KR20070101143A - 식물성 오일 기재 폴리올을 함유하는 저장 안정성이소시아네이트 반응성 성분 - Google Patents
식물성 오일 기재 폴리올을 함유하는 저장 안정성이소시아네이트 반응성 성분 Download PDFInfo
- Publication number
- KR20070101143A KR20070101143A KR1020070034939A KR20070034939A KR20070101143A KR 20070101143 A KR20070101143 A KR 20070101143A KR 1020070034939 A KR1020070034939 A KR 1020070034939A KR 20070034939 A KR20070034939 A KR 20070034939A KR 20070101143 A KR20070101143 A KR 20070101143A
- Authority
- KR
- South Korea
- Prior art keywords
- reactive component
- isocyanate
- oil
- weight
- vegetable oil
- 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- Withdrawn
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- 150000003839 salts Chemical class 0.000 description 1
- 235000019337 sorbitan trioleate Nutrition 0.000 description 1
- 229960000391 sorbitan trioleate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- BUXTXUBQAKIQKS-UHFFFAOYSA-N sulfuryl diisocyanate Chemical class O=C=NS(=O)(=O)N=C=O BUXTXUBQAKIQKS-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- IUTCEZPPWBHGIX-UHFFFAOYSA-N tin(2+) Chemical compound [Sn+2] IUTCEZPPWBHGIX-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
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
-
- 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
-
- 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
-
- 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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- 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
-
- 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
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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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- C08G18/65—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
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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
- C08G18/70—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)
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| US11/401,510 | 2006-04-11 | ||
| US11/401,510 US20070238800A1 (en) | 2006-04-11 | 2006-04-11 | Storage stable isocyanate-reactive component containing vegetable oil-based polyol |
Publications (1)
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| KR20070101143A true KR20070101143A (ko) | 2007-10-16 |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20190078630A (ko) * | 2016-11-11 | 2019-07-04 | 에보니크 데구사 게엠베하 | 폴리우레탄 기재 발포체용 유화제 |
Families Citing this family (67)
| 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 |
| EP2074157B1 (en) * | 2006-09-21 | 2017-02-01 | Dow Global Technologies LLC | 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 |
| CN101778913A (zh) * | 2007-08-10 | 2010-07-14 | 大金工业株式会社 | 涂布用组合物 |
| 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 |
| AU2009270862B2 (en) * | 2008-07-18 | 2015-04-30 | Dow Global Technologies Inc. | Natural resource based viscoelastic foams |
| 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 |
| KR20120103720A (ko) | 2009-12-22 | 2012-09-19 | 비와이케이-케미 게엠베하 | 안정한 폴리올 혼합물을 포함하는 조성물 |
| 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 |
| DE102011007479A1 (de) | 2011-04-15 | 2012-10-18 | Evonik Goldschmidt Gmbh | Zusammensetzung, enthaltend spezielle Amide und organomodifizierte Siloxane, geeignet zur Herstellung von Polyurethanschäumen |
| DE102011007468A1 (de) | 2011-04-15 | 2012-10-18 | Evonik Goldschmidt Gmbh | Zusammensetzung, enthaltend spezielle Carbamat-artige Verbindungen, 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 |
| PT2800767T (pt) * | 2012-01-06 | 2019-06-07 | Evonik Degussa Gmbh | Dispersões de melamina em poliol e suas utilizações na produção de poliuretano |
| 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 |
| 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 |
| EP2886591A1 (de) | 2013-12-19 | 2015-06-24 | Evonik Industries AG | Zusammensetzung, geeignet zur Herstellung von Polyurethanschäumen, enthaltend mindestens ein Nukleierungsmittel |
| DE102014215387B4 (de) | 2014-08-05 | 2020-06-10 | 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 |
| 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 |
| DE102014215388A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa Gmbh | Stickstoffhaltige Verbindungen, geeignet zur Verwendung bei der Herstellung von Polyurethanen |
| DE102014215384A1 (de) | 2014-08-05 | 2016-02-11 | Evonik Degussa 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 |
| EP3268406B8 (en) * | 2015-03-12 | 2019-09-18 | Huntsman Advanced Materials Licensing (Switzerland) GmbH | Polyol component for the production of pur foams |
| 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 |
| CN109196014B (zh) * | 2016-04-12 | 2021-11-09 | 赢创运营有限公司 | 硅氧烷-氧化烯共聚物表面活性剂组合物 |
| 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 |
| SG11201903596UA (en) * | 2016-11-10 | 2019-05-30 | Ppg Coatings Europe Bv | Surfactants for intumescent foam stabilization |
| US11312816B2 (en) * | 2017-04-12 | 2022-04-26 | Basf Se | Thermoplastic polyurethane and composite article |
| WO2019170484A1 (en) * | 2018-03-06 | 2019-09-12 | Basf Se | A preparation comprising thermoplastic polyisocyanate polyaddition product, a process for preparing the same and use thereof |
| EP3765540B1 (en) * | 2018-03-13 | 2023-01-25 | 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 |
| JP2022546564A (ja) | 2019-09-03 | 2022-11-04 | ダウ グローバル テクノロジーズ エルエルシー | フォーム配合物 |
| PT3819323T (pt) | 2019-11-07 | 2025-11-07 | Evonik Operations GmbH | Conjunto de compressão |
| 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 |
| CA3222682A1 (en) | 2021-06-17 | 2022-12-22 | Daniela HERMANN | Shaped flexible pu foam articles |
| 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 |
| CN117597373A (zh) | 2021-07-02 | 2024-02-23 | 赢创运营有限公司 | Pu泡沫的生产 |
| 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 |
| EP4257325A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | Optical prediction of polyurethane foam parameters |
| EP4257324A1 (en) | 2022-04-08 | 2023-10-11 | Evonik Operations GmbH | System and method for automatically setting parameters for 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 |
| WO2025040585A1 (en) | 2023-08-24 | 2025-02-27 | Evonik Operations Gmbh | Improved process for the depolymerization of polyurethane |
Family Cites Families (10)
| 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 |
| 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 |
| 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 |
| AU727456B2 (en) * | 1997-03-20 | 2000-12-14 | Huntsman International Llc | Process for rigid polyurethane foams |
| 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 |
| WO2000046266A1 (en) * | 1999-02-03 | 2000-08-10 | Huntsman Petrochemical Corporation | Compatibilization of blowing agent polyol mixtures for polyurethane foam manufacture |
| US20030083394A1 (en) * | 2001-06-07 | 2003-05-01 | Clatty Jan L. | Polyurethane foams having improved heat sag and a process for their production |
| 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 DE DE602007001550T patent/DE602007001550D1/de active Active
- 2007-03-29 ES ES07006484T patent/ES2327456T3/es active Active
- 2007-03-29 EP EP07006484A patent/EP1845121B1/en not_active Not-in-force
- 2007-04-04 CA CA002583950A patent/CA2583950A1/en not_active Abandoned
- 2007-04-10 KR KR1020070034939A patent/KR20070101143A/ko not_active Withdrawn
- 2007-04-10 SG SG200702618-0A patent/SG136890A1/en unknown
- 2007-04-10 BR BRPI0701994-7A patent/BRPI0701994A/pt not_active IP Right Cessation
- 2007-04-10 CN CN2007100971496A patent/CN101054433B/zh not_active Expired - Fee Related
- 2007-04-10 RU RU2007113125/04A patent/RU2007113125A/ru not_active Application Discontinuation
- 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
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20190078630A (ko) * | 2016-11-11 | 2019-07-04 | 에보니크 데구사 게엠베하 | 폴리우레탄 기재 발포체용 유화제 |
| KR20230125109A (ko) * | 2016-11-11 | 2023-08-28 | 에보니크 오퍼레이션즈 게엠베하 | 폴리우레탄 기재 발포체용 유화제 |
| US11814468B2 (en) | 2016-11-11 | 2023-11-14 | Evonik Operations Gmbh | Emulsifiers for polyurethane based foam |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2583950A1 (en) | 2007-10-11 |
| EP1845121A1 (en) | 2007-10-17 |
| MX2007004222A (es) | 2009-02-16 |
| ES2327456T3 (es) | 2009-10-29 |
| US20070238800A1 (en) | 2007-10-11 |
| SG136890A1 (en) | 2007-11-29 |
| RU2007113125A (ru) | 2008-10-20 |
| JP5289722B2 (ja) | 2013-09-11 |
| EP1845121B1 (en) | 2009-07-15 |
| BRPI0701994A (pt) | 2007-12-11 |
| CN101054433A (zh) | 2007-10-17 |
| CN101054433B (zh) | 2011-09-21 |
| DE602007001550D1 (de) | 2009-08-27 |
| JP2007277560A (ja) | 2007-10-25 |
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