FR2879616A1 - Composition polyisacyanate a proprietes anti-chocs ameliorees - Google Patents
Composition polyisacyanate a proprietes anti-chocs ameliorees Download PDFInfo
- Publication number
- FR2879616A1 FR2879616A1 FR0413669A FR0413669A FR2879616A1 FR 2879616 A1 FR2879616 A1 FR 2879616A1 FR 0413669 A FR0413669 A FR 0413669A FR 0413669 A FR0413669 A FR 0413669A FR 2879616 A1 FR2879616 A1 FR 2879616A1
- Authority
- FR
- France
- Prior art keywords
- isocyanate
- composition
- composition according
- poly
- advantageously
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 183
- 230000000703 anti-shock Effects 0.000 title 1
- 239000012948 isocyanate Substances 0.000 claims abstract description 62
- 238000000576 coating method Methods 0.000 claims abstract description 59
- 150000002513 isocyanates Chemical class 0.000 claims abstract description 53
- 239000004094 surface-active agent Substances 0.000 claims description 68
- 239000005056 polyisocyanate Substances 0.000 claims description 61
- 229920001228 polyisocyanate Polymers 0.000 claims description 61
- 150000001875 compounds Chemical class 0.000 claims description 55
- -1 hydrocarbon radical Chemical class 0.000 claims description 52
- 239000011248 coating agent Substances 0.000 claims description 39
- 229920005862 polyol Polymers 0.000 claims description 32
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 claims description 29
- 239000003795 chemical substances by application Substances 0.000 claims description 28
- 150000003077 polyols Chemical class 0.000 claims description 27
- 229920005989 resin Polymers 0.000 claims description 26
- 239000011347 resin Substances 0.000 claims description 26
- 239000004848 polyfunctional curative Substances 0.000 claims description 24
- 239000000758 substrate Substances 0.000 claims description 24
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 23
- 230000000873 masking effect Effects 0.000 claims description 23
- 238000006243 chemical reaction Methods 0.000 claims description 21
- 150000003254 radicals Chemical class 0.000 claims description 18
- 229920003180 amino resin Polymers 0.000 claims description 17
- 238000004132 cross linking Methods 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 15
- 238000010438 heat treatment Methods 0.000 claims description 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
- 239000003054 catalyst Substances 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 12
- 229920000877 Melamine resin Polymers 0.000 claims description 12
- 239000000178 monomer Substances 0.000 claims description 11
- 239000004814 polyurethane Substances 0.000 claims description 11
- 229920002635 polyurethane Polymers 0.000 claims description 11
- 239000007787 solid Substances 0.000 claims description 11
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- WHIVNJATOVLWBW-UHFFFAOYSA-N n-butan-2-ylidenehydroxylamine Chemical compound CCC(C)=NO WHIVNJATOVLWBW-UHFFFAOYSA-N 0.000 claims description 10
- 229910052698 phosphorus Inorganic materials 0.000 claims description 10
- 229920000728 polyester Polymers 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 9
- 125000001931 aliphatic group Chemical group 0.000 claims description 9
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 150000002989 phenols Chemical group 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- 239000000126 substance Substances 0.000 claims description 9
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 9
- 239000005058 Isophorone diisocyanate Substances 0.000 claims description 8
- 239000003945 anionic surfactant Substances 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 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 description 8
- 150000003141 primary amines Chemical group 0.000 claims description 8
- 239000013638 trimer Substances 0.000 claims description 8
- 125000000129 anionic group Chemical group 0.000 claims description 7
- 229920001223 polyethylene glycol Polymers 0.000 claims description 7
- 150000003512 tertiary amines Chemical class 0.000 claims description 7
- 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 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 6
- 239000005977 Ethylene Substances 0.000 claims description 6
- 239000005057 Hexamethylene diisocyanate Substances 0.000 claims description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 6
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 claims description 6
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 claims description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 6
- 238000006386 neutralization reaction Methods 0.000 claims description 6
- 239000002736 nonionic surfactant Substances 0.000 claims description 6
- 239000003960 organic solvent Substances 0.000 claims description 6
- 239000011574 phosphorus Substances 0.000 claims description 6
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- 229920001807 Urea-formaldehyde Polymers 0.000 claims description 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- 150000004657 carbamic acid derivatives Chemical class 0.000 claims description 5
- 239000000539 dimer Substances 0.000 claims description 5
- 125000000524 functional group Chemical group 0.000 claims description 5
- 239000002563 ionic surfactant Substances 0.000 claims description 5
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 claims description 5
- 229920005906 polyester polyol Polymers 0.000 claims description 5
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 claims description 5
- 239000002243 precursor Substances 0.000 claims description 5
- 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 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 4
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 4
- 239000012634 fragment Substances 0.000 claims description 4
- 230000000737 periodic effect Effects 0.000 claims description 4
- 235000021317 phosphate Nutrition 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 239000011593 sulfur Substances 0.000 claims description 4
- 150000003672 ureas Chemical class 0.000 claims description 4
- 239000004215 Carbon black (E152) Substances 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 150000001721 carbon Chemical group 0.000 claims description 3
- 125000005442 diisocyanate group Chemical group 0.000 claims description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 claims description 3
- 229930195733 hydrocarbon Natural products 0.000 claims description 3
- 150000003951 lactams Chemical class 0.000 claims description 3
- 150000002690 malonic acid derivatives Chemical class 0.000 claims description 3
- NGKKXKRXUOBKGI-UHFFFAOYSA-N 1,2,9-triisocyanatononane Chemical compound O=C=NCCCCCCCC(N=C=O)CN=C=O NGKKXKRXUOBKGI-UHFFFAOYSA-N 0.000 claims description 2
- AHBNSOZREBSAMG-UHFFFAOYSA-N 1,5-diisocyanato-2-methylpentane Chemical compound O=C=NCC(C)CCCN=C=O AHBNSOZREBSAMG-UHFFFAOYSA-N 0.000 claims description 2
- 229940008841 1,6-hexamethylene diisocyanate Drugs 0.000 claims description 2
- KNBYXBYFRFFKLU-UHFFFAOYSA-N 1-(diisocyanatomethyl)-5-isocyanato-1,3,3-trimethylcyclohexane Chemical compound CC1(C)CC(N=C=O)CC(C)(C(N=C=O)N=C=O)C1 KNBYXBYFRFFKLU-UHFFFAOYSA-N 0.000 claims description 2
- 239000005711 Benzoic acid Substances 0.000 claims description 2
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 claims description 2
- 239000004472 Lysine Substances 0.000 claims description 2
- NQTADLQHYWFPDB-UHFFFAOYSA-N N-Hydroxysuccinimide Chemical compound ON1C(=O)CCC1=O NQTADLQHYWFPDB-UHFFFAOYSA-N 0.000 claims description 2
- 150000007945 N-acyl ureas Chemical class 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical group CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 235000010233 benzoic acid Nutrition 0.000 claims description 2
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 claims description 2
- 150000001732 carboxylic acid derivatives Chemical group 0.000 claims description 2
- 229910052798 chalcogen Inorganic materials 0.000 claims description 2
- 150000001787 chalcogens Chemical class 0.000 claims description 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims description 2
- XRZIOLZRKBOXPA-UHFFFAOYSA-N diazetidine-3,4-dione Chemical compound O=C1NNC1=O XRZIOLZRKBOXPA-UHFFFAOYSA-N 0.000 claims description 2
- 150000002429 hydrazines Chemical class 0.000 claims description 2
- 150000002443 hydroxylamines Chemical class 0.000 claims description 2
- 150000002460 imidazoles Chemical class 0.000 claims description 2
- 150000003949 imides Chemical class 0.000 claims description 2
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 claims description 2
- 229910052752 metalloid Inorganic materials 0.000 claims description 2
- 239000012038 nucleophile Substances 0.000 claims description 2
- HXSACZWWBYWLIS-UHFFFAOYSA-N oxadiazine-4,5,6-trione Chemical compound O=C1ON=NC(=O)C1=O HXSACZWWBYWLIS-UHFFFAOYSA-N 0.000 claims description 2
- 150000002923 oximes Chemical class 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
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- 150000003003 phosphines Chemical class 0.000 claims description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 2
- IUGYQRQAERSCNH-UHFFFAOYSA-N pivalic acid Chemical compound CC(C)(C)C(O)=O IUGYQRQAERSCNH-UHFFFAOYSA-N 0.000 claims description 2
- 229920000058 polyacrylate Polymers 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- 150000003217 pyrazoles Chemical class 0.000 claims description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound 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 claims description 2
- 150000003335 secondary amines Chemical group 0.000 claims description 2
- 150000003871 sulfonates Chemical class 0.000 claims description 2
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 claims description 2
- 150000003573 thiols Chemical group 0.000 claims description 2
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims 1
- 125000005600 alkyl phosphonate group Chemical group 0.000 claims 1
- 150000008430 aromatic amides Chemical class 0.000 claims 1
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 claims 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims 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 claims 1
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- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 229910018138 Al-Y Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920000049 Carbon (fiber) Polymers 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 101000848724 Homo sapiens Rap guanine nucleotide exchange factor 3 Proteins 0.000 description 1
- 238000005684 Liebig rearrangement reaction Methods 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical class OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 102100034584 Rap guanine nucleotide exchange factor 3 Human genes 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
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- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229920006397 acrylic thermoplastic Polymers 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000004917 carbon fiber Substances 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000001767 cationic compounds Chemical class 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 150000003983 crown ethers Chemical class 0.000 description 1
- 150000005676 cyclic carbonates Chemical group 0.000 description 1
- 150000004292 cyclic ethers Chemical group 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- PDXRQENMIVHKPI-UHFFFAOYSA-N cyclohexane-1,1-diol Chemical compound OC1(O)CCCCC1 PDXRQENMIVHKPI-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 238000007306 functionalization reaction Methods 0.000 description 1
- 239000003365 glass fiber Substances 0.000 description 1
- 150000002334 glycols Chemical group 0.000 description 1
- 238000007542 hardness measurement Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N hydrogen peroxide Substances OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 1
- 150000002433 hydrophilic molecules Chemical class 0.000 description 1
- 229910001411 inorganic cation Inorganic materials 0.000 description 1
- LYBKPDDZTNUNNM-UHFFFAOYSA-N isopropylbenzylamine Chemical compound CC(C)NCC1=CC=CC=C1 LYBKPDDZTNUNNM-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- RMIODHQZRUFFFF-UHFFFAOYSA-M methoxyacetate Chemical compound COCC([O-])=O RMIODHQZRUFFFF-UHFFFAOYSA-M 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 238000010422 painting Methods 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
- 238000013379 physicochemical characterization Methods 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229940068917 polyethylene glycols Drugs 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940005657 pyrophosphoric acid Drugs 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 239000004634 thermosetting polymer Substances 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000012855 volatile organic compound Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
- C09D175/04—Polyurethanes
-
- 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
- C08G18/54—Polycondensates of aldehydes
-
- 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
- C08G18/54—Polycondensates of aldehydes
- C08G18/544—Polycondensates of aldehydes with nitrogen 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
- C08G18/80—Masked polyisocyanates
-
- 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
- C08G18/80—Masked polyisocyanates
- C08G18/8061—Masked polyisocyanates masked with compounds having only one group containing active hydrogen
- C08G18/807—Masked polyisocyanates masked with compounds having only one group containing active hydrogen with nitrogen containing compounds
- C08G18/8077—Oximes
Abstract
Description
Claims (35)
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0413669A FR2879616B1 (fr) | 2004-12-21 | 2004-12-21 | Composition polyisacyanate a proprietes anti-chocs ameliorees |
KR1020077016583A KR101268988B1 (ko) | 2004-12-21 | 2005-12-20 | 개선된 내-충격성을 갖는 폴리이소시아네이트 조성물 |
CN2005800471282A CN101107336B (zh) | 2004-12-21 | 2005-12-20 | 具有改进的抗冲击性能的多异氰酸酯组合物 |
EP05850546A EP1833935A1 (fr) | 2004-12-21 | 2005-12-20 | Composition polyisocyanate a proprietes anti-chocs ameliorees |
PCT/FR2005/003197 WO2006067326A1 (fr) | 2004-12-21 | 2005-12-20 | Composition polyisocyanate a proprietes anti-chocs ameliorees |
US11/793,489 US8188171B2 (en) | 2004-12-21 | 2005-12-20 | Polyisocyanate composition having improved impact-proof properties |
JP2007547567A JP2008524422A (ja) | 2004-12-21 | 2005-12-20 | 改良された耐衝撃性を有するポリイソシアネート組成物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0413669A FR2879616B1 (fr) | 2004-12-21 | 2004-12-21 | Composition polyisacyanate a proprietes anti-chocs ameliorees |
Publications (2)
Publication Number | Publication Date |
---|---|
FR2879616A1 true FR2879616A1 (fr) | 2006-06-23 |
FR2879616B1 FR2879616B1 (fr) | 2007-05-25 |
Family
ID=34953797
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FR0413669A Active FR2879616B1 (fr) | 2004-12-21 | 2004-12-21 | Composition polyisacyanate a proprietes anti-chocs ameliorees |
Country Status (7)
Country | Link |
---|---|
US (1) | US8188171B2 (fr) |
EP (1) | EP1833935A1 (fr) |
JP (1) | JP2008524422A (fr) |
KR (1) | KR101268988B1 (fr) |
CN (1) | CN101107336B (fr) |
FR (1) | FR2879616B1 (fr) |
WO (1) | WO2006067326A1 (fr) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8563636B2 (en) * | 2006-10-23 | 2013-10-22 | Kansai Paint Co., Ltd. | Aqueous two-package type clear coating composition and process for the formation of multilayer finish coating film |
ITVA20070066A1 (it) * | 2007-07-26 | 2009-01-27 | Lamberti Spa | Composizioni idrodisperdibili di poliisocianati |
FR2923835B1 (fr) * | 2007-11-20 | 2009-12-11 | Rhodia Operations | Nouvelles compositions polyisocyanates hydrophiles a base d'esters de phosphate. |
US9587140B2 (en) | 2012-02-21 | 2017-03-07 | Azalta Coating Systems Ip Co., Llc | Low foaming waterborne coating composition and use thereof |
WO2013126184A1 (fr) * | 2012-02-21 | 2013-08-29 | U.S. Coatings Ip Co. Llc | Composition de revêtement durcissable à basse température low et utilisation associée |
CN103044998B (zh) * | 2012-12-05 | 2015-06-10 | 燕山大学 | 一种适用于海雾环境下的镁合金防腐涂层及其制备方法 |
KR101701687B1 (ko) * | 2013-09-26 | 2017-02-01 | 미쓰이 가가쿠 가부시키가이샤 | 아이웨어 재료, 아이웨어 프레임 및 아이웨어 |
CN103739816B (zh) * | 2013-12-12 | 2016-03-02 | 苏州博纳化学科技有限公司 | 农乳类疏水单体的合成方法 |
EP3387037B1 (fr) * | 2015-12-09 | 2019-11-06 | Basf Se | Polyisocyanates dispersibles dans l'eau |
EP3517559B1 (fr) * | 2016-09-23 | 2021-02-24 | Asahi Kasei Kabushiki Kaisha | Composition de polyisocyanate, composition de polyisocyanate à blocs, composition de revêtement, composition aqueuse de revêtement, et matériau de support |
EP3305863A1 (fr) * | 2016-10-07 | 2018-04-11 | Basf Se | Procédé de production de polyisocyanates de diisocyanates (cyclo)aliphatiques résistants à la floculation dans les solvants |
CN114195971B (zh) * | 2016-10-14 | 2023-08-25 | 旭化成株式会社 | 多异氰酸酯组合物、封端多异氰酸酯组合物、亲水性多异氰酸酯组合物、涂料组合物和涂膜 |
EP3318337A1 (fr) * | 2016-11-03 | 2018-05-09 | PPG Industries Ohio, Inc. | Composition de revêtement et système de revêtement |
CN110621712B (zh) * | 2017-05-19 | 2021-09-10 | 旭化成株式会社 | 多异氰酸酯组合物 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2243983A1 (fr) * | 1973-09-18 | 1975-04-11 | Veba Chemie Ag | |
DE19725507A1 (de) * | 1997-06-17 | 1998-12-24 | Eckard Zuelch Gmbh & Co Lackfa | Trommellack |
WO2001005861A1 (fr) * | 1999-07-20 | 2001-01-25 | Rhodia Chimie | Procede pour conferer a un substrat un revetement ayant des proprietes de resistance elevee au choc |
EP1074590A2 (fr) * | 1999-08-04 | 2001-02-07 | Wolff Walsrode AG | Revêtement contenant un matériau cellulosique ainsi que son utilisation dans des peintures |
US20010018537A1 (en) * | 1997-02-28 | 2001-08-30 | Jean-Marie Bernard | Isocyanates modified to give them a surfactant property, composition containing them and coating resulting therefrom |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH08176477A (ja) | 1994-12-26 | 1996-07-09 | Nippon Paint Co Ltd | 電着塗料組成物及び高耐候性電着塗膜の形成方法 |
GB9602957D0 (en) * | 1996-02-17 | 1996-04-10 | Ici Plc | Coating compositions |
US20010021746A1 (en) | 1996-02-29 | 2001-09-13 | Minou Nabavi | Isocyanate-based compositions, their process for utilization, their utilization for producing coatings and coating thus obtained |
FR2745577B1 (fr) | 1996-02-29 | 2004-09-24 | Rhone Poulenc Chimie | Compositions a base d'isocyanate, leur procede d'utilisation leur utilisation pour realiser des revetements et revetement ainsi obtenu |
US5877254A (en) * | 1996-07-22 | 1999-03-02 | Film Specialties, Inc. | Scratch-resistant anti-fog coating composition incorporating isocyanate-reactive surfactants |
CO4870712A1 (es) * | 1997-03-17 | 1999-12-27 | Dow Chemical Co | Latex de poliuretano, procesos para su preparacion, y poli- meros preparados con los mismos |
US6258867B1 (en) * | 1999-07-23 | 2001-07-10 | Bayer Corporation | Method for making semi-rigid energy-absorbing foam with polyurethane fillers |
JP2001323123A (ja) | 2000-05-12 | 2001-11-20 | Asahi Kasei Corp | 高分子水性分散体組成物 |
FR2826366B1 (fr) | 2001-06-25 | 2005-03-11 | Rhodia Chimie Sa | Preparation d'isocyanates masques, notamment de polyisocyanates masques |
JP2003292887A (ja) | 2002-04-03 | 2003-10-15 | Dainippon Toryo Co Ltd | 上塗り塗料 |
-
2004
- 2004-12-21 FR FR0413669A patent/FR2879616B1/fr active Active
-
2005
- 2005-12-20 JP JP2007547567A patent/JP2008524422A/ja active Pending
- 2005-12-20 WO PCT/FR2005/003197 patent/WO2006067326A1/fr active Application Filing
- 2005-12-20 EP EP05850546A patent/EP1833935A1/fr not_active Withdrawn
- 2005-12-20 US US11/793,489 patent/US8188171B2/en active Active
- 2005-12-20 CN CN2005800471282A patent/CN101107336B/zh active Active
- 2005-12-20 KR KR1020077016583A patent/KR101268988B1/ko active IP Right Grant
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2243983A1 (fr) * | 1973-09-18 | 1975-04-11 | Veba Chemie Ag | |
US20010018537A1 (en) * | 1997-02-28 | 2001-08-30 | Jean-Marie Bernard | Isocyanates modified to give them a surfactant property, composition containing them and coating resulting therefrom |
DE19725507A1 (de) * | 1997-06-17 | 1998-12-24 | Eckard Zuelch Gmbh & Co Lackfa | Trommellack |
WO2001005861A1 (fr) * | 1999-07-20 | 2001-01-25 | Rhodia Chimie | Procede pour conferer a un substrat un revetement ayant des proprietes de resistance elevee au choc |
EP1074590A2 (fr) * | 1999-08-04 | 2001-02-07 | Wolff Walsrode AG | Revêtement contenant un matériau cellulosique ainsi que son utilisation dans des peintures |
Also Published As
Publication number | Publication date |
---|---|
CN101107336B (zh) | 2012-04-04 |
US8188171B2 (en) | 2012-05-29 |
FR2879616B1 (fr) | 2007-05-25 |
KR101268988B1 (ko) | 2013-05-31 |
CN101107336A (zh) | 2008-01-16 |
US20080044578A1 (en) | 2008-02-21 |
EP1833935A1 (fr) | 2007-09-19 |
KR20070091025A (ko) | 2007-09-06 |
JP2008524422A (ja) | 2008-07-10 |
WO2006067326A1 (fr) | 2006-06-29 |
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