JP2023126659A - Coating agent - Google Patents
Coating agent Download PDFInfo
- Publication number
- JP2023126659A JP2023126659A JP2023119318A JP2023119318A JP2023126659A JP 2023126659 A JP2023126659 A JP 2023126659A JP 2023119318 A JP2023119318 A JP 2023119318A JP 2023119318 A JP2023119318 A JP 2023119318A JP 2023126659 A JP2023126659 A JP 2023126659A
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- coating agent
- coating
- weight
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000011248 coating agent Substances 0.000 title claims abstract description 67
- 239000000049 pigment Substances 0.000 claims abstract description 83
- 229920005989 resin Polymers 0.000 claims abstract description 43
- 239000011347 resin Substances 0.000 claims abstract description 43
- 239000000843 powder Substances 0.000 claims abstract description 27
- 239000007787 solid Substances 0.000 claims abstract description 13
- 239000004606 Fillers/Extenders Substances 0.000 claims abstract description 9
- 238000000576 coating method Methods 0.000 claims description 25
- 230000001747 exhibiting effect Effects 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 5
- 239000008199 coating composition Substances 0.000 claims description 2
- 239000006224 matting agent Substances 0.000 claims description 2
- 239000012508 resin bead Substances 0.000 claims description 2
- 238000007761 roller coating Methods 0.000 abstract description 8
- 238000004040 coloring Methods 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 description 17
- -1 alicyclic hydrocarbon Chemical class 0.000 description 16
- 239000002245 particle Substances 0.000 description 14
- 229920005862 polyol Polymers 0.000 description 12
- 229910052782 aluminium Inorganic materials 0.000 description 11
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- 238000004132 cross linking Methods 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 229910044991 metal oxide Inorganic materials 0.000 description 7
- 150000004706 metal oxides Chemical class 0.000 description 7
- 239000002562 thickening agent Substances 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 239000002131 composite material Substances 0.000 description 6
- 238000010422 painting Methods 0.000 description 6
- 239000005056 polyisocyanate Substances 0.000 description 6
- 229920001228 polyisocyanate Polymers 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000009792 diffusion process Methods 0.000 description 5
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 4
- 238000006757 chemical reactions by type Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 239000010445 mica Substances 0.000 description 4
- 229910052618 mica group Inorganic materials 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical compound O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- AVWRKZWQTYIKIY-UHFFFAOYSA-N urea-1-carboxylic acid Chemical compound NC(=O)NC(O)=O AVWRKZWQTYIKIY-UHFFFAOYSA-N 0.000 description 3
- UPMLOUAZCHDJJD-UHFFFAOYSA-N 4,4'-Diphenylmethane Diisocyanate Chemical compound C1=CC(N=C=O)=CC=C1CC1=CC=C(N=C=O)C=C1 UPMLOUAZCHDJJD-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
- 239000004721 Polyphenylene oxide Substances 0.000 description 2
- 239000004113 Sepiolite Substances 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000005456 alcohol based solvent Substances 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000003125 aqueous solvent Substances 0.000 description 2
- 229960000892 attapulgite Drugs 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- 125000003700 epoxy group Chemical group 0.000 description 2
- 239000003759 ester based solvent Substances 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 210000004209 hair Anatomy 0.000 description 2
- 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 2
- 230000001771 impaired effect Effects 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- BKIMMITUMNQMOS-UHFFFAOYSA-N nonane Chemical compound CCCCCCCCC BKIMMITUMNQMOS-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229910052625 palygorskite Inorganic materials 0.000 description 2
- 239000011120 plywood Substances 0.000 description 2
- 229920000570 polyether Polymers 0.000 description 2
- 229920005749 polyurethane resin Polymers 0.000 description 2
- 230000009257 reactivity Effects 0.000 description 2
- 238000005096 rolling process Methods 0.000 description 2
- DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide group Chemical group NNC(=O)N DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 description 2
- 229910052624 sepiolite Inorganic materials 0.000 description 2
- 235000019355 sepiolite Nutrition 0.000 description 2
- 229920002050 silicone resin Polymers 0.000 description 2
- 238000007592 spray painting technique Methods 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 2
- 239000010456 wollastonite Substances 0.000 description 2
- 229910052882 wollastonite Inorganic materials 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- HZVFRKSYUGFFEJ-YVECIDJPSA-N (2r,3r,4s,5r)-7-phenylhept-6-ene-1,2,3,4,5,6-hexol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=CC1=CC=CC=C1 HZVFRKSYUGFFEJ-YVECIDJPSA-N 0.000 description 1
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 1
- 125000003504 2-oxazolinyl group Chemical group O1C(=NCC1)* 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- GXDVEXJTVGRLNW-UHFFFAOYSA-N [Cr].[Cu] Chemical compound [Cr].[Cu] GXDVEXJTVGRLNW-UHFFFAOYSA-N 0.000 description 1
- WBWJXRJARNTNBL-UHFFFAOYSA-N [Fe].[Cr].[Co] Chemical compound [Fe].[Cr].[Co] WBWJXRJARNTNBL-UHFFFAOYSA-N 0.000 description 1
- BQCFCWXSRCETDO-UHFFFAOYSA-N [Fe].[Mn].[Cu] Chemical compound [Fe].[Mn].[Cu] BQCFCWXSRCETDO-UHFFFAOYSA-N 0.000 description 1
- RJDOZRNNYVAULJ-UHFFFAOYSA-L [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] RJDOZRNNYVAULJ-UHFFFAOYSA-L 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000003463 adsorbent Substances 0.000 description 1
- 239000003619 algicide Substances 0.000 description 1
- 125000003545 alkoxy group Chemical group 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
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000004069 aziridinyl group Chemical group 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- VPKDCDLSJZCGKE-UHFFFAOYSA-N carbodiimide group Chemical group N=C=N VPKDCDLSJZCGKE-UHFFFAOYSA-N 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- SXKJCXWNWBRZGB-UHFFFAOYSA-N chromium copper manganese Chemical compound [Mn][Cr][Cu] SXKJCXWNWBRZGB-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- KORSJDCBLAPZEQ-UHFFFAOYSA-N dicyclohexylmethane-4,4'-diisocyanate Chemical compound C1CC(N=C=O)CCC1CC1CCC(N=C=O)CC1 KORSJDCBLAPZEQ-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000005315 distribution function Methods 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 239000004210 ether based solvent Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- DALUDRGQOYMVLD-UHFFFAOYSA-N iron manganese Chemical compound [Mn].[Fe] DALUDRGQOYMVLD-UHFFFAOYSA-N 0.000 description 1
- WTFXARWRTYJXII-UHFFFAOYSA-N iron(2+);iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+2].[Fe+3].[Fe+3] WTFXARWRTYJXII-UHFFFAOYSA-N 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- NIMLQBUJDJZYEJ-UHFFFAOYSA-N isophorone diisocyanate Chemical compound CC1(C)CC(N=C=O)CC(C)(CN=C=O)C1 NIMLQBUJDJZYEJ-UHFFFAOYSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 239000004611 light stabiliser Substances 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000010534 mechanism of action Effects 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- NDLPOXTZKUMGOV-UHFFFAOYSA-N oxo(oxoferriooxy)iron hydrate Chemical compound O.O=[Fe]O[Fe]=O NDLPOXTZKUMGOV-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920005906 polyester polyol Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000015096 spirit Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- RSJKGSCJYJTIGS-UHFFFAOYSA-N undecane Chemical compound CCCCCCCCCCC RSJKGSCJYJTIGS-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
Abstract
Description
本発明は、新規なコーティング剤に関するものである。 The present invention relates to a novel coating agent.
従来、光輝性を示すコーティング剤は、例えば、構造物、建築物、車両、家電等に用いられている。このようなコーティング剤には、光輝性顔料が含まれており、その光輝性を発揮させるため、コーティング剤の塗装はスプレーによって行われることが一般的である。 Conventionally, coating agents exhibiting glittering properties have been used for, for example, structures, buildings, vehicles, home appliances, and the like. Such a coating agent contains a glittering pigment, and in order to exhibit its glittering properties, the coating agent is generally applied by spraying.
例えば、特許文献1(特開2010-209276号公報)には、ウレタン樹脂、有機溶剤、及び光輝性顔料等を含むコーティング剤をスプレー塗装によって被塗物に塗着すると、有機溶剤の揮発に伴う光輝性顔料の配向によって、光輝性に優れた被膜が形成されることが記載されている。 For example, Patent Document 1 (Japanese Unexamined Patent Publication No. 2010-209276) states that when a coating agent containing a urethane resin, an organic solvent, a bright pigment, etc. is applied to an object by spray painting, the organic solvent evaporates and It is described that a film with excellent glitter can be formed by aligning the glitter pigment.
しかしながら、特許文献1のようにスプレー塗装を行う場合、塗装時に周辺への飛散が生じるため、塗装前に入念な養生が必要となり、また、飛散による材料ロスも多くなるおそれがある。 However, when spray painting is performed as in Patent Document 1, scattering occurs to the surrounding area during painting, so careful curing is required before painting, and there is also a risk that material loss due to scattering may increase.
このような問題点を解消するには、ローラー等で塗装を行う方法がある。ところが、光輝性を示すコーティング剤をローラー塗装すると、塗り継ぎ部分が目立つ仕上りとなりやすく、光輝性の外観が損なわれるおそれがある。 To solve this problem, there is a method of painting with a roller or the like. However, when a coating agent exhibiting glittering properties is applied with a roller, the finished area tends to be noticeable at the joints, and there is a risk that the glittering appearance may be impaired.
本発明は、このような点に鑑みなされたものであり、ローラー塗装等によって光輝性被膜が形成可能なコーティング剤を提供することを目的とするものである。 The present invention has been made in view of these points, and an object of the present invention is to provide a coating agent that can form a glittering film by roller coating or the like.
このような課題を解決するために本発明者は、鋭意検討の結果、樹脂成分、光輝性顔料、及び体質顔料として鱗片状粉体を特定比率で含むコーティング剤に想到し、本発明の完成に到った。 In order to solve these problems, the inventor of the present invention, as a result of intensive studies, came up with a coating agent containing a resin component, a bright pigment, and a scaly powder as an extender pigment in a specific ratio, and completed the present invention. It has arrived.
すなわち、本発明は以下の特徴を有するものである。
1.光輝性を示すコーティング剤であって、
樹脂成分(A)、光輝性顔料(B)、及び、体質顔料として鱗片状粉体(C)を含み、
前記樹脂成分(A)の固形分100重量部に対し、前記光輝性顔料(B)を1~20重量部、前記鱗片状粉体(C)を0.1~50重量部含むことを特徴とするコーティング剤(但し、艶消し剤、樹脂ビーズ、及び光輝材を含む塗料組成物を除く)。
2.さらに着色顔料(D)を含むことを特徴とする1.記載のコーティング剤。
3.繊維質ローラー塗装によって光輝性被膜が形成可能なものであることを特徴とする1.記載のコーティング剤。
That is, the present invention has the following features.
1. A coating agent exhibiting glittering properties,
A resin component (A), a bright pigment (B), and a scaly powder (C) as an extender pigment,
It is characterized by containing 1 to 20 parts by weight of the glittering pigment (B) and 0.1 to 50 parts by weight of the scaly powder (C) based on 100 parts by weight of the solid content of the resin component (A). (excluding coating compositions containing matting agents, resin beads, and glittering materials) .
2. 1. characterized by further containing a coloring pigment (D); Coating agent as described.
3. 1. A glittering film can be formed by coating with a fibrous roller. Coating agent as described.
本発明によれば、ローラー塗装等によって光輝性被膜が形成可能なコーティング剤を得ることができる。 According to the present invention, a coating agent that can form a glittering film by roller coating or the like can be obtained.
以下、本発明を実施するための形態について説明する。 EMBODIMENT OF THE INVENTION Hereinafter, the form for implementing this invention is demonstrated.
本発明のコーティング剤は、その形成被膜が光輝性を示すものであり、構成成分として、樹脂成分(A)、光輝性顔料(B)、及び、体質顔料として鱗片状粉体(C)を含む。 The coating agent of the present invention exhibits a glittering film formed thereon, and contains a resin component (A), a glittering pigment (B), and a scaly powder (C) as an extender pigment. .
このうち、樹脂成分(A)としては、例えば、アクリル樹脂、ポリエステル樹脂、ポリエーテル樹脂、ポリウレタン樹脂、アクリルシリコン樹脂、フッ素樹脂、酢酸ビニル樹脂、エポキシ樹脂等、あるいはこれらの複合系等を挙げることができる。これらは1種または2種以上で使用することができる。このような樹脂成分(A)の形態としては、水溶性樹脂、水分散性樹脂等の水性樹脂、溶剤可溶性樹脂、非水分散性樹脂等の非水系樹脂、あるいは無溶剤型樹脂等が挙げられる。樹脂成分(A)のガラス転移温度は、好ましくは-20~80℃、より好ましくは-10~60℃である。なお、本発明において、「a~b」は「a以上b以下」と同義である。 Among these, examples of the resin component (A) include acrylic resins, polyester resins, polyether resins, polyurethane resins, acrylic silicone resins, fluorine resins, vinyl acetate resins, epoxy resins, and composite systems thereof. I can do it. These can be used alone or in combination of two or more. Examples of the form of the resin component (A) include water-based resins such as water-soluble resins and water-dispersible resins, non-aqueous resins such as solvent-soluble resins and non-water-dispersible resins, and solvent-free resins. . The glass transition temperature of the resin component (A) is preferably -20 to 80°C, more preferably -10 to 60°C. In the present invention, "a to b" has the same meaning as "a or more and b or less".
上記樹脂成分(A)のうち、水性樹脂は、媒体として水を含むものである。一方、非水系樹脂は、非水系溶剤を媒体とするものである。非水系溶剤としては、例えば、n-へプタン、n-ヘキサン、n-ペンタン、n-オクタン、n-ノナン、n-デカン、n-ウンデカン、n-ドデカン等の脂肪族炭化水素溶剤、メチルシクロヘキサン、エチルシクロヘキサン等の脂環族炭化水素溶剤、ミネラルスピリット等の脂肪族炭化水素含有混合溶剤、石油エーテル、石油ナフサ、ソルベントナフサ、ケロシン等の石油系溶剤等の他、イソパラフィン系溶剤、アルコール系溶剤、エーテルアルコール系溶剤、エーテル系溶剤、エステル系溶剤、エーテルエステル系溶剤、ケトン系溶剤等が挙げられる。これらは、1種または2種以上で使用できる。 Among the resin components (A), the aqueous resin contains water as a medium. On the other hand, non-aqueous resins use non-aqueous solvents as a medium. Examples of non-aqueous solvents include aliphatic hydrocarbon solvents such as n-heptane, n-hexane, n-pentane, n-octane, n-nonane, n-decane, n-undecane, and n-dodecane, and methylcyclohexane. , alicyclic hydrocarbon solvents such as ethylcyclohexane, mixed solvents containing aliphatic hydrocarbons such as mineral spirits, petroleum solvents such as petroleum ether, petroleum naphtha, solvent naphtha, kerosene, isoparaffin solvents, alcohol solvents, etc. , ether-alcohol solvents, ether-based solvents, ester-based solvents, ether-ester-based solvents, ketone-based solvents, and the like. These can be used alone or in combination of two or more.
本発明における樹脂成分(A)は架橋反応性を有するものであってもよい。樹脂成分(A)が架橋反応型樹脂である場合は、被膜の強度、耐水性、耐候性、密着性等を高めることができる。架橋反応型樹脂は、それ自体で架橋反応を生じるもの、あるいは別途混合する架橋剤によって架橋反応を生じるもののいずれであってもよい。このような架橋反応性は、例えば、水酸基とイソシアネート基、カルボニル基とヒドラジド基、エポキシ基とアミノ基、アルド基とセミカルバジド基、ケト基とセミカルバジド基、アルコキシル基どうし、カルボキシル基と金属イオン、カルボキシル基とカルボジイミド基、カルボキシル基とエポキシ基、カルボキシル基とアジリジン基、カルボキシル基とオキサゾリン基等の反応性官能基を組み合わせることによって付与することができる。この中でも水酸基-イソシアート基架橋反応型樹脂が好適である。 The resin component (A) in the present invention may have crosslinking reactivity. When the resin component (A) is a crosslinking reaction type resin, the strength, water resistance, weather resistance, adhesion, etc. of the coating can be improved. The crosslinking reaction type resin may be one that causes a crosslinking reaction by itself, or one that causes a crosslinking reaction by a crosslinking agent that is mixed separately. Such crosslinking reactivity is caused by, for example, hydroxyl groups and isocyanate groups, carbonyl groups and hydrazide groups, epoxy groups and amino groups, aldo groups and semicarbazide groups, keto groups and semicarbazide groups, alkoxyl groups, carboxyl groups and metal ions, and carboxyl groups. It can be provided by combining reactive functional groups such as a group and a carbodiimide group, a carboxyl group and an epoxy group, a carboxyl group and an aziridine group, and a carboxyl group and an oxazoline group. Among these, hydroxyl group-isocyanate group crosslinking reaction type resins are preferred.
水酸基-イソシアート基架橋反応型樹脂としては、例えば、樹脂成分(A)として、ポリオール化合物と、ポリイソシアネート化合物とを含む態様が挙げられる。これら両成分は、被膜形成時に反応硬化して、ポリウレタン樹脂被膜を形成することができるものである。 Examples of the hydroxyl group-isocyanate group crosslinking reaction type resin include an embodiment containing a polyol compound and a polyisocyanate compound as the resin component (A). Both of these components can be reacted and cured during film formation to form a polyurethane resin film.
このうち、ポリオール化合物としては、例えば、例えば、ポリエーテルポリオール、ポリエステルポリオール、アクリルポリオール、含フッ素ポリオール、ポリイソプレンポリオール、カーボネートポリオール等が挙げられ、これらの1種または2種以上が使用できる。ポリオール化合物の水酸基価は、好ましくは10~200KOHmg/g、より好ましくは20~100KOHmg/gである。水酸基価は、樹脂固形分1gに含まれる水酸基と等モルの水酸化カリウムのmg数によって表される値である。また、ポリオール化合物の重量平均分子量は、好ましくは10000~150000である。重量平均分子量は、ゲルパーミエーションクロマトグラフィーを用いて測定して得られる値である。 Among these, examples of the polyol compound include polyether polyol, polyester polyol, acrylic polyol, fluorine-containing polyol, polyisoprene polyol, carbonate polyol, etc., and one or more of these can be used. The hydroxyl value of the polyol compound is preferably 10 to 200 KOHmg/g, more preferably 20 to 100 KOHmg/g. The hydroxyl value is a value expressed by the number of mg of potassium hydroxide equivalent to the hydroxyl group contained in 1 g of resin solid content. Further, the weight average molecular weight of the polyol compound is preferably 10,000 to 150,000. The weight average molecular weight is a value obtained by measurement using gel permeation chromatography.
ポリイソシアネート化合物は、1分子中に2以上のイソシアネート基を有するものであり、上記ポリオール化合物と架橋反応して被膜を形成するものである。ポリイソシアネート化合物としては、例えば、トルエンジイソシアネート(TDI)、4,4-ジフェニルメタンジイソシアネート(pure-MDI)、ポリメリックMDI、キシリレンジイソシアネート(XDI)、ヘキサメチレンジイソシアネート(HMDI)、イソホロンジイソシアネート(IPDI)、水添XDI、水添MDI等、あるいはこれらの誘導体(例えば、ウレタン化反応、アロファネート化反応、イソシアヌレート化反応等によって得られる化合物)が挙げられ、アロファネート基を有するもの、アロファネート基及びイソシアヌレート基を有するもの等も使用することができる。これらは、1種または2種以上で使用できる。 The polyisocyanate compound has two or more isocyanate groups in one molecule, and forms a film by crosslinking with the polyol compound. Examples of the polyisocyanate compound include toluene diisocyanate (TDI), 4,4-diphenylmethane diisocyanate (pure-MDI), polymeric MDI, xylylene diisocyanate (XDI), hexamethylene diisocyanate (HMDI), isophorone diisocyanate (IPDI), and water. Examples include doped XDI, hydrogenated MDI, etc., or derivatives thereof (for example, compounds obtained by urethanation reaction, allophanate reaction, isocyanurate reaction, etc.), and those having allophanate groups, allophanate groups and isocyanurate groups. You can also use what you have. These can be used alone or in combination of two or more.
ポリイソシアネート化合物の混合比率は、ポリオール化合物の水酸基に対する、ポリイソシアネート化合物のイソシアネート基の当量比、すなわちNCO/OH比を考慮して設定すればよい。NCO/OH比は、好ましくは0.6~1.4、より好ましくは0.8~1.2である。 The mixing ratio of the polyisocyanate compound may be set in consideration of the equivalent ratio of the isocyanate groups of the polyisocyanate compound to the hydroxyl groups of the polyol compound, that is, the NCO/OH ratio. The NCO/OH ratio is preferably between 0.6 and 1.4, more preferably between 0.8 and 1.2.
光輝性顔料(B)は、形成被膜に光輝性を付与する成分である。光輝性顔料としては、例えば、アルミニウムフレーク顔料、蒸着アルミニウムフレーク顔料、金属酸化物被覆アルミニウムフレーク顔料、着色アルミニウムフレーク顔料等のアルミニウムフレーク顔料;金属酸化物被覆マイカ顔料、金属酸化物被覆合成マイカ顔料、金属めっきマイカ顔料等のマイカ顔料;金属被覆ガラスフレーク顔料、金属酸化物被覆ガラスフレーク顔料、金属めっきガラスフレーク顔料等のガラスフレーク顔料;あるいは、チタンフレーク顔料、ステンレスフレーク顔料、金属酸化物被覆板状酸化鉄、金属酸化物被覆シリカフレーク顔料、金属酸化物被覆アルミナフレーク顔料等が挙げられる。これらは、1種または2種以上で使用できる。このうち、光輝性顔料(B)としては、アルミニウムフレーク顔料が好ましい。アルミニウムフレーク顔料としては、リーフィング型、及び/またはノンリーフィング型が使用できる。 The glitter pigment (B) is a component that imparts glitter to the formed film. Examples of bright pigments include aluminum flake pigments such as aluminum flake pigments, vapor-deposited aluminum flake pigments, metal oxide-coated aluminum flake pigments, and colored aluminum flake pigments; metal oxide-coated mica pigments, metal oxide-coated synthetic mica pigments, Mica pigments such as metal-plated mica pigments; glass flake pigments such as metal-coated glass flake pigments, metal oxide-coated glass flake pigments, and metal-plated glass flake pigments; or titanium flake pigments, stainless steel flake pigments, and metal oxide-coated platelets. Examples include iron oxide, metal oxide-coated silica flake pigments, metal oxide-coated alumina flake pigments, and the like. These can be used alone or in combination of two or more. Among these, aluminum flake pigments are preferred as the glitter pigment (B). As the aluminum flake pigment, leafing type and/or non-leafing type can be used.
光輝性顔料(B)の平均粒子径は、好ましくは1~20μm、より好ましくは3~15μmである。本発明では、このような平均粒子径を有する光輝性顔料(B)の使用により、光輝性を付与しつつ、被膜の透け等に起因するムラを抑制することができ、美観性を高めることができる。なお、本発明において、平均粒子径はメディアン径(d50)、すなわち正規分布関数から求められる体積基準の50%粒径の値であり、レーザー回折式粒度分布測定装置を用いて測定することができる。光輝性顔料(B)の平均厚みは、好ましくは0.05~0.3μmである。 The average particle diameter of the bright pigment (B) is preferably 1 to 20 μm, more preferably 3 to 15 μm. In the present invention, by using the glitter pigment (B) having such an average particle diameter, it is possible to impart glitter while suppressing unevenness caused by transparency of the coating, thereby improving the aesthetic appearance. can. In addition, in the present invention, the average particle diameter is the median diameter (d50), that is, the value of 50% particle diameter on a volume basis determined from a normal distribution function, and can be measured using a laser diffraction particle size distribution measuring device. . The average thickness of the glitter pigment (B) is preferably 0.05 to 0.3 μm.
光輝性顔料(B)は、JIS K5906:2009で規定される水面拡散面積が10000~50000cm 2/gであることが好ましく、より好ましくは15000~45000cm 2/g、さらに好ましくは16000~40000cm 2/gである。このような物性値を有する光輝性顔料(B)の使用は、被膜の透け等に起因するムラの抑制、美観性の向上等の点で有利に作用する。 The bright pigment (B) preferably has a water surface diffusion area defined by JIS K5906:2009 of 10,000 to 50,000 cm 2 /g, more preferably 15,000 to 45,000 cm 2 /g, and even more preferably 16,000 to 40,000 cm 2 /g . It is g. The use of the glittering pigment (B) having such physical properties is advantageous in terms of suppressing unevenness caused by transparency of the film, improving aesthetics, and the like.
光輝性顔料(B)の混合比率は、樹脂成分(A)の固形分100重量部に対し1~20重量部であり、好ましくは2~17重量部、より好ましくは3~15重量部である。光輝性顔料(B)の混合比率が上記下限以上であることにより、形成被膜に光輝性を付与することができ、被膜の透け等に起因するムラを抑制することも可能となる。光輝性顔料(B)の混合比率が上記上限以下であることにより、ローラー塗装時等において、塗り継ぎ部分が目立ちにくい仕上りを得ることができ、美観性を高めることができる。 The mixing ratio of the bright pigment (B) is 1 to 20 parts by weight, preferably 2 to 17 parts by weight, and more preferably 3 to 15 parts by weight based on 100 parts by weight of the solid content of the resin component (A). . When the mixing ratio of the glittering pigment (B) is at least the above-mentioned lower limit, glittering properties can be imparted to the formed film, and it is also possible to suppress unevenness due to transparency of the film and the like. When the mixing ratio of the bright pigment (B) is below the above upper limit, it is possible to obtain a finish in which the joint area is less noticeable during roller coating, etc., and the aesthetic appearance can be improved.
本発明では、体質顔料として鱗片状粉体(C)を含む。本発明では、この鱗片状粉体(C)を必須成分として含むことにより、ローラー塗装時等における塗り継ぎ部分を目立ちにくくし、光輝性を示す美観性の高い被膜を形成することができる。その作用機構は以下に限定されるものではないが、鱗片状粉体(C)は、光輝性顔料(B)の光輝性を阻害することなく、被膜形成時に光輝性顔料(B)の配向性を促していることが寄与しているものと推察される。 In the present invention, a scaly powder (C) is included as an extender pigment. In the present invention, by including this scaly powder (C) as an essential component, it is possible to make the joint parts during roller coating etc. less noticeable and to form a highly aesthetically pleasing coating that exhibits glitter. The mechanism of action is not limited to the following, but the scaly powder (C) can improve the orientation of the bright pigment (B) during film formation without inhibiting the brightness of the bright pigment (B). It is assumed that this is due to the promotion of
鱗片状粉体(C)の具体例としては、例えば、タルク、マイカ、カオリン、クレー等、あるいはこれらの焼成品等が挙げられ、これらは1種または2種以上で使用できる。鱗片状粉体(C)の平均粒子径は、好ましくは0.1~20μm、より好ましくは0.3~12μmである。このような平均粒子径を有する鱗片状粉体(C)の使用により、本発明の効果を安定的に得ることができる。 Specific examples of the scale-like powder (C) include talc, mica, kaolin, clay, etc., and baked products thereof, and these can be used alone or in combination of two or more. The average particle diameter of the scaly powder (C) is preferably 0.1 to 20 μm, more preferably 0.3 to 12 μm. By using the scale-like powder (C) having such an average particle diameter, the effects of the present invention can be stably obtained.
鱗片状粉体(C)の混合比率は、樹脂成分(A)の固形分100重量部に対し0.1~50重量部であり、好ましくは0.3~30重量部、より好ましくは0.5~20重量部、さらに好ましくは1~15重量部である。鱗片状粉体(C)の混合比率が上記下限以上であることにより、光輝性を付与しつつ、ローラー塗装時等において塗り継ぎ部分が目立ちにくい仕上りを得ることができ、美観性を高めることができる。鱗片状粉体(C)の混合比率が上記上限以下であることにより、十分な光輝性を示す被膜が形成でき、光沢感等の点でも好適である。 The mixing ratio of the scaly powder (C) is 0.1 to 50 parts by weight, preferably 0.3 to 30 parts by weight, more preferably 0.3 to 30 parts by weight, based on 100 parts by weight of the solid content of the resin component (A). The amount is 5 to 20 parts by weight, more preferably 1 to 15 parts by weight. By having the mixing ratio of the scale-like powder (C) equal to or higher than the above lower limit, it is possible to obtain a finish that makes the joints less noticeable during roller coating, etc., while imparting shine, and improves aesthetics. can. When the mixing ratio of the scale-like powder (C) is at most the above upper limit, a film exhibiting sufficient glitter can be formed, which is also suitable in terms of glossiness and the like.
本発明コーティング剤では、上述の成分に加え、さらに着色顔料(D)を含むことができる。本発明では、着色顔料(D)の混合により、種々の色調を呈する光輝性被膜を形成することができる。 The coating agent of the present invention may further contain a colored pigment (D) in addition to the above-mentioned components. In the present invention, by mixing the colored pigments (D), glitter coatings exhibiting various tones can be formed.
着色顔料(D)としては、例えば、酸化第二鉄(弁柄)、黄色酸化鉄、群青、コバルトグリーン等の無機有彩色顔料;アゾ系、ナフトール系、ピラゾロン系、アントラキノン系、ペリレン系、キナクリドン系、ジスアゾ系、イソインドリノン系、ベンゾイミダゾール系、フタロシアニン系、キノフタロン系等の有機有彩色顔料;カーボンブラック、鉄‐マンガン複合酸化物、鉄‐銅‐マンガン複合酸化物、鉄‐クロム‐コバルト複合酸化物、銅‐クロム複合酸化物、銅‐マンガン‐クロム複合酸化物、黒色酸化鉄等の黒色顔料;酸化チタン、酸化亜鉛、アルミナ等の白色顔料等が挙げられる。これら着色顔料(D)の1種または2種以上を用いることにより、コーティング剤を所望の色調に着色することができる。 Coloring pigments (D) include, for example, inorganic chromatic pigments such as ferric oxide (bengara), yellow iron oxide, ultramarine, and cobalt green; azo-based, naphthol-based, pyrazolone-based, anthraquinone-based, perylene-based, and quinacridone. Organic chromatic pigments such as chromatic, disazo, isoindolinone, benzimidazole, phthalocyanine, and quinophthalone; carbon black, iron-manganese composite oxide, iron-copper-manganese composite oxide, iron-chromium-cobalt Examples include black pigments such as composite oxide, copper-chromium composite oxide, copper-manganese-chromium composite oxide, and black iron oxide; white pigments such as titanium oxide, zinc oxide, and alumina. By using one or more of these color pigments (D), the coating agent can be colored in a desired color tone.
着色顔料(D)の混合比率は、樹脂成分(A)の固形分100重量部に対し、好ましくは0.01~20重量部であり、より好ましくは0.05~15重量部である。着色顔料(D)の混合比率が上記下限以上であることにより、所望の色調を付与することが可能となり、淡色から濃色にわたる種々の光輝性被膜が形成でき、被膜の透け等に起因するムラ抑制の点でも有利となる。着色顔料(D)の混合比率が上記上限以下であることにより、十分な光輝性を示す被膜が形成できる。 The mixing ratio of the colored pigment (D) is preferably 0.01 to 20 parts by weight, more preferably 0.05 to 15 parts by weight, based on 100 parts by weight of the solid content of the resin component (A). When the mixing ratio of the coloring pigment (D) is equal to or higher than the above lower limit, it becomes possible to impart a desired color tone, form a variety of bright coatings ranging from light colors to dark colors, and prevent unevenness caused by transparency of the coating, etc. It is also advantageous in terms of suppression. When the mixing ratio of the color pigment (D) is at most the above upper limit, a film exhibiting sufficient glitter can be formed.
本発明コーティング剤では、上記鱗片状粉体(C)以外の体質顔料を含むことができる。このような体質顔料としては、例えば、重質炭酸カルシウム、軽微性炭酸カルシウム、カオリン、陶土、珪藻土、含水微粉珪酸、バライト粉、硫酸バリウム、沈降性硫酸バリウム、炭酸バリウム、炭酸マグネシウム、シリカ粉、水酸化アルミニウム、セピオライト、モンロリロナイト、ウォラストナイト、アタパルジャイト等が挙げられる。これらは1種または2種以上で使用できる。 The coating agent of the present invention may contain extender pigments other than the scale-like powder (C). Examples of such extender pigments include heavy calcium carbonate, light calcium carbonate, kaolin, china clay, diatomaceous earth, hydrated fine silicic acid, barite powder, barium sulfate, precipitated barium sulfate, barium carbonate, magnesium carbonate, silica powder, Examples include aluminum hydroxide, sepiolite, montrollilonite, wollastonite, and attapulgite. These can be used alone or in combination of two or more.
上記体質顔料としては、例えば、セピオライト、モンロリロナイト、ウォラストナイト、アタパルジャイト等の針状粉体が好適である。このような針状粉体を混合することにより、光輝性の向上化、塗り継ぎ部分の仕上り性向上化等を図ることができる。このような針状粉体は、光輝性顔料(B)の配向性を補助するように作用するものと考えられる。 As the extender pigment, for example, acicular powders such as sepiolite, montrorillonite, wollastonite, and attapulgite are suitable. By mixing such acicular powder, it is possible to improve the shine, the finish of the joint area, and the like. It is thought that such acicular powder acts to assist the orientation of the glitter pigment (B).
針状粉体の混合比率は、樹脂成分(A)の固形分100重量部に対し、好ましくは0.1~20重量部であり、好ましくは0.5~13重量部、より好ましくは1~10重量部である。 The mixing ratio of the acicular powder is preferably 0.1 to 20 parts by weight, preferably 0.5 to 13 parts by weight, more preferably 1 to 13 parts by weight, based on 100 parts by weight of the solid content of the resin component (A). It is 10 parts by weight.
本発明コーティング剤は、増粘剤を含むことができる。増粘剤としては、例えば、有機ベントナイト、微粉シリカ、表面処理炭酸カルシウム、アマイドワックス、水添ヒマシ油ワックス、ベンジリデンソルビトール、金属石鹸、酸化ポリエチレン、重合植物油、ポリカルボン酸アミン塩等が挙げられる。これらは、1種または2種以上で使用できる。本発明では、光輝性の向上化、塗り継ぎ部分の仕上り性向上化等の観点から、酸化ポリエチレンを含むことが望ましい。 The coating agent of the present invention can contain a thickener. Examples of the thickener include organic bentonite, finely divided silica, surface-treated calcium carbonate, amide wax, hydrogenated castor oil wax, benzylidene sorbitol, metal soap, polyethylene oxide, polymerized vegetable oil, and polycarboxylic acid amine salt. These can be used alone or in combination of two or more. In the present invention, it is desirable to include oxidized polyethylene from the viewpoints of improving glitter, improving finish of joint areas, etc.
増粘剤の混合比率は、樹脂成分(A)の固形分100重量部に対して、固形分換算で好ましくは0.01~10重量部、より好ましくは0.05~5重量部である。 The mixing ratio of the thickener is preferably 0.01 to 10 parts by weight, more preferably 0.05 to 5 parts by weight in terms of solid content, based on 100 parts by weight of the solid content of resin component (A).
本発明コーティング剤は、本発明の効果が著しく損われない範囲内であれば、上記成分以外の各種添加剤を含むものであってもよい。このような添加剤としては、例えば、レベリング剤、造膜助剤、凍結防止剤、pH調整剤、湿潤剤、可塑剤、防腐剤、防黴剤、防藻剤、抗菌剤、分散剤、消泡剤、吸着剤、架橋剤、紫外線吸収剤、光安定剤、酸化防止剤、低汚染化剤、親水化剤、撥水剤、触媒、溶剤等が挙げられる。本発明コーティング剤は、上記成分、及び必要に応じこのような添加剤を常法によって均一に混合することで製造できる。コーティング剤の形態は、例えば、1液型、2液型、またはそれ以上の多液型とすることができる。 The coating agent of the present invention may contain various additives other than the above-mentioned components, as long as the effects of the present invention are not significantly impaired. Examples of such additives include leveling agents, film-forming aids, antifreeze agents, pH adjusters, wetting agents, plasticizers, preservatives, fungicides, algaecides, antibacterial agents, dispersants, and disinfectants. Examples include foaming agents, adsorbents, crosslinking agents, ultraviolet absorbers, light stabilizers, antioxidants, anti-staining agents, hydrophilic agents, water repellents, catalysts, and solvents. The coating agent of the present invention can be produced by uniformly mixing the above components and, if necessary, such additives by a conventional method. The form of the coating agent can be, for example, a one-part type, a two-part type, or a multi-part type.
本発明コーティング剤の加熱残分は、好ましくは60重量%以下であり、より好ましくは30~60重量%、さらに好ましくは40~55重量%である。加熱残分が上記下限以上であることにより、被膜の透け抑制等の点で好適であり、ムラの発生を抑制し、美観性を高めることができる。加熱残分が上記上限以下であることにより、コーティング剤の粘度が調整しやすく、塗り継ぎ部分の仕上り性等を高めることができる。なお、加熱残分は、JIS K5601-1-2の方法にて測定される値であり、加熱温度は105℃、加熱時間は60分である。 The heating residue of the coating agent of the present invention is preferably 60% by weight or less, more preferably 30 to 60% by weight, still more preferably 40 to 55% by weight. When the heating residue is at least the above lower limit, it is suitable for suppressing the film from showing through, suppressing the occurrence of unevenness, and improving the aesthetic appearance. When the heating residue is below the above-mentioned upper limit, the viscosity of the coating agent can be easily adjusted, and the finish of the joint area can be improved. Note that the heating residue is a value measured by the method of JIS K5601-1-2, the heating temperature is 105° C., and the heating time is 60 minutes.
本発明コーティング剤の顔料体積濃度は、好ましくは15%以下、より好ましくは3~10%、さらに好ましくは5~9.8%である。顔料体積濃度をこのような範囲内に設定することにより、本発明の効果を十分に得ることができる。なお、顔料体積濃度は、乾燥被膜中に含まれる顔料の容積百分率であり、コーティング剤を構成する樹脂成分及び顔料の混合量から計算により求められる値である。 The pigment volume concentration of the coating agent of the present invention is preferably 15% or less, more preferably 3 to 10%, and even more preferably 5 to 9.8%. By setting the pigment volume concentration within such a range, the effects of the present invention can be fully obtained. Note that the pigment volume concentration is the volume percentage of the pigment contained in the dry coating, and is a value calculated from the mixed amount of the resin component and pigment that constitute the coating agent.
本発明コーティング剤の塗装においては、公知の塗装器具を用いることができる。塗装器具としては、例えば、スプレー、ローラー、刷毛等を使用することができる。本発明コーティング剤は、この中でも特にローラー塗装に適したものである。ローラーとしては、ウールローラー等の繊維質ローラーが使用でき、その毛丈は好ましくは20mm以下、より好ましくは2~10mmである。 In applying the coating agent of the present invention, known painting equipment can be used. As the painting tool, for example, a spray, a roller, a brush, etc. can be used. The coating agent of the present invention is particularly suitable for roller coating. As the roller, a fibrous roller such as a wool roller can be used, and the hair length thereof is preferably 20 mm or less, more preferably 2 to 10 mm.
本発明コーティング剤の塗付け量(1回の塗装当たり)は、好ましくは0.02~0.5kg/m 2、より好ましくは0.03~0.3kg/m 2である。このような塗付け量であれば、光輝性の向上化、塗り継ぎ部分の仕上り性向上化等を図ることができる。 The coating amount of the coating agent of the present invention (per coating) is preferably 0.02 to 0.5 kg/m 2 , more preferably 0.03 to 0.3 kg/m 2 . With such a coating amount, it is possible to improve the shine, the finish of the joint area, and the like.
本発明では、上記塗付け量で1回目の塗装を行い、その被膜の乾燥後、上記塗付け量で2回目以降の塗装を繰り返し行い、コーティング剤を塗り重ねることができる。塗装時には溶剤等でコーティング剤を適宜希釈することができ、加熱残分が上記範囲内となるように設定することが望ましい。 In the present invention, the first coating is performed with the above coating amount, and after the film dries, the second and subsequent coatings are repeatedly performed with the above coating amount, so that the coating agent can be coated over and over again. At the time of painting, the coating agent can be appropriately diluted with a solvent, etc., and it is desirable to set the heating residue to be within the above range.
本発明では、コーティング剤の塗装後、必要に応じ透明保護層を設けることもできる。透明保護層を設けることで、耐候性、耐久性等を高めることができる。このような透明保護層は、例えば、アクリル樹脂、ウレタン樹脂、アクリルシリコン樹脂、フッ素樹脂等を結合材とする透明コーティング剤によって形成することができる。透明コーティング剤は、水系または溶剤系、艶消しタイプまたは艶有りタイプのいずれであってもよく、本発明の効果を阻害しない限り、着色することも可能である。 In the present invention, a transparent protective layer can be provided after application of the coating agent, if necessary. By providing a transparent protective layer, weather resistance, durability, etc. can be improved. Such a transparent protective layer can be formed using, for example, a transparent coating agent containing acrylic resin, urethane resin, acrylic silicone resin, fluororesin, or the like as a binder. The transparent coating agent may be water-based or solvent-based, matte type or glossy type, and may be colored as long as it does not impede the effects of the present invention.
透明コーティング剤の塗装方法としては、例えば、刷毛塗り、スプレー塗装、ローラー塗装等種々の方法を採用することができる。塗付け量(1回の塗装当たり)は、好ましくは0.02~0.3kg/m 2、より好ましくは0.05~0.15kg/m 2である。このような塗付け量で1回目の塗装を行い、その被膜の乾燥後、同様の塗付け量で2回目以降の塗装を繰り返し行い、透明コーティング剤を塗り重ねることもできる。 Various methods can be used to apply the transparent coating agent, such as brush coating, spray coating, and roller coating. The coating amount (per one coating) is preferably 0.02 to 0.3 kg/m 2 , more preferably 0.05 to 0.15 kg/m 2 . It is also possible to apply the first coat with such a coating amount, and after the film dries, to repeat the second and subsequent coatings with the same coating amount, thereby applying the transparent coating agent over and over again.
以下に実施例及び比較例を示して、本発明の特徴をより明確にする。 Examples and comparative examples are shown below to clarify the characteristics of the present invention.
(コーティング剤の製造)
樹脂成分1、光輝性顔料、粉体、着色顔料、増粘剤、及び溶媒を常法により混合・攪拌することによって主剤を製造し、これに硬化剤として樹脂成分2を混合し、さらに溶媒を混合することによって、各コーティング剤(加熱残分:45重量%)を製造した。表1には、各コーティング剤の配合(固形分換算)を示す。原料としては下記のものを使用した。
(Manufacture of coating agent)
A base resin is produced by mixing and stirring resin component 1, a bright pigment, a powder, a coloring pigment, a thickener, and a solvent in a conventional manner.Resin component 2 is mixed therein as a hardening agent, and then a solvent is added. Each coating agent (heating residue: 45% by weight) was manufactured by mixing. Table 1 shows the formulation (in terms of solid content) of each coating agent. The following materials were used as raw materials.
・樹脂成分1:アクリルポリオール分散液(水酸基価:40KOHmg/g、重量平均分子量:70000、固形分:50重量%、媒体:ミネラルスピリット)
・樹脂成分2:ポリイソシアネート化合物(ヘキサメチレンジイソシアネート誘導体、固形分:100重量%)
・光輝性顔料1:ノンリーフィング型アルミニウムフレーク顔料(平均粒子径:9μm、水面拡散面積:28000cm 2/g)
・光輝性顔料2:ノンリーフィング型アルミニウムフレーク顔料(平均粒子径:9μm、水面拡散面積:29500cm 2/g)
・光輝性顔料3:ノンリーフィング型アルミニウムフレーク顔料(平均粒子径:12μm、水面拡散面積:21000cm 2/g)
・光輝性顔料4:ノンリーフィング型アルミニウムフレーク顔料(平均粒子径:20μm、水面拡散面積:14000cm 2/g)
・鱗片状粉体1:タルク(平均粒子径:5μm)
・鱗片状粉体2:焼成カオリン(平均粒子径:0.6μm)
・粒状粉体1:シリカ(平均粒子径:3μm)
・着色顔料:カーボンブラック
・増粘剤:アマイドワックス系増粘剤、酸化ポリエチレン系増粘剤
・溶媒:ミネラルスピリット
・Resin component 1: Acrylic polyol dispersion (hydroxyl value: 40 KOHmg/g, weight average molecular weight: 70,000, solid content: 50% by weight, medium: mineral spirit)
・Resin component 2: Polyisocyanate compound (hexamethylene diisocyanate derivative, solid content: 100% by weight)
・Glitter pigment 1: Non-leafing aluminum flake pigment (average particle size: 9 μm, water surface diffusion area: 28000 cm 2 /g)
・Glitter pigment 2: Non-leafing aluminum flake pigment (average particle size: 9 μm, water surface diffusion area: 29500 cm 2 /g)
・Glitter pigment 3: Non-leafing aluminum flake pigment (average particle size: 12 μm, water surface diffusion area: 21000 cm 2 /g)
・Glitter pigment 4: Non-leafing aluminum flake pigment (average particle size: 20 μm, water surface diffusion area: 14000 cm 2 /g)
・Scaly powder 1: Talc (average particle size: 5 μm)
・Scaly powder 2: Calcined kaolin (average particle size: 0.6 μm)
・Granular powder 1: Silica (average particle size: 3 μm)
・Coloring pigment: carbon black ・Thickener: amide wax thickener, polyethylene oxide thickener ・Solvent: Mineral spirit
(試験方法)
シーラー処理を施した合板(60cm×60cm)に対し、各コーティング剤をウールローラー(毛丈6mm)にて塗付け量0.1kg/m 2で塗装し、16時間乾燥させた。このとき、合板は垂直に設置した。また、塗装は、コーティング剤を含ませたローラーをランダムに転動させてネタ配りを行った後、仕上げとしてローラーを同一方向に転動させることにより行った。塗装及び乾燥は、標準状態下(気温23℃、相対湿度50%)にて行った。
(Test method)
Each coating agent was applied to a sealer-treated plywood (60 cm x 60 cm) using a wool roller (hair length 6 mm) at a coating amount of 0.1 kg/m 2 and dried for 16 hours. At this time, the plywood was installed vertically. Further, the coating was carried out by randomly rolling a roller impregnated with a coating agent to distribute the material, and then for finishing by rolling the roller in the same direction. Coating and drying were performed under standard conditions (temperature 23° C., relative humidity 50%).
以上の方法で得られた試験板の外観(全体的な光輝性、及び塗り継ぎ部の目立ちにくさ)を評価した。全体的な光輝性(評価1)については、光輝性が高いものを「AA」とする4段階(優:AA>A>B>C:劣)にて行った。塗り継ぎ部分の目立ちにくさ(評価2)については、目立ちにくいものを「AA」とする4段階(優:AA>A>B>C:劣)にて行った。 The appearance of the test plate obtained by the above method (overall brightness and inconspicuousness of the painted joint) was evaluated. The overall brightness (evaluation 1) was evaluated on a four-level scale (excellent: AA>A>B>C: poor) with "AA" indicating high brightness. The inconspicuousness of the painted joint portion (evaluation 2) was evaluated on a four-level scale (excellent: AA>A>B>C: poor) with "AA" indicating less noticeable.
(試験結果)
試験結果を表1に示す。実施例1~8(特に実施例1~5)では、各試験において良好な結果が得られた。
(Test results)
The test results are shown in Table 1. In Examples 1 to 8 (especially Examples 1 to 5), good results were obtained in each test.
Claims (3)
樹脂成分(A)、光輝性顔料(B)、及び、体質顔料として鱗片状粉体(C)を含み、
前記樹脂成分(A)の固形分100重量部に対し、前記光輝性顔料(B)を1~20重量部、前記鱗片状粉体(C)を0.1~50重量部含むことを特徴とするコーティング剤(但し、艶消し剤、樹脂ビーズ、及び光輝材を含む塗料組成物を除く)。 A coating agent exhibiting glittering properties,
A resin component (A), a bright pigment (B), and a scaly powder (C) as an extender pigment,
It is characterized by containing 1 to 20 parts by weight of the glittering pigment (B) and 0.1 to 50 parts by weight of the scaly powder (C) based on 100 parts by weight of the solid content of the resin component (A). (excluding coating compositions containing matting agents, resin beads, and glittering materials) .
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US5166255A (en) * | 1990-09-10 | 1992-11-24 | Basf Corporation | Metallic water borne base coat composition based on acrylic latex resins using an acrylic resin having acid and nonionic functionality for aluminum storage and a pregelled hetorite clay for rheology control--water base 4 |
JP2000007954A (en) * | 1998-06-19 | 2000-01-11 | Fujikura Kasei Co Ltd | Multicolor coating material |
JP2002069380A (en) * | 2000-08-25 | 2002-03-08 | Nippon Bee Chemical Co Ltd | Coating composition and coated article |
JP2002188045A (en) * | 2000-12-20 | 2002-07-05 | Nippon Bee Chemical Co Ltd | Coating composition and coated article |
JP3994434B2 (en) * | 2001-03-13 | 2007-10-17 | 日産自動車株式会社 | Metallic appearance multilayer coating film and method for forming the same |
JP2002273329A (en) * | 2001-03-21 | 2002-09-24 | Nippon Paint Co Ltd | Method for forming brilliant coating film and coated article |
JP5563732B2 (en) * | 2007-01-19 | 2014-07-30 | 日本光研工業株式会社 | Smooth flaky powder, highly bright pigment and method for producing the same |
JP5382933B2 (en) * | 2009-03-14 | 2014-01-08 | ベック株式会社 | Laminated body |
JP5863589B2 (en) * | 2012-07-18 | 2016-02-16 | 関西ペイント株式会社 | Decorative film |
JP6212300B2 (en) * | 2012-09-13 | 2017-10-11 | 株式会社エフコンサルタント | Composition for decorative material |
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