JP4265473B2 - MULTILAYER COATING FORMATION METHOD AND COATED PRODUCT - Google Patents
MULTILAYER COATING FORMATION METHOD AND COATED PRODUCT Download PDFInfo
- Publication number
- JP4265473B2 JP4265473B2 JP2004125725A JP2004125725A JP4265473B2 JP 4265473 B2 JP4265473 B2 JP 4265473B2 JP 2004125725 A JP2004125725 A JP 2004125725A JP 2004125725 A JP2004125725 A JP 2004125725A JP 4265473 B2 JP4265473 B2 JP 4265473B2
- Authority
- JP
- Japan
- Prior art keywords
- coating
- mass
- resin
- coating film
- film
- 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.)
- Expired - Lifetime
Links
- 238000000576 coating method Methods 0.000 title claims description 38
- 239000011248 coating agent Substances 0.000 title claims description 37
- 238000000034 method Methods 0.000 title claims description 23
- 230000015572 biosynthetic process Effects 0.000 title description 2
- 239000000049 pigment Substances 0.000 claims description 46
- 239000003973 paint Substances 0.000 claims description 31
- 239000012508 resin bead Substances 0.000 claims description 25
- 239000008199 coating composition Substances 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 20
- 239000011347 resin Substances 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 18
- 239000002245 particle Substances 0.000 claims description 18
- 239000007787 solid Substances 0.000 claims description 12
- 238000002156 mixing Methods 0.000 claims description 6
- 239000011324 bead Substances 0.000 description 18
- 229910052782 aluminium Inorganic materials 0.000 description 14
- 239000011521 glass Substances 0.000 description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 11
- 238000005266 casting Methods 0.000 description 10
- 239000002184 metal Substances 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 8
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- GJRQTCIYDGXPES-UHFFFAOYSA-N iso-butyl acetate Natural products CC(C)COC(C)=O GJRQTCIYDGXPES-UHFFFAOYSA-N 0.000 description 6
- FGKJLKRYENPLQH-UHFFFAOYSA-M isocaproate Chemical compound CC(C)CCC([O-])=O FGKJLKRYENPLQH-UHFFFAOYSA-M 0.000 description 6
- OQAGVSWESNCJJT-UHFFFAOYSA-N isovaleric acid methyl ester Natural products COC(=O)CC(C)C OQAGVSWESNCJJT-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000012046 mixed solvent Substances 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- -1 polytetrafluoroethylene Polymers 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- 230000005484 gravity Effects 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 229920001228 polyisocyanate Polymers 0.000 description 4
- 239000005056 polyisocyanate Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 3
- XECAHXYUAAWDEL-UHFFFAOYSA-N acrylonitrile butadiene styrene Chemical compound C=CC=C.C=CC#N.C=CC1=CC=CC=C1 XECAHXYUAAWDEL-UHFFFAOYSA-N 0.000 description 3
- 239000004676 acrylonitrile butadiene styrene Substances 0.000 description 3
- 229920000122 acrylonitrile butadiene styrene Polymers 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000011247 coating layer Substances 0.000 description 3
- 229910052802 copper Inorganic materials 0.000 description 3
- 239000010949 copper Substances 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
- 150000004706 metal oxides Chemical class 0.000 description 3
- 239000010445 mica Substances 0.000 description 3
- 229910052618 mica group Inorganic materials 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000007921 spray Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- PQJZHMCWDKOPQG-UHFFFAOYSA-N 2-anilino-2-oxoacetic acid Chemical compound OC(=O)C(=O)NC1=CC=CC=C1 PQJZHMCWDKOPQG-UHFFFAOYSA-N 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- 235000000177 Indigofera tinctoria Nutrition 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000006096 absorbing agent Substances 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- 239000005456 alcohol based solvent Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
- 239000012964 benzotriazole Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 239000003759 ester based solvent Substances 0.000 description 2
- 239000004210 ether based solvent Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000003365 glass fiber Substances 0.000 description 2
- 229940097275 indigo Drugs 0.000 description 2
- COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011147 inorganic material Substances 0.000 description 2
- 239000005453 ketone based solvent Substances 0.000 description 2
- 239000012860 organic pigment Substances 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 2
- 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 2
- 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 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
- 239000004926 polymethyl methacrylate Substances 0.000 description 2
- 229920005672 polyolefin resin Polymers 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 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 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229920006026 co-polymeric resin Polymers 0.000 description 1
- 239000004567 concrete Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- 150000005125 dioxazines Chemical class 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004049 embossing Methods 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 239000005038 ethylene vinyl acetate Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 229920000728 polyester 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
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 230000035807 sensation Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Description
本発明は、複層塗膜形成方法およびこの方法により塗装された物品に関する。
さらに詳しくは、本発明は、鋳物(鋳肌)の様なゴツゴツとした質感のある金属調が得ることができる塗膜形成方法およびこの方法により塗装された物品に関する。
The present invention relates to a method for forming a multilayer coating film and an article coated by this method.
More specifically, the present invention relates to a coating film forming method capable of obtaining a metallic texture with a rough texture such as a casting (casting surface) and an article coated by this method.
現在、自動車・オ−トバイ・パソコン・携帯電話等の塗装物品においては、高い意匠性が必要とされている。そして、新規なデザインとして、鋳物(鋳肌)の様なゴツゴツとした質感のある金属調が求められている。 Currently, high design properties are required for painted articles such as automobiles, auto-bys, personal computers, and mobile phones. As a new design, there is a demand for a metallic texture with a rough texture such as a casting (casting surface).
従来から、この様なデザインを発現するため、被塗物として鋳物の上に直接、光輝性のあるフレーク顔料を含有するメタリック塗料が塗装されている。このような方式では、下地の鋳肌の表面粗度を利用しているため、下地の凹凸の小さい場合や下地に素材傷が発生し部分的なサンディング処理を施した場合には、光輝性のあるフレーク顔料を含有するメタリック塗料が塗装すると、下地の凹凸の影響を受け、被塗物全体が、均一なゴツゴツとした質感のある金属調とはならないという欠点があった。 Conventionally, in order to develop such a design, a metallic paint containing a flake pigment having a glittering property is applied directly on a casting as an object to be coated. In such a method, the surface roughness of the casting surface of the base is used, so if the surface of the base is small or if the material is scratched and partially sanded, When a metallic paint containing a certain flake pigment is applied, there is a drawback that the whole object to be coated does not have a uniform rugged metallic tone due to the influence of the unevenness of the base.
また、被塗物を切削し、凹凸を施すか、シボ加工した上に光輝性のあるフレーク顔料を含有するメタリック塗料が塗装されている方式も採用されている。このような方式では、下地の表面粗度が均一であるため、被塗物全体が、均一なゴツゴツとした質感のある金属調となる。しかし、下地への切削加工・シボ加工に多大な労力が必要であり、生産性に劣るという欠点があった。一方、被塗物に切削加工・シボ加工を施すことなく、鋳物の様なゴツゴツとした質感のある金属調塗膜をえるために球形ビーズと光輝性を有するフレーク顔料とを含有する塗料組成物を塗装する方式も採用されている。このような方式では、球形ビーズを配合することにより、被塗物全体が、均一なゴツゴツとした質感をえることができるが、光輝性を有するフレーク顔料の配向性が低下し、金属感をえることはできないという欠点があった。 In addition, a method is also employed in which a coated object is cut and textured or textured, and then a metallic paint containing a brilliant flake pigment is applied. In such a system, since the surface roughness of the base is uniform, the entire object to be coated has a uniform metallic texture with a rugged texture. However, a great amount of labor is required for cutting and embossing on the base, and there is a disadvantage that the productivity is inferior. On the other hand, a coating composition containing spherical beads and brilliant flake pigments in order to obtain a metal-like coating film with a rugged texture such as casting without subjecting the workpiece to cutting or graining. The method of painting is also adopted. In such a system, by blending the spherical beads, the entire coated object can have a uniform rugged texture, but the orientation of the brilliant flake pigment is lowered and a metallic feeling is obtained. There was a drawback that it was not possible.
また、反射屈折材が有する輝度や宝石調の輝きをえるため、反射屈折材のガラスまたはプラスティックビーズの一部に導電層を形成した後、帯電させて反射屈折材を被塗物の表面に吹き付ける塗装方法が提案されている。(特許文献1参照)しかし、この方式では、ビーズの一部に導電層を形成するためにアルミ蒸着設備が必要であり、生産性に劣るという欠点がある。 In addition, in order to increase the brightness and jewel-like brightness of the catadioptric material, a conductive layer is formed on part of the glass or plastic bead of the catadioptric material, and then charged and sprayed onto the surface of the object to be coated. A painting method has been proposed. However, in this method, an aluminum vapor deposition facility is required to form a conductive layer on a part of the beads, and there is a disadvantage that productivity is inferior.
また、玉虫色の干渉光を維持しつつ、多方面反射のキラキラとした光輝感と深み感をえるため、蒸着金属箔を含有するメタリック塗膜層の上にガラスビーズを含有する塗膜層を塗装し、さらに燐片状光輝性顔料を1%以下含有するトップクリヤーを塗装する光輝性塗膜の形成方法が提案されている。(特許文献2参照)この方法は、下層の蒸着金属箔を含有するメタリック塗膜層とガラスビーズ層の上に隠蔽力のないトップクリヤーを塗装しているため、キラキラとした光輝感に優れるが、求める鋳物の様なゴツゴツとした質感のある金属調の外観ではない。 In addition, a coating layer containing glass beads is applied on the metallic coating layer containing vapor-deposited metal foil in order to maintain the iridescent interference light and give the glittering and deep feeling of multi-directional reflection. Further, a method for forming a glitter coating film is proposed in which a top clear containing 1% or less of a scaly glitter pigment is applied. (Refer to Patent Document 2) This method is excellent in glittering radiance because the top clear with no hiding power is coated on the metallic coating layer containing the lower vapor-deposited metal foil and the glass bead layer. It is not a metal-like appearance with a rugged texture such as the desired casting.
さらに、球状ガラスビーズまたはガラス繊維を含有した下塗りの上に100メッシュのフルイを通過したガラスフレークを含有する上塗りを塗装する骨材含有塗装金属板が提案されている。(特許文献3)この方法は、比重の大きいガラスビーズまたはガラス繊維を塗料組成物に配合すると、塗料の貯蔵時に沈殿が生じる。また、得られる効果も全く異なる。
本発明は、従来のこのような問題点に着目してなされたもので、被塗物に切削加工・シボ加工を施すことなく、鋳物の様なゴツゴツとした質感のある金属調塗膜を安定的に形成できるようにしたものである。 The present invention has been made by paying attention to such conventional problems, and it is possible to stably produce a metal-like coating film having a rugged texture like a casting without subjecting the workpiece to cutting or graining. It can be formed automatically.
すなわち本発明は、被塗物に、平均粒子径60〜200μmの球形樹脂ビーズを塗膜形成樹脂の固形分に対して10〜40質量%配合してなるベースコート塗料組成物(A)を塗装することで形成されたベースコート塗膜の上に、ウエットオンウエットで、光輝性を有するフレーク顔料を塗膜形成樹脂の固形分に対して5〜15質量%配合してなるトップコート塗料組成物(B)を塗装することを特徴とする複層塗膜形成方法を提供する。 That is, the present invention is coated on a coating object, the average particle diameter of 60 to 200 DEG [mu] m base coating composition obtained by blending 10 to 40 wt% of spherical resin beads with respect to the solid content of the film-forming resin of the (A) A top coat coating composition comprising 5 to 15 % by mass of a flake pigment having glitter on the solid content of the coating film-forming resin on a base coat film formed by wet-on-wetting ( A method for forming a multilayer coating film characterized by coating B) is provided.
また、本発明は、被塗物に、プライマー層を塗装した後、平均粒子径60〜200μmの球形樹脂ビーズを塗膜形成樹脂の固形分に対して10〜40質量%配合してなるベースコート塗料組成物(A)を塗装することで形成されたベースコート塗膜の上に、ウエットオンウエットで、光輝性を有するフレーク顔料を塗膜形成樹脂の固形分に対して5〜15質量%配合してなるトップコート塗料組成物(B)を塗装することを特徴とする複層塗膜形成方法を提供する。 Further, the present invention provides a base coat comprising 10 to 40 % by mass of spherical resin beads having an average particle diameter of 60 to 200 μm based on the solid content of the film-forming resin after a primer layer is applied to an object to be coated. On the base coat film formed by applying the coating composition (A), 5-15 % by mass of a flake pigment having a glittering property is blended by wet-on-wet with respect to the solid content of the film-forming resin. A method for forming a multilayer coating film is provided, which comprises coating the topcoat coating composition (B).
また、本発明は、上記の塗膜形成方法により塗装された物品を提供する。 Moreover, this invention provides the articles | goods coated by said coating-film formation method.
本発明の複層塗膜形成方法によって、被塗物に切削加工・シボ加工を施すことなく、鋳物の様なゴツゴツとした質感のある金属調塗膜を安定的に形成できる。 By the method for forming a multilayer coating film of the present invention, it is possible to stably form a metal-like coating film having a rugged texture such as a casting without subjecting an object to be cut or textured.
以下、本発明について詳細に説明する。 Hereinafter, the present invention will be described in detail.
本発明に用いられるベースコート塗料組成物(A)は、平均粒子径60μm以上の球形樹脂ビーズを配合する。 The base coat coating composition (A) used in the present invention contains spherical resin beads having an average particle diameter of 60 μm or more.
球形ビーズの種類としては、一般に、鉄・銅などの金属ビーズ、ガラスビーズ、樹脂ビーズ等が知られている。しかし、鉄・銅などの金属ビーズの場合、ベースコート塗料組成物として用いたときに、金属イオンを溶出し易く、その溶出イオンによって、塗料が着色したり、ゲル化したりする問題点があり、適していない。また、ガラスビーズの場合、比重が大きいため、平均粒子径60μm以上のガラスビーズをベースコート塗料組成物に配合すると、ベースコート塗料の貯蔵時に沈殿が生じる問題があり、適していない。本発明に用いられる球形ビーズとしては、比重が小さく、ベースコート塗料中で安定である樹脂ビーズが好ましい。特に、好ましい球形ビーズの比重の範囲は、1.0〜1.5である。 As types of spherical beads, metal beads such as iron and copper, glass beads, resin beads and the like are generally known. However, in the case of metal beads such as iron and copper, when used as a base coat paint composition, metal ions are easily eluted, and there is a problem that the paint is colored or gelled by the eluted ions. Not. In the case of glass beads, since the specific gravity is large, if glass beads having an average particle diameter of 60 μm or more are blended in the base coat paint composition, there is a problem that precipitation occurs when the base coat paint is stored, which is not suitable. The spherical beads used in the present invention are preferably resin beads having a small specific gravity and being stable in the base coat paint. In particular, the preferred specific gravity range of the spherical beads is 1.0 to 1.5.
本発明に用いられる樹脂ビーズは、PMMA(ポリメチルメタクリレート)樹脂ビーズ、MMA−EGDM(エチレングリコールジメタクリレート)共重合樹脂ビーズ、ナイロン樹脂ビーズ、ポリテトラフルオロエチレン樹脂ビーズ等が挙げられる。
本発明に用いられる樹脂ビーズは、レーザー回折式粒度測定器にて測定し、平均粒子径60μm〜200μmである。好ましくは、平均粒子径80μm〜130μmである。平均粒径60μmより小さい場合は、ベースコート塗料組成物(A)の凹凸が小さく、ゴツゴツとした質感のある金属調塗膜を形成できない。また、平均粒径が200 μmより大きい場合は、エアスプレー塗装時にガンづまりが発生するという問題が生じるため好ましくない。
Examples of the resin beads used in the present invention include PMMA (polymethyl methacrylate) resin beads, MMA-EGDM (ethylene glycol dimethacrylate) copolymer resin beads, nylon resin beads, and polytetrafluoroethylene resin beads.
The resin beads used in the present invention are measured with a laser diffraction particle size analyzer and have an average particle size of 60 μm to 200 μm. The average particle diameter is preferably 80 μm to 130 μm. When the average particle size is smaller than 60 μm, the unevenness of the base coat coating composition (A) is small, and a metal-like coating film with a rough texture cannot be formed. On the other hand, if the average particle size is larger than 200 μm, there is a problem in that gun clogging occurs during air spray coating, which is not preferable.
上記の樹脂ビーズとしては、東洋紡績株式会社製「タフチックシリーズ(商品名)」、積水化成品工業株式会社製「テクポリマーシリーズ(商品名)」、住友スリーエム株式会社製「ダイニオンシリーズ(商品名)」等が挙げられる。 The above resin beads include “Toughtick Series (trade name)” manufactured by Toyobo Co., Ltd., “Tech Polymer Series (trade name)” manufactured by Sekisui Plastics Co., Ltd., and “Dinion Series (product) manufactured by Sumitomo 3M Limited”. Name) "and the like.
本発明のベースコート塗料組成物(A)に配合される球形樹脂ビーズは、各々単独で使用してもよい。また、球形樹脂ビーズを2種類以上組み合わせて使用してもよい。 The spherical resin beads blended in the base coat coating composition (A) of the present invention may be used alone. Two or more spherical resin beads may be used in combination.
本発明のベースコート塗料組成物(A)に用いられる塗膜形成樹脂としては、通常、塗料用として使用されている樹脂を制限なく使用できる。例えばアクリル樹脂、ポリエステル樹脂、アルキッド樹脂、繊維素系樹脂、ポリオレフィン樹脂、塩素化ポリオレフィン樹脂、フッ素樹脂、シリコン樹脂等を単独あるいは組み合わせて非架橋のラッカータイプとすることも例えば、アミノ樹脂、(ブロック)ポリイソシアネ−ト化合物、エポキシ化合物等の架橋形成樹脂と組み合わせて架橋硬化型とすることもできる。 As the film-forming resin used in the base coat paint composition (A) of the present invention, a resin usually used for paint can be used without limitation. For example, an acrylic resin, a polyester resin, an alkyd resin, a fiber resin, a polyolefin resin, a chlorinated polyolefin resin, a fluororesin, a silicon resin, etc. may be used alone or in combination to form a non-crosslinked lacquer type. ) It can also be made into a cross-linking curable type in combination with a cross-linking resin such as a polyisocyanate compound or an epoxy compound.
また、本発明に用いられるソリッドベースコート塗料の形態としては、溶剤型に限定されることはなく、水溶性、水分散型などの水性塗料を用いることができる。 The form of the solid base coat paint used in the present invention is not limited to the solvent type, and water-soluble or water-dispersed water-based paints can be used.
本発明におけるベースコート塗料組成物(A)が溶剤型塗料である場合は、有機溶剤に溶解して使用する。有機溶剤としては、芳香族炭化水素系溶剤、エステル系溶剤、ケトン系溶剤、アルコール系溶剤、エーテル系溶剤等が使用できる。
本発明のベースコート塗料組成物(A)は、平均粒子径60〜200μmの球形樹脂ビーズを塗膜形成樹脂の固形分に対して、10質量%〜40質量%配合する。配合量が、10質量%より少ない場合は、ベースコート塗料組成物(A)の凹凸が小さく、ゴツゴツとした質感のある金属調塗膜を形成できない。また、配合量が40質量%より多い場合は、塗膜形成樹脂が少ないため付着性が劣るという問題が生じるため好ましくない。
When the base coat paint composition (A) in the present invention is a solvent-type paint, it is used after being dissolved in an organic solvent. As the organic solvent, aromatic hydrocarbon solvents, ester solvents, ketone solvents, alcohol solvents, ether solvents and the like can be used.
In the base coat coating composition (A) of the present invention, spherical resin beads having an average particle size of 60 to 200 μm are blended in an amount of 10% by mass to 40 % by mass with respect to the solid content of the film forming resin . When the blending amount is less than 10% by mass, the unevenness of the base coat coating composition (A) is small, and a rough metallic texture film cannot be formed. Moreover, when there are more compounding quantities than 40 mass%, since there is a problem that adhesiveness is inferior because there are few coating film forming resins, it is not preferable.
本発明におけるベースコート塗料組成物(A)は、必要に応じてその他の着色顔料および各種添加剤などを配合することができる。着色顔料としては、従来から塗料用に常用されているものが用いられ、例えば有機系としてはアゾレ−キ系顔料、フタロシアニン顔料、インジゴ系顔料、ペリノン系顔料、ペリレン系顔料、キノフタロン系顔料、ジオキサジン系顔料、キナクリドン系顔料等を挙げる事ができ、無機系としては黄鉛、黄色酸化鉄、ベンガラ等が挙げられる。添加剤としては、ベンゾトリアゾール、蓚酸アニリド系等の紫外線吸収剤、ベンゾフェノ−ル系等の酸化防止剤、シリコ−ン系等のレベリング剤、ワックス、有機ベントナイト等の粘性制御剤、硬化触媒等が挙げられる。 The base coat coating composition (A) in the present invention may contain other color pigments and various additives as required. As the color pigment, those conventionally used for paints are used. For example, organic pigments include azo lake pigments, phthalocyanine pigments, indigo pigments, perinone pigments, perylene pigments, quinophthalone pigments, dioxazines. Pigments, quinacridone pigments, and the like, and examples of inorganic pigments include yellow lead, yellow iron oxide, and bengara. Additives include UV absorbers such as benzotriazole and oxalic acid anilide, antioxidants such as benzophenol, leveling agents such as silicone, viscosity control agents such as wax and organic bentonite, curing catalysts, etc. Can be mentioned.
本発明のトップコート塗料組成物(B)は、光輝性を有するフレーク顔料を含有する。
光輝性を有するフレーク顔料としては、従来から塗料に配合されている公知の光輝性を有するフレーク顔料を制限なく使用することができる。代表的な光輝性を有するフレーク顔料としては、リーフィング型アルミニウムフレーク、ノンリーフィング型アルミニウムフレーク、ニッケルフレーク、銅フレーク、チタンフレーク、ガラスフレーク等のフレーク;パールマイカ、着色パールマイカ等のマイカ粉末;シリカフレーク、アルミナフレーク等の偏光性顔料;金属または二酸化チタンで被覆されたガラスフレーク顔料;着色アルミニウムフレーク顔料、金属酸化物被覆アルミナフレーク、金属酸化物被覆シリカフレーク顔料、板状酸化鉄等が挙げられる。
本発明のトップコート塗料組成物(B)は、光輝性を有するフレーク顔料を塗膜形成樹脂の固形分に対して5質量%〜15質量%配合する。光輝性を有するフレーク顔料を塗膜形成樹脂の固形分に対して5質量%
未満の場合、光輝感が低下する。また、配合量が、15質量%より多い場合、耐湿性等の塗膜性能が低下するという問題が生じるため好ましくない。
The topcoat coating composition (B) of the present invention contains a flake pigment having glitter.
As the flake pigment having brilliant properties, any known flake pigment having brilliant properties that has been conventionally blended in paints can be used without limitation. Typical flake pigments having glittering properties include leafing type aluminum flakes, non-leafing type aluminum flakes, nickel flakes, copper flakes, titanium flakes, glass flakes, etc .; mica powders such as pearl mica and colored pearl mica; silica Polarizing pigments such as flakes and alumina flakes; glass flake pigments coated with metal or titanium dioxide; colored aluminum flake pigments, metal oxide-coated alumina flakes, metal oxide-coated silica flake pigments, plate-like iron oxide, etc. .
The top coat coating composition (B) of the present invention contains 5 % by mass to 15 % by mass of a flake pigment having a glittering property with respect to the solid content of the coating film-forming resin . 5 % by mass of flake pigment having brilliant properties with respect to the solid content of the film-forming resin
If it is less than 1, the glitter feeling is lowered. Moreover, when there are more compounding quantities than 15 mass%, since the problem that coating-film performance, such as moisture resistance, falls arises, it is unpreferable.
本発明におけるトップコート塗料組成物(B)は、必要に応じて、光輝性を失わない程度に、その他の着色顔料および各種添加剤などを配合することができる。着色顔料としては従来から塗料用に常用されているものが用いられ、例えば有機系としてはアゾレ−キ系顔料、フタロシアニン顔料、インジゴ系顔料、ペリノン系顔料、ペリレン系顔料、キノフタロン系顔料、ジオキサジン系顔料、キナクリドン系顔料等を挙げる事ができ、無機系としては黄鉛、黄色酸化鉄、ベンガラ等が挙げられる。添加剤としてはベンゾトリアゾール、蓚酸アニリド系等の紫外線吸収剤、ベンゾフェノ−ル系等の酸化防止剤、シリコ−ン系等のレベリング剤、ワックス、有機ベントナイト等の粘性制御剤、硬化触媒等が挙げられる。 The top coat coating composition (B) in the present invention can be blended with other color pigments and various additives as needed so as not to lose the glitter. As color pigments, those conventionally used for paints are used. For example, organic pigments include azo lake pigments, phthalocyanine pigments, indigo pigments, perinone pigments, perylene pigments, quinophthalone pigments, dioxazine pigments. Pigments, quinacridone pigments, and the like can be mentioned. Examples of inorganic materials include yellow lead, yellow iron oxide, and bengara. Additives include UV absorbers such as benzotriazole and oxalic acid anilide, antioxidants such as benzophenol, leveling agents such as silicone, viscosity control agents such as wax and organic bentonite, curing catalysts, etc. It is done.
本発明におけるトップコート塗料組成物(B)は、有機溶剤に溶解して使用する。有機溶剤としては、芳香族炭化水素系溶剤、エステル系溶剤、ケトン系溶剤、アルコ−ル系溶剤、エ−テル系溶剤等が使用できる。 The topcoat coating composition (B) in the present invention is used after being dissolved in an organic solvent. As the organic solvent, aromatic hydrocarbon solvents, ester solvents, ketone solvents, alcohol solvents, ether solvents and the like can be used.
本発明に用いられる複膜塗膜形成方法の塗装は、霧化式塗装機を用い、エアスプレ−方式、静電方式等、従来から公知の塗装方法により行うことができる。 The coating of the method for forming a multi-layer coating film used in the present invention can be performed by a conventionally known coating method such as an air spray method or an electrostatic method using an atomizing coater.
本発明が適応される被塗物としては、鉄、アルミニウム、マグネシウムもしくはこれらの合金を含む金属類、ガラス、コンクリ−ト等の無機材料、ポリエチレン、ポリプロピレン、エチレン−酢酸ビニル共重合体、ポリアミド、ポリアクリル、ポリエステル、塩化ビニル樹脂、塩化ビニリデン樹脂、ポリカ−ボネ−ト、ポリウレタン、アクリロニトリル−ブタジエン−スチレン共重合体等の樹脂成形品および各種FRPなどのプラスチック材料、木材、紙などが挙げられる。なお、これら被塗基材に予め適宜な化成処理を施したり、プライマ−等の下塗り塗装を施したりすることは任意である。
<実施例>
以下、本発明を実施例および比較例によりさらに具体的に説明する。しかし、本発明の範囲はこれらの例になんら限定されるものではない。なお各例中、特に断らない限り、部は質量部を表す。
<ベースコート塗料組成物1の調製>
アクリル樹脂として、「アクリディックA−190」(商品名、大日本インキ化学工業(株)製、加熱残分50質量%)40質量部と、酸化チタン「JR603」 (商品名、テイカ(株)製)10質量部と、キシレンと酢酸イソブチルとの比率が50:50の混合溶剤10質量部とを、ガラスビーズを分散媒体とするアトライターで粒度10μm以下になるまで分散し、酸化チタンペ−ストを作成した。次に、アクリル樹脂 20重量部、球形ビーズ「タフチックAR650MZ」 (商品名、東洋紡績(株)製、平均粒子径60μm) 7.5質量部を順次、加えて攪拌する。さらに、クリヤーの硬化剤として、ポリイソシアネ−ト化合物「スミジュ−ルN−75」(商品名、バイエルポリマー(株)製、加熱残分75質量%) 10質量部を加え、さらにキシレンと酢酸イソブチルとの比率が50:50の混合溶剤2.5質量部を加えて撹拌し、ベースコート塗料組成物1を調整した。
<ベースコート塗料組成物2〜8の調整>
混合物の割合を表1に示した通りとする以外は、ベースコート塗料組成物1と同様にベースコート塗料組成物2〜8を調製した。
The objects to which the present invention is applied include metals including iron, aluminum, magnesium or alloys thereof, glass, inorganic materials such as concrete, polyethylene, polypropylene, ethylene-vinyl acetate copolymer, polyamide, Examples thereof include resin molded products such as polyacryl, polyester, vinyl chloride resin, vinylidene chloride resin, polycarbonate, polyurethane, acrylonitrile-butadiene-styrene copolymer, plastic materials such as various FRPs, wood, and paper. In addition, it is arbitrary to perform an appropriate chemical conversion treatment on these coated substrates in advance, or to apply an undercoating such as a primer.
<Example>
Hereinafter, the present invention will be described more specifically with reference to Examples and Comparative Examples. However, the scope of the present invention is not limited to these examples. In addition, unless otherwise indicated in each example, a part represents a mass part.
<Preparation of base coat coating composition 1>
As an acrylic resin, 40 parts by weight of “Acridic A-190” (trade name, manufactured by Dainippon Ink & Chemicals, Inc., heating residue 50% by mass) and titanium oxide “JR603” (trade name, Takeca Co., Ltd.) 10 parts by mass) and 10 parts by mass of a mixed solvent having a ratio of xylene and isobutyl acetate of 50:50 are dispersed with an attritor using glass beads as a dispersion medium until the particle size becomes 10 μm or less, and titanium oxide paste is used. It was created. Next, 20 parts by weight of acrylic resin and 7.5 parts by weight of spherical beads “Toughtic AR650MZ” (trade name, manufactured by Toyobo Co., Ltd., average particle size 60 μm) are sequentially added and stirred. Furthermore, as a curing agent for the clear, 10 parts by mass of a polyisocyanate compound “Sumidur N-75” (trade name, manufactured by Bayer Polymer Co., Ltd., heated residue: 75% by mass), xylene, isobutyl acetate, A base coat coating composition 1 was prepared by adding 2.5 parts by mass of a mixed solvent having a ratio of 50:50 and stirring.
<Adjustment of base coat paint compositions 2-8>
Base coat paint compositions 2 to 8 were prepared in the same manner as the base coat paint composition 1 except that the ratio of the mixture was as shown in Table 1.
<注>
1)球形樹脂ビーズ:東洋紡績(株)製、タフチックAR650MZ、ポリMMA樹脂ビーズ、平均粒子径60μm、100質量%
2)球形樹脂ビーズ:東洋紡績(株)製、タフチックAR650ML、ポリMMA樹脂ビーズ、平均粒子径80μm、100質量%
3)球形樹脂ビーズ:東洋紡績(株)製、タフチックAR650MX、ポリMMA樹脂ビーズ、平均粒子径40μm、100質量%
4)球形樹脂ビーズ:東洋紡績(株)製、タフチックAR650M、ポリMMA樹脂ビーズ、平均粒子径30μm、100質量%
5)酸化チタン:テイカ(株)社製、JR603、
6)光輝性フレーク顔料:東洋アルミニウム(株)製、アルミニウムペーストTCR2020、アルミフレーク、加熱残分75%、
7)アクリル樹脂:大日本インキ化学工業(株)製、アクリディックA−190、加熱残分50%、
8)ポリイソシアネ−ト化合物:バイエルポリマー社製、スミジュ−ルN−75、加熱残分75%
9)キシレン/酢酸イソブチル:混合溶剤、質量比50/50
<トップコート塗料組成物1の調整>
アクリルウレタン樹脂系クリヤー塗料として、「ハイウレタンNo.5000クリヤー」(商品名、日本油脂BASFコ−ティングス(株)製、加熱残分45質量%) 60質量部、光輝性フレーク顔料として、「アルミニウムペーストTCR2020」(商品名、東洋アルミニウム(株)製、アルミフレーク) 5質量部を順次、加えて攪拌する。次に、クリヤーの硬化剤として、ポリイソシアネ−ト化合物「スミジュ−ルN−75」(商品名、バイエルポリマー社製、加熱残分75質量%) 15質量部を加え、さらにキシレンと酢酸イソブチルとの比率が50:50の混合溶剤 20質量部を加えて撹拌し、トップコート塗料組成物1を調整した。
<トップコート塗料組成物2〜4の調整>
混合物の割合を表2に示した通りとする以外は、トップコート塗料組成物1と同様にトップコート塗料組成物2〜4を調製した。
<Note>
1) Spherical resin beads: manufactured by Toyobo Co., Ltd., Tufic AR650MZ, polyMMA resin beads, average particle size 60 μm, 100% by mass
2) Spherical resin beads: manufactured by Toyobo Co., Ltd., Tufic AR650ML, polyMMA resin beads, average particle size of 80 μm, 100% by mass
3) Spherical resin beads: manufactured by Toyobo Co., Ltd., Tufic AR650MX, poly MMA resin beads, average particle size 40 μm, 100% by mass
4) Spherical resin beads: manufactured by Toyobo Co., Ltd., Tufic AR650M, poly MMA resin beads, average particle size 30 μm, 100% by mass
5) Titanium oxide: manufactured by Teika Co., Ltd., JR603,
6) Bright flake pigment: Toyo Aluminum Co., Ltd., aluminum paste TCR2020, aluminum flake, heating residue 75%,
7) Acrylic resin: manufactured by Dainippon Ink & Chemicals, Inc., Acrydic A-190, heating residue 50%,
8) Polyisocyanate compound: Bayer Polymer Co., Ltd., Smith N-75, heating residue 75%
9) Xylene / isobutyl acetate: mixed solvent, mass ratio 50/50
<Adjustment of Topcoat Paint Composition 1>
As an acrylic urethane resin-based clear paint, “High Urethane No. 5000 Clear” (trade name, manufactured by Nippon Oil & Fats BASF Co., Ltd., heated residue 45% by mass) 60 parts by mass, as a glitter flake pigment, “ 5 parts by mass of aluminum paste TCR2020 "(trade name, manufactured by Toyo Aluminum Co., Ltd., aluminum flakes) are sequentially added and stirred. Next, 15 parts by mass of a polyisocyanate compound “Sumidur N-75” (trade name, manufactured by Bayer Polymer Co., Ltd., heated residue: 75% by mass) is added as a clear curing agent, and xylene and isobutyl acetate are further added. 20 parts by mass of a mixed solvent having a ratio of 50:50 was added and stirred to prepare a topcoat coating composition 1.
<Adjustment of topcoat paint compositions 2 to 4>
Topcoat paint compositions 2 to 4 were prepared in the same manner as the topcoat paint composition 1 except that the ratio of the mixture was as shown in Table 2.
<注>
6)光輝性フレーク顔料:東洋アルミニウム(株)製、アルミニウムペーストTCR2020、アルミフレーク、加熱残分75%、
10)光輝性フレーク顔料:メルク(株)製、シラリックT60−WNTクリスタルシルバー、アルミナフレーク、加熱残分100質量%
11)光輝性フレーク顔料:日本板硝子(株)製、マイクログラスメタシャインMC1020RS、ガラスフレーク、加熱残分100質量%
12)アクリルウレタン樹脂系塗料:日本油脂BASFコ−ティングス(株)製、ハイウレタンNo.5000クリヤー、加熱残分45質量%
<実施例1>
厚さ3mm、7cm×12cmの日本A&L(株)製ABS基材、「クララスチックMVF」を試験片として用いた。この試験片をイソプロピルアルコールを用いて脱脂し、被塗物とした。フォードカップNo.4(25℃)で15秒となるように、キシレンと酢酸イソブチルとの混合溶剤(質量比50/50)にて粘度を調製したベースコート用塗料組成物1を乾燥膜厚20μmとなるようにエアスプレ−で塗装した。室温にて約10分間放置した後、フォードカップNo.4(25℃)で20秒となるように、キシレンと酢酸イソブチルとの混合溶剤(質量比50/50)にて粘度を調製した希釈したトップコート塗料組成物1を、ウエットオンウエットで、乾燥膜厚25μmとなるようにエアスプレ−で塗装し、室温にて約10分間放置した後、75℃で30分間焼き付け、試験板を得た。
<実施例2〜4、比較例1〜5>
ベースコート塗料組成物と、トップコート塗料組成物を表3に示した組合せとする以外は、実施例1と同様に行い、試験板を得た。
<実施例5>
厚さ3mm、7cm×12cmの日本A&L(株)製ABS基材「クララスチックMVF」をイソプロピルアルコールを用いて脱脂した後、塩素化ポリオレフィン樹脂系プライマーとして、「プライマックNo.1500プライマー」(商品名、日本油脂BASFコ−ティングス(株)製、)を乾燥膜厚が8μmとなるようにエアスプレ−で塗装し、室温にて約10分間放置した。次に、実施例1と同様の要領にて、ベースコート塗料組成物1とトップコート塗料組成物1とを順次、ウェットオンウェットにて塗装し、75℃で30分間焼き付け、試験板を得た。
<Note>
6) Bright flake pigment: Toyo Aluminum Co., Ltd., aluminum paste TCR2020, aluminum flake, heating residue 75%,
10) Bright flake pigment: Merck & Co., Inc., Silical T60-WNT crystal silver, alumina flake, heating residue 100% by mass
11) Bright flake pigment: manufactured by Nippon Sheet Glass Co., Ltd., Microglass Metashine MC1020RS, glass flake, heating residue 100% by mass
12) Acrylic urethane resin-based paint: Nippon Oil & Fats BASF Coatings Co., Ltd., High Urethane No.5000 clear, heating residue 45% by mass
<Example 1>
An ABS base material made by Japan A & L Co., Ltd. having a thickness of 3 mm and 7 cm × 12 cm, “Clarastic MVF” was used as a test piece. This test piece was degreased using isopropyl alcohol to obtain a coating object. Ford Cup No. The base coat coating composition 1 having a viscosity adjusted with a mixed solvent of xylene and isobutyl acetate (mass ratio 50/50) so as to be 15 seconds at 4 (25 ° C.) is air sprayed to a dry film thickness of 20 μm. Painted with-. After leaving at room temperature for about 10 minutes, Ford Cup No. The diluted topcoat coating composition 1 having a viscosity adjusted with a mixed solvent of xylene and isobutyl acetate (mass ratio 50/50) so as to be 20 seconds at 4 (25 ° C.) is dried on a wet on wet basis. After coating with an air spray to a film thickness of 25 μm and leaving at room temperature for about 10 minutes, baking was performed at 75 ° C. for 30 minutes to obtain a test plate.
<Examples 2-4, Comparative Examples 1-5>
A test plate was obtained in the same manner as in Example 1 except that the base coat paint composition and the top coat paint composition were combined as shown in Table 3.
<Example 5>
After degreasing ABS base material “Clarastic MVF” made by Japan A & L Co., Ltd. with a thickness of 3 mm and 7 cm × 12 cm using isopropyl alcohol, “Primac No. 1500 Primer” (product) Name, Nippon Oil & Fats BASF Coatings Co., Ltd.) was applied with an air spray so that the dry film thickness was 8 μm, and allowed to stand at room temperature for about 10 minutes. Next, in the same manner as in Example 1, the base coat paint composition 1 and the top coat paint composition 1 were sequentially applied by wet-on-wet and baked at 75 ° C. for 30 minutes to obtain a test plate.
これらの試験板を用いて、ゴツゴツとした質感と金属調感を評価した。評価結果を表3に示した。
(1)ゴツゴツとした質感
塗膜の仕上がり外観を評価できる10人により、目視による評価を行った。質感を下記の評価基準で判定した。
2;ゴツゴツとした質感がある
1;ゴツゴツとした質感に乏しい
2を合格とした。
(2)金属調感
塗膜の仕上がり外観を評価できる10人により、目視による評価を行った。金属感を下記の評価基準で判定した。
2;金属調感を有している
1;金属調感に乏しい
2を合格とした。
Using these test plates, the rough texture and metal feel were evaluated. The evaluation results are shown in Table 3.
(1) Rough texture A 10 person who can evaluate the finished appearance of the coating film was visually evaluated. The texture was judged according to the following evaluation criteria.
2: A rough texture 1; A rough texture 2 was accepted.
(2) Metallic sensation Visual evaluation was performed by 10 people who can evaluate the finished appearance of the coating film. The metal feeling was determined according to the following evaluation criteria.
2; 1 which has a metallic tone;
Claims (3)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004125725A JP4265473B2 (en) | 2004-04-21 | 2004-04-21 | MULTILAYER COATING FORMATION METHOD AND COATED PRODUCT |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004125725A JP4265473B2 (en) | 2004-04-21 | 2004-04-21 | MULTILAYER COATING FORMATION METHOD AND COATED PRODUCT |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2005305301A JP2005305301A (en) | 2005-11-04 |
JP4265473B2 true JP4265473B2 (en) | 2009-05-20 |
Family
ID=35434678
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2004125725A Expired - Lifetime JP4265473B2 (en) | 2004-04-21 | 2004-04-21 | MULTILAYER COATING FORMATION METHOD AND COATED PRODUCT |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4265473B2 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2008260872A (en) * | 2007-04-13 | 2008-10-30 | Pialex Technologies Corp | Clear coating material, and coating film inspection method |
EP3627988B1 (en) * | 2017-09-29 | 2021-01-13 | NIKE Innovate C.V. | Structurally-colored articles and methods for making and using structurally-colored articles |
-
2004
- 2004-04-21 JP JP2004125725A patent/JP4265473B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP2005305301A (en) | 2005-11-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4916319B2 (en) | Multilayer pattern coating film forming method | |
JPWO2013154168A1 (en) | Coating method | |
JP4851393B2 (en) | Coating method | |
JP2004018774A (en) | Matte coating composition, method for forming coating film, and coated object | |
JP4265473B2 (en) | MULTILAYER COATING FORMATION METHOD AND COATED PRODUCT | |
JP2004358329A (en) | Method for forming bright metallic coating film | |
JP4314469B2 (en) | LAMINATED COATING FORMATION METHOD, LAMINATED COATING AND COATED PRODUCT | |
JP4754056B2 (en) | Method for forming glitter coating film | |
JP4751043B2 (en) | MULTILAYER COATING FORMATION METHOD AND COATED ARTICLE | |
JP3285082B2 (en) | Coating method | |
JP4314466B2 (en) | LAMINATED COATING FORMATION METHOD, LAMINATED COATING AND COATED PRODUCT | |
JP2001314807A (en) | Method for forming coating film with sophisticated design properties | |
JP2002233815A (en) | Method of forming photoluminescent coating film and coated material | |
JP3994434B2 (en) | Metallic appearance multilayer coating film and method for forming the same | |
JP4058829B2 (en) | Paint composition | |
JP2001226612A (en) | Metallic coating composition, method of forming coating film, and coated product | |
JP2003245602A (en) | Method for forming luster color coating film and coated article | |
JP4507288B2 (en) | Multi-layer coating formation method | |
JP3982108B2 (en) | Coating method | |
JP2001104872A (en) | Method of forming coating film | |
JP2003119417A (en) | Brilliant material coating composition, method for forming coating film and coated product | |
JPH10244213A (en) | Method for formation of bright paint film and article coated therewith | |
JP2005306962A (en) | Coating composition, coating film formation method, and coated object | |
JP2005177642A (en) | Method of forming multilayer coating film, and coated article | |
JP4315001B2 (en) | Method for coating overcoat clear coating composition and coated article |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20060519 |
|
RD02 | Notification of acceptance of power of attorney |
Free format text: JAPANESE INTERMEDIATE CODE: A7422 Effective date: 20060519 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20081030 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20081111 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20081225 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20090127 |
|
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20090209 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 4265473 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20120227 Year of fee payment: 3 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130227 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20130227 Year of fee payment: 4 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20140227 Year of fee payment: 5 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20140227 Year of fee payment: 5 |
|
S111 | Request for change of ownership or part of ownership |
Free format text: JAPANESE INTERMEDIATE CODE: R313111 |
|
FPAY | Renewal fee payment (event date is renewal date of database) |
Free format text: PAYMENT UNTIL: 20140227 Year of fee payment: 5 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
S531 | Written request for registration of change of domicile |
Free format text: JAPANESE INTERMEDIATE CODE: R313531 |
|
R350 | Written notification of registration of transfer |
Free format text: JAPANESE INTERMEDIATE CODE: R350 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |