JP5567242B2 - 自己触媒特性をもったポリオールおよびこれから製造されたポリウレタン製品 - Google Patents
自己触媒特性をもったポリオールおよびこれから製造されたポリウレタン製品 Download PDFInfo
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- JP5567242B2 JP5567242B2 JP2002526949A JP2002526949A JP5567242B2 JP 5567242 B2 JP5567242 B2 JP 5567242B2 JP 2002526949 A JP2002526949 A JP 2002526949A JP 2002526949 A JP2002526949 A JP 2002526949A JP 5567242 B2 JP5567242 B2 JP 5567242B2
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- polyol
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- polyurethane
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- 229910015900 BF3 Inorganic materials 0.000 description 1
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- PQYJRMFWJJONBO-UHFFFAOYSA-N Tris(2,3-dibromopropyl) phosphate Chemical compound BrCC(Br)COP(=O)(OCC(Br)CBr)OCC(Br)CBr PQYJRMFWJJONBO-UHFFFAOYSA-N 0.000 description 1
- 229920013701 VORANOL™ Polymers 0.000 description 1
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- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- LNWBFIVSTXCJJG-UHFFFAOYSA-N [diisocyanato(phenyl)methyl]benzene Chemical class C=1C=CC=CC=1C(N=C=O)(N=C=O)C1=CC=CC=C1 LNWBFIVSTXCJJG-UHFFFAOYSA-N 0.000 description 1
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- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
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- NEHMKBQYUWJMIP-NJFSPNSNSA-N chloro(114C)methane Chemical compound [14CH3]Cl NEHMKBQYUWJMIP-NJFSPNSNSA-N 0.000 description 1
- KYKAJFCTULSVSH-UHFFFAOYSA-N chloro(fluoro)methane Chemical class F[C]Cl KYKAJFCTULSVSH-UHFFFAOYSA-N 0.000 description 1
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- 239000006071 cream Substances 0.000 description 1
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- 229960002887 deanol Drugs 0.000 description 1
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- 238000007033 dehydrochlorination reaction Methods 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 229940087091 dichlorotetrafluoroethane Drugs 0.000 description 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
- IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 description 1
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- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
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- UHCBBWUQDAVSMS-UHFFFAOYSA-N fluoroethane Chemical compound CCF UHCBBWUQDAVSMS-UHFFFAOYSA-N 0.000 description 1
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- 150000002334 glycols Chemical class 0.000 description 1
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- 150000008282 halocarbons Chemical class 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- WMIYKQLTONQJES-UHFFFAOYSA-N hexafluoroethane Chemical compound FC(F)(F)C(F)(F)F WMIYKQLTONQJES-UHFFFAOYSA-N 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
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- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 description 1
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- 239000002184 metal Substances 0.000 description 1
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- RCZLVPFECJNLMZ-UHFFFAOYSA-N n,n,n',n'-tetraethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN(CC)CC RCZLVPFECJNLMZ-UHFFFAOYSA-N 0.000 description 1
- XFLSMWXCZBIXLV-UHFFFAOYSA-N n,n-dimethyl-2-(4-methylpiperazin-1-yl)ethanamine Chemical compound CN(C)CCN1CCN(C)CC1 XFLSMWXCZBIXLV-UHFFFAOYSA-N 0.000 description 1
- ZUHZZVMEUAUWHY-UHFFFAOYSA-N n,n-dimethylpropan-1-amine Chemical compound CCCN(C)C ZUHZZVMEUAUWHY-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 1
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 1
- QYSGYZVSCZSLHT-UHFFFAOYSA-N octafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)F QYSGYZVSCZSLHT-UHFFFAOYSA-N 0.000 description 1
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- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
- KAVGMUDTWQVPDF-UHFFFAOYSA-N perflubutane Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)(F)F KAVGMUDTWQVPDF-UHFFFAOYSA-N 0.000 description 1
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- TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 1
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- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- DHNUXDYAOVSGII-UHFFFAOYSA-N tris(1,3-dichloropropyl) phosphate Chemical compound ClCCC(Cl)OP(=O)(OC(Cl)CCCl)OC(Cl)CCCl DHNUXDYAOVSGII-UHFFFAOYSA-N 0.000 description 1
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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
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
-
- 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
- C08G18/48—Polyethers
- C08G18/50—Polyethers having heteroatoms other than oxygen
- C08G18/5021—Polyethers having heteroatoms other than oxygen having nitrogen
-
- 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
- C08G18/48—Polyethers
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/482—Mixtures of polyethers containing at least one polyether containing nitrogen
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US23248000P | 2000-09-13 | 2000-09-13 | |
| US60/232,480 | 2000-09-13 | ||
| PCT/US2001/025633 WO2002022702A1 (en) | 2000-09-13 | 2001-08-16 | Polyols with autocatalytic characteristics and polyurethane products made therefrom |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004509188A JP2004509188A (ja) | 2004-03-25 |
| JP2004509188A5 JP2004509188A5 (enExample) | 2008-10-02 |
| JP5567242B2 true JP5567242B2 (ja) | 2014-08-06 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2002526949A Expired - Fee Related JP5567242B2 (ja) | 2000-09-13 | 2001-08-16 | 自己触媒特性をもったポリオールおよびこれから製造されたポリウレタン製品 |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP1319034B1 (enExample) |
| JP (1) | JP5567242B2 (enExample) |
| KR (1) | KR100848190B1 (enExample) |
| CN (1) | CN1239554C (enExample) |
| AT (1) | ATE530588T1 (enExample) |
| AU (1) | AU2001284971A1 (enExample) |
| BR (1) | BR0114130B1 (enExample) |
| CA (1) | CA2422266C (enExample) |
| ES (1) | ES2371747T3 (enExample) |
| MX (1) | MXPA03002158A (enExample) |
| PT (1) | PT1319034E (enExample) |
| WO (1) | WO2002022702A1 (enExample) |
| ZA (1) | ZA200302807B (enExample) |
Families Citing this family (45)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1442070A1 (en) * | 2001-10-01 | 2004-08-04 | Dow Global Technologies Inc. | Autocatalytic polyols with gelling characteristics and polyurethane products made therefrom |
| DE10240186A1 (de) * | 2002-08-28 | 2004-03-11 | Basf Ag | Verfahren zur Herstellung von emissionsarmen Polyurethan-Weichschaumstoffen |
| DE10337319A1 (de) | 2003-08-12 | 2005-03-17 | Basf Ag | Verfahren zur Herstellung von Polyetheralkoholen |
| JPWO2005054327A1 (ja) * | 2003-12-05 | 2007-06-28 | 株式会社ブリヂストン | 軟質ポリウレタンフォーム及び布貼り軟質ポリウレタンフォーム製品 |
| PT1699842E (pt) * | 2003-12-23 | 2012-01-06 | Dow Global Technologies Llc | Processo para produzir produtos em poliuretano autocatalíticos utilizando polióis com aminas terciárias em extremidades |
| CN1898287B (zh) | 2003-12-23 | 2011-01-19 | 陶氏环球技术公司 | 含有亚胺键和叔胺的非短效催化剂以及用其制备的聚氨酯产品 |
| BRPI0506654B1 (pt) * | 2004-03-31 | 2016-01-26 | Dow Global Technologies Inc | composição de isocianato modificado com uretano, polímero de poliuretano hidrofílico, processos para fazer uma espuma e um gel de poliuretano hidrofílico, meio de crescimento horticultural e uso de uma composição de isocianato modificado com uretano |
| US8017686B2 (en) * | 2005-08-23 | 2011-09-13 | Akzo Nobel Coating International B.V. | Polyurethane dispersant resin |
| EP1951777B1 (en) | 2005-11-14 | 2017-05-17 | Dow Global Technologies LLC | Method of molding rigid polyurethane foams with enhanced thermal conductivity |
| EP2104696B1 (en) | 2006-12-21 | 2013-09-11 | Dow Global Technologies LLC | Polyurethane catalysis based on the combination of autocatalytic polyol and urea |
| KR100871433B1 (ko) * | 2008-01-24 | 2008-12-03 | 듀라케미 (주) | 고탄성 고내구성을 지닌 건축용 내외장재 조성물 및 그제조방법 |
| EP2403887A1 (en) * | 2009-03-05 | 2012-01-11 | Dow Global Technologies LLC (formerly Known As Dow Global Technologies Inc.) | Polyols from hppo and polyurethane products made therefrom |
| US8598248B2 (en) | 2010-07-16 | 2013-12-03 | Bayer Materialscience Llc | Flexible polyurethane foams made from alkoxylated natural oil |
| WO2013102053A1 (en) * | 2011-12-29 | 2013-07-04 | Dow Global Technologies Llc | Amine polyether polyols and polyurethane foam compositions made from cyclic amine compounds |
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| EP3078696A1 (de) | 2015-04-08 | 2016-10-12 | Evonik Degussa GmbH | Herstellung emissionsarmer polyurethane |
| PL3133097T3 (pl) | 2015-08-17 | 2023-01-09 | Evonik Operations Gmbh | Wytwarzanie miękkich pianek poliuretanowych o ulepszonej twardości |
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-
2001
- 2001-08-16 ES ES01964076T patent/ES2371747T3/es not_active Expired - Lifetime
- 2001-08-16 JP JP2002526949A patent/JP5567242B2/ja not_active Expired - Fee Related
- 2001-08-16 WO PCT/US2001/025633 patent/WO2002022702A1/en not_active Ceased
- 2001-08-16 KR KR1020037003668A patent/KR100848190B1/ko not_active Expired - Fee Related
- 2001-08-16 CN CNB018155634A patent/CN1239554C/zh not_active Expired - Fee Related
- 2001-08-16 AU AU2001284971A patent/AU2001284971A1/en not_active Abandoned
- 2001-08-16 PT PT01964076T patent/PT1319034E/pt unknown
- 2001-08-16 CA CA2422266A patent/CA2422266C/en not_active Expired - Fee Related
- 2001-08-16 EP EP01964076A patent/EP1319034B1/en not_active Expired - Lifetime
- 2001-08-16 AT AT01964076T patent/ATE530588T1/de not_active IP Right Cessation
- 2001-08-16 MX MXPA03002158A patent/MXPA03002158A/es active IP Right Grant
- 2001-08-16 BR BRPI0114130-9A patent/BR0114130B1/pt not_active IP Right Cessation
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Also Published As
| Publication number | Publication date |
|---|---|
| MXPA03002158A (es) | 2004-12-13 |
| BR0114130B1 (pt) | 2012-01-24 |
| BR0114130A (pt) | 2003-12-09 |
| ZA200302807B (en) | 2004-05-07 |
| AU2001284971A1 (en) | 2002-03-26 |
| CA2422266C (en) | 2011-07-12 |
| JP2004509188A (ja) | 2004-03-25 |
| ES2371747T3 (es) | 2012-01-09 |
| PT1319034E (pt) | 2011-12-21 |
| CA2422266A1 (en) | 2002-03-21 |
| ATE530588T1 (de) | 2011-11-15 |
| CN1239554C (zh) | 2006-02-01 |
| KR100848190B1 (ko) | 2008-07-24 |
| CN1455791A (zh) | 2003-11-12 |
| KR20030033058A (ko) | 2003-04-26 |
| EP1319034A1 (en) | 2003-06-18 |
| WO2002022702A1 (en) | 2002-03-21 |
| EP1319034B1 (en) | 2011-10-26 |
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