JPH0662743B2 - 環境温度で硬化しうる液状コーテイング組成物 - Google Patents

環境温度で硬化しうる液状コーテイング組成物

Info

Publication number: JPH0662743B2
Authority: JP; Japan
Prior art keywords: group; compound; coating composition; malonate; weight
Prior art date: 1984-03-29
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.): Expired - Lifetime

Application number

JP60064069A

Other languages

English (en)

Japanese (ja)

Other versions

JPS60223816A (ja

Inventor

ヤープ・ミシエル・アツカーマン

Original Assignee

アクゾ・ナームローゼ・フエンノートシヤツプ

Priority date (The priority date 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 date listed.)

1984-03-29

Filing date

1985-03-29

Publication date

1994-08-17

1985-03-29 Application filed by アクゾ・ナームローゼ・フエンノートシヤツプ filed Critical アクゾ・ナームローゼ・フエンノートシヤツプ

1985-11-08 Publication of JPS60223816A publication Critical patent/JPS60223816A/ja

1994-08-17 Publication of JPH0662743B2 publication Critical patent/JPH0662743B2/ja

2009-08-17 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

239000008199 coating composition Substances 0.000 title claims abstract description 23
239000007788 liquid Substances 0.000 title claims abstract description 4
150000001875 compounds Chemical class 0.000 claims abstract description 30
150000001728 carbonyl compounds Chemical class 0.000 claims abstract description 7
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical group OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 30
239000000203 mixture Substances 0.000 claims description 23
238000000576 coating method Methods 0.000 claims description 16
239000011248 coating agent Substances 0.000 claims description 15
239000002253 acid Substances 0.000 claims description 13
150000002148 esters Chemical class 0.000 claims description 12
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
-1 malonate compound Chemical class 0.000 claims description 12
229920000728 polyester Polymers 0.000 claims description 11
238000006243 chemical reaction Methods 0.000 claims description 10
239000003054 catalyst Substances 0.000 claims description 9
239000004814 polyurethane Substances 0.000 claims description 9
229920002635 polyurethane Polymers 0.000 claims description 9
239000003822 epoxy resin Substances 0.000 claims description 7
229920000647 polyepoxide Polymers 0.000 claims description 7
239000004952 Polyamide Substances 0.000 claims description 5
125000004432 carbon atom Chemical group C* 0.000 claims description 5
229920000570 polyether Polymers 0.000 claims description 5
LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
229920000058 polyacrylate Polymers 0.000 claims description 4
229920000915 polyvinyl chloride Polymers 0.000 claims description 4
239000004593 Epoxy Substances 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
150000002430 hydrocarbons Chemical class 0.000 claims description 3
230000007935 neutral effect Effects 0.000 claims description 3
229920006122 polyamide resin Polymers 0.000 claims description 3
229920000193 polymethacrylate Polymers 0.000 claims description 3
125000003700 epoxy group Chemical group 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
238000000034 method Methods 0.000 claims description 2
WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
229920000642 polymer Polymers 0.000 abstract description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
229920005989 resin Polymers 0.000 description 19
239000011347 resin Substances 0.000 description 19
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 15
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 14
239000008096 xylene Substances 0.000 description 14
OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical compound [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 description 11
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
239000005056 polyisocyanate Substances 0.000 description 7
229920001228 polyisocyanate Polymers 0.000 description 7
229910000831 Steel Inorganic materials 0.000 description 6
ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 6
YRKCREAYFQTBPV-UHFFFAOYSA-N acetylacetone Chemical compound CC(=O)CC(C)=O YRKCREAYFQTBPV-UHFFFAOYSA-N 0.000 description 6
BEPAFCGSDWSTEL-UHFFFAOYSA-N dimethyl malonate Chemical compound COC(=O)CC(=O)OC BEPAFCGSDWSTEL-UHFFFAOYSA-N 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
229920005862 polyol Polymers 0.000 description 6
239000010959 steel Substances 0.000 description 6
NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 5
239000005058 Isophorone diisocyanate Substances 0.000 description 5
DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
SMTUJUHULKBTBS-UHFFFAOYSA-N benzyl(trimethyl)azanium;methanolate Chemical compound [O-]C.C[N+](C)(C)CC1=CC=CC=C1 SMTUJUHULKBTBS-UHFFFAOYSA-N 0.000 description 5
238000001035 drying Methods 0.000 description 5
150000002440 hydroxy compounds Chemical class 0.000 description 5
NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 5
150000002690 malonic acid derivatives Chemical class 0.000 description 5
150000003077 polyols Chemical class 0.000 description 5
239000005057 Hexamethylene diisocyanate Substances 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
238000001816 cooling Methods 0.000 description 4
JGFBRKRYDCGYKD-UHFFFAOYSA-N dibutyl(oxo)tin Chemical compound CCCC[Sn](=O)CCCC JGFBRKRYDCGYKD-UHFFFAOYSA-N 0.000 description 4
JQVDAXLFBXTEQA-UHFFFAOYSA-N dibutylamine Chemical compound CCCCNCCCC JQVDAXLFBXTEQA-UHFFFAOYSA-N 0.000 description 4
125000005442 diisocyanate group Chemical group 0.000 description 4
RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 4
125000005395 methacrylic acid group Chemical group 0.000 description 4
238000002156 mixing Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000000047 product Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
239000004721 Polyphenylene oxide Substances 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
150000001252 acrylic acid derivatives Chemical class 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
230000032050 esterification Effects 0.000 description 3
238000005886 esterification reaction Methods 0.000 description 3
125000002768 hydroxyalkyl group Chemical group 0.000 description 3
125000001453 quaternary ammonium group Chemical group 0.000 description 3
239000000758 substrate Substances 0.000 description 3
QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 description 2
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 2
IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
ORLQHILJRHBSAY-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1(CO)CCCCC1 ORLQHILJRHBSAY-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
229920003180 amino resin Polymers 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
XXMIOPMDWAUFGU-UHFFFAOYSA-N hexane-1,6-diol Chemical compound OCCCCCCO XXMIOPMDWAUFGU-UHFFFAOYSA-N 0.000 description 2
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 2
239000003960 organic solvent Substances 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
238000006068 polycondensation reaction Methods 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
239000011734 sodium Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
MGAXYKDBRBNWKT-UHFFFAOYSA-N (5-oxooxolan-2-yl)methyl 4-methylbenzenesulfonate Chemical compound C1=CC(C)=CC=C1S(=O)(=O)OCC1OC(=O)CC1 MGAXYKDBRBNWKT-UHFFFAOYSA-N 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
OKGNMRKOGWTADH-UHFFFAOYSA-N 1,4-dihydropyrimidine Chemical compound C1C=CNC=N1 OKGNMRKOGWTADH-UHFFFAOYSA-N 0.000 description 1
VOBUAPTXJKMNCT-UHFFFAOYSA-N 1-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound CCCCCC(OC(=O)C=C)OC(=O)C=C VOBUAPTXJKMNCT-UHFFFAOYSA-N 0.000 description 1
LTMRRSWNXVJMBA-UHFFFAOYSA-L 2,2-diethylpropanedioate Chemical compound CCC(CC)(C([O-])=O)C([O-])=O LTMRRSWNXVJMBA-UHFFFAOYSA-L 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
MLIREBYILWEBDM-UHFFFAOYSA-M 2-cyanoacetate Chemical compound [O-]C(=O)CC#N MLIREBYILWEBDM-UHFFFAOYSA-M 0.000 description 1
OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
OMQHDIHZSDEIFH-UHFFFAOYSA-N 3-Acetyldihydro-2(3H)-furanone Chemical compound CC(=O)C1CCOC1=O OMQHDIHZSDEIFH-UHFFFAOYSA-N 0.000 description 1
QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 1
HOSGXJWQVBHGLT-UHFFFAOYSA-N 6-hydroxy-3,4-dihydro-1h-quinolin-2-one Chemical group N1C(=O)CCC2=CC(O)=CC=C21 HOSGXJWQVBHGLT-UHFFFAOYSA-N 0.000 description 1
WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 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
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
238000006845 Michael addition reaction Methods 0.000 description 1
VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical group O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 1
HVVWZTWDBSEWIH-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(CO)(COC(=O)C=C)COC(=O)C=C HVVWZTWDBSEWIH-UHFFFAOYSA-N 0.000 description 1
GCPWJFKTWGFEHH-UHFFFAOYSA-N acetoacetamide Chemical compound CC(=O)CC(N)=O GCPWJFKTWGFEHH-UHFFFAOYSA-N 0.000 description 1
WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
229920000180 alkyd Polymers 0.000 description 1
150000001409 amidines Chemical class 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
UFMOVMDZFREWNZ-UHFFFAOYSA-M benzyl(trimethyl)azanium 3-oxobutanoate Chemical compound CC(=O)CC([O-])=O.C[N+](C)(C)CC1=CC=CC=C1 UFMOVMDZFREWNZ-UHFFFAOYSA-M 0.000 description 1
OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
229930016911 cinnamic acid Natural products 0.000 description 1
235000013985 cinnamic acid Nutrition 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
239000012973 diazabicyclooctane Substances 0.000 description 1
LNGAGQAGYITKCW-UHFFFAOYSA-N dimethyl cyclohexane-1,4-dicarboxylate Chemical compound COC(=O)C1CCC(C(=O)OC)CC1 LNGAGQAGYITKCW-UHFFFAOYSA-N 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
239000000975 dye Substances 0.000 description 1
XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
229940093858 ethyl acetoacetate Drugs 0.000 description 1
UKFXDFUAPNAMPJ-UHFFFAOYSA-N ethylmalonic acid Chemical compound CCC(C(O)=O)C(O)=O UKFXDFUAPNAMPJ-UHFFFAOYSA-N 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
239000001530 fumaric acid Substances 0.000 description 1
229920001002 functional polymer Polymers 0.000 description 1
125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
ROBFUDYVXSDBQM-UHFFFAOYSA-N hydroxymalonic acid Chemical compound OC(=O)C(O)C(O)=O ROBFUDYVXSDBQM-UHFFFAOYSA-N 0.000 description 1
239000012948 isocyanate Substances 0.000 description 1
IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
150000002513 isocyanates Chemical class 0.000 description 1
ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000010985 leather Substances 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
230000014759 maintenance of location Effects 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
229910001507 metal halide Inorganic materials 0.000 description 1
150000005309 metal halides Chemical class 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
NBTOZLQBSIZIKS-UHFFFAOYSA-N methoxide Chemical compound [O-]C NBTOZLQBSIZIKS-UHFFFAOYSA-N 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
229910000510 noble metal Inorganic materials 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920000768 polyamine Polymers 0.000 description 1
229920005906 polyester polyol Polymers 0.000 description 1
229920001225 polyester resin Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
FEMRXDWBWXQOGV-UHFFFAOYSA-N potassium amide Chemical class [NH2-].[K+] FEMRXDWBWXQOGV-UHFFFAOYSA-N 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
IMNIMPAHZVJRPE-UHFFFAOYSA-N triethylenediamine Chemical compound C1CN2CCN1CC2 IMNIMPAHZVJRPE-UHFFFAOYSA-N 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000002023 wood Substances 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
- C09D201/00—Coating compositions based on unspecified macromolecular compounds
- C09D201/02—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups
- C09D201/06—Coating compositions based on unspecified macromolecular compounds characterised by the presence of specified groups, e.g. terminal or pendant functional groups containing oxygen atoms
- C09D201/08—Carboxyl groups
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F283/00—Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass C08G
- 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
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- 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
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy 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
- C08G85/00—General processes for preparing compounds provided for in this subclass

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Wood Science & Technology (AREA)
Paints Or Removers (AREA)
Polyurethanes Or Polyureas (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Epoxy Resins (AREA)
Micro-Organisms Or Cultivation Processes Thereof (AREA)
Saccharide Compounds (AREA)
Medicinal Preparation (AREA)
Polymerisation Methods In General (AREA)
Polyesters Or Polycarbonates (AREA)
Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
Macromonomer-Based Addition Polymer (AREA)
Dental Preparations (AREA)
Fluid-Pressure Circuits (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Materials For Medical Uses (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Orthopedics, Nursing, And Contraception (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP60064069A 1984-03-29 1985-03-29 環境温度で硬化しうる液状コーテイング組成物 Expired - Lifetime JPH0662743B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
NL8401007		1984-03-29
NL8401007		1984-03-29

Publications (2)

Publication Number	Publication Date
JPS60223816A JPS60223816A (ja)	1985-11-08
JPH0662743B2 true JPH0662743B2 (ja)	1994-08-17

Family

ID=19843724

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP60064069A Expired - Lifetime JPH0662743B2 (ja)	1984-03-29	1985-03-29	環境温度で硬化しうる液状コーテイング組成物

Country Status (13)

Country	Link
US (1)	US4602061A (2)
EP (1)	EP0161697B1 (2)
JP (1)	JPH0662743B2 (2)
AT (1)	ATE32910T1 (2)
AU (1)	AU576837B2 (2)
BR (1)	BR8501408A (2)
CA (1)	CA1252240A (2)
DE (1)	DE3561824D1 (2)
DK (1)	DK166362C (2)
FI (1)	FI81372C (2)
GR (1)	GR850785B (2)
NO (1)	NO166492C (2)
ZA (1)	ZA852044B (2)

Families Citing this family (65)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3733182A1 (de) *	1987-10-01	1989-04-20	Hoechst Ag	Haertungskomponente und deren verwendung
DE3879669T2 (de) *	1988-02-01	1993-10-14	Rohm & Haas	Verfahren zum Reagieren von zwei Komponenten, Zusammensetzungen, Beschichtungszusammensetzungen und Verwendung davon.
US5177152A (en) *	1988-08-09	1993-01-05	Akzo N.V.	Water-dilutable, crosslinkable binder resin
ATE117326T1 (de) *	1988-08-09	1995-02-15	Akzo Nobel Nv	Beschichtungsmittel.
EP0448154A1 (en) *	1990-03-20	1991-09-25	Akzo Nobel N.V.	Coating composition including a blocked basic catalyst
CA2032219A1 (en) *	1990-10-01	1992-04-02	Jim D. Elmore	Two package ambient temperature curing coating composition
US5589534A (en) *	1990-10-16	1996-12-31	Akzo Nobel N.V.	Aqueous coating compositions including a reactive emulsifier
MY108731A (en) *	1992-04-16	1996-11-30	Akzo Nv	Aqueous coating compositions
BE1005775A3 (nl) *	1992-04-29	1994-01-25	Dsm Nv	Bindmiddelsamenstelling voor oplosmiddel- of watergebaseerde coatings.
AU672337B2 (en) *	1993-10-27	1996-09-26	Nippon Paint Co., Ltd.	Curable resin composition for coating uses
ATE176270T1 (de)	1995-11-22	1999-02-15	Akzo Nobel Nv	Feuchtigkeitshärtende beschichtungszusammensetzung
US5959028A (en) *	1996-05-22	1999-09-28	Nippon Paint Co., Ltd.	Curable resin composition for coating use
DE69620038T2 (de) *	1996-12-11	2002-10-02	Minnesota Mining And Mfg. Co., St. Paul	Bei raumtemperatur härtbares harz
US6204343B1 (en)	1996-12-11	2001-03-20	3M Innovative Properties Company	Room temperature curable resin
WO1998032756A1 (en) *	1997-01-22	1998-07-30	Ciba Specialty Chemicals Holding Inc.	Substituted aminoalkylidenamino triazines as herbicides
GB2323599A (en)	1997-03-18	1998-09-30	Courtaulds Plc	Compositions curable by a Michael reaction
US5945489A (en) *	1997-09-19	1999-08-31	Ashland, Inc.	Liquid oligomers containing unsaturation
AU2001258304A1 (en) *	2000-03-28	2001-10-08	Akzo Nobel N.V.	Photoactivatable coating composition and its use for the preparation of coatings with a rapidly processable surface at ambient temperature
ES2250489T3 (es)	2000-10-25	2006-04-16	Akzo Nobel Coatings International B.V.	Composicion de revestimiento en suspension en agua fotoactivable.
AU4885002A (en) *	2001-07-03	2003-01-09	Rohm And Haas Company	Composition method of making and method of using adhesive composition
US20030165701A1 (en) *	2001-12-13	2003-09-04	Straw Thomas Allen	Water borne ambient temperature curable coating composition
EP1371689A1 (en) *	2002-06-14	2003-12-17	Dainippon Ink And Chemicals, Inc.	Storage stable curable coating compositions
US8013068B2 (en) *	2003-01-02	2011-09-06	Rohm And Haas Company	Michael addition compositions
EP1640388B1 (en) *	2004-09-24	2015-02-25	Rohm and Haas Company	Biomass based Michael addition composition
DE102006055944A1 (de) *	2006-11-24	2008-05-29	Henkel Kgaa	Vernetzende Folienklebstoffe
JP5627684B2 (ja)	2009-08-21	2014-11-19	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	超顕微鏡的及び光学的可変像を有するデバイスのための装置及び方法
EP2374836A1 (en)	2010-04-07	2011-10-12	Nuplex Resins B.V.	Crosslinkable composition crosslinkable with a latent base catalyst.
EP2764037B1 (en) *	2011-10-07	2017-03-22	Nuplex Resins B.V.	A crosslinkable composition cross-linkable by real michael addition reaction and resins for use in said composition
NO2984133T3 (2)	2013-04-08	2018-08-25
US9023976B2 (en)	2013-05-01	2015-05-05	Robert Bernard Login	Amide-imide compounds and their corresponding polymers
US10774238B2 (en)	2015-04-17	2020-09-15	Allnex Netherlands B.V.	Method for curing a RMA crosslinkable resin coating, RMA crosslinkable compositions and resins for use therein
JP6833716B2 (ja)	2015-04-17	2021-02-24	オールネックス・ネザーランズ・ビー．ブイ．ＡｌｌｎｅｘＮｅｔｈｅｒｌａｎｄｓＢ．Ｖ．	Ｒｍａ架橋性コーティング組成物の接着の改善のための改質エポキシプライマー
JP6837991B2 (ja)	2015-04-17	2021-03-03	オールネックス・ネザーランズ・ビー．ブイ．ＡｌｌｎｅｘＮｅｔｈｅｒｌａｎｄｓＢ．Ｖ．	フロアコーティング組成物
US10767074B2 (en)	2015-04-17	2020-09-08	Allnex Netherlands B.V.	Process for the manufacture of a crosslinkable composition
PL3085748T3 (pl)	2015-04-20	2018-07-31	Jotun A/S	Powłoki
KR102583063B1 (ko)	2016-06-30	2023-09-26	엘리멘티스 스페셜티즈, 인크.	휴면 카르바메이트 개시제와 배합된 가교성 코팅 조성물
US11732165B2 (en)	2017-06-13	2023-08-22	Eastman Chemical Company	Low-temperature curable compositions
WO2018231922A1 (en)	2017-06-13	2018-12-20	Elementis Specialties, Inc.	Coating system
US10563040B2 (en)	2017-06-13	2020-02-18	Eastman Chemical Company	Low-temperature curable compositions
US20180355105A1 (en) *	2017-06-13	2018-12-13	Eastman Chemical Company	Self-cureable and low temperature cureable polyesters
AU2019212991B2 (en)	2018-01-26	2024-05-23	Allnex Netherlands B.V.	Powder coating composition
CA3099108A1 (en)	2018-05-07	2019-11-14	Swimc Llc	Corrosion-resistant primer and topcoat composition
US11518904B2 (en)	2018-09-26	2022-12-06	Swimc Llc	Curable coating compositions
EP3663326A1 (en)	2018-12-04	2020-06-10	Allnex Netherlands B.V.	Rma crosslinkable polymer
US11920050B2 (en)	2018-12-11	2024-03-05	Eastman Chemical Company	Self-curable and low temperature curable coating compositions
US20200181338A1 (en)	2018-12-11	2020-06-11	Eastman Chemical Company	Bis-primary amines as cross-linkers for the curing of acetoacetylated resin compositions
US12378434B2 (en)	2018-12-11	2025-08-05	Eastman Chemical Company	Curable coating compositions
EP3712190A1 (en)	2019-03-18	2020-09-23	ALLNEX AUSTRIA GmbH	Binder for an aqueous coating composition
CA3125005A1 (en)	2019-02-01	2020-08-06	Allnex Austria Gmbh	Binder for an aqueous coating composition
EP3689986A1 (en)	2019-02-01	2020-08-05	ALLNEX AUSTRIA GmbH	Binder for aqueous coating compositions
CN110240821B (zh)	2019-05-07	2021-04-02	广东华润涂料有限公司	木器用涂料组合物以及由其制成的木制品
CN110105799B (zh)	2019-05-07	2021-10-01	广东华润涂料有限公司	木器用涂料组合物以及由其制成的木制品
US12421348B2 (en)	2019-09-18	2025-09-23	Swimc Llc	Coating compositions and methods with polyfunctional carbamate salt
DE102020128717A1 (de)	2019-12-04	2021-06-10	Fischerwerke Gmbh & Co. Kg	Michael-Additions-härtendes Kunstharz für die chemische Befestigungstechnik
WO2021122978A1 (en)	2019-12-19	2021-06-24	Allnex Netherlands B.V.	Non aqueous crosslinkable composition
EP4330337A1 (en)	2021-04-28	2024-03-06	Allnex Netherlands B.V.	Process for overspray-free application of a resin composition and resin compositions for use in the process
WO2022236519A1 (en)	2021-05-10	2022-11-17	Allnex Resins (Shanghai) Co., Ltd.	Powder coating compostion blend
KR20240024222A (ko)	2021-06-22	2024-02-23	알넥스 네덜란드 비. 브이.	비수성 가교성 조성물
AU2022308331A1 (en)	2021-07-05	2023-11-16	Allnex Netherlands B.V.	Powder coating and crystalline donor and/or acceptor
MX2023013602A (es)	2021-07-05	2023-11-29	Allnex Netherlands Bv	Recubrimiento en polvo y catalizador precursor cristalino.
JP7518128B2 (ja) *	2021-09-22	2024-07-17	三洋化成工業株式会社	ポリエステル樹脂及び樹脂粒子の製造方法
JP7679271B2 (ja) *	2021-09-28	2025-05-19	三洋化成工業株式会社	樹脂粒子の製造方法
AU2023376145A1 (en)	2022-11-07	2025-04-03	Allnex Netherlands B.V.	Two component powder coating composition with separated catalyst system
WO2025153683A1 (en)	2024-01-19	2025-07-24	Jotun A/S	Intumescent coating composition
WO2025153696A1 (en)	2024-01-19	2025-07-24	Jotun A/S	Intumescent coating composition

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE835809C (de) *	1950-02-28	1952-04-03	Bayer Ag	Verfahren zur Herstellung von Polyadditionsprodukten
US4006122A (en) *	1974-03-11	1977-02-01	The Upjohn Company	Polyester-amides prepared from polymalonates and isocyanates

1985
- 1985-03-19 ZA ZA852044A patent/ZA852044B/xx unknown
- 1985-03-26 US US06/716,273 patent/US4602061A/en not_active Expired - Lifetime
- 1985-03-27 DE DE8585200459T patent/DE3561824D1/de not_active Expired
- 1985-03-27 EP EP85200459A patent/EP0161697B1/en not_active Expired
- 1985-03-27 AT AT85200459T patent/ATE32910T1/de not_active IP Right Cessation
- 1985-03-28 GR GR850785A patent/GR850785B/el unknown
- 1985-03-28 FI FI851258A patent/FI81372C/fi not_active IP Right Cessation
- 1985-03-28 DK DK139485A patent/DK166362C/da not_active IP Right Cessation
- 1985-03-28 AU AU40458/85A patent/AU576837B2/en not_active Ceased
- 1985-03-28 CA CA000477745A patent/CA1252240A/en not_active Expired
- 1985-03-28 NO NO851266A patent/NO166492C/no not_active IP Right Cessation
- 1985-03-28 BR BR8501408A patent/BR8501408A/pt not_active IP Right Cessation
- 1985-03-29 JP JP60064069A patent/JPH0662743B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
DK139485D0 (da)	1985-03-28
US4602061A (en)	1986-07-22
DK166362B (da)	1993-04-13
DK139485A (da)	1985-09-30
BR8501408A (pt)	1985-11-26
EP0161697B1 (en)	1988-03-09
ATE32910T1 (de)	1988-03-15
CA1252240A (en)	1989-04-04
NO166492C (no)	1991-07-31
GR850785B (2)	1985-11-25
AU4045885A (en)	1985-10-03
AU576837B2 (en)	1988-09-08
FI851258A0 (fi)	1985-03-28
NO166492B (no)	1991-04-22
DE3561824D1 (en)	1988-04-14
JPS60223816A (ja)	1985-11-08
NO851266L (no)	1985-09-30
FI851258L (fi)	1985-09-30
EP0161697A1 (en)	1985-11-21
FI81372C (fi)	1990-10-10
FI81372B (fi)	1990-06-29
DK166362C (da)	1993-09-06
ZA852044B (en)	1985-11-27

Publication	Publication Date	Title
EP0161697B1 (en)	1988-03-09	Liquid coating composition curable at ambient temperature
KR100612537B1 (ko)	2006-08-11	분말 페인트 결합제 조성물
US5134205A (en)	1992-07-28	Certain hydroxyalkyl carbamate compounds, homopolymers and copolymers thereof and uses thereof
CA1341178C (en)	2001-02-13	Certain hydroxyalkyl carbamates, polymers and uses thereof
JP3537955B2 (ja)	2004-06-14	超分枝ポリアスパラギン酸エステル及びその調製方法
JP5128247B2 (ja)	2013-01-23	コーティング組成物
KR20010030571A (ko)	2001-04-16	카르바메이트 작용성 화합물의 혼합물을 함유하는 경화성코팅 조성물
JPS5944310B2 (ja)	1984-10-29	ブロツクトイソシアネ−ト基を有するポリイソシアネ−ト混合物の製造方法
CZ14693A3 (en)	1993-12-15	Coating compositions, process of their preparation and their use for producing coating
JPS60104119A (ja)	1985-06-08	貯蔵安定性の一成分系ウレタン化合物並びにその製造法および使用法
JPS58501123A (ja)	1983-07-14	１，４−シクロヘキサンビス（メチルイソシアネ−ト）ベ−スの固形ブロックト架橋剤
JPS61113658A (ja)	1986-05-31	硬化性塗料組成物
US5925711A (en)	1999-07-20	Polyamines and their use in aqueous coating compositions
MXPA01006298A (es)	2005-06-20	Composicion de recubrimiento.
JP2003128989A (ja)	2003-05-08	ハイソリッド塗料組成物
SU784790A3 (ru)	1980-11-30	Способ получени термоотверждаемого св зующего дл покрыти , осаждаемого на катоде
CZ196495A3 (en)	1996-02-14	(poly)anhydride-modified polyisocyanates of dicarboxylic acids
JP2742816B2 (ja)	1998-04-22	硬化性樹脂組成物
JP3697562B2 (ja)	2005-09-21	熱硬化性樹脂組成物
JPH02276878A (ja)	1990-11-13	一液型ポリウレタン熱硬化性被覆用組成物
WO1997004881A1 (en)	1997-02-13	Polyester oligomer acrylates
JPS6120591B2 (2)	1986-05-22
JP4234318B2 (ja)	2009-03-04	つや消し又は梨地のコーティングを得るために有益な組成物、この組成物の使用、及びこれによって得られたコーティング
KR20060054132A (ko)	2006-05-22	블록킹된 뷰렛화 이소시아네이트
JP2521285B2 (ja)	1996-08-07	溶剤ベ―ス可撓性コ―ティング組成物