CZ296406B6 - Polyetherové polyoly s dlouhým retezcem a vysokýmobsahem primárních hydroxylových skupin, zpusob jejich výroby a pouzití - Google Patents
Polyetherové polyoly s dlouhým retezcem a vysokýmobsahem primárních hydroxylových skupin, zpusob jejich výroby a pouzití Download PDFInfo
- Publication number
- CZ296406B6 CZ296406B6 CZ20013761A CZ20013761A CZ296406B6 CZ 296406 B6 CZ296406 B6 CZ 296406B6 CZ 20013761 A CZ20013761 A CZ 20013761A CZ 20013761 A CZ20013761 A CZ 20013761A CZ 296406 B6 CZ296406 B6 CZ 296406B6
- Authority
- CZ
- Czechia
- Prior art keywords
- hydroxyl groups
- mixture
- grams
- range
- dmc catalyst
- Prior art date
Links
- 229920005862 polyol Polymers 0.000 title claims abstract description 64
- 150000003077 polyols Chemical class 0.000 title claims abstract description 62
- 229920000570 polyether Polymers 0.000 title claims abstract description 44
- 239000004721 Polyphenylene oxide Substances 0.000 title claims abstract description 41
- 125000002887 hydroxy group Chemical group [H]O* 0.000 title claims abstract description 38
- 238000000034 method Methods 0.000 title claims description 25
- 238000002360 preparation method Methods 0.000 title description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 46
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 45
- 239000000203 mixture Substances 0.000 claims abstract description 34
- 239000007858 starting material Substances 0.000 claims abstract description 23
- 125000006353 oxyethylene group Chemical group 0.000 claims abstract description 21
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 11
- 239000003054 catalyst Substances 0.000 claims description 48
- 239000003960 organic solvent Substances 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 abstract description 5
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 18
- 239000011541 reaction mixture Substances 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 11
- -1 ether polyol Chemical class 0.000 description 10
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000012153 distilled water Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 229920002635 polyurethane Polymers 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 125000005702 oxyalkylene group Chemical group 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000003039 volatile agent Substances 0.000 description 3
- HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 238000010923 batch production Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- RKBAPHPQTADBIK-UHFFFAOYSA-N cobalt;hexacyanide Chemical compound [Co].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] RKBAPHPQTADBIK-UHFFFAOYSA-N 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000010107 reaction injection moulding Methods 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 229960004793 sucrose Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/08—Saturated oxiranes
- C08G65/10—Saturated oxiranes characterised by the catalysts used
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2642—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds characterised by the catalyst used
- C08G65/2645—Metals or compounds thereof, e.g. salts
- C08G65/2663—Metal cyanide catalysts, i.e. DMC's
-
- 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
- C08G18/4841—Polyethers containing oxyethylene units and other oxyalkylene units containing oxyethylene 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
- C08G18/4866—Polyethers having a low unsaturation value
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Toxicology (AREA)
- Polyethers (AREA)
- Polyurethanes Or Polyureas (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Cephalosporin Compounds (AREA)
- Investigating Or Analysing Materials By Optical Means (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19918727A DE19918727A1 (de) | 1999-04-24 | 1999-04-24 | Langkettige Polyetherpolyole mit hohem Anteil primärer OH-Gruppen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CZ20013761A3 CZ20013761A3 (cs) | 2002-04-17 |
| CZ296406B6 true CZ296406B6 (cs) | 2006-03-15 |
Family
ID=7905780
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CZ20013761A CZ296406B6 (cs) | 1999-04-24 | 2000-04-11 | Polyetherové polyoly s dlouhým retezcem a vysokýmobsahem primárních hydroxylových skupin, zpusob jejich výroby a pouzití |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US6617419B1 (enExample) |
| EP (1) | EP1173498B1 (enExample) |
| JP (1) | JP2002543228A (enExample) |
| KR (1) | KR100610285B1 (enExample) |
| CN (1) | CN1183180C (enExample) |
| AT (1) | ATE273339T1 (enExample) |
| AU (1) | AU3819600A (enExample) |
| BR (1) | BR0010002B1 (enExample) |
| CA (1) | CA2367670C (enExample) |
| CZ (1) | CZ296406B6 (enExample) |
| DE (2) | DE19918727A1 (enExample) |
| ES (1) | ES2226804T3 (enExample) |
| HK (1) | HK1046147B (enExample) |
| HU (1) | HU228388B1 (enExample) |
| ID (1) | ID30542A (enExample) |
| MX (1) | MXPA01010737A (enExample) |
| PL (1) | PL199860B1 (enExample) |
| PT (1) | PT1173498E (enExample) |
| RU (1) | RU2242485C2 (enExample) |
| WO (1) | WO2000064963A1 (enExample) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19928156A1 (de) * | 1999-06-19 | 2000-12-28 | Bayer Ag | Aus Polyetherpolyolen hergestellte Polyurethan-Weichschäume |
| EP1469027B1 (en) | 2002-01-22 | 2014-07-16 | Asahi Glass Company, Limited | Process for continuously producing polyether |
| JP4273876B2 (ja) * | 2003-08-25 | 2009-06-03 | 旭硝子株式会社 | ポリエーテルモノオールまたはポリエーテルポリオールおよびその製造方法 |
| CN100549063C (zh) * | 2003-10-10 | 2009-10-14 | 国际壳牌研究有限公司 | 制备聚醚多元醇的方法 |
| JP4899508B2 (ja) * | 2006-02-03 | 2012-03-21 | 旭硝子株式会社 | ポリエーテルポリオールの製造方法 |
| CN100588669C (zh) * | 2006-11-28 | 2010-02-10 | 王伟松 | 烯丙醇无规聚醚的制备方法 |
| DE102007002555A1 (de) * | 2007-01-17 | 2008-07-24 | Bayer Materialscience Ag | Doppelmetallcyanid-Katalysatoren für die Herstellung von Polyetherpolyolen |
| DE102007057147A1 (de) | 2007-11-28 | 2009-06-04 | Evonik Goldschmidt Gmbh | Verfahren zur Alkoxylierung mit DMC-Katalysatoren im Schlaufenreaktor mit Strahlsauger |
| EP2241584B1 (en) * | 2008-01-25 | 2012-03-21 | Kaneka Corporation | Process for producing polyalkylene oxide |
| TW201120076A (en) * | 2009-10-05 | 2011-06-16 | Asahi Glass Co Ltd | Method for producing soft polyurethane foam and sheet |
| US20110230581A1 (en) * | 2010-03-17 | 2011-09-22 | Bayer Materialscience Llc | Process for the production of polyether polyols with a high ethylene oxide content |
| WO2011136367A1 (ja) * | 2010-04-30 | 2011-11-03 | 旭硝子株式会社 | ポリオキシアルキレンポリオール、ポリマー分散ポリオール、および軟質ポリウレタンフォーム、ならびにこれらの製造方法 |
| JP5648797B2 (ja) * | 2010-11-22 | 2015-01-07 | 旭硝子株式会社 | ポリエーテルヒドロキシ化合物の製造方法 |
| EP2530101A1 (de) * | 2011-06-01 | 2012-12-05 | Bayer MaterialScience AG | Verfahren zur Herstellung von Polyetherpolyolen |
| CN102417594A (zh) * | 2011-10-14 | 2012-04-18 | 滨州市华茂工贸有限公司 | 缩合醇无规聚醚的配方、生产工艺及应用 |
| SG10201604976RA (en) | 2011-12-20 | 2016-08-30 | Bayer Ip Gmbh | Hydroxy-aminopolymers and method for producing same |
| EP2840103A4 (en) * | 2012-04-18 | 2015-09-23 | Asahi Glass Co Ltd | PROCESS FOR PREPARING POLYETHERES |
| US9051412B2 (en) * | 2013-03-14 | 2015-06-09 | Bayer Materialscience Llc | Base-catalyzed, long chain, active polyethers from short chain DMC-catalyzed starters |
| US20170355818A1 (en) * | 2014-11-07 | 2017-12-14 | Idemitsu Kosan Co., Ltd. | Method for producing polyalkylene glycol, viscosity index improver, lubricating oil composition, and method for producing lubricating oil composition |
| AR104981A1 (es) * | 2015-06-20 | 2017-08-30 | Dow Global Technologies Llc | Proceso continuo para producir polioles de poliéter que tienen un elevado contenido de óxido de etileno polimerizado, mediante el uso de un complejo catalizador de cianuro de metal doble y un compuesto metálico de la serie de lantanida o metal del grupo 3 - grupo 15, magnesio |
| PL3681925T3 (pl) * | 2017-09-15 | 2022-10-31 | Dow Global Technologies Llc | Ciągły sposób wytwarzania polieteropolioli |
| PL3707192T3 (pl) | 2017-11-06 | 2023-07-31 | Shell Internationale Research Maatschappij B.V. | Sposób wytwarzania poliolu polieterowego o wysokiej zawartości tlenku etylenu |
| JP7202524B2 (ja) * | 2019-01-21 | 2023-01-12 | 日油株式会社 | アルキレンオキシド誘導体、潤滑剤、消泡剤、化粧品用基材およびそれを含む化粧料 |
| WO2020153223A1 (ja) * | 2019-01-21 | 2020-07-30 | 日油株式会社 | アルキレンオキシド誘導体、消泡剤、潤滑剤、化粧料用基材およびそれを含む化粧料、毛髪用洗浄剤組成物および身体用洗浄剤組成物 |
| CN111303403B (zh) * | 2020-04-13 | 2022-06-14 | 山东蓝星东大有限公司 | 端多羟基聚醚多元醇制备方法 |
| US11753516B2 (en) | 2021-10-08 | 2023-09-12 | Covestro Llc | HFO-containing compositions and methods of producing foams |
| EP4279534A1 (en) | 2022-05-20 | 2023-11-22 | PCC ROKITA Spolka Akcyjna | A method for producing low unsaturation level oxyalkylates, an oxyalkylate, a use thereof and a polyurethane foam |
| PL442356A1 (pl) * | 2022-09-26 | 2024-04-02 | Pcc Rokita Spółka Akcyjna | Poliol polieterowy, sposób jego wytwarzania i jego zastosowanie oraz elastyczna pianka poliuretanowa |
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|---|---|---|---|---|
| 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 |
| CA1155871A (en) | 1980-10-16 | 1983-10-25 | Gencorp Inc. | Method for treating polypropylene ether and poly-1,2- butylene ether polyols |
| US5103062A (en) * | 1987-04-10 | 1992-04-07 | Texaco Inc. | Modified normally liquid, water-soluble polyoxyalkylene polyamines |
| US4942214A (en) * | 1988-06-29 | 1990-07-17 | W. L. Gore & Assoc. Inc. | Flexible breathable polyurethane coatings and films, and the prepolymers from which they are made |
| JPH02191628A (ja) * | 1989-01-19 | 1990-07-27 | Dai Ichi Kogyo Seiyaku Co Ltd | ポリエーテルポリオール |
| JP2999789B2 (ja) * | 1990-02-23 | 2000-01-17 | 旭硝子株式会社 | ポリエーテル類の製造方法 |
| US5158922A (en) | 1992-02-04 | 1992-10-27 | Arco Chemical Technology, L.P. | Process for preparing metal cyanide complex catalyst |
| JP3299803B2 (ja) * | 1993-02-26 | 2002-07-08 | 旭硝子株式会社 | ポリエーテルポリオールの製造方法 |
| US5482908A (en) | 1994-09-08 | 1996-01-09 | Arco Chemical Technology, L.P. | Highly active double metal cyanide catalysts |
| US5563221A (en) | 1995-06-21 | 1996-10-08 | Arco Chemical Technology, L.P. | Process for making ethylene oxide-capped polyols from double metal cyanide-catalyzed polyols |
| US5545601A (en) | 1995-08-22 | 1996-08-13 | Arco Chemical Technology, L.P. | Polyether-containing double metal cyanide catalysts |
| US5700847A (en) * | 1995-12-04 | 1997-12-23 | Arco Chemical Technology, L.P. | Molded polyurethane foam with enhanced physical properties |
| US5668191A (en) | 1995-12-21 | 1997-09-16 | Arco Chemical Technology, L.P. | One-shot cold molded flexible polyurethane foam from low primary hydroxyl polyols and process for the preparation thereof |
| US5605939A (en) * | 1996-01-26 | 1997-02-25 | Arco Chemical Technology, L.P. | Poly(oxypropylene/oxyethylene) random polyols useful in preparing flexible high resilience foam with reduced tendencies toward shrinkage and foam prepared therewith |
| 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 |
| RU2115667C1 (ru) * | 1997-04-22 | 1998-07-20 | Научно-исследовательский институт по нефтепромысловой химии | Продукт последовательного присоединения окиси этилена и окиси пропилена к высшему жирному спирту и состав для предотвращения асфальтено-смолопарафиновых отложений |
| CA2306378C (en) | 1997-10-13 | 2007-07-17 | Bayer Aktiengesellschaft | Crystalline double metal cyanide catalysts for producing polyether polyols |
| DE19810269A1 (de) | 1998-03-10 | 2000-05-11 | Bayer Ag | Verbesserte Doppelmetallcyanid-Katalysatoren für die Herstellung von Polyetherpolyolen |
| US6066683A (en) | 1998-04-03 | 2000-05-23 | Lyondell Chemical Worldwide, Inc. | Molded and slab polyurethane foam prepared from double metal cyanide complex-catalyzed polyoxyalkylene polyols and polyols suitable for the preparation thereof |
| US6008263A (en) | 1998-04-03 | 1999-12-28 | Lyondell Chemical Worldwide, Inc. | Molded and slab polyurethane foam prepared from double metal cyanide complex-catalyzed polyoxyalkylene polyols and polyols suitable for the preparation thereof |
-
1999
- 1999-04-24 DE DE19918727A patent/DE19918727A1/de not_active Withdrawn
-
2000
- 2000-04-11 RU RU2001131893/04A patent/RU2242485C2/ru not_active IP Right Cessation
- 2000-04-11 HU HU0200782A patent/HU228388B1/hu not_active IP Right Cessation
- 2000-04-11 WO PCT/EP2000/003217 patent/WO2000064963A1/de not_active Ceased
- 2000-04-11 HK HK02107758.5A patent/HK1046147B/zh not_active IP Right Cessation
- 2000-04-11 CN CNB008067120A patent/CN1183180C/zh not_active Expired - Lifetime
- 2000-04-11 MX MXPA01010737A patent/MXPA01010737A/es active IP Right Grant
- 2000-04-11 BR BRPI0010002-1A patent/BR0010002B1/pt not_active IP Right Cessation
- 2000-04-11 PL PL351384A patent/PL199860B1/pl unknown
- 2000-04-11 ES ES00917070T patent/ES2226804T3/es not_active Expired - Lifetime
- 2000-04-11 AU AU38196/00A patent/AU3819600A/en not_active Abandoned
- 2000-04-11 KR KR1020017013535A patent/KR100610285B1/ko not_active Expired - Lifetime
- 2000-04-11 EP EP00917070A patent/EP1173498B1/de not_active Expired - Lifetime
- 2000-04-11 DE DE50007388T patent/DE50007388D1/de not_active Expired - Lifetime
- 2000-04-11 ID IDW00200102276A patent/ID30542A/id unknown
- 2000-04-11 JP JP2000614312A patent/JP2002543228A/ja active Pending
- 2000-04-11 PT PT00917070T patent/PT1173498E/pt unknown
- 2000-04-11 CZ CZ20013761A patent/CZ296406B6/cs not_active IP Right Cessation
- 2000-04-11 US US10/009,889 patent/US6617419B1/en not_active Expired - Lifetime
- 2000-04-11 AT AT00917070T patent/ATE273339T1/de not_active IP Right Cessation
- 2000-04-11 CA CA002367670A patent/CA2367670C/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| HUP0200782A2 (en) | 2002-06-29 |
| EP1173498A1 (de) | 2002-01-23 |
| AU3819600A (en) | 2000-11-10 |
| ATE273339T1 (de) | 2004-08-15 |
| CZ20013761A3 (cs) | 2002-04-17 |
| CA2367670A1 (en) | 2000-11-02 |
| MXPA01010737A (es) | 2002-06-04 |
| PL199860B1 (pl) | 2008-11-28 |
| HU228388B1 (en) | 2013-03-28 |
| PT1173498E (pt) | 2005-01-31 |
| CN1348476A (zh) | 2002-05-08 |
| HUP0200782A3 (en) | 2004-03-29 |
| RU2242485C2 (ru) | 2004-12-20 |
| PL351384A1 (en) | 2003-04-07 |
| BR0010002B1 (pt) | 2010-06-15 |
| DE50007388D1 (de) | 2004-09-16 |
| CN1183180C (zh) | 2005-01-05 |
| ES2226804T3 (es) | 2005-04-01 |
| BR0010002A (pt) | 2002-01-08 |
| HK1046147A1 (en) | 2002-12-27 |
| WO2000064963A1 (de) | 2000-11-02 |
| US6617419B1 (en) | 2003-09-09 |
| DE19918727A1 (de) | 2000-10-26 |
| EP1173498B1 (de) | 2004-08-11 |
| KR100610285B1 (ko) | 2006-08-09 |
| HK1046147B (zh) | 2005-08-19 |
| CA2367670C (en) | 2008-10-07 |
| KR20010110796A (ko) | 2001-12-13 |
| JP2002543228A (ja) | 2002-12-17 |
| ID30542A (id) | 2001-12-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Patent lapsed due to non-payment of fee |
Effective date: 20160411 |