NO313555B1 - Mykelastiske polyuretanskumstoffer og en fremgangsmåte for fremstilling derav - Google Patents
Mykelastiske polyuretanskumstoffer og en fremgangsmåte for fremstilling derav Download PDFInfo
- Publication number
- NO313555B1 NO313555B1 NO19975512A NO975512A NO313555B1 NO 313555 B1 NO313555 B1 NO 313555B1 NO 19975512 A NO19975512 A NO 19975512A NO 975512 A NO975512 A NO 975512A NO 313555 B1 NO313555 B1 NO 313555B1
- Authority
- NO
- Norway
- Prior art keywords
- chain
- weight
- polyether
- functionality
- polyether polyol
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 9
- 229920005830 Polyurethane Foam Polymers 0.000 title claims description 9
- 239000011496 polyurethane foam Substances 0.000 title claims description 9
- 229920005862 polyol Polymers 0.000 claims abstract description 30
- 150000003077 polyols Chemical class 0.000 claims abstract description 25
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 22
- 229920000570 polyether Polymers 0.000 claims abstract description 22
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims abstract description 16
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920001228 polyisocyanate Polymers 0.000 claims abstract description 11
- 239000005056 polyisocyanate Substances 0.000 claims abstract description 11
- 238000004519 manufacturing process Methods 0.000 claims abstract description 8
- 239000000654 additive Substances 0.000 claims abstract description 5
- 239000003381 stabilizer Substances 0.000 claims abstract description 4
- 239000012190 activator Substances 0.000 claims abstract description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 8
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 4
- 239000003380 propellant Substances 0.000 claims description 4
- JXCHMDATRWUOAP-UHFFFAOYSA-N diisocyanatomethylbenzene Chemical compound O=C=NC(N=C=O)C1=CC=CC=C1 JXCHMDATRWUOAP-UHFFFAOYSA-N 0.000 claims description 3
- PCHXZXKMYCGVFA-UHFFFAOYSA-N 1,3-diazetidine-2,4-dione Chemical group O=C1NC(=O)N1 PCHXZXKMYCGVFA-UHFFFAOYSA-N 0.000 claims description 2
- 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 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical group NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 2
- 239000004202 carbamide Chemical group 0.000 claims description 2
- 150000001718 carbodiimides 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
- 239000007788 liquid Substances 0.000 claims description 2
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical group NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 2
- 239000006260 foam Substances 0.000 abstract description 10
- 239000004604 Blowing Agent Substances 0.000 abstract 1
- 229920003225 polyurethane elastomer Polymers 0.000 abstract 1
- 235000019589 hardness Nutrition 0.000 description 11
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 229920001821 foam rubber Polymers 0.000 description 6
- 238000005482 strain hardening Methods 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 4
- -1 ester polyols Chemical class 0.000 description 4
- 239000006261 foam material Substances 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- 239000004814 polyurethane Substances 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000004872 foam stabilizing agent Substances 0.000 description 3
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- 206010024453 Ligament sprain Diseases 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 208000010040 Sprains and Strains Diseases 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- GIWQSPITLQVMSG-UHFFFAOYSA-N 1,2-dimethylimidazole Chemical compound CC1=NC=CN1C GIWQSPITLQVMSG-UHFFFAOYSA-N 0.000 description 1
- AXFVIWBTKYFOCY-UHFFFAOYSA-N 1-n,1-n,3-n,3-n-tetramethylbutane-1,3-diamine Chemical compound CN(C)C(C)CCN(C)C AXFVIWBTKYFOCY-UHFFFAOYSA-N 0.000 description 1
- LXBGSDVWAMZHDD-UHFFFAOYSA-N 2-methyl-1h-imidazole Chemical compound CC1=NC=CN1 LXBGSDVWAMZHDD-UHFFFAOYSA-N 0.000 description 1
- HVCNXQOWACZAFN-UHFFFAOYSA-N 4-ethylmorpholine Chemical compound CCN1CCOCC1 HVCNXQOWACZAFN-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
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ISKQADXMHQSTHK-UHFFFAOYSA-N [4-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=C(CN)C=C1 ISKQADXMHQSTHK-UHFFFAOYSA-N 0.000 description 1
- CQQXCSFSYHAZOO-UHFFFAOYSA-L [acetyloxy(dioctyl)stannyl] acetate Chemical compound CCCCCCCC[Sn](OC(C)=O)(OC(C)=O)CCCCCCCC CQQXCSFSYHAZOO-UHFFFAOYSA-L 0.000 description 1
- UKLDJPRMSDWDSL-UHFFFAOYSA-L [dibutyl(dodecanoyloxy)stannyl] dodecanoate Chemical compound CCCCCCCCCCCC(=O)O[Sn](CCCC)(CCCC)OC(=O)CCCCCCCCCCC UKLDJPRMSDWDSL-UHFFFAOYSA-L 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- RGAMPJYGTCSRAG-UHFFFAOYSA-N bis[2-(diethylamino)ethyl] hexanedioate Chemical compound CCN(CC)CCOC(=O)CCCCC(=O)OCCN(CC)CC RGAMPJYGTCSRAG-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- RJGHQTVXGKYATR-UHFFFAOYSA-L dibutyl(dichloro)stannane Chemical compound CCCC[Sn](Cl)(Cl)CCCC RJGHQTVXGKYATR-UHFFFAOYSA-L 0.000 description 1
- JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 1
- 239000012975 dibutyltin dilaurate Substances 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- HGQSXVKHVMGQRG-UHFFFAOYSA-N dioctyltin Chemical compound CCCCCCCC[Sn]CCCCCCCC HGQSXVKHVMGQRG-UHFFFAOYSA-N 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 230000001408 fungistatic effect Effects 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
- 150000005828 hydrofluoroalkanes Chemical class 0.000 description 1
- QWTDNUCVQCZILF-UHFFFAOYSA-N iso-pentane Natural products CCC(C)C QWTDNUCVQCZILF-UHFFFAOYSA-N 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- XFLSMWXCZBIXLV-UHFFFAOYSA-N n,n-dimethyl-2-(4-methylpiperazin-1-yl)ethanamine Chemical compound CN(C)CCN1CCN(C)CC1 XFLSMWXCZBIXLV-UHFFFAOYSA-N 0.000 description 1
- ZWRDBWDXRLPESY-UHFFFAOYSA-N n-benzyl-n-ethylethanamine Chemical compound CCN(CC)CC1=CC=CC=C1 ZWRDBWDXRLPESY-UHFFFAOYSA-N 0.000 description 1
- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- SYRHIZPPCHMRIT-UHFFFAOYSA-N tin(4+) Chemical class [Sn+4] SYRHIZPPCHMRIT-UHFFFAOYSA-N 0.000 description 1
- RUELTTOHQODFPA-UHFFFAOYSA-N toluene 2,6-diisocyanate Chemical compound CC1=C(N=C=O)C=CC=C1N=C=O RUELTTOHQODFPA-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 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
- 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
- C08G18/4804—Two or more polyethers of different physical or chemical nature
- C08G18/4812—Mixtures of polyetherdiols with polyetherpolyols having at least three hydroxy 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
- C08G2110/00—Foam properties
- C08G2110/0008—Foam properties flexible
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0041—Foam properties having specified density
- C08G2110/005—< 50kg/m3
-
- 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
- C08G2110/00—Foam properties
- C08G2110/0083—Foam properties prepared using water as the sole blowing agent
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S521/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S521/914—Polyurethane cellular product formed from a polyol which has been derived from at least two 1,2 epoxides as reactants
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)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Materials For Medical Uses (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19649829A DE19649829A1 (de) | 1996-12-02 | 1996-12-02 | Weichelastische Polyurethanschaumstoffe und ein Verfahren zu deren Herstellung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO975512D0 NO975512D0 (no) | 1997-12-01 |
| NO975512L NO975512L (no) | 1998-06-03 |
| NO313555B1 true NO313555B1 (no) | 2002-10-21 |
Family
ID=7813325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19975512A NO313555B1 (no) | 1996-12-02 | 1997-12-01 | Mykelastiske polyuretanskumstoffer og en fremgangsmåte for fremstilling derav |
Country Status (10)
| Country | Link |
|---|---|
| US (2) | US5814676A (fr) |
| EP (1) | EP0845485B1 (fr) |
| JP (1) | JP4106116B2 (fr) |
| AT (1) | ATE281484T1 (fr) |
| CA (1) | CA2223191C (fr) |
| DE (2) | DE19649829A1 (fr) |
| DK (1) | DK0845485T3 (fr) |
| ES (1) | ES2231838T3 (fr) |
| NO (1) | NO313555B1 (fr) |
| PT (1) | PT845485E (fr) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5889068A (en) * | 1997-07-24 | 1999-03-30 | Bayer Corporation | Water blown polyurethane soling systems |
| DE19813107A1 (de) * | 1998-03-25 | 1999-09-30 | Basf Ag | Verfahren zur Herstellung von Polyurethanschaumstoffen |
| DE19924802B4 (de) * | 1999-05-29 | 2008-02-28 | Basf Ag | Verfahren zur Herstellung von schalldämpfenden und energieabsorbierenden Polyurethanschäumen |
| DE19924804C5 (de) * | 1999-05-29 | 2009-02-12 | Basf Se | Verfahren zur Herstellung von schallabsorbierenden Polyurethanschäumen mit adhäsiver Oberfläche |
| CZ20021747A3 (cs) * | 1999-11-22 | 2002-08-14 | Shell Internationale Research Maatschappij B. V. | Způsob výroby pruľné polyuretanové pěny |
| AU2004901A (en) | 2000-01-17 | 2001-07-31 | Huntsman International Llc | Process for preparing a free rise or slabstock flexible polyurethane foam |
| US6344494B1 (en) * | 2000-05-24 | 2002-02-05 | Basf Corporation | Use of low unsaturated polyether polyols in slabstock foam applications |
| EP1164153A1 (fr) * | 2000-06-13 | 2001-12-19 | Huntsman International Llc | Procédé pour la préparation de mousses flexibles de polyuréthane |
| DE10105558A1 (de) * | 2001-02-06 | 2005-04-07 | Basf Ag | Verfahren zur Herstellung von in-situ retikulierten Polyurethanweichschaumstoffen |
| DE10105559A1 (de) * | 2001-02-06 | 2002-08-08 | Basf Ag | Verfahren zur Herstellung von niedrigdichten hydrophilen Polyurethanweichschaumstoffen |
| DE10105560A1 (de) * | 2001-02-06 | 2002-08-08 | Basf Ag | Verfahren zur Herstellung von Polyurethanweichschäumen |
| US7572837B2 (en) | 2001-10-31 | 2009-08-11 | Tosoh Corporation | Process for the production of flexible polyurethane foams |
| US7179845B2 (en) * | 2003-01-10 | 2007-02-20 | Fomo Products, Inc. | Elastomeric latex foams |
| US20040154718A1 (en) * | 2003-02-06 | 2004-08-12 | Doesburg Van I. | Polyurethane filled tire and method of making same |
| DE102004010983A1 (de) * | 2004-03-03 | 2005-09-22 | Georg-August-Universität Göttingen | Vorrichtung zur Entnahme und Ausstrich von Zellen |
| EP1600571B2 (fr) † | 2004-05-27 | 2011-12-21 | ISO-Chemie GmbH | Elément d'étanchéité |
| DE102004059724A1 (de) * | 2004-12-11 | 2006-06-14 | Bayer Materialscience Ag | Verfahren und Anlage zur Herstellung von Schaumstoff in einem kontinuierlichen Schaumprozess |
| DE102005003341A1 (de) * | 2005-01-25 | 2006-07-27 | Bayer Materialscience Ag | Verfahren und Anlage zur optimierten Herstellung von Schaumstoff in einem kontinuierlichen Blockschaumprozess |
| JP5710654B2 (ja) * | 2013-01-09 | 2015-04-30 | 東洋ゴム工業株式会社 | ポリウレタンフォームパネル |
| JP5710653B2 (ja) * | 2013-01-09 | 2015-04-30 | 東洋ゴム工業株式会社 | ポリウレタンフォームパネル |
| JP5615389B2 (ja) * | 2013-01-09 | 2014-10-29 | 東洋ゴム工業株式会社 | 建築構造体及びその製造方法 |
| EP3133097B1 (fr) * | 2015-08-17 | 2022-10-05 | Evonik Operations GmbH | Mousses souples de polyuréthane a durete elevee |
| CN106632985B (zh) * | 2015-11-04 | 2019-04-23 | 万华化学（北京）有限公司 | 一种聚氨酯泡沫材料及其制备方法和用途 |
| LT3394137T (lt) * | 2015-12-21 | 2021-06-10 | Shell Internationale Research Maatschappij B.V. | Poliuretano putplasčio gamybos būdas |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4008189A (en) * | 1974-06-03 | 1977-02-15 | Olin Corporation | Hydrophilic polyurethane foam |
| DE3806476A1 (de) * | 1988-03-01 | 1989-09-14 | Bayer Ag | Verfahren zur herstellung von kalthaertenden polyurethan-weichformschaumstoffen mit hervorragenden daempfungseigenschaften |
| DE3901189A1 (de) * | 1989-01-17 | 1990-09-20 | Bayer Ag | Verfahren zur herstellung von polyurethan-weichformschaumstoffen niedriger rohdichte |
| DE4202992A1 (de) * | 1992-02-03 | 1993-08-05 | Bayer Ag | Verfahren zur herstellung von elastischen, offenzelligen pur-weichschaumstoffen |
| CA2132595C (fr) * | 1993-09-22 | 1999-03-16 | Thomas L. Fishback | Composition de polyol a bonnes caracteristiques d'ecoulement et mousses de polyurethane rigides gonflees a l'eau obtenues avec celles-ci, a bonne stabilite dimensionnelle |
| US5478494A (en) * | 1993-09-22 | 1995-12-26 | Basf Corporation | Polyol composition having good flow and formic acid blown rigid polyurethane foams made thereby having good dimensional stability |
-
1996
- 1996-12-02 DE DE19649829A patent/DE19649829A1/de not_active Withdrawn
-
1997
- 1997-11-20 DE DE59712060T patent/DE59712060D1/de not_active Expired - Fee Related
- 1997-11-20 PT PT97120331T patent/PT845485E/pt unknown
- 1997-11-20 DK DK97120331T patent/DK0845485T3/da active
- 1997-11-20 AT AT97120331T patent/ATE281484T1/de not_active IP Right Cessation
- 1997-11-20 EP EP97120331A patent/EP0845485B1/fr not_active Expired - Lifetime
- 1997-11-20 ES ES97120331T patent/ES2231838T3/es not_active Expired - Lifetime
- 1997-11-24 US US08/976,929 patent/US5814676A/en not_active Expired - Fee Related
- 1997-11-26 CA CA002223191A patent/CA2223191C/fr not_active Expired - Fee Related
- 1997-12-01 NO NO19975512A patent/NO313555B1/no not_active IP Right Cessation
- 1997-12-01 JP JP34365497A patent/JP4106116B2/ja not_active Expired - Fee Related
-
1998
- 1998-06-10 US US09/095,201 patent/US5863961A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| NO975512D0 (no) | 1997-12-01 |
| ES2231838T3 (es) | 2005-05-16 |
| JPH10168153A (ja) | 1998-06-23 |
| EP0845485A1 (fr) | 1998-06-03 |
| US5814676A (en) | 1998-09-29 |
| EP0845485B1 (fr) | 2004-11-03 |
| CA2223191A1 (fr) | 1998-06-02 |
| MX9709391A (es) | 1998-06-30 |
| CA2223191C (fr) | 2009-04-07 |
| ATE281484T1 (de) | 2004-11-15 |
| DE19649829A1 (de) | 1998-06-04 |
| DE59712060D1 (de) | 2004-12-09 |
| JP4106116B2 (ja) | 2008-06-25 |
| US5863961A (en) | 1999-01-26 |
| PT845485E (pt) | 2005-02-28 |
| NO975512L (no) | 1998-06-03 |
| DK0845485T3 (da) | 2005-01-31 |
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