WO1996011961B1 - Polymerization catalyst systems, their production and use - Google Patents
Polymerization catalyst systems, their production and useInfo
- Publication number
- WO1996011961B1 WO1996011961B1 PCT/US1995/012789 US9512789W WO9611961B1 WO 1996011961 B1 WO1996011961 B1 WO 1996011961B1 US 9512789 W US9512789 W US 9512789W WO 9611961 B1 WO9611961 B1 WO 9611961B1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- group
- different
- halogen atom
- alkyl
- catalyst system
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title claims 3
- 239000002685 polymerization catalyst Substances 0.000 title 1
- 238000000034 method Methods 0.000 claims abstract 17
- 239000003054 catalyst Substances 0.000 claims abstract 13
- 230000000379 polymerizing effect Effects 0.000 claims abstract 3
- 150000001336 alkenes Chemical class 0.000 claims abstract 2
- 229910052723 transition metal Inorganic materials 0.000 claims abstract 2
- 150000003624 transition metals Chemical class 0.000 claims abstract 2
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims 9
- 125000005843 halogen group Chemical group 0.000 claims 9
- 125000002877 alkyl aryl group Chemical group 0.000 claims 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims 7
- 125000000041 C6-C10 aryl group Chemical group 0.000 claims 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims 5
- 125000005018 aryl alkenyl group Chemical group 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 4
- 125000004122 cyclic group Chemical group 0.000 claims 4
- 239000012968 metallocene catalyst Substances 0.000 claims 4
- 239000003607 modifier Substances 0.000 claims 4
- 239000007795 chemical reaction product Substances 0.000 claims 3
- 229910052710 silicon Inorganic materials 0.000 claims 3
- 239000010703 silicon Substances 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 claims 2
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims 2
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims 2
- FLFNHHSXSLXYQB-UHFFFAOYSA-L CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 Chemical compound CC1=CC(C(=CC=C2)C=3C=CC=CC=3)=C2C1[Zr](Cl)(Cl)(=[Si](C)C)C1C(C)=CC2=C1C=CC=C2C1=CC=CC=C1 FLFNHHSXSLXYQB-UHFFFAOYSA-L 0.000 claims 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000004407 fluoroaryl group Chemical group 0.000 claims 2
- 229910052732 germanium Inorganic materials 0.000 claims 2
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 230000000737 periodic effect Effects 0.000 claims 2
- 239000011148 porous material Substances 0.000 claims 2
- 229910052718 tin Inorganic materials 0.000 claims 2
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims 1
- 125000000172 C5-C10 aryl group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- CGELJBSWQTYCIY-UHFFFAOYSA-L [Cl-].[Cl-].CC1=Cc2ccccc2[C@H]1[Zr++]([C@@H]1C(C)=Cc2ccccc12)=[Si](C)C Chemical compound [Cl-].[Cl-].CC1=Cc2ccccc2[C@H]1[Zr++]([C@@H]1C(C)=Cc2ccccc12)=[Si](C)C CGELJBSWQTYCIY-UHFFFAOYSA-L 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 abstract 2
- 239000007789 gas Substances 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 239000002002 slurry Substances 0.000 abstract 1
Abstract
This invention is generally directed toward a supported catalyst system useful for polymerizing olefins. The method for supporting the catalyst of the invention provides for a supported bulky ligand transition metal catalyst which when utilized in a polymerization process substantially reduces the reactor fouling and sheeting in a gas, slurry or liquid pool polymerization process.
Claims
1. A method for producing a supported catalyst system, said method comprising the steps of combining an alumoxane, a surface modifier, a porous carrier, and a metallocene catalyst component in a solvent to form a solution wherein the metallocene catalyst component is represented by the following formula:
R1 and R2 are identical or different, are one of a hydrogen atom, a C1-C10 alkyl group, a C1-C10 alkoxy group, a C5-C10 aryl group, a C5-C10 aryloxy group, a C2-C10 alkenyl group, a C7-C40 arylalkyl group, a C7-C40 alkylaryl group, a C8-C40 arylalkenyl group, or a halogen atom;
R3 and R4 are hydrogen atoms;
R5 and R6 are identical or different, preferably identical, are one of a halogen atom, a C1-C10 alkyl group, which may be halogensted, a C6-C10 aryl group, which may be halogenated, a C2-C10 alkenyl group, a C7-C40 arylalkyl group, a C7-C40 alkylaryl group, a C8-C40 arylalkanyl group, a -NR2 15, -SR15, OR15, -OSiR3 15 or -PR2 15 radical, wherein R15 is one of a halogen atom, a C1-C10 alkyl group, or a C6-C10 aryl group; R5 and R6 are identical or different, preferably identical, are one of a halogen atom, a C1-C10 alkyl group, which may be halogenated, a C6-C10 aryl group, which may be halogenated, a C2-C10 alkenyl group, a C7-C40 arylalkyl group, a C7-C40 alkylaryl group, a C8-C40 arylalkenyl group, a -NR2 15, SR15, - OR15, -OSiR3 15 or -PR2 15 radical, wherein R15 is one of a halogen atom, a C1-C10 alkyl group, or a C6-C10 aryl group;
-BR1 1, =AlR11, -Ge-, -Sn-, -O-, -S-, - SO, -SO2, -NR11, =CO, PR11, or -P(O)R11;
wherein:
R11, R12 and R13 are identical or different and are a hydrogen atom, a halogen atom, a C1-C20 alkyl group, a C1-C20 fluoroalkyl group, a C6-C30 aryl group, a C6-C30 fluoroaryl group, a C1-C20 alkoxy group, a C2-C20 alkeayl group, a C7-C40 arylalkyl group, a C8-C40 arylalkonyl group, C7-C40 alkylaryl group, or R11 and R12, or R1 1 and R13, together with the atoms binding them, can form ring systems;
M2 is silicon, germanium or tin;
R8 and R9 are identical or different and have the meanings as stated for R11;
m and n are identical or different and are zero, 1 or 2, m plus n being aero, 1 or 2; and the radicals R10 are Identical or different and have the meanings stated for R1 1, R12 and R13 wherein further two adjacent R10 radicals can be joined together to form a ring system.
2. The method of claim 1 wherein the total volume of the solution is from 0.8 to 3.0 times the total pore volume of the porous support.
3. The method of claims 1 or 2 wherein the metallocene catalyst component comprises two or more metallocene catalyst components.
4. The method of any of the preceding claims further comprising the step of prepolymerizing the supported catalyst system with an olefinlc monomer.
5. The method of any of the preceding claims wherein m=n=0 and
M2-silicon.
6. The method of any of the preceding claims wherein R5 = R6 = C1-10 alkyl.
7. The method of any of the preceding claims wherein three of the R10 radicals = hydrogen and one ia a C6-30 aryl group.
8. The method of any of the preceding claims wherein at least one of the R10 radicals is C1-10 alkyl.
9. The method of any of the preceding claims wherein the metailocene component is selected from the group consisting of:
rac-dimethylsilandiylbis(2-methyl-4,5-benzoindenyl)- zirconium dichloride, rac-dimethylsilandiylbis(2-methylindenyl)-zirconium dichloride,
rac-dimethylsilandiyl-bis(2-methyl-4,6-diianpropylindenyl)-zirconium dichloride, rac-dimethylsilandiylbis(2-methyl-4-phenylindenyl)zirconium dichloride, and rac-dimethylsilandiylbis(2-methyl-4-phenylindenyl)zirconium dichloride.
10. The method of any of the preceding claims wherein the surface modifier is present in an amount in the range of 0.2 weight percent to lets than 5 weight percent of the total weight of the supported catalyst system.
11. The method of any of the preceding claims wherein the surface modifier is selected from at least one of the group of compounds represented by the following chemical formulas. C18H37N(CH2CH2OH)2, C12H25N(CH2CH2OH)2 and (CH3(CH2)7(CH)2(CH2)7OCOCH2(CHOH)4CH2OH.
12. A method for producing a supported catalyst system, said catalyst system comprising a first component comprising a chiral, Group 4 transition metal, bridged, substituted bisindenyl metailocene catalyst and a first solvent, a second component comprising an akumoxane and a second solvent, and a porous support, said method comprising the step of
a) combining the first component and the second component to form a reaction product solution;
b) combining the reaction product and the porous support, such that at any point during the formation of the supported catalyst system the total volume of the reaction product added to the porous support is leas than four times the total pore volume of the porous support; and
e) introducing a surface modifier.
13. The method of claim 13 wherein the metailocene catalyst component is represented by the general formula:
R1 and R2 are identical or different, are one of a hydrogen atom, a C1-C10 alkyl group, a C1-C10 alkoxy group, a C6-C10 aryl group, a C6-C10 aryloxy group, a C2-C10 alkenyl group, a C7-C40 arylalkyl group, a C7-C40 alkylaryl group, a C8-C40 arylalkenyl group, or a halogen atom.
R3 and R4 am hydrogen atoms;
R5 and R6 are identical or different, preferably identical, are one of a halogen nom, a C1-C10 alkyl group, which may be halogenated, a C6-C10 aryl group, which may be halogenated, a C2-C10 alkenyl group, a C7-C40 arylalkyl group, a C7-C40 alkylaryl group, a C8-C40) arylalkenyl group, a -NR2 15, -SR15, - OR15, -OSiR3 15 or -PR2 15 radical, wherein R1 5 is one of a halogen atom, a C1-C10 alky, group, or a C6-C40 aryl group,
R7 is
=_BR1 1,=AlR1 1, -Ge-, -Sn-, -O-, -S-, - SO, -SO2, =NR1 1, -CO, PR1 1, or
=P(O)R1 1;
wherein:
R11, R12 and R13 are identical or different and are a hydrogen atom, a halogen atom, a C1-C20 alkyl group, a C1-C20 fluoroalkyl group, a C6-C30 aryl group, a C6-C30 fluoroaryl group, a C1-C20 alkoxy group, a C2-C20 alkenyl group, a C7-C40 arylalkyl group, a C8-G40 arylalkaryl group, C7-C40 alkylaryl group, or R1 1 and R12, or R11 and R13, together with the atoms binding them, can form ring systems; M2 is silicon, germanium or tin,
R8 and R9 are identical or different and have the meanings as stated for
R1 1;
m and n are identical or different and are zero, 1 or 2, m plus n being zero, 1 or 2; and
the radicals R10 are identical or different and have the meanings stated for R11, R12 and R13 wherein further two adjacent R10 radicals can be joined together to form a ring system.
14. A supported catalyst system produced by the method of any of the preceding claims.
15. A process for polymerizing propylene alone or in combination with one or more other olefins, said process comprising polymerizing in the presence of the supported catalyst system of claim 14.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE69509403T DE69509403T2 (en) | 1994-10-13 | 1995-10-12 | Polymerization catalyst systems, their manufacture and their use |
CA002202404A CA2202404C (en) | 1994-10-13 | 1995-10-12 | Polymerization catalyst systems, their production and use |
JP8513296A JPH10511706A (en) | 1994-10-13 | 1995-10-12 | Polymerization catalyst systems, their production and use |
EP95938716A EP0785956B1 (en) | 1994-10-13 | 1995-10-12 | Polymerization catalyst systems, their production and use |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US32267594A | 1994-10-13 | 1994-10-13 | |
US08/322,675 | 1994-10-13 | ||
US08/502,231 | 1995-07-13 | ||
US08/502,231 US6124230A (en) | 1995-07-13 | 1995-07-13 | Polymerization catalyst systems, their production and use |
Publications (2)
Publication Number | Publication Date |
---|---|
WO1996011961A1 WO1996011961A1 (en) | 1996-04-25 |
WO1996011961B1 true WO1996011961B1 (en) | 1996-06-27 |
Family
ID=26983548
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1995/012789 WO1996011961A1 (en) | 1994-10-13 | 1995-10-12 | Polymerization catalyst systems, their production and use |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP0785956B1 (en) |
JP (1) | JPH10511706A (en) |
KR (1) | KR100367964B1 (en) |
CN (1) | CN1096470C (en) |
DE (1) | DE69509403T2 (en) |
ES (1) | ES2132744T3 (en) |
WO (1) | WO1996011961A1 (en) |
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KR102035310B1 (en) * | 2015-06-26 | 2019-10-22 | 주식회사 엘지화학 | Catalyst system and process for preparing polyolefins |
KR102569384B1 (en) * | 2016-04-01 | 2023-08-23 | 주식회사 레이크머티리얼즈 | The manufacturing method of the supported catalyst for olefin polymerization |
CN107987191B (en) * | 2016-10-26 | 2021-03-16 | 中国石油化工股份有限公司 | Supported metallocene catalyst and preparation method and application thereof |
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DE4242486A1 (en) * | 1992-12-16 | 1994-06-23 | Basf Ag | Propylene homopolymers |
CA2129794A1 (en) * | 1993-08-10 | 1995-02-11 | Toshiyuki Tsutsui | Olefin polymerization catalysts and methods of olefin polymerization |
-
1995
- 1995-10-12 WO PCT/US1995/012789 patent/WO1996011961A1/en active IP Right Grant
- 1995-10-12 DE DE69509403T patent/DE69509403T2/en not_active Expired - Lifetime
- 1995-10-12 JP JP8513296A patent/JPH10511706A/en active Pending
- 1995-10-12 KR KR1019970702394A patent/KR100367964B1/en not_active Expired - Lifetime
- 1995-10-12 ES ES95938716T patent/ES2132744T3/en not_active Expired - Lifetime
- 1995-10-12 CN CN95195652A patent/CN1096470C/en not_active Expired - Lifetime
- 1995-10-12 EP EP95938716A patent/EP0785956B1/en not_active Expired - Lifetime
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