JP2002510740A5 - - Google Patents
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- JP2002510740A5 JP2002510740A5 JP2000542412A JP2000542412A JP2002510740A5 JP 2002510740 A5 JP2002510740 A5 JP 2002510740A5 JP 2000542412 A JP2000542412 A JP 2000542412A JP 2000542412 A JP2000542412 A JP 2000542412A JP 2002510740 A5 JP2002510740 A5 JP 2002510740A5
- Authority
- JP
- Japan
- Prior art keywords
- monomer
- weight
- dicarboxylic acid
- unsaturated polyester
- component
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 239000000178 monomer Substances 0.000 description 59
- 229920006305 unsaturated polyester Polymers 0.000 description 27
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 23
- 239000005977 Ethylene Substances 0.000 description 23
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 19
- 239000002270 dispersing agent Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 18
- 229920001577 copolymer Polymers 0.000 description 17
- 229920000578 graft copolymer Polymers 0.000 description 17
- 239000002491 polymer binding agent Substances 0.000 description 17
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 16
- 239000003822 epoxy resin Substances 0.000 description 16
- 229920000647 polyepoxide Polymers 0.000 description 16
- 229920005596 polymer binder Polymers 0.000 description 16
- 239000008199 coating composition Substances 0.000 description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 14
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 14
- 229920005862 polyol Polymers 0.000 description 13
- 150000003077 polyols Chemical class 0.000 description 13
- 239000000839 emulsion Substances 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 10
- 150000001991 dicarboxylic acids Chemical class 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
- 239000011230 binding agent Substances 0.000 description 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 8
- 238000000576 coating method Methods 0.000 description 7
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 238000011065 in-situ storage Methods 0.000 description 6
- 239000000049 pigment Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 125000001931 aliphatic group Chemical group 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 5
- 239000003973 paint Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000011253 protective coating Substances 0.000 description 5
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- 239000012855 volatile organic compound Substances 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
- VPWNQTHUCYMVMZ-UHFFFAOYSA-N 4,4'-sulfonyldiphenol Chemical class C1=CC(O)=CC=C1S(=O)(=O)C1=CC=C(O)C=C1 VPWNQTHUCYMVMZ-UHFFFAOYSA-N 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 230000032050 esterification Effects 0.000 description 3
- 238000005886 esterification reaction Methods 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 239000003999 initiator Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000002978 peroxides Chemical group 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- RUMACXVDVNRZJZ-UHFFFAOYSA-N 2-methylpropyl 2-methylprop-2-enoate Chemical compound CC(C)COC(=O)C(C)=C RUMACXVDVNRZJZ-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical group C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 125000005907 alkyl ester group Chemical group 0.000 description 2
- 235000013361 beverage Nutrition 0.000 description 2
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- 150000003944 halohydrins Chemical class 0.000 description 2
- 229940087305 limonene Drugs 0.000 description 2
- 235000001510 limonene Nutrition 0.000 description 2
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 2
- 239000010665 pine oil Substances 0.000 description 2
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 230000002087 whitening effect Effects 0.000 description 2
- PSGCQDPCAWOCSH-UHFFFAOYSA-N (4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl) prop-2-enoate Chemical compound C1CC2(C)C(OC(=O)C=C)CC1C2(C)C PSGCQDPCAWOCSH-UHFFFAOYSA-N 0.000 description 1
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 1
- ZXCYIJGIGSDJQQ-UHFFFAOYSA-N 2,3-dichloropropan-1-ol Chemical compound OCC(Cl)CCl ZXCYIJGIGSDJQQ-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- WDQMWEYDKDCEHT-UHFFFAOYSA-N 2-ethylhexyl 2-methylprop-2-enoate Chemical compound CCCCC(CC)COC(=O)C(C)=C WDQMWEYDKDCEHT-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical compound OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000001253 acrylic acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 235000013405 beer Nutrition 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 235000014171 carbonated beverage Nutrition 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 description 1
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- 239000006115 industrial coating Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- ULDDEWDFUNBUCM-UHFFFAOYSA-N pentyl prop-2-enoate Chemical compound CCCCCOC(=O)C=C ULDDEWDFUNBUCM-UHFFFAOYSA-N 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical class OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9807213.5 | 1998-04-04 | ||
| GBGB9807213.5A GB9807213D0 (en) | 1998-04-04 | 1998-04-04 | Aqueous coating composition |
| PCT/EP1999/002279 WO1999051696A1 (en) | 1998-04-04 | 1999-03-30 | Aqueous coating composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002510740A JP2002510740A (ja) | 2002-04-09 |
| JP2002510740A5 true JP2002510740A5 (https=) | 2006-05-11 |
Family
ID=10829832
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000542412A Pending JP2002510740A (ja) | 1998-04-04 | 1999-03-30 | 水性被覆剤組成物 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6306934B1 (https=) |
| EP (1) | EP1086183B1 (https=) |
| JP (1) | JP2002510740A (https=) |
| KR (1) | KR100528252B1 (https=) |
| AT (1) | ATE269888T1 (https=) |
| AU (1) | AU743096B2 (https=) |
| DE (1) | DE69918301T2 (https=) |
| ES (1) | ES2228036T3 (https=) |
| GB (1) | GB9807213D0 (https=) |
| WO (1) | WO1999051696A1 (https=) |
| ZA (1) | ZA200005295B (https=) |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1169382B1 (en) * | 1999-03-15 | 2003-06-04 | Kao Corporation | Water-based resin composition |
| DE60314734T2 (de) * | 2002-03-08 | 2008-03-06 | Valspar Sourcing, Inc., Minneapolis | Beschichtungen mit niedrigem gehalt an flüchtigen organischen verbindungen |
| WO2003076536A1 (en) * | 2002-03-08 | 2003-09-18 | Valspar Sourcing, Inc | Polymerization of a reactive diluent in the presence of an epoxy-amine material, and coating compositions prepared thereby |
| US20040132895A1 (en) * | 2002-08-30 | 2004-07-08 | Ambrose Ronald R. | Compositions and methods for coating food cans |
| US7745508B2 (en) * | 2002-08-30 | 2010-06-29 | Ppg Industries Ohio, Inc. | Compositions and methods for coating food cans |
| US7341762B2 (en) * | 2003-01-08 | 2008-03-11 | The Glidden Company | Coating composition having improved release properties and the process for making the same |
| EP1615966B2 (en) | 2003-04-02 | 2019-10-09 | Swimc Llc | Aqueous dispersions and coatings |
| JP4591653B2 (ja) * | 2003-08-08 | 2010-12-01 | 東洋インキ製造株式会社 | 複合樹脂エマルジョン含有水性塗料組成物 |
| JP2007521996A (ja) * | 2004-02-12 | 2007-08-09 | ヴァルスパー・ソーシング・インコーポレーテッド | 容器内面のコーティング方法、および、内部コーティングを含む容器 |
| PL3037488T3 (pl) | 2004-10-20 | 2022-11-14 | Swimc Llc | Kompozycje powlekające dla pojemników i sposoby powlekania |
| US9758665B2 (en) * | 2004-12-22 | 2017-09-12 | Imperial Chemical Industries Limited | Aqueous polymer dispersions |
| AU2007297378B2 (en) | 2006-09-19 | 2013-05-30 | Swimc Llc | Food and beverage coated containers, method of coating and coating composition |
| WO2009148988A2 (en) * | 2008-06-03 | 2009-12-10 | Valspar Sourcing, Inc. | Easy-open container and container coating |
| US20100260954A1 (en) * | 2008-11-26 | 2010-10-14 | Valspar Sourcing, Inc. | Polymer having polycyclic groups and coating compositions thereof |
| AU2009319797B2 (en) | 2008-11-26 | 2015-09-03 | Swimc Llc | Polyester polymer and coating compositions thereof |
| AU2009319890B2 (en) | 2008-11-26 | 2015-09-10 | Swimc Llc | Polyester-carbamate polymer and coating compositions thereof |
| US8367171B2 (en) | 2008-11-26 | 2013-02-05 | Valspar Sourcing, Inc. | Polymer having polycyclic groups and coating compositions thereof |
| WO2010118349A1 (en) | 2009-04-09 | 2010-10-14 | Valspar Sourcing, Inc. | Polyester coating composition |
| MX338773B (es) | 2009-04-09 | 2016-05-02 | Valspar Sourcing Inc | Polimero que tiene funcionalidad cicloalifatica insaturada y composiciones de recubrimiento formadas de este. |
| US8747979B2 (en) | 2009-07-17 | 2014-06-10 | Valspar Sourcing, Inc. | Coating compositions and articles coated therewith |
| US9011999B2 (en) | 2009-09-18 | 2015-04-21 | Valspar Sourcing, Inc. | Coating composition including an unsaturated polymer |
| EP2558543B1 (en) | 2010-04-16 | 2017-08-30 | Valspar Sourcing, Inc. | Coating compositions for packaging articles and methods of coating |
| US20130178590A1 (en) * | 2010-09-30 | 2013-07-11 | Dow Global Technologies Llc | Advanced epoxy resin compositions |
| EP2621998A1 (en) | 2010-09-30 | 2013-08-07 | Dow Global Technologies LLC | Coating compositions |
| JP5795804B2 (ja) | 2010-09-30 | 2015-10-14 | ダウ グローバル テクノロジーズ エルエルシー | コーティング組成物 |
| WO2012050777A1 (en) | 2010-09-30 | 2012-04-19 | Dow Global Technologies Llc | Advanced poly epoxy ester resin compositions |
| EP3878912B1 (en) | 2011-02-07 | 2023-04-05 | Swimc Llc | Coating compositions for containers and other articles and methods of coating |
| EP2599844A1 (en) * | 2011-12-02 | 2013-06-05 | PPG Industries Ohio Inc. | Coating composition for a food or beverage can |
| US20150108144A1 (en) * | 2011-12-05 | 2015-04-23 | Blue Wave Co S.A. | Cyclopentadiene polymer liner for pressurized fluid transport systems |
| EP2882658B1 (en) | 2012-08-09 | 2021-09-08 | Swimc Llc | Container coating system |
| AU2013299578A1 (en) | 2012-08-09 | 2015-02-19 | Valspar Sourcing, Inc. | Compositions for containers and other articles and methods of using same |
| CN104045808A (zh) | 2013-03-12 | 2014-09-17 | 陶氏环球技术有限公司 | 环氧树脂组合物、其制备方法及其制品 |
| CN110790914A (zh) | 2014-04-14 | 2020-02-14 | 宣伟投资管理有限公司 | 制备用于容器和其它制品的组合物的方法以及使用所述组合物的方法 |
| US9718983B2 (en) | 2014-05-30 | 2017-08-01 | Ppg Industries Ohio, Inc. | Coating composition for a food or beverage can |
| KR20180002745A (ko) * | 2015-05-29 | 2018-01-08 | 피피지 인더스트리즈 오하이오 인코포레이티드 | 에멀젼 중합된 라텍스 중합체로 코팅된 포장재 |
| TWI614275B (zh) | 2015-11-03 | 2018-02-11 | Valspar Sourcing Inc | 用於製備聚合物的液體環氧樹脂組合物 |
| CN109071828A (zh) | 2016-02-29 | 2018-12-21 | 米切尔曼公司 | 可生物降解聚合物的水基的水解稳定分散体 |
| JP7241001B2 (ja) * | 2019-10-23 | 2023-03-16 | トヨタ自動車東日本株式会社 | 着色コート層用塗料およびその塗装方法 |
| CN118284643A (zh) | 2021-12-16 | 2024-07-02 | 湛新奥地利有限公司 | 涂料组合物 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4212781A (en) * | 1977-04-18 | 1980-07-15 | Scm Corporation | Modified epoxy resins, processes for making and using same and substrates coated therewith |
| US4683273A (en) | 1986-05-27 | 1987-07-28 | The Glidden Company | Polyester and epoxy resin coating |
| DE4242518C2 (de) | 1992-12-16 | 1996-10-02 | Bollig & Kemper | Wäßrige Polymerdispersionen für Klarlacke |
| DE4314306A1 (de) * | 1993-04-30 | 1995-02-02 | Basf Ag | Verdunstungsarme ungesättigte Polyesterharze |
| US5290828A (en) | 1993-06-11 | 1994-03-01 | The Glidden Company | Aqueous dispersed acrylic grafted epoxy polyester protective coatings |
| DE4325886A1 (de) | 1993-08-02 | 1995-02-09 | Basf Ag | Thixotrope ungesättigte Polyesterharze |
| US5464885A (en) | 1994-04-04 | 1995-11-07 | The Glidden Company | Low VOC, aqueous dispersed, epoxy-ester acrylic graft coatings |
| US5532297A (en) | 1995-05-26 | 1996-07-02 | The Glidden Company | Divinyl benzene modified, aqueous dispersed, acrylic graft coatings |
| US5830928A (en) | 1996-02-20 | 1998-11-03 | Ppg Industries, Inc. | Waterborne coating compositions |
-
1998
- 1998-04-04 GB GBGB9807213.5A patent/GB9807213D0/en not_active Ceased
-
1999
- 1999-03-29 US US09/280,639 patent/US6306934B1/en not_active Expired - Lifetime
- 1999-03-30 EP EP99919183A patent/EP1086183B1/en not_active Expired - Lifetime
- 1999-03-30 KR KR10-2000-7010963A patent/KR100528252B1/ko not_active Expired - Lifetime
- 1999-03-30 WO PCT/EP1999/002279 patent/WO1999051696A1/en not_active Ceased
- 1999-03-30 JP JP2000542412A patent/JP2002510740A/ja active Pending
- 1999-03-30 AT AT99919183T patent/ATE269888T1/de not_active IP Right Cessation
- 1999-03-30 DE DE69918301T patent/DE69918301T2/de not_active Expired - Lifetime
- 1999-03-30 ES ES99919183T patent/ES2228036T3/es not_active Expired - Lifetime
- 1999-03-30 AU AU37048/99A patent/AU743096B2/en not_active Expired
-
2000
- 2000-09-29 ZA ZA200005295A patent/ZA200005295B/en unknown
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