JP2004231962A5 - - Google Patents
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- Publication number
- JP2004231962A5 JP2004231962A5 JP2004019319A JP2004019319A JP2004231962A5 JP 2004231962 A5 JP2004231962 A5 JP 2004231962A5 JP 2004019319 A JP2004019319 A JP 2004019319A JP 2004019319 A JP2004019319 A JP 2004019319A JP 2004231962 A5 JP2004231962 A5 JP 2004231962A5
- Authority
- JP
- Japan
- Prior art keywords
- rigid
- bis
- semi
- polyurethane foam
- urea
- 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.)
- Granted
Links
- 229920005830 Polyurethane Foam Polymers 0.000 claims 11
- 239000011496 polyurethane foam Substances 0.000 claims 11
- 229910052797 bismuth Inorganic materials 0.000 claims 7
- 239000003054 catalyst Substances 0.000 claims 5
- 125000002524 organometallic group Chemical group 0.000 claims 5
- -1 bismuth carboxylate Chemical class 0.000 claims 4
- 239000011541 reaction mixture Substances 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 claims 3
- 239000005056 polyisocyanate Substances 0.000 claims 3
- 229920001228 polyisocyanate Polymers 0.000 claims 3
- 229920005862 polyol Polymers 0.000 claims 3
- 150000003077 polyols Chemical class 0.000 claims 3
- FDAWBMYJDPMZIA-UHFFFAOYSA-N 2-piperidin-1-ylethylurea Chemical compound NC(=O)NCCN1CCCCC1 FDAWBMYJDPMZIA-UHFFFAOYSA-N 0.000 claims 2
- 239000004604 Blowing Agent Substances 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 150000007942 carboxylates Chemical class 0.000 claims 2
- 238000006555 catalytic reaction Methods 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 2
- 239000012970 tertiary amine catalyst Substances 0.000 claims 2
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical group C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 claims 2
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 claims 1
- ICWWRTAZKLRCOD-UHFFFAOYSA-N 1,1-bis[2-(dimethylamino)ethyl]urea Chemical compound CN(C)CCN(C(N)=O)CCN(C)C ICWWRTAZKLRCOD-UHFFFAOYSA-N 0.000 claims 1
- FEBQQCUMEMUCCG-UHFFFAOYSA-N 1,1-dimethyl-3-pyrrolidin-1-ylurea Chemical compound CN(C)C(=O)NN1CCCC1 FEBQQCUMEMUCCG-UHFFFAOYSA-N 0.000 claims 1
- BXKZTHFWTIEYSG-UHFFFAOYSA-N 1,3-bis(2-morpholin-4-ylethyl)urea Chemical compound C1COCCN1CCNC(=O)NCCN1CCOCC1 BXKZTHFWTIEYSG-UHFFFAOYSA-N 0.000 claims 1
- XTUPRKONHBQJHJ-UHFFFAOYSA-N 1,3-bis(3-morpholin-4-ylpropyl)urea Chemical compound C1COCCN1CCCNC(=O)NCCCN1CCOCC1 XTUPRKONHBQJHJ-UHFFFAOYSA-N 0.000 claims 1
- ASPVUEBKOVRENF-UHFFFAOYSA-N 1,3-bis(3-piperidin-1-ylpropyl)urea Chemical compound C1CCCCN1CCCNC(=O)NCCCN1CCCCC1 ASPVUEBKOVRENF-UHFFFAOYSA-N 0.000 claims 1
- BRLHUTYQAUOXSB-UHFFFAOYSA-N 1,3-bis[2-(dimethylamino)ethyl]urea Chemical compound CN(C)CCNC(=O)NCCN(C)C BRLHUTYQAUOXSB-UHFFFAOYSA-N 0.000 claims 1
- FCQPNTOQFPJCMF-UHFFFAOYSA-N 1,3-bis[3-(dimethylamino)propyl]urea Chemical compound CN(C)CCCNC(=O)NCCCN(C)C FCQPNTOQFPJCMF-UHFFFAOYSA-N 0.000 claims 1
- VDEJXKBCCWFYRL-UHFFFAOYSA-N 2-morpholin-4-ylethylurea Chemical compound NC(=O)NCCN1CCOCC1 VDEJXKBCCWFYRL-UHFFFAOYSA-N 0.000 claims 1
- UMLZJALTCYNZCE-UHFFFAOYSA-N 3-morpholin-4-ylpropylurea Chemical compound NC(=O)NCCCN1CCOCC1 UMLZJALTCYNZCE-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- YPIFGDQKSSMYHQ-UHFFFAOYSA-N 7,7-dimethyloctanoic acid Chemical compound CC(C)(C)CCCCCC(O)=O YPIFGDQKSSMYHQ-UHFFFAOYSA-N 0.000 claims 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 claims 1
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 claims 1
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/353,642 US6825238B2 (en) | 2003-01-29 | 2003-01-29 | Low acid organometallic catalyst for the production of flexible, semi-flexible and rigid polyurethane foams |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2004231962A JP2004231962A (ja) | 2004-08-19 |
| JP2004231962A5 true JP2004231962A5 (enExample) | 2005-05-26 |
| JP4081449B2 JP4081449B2 (ja) | 2008-04-23 |
Family
ID=32655531
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2004019319A Expired - Fee Related JP4081449B2 (ja) | 2003-01-29 | 2004-01-28 | 軟質、半硬質および硬質ポリウレタンフォームを製造するための低酸性の有機金属触媒 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6825238B2 (enExample) |
| EP (1) | EP1443065B1 (enExample) |
| JP (1) | JP4081449B2 (enExample) |
| KR (1) | KR100523419B1 (enExample) |
| CN (1) | CN1519264B (enExample) |
| AT (1) | ATE339457T1 (enExample) |
| BR (1) | BRPI0400127A (enExample) |
| DE (1) | DE602004002308T2 (enExample) |
| MX (1) | MXPA04000863A (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040222310A1 (en) * | 2003-05-07 | 2004-11-11 | Lear Corporation | Method of spray polyurethane application utilizing internally mixed components applied with a flat fan spray |
| DE102004009740A1 (de) * | 2004-02-25 | 2005-09-15 | Basf Ag | Zinn- und Übergangsmetallfreie Polyurethanschaumstoffe |
| EP1602676A1 (en) * | 2004-06-01 | 2005-12-07 | SOLVAY (Société Anonyme) | Catalytic compositions |
| CN101103084B (zh) * | 2005-01-13 | 2010-09-29 | 旭硝子株式会社 | 涂层剂组合物及其用途 |
| AU2006218395A1 (en) | 2005-03-03 | 2006-09-08 | South Dakota Soybean Processors, Llc | Novel polyols derived from a vegetable oil using an oxidation process |
| JP2006348099A (ja) * | 2005-06-14 | 2006-12-28 | Bridgestone Corp | ポリウレタン発泡原液及び低密度ポリウレタン断熱材 |
| KR100682398B1 (ko) * | 2005-07-20 | 2007-02-15 | 에스엔케이폴리텍(주) | 우수한 충격흡수성 및 복원력을 갖는 폴리우레탄 폼 및이의 제조방법 |
| JP4989623B2 (ja) * | 2006-02-21 | 2012-08-01 | 三井化学株式会社 | ポリチオウレタン系光学材料用重合性組成物 |
| US20070225393A1 (en) * | 2006-03-27 | 2007-09-27 | Arnold Allen R Jr | Crosslinkers for minimizing deterioration of polyurethane foams |
| US8530534B2 (en) | 2006-05-04 | 2013-09-10 | Air Products And Chemicals, Inc. | Trimerization catalysts from sterically hindered salts |
| WO2008021034A2 (en) * | 2006-08-10 | 2008-02-21 | Dow Global Technologies, Inc. | Method for preparing viscoelastic polyurethane foam |
| JP5563980B2 (ja) * | 2007-08-27 | 2014-07-30 | ダウ グローバル テクノロジーズ エルエルシー | 粘弾性フォームのビスマス塩による触媒作用 |
| JP2014506947A (ja) * | 2011-02-21 | 2014-03-20 | ハネウェル・インターナショナル・インコーポレーテッド | ハロゲン化オレフィン発泡剤を含むポリウレタンフォームプレミックス及びそれから製造されるフォーム |
| CN102733198B (zh) * | 2012-07-11 | 2013-12-25 | 山东天庆科技发展有限公司 | 水性聚氨酯光油及制备方法 |
| US10023681B2 (en) | 2012-10-24 | 2018-07-17 | Evonik Degussa Gmbh | Delay action catalyst for improving the stability of polyurethane systems having halogen containing blowing agents |
| WO2014133986A1 (en) * | 2013-02-26 | 2014-09-04 | Honeywell International Inc. | Polyurethane foam premixes containing halogenated olefin blowing agents and foams made from same |
| EP3110546B1 (en) | 2014-02-26 | 2022-03-30 | Evonik Operations GmbH | Method for making a polyisocyanurate/polyurethane foam |
| KR102465028B1 (ko) * | 2014-10-13 | 2022-11-08 | 에보닉 오퍼레이션스 게엠베하 | 황 기반 염으로부터의 폴리우레탄 촉매 |
| JP6689858B2 (ja) * | 2015-01-13 | 2020-04-28 | ザ・シェファード・ケミカル・カンパニーＴｈｅ Ｓｈｅｐｈｅｒｄ Ｃｈｅｍｉｃａｌ Ｃｏｍｐａｎｙ | 新規ポリウレタン硬化剤 |
| CN108659195B (zh) * | 2017-03-28 | 2022-05-24 | 科思创德国股份有限公司 | 一种制备聚氨酯高回弹软质海绵的方法 |
| US11046850B2 (en) | 2017-09-27 | 2021-06-29 | Evonik Operations Gmbh | Mixed metal catalyst compositions and methods for making polyurethane foam |
| CN108892769B (zh) * | 2018-06-19 | 2021-07-06 | 石家庄合汇化工有限公司 | 一种用于制备聚氨酯的酸封延迟性催化剂 |
| JP7123483B2 (ja) * | 2018-09-28 | 2022-08-23 | 株式会社イノアックコーポレーション | ポリウレタンフォーム、パッド、ポリウレタンフォームの製造方法、及び、パッドの製造方法 |
| CN111607061B (zh) * | 2020-04-15 | 2022-04-15 | 黎明化工研究设计院有限责任公司 | 一种无阻燃剂高阻燃低气味全水自结皮聚氨酯泡沫及其制备方法 |
| US11738487B2 (en) | 2021-01-22 | 2023-08-29 | Covestro Llc | Processes for making molded flexible foams and flexible foams produced thereby |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1299886B (de) | 1961-06-01 | 1969-07-24 | M & T Chemicals Inc | Verfahren zur Herstellung von Polyurethanen |
| DE2019767A1 (de) | 1970-04-23 | 1971-12-23 | Gen Tire & Rubber Co | Katalysatorsysteme fuer Urethanschaeume |
| US4105595A (en) | 1974-09-17 | 1978-08-08 | Bayer Aktiengesellschaft | Process for the production of highly elastic polyurethane foams |
| US4256848A (en) | 1978-03-06 | 1981-03-17 | Basf Wyandotte Corporation | Synergistic polyurethane co-catalysts which are a combination of an organo-mercuric compound and a zinc salt of an alkyl carboxylic acid |
| US4200699A (en) | 1978-10-12 | 1980-04-29 | M&T Chemicals Inc. | Catalyst composition for rigid polyurethane foams |
| US4256847A (en) | 1979-10-17 | 1981-03-17 | Mooney Chemicals, Inc. | Rigid polyurethane foam process using lithium/zinc catalyst |
| US5342859A (en) | 1991-06-25 | 1994-08-30 | Atlas Roofing Corporation | Method of producing rigid foams and products produced therefrom |
| US5324754A (en) | 1992-12-14 | 1994-06-28 | Basf Corporation | Lithium-based salts in flexible foams |
| DE19506671C2 (de) | 1995-02-25 | 1999-11-18 | Basf Ag | Verfahren zur Herstellung von Polyurethan-Schaumstoffen |
| IN1997CH00157A (enExample) | 1996-10-01 | 2006-06-09 | Recticel | |
| US6005016A (en) * | 1998-10-06 | 1999-12-21 | Bayer Corporation | Rigid polyurethane foam based on polyethers of TDA |
| DE10142296C1 (de) * | 2001-08-29 | 2003-02-13 | Bayer Ag | Polyurethanelastomere, Verfahren zu ihrer Herstellung und ihre Verwendung |
-
2003
- 2003-01-29 US US10/353,642 patent/US6825238B2/en not_active Expired - Lifetime
-
2004
- 2004-01-23 BR BR0400127-3A patent/BRPI0400127A/pt not_active IP Right Cessation
- 2004-01-27 EP EP04001660A patent/EP1443065B1/en not_active Expired - Lifetime
- 2004-01-27 KR KR10-2004-0004961A patent/KR100523419B1/ko not_active Expired - Fee Related
- 2004-01-27 DE DE602004002308T patent/DE602004002308T2/de not_active Expired - Lifetime
- 2004-01-27 AT AT04001660T patent/ATE339457T1/de not_active IP Right Cessation
- 2004-01-28 MX MXPA04000863A patent/MXPA04000863A/es active IP Right Grant
- 2004-01-28 JP JP2004019319A patent/JP4081449B2/ja not_active Expired - Fee Related
- 2004-01-29 CN CN2004100035562A patent/CN1519264B/zh not_active Expired - Lifetime
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