ES2327456T3 - Componente reactivo con isocianato estable durante el almacenamiento que contiene poliol basado en aceite vegetal. - Google Patents
Componente reactivo con isocianato estable durante el almacenamiento que contiene poliol basado en aceite vegetal. Download PDFInfo
- Publication number
- ES2327456T3 ES2327456T3 ES07006484T ES07006484T ES2327456T3 ES 2327456 T3 ES2327456 T3 ES 2327456T3 ES 07006484 T ES07006484 T ES 07006484T ES 07006484 T ES07006484 T ES 07006484T ES 2327456 T3 ES2327456 T3 ES 2327456T3
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- ES
- Spain
- Prior art keywords
- oil
- isocyanate
- weight
- reactive component
- component
- 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.)
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- 150000003077 polyols Chemical class 0.000 title claims abstract description 74
- 229920005862 polyol Polymers 0.000 title claims abstract description 66
- 235000015112 vegetable and seed oil Nutrition 0.000 title claims abstract description 42
- 239000008158 vegetable oil Substances 0.000 title claims abstract description 38
- 238000003860 storage Methods 0.000 title claims abstract description 35
- 239000012948 isocyanate Substances 0.000 claims abstract description 116
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 116
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 39
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 25
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 22
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims abstract description 21
- -1 and optionally Substances 0.000 claims abstract description 19
- 239000003054 catalyst Substances 0.000 claims abstract description 19
- 239000004094 surface-active agent Substances 0.000 claims abstract description 19
- 239000012875 nonionic emulsifier Substances 0.000 claims abstract description 16
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000000049 pigment Substances 0.000 claims abstract description 9
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims abstract description 8
- 239000004604 Blowing Agent Substances 0.000 claims abstract 4
- 239000003995 emulsifying agent Substances 0.000 claims description 42
- 239000005056 polyisocyanate Substances 0.000 claims description 34
- 229920001228 polyisocyanate Polymers 0.000 claims description 34
- 239000003921 oil Substances 0.000 claims description 30
- 235000019198 oils Nutrition 0.000 claims description 30
- 229920003225 polyurethane elastomer Polymers 0.000 claims description 28
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- 229920000570 polyether Polymers 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 22
- 229920000728 polyester Polymers 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 16
- 235000013311 vegetables Nutrition 0.000 claims description 15
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 9
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical group CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 6
- 235000010469 Glycine max Nutrition 0.000 claims description 6
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 claims description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 5
- 239000005977 Ethylene Substances 0.000 claims description 5
- 239000003549 soybean oil Substances 0.000 claims description 5
- 235000012424 soybean oil Nutrition 0.000 claims description 5
- 239000004952 Polyamide Substances 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical group NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
- 239000004359 castor oil Substances 0.000 claims description 4
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- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- 229920002857 polybutadiene Polymers 0.000 claims description 4
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- 235000008753 Papaver somniferum Nutrition 0.000 claims description 3
- 125000003118 aryl group Chemical group 0.000 claims description 3
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 3
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 239000003153 chemical reaction reagent Substances 0.000 claims description 3
- 235000012343 cottonseed oil Nutrition 0.000 claims description 3
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical group OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 3
- 229920006389 polyphenyl polymer Polymers 0.000 claims description 3
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 3
- ZTNJGMFHJYGMDR-UHFFFAOYSA-N 1,2-diisocyanatoethane Chemical compound O=C=NCCN=C=O ZTNJGMFHJYGMDR-UHFFFAOYSA-N 0.000 claims description 2
- ALQLPWJFHRMHIU-UHFFFAOYSA-N 1,4-diisocyanatobenzene Chemical compound O=C=NC1=CC=C(N=C=O)C=C1 ALQLPWJFHRMHIU-UHFFFAOYSA-N 0.000 claims description 2
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims description 2
- CEZWFBJCEWZGHX-UHFFFAOYSA-N 4-isocyanato-n-(oxomethylidene)benzenesulfonamide Chemical class O=C=NC1=CC=C(S(=O)(=O)N=C=O)C=C1 CEZWFBJCEWZGHX-UHFFFAOYSA-N 0.000 claims description 2
- 244000105624 Arachis hypogaea Species 0.000 claims description 2
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 claims description 2
- 235000006008 Brassica napus var napus Nutrition 0.000 claims description 2
- 240000000385 Brassica napus var. napus Species 0.000 claims description 2
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 claims description 2
- 235000004977 Brassica sinapistrum Nutrition 0.000 claims description 2
- 235000003222 Helianthus annuus Nutrition 0.000 claims description 2
- 244000020551 Helianthus annuus Species 0.000 claims description 2
- 240000001090 Papaver somniferum Species 0.000 claims description 2
- 235000010678 Paulownia tomentosa Nutrition 0.000 claims description 2
- 240000002834 Paulownia tomentosa Species 0.000 claims description 2
- 240000008042 Zea mays Species 0.000 claims description 2
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 claims description 2
- 150000001718 carbodiimides Chemical group 0.000 claims description 2
- 235000005822 corn Nutrition 0.000 claims description 2
- 125000005442 diisocyanate group Chemical group 0.000 claims description 2
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 2
- 235000019482 Palm oil Nutrition 0.000 claims 3
- 235000019483 Peanut oil Nutrition 0.000 claims 3
- 239000000944 linseed oil Substances 0.000 claims 3
- 235000021388 linseed oil Nutrition 0.000 claims 3
- 239000002540 palm oil Substances 0.000 claims 3
- 239000000312 peanut oil Substances 0.000 claims 3
- 235000019486 Sunflower oil Nutrition 0.000 claims 2
- 239000000828 canola oil Substances 0.000 claims 2
- 235000019519 canola oil Nutrition 0.000 claims 2
- 239000002285 corn oil Substances 0.000 claims 2
- 235000005687 corn oil Nutrition 0.000 claims 2
- 239000002600 sunflower oil Substances 0.000 claims 2
- 239000002383 tung oil Substances 0.000 claims 2
- 229920000742 Cotton Polymers 0.000 claims 1
- 239000004202 carbamide Chemical group 0.000 claims 1
- 239000002385 cottonseed oil Substances 0.000 claims 1
- HLJDOURGTRAFHE-UHFFFAOYSA-N isocyanic acid;3,5,5-trimethylcyclohex-2-en-1-one Chemical compound N=C=O.N=C=O.CC1=CC(=O)CC(C)(C)C1 HLJDOURGTRAFHE-UHFFFAOYSA-N 0.000 claims 1
- 239000010491 poppyseed oil Substances 0.000 claims 1
- 239000000945 filler Substances 0.000 abstract description 6
- 239000006260 foam Substances 0.000 description 17
- 238000004519 manufacturing process Methods 0.000 description 16
- 239000000126 substance Substances 0.000 description 13
- 229920002635 polyurethane Polymers 0.000 description 12
- 239000004814 polyurethane Substances 0.000 description 12
- 239000000047 product Substances 0.000 description 8
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 5
- 239000000654 additive Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- 229920000847 nonoxynol Polymers 0.000 description 5
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 5
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 229920001971 elastomer Polymers 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 4
- 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 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- 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
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 235000004443 Ricinus communis Nutrition 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 229920001400 block copolymer Polymers 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
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- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- PLFJWWUZKJKIPZ-UHFFFAOYSA-N 2-[2-[2-(2,6,8-trimethylnonan-4-yloxy)ethoxy]ethoxy]ethanol Chemical compound CC(C)CC(C)CC(CC(C)C)OCCOCCOCCO PLFJWWUZKJKIPZ-UHFFFAOYSA-N 0.000 description 2
- MWRSABPHNREIIX-UHFFFAOYSA-N 9,9-dimethyldecan-1-ol Chemical class CC(C)(C)CCCCCCCCO MWRSABPHNREIIX-UHFFFAOYSA-N 0.000 description 2
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 238000006555 catalytic reaction Methods 0.000 description 2
- 239000004872 foam stabilizing agent Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
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- MJYQFWSXKFLTAY-OVEQLNGDSA-N (2r,3r)-2,3-bis[(4-hydroxy-3-methoxyphenyl)methyl]butane-1,4-diol;(2r,3r,4s,5s,6r)-6-(hydroxymethyl)oxane-2,3,4,5-tetrol Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O.C1=C(O)C(OC)=CC(C[C@@H](CO)[C@H](CO)CC=2C=C(OC)C(O)=CC=2)=C1 MJYQFWSXKFLTAY-OVEQLNGDSA-N 0.000 description 1
- 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
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- 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
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- UKODFQOELJFMII-UHFFFAOYSA-N pentamethyldiethylenetriamine Chemical compound CN(C)CCN(C)CCN(C)C UKODFQOELJFMII-UHFFFAOYSA-N 0.000 description 1
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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
- 241000894007 species Species 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
- 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
- KSBAEPSJVUENNK-UHFFFAOYSA-L tin(ii) 2-ethylhexanoate Chemical compound [Sn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O KSBAEPSJVUENNK-UHFFFAOYSA-L 0.000 description 1
- YJGJRYWNNHUESM-UHFFFAOYSA-J triacetyloxystannyl acetate Chemical class [Sn+4].CC([O-])=O.CC([O-])=O.CC([O-])=O.CC([O-])=O YJGJRYWNNHUESM-UHFFFAOYSA-J 0.000 description 1
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Classifications
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/40—High-molecular-weight compounds
- C08G18/63—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers
- C08G18/632—Block or graft polymers obtained by polymerising compounds having carbon-to-carbon double bonds on to polymers onto polyethers
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/16—Catalysts
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/2805—Compounds having only one group containing active hydrogen
- C08G18/2815—Monohydroxy compounds
- C08G18/283—Compounds containing ether groups, e.g. oxyalkylated monohydroxy compounds
-
- 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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- C08G18/30—Low-molecular-weight compounds
- C08G18/36—Hydroxylated esters of higher fatty acids
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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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
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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
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- C08G18/4845—Polyethers containing oxyethylene units and other oxyalkylene units containing oxypropylene or higher oxyalkylene end groups
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
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- 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
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
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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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- C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polyurethanes Or Polyureas (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (2)
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| US401510 | 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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| ES2327456T3 true ES2327456T3 (es) | 2009-10-29 |
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| ES07006484T Active ES2327456T3 (es) | 2006-04-11 | 2007-03-29 | Componente reactivo con isocianato estable durante el almacenamiento que contiene poliol basado en aceite vegetal. |
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| MX (1) | MX2007004222A (enExample) |
| RU (1) | RU2007113125A (enExample) |
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| 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 |
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| 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 |
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| SG11201903596UA (en) * | 2016-11-10 | 2019-05-30 | Ppg Coatings Europe Bv | Surfactants for intumescent foam stabilization |
| PL3538582T3 (pl) * | 2016-11-11 | 2022-07-18 | Evonik Operations Gmbh | Emulgatory przeznaczone do pianki na bazie poliuretanu |
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| JPS62100513A (ja) * | 1985-10-28 | 1987-05-11 | Ito Seiyu Kk | 硬化性組成物 |
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| 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
Also Published As
| Publication number | Publication date |
|---|---|
| CA2583950A1 (en) | 2007-10-11 |
| EP1845121A1 (en) | 2007-10-17 |
| MX2007004222A (es) | 2009-02-16 |
| KR20070101143A (ko) | 2007-10-16 |
| 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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