao A hardness is measured according to ASTM 2240.The air cooling point of tackiness agent is carried out acupuncture, and by the calibration summary deflection.

Point T shape peeling force is pressed ASTM D 1876 and is measured, except sample is produced as follows: two 1 inch x3 inch (2.54cmx7.62cm) base material that will cut out combines by adhesive spots, and the volume of tackiness agent is for it occupies about 1 square inch (1 inch=2.54cm) area when suppressing under about 500g weight.After sample was made, the instrument of the destructive force that the damage that all samples are applied by record produces carried out the in harness test (speed is 2 inch per minute clocks) of drawing back.Write down maximum, force that each specimen reaches and it is average, so produce average maximum, force, with its record as putting T shape peeling force.

Adhesive melt viscosity (ASTM D-3236) (being also referred to as " viscosity ", " brookfield viscosity " or " melt viscosity "): the melt viscosity distribution plan is generally measured with Brookfield Thermosel viscometer and No. 27 axles down for 120 ℃ to 190 ℃ in temperature.

Stripping strength (the ASTM D1876 of modification): base material (1x3 inch (25x76mm)) is sealed 1 to 2 second with binder film (5mil (130 μ m) is thick) under 135 ℃ and 40psi (0.28MPa) pressure.Should on tester for elongation, oppositely peel off by bonding sample with constant pinblock speed 2in/min (51mm/min).Record is peeled away required mean force with bonding (5 samples).

The ability of the temperature that rises with 10 (5.5 ℃)/15min is born in shear adhesion fail temperature (SAFT) (the ASTM D4498 of modification) measurement bonding place under the constant force of drawing back the bonding place with shear mode.1 inch x1 inch of binding (25mmx25mm) (kraft paper) is formed by the heat-sealing 1.5s according to above-mentioned operation " (b) " by tackiness agent.Will be in 32 ℃ baking oven at the sample vertical hanging of its bottom-loaded 500g load.Temperature when the record weight falls.Tackiness agent with high fail temperature is necessary for will often experience pyritous connection with wrapping of piece assembly between storage and delivery period.

Release adhesive fail temperature (PAFT) is measured with the following operation of revising according to TAPPI T814 PM-77 operation.With a hot-melt adhesive bar that is heated to 177 ℃ two 6 " x12 " layers of kraft paper are forced together.With this laminate deburring and be cut into the wide bar of 1-inch.To have with these that peel off 100-g weight that mode hangs and put into baking oven.Temperature of oven raises with 30 ℃/hr of speed.Sample is hung on the switch, and this switch can trip when sample destroys with the record fail temperature.

Low temperature substrates fiber tearing: according to above-mentioned operation " (b) " preparation kraft paper binding.The binding sample is put into icebox or the required probe temperature of refrigerator acquisition.This binding is separated with hand, and observe the destruction type of measuring.The matrix fiber amount of tearing is represented with per-cent." SF " represents wood destruction.

By adhesive blends being heated to 121 ℃ and hot-melt adhesive beads (about 1g) is applied on the ASTM thermometer bulb measures cloud point.Note the temperature of this hot-melt adhesive muddiness then.These observed values of cloud point provide the overall compatibility of hot melts, i.e. the mutual consistency indication of each component.

Compression moulding: compacting is fit to the plate of physicals test on the Carver hydropress.The 6.5g polymkeric substance is being lined with Teflon ^TMMolding between the copper coin (0.05 " thick) of the aluminium foil of coating.To have the square perforate of 4 " x4 " 0.033 " thick sheet frame (chase) is used to control thickness of sample.Under minimum pressure 170 ℃ or 180 ℃ of following preheatings after 1 minute, the hydraulic pressure load is risen to gradually about 10,000-15,000lb keeps them 3 minutes under this pressure.Subsequently with sample and molded plate about 10,000 to 15, cooling 3 minutes between the water-cooled pressing plate of press under the 000lb load.With the at room temperature minimum balance of this plate 2 days, carry out the physicals test then.

One directional tensile test: from holoplast, cut out the dog-bone that is used for tension test with mallet handle die.Sample is of a size of those that stipulate among the ASTM D 1708.Tensile property is at Instron ^TM4502 type Elongation test airborne measurements, this test machine are equipped with a 22.48lb loading compartment and the pneumatic pawl (pneumatic jaws) of spination anchor clamps face are housed.Be out of shape under constant pinblock speed 5.0in/min, wherein data sampling speed is 25 point/seconds.The test fore paw separates 0.876 ", under the supposition affine deformation, calculate strain by it.Calculate initial modulus, surrender (when obvious) stress and strain, the most heavily stressed, fracture tensile strength and breaking strain.Test is from minimum 5 samples of each plate, and the result who provides is a mean value.All stress of quoting all calculate based on the original cross-sectional area of sample, and the cross section that is not considered as rising strained function reduces.

Rheological property (G ', G ") measures on the ARES instrument, and this instrument is by Rheometric Scientific, Piscataway, New Jersey makes.At first, cool off with 1 ℃/min then this polymer melted.Begin to drop to about 80 ℃ cooling period record dynamic modulus at least 30 ℃ being higher than material melting point certainly.Therefore test result is the evolution (evolution) of storage modulus G ', out-of-phase modulus G the ratio tan δ=G of temperature function " and as "/G '.Measure and under constant frequency 10rad/s and 20% strain, carry out with the plate fishplate bar geometrical shape (plate-and-plate geometry) of 12.5mm diameter.

Embodiment

General provisions

All polymerizations are all carried out with the mixed metallocene catalyst system in the single hop flow reactor of full of liquid.Reactor is 0.5 liter of stainless steel autoclave reactor, and the water cooling/steam heating member and the pressure controller of agitator, band temperature regulator is housed.At first by passing through three column purification systems with solvent, propylene and comonomer (as butylene and hexene) (if existence) purifying.Purification system is made up of Oxiclear post (Model #RGP-R1-500 is available from Labclear), the 5A that is connected on its back and 3A molecular sieve column.When having polymerization low activity sign, with the purification column regular regeneration.3A and 5A molecular sieve are all dividing 260 ℃ of other design temperatures and 315 ℃ of regeneration down in inside under nitrogen.Molecular screen material is available from Aldrich.The regeneration in initial manufacturing of Oxiclear post.To add in the manifold from the purifying ethene of internal material-feeding, then reactor be passed through Brookfield streams controller.Ethene is carried with the gas form that is dissolved in cold solvent/monomer mixture.Then with the solvent of purifying and monomer by be cooled to-15 ℃ approximately by refrigerator, add in the reactor through manifold then.With solvent with monomer mixes in manifold and add in the reactor through single pipe.The all liquid flow velocity is all used Brooksfield mass flow meter or Micro-Motion Coriolis type flowmeter survey.

Except as otherwise noted, catalyst compound is bought by Albemarle.

Being used to produce the polyacrylic catalyst compound of hypocrystalline and being racemize-dichloro-dimethyl silyl two (2-methyl-4-phenyl indenyl) closes zirconium, racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) and closes that zirconium, racemize-dimethylformamide dimethyl base silyl two (2-methyl indenyl) close zirconium, racemize-dimethylformamide dimethyl base silyl two (indenyl) closes hafnium and racemize-dimethyl 1,2-ethylidene-two (4,7-dimethyl indenyl) closes hafnium (available from Boulder Scientific Company).

Being used for the polyacrylic catalyst compound of production non-crystalline state is that dichloro-dimethyl silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) closes titanium, dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) closes titanium, dimethylformamide dimethyl base silyl (tertiary butyl amino) (tetramethyl-ring pentadienyl) closes titanium (available from Boulder Scientific Company), dimethyl [two (right-the triethylsilyl phenyl) methylene radical] (cyclopentadienyl) (3,8-di-t-butyl fluorenyl) closes hafnium and (press US 6,528, embodiment production in 670) and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (N-1-adamantyl) close titanium (according to US 5, embodiment production in 955,625).

Dichloro-dimethyl silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) closes titanium according to US 5,057, the embodiment production in 475.This dimethyl variant is by making the acquisition of described dichloride dimethyl.

Racemize-dichloro-dimethyl silyl two (2-methyl-4-phenyl indenyl) closes zirconium and dichloro-dimethyl silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) closes titanium MAO (methylaluminoxane) activation.Racemize-dimethyl ethylene two (4,7-dimethyl indenyl) closes hafnium and (available from Single-Site Catalysts, LLC) activates in advance with trityl four (pentafluorophenyl group) borate.All the other catalyzer are with four (pentafluorophenyl group) boric acid N, accelerine

(available from Albemarle) pre-activation.For preactivated catalyst system, before polyreaction, this catalyzer was activated at least 10 minutes in 1: 1 in molar ratio to 1: 1.1 with promotor in 700ml toluene.Then this catalyst body is tied up to the catalyst concn that is diluted to concentration 0.2 to 1.4mg/ml in the toluene.This catalyst solution is used for all polymerization experiment of carrying out on the same day.When the catalyst solution that consumed more than the 700ml milliliter in one day, prepare new catalyst solution batch of material.With each catalyst solution through independent pipeline suction.Catalyzer is mixed in manifold, add in the reactor through single pipeline then.In methylaluminoxane activatory system, (MAO, 10wt.% in toluene is available from Albemarle) dilutes in 1000ml toluene with the 280ml methylaluminoxane, and this solution is stored in 5 liters of stainless steel cylinders.This catalyzer is diluted to concentration 0.2 to 1.4mg/ml in toluene.With each catalyst solution and methylaluminoxane solution through dividing other pipeline suction.Catalyzer and MAO are mixed in manifold, add in the reactor through single pipeline then.Pipe connecting between catalyzer manifold and the reactor inlet is long for about 1m.

All catalyst solutions are remained in the inert atmosphere of water content＜1.5ppm and and add in the reactor by volume pump.Catalyzer carries out with monomeric the contact in reactor.Adopt toluene regularly catalyst pump to be calibrated as calibrate medium.Catalyst concn in the raw material is by the suction rate-controlling of catalyst concn in the change catalyst solution and/or change catalyst solution.The suction speed of catalyst solution changes in 0.2 to 5ml/min scope.

As the impurity scavenging agent, 55ml triisobutyl aluminium (25wt.%, in toluene, Akzo Noble) is diluted in the 22.83kg hexane.The triisobutyl aluminum solutions of dilution under covering, nitrogen is stored in 37.9 litre flasks.It is about 90% until consuming that this solution is used for all polymerization experiment, prepares new batch of material then.The suction speed of triisobutyl aluminum solutions changes with polyreaction is different, can be from 0 (no scavenging agent) to 4ml/min.

For relating to α, the polyreaction of ω-diolefine, with 1, the 9-decadiene is diluted to concentration 4.8 to 9.5vol.% in toluene.Then this diluting soln is added in the reactor through the comonomer pipeline by volume pump.(this 1, the 9-decadiene is available from Aldrich, and by by at high temperature activatory aluminum oxide under the nitrogen, then by at high temperature under nitrogen the activatory molecular sieve carry out purifying.)

At first came cleaning reactor at least one hour by under maximum permissible temperature (about 150 ℃), reactor assembly being crossed in solvent (for example hexane) and scavenging agent uninterrupted pumping.After the cleaning, with this reactor use through water/vapour mixture that reactor jacket flows through heat/be cooled to temperature required and by control the solvent streams controlling reactor under setting pressure.When reaching the steady state of operation, monomer and catalyst solution are added in the reactor then.The automatic temp Controlling System is used for reactor control and remains under the design temperature.Determine that by the reduction temperature of observing viscous product and water-steam mixture polymerization activity begins.In case after the activity of foundation and system reach balance, before collecting sample,, reactor is marked (lined out) by 5 times the time of mean residence time at least of this system of operate continuously under the condition of setting up.After system reached the stable state operation, collection mainly contained solvent, polymkeric substance and unreacted monomeric gained mixture in collection box.With the sample collected at first in stink cupboard dry air to evaporate most of solvent, then in vacuum drying oven temperature about 90 ℃ dry about 12 hours down.This vacuum drying oven exsiccant samples weighing is obtained yield.Institute responds all and to carry out under 45 to 130 ℃ of 2.41MPa-g pressure and temperatures.

Embodiment 1-4

With racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) close zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) close titanium under 115 ℃ of temperature in the catalyst ratio scope 4 samples of preparation.Polyreaction is carried out according to above-mentioned general operation.Detailed experiments condition and result provide in table 1.

Embodiment 5-8

With racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) close zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (tertiary butyl amino) close titanium under 100 ℃ of temperature in the catalyst ratio scope 4 samples of preparation.Polyreaction is carried out according to above-mentioned general operation.Detailed experiments condition and result provide in table 2.

Embodiment 9-15

Closing hafnium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) with dimethylformamide dimethyl base silyl two (indenyls) closes titanium prepare 7 samples under the about 80.0mol% of catalyst ratio in certain temperature range.Polyreaction is carried out according to above-mentioned general operation.Detailed experiments condition and result provide in table 3.These data presentation temperature have a significant effect to degree of crystallinity, Mw, Mw/Mn and branching measurer.Total amount can be controlled by temperature of reaction, and this is because the reaction kinetics of each catalyzer has unique response to polymerization temperature.

Embodiment 16-19

With racemize-dimethylformamide dimethyl base silyl two (indenyls) close hafnium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) close titanium under 100 ℃ of temperature under various catalyst ratios 4 samples of preparation.Polyreaction is carried out according to above-mentioned general operation.Detailed experiments condition and result provide in table 4.These data presentation catalyst ratios have a significant effect to degree of crystallinity, Mw, Mw/Mn and branching measurer.Total amount can be controlled by temperature of reaction, and this is because the reaction kinetics of each catalyzer has unique response to polymerization temperature.

Embodiment 20-34

Close zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) closes titanium catalyst according to 15 samples of above-mentioned general operation preparation with racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl), different is will be a small amount of as 1 of diolefinic monomer, 9-decadiene and add together as the propylene of 'alpha '-olefin monomers.Detailed experiments condition and result provide in table 5 and 6.

Embodiment 35-39

With dimethylformamide dimethyl base silyl two (indenyls) close hafnium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) close titanium catalyst under the catalyst ratio 75mol% and in 85 to 105 ℃ of temperature ranges according to 5 samples of above-mentioned general operation preparation, different is will be a small amount of as 1 of diolefinic monomer, 9-decadiene and add together as the propylene of 'alpha '-olefin monomers.Detailed experiments condition and result provide in table 7.

Embodiment 40-43

Close hafnium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) closes titanium according to 4 samples of above-mentioned general operation preparation with racemize-dimethylformamide dimethyl base silyl two (indenyls), different is will be a small amount of as 1 of diolefinic monomer, 9-decadiene and add together as the propylene of 'alpha '-olefin monomers.Detailed experiments condition and result provide in table 8.

Embodiment 44-47

Close hafnium and dimethylformamide dimethyl base silyl-(tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) with racemize-dimethyl ethylene-two (4,7-dimethyl indenyl) and close titanium 4 samples of preparation in 110 ℃ of temperature and certain catalyst ratio scope.The condition that embodiment 44 to 47 uses (comprising that diolefine adds) is according to above-mentioned general operation, and different is will be a small amount of as 1 of diolefinic monomer, 9-decadiene and add together as the propylene of 'alpha '-olefin monomers.Detailed experiments condition and result provide in table 9.

Embodiment 48-51

With racemize-dimethylformamide dimethyl base silyl two (2-methyl indenyls) close zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) close titanium in 80 ℃ of temperature and catalyst ratio 74 to 84mol% scopes according to 4 samples of above-mentioned general operation preparation, different is will be a small amount of as 1 of diolefinic monomer, 9-decadiene and add together as the propylene of 'alpha '-olefin monomers.Detailed experiments condition and result provide in table 10.

Embodiment 52-57

Closing zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) with racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) closes titanium prepare 6 samples according to above-mentioned general operation under 80 to 95 ℃ of temperature and the about 87mol% of catalyst ratio, different is (1) will be a small amount of as 1 of diolefine raw material, 9-decadiene and add together as the propylene of 'alpha '-olefin monomers; (2) small quantity of hydrogen is also added in the reactor.Detailed experiments condition and result provide in table 11.Embodiment 52-57 shows: except the control by selecting catalyst and processing condition such as temperature acquisition, the adding of hydrogen can be handled Mw effectively, Mw/Mn, degree of crystallinity, crystallization phases and non-crystalline state ratio mutually.

Embodiment 58-60

Closing zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) with racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) closes titanium prepare 3 samples according to above-mentioned general operation in 115 ℃ of temperature and the about 87mol% scope of catalyst ratio, different is (1) adds on a small quantity 1, and the 9-decadiene is as diolefinic monomer; (2) racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) closes zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) and closes titanium catalyst and carry out premix and dilute in toluene, is not adding in the catalyzer manifold under the activation in advance then; (3) with four (pentafluorophenyl group) boric acid N, accelerine

In toluene, dilute, add then in the catalyzer manifold; (4) in the catalyzer manifold, begin catalyst activation.Detailed experiments condition and result provide in table 12.Embodiment 58-60 show catalyzer can be before just will adding reactor online activation and in reactor, activating.

Embodiment 61-66

Closing zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) with dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) closes titanium prepare 6 samples according to above-mentioned general operation under 105 to 130 ℃ of temperature and the about 84.6mol% of catalyst ratio, different is (1) adds on a small quantity 1, and the 9-decadiene is as diolefinic monomer; (2) ethene is added in the reactor.Detailed experiments condition and result provide in table 13.Ethylene content in the polymkeric substance obtains by fourier transform infrared analysis (FTIR).

Embodiment 67-71

Closing zirconium and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) with dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) closes titanium (except that embodiment 69) under 105 to 115 ℃ of temperature and prepares all these samples according to above-mentioned general operation, different is (1) uses a small amount of Dicyclopentadiene (DCPD) (this Dicyclopentadiene (DCPD) is available from aldrich in embodiment 67,, at first it is dissolved in the toluene.Then with this solution through under the nitrogen at high temperature the activatory aluminum oxide, then through under nitrogen at high temperature the activatory molecular sieve carry out purifying); (2) in embodiment 68 and 70, use 1-butylene; (3) add 1 in embodiment 71,9-decadiene and 1-hexene are respectively as diolefinic monomer and comonomer.Embodiment 69 usefulness dimethylformamide dimethyl base silyls (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) close titanium and racemize-dimethylformamide dimethyl base silyl two (2-methyl indenyl) and close Zr catalyst and carry out.Detailed experiments condition and result provide in table 14.

Embodiment 72

Embodiment 72 carries out in 500-ml autoclave batch reactor.At first 125ml purifying toluene is added in the stainless steel autoclave reactor, then add 0.1ml triisobutyl aluminium (TIBAL) solution (25wt.%TIBAL dilutes) in 5ml toluene.Then this mixture is stirred and be heated to 120 ℃ until pressure-stabilisation.This reactor is remained under the slight positive pressure.Then under agitation add 125ml prepurification propylene.Reaction mixture is heated to 120 ℃.Under this temperature of reactor, 1.5ml pre-mixing and preactivated catalyst solution are added in the reactor by the sleeve pipe that inserts with nitrogen.This catalyst solution closes titanium, 1.9mg racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) by 32mg dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) and closes zirconium and 1.6mg dimethylformamide dimethyl base silyl two (indenyl) and close hafnium and form, and with 62.1mg four (pentafluorophenyl group) boric acid N, accelerine

Be dissolved in the 50ml toluene.This polymerization was carried out 15 minutes.Then with reactor cooling and to atmosphere emptying.In collection box, collect the gained mixture mainly contain solvent, polymkeric substance and unreacted monomer, and with this mixture at first in stink cupboard dry air to evaporate most of solvent, then in vacuum drying oven about 90 ℃ dry about 12 hours down.102.9 ℃ of resulting polymers (12.79g) peak value display Tcs (measuring), second-order transition temperature (Tg)-8.7 ℃ and melting heat 51.9J/g by DSC.Average molecular mass Mn/Mw/Mz is 33825/66387/267680.

Embodiment 73-75 (Comparative Examples)

Close zirconium or dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) closes titanium according to 3 samples of above-mentioned general operation preparation with racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl), different is only to use a kind of catalyzer.Racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) is closed zirconium be used to prepare isotactic polyprophlene, be used to prepare the amorphous poly propylene and dimethylformamide dimethyl base silyl (tetramethyl-ring pentadienyl) (cyclo-dodecyl amino) is closed titanium.The experiment condition and the viscosity of polymer samples provide in table 15.

To analyze to measure its degree of branching from several samples of front embodiment.In the present invention, degree of crystallinity is measured under branched polymer molecular weight Mz with the value of branch index g '.The result provides in to 13 at table 1.

The sample solvent extraction classification of describing among embodiment 4 and the embodiment 31-34.The result provides in table 16.The classification fraction of choosing GPC-DRI-VIS-LS and dsc analysis.Result from these analyses also provides in table 17.Complex viscosity scope from the classification fraction of the sample of description among the embodiment 31 is measured in 80 to 130 ℃ of scopes of temperature, provides in Fig. 5.

The sample of describing among the embodiment 4 and its fraction that extracts from solvent extraction are used ¹³C NMR analyzes.

Mm triad per-cent is directly measured by C-13NMR spectrum; The amount of supposing the mm triad in this mixture only depends on the aPP in the sample and the amount of scPP (" being respectively Atactic Polypropelene and hypocrystalline polypropylene ") component.By knowing tacticity (mm) amount of pure aPP and scPP component, can calculate the ratio of each component, it is equivalent to mm amount in the observed mixture.Value given below shows the per-cent of isotactic triad based on whole not classification polymkeric substance and three kinds of fractions.The data of calculating use following supposition to generate: isotaxy and atactic are the sign of the regularity in the bulk polymer segment with reference to polymkeric substance.Use methyl triad district, calculate isotaxy and have 94.7%mm, randomly contain 13.6% with reference to polymkeric substance with reference to polymkeric substance.

The viscosity of embodiment 12,22 and 49 product is measured in 80 to 130 ℃ of temperature ranges.This complex viscosity distribution plan provides in Fig. 1.The above-mentioned three sections features of these digital proofs.

With the sample of choosing and its blend test binder performance.With straight polymer and tackifier, oil or wax and stablizer compounding formation hot-melt adhesive blend.The performance of these polymkeric substance and its blend is with respect to typical EVA blend test available from Henkel and Chief.Blend is at high temperature carried out to form the fluid melt under low the shearing.Mixing temperature can be about 130 to 190 ℃.

Escorez ^TM5637 for the aromatic modified resin of hydrogenation with 130 ℃ of ring and ball softening points by the Dicyclopentadiene (DCPD) raw material production, available from ExxonMobil Chemical Company inHouston, and Texas.

Paraflint H-1 is a Fisher-Tropsch wax, shows melt viscosity 10mPas down at 250 °F, available from Moore and Munger.

Aristowax 165 is the refining paraffin wax, available from Frank B Ross Co in Jersey City New Jersey.It is separated from oil, has 158 to 165 of fusing points.

Henkel Hot Melt 80-8368 is commercial hot melts, is made by the blend of EVA, tackifier and wax, available from Henkel Corp.

MAPP40 is maleic anhydride modified polypropylene, has 149 ℃ of acid number 50, the viscosity 300cps under 190 ℃ and softening temperatures, available from Chusei, and USA.

Chief Hot Melt 268 is commercial hot melts, is made by EVA, tackifier and wax, available from Chief Adhesives.

Be high refining white mineral oil, form to have pour point-20 ℃, in the time of 40 ℃, have dynamic viscosity 64 to 70cSt, available from Witco by radical of saturated aliphatic and cyclic aliphatic non-polar hydrocarbon.

Licomont AR 504 is a maleic anhydride inoculated polypropylene wax, has 156 ℃ of acid number 41, the viscosity 373mPas under 190 ℃ and softening temperatures, available from Clarient.

AC 540 is an ethylene acrylic acid co polymer, has 105 ℃ of acid number 40, the viscosity under 140 ℃ 575 and dropping points, available from Honeywell.

Polywax 2000 is a polyethylene wax, and available from Baker Petrolite Plain BOPP (biaxially oriented polypropylene film), the film of 28 micron thickness is available from Mobil Films.

The BOPP of corona treatment (biaxially oriented polypropylene film), the film of 28 micron thickness is available from Mobil Films.

Cardboard 84A has the cardboard that the grey Poster Board 20pt waste paper of 20% regenerated fibre is made, available from Huckster packaging and supply, Inc.in Houston, Texas.

Cardboard 84B is common placard cardboard clay coated newsprinting paper (poster board clay coated news print), available from Huckster packaging and supply, Inc.in Houston, Texas.

Card board kai 84C is common ripple card board kai 200# blank, available from Huckster packaging and supply, Inc.in Houston, Texas.

REXTAC RT 2730 is the multipolymer of propylene, butylene and ethene, has about 67.5mol% propylene, about 30.5mol% butylene and about 2mol% ethene, and by Huntsman, Company produces.This multipolymer has about 15mol%BB diad, about 43mol%PB diad and about 43mol%PP diad.Fusing point is 70 ℃ (having 25 to 116 ℃ of melting ranges), and Tg is-25 ℃, and degree of crystallinity is that about 7%, enthalpy is 10J/g (passing through dsc measurement).Mn is 8260, Mw be 59100 and Mz be 187900 (passing through gpc measurement).Mw/Mn is 7.15.

REXTAC RT 2715 is the multipolymer of propylene, butylene and ethene, has about 67.5mol% propylene, about 30.5mol% butylene and about 2mol% ethene, and by Huntsman, Company produces.This multipolymer has about 11mol%BB diad, about 40mol%PB diad and about 49mol%PP diad.Fusing point is 76 ℃ (having 23 to 124 ℃ of melting ranges), and Tg is-22 ℃, and degree of crystallinity is that about 7%, enthalpy is 11J/g (passing through dsc measurement).Mn is 6630, Mw be 51200 and Mz be 166,700 (passing through gpc measurement).Mw/Mn is 7.7.

All adhesive formulations are all by wt%, unless in the composition that table 18 is listed to the table 50 explanation is arranged in addition.

C3/C2 is a Comparative Examples.This polymkeric substance is the ethylene/propene copolymer with the about 10wt% of ethylene content.This polymkeric substance uses racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) to close zirconium general operation preparation according to the foregoing description 1 under 70 ℃ of polymerization temperatures, and different is only to use a kind of catalyzer.This polymkeric substance has the viscosity 1368cps under 95 ℃ and 190 ℃ of the peak value temperature of fusion.

There is not table 24.

Embodiment E X1-EX13

Below sample under 70 to 125 ℃ of temperature according to above-mentioned general operation preparation, different is: (1) adds a small amount of 1 in embodiment E X1-EX3, EX5 and EX9, and the 9-decadiene is as diolefinic monomer; (2) in embodiment E X13-EX17, use ethene.Detailed experiments condition and result provide in table 30,31 and 32.

Polymerizing condition

To merge the reactor feedstocks solution that forms 25lb/hr with speed 8lb/hr propylene material that adds and the hexane that adds with 17lb/hr.The tri-n-octylaluminium (TNOA) (available from Albemarle) of 3wt.% solution form that will be in hexane is introduced in this logistics with speed 0.0006lb/hr.

Catalyzer and activator add the reactor from independent inlet.This catalyst solution is by dimethyl two (right-the triethylsilyl phenyl) methylene radical] (cyclopentadienyl) (3,8-di-t-butyl fluorenyl) closes the mixture composition that hafnium (catalyzer G) and racemize-dimethylformamide dimethyl base silyl two (2-methyl-4-phenyl indenyl) closes zirconium (catalyst B), wherein have 97mol% catalyzer G.Formation 0.5wt% solution prepares catalyst solution in the toluene by this catalyst mixture is dissolved in.The activator feedstream is by four (pentafluorophenyl group) boric acid N, accelerine 0.2wt% solution in toluene constitutes.Catalyzer and activator are all available from Albemarle.It is mixed at once catalyzer and traditional thread binding being made into of activator materail tube in the reactor upstream in pipeline, estimate that wherein be 2-4 minute duration of contact.Catalyzer and activator feeding rate are respectively 0.04g/hr and 0.1g/hr.

Reactor feedstocks is converted into polymkeric substance through two placed in-line continuously stirring jar reactors.The temperature of two reactors is controlled under 135 ℃.These two reactors are full liquid operation under 530psig pressure.The residence time of raw material in each reactor is 45 minutes.The transformation efficiency that propylene is converted into polymeric articles is about 91%.

From solution, reclaim molten polymer through two flash stage (all there is preheater in per stage).Fs (20psig) polymkeric substance comprises about 2% solvent, and second rank (50 torr vacuum) introduces about 800ppm volatile matter.Water is injected subordinate phase flash distillation (devolatilizer) material with the quenching remainder catalyst and be aided with the solvent stripping.The performance of polymkeric substance and final tackiness agent is generally listed in the table 33.

Make masterbatch blend and granulation under water in static mixer of polymkeric substance and additive for fusing (wax, tackifier and antioxidant).The rate of pumping of controlling polymers and masterbatch is introduced 20% masterbatch in the finished product tackiness agent.The performance of the tackiness agent of preparing is shown in the table 34.

Make the blend under intensification and low shear-mixed of described polymkeric substance, tackifier, wax, antioxidant and other composition form the mobile melt and prepare multiple hotmelt.Mixing temperature from about 130 to about 190 ℃ of changes.As an example, table 35 is listed the detailed prescription and the performance of blend.

The preparation of point: 190 ℃ of 0.2g tackiness agent/use temperatures on the base material/then weight of 0.5kg was placed on base material 2 minutes, wear out and after one day sample carried out T shape and peel off.

The bar of the preparation of sample: 2.5cm * 7.5cm size.

Except as otherwise noted, described value is the mean value of 5 samples.

The CF=cohesive failure, the AF=adhesion failure, the sliding sticking habit of SS=, the SF=base material damages, the fracture of AB=tackiness agent.When observing several classes and losing efficacy, by the most frequent destruction type of listing.

Described EVA Test prescription is by the laboratory blend that raw material is made that is purchased from ExxonMobil Chemical Company or other material supplier.Concrete prescription is 35%Escorene (tm) UL 7720,50% Escorez (tm) 2393,15% Paraflint (tm) H-1, adds about 0.5% Irganox 1010.

The polymkeric substance of preparation embodiment E X1, EX3, EX5, EX7 and EX8 is used to estimate Pressuresensitive Tape and tag application.180 ° of peel adhesion are pressed PSTC 101 and are measured, and the spin adhesive test carries out with the PSTC6 method, and loops viscosity obtains with PSTC 16.The prescription and the performance of these blends are shown in the table 45.PSTC=Pressuresensitive Tape association.

Prepare following formulation as thermoplasticity road marking compositions (TRM) and estimate viscosity, softening temperature, high temperature sedimentation and color coordinate.Described being compounded in the aluminium pot (diameter 78mm, high 95mm) that places in the heating jacket carried out.The capacity of this aluminium pot is about 500g.The all the components of listed prescription added in the aluminium pot in 30 minutes in 180 ℃ are descended table 46.Then before test with mixture 180 ℃ of following restir 30 minutes (partly to begin total mixing time be 60 minutes from adding mineral).The sample for preparing thermoplasticity road sign formulation after the mixing immediately.Be to measure color coordinate, the formulation of heat is poured in the tubular silicone mold of the about 41mm of diameter, high about 6mm and prepared the sample piece.Under the room temperature the top of new sample preparation piece (on) and the end (descending) face on measure color coordinate, the sample piece was worn out 96 hours under about 32 ℃ temperature.Go up measurement CIE coordinate X, Y and Z at Hunterlab chromascope (Standard Illuminant C).Huang Du and whiteness index are measured by ASTM D1925 and ASTM E313 respectively.

Be to measure the high temperature sedimentation, the formulation of heat is poured in the tubular silicone mold of the about 50mm of diameter, high about 70mm and prepared cylindrical sample.Sample was kept 6 hours under 200 ℃ in baking oven, do not stir so that particles settling.Make cylindrical sample be cooled to room temperature (spending the night) then, along cylinder the axle cut in half by the centre.On the cross section of new tangent plane, observe the high temperature sedimentation.Amount with percentage report settling area.

The compounding of thermoplasticity road sign formulation is measured Zahn cap viscosity after finishing immediately.Use the aperture to be extended to No. 5 Zahn caps (from Braive instruments, Liege Belgium) of 6mm diameter.Praise grace viscosity in the identical aluminium pot measurement that is used for compounding.During the compounding end cycle, from the TRM blend composition, take out mixing device, Zahn cap is immersed in the blend composition.Make the complete submergence of this glass need abundant blend (500g).Measure Zahn cap viscosity in order to following method:

1. for example nurse one's health described formulation and cup for 170 ℃ and 190 ℃ times at probe temperature.Importantly in the TRM formulation, stir lightly to obtain uniform temperature and to avoid deposition with described cup.

2. on the indicating meter of heating jacket controller, check the temperature of formulation.

3. make the complete submergence of Zahn cap and make it to be full of the thermoplasticity formulation.

4. make the cup vertical uplift that is full of leave melt and make TRM pass through aperture unrestricted flow.(when cup rises) opened chronoscope when the liquid level of formulation reached the Zahn cap top.

5. make formulation unrestricted flow, final eddy current stops chronoscope and writing time when forming " stain ".

This test repeats for several times until obtaining the even test result.Tolerance deviation depends on actual result: for low viscosity (for example 20 to 60s), and several seconds discrete can acceptance; For high viscosity formulation (about 2 minutes of Zahn cap time), dispersing can be obviously higher.The Zahn cap time was designated as "＞3min " greater than 3 minutes, because test no longer valid.

Softening temperature is by ring ﹠amp; The ball method is measured based on ASTM E-28.

Use embodiment E X2, EX6 and the prescription of EX9 polymkeric substance and the performance of these formulations to be shown in the table 46.

Supatex fabric

The diaper structure tackiness agent makes non-woven polypropylene lining and polyethylene back sheet bonding.Described tackiness agent can be coated with by several method.So that the required mean force of supatex fabric and PE membrane sepn is measured bounding force.Use Zwick tensiometer measure force by peeling off (T shape is peeled off) with 180 ° of angles under differing temps and after the different time.Peeling rate is 300mm/min.Described tackiness agent CT325-150Meltex coating machine wide bonding helical of list and the 5g/m of 20mm ²Added weight be coated with.10 meters supatex fabric/PE structure is cut into the long sample of several about 20cm.Then sample is peeled off a little with on the pawl that is fixed on the Zwick tester.Peel off the structure of 6cm, calculate the mean value of described power with data acquisition computer.

The jet velocity limit is the tolerance of producing the maximum rate of this structure.Because Meltex does not have these speed, so simulation can be sprayed speed.The card board kai box is placed under the nozzle, improves the tackiness agent rate of pumping, observe spiral shape with photoflash lamp.When through-put surpasses the ability that produces even helical, the recording quality flow velocity.Computing machine speed then.The speed of two nozzles of 0.018 inch of calculated diameter and 0.030 inch.

The ST=base material is torn, CF=cohesive failure, AF=adhesion failure

Polymkeric substance C3/C4 is propene-1-butene-1 multipolymer in the last table, with dimethyl two (right-the triethylsilyl phenyl) methylene radical]-(cyclopentadienyl) (3,8-di-t-butyl fluorenyl) close the hafnium preparation; ScPP is the hypocrystalline polypropylene, closes zirconium preparation with racemize-dimethylformamide dimethyl base silyl-two (2-methyl-4-phenyl indenyl), according to the method for above-mentioned general provisions but only use a kind of catalyzer.The detailed test conditions and the character of these polymkeric substance are shown in the table 48.

Mixture 404 is a Comparative Examples.

Table 49 illustrates prescription and the performance with the Rextac tackiness agent of the tackiness agent of EVA, SIS and the preparation of SBS based polyalcohol and preparation.

The ST=base material is torn, CF=cohesive failure, AF=adhesion failure

It is for reference that all documents described herein comprise that any priority documents and/or testing method all are incorporated herein.From above-mentioned general describe and specific embodiments apparent, although illustrated and described form of the present invention, can carry out various modifications under the spirit and scope of the invention situation not deviating from.Therefore.The present invention is not limited by these forms.

Claims

1. tackiness agent comprises and contains 50wt% or more one or more has the polymkeric substance of the alpha-olefin of 3 to 12 carbon atoms that wherein said polymkeric substance has following feature: some T shape peeling force is 1 newton or higher; Mw is 10000 to 60000; The branch index g ' that measures under the Mz of polymkeric substance is 0.95 or lower; With melting heat be 1 to 70J/g; Non-crystalline region content is at least 50%.

2. the tackiness agent of claim 1, wherein said crystallinity of polymer is between 5 and 40%.

3. the tackiness agent of claim 1, wherein branch index g ' is 0.90 or lower.

4. the tackiness agent of claim 1, wherein branch index g ' is 0.80 or lower.

5. the tackiness agent of claim 1, the viscosity of wherein said polymkeric substance under 190 ℃ is 90000mPas or lower.

6. the tackiness agent of claim 1, the viscosity of wherein said polymkeric substance under 160 ℃ is 8000mPas or lower.

7. the tackiness agent of claim 1, the melting heat of wherein said polymkeric substance is greater than 10J/g.

8. the tackiness agent of claim 1, the melting heat of wherein said polymkeric substance are 20 to 70J/g.

9. the tackiness agent of claim 1, the melting heat of wherein said polymkeric substance are 30 to 60J/g.

10. the tackiness agent of claim 1, wherein said crystallinity of polymer is 10-30%.

11. the tackiness agent of claim 1, the fracture tensile strength of wherein said polymkeric substance are 0.75MPa or higher.

12. the tackiness agent of claim 1, the shear adhesion fail temperature of wherein said polymkeric substance is 100-130 ℃.

13. the tackiness agent of claim 1, the Mz/Mn of wherein said polymkeric substance are 2 to 200.

14. the tackiness agent of claim 1, the Xiao A hardness of wherein said polymkeric substance are 20-90.

15. the tackiness agent of claim 1, the some T shape peeling force of wherein said polymkeric substance 3 and 10000N between.

16. the tackiness agent of claim 1, the some T shape peeling force of wherein said polymkeric substance 10 and 2000N between.

17. the tackiness agent of claim 1, the fracture tensile strength of wherein said polymkeric substance are 0.6MPa or higher.

18. the tackiness agent of claim 1, the Tg of wherein said polymkeric substance is between 5 and-65 ℃.

19. arbitrary tackiness agent of claim 2-18, wherein said polymkeric substance comprise the propylene of 50wt% at least.

20. arbitrary tackiness agent of claim 2-18, wherein said polymkeric substance comprise the propylene of 50wt% at least and at most 50wt% be selected from ethene, butylene, hexene, octene, decene, dodecylene, amylene, heptene, nonene, 4-methyl-amylene-1,3-methyl-amylene-1,3,5, the comonomer of 5-trimethylammonium-hexene-1 and 5-ethyl-1-nonene.

21. arbitrary tackiness agent of claim 2-18, wherein said polymkeric substance comprise propylene and 5wt% or the ethene still less of 50wt% at least.

22. arbitrary tackiness agent of claim 2-18, wherein said polymkeric substance comprise the divinyl that is selected from of maximum 10wt%, pentadiene, hexadiene, heptadiene, octadiene, nonadiene, decadiene, 11 carbon diene, 12 carbon diene, oleatridecadiene, 14 carbon diene, 15 carbon diene, 16 carbon diene, 17 carbon diene, 18 carbon diene, 19 carbon diene, 20 carbon diene, 21 carbon diene, 22 carbon diene, two oleatridecadienes, the tetracosa carbon diene, 25 carbon diene, 26 carbon diene, heptacosadiene, 28 carbon diene, 29 carbon diene, 30 carbon diene, cyclopentadiene, vinyl norbornene, norbornadiene, ethylidene norbornene, Vinylstyrene, diene with Dicyclopentadiene (DCPD).

23. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprises one or more tackifier.

24. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprise one or more tackifier that are selected from aliphatic hydrocarbon resins, aromatic modified aliphatic hydrocarbon resins, hydrogenation polycyclopentadiene resin, polycyclopentadiene resin, rosin, rosin ester, wood rosin, wood rosin ester, starex, starex ester, polyterpene, aromatic modified polyterpene, terpene phenolic resin, aromatic modified hydrogenation polycyclopentadiene resin, Hydrogenated aliphatic resin, Hydrogenated aliphatic aromatic resin, hydriding terpene and modification terpenes, hydroabietic acid and hydrogenated wood rosin glycerol ester.

25. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprise one or more wax of the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax and the wax modifiers that are selected from f-t synthetic wax, oxidation.

26. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprise one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler and water.

27. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprise one or more aliphatic naphthenic oil and white oil.

28. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprise the multipolymer that is selected from equal poly-alpha olefins, alpha-olefin, the binary of diolefine and one or more polymeric additive of terpolymer, elastomerics, segmented copolymer, acrylic ester polymer, acrylic acid alkyl ester polymer and vinyl acetate polymer.

29. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprise one or more softening agent that is selected from mineral oil, polybutene and phthalic ester.

30. arbitrary tackiness agent of claim 2-18, wherein said tackiness agent also comprise one or more softening agent that is selected from phthalic acid two different undecyl esters, phthalic acid diisononyl esters and dioctyl phthalate (DOP).

31. arbitrary tackiness agent of claim 2-18, the peak value fusing point of wherein said polymkeric substance is between 80 and 140 ℃.

32. arbitrary tackiness agent of claim 2-18, the Tg of wherein said polymkeric substance are 0 ℃ or lower.

33. arbitrary tackiness agent of claim 2-18, the melt index of wherein said polymkeric substance are 50dg/min or higher, this melt index is pressed ASTM 1238 D in 2.16kg, 190 ℃ of measurements down.

34. arbitrary tackiness agent of claim 2-18, be 30 seconds or shorter the set time of wherein said polymkeric substance.

35. arbitrary tackiness agent of claim 2-18, the ctystallizing point Tc of wherein said polymkeric substance is than low at least 10 ℃ of peak value fusing point Tm.

36. arbitrary tackiness agent of claim 2-18, the crystallisation range of wherein said polymkeric substance are 10 to 60 ℃.

37. a packaging tackiness agent comprises arbitrary tackiness agent of claim 1-36.

38. packing, the packaging tackiness agent that comprises claim 37, wherein said tackiness agent are applied at least a portion of one or more packaging member that is selected from cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, plastic resin, metal, metal alloy, tinsel, film, plastic film, laminating material and sheet material.

39. a packing comprises the packaging tackiness agent of claim 37, wherein said tackiness agent is applied at least a portion of one or more packaging member that is selected from cardboard case, crate, chamber, Corrugated Box and pallet.

40. packing, the packaging tackiness agent that comprises claim 37, wherein said tackiness agent are applied at least a portion of one or more packaging member that is selected from cereal product, biscuit product, beer packed, frozen product, paper bag, drinking glasses, milk box, juice box and is used to transport the container of product.

41. arbitrary packing of claim 38-40, the substrate fiber of the wherein said tackiness agent rate of tearing is 75% to 100% under 22 ℃.

42. arbitrary packing of claim 38-40, the substrate fiber of the wherein said tackiness agent rate of tearing is 95% to 100% under 22 ℃.

43. arbitrary packing of claim 38-40, the substrate fiber of the wherein said tackiness agent rate of tearing is 50% to 100% under-20 ℃.

44. arbitrary packing of claim 38-40, the substrate fiber of the wherein said tackiness agent rate of tearing is 90% to 100% under-20 ℃.

45. arbitrary packing of claim 38-40, the substrate fiber of the wherein said tackiness agent rate of tearing is 20% to 100% under 50 ℃.

46. arbitrary packing of claim 38-40, the substrate fiber of the wherein said tackiness agent rate of tearing is 50% to 100% under 50 ℃.

47. disposable, the arbitrary tackiness agent that comprises claim 1-36, wherein said tackiness agent imposes at least a portion of one or more disposable member, and described disposable member is selected from non-woven webs, non-elastic nonwoven, elastic nonwovens, shrink the adherent laminating material, tension adherent laminating material, spunbond-as to melt and spray-the spunbonded type laminating material, polypropylene spunbond layer, polyethylene layer, composite polyethylene and polypropylene spunbond layer, elastic wire, styrene-isoprene-phenylethene, styrene-ethylene/propylene-styrene, vinylbenzene-altogether-butadiene-styrene, urethane, Woven fabric, polypropylene, polyester, not saturating body fluid layer, the permeable mass liquid layer, absorption agent, tissue paper, polyolefin film, polyester film, polychloroethylene film, polyvinylidene chlorida film, the polyvinyl acetate film, the flexible fastening adhesive tape, preceding tape backing, timber, paper, barrier film, film laminate, non-woven composite, textile material, durable fabrics, elastic webs, cladding material, non-woven polyethylene, porous polyethylene, long filament, the multiporous fiber net, the latch closure material, the spunbonded type non-woven fleece, lining, elastomeric side panels, fixation adhesive tape, elastic tape, regenerated fiber, nylon, the cellulose paper dregs of rice, cellulose villus, with the superabsorbent cotton-wool.

48. disposable, comprise arbitrary tackiness agent of claim 1-36, wherein said tackiness agent imposes at least a portion of one or more the disposable member that is selected from diaper, training pants, sanitary towel, pantiliner, incontinence garments either, mattress, surgical gown, surgical drape, mousetrap, hook and eye, medical clothes and swim suit.

49. the disposable of claim 47 or 48 wherein makes described disposable member adhere to the second disposable member by described tackiness agent.

50. the disposable of claim 47 or 48, wherein said tackiness agent also comprise one or more solvent that is selected from hexane, heptane, mineral turpentine, dimethylbenzene, toluene, benzene and hydrochloric ether.

51. the disposable of claim 47 or 48, wherein said tackiness agent also comprises and is selected from three (di-t-butyl-to acrinyl)-Three methyl Benzene, alkylation bis-phenol, zinc dibutyl dithiocarbamate, 4,4 '-methylene-bis (2, the 6-DI-tert-butylphenol compounds), four [methylene radical (3,5-di-t-butyl-4-hydroxyl hydrogenated cinnamate) methane], thio-2 acid lauryl stearyl, 3, one or more antioxidant of 3 '-thiodipropionate dilauryl and 2,6 ditertiary butyl p cresol.

52. the disposable of claim 47 or 48, wherein said tackiness agent also comprises and is selected from hindered phenol, thiophenol, phosphorated phenol, 1,3,5-trimethylammonium-2,4,6-three (3,5-di-t-butyl-4-acrinyl) benzene, four-3-(3,5-di-t-butyl-4-hydroxyphenyl) propionic acid pentaerythritol ester, 3-(3,5-di-t-butyl-4-hydroxyphenyl) propionic acid Octadecane base ester, 4,4 '-methylene-bis (4-methyl-6-tert butyl phenol), 4,4 '-thiobis (6-tert-butyl o cresols), 2,6 di t butyl phenol, 6-(4-hydroxyl phenoxy group)-2, two (the positive hot sulfenyls)-1 of 4-, 3, the 5-triazine, 2,4,6-three (4-hydroxyl-3,5-di-t-butyl-phenoxy group)-1,3,5-triazines, 3,5-di-t-butyl-4-acrinyl phosphonic acids two Octadecane base esters, 3, one or more stablizer of 5-di-tert-butyl-4-hydroxybenzoic acid 2-(positive hot sulfenyl) ethyl ester and six (3,3,5-di-t-butyl-4-hydroxyphenyl) propionic acid sorbitol ester.

53. the disposable of claim 47 or 48, the melt index of wherein said polymkeric substance are 50dg/min or higher, this melt index is pressed ASTM 1238 D in 2.16kg, 190 ℃ of measurements down.

54. the disposable of claim 47 or 48, the release adhesive fail temperature of wherein said tackiness agent are 30 to 110 ℃.

55. the disposable of claim 47 or 48, the shear adhesion fail temperature of wherein said tackiness agent is 50 ℃ or higher.

56. the disposable of claim 47 or 48, the fracture tensile strength of wherein said tackiness agent is 0.69MPa or higher down at 25 ℃.

57. the disposable of claim 48 or 49, the tensile strength of wherein said tackiness agent are 1.38 to 3.45MPa under 25 ℃.

58. the disposable of claim 47 or 48, the brookfield viscosity of wherein said tackiness agent are 50 to 25000mPas under 177 ℃.

59. the disposable of claim 47 or 48, the brookfield viscosity of wherein said tackiness agent are 500 to 7000mPas under 177 ℃.

60. the disposable of claim 47 or 48, the cloud point of wherein said tackiness agent are 200 ℃ or lower.

61. the disposable of claim 47 or 48, the second-order transition temperature of wherein said tackiness agent are-65 to 25 ℃.

62. the disposable of claim 47 or 48, the stripping strength of wherein said tackiness agent are 90 to 1000g/cm.

63. the disposable of claim 47 or 48, the complex viscosity of wherein said tackiness agent are 50 pools or lower under the shearing rate of 177 ℃ and 1000rad/s.

64. the disposable of claim 47 or 48, the use temperature of wherein said tackiness agent are 100 to 200 ℃.

65. the disposable of claim 47 or 48, the stripping strength of wherein said tackiness agent are 90 to 625g/cm.

66. the disposable of claim 47 or 48, the stripping strength of wherein said tackiness agent are 265 to 625g/cm.

67. the disposable of claim 47 or 48, the stripping strength of wherein said tackiness agent are 15 to 450g/cm.

68. the disposable of claim 47 or 48, wherein said disposable are the consumer's goods.

69. a film comprises arbitrary tackiness agent of claim 1-36.

70. the film of claim 69 also comprises one or more other polymeric constituent that is selected from polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer and multipolymer thereof.

71. the film of claim 69, wherein said film comprise the layer that is selected from paper, tinsel, metal, metal alloy, polyethylene, polypropylene, polyester, polyethylene terephthalate, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, polymeric amide, its homopolymer and multipolymer thereof.

72. the film of claim 69, wherein said film comprises polypropylene layer.

73. the film of claim 69, wherein said film comprises the oriented polypropylene layer.

74. the film of claim 69, wherein said film comprises the Biaially oriented polypropylene layer.

75. a pressure sensitive adhesive comprises arbitrary tackiness agent of claim 1-36.

76. the pressure sensitive adhesive of claim 75, the second-order transition temperature of wherein said pressure sensitive adhesive are-65 to 30 ℃.

77. the pressure sensitive adhesive of claim 75 or 76, the storage modulus of wherein said pressure sensitive adhesive is 1 * 10 under 25 ℃ and 1 radian per second ⁴To 1 * 10 ⁷Dynes/cm.

78. the pressure sensitive adhesive of claim 75 or 76, the brookfield viscosity of wherein said pressure sensitive adhesive is 20000mPas or lower down at 150 ℃.

79. the pressure sensitive adhesive of claim 75 or 76, the trace of the size exclusion chromatography, of wherein said polymkeric substance is bimodal.

80. the pressure sensitive adhesive of claim 75 or 76, the brookfield viscosity of wherein said pressure sensitive adhesive is 10000mPas or lower down at 190 ℃.

81. the pressure sensitive adhesive of claim 75 or 76, be 30 minutes or shorter the set time of wherein said pressure sensitive adhesive.

82. the pressure sensitive adhesive of claim 75 or 76, wherein said pressure sensitive adhesive is the consumer's goods.

83. a laminated product comprises arbitrary tackiness agent bonded two or multilayer with claim 1-36.

84. the laminated product of claim 83, wherein said tackiness agent are present between the described layer.

85. comprising one of at least, the laminated product of claim 83 or 84, wherein said layer be selected from one or more material of timber, plastics, paper, rubber, metal, tinsel, metalized surface, cloth, non-woven fabrics, spun-bonded fibre, stone, gypsum, glass, pottery, film and foamy.

86. the laminated product of claim 83 or 84, comprise that more than two-layer wherein every layer is independently selected from timber, plastics, paper, rubber, metal, tinsel, metalized surface, cloth, non-woven fabrics, spun-bonded fibre, stone, gypsum, glass, pottery, film and foams.

87. the laminated product of claim 83 or 84, wherein said two or multilayer comprise the first layer and the second layer, the described second layer is formed by the material different with the first layer.

88. the laminated product of claim 83 or 84 also comprises the interleaving paper or the stripper that are present on the top layer.

89. the laminated product of claim 83 or 84, wherein said laminar structure is by being selected from spraying, extrusion molding, melt bonded, the method production of injecting described polymkeric substance and hot melt adhesive technology.

90. the laminated product of claim 83 or 84, wherein said layer comprise one of at least described tackiness agent and one or more material that is selected from timber, plastics, paper, rubber, metal, tinsel, metalized surface, cloth, non-woven fabrics, spun-bonded fibre, stone, gypsum, glass, pottery, film and foams.

91. the laminated product of claim 83 or 84, the open hour of wherein said tackiness agent are 60 seconds or shorter.

92. the laminated product of claim 83 or 84, be 3 seconds or longer the set time of wherein said tackiness agent.

93. the laminated product of claim 83 or 84, the substrate fiber of the wherein said tackiness agent rate of tearing is 75% to 100% under 22 ℃.

94. the laminated product of claim 83 or 84, the release adhesive fail temperature of wherein said tackiness agent is 60 ℃ or higher.

95. the laminated product of claim 83 or 84, the shear adhesion fail temperature of wherein said tackiness agent is 50 ℃ or higher.

96. being 177 ℃, the laminated product of claim 83 or 84, the viscosity of wherein said tackiness agent descend 0.2 to 8Pas.

97. being 177 ℃, the laminated product of claim 83 or 84, the viscosity of wherein said tackiness agent descend 0.5 to 2.5Pas.

98. the laminated product of claim 83 or 84, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

99. the laminated product of claim 83 or 84, the some T shape peeling force of wherein said tackiness agent are 3 to 4000N.

100. the laminated product of claim 83 or 84, the some T shape peeling force of wherein said tackiness agent are 5 to 3000N.

101. the laminated product of claim 83 or 84, the some T shape peeling force of wherein said tackiness agent are 15 to 1000N.

102. the laminated product of claim 83 or 84, wherein said laminated product are the consumer's goods.

103. a fiber product comprises arbitrary tackiness agent of one or more filamentary material and claim 1-36.

104. the fiber product of claim 103, wherein said filamentary material are monocomponent fibre, multicomponent fibre or its combination.

105. the fiber product of claim 103 or 104, wherein said filamentary material comprise be selected from that cotton, hemp, cellulose ester, polyester, wool, people send out, Kev draws, nylon, Nomex (Nomex nylon), polyacrylic ester and polyolefinic one or more material.

106. the fiber product of claim 103 or 104, wherein said filamentary material comprise one or more polymkeric substance or the multipolymer that is selected from polyethylene terephthalate, polybutylene terephthalate, poly terephthalic acid first diester and poly-hydroxy-benzoic acid second diester.

107. the fiber product of claim 103 or 104, wherein said filamentary material comprise one or more polymkeric substance or the multipolymer that is selected from polyethylene, polypropylene, ethylene-acrylic acid ester polymer, ethylene/alkyl acrylate polymkeric substance and ethane-acetic acid ethyenyl ester polymkeric substance.

108. the fiber product of claim 103 or 104, wherein said fiber product are nonwoven articles.

109. the fiber product of claim 108, wherein said filamentary material comprise one or more material that is selected from polypropylene, regenerated fiber, polyester, polyethylene, nylon, Mierocrystalline cellulose, viscose glue, ethylene-propylene copolymer, polycarbonate, thermoplastic elastomer, fluoropolymer, vinyl based polymer, carbon, glass, mineral, wool, acrylic acid or the like, polyvinyl chloride, urethane and organic binder bond.

110. the fiber product of claim 109, wherein said fiber product are selected from diaper, swim suit, child's training pants, adult-incontinence clothes, feminine care products, medical clothes, mattress, surgical drape, cloth lining, scouring pad, automotive interior member, adhesive tape, face shield and respirator, air filter, vacuum bag, oil and chemical leakage absorption agent, thermal insulation, first aid dressing, medical binder, fiberfill, coat, cotton-wadded quilt stopping composition, furniture liner, filtration medium and Wiping material.

111. the fiber product of claim 103 or 104, wherein said fiber product are the carpet backing goods.

112. the fiber product of claim 111 also comprises basic back lining materials, wherein said filamentary material is fixed on the described basic back lining materials, and described tackiness agent places at least a portion of described filamentary material.

113. the fiber product of claim 112 also comprises the second layer back lining materials that adheres to described tackiness agent.

114. the fiber product of claim 112, wherein said basic back lining materials are selected from one or more material of woven jute, woven finedraw polypropylene screen, sack cloth, needling material and non-woven polypropylene.

115. the fiber product of claim 103 or 104, wherein said filamentary material have the cross section of the circle of being selected from, ellipse, T shape, Y shape, cruciform, hollow shape, square, leafy shape, band shape and polygonal shape.

116. the fiber product of claim 103 or 104, wherein said fiber product are clothes, felt, insulant, carpet, matrix material, printed circuit board (PCB) prepreg and wig.

117. the fiber product of claim 103 or 104, wherein said tackiness agent also comprise one or more additive that is selected from tensio-active agent, whipping agent, polymer compatibilizer, fire retardant and water.

118. the fiber product of claim 103 or 104, the substrate fiber of the wherein said tackiness agent rate of tearing is 75% to 100% under 22 ℃.

119. the fiber product of claim 103 or 104, the release adhesive fail temperature of wherein said tackiness agent is 50 ℃ or higher.

120. the fiber product of claim 103 or 104, the release adhesive fail temperature of wherein said tackiness agent is 75 ℃ or higher.

121. the fiber product of claim 103 or 104, the shear adhesion fail temperature of wherein said tackiness agent is 70 ℃ or higher.

122. the fiber product of claim 103 or 104, the fracture tensile strength of wherein said tackiness agent is down 1MPa at least at 25 ℃.

123. the fiber product of claim 103 or 104, the brookfield viscosity of wherein said tackiness agent are to be lower than 9Pas under 177 ℃.

124. being 177 ℃, the fiber product of claim 103 or 104, the brookfield viscosity of wherein said tackiness agent descend 0.2 to 8Pas.

125. being 177 ℃, the fiber product of claim 103 or 104, the viscosity of wherein said tackiness agent descend 0.5 to 2.5Pas.

126. the fiber product of claim 103 or 104, the cloud point of wherein said tackiness agent are 200 ℃ or lower.

127. the fiber product of claim 103 or 104, the cloud point of wherein said tackiness agent are 190 ℃ or lower.

128. the fiber product of claim 103 or 104, the cloud point of wherein said tackiness agent are 130 ℃ or lower.

129. the fiber product of claim 103 or 104, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

130. the fiber product of claim 111, the tufting bounding force of wherein said tackiness agent is 1kg or higher.

131. the fiber product of claim 111, the tufting bounding force of wherein said tackiness agent is 3kg or higher.

132. the fiber product of claim 111, the tufting bounding force of wherein said tackiness agent is 5kg or higher.

133. the fiber product of claim 112, the tufting bounding force of wherein said tackiness agent is 15kg or higher.

134. the fiber product of claim 103 or 104, the flexible of wherein said tackiness agent is 10 ℃ or lower.

135. the fiber product of claim 103 or 104, the flexible of wherein said tackiness agent is 5 ℃ or lower.

136. the fiber product of claim 103 or 104, wherein said fiber product are the consumer's goods.

137. a hot-melt adhesive composition comprises arbitrary tackiness agent of claim 1-36.

138. the hot-melt adhesive composition of claim 137, the substrate fiber of the wherein said binder composition rate of tearing is 75% to 100% under 25 ℃.

139. the hot-melt adhesive composition of claim 137 or 138, the substrate fiber of the wherein said binder composition rate of tearing is 95% to 100% under 25 ℃.

140. the hot-melt adhesive composition of claim 137 or 138, the substrate fiber of the wherein said binder composition rate of tearing is 50% to 100% under-20 ℃.

141. the hot-melt adhesive composition of claim 137 or 138, the substrate fiber of the wherein said binder composition rate of tearing is 95% to 100% under-20 ℃.

142. the hot-melt adhesive composition of claim 137 or 138, the release adhesive fail temperature of wherein said binder composition is 200 ℃ or lower.

143. the hot-melt adhesive composition of claim 137 or 138, the shear adhesion fail temperature of wherein said binder composition is 200 ℃ or lower.

144. the hot-melt adhesive composition of claim 137 or 138, the fracture tensile strength of wherein said binder composition is 20bar or higher down at 25 ℃.

145. the hot-melt adhesive composition of claim 137 or 138, the fracture tensile strength of wherein said binder composition is 27bar or higher down at 25 ℃.

146. the hot-melt adhesive composition of claim 137 or 138, the fracture tensile strength of wherein said binder composition is 34bar or higher down at 25 ℃.

147. the hot-melt adhesive composition of claim 137 or 138, the fracture tensile strength of wherein said binder composition is 55bar or higher down at 25 ℃.

148. the hot-melt adhesive composition of claim 137 or 138, the elongation of wherein said binder composition is 200% or higher strain of raw footage down at 25 ℃.

149. the hot-melt adhesive composition of claim 137 or 138, the cloud point of wherein said binder composition are 200 ℃ or lower.

150. the hot-melt adhesive composition of claim 137 or 138, the cloud point of wherein said binder composition are 120 ℃ or lower.

151. the hot-melt adhesive composition of claim 137 or 138, the cloud point of wherein said binder composition are 100 ℃ or lower.

152. the hot-melt adhesive composition of claim 137 or 138, wherein said hot-melt adhesive composition are the consumer's goods.

153. a carpet comprises arbitrary hot-melt adhesive composition of claim 137 to 151.

154. an adhesive tape comprises arbitrary hot-melt adhesive composition of claim 137 to 151.

155. a roofing board comprises arbitrary tackiness agent of claim 1-36; With

The roofing element of first side and second side is arranged, and wherein said tackiness agent is applied at least a portion of described second side.

156. the roofing board of claim 155, wherein said roofing element comprises metal sheet.

157. the roofing board of claim 156, wherein said roofing element is selected from copper, steel, zinc, aluminium and alloy thereof.

158. arbitrary roofing board of claim 155 to 157, wherein said first side comprises one or more material that is selected from roof pitch and fabric.

159. arbitrary roofing board of claim 155 to 157, wherein said second side comprises one or more material that is selected from rubber, fiberglass, aromatic poly, carbon, polyester, nylon, pitch and metal sheet.

160. arbitrary roofing board of claim 155 to 157, wherein said metal sheet comprise copper, aluminium or its alloy.

161. arbitrary roofing board of claim 155 to 157, wherein said tackiness agent also comprises one or more bituminous material.

162. arbitrary roofing board of claim 155 to 157, wherein said one or more bituminous material comprises pitch.

163. arbitrary roofing board of claim 155 to 157, wherein said tackiness agent comprise 80wt% or one or more bituminous material still less.

164. arbitrary roofing board of claim 155 to 157, the shear adhesion fail temperature of wherein said tackiness agent is 90 ℃ or higher.

165. arbitrary roofing board of claim 155 to 157, the fracture tensile strength of wherein said tackiness agent is 6.5bar or higher down at 25 ℃.

166. arbitrary roofing board of claim 155 to 157, the elongation of wherein said tackiness agent is 5% strain of raw footage or higher down at 25 ℃.

167. being 177 ℃, arbitrary roofing board of claim 155 to 157, the viscosity of wherein said tackiness agent descend 0.2 to 10Pas.

168. arbitrary roofing board of claim 155 to 157, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

169. arbitrary roofing board of claim 155 to 157, the softening temperature of wherein said tackiness agent are 80 to 200 ℃.

170. a reflective article comprises the reflecting material that imposes at least in part on the substrate surface; With

Arbitrary tackiness agent of claim 1-36.

171. the reflective article of claim 170, wherein said reflecting material is selected from prism and granulated glass sphere.

172. the reflective article of claim 170 or 171, wherein said substrate surface is selected from cycle track, traffic sign, ground, playground, ship, runway, crossing, buildings, the tennis court, traffic route, the synthetic rubber surrogate, oil rig, the tunnel, concrete, metal, pitch, brick, paving stone, ceramic tile, steel plate, timber, pottery, polymeric material, glass, abutment, the traffic roadblock, fence, pipeline, electric pole, guardrail, concrete blocks, curb, the parking lot, porcelain, stone, plank, shaving board, wooden auto parts, glass port, beaujolais, liquid-crystal display, lamp, duplicating machine, the electronics backboard, scattering whiteness standard substance.

173. the reflective article of claim 170 or 171, the solidification value of wherein said tackiness agent are-20 to 250 ℃.

174. arbitrary reflective article of claim 170 or 171, the open temperature of wherein said tackiness agent are-20 to 250 ℃.

175. the reflective article of claim 170 or 171, the viscosity of wherein said tackiness agent are 177 ℃ of following 9Pas or lower.

176. being 177 ℃, the reflective article of claim 170 or 171, the viscosity of wherein said tackiness agent descend 0.2 to 8Pas.

177. being 177 ℃, the reflective article of claim 170 or 171, the viscosity of wherein said tackiness agent descend 0.5 to 2.5Pas.

178. the reflective article of claim 170 or 171, the cloud point of wherein said tackiness agent are 275 ℃ or lower.

179. the reflective article of claim 170 or 171, the density of wherein said tackiness agent is 0.99g/cm down at 25 ℃ ³Or it is lower.

180. the reflective article of claim 170 or 171, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

181. the reflective article of claim 170 or 171, the brightness of wherein said tackiness agent are 70 or higher.

182. the reflective article of claim 170 or 171, the brightness of wherein said tackiness agent are 75 or higher.

183. the reflective article of claim 170 or 171, wherein said reflective article are the consumer's goods.

184. an adhesive tape comprises arbitrary tackiness agent and the backing spare of claim 1-36.

185. the adhesive tape of claim 184, wherein said backing spare have two opposite faces, described tackiness agent is applied to the one side at least of described backing spare.

186. the adhesive tape of claim 185, wherein said tackiness agent are applied on the part on two sides of described two opposite faces.

187. the adhesive tape of claim 184 or 185 also comprises the release liner that places described tackiness agent opposite.

188. the adhesive tape of claim 187, wherein said tackiness agent strippingly contacts described release liner.

189. arbitrary adhesive tape of claim 184 to 186, wherein said backing spare itself twines rolling.

190. arbitrary adhesive tape of claim 184 to 186, it adheres on the base material that is selected from polyolefine, stainless steel, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, metal, metal alloy, tinsel, skin, film, laminating material, cloth, container, instruments, medical devices, glass and sheet material.

191. arbitrary adhesive tape of claim 184 to 186, wherein said backing spare be selected from polyester film, polyolefine thin film, polyurethane film, polyvinyl chloride foam, polyethylene, non-woven urethane, non-woven polyester, knit goods, polyethylene, polypropylene, polyethylene terephthalate, polyvinyl chloride, kraft paper, laminating material, latex dipping paper, tinsel, building stones, styrenic foams, laminated foam, cloth, crepe paper, and composition thereof.

192. arbitrary adhesive tape of claim 184 to 186, wherein said tackiness agent also comprise one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, thickening material, rheology modifier, filler, antiblocking additive, polymeric additive, tensio-active agent, processing aid, linking agent, neutralizing agent, fire retardant, compatilizer and biocide.

193. arbitrary adhesive tape of claim 184 to 186, the viscosity of wherein said tackiness agent are to be lower than 200Pas under 160 ℃.

194. arbitrary adhesive tape of claim 184 to 186, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

195. arbitrary adhesive tape of claim 184 to 186, when wherein said base material comprised glass, 180 ° of peel angle peel adhesion of described tackiness agent were 90 to 1800g/cm.

196. arbitrary adhesive tape of claim 184 to 186, when wherein said base material comprised stainless steel, 180 ° of peel angle peel adhesion of described tackiness agent were 100 to 2000g/cm.

197. arbitrary adhesive tape of claim 184 to 186, the spin viscosity of wherein said tackiness agent are 0.5 to 30cm.

198. arbitrary adhesive tape of claim 184 to 186, when wherein said base material comprises stainless steel, the hot shearing intensity of described tackiness agent be 40 ℃ following 10 minutes or longer.

199. arbitrary adhesive tape of claim 184 to 186, when wherein said base material comprised stainless steel, the cement strength of described tackiness agent under 12.5 * 25.0mm and 1kg load was 1 minute or longer.

200. arbitrary adhesive tape of claim 184 to 186, the probe tack of wherein said tackiness agent are 1 to 1000g.

201. arbitrary adhesive tape of claim 184 to 186, the plateau region shearing modulus of wherein said tackiness agent are 25 ℃ following 1 * 10 ⁴To 1 * 10 ⁷Dynes/cm.

202. being 175 ℃, arbitrary adhesive tape of claim 184 to 186, the melt viscosity of wherein said tackiness agent descend 1000 to 250000mPas.

203. arbitrary adhesive tape of claim 184 to 186, wherein said adhesive tape are the consumer's goods.

204. wood working goods comprise arbitrary tackiness agent and the structural member of claim 1-36, wherein said tackiness agent is applied at least a portion of described structural member.

205. the wood working goods of claim 204, wherein said structural member comprise timber or glued board or plastics or facing plate.

206. the wood working goods of claim 204, wherein said structural member is selected from plank, fiberboard, plasterboard, plaster board, glued board, PVC, melamine, polyester, impregnated paper and asbestos cement plate.

207. the wood working goods of claim 204, wherein said wood working goods are selected from indoor furniture, outdoor furniture, ornament, filler rod, door, frame, window and factory's woodwork.

208. arbitrary wood working goods of claim 204 to 207, the brookfield viscosity of wherein said tackiness agent are 10 to 150Pas.

209. arbitrary wood working goods of claim 204 to 207, the plateau modulus of wherein said tackiness agent is 1 * 10 under 25 ℃ and 1 radian per second ⁶To 1 * 10 ⁸Dynes/cm.

210. arbitrary wood working goods of claim 204 to 207, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

211. arbitrary wood working goods of claim 204 to 207, the open hour of wherein said tackiness agent are 5 minutes or longer.

212. arbitrary wood working goods of claim 204 to 207, the open hour of wherein said tackiness agent are 10 minutes or longer.

213. arbitrary wood working goods of claim 204 to 207, the open hour of wherein said tackiness agent are 20 minutes or longer.

214. arbitrary wood working goods of claim 204 to 207, be 1 minute or shorter the set time of wherein said tackiness agent.

215. arbitrary wood working goods of claim 204 to 207, be 5 minutes or shorter the set time of wherein said tackiness agent.

216. arbitrary wood working goods of claim 204 to 207, be 10 minutes or shorter the set time of wherein said tackiness agent.

217. wooden consumer's goods comprise arbitrary tackiness agent of claim 1-36.

218. a label that is used to adhere to base material comprises arbitrary tackiness agent, backing spare and the peeling liner of claim 1-36, wherein makes described peeling liner adhere to described backing spare with described tackiness agent.

219. the label of claim 218, wherein said backing spare are selected from polyolefine, stainless steel, cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, metal, metal alloy, tinsel, skin, film, laminating material, cloth, container, instruments, medical devices, glass and sheet material.

220. the label of claim 218, wherein said backing spare are selected from polyester film, polyolefine thin film, polyurethane film, polyvinyl chloride foam, polyethylene, non-woven urethane, non-woven polyester, knit goods, polyethylene, polypropylene, polyethylene terephthalate, polyvinyl chloride, kraft paper, laminating material, latex dipping paper, tinsel, building stones, styrenic foams, laminated foam body, cloth, crepe paper, reach polyethylene and polyacrylic mixture.

221. two opposite faces that arbitrary label of claim 218 to 220, wherein said backing spare and peel off and be lined with two opposite faces, described tackiness agent are applied to described backing spare one of at least or two opposite faces of described peeling liner one of at least on.

222. arbitrary label of claim 218 to 220, the brookfield viscosity of wherein said tackiness agent are 177 ℃ of following 50000mPas or lower.

223. arbitrary label of claim 218 to 220, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

224. arbitrary label of claim 218 to 220, the plateau region shearing modulus of wherein said tackiness agent are 25 ℃ following 1 * 10 ⁴To 1 * 10 ⁷Dynes/cm.

225. arbitrary label of claim 218 to 220, when described base material comprised glass, 180 ° of peel angle peel adhesion of described tackiness agent were 1 to 1800g/cm.

226. arbitrary label of claim 218 to 220, when described base material comprised polyethylene film, 180 ° of peel angle peel adhesion of described tackiness agent were 1 to 1800g/cm.

227. arbitrary label of claim 218 to 220, the spin viscosity of wherein said tackiness agent are 0.1 to 30cm.

228. arbitrary label of claim 218 to 220, when wherein said base material comprised glass, the loops viscosity of described tackiness agent was 1 to 10N/cm.

229. arbitrary label of claim 218 to 220, when wherein said base material comprised polyethylene film, the loops viscosity of described tackiness agent was 1 to 10N/cm.

230. arbitrary label of claim 218 to 220, when wherein said base material comprised stainless steel, the hot shearing intensity of described tackiness agent was greater than 40 minutes under 40 ℃.

231. arbitrary label of claim 218 to 220, when wherein said base material comprises stainless steel, described tackiness agent under 12.5 * 25.0mm and 1kg load cement strength greater than 1 minute.

232. arbitrary label of claim 218 to 220, the Polyken probe tack of wherein said tackiness agent are 1 to 900g.

233. bind goods for one kind, comprise arbitrary tackiness agent and the adhesive of claim 1-36, wherein said tackiness agent is applied at least a portion of described adhesive.

234. the bookbinding goods of claim 233, wherein said bookbinding goods are selected from hardcover, periodical, textbook, handbook, magazine, moccasin textbook, paperbound, magazine and catalogue.

235. the bookbinding goods of claim 233 or 234, wherein said adhesive comprise paper or thick material paper.

236. the bookbinding goods of claim 233 or 234, the substrate fiber of the wherein said tackiness agent rate of tearing is 75% to 100% under 22 ℃.

237. the bookbinding goods of claim 233 or 234, the substrate fiber of the wherein said tackiness agent rate of tearing is 95% to 100% under 22 ℃.

238. the bookbinding goods of claim 233 or 234, the release adhesive fail temperature of wherein said tackiness agent is 60 ℃ or higher.

239. the bookbinding goods of claim 233 or 234, the release adhesive fail temperature of wherein said tackiness agent is 200 ℃ or lower.

240. the bookbinding goods of claim 233 or 234, the shear adhesion fail temperature of wherein said tackiness agent is 70 ℃ or higher.

241. the bookbinding goods of claim 233 or 234, the shear adhesion fail temperature of wherein said tackiness agent is 200 ℃ or lower.

242. the bookbinding goods of claim 233 or 234, the fracture tensile strength of wherein said tackiness agent are 27.5 to 82bar under 25 ℃.

243. the bookbinding goods of claim 233 or 234, the fracture tensile strength of wherein said tackiness agent are 27.5 to 65bar under 25 ℃.

244. the bookbinding goods of claim 233 or 234, the fracture tensile strength of wherein said tackiness agent are 27.5 to 40bar under 25 ℃.

245. the bookbinding goods of claim 233 or 234, the elongation of wherein said tackiness agent is 100% to 1000% strain of raw footage down at 25 ℃.

246. the bookbinding goods of claim 233 or 234, the elongation of wherein said tackiness agent is 100% to 750% strain of raw footage down at 25 ℃.

247. the bookbinding goods of claim 233 or 234, the elongation of wherein said tackiness agent is 100% to 600% strain of raw footage down at 25 ℃.

248. the bookbinding goods of claim 233 or 234, the fracture tensile strength of wherein said tackiness agent is 1.5 or lower with the ratio of extension at break.

249. the bookbinding goods of claim 233 or 234, the fracture tensile strength of wherein said tackiness agent is 1.25 or lower with the ratio of extension at break.

250. the bookbinding goods of claim 233 or 234, the fracture tensile strength of wherein said tackiness agent is 0.9 or lower with the ratio of extension at break.

251. the bookbinding goods of claim 233 or 234, the viscosity of wherein said tackiness agent are 177 ℃ of following 2.5Pas or lower.

252. the bookbinding goods of claim 233 or 234, the viscosity of wherein said tackiness agent are 177 ℃ of following 10Pas or lower.

253. the bookbinding goods of claim 233 or 234, the second-order transition temperature of wherein said tackiness agent are-65 to 30 ℃.

254. the bookbinding goods of claim 233 or 234, the Young's modulus of wherein said tackiness agent are 65 to 690bar.

255. the bookbinding goods of claim 233 or 234, the some T shape peeling force of wherein said tackiness agent are 3 to 4000N.

256. the bookbinding goods of claim 233 or 234, the some T shape peeling force of wherein said tackiness agent are 5 to 3000N.

257. the bookbinding goods of claim 233 or 234, the some T shape peeling force of wherein said tackiness agent are 15 to 1000N.

258. the bookbinding goods of claim 233 or 234, wherein said bookbinding goods are the consumer's goods.

259. a road marking compositions comprises binder composition and one or more filler, described binder composition comprises arbitrary tackiness agent of claim 1-36.

260. the road marking compositions of claim 259, wherein said road marking compositions are applied to one or more base material that is selected from pitch, concrete, metal, brick, paving stone, pottery, cinder brick, ground, playground, runway, synthetic rubber surrogate, concrete, ceramic tile, steel plate, timber, pottery, polymeric material, glass, porcelain, stone, plank, shaving board, wooden auto parts and beaujolais.

261. it is 100000 to 250000 multipolymer that the road marking compositions of claim 259 or 260, wherein said binder composition also comprise Mw.

262. it is 250000 to 500000 multipolymer that the road marking compositions of claim 260 or 261, wherein said binder composition also comprise Mw.

263. it is that 100000 to 250000 first multipolymer and Mw are 250000 to 500000 second multipolymer that the road marking compositions of claim 259 or 260, wherein said binder composition also comprise Mw.

264. also comprising the f-t synthetic wax, hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers, the maleic anhydride grafted that are selected from f-t synthetic wax, oxidation, the road marking compositions of claim 259 or 260, wherein said binder composition have side to hang one or more wax of polyethylene, paraffin and the Microcrystalline Wax of acid functional group part.

265. the road marking compositions of claim 259 or 260, wherein said binder composition also comprises one or more additive.

266. the road marking compositions of claim 259 or 260, wherein said binder composition also comprise one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, extender, hindered phenol, phosphoric acid ester, antiblocking additive, lubricant, photostabilizer, UV light absorber, dispersion agent, alkali, wetting agent, fire retardant, linking agent, solidifying agent, covering agent and water.

267. the road marking compositions of claim 259 or 260, wherein said one or more oil comprises aliphatic oil, naphthenic oil, white oil, soya-bean oil, its combination.

268. the road marking compositions of claim 259 or 260, wherein said binder composition also comprise one or more softening agent that is selected from mineral oil, polybutene, phthalic ester, hydrocarbon ils, soya-bean oil, elastomerics, olefin oligomer, vegetables oil and cyclohexane dimethanol bisbenzoate.

269. the road marking compositions of claim 259 or 260, wherein said one or more filler is selected from sand, pigment, granulated glass sphere, the polymer-based carbon bead, lime carbonate, crushed marble, rhombspar, talcum, prismatic tamper, the reflection from lens body, the calcite spar, silica sand, graphite, floating dust, cement flour, clay, feldspar, nepheline, fumed silica, aluminum oxide, magnesium oxide, zinc oxide, barium sulfate, pure aluminium silicate, Calucium Silicate powder, titanate, chalk, the reflective mineral filler, calcium sulfate, calcium metasilicate, silica powder, the calcining flint powder, mica, the calcium silicate glass fiber, dyestuff, grouan, gypsum, slaked lime, diatomite, tamper, white lead, lithopone, chrome yellow, cadmium yellow, polymer gel, stupalith, corundum, aluminium hydroxide, and zinc neodecanoate.

270. the road marking compositions of claim 259 or 260, wherein said binder composition also comprise the polymkeric substance that is selected from the succinyl oxide modification and one or more properties-correcting agent of metal oxide.

271. the road marking compositions of claim 259 or 260, wherein said road marking compositions comprises 10 to 80wt% binder composition.

272. the road marking compositions of claim 259 or 260, wherein said binder composition comprise 30wt% or one or more wax still less.

273. the road marking compositions of claim 259 or 260, wherein said binder composition comprise 80wt% or one or more tackifier still less.

274. the road marking compositions of claim 259 or 260, wherein said binder composition comprise 20wt% or one or more softening agent still less.

275. the road marking compositions of claim 259 or 260, wherein said binder composition comprise the tackifier or the polymkeric substance of 5wt% or one or more sour modification still less.

276. the road marking compositions of claim 259 or 260, wherein said binder composition comprise 5wt% or one or more stablizer still less.

277. the road marking compositions of claim 259 or 260, wherein said binder composition comprise 40wt% or one or more polymeric additive still less.

278. the road marking compositions of claim 259 or 260, wherein said binder composition comprise 10wt% or one or more covering agent still less.

279. the road marking compositions of claim 259 or 260, wherein said binder composition comprise 1wt% or one or more antioxidant still less.

280. the road marking compositions of claim 259 or 260, wherein said road marking compositions comprise one or more filler of 20 to 90wt%.

281. the road marking compositions of claim 259 or 260, wherein said one or more filler comprise 50wt% or one or more bead still less.

282. the road marking compositions of claim 259 or 260, wherein said one or more filler comprises one or more bead of 10 to 40wt%.

283. the road marking compositions of claim 259 or 260, wherein said one or more filler comprises one or more bead of 15 to 30wt%.

284. the road marking compositions of claim 259 or 260, wherein said one or more filler comprise 20wt% or one or more pigment still less.

285. the road marking compositions of claim 259 or 260, wherein said one or more filler comprises one or more pigment of 2 to 15wt%.

286. the road marking compositions of claim 259 or 260, wherein said one or more filler comprises one or more pigment of 3 to 10wt%.

287. the road marking compositions of claim 259 or 260, the grace viscosity of praising of wherein said binder composition is 190 ℃ times 35 to 180 seconds.

288. the road marking compositions of claim 259 or 260, the grace viscosity of praising of wherein said binder composition is to be lower than 120 seconds under 190 ℃.

289. the road marking compositions of claim 259 or 260, the second-order transition temperature of wherein said binder composition are-65 to 30 ℃.

290. the road marking compositions of claim 259 or 260, the some T shape peeling force of wherein said binder composition are 3 to 4000N.

291. the road marking compositions of claim 259 or 260, the some T shape peeling force of wherein said binder composition are 5 to 3000N.

292. the road marking compositions of claim 259 or 260, the some T shape peeling force of wherein said binder composition are 15 to 1000N.

293. the road marking compositions of claim 259 or 260, the bounding force on wherein said binder composition and road surface are 1.0N/mm ²Or it is bigger.

294. the road marking compositions of claim 259 or 260, the bounding force on wherein said binder composition and road surface are 1.2N/mm ²Or it is bigger.

295. the road marking compositions of claim 259 or 260, the bounding force on wherein said binder composition and road surface are 1.3N/mm ²Or it is bigger.

296. the road marking compositions of claim 259 or 260, the bounding force on wherein said binder composition and road surface are 1.5N/mm ²Or it is bigger.

297. the road marking compositions of claim 259 or 260, the softening temperature of wherein said binder composition are 90 ℃ or higher.

298. the road marking compositions of claim 259 or 260, the softening temperature of wherein said binder composition are 95 ℃ or higher.

299. the road marking compositions of claim 259 or 260, the softening temperature of wherein said binder composition are 98 ℃ or higher.

300. the road marking compositions of claim 259 or 260, the softening temperature of wherein said binder composition are 100 ℃ or higher.

301. the road marking compositions of claim 259 or 260, the acupuncture degree of described binder composition are 5 to 120s/10mm.

302. the road marking compositions of claim 259 or 260, the brightness of wherein said binder composition are 70 or higher.

303. the road marking compositions of claim 259 or 260, the brightness of wherein said binder composition are 75 or higher.

304. the road marking compositions of claim 259 or 260, the brightness of wherein said binder composition are 76 or higher.

305. the road marking compositions of claim 259 or 260, the brightness of wherein said binder composition are 78 or higher.

306. being 177 ℃, the road marking compositions of claim 259 or 260, the melt viscosity of wherein said binder composition descend 0.4 to 30Pas.

307. an encapsulant composition that comprises mixture, described mixture comprise arbitrary tackiness agent of claim 1-36, wherein said mixture imposes at least a portion of sealed substrate surface.

308. the encapsulant composition of claim 307, wherein said base material is selected from concrete, roof Material, marble, anodized aluminum, brick, mortar, grouan, Wingdale, porcelain, glass, painted surface, timber, polyvinyl chloride, polyacrylic ester, polycarbonate, polystyrene, fabric, packing ring, pipeline, metal, distribution, sled, polyethylene, polypropylene, acrylic resin, PVDC, paper, ethane-acetic acid ethyenyl ester, automobile, buildings, aircraft, dashboard, the deck, skeleton, the road surface, rear deflector door, door-plate, wheel house, panel, fireproof brickwork, the flange at edge, ground, vehicle body, and floor pan.

309. also comprising, the encapsulant composition of claim 307 or 308, wherein said mixture be selected from f-t synthetic wax, the f-t synthetic wax of oxidation, the hydroxyl stearamide wax, functionalized waxes, Poly Propylene Wax, polyethylene wax, wax modifiers, non-crystalline state wax, carnauba wax, Viscotrol C wax, Microcrystalline Wax, beeswax, carnauba wax, castor wax, spermaceti, vegetable wax, gama wax, Japan wax, ouricury wax, Pseudotsuga menziesii (Mirbel) Franco bark wax, rice bran wax, jojoba wax, fruit of Grecian Laurel wax, montanin wax, peat wax, ceresine, petroleum wax, paraffin, one or more wax of the chloroflo of chemical modification and the amide waxe of replacement.

310. the encapsulant composition of claim 307 or 308, wherein said mixture also comprise one or more additive that is selected from softening agent, oil, stablizer, antioxidant, pigment, antiblocking additive, processing aid, neutralizing agent, water, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, linking agent, thixotropic agent, tensio-active agent, adhesion promotor, toughener, chainextender, ultra-violet stabilizer, tinting material, organic solvent, siccative, wetting agent, nucleator, promotor and solidifying agent.

311. also comprising, the encapsulant composition of claim 307 or 308, wherein said mixture be selected from diatomite, lime carbonate, ferric oxide, hydrogenated castor oil, fumed silica, precipitated chalk, talcum, zinc oxide, polyvinyl chloride powder, mycocide, graphite, carbon black, pitch, carbon packing, clay, mica, fiber, titanium dioxide, Cadmium Sulfide, asbestos, wood powder, polyethylene powder, bubble shape thing, bead, thixotrope, wilkinite, calcium sulfate, calcium oxide and magnesian one or more filler.

312. the encapsulant composition of claim 307 or 308, wherein said mixture also comprises and is selected from silane, titanic acid ester, acrylic acid or the like, acid, acid anhydride, Resins, epoxy, stiffening agent, polymeric amide, methyl acrylate, epoxide, resol, polyisobutene, aminoalkyl, the mercapto alkyl, epoxy alkyl, the urea alkyl, carboxyl, the functional silane of acrylate and isocyanuric acid ester, mercaptopropyl trimethoxysilane, glycidoxy-propyltrimethoxy silane, aminopropyl triethoxysilane, the aminoethyl aminopropyl trimethoxysilane, the urea propyl trimethoxy silicane, two-γ-trimethoxysilyl-third ureas, 1,3,5-three-γ-trimethoxy-silylpropyl isocyanuric acid ester, two-γ-the trimethoxy-silylpropyl maleic acid ester, one or more adhesion promotor of fumarate and gamma-methyl allyl acyloxypropyl trimethoxysilane and aminopropyl triethoxysilane.

313. the encapsulant composition of claim 307 or 308, wherein said mixture also comprise one or more linking agent that is selected from oxime linking agent, organoalkoxysilane, epoxy alkyl organoalkoxysilane, amido silane, aminosilane, alkene TMOS, tetraethoxysilane, methyltrimethoxy silane, vinyltrimethoxy silane, glycidoxy-propyltrimethoxy silane, vinyl three iso-propenyloxysilanes, methyl three iso-propenyloxysilanes, methyl three hexamethylene aminosilanes, methyl three Zhong Ding aminosilanes and polyisocyanates.

314. the encapsulant composition of claim 307 or 308, wherein said mixture also comprise one or more organic solvent that is selected from aliphatic solvents, alicyclic solvents, mineral turpentine and aromatic solvent.

315. the encapsulant composition of claim 307 or 308, wherein said mixture also comprise one or more tensio-active agent of the polydimethylsiloxanemacromer macromer that is selected from the organopolysiloxane that contains vinyl, the organopolysiloxane that contains sulfydryl and ethenyl blocking.

316. the encapsulant composition of claim 307 or 308, wherein said mixture also comprise be selected from aminosilane, amido silane, acetoxysilane and aminooxy silane, methyl ethylene two-N-methyl kharophen silane, methyl hydrogen diacetoxy silane, dimethyl is two-diethyl hydroxylamino silane, dimethyl is two-one or more chainextender of Zhong Ding aminosilane and polyisocyanates.

317. the encapsulant composition of claim 307 or 308, wherein said mixture also comprises and is selected from thioesters, phosphoric acid ester, hindered phenol, four (3-(3 ', 5 '-di-t-butyl-4-hydroxyphenyl) methane propionic acid methylene ester), 2,2 '-ethylenebis (4, the 6-DI-tert-butylphenol compounds), 1,1,3-three (2-methyl-4-hydroxyl-5-tert-butyl-phenyl) butane, 1,3,5-trimethylammonium-2,4,6-three (3,5-di-t-butyl-4-acrinyl) benzene, Tyox B, tetramethylolmethane four (β-lauryl sulfo-propionic ester), alkyl-aryl two-and one or more antioxidant of many-phosphoric acid ester and thiophosphite.

318. the encapsulant composition of claim 309, wherein said mixture comprise 30wt% or one or more wax still less.

319. the encapsulant composition of claim 309, wherein said mixture comprise 20wt% or one or more wax still less.

320. the encapsulant composition of claim 311, wherein said mixture comprise 10wt% or one or more wax still less.

321. the encapsulant composition of claim 312, wherein said mixture comprise 95wt% or one or more described additive still less.

322. the encapsulant composition of claim 310, wherein said mixture comprise 50wt% or one or more described additive still less.

323. the encapsulant composition of claim 310, wherein said mixture comprise 10wt% or one or more described additive still less.

324. the encapsulant composition of claim 313, wherein said mixture comprise 5wt% or one or more linking agent still less.

325. the encapsulant composition of claim 311, wherein said mixture comprise 50wt% or one or more filler still less.

326. the encapsulant composition of claim 315, wherein said mixture comprise 15wt% or one or more tensio-active agent still less.

327. the encapsulant composition of claim 312, wherein said mixture comprise 15wt% or one or more adhesion promotor still less.

328. the encapsulant composition of claim 307 or 308, wherein said mixture comprise 75wt% or one or more toughener still less.

329. the encapsulant composition of claim 307 or 308, wherein said mixture comprise 30wt% or one or more toughener still less.

330. the encapsulant composition of claim 307 or 308, wherein said mixture comprise 50wt% or one or more polymeric additive still less.

331. the encapsulant composition of claim 317, wherein said mixture comprises 0.01 to 10wt% antioxidant.

332. the encapsulant composition of claim 317, wherein said mixture comprises 0.05 to 5wt% antioxidant.

333. the encapsulant composition of claim 307 or 308, the tensile strength modulus under 100% elongation of wherein said mixture is 0.003 to 0.06bar under 20 ℃.

334. the encapsulant composition of claim 307 or 308, the elongation at break of wherein said mixture are 190% or higher under 20 ℃.

335. the encapsulant composition of claim 307 or 308, the viscosity of wherein said mixture are 177 ℃ of following 9Pas or lower.

336. the encapsulant composition of claim 307 or 308, the second-order transition temperature of wherein said mixture are-65 to 30 ℃.

337. the encapsulant composition of claim 307 or 308, the some T shape peeling force of wherein said mixture are 3 to 4000N.

338. dropping down stream after 70 ℃ of following 1 weeks, the encapsulant composition of claim 307 or 308, wherein said mixture be 7.5cm or lower.

339. the encapsulant composition of claim 307 or 308, the Xiao A hardness of wherein said mixture are 3 to 45.

340. the encapsulant composition of claim 307 or 308, the tensile strength of wherein said mixture are 0.0095 to 0.2bar.

341. the encapsulant composition of claim 307 or 308, the stress relaxation rate of wherein said mixture are 75% or lower under 25 ℃.

342. the encapsulant composition of claim 307 or 308, wherein said mixture is 0.01bar or higher in shear adhesion power on glass.

343. the encapsulant composition of claim 307 or 308, the fusing point of wherein said mixture are 200 ℃ or lower.

344. the encapsulant composition of claim 307 or 308, wherein said mixture is 10pli or higher with respect to 180 ° of stripping strengths of glass.

345. a paving compositions comprises pitch, gathers materials and arbitrary tackiness agent of claim 1-36, wherein said gathering materials is selected from clay, stone, sand, rock, gravel and slag.

346. the paving compositions of claim 345, wherein said pitch are one or more rock asphalt, petroleum pitch or its arbitrary combination.

347. the paving compositions of claim 345, wherein said pitch comprises asphalite, stellar coal, grahamite, manjak, lake pitch, Trinidad asphalt or rock asphalt.

348. arbitrary paving compositions of claim 345 to 347, wherein said composition also comprise the filler that is selected from carbon black, broken ore, mine tailing, cinder, slag, lime-ash, broken tire, clay and glass.

349. arbitrary paving compositions of claim 345 to 347, wherein said paving compositions comprise 95wt% or gathering materials still less.

350. arbitrary paving compositions of claim 345 to 347, wherein said paving compositions comprise 90 to 96wt% gather materials.

351. arbitrary paving compositions of claim 345 to 347, wherein said paving compositions comprises 80 to 99wt% pitch.

352. arbitrary paving compositions of claim 345 to 347, the release adhesive fail temperature of wherein said tackiness agent is 60 ℃ or higher.

353. arbitrary paving compositions of claim 345 to 347, the shear adhesion fail temperature of wherein said tackiness agent is 70 ℃ or higher.

354. arbitrary paving compositions of claim 345 to 347, the solidification value of wherein said tackiness agent are-20 to 250 ℃.

355. arbitrary paving compositions of claim 345 to 347, the Xiao A hardness of wherein said tackiness agent are 3 to 45.

356. a glue rod comprises containing the slender member that right requires arbitrary tackiness agent of 1-36.

357. the glue rod of claim 356, wherein exert pressure or when heating described glue rod on base material, produce binder deposition.

358. the glue rod of claim 357, wherein said base material are selected from cardboard, container board, shipping tag hardboard paper, corrugated cardboard, chipboard, kraft paper, card board kai, fiberboard, metal, metal alloy, tinsel, film, laminating material, sheet material, timber, polystyrene, nylon, polycarbonate, polypropylene, styrenic porous plastics, porous substrate, polyvinyl chloride, wall and polyester.

359. arbitrary glue rod of claim 356 to 358, wherein said tackiness agent also comprises one or more additive that is selected from softening agent, oil, stablizer, antioxidant, synergistic agent, pigment, dyestuff, polymeric additive, defoamer, sanitas, thickening material, rheology modifier, wetting Agent for Printing Inks, filler, water, spices, fire retardant, tinting material, microbiotic, sterilant, anti-mycotic agent, inorganic salt, jelling agent, tackiness agent, tensio-active agent, alkali, biocide and suds suppressor.

360. arbitrary glue rod of claim 356 to 358, wherein said tackiness agent also comprises one or more filler that is selected from polyethylene, titanium oxide and lime carbonate.

361. arbitrary glue rod of claim 356 to 358, wherein said tackiness agent comprise one or more described inorganic salt of 5 to 30wt%.

362. arbitrary glue rod of claim 356 to 358, wherein said tackiness agent comprise 5wt% or still less one or more tinting material, dyestuff, antioxidant, spices or pigment.

363. arbitrary glue rod of claim 356 to 358, wherein said tackiness agent comprise 1wt% or one or more biocide still less.

364. arbitrary glue rod of claim 356 to 358, the substrate fiber of the wherein said tackiness agent rate of tearing is 75% to 100% under 25 ℃.

365. arbitrary glue rod of claim 356 to 358, the substrate fiber of the wherein said tackiness agent rate of tearing is 95% to 100% under 25 ℃.

366. arbitrary glue rod of claim 356 to 358, the release adhesive fail temperature of wherein said tackiness agent is 60 ℃ or higher.

367. arbitrary glue rod of claim 356 to 358, the shear adhesion fail temperature of wherein said tackiness agent is 70 ℃ or higher.

368. being 177 ℃, arbitrary glue rod of claim 356 to 358, the viscosity of wherein said tackiness agent descend 1 to 50Pas.

369. arbitrary glue rod of claim 356 to 358, the softening temperature of wherein said tackiness agent are 70 to 100 ℃.

370. arbitrary glue rod of claim 356 to 358, the use temperature of wherein said tackiness agent is 190 ℃ or lower.

371. arbitrary glue rod of claim 356 to 358, the some T shape peeling force of wherein said tackiness agent are 3 to 4000N.

372. pipeline parcel goods comprise arbitrary tackiness agent and the parcel member of claim 1-36, wherein said tackiness agent place at least in part on the described parcel member or within.

373. the pipeline of claim 372 parcel goods, wherein said parcel member is selected from fiberglass, fiber, Woven fabric, supatex fabric, cloth, polyethylene, polypropylene, acrylic rubber, EPDM, paracril, nylon, epichlorohydrin elastomer, polysulphide, acrylic elastomer and isoprene-isobutylene rubber.

374. the pipeline of claim 372 parcel goods, wherein said pipeline parcel goods are selected from pipeline, accessory, jar, vessel and container.

375. arbitrary pipeline parcel goods of claim 372-374, wherein said pipeline parcel goods are made by the material that is selected from timber, cement, concrete, supatex fabric, Woven fabric, aluminium, stainless steel, brass, nickel, glass, glazed ceramics, unglazed pottery, ceramic tile, polyvinyl chloride, polyethylene terephthalate, gypsum, plaster, bituminous coating, roofing felt, synthetic polymer membranes and polyurathamc isolator.

376. arbitrary pipeline parcel goods of claim 372-374, wherein said tackiness agent also comprises one or more polymeric additive that is selected from isoprene-isobutylene rubber and polyisobutene.

377. arbitrary pipeline parcel goods of claim 372-374, the release adhesive fail temperature of wherein said tackiness agent is 60 ℃ or higher.

378. arbitrary pipeline parcel goods of claim 372-374, the shear adhesion fail temperature of wherein said tackiness agent is 70 ℃ or higher.

379. the arbitrary pipeline of claim 372-374 parcel goods, the fracture tensile strength of wherein said tackiness agent are 0.7 to 1.5bar under 23 ℃.

380. arbitrary pipeline parcel goods of claim 372-374, the elongation of wherein said tackiness agent is 50% strain of raw footage or higher down at 23 ℃.

381. arbitrary pipeline parcel goods of claim 372-374, the solidification value of wherein said tackiness agent is-20 to 250 ℃.

382. arbitrary pipeline parcel goods of claim 372-374, the open hour of wherein said tackiness agent are-20 to 250 ℃.

383. arbitrary pipeline parcel goods of claim 372-374, the cloud point of wherein said tackiness agent is 275 ℃ or lower.

384. arbitrary pipeline parcel goods of claim 372-374, the cloud point of wherein said tackiness agent is 190 ℃ or lower.

385. arbitrary pipeline parcel goods of claim 372-374, the cloud point of wherein said tackiness agent is 130 ℃ or lower.

386. arbitrary pipeline parcel goods of claim 372-374, the second-order transition temperature of wherein said tackiness agent is 0 ℃ or lower.

387. arbitrary pipeline parcel goods of claim 372-374, wherein said pipeline parcel goods are the consumer's goods.

388. the goods that transparent panel is arranged comprise:

One or more transparent panel; With

Be applied to the arbitrary tackiness agent of the claim 1-36 at least a portion of described one or more panel.

389. the goods of claim 388, wherein said one or more transparent panel comprises one or more material that is selected from polyvinyl butyral acetal, urethane, vinyl-acetic ester, polyethylene, polypropylene, polycarbonate, glass and silicate glass.

390. the goods of claim 388 or 389, wherein said goods are selected from splinter-proof glass, sound control glass and shatter proof glass.

391. the goods of claim 388 or 389, wherein said tackiness agent forms film on described one or more transparent panel.