CA2174085A1 - Reactive diluent aldimine oxazolidines - Google Patents
Reactive diluent aldimine oxazolidinesInfo
- Publication number
- CA2174085A1 CA2174085A1 CA002174085A CA2174085A CA2174085A1 CA 2174085 A1 CA2174085 A1 CA 2174085A1 CA 002174085 A CA002174085 A CA 002174085A CA 2174085 A CA2174085 A CA 2174085A CA 2174085 A1 CA2174085 A1 CA 2174085A1
- Authority
- CA
- Canada
- Prior art keywords
- group
- hydrogen atoms
- groups
- composition
- compound
- 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.)
- Abandoned
Links
- -1 aldimine oxazolidines Chemical class 0.000 title claims abstract description 25
- 239000003085 diluting agent Substances 0.000 title description 22
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 33
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 21
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 19
- 150000003573 thiols Chemical group 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 18
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 17
- 150000002367 halogens Chemical group 0.000 claims abstract description 17
- 238000002360 preparation method Methods 0.000 claims abstract description 17
- 125000000524 functional group Chemical group 0.000 claims abstract description 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 14
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims abstract description 14
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims abstract description 13
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 12
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 11
- 125000000732 arylene group Chemical group 0.000 claims abstract description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical group CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 9
- 125000003118 aryl group Chemical group 0.000 claims abstract description 9
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 8
- 125000002993 cycloalkylene group Chemical group 0.000 claims abstract description 8
- 239000011248 coating agent Substances 0.000 claims description 28
- 238000000576 coating method Methods 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 17
- 150000004705 aldimines Chemical group 0.000 claims description 9
- 229910052757 nitrogen Inorganic materials 0.000 claims description 9
- 125000004429 atom Chemical group 0.000 claims description 8
- 239000000853 adhesive Substances 0.000 claims description 6
- 230000001070 adhesive effect Effects 0.000 claims description 6
- 239000012948 isocyanate Substances 0.000 claims description 5
- 150000002513 isocyanates Chemical class 0.000 claims description 5
- 239000003822 epoxy resin Substances 0.000 claims description 4
- 229920000647 polyepoxide Polymers 0.000 claims description 4
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 claims description 3
- 239000000976 ink Substances 0.000 claims description 3
- 239000000565 sealant Substances 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 8
- 125000000160 oxazolidinyl group Chemical group 0.000 claims 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000009472 formulation Methods 0.000 description 7
- 239000002904 solvent Substances 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- AMIMRNSIRUDHCM-UHFFFAOYSA-N Isopropylaldehyde Chemical compound CC(C)C=O AMIMRNSIRUDHCM-UHFFFAOYSA-N 0.000 description 2
- 241001024304 Mino Species 0.000 description 2
- 241000282320 Panthera leo Species 0.000 description 2
- NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 2
- 229910000564 Raney nickel Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000012263 liquid product Substances 0.000 description 2
- 229920000582 polyisocyanurate Polymers 0.000 description 2
- 239000011495 polyisocyanurate Substances 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 241001136792 Alle Species 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- 229920001730 Moisture cure polyurethane Polymers 0.000 description 1
- YFONKFDEZLYQDH-OPQQBVKSSA-N N-[(1R,2S)-2,6-dimethyindan-1-yl]-6-[(1R)-1-fluoroethyl]-1,3,5-triazine-2,4-diamine Chemical compound C[C@@H](F)C1=NC(N)=NC(N[C@H]2C3=CC(C)=CC=C3C[C@@H]2C)=N1 YFONKFDEZLYQDH-OPQQBVKSSA-N 0.000 description 1
- 101150050192 PIGM gene Proteins 0.000 description 1
- 229930040373 Paraformaldehyde Natural products 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 235000014328 Schoenoplectus acutus var occidentalis Nutrition 0.000 description 1
- 244000136421 Scirpus acutus Species 0.000 description 1
- 235000014326 Scirpus californicus Nutrition 0.000 description 1
- 235000017913 Scirpus lacustris Nutrition 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 150000007982 azolidines Chemical class 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000004710 electron pair approximation Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 1
- MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229920002866 paraformaldehyde Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3296—Hydroxyamines being in latent form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Epoxy Resins (AREA)
- Paints Or Removers (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/143,470 US5466769A (en) | 1993-10-26 | 1993-10-26 | Reactive diluent aldimine oxazolidines |
| US08/143,470 | 1993-10-26 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2174085A1 true CA2174085A1 (en) | 1995-05-04 |
Family
ID=22504227
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002174085A Abandoned CA2174085A1 (en) | 1993-10-26 | 1994-10-21 | Reactive diluent aldimine oxazolidines |
Country Status (8)
| Country | Link |
|---|---|
| US (4) | US5466769A (OSRAM) |
| EP (1) | EP0748344A1 (OSRAM) |
| JP (1) | JPH09504328A (OSRAM) |
| KR (1) | KR960705864A (OSRAM) |
| AU (1) | AU8051194A (OSRAM) |
| CA (1) | CA2174085A1 (OSRAM) |
| TW (1) | TW287161B (OSRAM) |
| WO (1) | WO1995011933A1 (OSRAM) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5466769A (en) * | 1993-10-26 | 1995-11-14 | Angus Chemical Company | Reactive diluent aldimine oxazolidines |
| US5977285A (en) * | 1997-08-07 | 1999-11-02 | Akzo Nobel N.V. | Sprayable coating compositions comprising oxazolidines, isocyanates and hydroxyl or amine functional resins |
| US6545117B1 (en) | 1997-08-07 | 2003-04-08 | Akzo Noble N.V. | Sprayable coating compositions comprising an oxazolidine functional compound, an isocyanate functional compound, and a compound selected from a mercapto and a sulfonic acid functional compound |
| US5955199A (en) * | 1997-09-26 | 1999-09-21 | Ashland Inc. | Imine-containing curative for two component polyurethane structural adhesives |
| US6001274A (en) * | 1999-01-04 | 1999-12-14 | Gabriel J. Farkas | Composition to detoxify and to convert formaldehyde in gaseous state and in aqueous and non-aqueous solutions |
| WO2001023103A1 (en) * | 1999-09-29 | 2001-04-05 | American Spray Coatings | Method, solution and paint for forming a metallic mirror surface or metallic luster |
| US7111950B2 (en) * | 1999-09-29 | 2006-09-26 | American Spray Coatings | Method for forming a metallic mirror surface on a receiving surface |
| CA2284342C (en) | 1999-09-29 | 2011-11-01 | Meaney, Daniel J., Jr. | Method, solution and paint for forming a metallic mirror surface or metallic luster |
| US6362302B1 (en) | 1999-11-29 | 2002-03-26 | Carl E. Boddie | Method and compositions for spray molding polyurethane three dimensional objects |
| KR100366564B1 (ko) * | 2000-05-23 | 2003-01-09 | 삼화페인트공업주식회사 | 잠재성 경화재의 제조방법 및 그 경화제를 포함하는폴리우레탄 일액형도료 조성물 |
| AU2005284095B2 (en) * | 2004-09-17 | 2011-04-07 | Sonec B.V. | Coating composition based on thiol-nco curing |
| KR100777429B1 (ko) * | 2005-08-04 | 2007-11-28 | 에스케이씨 주식회사 | 저장성이 우수한 습기경화형 폴리우레탄 조성물 및 그제조방법 |
| EP1772447A1 (de) * | 2005-09-30 | 2007-04-11 | Sika Technology AG | Aldimine mit aktivem Wasserstoff aufweisenden Reaktivgruppen sowie deren Verwendung |
| WO2009114329A2 (en) * | 2008-03-07 | 2009-09-17 | Dow Global Technologies Inc. | Polyurethanes having low levels of aldehyde emissions |
| US8236263B2 (en) * | 2008-11-17 | 2012-08-07 | Dow Global Technologies Llc | Methods for reducing airborne formaldehyde |
| EP2327733A1 (en) * | 2009-10-30 | 2011-06-01 | Sika Technology AG | Non-Crystallising Bis-Oxazolidines |
| AU2014209986A1 (en) | 2013-01-22 | 2015-06-11 | Sika Technology Ag | Liquid-applied waterproofing membrane for roofs comprising a long-chain aldimine |
| BR112015015286B1 (pt) | 2013-01-22 | 2020-12-22 | Sika Technology Ag | membrana de impermeabilização de uma parte líquidoaplicada de cura por umidade, uso da mesma em um telhado, sistema e método de impermeabilização, estrutura de telhado impermeável e uso de trialdimina em uma membrana de impermeabilização |
| CN104884494B (zh) | 2013-01-22 | 2018-07-20 | Sika技术股份公司 | 用于屋顶的包含两种不同醛亚胺的液体施加防水膜 |
| US10415250B2 (en) | 2013-01-22 | 2019-09-17 | Sika Technology Ag | Liquid-applied waterproofing membrane comprising oxazolidine and aldimine |
| KR102243100B1 (ko) | 2013-08-26 | 2021-04-22 | 헌츠만 페트로케미칼 엘엘씨 | 아민 촉매 내의 알데하이드의 감소 |
| CN105026438B (zh) | 2013-10-01 | 2021-07-06 | 亨斯迈石油化学有限责任公司 | 降低胺催化剂中的醛 |
| US10766994B2 (en) | 2014-12-31 | 2020-09-08 | Huntsman Petrochemical Llc | Reduction of aldehydes in amine catalysts |
| IL243898B (en) * | 2015-02-03 | 2020-04-30 | Seagrave Coatings Corp | Coating compositions |
| BR112019016446A2 (pt) | 2017-02-09 | 2020-04-07 | Dow Global Technologies Llc | espuma de poliuretano com baixos níveis de emissões de aldeído |
| US11136444B2 (en) | 2017-02-20 | 2021-10-05 | Dow Global Technologies Llc | Polyurethanes having reduced aldehyde emissions |
| CN107043447B (zh) * | 2017-04-19 | 2019-12-03 | 江苏湘园化工有限公司 | 一种非对称潜伏性聚氨酯固化剂及其制备方法 |
| CN112585184B (zh) | 2018-08-02 | 2023-04-11 | 陶氏环球技术有限责任公司 | 减少聚氨酯泡沫中醛排放的方法 |
| EP3830157B1 (en) | 2018-08-02 | 2024-12-04 | Dow Global Technologies, LLC | Methods for reducing aldehyde emissions in polyurethane foams |
| EP3830164B1 (en) | 2018-08-02 | 2023-12-06 | Dow Global Technologies LLC | Methods for reducing aldehyde emissions in polyurethane foams |
| EP3830160B1 (en) | 2018-08-02 | 2025-06-25 | Dow Global Technologies LLC | Methods for reducing aldehyde emissions in polyurethane foams |
| US11453742B2 (en) | 2018-08-02 | 2022-09-27 | Dow Global Technologies Llc | Methods for reducing aldehyde emissions in polyurethane foams |
| JP7421638B2 (ja) | 2019-08-30 | 2024-01-24 | ダウ グローバル テクノロジーズ エルエルシー | ポリエーテルポリオールおよびポリウレタン発泡体のアルデヒド排出量を減少させるための方法 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3743626A (en) * | 1968-10-18 | 1973-07-03 | Rohm & Haas | Hydrocurable oxazolidine-isocyanate compositions |
| US4054717A (en) * | 1975-11-19 | 1977-10-18 | Rohm And Haas Company | Mineral paper coating compositions containing latex and amphoteric polymer |
| US4046744A (en) * | 1976-07-28 | 1977-09-06 | Rohm And Haas Company | Thermosetting coatings based on ketoxime-blocked isocyanates and oxazolidines |
| JPS6029730B2 (ja) * | 1977-08-06 | 1985-07-12 | 三菱電機株式会社 | エポキシ樹脂組成物 |
| DE3019356A1 (de) * | 1980-05-21 | 1981-11-26 | Sika AG, vorm. Kaspar Winkler & Co., 8048 Zürich | Neue, adimin- und oxazolidingruppen aufweisende verbindungen sowie verfahren zu deren herstellung und ihre verwendung als haerter fuer polyisocyanate |
| US4772716A (en) * | 1986-07-14 | 1988-09-20 | Ciba-Geigy Corporation | Oxazolidines containing silane groups |
| US5104955A (en) * | 1987-04-27 | 1992-04-14 | The Sherwin-Williams Company | Hydroxy-functional polyester diluents as additives in coating compositions |
| US5223174A (en) * | 1991-08-15 | 1993-06-29 | Angus Chemical Company | Moisture-scavenging iminoalcohol-oxazolidine mixtures |
| US5214086A (en) * | 1991-09-04 | 1993-05-25 | Basf Corporation | Coating compositions which may be ambient cured |
| US5466769A (en) * | 1993-10-26 | 1995-11-14 | Angus Chemical Company | Reactive diluent aldimine oxazolidines |
-
1993
- 1993-10-26 US US08/143,470 patent/US5466769A/en not_active Expired - Fee Related
-
1994
- 1994-10-11 US US08/321,227 patent/US5591819A/en not_active Expired - Fee Related
- 1994-10-11 US US08/321,436 patent/US5506329A/en not_active Expired - Fee Related
- 1994-10-21 JP JP7512721A patent/JPH09504328A/ja active Pending
- 1994-10-21 AU AU80511/94A patent/AU8051194A/en not_active Abandoned
- 1994-10-21 WO PCT/US1994/012041 patent/WO1995011933A1/en not_active Ceased
- 1994-10-21 EP EP94931423A patent/EP0748344A1/en not_active Withdrawn
- 1994-10-21 CA CA002174085A patent/CA2174085A1/en not_active Abandoned
- 1994-10-21 KR KR1019960702093A patent/KR960705864A/ko not_active Withdrawn
- 1994-10-27 TW TW083109916A patent/TW287161B/zh active
-
1995
- 1995-11-13 US US08/556,025 patent/US5571922A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| AU8051194A (en) | 1995-05-22 |
| EP0748344A1 (en) | 1996-12-18 |
| US5466769A (en) | 1995-11-14 |
| TW287161B (OSRAM) | 1996-10-01 |
| EP0748344A4 (en) | 1996-09-19 |
| JPH09504328A (ja) | 1997-04-28 |
| KR960705864A (ko) | 1996-11-08 |
| US5506329A (en) | 1996-04-09 |
| US5571922A (en) | 1996-11-05 |
| US5591819A (en) | 1997-01-07 |
| WO1995011933A1 (en) | 1995-05-04 |
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