JP2003522817A5 - - Google Patents
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- Publication number
- JP2003522817A5 JP2003522817A5 JP2000511821A JP2000511821A JP2003522817A5 JP 2003522817 A5 JP2003522817 A5 JP 2003522817A5 JP 2000511821 A JP2000511821 A JP 2000511821A JP 2000511821 A JP2000511821 A JP 2000511821A JP 2003522817 A5 JP2003522817 A5 JP 2003522817A5
- Authority
- JP
- Japan
- Prior art keywords
- acrylate
- agent
- acetoacetoxy
- group
- weight
- 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
Links
- 229920000642 polymer Polymers 0.000 description 16
- -1 Acetoacetoxy Chemical group 0.000 description 14
- 239000000203 mixture Substances 0.000 description 10
- 239000000178 monomer Substances 0.000 description 10
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 9
- 229920002554 vinyl polymer Polymers 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- WQAQPCDUOCURKW-UHFFFAOYSA-N butanethiol Chemical group CCCCS WQAQPCDUOCURKW-UHFFFAOYSA-N 0.000 description 4
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical group CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 2
- YHSYGCXKWUUKIK-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C=C YHSYGCXKWUUKIK-UHFFFAOYSA-N 0.000 description 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-M 2-sulfanylpropanoate Chemical compound CC(S)C([O-])=O PMNLUUOXGOOLSP-UHFFFAOYSA-M 0.000 description 2
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 2
- FJKZPONBPMKPLO-UHFFFAOYSA-N 3-prop-2-enoyloxypropyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCCOC(=O)C=C FJKZPONBPMKPLO-UHFFFAOYSA-N 0.000 description 2
- PICTWXAWDCLLKO-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCCCOC(=O)C=C PICTWXAWDCLLKO-UHFFFAOYSA-N 0.000 description 2
- COGACLHOGIPEFQ-UHFFFAOYSA-N 8-methylnonane-1-thiol Chemical compound CC(C)CCCCCCCS COGACLHOGIPEFQ-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 229920002873 Polyethylenimine Polymers 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000012986 chain transfer agent Substances 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 239000008199 coating composition Substances 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- WNAHIZMDSQCWRP-UHFFFAOYSA-N dodecane-1-thiol Chemical compound CCCCCCCCCCCCS WNAHIZMDSQCWRP-UHFFFAOYSA-N 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- QJAOYSPHSNGHNC-UHFFFAOYSA-N octadecane-1-thiol Chemical compound CCCCCCCCCCCCCCCCCCS QJAOYSPHSNGHNC-UHFFFAOYSA-N 0.000 description 2
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-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
- 239000010452 phosphate Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000004014 plasticizer Substances 0.000 description 2
- AXLMPTNTPOWPLT-UHFFFAOYSA-N prop-2-enyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCC=C AXLMPTNTPOWPLT-UHFFFAOYSA-N 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 229940113165 trimethylolpropane Drugs 0.000 description 2
- IICRHVJNHYVVKT-UHFFFAOYSA-N 2-(2-ethylhexylsulfanyl)propanoic acid Chemical compound CCCCC(CC)CSC(C)C(O)=O IICRHVJNHYVVKT-UHFFFAOYSA-N 0.000 description 1
- VVXUMDXOTNQMQQ-UHFFFAOYSA-N 2-butylsulfanylpropanoic acid Chemical compound CCCCSC(C)C(O)=O VVXUMDXOTNQMQQ-UHFFFAOYSA-N 0.000 description 1
- PJEKREDJLDASAE-UHFFFAOYSA-N 2-ethylhexyl 2-sulfanylpropanoate Chemical compound CCCCC(CC)COC(=O)C(C)S PJEKREDJLDASAE-UHFFFAOYSA-N 0.000 description 1
- JYCQQPHGFMYQCF-UHFFFAOYSA-N 4-tert-Octylphenol monoethoxylate Chemical class CC(C)(C)CC(C)(C)C1=CC=C(OCCO)C=C1 JYCQQPHGFMYQCF-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- XOCSLJFIGMLQLF-UHFFFAOYSA-N butyl 2-sulfanylpropanoate Chemical compound CCCCOC(=O)C(C)S XOCSLJFIGMLQLF-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 125000002993 cycloalkylene group Chemical group 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- URXNVXOMQQCBHS-UHFFFAOYSA-N naphthalene;sodium Chemical compound [Na].C1=CC=CC2=CC=CC=C21 URXNVXOMQQCBHS-UHFFFAOYSA-N 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000006223 plastic coating Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- AAMCVENDCXWDPJ-UHFFFAOYSA-N sulfanyl acetate Chemical compound CC(=O)OS AAMCVENDCXWDPJ-UHFFFAOYSA-N 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 description 1
- 239000000326 ultraviolet stabilizing agent Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6427497P | 1997-09-18 | 1997-09-18 | |
| US60/064,274 | 1997-09-18 | ||
| US09/023,522 US6201048B1 (en) | 1997-09-18 | 1998-02-13 | Stable waterborne polymer compositions containing poly(alkyleneimines) |
| US09/023,522 | 1998-02-13 | ||
| PCT/US1998/018609 WO1999014278A1 (en) | 1997-09-18 | 1998-09-04 | Stable waterborne polymer compositions containing poly(alkyleneimines) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2003522817A JP2003522817A (ja) | 2003-07-29 |
| JP2003522817A5 true JP2003522817A5 (enExample) | 2006-01-05 |
Family
ID=26697271
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000511821A Pending JP2003522817A (ja) | 1997-09-18 | 1998-09-04 | 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 (9)
| Country | Link |
|---|---|
| US (1) | US6201048B1 (enExample) |
| EP (1) | EP1019455A1 (enExample) |
| JP (1) | JP2003522817A (enExample) |
| KR (1) | KR20010024054A (enExample) |
| CN (1) | CN1290286A (enExample) |
| AU (1) | AU9306398A (enExample) |
| BR (1) | BR9812468A (enExample) |
| CA (1) | CA2303333A1 (enExample) |
| WO (1) | WO1999014278A1 (enExample) |
Families Citing this family (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6417267B1 (en) * | 1996-05-28 | 2002-07-09 | Eastman Chemical Company | Adhesive compositions containing stable amino-containing polymer latex blends |
| US6649679B1 (en) * | 1997-09-18 | 2003-11-18 | Eastman Chemical Company | Stable waterborne polymer compositions containing poly(alkylenimines) |
| CN100412149C (zh) * | 1999-07-08 | 2008-08-20 | 赫尔克里士公司 | 赋予材料期望性质的组合物 |
| US6310125B1 (en) | 2000-04-05 | 2001-10-30 | 3M Innovative Properties Company | Water-dispersed adhesive compositions |
| US6541550B1 (en) | 2000-04-05 | 2003-04-01 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesive compositions |
| US6306942B1 (en) | 2000-04-05 | 2001-10-23 | 3M Innovative Properties Company | Low temperature thermally activated water-dispersed adhesives |
| US6444737B1 (en) | 2000-04-05 | 2002-09-03 | 3M Innovative Properties Company | Water-dispersed polymer stabilizer |
| US7317053B1 (en) | 2000-07-10 | 2008-01-08 | Hercules Incorporated | Compositions for imparting desired properties to materials |
| US20030134973A1 (en) * | 2002-01-15 | 2003-07-17 | Chen Robert Gow-Sheng | Waterborne latexes for anti-corrosive and solvent-resistant coating compositions |
| EP1529815B1 (en) * | 2003-11-10 | 2015-03-25 | Rohm And Haas Company | Aqueous polymer dispersion and method for preparing a coated substrate |
| US8364670B2 (en) | 2004-12-28 | 2013-01-29 | Dt Labs, Llc | System, method and apparatus for electronically searching for an item |
| US8571075B2 (en) | 2010-11-29 | 2013-10-29 | Imra America, Inc. | Frequency comb source with large comb spacing |
| US20080199706A1 (en) * | 2007-02-21 | 2008-08-21 | Kristy Bacher | Polyurethane elastomeric adhesive composition and composite article formed therefrom |
| US9492063B2 (en) | 2009-06-18 | 2016-11-15 | Endochoice Innovation Center Ltd. | Multi-viewing element endoscope |
| EP2374836A1 (en) * | 2010-04-07 | 2011-10-12 | Nuplex Resins B.V. | Crosslinkable composition crosslinkable with a latent base catalyst. |
| US8809447B2 (en) | 2010-12-15 | 2014-08-19 | Eastman Chemical Company | Acetoacetate-functional monomers 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 |
| US8809446B2 (en) | 2010-12-15 | 2014-08-19 | Eastman Chemical Company | Substituted 3-oxopentanoates and their uses in coating compositions |
| EP2668236A1 (de) * | 2011-01-25 | 2013-12-04 | BASF Coatings GmbH | Basislacke für überbrannte mehrschichtlackierungen |
| CN105985724A (zh) | 2011-10-07 | 2016-10-05 | 树脂核动力工业有限公司 | 可交联组合物 |
| ES2669524T3 (es) | 2013-04-08 | 2018-05-28 | Allnex Netherlands B.V. | Composición reticulable por reacción de adición de Michael Real (RMA) |
| CA2927629C (en) | 2013-10-29 | 2021-04-13 | Dow Global Technologies Llc | An aqueous coating composition |
| US9505942B2 (en) * | 2014-06-23 | 2016-11-29 | Eastman Kodak Company | Preparation of patterned or electrically-conductive articles |
| EP3037486A1 (en) * | 2014-12-24 | 2016-06-29 | Akzo Nobel Coatings International B.V. | Method for protecting wood |
| CN107660227B (zh) | 2015-04-17 | 2021-07-16 | 欧尼克斯荷兰有限公司 | 地板涂料组合物 |
| EP3283588B1 (en) | 2015-04-17 | 2025-06-18 | Allnex Netherlands B.V. | A method for curing a rma crosslinkable resin coating, rma crosslinkable compositions and resins for use therein |
| CN107667146B (zh) | 2015-04-17 | 2021-01-01 | 欧尼克斯荷兰有限公司 | 制造可交联组合物的方法 |
| EP3283585B1 (en) | 2015-04-17 | 2023-11-15 | Allnex Netherlands B.V. | Adhesion promotor for real michael addition crosslinkable compositions |
| EP3824893B1 (en) | 2016-06-30 | 2023-11-01 | Elementis Specialties, Inc. | Crosslinkable coating compositions formulated with dormant carbamate initiator |
| EP3434701A1 (en) * | 2017-07-25 | 2019-01-30 | Arkema France | Stable aqueous polymer dispersions |
| EP3663326A1 (en) | 2018-12-04 | 2020-06-10 | Allnex Netherlands B.V. | Rma crosslinkable polymer |
| EP3712190A1 (en) | 2019-03-18 | 2020-09-23 | ALLNEX AUSTRIA GmbH | Binder for an aqueous coating composition |
| EP3689986A1 (en) | 2019-02-01 | 2020-08-05 | ALLNEX AUSTRIA GmbH | Binder for aqueous coating compositions |
| CA3125005A1 (en) | 2019-02-01 | 2020-08-06 | Allnex Austria Gmbh | Binder for an aqueous coating composition |
| JP7168595B2 (ja) * | 2020-02-04 | 2022-11-09 | 株式会社日本触媒 | 窯業建材用樹脂エマルション |
| CN111808228B (zh) * | 2020-07-15 | 2022-07-12 | 万华化学集团股份有限公司 | 超支化聚乙烯亚胺掺杂改性的丙烯酸乳液及其制备方法 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3642485A1 (de) | 1986-12-12 | 1988-06-23 | Basf Ag | Klebstoffe fuer verklebungen mit erhoehter waermestandfestigkeit |
| US5391624A (en) | 1992-02-10 | 1995-02-21 | S. C. Johnson & Son, Inc. | Thermosettable compositions |
| US5296530A (en) | 1992-07-28 | 1994-03-22 | Rohm And Haas Company | Method for light-assisted curing of coatings |
| JP2734905B2 (ja) | 1992-10-07 | 1998-04-02 | 日本電気株式会社 | 画像符号化装置 |
| US5525662A (en) | 1993-07-14 | 1996-06-11 | Rohm And Haas Company | Functionalization of polymers via enamine of acetoacetate |
| JP3114440B2 (ja) | 1993-07-22 | 2000-12-04 | 日産自動車株式会社 | スポット溶接装置 |
| US5770650A (en) * | 1995-10-06 | 1998-06-23 | Basf Corporation | Curable compositions for coatings |
| ATE176919T1 (de) | 1995-01-18 | 1999-03-15 | Dow Chemical Co | Schnellhärtende wässrige beschichtungszusammensetzung und farbe |
| US5783626A (en) * | 1995-04-12 | 1998-07-21 | Taylor; James Wayne | Waterborne polymers with pendant crosslinkable groups |
| US5891950A (en) * | 1996-05-28 | 1999-04-06 | Eastman Chemical Company | Use of stable amino-functional latexes in water-based inks |
| WO1997045468A1 (en) | 1996-05-28 | 1997-12-04 | Eastman Chemical Company | Surfactant-containing acetoacetoxy-functional and enamine-functional polymers |
| US5990224A (en) * | 1997-09-18 | 1999-11-23 | Eastman Chemical Company | Stable low foam waterborne polymer compositions containing poly(alkyleneimines) |
-
1998
- 1998-02-13 US US09/023,522 patent/US6201048B1/en not_active Expired - Lifetime
- 1998-09-04 WO PCT/US1998/018609 patent/WO1999014278A1/en not_active Ceased
- 1998-09-04 KR KR1020007002792A patent/KR20010024054A/ko not_active Withdrawn
- 1998-09-04 CA CA002303333A patent/CA2303333A1/en not_active Abandoned
- 1998-09-04 BR BR9812468-4A patent/BR9812468A/pt not_active IP Right Cessation
- 1998-09-04 AU AU93063/98A patent/AU9306398A/en not_active Abandoned
- 1998-09-04 JP JP2000511821A patent/JP2003522817A/ja active Pending
- 1998-09-04 EP EP98945927A patent/EP1019455A1/en not_active Withdrawn
- 1998-09-04 CN CN98811219A patent/CN1290286A/zh active Pending
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