JP2006526044A - Ｐｉｐａ−ポリオールの製造方法 - Google Patents
Ｐｉｐａ−ポリオールの製造方法 Download PDFInfo
- Publication number
- JP2006526044A JP2006526044A JP2006505493A JP2006505493A JP2006526044A JP 2006526044 A JP2006526044 A JP 2006526044A JP 2006505493 A JP2006505493 A JP 2006505493A JP 2006505493 A JP2006505493 A JP 2006505493A JP 2006526044 A JP2006526044 A JP 2006526044A
- Authority
- JP
- Japan
- Prior art keywords
- polyol
- weight
- equivalent
- polyisocyanate
- equivalent 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.)
- Withdrawn
Links
- 229920005862 polyol Polymers 0.000 title claims abstract description 142
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 150000003077 polyols Chemical class 0.000 claims abstract description 127
- 239000000203 mixture Substances 0.000 claims abstract description 64
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 43
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 43
- 239000011236 particulate material Substances 0.000 claims abstract description 17
- 238000000034 method Methods 0.000 claims abstract description 15
- 125000006353 oxyethylene group Chemical group 0.000 claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 11
- 125000005702 oxyalkylene group Chemical group 0.000 claims abstract description 7
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 claims abstract description 6
- 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 29
- 238000002156 mixing Methods 0.000 claims description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 11
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 11
- 229920005830 Polyurethane Foam Polymers 0.000 claims description 7
- 239000011496 polyurethane foam Substances 0.000 claims description 7
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 6
- 229920000570 polyether Polymers 0.000 claims description 6
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 239000000839 emulsion Substances 0.000 claims description 2
- 239000011541 reaction mixture Substances 0.000 claims description 2
- 241001425800 Pipa Species 0.000 description 19
- 239000006260 foam Substances 0.000 description 14
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
- 229940125782 compound 2 Drugs 0.000 description 10
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 9
- 229940125904 compound 1 Drugs 0.000 description 9
- 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 8
- -1 carbodiimide modified MDI Chemical class 0.000 description 7
- 239000004814 polyurethane Substances 0.000 description 7
- 229920002635 polyurethane Polymers 0.000 description 7
- 238000002360 preparation method Methods 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 239000003999 initiator Substances 0.000 description 6
- 238000011068 loading method Methods 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 229920000768 polyamine Polymers 0.000 description 5
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 125000005442 diisocyanate group Chemical group 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000004604 Blowing Agent Substances 0.000 description 3
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 239000004202 carbamide Substances 0.000 description 3
- 150000001718 carbodiimides Chemical class 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 108010026961 trifluoroacetyl-leucyl-alanyl-4-trifluoromethylanilide Proteins 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 229920000265 Polyparaphenylene Polymers 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical compound C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- AICOOMRHRUFYCM-ZRRPKQBOSA-N oxazine, 1 Chemical compound C([C@@H]1[C@H](C(C[C@]2(C)[C@@H]([C@H](C)N(C)C)[C@H](O)C[C@]21C)=O)CC1=CC2)C[C@H]1[C@@]1(C)[C@H]2N=C(C(C)C)OC1 AICOOMRHRUFYCM-ZRRPKQBOSA-N 0.000 description 2
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 2
- PBWHJRFXUPLZDS-UHFFFAOYSA-N (1-Ethylpropyl)benzene Chemical compound CCC(CC)C1=CC=CC=C1 PBWHJRFXUPLZDS-UHFFFAOYSA-N 0.000 description 1
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
- VOZKAJLKRJDJLL-UHFFFAOYSA-N 2,4-diaminotoluene Chemical compound CC1=CC=C(N)C=C1N VOZKAJLKRJDJLL-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 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 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 210000004027 cell Anatomy 0.000 description 1
- 230000001413 cellular effect Effects 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- YMHQVDAATAEZLO-UHFFFAOYSA-N cyclohexane-1,1-diamine Chemical compound NC1(N)CCCCC1 YMHQVDAATAEZLO-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 210000000497 foam cell Anatomy 0.000 description 1
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000013518 molded foam Substances 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920002959 polymer blend Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 150000003141 primary amines Chemical group 0.000 description 1
- 150000003335 secondary amines Chemical group 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 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
- C08G18/28—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
- C08G18/409—Dispersions of polymers of C08G in organic compounds having 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
- C08G18/40—High-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
- C08G18/08—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
- C08G18/0871—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 organic
- C08G18/0876—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 organic the dispersing or dispersed phase being a polyol
-
- 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
- C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
- C08G18/76—Polyisocyanates or polyisothiocyanates cyclic aromatic
- C08G18/7657—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings
- C08G18/7664—Polyisocyanates or polyisothiocyanates cyclic aromatic containing two or more aromatic rings containing alkylene polyphenyl groups
-
- 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
- C08G2110/0041—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)
- 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP03010560 | 2003-05-12 | ||
| PCT/EP2004/050369 WO2004099281A1 (en) | 2003-05-12 | 2004-03-26 | Process for making a pipa-polyol |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010202079A Division JP2011006698A (ja) | 2003-05-12 | 2010-09-09 | Ｐｉｐａポリオールの製造方法 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2006526044A true JP2006526044A (ja) | 2006-11-16 |
| JP2006526044A5 JP2006526044A5 (enExample) | 2010-04-02 |
Family
ID=33427048
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006505493A Withdrawn JP2006526044A (ja) | 2003-05-12 | 2004-03-26 | Ｐｉｐａ−ポリオールの製造方法 |
| JP2010202079A Withdrawn JP2011006698A (ja) | 2003-05-12 | 2010-09-09 | Ｐｉｐａポリオールの製造方法 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010202079A Withdrawn JP2011006698A (ja) | 2003-05-12 | 2010-09-09 | Ｐｉｐａポリオールの製造方法 |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20060058410A1 (enExample) |
| EP (1) | EP1631605A1 (enExample) |
| JP (2) | JP2006526044A (enExample) |
| KR (1) | KR20060009322A (enExample) |
| CN (1) | CN100379783C (enExample) |
| AR (1) | AR044311A1 (enExample) |
| AU (1) | AU2004236428B2 (enExample) |
| BR (1) | BRPI0409646A (enExample) |
| CA (1) | CA2520890A1 (enExample) |
| MX (1) | MXPA05012176A (enExample) |
| RU (1) | RU2357976C2 (enExample) |
| TW (1) | TW200424224A (enExample) |
| WO (1) | WO2004099281A1 (enExample) |
| ZA (1) | ZA200508778B (enExample) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010516877A (ja) * | 2007-01-31 | 2010-05-20 | バイエル・マテリアルサイエンス・アクチェンゲゼルシャフト | ナノウレア分散体 |
| JP2014514428A (ja) * | 2011-05-09 | 2014-06-19 | ダウ グローバル テクノロジーズ エルエルシー | 微粒子の高濃度ポリイソシアネート重付加物／ポリウレタン−尿素ポリオール |
| JP2016531193A (ja) * | 2013-09-13 | 2016-10-06 | ダウ グローバル テクノロジーズ エルエルシー | Ｐｉｐａポリオール系の従来の軟質発泡体 |
| JP2016537483A (ja) * | 2013-09-13 | 2016-12-01 | ダウ グローバル テクノロジーズ エルエルシー | 分散ウレタン変性ポリイソシアヌレートを含有する揺変性ポリオール組成物 |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102005050701A1 (de) * | 2005-10-22 | 2007-05-03 | Bayer Materialscience Ag | Verfahren zur Herstellung von PIPA-Polyolen |
| JP5224715B2 (ja) | 2007-04-27 | 2013-07-03 | 三井化学株式会社 | 制振吸音材、およびその製造方法 |
| EP2275466A1 (de) * | 2009-07-16 | 2011-01-19 | Bayer MaterialScience AG | Polyharnstoff-basierter Gewebekleber |
| DK2673311T3 (en) * | 2011-02-09 | 2014-12-01 | Bayer Materialscience Ag | Tissue adhesive based on trifunctional aspartate |
| WO2012107375A1 (de) * | 2011-02-09 | 2012-08-16 | Bayer Materialscience Ag | Gewebekleber auf basis stickstoffmodifizierter aspartate |
| ES2544935T3 (es) * | 2011-04-19 | 2015-09-07 | Medical Adhesive Revolution Gmbh | Adhesivo médico para detener hemorragias |
| WO2013148252A1 (en) * | 2012-03-30 | 2013-10-03 | Dow Global Technologies Llc | Tin free polymer polyols |
| MX2014004304A (es) * | 2013-04-09 | 2015-05-07 | Dow Quimica Mexicana S A De C V | Composicion adhesiva de curado rapido. |
| AU2014318648B2 (en) | 2013-09-13 | 2017-09-07 | Dow Global Technologies Llc | PIPA polyol based viscoelastic foams |
| EP3263620B1 (en) * | 2016-06-30 | 2019-03-13 | Polytex Sportbeläge Produktions-GmbH | Pu flooring production for a sports field |
| MX2019003055A (es) * | 2016-09-29 | 2019-06-06 | Dow Global Technologies Llc | Espuma de poliuretano flexible de inflamabilidad reducida. |
| EP3519478B1 (en) | 2016-09-30 | 2020-07-08 | Dow Global Technologies LLC | Polyol compositions |
| CA3044897A1 (en) | 2016-11-28 | 2018-05-31 | Univation Technologies, Llc | Producing a polyethylene polymer |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05287046A (ja) * | 1992-04-06 | 1993-11-02 | Mitsui Toatsu Chem Inc | 発泡成形性の良い半硬質ポリウレタンフォームの製造法 |
| JPH06256454A (ja) * | 1993-02-02 | 1994-09-13 | Imperial Chem Ind Plc <Ici> | 軟質フォームの製造方法 |
| JP2003501501A (ja) * | 1999-05-31 | 2003-01-14 | ハンツマン・インターナショナル・エルエルシー | ポリマー変性ポリオール類、これらをポリウレタン生成物の製造に使用する方法 |
| JP2003501502A (ja) * | 1999-05-31 | 2003-01-14 | ハンツマン・インターナショナル・エルエルシー | Ｐｉｐａポリオールの製造方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4049590A (en) * | 1975-11-24 | 1977-09-20 | Basf Aktiengesellschaft | Manufacture of polyurethane compositions |
| CA1051271A (en) * | 1978-01-20 | 1979-03-27 | Paul Gorse | Folding door |
| GB2072204B (en) * | 1980-02-14 | 1983-12-07 | Rowlands J P | Polymer-modified polyols useful in polyurethane manufacture |
| US4374209A (en) * | 1980-10-01 | 1983-02-15 | Interchem International S.A. | Polymer-modified polyols useful in polyurethane manufacture |
| EP0072096B2 (en) * | 1981-08-11 | 1988-04-06 | Imperial Chemical Industries Plc | Polymer-modified polyols, a method of forming them, their use in the manufacture of polyurethane products and the products so obtained |
| DE3270603D1 (en) * | 1981-10-28 | 1986-05-22 | Ici Plc | Polymer-modified polyols |
| GB8317354D0 (en) * | 1983-06-27 | 1983-07-27 | Ici Plc | Polymer-modified polyols |
| US4559366A (en) * | 1984-03-29 | 1985-12-17 | Jaquelyn P. Pirri | Preparation of microcellular polyurethane elastomers |
| US4863976A (en) * | 1988-04-26 | 1989-09-05 | Dow Chemical Company | Polyurethane foam prepared using high functionalilty cell openers |
| US5068280A (en) * | 1989-09-12 | 1991-11-26 | The Dow Chemical Company | Polyurethane and/or polyurea dispersions in active hydrogen-containing compositions |
| US5292778A (en) * | 1992-11-20 | 1994-03-08 | Woodbridge Foam Corporation | Polymer-modified polyol dispersions and processes for production and use thereof |
| US5565498A (en) * | 1993-02-02 | 1996-10-15 | Imperial Chemical Industries Plc | Process for making flexible foams |
| US5484820A (en) * | 1994-08-05 | 1996-01-16 | The Dow Chemical Company | Polyurethane foam for packaging applications |
| CN1131256C (zh) * | 1997-03-25 | 2003-12-17 | 亨茨曼Ici化学品有限公司 | 可挠性聚氨基甲酸酯发泡体的制法 |
| US6066683A (en) * | 1998-04-03 | 2000-05-23 | Lyondell Chemical Worldwide, Inc. | Molded and slab polyurethane foam prepared from double metal cyanide complex-catalyzed polyoxyalkylene polyols and polyols suitable for the preparation thereof |
| TW568921B (en) * | 1998-08-07 | 2004-01-01 | Huntsman Int Llc | Process for preparing a moulded flexible polyurethane foam |
| CN1126770C (zh) * | 1999-03-17 | 2003-11-05 | 亨兹曼国际有限公司 | 制备模塑聚氨酯材料的方法 |
| DE19962911C2 (de) * | 1999-12-23 | 2002-11-21 | Bayer Ag | Flammwidriger HR-Kaltformschaum mit reduzierter Rauchgasintensität und -toxizität |
-
2004
- 2004-03-26 CN CNB2004800126714A patent/CN100379783C/zh not_active Expired - Fee Related
- 2004-03-26 RU RU2005138510/04A patent/RU2357976C2/ru not_active IP Right Cessation
- 2004-03-26 BR BRPI0409646-0A patent/BRPI0409646A/pt not_active Application Discontinuation
- 2004-03-26 WO PCT/EP2004/050369 patent/WO2004099281A1/en not_active Ceased
- 2004-03-26 JP JP2006505493A patent/JP2006526044A/ja not_active Withdrawn
- 2004-03-26 EP EP04723615A patent/EP1631605A1/en not_active Withdrawn
- 2004-03-26 KR KR1020057021355A patent/KR20060009322A/ko not_active Abandoned
- 2004-03-26 AU AU2004236428A patent/AU2004236428B2/en not_active Ceased
- 2004-03-26 CA CA002520890A patent/CA2520890A1/en not_active Abandoned
- 2004-03-26 MX MXPA05012176A patent/MXPA05012176A/es active IP Right Grant
- 2004-04-08 TW TW093109812A patent/TW200424224A/zh unknown
- 2004-05-11 AR ARP040101616A patent/AR044311A1/es active IP Right Grant
-
2005
- 2005-10-28 ZA ZA200508778A patent/ZA200508778B/en unknown
- 2005-11-03 US US11/267,921 patent/US20060058410A1/en not_active Abandoned
-
2010
- 2010-09-09 JP JP2010202079A patent/JP2011006698A/ja not_active Withdrawn
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH05287046A (ja) * | 1992-04-06 | 1993-11-02 | Mitsui Toatsu Chem Inc | 発泡成形性の良い半硬質ポリウレタンフォームの製造法 |
| JPH06256454A (ja) * | 1993-02-02 | 1994-09-13 | Imperial Chem Ind Plc <Ici> | 軟質フォームの製造方法 |
| JP2003501501A (ja) * | 1999-05-31 | 2003-01-14 | ハンツマン・インターナショナル・エルエルシー | ポリマー変性ポリオール類、これらをポリウレタン生成物の製造に使用する方法 |
| JP2003501502A (ja) * | 1999-05-31 | 2003-01-14 | ハンツマン・インターナショナル・エルエルシー | Ｐｉｐａポリオールの製造方法 |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010516877A (ja) * | 2007-01-31 | 2010-05-20 | バイエル・マテリアルサイエンス・アクチェンゲゼルシャフト | ナノウレア分散体 |
| JP2014514428A (ja) * | 2011-05-09 | 2014-06-19 | ダウ グローバル テクノロジーズ エルエルシー | 微粒子の高濃度ポリイソシアネート重付加物／ポリウレタン−尿素ポリオール |
| JP2016531193A (ja) * | 2013-09-13 | 2016-10-06 | ダウ グローバル テクノロジーズ エルエルシー | Ｐｉｐａポリオール系の従来の軟質発泡体 |
| JP2016537483A (ja) * | 2013-09-13 | 2016-12-01 | ダウ グローバル テクノロジーズ エルエルシー | 分散ウレタン変性ポリイソシアヌレートを含有する揺変性ポリオール組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2520890A1 (en) | 2004-11-18 |
| WO2004099281A9 (en) | 2006-02-23 |
| ZA200508778B (en) | 2007-06-27 |
| AU2004236428B2 (en) | 2008-05-01 |
| AR044311A1 (es) | 2005-09-07 |
| BRPI0409646A (pt) | 2006-04-25 |
| MXPA05012176A (es) | 2006-02-08 |
| CN100379783C (zh) | 2008-04-09 |
| US20060058410A1 (en) | 2006-03-16 |
| EP1631605A1 (en) | 2006-03-08 |
| CN1784442A (zh) | 2006-06-07 |
| JP2011006698A (ja) | 2011-01-13 |
| RU2357976C2 (ru) | 2009-06-10 |
| RU2005138510A (ru) | 2006-07-27 |
| KR20060009322A (ko) | 2006-01-31 |
| AU2004236428A1 (en) | 2004-11-18 |
| TW200424224A (en) | 2004-11-16 |
| AU2004236428A2 (en) | 2004-11-18 |
| WO2004099281A1 (en) | 2004-11-18 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2011006698A (ja) | Ｐｉｐａポリオールの製造方法 | |
| JP5367674B2 (ja) | フリーライズまたはスラブストック軟質ポリウレタンフォームの製造方法 | |
| EP3044247B1 (en) | Pipa based combustion-modified polyurethane foam | |
| JP2002522581A (ja) | 軟質ポリウレタンフォームの製造方法 | |
| JP4109545B2 (ja) | 軟質ポリウレタンフォームの製造方法 | |
| US6579912B2 (en) | Process for preparing a flexible polyurethane foam | |
| US20030158281A1 (en) | Process for preparing a flexible polyurethane foam | |
| EP1527117B1 (en) | Polyols | |
| AU726924B2 (en) | New isocyanate-terminated prepolymers | |
| RU2386644C2 (ru) | Способ получения пипп-полиола | |
| CN101945910A (zh) | 具有高的硬嵌段含量的弹性体材料和制备它们的方法 | |
| CN109937220A (zh) | 具有足够硬度和良好挠性的聚氨酯泡沫 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20070322 |
|
| A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20091013 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20091016 |
|
| A601 | Written request for extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A601 Effective date: 20100118 |
|
| A602 | Written permission of extension of time |
Free format text: JAPANESE INTERMEDIATE CODE: A602 Effective date: 20100125 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100205 |
|
| A524 | Written submission of copy of amendment under article 19 pct |
Free format text: JAPANESE INTERMEDIATE CODE: A524 Effective date: 20100205 |
|
| A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20100305 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100603 |
|
| A02 | Decision of refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A02 Effective date: 20100706 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100909 |
|
| A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20100909 |
|
| A911 | Transfer to examiner for re-examination before appeal (zenchi) |
Free format text: JAPANESE INTERMEDIATE CODE: A911 Effective date: 20101026 |
|
| A912 | Re-examination (zenchi) completed and case transferred to appeal board |
Free format text: JAPANESE INTERMEDIATE CODE: A912 Effective date: 20101126 |
|
| A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20120419 |