JP5478803B2 - 超高固形分含量を有するポリマーポリオール - Google Patents
超高固形分含量を有するポリマーポリオール Download PDFInfo
- Publication number
- JP5478803B2 JP5478803B2 JP2005224330A JP2005224330A JP5478803B2 JP 5478803 B2 JP5478803 B2 JP 5478803B2 JP 2005224330 A JP2005224330 A JP 2005224330A JP 2005224330 A JP2005224330 A JP 2005224330A JP 5478803 B2 JP5478803 B2 JP 5478803B2
- Authority
- JP
- Japan
- Prior art keywords
- polyol
- polymer
- polymer polyol
- radical polymerization
- chain transfer
- 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.)
- Expired - Fee Related
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- 239000003381 stabilizer Substances 0.000 claims abstract description 88
- 239000012986 chain transfer agent Substances 0.000 claims abstract description 76
- 239000000178 monomer Substances 0.000 claims abstract description 72
- 238000000034 method Methods 0.000 claims abstract description 33
- 239000007870 radical polymerization initiator Substances 0.000 claims abstract description 32
- 230000008569 process Effects 0.000 claims abstract description 14
- 238000010526 radical polymerization reaction Methods 0.000 claims abstract description 8
- 239000000203 mixture Substances 0.000 claims description 67
- 239000000047 product Substances 0.000 claims description 24
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- 125000000962 organic group Chemical group 0.000 claims description 11
- 239000005056 polyisocyanate Substances 0.000 claims description 11
- 229920001228 polyisocyanate Polymers 0.000 claims description 11
- 239000007788 liquid Substances 0.000 claims description 9
- 239000007795 chemical reaction product Substances 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 229920005601 base polymer Polymers 0.000 claims description 5
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- FVQMJJQUGGVLEP-UHFFFAOYSA-N (2-methylpropan-2-yl)oxy 2-ethylhexaneperoxoate Chemical compound CCCCC(CC)C(=O)OOOC(C)(C)C FVQMJJQUGGVLEP-UHFFFAOYSA-N 0.000 description 6
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- 229920002635 polyurethane Polymers 0.000 description 6
- 239000004814 polyurethane Substances 0.000 description 6
- OPQYOFWUFGEMRZ-UHFFFAOYSA-N tert-butyl 2,2-dimethylpropaneperoxoate Chemical compound CC(C)(C)OOC(=O)C(C)(C)C OPQYOFWUFGEMRZ-UHFFFAOYSA-N 0.000 description 6
- AQKYLAIZOGOPAW-UHFFFAOYSA-N 2-methylbutan-2-yl 2,2-dimethylpropaneperoxoate Chemical compound CCC(C)(C)OOC(=O)C(C)(C)C AQKYLAIZOGOPAW-UHFFFAOYSA-N 0.000 description 5
- 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 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 5
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 5
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229930182470 glycoside Natural products 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
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- 235000000346 sugar Nutrition 0.000 description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 description 4
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 4
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 4
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- 101000911390 Homo sapiens Coagulation factor VIII Proteins 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
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- 125000003118 aryl group Chemical group 0.000 description 4
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- GJBRNHKUVLOCEB-UHFFFAOYSA-N tert-butyl benzenecarboperoxoate Chemical compound CC(C)(C)OOC(=O)C1=CC=CC=C1 GJBRNHKUVLOCEB-UHFFFAOYSA-N 0.000 description 4
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- 239000003607 modifier Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229920003986 novolac Polymers 0.000 description 1
- QJAOYSPHSNGHNC-UHFFFAOYSA-N octadecane-1-thiol Chemical compound CCCCCCCCCCCCCCCCCCS QJAOYSPHSNGHNC-UHFFFAOYSA-N 0.000 description 1
- OEIJHBUUFURJLI-UHFFFAOYSA-N octane-1,8-diol Chemical compound OCCCCCCCCO OEIJHBUUFURJLI-UHFFFAOYSA-N 0.000 description 1
- KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- WPPLKRDOKPISSC-UHFFFAOYSA-N pentyl 2,2-dimethylpropaneperoxoate Chemical group CCCCCOOC(=O)C(C)(C)C WPPLKRDOKPISSC-UHFFFAOYSA-N 0.000 description 1
- 229920000233 poly(alkylene oxides) Polymers 0.000 description 1
- 239000004632 polycaprolactone Substances 0.000 description 1
- 229920001610 polycaprolactone Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- YPVDWEHVCUBACK-UHFFFAOYSA-N propoxycarbonyloxy propyl carbonate Chemical compound CCCOC(=O)OOC(=O)OCCC YPVDWEHVCUBACK-UHFFFAOYSA-N 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-N triphosphoric acid Chemical compound OP(O)(=O)OP(O)(=O)OP(O)(O)=O UNXRWKVEANCORM-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- VYCMMFXHSBVRGP-UHFFFAOYSA-N undecyl cyanate Chemical compound C(CCCCCCCCCC)OC#N VYCMMFXHSBVRGP-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 239000000811 xylitol Substances 0.000 description 1
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 description 1
- 235000010447 xylitol Nutrition 0.000 description 1
- 229960002675 xylitol Drugs 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/702—Isocyanates or isothiocyanates containing compounds having carbon-to-carbon double bonds; Telomers thereof
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- C08F283/06—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G on to polyethers, polyoxymethylenes or polyacetals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/06—Polymers provided for in subclass C08G
- C08F290/062—Polyethers
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/632—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers onto polyethers
-
- 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
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/636—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers characterised by the presence of a dispersion-stabiliser
-
- 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
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/671—Unsaturated compounds having only one group containing active hydrogen
- C08G18/672—Esters of acrylic or alkyl acrylic acid having only one group 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
- C08G18/67—Unsaturated compounds having active hydrogen
- C08G18/68—Unsaturated polyesters
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
-
- 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
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- 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
- C08G2110/0041—Foam properties having specified density
- C08G2110/005—< 50kg/m3
-
- 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)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Dispersion Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Graft Or Block Polymers (AREA)
- Polymerisation Methods In General (AREA)
- Biological Depolymerization Polymers (AREA)
- Polymerization Catalysts (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Polyethers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/909,493 US7759423B2 (en) | 2004-08-02 | 2004-08-02 | Polymer polyols with ultra-high solids contents |
| US10/909493 | 2004-08-02 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2006045568A JP2006045568A (ja) | 2006-02-16 |
| JP2006045568A5 JP2006045568A5 (enExample) | 2008-09-18 |
| JP5478803B2 true JP5478803B2 (ja) | 2014-04-23 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2005224330A Expired - Fee Related JP5478803B2 (ja) | 2004-08-02 | 2005-08-02 | 超高固形分含量を有するポリマーポリオール |
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| EP (1) | EP1624005B1 (enExample) |
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| CA (1) | CA2513480C (enExample) |
| DE (1) | DE602005004457T2 (enExample) |
| ES (1) | ES2299925T3 (enExample) |
| MX (1) | MXPA05008065A (enExample) |
| PL (1) | PL1624005T3 (enExample) |
| PT (1) | PT1624005E (enExample) |
| RU (1) | RU2005124357A (enExample) |
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| RU2380388C2 (ru) | 2005-07-07 | 2010-01-27 | Санио Кемикал Индастриз, Лтд. | Полиольная композиция, содержащая диспергированные мелкие частицы, способ получения полимерного полиола и способ получения полиуретановой смолы |
| US20070060690A1 (en) | 2005-09-09 | 2007-03-15 | Bayer Materialscience Llc | Low viscosity polymer polyols characterized by a high hydroxyl number |
| DE102006029588A1 (de) * | 2006-06-26 | 2007-12-27 | Bayer Materialscience Ag | Verfahren zum Strippen von Polymerpolyolen |
| CA2656799A1 (en) * | 2006-07-05 | 2008-01-10 | Dow Global Technologies Inc. | Copolymer polyols and a process for the production thereof |
| US20080071056A1 (en) * | 2006-09-14 | 2008-03-20 | Borst Joseph P | Method of forming a graft polyol and polyurethane article formed from the graft polyol |
| EP2066717B2 (de) † | 2006-09-15 | 2013-11-20 | Basf Se | Verfahren zur herstellung von polyurethan-hartschaumstoffen |
| KR100749339B1 (ko) | 2007-03-27 | 2007-08-21 | 티엠에스 주식회사 | 높은 고형분 함량을 가지는 폴리머 폴리올의 제조방법 |
| US20080262119A1 (en) * | 2007-04-04 | 2008-10-23 | Jeroen Patrick Michel Bouwman | Process for preparing polymer polyols |
| EP2194097B1 (en) | 2007-09-28 | 2013-07-03 | Sanyo Chemical Industries, Ltd. | Polymer polyol, method for producing the same, and method for producing polyurethane resin |
| JP4851503B2 (ja) * | 2007-10-10 | 2012-01-11 | 三洋化成工業株式会社 | 微粒子分散ポリオールの製造方法及びポリウレタン樹脂の製造方法 |
| US8822581B2 (en) * | 2008-06-19 | 2014-09-02 | Dow Global Technologies Llc | Melt dispersion process for making polymer polyols |
| ES2420612T3 (es) | 2009-09-03 | 2013-08-26 | Shell Internationale Research Maatschappij B.V. | Proceso para preparar un poliol polímero |
| EP2601231A1 (en) * | 2010-08-03 | 2013-06-12 | Shell Internationale Research Maatschappij B.V. | Process for preparing polymer polyols |
| SG187177A1 (en) * | 2010-08-03 | 2013-02-28 | Shell Int Research | Process for preparing polymer polyols |
| CN101962427B (zh) * | 2010-09-28 | 2012-07-25 | 山东蓝星东大化工有限责任公司 | 高固含量低粘度聚合物多元醇的合成方法 |
| SG11201400544RA (en) | 2011-09-12 | 2014-04-28 | Basf Se | Graft polyol and method of forming the same |
| CN103030750A (zh) * | 2011-10-09 | 2013-04-10 | 中国石油化工集团公司 | 制备聚合物多元醇的方法 |
| US8946313B2 (en) | 2011-12-16 | 2015-02-03 | Bayer Materialscience Llc | Hybrid PHD/PMPO polyols for polyurethane foam applications |
| US10066047B2 (en) | 2012-02-02 | 2018-09-04 | Covestro Llc | Polyurethane foams with decreased aldehyde emissions, a process for preparing these foams and a method for decreasing aldehyde in polyurethane foams |
| US20140066536A1 (en) | 2012-08-30 | 2014-03-06 | Bayer Materialscience Llc | Polymer polyols having improved quality |
| WO2014055282A1 (en) | 2012-10-05 | 2014-04-10 | Dow Global Technologies Llc | Macromer and process for making polymer polyols |
| US20140249274A1 (en) * | 2013-03-04 | 2014-09-04 | Bayer Materialscience Llc | High functionality isocyanates as polymer polyol stabilizers and the polymer polyols prepared from these stabilizers |
| US9163099B2 (en) | 2013-03-08 | 2015-10-20 | Bayer Materialscience Llc | Polybutadiene modified polymer polyols, foams prepared from polybutadiene modified polymer polyols, and processes for the production thereof |
| CN104045791A (zh) * | 2013-03-11 | 2014-09-17 | 中国石油化工集团公司 | 聚合物多元醇的制备方法 |
| US8987396B2 (en) * | 2013-03-15 | 2015-03-24 | Bayer Materialscience Llc | Active polymer polyols and a process for their production |
| US9840603B2 (en) * | 2013-09-13 | 2017-12-12 | Dow Global Technologies Llc | PIPA based combustion-modified flexible foam |
| CN103601860B (zh) * | 2013-10-24 | 2016-03-30 | 江苏钟山化工有限公司 | 一种聚合物多元醇的制法及其制得的聚合物多元醇和用途 |
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| US9951174B2 (en) | 2015-05-20 | 2018-04-24 | Covestro Llc | Polyol compositions, a process for the production of these polyol compositions, and their use in the production of open celled polyurethane foams having high airflow |
| US9505881B1 (en) | 2015-06-10 | 2016-11-29 | Covestro Llc | Polymer polyol compositions, a process for preparing these novel polymer polyol compositions, flexible foams prepared from these novel polymer polyols and a process for the preparation of these flexible foams |
| JP6936810B2 (ja) * | 2016-03-31 | 2021-09-22 | ダウ グローバル テクノロジーズ エルエルシー | 単分散分散ポリマー粒子を有するポリマーポリオールを作製するプロセス |
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| US10767008B2 (en) | 2017-01-16 | 2020-09-08 | Covestro Llc | Polymer polyols comprising amine based polyether polyols and a process for preparing these polymer polyols |
| CN110402263B (zh) | 2017-03-15 | 2022-06-07 | 科思创有限公司 | 具有降低的温度敏感性的粘弹性聚氨酯泡沫 |
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| TWI650159B (zh) * | 2017-11-27 | 2019-02-11 | 三芳化學工業股份有限公司 | 球體結構及其製造方法 |
| US10479862B2 (en) * | 2017-12-07 | 2019-11-19 | Covestro Llc | Amine based polymer polyol stabilizers |
| CN109925683A (zh) * | 2017-12-15 | 2019-06-25 | 三芳化学工业股份有限公司 | 球体结构及其制造方法 |
| US10526484B2 (en) | 2017-12-20 | 2020-01-07 | Covestro Llc | Dithiocarbonate containing polyols as polymer polyol stabilizers |
| KR101998849B1 (ko) * | 2018-03-02 | 2019-07-11 | 금호석유화학 주식회사 | 저점도를 갖는 고고형분 폴리머 폴리올의 제조방법 |
| CA3095462A1 (en) * | 2018-03-28 | 2019-10-03 | Benjamin Lund | Thiol-acrylate polymers, methods of synthesis thereof and use in additive manufacturing technologies |
| US11739177B2 (en) | 2018-04-20 | 2023-08-29 | Adaptive 3D Technologies | Sealed isocyanates |
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| US10793692B2 (en) | 2018-10-24 | 2020-10-06 | Covestro Llc | Viscoelastic flexible foams comprising hydroxyl-terminated prepolymers |
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| US11911956B2 (en) | 2018-11-21 | 2024-02-27 | Adaptive 3D Technologies | Using occluding fluids to augment additive manufacturing processes |
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| CN113557251B (zh) * | 2020-02-25 | 2024-02-20 | 雷普索尔有限公司 | 用于制备聚合物多元醇的方法 |
| US11572433B2 (en) | 2021-03-12 | 2023-02-07 | Covestro Llc | In-situ formed polyols, a process for their preparation, foams prepared from these in-situ formed polyols and a process for their preparation |
| CN115232256B (zh) * | 2021-04-22 | 2024-07-23 | 中国石油化工股份有限公司 | 一种高回弹聚合物多元醇的制备方法及得到的聚合物多元醇与应用 |
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-
2004
- 2004-08-02 US US10/909,493 patent/US7759423B2/en not_active Expired - Lifetime
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2005
- 2005-07-20 DE DE602005004457T patent/DE602005004457T2/de not_active Expired - Lifetime
- 2005-07-20 ES ES05015715T patent/ES2299925T3/es not_active Expired - Lifetime
- 2005-07-20 EP EP05015715A patent/EP1624005B1/en not_active Expired - Lifetime
- 2005-07-20 AT AT05015715T patent/ATE384749T1/de not_active IP Right Cessation
- 2005-07-20 PT PT05015715T patent/PT1624005E/pt unknown
- 2005-07-20 PL PL05015715T patent/PL1624005T3/pl unknown
- 2005-07-26 CA CA2513480A patent/CA2513480C/en not_active Expired - Fee Related
- 2005-07-28 MX MXPA05008065A patent/MXPA05008065A/es active IP Right Grant
- 2005-08-01 RU RU2005124357/04A patent/RU2005124357A/ru not_active Application Discontinuation
- 2005-08-01 KR KR1020050070327A patent/KR101285912B1/ko not_active Expired - Fee Related
- 2005-08-02 CN CNB2005101038505A patent/CN100500736C/zh not_active Expired - Fee Related
- 2005-08-02 BR BRPI0503174A patent/BRPI0503174B1/pt not_active IP Right Cessation
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Also Published As
| Publication number | Publication date |
|---|---|
| KR101285912B1 (ko) | 2013-07-12 |
| MXPA05008065A (es) | 2006-02-07 |
| PL1624005T3 (pl) | 2008-07-31 |
| RU2005124357A (ru) | 2007-02-10 |
| BRPI0503174B1 (pt) | 2016-03-15 |
| CN100500736C (zh) | 2009-06-17 |
| ES2299925T3 (es) | 2008-06-01 |
| ATE384749T1 (de) | 2008-02-15 |
| EP1624005B1 (en) | 2008-01-23 |
| DE602005004457T2 (de) | 2009-01-22 |
| US7759423B2 (en) | 2010-07-20 |
| CA2513480C (en) | 2012-11-27 |
| CN1740210A (zh) | 2006-03-01 |
| JP2006045568A (ja) | 2006-02-16 |
| EP1624005A1 (en) | 2006-02-08 |
| US20060025492A1 (en) | 2006-02-02 |
| HK1089195A1 (zh) | 2006-11-24 |
| KR20060049009A (ko) | 2006-05-18 |
| PT1624005E (pt) | 2008-04-08 |
| CA2513480A1 (en) | 2006-02-02 |
| DE602005004457D1 (de) | 2008-03-13 |
| BRPI0503174A (pt) | 2006-03-14 |
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