JP2003501499A5 - - Google Patents
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- Publication number
- JP2003501499A5 JP2003501499A5 JP2001500685A JP2001500685A JP2003501499A5 JP 2003501499 A5 JP2003501499 A5 JP 2003501499A5 JP 2001500685 A JP2001500685 A JP 2001500685A JP 2001500685 A JP2001500685 A JP 2001500685A JP 2003501499 A5 JP2003501499 A5 JP 2003501499A5
- Authority
- JP
- Japan
- Prior art keywords
- methacrylate
- latent
- alkyd
- group
- oxidative
- 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.)
- Granted
Links
- 230000001590 oxidative effect Effects 0.000 description 33
- 229920000180 alkyd Polymers 0.000 description 26
- 238000000034 method Methods 0.000 description 21
- 239000004816 latex Substances 0.000 description 16
- 239000000178 monomer Substances 0.000 description 15
- 229920000126 latex Polymers 0.000 description 11
- 125000000524 functional group Chemical group 0.000 description 10
- -1 allyl maleate Chemical compound 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 4
- 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 description 4
- BEWCNXNIQCLWHP-UHFFFAOYSA-N 2-(tert-butylamino)ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCNC(C)(C)C BEWCNXNIQCLWHP-UHFFFAOYSA-N 0.000 description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 4
- AEMJIUOEWGKFER-UHFFFAOYSA-N 4-hydroxybut-1-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC=CCCO AEMJIUOEWGKFER-UHFFFAOYSA-N 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 description 4
- ZPOLOEWJWXZUSP-WAYWQWQTSA-N bis(prop-2-enyl) (z)-but-2-enedioate Chemical compound C=CCOC(=O)\C=C/C(=O)OCC=C ZPOLOEWJWXZUSP-WAYWQWQTSA-N 0.000 description 4
- 150000002081 enamines Chemical class 0.000 description 4
- FFYWKOUKJFCBAM-UHFFFAOYSA-N ethenyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC=C FFYWKOUKJFCBAM-UHFFFAOYSA-N 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 3
- IWTYTFSSTWXZFU-UHFFFAOYSA-N 3-chloroprop-1-enylbenzene Chemical compound ClCC=CC1=CC=CC=C1 IWTYTFSSTWXZFU-UHFFFAOYSA-N 0.000 description 3
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 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
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- SJIXRGNQPBQWMK-UHFFFAOYSA-N 2-(diethylamino)ethyl 2-methylprop-2-enoate Chemical compound CCN(CC)CCOC(=O)C(C)=C SJIXRGNQPBQWMK-UHFFFAOYSA-N 0.000 description 2
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 2
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-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
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- TVWTZAGVNBPXHU-FOCLMDBBSA-N dioctyl (e)-but-2-enedioate Chemical compound CCCCCCCCOC(=O)\C=C\C(=O)OCCCCCCCC TVWTZAGVNBPXHU-FOCLMDBBSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- QSVXXWUAIOHMFG-UHFFFAOYSA-N n-but-3-enyl-2-methylprop-2-enamide;urea Chemical compound NC(N)=O.CC(=C)C(=O)NCCC=C QSVXXWUAIOHMFG-UHFFFAOYSA-N 0.000 description 2
- KCAMXZBMXVIIQN-UHFFFAOYSA-N octan-3-yl 2-methylprop-2-enoate Chemical compound CCCCCC(CC)OC(=O)C(C)=C KCAMXZBMXVIIQN-UHFFFAOYSA-N 0.000 description 2
- NZIDBRBFGPQCRY-UHFFFAOYSA-N octyl 2-methylprop-2-enoate Chemical compound CCCCCCCCOC(=O)C(C)=C NZIDBRBFGPQCRY-UHFFFAOYSA-N 0.000 description 2
- 229940065472 octyl acrylate Drugs 0.000 description 2
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 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
- 239000000049 pigment Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- NIXVAPHNPNMUIX-UHFFFAOYSA-N 6-amino-2-methylhex-2-enamide Chemical compound NC(=O)C(C)=CCCCN NIXVAPHNPNMUIX-UHFFFAOYSA-N 0.000 description 1
- 206010013642 Drooling Diseases 0.000 description 1
- 208000008630 Sialorrhea Diseases 0.000 description 1
- 239000013036 UV Light Stabilizer Substances 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000005399 allylmethacrylate group Chemical group 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000007720 emulsion polymerization reaction Methods 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/321,610 | 1999-05-28 | ||
| US09/321,610 US6333378B1 (en) | 1997-08-12 | 1999-05-28 | Acrylic modified waterborne alkyd or uralkyd dispersions |
| PCT/US2000/014557 WO2000073361A1 (en) | 1999-05-28 | 2000-05-26 | Acrylic modified waterborne alkyd or uralkyd dispersions |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2003501499A JP2003501499A (ja) | 2003-01-14 |
| JP2003501499A5 true JP2003501499A5 (enExample) | 2007-06-14 |
| JP4833465B2 JP4833465B2 (ja) | 2011-12-07 |
Family
ID=23251275
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2001500685A Expired - Fee Related JP4833465B2 (ja) | 1999-05-28 | 2000-05-26 | アクリル変性水性アルキド又はウラルキド分散液 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US6333378B1 (enExample) |
| EP (1) | EP1185567B1 (enExample) |
| JP (1) | JP4833465B2 (enExample) |
| CN (1) | CN1131252C (enExample) |
| AT (1) | ATE286926T1 (enExample) |
| AU (1) | AU5046800A (enExample) |
| BR (1) | BR0010994A (enExample) |
| DE (1) | DE60017394T2 (enExample) |
| ES (1) | ES2231205T3 (enExample) |
| MX (1) | MXPA01012195A (enExample) |
| WO (1) | WO2000073361A1 (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1164706C (zh) * | 2001-03-10 | 2004-09-01 | 海洋化工研究院 | 环氧酯乳液和以该乳液为基料的水性防锈底漆 |
| US7396871B2 (en) * | 2002-01-14 | 2008-07-08 | Eastman Chemical Comapny | Rubber modified acrylic and/or vinyl hybrid resins |
| AU2003261432A1 (en) * | 2002-08-10 | 2004-02-25 | The Sherwin-Williams Company | Aerosol paint composition for adherence to plastic |
| AT412347B (de) * | 2003-03-12 | 2005-01-25 | Surface Specialties Austria | Wasserverdünnbare polyesterharze |
| CN1957048B (zh) * | 2004-05-25 | 2010-10-13 | 阿克佐诺贝尔国际涂料股份有限公司 | 含有乙烯基改性的醇酸树脂的涂料组合物 |
| US20060270769A1 (en) * | 2005-05-24 | 2006-11-30 | Shoaf Glenn L | Acrylic-modified alkyd hybrid latexes and their use as viscosity modifiers |
| WO2008006580A2 (en) * | 2006-07-14 | 2008-01-17 | Dsm Ip Assets B.V. | Process for preparing organic nanoparticles |
| JP5665536B2 (ja) * | 2007-06-15 | 2015-02-04 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 低ｖｏｃ水性ハイブリッド結合剤 |
| WO2009007446A1 (en) * | 2007-07-12 | 2009-01-15 | Dsm Ip Assets B.V. | Organic nano-particles and process for their preparation |
| DE102007048192A1 (de) * | 2007-10-08 | 2009-04-09 | Evonik Röhm Gmbh | Emulsionspolymere, wässrige Dispersionen und Verfahren zu deren Herstellung |
| US20090163635A1 (en) * | 2007-12-19 | 2009-06-25 | Eastman Chemical Company | Aqueous dispersions of adhesion promoters |
| US20100104872A1 (en) * | 2008-09-17 | 2010-04-29 | Archer-Daniels-Midland Company | Biobased waterborne synthetic polyurethane hybrid latexes and films |
| MX341522B (es) | 2008-12-22 | 2016-08-24 | Sherwin Williams Co | Mini-emulsiones y latex de las mismas. |
| US20110086969A1 (en) * | 2009-10-09 | 2011-04-14 | Eric Cline | Fast dry polyester latex for coatings |
| US8785557B2 (en) * | 2009-12-16 | 2014-07-22 | Basf Se | Use of aqueous hybrid binders for gloss paints |
| AU2010341014B2 (en) | 2009-12-16 | 2015-02-05 | Basf Se | Use of aqueous hybrid binding agents for gloss paints |
| CN102093764B (zh) * | 2010-12-31 | 2013-04-10 | 长安大学 | 沥青路面用多色系选择性太阳热反射涂料 |
| CN102127213B (zh) * | 2011-01-17 | 2013-05-22 | 华中科技大学 | 一种水性丙烯酸醇酸树脂及其制备方法和应用 |
| EP2481763A1 (en) * | 2011-01-27 | 2012-08-01 | Cytec Surface Specialties S.A./N.V. | Graft copolymer latices |
| CN102746762B (zh) * | 2012-05-29 | 2014-08-06 | 兰州理工大学 | 醇酸丙烯酸杂化乳胶涂料及其制备方法 |
| CN102746465A (zh) * | 2012-05-29 | 2012-10-24 | 西北永新化工股份有限公司 | 醇酸丙烯酸杂化乳液及其制备方法 |
| EP2945994B1 (en) | 2013-01-18 | 2018-07-11 | Basf Se | Acrylic dispersion-based coating compositions |
| CN104151537A (zh) * | 2014-07-25 | 2014-11-19 | 青岛展辰新材料有限公司 | 一种低气味丙烯酸改性醇酸树脂及其制备方法 |
| US10294320B2 (en) * | 2014-11-03 | 2019-05-21 | Arkema Inc. | Latex comprising water-soluble acrylic modified alkyd dispersion and method of production thereof |
| US10696771B2 (en) | 2015-03-26 | 2020-06-30 | Performance Materials Na, Inc. | Method of incorporating ethylene copolymers into latex |
| CN105568701A (zh) * | 2015-12-28 | 2016-05-11 | 杭州富阳伟文环保科技有限公司 | 一种珠光抗折皱防水透湿聚氨酯合成革的制备方法 |
| KR102027935B1 (ko) * | 2017-01-20 | 2019-11-04 | 한화케미칼 주식회사 | 알칼리 수용성 수지, 이의 제조 방법 및 알칼리 수용성 수지를 포함하는 에멀젼 중합체 |
| EP3575333B1 (en) | 2017-01-25 | 2023-09-06 | DIC Corporation | Active-energy-ray-curable aqueous resin composition and undercoat agent for inorganic-material thin film |
| MX2019012843A (es) * | 2017-04-26 | 2019-11-28 | Arkema Inc | Recubrimiento aislante termico con baja conductividad termica. |
| CN112789332A (zh) * | 2018-10-11 | 2021-05-11 | 伊士曼化工公司 | 具有改进的耐刮擦性的热固性涂层组合物 |
| CN113583207B (zh) * | 2021-07-01 | 2022-08-26 | 山西省应用化学研究所(有限公司) | 基于蓖麻油的水性聚氨酯乳液及胶粘剂的制备方法 |
Family Cites Families (44)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3345313A (en) | 1963-02-20 | 1967-10-03 | Trojan Powder Co | Alkyd resins and their preparation from reaction mixtures comprising a polymethylolalkanoic acid |
| US3734874A (en) | 1970-02-27 | 1973-05-22 | Eastman Kodak Co | Polyesters and polyesteramides containing ether groups and sulfonate groups in the form of a metallic salt |
| US3778395A (en) | 1972-02-18 | 1973-12-11 | Borden Inc | Printing inks comprising a uralkyd |
| IT981904B (it) | 1973-04-09 | 1974-10-10 | Duco Spa | Resine alchidiche all acqua modi ficate con acido acrilico o meta crilico |
| US3979346A (en) | 1973-11-08 | 1976-09-07 | Vianova-Kunstharz A.G. | Emulsifiers for preparing aqueous dispersions of alkyd resins |
| US4011388A (en) | 1974-07-02 | 1977-03-08 | E. I. Du Pont De Nemours And Company | Process for preparing emulsions by polymerization of aqueous monomer-polymer dispersions |
| DE2440267C2 (de) | 1974-08-22 | 1984-10-11 | Bayer Ag, 5090 Leverkusen | Thixotrope Urethanalkydharze |
| US4178425A (en) | 1976-07-07 | 1979-12-11 | Rohm And Haas Company | Polyurethane coating compositions containing unsaturated esters of glycol monodicyclopentenyl ethers |
| NL7806349A (nl) | 1977-06-13 | 1978-12-15 | Unilever Nv | In water dispergeerbare alkydharsen, waterige alkyd- dispersies, alsmede werkwijze ter bereiding van deze dispersies. |
| US4116902A (en) | 1977-10-05 | 1978-09-26 | International Minerals & Chemical Corp. | Polyurethane-modified alkyd resin |
| US4180645A (en) | 1978-05-22 | 1979-12-25 | Rohm And Haas Company | Polyurethane coating compositions from dicyclopentenyl acrylate and/or methacrylate |
| US4222911A (en) | 1978-08-07 | 1980-09-16 | Ppg Industries, Inc. | Polyester diol extended uralkyd resin and coating compositions containing the same |
| US4293471A (en) | 1979-03-16 | 1981-10-06 | E. I. Du Pont De Nemours And Company | Fast-drying alkyd latex |
| JPS5641221A (en) | 1979-09-10 | 1981-04-17 | Hitachi Chem Co Ltd | Water-dispersed resin composition |
| AT365216B (de) | 1979-10-29 | 1981-12-28 | Vianova Kunstharz Ag | Verfahren zur herstellung wasseremulgierbarer lufttrocknender lackbindemittel auf basis von modifizierten alkydharzen und emulsionen auf dieser basis |
| US4414357A (en) | 1979-11-27 | 1983-11-08 | Glasurit America, Inc. | Polyester or alkyd resin composition containing acrylic microgels |
| WO1983000151A1 (en) | 1981-06-29 | 1983-01-20 | Dulux Australia Ltd | Stable aqueous film-forming dispersions |
| DE3132937A1 (de) | 1981-08-20 | 1983-03-03 | Henkel KGaA, 4000 Düsseldorf | Wasserverduennbare harzzubereitung auf basis von alkydharzen und polyacrylatharzen sowie deren verwendung als wasserverduennbare lackharze |
| US4436849A (en) | 1981-10-26 | 1984-03-13 | Kansai Paint Company, Limited | Aqueous resin composition |
| CA1208835A (en) | 1982-10-04 | 1986-07-29 | Teruaki Kuwajima | Aqueous coating composition |
| DE3246614A1 (de) | 1982-12-16 | 1984-06-20 | Henkel KGaA, 4000 Düsseldorf | Emulgator- und loesungsmittelfreie alkydharzwasserlacke |
| US4737551A (en) | 1986-06-23 | 1988-04-12 | E. I. Dupont De Nemours And Company | Coating composition of a hydroxy group-containing modified polyester with polymerized lactone monomers |
| US4698391A (en) | 1986-07-30 | 1987-10-06 | Eastman Kodak Company | Crosslinked polymers with lowered resistivity and materials and methods for their preparation |
| US4946932A (en) | 1988-12-05 | 1990-08-07 | Eastman Kodak Company | Water-dispersible polyester blends |
| JPH02214787A (ja) | 1989-02-14 | 1990-08-27 | Nippon Paint Co Ltd | 常温乾燥性塗料組成物 |
| US5011883A (en) | 1990-02-07 | 1991-04-30 | Ici Americas Inc. | Stabilized polymer latex composition |
| IT1241142B (it) | 1990-05-16 | 1993-12-29 | Alusuisse Italia Spa | Monomeri acceleranti della polimerizzazione delle resine poliestere insature |
| FR2664533B1 (fr) | 1990-07-16 | 1994-09-30 | Rhone Poulenc Films | Films polyesters composites et leur utilisation comme couche de protection pour plaques photopolymeres et plaques photopolymeres les comportant. |
| EP0492847B2 (en) | 1990-12-21 | 2002-11-20 | Rohm And Haas Company | Air curing polymer composition |
| EP0555903A1 (en) | 1992-02-04 | 1993-08-18 | Akzo Nobel N.V. | Water-dispersible hybrid core-shell polymer, an aqueous dispersion thereof, and a coating composition made therefrom |
| US5296530A (en) | 1992-07-28 | 1994-03-22 | Rohm And Haas Company | Method for light-assisted curing of coatings |
| US5349026A (en) | 1992-11-20 | 1994-09-20 | Rohm And Haas Company | Reactive coalescents |
| US5326808A (en) | 1993-02-18 | 1994-07-05 | The Glidden Company | Odor free, air dry, aqueous emulsion paints |
| US5371148A (en) | 1993-06-23 | 1994-12-06 | Union Carbide Chemicals & Plastics Technology Corporation | Reactive polymers having pendant flexible side chains prepared from ethylenically unsaturated carbodiimides |
| BE1007263A3 (nl) | 1993-07-09 | 1995-05-02 | Dsm Nv | Alkydhars en emulsies daarvan. |
| US5525662A (en) | 1993-07-14 | 1996-06-11 | Rohm And Haas Company | Functionalization of polymers via enamine of acetoacetate |
| US5686518A (en) | 1993-10-12 | 1997-11-11 | Georgia Tech | Miniemulsion polymerization process using polymeric co-surfactant |
| US5378757A (en) | 1993-11-15 | 1995-01-03 | Eastman Chemical Company | Water-dissipatable alkyd resins and coatings prepared therefrom |
| US5869590A (en) | 1995-04-12 | 1999-02-09 | Eastman Chemical Company | Waterborne polymers having pendant allyl groups |
| US5539073A (en) | 1995-04-12 | 1996-07-23 | Eastman Chemical Company | Waterborne polymers having pendant allyl groups |
| US5538760A (en) | 1995-05-22 | 1996-07-23 | Eastman Chemical Company | Alkyd/acrylic latexes for cleaning and protecting hard surfaces |
| US5569715A (en) | 1995-07-24 | 1996-10-29 | Basf Corporation | Process for obtaining hydrophobically modified emulsion polymers and polymers obtained thereby |
| EP0755946A3 (en) * | 1995-07-24 | 1997-10-01 | Basf Corp | Method for the preparation of hydrophobic emulsion polymers, the polymers thus obtained and the aqueous coating compositions containing these polymers |
| EP1003798B1 (en) * | 1997-08-12 | 2005-10-19 | Eastman Chemical Company | Acrylic modified waterborne sulfonated alkyd dispersions |
-
1999
- 1999-05-28 US US09/321,610 patent/US6333378B1/en not_active Expired - Lifetime
-
2000
- 2000-05-26 JP JP2001500685A patent/JP4833465B2/ja not_active Expired - Fee Related
- 2000-05-26 MX MXPA01012195A patent/MXPA01012195A/es not_active Application Discontinuation
- 2000-05-26 DE DE60017394T patent/DE60017394T2/de not_active Expired - Lifetime
- 2000-05-26 AU AU50468/00A patent/AU5046800A/en not_active Abandoned
- 2000-05-26 CN CN00810902A patent/CN1131252C/zh not_active Expired - Fee Related
- 2000-05-26 EP EP00932794A patent/EP1185567B1/en not_active Expired - Lifetime
- 2000-05-26 BR BR0010994-0A patent/BR0010994A/pt not_active IP Right Cessation
- 2000-05-26 AT AT00932794T patent/ATE286926T1/de not_active IP Right Cessation
- 2000-05-26 WO PCT/US2000/014557 patent/WO2000073361A1/en not_active Ceased
- 2000-05-26 ES ES00932794T patent/ES2231205T3/es not_active Expired - Lifetime
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