JP2013537565A5 - - Google Patents
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- Publication number
- JP2013537565A5 JP2013537565A5 JP2013517327A JP2013517327A JP2013537565A5 JP 2013537565 A5 JP2013537565 A5 JP 2013537565A5 JP 2013517327 A JP2013517327 A JP 2013517327A JP 2013517327 A JP2013517327 A JP 2013517327A JP 2013537565 A5 JP2013537565 A5 JP 2013537565A5
- Authority
- JP
- Japan
- Prior art keywords
- raw material
- polyol
- production
- polyol mixture
- functional
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 claims description 15
- 229920005903 polyol mixture Polymers 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 8
- 239000002994 raw material Substances 0.000 claims description 8
- 229920002635 polyurethane Polymers 0.000 claims description 6
- 239000004814 polyurethane Substances 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 4
- 229920005862 polyol Polymers 0.000 claims description 4
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 3
- -1 carbonate polyol Chemical class 0.000 claims description 3
- 239000004922 lacquer Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 239000000853 adhesive Substances 0.000 claims description 2
- 230000001070 adhesive effect Effects 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 2
- 239000001569 carbon dioxide Substances 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000007334 copolymerization reaction Methods 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000004033 plastic Substances 0.000 claims description 2
- 229920003023 plastic Polymers 0.000 claims description 2
- 229920001228 polyisocyanate Polymers 0.000 claims description 2
- 239000005056 polyisocyanate Substances 0.000 claims description 2
- 150000003077 polyols Chemical class 0.000 claims description 2
- 229920003009 polyurethane dispersion Polymers 0.000 claims description 2
- 239000000565 sealant Substances 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 4
- 150000004985 diamines Chemical class 0.000 description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 150000005676 cyclic carbonates Chemical class 0.000 description 2
- RHPBLLCTOLJFPH-UHFFFAOYSA-N piperidin-2-ylmethanamine Chemical compound NCC1CCCCN1 RHPBLLCTOLJFPH-UHFFFAOYSA-N 0.000 description 2
- LTEKQAPRXFBRNN-UHFFFAOYSA-N piperidin-4-ylmethanamine Chemical compound NCC1CCNCC1 LTEKQAPRXFBRNN-UHFFFAOYSA-N 0.000 description 2
- KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- PWGJDPKCLMLPJW-UHFFFAOYSA-N 1,8-diaminooctane Chemical compound NCCCCCCCCN PWGJDPKCLMLPJW-UHFFFAOYSA-N 0.000 description 1
- HXKKHQJGJAFBHI-UHFFFAOYSA-N 1-aminopropan-2-ol Chemical compound CC(O)CN HXKKHQJGJAFBHI-UHFFFAOYSA-N 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- PQMCFTMVQORYJC-UHFFFAOYSA-N 2-aminocyclohexan-1-ol Chemical compound NC1CCCCC1O PQMCFTMVQORYJC-UHFFFAOYSA-N 0.000 description 1
- JFFOUICIRBXFRC-UHFFFAOYSA-N 2-aminocyclopentan-1-ol Chemical compound NC1CCCC1O JFFOUICIRBXFRC-UHFFFAOYSA-N 0.000 description 1
- BKMMTJMQCTUHRP-UHFFFAOYSA-N 2-aminopropan-1-ol Chemical compound CC(N)CO BKMMTJMQCTUHRP-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- DZIHTWJGPDVSGE-UHFFFAOYSA-N 4-[(4-aminocyclohexyl)methyl]cyclohexan-1-amine Chemical compound C1CC(N)CCC1CC1CCC(N)CC1 DZIHTWJGPDVSGE-UHFFFAOYSA-N 0.000 description 1
- BLFRQYKZFKYQLO-UHFFFAOYSA-N 4-aminobutan-1-ol Chemical compound NCCCCO BLFRQYKZFKYQLO-UHFFFAOYSA-N 0.000 description 1
- IMLXLGZJLAOKJN-UHFFFAOYSA-N 4-aminocyclohexan-1-ol Chemical compound NC1CCC(O)CC1 IMLXLGZJLAOKJN-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- QQKNRSWPDPPDGN-UHFFFAOYSA-N N1CCC(CC1)CCO.N1CCC(CC1)CCO Chemical compound N1CCC(CC1)CCO.N1CCC(CC1)CCO QQKNRSWPDPPDGN-UHFFFAOYSA-N 0.000 description 1
- 239000005700 Putrescine Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- SSJXIUAHEKJCMH-UHFFFAOYSA-N cyclohexane-1,2-diamine Chemical compound NC1CCCCC1N SSJXIUAHEKJCMH-UHFFFAOYSA-N 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- QFTYSVGGYOXFRQ-UHFFFAOYSA-N dodecane-1,12-diamine Chemical compound NCCCCCCCCCCCCN QFTYSVGGYOXFRQ-UHFFFAOYSA-N 0.000 description 1
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- KVKFRMCSXWQSNT-UHFFFAOYSA-N n,n'-dimethylethane-1,2-diamine Chemical compound CNCCNC KVKFRMCSXWQSNT-UHFFFAOYSA-N 0.000 description 1
- SXJVFQLYZSNZBT-UHFFFAOYSA-N nonane-1,9-diamine Chemical compound NCCCCCCCCCN SXJVFQLYZSNZBT-UHFFFAOYSA-N 0.000 description 1
- WTSXICLFTPPDTL-UHFFFAOYSA-N pentane-1,3-diamine Chemical compound CCC(N)CCN WTSXICLFTPPDTL-UHFFFAOYSA-N 0.000 description 1
- PEUGKEHLRUVPAN-UHFFFAOYSA-N piperidin-3-amine Chemical compound NC1CCCNC1 PEUGKEHLRUVPAN-UHFFFAOYSA-N 0.000 description 1
- BCIIMDOZSUCSEN-UHFFFAOYSA-N piperidin-4-amine Chemical compound NC1CCNCC1 BCIIMDOZSUCSEN-UHFFFAOYSA-N 0.000 description 1
- AUKXFNABVHIUAC-UHFFFAOYSA-N pyrrolidin-2-ylmethylamine Chemical compound NCC1CCCN1 AUKXFNABVHIUAC-UHFFFAOYSA-N 0.000 description 1
- NGXSWUFDCSEIOO-UHFFFAOYSA-N pyrrolidin-3-amine Chemical compound NC1CCNC1 NGXSWUFDCSEIOO-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102010030950 | 2010-07-05 | ||
| DE102010030950.8 | 2010-07-05 | ||
| PCT/EP2011/061174 WO2012004209A1 (de) | 2010-07-05 | 2011-07-04 | Verfahren zur herstellung von polyolgemischen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013537565A JP2013537565A (ja) | 2013-10-03 |
| JP2013537565A5 true JP2013537565A5 (OSRAM) | 2014-06-26 |
Family
ID=44630253
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013517327A Pending JP2013537565A (ja) | 2010-07-05 | 2011-07-04 | ポリオール混合物の製造方法 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9096717B2 (OSRAM) |
| EP (1) | EP2591036B1 (OSRAM) |
| JP (1) | JP2013537565A (OSRAM) |
| KR (1) | KR20130089642A (OSRAM) |
| CN (1) | CN103097425B (OSRAM) |
| BR (1) | BR112013000260A2 (OSRAM) |
| CA (1) | CA2804134A1 (OSRAM) |
| ES (1) | ES2463967T3 (OSRAM) |
| MX (1) | MX2013000190A (OSRAM) |
| SG (1) | SG186833A1 (OSRAM) |
| WO (1) | WO2012004209A1 (OSRAM) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN114774053A (zh) * | 2012-04-16 | 2022-07-22 | 沙特阿美技术公司 | 粘合剂组合物和方法 |
| EP2886572A1 (de) * | 2013-12-17 | 2015-06-24 | Bayer MaterialScience AG | Einsatz von Urethan-Alkoholen zur Herstellung von Polyethercarbonatpolyolen |
| US10308759B2 (en) | 2014-04-03 | 2019-06-04 | Saudi Aramco Technologies Company | Aliphatic polycarbonate polyol compositions |
| WO2016120406A1 (en) * | 2015-01-28 | 2016-08-04 | Repsol, S.A. | A polyurethane adhesive formulation based on polyether carbonate polyol |
| EP3098251A1 (de) * | 2015-05-26 | 2016-11-30 | Covestro Deutschland AG | Einsatz von alkoholen, die mindestens zwei urethangruppen enthalten, zur herstellung von polyetherpolyolen |
| EP3098252A1 (de) * | 2015-05-26 | 2016-11-30 | Covestro Deutschland AG | Einsatz von alkoholen, die mindestens zwei urethangruppen enthalten, zur herstellung von polyethercarbonatpolyolen |
| JP2018528997A (ja) * | 2015-08-04 | 2018-10-04 | レプソル・ソシエダッド・アノニマＲｅｐｓｏｌ．Ｓ．Ａ． | 感圧接着剤のための新規調製物 |
| US10119223B2 (en) | 2016-07-15 | 2018-11-06 | Covestro Llc | Carpet and synthetic turf backings prepared from a polyether carbonate polyol |
| CN109970994A (zh) * | 2017-12-28 | 2019-07-05 | 科思创德国股份有限公司 | 水性分散体 |
| JP2021508753A (ja) * | 2017-12-28 | 2021-03-11 | コベストロ、ドイチュラント、アクチエンゲゼルシャフトＣｏｖｅｓｔｒｏ Ｄｅｕｔｓｃｈｌａｎｄ Ａｇ | 水性分散液 |
| CN111138623B (zh) * | 2020-01-10 | 2021-02-19 | 浙江大学 | 一种有机硅改性聚醚-聚碳酸酯水性聚氨酯及其制备方法 |
| KR102566314B1 (ko) * | 2021-01-29 | 2023-08-14 | 한국화학연구원 | 에폭시 화합물, 이를 포함하는 에폭시 수지 조성물 및 이를 포함하는 일액형 에폭시 접착제 조성물 |
| WO2025179411A1 (en) * | 2024-02-26 | 2025-09-04 | Dic Corporation | Moisture-curable polyurethane hot-melt resin composition, adhesive, and laminate |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1063525A (en) | 1963-02-14 | 1967-03-30 | Gen Tire & Rubber Co | Organic cyclic oxide polymers, their preparation and tires prepared therefrom |
| US3829505A (en) | 1970-02-24 | 1974-08-13 | Gen Tire & Rubber Co | Polyethers and method for making the same |
| US3941849A (en) | 1972-07-07 | 1976-03-02 | The General Tire & Rubber Company | Polyethers and method for making the same |
| DE2832253A1 (de) | 1978-07-22 | 1980-01-31 | Bayer Ag | Verfahren zur herstellung von formschaumstoffen |
| GB8528071D0 (en) | 1985-11-14 | 1985-12-18 | Shell Int Research | Polycarbonates |
| NL8600166A (nl) | 1986-01-27 | 1987-08-17 | Gen Electric | Polymeermengsel, dat een polyamide, een polyfenyleenether en een middel voor het verbeteren van de slagsterkte bevat. |
| DE3617705A1 (de) * | 1986-05-26 | 1987-12-03 | Hoechst Ag | Urethangruppenhaltige polymere, deren loesungen und deren waessrige dispersionen, verfahren zu ihrer herstellung und ihre verwendung |
| US5158922A (en) | 1992-02-04 | 1992-10-27 | Arco Chemical Technology, L.P. | Process for preparing metal cyanide complex catalyst |
| US5470813A (en) | 1993-11-23 | 1995-11-28 | Arco Chemical Technology, L.P. | Double metal cyanide complex catalysts |
| US5712216A (en) | 1995-05-15 | 1998-01-27 | Arco Chemical Technology, L.P. | Highly active double metal cyanide complex catalysts |
| US5482908A (en) | 1994-09-08 | 1996-01-09 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| US5545601A (en) | 1995-08-22 | 1996-08-13 | Arco Chemical Technology, L.P. | Polyether-containing double metal cyanide catalysts |
| US5627120A (en) | 1996-04-19 | 1997-05-06 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| US5714428A (en) | 1996-10-16 | 1998-02-03 | Arco Chemical Technology, L.P. | Double metal cyanide catalysts containing functionalized polymers |
| DE19905611A1 (de) | 1999-02-11 | 2000-08-17 | Bayer Ag | Doppelmetallcyanid-Katalysatoren für die Herstellung von Polyetherpolyolen |
| KR100769003B1 (ko) | 2000-04-20 | 2007-10-22 | 바이엘 악티엔게젤샤프트 | 이중 금속 시아나이드 (ｄｍｃ) 촉매의 제조 방법 |
| US6646153B1 (en) * | 2000-07-19 | 2003-11-11 | E. I. Du Pont De Nemours And Company | Hydroxyl functional urethanes having a tertiary carbamate bond |
| EP1432488A4 (en) * | 2001-10-01 | 2005-02-02 | Eurotech Ltd | PREPARATION OF OLIGOMERIC CYCLOCARBONATES AND THEIR USE IN NON-ISOCYANATE OR HYBRID NOTISOCYANATE POLYURETHANES |
| DE10219028A1 (de) | 2002-04-29 | 2003-11-06 | Bayer Ag | Herstellung und Verwendung von hochmolekularen aliphatischen Polycarbonaten |
| US6713599B1 (en) * | 2003-03-31 | 2004-03-30 | Basf Corporation | Formation of polymer polyols with a narrow polydispersity using double metal cyanide (DMC) catalysts |
| EP1506975A1 (en) * | 2003-08-13 | 2005-02-16 | Vantico GmbH | Nanocomposites based on polyurethane or polyurethane-epoxy hybrid resins prepared avoiding isocyanates |
| JP2006009001A (ja) * | 2004-05-26 | 2006-01-12 | Japan Paint Manufacturers Association | ポリヒドロキシウレタンの製造方法 |
| US7268204B2 (en) | 2005-03-29 | 2007-09-11 | Basf Corporation | Complex of a multimetal cyanide compound and methods of forming polyethercarbonate polyols |
| US7671228B2 (en) * | 2005-03-29 | 2010-03-02 | Basf Corporation | Method of forming a polyethercarbonate polyol using a CO2-philic compound or substituent |
| US7977501B2 (en) * | 2006-07-24 | 2011-07-12 | Bayer Materialscience Llc | Polyether carbonate polyols made via double metal cyanide (DMC) catalysis |
| ATE514726T1 (de) * | 2006-11-15 | 2011-07-15 | Basf Se | Verfahren zur herstellung von polyurethan- weichschaumstoffen |
| CN101611074B (zh) | 2007-01-30 | 2012-07-25 | 巴斯夫欧洲公司 | 制备聚醚碳酸酯多元醇的方法 |
| EP2015014A1 (de) * | 2007-07-11 | 2009-01-14 | Bayer MaterialScience AG | Verfahren zur Trocknung von Schäumen aus wässrigen PUR-Dispersionen |
| JP5381977B2 (ja) * | 2008-03-25 | 2014-01-08 | 旭硝子株式会社 | ヒドロキシ化合物の製造方法、ならびにプレポリマーおよびポリウレタンの製造方法 |
| EP2274385B1 (en) * | 2008-05-08 | 2014-08-20 | E. I. Du Pont de Nemours and Company | Inkjet inks for textiles containing crosslinked polyurethanes and further containing additional reactive components |
| JP5781939B2 (ja) * | 2008-12-23 | 2015-09-24 | ノボマー， インコーポレイテッド | 調整可能なポリマー組成物 |
| DE102009033637A1 (de) * | 2009-07-17 | 2011-01-20 | Bayer Materialscience Ag | Prepolymere |
-
2011
- 2011-07-04 BR BR112013000260A patent/BR112013000260A2/pt not_active IP Right Cessation
- 2011-07-04 MX MX2013000190A patent/MX2013000190A/es active IP Right Grant
- 2011-07-04 EP EP11743458.9A patent/EP2591036B1/de not_active Not-in-force
- 2011-07-04 US US13/808,470 patent/US9096717B2/en not_active Expired - Fee Related
- 2011-07-04 KR KR1020137002890A patent/KR20130089642A/ko not_active Withdrawn
- 2011-07-04 ES ES11743458.9T patent/ES2463967T3/es active Active
- 2011-07-04 WO PCT/EP2011/061174 patent/WO2012004209A1/de not_active Ceased
- 2011-07-04 JP JP2013517327A patent/JP2013537565A/ja active Pending
- 2011-07-04 CA CA2804134A patent/CA2804134A1/en not_active Abandoned
- 2011-07-04 CN CN201180042617.4A patent/CN103097425B/zh not_active Expired - Fee Related
- 2011-07-04 SG SG2012095717A patent/SG186833A1/en unknown
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