US20060048464A1 - Free laying floor tile having pvc based backing material for preventing tile from slipping provided on back surface thereof - Google Patents
Free laying floor tile having pvc based backing material for preventing tile from slipping provided on back surface thereof Download PDFInfo
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- US20060048464A1 US20060048464A1 US10/527,534 US52753405A US2006048464A1 US 20060048464 A1 US20060048464 A1 US 20060048464A1 US 52753405 A US52753405 A US 52753405A US 2006048464 A1 US2006048464 A1 US 2006048464A1
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- United States
- Prior art keywords
- floor tile
- loose
- tile according
- lay floor
- plasticizer
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- Abandoned
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- 239000000463 material Substances 0.000 title claims abstract description 111
- 239000004800 polyvinyl chloride Substances 0.000 claims abstract description 47
- 229920000915 polyvinyl chloride Polymers 0.000 claims abstract description 41
- 239000004014 plasticizer Substances 0.000 claims abstract description 28
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000011118 polyvinyl acetate Substances 0.000 claims abstract description 14
- 229920002689 polyvinyl acetate Polymers 0.000 claims abstract description 14
- 229920001577 copolymer Polymers 0.000 claims abstract description 11
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 229920001756 Polyvinyl chloride acetate Polymers 0.000 claims abstract description 6
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid group Chemical group C(C=1C(C(=O)O)=CC=CC1)(=O)O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 claims description 20
- 239000011347 resin Substances 0.000 claims description 17
- 229920005989 resin Polymers 0.000 claims description 17
- 239000003381 stabilizer Substances 0.000 claims description 12
- 238000005187 foaming Methods 0.000 claims description 10
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical group CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 claims description 5
- 239000006260 foam Substances 0.000 claims description 5
- 230000002209 hydrophobic effect Effects 0.000 claims description 5
- 239000000178 monomer Substances 0.000 claims description 4
- 229920001296 polysiloxane Polymers 0.000 claims description 4
- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 3
- 239000004803 Di-2ethylhexylphthalate Substances 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 25
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 abstract description 15
- 238000010521 absorption reaction Methods 0.000 abstract description 12
- 239000003513 alkali Substances 0.000 abstract description 10
- 238000010438 heat treatment Methods 0.000 description 9
- 238000012360 testing method Methods 0.000 description 9
- 239000000839 emulsion Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 230000001070 adhesive effect Effects 0.000 description 6
- 239000000853 adhesive Substances 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- 238000007598 dipping method Methods 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003672 ureas Chemical class 0.000 description 2
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
- -1 ACRYL Chemical class 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000012612 commercial material Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004872 foam stabilizing agent Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000011369 resultant mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Images
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N7/00—Flexible sheet materials not otherwise provided for, e.g. textile threads, filaments, yarns or tow, glued on macromolecular material
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F15/00—Flooring
- E04F15/02—Flooring or floor layers composed of a number of similar elements
- E04F15/10—Flooring or floor layers composed of a number of similar elements of other materials, e.g. fibrous or chipped materials, organic plastics, magnesite tiles, hardboard, or with a top layer of other materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B27/00—Layered products comprising a layer of synthetic resin
- B32B27/30—Layered products comprising a layer of synthetic resin comprising vinyl (co)polymers; comprising acrylic (co)polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B60—VEHICLES IN GENERAL
- B60N—SEATS SPECIALLY ADAPTED FOR VEHICLES; VEHICLE PASSENGER ACCOMMODATION NOT OTHERWISE PROVIDED FOR
- B60N3/00—Arrangements or adaptations of other passenger fittings, not otherwise provided for
- B60N3/04—Arrangements or adaptations of other passenger fittings, not otherwise provided for of floor mats or carpets
- B60N3/046—Arrangements or adaptations of other passenger fittings, not otherwise provided for of floor mats or carpets characterised by the fixing means
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F15/00—Flooring
- E04F15/02—Flooring or floor layers composed of a number of similar elements
-
- E—FIXED CONSTRUCTIONS
- E04—BUILDING
- E04F—FINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
- E04F15/00—Flooring
- E04F15/02—Flooring or floor layers composed of a number of similar elements
- E04F15/02172—Floor elements with an anti-skid main surface, other than with grooves
Definitions
- the present invention relates to a loose-lay floor tile which has on the back face a nonskid backing material using a polyvinyl chloride-based raw material (“polyvinyl chloride” will be referred to as “PVC”, hereinafter).
- PVC polyvinyl chloride
- the strength is one-third or smaller of a PVC-based mechanically foamed material described later when the expansion rate is the same.
- the present invention has an object of providing a loose-lay floor tile which has on the back face a nonskid backing material prepared by using a PVC-based raw material in place of an acrylic mechanically foamed material.
- the present invention provides:
- FIG. 1 shows a sectional view of a loose-lay floor tile which has a nonskid backing material on the back face of the floor tile as stripes.
- the backing material must be a flexible elastomer.
- Examples of the above material include elastomers having an elongation of 300% or greater.
- a foamed material is preferable to a non-foamed material from the standpoint of the flexibility.
- Examples of the above material include foamed materials based on acrylic materials, urethanes and PVC.
- a material having a suitable tackiness must be selected since separation of sheets of the material having excessively great tackiness becomes difficult when the sheets are packaged and stored for a long time in the condition such that adhesive faces of the sheets are faced to each other although the greater the tackiness of the material, the greater the adhesive effect.
- Examples of the above material include adhesive coating materials curable with ultraviolet ray and conventional products coated with adhesives.
- a PVC paste is foamed mechanically, and the foamed paste is solidified and used.
- foam stabilizers, thixotropy agents, stabilizers, fillers and flame retardants are added, where necessary, in combination with the resin and the plasticizer which are the main components of the paste.
- the polyvinyl chloride resin as the main component of the PVC paste may be a polymer comprising the vinyl chloride unit alone, it is preferable that a copolymer of vinyl chloride and vinyl acetate or a mixture of PVC and polyvinyl acetate is used since curing can be conducted at a low temperature and the productivity is improved.
- the content of vinyl acetate in the copolymer is about 3 to 10% by mole and more preferably about 5 to 8% by mole as the monomer unit.
- a commercial material containing vinyl acetate in the above range may be used.
- the content of polyvinyl acetate is about 1.5 to 5% by weight and more preferably about 2 to 3% by weight.
- the content of polyvinyl acetate is smaller than about 1.5% by weight, workability is insufficient, and there is the possibility that the desired strength is not obtained.
- the content of polyvinyl acetate exceeds about 5% by weight, heat stability during working decreases.
- the plasticizer is used in an amount of about 50 to 200 parts by weight and preferably about 80 to 120 parts by weight per 100 parts by weight of the resin.
- the amount of the plasticizer is less than about 50 parts by weight, flexibility of the obtained material is insufficient, and there is the possibility that an excellent foamed material is not obtained.
- the amount of the plasticizer exceeds about 200 parts by weight, the obtained material is excessively flexible, and there is the possibility that strength of the backing material is small.
- phthalic ester-based plasticizers such as di-2-ethylhexyl phthalate (DOP) and diisononyl phthalate (DINP) are preferable, and DOP is more preferable for the PVC-based mechanically foamed material.
- the foaming stabilizer is used when the material is mechanically foamed. It is preferable that a silicone-based surfactant of the hydrophobic type is used as the foaming stabilizer so that the water-repelling property is also exhibited and penetration of water into the foamed material is prevented. It is preferable that the foaming stabilizer is used in an amount of 5% by weight or less. However, it is necessary that at least 3% by weight of the foaming stabilizer be used when the expansion rate of the foamed material is 3 or greater.
- the expansion rate is about 1.5 to 4 and preferably about 2.5 to 3.
- the expansion rate exceeds about 4, the material shows marked shrinking during curing by heating, and there is the possibility that workability in coating decreases during application of the foamed sol at a speed of coating of 10 m/minute or greater (the sol does not extend smoothly due to the great expansion rate, i.e., due to a great viscosity).
- the expansion rate is smaller than about 1.5, there is the possibility that the sufficient nonskid property is not exhibited.
- the foamed material is preferable to a non-foamed material due to the more excellent nonskid property.
- Foamed PVC includes the mechanically foamed material described above and chemically foamed materials which are obtained by chemical foaming.
- the PVC-based mechanically foamed material is preferable since the chemically foamed materials have the following drawbacks (i) to (iv):
- a high temperature of 200° C. or higher is necessary for the chemical foaming, and the floor tile itself is damaged by the high temperature.
- the thixotropy agent is used when the plasticizer is used in a great amount or for improving the coating property of the material and preventing flow and deformation of the material applied to the back face.
- examples of the thixotropy agent include modified urea solutions.
- the filler and the flame retardant conventional stabilizers, fillers and flame retardants can be used.
- a nonskid backing material in accordance with the present invention was prepared by mixing the following components, followed by mechanically foaming the resultant mixture (the expansion rate: 2.8).
- “part” means “part by weight”.
- a paste of a PVC resin 80 parts (a copolymer containing 7% of vinyl acetate; the number-average molecular weight: 1,700)
- a PVC resin for blending 20 parts (a copolymer containing 5% of vinyl acetate; the number-average molecular weight: 1,100)
- a plasticizer (DOP) 120 parts Calcium carbonate treated with fatty 10 parts acids on the surface
- a silicone-based foam stabilizer 7 parts A modified urea-based thixotropy agent 0.2 parts
- FIG. 1 On the back face of one loose-lay floor tile which had a size of a 50 cm square and a thickness of 5 mm and made of a plastic, stripes were formed with 50 g of the nonskid backing material prepared above.
- the floor tile having the backing material was heated by an infra-heater at 165° C. for 5 seconds to solidify the backing material.
- the sectional view of the obtained floor tile is shown in FIG. 1 .
- the height of the stripe of the nonskid backing material was 0.3 to 0.5 mm, and the width of the stripe on the face of the floor tile was about 2 mm.
- the distance between the stripes of the nonskid backing material was about 3 mm.
- a nonskid backing material was prepared by adding 2 parts by weight of a crosslinking agent “CR-5L” manufactured by E-TEC Co., Ltd. to 100 parts by weight of a nonskid backing material which was a mechanically foamed material prepared by using a commercial acrylic emulsion [manufactured by E-TEC Co., Ltd.; ACRYL EMULSION “A-412A”].
- the C. S. R. value was measured in accordance with the same method as that used in Example 1 using the obtained floor tile having the backing material. The results of the measurement are shown in Table 1.
- Example 1 and Comparative Example 1 were each mechanically foamed, applied each to a glass plate of a 500 mm square and solidified by heating in a drying oven at 165° C. for 5 minutes, and sheets of the mechanically foamed materials having a thickness of about 1 mm were prepared.
- the obtained foamed sheets were separated from the glass plates, and test pieces necessary for the following evaluations were cut out from the sheets. Using the obtained test pieces, properties of the nonskid backing materials were evaluated.
- a test piece having a size of 40 mm ⁇ 100 mm was dipped into warm water at 46° C., and the water absorption was measured after 1 minute, 1 hour and 24 hours.
- the PVC-based mechanically foamed material in accordance with the present invention absorbed almost no water.
- the mechanically foamed material of Comparative Example 1 prepared by using an acrylic emulsion rapidly absorbed water immediately after being dipped into water, and the water absorption reached 172% after 1 minute.
- a test piece prepared by cutting out into the shape of the No. 3 dumbbell defined in Japanese Industrial Standard K-6301 was dipped into a 2% aqueous solution of sodium hydroxide.
- the tensile strength and the elongation at break were measured after one week and two weeks in accordance with the method of Japanese Industrial Standard A-6008 at a temperature of 20° C. and a speed of extension of 200 mm/minute. The results are shown in Table 1.
- the nonskid backing material in accordance with the present invention prepared by using the PVC-based raw material exhibited smaller water absorption, more excellent resistance to alkali and greater strength of the foamed material than those of conventional mechanically foamed materials prepared by using an acrylic emulsion, the same coefficient of slipping resistance (the C. S. R. value) as that of the conventional mechanically foamed materials and excellent properties as the backing material for floor tiles used by simply laying on a floor.
- Example 1 1 hour 24 hours initial 1 week 2 weeks strength, N/mm 2 Example 1 0.75 0.9 2.5 18.8 0.35 0.57 0.45 0.35 (130) (140) (140) Comparative 0.75 172 186 200 0.13 0 0 0.13 Example 1 (250) (80) (0) Note Control 0.51 — — — — — — — Note: The test piece was swollen to a volume twice as much as the initial volume.
- the nonskid backing material exhibiting more excellent water-repelling property, resistance to alkali and resistance to moisture, water and alkaline water from the ground coat than those of mechanically foamed materials containing an acrylic emulsion as the main component can be provided.
- the backing material which provides a foamed material exhibiting a great strength and can bear ordinary dynamic loads can be provided.
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- Engineering & Computer Science (AREA)
- Architecture (AREA)
- Civil Engineering (AREA)
- Structural Engineering (AREA)
- Transportation (AREA)
- Mechanical Engineering (AREA)
- Textile Engineering (AREA)
- Floor Finish (AREA)
- Laminated Bodies (AREA)
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Road Paving Structures (AREA)
Abstract
A loose-lay floor tile which has on a back face a nonskid backing material obtained by solidifying a paste sol containing a plasticizer and one of polyvinyl chloride, copolymers of vinyl chloride and vinyl acetate and mixtures of polyvinyl chloride and polyvinyl acetate. Drawbacks of conventional acrylic mechanically foamed materials such as water absorption, resistance to water, resistance to alkali and strength of a foamed material are improved.
Description
- The present invention relates to a loose-lay floor tile which has on the back face a nonskid backing material using a polyvinyl chloride-based raw material (“polyvinyl chloride” will be referred to as “PVC”, hereinafter).
- As the material for providing the nonskid property to a loose-lay floor tile, mechanically foamed materials containing an emulsion of an acrylic resin as the main component (referred to as “acrylic mechanically foamed materials, hereinafter) are conventionally used. The production of the above material has been studied, and the properties of the material have been evaluated. The results of the study and the evaluation show that the above material has the following drawbacks (a) to (d):
- (a) Markedly Great Water Absorption
- Water is absorbed through joints during maintenance.
- Water is absorbed during washing for recycling.
- Water in a moist ground coat is absorbed.
- (b) Poor Resistance to Water
- Strength decreases after being dipped into water for one week or longer.
- (c) Poor Resistance to Alkali
- Strength markedly decreases when the material is dipped into a 2% aqueous solution of sodium hydroxide.
- (d) Small Strength of a Foamed Material
- The strength is one-third or smaller of a PVC-based mechanically foamed material described later when the expansion rate is the same.
- When sheets of the material are packaged and stored for a long time in the condition such that adhesive faces of the sheets are faced to each other, separation of the sheets becomes difficult, and the sheets of the foamed material are occasionally fractured when the sheets are forced to be separated.
- Therefore, it is inevitable that the quality of the acrylic mechanically foamed materials remains unreliable when tiles having the material are used by directly laying on a floor.
- The present invention has an object of providing a loose-lay floor tile which has on the back face a nonskid backing material prepared by using a PVC-based raw material in place of an acrylic mechanically foamed material.
- As the result of intensive studies by the present inventors to achieve the above object, it was found that the drawbacks of the acrylic mechanically foamed materials could be overcome with a loose-lay floor tile which has on the back face a nonskid backing material obtained by solidifying a paste sol comprising a plasticizer and a polyvinyl chloride-based resin.
- The present invention provides:
- (1) A loose-lay floor tile which has on a back face a nonskid backing material obtained by solidifying a paste sol comprising a plasticizer and at least one polyvinyl chloride-based resin selected from the group consisting of a polyvinyl chloride, a copolymer of vinyl chloride and vinyl acetate and a mixture of polyvinyl chloride and polyvinyl acetate;
- (2) A loose-lay floor tile described in (1), wherein the paste sol further comprises a foam stabilizer of a hydrophobic type, and a foamed material obtained by mechanically foaming and then solidifying the paste sol is disposed on the back face of the tile;
- (3) A loose-lay floor tile described in (1) or (2), wherein the polyvinyl chloride-based resin is a copolymer of vinyl chloride and vinyl acetate which comprises about 3 to 10% by mole of vinyl acetate as a monomer unit;
- (4) A loose-lay floor tile described in (1) or (2), wherein the polyvinyl chloride-based resin is a mixture of polyvinyl chloride and polyvinyl acetate comprising about 1.5 to 5% by weight of polyvinyl acetate;
- (5) A loose-lay floor tile described in any one of (1) to (4), wherein the plasticizer is a phthalic acid-based plasticizer;
- (6) A loose-lay floor tile described in (5), wherein a content of the phthalic acid-based plasticizer is about 50 to 200 parts by weight per 100 parts by weight of the polyvinyl chloride-based resin; and
- (7) A loose-lay floor tile described in (2), wherein the foamed material has an expansion rate of 1.5 to 4.
-
FIG. 1 shows a sectional view of a loose-lay floor tile which has a nonskid backing material on the back face of the floor tile as stripes. - The present invention will be described more specifically in the following.
- To provide the “nonskid property” necessary for the nonskid backing material, the following points 1) to 3) must be considered.
- 1) The backing material must be a flexible elastomer.
- Examples of the above material include elastomers having an elongation of 300% or greater.
- 2) A foamed material is preferable to a non-foamed material from the standpoint of the flexibility.
- Examples of the above material include foamed materials based on acrylic materials, urethanes and PVC.
- 3) A material having a suitable tackiness must be selected since separation of sheets of the material having excessively great tackiness becomes difficult when the sheets are packaged and stored for a long time in the condition such that adhesive faces of the sheets are faced to each other although the greater the tackiness of the material, the greater the adhesive effect.
- Examples of the above material include adhesive coating materials curable with ultraviolet ray and conventional products coated with adhesives.
- The above points of consideration have been studied by the present inventors, and the result of the study shows that, when a material comprising PVC is used, the above points of consideration 1) and 2) can be satisfied, the drawbacks of acrylic mechanically foamed materials, i.e., the great absorption of water, poor resistances to water and alkali and small strength of the foamed material, can be improved, and advantages are exhibited on the productivity and production facilities.
- When an acrylic mechanically foamed material is used, at least 20 minutes at 140° C. is required for drying and curing, and an apparatus for the drying step (such as a long drying oven with the hot air) is necessary for improving the productivity. In contrast, when a PVC mechanically foamed material is used, “heating using an infra-heater (heating with far infrared ray)” or “Schwank heating (heating using a gas burner)” can be used, and the curing can be achieved in ten and several seconds. Moreover, PVC is more resistant to alkali than acrylic resins, and strength of a PVC-based mechanically foamed material is three times or more as great as that of acrylic mechanically foamed materials when the expansion rate is the same.
- With respect to the point of consideration 3), it is found to be effective that not the tackiness of an adhesive but the working mechanism that slippage is prevented by the combination of the friction coefficient with the ground coat surely kept at a specific value and the absorption of stress by deformation of the backing material (the working mechanism that the stress in the direction of slippage is absorbed by friction and deformation) is utilized.
- In the practical application, it is preferable that a PVC paste is foamed mechanically, and the foamed paste is solidified and used. To satisfy the above points of consideration and the requirements on the productivity and the properties in relation to the ground coat such as mortar, it is preferable that foam stabilizers, thixotropy agents, stabilizers, fillers and flame retardants are added, where necessary, in combination with the resin and the plasticizer which are the main components of the paste.
- Although the polyvinyl chloride resin as the main component of the PVC paste may be a polymer comprising the vinyl chloride unit alone, it is preferable that a copolymer of vinyl chloride and vinyl acetate or a mixture of PVC and polyvinyl acetate is used since curing can be conducted at a low temperature and the productivity is improved. When the copolymer of vinyl chloride and vinyl acetate is used, it is preferable that the content of vinyl acetate in the copolymer is about 3 to 10% by mole and more preferably about 5 to 8% by mole as the monomer unit. A commercial material containing vinyl acetate in the above range may be used. When a mixture of PVC and polyvinyl acetate is used, the content of polyvinyl acetate is about 1.5 to 5% by weight and more preferably about 2 to 3% by weight. When the content of polyvinyl acetate is smaller than about 1.5% by weight, workability is insufficient, and there is the possibility that the desired strength is not obtained. When the content of polyvinyl acetate exceeds about 5% by weight, heat stability during working decreases.
- The plasticizer is used in an amount of about 50 to 200 parts by weight and preferably about 80 to 120 parts by weight per 100 parts by weight of the resin. When the amount of the plasticizer is less than about 50 parts by weight, flexibility of the obtained material is insufficient, and there is the possibility that an excellent foamed material is not obtained. When the amount of the plasticizer exceeds about 200 parts by weight, the obtained material is excessively flexible, and there is the possibility that strength of the backing material is small. As the plasticizer, phthalic ester-based plasticizers such as di-2-ethylhexyl phthalate (DOP) and diisononyl phthalate (DINP) are preferable, and DOP is more preferable for the PVC-based mechanically foamed material.
- The foaming stabilizer is used when the material is mechanically foamed. It is preferable that a silicone-based surfactant of the hydrophobic type is used as the foaming stabilizer so that the water-repelling property is also exhibited and penetration of water into the foamed material is prevented. It is preferable that the foaming stabilizer is used in an amount of 5% by weight or less. However, it is necessary that at least 3% by weight of the foaming stabilizer be used when the expansion rate of the foamed material is 3 or greater.
- For the PVC-based mechanically foamed material, it is suitable that the expansion rate is about 1.5 to 4 and preferably about 2.5 to 3. When the expansion rate exceeds about 4, the material shows marked shrinking during curing by heating, and there is the possibility that workability in coating decreases during application of the foamed sol at a speed of coating of 10 m/minute or greater (the sol does not extend smoothly due to the great expansion rate, i.e., due to a great viscosity). When the expansion rate is smaller than about 1.5, there is the possibility that the sufficient nonskid property is not exhibited. The foamed material is preferable to a non-foamed material due to the more excellent nonskid property. In the present invention, the expansion rate is defined as follows:
Expansion rate=(Density of a material before being foamed)/(Density of the material after being foamed) - Foamed PVC includes the mechanically foamed material described above and chemically foamed materials which are obtained by chemical foaming. When a foamed PVC is used as the backing material, the PVC-based mechanically foamed material is preferable since the chemically foamed materials have the following drawbacks (i) to (iv):
- (i) A high temperature of 200° C. or higher is necessary for the chemical foaming, and the floor tile itself is damaged by the high temperature.
- (ii) Controlling the thickness of the foamed material is difficult.
- (iii) A heating apparatus of the direct heating type cannot be used, and the heated air must be used. Therefore, the heating apparatus becomes great and complicated.
- (iv) It is difficult that the foaming is controlled and fine cells are formed.
- The thixotropy agent is used when the plasticizer is used in a great amount or for improving the coating property of the material and preventing flow and deformation of the material applied to the back face. Examples of the thixotropy agent include modified urea solutions. Although the greater the amount of the thixotropy agent, the better for this purpose, an excessively great amount causes a marked increase in the viscosity of the sol and is not practical. Therefore, the amount is about 3.0% by weight or less and preferably about 1.5% by weight or less.
- As the stabilizer, the filler and the flame retardant, conventional stabilizers, fillers and flame retardants can be used.
- The present invention will be described more specifically with reference to examples in the following. However, the present invention is not limited to the examples.
- A nonskid backing material in accordance with the present invention was prepared by mixing the following components, followed by mechanically foaming the resultant mixture (the expansion rate: 2.8). As for the amount of the component, “part” means “part by weight”.
A paste of a PVC resin 80 parts (a copolymer containing 7% of vinyl acetate; the number-average molecular weight: 1,700) A PVC resin for blending 20 parts (a copolymer containing 5% of vinyl acetate; the number-average molecular weight: 1,100) A plasticizer (DOP) 120 parts Calcium carbonate treated with fatty 10 parts acids on the surface A silicone-based foam stabilizer 7 parts A modified urea-based thixotropy agent 0.2 parts - On the back face of one loose-lay floor tile which had a size of a 50 cm square and a thickness of 5 mm and made of a plastic, stripes were formed with 50 g of the nonskid backing material prepared above. The floor tile having the backing material was heated by an infra-heater at 165° C. for 5 seconds to solidify the backing material. The sectional view of the obtained floor tile is shown in
FIG. 1 . The height of the stripe of the nonskid backing material was 0.3 to 0.5 mm, and the width of the stripe on the face of the floor tile was about 2 mm. The distance between the stripes of the nonskid backing material was about 3 mm. - The coefficient of slipping resistance [the C. S. R. value=maximum pulling force/applied weight (80 kg)] was measured in accordance with the method of Japanese Industrial Standard A 1454 using the obtained floor tile having the backing material and the floor tile without the backing material (the control). The results of the measurement are shown in Table 1.
- A nonskid backing material was prepared by adding 2 parts by weight of a crosslinking agent “CR-5L” manufactured by E-TEC Co., Ltd. to 100 parts by weight of a nonskid backing material which was a mechanically foamed material prepared by using a commercial acrylic emulsion [manufactured by E-TEC Co., Ltd.; ACRYL EMULSION “A-412A”].
- On the back face of one loose-lay floor tile which had a size of a 50 cm square and a thickness of 5 mm and made of a plastic, stripes were formed with 50 g of the nonskid backing material prepared above in the same manner as that in Example 1. The floor tile having the backing material was heated in a drying oven at 150° C. for 1 minute to solidify the backing material.
- The C. S. R. value was measured in accordance with the same method as that used in Example 1 using the obtained floor tile having the backing material. The results of the measurement are shown in Table 1.
- It is shown by the results in Table 1 that the mechanically foamed nonskid floor tile of Example 1 exhibited the same slipping resistance as that of the mechanically foamed floor tile of Comparative Example 1 prepared by using an acrylic emulsion.
- The nonskid backing materials used in Example 1 and Comparative Example 1 were each mechanically foamed, applied each to a glass plate of a 500 mm square and solidified by heating in a drying oven at 165° C. for 5 minutes, and sheets of the mechanically foamed materials having a thickness of about 1 mm were prepared. The obtained foamed sheets were separated from the glass plates, and test pieces necessary for the following evaluations were cut out from the sheets. Using the obtained test pieces, properties of the nonskid backing materials were evaluated.
- (1) Water Absorption
- A test piece having a size of 40 mm×100 mm was dipped into warm water at 46° C., and the water absorption was measured after 1 minute, 1 hour and 24 hours. The water absorption was calculated from the weights of the test piece before and after the dipping in accordance with the following equation:
Water absorption=(weight of test piece after dipping−weight of test piece before dipping)/(weight of test piece before dipping) - The results of the measurement of the water absorption are shown in Table 1.
- As shown in Table 1, the PVC-based mechanically foamed material in accordance with the present invention absorbed almost no water. In contrast, the mechanically foamed material of Comparative Example 1 prepared by using an acrylic emulsion rapidly absorbed water immediately after being dipped into water, and the water absorption reached 172% after 1 minute.
- (2) Resistance to Alkali
- A test piece prepared by cutting out into the shape of the No. 3 dumbbell defined in Japanese Industrial Standard K-6301 was dipped into a 2% aqueous solution of sodium hydroxide. The tensile strength and the elongation at break were measured after one week and two weeks in accordance with the method of Japanese Industrial Standard A-6008 at a temperature of 20° C. and a speed of extension of 200 mm/minute. The results are shown in Table 1.
- As shown in Table 1, almost no effects of the alkali were found on the PVC-based mechanically foamed material in accordance with the present invention. In contrast, the mechanically foamed material of Comparative Example 1 prepared by using an acrylic emulsion had an initial strength which was one third as small as that of the PVC-based mechanically foamed material in accordance with the present invention. Moreover, after being dipped into the alkali for 2 weeks, the mechanically foamed material of Comparative Example 1 was swollen to a volume twice as much as that of the initial volume, and the strength and the elongation at break decreased to zero.
- It is shown by the above results that the nonskid backing material in accordance with the present invention prepared by using the PVC-based raw material exhibited smaller water absorption, more excellent resistance to alkali and greater strength of the foamed material than those of conventional mechanically foamed materials prepared by using an acrylic emulsion, the same coefficient of slipping resistance (the C. S. R. value) as that of the conventional mechanically foamed materials and excellent properties as the backing material for floor tiles used by simply laying on a floor.
TABLE 1 Resistance to alkali, N/mm2 Strength of foamed C.R.S. Water absorption, %, after (elongation, %), after material, tensile value 1 min. 1 hour 24 hours initial 1 week 2 weeks strength, N/mm2 Example 1 0.75 0.9 2.5 18.8 0.35 0.57 0.45 0.35 (130) (140) (140) Comparative 0.75 172 186 200 0.13 0 0 0.13 Example 1 (250) (80) (0) Note Control 0.51 — — — — — — —
Note:
The test piece was swollen to a volume twice as much as the initial volume.
- In accordance with the present invention, the nonskid backing material exhibiting more excellent water-repelling property, resistance to alkali and resistance to moisture, water and alkaline water from the ground coat than those of mechanically foamed materials containing an acrylic emulsion as the main component can be provided. The backing material which provides a foamed material exhibiting a great strength and can bear ordinary dynamic loads can be provided.
Claims (21)
1-7. (canceled)
8. A loose-lay floor tile which has on a back face a nonskid backing material obtained by solidifying a paste sol comprising a plasticizer and at least one polyvinyl chloride-based resin selected from the group consisting of a polyvinyl chloride, a copolymer of vinyl chloride and vinyl acetate and a mixture of polyvinyl chloride and polyvinyl acetate.
9. A loose-lay floor tile according to claim 8 , wherein the paste sol further comprises a foam stabilizer of a hydrophobic type, and a foamed material obtained by mechanically foaming and then solidifying the paste sol so as to be disposed on the back face of the tile.
10. A loose-lay floor tile according to claim 8 , wherein the polyvinyl chloride-based resin is a copolymer of vinyl chloride and vinyl acetate which comprises about 3 to 10% by mole of vinyl acetate as a monomer unit.
11. A loose-lay floor tile according to claim 9 , wherein the polyvinyl chloride-based resin is a copolymer of vinyl chloride and vinyl acetate which comprises about 3 to 10% by mole of vinyl acetate as a monomer unit.
12. A loose-lay floor tile according to claim 8 , wherein the polyvinyl chloride-based resin is a mixture of polyvinyl chloride and polyvinyl acetate comprising about 1.5 to 5% by weight of polyvinyl acetate.
13. A loose-lay floor tile according to claim 9 , wherein the polyvinyl chloride-based resin is a mixture of polyvinyl chloride and polyvinyl acetate comprising about 1.5 to 5% by weight of polyvinyl acetate.
14. A loose-lay floor tile according to claim 9 , wherein the plasticizer is a phthalic acid-based plasticizer.
15. A loose-lay floor tile according to claim 10 , wherein the plasticizer is a phthalic acid-based plasticizer.
16. A loose-lay floor tile according to claim 11 , wherein the plasticizer is a phthalic acid-based plasticizer.
17. A loose-lay floor tile according to claim 12 , wherein the plasticizer is a phthalic acid-based plasticizer.
18. A loose-lay floor tile according to claim 13 , wherein the plasticizer is a phthalic acid-based plasticizer.
19. A loose-lay floor tile according to claim 15 , wherein a content of the phthalic acid-based plasticizer is about 50 to 200 parts by weight per 100 parts by weight of the polyvinyl chloride-based resin.
20. A loose-lay floor tile according to claim 16 , wherein a content of the phthalic acid-based plasticizer is about 50 to 200 parts by weight per 100 parts by weight of the polyvinyl chloride-based resin.
21. A loose-lay floor tile according to claim 20 , wherein the phthalic acid-based plasticizer is selected from the group consisting of di-2-ethylhexyl phthalate and diisononyl phthalate.
22. A loose-lay floor tile according to claim 20 , wherein the foam stabilizer of a hydrophobic type comprises a silicone-based surfactant.
23. A loose-lay floor tile according to claim 21 , wherein the foam stabilizer of a hydrophobic type comprises a silicone-based surfactant.
24. A loose-lay floor tile according to claim 9 , wherein the foamed material has an expansion rate of about 1.5 to 4.
25. A loose-lay floor tile according to claim 13 , wherein the foamed material has an expansion rate of about 1.5 to 4.
26. A loose-lay floor tile according to claim 24 , wherein the foamed material is disposed in a manner such that said foamed material forms stripes on the back face of said tile.
27. A loose-lay floor tile according to claim 18 , wherein the foamed material is disposed in a manner such that said foamed material forms stripes on the back face of said tile.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002-276034 | 2002-09-20 | ||
JP2002276034A JP4053391B2 (en) | 2002-09-20 | 2002-09-20 | Floor tiles with non-slip backing material made of PVC on the back |
PCT/JP2003/012036 WO2004027142A1 (en) | 2002-09-20 | 2003-09-19 | Free laying floor tile having pvc based backing material for preventing tile from slipping provided on back surface thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
US20060048464A1 true US20060048464A1 (en) | 2006-03-09 |
Family
ID=32025054
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US10/527,534 Abandoned US20060048464A1 (en) | 2002-09-20 | 2003-09-19 | Free laying floor tile having pvc based backing material for preventing tile from slipping provided on back surface thereof |
Country Status (9)
Country | Link |
---|---|
US (1) | US20060048464A1 (en) |
EP (1) | EP1548181B1 (en) |
JP (1) | JP4053391B2 (en) |
KR (1) | KR20050057322A (en) |
AT (1) | ATE470751T1 (en) |
AU (1) | AU2003264534A1 (en) |
DE (1) | DE60332946D1 (en) |
ES (1) | ES2346138T3 (en) |
WO (1) | WO2004027142A1 (en) |
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US20050229524A1 (en) * | 2004-02-23 | 2005-10-20 | Bennett John L | Wall sheathing system and method of installation |
US20050229504A1 (en) * | 2004-02-23 | 2005-10-20 | Bennett John L | Panel for sheathing system and method |
US20050257469A1 (en) * | 2004-02-23 | 2005-11-24 | Bennett John L | Panelized roofing system and method |
EP2182135A1 (en) * | 2008-10-28 | 2010-05-05 | Tarkett GDL S.A. | Removable surface covering |
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US20220136259A1 (en) * | 2018-11-20 | 2022-05-05 | Wellmade Floor Covering Int'l Inc. | Anti-Slip, Noise Reducing Pad Directly Applied And Adhered To The Back of Flooring Materials and Method |
CN116922904A (en) * | 2023-08-01 | 2023-10-24 | 上海舜睿新材料股份有限公司 | PVC floor with anti-skid performance and preparation method thereof |
US12257820B2 (en) | 2020-04-29 | 2025-03-25 | Kcc Glass Corporation | Multilayered flooring decorative material |
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JP2006008860A (en) * | 2004-06-25 | 2006-01-12 | Daicel Novafoam Ltd | Foam molding and method for producing the same |
US20090061168A1 (en) * | 2007-08-28 | 2009-03-05 | D&J Art Co., Ltd. | Method for manufacturing floor covering and floor covering manufactured thereby |
JP6077692B1 (en) | 2016-03-04 | 2017-02-08 | 伸興化成株式会社 | Recyclable synthetic resin tile and manufacturing method thereof |
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Also Published As
Publication number | Publication date |
---|---|
EP1548181A4 (en) | 2008-04-02 |
ATE470751T1 (en) | 2010-06-15 |
JP2004107845A (en) | 2004-04-08 |
AU2003264534A8 (en) | 2004-04-08 |
KR20050057322A (en) | 2005-06-16 |
WO2004027142A1 (en) | 2004-04-01 |
ES2346138T3 (en) | 2010-10-11 |
EP1548181A1 (en) | 2005-06-29 |
AU2003264534A1 (en) | 2004-04-08 |
JP4053391B2 (en) | 2008-02-27 |
EP1548181B1 (en) | 2010-06-09 |
DE60332946D1 (en) | 2010-07-22 |
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Owner name: SHINKOKASEI CO., LTD., JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SUZUKI, NAOYUKI;PAN, QINGYANG;ISHIYAMA, SEISHIRO;REEL/FRAME:017194/0399;SIGNING DATES FROM 20050125 TO 20050128 Owner name: TAJIMA INCORPORATED, JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:SUZUKI, NAOYUKI;PAN, QINGYANG;ISHIYAMA, SEISHIRO;REEL/FRAME:017194/0399;SIGNING DATES FROM 20050125 TO 20050128 |
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