JPS62244476A - Improved method for anticorrosion painting of metal cast and forged product - Google Patents
Improved method for anticorrosion painting of metal cast and forged productInfo
- Publication number
- JPS62244476A JPS62244476A JP8781686A JP8781686A JPS62244476A JP S62244476 A JPS62244476 A JP S62244476A JP 8781686 A JP8781686 A JP 8781686A JP 8781686 A JP8781686 A JP 8781686A JP S62244476 A JPS62244476 A JP S62244476A
- Authority
- JP
- Japan
- Prior art keywords
- paint
- coating
- resin
- curing
- polyol
- 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
- 238000000034 method Methods 0.000 title claims abstract description 13
- 238000010422 painting Methods 0.000 title claims abstract description 9
- 229910052751 metal Inorganic materials 0.000 title abstract description 6
- 239000002184 metal Substances 0.000 title abstract description 6
- 238000000576 coating method Methods 0.000 claims abstract description 44
- 239000003973 paint Substances 0.000 claims abstract description 37
- 239000011248 coating agent Substances 0.000 claims abstract description 31
- 150000001412 amines Chemical class 0.000 claims abstract description 22
- 239000012298 atmosphere Substances 0.000 claims abstract description 15
- 238000005260 corrosion Methods 0.000 claims abstract description 15
- 229920002803 thermoplastic polyurethane Polymers 0.000 claims abstract description 15
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 229920002635 polyurethane Polymers 0.000 claims abstract description 8
- 239000004814 polyurethane Substances 0.000 claims abstract description 8
- NDKWCCLKSWNDBG-UHFFFAOYSA-N zinc;dioxido(dioxo)chromium Chemical compound [Zn+2].[O-][Cr]([O-])(=O)=O NDKWCCLKSWNDBG-UHFFFAOYSA-N 0.000 claims abstract description 7
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 claims abstract description 6
- 229920005862 polyol Polymers 0.000 claims description 18
- 238000005242 forging Methods 0.000 claims description 17
- 150000003077 polyols Chemical class 0.000 claims description 17
- 238000005058 metal casting Methods 0.000 claims description 15
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
- 239000003822 epoxy resin Substances 0.000 claims description 7
- 229920000647 polyepoxide Polymers 0.000 claims description 7
- 239000004593 Epoxy Substances 0.000 claims description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 229920000180 alkyd Polymers 0.000 claims description 3
- 239000004925 Acrylic resin Substances 0.000 claims description 2
- 229920000178 Acrylic resin Polymers 0.000 claims description 2
- 229920001225 polyester resin Polymers 0.000 claims description 2
- 239000004645 polyester resin Substances 0.000 claims description 2
- 239000005056 polyisocyanate Substances 0.000 claims description 2
- 229920001228 polyisocyanate Polymers 0.000 claims description 2
- 230000007797 corrosion Effects 0.000 abstract description 13
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 6
- 229910052742 iron Inorganic materials 0.000 abstract description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052782 aluminium Inorganic materials 0.000 abstract description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 3
- 229910019142 PO4 Inorganic materials 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 abstract 1
- 239000010452 phosphate Substances 0.000 abstract 1
- 238000001723 curing Methods 0.000 description 13
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000049 pigment Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 238000005266 casting Methods 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 3
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 3
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229960002887 deanol Drugs 0.000 description 3
- -1 diisocyanate compound Chemical class 0.000 description 3
- 239000012972 dimethylethanolamine Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229920000298 Cellophane Polymers 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000004512 die casting Methods 0.000 description 2
- GGSUCNLOZRCGPQ-UHFFFAOYSA-N diethylaniline Chemical compound CCN(CC)C1=CC=CC=C1 GGSUCNLOZRCGPQ-UHFFFAOYSA-N 0.000 description 2
- 125000005442 diisocyanate group Chemical group 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000003746 surface roughness Effects 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- FKTHNVSLHLHISI-UHFFFAOYSA-N 1,2-bis(isocyanatomethyl)benzene Chemical class O=C=NCC1=CC=CC=C1CN=C=O FKTHNVSLHLHISI-UHFFFAOYSA-N 0.000 description 1
- RJDYKQDRMZDDOM-UHFFFAOYSA-N 1,6-diaminohexane-2,5-diol Chemical compound NCC(O)CCC(O)CN RJDYKQDRMZDDOM-UHFFFAOYSA-N 0.000 description 1
- IWSZDQRGNFLMJS-UHFFFAOYSA-N 2-(dibutylamino)ethanol Chemical compound CCCCN(CCO)CCCC IWSZDQRGNFLMJS-UHFFFAOYSA-N 0.000 description 1
- FMFWSIARXFCACS-UHFFFAOYSA-N 2-[bis(2-ethylhexyl)amino]ethanol Chemical compound CCCCC(CC)CN(CCO)CC(CC)CCCC FMFWSIARXFCACS-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 1
- 239000005058 Isophorone diisocyanate Substances 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- QFFVPLLCYGOFPU-UHFFFAOYSA-N barium chromate Chemical compound [Ba+2].[O-][Cr]([O-])(=O)=O QFFVPLLCYGOFPU-UHFFFAOYSA-N 0.000 description 1
- 229940083898 barium chromate Drugs 0.000 description 1
- 238000005422 blasting Methods 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 238000013007 heat curing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- 239000001023 inorganic pigment Substances 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
- PIJPYDMVFNTHIP-UHFFFAOYSA-L lead sulfate Chemical compound [PbH4+2].[O-]S([O-])(=O)=O PIJPYDMVFNTHIP-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- AYLRODJJLADBOB-QMMMGPOBSA-N methyl (2s)-2,6-diisocyanatohexanoate Chemical compound COC(=O)[C@@H](N=C=O)CCCCN=C=O AYLRODJJLADBOB-QMMMGPOBSA-N 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- MXHTZQSKTCCMFG-UHFFFAOYSA-N n,n-dibenzyl-1-phenylmethanamine Chemical compound C=1C=CC=CC=1CN(CC=1C=CC=CC=1)CC1=CC=CC=C1 MXHTZQSKTCCMFG-UHFFFAOYSA-N 0.000 description 1
- OOHAUGDGCWURIT-UHFFFAOYSA-N n,n-dipentylpentan-1-amine Chemical compound CCCCCN(CCCCC)CCCCC OOHAUGDGCWURIT-UHFFFAOYSA-N 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000005498 polishing Methods 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- YFTHZRPMJXBUME-UHFFFAOYSA-N tripropylamine Chemical compound CCCN(CCC)CCC YFTHZRPMJXBUME-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、鉄系材料及び被鉄金属材料等の鋳物または、
鍛造品、即ち各種金属鋳鍛造品の改良された防錆塗装方
法に関する。[Detailed Description of the Invention] [Industrial Field of Application] The present invention relates to castings of ferrous materials and ferrous metal materials, etc.
This invention relates to an improved anti-rust coating method for forged products, that is, various metal casting and forging products.
従来鉄鋳物、アルミダイカスト製品等の各種金属鋳鍛造
品の防錆塗装方法としては、速乾性アルキッド樹脂塗料
あるいはラッカー型塗料を塗装し、常温で塗膜を乾燥す
るか、比帥的イl厄掘I テ lイEl Q n0ρ
〜 1 区 n0ρ箇但向φ乾燥する方法が行われてい
る。かかる従来の塗装方法で得られる金属鋳鍛造品の塗
膜の耐蝕性は、ツルトスプレー法で72〜120時間程
度の耐蝕性でしかなく、このため更にすぐれた耐蝕性を
有する塗膜を得るためには、アルキッド−メラミン系の
焼付硬化型の塗料を用い、塗装した塗膜を焼付ける方法
が行われている。Conventional anti-rust coating methods for various metal castings and forgings, such as iron castings and aluminum die-casting products, include coating with quick-drying alkyd resin paint or lacquer-type paint and drying the coating at room temperature, or drying the paint film at room temperature. Hori Te El Q n0ρ
~ 1 ward n0ρkadankoφ drying method is used. The corrosion resistance of coatings on metal castings and forgings obtained by such conventional coating methods is only about 72 to 120 hours using the Tsuruto spray method. Therefore, in order to obtain coatings with even better corrosion resistance, A method of baking the painted film using an alkyd-melamine baking-curing paint is used.
しかしながら上述した焼付硬化型塗料を使用する塗装方
法においては、焼付硬化するに当って、被塗物である金
属鋳鍛造品が一般に比熱が大であり、しかも通常肉厚で
あるために焼付加熱のために非常に大なる熱量を必要と
し、更に被塗物の温度上昇が遅く、焼付けに時間がかか
る欠点を有している。また金属鋳鍛造品の表面における
温度分布に差異を生ずることがあり、このため塗膜の硬
化が均一に行なわれず、特に硬化不足となった部分の塗
膜には充分な性能が得られないという欠点も有していた
。However, in the painting method using the above-mentioned bake-hardening paint, the metal castings and forgings to be coated generally have a large specific heat and are usually thick, so the heat added by baking increases. This method requires a very large amount of heat, and also has the disadvantage that the temperature of the object to be coated increases slowly and baking takes time. Additionally, there may be differences in temperature distribution on the surface of metal castings and forgings, which prevents the coating from curing uniformly, making it difficult to obtain sufficient performance, especially in areas where the coating is insufficiently cured. It also had drawbacks.
また一般に金属錆F2造品は表面粗度が大であり、この
ため加熱硬化時のヒートフローにより、突起部では塗膜
が薄くなり、いわゆる透けを生じ、塗膜不足による耐蝕
性の低下がみられる。In addition, metal rust F2 products generally have a high surface roughness, so the heat flow during heat curing causes the coating film to become thinner at the protruding parts, resulting in so-called see-through, resulting in a decrease in corrosion resistance due to insufficient coating film. It will be done.
従って本発明の目的は、高温焼付加熱を必要とせず表面
粗度の一般に大なる金属鋳鍛造品にすぐれた耐蝕性を有
する塗膜を形成するための塗装方法を提供することであ
り、ウレタン樹脂塗料を使用し、常温ないしは100°
C以下の低温で硬化することにより前記ヒートフローに
よる透けの問題を解決すると共に、その下塗りとしてい
わゆるウォッシュプライマーを塗装することにより、さ
らに耐蝕性の向上をはかるものである。Therefore, an object of the present invention is to provide a coating method for forming a coating film having excellent corrosion resistance on metal castings and forgings, which generally have a large surface roughness, without requiring high-temperature baking heat. Use paint at room temperature or 100°
By curing at a low temperature below C, the problem of see-through due to heat flow is solved, and by applying a so-called wash primer as an undercoat, corrosion resistance is further improved.
本発明は、金属鋳鍛造品を二液型ウオシュプライマーで
塗装し、引き続き(A)ウレタン樹脂塗料で塗装し、気
化したアミン雰囲気中にて、塗膜を硬化させる又は(B
)ウレタン塗料を気化したアミンを含有する空気で、霧
化塗装するものであり、金属錆鍛造物を防錆塗装するに
際し、まずブチラール樹脂、ジンククロメート、リン酸
からなるウォッシュプライマーを塗布し、しかる後、ウ
レタン樹脂塗料で塗装し、気相状態にあるアミン雰囲気
中で、ウレタン樹脂塗料塗膜を硬化させることを特徴と
する塗装方法、及び金属鋳鍛造品を防錆塗装するに際し
、まずブチラール樹脂、ジンククロメート、リン酸から
なるウォッシュプライマーを塗布し、しかる後、ウレタ
ン樹脂塗料を気化したアミンを含有する空気で、霧化塗
装することを特徴とする塗装方法である。The present invention involves painting metal castings and forgings with a two-component wash primer, followed by (A) painting with a urethane resin paint, and curing the paint film in a vaporized amine atmosphere, or (B)
) The urethane paint is atomized with air containing vaporized amine, and when applying rust-preventive coating to metal rust forgings, first apply a wash primer consisting of butyral resin, zinc chromate, and phosphoric acid, and then A coating method characterized by coating with a urethane resin paint and curing the urethane resin paint film in an amine atmosphere in a gaseous state, and when applying anti-corrosion coating to metal castings and forgings, first apply butyral resin. This coating method is characterized by applying a wash primer consisting of , zinc chromate, and phosphoric acid, and then atomizing the urethane resin paint with air containing vaporized amine.
本発明方法で塗装しうる金属鋳鍛造品としては、各種鉄
系材料の鋳鍛造品、アルミダイカスト製品の如き、鉄、
非鉄金属の鋳形品および鍛造品がある。Metal castings and forgings that can be coated using the method of the present invention include castings and forgings made of various iron-based materials, aluminum die-casting products, iron,
There are non-ferrous metal castings and forgings.
本発明で使用されるウォッシュプライマーは、ブチラー
ル樹脂及びジンククロメートを主成分とする基材とリン
酸を主成分とする硬化剤とからなる通常公知の二液型ウ
ォッシュプライマーであればよい。The wash primer used in the present invention may be any commonly known two-component wash primer consisting of a base material mainly composed of butyral resin and zinc chromate and a curing agent mainly composed of phosphoric acid.
本発明で使用しうるウレタン樹脂塗料は、ビヒクル中に
インシアネート基を有する化合物もしくは樹脂を含有す
る塗料であればよく、任意のものを使用しうるが、特に
二液型ポリウレタン塗料が好ましい。The urethane resin paint that can be used in the present invention may be any paint that contains a compound or resin having an incyanate group in the vehicle, but two-component polyurethane paints are particularly preferred.
二液型ポリウレタン塗料とは、分子中に2個以上の水酸
基を有する樹脂を含有する塗料成分(基材)と、分子中
に2個以上のイソシアネート基を有する化合物もしくは
モノマーまたはプレポリマー(硬化剤)とを塗装前に所
定量混合して使用する塗料である。A two-component polyurethane paint consists of a paint component (base material) containing a resin having two or more hydroxyl groups in the molecule, and a compound or monomer or prepolymer (hardening agent) having two or more isocyanate groups in the molecule. ) is a paint that is used by mixing a predetermined amount with before painting.
本発明方法においては上記二液型ポリウレタン塗料の基
材ポリオール成分として、特に水酸基価が10以上のア
クリル樹脂ポリオール、アルキド樹脂ポリオールまたは
ポリエステル樹脂ポリオール20〜95重量%およびエ
ポキシ価300〜4000を有するエポキシ樹脂ポリオ
ール5〜80重量%よりなるのが好ましい。In the method of the present invention, as the base polyol component of the two-component polyurethane paint, 20 to 95% by weight of an acrylic resin polyol, an alkyd resin polyol, or a polyester resin polyol having a hydroxyl value of 10 or more and an epoxy resin having an epoxy value of 300 to 4,000 are used. Preferably, it consists of 5 to 80% by weight of the resin polyol.
才な本発明で使用する二液型ポリウレタン塗料の硬化剤
成分としてはトリレンジイソシアネート、キシレンジイ
ソシアネー?−、ヘキサンメチレンジイソシアネート、
イソホロンジイソシアネート、4,4′−ジフェニルメ
タンジイソシアネート、4,4′−ジシクロヘキシルメ
タンジイソシアネート、リジンジイソシアネート、水素
添加キシリレンジイソシアネート、水素添加インホロン
ジイソシアネートの如きジイソシアネート化合物の3〜
5量体、更には過剰モルの上記ジイソシアネート化合物
とエチレングリコール、プロピレングリコール等の2価
アルコールまたはグリセリン、トリメチロールプロパン
等の3価アルコールとを反応させて得られる付加物、更
にはこれらの重合体を使用できる。The curing agent components of the two-component polyurethane paint used in the present invention include tolylene diisocyanate and xylene diisocyanate. −, hexamethylene diisocyanate,
3 to 3 of diisocyanate compounds such as isophorone diisocyanate, 4,4'-diphenylmethane diisocyanate, 4,4'-dicyclohexylmethane diisocyanate, lysine diisocyanate, hydrogenated xylylene diisocyanate, and hydrogenated inphorone diisocyanate.
Pentamer, furthermore, an adduct obtained by reacting an excess molar amount of the above diisocyanate compound with a dihydric alcohol such as ethylene glycol or propylene glycol or a trihydric alcohol such as glycerin or trimethylolpropane, and furthermore, a polymer thereof. can be used.
硬化剤は基材ポリオール成分中の水酸基1モルに対して
イソシアネート基が0.8〜1.2モルとなる割合で混
合して使用する。The curing agent is used by mixing in a ratio of 0.8 to 1.2 moles of isocyanate groups per mole of hydroxyl groups in the base polyol component.
本発明で使用しうる上述した基材ポリオール成分には所
望により、塗膜の乾燥性向上、物性改良、外観改良の目
的で他の樹脂例えば繊維素誘導体、ポリ塩化ビニル、ポ
リ酢酸ビニル、塩化ビニル、酢酸ビニル共重合体等を混
入してもよく、また顔料溶剤、各種添加剤を加えること
ができる。The above-mentioned base polyol component that can be used in the present invention may optionally contain other resins such as cellulose derivatives, polyvinyl chloride, polyvinyl acetate, and vinyl chloride for the purpose of improving the drying properties, physical properties, and appearance of the coating film. , vinyl acetate copolymer, etc. may be mixed, and pigment solvents and various additives may also be added.
顔料としては着色顔料例えばカーボンブラック、酸化鉄
、酸化チタン、黄鉛等の無機顔料、シアニンググリーン
、シアニングブルーその他の有機顔料:防錆顔料として
ストロンチウムクロメ−1−、鉛白、鉛酸カルシウム、
塩基性硫酸鉛、鉛丹、ジンククロメート、クロム酸バリ
ウム:体質顔料として例えば炭酸カルシウム、タルク、
クレー、硫酸バリウム、ケイ石粉等が使用できる。溶剤
としては硬化剤と反応しないものであれば任意の溶剤を
使用でき、例えばアセトン、メチルエチルケトン、メチ
ルイソブチルケトン、酢酸エチル、酢酸ブチル、セロソ
ルブアセテート、トルエン、キシレン等を使用できる。Pigments include colored pigments such as carbon black, iron oxide, titanium oxide, inorganic pigments such as yellow lead, cyanine green, cyanine blue and other organic pigments, and anti-rust pigments such as strontium chrome-1-, lead white, and calcium leadate. ,
Basic lead sulfate, red lead, zinc chromate, barium chromate: Extender pigments such as calcium carbonate, talc,
Clay, barium sulfate, silica powder, etc. can be used. Any solvent can be used as long as it does not react with the curing agent, such as acetone, methyl ethyl ketone, methyl isobutyl ketone, ethyl acetate, butyl acetate, cellosolve acetate, toluene, xylene, and the like.
各種添加剤としては沈殿防止剤、酸化防止剤、粘度調整
剤、表面調整剤等を使用できる。As various additives, a suspending agent, an antioxidant, a viscosity modifier, a surface modifier, etc. can be used.
本発明で使用する二液型ポリウレタン塗料の上記基材ポ
リオール成分の水酸基価は10以上、好ましくは]−〇
〜300である。水酸基価が10未満であるとインシア
ネート化合物との反応により生成するウレタン結合が少
なくなりすぎ、形成される塗膜に充分な防蝕性が得られ
ず、また水酸基価が300を超えると後述する如く、本
発明に従ってアミン雰囲気中に暴露したとき常温での硬
化に長時間を要するようになるので好ましくない。また
併用するエポキシ樹脂としてはエポキシ価300〜40
00のものが好ましく、300未満では形成される塗膜
の硬化不充分となり、4000を超えると塗料粘度が大
となりすぎ塗装困難を生ずることがあり、また塗膜の膜
厚低下を生ずることがあるので奸才しくない本発明方法
で使用するウレタン樹脂塗料においては水酸基価10以
上のポリオール成分を20〜95重量%、エポキシ価3
00〜4000のエポキシ樹脂を5〜80重量%の割1
゛
合で使用するのが好ましく、エポキシ樹脂成分が5重量
%未満となると、形成される塗膜の耐蝕性が低下し、ま
た80重量%を超えると後述するアミン雰囲気中に曝し
て塗膜を硬化させるのに長時間を要するので好ましくな
い。The base polyol component of the two-component polyurethane paint used in the present invention has a hydroxyl value of 10 or more, preferably from -0 to 300. If the hydroxyl value is less than 10, the number of urethane bonds generated by the reaction with the incyanate compound will be too small, and the resulting coating will not have sufficient corrosion resistance.If the hydroxyl value exceeds 300, as will be described later, According to the present invention, when exposed to an amine atmosphere, curing at room temperature takes a long time, which is not preferable. In addition, the epoxy resin used in combination has an epoxy value of 300 to 40.
A value of 0.00 is preferable; if it is less than 300, the coating film formed will be insufficiently cured, and if it exceeds 4000, the viscosity of the paint may become too high, making it difficult to coat, and may also cause a decrease in the thickness of the coating film. Therefore, the urethane resin paint used in the unsophisticated method of the present invention contains 20 to 95% by weight of a polyol component with a hydroxyl value of 10 or more, and an epoxy value of 3.
5 to 80% by weight of 00 to 4000 epoxy resin
If the epoxy resin component is less than 5% by weight, the corrosion resistance of the coating film formed will decrease, and if it exceeds 80% by weight, the coating film may be exposed to the amine atmosphere described below. This is not preferred because it takes a long time to cure.
本発明方法を実施するには、まず、前述したウォッシュ
プライマーの基材と硬化剤を定率で混合して、5〜10
μの膜厚を得る様に塗布する。次に(A>前述の基材ポ
リオール成分と、硬化剤ポリイソシアネートとを混合し
、金属の鋳鍛造品に塗布する。更にアミン雰囲気中に曝
露することにより硬化させれば良い。To carry out the method of the present invention, first, the base material of the wash primer described above and a curing agent are mixed at a fixed ratio,
Apply to obtain a film thickness of μ. Next (A> The above-mentioned base polyol component and hardening agent polyisocyanate are mixed and applied to a metal cast and forged product. Furthermore, it may be hardened by exposing it to an amine atmosphere.
又(A)の代りに(B)気化したアミンを含有する空気
で、ウレタン樹脂塗料を霧化して塗装しても良い。Alternatively, instead of (A), (B) the urethane resin paint may be atomized and applied using air containing vaporized amine.
このとき使用しうるアミンとしては第三級アミンが好ま
しく、例えばトリメチルアミン、トリエチルアミン、ト
リプロピルアミン、トリブチルアミン、トリアミルアミ
ン、テトラメチルエチレンジアミン等の脂肪族アミン、
ジエチルアニリン、ジエチルアニリン、トリベンジルア
ミン等の芳香族アミン、N−メチルモルホリン、N−エ
チルモルボリン、あるいはメチルジェタノールアミン、
ジメチルエタノールアミン、ジエチルエタノールアミン
、ジブチルエタノールアミン、ジ(2−エチルヘキシル
)エタノールアミン、エチレンジエタノールアミン、ジ
ブデルイソプロパノールアミン等のアルカノールアミン
があり、なかでもジメチルエタノールアミン、テトラメ
チルエチレンジアミンが好ましい。The amines that can be used at this time are preferably tertiary amines, such as aliphatic amines such as trimethylamine, triethylamine, tripropylamine, tributylamine, triamylamine, and tetramethylethylenediamine;
Aromatic amines such as diethylaniline, diethylaniline, tribenzylamine, N-methylmorpholine, N-ethylmorboline, or methyljetanolamine,
There are alkanolamines such as dimethylethanolamine, diethylethanolamine, dibutylethanolamine, di(2-ethylhexyl)ethanolamine, ethylenediethanolamine, and dibdelisopropanolamine, among which dimethylethanolamine and tetramethylethylenediamine are preferred.
上記アミンによる雰囲気又は、霧化用空気中のアミン濃
度が約10〜3000ppm、好ましくは約600〜2
000 p p mとなるようにし、雰囲気温度は常温
が望ましい、しかし0〜]−00°Cの温度、好ましく
は10〜50℃の温度を使用しうる。なおアミン雰囲気
は静止状態よりもその触媒作用を効果的にするため0.
5〜2.0m/秒の風速で循環させるのが好ましい。The amine concentration in the above amine atmosphere or atomizing air is about 10 to 3000 ppm, preferably about 600 to 2
000 ppm, and the ambient temperature is preferably room temperature, but a temperature of 0 to -00°C, preferably 10 to 50°C may be used. It should be noted that the amine atmosphere has a 0.0.
It is preferable to circulate at a wind speed of 5 to 2.0 m/sec.
アミン雰囲気に曝露する時間、即ち塗膜を硬化させるの
に要する時間は、塗膜の膜厚によって異なるが一般に1
〜10分、好ましくは2〜3分で充分である。一般にア
ミン雰囲気中で処理をした後、常温でアミンを含まぬ空
気を吹きつけて乾燥硬化を促進させるのが好ましい。こ
のときの空気温度は常温で充分であるが、場合によって
は100℃以下、好ましくは25〜50°Cの温度を使
用しても良い。The time of exposure to the amine atmosphere, that is, the time required to cure the coating film, varies depending on the thickness of the coating film, but is generally 1.
~10 minutes, preferably 2-3 minutes is sufficient. Generally, after processing in an amine atmosphere, it is preferable to blow amine-free air at room temperature to accelerate drying and curing. At this time, room temperature is sufficient as the air temperature, but in some cases, a temperature of 100°C or less, preferably 25 to 50°C may be used.
本発明方法によれば、上述したウォッシュブライマーと
ウレタン樹脂塗料を用いて金属鋳鍛造品を重ね塗りした
後、従来の塗装方法の如く塗膜もしくは金属鋳鍛造品を
加熱する必要はなく、単に上述した如く、アミン雰囲気
に短時間曝露することによって塗膜を硬化させることが
できる。このため塗膜に従来法の如きヒートフローによ
る膜厚低下もなく、また局部加熱もしくは不均一加熱に
よる塗膜性能のバラツキも生ぜず、後述する実施例にも
示す如く、塩水噴霧試験による耐蝕性においてもすぐれ
た塗膜が得られる。According to the method of the present invention, it is not necessary to heat the coating film or the metal casting and forgings as in the conventional coating method after overcoating the metal castings and forgings using the above-mentioned wash primer and urethane resin paint. As mentioned above, the coating can be cured by brief exposure to an amine atmosphere. As a result, there is no reduction in film thickness due to heat flow as in conventional methods, and there is no variation in film performance due to localized or uneven heating, and as shown in the examples below, corrosion resistance in salt spray tests has been confirmed. An excellent coating film can also be obtained.
以下に実施例を挙げて本発明を説明する。 The present invention will be explained below with reference to Examples.
文中、部は重量部である。In the text, parts are parts by weight.
実施例1
鋳鉄の鋳物をショツトブラストで研磨した後、二液型ウ
ォッシュプライマー(神東塗料社製商品名ウォッシュプ
ライマー#20;基剤/硬化剤−80/20 )を7μ
になる様に塗布した。Example 1 After polishing a cast iron casting by shot blasting, 7μ of a two-component wash primer (trade name: Wash Primer #20, manufactured by Shinto Toyo Co., Ltd.; base/hardener: 80/20) was applied.
I applied it to make it look like this.
ソト I−方 古、l−1−下台−勇2 イト /7’
l−一 臂蔓斤J カ 1ノ 々 ソ 倉−脂塗料を乾
燥塗膜が30μになる様に塗布した。Soto I-way old, l-1-shitadai-yu 2 ito /7'
The paint was applied so that the dry coating film was 30μ.
基剤成分(アクリルポリオール/エポキシ樹脂−60/
40 )
カーボンブラック 3.0部りロム酸
スl−ロチウム 5.0部タルク
10.0部クレー
15.0部ポリアクリルポリオール(
水酸基価
25、大日本インキ社製、不揮発分
50%) 35.0部エ
ピコート1001 (エポキシ価4
50〜500のエポキシ樹脂、油化
シェルエポキシ社製> 12.0部シンナ
ー 20.0部合 計
100.0部硬化剤成分
スミジュールL−75()ルエンジイソシアネート、住
友バイエルウレタン
社製) 14.5部塗装
後2分間室温で放置し、次いでジメチルエタノールアミ
ン800ppmの雰囲気中で風速1.2m/秒で塗膜を
曝露した。その後更に10分間室温の空気を吹き付は乾
燥硬化させた。Base component (acrylic polyol/epoxy resin-60/
40) Carbon black 3.0 parts Sl-rotium romate 5.0 parts Talc
10.0 parts clay
15.0 parts polyacrylic polyol (
Hydroxyl value 25, manufactured by Dainippon Ink Co., Ltd., non-volatile content 50%) 35.0 parts Epicoat 1001 (Epoxy resin with an epoxy value 4 50-500, manufactured by Yuka Shell Epoxy Co., Ltd. > 12.0 parts Thinner 20.0 parts total
100.0 parts Curing agent component: SUMIDULE L-75 (2) (renediisocyanate, manufactured by Sumitomo Bayer Urethane) 14.5 parts After painting, leave to stand at room temperature for 2 minutes, then blow in an atmosphere containing 800 ppm of dimethylethanolamine at a wind speed of 1.2 m/min. The coating was exposed in seconds. Thereafter, it was dried and cured by blowing room temperature air for another 10 minutes.
更に1日経過後塗膜にナイフでクロスカッ)・を入れ、
塩水噴霧試験機に480時間入れた後取り出し、水洗し
、乾燥したのち、クロスカット部にセロファンテープを
圧着し、引き剥してクロスカット部からの塗膜の剥離幅
を測定したところ、片幅で3關以内であり、良好な耐蝕
性を得た。また鋳形品突部の直鎖は全くなく外観良好で
あった。After another day, cross-cut the paint film with a knife,
After placing it in a salt spray tester for 480 hours, it was taken out, washed with water, and dried. Cellophane tape was pressed onto the cross-cut area, and the tape was peeled off to measure the peeling width of the coating film from the cross-cut area. Within 3 degrees, good corrosion resistance was obtained. In addition, there were no straight chains in the protrusions of the molded product, and the appearance was good.
実施例2
実施例]と同様にし、て、ウォッシュプライマーを7μ
になる様に塗布した。Example 2 In the same manner as in Example], add 7μ of wash primer.
I applied it to make it look like this.
次に、直ちに実施例1と同様の二液型ウレタン樹脂塗料
をアミンを気化した空気で霧化し、30μになる様に塗
装した。Next, immediately a two-component urethane resin paint similar to that in Example 1 was atomized with air containing vaporized amine, and coated to a thickness of 30 μm.
使用したアミンはトリエチルアミンで空気中の濃度は6
00ppmであった。The amine used was triethylamine, and its concentration in the air was 6.
It was 00 ppm.
実施例1と同様にして、塗膜性能テストした。The coating film performance was tested in the same manner as in Example 1.
塩化噴霧試験機に360時間入れた後、取り出し水洗し
、乾燥した後、クロスカット部からの塗膜の剥離中を測
定したところ、片山で3關以内であり、良好な耐蝕性を
得た。After being placed in a chloride spray tester for 360 hours, it was taken out, washed with water, and dried. When the peeling of the coating film from the cross-cut portion was measured, it was within 3 degrees at Katayama, indicating good corrosion resistance.
また、鋳形晶突部の直鎖は、10c+++2当り、2〜
3点であった。In addition, the straight chain of the mold crystal protrusion is 2 to 2 per 10c+++2.
It was 3 points.
〔比較例1〕
塗膜の硬化処理をアミンを含まぬ雰囲気で120℃で2
0分焼付な以外は実施例1と同様に塗装した。[Comparative Example 1] The coating film was cured at 120°C for 2 hours in an amine-free atmosphere.
Painting was carried out in the same manner as in Example 1, except that baking was performed for 0 minutes.
塩水噴霧試験240時間後、クロスカット部のセロファ
ンテープを引き剥したところ、剥離幅は3關以内であっ
たが、凸部より直鎖が多数発生し、外観不良となった。After 240 hours of the salt spray test, the cellophane tape at the cross-cut portion was peeled off, and although the peeling width was within 3 degrees, many straight chains were generated from the convex portions, resulting in poor appearance.
本発明の方法に従うと、常温で短時間で乾燥でき、また
常温で乾燥できるなめ省エネルギーとなる等の効果があ
るうえ、従来の塗装方法によって得られる塗膜のヒート
フローによる膜厚低下に起因する耐蝕性紙下等の欠点が
除かれるので金属鋳鍛造品の塗装方法としては好適であ
る。According to the method of the present invention, it can be dried at room temperature in a short time, and it can be dried at room temperature, which saves energy. It is suitable as a coating method for metal castings and forgings because it eliminates defects such as corrosion-resistant paper coating.
Claims (1)
ル樹脂、ジンククロメート、リン酸からなるウォッシュ
プライマーを塗布し、しかる後、ウレタン樹脂塗料で塗
装し、気相状態にあるアミン雰囲気中で、ウレタン樹脂
塗料塗膜を硬化させることを特徴とする塗装方法。 2、金属鋳鍛造品を防錆塗装するに際し、まずブチラー
ル樹脂、ジンククロメート、リン酸からなるウォッシュ
プライマーを塗布し、しかる後、ウレタン樹脂塗料を気
化したアミンを含有する空気で、霧化塗装することを特
徴とする塗装方法。 3、ウレタン樹脂塗料が二液型ポリウレタン塗料である
特許請求の範囲第1及び第2項記載の塗装方法。 4、二液ポリウレタン塗料の基材ポリオール成分が、水
酸基価10以上のアクリル樹脂ポリオール、アルキド樹
脂ポリオールまたはポリエステル樹脂ポリオール20〜
95重量%およびエポキシ価300〜4000を有する
エポキシ樹脂ポリオール5〜80重量%よりなり、硬化
剤成分がポリイソシアネート化合物からなる特許請求の
範囲第3項記載の塗装方法。[Claims] 1. When applying anti-corrosion coating to metal castings and forgings, first apply a wash primer consisting of butyral resin, zinc chromate, and phosphoric acid, then apply urethane resin paint, and leave it in a gas phase. A coating method characterized by curing a urethane resin paint film in an amine atmosphere. 2. When applying anti-rust coating to metal castings and forgings, first apply a wash primer consisting of butyral resin, zinc chromate, and phosphoric acid, and then atomize the urethane resin paint with air containing amine. A painting method characterized by: 3. The coating method according to claims 1 and 2, wherein the urethane resin paint is a two-component polyurethane paint. 4. The base polyol component of the two-component polyurethane paint is an acrylic resin polyol, an alkyd resin polyol, or a polyester resin polyol with a hydroxyl value of 10 or more from 20 to 20.
4. The coating method according to claim 3, comprising 95% by weight of an epoxy resin polyol and 5 to 80% by weight of an epoxy resin polyol having an epoxy value of 300 to 4000, and the curing agent component comprising a polyisocyanate compound.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8781686A JPS62244476A (en) | 1986-04-16 | 1986-04-16 | Improved method for anticorrosion painting of metal cast and forged product |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8781686A JPS62244476A (en) | 1986-04-16 | 1986-04-16 | Improved method for anticorrosion painting of metal cast and forged product |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS62244476A true JPS62244476A (en) | 1987-10-24 |
Family
ID=13925494
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8781686A Pending JPS62244476A (en) | 1986-04-16 | 1986-04-16 | Improved method for anticorrosion painting of metal cast and forged product |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS62244476A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04335501A (en) * | 1991-05-11 | 1992-11-24 | Sumitomo Special Metals Co Ltd | Permanent magnet excellent in corrosion resistance |
CN105925156A (en) * | 2016-06-20 | 2016-09-07 | 无锡市虎皇漆业有限公司 | One-step forming solvent type single-component quick drying hammer finish and preparation method |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS518131A (en) * | 1974-07-11 | 1976-01-22 | Riken Keikinzoku Kogyo Kk | Aruminiumumoshikuha aruminiumugokinzaino chakushokusankahimakuseiseiho |
JPS59170153A (en) * | 1983-03-10 | 1984-09-26 | シユランド・オイル・インコ−ポレ−テツド | Adhesion of liquid paint coating to substrate |
JPS59216661A (en) * | 1983-05-25 | 1984-12-06 | Mitsubishi Electric Corp | Method for curing polyurethane film |
JPS6075356A (en) * | 1983-09-30 | 1985-04-27 | Trinity Ind Corp | Device for forming coated film |
-
1986
- 1986-04-16 JP JP8781686A patent/JPS62244476A/en active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS518131A (en) * | 1974-07-11 | 1976-01-22 | Riken Keikinzoku Kogyo Kk | Aruminiumumoshikuha aruminiumugokinzaino chakushokusankahimakuseiseiho |
JPS59170153A (en) * | 1983-03-10 | 1984-09-26 | シユランド・オイル・インコ−ポレ−テツド | Adhesion of liquid paint coating to substrate |
JPS59216661A (en) * | 1983-05-25 | 1984-12-06 | Mitsubishi Electric Corp | Method for curing polyurethane film |
JPS6075356A (en) * | 1983-09-30 | 1985-04-27 | Trinity Ind Corp | Device for forming coated film |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH04335501A (en) * | 1991-05-11 | 1992-11-24 | Sumitomo Special Metals Co Ltd | Permanent magnet excellent in corrosion resistance |
CN105925156A (en) * | 2016-06-20 | 2016-09-07 | 无锡市虎皇漆业有限公司 | One-step forming solvent type single-component quick drying hammer finish and preparation method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS585345A (en) | Vapor permeable curable coating for surface porous base material | |
KR940011198B1 (en) | Process for painting a polyolefinic resin component | |
US5283084A (en) | Process for making wrinkle-free coating using solventborne clearcoat composition over waterborne basecoat composition | |
JPH0238129B2 (en) | ||
JPS62244476A (en) | Improved method for anticorrosion painting of metal cast and forged product | |
US2798009A (en) | Coating composition for metals | |
JPH0331382A (en) | Manufacture of coating material and coated material, coated base | |
JPS6153366A (en) | Coating of thick-coating sealer paint for mending | |
JP2000140748A (en) | Coating of wheel for vehicle with plating tone appearance and wheel for vehicle | |
JPS6214972A (en) | Method for painting metal cast and forged products | |
JPH09131567A (en) | Coating method of aluminum foil | |
JP2002035685A (en) | Method for preventing rusting of weatherable steel | |
JPH0860090A (en) | Coating composition curable with amine catalyst and coating method | |
JPS60203437A (en) | Metallic coated metallic plate | |
Kurata et al. | Development of High Appearance Water Born Primer Surfacer Coating for Short Process Body Paint | |
JP3001812B2 (en) | Automotive coating composition | |
JPS63161034A (en) | Improved method for painting reaction injection molded article | |
JP3987884B2 (en) | How to paint counterweight | |
CN114316749A (en) | Vehicle-mounted magnesium alloy UV piano black paint | |
JP3969462B2 (en) | Painting method | |
CA1234441A (en) | Multiple use acrylic primer composition | |
JPH01151978A (en) | Automotive coating method | |
JPS6054115B2 (en) | How to paint a car body | |
JP2002273330A (en) | Coating film forming method and coated article | |
JPH06279728A (en) | Coating application method |