JP6904529B1 - A method for forming an aqueous resin composition containing an aluminum pigment, an aqueous electrodeposition resin solution, an aqueous electrodeposition coating film, a coating film, and an electrodeposition coating film. - Google Patents
A method for forming an aqueous resin composition containing an aluminum pigment, an aqueous electrodeposition resin solution, an aqueous electrodeposition coating film, a coating film, and an electrodeposition coating film. Download PDFInfo
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- JP6904529B1 JP6904529B1 JP2020195923A JP2020195923A JP6904529B1 JP 6904529 B1 JP6904529 B1 JP 6904529B1 JP 2020195923 A JP2020195923 A JP 2020195923A JP 2020195923 A JP2020195923 A JP 2020195923A JP 6904529 B1 JP6904529 B1 JP 6904529B1
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- Prior art keywords
- water
- mass
- aqueous
- parts
- electrodeposition coating
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- 238000000576 coating method Methods 0.000 title claims abstract description 165
- 238000004070 electrodeposition Methods 0.000 title claims abstract description 163
- 239000011248 coating agent Substances 0.000 title claims abstract description 161
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 98
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 95
- 239000000049 pigment Substances 0.000 title claims abstract description 90
- 239000011342 resin composition Substances 0.000 title claims abstract description 74
- 229920005989 resin Polymers 0.000 title claims abstract description 62
- 239000011347 resin Substances 0.000 title claims abstract description 62
- 238000000034 method Methods 0.000 title claims abstract description 34
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 94
- 229920003180 amino resin Polymers 0.000 claims abstract description 48
- 239000007788 liquid Substances 0.000 claims abstract description 39
- 229920001577 copolymer Polymers 0.000 claims abstract description 31
- 239000000463 material Substances 0.000 claims abstract description 30
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 30
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 28
- 239000003125 aqueous solvent Substances 0.000 claims abstract description 19
- 239000002253 acid Substances 0.000 claims abstract description 17
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims abstract description 15
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 claims abstract description 14
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 12
- 125000001424 substituent group Chemical group 0.000 claims abstract description 5
- 229920006163 vinyl copolymer Polymers 0.000 claims description 43
- 150000001875 compounds Chemical class 0.000 claims description 8
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 claims description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 4
- 239000011733 molybdenum Substances 0.000 claims description 4
- 229910052750 molybdenum Inorganic materials 0.000 claims description 4
- 229910052698 phosphorus Inorganic materials 0.000 claims description 4
- 239000011574 phosphorus Substances 0.000 claims description 4
- 239000002210 silicon-based material Substances 0.000 claims description 3
- 238000005260 corrosion Methods 0.000 abstract description 16
- 230000007797 corrosion Effects 0.000 abstract description 16
- 239000003513 alkali Substances 0.000 abstract description 8
- 239000002904 solvent Substances 0.000 abstract description 7
- 239000002585 base Substances 0.000 abstract description 6
- 239000000126 substance Substances 0.000 abstract description 4
- 238000010586 diagram Methods 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 82
- 239000008367 deionised water Substances 0.000 description 49
- 229910021641 deionized water Inorganic materials 0.000 description 49
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 40
- 229960002887 deanol Drugs 0.000 description 40
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 34
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 31
- 238000003756 stirring Methods 0.000 description 27
- 239000000203 mixture Substances 0.000 description 26
- 239000011550 stock solution Substances 0.000 description 24
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 20
- 239000004480 active ingredient Substances 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 15
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- 239000003795 chemical substances by application Substances 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 239000003973 paint Substances 0.000 description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 7
- 241000209094 Oryza Species 0.000 description 7
- 235000007164 Oryza sativa Nutrition 0.000 description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 235000019441 ethanol Nutrition 0.000 description 7
- 238000011156 evaluation Methods 0.000 description 7
- 235000009566 rice Nutrition 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 6
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 6
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 6
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 6
- 229920000877 Melamine resin Polymers 0.000 description 5
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- 229910052710 silicon Inorganic materials 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000013461 design Methods 0.000 description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000007769 metal material Substances 0.000 description 4
- 239000011259 mixed solution Substances 0.000 description 4
- 230000003472 neutralizing effect Effects 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 239000004640 Melamine resin Substances 0.000 description 3
- 239000004264 Petrolatum Substances 0.000 description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 230000001804 emulsifying effect Effects 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 235000019271 petrolatum Nutrition 0.000 description 3
- 229940066842 petrolatum Drugs 0.000 description 3
- 239000003505 polymerization initiator Substances 0.000 description 3
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 3
- 150000003377 silicon compounds Chemical class 0.000 description 3
- 239000010935 stainless steel Substances 0.000 description 3
- 229910001220 stainless steel Inorganic materials 0.000 description 3
- 229920001187 thermosetting polymer Polymers 0.000 description 3
- GWZMWHWAWHPNHN-UHFFFAOYSA-N 2-hydroxypropyl prop-2-enoate Chemical compound CC(O)COC(=O)C=C GWZMWHWAWHPNHN-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 2
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 description 2
- NDWUBGAGUCISDV-UHFFFAOYSA-N 4-hydroxybutyl prop-2-enoate Chemical compound OCCCCOC(=O)C=C NDWUBGAGUCISDV-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-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
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
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- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
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- IAXXETNIOYFMLW-COPLHBTASA-N [(1s,3s,4s)-4,7,7-trimethyl-3-bicyclo[2.2.1]heptanyl] 2-methylprop-2-enoate Chemical compound C1C[C@]2(C)[C@@H](OC(=O)C(=C)C)C[C@H]1C2(C)C IAXXETNIOYFMLW-COPLHBTASA-N 0.000 description 1
- AFSQFGXTYWXFPP-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1(CO)CCCCC1 AFSQFGXTYWXFPP-UHFFFAOYSA-N 0.000 description 1
- KKVKUNIBLLLFHA-UHFFFAOYSA-N [1-(hydroxymethyl)cyclohexyl]methyl prop-2-enoate Chemical compound C=CC(=O)OCC1(CO)CCCCC1 KKVKUNIBLLLFHA-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000008360 acrylonitriles Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- APUPEJJSWDHEBO-UHFFFAOYSA-P ammonium molybdate Chemical compound [NH4+].[NH4+].[O-][Mo]([O-])(=O)=O APUPEJJSWDHEBO-UHFFFAOYSA-P 0.000 description 1
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- 125000000129 anionic group Chemical group 0.000 description 1
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- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 description 1
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- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
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- OIWOHHBRDFKZNC-UHFFFAOYSA-N cyclohexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC1CCCCC1 OIWOHHBRDFKZNC-UHFFFAOYSA-N 0.000 description 1
- KBLWLMPSVYBVDK-UHFFFAOYSA-N cyclohexyl prop-2-enoate Chemical compound C=CC(=O)OC1CCCCC1 KBLWLMPSVYBVDK-UHFFFAOYSA-N 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
- 229940043279 diisopropylamine Drugs 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 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 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- MDNFYIAABKQDML-UHFFFAOYSA-N heptyl 2-methylprop-2-enoate Chemical compound CCCCCCCOC(=O)C(C)=C MDNFYIAABKQDML-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 1
- LNMQRPPRQDGUDR-UHFFFAOYSA-N hexyl prop-2-enoate Chemical compound CCCCCCOC(=O)C=C LNMQRPPRQDGUDR-UHFFFAOYSA-N 0.000 description 1
- 229940119545 isobornyl methacrylate Drugs 0.000 description 1
- 229940035429 isobutyl alcohol Drugs 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- 239000002932 luster Substances 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
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- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- LVQPBIMCRZQQBC-UHFFFAOYSA-N methoxymethyl 2-methylprop-2-enoate Chemical compound COCOC(=O)C(C)=C LVQPBIMCRZQQBC-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
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
- 239000005078 molybdenum compound Substances 0.000 description 1
- 150000002752 molybdenum compounds Chemical class 0.000 description 1
- KCTMTGOHHMRJHZ-UHFFFAOYSA-N n-(2-methylpropoxymethyl)prop-2-enamide Chemical compound CC(C)COCNC(=O)C=C KCTMTGOHHMRJHZ-UHFFFAOYSA-N 0.000 description 1
- UTSYWKJYFPPRAP-UHFFFAOYSA-N n-(butoxymethyl)prop-2-enamide Chemical compound CCCCOCNC(=O)C=C UTSYWKJYFPPRAP-UHFFFAOYSA-N 0.000 description 1
- LSWADWIFYOAQRZ-UHFFFAOYSA-N n-(ethoxymethyl)prop-2-enamide Chemical compound CCOCNC(=O)C=C LSWADWIFYOAQRZ-UHFFFAOYSA-N 0.000 description 1
- ULYOZOPEFCQZHH-UHFFFAOYSA-N n-(methoxymethyl)prop-2-enamide Chemical compound COCNC(=O)C=C ULYOZOPEFCQZHH-UHFFFAOYSA-N 0.000 description 1
- QYZFTMMPKCOTAN-UHFFFAOYSA-N n-[2-(2-hydroxyethylamino)ethyl]-2-[[1-[2-(2-hydroxyethylamino)ethylamino]-2-methyl-1-oxopropan-2-yl]diazenyl]-2-methylpropanamide Chemical compound OCCNCCNC(=O)C(C)(C)N=NC(C)(C)C(=O)NCCNCCO QYZFTMMPKCOTAN-UHFFFAOYSA-N 0.000 description 1
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 229940105570 ornex Drugs 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920013716 polyethylene resin Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- BOQSSGDQNWEFSX-UHFFFAOYSA-N propan-2-yl 2-methylprop-2-enoate Chemical compound CC(C)OC(=O)C(C)=C BOQSSGDQNWEFSX-UHFFFAOYSA-N 0.000 description 1
- LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
- NHARPDSAXCBDDR-UHFFFAOYSA-N propyl 2-methylprop-2-enoate Chemical compound CCCOC(=O)C(C)=C NHARPDSAXCBDDR-UHFFFAOYSA-N 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000012966 redox initiator Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000008096 xylene Substances 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
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C08G81/024—Block or graft polymers containing sequences of polymers of C08C or C08F and of polymers of C08G
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/24—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials for applying particular liquids or other fluent materials
-
- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/14—Methyl esters, e.g. methyl (meth)acrylate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2507/00—Polyolefins
- B05D2507/01—Polyethylene
- B05D2507/015—Polyethylene modified
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/20—Air quality improvement or preservation, e.g. vehicle emission control or emission reduction by using catalytic converters
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Abstract
【課題】低VOC性を有し、経時安定性に優れ、電着塗装による塗着効率、被塗装物への密着性、下地の隠蔽性に優れた、アルミニウム顔料を含有する水性樹脂組成物及び該水性樹脂組成物からなる水性電着樹脂液、水性電着塗料、金属調の外観(メタリック感、光沢、色調)を有し、耐食性(耐候性及び、耐酸性、耐アルカリ性、耐溶剤性等の耐薬品性)に優れた塗膜、及び該塗膜の形成方法を提供する。【解決手段】(A)水分散性ビニル系共重合体、(B)アミノ樹脂及び(C)水分散性アルミニウム顔料を含有し、(A)水分散性ビニル系共重合体は、置換基としてカルボキシル基を有し、酸価が20〜100mgKOHであり、水性溶媒への分散性を有し、炭素−炭素不飽和結合が(共)重合した(共)重合体であり、質量比(A)/(B)は、40/60〜80/20であり、質量比(C)/{(A)+(B)}は、0.1/99.9〜15/85である水性樹脂組成物。【選択図】なしPROBLEM TO BE SOLVED: To provide an aqueous resin composition containing an aluminum pigment, which has low VOC properties, is excellent in stability over time, is excellent in coating efficiency by electrodeposition coating, adhesion to an object to be coated, and concealment of a base. A water-based electrodeposition resin liquid composed of the water-based resin composition, a water-based electrodeposition coating material, having a metallic appearance (metallic feeling, gloss, color tone), and corrosion resistance (weather resistance, acid resistance, alkali resistance, solvent resistance, etc.) A coating film having excellent chemical resistance) and a method for forming the coating film are provided. SOLUTION: The (A) water-dispersible vinyl-based copolymer, (B) amino resin and (C) water-dispersible aluminum pigment are contained, and (A) the water-dispersible vinyl-based copolymer is used as a substituent. It is a (co) polymer having a carboxyl group, an acid value of 20 to 100 mgKOH, dispersibility in an aqueous solvent, and a carbon-carbon unsaturated bond (co) polymerized, and has a mass ratio (A). / (B) is 40/60 to 80/20, and the mass ratio (C) / {(A) + (B)} is 0.1 / 99.9 to 15/85. .. [Selection diagram] None
Description
本発明は、アルミニウム顔料を含有する水性樹脂組成物、該水性樹脂組成物からなる水性電着樹脂液、水性電着塗料、それらから形成された、金属素材(アルミニウム、ステンレス及び各種合金などの)等の導電性素材からなる被塗装物に対して優れた密着性及び下地の隠蔽性を有し、金属調で均一な外観を有する塗膜、及びその塗装方法に関する。 The present invention relates to an aqueous resin composition containing an aluminum pigment, an aqueous electrodeposition resin solution comprising the aqueous resin composition, an aqueous electrodeposition coating material, and a metal material (such as aluminum, stainless steel, and various alloys) formed from the aqueous electrodeposition resin composition. The present invention relates to a coating film having excellent adhesion to an object to be coated made of a conductive material such as the above, and having a metallic and uniform appearance, and a coating method thereof.
従来から金属素材に対し、耐食性や意匠性を付与するために電着塗装法が検討されている。電着塗装法は他の塗装方法と比較して塗着効率に優れるなどの利点があるが、比重の大きな顔料などは沈降するため電着塗装では使用が制限されている。また、高輝性や、様々な意匠性を付与することが容易で、アルミニウム顔料を含有してメタリック外観が得られる塗料は、主にスプレー塗装により塗膜を形成されている。
スプレー塗装は優れた意匠性が得られるが、塗着効率が悪く、多量のVOCを発生させるため近年では低VOC型の塗料が望まれている。
Conventionally, an electrodeposition coating method has been studied in order to impart corrosion resistance and design to metal materials. The electrodeposition coating method has advantages such as excellent coating efficiency as compared with other coating methods, but its use is restricted in electrodeposition coating because pigments having a large specific density settle. In addition, a paint that easily imparts high brilliance and various design properties and that contains an aluminum pigment to obtain a metallic appearance is mainly formed by spray painting.
Although spray coating can obtain excellent designability, coating efficiency is poor and a large amount of VOC is generated. Therefore, in recent years, low VOC type coating materials have been desired.
上記の問題点を解決するための方法として、古くからアルミニウム顔料などを配合した電着塗料が検討されている(特許文献1)。
しかしながら、1μm〜100μmと粒子径が大きく、また比重が2.7g/cm3と大きなアルミニウム顔料は電着塗装時に沈降しやすいため、電着塗装によって得られる外観は、塗装対象物の上部と下部、また側面と天面とではアルミニウム顔料の塗着度合い(付着量)が異なり、ムラが発生しやすい。また水系においてアルミニウムが水と反応し水素ガスを発生して経時劣化するなど、課題が多かった。
その後、アルミニウムと水との反応を抑制する為の表面処理したアルミニウム顔料が開発され、それらを用いた電着塗料が提案されている(特許文献2、3)。
しかしながら、上記と同様な塗着度合い(付着量)の差異が生じてしまい、下地を隠蔽し金属調を満足する外観を得られない、または均一な金属調の外観を得ることができなかった。
また、沈降しにくいリーフィング形状のアルミニウム顔料を含有したアニオン電着塗料が提案されているが(特許文献4)、リーフィング形状のアルミニウム顔料は、沈降は抑制されているが液面に浮遊しやすく、塗装対象物の上部と下部とでアルミニウム顔料の付着量に差が生じ、下地の隠蔽性が不十分になり、十分な金属調外観が得られなかった。
As a method for solving the above problems, an electrodeposition coating material containing an aluminum pigment or the like has been studied for a long time (Patent Document 1).
However, since aluminum pigments having a large particle size of 1 μm to 100 μm and a large specific gravity of 2.7 g / cm 3 tend to settle during electrodeposition coating, the appearance obtained by electrodeposition coating is the upper and lower parts of the object to be coated. In addition, the degree of coating (adhesion amount) of the aluminum pigment differs between the side surface and the top surface, and unevenness is likely to occur. In addition, there are many problems such as aluminum reacting with water in an aqueous system to generate hydrogen gas and deteriorating with time.
Subsequently, surface-treated aluminum pigments for suppressing the reaction between aluminum and water have been developed, and electrodeposition coating materials using them have been proposed (Patent Documents 2 and 3).
However, the same difference in the degree of coating (adhesion amount) as described above occurs, and it is not possible to obtain an appearance satisfying the metallic tone by concealing the base, or it is not possible to obtain a uniform metallic appearance.
Further, an anion electrodeposition coating material containing a leafing-shaped aluminum pigment that does not easily settle has been proposed (Patent Document 4), but the leaving-shaped aluminum pigment is suppressed from settling but easily floats on the liquid surface. There was a difference in the amount of aluminum pigment adhered between the upper part and the lower part of the object to be painted, the hiding property of the base was insufficient, and a sufficient metallic appearance could not be obtained.
以上のように、アルミニウム顔料を用い、十分な金属調外観の得られる電着塗料はこれまでになかった。 As described above, there has never been an electrodeposition paint that uses an aluminum pigment and can obtain a sufficient metallic appearance.
本発明は、前記のような従来技術における問題点を解決し、低VOC性を有し、経時安定性に優れ、電着塗装による塗着効率、被塗装物への密着性、下地の隠蔽性に優れた、ア
ルミニウム顔料を含有する水性樹脂組成物及び該水性樹脂組成物からなる水性電着樹脂液、水性電着塗料、更には、それらから形成される、均一な膜厚及び均一な金属調の外観(メタリック感、光沢、色調)を有し、密着性、意匠性、耐食性(耐候性及び、耐酸性、耐アルカリ性、耐溶剤性等の耐薬品性)、経時安定性に優れた、アルミニウム顔料を含有する塗膜、及び該塗膜の形成方法を提供することを課題としている。
The present invention solves the above-mentioned problems in the prior art, has low VOC property, is excellent in stability over time, coating efficiency by electrodeposition coating, adhesion to an object to be coated, and hiding property of a base. An aqueous resin composition containing an aluminum pigment, an aqueous electrodeposition resin solution comprising the aqueous resin composition, an aqueous electrodeposition coating material, and a uniform film thickness and a uniform metallic tone formed from them. Aluminum with excellent appearance (metallic feeling, luster, color tone), adhesion, design, corrosion resistance (weather resistance and chemical resistance such as acid resistance, alkali resistance, solvent resistance), and stability over time. An object of the present invention is to provide a coating film containing a pigment and a method for forming the coating film.
本発明者は、鋭意研究の結果、特定のビニル系共重合体、アミノ樹脂、アルミニウム顔料を含有する水性樹脂組成物、それにより得られる水性樹脂組成物を用いて、定電流法で電着塗装することにより、金属調の外観を有するアルミニウム顔料含有電着塗膜を形成することで、上記問題点を克服できることを見出して本発明に至った。
そして本発明は、以下の点を特徴とする。
As a result of diligent research, the present inventor has conducted electrodeposition coating by a constant current method using an aqueous resin composition containing a specific vinyl-based copolymer, an amino resin, and an aluminum pigment, and an aqueous resin composition obtained thereby. The present invention has been made by finding that the above problems can be overcome by forming an aluminum pigment-containing electrodeposited coating film having a metallic appearance.
The present invention is characterized by the following points.
1.(A)水分散性ビニル系共重合体、(B)アミノ樹脂及び(C)水分散性アルミニウム顔料を含有する水性樹脂組成物であって、
(A)水分散性ビニル系共重合体は、置換基としてカルボキシル基を有し、酸価が20〜100mgKOHであり、水性溶媒への分散性を有し、炭素−炭素不飽和結合が(共)重合した(共)重合体であり、
質量比(A)/(B)は、40/60〜80/20であり、
質量比(C)/{(A)+(B)}は、0.1/99.9〜15/85であることを特徴とする、水性樹脂組成物。
2.前記水分散性アルミニウム顔料が、表面処理アルミニウム顔料からなり、
該表面処理アルミニウム顔料の表面は、無機リン系化合物、モリブデン系化合物、珪素系化合物、有機樹脂からなる群から選ばれる1種、または2種以上の組み合わせを含有する
ことを特徴とする、上記1記載の水性樹脂組成物。
3.上記1又は2に記載の水性樹脂組成物からなることを特徴とする、水性電着樹脂液。4.上記3に記載の水性電着樹脂液からなることを特徴とする、水性電着塗料。
5.上記4に記載の水性電着塗料から形成され、金属調の外観を有することを特徴とする、電着塗膜。
6.上記3に記載の水性電着樹脂液または上記4に記載の水性電着塗料を、定電流法で電着塗装することを特徴とする、電着塗膜の形成方法。
1. 1. An aqueous resin composition containing (A) a water-dispersible vinyl-based copolymer, (B) an amino resin, and (C) a water-dispersible aluminum pigment.
The water-dispersible vinyl-based copolymer has a carboxyl group as a substituent, an acid value of 20 to 100 mgKOH, dispersibility in an aqueous solvent, and a carbon-carbon unsaturated bond (co). ) It is a polymerized (co) polymer,
The mass ratio (A) / (B) is 40/60 to 80/20.
An aqueous resin composition having a mass ratio (C) / {(A) + (B)} of 0.1 / 99.9 to 15/85.
2. The water-dispersible aluminum pigment comprises a surface-treated aluminum pigment.
The surface of the surface-treated aluminum pigment is characterized by containing one kind selected from the group consisting of an inorganic phosphorus-based compound, a molybdenum-based compound, a silicon-based compound, and an organic resin, or a combination of two or more kinds. The aqueous resin composition according to the above.
3. 3. An aqueous electrodeposition resin liquid comprising the aqueous resin composition according to 1 or 2 above. 4. An aqueous electrodeposition coating material comprising the aqueous electrodeposition resin solution according to 3 above.
5. An electrodeposition coating film formed from the water-based electrodeposition coating material according to 4 above, which has a metallic appearance.
6. A method for forming an electrodeposition coating film, which comprises electrodepositing the aqueous electrodeposition resin liquid according to 3 above or the aqueous electrodeposition coating material according to 4 above by a constant current method.
本発明により、低VOCの塗装プロセスを実現できることで産業上極めて有用であり、安定性に優れ、電着塗装による塗着効率、金属素材への密着性、下地の隠蔽性に優れた、アルミニウム顔料を含有する水性樹脂組成物及び該水性樹脂組成物からなる水性樹脂組成物、更には、それらから形成されるアルミニウム顔料を含有して金属調の外観を有して、密着性、意匠性、耐食性、経時安定性に優れた塗膜、及び該塗膜の形成方法を提供することができる。 According to the present invention, it is extremely useful in industry because a low VOC coating process can be realized, and an aluminum pigment having excellent stability, coating efficiency by electrodeposition coating, adhesion to a metal material, and concealment of a base is excellent. A water-based resin composition containing the above, an water-based resin composition composed of the water-based resin composition, and an aluminum pigment formed from the water-based resin composition, which has a metallic appearance, and has adhesiveness, designability, and corrosion resistance. , A coating film having excellent stability over time, and a method for forming the coating film can be provided.
本発明について更に詳しく説明する。
本発明は、アルミニウム顔料を含有する低VOC性の水性樹脂組成物、該水性樹脂組成物からなる水性樹脂液、該水性樹脂液からなる水性電着塗料、更には、それらから形成される金属調の外観を有する均一で経時安定性に優れ塗膜、及び該塗膜の形成方法に関する。
The present invention will be described in more detail.
The present invention relates to a low VOC water-based resin composition containing an aluminum pigment, a water-based resin liquid composed of the water-based resin composition, a water-based electrodeposition coating material composed of the water-based resin liquid, and a metallic tone formed from the water-based resin composition. The present invention relates to a coating film having the appearance of the above, which is uniform and has excellent stability over time, and a method for forming the coating film.
<水性樹脂組成物>
本発明の水性樹脂組成物は、有効成分(固形分、非溶剤成分)として、(A)水分散性
ビニル系共重合体、(B)アミノ樹脂、(C)水分散性アルミニウム顔料を含有することが好ましい。
そして、必要に応じて、(D)中和剤や、(E)水性溶剤を更に含有することができる。
<Aqueous resin composition>
The aqueous resin composition of the present invention contains (A) a water-dispersible vinyl copolymer, (B) an amino resin, and (C) a water-dispersible aluminum pigment as active ingredients (solid content, non-solvent component). Is preferable.
Then, if necessary, (D) a neutralizing agent and (E) an aqueous solvent can be further contained.
また、塗膜が意匠性を有し易いように顔料、染料、フィラー等を更に含有したり、塗膜形成時の作業性の向上や塗膜への様々な機能付与の為に、光安定剤、酸化防止剤、湿潤剤、レベリング剤、消泡剤等の各種添加剤や、ウレタン樹脂やエポキシ樹脂等の他の樹脂を更に含有したりできる。 In addition, a light stabilizer is added to further contain pigments, dyes, fillers, etc. so that the coating film has a design property, and to improve workability at the time of forming the coating film and to impart various functions to the coating film. , Various additives such as antioxidants, wetting agents, leveling agents, defoaming agents, and other resins such as urethane resin and epoxy resin can be further contained.
本発明の水性樹脂組成物中の、(A)水分散性ビニル系共重合体と(B)アミノ樹脂との質量比(A)/(B)は、40/60〜80/20が好ましく、50/50〜75/25がより好ましい。
質量比(A)/(B)が上記範囲未満であると、水性樹脂組成物中での、樹脂成分である(A)水分散性ビニル系共重合体及び(B)アミノ樹脂の水分散性(水溶性または乳化性)が低下して、液分離や沈降を生じ易くなり、また、塗膜の硬度が不十分になり易く、製造コストも大きく上昇する。
質量比(A)/(B)が上記範囲よりも大きいと、十分な塗膜性能(耐薬品性、塗膜硬度)を得ることが困難になる。
The mass ratio (A) / (B) of the (A) water-dispersible vinyl-based copolymer and the (B) amino resin in the aqueous resin composition of the present invention is preferably 40/60 to 80/20. More preferably, 50/50 to 75/25.
When the mass ratio (A) / (B) is less than the above range, the water dispersibility of the (A) water-dispersible vinyl copolymer and (B) amino resin, which are the resin components, in the aqueous resin composition. (Water solubility or emulsifying property) is lowered, liquid separation and sedimentation are likely to occur, the hardness of the coating film is likely to be insufficient, and the production cost is greatly increased.
If the mass ratio (A) / (B) is larger than the above range, it becomes difficult to obtain sufficient coating film performance (chemical resistance, coating film hardness).
本発明の水性樹脂組成物中の、(C)水分散性アルミニウム顔料と、(A)水分散性ビニル系共重合体及び(B)アミノ樹脂の合計の質量比(C)/{(A)+(B)}は、0.1/99.9〜15/85が好ましく、5/95〜11/89がより好ましい。
上記範囲未満であると、十分な金属調外観(メタリック感)の塗膜を得ることが困難であり、上記範囲よりも大きいと、塗膜性能や耐アルカリ性が悪くなり、製造コストが著しく上昇する。
Total mass ratio of (C) water-dispersible aluminum pigment, (A) water-dispersible vinyl copolymer and (B) amino resin in the aqueous resin composition of the present invention (C) / {(A) + (B)} is preferably 0.1 / 99.9 to 15/85, and more preferably 5/95 to 11/89.
If it is less than the above range, it is difficult to obtain a coating film having a sufficient metallic appearance (metallic feeling), and if it is larger than the above range, the coating film performance and alkali resistance deteriorate, and the manufacturing cost increases remarkably. ..
[(A)水分散性ビニル系共重合体]
(A)水分散性ビニル系共重合体は、水性溶媒への可溶性または水性溶媒中での乳化性を有することによって水性溶媒中での分散が可能なビニル系共重合体である。
(A)水分散性ビニル系共重合体の主骨格は、重合性炭素−炭素2重結合または3重結合等の重合性炭素−炭素不飽和結合基同士の(共)重合によって主に形成されている。
炭素−炭素不飽和結合基の具体例としては、ビニル基、アリル基、(メタ)アクリル基、αβ不飽和カルボニル基等が挙げられ、これらは単独で重合してもよく、2種以上が共重合してもよい。
[(A) Water-dispersible vinyl copolymer]
The water-dispersible vinyl-based copolymer (A) is a vinyl-based copolymer that is soluble in an aqueous solvent or emulsible in an aqueous solvent so that it can be dispersed in an aqueous solvent.
The main skeleton of the (A) water-dispersible vinyl-based copolymer is mainly formed by (co) polymerization of polymerizable carbon-carbon unsaturated bond groups such as a polymerizable carbon-carbon double bond or a triple bond. ing.
Specific examples of the carbon-carbon unsaturated bond group include a vinyl group, an allyl group, a (meth) acrylic group, an αβ unsaturated carbonyl group and the like, which may be polymerized alone or in combination of two or more. It may be polymerized.
(A)水分散性ビニル系共重合体は、置換基としてカルボキシル基を有することが好ましい。そして、カルボン酸エステル基および/または水酸基をさらに有していてもよい。
(A)水分散性ビニル系共重合体は、上記の置換基を有することによって、優れた水分散性を有することが容易になる。
そして、(A)水分散性ビニル系共重合体は、水酸基および/またはカルボキシル基を有することによって、(B)アミノ樹脂と架橋を形成することができ、塗膜に耐食性(耐候性、耐薬品性)、高硬度などを付与することができる。
The water-dispersible vinyl-based copolymer (A) preferably has a carboxyl group as a substituent. Then, it may further have a carboxylic acid ester group and / or a hydroxyl group.
By having the above-mentioned substituent, the water-dispersible vinyl-based copolymer (A) can easily have excellent water dispersibility.
By having a hydroxyl group and / or a carboxyl group, the (A) water-dispersible vinyl-based copolymer can form a crosslink with the (B) amino resin, and the coating film has corrosion resistance (weather resistance, chemical resistance). (Sex), high hardness, etc. can be imparted.
(A)水分散性ビニル系共重合体は、酸価が20〜100mgKOHであることが好ましく、30〜80mgKOHであることがより好ましい。上記範囲未満であると十分な水分散性が得ることが困難になり易く、上記範囲よりも高いと耐水性が低下し易く、十分な塗膜性能を得難くなり、また、表面処理した水分散性アルミニウム顔料の安定性を低下させ易くなる。なお、本発明において酸価はJIS K5601−2−1に準拠して測定した。 The water-dispersible vinyl-based copolymer (A) preferably has an acid value of 20 to 100 mgKOH, and more preferably 30 to 80 mgKOH. If it is less than the above range, it tends to be difficult to obtain sufficient water dispersibility, and if it is higher than the above range, water resistance tends to decrease, it becomes difficult to obtain sufficient coating film performance, and surface-treated water dispersion. It tends to reduce the stability of the aluminum pigment. In the present invention, the acid value was measured according to JIS K5601-2-1.
上記のような水分散性ビニル系共重合体は、重合性炭素−炭素不飽和結合基とカルボキシル基とを有する単量体、重合性炭素−炭素不飽和結合基とカルボキシル基と水酸基とを有する単量体、重合性炭素−炭素不飽和結合基とカルボン酸エステル基とを有する単量体、重合性炭素−炭素不飽和結合基とカルボン酸エステル基と水酸基とを有する単量体からなる群から選ばれる1種または2種以上を組み合わせて、(共)重合させることによって得ることができる。
また、共重合成分として、重合性炭素−炭素不飽和結合基を有する他の単量体を併用することもできる。
The water-dispersible vinyl-based copolymer as described above has a monomer having a polymerizable carbon-carbon unsaturated bond group and a carboxyl group, and a polymerizable carbon-carbon unsaturated bond group, a carboxyl group and a hydroxyl group. A group consisting of a monomer, a monomer having a polymerizable carbon-carbon unsaturated bond group and a carboxylic acid ester group, and a monomer having a polymerizable carbon-carbon unsaturated bond group, a carboxylic acid ester group and a hydroxyl group. It can be obtained by (co) polymerizing one kind or a combination of two or more kinds selected from the above.
Further, as a copolymerization component, another monomer having a polymerizable carbon-carbon unsaturated bond group can also be used in combination.
重合性炭素−炭素不飽和結合基とカルボキシル基とを有する単量体の具体例としては、アクリル酸、α−クロロアクリル酸、メタクリル酸、イタコン酸、無水マレイン酸、マレイン酸、フマル酸、クロトン酸、シトラコン酸、メサコン酸等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。上記の中でもアクリル酸が好ましい。 Specific examples of the monomer having a polymerizable carbon-carbon unsaturated bond group and a carboxyl group include acrylic acid, α-chloroacrylic acid, methacrylic acid, itaconic acid, maleic anhydride, maleic acid, fumaric acid, and crotonic acid. Acids, citraconic acid, methacrylic acid and the like can be mentioned, and one or a combination of two or more selected from these groups can be used. Among the above, acrylic acid is preferable.
重合性炭素−炭素不飽和結合基とカルボン酸エステル基とを有する単量体は、炭素数約20までのアルキル基や脂環式炭化水素基を有する(メタ)アクリレート等が好ましく用いられ、具体例としては、メチルアクリレート、メチルメタクリレート、エチルアクリレート、エチルメタクリレート、n−プロピルアクリレート、n−プロピルメタクリレート、イソプロピルアクリレート、イソプロピルメタクリレート、ノルマルブチルアクリレート、ノルマルブチルメタクリレート、ノルマルヘキシルアクリレート、ノルマルヘキシルメタクリレート、ノルマルヘプチルアクリレート、ノルマルヘプチルメタクリレート、2−エチルヘキシルアクリレート、2−エチルヘキシルメタクリレート、ノルマルラウリルアクリレート、ノルマルラウリルメタクリレート、ステアリルアクリレート、ステアリルメタクリレート、シクロヘキシルアクリレート、シクロヘキシルメタクリレート、イソボルニルアクリレート、イソボルニルメタクリレート等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。
上記の中でも、メチルメタクリレート、エチルアクリレート、ブチルアクリレート、2−エチルヘキシルアクリレートを組み合わせて用いることが好ましい。
As the monomer having a polymerizable carbon-carbon unsaturated bond group and a carboxylic acid ester group, an alkyl group having up to about 20 carbon atoms, a (meth) acrylate having an alicyclic hydrocarbon group, or the like is preferably used. Examples include methyl acrylate, methyl methacrylate, ethyl acrylate, ethyl methacrylate, n-propyl acrylate, n-propyl methacrylate, isopropyl acrylate, isopropyl methacrylate, normal butyl acrylate, normal butyl methacrylate, normal hexyl acrylate, normal hexyl methacrylate, normal heptyl. Examples thereof include acrylate, normal heptyl methacrylate, 2-ethylhexyl acrylate, 2-ethylhexyl methacrylate, normal lauryl acrylate, normal lauryl methacrylate, stearyl acrylate, stearyl methacrylate, cyclohexyl acrylate, cyclohexyl methacrylate, isobornyl acrylate, isobornyl methacrylate and the like. One kind or two or more kinds selected from these groups can be used in combination.
Among the above, it is preferable to use a combination of methyl methacrylate, ethyl acrylate, butyl acrylate, and 2-ethylhexyl acrylate.
重合性炭素−炭素不飽和結合基とカルボン酸エステル基と水酸基とを有する単量体の具体例としては、2−ヒドロキシエチルアクリレート、2−ヒドロキシエチルメタクリレート、2−ヒドロキシプロピルアクリレート、2−ヒドロキシプロピルメタクリレート、3−ヒドロキシプロピルアクリレート、3−ヒドロキシプロピルメタクリレート、4−ヒドロキシブチルアクリレート、4−ヒドロキシブチルメタクリレート、ジエチレングリコールモノアクリレート、シクロヘキサンジメタノールモノアクリレート、シクロヘキサンジメタノールモノメタクリレート等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。
上記の中でも、2−ヒドロキシエチルアクリレート、2−ヒドロキシエチルメタクリレート、2−ヒドロキシプロピルアクリレート、2−ヒドロキシプロピルメタクリレート、3−ヒドロキシプロピルアクリレート、3−ヒドロキシプロピルメタクリレート、4−ヒドロキシブチルアクリレート、4−ヒドロキシブチルメタクリレートからなる群から選ばれる1種または2種以上を組み合わせて用いることが好ましい。上記の中でも、2−ヒドロキシエチルアクリレートが好ましい。
Specific examples of the monomer having a polymerizable carbon-carbon unsaturated bond group, a carboxylic acid ester group and a hydroxyl group include 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate and 2-hydroxypropyl. Examples thereof include methacrylate, 3-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, 4-hydroxybutyl acrylate, 4-hydroxybutyl methacrylate, diethylene glycol monoacrylate, cyclohexanedimethanol monoacrylate, cyclohexanedimethanol monomethacrylate, and the like. One selected type or a combination of two or more types can be used.
Among the above, 2-hydroxyethyl acrylate, 2-hydroxyethyl methacrylate, 2-hydroxypropyl acrylate, 2-hydroxypropyl methacrylate, 3-hydroxypropyl acrylate, 3-hydroxypropyl methacrylate, 4-hydroxybutyl acrylate, 4-hydroxybutyl It is preferable to use one kind or a combination of two or more kinds selected from the group consisting of methacrylate. Among the above, 2-hydroxyethyl acrylate is preferable.
重合性炭素−炭素不飽和結合基を有する他の単量体の具体例としては、芳香族基を有するビニル系単量体、N−アルコキシアルキルアミド基を有する共重合性ビニル系単量体、末端にビニル基を有する高分子であるマクロモノマー、アクリロニトリル、酢酸ビニル、アリル基含有化合物等が挙げられ、これらの群から選ばれる1種または2種以上を組み合
わせて用いることができる。
Specific examples of other monomers having a polymerizable carbon-carbon unsaturated bond group include a vinyl-based monomer having an aromatic group, a copolymerizable vinyl-based monomer having an N-alkoxyalkylamide group, and the like. Examples thereof include macromonomers, acrylonitriles, vinyl acetates, and allyl group-containing compounds which are polymers having a vinyl group at the end, and one or a combination of two or more selected from these groups can be used.
芳香族基を有するビニル系単量体の具体例としては、スチレン、α−メチルスチレン、α−クロロスチレン、ビニルトルエン等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。上記の中でもスチレンが好ましい。 Specific examples of the vinyl-based monomer having an aromatic group include styrene, α-methylstyrene, α-chlorostyrene, vinyltoluene and the like, and one or a combination of two or more selected from these groups can be mentioned. Can be used. Among the above, styrene is preferable.
N−アルコキシアルキルアミド基を有する共重合性ビニル系単量体の具体例としては、N−メトキシメチルアクリルアミド、N−エトキシメチルアクリルアミド、N−ノルマルブトキシメチルアクリルアミド、N−イソブトキシメチルアクリルアミド、N−メトキシメチルメタクリルアミド、N−エトキシメチルメタクリルアミド、N−ノルマルブトキシメチルメタクリルアミド、N−イソブトキシメチルメタクリルアミド等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。 Specific examples of the copolymerizable vinyl-based monomer having an N-alkoxyalkylamide group include N-methoxymethylacrylamide, N-ethoxymethylacrylamide, N-normalbutoxymethylacrylamide, N-isobutoxymethylacrylamide, and N-. Examples thereof include methoxymethylmethacrylate, N-ethoxymethylmethacrylate, N-normalbutoxymethylmethacrylate, N-isobutoxymethylmethacrylate, etc., and one or a combination of two or more selected from these groups can be used. can.
上記の(共)重合成分を(共)重合させて(共)重合体を合成する際には、各種水性溶媒中で合成することが好ましく、必要に応じて、各種の重合開始剤を用いることができる。 When synthesizing a (co) polymer by (co) polymerizing the above (co) polymerization components, it is preferable to synthesize in various aqueous solvents, and various polymerization initiators are used as necessary. Can be done.
水性溶媒の具体例としては、水、アルコール類、エチレングリコールエーテル類、プロピレングリコールエーテル類が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。
上記の中でも、イソプロパノール、エチレングリコールモノノルマルブチルエーテル等が好ましく用いられる。
Specific examples of the aqueous solvent include water, alcohols, ethylene glycol ethers, and propylene glycol ethers, and one or a combination of two or more selected from these groups can be used, but the present invention is limited to these. Not done.
Among the above, isopropanol, ethylene glycol mononormal butyl ether and the like are preferably used.
重合開始剤には、ラジカル開始剤を用いることが好ましい。
ラジカル開始剤の具体例としては、ジハロゲン化合物、アゾ化合物、有機過酸化物、レドックス開始剤等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるがこれらに限定されない。
上記の中でもアゾ化合物が好ましく用いられ、アゾ化合物の中でも、2,2′−アゾビスイソブチロニトリル、2,2′−アゾビスイソ(2−メチルブチロニトリル)、2,2′−アゾビス(2,4−ジメチルバレロニトリル)が好ましく用いられる。
It is preferable to use a radical initiator as the polymerization initiator.
Specific examples of the radical initiator include dihalogen compounds, azo compounds, organic peroxides, redox initiators, and the like, and one or a combination of two or more selected from these groups can be used. Not limited.
Among the above, azo compounds are preferably used, and among the azo compounds, 2,2'-azobisisobutyronitrile, 2,2'-azobisiso (2-methylbutyronitrile), and 2,2'-azobis (2). , 4-Dimethylvaleronitrile) is preferably used.
[(B)アミノ樹脂]
(B)アミノ樹脂の具体例としては、メラミン樹脂、ベンゾグアナミン樹脂、尿素樹脂からなる群から選ばれる1種または2種以上を組み合わせて用いることができる。
特にメラミン樹脂を用いることが好ましく、そして、メラミン樹脂の中でも、メチロール基の少なくとも一部を低級アルコールでアルコキシ化したアルコキシ化メラミンを含むことがより好ましい。
低級アルコールとしては、メチルアルコール、エチルアルコール、n−プロピルアルコール、イソプロピルアルコール、n−ブチルアルコール、イソブチルアルコールからなる群から選ばれる1種または2種以上を組み合わせて用いることが好ましい。
(B)アミノ樹脂は加熱によって硬化させることが可能であり、水酸基やカルボキシル基を有する化合物を硬化剤として用いてもよく、各種の硬化促進剤を用いてもよい。
[(B) Amino resin]
As a specific example of the (B) amino resin, one kind or a combination of two or more kinds selected from the group consisting of a melamine resin, a benzoguanamine resin, and a urea resin can be used.
In particular, it is preferable to use a melamine resin, and among the melamine resins, it is more preferable to contain an alkoxylated melamine in which at least a part of the methylol group is alkoxylated with a lower alcohol.
As the lower alcohol, it is preferable to use one or a combination of two or more selected from the group consisting of methyl alcohol, ethyl alcohol, n-propyl alcohol, isopropyl alcohol, n-butyl alcohol and isobutyl alcohol.
The amino resin (B) can be cured by heating, and a compound having a hydroxyl group or a carboxyl group may be used as a curing agent, or various curing accelerators may be used.
[(C)水分散性アルミニウム顔料]
(C)水分散性アルミニウム顔料は、水性溶媒への分散性に優れたアルミニウム顔料である。水分散性アルミニウム顔料が塗膜に含有されていることで、立体感のある金属調外観を示すことができる。
水分散性アルミニウム顔料とは、粉体のまま水性溶剤への均一に分散することに優れたアルミニウム顔料である。
(C)水分散性アルミニウム顔料は、アルミニウム粉末の表面を表面処理剤によって処
理して得られた顔料であり、形成された表面処理面によって、金属アルミニウムと水との反応が抑制され、優れた水分散性が得られている。
(C)水分散性アルミニウム顔料は、アルミニウム粉含有量が40〜60質量%のペースト状にした状態で用いることが好ましい。
[(C) Water-dispersible aluminum pigment]
(C) The water-dispersible aluminum pigment is an aluminum pigment having excellent dispersibility in an aqueous solvent. Since the water-dispersible aluminum pigment is contained in the coating film, it is possible to exhibit a metallic appearance with a three-dimensional effect.
The water-dispersible aluminum pigment is an aluminum pigment that is excellent in being uniformly dispersed in an aqueous solvent as a powder.
(C) The water-dispersible aluminum pigment is a pigment obtained by treating the surface of aluminum powder with a surface treatment agent, and the formed surface treatment surface suppresses the reaction between metallic aluminum and water, which is excellent. Water dispersibility is obtained.
The water-dispersible aluminum pigment (C) is preferably used in the form of a paste having an aluminum powder content of 40 to 60% by mass.
金属アルミニウムは水と反応して水酸化アルミニウムと水素ガスを発生させる。このような反応が進行すると、アルミニウム顔料は金属調の外観を損ない、アルミニウム顔料を含有する水性樹脂組成物は、発泡し、アルミニウム顔料の凝集物が派生し、粘度が変化して、経時安定性が低下する。また、該水性樹脂組成物から形成された塗膜も同様に金属調の外観を損い、経時安定性が低下する。 Metallic aluminum reacts with water to generate aluminum hydroxide and hydrogen gas. When such a reaction proceeds, the aluminum pigment impairs the metallic appearance, and the aqueous resin composition containing the aluminum pigment foams, agglomerates of the aluminum pigment are derived, the viscosity changes, and the stability with time is changed. Decreases. Further, the coating film formed from the aqueous resin composition also impairs the metallic appearance and the stability with time is lowered.
(C)水分散性アルミニウム顔料の粒子の形状は、塗膜中に敷き詰められて、下地を隠蔽する効果も得ら為に、鱗片状が好ましい。
また、電着用途で従来用いられているリーフィングタイプは浮遊しやすく隠蔽性に劣ることから、塗膜中に一様に分散配列することができるノンリーフィングタイプがより好ましい。
(C) The shape of the particles of the water-dispersible aluminum pigment is preferably scaly because it is spread in the coating film and has an effect of concealing the base.
Further, since the leafing type conventionally used for electrodeposition applications is easily suspended and inferior in concealing property, the non-leafing type that can be uniformly dispersed and arranged in the coating film is more preferable.
(C)水分散性アルミニウム顔料の平均粒子径は、一般塗料用途には平均粒子径7〜50μmが好ましく、水性樹脂組成物用途には7〜20μmが好ましく、7〜15μmがより好ましい。上記範囲よりも小さいものは、入手困難な割には性能があまり変わらず、上記範囲よりも大きいと、(C)水分散性アルミニウム顔料は比重が約2.7g/cm3と大きい為に自重による沈降を生じ易くなる。
(C)水分散性アルミニウム顔料の表面を構成する化合物の具体例としては、無機リン系化合物、モリブデン系化合物、珪素系化合物、有機樹脂等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。特に、有機珪素系化合物及び有機樹脂のハイブリッドが好ましい。
The average particle size of the water-dispersible aluminum pigment (C) is preferably 7 to 50 μm, more preferably 7 to 20 μm, and more preferably 7 to 15 μm for general coating applications and 7 to 20 μm for aqueous resin composition applications. If it is smaller than the above range, the performance does not change much even though it is difficult to obtain, and if it is larger than the above range, (C) the water-dispersible aluminum pigment has a large specific gravity of about 2.7 g / cm 3 , so its own weight. Is likely to cause sedimentation due to.
Specific examples of the compound constituting the surface of the (C) water-dispersible aluminum pigment include inorganic phosphorus compounds, molybdenum compounds, silicon compounds, organic resins and the like, and one or two selected from these groups A combination of seeds and above can be used. In particular, a hybrid of an organic silicon compound and an organic resin is preferable.
表面処理剤には、市販のものを用いることが可能であり、無機リン系表面処理剤、モリブデン系表面処理剤、珪素系表面処理剤、有機樹脂系表面処理剤が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。
表面処理剤は、1種単独よりも2種以上を組み合わせて用いることが好ましく、特に、珪素系表面処理剤と有機樹脂系表面処理剤との組み合わせが好ましい。
Commercially available surface treatment agents can be used, and examples thereof include inorganic phosphorus-based surface treatment agents, molybdenum-based surface treatment agents, silicon-based surface treatment agents, and organic resin-based surface treatment agents. One selected type or a combination of two or more types can be used.
It is preferable to use two or more types of surface treatment agents in combination rather than one type alone, and in particular, a combination of a silicon-based surface treatment agent and an organic resin-based surface treatment agent is preferable.
無機リン系表面処理剤の具体例としてはリン酸等が、モリブデン系表面処理剤の具体例としてはモリブデン酸アンモニウム、ポリモリブデン酸等が、珪素系表面処理剤の具体例としてはアルコキシシラン等が挙げられる。 Phosphoric acid and the like are specific examples of the inorganic phosphorus-based surface treatment agent, ammonium molybdate, polymolybdate and the like are specific examples of the molybdate-based surface treatment agent, and alkoxysilane and the like are specific examples of the silicon-based surface treatment agent. Can be mentioned.
有機樹脂系表面処理剤は、各種の樹脂を含むことができ、含まれる樹脂は、熱可塑性樹脂または熱硬化性樹脂の何れか、または両方を含んでもよいが、堅固な三次元架橋構造を生じて不溶及び不融化する熱硬化性樹脂を含むことが好ましい。 The organic resin-based surface treatment agent can contain various resins, and the contained resin may contain either or both of a thermoplastic resin and a thermosetting resin, but produces a solid three-dimensional crosslinked structure. It is preferable to contain a thermosetting resin that is insoluble and infusible.
熱可塑性樹脂の具体例としては、アクリル酸エステル共重合体、ポリエステル樹脂、ポリエチレン樹脂、ポリスチレン樹脂等が挙げられる。
熱硬化性樹脂の具体例としては、アクリル酸エステル共重合体、エポキシ樹脂、ポリウレタン樹脂等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができる。上記の中でも、三次元架橋構造を形成し得るアクリル酸エステル共重合体を含むことがより好ましい。
Specific examples of the thermoplastic resin include acrylic acid ester copolymers, polyester resins, polyethylene resins, polystyrene resins and the like.
Specific examples of the thermosetting resin include acrylic acid ester copolymers, epoxy resins, polyurethane resins, and the like, and one or a combination of two or more selected from these groups can be used. Among the above, it is more preferable to contain an acrylic acid ester copolymer capable of forming a three-dimensional crosslinked structure.
市販されている(C)水分散性アルミニウム顔料の具体例としては、例えば、東洋アルミニウム株式会社製の水性アルペーストが有り、処理方法によって、WXMシリーズ(無
機リン酸化合物系処理剤による処理)、WLシリーズ(モリブデン系処理剤による処理)、EMRシリーズ(有機珪素系処理剤による処理)、BPシリーズ(アクリル樹脂コート処理剤による処理)、WRAシリーズ(アクリル樹脂コート剤及び有機珪素系処理剤によるハイブリッド処理)等が上市されており、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。
Specific examples of the commercially available (C) water-dispersible aluminum pigment include an aqueous polypaste manufactured by Toyo Aluminum Co., Ltd., and depending on the treatment method, WXM series (treatment with an inorganic phosphoric acid compound-based treatment agent), WL series (treatment with molybdenum-based treatment agent), EMR series (treatment with organic silicon-based treatment agent), BP series (treatment with acrylic resin coating treatment agent), WRA series (hybrid with acrylic resin coating agent and organic silicon-based treatment agent) Treatment) and the like are on the market, and one kind or two or more kinds selected from these groups can be used in combination, but the present invention is not limited to these.
[(D)中和剤]
本発明の水性樹脂組成物は、(A)水分散性ビニル系共重合体が有するカルボキシル基を中和する為の(D)中和剤を含有することができる。
[(D) Neutralizer]
The aqueous resin composition of the present invention can contain (A) a neutralizing agent for neutralizing the carboxyl group of the water-dispersible vinyl-based copolymer.
(D)中和剤は、有機アミン類を含むことが好ましい。
有機アミン類の具体例としては、アルキルアミン類、アルカノールアミン類、アルキレンポリアミン類、アルキレンイミン類、環状アミン類等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。上記の中でも、アルカノールアミン類を含むことがより好ましい。
The neutralizer (D) preferably contains organic amines.
Specific examples of organic amines include alkylamines, alkanolamines, alkylenepolyamines, alkyleneimines, cyclic amines, etc., and one or a combination of two or more selected from these groups may be used. However, it is not limited to these. Among the above, it is more preferable to contain alkanolamines.
アルキルアミン類の具体例としては、モノメチルアミン、ジメチルアミン、トリメチルアミン、モノエチルアミン、ジエチルアミン、トリエチルアミン、モノイソプロピルアミン、ジイソプロピルアミン、トリイソプロピルアミン、モノブチルアミン、ジブチルアミン、トリブチルアミン等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of alkylamines include monomethylamine, dimethylamine, trimethylamine, monoethylamine, diethylamine, triethylamine, monoisopropylamine, diisopropylamine, triisopropylamine, monobutylamine, dibutylamine, tributylamine and the like. One or a combination of two or more selected from the group can be used, but is not limited thereto.
アルカノールアミン類の具体例としては、モノエタノールアミン、ジエタノールアミン、トリエタノールアミン、モノ(2−ヒドロキシプロピル)アミン、ジ(2−ヒドロキシプロピル)アミン、トリ(2−ヒドロキシプロピル)アミン、ジメチルアミノエタノール、ジエチルアミノエタノール等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of alkanolamines include monoethanolamine, diethanolamine, triethanolamine, mono (2-hydroxypropyl) amine, di (2-hydroxypropyl) amine, tri (2-hydroxypropyl) amine, dimethylaminoethanol, and the like. Examples thereof include diethylaminoethanol, and one or a combination of two or more selected from these groups can be used, but the present invention is not limited thereto.
アルキレンポリアミン類の具体例としては、エチレンジアミン、プロピレンジアミン、ジエチレントリアミン、トリエチレンテトラミン等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of the alkylene polyamines include ethylenediamine, propylenediamine, diethylenetriamine, triethylenetetramine and the like, and one or a combination of two or more selected from these groups can be used, but the present invention is not limited thereto.
アルキレンイミン類の具体例としては、エチレンイミン、プロピレンイミン等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of the alkyleneimines include ethyleneimine, propyleneimine, and the like, and one or a combination of two or more selected from these groups can be used, but the alkyleneimines are not limited thereto.
環状アミン類の具体例としては、ピペラジン、モルホリン、ピラジン、ピリジン等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of cyclic amines include piperazine, morpholine, pyrazine, pyridine and the like, and one or a combination of two or more selected from these groups can be used, but the cyclic amines are not limited thereto.
これらの有機アミン類は、(A)水分散性ビニル系共重合体が有するカルボキシル基に配向して塩化することで、(A)水分散性ビニル系共重合体の水性溶剤中での乳化性または水溶性を高めて、水性溶剤中での分散性を高めることができる。 These organic amines are oriented toward the carboxyl group of the (A) water-dispersible vinyl-based copolymer and chloride to form an emulsifying property of the (A) water-dispersible vinyl-based copolymer in an aqueous solvent. Alternatively, the water solubility can be increased to enhance the dispersibility in an aqueous solvent.
水性樹脂組成物中の(D)中和剤の含有量は、有機アミン類のアミノ基と(A)水分散性ビニル系共重合体が有するカルボキシル基とのモル比アミノ基/カルボキシル基が、好ましくは0.3〜0.9、より好ましくは0.4〜0.7になる割合が好ましい。
上記範囲よりも高いと、アルカリ成分の増加により水分散性アルミニウム顔料の安定性が低下し、上記範囲よりも低いと、(A)水分散性ビニル系共重合体の水溶性または乳化性を高める効果が不十分になり易い
The content of the (D) neutralizing agent in the aqueous resin composition is a molar ratio of the amino group of the organic amines and the carboxyl group of the (A) water-dispersible vinyl-based copolymer. The ratio is preferably 0.3 to 0.9, more preferably 0.4 to 0.7.
If it is higher than the above range, the stability of the water-dispersible aluminum pigment is lowered due to the increase in the alkaline component, and if it is lower than the above range, the water solubility or emulsifying property of the (A) water-dispersible vinyl copolymer is enhanced. The effect tends to be insufficient
[(E)水性溶剤]
水性樹脂組成物は、(A)水分散性ビニル系共重合体が固体や高粘度液体である場合には、(E)水性溶剤を含有することが好ましい。
(E)水性溶剤は、水性の溶剤であり、具体例としては、水、アルコール類、エチレングリコールエーテル類、プロピレングリコールエーテル類が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。
[(E) Aqueous solvent]
The aqueous resin composition preferably contains (E) an aqueous solvent when the (A) water-dispersible vinyl copolymer is a solid or a high-viscosity liquid.
The (E) aqueous solvent is an aqueous solvent, and specific examples thereof include water, alcohols, ethylene glycol ethers, and propylene glycol ethers, and one or a combination of two or more selected from these groups. However, the present invention is not limited to these.
アルコール類の具体例としては、メタノール、エタノール、ノルマルプロパノール、イソプロパノール、ノルマルブタノール、イソブタノール、ノルマルヘキシルアルコール、2−エチルヘキシルアルコール、ベンジルアルコール等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of alcohols include methanol, ethanol, normal propanol, isopropanol, normal butanol, isobutanol, normal hexyl alcohol, 2-ethylhexyl alcohol, benzyl alcohol and the like, and one or two selected from these groups. The above can be used in combination, but the present invention is not limited to these.
エチレングリコールエーテル類の具体例としては、エチレングリコールモノメチルエーテル、エチレングリコールモノエチルエーテル、エチレングリコールモノノルマルプロピルエーテル、エチレングリコールモノイソプロピルエーテル、エチレングリコールモノノルマルブチルエーテル、エチレングリコールモノイソブチルエーテル、エチレングリコールモノターシャリブチルエーテル、エチレングリコールモノノルマルヘキシルエーテル、エチレングリコールモノノルマルオクチルエーテル、エチレングリコールモノ−2−エチルヘキシルエーテル等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of ethylene glycol ethers include ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol mononormal propyl ether, ethylene glycol monoisopropyl ether, ethylene glycol mononormal butyl ether, ethylene glycol monoisobutyl ether, and ethylene glycol monotasha. Examples thereof include rebutyl ether, ethylene glycol mononormal hexyl ether, ethylene glycol mononormal octyl ether, ethylene glycol mono-2-ethylhexyl ether, and one or a combination of two or more selected from these groups can be used. , Not limited to these.
プロピレングリコールエーテル類の具体例としては、プロピレングリコールモノメチルエーテル、プロピレングリコールモノエチルエーテル、プロピレングリコールモノノルマルプロピルエーテル、プロピレングリコールモノイソプロピルエーテル、プロピレングリコールモノノルマルブチルエーテル、プロピレングリコールモノイソブチルエーテル、プロピレングリコールモノターシャリブチルエーテル、プロピレングリコールモノノルマルヘキシルエーテル、プロピレングリコールモノノルマルオクチルエーテル、プロピレングリコールモノ2−エチルヘキシルエーテル等が挙げられ、これらの群から選ばれる1種または2種以上を組み合わせて用いることができるが、これらに限定されない。 Specific examples of propylene glycol ethers include propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol mononormal propyl ether, propylene glycol monoisopropyl ether, propylene glycol mononormal butyl ether, propylene glycol monoisobutyl ether, and propylene glycol monotasha. Examples thereof include rebutyl ether, propylene glycol mononormal hexyl ether, propylene glycol mononormal octyl ether, propylene glycol mono2-ethylhexyl ether and the like, and one or a combination of two or more selected from these groups can be used. Not limited to these.
水性樹脂組成物中の(E)水性溶剤の含有量は、1〜10質量%が好ましく、2〜8質量%がより好ましい。 The content of the (E) aqueous solvent in the aqueous resin composition is preferably 1 to 10% by mass, more preferably 2 to 8% by mass.
<水性電着樹脂液>
本発明の水性電着樹脂液は、本発明の水性樹脂組成物からなる電着用の樹脂液であり、電着によって電着膜を形成することができる。
水性電着樹脂液の組成は水性樹脂組成物と同一であってもよく、必要に応じて他の成分を更に含有することもできる。
<Aqueous electrodeposition resin liquid>
The aqueous electrodeposition resin liquid of the present invention is an electrodeposited resin liquid comprising the aqueous resin composition of the present invention, and an electrodeposition film can be formed by electrodeposition.
The composition of the aqueous electrodeposition resin liquid may be the same as that of the aqueous resin composition, and other components may be further contained if necessary.
<水性電着塗料>
本発明の水性電着塗料は、本発明の水性電着樹脂液からなる塗料であり、電着塗装によって電着塗膜を形成することができる。
水性電着塗料の組成は、水性電着樹脂液と同一であってもよく、必要に応じて他の成分を更に含有することもできる。
<Aqueous electrodeposition paint>
The water-based electrodeposition coating material of the present invention is a coating material made of the water-based electrodeposition resin liquid of the present invention, and an electrodeposition coating film can be formed by electrodeposition coating.
The composition of the water-based electrodeposition coating material may be the same as that of the water-based electrodeposition resin liquid, and other components may be further contained if necessary.
<電着塗膜>
本発明の電着塗膜は、本発明の水性樹脂組成物、水性電着樹脂液、または水性電着塗料を、被塗装物に電着塗装することにより形成された塗膜であり、金属調の外観を有する。
該電着塗装は、定電流法による電着塗装が好ましい。
上記の被塗装物は、導電性を有する素材であれば特に限定されないが、金属素材(特に、アルミニウム、ステンレス及び各種合金)が好ましい。
<Electrodeposition coating>
The electrodeposition coating film of the present invention is a coating film formed by electrodeposition coating of the water-based resin composition, the water-based electrodeposition resin liquid, or the water-based electrodeposition coating material of the present invention on an object to be coated, and is metallic. Has the appearance of.
The electrodeposition coating is preferably electrodeposition coating by a constant current method.
The above-mentioned object to be coated is not particularly limited as long as it is a conductive material, but a metal material (particularly, aluminum, stainless steel and various alloys) is preferable.
<電着塗膜形成方法>
本発明の電着塗膜形成(電着塗装)方法は、本発明の水性樹脂組成物、水性電着樹脂液または水性電着塗料を用いて、電着塗装する形成方法である。
電着塗装は、定電流法で行われることが好ましい。
また、電着塗装は、被塗装物を陽極、電極を陰極として通電するアニオン電着塗装によって行うことが好ましい。
アニオン電着塗装は、カチオン電着塗装よりも、塗装色の安定性が高く、焼付温度を低くできる等の点で有利である。
そして、本発明の水性樹脂組成物が含有する(C)水分散性アルミニウム顔料は、比重が約2.7g/cm3と大きく、電着塗装時に沈降し易いため、被塗装物への通電条件としては、短時間で所定の膜厚を得られるように、印加電圧を高くすることが好ましい。
<Method for forming electrodeposition coating film>
The electrodeposition coating film forming (electrodeposition coating) method of the present invention is a forming method of electrodeposition coating using the aqueous resin composition, the aqueous electrodeposition resin liquid or the aqueous electrodeposition coating material of the present invention.
The electrodeposition coating is preferably performed by a constant current method.
Further, the electrodeposition coating is preferably performed by anion electrodeposition coating in which the object to be coated is used as an anode and the electrode is used as a cathode.
Anionic electrodeposition coating is more advantageous than cationic electrodeposition coating in that the coating color is more stable and the baking temperature can be lowered.
The water-dispersible aluminum pigment (C) contained in the aqueous resin composition of the present invention has a large specific gravity of about 2.7 g / cm 3 and easily settles during electrodeposition coating. It is preferable to increase the applied voltage so that a predetermined film thickness can be obtained in a short time.
定電流法による電着塗装における膜の形成プロセスの段階においては、膜形成の初期段階では相対的に低い電圧を印加し、膜厚が大きくなって膜抵抗が大きくなるにつれて、相対的に高い電圧を印加することが好ましい。このように膜厚に応じて印加電圧を変化させることによって、定電流で電着塗装して、膜厚ムラの発生を抑制して、均一な金属調外観を得ることができる。 In the stage of the film formation process in electrodeposition coating by the constant current method, a relatively low voltage is applied in the initial stage of film formation, and a relatively high voltage is applied as the film thickness increases and the film resistance increases. Is preferably applied. By changing the applied voltage according to the film thickness in this way, it is possible to perform electrodeposition coating with a constant current, suppress the occurrence of film thickness unevenness, and obtain a uniform metallic appearance.
これに対し、定電圧法による電着塗装の場合は、膜抵抗が大きくなるにつれて電流値が低下もしくは鈍化し、高電圧処理においても所定膜厚が容易には得られ難い、もしくは、後半の通電がアルミニウム顔料を含まない塗膜を形成させるため、金属調外観の不足やムラが生じ易い。 On the other hand, in the case of electrodeposition coating by the constant voltage method, the current value decreases or slows down as the film resistance increases, and it is difficult to easily obtain a predetermined film thickness even in high voltage processing, or energization in the latter half. However, since a coating film containing no aluminum pigment is formed, lack of metallic appearance and unevenness are likely to occur.
定電流法で電着塗装する形成方法の具体的な条件としては、例えば、電着塗装を施す被塗装物の表面積100cm2に対して、印加電圧を、好ましくは100〜250V、より好ましくは150〜200Vの範囲で変化させて、電流密度を、好ましくは1.0〜6.0mA/cm2、より好ましくは2.0〜4.0mA/cm2に保ち、通電時間を、好ましくは0.10分〜0.50分、より好ましくは0.20〜0.30分で、電着塗装することが挙げられる。
電着塗装された被塗装物は、水洗され、次いで150〜250℃で15〜60分間加熱されて、溶剤が除去され、電着塗膜の架橋による硬化が進行し、優れた耐食性や硬度を有する電着塗膜が形成される。
As a specific condition of the forming method for electrodeposition coating by the constant current method, for example, the applied voltage is preferably 100 to 250 V, more preferably 150, for a surface area of 100 cm 2 of the object to be electrodeposited. The current density is preferably maintained at 1.0 to 6.0 mA / cm 2 , more preferably 2.0 to 4.0 mA / cm 2 , and the energization time is preferably 0. Electrodeposition coating may be performed in 10 minutes to 0.50 minutes, more preferably 0.20 to 0.30 minutes.
The electrodeposited object to be coated is washed with water and then heated at 150 to 250 ° C. for 15 to 60 minutes to remove the solvent, and the electrodeposition coating film is cured by cross-linking to obtain excellent corrosion resistance and hardness. The electrodeposited coating film to have is formed.
以下に本発明の実施例及び比較例を挙げてさらに具体的に説明するが、これによって本発明が限定されるものではない。 Hereinafter, the present invention will be described in more detail with reference to Examples and Comparative Examples of the present invention, but the present invention is not limited thereto.
実施例で用いる(B)アミノ樹脂、(C)水分散性アルミニウム顔料は下記の通りである。
[(B)アミノ樹脂]
・アミノ樹脂1:オルネクスジャパン株式会社製メラミン樹脂 サイメル232、有効成分100%。
[(C)水分散性アルミニウム顔料]
・水分散性アルミニウム顔料1:東洋アルミニウム株式会社製、WRA−5660。有効成分50%、表面はアクリル樹脂及び珪素系化合物からなるハイブリッド組成を含有する。鱗片状、ノンリーフィングタイプ。平均粒子径10μm。
・水分散性アルミニウム顔料2:東洋アルミニウム株式会社製、EMR−D5620、有効成分60%、表面は珪素系化合物を含有する。鱗片状、ノンリーフィングタイプ平均粒子径17μm。
・水分散性アルミニウム顔料3:東洋アルミニウム株式会社製、BP−6360J。有効成分50%、表面はアクリル樹脂を含有する。鱗片状、ノンリーフィングタイプ。平均粒子径10μm。
The (B) amino resin and (C) water-dispersible aluminum pigment used in the examples are as follows.
[(B) Amino resin]
-Amino resin 1: Melamine resin Cymel 232 manufactured by Ornex Japan Co., Ltd., 100% active ingredient.
[(C) Water-dispersible aluminum pigment]
-Water-dispersible aluminum pigment 1: WRA-5660 manufactured by Toyo Aluminum K.K. The active ingredient is 50%, and the surface contains a hybrid composition composed of an acrylic resin and a silicon-based compound. Scale-like, non-reefing type. Average particle size 10 μm.
-Water-dispersible aluminum pigment 2: EMR-D5620 manufactured by Toyo Aluminum K.K., 60% active ingredient, and the surface contains a silicon compound. Scale-like, non-leafing type Average particle size 17 μm.
-Water-dispersible aluminum pigment 3: BP-6360J manufactured by Toyo Aluminum K.K. The active ingredient is 50%, and the surface contains acrylic resin. Scale-like, non-reefing type. Average particle size 10 μm.
<(A)水分散性ビニル系共重合体の製造>
[合成例1]
攪拌装置、還流冷却器及び窒素導入管を備えた3リットルの4つ口フラスコに下記原料を仕込み、90℃に昇温した。
イソプロパノール 12質量部
エチレングリコールモノノルマルブチルエーテル 8質量部
上記とは別に、下記原料の混合液を滴下ロートに仕込み、前記フラスコ内に120分かけて滴下した。ここで2,2′−アゾビスイソブチロニトリルは重合開始剤として作用する。
イソプロパノール 5質量部
エチレングリコールモノノルマルブチルエーテル 13質量部
アクリル酸 5質量部
2−ヒドロキシエチルアクリレート 15質量部
スチレン 10質量部
2−エチルヘキシルアクリレート 10質量部
エチルアクリレート 10質量部
ブチルアクリレート 10質量部
メチルメタクリレート 40質量部
2,2′−アゾビスイソブチロニトリル 1質量部
上記の滴下が終了した後に、さらに、下記の混合物を30分毎に3回添加した。
イソプロパノール 0.4質量部
2,2′−アゾビスイソブチロニトリル 0.2質量部
そしてさらに、90℃で90分反応を続け、水分散性ビニル系共重合体溶液1(固形分72.2質量%、固形分の酸価38.3mgKOH。)を得た。
<(A) Production of water-dispersible vinyl copolymer>
[Synthesis Example 1]
The following raw materials were charged into a 3-liter four-necked flask equipped with a stirrer, a reflux condenser and a nitrogen introduction tube, and the temperature was raised to 90 ° C.
Isopropanol 12 parts by mass Ethylene glycol mononormal butyl ether 8 parts by mass Separately from the above, a mixed solution of the following raw materials was charged into a dropping funnel and dropped into the flask over 120 minutes. Here, 2,2'-azobisisobutyronitrile acts as a polymerization initiator.
Isopropanol 5 parts by mass Ethylene glycol mononormal butyl ether 13 parts by mass Acrylic acid 5 parts by mass 2-Hydroxyethyl acrylate 15 parts by mass Stylus 10 parts by mass 2-Ethylhexyl acrylate 10 parts by mass Ethyl acrylate 10 parts by mass Butyl acrylate 10 parts by mass Methyl methacrylate 40 parts by mass Part 2,2'-Azobisisobutyronitrile 1 part by mass After the above dropping was completed, the following mixture was further added 3 times every 30 minutes.
Isopropanol 0.4 parts by mass 2,2'-azobisisobutyronitrile 0.2 parts by mass Then, the reaction was continued at 90 ° C. for 90 minutes, and the water-dispersible vinyl copolymer solution 1 (solid content 72.2) was continued. Mass%, acid value of solid content 38.3 mgKOH.) Was obtained.
[合成例2]
攪拌装置、還流冷却器及び窒素導入管を備えた3リットルの4つ口フラスコに下記を仕込み、90℃に昇温した。
イソプロパノール 12.0質量部
エチレングリコールモノノルマルブチルエーテル 8.0質量部
上記とは別に、下記の混合液を滴下ロートに仕込み、前記フラスコ内に120分かけて滴下した。
イソプロパノール 5質量部
エチレングリコールモノノルマルブチルエーテル 13質量部
アクリル酸 7質量部
2−ヒドロキシエチルアクリレート 15質量部
スチレン 10質量部
2−エチルヘキシルアクリレート 10質量部
エチルアクリレート 10質量部
ブチルアクリレート 10質量部
メチルメタクリレート 38質量部
2,2′−アゾビスイソブチロニトリル 1質量部
滴下終了後、さらに下記の混合物を、30分毎に3回添加した。
イソプロパノール 0.4質量部
2,2′−アゾビスイソブチロニトリル 0.2質量部
そしてさらに、90℃で90分反応を続け、水分散性ビニル系共重合体溶液2(固形分72.2質量%、固形分の酸価53.6mgKOH。)を得た。
[Synthesis Example 2]
The following was placed in a 3-liter four-necked flask equipped with a stirrer, a reflux condenser and a nitrogen introduction tube, and the temperature was raised to 90 ° C.
Isopropanol 12.0 parts by mass Ethylene glycol mononormal butyl ether 8.0 parts by mass Separately from the above, the following mixed solution was charged into a dropping funnel and dropped into the flask over 120 minutes.
Isopropanol 5 parts by mass Ethylene glycol mononormal butyl ether 13 parts by mass Acrylic acid 7 parts by mass 2-Hydroxyethyl acrylate 15 parts by mass Stylus 10 parts by mass 2-Ethylhexyl acrylate 10 parts by mass Ethyl acrylate 10 parts by mass Butyl acrylate 10 parts by mass Methyl methacrylate 38 parts by mass Part 2,2'-Azobisisobutyronitrile 1 part by mass After completion of the dropping, the following mixture was further added 3 times every 30 minutes.
Isopropanol 0.4 parts by mass 2,2'-azobisisobutyronitrile 0.2 parts by mass Then, the reaction was continued at 90 ° C. for 90 minutes, and the water-dispersible vinyl copolymer solution 2 (solid content 72.2) was continued. Mass%, acid value of solid content 53.6 mgKOH.) Was obtained.
[合成例3]
攪拌装置、還流冷却器及び窒素導入管を備えた3リットルの4つ口フラスコに下記を仕込み、90℃に昇温した。
イソプロパノール 12質量部
エチレングリコールモノノルマルブチルエーテル 8質量部
上記とは別に、下記の混合液を滴下ロートに仕込み、前記フラスコ内に120分かけて滴下した。
イソプロパノール 5質量部
エチレングリコールモノノルマルブチルエーテル 13質量部
アクリル酸 2質量部
2−ヒドロキシエチルアクリレート 15質量部
スチレン 10質量部
2−エチルヘキシルアクリレート 10質量部
エチルアクリレート 10質量部
ブチルアクリレート 10質量部
メチルメタクリレート 43質量部
2,2′−アゾビスイソブチロニトリル 1質量部
滴下終了後、さらに下記の混合物を、30分毎に3回添加した。
イソプロパノール 0.4質量部
2,2′−アゾビスイソブチロニトリル 0.2質量部
さらに90℃で90分反応を続け、水分散性ビニル系共重合体溶液3(固形分72.2質量%、固形分の酸価15.3mgKOH。)を得た。
[Synthesis Example 3]
The following was placed in a 3-liter four-necked flask equipped with a stirrer, a reflux condenser and a nitrogen introduction tube, and the temperature was raised to 90 ° C.
Isopropanol 12 parts by mass Ethylene glycol mononormal butyl ether 8 parts by mass Separately from the above, the following mixed solution was charged into a dropping funnel and dropped into the flask over 120 minutes.
Isopropanol 5 parts by mass Ethylene glycol mononormal butyl ether 13 parts by mass Acrylic acid 2 parts by mass 2-Hydroxyethyl acrylate 15 parts by mass styrene 10 parts by mass 2-Ethylhexyl acrylate 10 parts by mass Ethyl acrylate 10 parts by mass Butyl acrylate 10 parts by mass Methyl methacrylate 43 parts by mass Part 2,2'-Azobisisobutyronitrile 1 part by mass After completion of the dropping, the following mixture was further added 3 times every 30 minutes.
Isopropanol 0.4 parts by mass 2,2'-azobisisobutyronitrile 0.2 parts by mass Further, the reaction was continued at 90 ° C. for 90 minutes, and the water-dispersible vinyl copolymer solution 3 (solid content 72.2% by mass) was continued. , The acid value of the solid content was 15.3 mgKOH.).
[合成例4]
攪拌装置、還流冷却器及び窒素導入管を備えた3リットルの4つ口フラスコに下記を仕込み、90℃に昇温した。
イソプロパノール 12質量部
エチレングリコールモノノルマルブチルエーテル 8質量部
上記とは別に、下記の混合液を滴下ロートに仕込み、前記フラスコ内に120分かけて滴下した。
イソプロパノール 5質量部
エチレングリコールモノノルマルブチルエーテル 13質量部
アクリル酸 14質量部
2−ヒドロキシエチルアクリレート 15質量部
スチレン 10質量部
2−エチルヘキシルアクリレート 10質量部
エチルアクリレート 10質量部
ブチルアクリレート 10質量部
メチルメタクリレート 31質量部
2,2′−アゾビスイソブチロニトリル 1質量部
滴下終了後、さらに下記の混合物を、30分毎に3回添加した。
イソプロパノール 0.4質量部
2,2′−アゾビスイソブチロニトリル 0.2質量部
さらに90℃で90分反応を続け、水分散性ビニル系共重合体溶液4(固形分72.2質量%、固形分の酸価107.2mgKOH。)を得た。
[Synthesis Example 4]
The following was placed in a 3-liter four-necked flask equipped with a stirrer, a reflux condenser and a nitrogen introduction tube, and the temperature was raised to 90 ° C.
Isopropanol 12 parts by mass Ethylene glycol mononormal butyl ether 8 parts by mass Separately from the above, the following mixed solution was charged into a dropping funnel and dropped into the flask over 120 minutes.
Isopropanol 5 parts by mass Ethylene glycol mononormal butyl ether 13 parts by mass Acrylic acid 14 parts by mass 2-Hydroxyethyl acrylate 15 parts by mass Stylus 10 parts by mass 2-Ethylhexyl acrylate 10 parts by mass Ethyl acrylate 10 parts by mass Butyl acrylate 10 parts by mass Methyl methacrylate 31 parts by mass Part 2,2'-Azobisisobutyronitrile 1 part by mass After completion of the dropping, the following mixture was further added 3 times every 30 minutes.
Isopropanol 0.4 parts by mass 2,2'-azobisisobutyronitrile 0.2 parts by mass Further, the reaction was continued at 90 ° C. for 90 minutes, and the water-dispersible vinyl copolymer solution 4 (solid content 72.2% by mass) was continued. , The acid value of the solid content was 107.2 mgKOH.).
[実施例1]
(水性樹脂組成物(水性電着樹脂液)の製造)
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液1を得た。
水分散性ビニル系共重合体溶液1 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 1.2質量部
脱イオン水 123.8質量部
ここで、原液1中の水分散性ビニル系共重合体1の濃度は、90×0.722/(90+35+1.2+123.8)×100=25.99質量%である。
また、原液1中のアミノ樹脂1の濃度は、35/(90+35+1.2+123.8)×100=14.00質量%である。
そしてさらに、90℃で90分反応を続け、水分散性ビニル系共重合体溶液1(固形分72.2質量%、固形分の酸価38.3mgKOH。)を得た。
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液1を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液1(有効成分8%)を得た。
脱イオン水 789.4質量部
原液1 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.6質量部
ここで、原液1中の水分散性ビニル系共重合体1の濃度は、200×0.2599/(789.4+200+10+0.6)×100=5.20質量%である。
また、原液1中のアミノ樹脂1の濃度は、200×0.14/(789.4+200+10+0.6)×100=2.80質量%である。
得られた電着塗料用希釈液1と水分散性アルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)1を得た。
電着塗料用希釈液1 100質量部
水分散性アルミニウム顔料1 1質量部
ここで、水性樹脂組成物中の水分散性ビニル系共重合体1/アミノ樹脂1/水分散性アルミニウム顔料1、の質量比は、5.20/2.80/1×0.5であることから、下記
の質量比が算出される。
水分散性ビニル系共重合体1/アミノ樹脂1=5.20/2.80=65.0/35.0。
水分散性アルミニウム顔料1/(水分散性ビニル系共重合体1+アミノ樹脂1)=6.3/100.0
また、水性樹脂組成物の固形分中の各々の質量%は、下記の通りに算出される。
水分散性ビニル系共重合体1:5.20/(5.20+2.80+0.5)×100=61.2質量%。
アミノ樹脂1:2.80/(5.20+2.80+0.5)×100=32.9質量%。
水分散性アルミニウム顔料1:0.5/(5.20+2.80+0.5)×100=5.9質量%。
[Example 1]
(Production of water-based resin composition (water-based electrodeposition resin liquid))
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 1.
Water-dispersible vinyl-based copolymer solution 1 90.0 parts by mass Amino resin 1 35.0 parts by mass Didimethylaminoethanol 1.2 parts by mass Deionized water 123.8 parts by mass Here, the water-dispersible vinyl in the stock solution 1 The concentration of the system copolymer 1 is 90 × 0.722 / (90 + 35 + 1.2 + 123.8) × 100 = 25.99% by mass.
The concentration of the amino resin 1 in the stock solution 1 is 35 / (90 + 35 + 1.2 + 123.8) × 100 = 14.00% by mass.
Further, the reaction was continued at 90 ° C. for 90 minutes to obtain an aqueous dispersible vinyl copolymer solution 1 (solid content 72.2% by mass, acid value 38.3 mgKOH of solid content).
Then, deionized water is charged into another container at the following ratio, the stock solution 1 obtained above is added while stirring, and then butyl cellosolve and dimethylaminoethanol are added to homogenize the mixture for electrodeposition coating. Diluted solution 1 (active ingredient 8%) was obtained.
Deionized water 789.4 parts by mass Stock solution 1 200.0 parts by mass Butyl cellosolve 10.0 parts by mass dimethylaminoethanol 0.6 parts by mass Here, the concentration of the water-dispersible vinyl copolymer 1 in the stock solution 1 is 200. × 0.2599 / (789.4 + 200 + 10 + 0.6) × 100 = 5.20% by mass.
The concentration of the amino resin 1 in the stock solution 1 is 200 × 0.14 / (789.4 + 200 + 10 + 0.6) × 100 = 2.80% by mass.
The obtained diluent 1 for electrodeposition coating material and the water-dispersible aluminum pigment 1 were mixed and stirred at the following ratios to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 1.
Diluting Liquid for Electrodeposition Paint 1 100 parts by mass Water-dispersible aluminum pigment 1 1 part by mass Here, the water-dispersible vinyl copolymer 1 / amino resin 1 / water-dispersible aluminum pigment 1 in the aqueous resin composition. Since the mass ratio is 5.20 / 2.80 / 1 × 0.5, the following mass ratio is calculated.
Water-dispersible vinyl copolymer 1 / amino resin 1 = 5.20 / 2.80 = 65.0 / 35.0.
Water-dispersible aluminum pigment 1 / (water-dispersible vinyl copolymer 1 + amino resin 1) = 6.3 / 100.0
In addition, each mass% in the solid content of the aqueous resin composition is calculated as follows.
Water-dispersible vinyl copolymer 1: 5.20 / (5.20 + 2.80 + 0.5) × 100 = 61.2% by mass.
Amino resin 1: 2.80 / (5.20 + 2.80 + 0.5) × 100 = 32.9% by mass.
Water-dispersible aluminum pigment 1: 0.5 / (5.20 + 2.80 + 0.5) × 100 = 5.9% by mass.
(塗膜の形成)
水性樹脂組成物1と下記の被塗装物及び陰極を用いて、下記条件の定電流法にて両極間に電圧印加して、定電圧法アニオン電着塗装を行った。印加電圧は、下記範囲の電流密度を維持できるように、初期では低い電圧を印加し、塗膜の電気抵抗の上昇に応じて高い電圧が印加した。
被塗装物:アルカリ脱脂後に酸洗処理された厚さ1mmのA1100板材をコの字状に曲げて、上面部、側面部、下面部を有する形状にした。
陰極:18−8ステンレス鋼板
浴温:20℃
電流密度:3.0mA/cm2
通電時間:10秒
次いで、電着塗装された被塗装物を取り出して充分に水洗したのちに、170℃の温度で20分間加熱して、電着塗膜を乾燥及び硬化(焼付乾燥)させて、金属調の外観を有する電着塗膜を得た。
そして、各種評価を行い、上記の算出結果と各種評価結果を表2に示した。
(Formation of coating film)
Using the aqueous resin composition 1 and the following object to be coated and the cathode, a voltage was applied between the two poles by the constant current method under the following conditions to perform constant voltage anion electrodeposition coating. As the applied voltage, a low voltage was initially applied so that the current density in the following range could be maintained, and a high voltage was applied as the electrical resistance of the coating film increased.
Object to be coated: An A1100 plate having a thickness of 1 mm, which was pickled after being degreased with alkali, was bent into a U shape to have a shape having an upper surface portion, a side surface portion, and a lower surface portion.
Cathode: 18-8 stainless steel plate Bath temperature: 20 ° C
Current density: 3.0mA / cm 2
Energization time: 10 seconds Next, after taking out the electrodeposited object to be coated and thoroughly washing it with water, it is heated at a temperature of 170 ° C. for 20 minutes to dry and cure (baking and drying) the electrodeposited coating film. , An electrodeposition coating film having a metallic appearance was obtained.
Then, various evaluations were performed, and the above calculation results and various evaluation results are shown in Table 2.
[実施例2]
下記の割合で、水分散性ビニル系共重合体溶液2とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液2を得た。
水分散性ビニル系共重合体溶液2 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 1.7質量部
脱イオン水 123.3質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液2を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液2(有効成分8%)を得た。
脱イオン水 789.1質量部
原液2 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.9質量部
得られた電着塗料用希釈液2と水分散性アルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)2を得た。
電着塗料用希釈液2 100質量部
水分散性アルミニウム顔料1 1質量部
そして、水性樹脂組成物(水性電着樹脂液)2を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Example 2]
The water-dispersible vinyl copolymer solution 2 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 2.
Water-dispersible vinyl copolymer solution 2 90.0 parts by mass Amino resin 1 35.0 parts by mass Didimethylaminoethanol 1.7 parts by mass Deionized water 123.3 parts by mass Then, in another container at the following ratio. Deionized water was charged, and the undiluted solution 2 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 2 for electrodeposition paint (active ingredient 8%). rice field.
Deionized water 789.1 parts by mass Stock solution 2 200.0 parts by mass Butyl cellosolve 10.0 parts by mass dimethylaminoethanol 0.9 parts by mass The obtained diluent 2 for electrodeposition coating and water-dispersible aluminum pigment 1 are mixed in the following proportions. The mixture was mixed and stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 2.
Diluting liquid for electrodeposition coating 2 100 parts by mass Water-dispersible aluminum pigment 1 1 part by mass The electrodeposition coating film is applied in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin solution) 2 is used. It was formed and evaluated in the same manner.
[実施例3]
下記の割合で、水分散性ビニル系共重合体溶液2とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液3を得た。
水分散性ビニル系共重合体溶液2 83.1質量部
アミノ樹脂1 40.0質量部
ジメチルアミノエタノール 1.5質量部
脱イオン水 125.4質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液3を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液3(有効成分8%)を得た。
脱イオン水 789.2質量部
原液3 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.8質量部
得られた電着塗料用希釈液3と水分散性アルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)3を得た。
電着塗料用希釈液3 100質量部
水分散性アルミニウム顔料1 1質量部
そして、水性樹脂組成物(水性電着樹脂液)3を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Example 3]
The water-dispersible vinyl copolymer solution 2 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 3.
Water-dispersible vinyl copolymer solution 2 83.1 parts by mass Amino resin 1 40.0 parts by mass Didimethylaminoethanol 1.5 parts by mass Deionized water 125.4 parts by mass And in another container at the following ratio Deionized water was charged, and the undiluted solution 3 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 3 for electrodeposition paint (active ingredient 8%). rice field.
Deionized water 789.2 parts by mass Stock solution 3 200.0 parts by mass Butyl cellosolve 10.0 parts by mass dimethylaminoethanol 0.8 parts by mass The obtained diluent 3 for electrodeposition coating and water-dispersible aluminum pigment 1 are mixed in the following proportions. 3 was mixed and stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 3.
Diluting liquid for electrodeposition coating material 3 100 parts by mass Water-dispersible aluminum pigment 1 1 part by mass The electrodeposition coating film is applied in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin solution) 3 is used. It was formed and evaluated in the same manner.
[実施例4]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液4を得た。
水分散性ビニル系共重合体溶液 1 66.4質量部
アミノ樹脂1 58.6質量部
ジメチルアミノエタノール 0.9質量部
脱イオン水 124.1質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液4(有効成分8%)を得た。
脱イオン水 789.4質量部
原液4 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.6質量部
得られた電着塗料用希釈液4と水分散性アルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)4を得た。
電着塗料用希釈液4 100質量部
水分散性アルミニウム顔料1 1質量部
そして、水性樹脂組成物(水性電着樹脂液)2を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Example 4]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 4.
Water-dispersible vinyl copolymer solution 1 66.4 parts by mass Amino resin 1 58.6 parts by mass Didimethylaminoethanol 0.9 parts by mass Deionized water 124.1 parts by mass Then, in another container at the following ratio. Deionized water was charged, and the undiluted solution obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 4 (active ingredient 8%) for electrodeposition coating. ..
Deionized water 789.4 parts by mass Undiluted solution 4 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.6 parts by mass The obtained diluent 4 for electrodeposition coating and water-dispersible aluminum pigment 1 are mixed in the following proportions. Aqueous resin composition (aqueous electrodeposition resin solution) 4 was obtained by mixing and stirring with.
Diluting liquid for electrodeposition coating material 4 100 parts by mass Water-dispersible aluminum pigment 1 1 part by mass The electrodeposition coating film is applied in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin solution) 2 is used. It was formed and evaluated in the same manner.
[実施例5]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液5を得た。
水分散性ビニル系共重合体溶液1 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 1.2質量部
脱イオン水 123.8質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液5を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液5(有効成分8%)を得た。
脱イオン水 789.4質量部
原液4 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.6質量部
得られた電着塗料用希釈液5と水分散性アルミニウム顔料2とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)5を得た。
電着塗料用希釈液5 100質量部
アルミニウム顔料2 1質量部
そして、水性樹脂組成物(水性電着樹脂液)5を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Example 5]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 5.
Water-dispersible vinyl copolymer solution 1 90.0 parts by mass Amino resin 1 35.0 parts by mass Didimethylaminoethanol 1.2 parts by mass Deionized water 123.8 parts by mass Then, in another container at the following ratio. Deionized water was charged, and the undiluted solution 5 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 5 (active ingredient 8%) for electrodeposition coating. rice field.
Deionized water 789.4 parts by mass Undiluted solution 4 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.6 parts by mass The obtained diluent 5 for electrodeposition coating and water-dispersible aluminum pigment 2 are mixed in the following proportions. Aqueous resin composition (aqueous electrodeposition resin solution) 5 was obtained by mixing and stirring with.
Diluting liquid for electrodeposition paint 5 100 parts by mass Aluminum pigment 2 1 part by mass Then, an electrodeposition coating film was formed by the same method as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin liquid) 5 was used. , The same evaluation was performed.
[実施例6]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液6を得た。
水分散性ビニル系共重合体溶液1 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 1.2質量部
脱イオン水 123.8質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液6を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液6(有効成分8%)を得た。
脱イオン水 789.4質量部
原液5 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.6質量部
得られた電着塗料用希釈液6とアルミニウム顔料3とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)6を得た。
電着塗料用希釈液6 100質量部
水分散性アルミニウム顔料3 1質量部
そして、水性樹脂組成物(水性電着樹脂液)6を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Example 6]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 6.
Water-dispersible vinyl copolymer solution 1 90.0 parts by mass Amino resin 1 35.0 parts by mass Didimethylaminoethanol 1.2 parts by mass Deionized water 123.8 parts by mass Then, in another container at the following ratio. Deionized water was charged, and the undiluted solution 6 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 6 (active ingredient 8%) for electrodeposition coating. rice field.
Deionized water 789.4 parts by mass Stock solution 5 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.6 parts by mass The obtained diluent 6 for electrodeposition coating and aluminum pigment 3 are mixed in the following ratios. The mixture was stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 6.
Diluting liquid for electrodeposition coating material 6 100 parts by mass Water-dispersible aluminum pigment 3 1 part by mass The electrodeposition coating film is applied in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin liquid) 6 is used. It was formed and evaluated in the same manner.
[実施例7]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液7を得た。
水分散性ビニル系共重合体溶液1 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 1.2質量部
脱イオン水 123.8質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液7を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液7(有効成分8%)を得た。
脱イオン水 789.4質量部
原液6 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.6質量部
得られた電着塗料用希釈液7とアルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)7を得た。
電着塗料用希釈液7 100.0質量部
アルミニウム顔料1 1.8質量部
そして、水性樹脂組成物(水性電着樹脂液)7を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Example 7]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 7.
Water-dispersible vinyl copolymer solution 1 90.0 parts by mass Amino resin 1 35.0 parts by mass Didimethylaminoethanol 1.2 parts by mass Deionized water 123.8 parts by mass Then, in another container at the following ratio. Deionized water was charged, and the undiluted solution 7 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 7 (active ingredient 8%) for electrodeposition coating. rice field.
Deionized water 789.4 parts by mass Stock solution 6 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.6 parts by mass The obtained diluent 7 for electrodeposition coating and aluminum pigment 1 are mixed in the following ratios. The mixture was stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 7.
Diluting liquid for electrodeposition paint 7 100.0 parts by mass Aluminum pigment 1 1.8 parts by mass Then, the electrodeposition coating film was formed in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin liquid) 7 was used. Was formed and evaluated in the same manner.
[比較例1]
下記の割合で、ビニル系共重合体溶液3とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液8を得た。
水分散性ビニル系共重合体溶液3 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 0.5質量部
脱イオン水 124.5質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液8を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液8(有効成分8%)を得た。
脱イオン水 789.7質量部
原液8 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.3質量部
得られた電着塗料用希釈液8と水分散性アルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)8を得た。
電着塗料用希釈液8 100質量部
水分散性アルミニウム顔料1 1質量部
そして、水性樹脂組成物(水性電着樹脂液)8を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Comparative Example 1]
The vinyl copolymer solution 3 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 8.
Water-dispersible vinyl copolymer solution 3 90.0 parts by mass Amino resin 1 35.0 parts by mass dimethylaminoethanol 0.5 parts by mass Deionized water 124.5 parts by mass And in another container at the following ratio Deionized water was charged, and the undiluted solution 8 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 8 (active ingredient 8%) for electrodeposition coating. rice field.
Deionized water 789.7 parts by mass Undiluted solution 8 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.3 parts by mass The obtained diluent 8 for electrodeposition coating and water-dispersible aluminum pigment 1 are mixed in the following proportions. Aqueous resin composition (aqueous electrodeposition resin solution) 8 was obtained by mixing and stirring with.
Diluting liquid for electrodeposition coating 8 100 parts by mass Water-dispersible aluminum pigment 1 1 part by mass The electrodeposition coating film is applied in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin liquid) 8 is used. It was formed and evaluated in the same manner.
[比較例2]
下記の割合で、ビニル系共重合体溶液4とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液9を得た。
水分散性ビニル系共重合体溶液4 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 3.4質量部
脱イオン水 121.6質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液9を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液9(有効成分8%)を得た。
脱イオン水 788.2質量部
原液9 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 1.8質量部
得られた電着塗料用希釈液9とアルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)9を得た。
電着塗料用希釈液9 100質量部
水分散性アルミニウム顔料1 1質量部
そして、水性樹脂組成物(水性電着樹脂液)9を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Comparative Example 2]
The vinyl copolymer solution 4 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 9.
Water-dispersible vinyl copolymer solution 4 90.0 parts by mass Amino resin 1 35.0 parts by mass Didimethylaminoethanol 3.4 parts by mass Deionized water 121.6 parts by mass Then, in another container at the following ratio. Deionized water was charged, and the undiluted solution 9 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 9 (active ingredient 8%) for electrodeposition coating. rice field.
Deionized water 788.2 parts by mass Undiluted solution 9 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 1.8 parts by mass The obtained diluent 9 for electrodeposition coating and aluminum pigment 1 are mixed in the following ratios. The mixture was stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 9.
Diluting liquid for electrodeposition coating material 9 100 parts by mass Water-dispersible aluminum pigment 1 1 part by mass The electrodeposition coating film is applied in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin solution) 9 is used. It was formed and evaluated in the same manner.
[比較例3]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液10を得た。
水分散性ビニル系共重合体溶液1 90.0質量部
アミノ樹脂1 35.0質量部
ジメチルアミノエタノール 1.2質量部
脱イオン水を 123.8質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液10を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液10(有効成分8%)を得た。
脱イオン水 789.4質量部
原液10 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.6質量部
得られた電着塗料用希釈液10とアルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)10を得た。
電着塗料用希釈液10 100質量部
水分散性アルミニウム顔料1 0.01質量部
そして、水性樹脂組成物(水性電着樹脂液)10を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Comparative Example 3]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 10.
Water-dispersible vinyl copolymer solution 1 90.0 parts by mass Amino resin 1 35.0 parts by mass Didimethylaminoethanol 1.2 parts by mass 123.8 parts by mass Deionized water And another container at the following ratio Deionized water was added to the mixture, and the undiluted solution 10 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the solution 10 (active ingredient 8%) for electrodeposition coating. Obtained.
Deionized water 789.4 parts by mass Undiluted solution 10 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.6 parts by mass The obtained diluent 10 for electrodeposition coating and aluminum pigment 1 are mixed in the following ratios. The mixture was stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 10.
Diluting liquid for electrodeposition coating 10 100 parts by mass Water-dispersible aluminum pigment 1 0.01 part by mass Electrodeposition coating by the same method as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin liquid) 10 was used. A film was formed and evaluated in the same manner.
[比較例4]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液11を得た。
水分散性ビニル系共重合体溶液1 90質量部
アミノ樹脂1 35質量部
ジメチルアミノエタノール 1.2質量部
脱イオン水 123.8質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液11を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液11(有効成分8%)を得た。
脱イオン水 789.4質量部
原液11 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.6質量部
得られた電着塗料用希釈液11とアルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)11を得た。
電着塗料用希釈液11 100質量部
水分散性アルミニウム顔料1 3質量部
そして、水性樹脂組成物(水性電着樹脂液)11を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Comparative Example 4]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 11.
Water-dispersible vinyl copolymer solution 1 90 parts by mass Amino resin 1 35 parts by mass Didimethylaminoethanol 1.2 parts by mass Deionized water 123.8 parts by mass Then, deionized water is placed in another container at the following ratio. The stock solution 11 obtained above was added while being charged and stirred, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluent 11 for electrodeposition coating (active ingredient 8%).
Deionized water 789.4 parts by mass Undiluted solution 11 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.6 parts by mass The obtained diluent 11 for electrodeposition coating and aluminum pigment 1 are mixed in the following ratios. The mixture was stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 11.
Diluting liquid for electrodeposition coating material 11 100 parts by mass Water-dispersible aluminum pigment 13 parts by mass The electrodeposition coating film is applied in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin liquid) 11 is used. It was formed and evaluated in the same manner.
[比較例5]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて転相乳化を行ない、原液12を得た。
水分散性ビニル系共重合体溶液1 124.7質量部
アミノ樹脂1 10質量部
ジメチルアミノエタノール 1.7質量部
脱イオン水 114.6質量部
そして、下記の割合で、別の容器に脱イオン水を仕込み、攪拌しながら上記で得た原液12を投入し、次にブチルセロソルブとジメチルアミノエタノールとを添加して均一化して、電着塗料用希釈液12(有効成分8%)を得た。
脱イオン水 789.1質量部
原液12 200.0質量部
ブチルセロソルブ 10.0質量部
ジメチルアミノエタノール 0.9質量部
得られた電着塗料用希釈液12とアルミニウム顔料1とを下記割合で混合、攪拌して、水性樹脂組成物(水性電着樹脂液)12を得た。
電着塗料用希釈液12 100質量部
水分散性アルミニウム顔料1 1質量部
そして、水性樹脂組成物(水性電着樹脂ビニル系共重合体液)12を用いた以外は実施例1と同じ方法で電着塗膜を形成して、同様に評価を行った。
[Comparative Example 5]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to carry out phase inversion emulsification to obtain a stock solution 12.
Water-dispersible vinyl copolymer solution 1 124.7 parts by mass Amino resin 1 10 parts by mass Didimethylaminoethanol 1.7 parts by mass Deionized water 114.6 parts by mass Then, deionize in another container at the following ratio. Water was charged, and the undiluted solution 12 obtained above was added while stirring, and then butyl cellosolve and dimethylaminoethanol were added to homogenize the mixture to obtain a diluted solution 12 (active ingredient 8%) for electrodeposition coating.
Deionized water 789.1 parts by mass Undiluted solution 12 200.0 parts by mass Butyl cellosolve 10.0 parts by mass Dimethylaminoethanol 0.9 parts by mass The obtained diluent 12 for electrodeposition coating and aluminum pigment 1 are mixed in the following ratios. The mixture was stirred to obtain an aqueous resin composition (aqueous electrodeposition resin solution) 12.
Diluting Liquid for Electrodeposition Paint 12 100 parts by mass Water-dispersible aluminum pigment 1 1 part by mass And electroelectricity is carried out in the same manner as in Example 1 except that the aqueous resin composition (aqueous electrodeposition resin vinyl-based copolymer liquid) 12 is used. A coating film was formed and evaluated in the same manner.
[比較例6]
下記の割合で、水分散性ビニル系共重合体溶液1とアミノ樹脂1とを混合し、さらにジメチルアミノエタノールを添加混合した。攪拌を続けながら、脱イオン水を加えて原液13を得た。
しかしながら、原液13は、水溶化も転相乳化も生じず不均一であった為、以降の作業及び評価を中止した。
水分散性ビニル系共重合体溶液1 41.6質量部
アミノ樹脂1 70質量部
ジメチルアミノエタノール 0.6質量部
脱イオン水 137.8質量部
[Comparative Example 6]
The water-dispersible vinyl copolymer solution 1 and the amino resin 1 were mixed at the following ratios, and dimethylaminoethanol was further added and mixed. While continuing stirring, deionized water was added to obtain a stock solution 13.
However, since the undiluted solution 13 was non-uniform without water solubilization or phase inversion emulsification, the subsequent work and evaluation were stopped.
Water-dispersible vinyl-based copolymer solution 1 41.6 parts by mass Amino resin 1 70 parts by mass Dimethylaminoethanol 0.6 parts by mass Deionized water 137.8 parts by mass
[比較例7]
実施例1で得た水性樹脂組成物(水性電着樹脂液)1を用いて、定電流法の代わりに定電圧法(250vで10秒間印加)を用いたこと以外は、実施例1と同じ方法で電着塗装を行って、塗膜を形成して、同様に評価を行った。
[Comparative Example 7]
Same as Example 1 except that the aqueous resin composition (aqueous electrodeposition resin solution) 1 obtained in Example 1 was used and the constant voltage method (applied at 250 v for 10 seconds) was used instead of the constant current method. Electrodeposition coating was performed by the method to form a coating film, and evaluation was performed in the same manner.
<電着塗膜の評価方法>
[メタリック感]
塗装物の電着塗膜のメタリック感(金属調外観)を、目視比較によって判定した。表中の記号の意味は下記の通り。
◎:メタリック感が良好で均一。
○:メタリック感がやや不足、または少々ムラ有り。
×:メタリック感が不足またはムラ多い。
<Evaluation method of electrodeposition coating film>
[Metallic feeling]
The metallic feeling (metallic appearance) of the electrodeposited coating film of the coated material was judged by visual comparison. The meanings of the symbols in the table are as follows.
⊚: Good metallic feeling and uniform.
◯: The metallic feeling is slightly insufficient or slightly uneven.
X: Insufficient metallic feeling or a lot of unevenness.
[膜厚均一性]
渦電流式膜厚計(Fisher製ISOSCOPE)を用いて、塗装物の上面部、側面部、下面部の電着塗膜の膜厚を測定して、σ(分散)を算出して判定した。表中の記号の意味は下記の通り。
◎:σが1.0μm未満。
○:σが1.0μm以上、2.0μm未満。
×:σが2.0μm以上。
[Film thickness uniformity]
Using an eddy current type film thickness meter (ISOCOPE manufactured by Fisher), the film thickness of the electrodeposited coating film on the upper surface portion, the side surface portion, and the lower surface portion of the coated material was measured, and σ (dispersion) was calculated and determined. The meanings of the symbols in the table are as follows.
⊚: σ is less than 1.0 μm.
◯: σ is 1.0 μm or more and less than 2.0 μm.
X: σ is 2.0 μm or more.
[光沢均一性]
塗装物の側面部、上面部、下面部の電着塗膜の光沢を、60°鏡面反射率を用いて測定して、σ(分散)を算出して判定した。表中の記号の意味は下記の通り。
◎:σが5%未満。
○:σが5%以上、10%未満。
×:σが10%以上。
[Gloss uniformity]
The gloss of the electrodeposited coating film on the side surface portion, the upper surface portion, and the lower surface portion of the coated material was measured using the 60 ° mirror surface reflectance, and σ (dispersion) was calculated and determined. The meanings of the symbols in the table are as follows.
⊚: σ is less than 5%.
◯: σ is 5% or more and less than 10%.
X: σ is 10% or more.
[色調均一性]
塗装物の側面部、上面部、下面部の電着塗膜の色調を、色彩色差計CR−400(コニカミノルタ製)を用いて測定し、側面部に対する上面部及び下面部の各々の色差ΔEを算出して、平均値で判定した。表中の記号の意味は下記の通り。
◎:ΔEが1未満。
○:ΔEが1以上2未満。
×:ΔEが2以上。
[Color tone uniformity]
The color tone of the electrodeposited coating film on the side surface, upper surface, and lower surface of the painted object was measured using a color difference meter CR-400 (manufactured by Konica Minolta), and the color difference ΔE of each of the upper surface and the lower surface with respect to the side surface was measured. Was calculated and judged by the average value. The meanings of the symbols in the table are as follows.
⊚: ΔE is less than 1.
◯: ΔE is 1 or more and less than 2.
X: ΔE is 2 or more.
[密着性]
JIS K 5600−5−6に従って、塗膜に5×5=25個の碁盤状の升目を刻み入れて、テープ貼り付け及び剥離操作によって、剥離や欠けを生じなかった升目の数を数えた。表中の記号の意味は下記の通り。
◎:25個。
〇:24個以上、25個未満。
×:24個未満。
[Adhesion]
According to JIS K 5600-5-6, 5 × 5 = 25 grid-shaped squares were engraved in the coating film, and the number of squares that did not peel or chip by the tape application and peeling operation was counted. The meanings of the symbols in the table are as follows.
⊚: 25 pieces.
〇: 24 or more, less than 25.
X: Less than 24 pieces.
[耐酸性]
内径32mm、高さ30mmのリングをワセリンで塗膜表面に接触させ、リング内に、リングの高さ1/2まで5%硫酸水溶液を入れ、24時間後の外観状態を評価した。表中の記号の意味は下記の通り。
◎:腐食や膨れが無い、または僅かである。
○:腐食と膨れが見られる。
×:著しい腐食または膨れが見られる。
[Acid resistance]
A ring having an inner diameter of 32 mm and a height of 30 mm was brought into contact with the surface of the coating film with petrolatum, and a 5% aqueous sulfuric acid solution was placed in the ring to a height of 1/2 of the ring, and the appearance state after 24 hours was evaluated. The meanings of the symbols in the table are as follows.
⊚: No corrosion or swelling, or slight swelling.
◯: Corrosion and swelling are observed.
X: Significant corrosion or swelling is observed.
[耐アルカリ性]
内径32mm、高さ30mmのリングをワセリンで塗膜表面に接触させ、リング内に、リングの高さ1/2まで0.5%水酸化ナトリウム水溶液を入れ、24時間後の外観状態を評価した。表中の記号の意味は下記の通り。
◎:腐食や膨れが無い、または僅かである。
○:腐食と膨れが見られる。
×:著しい腐食または膨れが見られる。
[Alkali resistance]
A ring having an inner diameter of 32 mm and a height of 30 mm was brought into contact with the surface of the coating film with petrolatum, and a 0.5% sodium hydroxide aqueous solution was placed in the ring to a height of 1/2 of the ring, and the appearance state after 24 hours was evaluated. .. The meanings of the symbols in the table are as follows.
⊚: No corrosion or swelling, or slight swelling.
◯: Corrosion and swelling are observed.
X: Significant corrosion or swelling is observed.
[耐溶剤性]
内径32mm、高さ30mmのリングをワセリンで塗膜表面に接触させ、リング内に、リングの高さ1/2までキシレンを入れ、24時間後の外観状態を評価した。表中の記号の意味は下記の通り。
◎:腐食や膨れが無い、または僅かである。
○:腐食と膨れが見られる。
×:著しい腐食または膨れが見られる。
[Solvent resistance]
A ring having an inner diameter of 32 mm and a height of 30 mm was brought into contact with the surface of the coating film with petrolatum, xylene was put into the ring to a height of 1/2 of the ring, and the appearance state after 24 hours was evaluated. The meanings of the symbols in the table are as follows.
⊚: No corrosion or swelling, or slight swelling.
◯: Corrosion and swelling are observed.
X: Significant corrosion or swelling is observed.
<結果のまとめ>
各実施例の水性樹脂組成物(水性電着樹脂液)及びそれを用いて定電流法で電着塗装された電着塗装膜は、水性溶媒を用いたことで低VOC性を有し、表面処理された水分散性アルミニウム顔料を用いたことで経時安定性に優れ、優れたメタリック感、膜厚均一性、
光沢均一性、色調均一性、密着性、耐酸性、耐アルカリ性、耐溶剤性のバランスを示し、本発明の課題を解決するものであった。
一方、水分散性ビニル系共重合体の酸価が低すぎる比較例1は劣った耐アルカリ性及び耐溶剤性を示し、高すぎる比較例2は劣った密着性を示した。
水分散性アルミニウム顔料の含有量が低すぎる比較例3は劣ったメタリック感を示し、高すぎる比較例4は劣った耐アルカリ性を示した。
質量比(A)水分散性ビニル系共重合体/(B)アミノ樹脂が高すぎる比較例5は光沢均一性に劣り、低すぎる比較例6は水性液状樹脂組成物が水溶化も乳化転相もせず不均一であった為に、以降の評価を中断した。
定電圧法で電着塗装した比較例7はメタリック感、膜厚均一性、光沢均一性、色調均一性に劣った結果を示した。
<Summary of results>
The aqueous resin composition (aqueous electrodeposition resin solution) of each example and the electrodeposition coating film electrodeposited by the constant current method using the aqueous resin composition have low VOC properties due to the use of an aqueous solvent, and have a surface surface. By using the treated water-dispersible aluminum pigment, it has excellent stability over time, excellent metallic feeling, film thickness uniformity,
It shows a balance of gloss uniformity, color tone uniformity, adhesion, acid resistance, alkali resistance, and solvent resistance, and solves the problem of the present invention.
On the other hand, Comparative Example 1 in which the acid value of the water-dispersible vinyl-based copolymer was too low showed inferior alkali resistance and solvent resistance, and Comparative Example 2 in which the acid value was too high showed inferior adhesion.
Comparative Example 3 in which the content of the water-dispersible aluminum pigment was too low showed a poor metallic feeling, and Comparative Example 4 in which the content of the water-dispersible aluminum pigment was too high showed a poor alkali resistance.
Mass ratio (A) Water-dispersible vinyl copolymer / (B) Amino resin is too high Comparative Example 5 is inferior in gloss uniformity, and Comparative Example 6 is too low. Since it was uneven, the subsequent evaluation was interrupted.
Comparative Example 7 in which electrodeposition coating was performed by the constant voltage method showed inferior results in metallic feeling, film thickness uniformity, gloss uniformity, and color tone uniformity.
本発明のアルミニウム顔料を含有する水性樹脂組成物及び該水性樹脂組成物からなる水性電着樹脂液、水性電着塗料及びこれを用いて形成された金属調の外観を有するアルミニウム顔料を含有する電着塗膜は、意匠性及び耐食性が要求され、低VOCの要求が高い分野において好適に使用される。 An aqueous resin composition containing the aluminum pigment of the present invention, an aqueous electrodeposition resin liquid comprising the aqueous resin composition, an aqueous electrodeposition coating material, and an electroelectron containing an aluminum pigment having a metallic appearance formed by using the aqueous electrodeposition coating material. The coating film is preferably used in a field where designability and corrosion resistance are required and low VOC is required.
Claims (6)
(A)水分散性ビニル系共重合体は、置換基としてカルボキシル基を有し、酸価が20〜100mgKOHであり、水性溶媒への分散性を有し、炭素−炭素不飽和結合が(共)重合した(共)重合体であり、
質量比(A)/(B)は、40/60〜80/20であり、
質量比(C)/{(A)+(B)}は、0.1/99.9〜15/85であることを特徴とする、定電流法電着塗装用水性樹脂組成物。 (A) a water-dispersible vinyl copolymer, a (B) an amino resin and (C) a constant current method electrodeposition coating the aqueous resin composition containing a water-dispersible aluminum pigment,
The water-dispersible vinyl-based copolymer has a carboxyl group as a substituent, an acid value of 20 to 100 mgKOH, dispersibility in an aqueous solvent, and a carbon-carbon unsaturated bond (co). ) It is a polymerized (co) polymer,
The mass ratio (A) / (B) is 40/60 to 80/20.
Mass ratio (C) / {(A) + (B)} is characterized by a 0.1 / 99.9 to 15/85, a constant current method electrodeposition coating aqueous resin composition.
該表面処理アルミニウム顔料の表面は、無機リン系化合物、モリブデン系化合物、珪素系化合物、有機樹脂からなる群から選ばれる1種、または2種以上の組み合わせを含有することを特徴とする、請求項1に記載の定電流法電着塗装用水性樹脂組成物。 The water-dispersible aluminum pigment comprises a surface-treated aluminum pigment.
The surface of the surface-treated aluminum pigment is characterized by containing one kind selected from the group consisting of an inorganic phosphorus-based compound, a molybdenum-based compound, a silicon-based compound, and an organic resin, or a combination of two or more kinds. constant current method electrodeposition coating the aqueous resin composition according to 1.
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