JP4846952B2 - ポリ(アルキレンイミン)を含む安定な水性ポリマー組成物 - Google Patents
ポリ(アルキレンイミン)を含む安定な水性ポリマー組成物 Download PDFInfo
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- JP4846952B2 JP4846952B2 JP2001546833A JP2001546833A JP4846952B2 JP 4846952 B2 JP4846952 B2 JP 4846952B2 JP 2001546833 A JP2001546833 A JP 2001546833A JP 2001546833 A JP2001546833 A JP 2001546833A JP 4846952 B2 JP4846952 B2 JP 4846952B2
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- acetoacetoxy
- weight
- polymer
- polymers
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 230
- 229920000642 polymer Polymers 0.000 title claims description 166
- -1 acetoacetoxy Chemical group 0.000 claims description 146
- 230000001070 adhesive effect Effects 0.000 claims description 107
- 239000000853 adhesive Substances 0.000 claims description 104
- 229920001002 functional polymer Polymers 0.000 claims description 79
- 239000000178 monomer Substances 0.000 claims description 62
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 42
- 238000000034 method Methods 0.000 claims description 40
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- 239000004820 Pressure-sensitive adhesive Substances 0.000 claims description 26
- 239000002736 nonionic surfactant Substances 0.000 claims description 24
- 238000000576 coating method Methods 0.000 claims description 22
- 125000000524 functional group Chemical group 0.000 claims description 20
- 239000011248 coating agent Substances 0.000 claims description 19
- 125000000217 alkyl group Chemical group 0.000 claims description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims description 17
- 239000001257 hydrogen Substances 0.000 claims description 17
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 16
- 150000002367 halogens Chemical class 0.000 claims description 16
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 14
- 125000002947 alkylene group Chemical group 0.000 claims description 14
- 238000006116 polymerization reaction Methods 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 11
- 238000003825 pressing Methods 0.000 claims description 10
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 claims description 9
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 9
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- 239000004925 Acrylic resin Substances 0.000 claims description 9
- 239000004952 Polyamide Substances 0.000 claims description 9
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- 229920002635 polyurethane Polymers 0.000 claims description 9
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- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 229920000180 alkyd Polymers 0.000 claims description 8
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 8
- HDERJYVLTPVNRI-UHFFFAOYSA-N ethene;ethenyl acetate Chemical group C=C.CC(=O)OC=C HDERJYVLTPVNRI-UHFFFAOYSA-N 0.000 claims description 8
- 229920001038 ethylene copolymer Polymers 0.000 claims description 8
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
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- 230000008569 process Effects 0.000 claims description 8
- 229910052717 sulfur Inorganic materials 0.000 claims description 8
- 239000002174 Styrene-butadiene Substances 0.000 claims description 7
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 claims description 7
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- 239000005020 polyethylene terephthalate Substances 0.000 claims description 7
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- 239000011347 resin Substances 0.000 claims description 7
- 239000011115 styrene butadiene Substances 0.000 claims description 7
- 229920003048 styrene butadiene rubber Polymers 0.000 claims description 7
- 239000004698 Polyethylene Substances 0.000 claims description 6
- 239000004743 Polypropylene Substances 0.000 claims description 6
- 238000010030 laminating Methods 0.000 claims description 6
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 6
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- 239000004800 polyvinyl chloride Substances 0.000 claims description 6
- 230000006872 improvement Effects 0.000 claims description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 4
- YHSYGCXKWUUKIK-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C=C YHSYGCXKWUUKIK-UHFFFAOYSA-N 0.000 claims description 3
- FJKZPONBPMKPLO-UHFFFAOYSA-N 3-prop-2-enoyloxypropyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCCOC(=O)C=C FJKZPONBPMKPLO-UHFFFAOYSA-N 0.000 claims description 3
- PICTWXAWDCLLKO-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCCCOC(=O)C=C PICTWXAWDCLLKO-UHFFFAOYSA-N 0.000 claims description 3
- 230000002776 aggregation Effects 0.000 claims description 3
- AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 18
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 6
- 241000220317 Rosa Species 0.000 claims 5
- 238000001035 drying Methods 0.000 claims 2
- 229920002587 poly(1,3-butadiene) polymer Polymers 0.000 claims 2
- 238000005054 agglomeration Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 41
- 239000004094 surface-active agent Substances 0.000 description 35
- 239000000243 solution Substances 0.000 description 34
- 239000004816 latex Substances 0.000 description 26
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- 239000008199 coating composition Substances 0.000 description 10
- 150000002081 enamines Chemical group 0.000 description 10
- CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
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- LCPVQAHEFVXVKT-UHFFFAOYSA-N 2-(2,4-difluorophenoxy)pyridin-3-amine Chemical compound NC1=CC=CN=C1OC1=CC=C(F)C=C1F LCPVQAHEFVXVKT-UHFFFAOYSA-N 0.000 description 8
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 8
- 239000001099 ammonium carbonate Substances 0.000 description 8
- 239000007787 solid Substances 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 7
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- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000000872 buffer Substances 0.000 description 6
- 238000001879 gelation Methods 0.000 description 6
- 238000005096 rolling process Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
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- 229910052751 metal Inorganic materials 0.000 description 5
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- 150000003141 primary amines Chemical class 0.000 description 5
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- 239000011734 sodium Substances 0.000 description 5
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
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- WDJHALXBUFZDSR-UHFFFAOYSA-N acetoacetic acid Chemical group CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 description 4
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 4
- 239000003431 cross linking reagent Substances 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 229910021641 deionized water Inorganic materials 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000123 paper Substances 0.000 description 4
- 150000003335 secondary amines Chemical class 0.000 description 4
- 239000012265 solid product Substances 0.000 description 4
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 3
- 239000004908 Emulsion polymer Substances 0.000 description 3
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 3
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
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- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
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- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
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- WXHBJKQCHSDHGL-UHFFFAOYSA-N methanediimine;2-methylprop-2-enoic acid Chemical compound N=C=N.CC(=C)C(O)=O WXHBJKQCHSDHGL-UHFFFAOYSA-N 0.000 description 2
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Classifications
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/12—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives
- C08J5/124—Bonding of a preformed macromolecular material to the same or other solid material such as metal, glass, leather, e.g. using adhesives using adhesives based on a macromolecular component
- C08J5/127—Aqueous adhesives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09J—ADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
- C09J201/00—Adhesives based on unspecified macromolecular compounds
- C09J201/02—Adhesives based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09J201/06—Adhesives based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing oxygen atoms
- C09J201/08—Carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2666/00—Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
- C08L2666/02—Organic macromolecular compounds, natural resins, waxes or and bituminous materials
- C08L2666/14—Macromolecular compounds according to C08L59/00 - C08L87/00; Derivatives thereof
- C08L2666/20—Macromolecular compounds having nitrogen in the main chain according to C08L75/00 - C08L79/00; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Materials Engineering (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Dispersion Chemistry (AREA)
- Manufacturing & Machinery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Adhesives Or Adhesive Processes (AREA)
- Laminated Bodies (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/467,071 | 1999-12-20 | ||
| US09/467,071 US6649679B1 (en) | 1997-09-18 | 1999-12-20 | Stable waterborne polymer compositions containing poly(alkylenimines) |
| PCT/US2000/033847 WO2001046332A1 (en) | 1999-12-20 | 2000-12-15 | Stable waterborne polymer compositions containing poly(alkylenimines) |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003518152A JP2003518152A (ja) | 2003-06-03 |
| JP2003518152A5 JP2003518152A5 (enExample) | 2008-02-21 |
| JP4846952B2 true JP4846952B2 (ja) | 2011-12-28 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001546833A Expired - Fee Related JP4846952B2 (ja) | 1999-12-20 | 2000-12-15 | ポリ(アルキレンイミン)を含む安定な水性ポリマー組成物 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6649679B1 (enExample) |
| EP (1) | EP1252251A1 (enExample) |
| JP (1) | JP4846952B2 (enExample) |
| CN (1) | CN1434845A (enExample) |
| BR (1) | BR0016588A (enExample) |
| MX (1) | MXPA02006126A (enExample) |
| WO (1) | WO2001046332A1 (enExample) |
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| US8013068B2 (en) | 2003-01-02 | 2011-09-06 | Rohm And Haas Company | Michael addition compositions |
| US7722733B2 (en) | 2004-03-29 | 2010-05-25 | Baxter International Inc. | Method for sterile connection of tubing |
| EP1593728B1 (en) | 2004-05-03 | 2012-05-09 | Rohm And Haas Company | Michael addition compositions |
| EP1637882B1 (de) * | 2004-09-09 | 2007-08-08 | Analyticon Biotechnologies AG | Lateralflussmessvorrichtung und Messverfahren für Analyten |
| US6969734B1 (en) * | 2004-11-10 | 2005-11-29 | Rohm And Haas Company | Aqueous polymer dispersion and method of use |
| CN101061192B (zh) * | 2004-12-17 | 2012-03-07 | 威士伯采购公司 | 包含乙酰乙酰基官能聚合物的水性涂料组合物、涂层及方法 |
| US8609762B2 (en) * | 2004-12-17 | 2013-12-17 | Valspar Sourcing, Inc. | Aqueous coating compositions containing acetoacetyl-functional polymers, coatings, and methods |
| CA2627509C (en) | 2005-11-15 | 2013-10-22 | Valspar Sourcing, Inc. | Crush resistant latex topcoat composition for fiber cement substrates |
| AU2007211046B2 (en) | 2006-01-31 | 2011-09-01 | Valspar Sourcing, Inc. | Method for coating a cement fiberboard article |
| WO2007089913A1 (en) | 2006-01-31 | 2007-08-09 | Valspar Sourcing, Inc. | Coating system for cement composite articles |
| US8293361B2 (en) | 2006-01-31 | 2012-10-23 | Valspar Sourcing, Inc. | Coating system for cement composite articles |
| US9783622B2 (en) | 2006-01-31 | 2017-10-10 | Axalta Coating Systems Ip Co., Llc | Coating system for cement composite articles |
| MX2008014749A (es) | 2006-05-19 | 2009-02-04 | Valspar Sourcing Inc | Sistema de recubrimiento para articulos compuestos de cemento. |
| EP2035516B2 (en) | 2006-06-02 | 2017-01-04 | Valspar Sourcing, Inc. | High performance aqueous coating compositions |
| US7812090B2 (en) * | 2006-06-02 | 2010-10-12 | Valspar Sourcing, Inc. | High performance aqueous coating compositions |
| EP2043967B1 (en) | 2006-07-07 | 2018-07-04 | Valspar Sourcing, Inc. | Coating systems for cement composite articles |
| JP4782025B2 (ja) * | 2007-01-19 | 2011-09-28 | 信越化学工業株式会社 | シリコーン共重合体およびそれを含有する化粧料 |
| US8202581B2 (en) | 2007-02-16 | 2012-06-19 | Valspar Sourcing, Inc. | Treatment for cement composite articles |
| US8980993B2 (en) | 2008-07-10 | 2015-03-17 | Arkema Inc. | Coating compositions for improved block resistance |
| BRPI0917455B1 (pt) | 2008-08-15 | 2018-11-21 | Valspar Sourcing Inc | composição de revestimento, método para preparar um artigo revestido, e, artigo revestido |
| AU2009316285A1 (en) | 2008-11-24 | 2010-05-27 | Valspar Sourcing, Inc. | Coating system for cement composite articles |
| JP5593093B2 (ja) * | 2009-03-30 | 2014-09-17 | リンテック株式会社 | アクリル系エマルション型粘着剤組成物、その製造方法および粘着シート |
| EP2473674B1 (en) * | 2009-09-01 | 2013-07-10 | Armstrong World Industries, Inc. | Cellulosic product forming process and wet formed cellulosic product |
| CN102863591A (zh) * | 2012-10-23 | 2013-01-09 | 南通市黄海电机有限公司 | 一种乳胶组合物及其制备方法 |
| CN103540217B (zh) * | 2013-10-08 | 2016-06-01 | 雅图高新材料有限公司 | 一种用氮丙啶交联的丙烯酸酯树脂双组份水性汽车涂料及其制备方法 |
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-
1999
- 1999-12-20 US US09/467,071 patent/US6649679B1/en not_active Expired - Fee Related
-
2000
- 2000-12-15 JP JP2001546833A patent/JP4846952B2/ja not_active Expired - Fee Related
- 2000-12-15 EP EP00984346A patent/EP1252251A1/en not_active Withdrawn
- 2000-12-15 BR BR0016588-3A patent/BR0016588A/pt not_active Application Discontinuation
- 2000-12-15 CN CN00819059A patent/CN1434845A/zh active Pending
- 2000-12-15 MX MXPA02006126A patent/MXPA02006126A/es not_active Application Discontinuation
- 2000-12-15 WO PCT/US2000/033847 patent/WO2001046332A1/en not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA02006126A (es) | 2002-12-05 |
| US6649679B1 (en) | 2003-11-18 |
| EP1252251A1 (en) | 2002-10-30 |
| BR0016588A (pt) | 2002-11-26 |
| JP2003518152A (ja) | 2003-06-03 |
| CN1434845A (zh) | 2003-08-06 |
| WO2001046332A1 (en) | 2001-06-28 |
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