CN101054433B - 储存稳定的含有植物油基多元醇的异氰酸酯-活性组分 - Google Patents
储存稳定的含有植物油基多元醇的异氰酸酯-活性组分 Download PDFInfo
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- CN101054433B CN101054433B CN2007100971496A CN200710097149A CN101054433B CN 101054433 B CN101054433 B CN 101054433B CN 2007100971496 A CN2007100971496 A CN 2007100971496A CN 200710097149 A CN200710097149 A CN 200710097149A CN 101054433 B CN101054433 B CN 101054433B
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- 238000007670 refining Methods 0.000 description 1
- 239000011342 resin composition Substances 0.000 description 1
- WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical compound [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 description 1
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical compound [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
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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
- C08G18/08—Processes
- C08G18/16—Catalysts
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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
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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
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/283—Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
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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
- C08G18/30—Low-molecular-weight compounds
- C08G18/36—Hydroxylated esters of higher fatty acids
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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
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- C08G18/4816—Two or more polyethers of different physical or chemical nature mixtures of two or more polyetherpolyols having at least three hydroxy groups
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- 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
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- 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
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- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
- C08G18/4845—Polyethers containing oxyethylene units and other oxyalkylene units containing oxypropylene or higher oxyalkylene end groups
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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
- C08G18/40—High-molecular-weight compounds
- C08G18/48—Polyethers
- C08G18/4833—Polyethers containing oxyethylene units
- C08G18/4837—Polyethers containing oxyethylene units and other oxyalkylene units
- C08G18/485—Polyethers containing oxyethylene units and other oxyalkylene units containing mixed oxyethylene-oxypropylene or oxyethylene-higher oxyalkylene end 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
- 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
- C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
- C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
- C08G18/6666—Compounds of group C08G18/48 or C08G18/52
- C08G18/6696—Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/36 or hydroxylated esters of higher fatty acids of C08G18/38
-
- 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
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)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/401,510 US20070238800A1 (en) | 2006-04-11 | 2006-04-11 | Storage stable isocyanate-reactive component containing vegetable oil-based polyol |
| US11/401,510 | 2006-04-11 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101054433A CN101054433A (zh) | 2007-10-17 |
| CN101054433B true CN101054433B (zh) | 2011-09-21 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
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| CN2007100971496A Expired - Fee Related CN101054433B (zh) | 2006-04-11 | 2007-04-10 | 储存稳定的含有植物油基多元醇的异氰酸酯-活性组分 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US20070238800A1 (https=) |
| EP (1) | EP1845121B1 (https=) |
| JP (1) | JP5289722B2 (https=) |
| KR (1) | KR20070101143A (https=) |
| CN (1) | CN101054433B (https=) |
| BR (1) | BRPI0701994A (https=) |
| CA (1) | CA2583950A1 (https=) |
| DE (1) | DE602007001550D1 (https=) |
| ES (1) | ES2327456T3 (https=) |
| MX (1) | MX2007004222A (https=) |
| RU (1) | RU2007113125A (https=) |
| SG (1) | SG136890A1 (https=) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BRPI0600782A (pt) * | 2006-02-24 | 2007-11-20 | Phb Ind Sa | composição para preparo de poliol poliéster degradável, processo para obtenção de poliol poliéster, de elastÈmero, de espumas, de tintas e de adesivos, e espuma degradável de um poliol poliéster |
| JP2007314672A (ja) * | 2006-05-26 | 2007-12-06 | Inoac Corp | ポリウレタン発泡体 |
| AU2007297828B2 (en) * | 2006-09-21 | 2013-06-27 | Dow Brasil Sudeste Industrial Ltda. | Viscoelastic foams having high air flow |
| WO2008134217A1 (en) * | 2007-04-27 | 2008-11-06 | Dow Global Technologies Inc. | Low volatiles coatings, sealants and binders from renewable oils |
| JP5505921B2 (ja) * | 2007-08-01 | 2014-05-28 | 株式会社イノアックコーポレーション | 軟質ポリウレタン発泡体 |
| WO2009022579A1 (ja) * | 2007-08-10 | 2009-02-19 | Daikin Industries, Ltd. | コーティング用組成物 |
| DE102008000243A1 (de) * | 2008-02-06 | 2009-08-13 | Evonik Goldschmidt Gmbh | Neuartige Kompatibilisierungsmittel zur Verbesserung der Lagerstabilität von Polyolmischungen |
| DE102008000255A1 (de) | 2008-02-08 | 2009-08-20 | Evonik Goldschmidt Gmbh | Siloxanzusammensetzungen |
| JP5288324B2 (ja) * | 2008-05-09 | 2013-09-11 | 日本ポリウレタン工業株式会社 | ポリウレタン樹脂形成性組成物、シール材及び中空糸膜モジュール |
| BRPI0911010A2 (pt) | 2008-07-18 | 2015-10-06 | Dow Global Technologies Llc | espuma viscoelástica, composição de poliol, sistema reagente para a preparação de uma espuma de poliuretano viscoelástica, material de poliuretano viscoelástico, e processo para preparar uma espuma de poliuretano viscoelástica |
| US20100055467A1 (en) * | 2008-09-02 | 2010-03-04 | Ppg Industries Ohio, Inc. | Coating compositions comprising the reaction product of a biomass derived polyol and a lactide |
| JP5346228B2 (ja) * | 2009-03-03 | 2013-11-20 | 三井化学株式会社 | ポリオール組成物およびその用途 |
| DE102009001595A1 (de) | 2009-03-17 | 2010-09-23 | Evonik Goldschmidt Gmbh | Kompatibilisierungsmittel zur Verbesserung der Lagerstabilität von Polyolmischungen |
| EP2516495B1 (de) | 2009-12-22 | 2015-07-29 | BYK-Chemie GmbH | Zusammensetzung umfassend stabile polyolmischungen |
| EP2368926B1 (de) * | 2010-03-25 | 2013-05-22 | Basf Se | Wasseremulgierbare Isocyanate mit verbesserten Eigenschaften |
| US9290604B2 (en) * | 2010-08-13 | 2016-03-22 | Air Products And Chemicals, Inc. | NPE-free emulsifiers for water-blown polyurethane spray foam |
| DE102010063241A1 (de) | 2010-12-16 | 2012-06-21 | Evonik Goldschmidt Gmbh | Siliconstabilisatoren für Polyurethan- oder Polyisocyanurat-Hartschaumstoffe |
| CN102153720B (zh) * | 2011-02-10 | 2012-09-26 | 中国科学院过程工程研究所 | 一种制备植物油基聚氨酯材料微球的方法 |
| DE102011007468A1 (de) | 2011-04-15 | 2012-10-18 | Evonik Goldschmidt Gmbh | Zusammensetzung, enthaltend spezielle Carbamat-artige Verbindungen, geeignet zur Herstellung von Polyurethanschäumen |
| DE102011007479A1 (de) | 2011-04-15 | 2012-10-18 | Evonik Goldschmidt Gmbh | Zusammensetzung, enthaltend spezielle Amide und organomodifizierte Siloxane, geeignet zur Herstellung von Polyurethanschäumen |
| DE102011109541A1 (de) | 2011-08-03 | 2013-02-07 | Evonik Goldschmidt Gmbh | Verwendung von Polysiloxanen enthaltend verzweigte Polyetherreste zur Herstellung von Polyurethanschäumen |
| US9822482B2 (en) * | 2011-11-16 | 2017-11-21 | Singtex Industrial Co., Ltd. | Method for preparing a functional film via coffee oil and textile thereof |
| EP2800767B1 (en) * | 2012-01-06 | 2019-03-06 | Evonik Degussa GmbH | Melamine-polyol dispersions and uses thereof in manufacturing polyurethane |
| DE102013201829A1 (de) | 2013-02-05 | 2014-08-07 | Evonik Industries Ag | Amine, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| MX370742B (es) * | 2013-05-29 | 2019-12-20 | Dow Quim Mexicana S A De C V | Una formulacion para preparar una espuma de poliuretano. |
| DE102013217395A1 (de) | 2013-09-02 | 2015-03-05 | Evonik Industries Ag | Verwendung von Mischungen organofunktionell modifizierter Polysiloxane mit Amiden bei der Herstellung von Polyurethanweichschäumen |
| CN103665267B (zh) * | 2013-12-16 | 2016-01-27 | 上海汇得化工有限公司 | 一种汽车座椅内饰用聚氨酯合成革树脂及制备方法 |
| EP2886591A1 (de) | 2013-12-19 | 2015-06-24 | Evonik Industries AG | Zusammensetzung, geeignet zur Herstellung von Polyurethanschäumen, enthaltend mindestens ein Nukleierungsmittel |
| DE102013226575B4 (de) | 2013-12-19 | 2021-06-24 | Evonik Operations Gmbh | Zusammensetzung, geeignet zur Herstellung von Polyurethanschäumen, enthaltend mindestens einen ungesättigten Fluorkohlenwasserstoff oder ungesättigten Fluorkohlenwasserstoff als Treibmittel, Polyurethanschäume, Verfahren zu deren Herstellung und deren Verwendung |
| DE102014215384A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215387B4 (de) | 2014-08-05 | 2020-06-10 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215381B4 (de) | 2014-08-05 | 2020-06-10 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215380B4 (de) | 2014-08-05 | 2022-04-28 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215383B4 (de) | 2014-08-05 | 2020-06-10 | Evonik Operations Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215382A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215388A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| MX375891B (es) * | 2015-03-12 | 2025-03-07 | Huntsman Adv Mat Licensing Switzerland Gmbh | Componente de poliol para la produccion de espumas de poliuretano. |
| JP6467660B2 (ja) * | 2015-03-26 | 2019-02-13 | 三井化学Ｓｋｃポリウレタン株式会社 | ポリオール組成物およびポリウレタンフォーム |
| EP3078696A1 (de) | 2015-04-08 | 2016-10-12 | Evonik Degussa GmbH | Herstellung emissionsarmer polyurethane |
| EP3176206A1 (de) | 2015-12-01 | 2017-06-07 | Evonik Degussa GmbH | Verfahren zur herstellung feinzelliger schaumstoffe unter verwendung eines zellalterungshemmers |
| EP3205678A1 (de) | 2016-02-10 | 2017-08-16 | Evonik Degussa GmbH | Alterungsbeständige und emissionsarme matratzen und/oder kissen |
| PL3443019T3 (pl) * | 2016-04-12 | 2021-01-11 | Evonik Operations Gmbh | Kompozycje środków powierzchniowo czynnych w postaci kopolimerów siloksanowooksyalkilenowych |
| CN106496504A (zh) * | 2016-10-31 | 2017-03-15 | 厦门艾美森新材料科技股份有限公司 | 一种聚氨酯泡沫组合料及其制备方法、聚氨酯泡沫 |
| KR102247366B1 (ko) * | 2016-11-10 | 2021-05-03 | 피피지 코팅스 유럽 비.브이. | 팽창성 발포체 안정화용 계면활성제 |
| PL3538582T3 (pl) * | 2016-11-11 | 2022-07-18 | Evonik Operations Gmbh | Emulgatory przeznaczone do pianki na bazie poliuretanu |
| CN110506065B (zh) * | 2017-04-12 | 2023-01-24 | 巴斯夫欧洲公司 | 热塑性聚氨酯和复合制品 |
| CN112088181B (zh) * | 2018-03-06 | 2023-06-27 | 巴斯夫聚氨酯特种产品（中国）有限公司 | 包含热塑性多异氰酸酯加聚产物的制剂、其制备方法及其用途 |
| WO2019177899A1 (en) * | 2018-03-13 | 2019-09-19 | Dow Global Technologies Llc | Viscoelastic foam |
| CN108976386A (zh) * | 2018-06-04 | 2018-12-11 | 张家港市顾乐仕生活家居科技有限公司 | 一种含有天然植物抗菌防霉聚氨酯复合材料及其制备方法 |
| DE102019127885A1 (de) * | 2018-10-26 | 2020-04-30 | Toyota Jidosha Kabushiki Kaisha | Wasser-basierte beschichtungszusammensetzung und herstellungsverfahren derselben |
| EP3744745A1 (de) | 2019-05-28 | 2020-12-02 | Evonik Operations GmbH | Herstellung von pu-schaumstoffen |
| US12458150B2 (en) | 2019-07-19 | 2025-11-04 | Evonik Operations Gmbh | Shaped PU foam articles |
| US20220243026A1 (en) * | 2019-09-03 | 2022-08-04 | Dow Global Technologies Llc | Foam formulation |
| RS67445B1 (sr) | 2019-11-07 | 2025-12-31 | Evonik Operations Gmbh | Trajna deformacija sabijanjem |
| EP3865527A1 (de) | 2020-02-14 | 2021-08-18 | Evonik Operations GmbH | Herstellung von pu-schaumstoffen |
| US20220106432A1 (en) | 2020-10-07 | 2022-04-07 | Evonik Operations Gmbh | Shaped flexible pu foam articles |
| CN113174034B (zh) * | 2021-04-09 | 2023-04-07 | 旭川化学（苏州）有限公司 | 一种聚酯多元醇及其制备方法 |
| CN112961302B (zh) * | 2021-04-20 | 2022-12-06 | 浙江清优材料科技有限公司 | 一种耐高温高湿聚氨酯发泡材料 |
| CN117529512A (zh) | 2021-06-17 | 2024-02-06 | 赢创运营有限公司 | 成型软质聚氨酯泡沫制品 |
| US11613604B2 (en) | 2021-06-28 | 2023-03-28 | Covestro Llc | Isocyanate-reactive compositions, polyurethane foams formed therefrom, multi-layer composite articles that include such foams, and methods for their preparation |
| CA3224261A1 (en) | 2021-07-02 | 2023-01-05 | Annegret Terheiden | Production of pu foams |
| CN118742583A (zh) | 2022-02-22 | 2024-10-01 | 赢创运营有限公司 | 使用来自基于胺的水解过程的回收多元醇生产pu泡沫 |
| EP4257327A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | Optical determination of a control signal for slabstock polyurethane foam production |
| EP4257326A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | Optical determination of a control signal in response to detection of macroscopic polyurethane foam defects |
| EP4257323A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | System and method for determining parameters for foam production |
| EP4257324A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | System and method for automatically setting parameters for foam production |
| EP4257325A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | Optical prediction of polyurethane foam parameters |
| CN121752648A (zh) | 2023-08-24 | 2026-03-27 | 赢创运营有限公司 | 用于解聚聚氨酯的改进方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000046266A1 (en) * | 1999-02-03 | 2000-08-10 | Huntsman Petrochemical Corporation | Compatibilization of blowing agent polyol mixtures for polyurethane foam manufacture |
| US6121337A (en) * | 1990-03-23 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Compositions containing 1,1,2,2-tetrafluoroethane (HFC-134) for closed-cell polymer foam production |
| CN1390869A (zh) * | 2001-06-07 | 2003-01-15 | 美国拜尔公司 | 经改进热挠度的聚氨酯泡沫塑料及其生产方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62100513A (ja) * | 1985-10-28 | 1987-05-11 | Ito Seiyu Kk | 硬化性組成物 |
| DE3626223A1 (de) * | 1986-08-02 | 1988-02-04 | Henkel Kgaa | Polyurethan-praepolymere auf basis oleochemischer polyole, ihre herstellung und verwendung |
| JPH05117619A (ja) * | 1991-10-31 | 1993-05-14 | Koatsu Gas Kogyo Co Ltd | 一液湿気硬化型ポリウレタン系接着剤 |
| DE69804952T2 (de) * | 1997-03-20 | 2002-10-17 | Huntsman International Llc, Salt Lake City | Verfahren zur herstellung von polyurethanhartschäumen |
| JP4107710B2 (ja) * | 1998-04-30 | 2008-06-25 | 三井化学ポリウレタン株式会社 | 変性ポリイソシアネートおよびその製造方法 |
| JP4621460B2 (ja) * | 2004-09-07 | 2011-01-26 | 出光サートマー株式会社 | 液状重合体組成物 |
| JP2007269849A (ja) * | 2006-03-30 | 2007-10-18 | Dainippon Ink & Chem Inc | 硬質ポリウレタンフォームの製造方法及び建築用断熱材 |
-
2006
- 2006-04-11 US US11/401,510 patent/US20070238800A1/en not_active Abandoned
-
2007
- 2007-03-29 ES ES07006484T patent/ES2327456T3/es active Active
- 2007-03-29 EP EP07006484A patent/EP1845121B1/en not_active Not-in-force
- 2007-03-29 DE DE602007001550T patent/DE602007001550D1/de active Active
- 2007-04-04 CA CA002583950A patent/CA2583950A1/en not_active Abandoned
- 2007-04-10 BR BRPI0701994-7A patent/BRPI0701994A/pt not_active IP Right Cessation
- 2007-04-10 RU RU2007113125/04A patent/RU2007113125A/ru not_active Application Discontinuation
- 2007-04-10 KR KR1020070034939A patent/KR20070101143A/ko not_active Withdrawn
- 2007-04-10 CN CN2007100971496A patent/CN101054433B/zh not_active Expired - Fee Related
- 2007-04-10 SG SG200702618-0A patent/SG136890A1/en unknown
- 2007-04-10 MX MX2007004222A patent/MX2007004222A/es active IP Right Grant
- 2007-04-11 JP JP2007103447A patent/JP5289722B2/ja not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6121337A (en) * | 1990-03-23 | 2000-09-19 | E. I. Du Pont De Nemours And Company | Compositions containing 1,1,2,2-tetrafluoroethane (HFC-134) for closed-cell polymer foam production |
| WO2000046266A1 (en) * | 1999-02-03 | 2000-08-10 | Huntsman Petrochemical Corporation | Compatibilization of blowing agent polyol mixtures for polyurethane foam manufacture |
| CN1390869A (zh) * | 2001-06-07 | 2003-01-15 | 美国拜尔公司 | 经改进热挠度的聚氨酯泡沫塑料及其生产方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2007277560A (ja) | 2007-10-25 |
| MX2007004222A (es) | 2009-02-16 |
| ES2327456T3 (es) | 2009-10-29 |
| SG136890A1 (en) | 2007-11-29 |
| KR20070101143A (ko) | 2007-10-16 |
| US20070238800A1 (en) | 2007-10-11 |
| BRPI0701994A (pt) | 2007-12-11 |
| RU2007113125A (ru) | 2008-10-20 |
| CN101054433A (zh) | 2007-10-17 |
| EP1845121B1 (en) | 2009-07-15 |
| JP5289722B2 (ja) | 2013-09-11 |
| EP1845121A1 (en) | 2007-10-17 |
| CA2583950A1 (en) | 2007-10-11 |
| DE602007001550D1 (de) | 2009-08-27 |
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