CA2640381A1 - Composition made from a diisocyanate and a monoamine and process for preparing it - Google Patents
Composition made from a diisocyanate and a monoamine and process for preparing it Download PDFInfo
- Publication number
- CA2640381A1 CA2640381A1 CA002640381A CA2640381A CA2640381A1 CA 2640381 A1 CA2640381 A1 CA 2640381A1 CA 002640381 A CA002640381 A CA 002640381A CA 2640381 A CA2640381 A CA 2640381A CA 2640381 A1 CA2640381 A1 CA 2640381A1
- Authority
- CA
- Canada
- Prior art keywords
- weight
- composition according
- polyisocyanate
- water
- polyol
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 58
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 8
- 125000005442 diisocyanate group Chemical group 0.000 title description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 43
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 32
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 32
- 229920005862 polyol Polymers 0.000 claims description 26
- 150000003077 polyols Chemical class 0.000 claims description 26
- 238000000034 method Methods 0.000 claims description 25
- 239000006260 foam Substances 0.000 claims description 19
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 claims description 12
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 239000011496 polyurethane foam Substances 0.000 claims description 10
- 125000006353 oxyethylene group Chemical group 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 150000002430 hydrocarbons Chemical class 0.000 claims description 7
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 6
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 claims description 6
- 239000004604 Blowing Agent Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- 229920000570 polyether Polymers 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 238000000518 rheometry Methods 0.000 claims description 3
- 239000004215 Carbon black (E152) Substances 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 230000001413 cellular effect Effects 0.000 abstract description 2
- 239000000047 product Substances 0.000 description 14
- PGYPOBZJRVSMDS-UHFFFAOYSA-N loperamide hydrochloride Chemical compound Cl.C=1C=CC=CC=1C(C=1C=CC=CC=1)(C(=O)N(C)C)CCN(CC1)CCC1(O)C1=CC=C(Cl)C=C1 PGYPOBZJRVSMDS-UHFFFAOYSA-N 0.000 description 12
- 239000006228 supernatant Substances 0.000 description 7
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 5
- -1 oxyethylene, oxypropylene Chemical group 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 238000007086 side reaction Methods 0.000 description 5
- 150000001412 amines Chemical class 0.000 description 4
- 238000012512 characterization method Methods 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 229910017053 inorganic salt Inorganic materials 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000002666 chemical blowing agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 150000005827 chlorofluoro hydrocarbons Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- XXKOQQBKBHUATC-UHFFFAOYSA-N cyclohexylmethylcyclohexane Chemical compound C1CCCCC1CC1CCCCC1 XXKOQQBKBHUATC-UHFFFAOYSA-N 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- YUWFEBAXEOLKSG-UHFFFAOYSA-N hexamethylbenzene Chemical group CC1=C(C)C(C)=C(C)C(C)=C1C YUWFEBAXEOLKSG-UHFFFAOYSA-N 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000004094 surface-active 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
- C08G18/08—Processes
-
- 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
- C08G18/0838—Manufacture of polymers in the presence of non-reactive compounds
- C08G18/0842—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents
- C08G18/0861—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers
- C08G18/0866—Manufacture of polymers in the presence of non-reactive compounds in the presence of liquid diluents in the presence of a dispersing phase for the polymers or a phase dispersed in the polymers the dispersing or dispersed phase being an aqueous medium
-
- 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
-
- 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
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/285—Nitrogen containing compounds
- C08G18/2865—Compounds having only one primary or secondary amino group; Ammonia
-
- 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
-
- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0008—Foam properties flexible
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Polyurethanes Or Polyureas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP06111114 | 2006-03-14 | ||
| EP06111114.2 | 2006-03-14 | ||
| PCT/EP2007/051335 WO2007104623A1 (en) | 2006-03-14 | 2007-02-12 | Composition made from a diisocyanate and a monoamine and process for preparing it |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2640381A1 true CA2640381A1 (en) | 2007-09-20 |
Family
ID=36940234
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002640381A Abandoned CA2640381A1 (en) | 2006-03-14 | 2007-02-12 | Composition made from a diisocyanate and a monoamine and process for preparing it |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US8143364B2 (enExample) |
| EP (1) | EP1996634B1 (enExample) |
| JP (1) | JP2009529597A (enExample) |
| KR (1) | KR20080112293A (enExample) |
| CN (1) | CN101400713B (enExample) |
| AT (1) | ATE438671T1 (enExample) |
| AU (1) | AU2007224541B2 (enExample) |
| BR (1) | BRPI0708263A2 (enExample) |
| CA (1) | CA2640381A1 (enExample) |
| DE (1) | DE602007001876D1 (enExample) |
| ES (1) | ES2327583T3 (enExample) |
| RU (1) | RU2441034C2 (enExample) |
| WO (1) | WO2007104623A1 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2072549A1 (en) * | 2007-12-19 | 2009-06-24 | Huntsman International Llc | Novel composition from a polyisocyanate and a polyether monoamine |
| BRPI0906674B1 (pt) * | 2008-02-14 | 2019-01-08 | Huntsman Int Llc | material elastomérico, e, processos para preparar e para fabricar um material elastomérico |
| US9018333B2 (en) * | 2009-04-21 | 2015-04-28 | Huntsman International Llc | Polyisocyanate composition |
| EP2440615B1 (en) * | 2009-06-09 | 2013-04-03 | Huntsman International LLC | Materials comprising a matrix and process for preparing them |
| US20130012609A1 (en) * | 2010-03-31 | 2013-01-10 | Dow Global Technologies Llc | Professional grade one component polyurethane foam with non-liquefied inert propellant |
| JP5972005B2 (ja) * | 2012-03-28 | 2016-08-17 | 株式会社ネオス | 水溶性消泡剤および低泡性加工油剤 |
| JP6732913B2 (ja) * | 2016-07-15 | 2020-07-29 | 関西ペイント株式会社 | 塗料組成物 |
| JP7113011B2 (ja) * | 2017-06-20 | 2022-08-04 | 株式会社ブリヂストン | 軟質ポリウレタンフォーム用組成物、軟質ポリウレタンフォーム並びに車両用シートパッド |
| JP7408586B2 (ja) * | 2019-02-15 | 2024-01-05 | 関西ペイント株式会社 | 塗料組成物 |
| JP7413287B2 (ja) * | 2019-02-15 | 2024-01-15 | 関西ペイント株式会社 | 粘性調整剤及び塗料組成物 |
| MX2021010983A (es) * | 2019-03-12 | 2021-10-13 | Huntsman Petrochemical Llc | Dispersantes elaborados a partir de isocianatos y aminas. |
| CN113474427B (zh) | 2019-03-26 | 2022-06-21 | 关西涂料株式会社 | 涂料组合物 |
| CN114349932B (zh) * | 2022-01-17 | 2024-05-31 | 亚士创能科技(上海)股份有限公司 | 可用于颜料包覆的聚合物、聚合物包覆颜料及其制备方法和无机涂料 |
Family Cites Families (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL209758A (enExample) * | 1955-08-12 | |||
| US2925387A (en) * | 1958-07-21 | 1960-02-16 | Standard Oil Co | Method of preparing ureido grease-thickener concentrate and lubricating greases containing same |
| GB956056A (en) * | 1961-10-02 | 1964-04-22 | Ici Ltd | Improvements in or relating to the manufacture of foamed polyurethanes |
| GB1169737A (en) | 1966-04-29 | 1969-11-05 | Internat Synthetic Rubber Comp | Thermoplastic Elastomer Block Polymers |
| US3401027A (en) * | 1967-04-10 | 1968-09-10 | Chevron Res | Light hydrocarbon liquids containing a jellifying agent comprising polyureas |
| GB1250401A (enExample) | 1968-01-08 | 1971-10-20 | ||
| US3741911A (en) * | 1970-12-21 | 1973-06-26 | Hart Chemical Ltd | Phosphate-free detergent composition |
| DE2418075A1 (de) | 1974-04-13 | 1975-10-30 | Bayer Ag | Thermoplastische polyurethan-elastomere mit verbesserter verarbeitbarkeit |
| NL176864C (nl) * | 1976-11-25 | 1985-06-17 | Akzo Nv | Werkwijze voor de bereiding van een thixotrope bekledingssamenstelling. |
| DE2738268A1 (de) * | 1977-08-25 | 1979-03-08 | Basf Ag | Hydrophobe polyurethanschaumstoffe zur oelabsorption |
| DE2902469A1 (de) * | 1979-01-23 | 1980-07-31 | Bayer Ag | Suspensionen von isocyanatoharnstoffen in isocyanatpraepolymeren, ein verfahren zu ihrer herstellung, sowie ihre verwendung bei der herstellung von hochmolekularen polyurethankunststoffen |
| US4261845A (en) * | 1980-01-18 | 1981-04-14 | Texaco Development Corporation | Novel polyureas and their use as grease thickening agents |
| DE3021293A1 (de) | 1980-06-06 | 1981-12-24 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von elastischen polyurethanschaumstoffen |
| DE3132760A1 (de) | 1981-08-19 | 1983-03-03 | Basf Ag, 6700 Ludwigshafen | Verfahren zur verbesserung der fliessfaehigkeit von polyurethan-elastomeren |
| DE3303442A1 (de) * | 1983-02-02 | 1984-08-16 | Optimol-Ölwerke GmbH, 8000 München | Schmierfettzusammensetzung, ihre herstellung und verwendung |
| US4499254A (en) * | 1984-02-13 | 1985-02-12 | Texaco Inc. | Reaction injection molded elastomers containing high molecular weight organic acids |
| US4751253A (en) * | 1986-10-06 | 1988-06-14 | Tylenda Eugene J | Method of preparing dimensionally stable, flexible urethane foam and the foam produced thereby |
| US4791146A (en) * | 1986-10-06 | 1988-12-13 | Tylenda Eugene J | Method of preparing dimensionally stable, flexible urethane foam and the foam produced thereby |
| GB8701993D0 (en) * | 1987-01-29 | 1987-03-04 | Bp Chem Int Ltd | Polyurethane foams |
| DE3724555A1 (de) * | 1987-07-24 | 1989-02-02 | Basf Ag | Viskositaetsregulierende stoffe fuer einkomponentige polyurethansysteme |
| US5145591A (en) * | 1989-07-07 | 1992-09-08 | Nippon Oil Co., Ltd. | Diurea grease composition |
| US5364909A (en) * | 1992-07-23 | 1994-11-15 | Arco Chemical Technology, L.P. | Graft polymer compositions containing mono-amine functionalized polyoxyalkylene ethers |
| DE4236901A1 (de) * | 1992-10-31 | 1994-05-05 | Herberts Gmbh | Als Rheologie-Beeinflusser geeignete Zusammensetzung, Verfahren zu deren Herstellung und deren Verwendung in Überzugsmitteln |
| GB9311838D0 (en) * | 1993-06-08 | 1993-07-28 | Ici Plc | Process for making flexible foams |
| GB9404127D0 (en) | 1994-03-03 | 1994-04-20 | Polyol Int Bv | Process for producing a soft, flexible, hot molded poyurethane foam |
| JP3312476B2 (ja) | 1994-03-22 | 2002-08-05 | 日本ポリウレタン工業株式会社 | 軟質ウレタンフォームの製造方法 |
| JP3500700B2 (ja) | 1994-05-31 | 2004-02-23 | 旭硝子株式会社 | 非フォーム状ポリウレタン樹脂の製造方法 |
| US5591779A (en) * | 1994-11-22 | 1997-01-07 | Imperial Chemical Industries Plc | Process for making flexible foams |
| JP2002511114A (ja) * | 1997-07-09 | 2002-04-09 | ハンツマン・アイシーアイ・ケミカルズ・エルエルシー | 圧縮された親水性ポリウレタンフォーム |
| US6218462B1 (en) * | 1999-12-03 | 2001-04-17 | Bayer Corporation | Liquid ultra-high molecular weight polyurethane plasticizers |
| US6355721B1 (en) * | 1999-12-03 | 2002-03-12 | Bayer Coporation | High molecular weight liquid, non-functional polyether polyurethane plasticizers |
| AU5626801A (en) * | 2000-04-12 | 2001-10-23 | Akzo Nobel Nv | Aqueous two-component cross-linkable composition |
| DE10111793A1 (de) * | 2001-03-12 | 2002-09-26 | Borchers Gmbh | Neue Polyurethane und ihre Verwendung zur Verdickung wässriger Systeme |
| DE10126647A1 (de) | 2001-06-01 | 2002-12-12 | Basf Coatings Ag | Rheologiehilfsmittel, Verfahren zu seiner Herstellung und seine Verwendung |
| WO2004014980A1 (en) | 2002-08-02 | 2004-02-19 | Huntsman International Llc | Polyols |
| US20050131095A1 (en) | 2002-08-02 | 2005-06-16 | Jianming Yu | Novel polyols |
| DE10241853B3 (de) * | 2002-09-09 | 2004-01-22 | Byk-Chemie Gmbh | Polymeres Harnstoffurethan als Rheologiesteuerungsmittel und Verfahren zur Herstellung |
| TWI314564B (en) * | 2003-08-27 | 2009-09-11 | Great Eastern Resins Ind Co Ltd | Water dispersible polyisocyanate composition bearing urea and/or biuret and its uses as aqueous resin adhesive |
| US20070148471A1 (en) * | 2004-09-01 | 2007-06-28 | Rukavina Thomas G | Impact resistant polyurethane and poly(ureaurethane) articles and methods of making the same |
-
2007
- 2007-02-12 CA CA002640381A patent/CA2640381A1/en not_active Abandoned
- 2007-02-12 BR BRPI0708263-0A patent/BRPI0708263A2/pt not_active IP Right Cessation
- 2007-02-12 US US12/282,540 patent/US8143364B2/en not_active Expired - Fee Related
- 2007-02-12 KR KR1020087024966A patent/KR20080112293A/ko not_active Ceased
- 2007-02-12 CN CN2007800088754A patent/CN101400713B/zh not_active Expired - Fee Related
- 2007-02-12 EP EP07704514A patent/EP1996634B1/en not_active Not-in-force
- 2007-02-12 JP JP2008558751A patent/JP2009529597A/ja active Pending
- 2007-02-12 WO PCT/EP2007/051335 patent/WO2007104623A1/en not_active Ceased
- 2007-02-12 AU AU2007224541A patent/AU2007224541B2/en not_active Ceased
- 2007-02-12 AT AT07704514T patent/ATE438671T1/de not_active IP Right Cessation
- 2007-02-12 RU RU2008140514/04A patent/RU2441034C2/ru not_active IP Right Cessation
- 2007-02-12 DE DE602007001876T patent/DE602007001876D1/de active Active
- 2007-02-12 ES ES07704514T patent/ES2327583T3/es active Active
Also Published As
| Publication number | Publication date |
|---|---|
| US20090069456A1 (en) | 2009-03-12 |
| CN101400713B (zh) | 2012-05-30 |
| JP2009529597A (ja) | 2009-08-20 |
| EP1996634B1 (en) | 2009-08-05 |
| DE602007001876D1 (de) | 2009-09-17 |
| RU2008140514A (ru) | 2010-04-20 |
| EP1996634A1 (en) | 2008-12-03 |
| US8143364B2 (en) | 2012-03-27 |
| BRPI0708263A2 (pt) | 2011-05-24 |
| WO2007104623A1 (en) | 2007-09-20 |
| KR20080112293A (ko) | 2008-12-24 |
| ATE438671T1 (de) | 2009-08-15 |
| AU2007224541B2 (en) | 2011-10-20 |
| RU2441034C2 (ru) | 2012-01-27 |
| AU2007224541A1 (en) | 2007-09-20 |
| CN101400713A (zh) | 2009-04-01 |
| ES2327583T3 (es) | 2009-10-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |
Effective date: 20140212 |