PT929586E - Moldados elastomericos de poliuretano estaveis a luz e processo para a sua producao - Google Patents
Moldados elastomericos de poliuretano estaveis a luz e processo para a sua producao Download PDFInfo
- Publication number
- PT929586E PT929586E PT97942719T PT97942719T PT929586E PT 929586 E PT929586 E PT 929586E PT 97942719 T PT97942719 T PT 97942719T PT 97942719 T PT97942719 T PT 97942719T PT 929586 E PT929586 E PT 929586E
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- Portugal
- Prior art keywords
- weight
- catalyst
- component
- process according
- isocyanate
- Prior art date
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- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 claims abstract description 44
- 238000010107 reaction injection moulding Methods 0.000 claims abstract description 43
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- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 44
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- 150000001412 amines Chemical class 0.000 claims description 31
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 29
- -1 polytetramethylene Polymers 0.000 claims description 23
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 20
- 239000003795 chemical substances by application Substances 0.000 claims description 18
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- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 13
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 12
- 150000001875 compounds Chemical class 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000003431 cross linking reagent Substances 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 238000007654 immersion Methods 0.000 claims description 5
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims description 5
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 4
- 239000004611 light stabiliser Substances 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000004604 Blowing Agent Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 238000000354 decomposition reaction Methods 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 2
- 150000002978 peroxides Chemical class 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- 125000005442 diisocyanate group Chemical group 0.000 claims 1
- 238000007789 sealing Methods 0.000 claims 1
- 238000005538 encapsulation Methods 0.000 abstract description 11
- 229920001971 elastomer Polymers 0.000 description 29
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- 101100494773 Caenorhabditis elegans ctl-2 gene Proteins 0.000 description 6
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- 101100112369 Fasciola hepatica Cat-1 gene Proteins 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 101100005271 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cat-1 gene Proteins 0.000 description 6
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- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 3
- 101100005280 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cat-3 gene Proteins 0.000 description 3
- 101100208039 Rattus norvegicus Trpv5 gene Proteins 0.000 description 3
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- 230000015556 catabolic process Effects 0.000 description 3
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- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003995 emulsifying agent Substances 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
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- BDERNNFJNOPAEC-UHFFFAOYSA-N 1-propanol Substances CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- SXFJDZNJHVPHPH-UHFFFAOYSA-N 3-methylpentane-1,5-diol Chemical compound OCCC(C)CCO SXFJDZNJHVPHPH-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical compound ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
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- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 2
- VQPKAMAVKYTPLB-UHFFFAOYSA-N lead;octanoic acid Chemical compound [Pb].CCCCCCCC(O)=O VQPKAMAVKYTPLB-UHFFFAOYSA-N 0.000 description 2
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 229910052724 xenon Inorganic materials 0.000 description 2
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- QWGRWMMWNDWRQN-UHFFFAOYSA-N 2-methylpropane-1,3-diol Chemical compound OCC(C)CO QWGRWMMWNDWRQN-UHFFFAOYSA-N 0.000 description 1
- RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 206010015946 Eye irritation Diseases 0.000 description 1
- 235000010650 Hyssopus officinalis Nutrition 0.000 description 1
- 240000001812 Hyssopus officinalis Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 101100286123 Mus musculus Hoxa1 gene Proteins 0.000 description 1
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- 229920005830 Polyurethane Foam Polymers 0.000 description 1
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- YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
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- 239000003513 alkali Substances 0.000 description 1
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- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- SXQXMCWCWVCFPC-UHFFFAOYSA-N aluminum;potassium;dioxido(oxo)silane Chemical compound [Al+3].[K+].[O-][Si]([O-])=O.[O-][Si]([O-])=O SXQXMCWCWVCFPC-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 229940053200 antiepileptics fatty acid derivative Drugs 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- JDIBGQFKXXXXPN-UHFFFAOYSA-N bismuth(3+) Chemical class [Bi+3] JDIBGQFKXXXXPN-UHFFFAOYSA-N 0.000 description 1
- CDQSJQSWAWPGKG-UHFFFAOYSA-N butane-1,1-diol Chemical compound CCCC(O)O CDQSJQSWAWPGKG-UHFFFAOYSA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 1
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- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 1
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- PMMYEEVYMWASQN-IMJSIDKUSA-N cis-4-Hydroxy-L-proline Chemical compound O[C@@H]1CN[C@H](C(O)=O)C1 PMMYEEVYMWASQN-IMJSIDKUSA-N 0.000 description 1
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
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- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N ethyl hexanoate Chemical compound CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
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- ACCCMOQWYVYDOT-UHFFFAOYSA-N hexane-1,1-diol Chemical compound CCCCCC(O)O ACCCMOQWYVYDOT-UHFFFAOYSA-N 0.000 description 1
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- WABPQHHGFIMREM-UHFFFAOYSA-N lead(0) Chemical compound [Pb] WABPQHHGFIMREM-UHFFFAOYSA-N 0.000 description 1
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- UWJJYHHHVWZFEP-UHFFFAOYSA-N pentane-1,1-diol Chemical compound CCCCC(O)O UWJJYHHHVWZFEP-UHFFFAOYSA-N 0.000 description 1
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- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical compound CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
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- 238000003756 stirring Methods 0.000 description 1
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- 238000003786 synthesis reaction Methods 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 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
- C08G18/08—Processes
- C08G18/16—Catalysts
- C08G18/161—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22
- C08G18/163—Catalysts containing two or more components to be covered by at least two of the groups C08G18/166, C08G18/18 or C08G18/22 covered by C08G18/18 and C08G18/22
-
- 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
- C08G18/22—Catalysts containing metal 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
- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
- C08G18/72—Polyisocyanates or polyisothiocyanates
- C08G18/77—Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
- C08G18/78—Nitrogen
- C08G18/79—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
- C08G18/791—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
- C08G18/792—Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
-
- 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
- C08G2110/0016—Foam properties semi-rigid
-
- 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
- C08G2110/0066—≥ 150kg/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
- C08G2120/00—Compositions for reaction injection moulding processes
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Polyurethanes Or Polyureas (AREA)
- Artificial Filaments (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Macromonomer-Based Addition Polymer (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
- Heating, Cooling, Or Curing Plastics Or The Like In General (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Vehicle Interior And Exterior Ornaments, Soundproofing, And Insulation (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 |
|---|---|---|---|
| EP96202738 | 1996-10-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PT929586E true PT929586E (pt) | 2001-09-28 |
Family
ID=8224452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PT97942719T PT929586E (pt) | 1996-10-01 | 1997-10-01 | Moldados elastomericos de poliuretano estaveis a luz e processo para a sua producao |
Country Status (22)
Families Citing this family (76)
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| JP4540079B2 (ja) * | 2000-04-28 | 2010-09-08 | Ｊｓｒ株式会社 | 光ファイバ用硬化性樹脂組成物およびその硬化物 |
| EP1177949A1 (en) * | 2000-08-01 | 2002-02-06 | Recticel | Method for manufacturing a trim part for the interior of an automobile vehicle or at least a skin therefor |
| DE10142296C1 (de) | 2001-08-29 | 2003-02-13 | Bayer Ag | Polyurethanelastomere, Verfahren zu ihrer Herstellung und ihre Verwendung |
| US6919486B2 (en) * | 2001-12-21 | 2005-07-19 | Basf Corporation | Polyetherols produced using aluminium phosphonate catalysts |
| US20030213189A1 (en) * | 2002-05-16 | 2003-11-20 | Goldman Arthur S. | Thermoplastic polymer extrusion bending |
| JP4538317B2 (ja) * | 2002-06-21 | 2010-09-08 | ビーエーエスエフ ソシエタス・ヨーロピア | 微細発泡性又は無発泡性の光安定性ポリウレタン材料及びその製造方法 |
| US6825238B2 (en) * | 2003-01-29 | 2004-11-30 | Air Products And Chemicals, Inc. | Low acid organometallic catalyst for the production of flexible, semi-flexible and rigid polyurethane foams |
| EP1620323B1 (en) | 2003-04-18 | 2008-07-16 | Mayex USA Kft. | Dispensing cup |
| WO2005089085A2 (en) | 2003-07-14 | 2005-09-29 | Rhodia Inc | Improved color stability of isocyanates |
| US7296388B2 (en) * | 2003-08-12 | 2007-11-20 | Valentz Arthur J | Skylight having a molded plastic frame |
| EP1510322A1 (en) | 2003-08-27 | 2005-03-02 | Recticel | Method for manufacturing a composite trim part for the interior of an automotive vehicle |
| US20050143478A1 (en) * | 2003-12-24 | 2005-06-30 | Kao Corporation | Catalyst for preparing polyurethane |
| DE102004009740A1 (de) * | 2004-02-25 | 2005-09-15 | Basf Ag | Zinn- und Übergangsmetallfreie Polyurethanschaumstoffe |
| US7021498B2 (en) | 2004-04-06 | 2006-04-04 | Advanced Controls And Engineering | Urethane spray gun assembly |
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| US7268170B2 (en) * | 2004-10-13 | 2007-09-11 | Bayer Materialscience Llc | Foam modifier, foams prepared from this novel foam modifier and a process for the preparation of these foams |
| EP1657267A1 (en) * | 2004-11-10 | 2006-05-17 | INSA (Institut National des Sciences Appliqées) | Two-part polyisocyanate/polyol composition and its use for making casted products, in particular ophthalmic lenses |
| US8188208B2 (en) * | 2005-01-13 | 2012-05-29 | Bayer Materialscience Llc | Solid polyurethane elastomers which exhibit reduced dimensional shrinkage |
| US20060160977A1 (en) * | 2005-01-14 | 2006-07-20 | Jung-Shun Ou | Prescription for preparation of non-yellowing polyurethane foam |
| WO2006083584A2 (en) * | 2005-02-04 | 2006-08-10 | The Procter & Gamble Company | Absorbent structure with improved water-absorbing material |
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| US20070142601A1 (en) * | 2005-12-15 | 2007-06-21 | Bayer Materialscience Llc | RIM elastomers based on isocyanurates of isophorone diisocyanate and prepolymers thereof |
| US20070142607A1 (en) * | 2005-12-15 | 2007-06-21 | Bayer Materialscience Llc | Weather resistant polyurethane elastomer |
| US20070142610A1 (en) * | 2005-12-15 | 2007-06-21 | Harasin Stephen J | Polyurethane elastomers comprising allophanate modified isocyanates |
| US7772353B2 (en) * | 2005-12-15 | 2010-08-10 | Bayer Materialscience Llc | Fast curing aliphatic RIM elastomers |
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| EP2183294B1 (en) * | 2007-07-23 | 2019-01-09 | Dow Global Technologies LLC | Two part polyurethane curable composition having substantially consistent g-modulus across the range of use temperatures |
| EP2185617B1 (en) * | 2007-08-27 | 2016-03-16 | Dow Global Technologies LLC | Catalysis of viscoelastic foams with bismuth salts |
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| US20100227985A1 (en) * | 2007-10-15 | 2010-09-09 | Mitsui Chemicals, Inc. | Granular polyurethane resin composition and molded article of the same |
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| DE102008008391A1 (de) * | 2008-02-09 | 2009-08-13 | Bayer Materialscience Ag | Geschäumte, lichtechte Polyurethanformteile |
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| JP2010214298A (ja) | 2009-03-17 | 2010-09-30 | Japan Gore Tex Inc | 透湿性隔膜材料 |
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| CN101768251B (zh) * | 2009-12-31 | 2012-08-08 | 南京汇科高分子材料有限公司 | 用于汽车玻璃包边的聚氨酯弹性体及其制备方法 |
| EP2365012A1 (en) * | 2010-03-05 | 2011-09-14 | RECTICEL Automobilsysteme GmbH | Method for producing a skin layer of a flexible, elastomeric, thermoset, phase-separated polyurethane material |
| JP2013535559A (ja) | 2010-08-12 | 2013-09-12 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | 耐光性ポリウレタンおよびその使用 |
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| EP2522684A1 (en) | 2011-05-12 | 2012-11-14 | Recticel | Method for functionalising a thermoset isocyanate-based polymeric solid material. |
| KR101319684B1 (ko) | 2011-06-07 | 2013-10-17 | 금호미쓰이화학 주식회사 | 내열성 변성 이소시아네이트 조성물 및 이를 포함하는 내열성을 갖는 파이프 단열용 폴리우레탄 발포체 조성물 및 그 발포방법 |
| EP2679380A1 (en) | 2012-06-28 | 2014-01-01 | RECTICEL Automobilsysteme GmbH | Method for manufacturing a flexible skin having at least one insert adhered thereto. |
| ITMI20131026A1 (it) * | 2013-06-20 | 2014-12-20 | Dow Global Technologies Llc | Processo per la produzione di un espanso poliuretanico che utilizza un catalizzatore tetraalchilstannossi |
| ES2560475T3 (es) | 2013-04-30 | 2016-02-19 | Webasto SE | Método y molde para producir un conjunto de panel |
| DE102013022173B4 (de) | 2013-12-23 | 2017-03-30 | Gt Elektrotechnische Produkte Gmbh | Polyurethan-Elastomere auf der Basis von Polyetheralkoholgemischen und trimerisierten Diisocyanaten |
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| DE102015218869B4 (de) | 2015-09-30 | 2017-10-26 | Lisa Dräxlmaier GmbH | Verfahren und Vorrichtung zur Herstellung eines Zuschnitts einer Sprühhaut |
| SI3559070T1 (sl) * | 2017-04-28 | 2020-08-31 | Recticel Automobilsysteme Gmbh | Elastomerni kompozitni poliuretanski filmi |
| US10717714B2 (en) * | 2017-07-07 | 2020-07-21 | Chitec Technology Co., Ltd. | Reactive ultraviolet absorber and application thereof |
| US11046850B2 (en) | 2017-09-27 | 2021-06-29 | Evonik Operations Gmbh | Mixed metal catalyst compositions and methods for making polyurethane foam |
| CN111196871A (zh) * | 2018-11-19 | 2020-05-26 | 科思创德国股份有限公司 | 一种制备聚氨酯弹性体的方法 |
| US20210388150A1 (en) | 2018-11-19 | 2021-12-16 | Covestro Intellectual Property Gmbh & Co. Kg | A process for producing a polyurethane elastomer |
| CN110183843B (zh) * | 2019-05-16 | 2021-12-14 | 美瑞新材料股份有限公司 | 一种耐黄变的热塑性聚氨酯发泡材料及其制备方法 |
| US20230041434A1 (en) * | 2019-12-24 | 2023-02-09 | Covestro Deutschland Ag | Flexible foam |
| BR112022011746A2 (pt) | 2020-01-16 | 2022-08-30 | Ascorium Gmbh | Forro para uma parte de acabamento de interior de veículo contendo um elemento operante |
| HUE058718T2 (hu) | 2020-01-16 | 2022-09-28 | Ascorium Gmbh | Burkolat fényforrással rendelkezõ jármûbelsõ-kárpitozásrészhez |
| EP3862375B1 (en) * | 2020-02-10 | 2024-09-04 | Indresmat BV | Use of aliphatic isocyanate as toxic fume supressant in polyurethane foams |
| JP7469611B2 (ja) * | 2020-02-27 | 2024-04-17 | 東ソー株式会社 | ウレタンプレポリマー組成物 |
| JP7413927B2 (ja) * | 2020-05-26 | 2024-01-16 | 東ソー株式会社 | ウレタンプレポリマー組成物 |
| US20240218591A1 (en) * | 2021-04-13 | 2024-07-04 | Basf Se | Non-solvent pu system, an artificial leather comprising the same and a process for producing the artificial leather |
| WO2023285453A1 (en) * | 2021-07-13 | 2023-01-19 | Akzo Nobel Coatings International B.V. | One-component moisture-curable adhesive composition |
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| US3931381A (en) * | 1970-09-04 | 1976-01-06 | The General Tire & Rubber Company | Mold release method for polyurethane integral-skin foam |
| LU81024A1 (fr) * | 1979-03-09 | 1980-09-24 | Prb Sa | Procede pour la preparation de polyurethanne a peau integrale et polyurethanne obtenu |
| DE2914134A1 (de) * | 1979-04-07 | 1980-10-23 | Bayer Ag | Verfahren zur herstellung von polyurethan-schaumstoffen |
| US4452924A (en) * | 1983-05-05 | 1984-06-05 | Mobay Chemical Corporation | Flexible polyurethane foams having improved load bearing characteristics |
| SU1275018A1 (ru) * | 1985-03-15 | 1986-12-07 | Казанский Ордена Трудового Красного Знамени Химико-Технологический Институт Им.С.М.Кирова | Способ получени эластичных пенополиуретанов |
| EP0275010B1 (de) * | 1987-01-14 | 1991-11-21 | Bayer Ag | Verfahren zur Herstellung von Polyurethan-Formteilen |
| US5656677A (en) * | 1989-01-20 | 1997-08-12 | Recticel | Method for preparing and applying a sprayable, light stable polyurethane |
| US5100997A (en) * | 1990-05-29 | 1992-03-31 | Olin Corporation | Preparation of elastomers using high molecular weight polyols or polyamines, said polyols prepared using a double metal cyanide complex catalyst |
| US5502147A (en) * | 1993-12-21 | 1996-03-26 | Bayer Corporation | Aliphatic rim elastomers |
| CA2174305C (en) * | 1995-06-07 | 2007-07-03 | Ronald A. Cageao | Method of producing gaskets from polyurethane/urea compositions and gaskets produced therefrom |
-
1997
- 1997-09-30 IN IN157CH1997 patent/IN1997CH00157A/en unknown
- 1997-10-01 SK SK400-99A patent/SK285340B6/sk not_active IP Right Cessation
- 1997-10-01 ID IDW990286A patent/ID21506A/id unknown
- 1997-10-01 HU HU0000054A patent/HU223496B1/hu not_active IP Right Cessation
- 1997-10-01 ZA ZA9708803A patent/ZA978803B/xx unknown
- 1997-10-01 DK DK97942719T patent/DK0929586T3/da active
- 1997-10-01 AU AU44466/97A patent/AU4446697A/en not_active Abandoned
- 1997-10-01 ES ES97942719T patent/ES2157600T3/es not_active Expired - Lifetime
- 1997-10-01 US US09/068,516 patent/US6242555B1/en not_active Expired - Lifetime
- 1997-10-01 EP EP97942719A patent/EP0929586B1/en not_active Expired - Lifetime
- 1997-10-01 WO PCT/BE1997/000112 patent/WO1998014492A1/en active IP Right Grant
- 1997-10-01 JP JP51606098A patent/JP3911030B2/ja not_active Expired - Lifetime
- 1997-10-01 DE DE69704626T patent/DE69704626T2/de not_active Expired - Lifetime
- 1997-10-01 MX MX9903192A patent/MX216281B/es not_active IP Right Cessation
- 1997-10-01 CZ CZ0109299A patent/CZ299115B6/cs not_active IP Right Cessation
- 1997-10-01 AT AT97942719T patent/ATE200683T1/de active
- 1997-10-01 PT PT97942719T patent/PT929586E/pt unknown
- 1997-10-01 KR KR1019997002826A patent/KR100551978B1/ko not_active Expired - Lifetime
- 1997-10-01 CA CA002266623A patent/CA2266623C/en not_active Expired - Fee Related
- 1997-10-01 PL PL332552A patent/PL192282B1/pl not_active IP Right Cessation
- 1997-10-01 BR BR9712182-7A patent/BR9712182A/pt not_active IP Right Cessation
- 1997-10-01 RU RU99108990/04A patent/RU2201940C2/ru not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| EP0929586B1 (en) | 2001-04-18 |
| EP0929586A1 (en) | 1999-07-21 |
| JP3911030B2 (ja) | 2007-05-09 |
| DE69704626T2 (de) | 2001-11-08 |
| MX216281B (es) | 2003-09-09 |
| HUP0000054A2 (hu) | 2000-05-28 |
| DE69704626D1 (de) | 2001-05-23 |
| CA2266623A1 (en) | 1998-04-09 |
| ID21506A (id) | 1999-06-17 |
| IN1997CH00157A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2006-06-09 |
| ZA978803B (en) | 1998-04-17 |
| SK40099A3 (en) | 2000-07-11 |
| CA2266623C (en) | 2009-12-15 |
| HU223496B1 (hu) | 2004-08-30 |
| PL332552A1 (en) | 1999-09-13 |
| CZ299115B6 (cs) | 2008-04-23 |
| KR20000048830A (ko) | 2000-07-25 |
| JP2001501241A (ja) | 2001-01-30 |
| KR100551978B1 (ko) | 2006-02-20 |
| HUP0000054A3 (en) | 2000-09-28 |
| PL192282B1 (pl) | 2006-09-29 |
| WO1998014492A1 (en) | 1998-04-09 |
| ES2157600T3 (es) | 2001-08-16 |
| MX9903192A (es) | 1999-08-31 |
| BR9712182A (pt) | 1999-08-31 |
| AU4446697A (en) | 1998-04-24 |
| SK285340B6 (sk) | 2006-11-03 |
| ATE200683T1 (de) | 2001-05-15 |
| DK0929586T3 (da) | 2001-08-13 |
| CZ109299A3 (cs) | 1999-09-15 |
| US6242555B1 (en) | 2001-06-05 |
| RU2201940C2 (ru) | 2003-04-10 |
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