JP2002514673A5 - - Google Patents
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- JP2002514673A5 JP2002514673A5 JP2000548405A JP2000548405A JP2002514673A5 JP 2002514673 A5 JP2002514673 A5 JP 2002514673A5 JP 2000548405 A JP2000548405 A JP 2000548405A JP 2000548405 A JP2000548405 A JP 2000548405A JP 2002514673 A5 JP2002514673 A5 JP 2002514673A5
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- JP
- Japan
- Prior art keywords
- acid
- polymer composition
- component
- amine
- meth
- 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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- 229920000642 polymer Polymers 0.000 description 40
- 239000000203 mixture Substances 0.000 description 32
- 239000004816 latex Substances 0.000 description 20
- 229920000126 latex Polymers 0.000 description 20
- 239000002253 acid Substances 0.000 description 14
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 10
- 239000000178 monomer Substances 0.000 description 10
- -1 Vinyl Chemical group 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- 238000004132 cross linking Methods 0.000 description 9
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- 238000009835 boiling Methods 0.000 description 6
- 229910052757 nitrogen Inorganic materials 0.000 description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 6
- 150000007524 organic acids Chemical class 0.000 description 6
- HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 4
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
- VHRGRCVQAFMJIZ-UHFFFAOYSA-N cadaverine Chemical compound NCCCCCN VHRGRCVQAFMJIZ-UHFFFAOYSA-N 0.000 description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 4
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 4
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
- 235000005985 organic acids Nutrition 0.000 description 4
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 4
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-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
- 239000011248 coating agent Substances 0.000 description 3
- YQXJHAJWNXVSTP-UHFFFAOYSA-N 1,2,2-trimethylcyclohexane-1,3-diamine Chemical compound CC1(C)C(N)CCCC1(C)N YQXJHAJWNXVSTP-UHFFFAOYSA-N 0.000 description 2
- VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
- MOFBDJIQKHNGPG-UHFFFAOYSA-N 2,2,4-trimethylhexane-1,1-diamine Chemical compound CCC(C)CC(C)(C)C(N)N MOFBDJIQKHNGPG-UHFFFAOYSA-N 0.000 description 2
- YVLHRYOHNHUVOA-UHFFFAOYSA-N 2,2-dimethylpropane-1,1-diamine Chemical compound CC(C)(C)C(N)N YVLHRYOHNHUVOA-UHFFFAOYSA-N 0.000 description 2
- BMXFFBCPBDWECJ-UHFFFAOYSA-N 2-(diaminoamino)ethanol Chemical compound NN(N)CCO BMXFFBCPBDWECJ-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical group COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 2
- HMJBXEZHJUYJQY-UHFFFAOYSA-N 4-(aminomethyl)octane-1,8-diamine Chemical compound NCCCCC(CN)CCCN HMJBXEZHJUYJQY-UHFFFAOYSA-N 0.000 description 2
- AWQSAIIDOMEEOD-UHFFFAOYSA-N 5,5-Dimethyl-4-(3-oxobutyl)dihydro-2(3H)-furanone Chemical compound CC(=O)CCC1CC(=O)OC1(C)C AWQSAIIDOMEEOD-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
- GKXVJHDEWHKBFH-UHFFFAOYSA-N [2-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC=C1CN GKXVJHDEWHKBFH-UHFFFAOYSA-N 0.000 description 2
- 235000011054 acetic acid Nutrition 0.000 description 2
- 125000002339 acetoacetyl group Chemical group O=C([*])C([H])([H])C(=O)C([H])([H])[H] 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 2
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 2
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 2
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N cyclohexanecarboxylic acid Chemical compound OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
- OYOFUEDXAMRQBB-UHFFFAOYSA-N cyclohexylmethanediamine Chemical compound NC(N)C1CCCCC1 OYOFUEDXAMRQBB-UHFFFAOYSA-N 0.000 description 2
- GPQWKLDEDGOJQH-UHFFFAOYSA-N ethane-1,1,1,2-tetramine Chemical compound NCC(N)(N)N GPQWKLDEDGOJQH-UHFFFAOYSA-N 0.000 description 2
- 125000003916 ethylene diamine group Chemical group 0.000 description 2
- 235000019253 formic acid Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 2
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- 229920000333 poly(propyleneimine) Polymers 0.000 description 2
- 235000019260 propionic acid Nutrition 0.000 description 2
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 2
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 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
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- OLIBHZVRLPRRHI-UHFFFAOYSA-N benzoic acid;carbonic acid Chemical compound OC(O)=O.OC(=O)C1=CC=CC=C1 OLIBHZVRLPRRHI-UHFFFAOYSA-N 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000005562 fading Methods 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/078,924 | 1998-05-14 | ||
| US09/078,924 US6262169B1 (en) | 1998-05-14 | 1998-05-14 | Protonated amines for controlled crosslinking of latex polymers |
| PCT/US1999/009750 WO1999058608A1 (en) | 1998-05-14 | 1999-05-05 | Protonated amines for controlled crosslinking of latex polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2002514673A JP2002514673A (ja) | 2002-05-21 |
| JP2002514673A5 true JP2002514673A5 (cg-RX-API-DMAC10.html) | 2006-06-29 |
Family
ID=22147053
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000548405A Pending JP2002514673A (ja) | 1998-05-14 | 1999-05-05 | ラテックスポリマーの制御架橋用プロトン化アミン |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6262169B1 (cg-RX-API-DMAC10.html) |
| EP (1) | EP1084193A1 (cg-RX-API-DMAC10.html) |
| JP (1) | JP2002514673A (cg-RX-API-DMAC10.html) |
| KR (1) | KR20010043556A (cg-RX-API-DMAC10.html) |
| CN (1) | CN1309683A (cg-RX-API-DMAC10.html) |
| AU (1) | AU758504B2 (cg-RX-API-DMAC10.html) |
| BR (1) | BR9910473A (cg-RX-API-DMAC10.html) |
| CA (1) | CA2331673A1 (cg-RX-API-DMAC10.html) |
| MY (1) | MY117044A (cg-RX-API-DMAC10.html) |
| WO (1) | WO1999058608A1 (cg-RX-API-DMAC10.html) |
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| JP3591808B2 (ja) * | 1998-03-17 | 2004-11-24 | 株式会社東芝 | 画像入力装置および方法および記録媒体 |
| US6869996B1 (en) | 1999-06-08 | 2005-03-22 | The Sherwin-Williams Company | Waterborne coating having improved chemical resistance |
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| DE10133727A1 (de) * | 2001-07-11 | 2003-01-23 | Borchers Gmbh | Verwendung von Mischungen spezieller organischer Verbindungen als Hautverhinderungsmittel in lufttrocknenden Lacken |
| US6673854B2 (en) * | 2001-10-05 | 2004-01-06 | National Starch And Chemical Investment Holding Corporation | Vinyl acetate/ethylene emulsion stabilized with a phosphate surfactant |
| US6770864B2 (en) * | 2001-12-22 | 2004-08-03 | Yong Yan | Light beam operated personal interfaces to computers |
| US20040003892A1 (en) * | 2002-07-08 | 2004-01-08 | Lehman Nicholas C. | One part woodworking adhesive composition |
| KR100863501B1 (ko) * | 2002-10-07 | 2008-10-15 | 주식회사 코오롱 | 광디바이스용 보호막 형성 재료로 유용한 감광성 수지조성물 |
| US6992156B2 (en) * | 2002-12-31 | 2006-01-31 | The Goodyear Tire & Rubber Company | Controlled polymerization |
| US7528204B2 (en) * | 2004-05-17 | 2009-05-05 | The Goodyear Tire & Rubber Company | Hydrogenation and epoxidation of polymers made by controlled polymerization |
| AU2005245950A1 (en) * | 2004-05-19 | 2005-12-01 | Flexcon Company, Inc. | Liquid formulations for coating and printing substrates |
| US20050260240A1 (en) * | 2004-05-20 | 2005-11-24 | Isp Investments Inc. | Rain-fast bioactive compositions |
| BRPI0518234A2 (pt) * | 2004-10-08 | 2008-11-11 | Sherwin Williams Co | revestimentos carregados de Água de auto-reticulaÇço |
| NL1031208C2 (nl) * | 2006-02-22 | 2007-08-24 | Univ Eindhoven Tech | Waterige dispersie en werkwijze voor het aanbrengen op een substraat van een coating op basis van een dergelijke dispersie. |
| US8222304B2 (en) | 2006-03-23 | 2012-07-17 | Rhodia Operations | Process for the treatment of a hydrophobic surface by an aqueous phase |
| DE102006039941A1 (de) * | 2006-08-25 | 2008-02-28 | Wacker Chemie Ag | Verfahren zur Behandlung von cellulosehaltigen Fasern oder Flächengebilde enthaltend cellulosehaltige Fasern |
| US8921477B2 (en) * | 2008-10-13 | 2014-12-30 | Eastern Michigan University | Conventional latex / nanolatex blends |
| EP2374836A1 (en) * | 2010-04-07 | 2011-10-12 | Nuplex Resins B.V. | Crosslinkable composition crosslinkable with a latent base catalyst. |
| US8809446B2 (en) | 2010-12-15 | 2014-08-19 | Eastman Chemical Company | Substituted 3-oxopentanoates and their uses in coating compositions |
| US9029451B2 (en) | 2010-12-15 | 2015-05-12 | Eastman Chemical Company | Waterborne coating compositions that include 2,2,4-trimethyl-3-oxopentanoate esters as reactive coalescents |
| US8809447B2 (en) | 2010-12-15 | 2014-08-19 | Eastman Chemical Company | Acetoacetate-functional monomers and their uses in coating compositions |
| CN104039869B (zh) * | 2011-10-07 | 2016-04-27 | 树脂核动力工业有限公司 | 含潜在碱催化剂的可交联组合物及潜在的碱催化剂组合物 |
| SI2995636T1 (sl) | 2011-10-07 | 2017-10-30 | Allnex Netherlands B.V. | Sestavek za uporabo v postopku priprave sestavka, premrežljivega z RMA |
| CN102504090A (zh) * | 2011-10-12 | 2012-06-20 | 辽宁恒星精细化工有限公司 | 一种纺织品涂料印花用粘合剂及其制备方法 |
| JP6059088B2 (ja) * | 2012-06-14 | 2017-01-11 | 日東電工株式会社 | 耐水性有機薄膜、耐水性有機薄膜の製造方法、及び、耐水性有機薄膜を有する画像表示装置 |
| US11535762B2 (en) | 2012-09-18 | 2022-12-27 | Ennis Flint | Fast drying aqueous amine free coating composition(s) |
| JP2014125512A (ja) * | 2012-12-25 | 2014-07-07 | Henkel Japan Ltd | 水性アミンエマルション |
| EP2945994B1 (en) | 2013-01-18 | 2018-07-11 | Basf Se | Acrylic dispersion-based coating compositions |
| EP2970697B1 (en) | 2013-03-15 | 2022-10-05 | Swimc Llc | Water-based compositions that resist dirt pick-up |
| US10196537B2 (en) | 2013-03-15 | 2019-02-05 | The Sherwin-Williams Company | Dirt pick-up resistant composition |
| US9120936B2 (en) | 2013-03-15 | 2015-09-01 | Valspar Sourcing, Inc. | Water-based compositions that resist dirt pick-up |
| US10221322B2 (en) | 2013-03-15 | 2019-03-05 | The Sherwin-Williams Company | Dirt pick-up resistant composition |
| CN105324426B (zh) | 2013-04-08 | 2018-07-03 | 欧尼克斯荷兰有限公司 | 通过真实迈克尔加成(rma)反应而可交联的组合物 |
| US9650542B2 (en) | 2013-08-13 | 2017-05-16 | Basf Se | Use of polypropyleneimine as curing agent for epoxide resins |
| CN117264491A (zh) | 2014-09-12 | 2023-12-22 | 宣伟投资管理有限公司 | 耐沾污性的水基涂料组合物 |
| JP6713796B2 (ja) * | 2015-03-28 | 2020-06-24 | 株式会社日本触媒 | 塗料用水性樹脂組成物 |
| WO2016166334A1 (en) | 2015-04-17 | 2016-10-20 | Nuplex Resins B.V. | Process for the manufacture of a crosslinkable composition |
| AU2016247589B2 (en) | 2015-04-17 | 2020-10-29 | Allnex Netherlands B.V. | Floor coating compositions |
| CA2982882C (en) | 2015-04-17 | 2022-11-22 | Allnex Netherlands B.V. | A method for curing a rma crosslinkable resin coating, rma crosslinkable compositions and resins for use therein |
| CN107667151A (zh) | 2015-04-17 | 2018-02-06 | 欧尼克斯荷兰有限公司 | 具有改善的粘附性的rma可交联组合物 |
| CN105154054B (zh) * | 2015-08-07 | 2017-12-22 | 中国石油化工股份有限公司胜利油田分公司勘探开发研究院 | 一种三元胺参与合成的交联型聚合物驱油剂及其制备方法 |
| US10717800B2 (en) | 2015-09-17 | 2020-07-21 | Ennis Paint, Inc. | Controlled crosslinking of latex polymers with polyfunctional amines |
| US10450475B2 (en) | 2015-11-17 | 2019-10-22 | Ennis Paint, Inc. | Traffic marking compositions containing polyfunctional amines |
| EP3630868A4 (en) * | 2017-05-29 | 2021-01-13 | Dow Global Technologies LLC | PROCESS FOR PREPARING AN ACETOACETYL-FUNCTION POLYMER |
| US10876014B2 (en) * | 2017-09-22 | 2020-12-29 | Natoco Co., Ltd. | Coating composition, coating material, cured film, article having cured film, and method for producing article having cured film |
| EP3802711B1 (en) | 2018-05-29 | 2025-10-01 | Swimc Llc | Water-based compositions with long term gloss retention |
| EP3663326A1 (en) | 2018-12-04 | 2020-06-10 | Allnex Netherlands B.V. | Rma crosslinkable polymer |
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| JPH08311407A (ja) | 1995-05-24 | 1996-11-26 | Rohm & Haas Co | アセトアセテート官能性ポリマー及び多官能性アミンを含有する水性組成物 |
| AU720104B2 (en) * | 1995-12-04 | 2000-05-25 | Rohm And Haas Company | Waterborne crosslinkable coating compositions |
| US6005035A (en) | 1997-09-18 | 1999-12-21 | Eastman Chemical Company | Stable waterborne polymer compositions containing poly(alkylenimines) |
-
1998
- 1998-05-14 US US09/078,924 patent/US6262169B1/en not_active Expired - Lifetime
-
1999
- 1999-05-05 JP JP2000548405A patent/JP2002514673A/ja active Pending
- 1999-05-05 EP EP99921650A patent/EP1084193A1/en not_active Withdrawn
- 1999-05-05 CA CA002331673A patent/CA2331673A1/en not_active Abandoned
- 1999-05-05 KR KR1020007012676A patent/KR20010043556A/ko not_active Withdrawn
- 1999-05-05 WO PCT/US1999/009750 patent/WO1999058608A1/en not_active Ceased
- 1999-05-05 BR BR9910473-3A patent/BR9910473A/pt not_active Application Discontinuation
- 1999-05-05 AU AU38802/99A patent/AU758504B2/en not_active Ceased
- 1999-05-05 MY MYPI99001785A patent/MY117044A/en unknown
- 1999-05-05 CN CN99808551A patent/CN1309683A/zh active Pending
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