JP2007513224A - 燃焼遅延剤、添加剤組成物、および燃焼遅延性ポリウレタン - Google Patents
燃焼遅延剤、添加剤組成物、および燃焼遅延性ポリウレタン Download PDFInfo
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- JP2007513224A JP2007513224A JP2006541291A JP2006541291A JP2007513224A JP 2007513224 A JP2007513224 A JP 2007513224A JP 2006541291 A JP2006541291 A JP 2006541291A JP 2006541291 A JP2006541291 A JP 2006541291A JP 2007513224 A JP2007513224 A JP 2007513224A
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- chlorophosphate
- anhydride
- reaction product
- dihydrocarbyl
- carbon atoms
- Prior art date
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- IHBVNSPHKMCPST-UHFFFAOYSA-N 3-bromopropanoyl chloride Chemical compound ClC(=O)CCBr IHBVNSPHKMCPST-UHFFFAOYSA-N 0.000 description 1
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- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- ONPYOCYQXOZWAI-UHFFFAOYSA-N CC1=C(C=CC(=C1)C(C)(C(=O)O)C(C)(C)C)O Chemical compound CC1=C(C=CC(=C1)C(C)(C(=O)O)C(C)(C)C)O ONPYOCYQXOZWAI-UHFFFAOYSA-N 0.000 description 1
- NBBUENBHDQWAMS-UHFFFAOYSA-N CCCCCC(CCCC)(C1=CC(=C(C=C1)O)C)C(=O)O Chemical compound CCCCCC(CCCC)(C1=CC(=C(C=C1)O)C)C(=O)O NBBUENBHDQWAMS-UHFFFAOYSA-N 0.000 description 1
- VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
- QONUJRHZWGPJPC-UHFFFAOYSA-N ClCC(Cl)COP(=O)(O)OCC(Cl)CCl Chemical compound ClCC(Cl)COP(=O)(O)OCC(Cl)CCl QONUJRHZWGPJPC-UHFFFAOYSA-N 0.000 description 1
- KKUKTXOBAWVSHC-UHFFFAOYSA-N Dimethylphosphate Chemical compound COP(O)(=O)OC KKUKTXOBAWVSHC-UHFFFAOYSA-N 0.000 description 1
- 238000001157 Fourier transform infrared spectrum Methods 0.000 description 1
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 229920013701 VORANOL™ Polymers 0.000 description 1
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- SVNGYUMAOUOHCE-UHFFFAOYSA-N [chloro(cyclopropyloxy)phosphoryl]oxycyclopropane Chemical compound C1CC1OP(=O)(Cl)OC1CC1 SVNGYUMAOUOHCE-UHFFFAOYSA-N 0.000 description 1
- LCXRVPWGRALHAD-UHFFFAOYSA-N [chloro(ethoxy)phosphoryl]oxybenzene Chemical compound CCOP(Cl)(=O)OC1=CC=CC=C1 LCXRVPWGRALHAD-UHFFFAOYSA-N 0.000 description 1
- NGFFLHMFSINFGB-UHFFFAOYSA-N [chloro(methoxy)phosphoryl]oxymethane Chemical compound COP(Cl)(=O)OC NGFFLHMFSINFGB-UHFFFAOYSA-N 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
- 238000010521 absorption reaction Methods 0.000 description 1
- FXXACINHVKSMDR-UHFFFAOYSA-N acetyl bromide Chemical compound CC(Br)=O FXXACINHVKSMDR-UHFFFAOYSA-N 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- NWCHELUCVWSRRS-UHFFFAOYSA-N atrolactic acid Chemical compound OC(=O)C(O)(C)C1=CC=CC=C1 NWCHELUCVWSRRS-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- SVYONMGCIOEHOO-UHFFFAOYSA-N bis(1,2-dibromoethyl) hydrogen phosphate Chemical compound BrCC(Br)OP(=O)(O)OC(Br)CBr SVYONMGCIOEHOO-UHFFFAOYSA-N 0.000 description 1
- CFRHVJAOAULIRG-UHFFFAOYSA-N bis(1-bromo-3-chloropropan-2-yl) hydrogen phosphate Chemical compound ClCC(CBr)OP(=O)(O)OC(CCl)CBr CFRHVJAOAULIRG-UHFFFAOYSA-N 0.000 description 1
- QZUZYRQEGHDUJR-UHFFFAOYSA-N bis(1-methylcyclohexyl) hydrogen phosphate Chemical compound C1CCCCC1(C)OP(O)(=O)OC1(C)CCCCC1 QZUZYRQEGHDUJR-UHFFFAOYSA-N 0.000 description 1
- ROLQPIOIXBZPFD-UHFFFAOYSA-N bis(2,2,2-trichloroethyl) hydrogen phosphate Chemical compound ClC(Cl)(Cl)COP(=O)(O)OCC(Cl)(Cl)Cl ROLQPIOIXBZPFD-UHFFFAOYSA-N 0.000 description 1
- XITRBUPOXXBIJN-UHFFFAOYSA-N bis(2,2,6,6-tetramethylpiperidin-4-yl) decanedioate Chemical compound C1C(C)(C)NC(C)(C)CC1OC(=O)CCCCCCCCC(=O)OC1CC(C)(C)NC(C)(C)C1 XITRBUPOXXBIJN-UHFFFAOYSA-N 0.000 description 1
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- AAYXTXGPYAJLSB-UHFFFAOYSA-N bis(2,3,4-trichlorobutyl) hydrogen phosphate Chemical compound ClCC(Cl)C(Cl)COP(=O)(O)OCC(Cl)C(Cl)CCl AAYXTXGPYAJLSB-UHFFFAOYSA-N 0.000 description 1
- FMYQTDSYXPAKKF-UHFFFAOYSA-N bis(2,4-dibromophenyl) hydrogen phosphate Chemical compound C=1C=C(Br)C=C(Br)C=1OP(=O)(O)OC1=CC=C(Br)C=C1Br FMYQTDSYXPAKKF-UHFFFAOYSA-N 0.000 description 1
- FAEDFEUORGJVOF-UHFFFAOYSA-N bis(2,5-dichlorophenyl) hydrogen phosphate Chemical compound C=1C(Cl)=CC=C(Cl)C=1OP(=O)(O)OC1=CC(Cl)=CC=C1Cl FAEDFEUORGJVOF-UHFFFAOYSA-N 0.000 description 1
- RNKDFEYVFWYXEK-UHFFFAOYSA-N bis(2,5-dimethylphenyl) hydrogen phosphate Chemical compound CC1=CC=C(C)C(OP(O)(=O)OC=2C(=CC=C(C)C=2)C)=C1 RNKDFEYVFWYXEK-UHFFFAOYSA-N 0.000 description 1
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- UUEFDGORLDWVJF-UHFFFAOYSA-N bis(2-bromoethenyl) hydrogen phosphate Chemical compound BrC=COP(=O)(O)OC=CBr UUEFDGORLDWVJF-UHFFFAOYSA-N 0.000 description 1
- VBSLONKXEFHWAG-UHFFFAOYSA-N bis(2-bromoethyl) hydrogen phosphate Chemical compound BrCCOP(=O)(O)OCCBr VBSLONKXEFHWAG-UHFFFAOYSA-N 0.000 description 1
- HKHQYFVEGSOYFG-UHFFFAOYSA-N bis(2-bromophenyl) chloro phosphate Chemical compound C=1C=CC=C(Br)C=1OP(=O)(OCl)OC1=CC=CC=C1Br HKHQYFVEGSOYFG-UHFFFAOYSA-N 0.000 description 1
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- HCZIEWHRARORGB-UHFFFAOYSA-N bis(2-chloronaphthalen-1-yl) hydrogen phosphate Chemical compound C1=CC=C2C(OP(=O)(OC=3C4=CC=CC=C4C=CC=3Cl)O)=C(Cl)C=CC2=C1 HCZIEWHRARORGB-UHFFFAOYSA-N 0.000 description 1
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- OHRCKPRYDGSBRN-UHFFFAOYSA-N bis(2-methylphenyl) hydrogen phosphate Chemical compound CC1=CC=CC=C1OP(O)(=O)OC1=CC=CC=C1C OHRCKPRYDGSBRN-UHFFFAOYSA-N 0.000 description 1
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- MZASWNNFDGQBFT-UHFFFAOYSA-N bis(trichloromethyl) hydrogen phosphate Chemical compound ClC(Cl)(Cl)OP(=O)(O)OC(Cl)(Cl)Cl MZASWNNFDGQBFT-UHFFFAOYSA-N 0.000 description 1
- ZMJAMLYPKVCMJX-UHFFFAOYSA-N bis[(3-bromocyclopentyl)oxy]-chloro-sulfanylidene-$l^{5}-phosphane Chemical compound C1CC(Br)CC1OP(=S)(Cl)OC1CCC(Br)C1 ZMJAMLYPKVCMJX-UHFFFAOYSA-N 0.000 description 1
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- ZRSPTVIRKWIYOG-UHFFFAOYSA-N chloro-dipentoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCCCCOP(Cl)(=S)OCCCCC ZRSPTVIRKWIYOG-UHFFFAOYSA-N 0.000 description 1
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- VZWIGIXJYOZQQJ-UHFFFAOYSA-N chloro-sulfanylidene-bis(2,2,2-trichloroethoxy)-$l^{5}-phosphane Chemical compound ClC(Cl)(Cl)COP(Cl)(=S)OCC(Cl)(Cl)Cl VZWIGIXJYOZQQJ-UHFFFAOYSA-N 0.000 description 1
- ITSPJTRLPJBJHU-UHFFFAOYSA-N chloro-sulfanylidene-bis(tribromomethoxy)-$l^{5}-phosphane Chemical compound BrC(Br)(Br)OP(=S)(Cl)OC(Br)(Br)Br ITSPJTRLPJBJHU-UHFFFAOYSA-N 0.000 description 1
- DLFMBNLZFSTQRS-UHFFFAOYSA-N chloro-sulfanylidene-bis(trichloromethoxy)-$l^{5}-phosphane Chemical compound ClC(Cl)(Cl)OP(Cl)(=S)OC(Cl)(Cl)Cl DLFMBNLZFSTQRS-UHFFFAOYSA-N 0.000 description 1
- PGQQOXWUXDKDDP-UHFFFAOYSA-N chloro-sulfanylidene-bis[2-(tribromomethyl)phenoxy]-$l^{5}-phosphane Chemical compound C=1C=CC=C(C(Br)(Br)Br)C=1OP(=S)(Cl)OC1=CC=CC=C1C(Br)(Br)Br PGQQOXWUXDKDDP-UHFFFAOYSA-N 0.000 description 1
- 125000000068 chlorophenyl group Chemical group 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000013068 control sample Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical compound C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 description 1
- FWFSEYBSWVRWGL-UHFFFAOYSA-N cyclohexene oxide Natural products O=C1CCCC=C1 FWFSEYBSWVRWGL-UHFFFAOYSA-N 0.000 description 1
- 239000012973 diazabicyclooctane Substances 0.000 description 1
- HDFFVHSMHLDSLO-UHFFFAOYSA-M dibenzyl phosphate Chemical compound C=1C=CC=CC=1COP(=O)([O-])OCC1=CC=CC=C1 HDFFVHSMHLDSLO-UHFFFAOYSA-M 0.000 description 1
- LXSZEGQOLMMPAJ-UHFFFAOYSA-N dichloro-[chloro(dichloromethoxy)phosphoryl]oxymethane Chemical compound ClC(Cl)OP(Cl)(=O)OC(Cl)Cl LXSZEGQOLMMPAJ-UHFFFAOYSA-N 0.000 description 1
- SWXUEJURRAEAMJ-UHFFFAOYSA-N dicyclobutyl hydrogen phosphate Chemical compound C1CCC1OP(=O)(O)OC1CCC1 SWXUEJURRAEAMJ-UHFFFAOYSA-N 0.000 description 1
- POVJEPOYXLSCLY-UHFFFAOYSA-N dicyclopentyl hydrogen phosphate Chemical compound C1CCCC1OP(=O)(O)OC1CCCC1 POVJEPOYXLSCLY-UHFFFAOYSA-N 0.000 description 1
- PYGPMDXRQICOAP-UHFFFAOYSA-N dicyclopropyl hydrogen phosphate Chemical compound C1CC1OP(=O)(O)OC1CC1 PYGPMDXRQICOAP-UHFFFAOYSA-N 0.000 description 1
- LGTLXDJOAJDFLR-UHFFFAOYSA-N diethyl chlorophosphate Chemical compound CCOP(Cl)(=O)OCC LGTLXDJOAJDFLR-UHFFFAOYSA-N 0.000 description 1
- UCQFCFPECQILOL-UHFFFAOYSA-N diethyl hydrogen phosphate Chemical compound CCOP(O)(=O)OCC UCQFCFPECQILOL-UHFFFAOYSA-N 0.000 description 1
- ITJPTURSPJESQC-UHFFFAOYSA-N diethyl pentyl phosphate Chemical compound CCCCCOP(=O)(OCC)OCC ITJPTURSPJESQC-UHFFFAOYSA-N 0.000 description 1
- WZPMZMCZAGFKOC-UHFFFAOYSA-N diisopropyl hydrogen phosphate Chemical compound CC(C)OP(O)(=O)OC(C)C WZPMZMCZAGFKOC-UHFFFAOYSA-N 0.000 description 1
- JFHGLVIOIANSIN-UHFFFAOYSA-N dimethyl butanedioate;1-(2-hydroxyethyl)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound COC(=O)CCC(=O)OC.CC1(C)CC(O)CC(C)(C)N1CCO JFHGLVIOIANSIN-UHFFFAOYSA-N 0.000 description 1
- WJZUIWBZDGBLKK-UHFFFAOYSA-M dipentyl phosphate Chemical compound CCCCCOP([O-])(=O)OCCCCC WJZUIWBZDGBLKK-UHFFFAOYSA-M 0.000 description 1
- ASMQGLCHMVWBQR-UHFFFAOYSA-M diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-M 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- YEWZQCDRZRYAEB-UHFFFAOYSA-N ditert-butyl hydrogen phosphate Chemical compound CC(C)(C)OP(O)(=O)OC(C)(C)C YEWZQCDRZRYAEB-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- XMNQCSOOUOJOLR-UHFFFAOYSA-N ethyl methyl hydrogen phosphate Chemical compound CCOP(O)(=O)OC XMNQCSOOUOJOLR-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 210000004124 hock Anatomy 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- LSACYLWPPQLVSM-UHFFFAOYSA-N isobutyric acid anhydride Chemical compound CC(C)C(=O)OC(=O)C(C)C LSACYLWPPQLVSM-UHFFFAOYSA-N 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N mandelic acid Chemical compound OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 1
- 238000010525 oxidative degradation reaction Methods 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 238000005191 phase separation Methods 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- WSDQIHATCCOMLH-UHFFFAOYSA-N phenyl n-(3,5-dichlorophenyl)carbamate Chemical compound ClC1=CC(Cl)=CC(NC(=O)OC=2C=CC=CC=2)=C1 WSDQIHATCCOMLH-UHFFFAOYSA-N 0.000 description 1
- CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 1
- 125000004482 piperidin-4-yl group Chemical group N1CCC(CC1)* 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical group O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 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
- 239000002904 solvent Substances 0.000 description 1
- 229940014800 succinic anhydride Drugs 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YIPZJTGXMJGCFV-UHFFFAOYSA-N tribromo-[chloro(tribromomethoxy)phosphoryl]oxymethane Chemical compound BrC(Br)(Br)OP(=O)(Cl)OC(Br)(Br)Br YIPZJTGXMJGCFV-UHFFFAOYSA-N 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- 230000004580 weight loss Effects 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
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0066—Flame-proofing or flame-retarding additives
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/521—Esters of phosphoric acids, e.g. of H3PO4
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K21/00—Fireproofing materials
- C09K21/14—Macromolecular materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Polyurethanes Or Polyureas (AREA)
- Fireproofing Substances (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/719,948 US7153901B2 (en) | 2003-11-21 | 2003-11-21 | Flame retardant, additive compositions, and flame retardant polyurethanes |
| PCT/US2004/038071 WO2005052018A2 (en) | 2003-11-21 | 2004-11-16 | Flame retardant, additive compositions, and flame retardant polyurethanes |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2007513224A true JP2007513224A (ja) | 2007-05-24 |
| JP2007513224A5 JP2007513224A5 (https=) | 2008-01-10 |
Family
ID=34591465
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2006541291A Withdrawn JP2007513224A (ja) | 2003-11-21 | 2004-11-16 | 燃焼遅延剤、添加剤組成物、および燃焼遅延性ポリウレタン |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US7153901B2 (https=) |
| EP (1) | EP1685176A2 (https=) |
| JP (1) | JP2007513224A (https=) |
| KR (1) | KR20060123176A (https=) |
| CN (1) | CN1882629A (https=) |
| AU (1) | AU2004292526A1 (https=) |
| BR (1) | BRPI0417049A (https=) |
| CA (1) | CA2546299A1 (https=) |
| IL (1) | IL175687A0 (https=) |
| MX (1) | MXPA06005648A (https=) |
| RU (1) | RU2006121970A (https=) |
| UA (1) | UA84722C2 (https=) |
| WO (1) | WO2005052018A2 (https=) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010535896A (ja) * | 2007-08-07 | 2010-11-25 | アルベマール・コーポレーシヨン | 粘弾性ポリウレタン発泡体中での使用に適切な火炎遅延剤 |
| JP2014514375A (ja) * | 2011-03-16 | 2014-06-19 | ケムチュア コーポレイション | 軟質ポリウレタンフォーム用反応性難燃剤ブレンド |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1574995A1 (en) * | 2004-03-12 | 2005-09-14 | Thomson Licensing S.A. | Method for encoding interlaced digital video data |
| MX2008012835A (es) * | 2006-04-06 | 2008-10-17 | Albemarle Corp | Composiciones de aditivo retardante de flama y uso de las mismas. |
| JP2010522268A (ja) * | 2007-03-26 | 2010-07-01 | アルベマール・ユーロプ・エスピーアールエル | 低煙性難燃性ポリウレタンフォーム製剤 |
| CN101476479B (zh) * | 2009-01-20 | 2011-01-05 | 中国科学技术大学 | 一种防治矿井煤自燃的泡沫型阻化剂及其使用方法 |
| US20120264839A1 (en) | 2011-04-14 | 2012-10-18 | Chemtura Corporation | Flame retardant blends for flexible polyurethane foams |
| TWI638005B (zh) | 2011-08-19 | 2018-10-11 | 法克斯聚合物股份有限公司 | 具優越耐火性之熱塑性聚胺基甲酸酯 |
| CN102585148B (zh) * | 2011-12-28 | 2014-04-16 | 万华化学集团股份有限公司 | 制备高阻燃性聚异氰脲酸酯泡沫用组合料 |
| CN103012739B (zh) * | 2012-12-21 | 2014-10-29 | 山东一诺威聚氨酯股份有限公司 | 阻燃改性mdi及其制备方法 |
| EP2948464A4 (en) | 2013-01-22 | 2016-12-07 | Frx Polymers Inc | PHOSPHORUS-BASED EPOXY BINDINGS AND COMPOSITIONS THEREOF |
| WO2014170316A1 (en) * | 2013-04-16 | 2014-10-23 | Basf Se | Phosphorous containing flame retardants |
| GB2523756B (en) * | 2014-03-03 | 2017-01-11 | Addivant Switzerland Gmbh | Antioxidant compositions |
| US10738176B2 (en) | 2016-12-06 | 2020-08-11 | International Business Machines Corporation | Flame-retardant polyallyl and polyalkenyl isocyanurate compounds |
| CN108795543A (zh) * | 2017-05-03 | 2018-11-13 | 中国石油天然气股份有限公司 | 一种工程机械专用液压油组合物 |
| CN112851909B (zh) * | 2021-01-14 | 2022-08-05 | 万华化学（宁波）有限公司 | 一种储存稳定的多异氰酸酯组合物 |
| CN117701239B (zh) * | 2023-12-26 | 2024-06-11 | 苏州添易朗科技有限公司 | 一种uv和热双重固化的改性有机硅胶粘剂及其制备方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5566917A (en) * | 1978-11-14 | 1980-05-20 | Toyo Tire & Rubber Co Ltd | Manufacture of non-yellowing integral polyurethane foam |
| JPS6150944A (ja) | 1984-08-20 | 1986-03-13 | Agency Of Ind Science & Technol | 新規臭素化フタル酸アリルエステル化合物 |
| JPS61227550A (ja) | 1986-01-24 | 1986-10-09 | Agency Of Ind Science & Technol | 臭素化フタル酸アリル系エステルの製造方法 |
| JPS62298560A (ja) | 1986-06-19 | 1987-12-25 | Nippon Shokubai Kagaku Kogyo Co Ltd | 新規臭素化フタル酸エステル化合物 |
| JPS63251408A (ja) | 1987-04-07 | 1988-10-18 | Nippon Shokubai Kagaku Kogyo Co Ltd | 高屈折率樹脂 |
| FR2681595B1 (fr) | 1991-09-24 | 1994-09-02 | Rhone Poulenc Chimie | Procede d'esterification de sels d'acides carboxyliques. |
| CA2302707A1 (en) * | 1997-09-30 | 1999-04-08 | Rosemarie A. Boccuzzi | Stabilized polyether polyol and polyurethane foam obtained therefrom |
| WO2000035999A1 (en) | 1998-12-18 | 2000-06-22 | The Dow Chemical Company | Polyurethane based foam containing exfoliating graphite and the process for the preparation thereof |
| US6812276B2 (en) | 1999-12-01 | 2004-11-02 | General Electric Company | Poly(arylene ether)-containing thermoset composition, method for the preparation thereof, and articles derived therefrom |
| AU2001230056A1 (en) | 2000-01-13 | 2001-07-24 | Shell Internationale Research Maatschappij B.V. | Polyol formulation |
| US6521703B2 (en) | 2000-01-18 | 2003-02-18 | General Electric Company | Curable resin composition, method for the preparation thereof, and articles derived thereform |
| WO2002062863A2 (en) | 2000-12-29 | 2002-08-15 | World Properties Inc. | Flame retardant polyurethane composition and method of manufacture thereof |
| EP1312630B1 (en) | 2001-10-31 | 2012-12-12 | Tosoh Corporation | Process for the production of flexible polyurethane foams |
| US20030153656A1 (en) | 2002-01-11 | 2003-08-14 | Rinus Sjerps | Flame retardant polyurethanes and polyisocyanurates, and additives therefor |
| AU2002256360A1 (en) | 2002-04-25 | 2003-11-10 | World Properties Inc. | Flame retardant polyurethane composition and method of manufacture thereof |
| US20040171722A1 (en) | 2003-02-28 | 2004-09-02 | Brown William R. | Flame retardant polyurethanes and additive compositions for use in producing them |
-
2003
- 2003-11-21 US US10/719,948 patent/US7153901B2/en not_active Expired - Fee Related
-
2004
- 2004-11-16 EP EP04819525A patent/EP1685176A2/en not_active Withdrawn
- 2004-11-16 CA CA002546299A patent/CA2546299A1/en not_active Abandoned
- 2004-11-16 RU RU2006121970/04A patent/RU2006121970A/ru not_active Application Discontinuation
- 2004-11-16 BR BRPI0417049-0A patent/BRPI0417049A/pt not_active IP Right Cessation
- 2004-11-16 CN CNA2004800342041A patent/CN1882629A/zh active Pending
- 2004-11-16 AU AU2004292526A patent/AU2004292526A1/en not_active Abandoned
- 2004-11-16 UA UAA200606949A patent/UA84722C2/ru unknown
- 2004-11-16 WO PCT/US2004/038071 patent/WO2005052018A2/en not_active Ceased
- 2004-11-16 MX MXPA06005648A patent/MXPA06005648A/es unknown
- 2004-11-16 KR KR1020067009827A patent/KR20060123176A/ko not_active Withdrawn
- 2004-11-16 JP JP2006541291A patent/JP2007513224A/ja not_active Withdrawn
-
2006
- 2006-05-16 IL IL175687A patent/IL175687A0/en unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2010535896A (ja) * | 2007-08-07 | 2010-11-25 | アルベマール・コーポレーシヨン | 粘弾性ポリウレタン発泡体中での使用に適切な火炎遅延剤 |
| JP2014514375A (ja) * | 2011-03-16 | 2014-06-19 | ケムチュア コーポレイション | 軟質ポリウレタンフォーム用反応性難燃剤ブレンド |
Also Published As
| Publication number | Publication date |
|---|---|
| US7153901B2 (en) | 2006-12-26 |
| CN1882629A (zh) | 2006-12-20 |
| BRPI0417049A (pt) | 2007-02-06 |
| US20050113495A1 (en) | 2005-05-26 |
| CA2546299A1 (en) | 2005-06-09 |
| KR20060123176A (ko) | 2006-12-01 |
| UA84722C2 (ru) | 2008-11-25 |
| MXPA06005648A (es) | 2006-08-17 |
| WO2005052018A3 (en) | 2005-08-18 |
| RU2006121970A (ru) | 2007-12-27 |
| IL175687A0 (en) | 2006-09-05 |
| WO2005052018A2 (en) | 2005-06-09 |
| EP1685176A2 (en) | 2006-08-02 |
| AU2004292526A1 (en) | 2005-06-09 |
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