JP2667886B2 - Repair method of coating film - Google Patents
Repair method of coating filmInfo
- Publication number
- JP2667886B2 JP2667886B2 JP63279977A JP27997788A JP2667886B2 JP 2667886 B2 JP2667886 B2 JP 2667886B2 JP 63279977 A JP63279977 A JP 63279977A JP 27997788 A JP27997788 A JP 27997788A JP 2667886 B2 JP2667886 B2 JP 2667886B2
- Authority
- JP
- Japan
- Prior art keywords
- coating film
- top coat
- paint
- coating
- repairing
- 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 68
- 239000011248 coating agent Substances 0.000 title claims description 66
- 238000000034 method Methods 0.000 title claims description 27
- 239000003973 paint Substances 0.000 claims description 35
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 23
- 239000000049 pigment Substances 0.000 claims description 22
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims description 21
- 238000005498 polishing Methods 0.000 claims description 15
- 239000011347 resin Substances 0.000 claims description 9
- 229920005989 resin Polymers 0.000 claims description 9
- 239000007787 solid Substances 0.000 claims description 4
- 239000008199 coating composition Substances 0.000 claims 3
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 12
- 239000000178 monomer Substances 0.000 description 12
- 238000010422 painting Methods 0.000 description 7
- 239000002987 primer (paints) Substances 0.000 description 7
- 239000005057 Hexamethylene diisocyanate Substances 0.000 description 6
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- RRAMGCGOFNQTLD-UHFFFAOYSA-N hexamethylene diisocyanate Chemical compound O=C=NCCCCCCN=C=O RRAMGCGOFNQTLD-UHFFFAOYSA-N 0.000 description 6
- 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 6
- 239000004925 Acrylic resin Substances 0.000 description 5
- 229920000178 Acrylic resin Polymers 0.000 description 5
- 239000005002 finish coating Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 239000004923 Acrylic lacquer Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 210000003298 dental enamel Anatomy 0.000 description 4
- 239000000463 material Substances 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
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 3
- 239000005056 polyisocyanate Substances 0.000 description 3
- 229920001228 polyisocyanate Polymers 0.000 description 3
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 2
- 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
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 239000005058 Isophorone diisocyanate Substances 0.000 description 2
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 238000005299 abrasion Methods 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- -1 hydroxypropyl Chemical group 0.000 description 2
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 239000004922 lacquer Substances 0.000 description 2
- 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 2
- 239000000203 mixture Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- 239000011342 resin composition Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- VZXPHDGHQXLXJC-UHFFFAOYSA-N 1,6-diisocyanato-5,6-dimethylheptane Chemical compound O=C=NC(C)(C)C(C)CCCCN=C=O VZXPHDGHQXLXJC-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- DPBJAVGHACCNRL-UHFFFAOYSA-N 2-(dimethylamino)ethyl prop-2-enoate Chemical compound CN(C)CCOC(=O)C=C DPBJAVGHACCNRL-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 244000137852 Petrea volubilis Species 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- GCTFWCDSFPMHHS-UHFFFAOYSA-M Tributyltin chloride Chemical compound CCCC[Sn](Cl)(CCCC)CCCC GCTFWCDSFPMHHS-UHFFFAOYSA-M 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- WCRDXYSYPCEIAK-UHFFFAOYSA-N dibutylstannane Chemical compound CCCC[SnH2]CCCC WCRDXYSYPCEIAK-UHFFFAOYSA-N 0.000 description 1
- AYOHIQLKSOJJQH-UHFFFAOYSA-N dibutyltin Chemical compound CCCC[Sn]CCCC AYOHIQLKSOJJQH-UHFFFAOYSA-N 0.000 description 1
- 125000005442 diisocyanate group Chemical group 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000007688 edging Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 150000002596 lactones Chemical class 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- AFCAKJKUYFLYFK-UHFFFAOYSA-N tetrabutyltin Chemical compound CCCC[Sn](CCCC)(CCCC)CCCC AFCAKJKUYFLYFK-UHFFFAOYSA-N 0.000 description 1
- JUYONNFUNDDKBE-UHFFFAOYSA-J tri(oct-2-enoyloxy)stannyl oct-2-enoate Chemical compound [Sn+4].CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O.CCCCCC=CC([O-])=O JUYONNFUNDDKBE-UHFFFAOYSA-J 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
【発明の詳細な説明】 [産業上の利用分野] 本発明は塗膜の補修方法、さらに詳しくは、自動車の
補修に特に好適な高級仕上げ塗膜を形成できる塗膜の補
修方法に関する。The present invention relates to a method for repairing a coating film, and more particularly, to a method for repairing a coating film capable of forming a high-grade finish coating film particularly suitable for repairing automobiles.
[従来の技術および課題] 近年、各自動車メーカーにおいては塗装の高級化が進
み、肉持ち感、ツヤ、深みのある高仕上りの塗膜を増加
してきている。[Prior art and problems] In recent years, each automobile manufacturer has been upgrading the quality of painting, and the number of highly finished coating films with a feeling of durability, gloss, and depth has been increasing.
一方、従来の塗膜の補修仕様は、一般にプライマーサ
ーフェーサー塗装−研磨−1種類の塗料による上塗塗
装、または1種類の塗料による上塗塗装のみとなってお
り、新車塗膜の仕上り性向上に対して、従来の補修方法
では仕上りの見劣りが目立ち実用性が乏しい現状にあ
る。On the other hand, the conventional specifications for repairing coating films are generally primer surfacer coating-polishing-overcoating with one type of paint or overcoating with one type of paint, to improve the finish of new car coatings. However, the conventional repair method is inferior in the finish and is not practical in practice.
このため、高級仕上げ塗膜を形成できる補修方法の確
立が望まれていた。For this reason, establishment of a repair method capable of forming a high-grade finish coating film has been desired.
[発明の開示] そこで本発明者らは高級仕上げ車の補修にも適用可能
な高級仕上げ塗膜を形成できる補修方法を鋭意検討した
結果、本発明に到達した。すなわち本発明は、 プライマーサーフェーサー塗膜を介して、もしくは介
さずに上塗り塗装を行なう塗膜の補修方法において、上
塗り塗装工程として、 (a)顔料を70〜170PHRの量含有するアクリルウレタン
塗料を塗装し、乾燥させて上塗第1層塗膜を形成する工
程、 (b)該上塗第1層塗膜を研磨する工程、 (c)研磨された上塗第1層塗膜上に色決めした着色上
塗塗料を塗装し、上塗第2層塗膜を形成する工程、 (d)上塗第2層塗膜上に、該着色上塗塗料における、
樹脂固形分に対する顔料分比率の0〜90%の顔料分比率
を有する仕上げ上塗塗料を塗装する工程 を有する塗膜の補修方法に関する。DISCLOSURE OF THE INVENTION Accordingly, the present inventors have intensively studied a repair method capable of forming a high-grade finish coating film that can also be applied to repair of a high-grade finish vehicle, and as a result, have reached the present invention. That is, the present invention provides a method for repairing a coating film in which a top coat is applied with or without a primer surfacer coating film, wherein (a) an acrylic urethane paint containing a pigment in an amount of 70 to 170 PHR is applied as a top coating process. And then drying to form a topcoat first-layer coating film, (b) a step of polishing the topcoat first-layer coating film, and (c) a colored topcoat that has been color-coded on the polished topcoat first-layer coating film. A step of applying a paint to form a top coat second layer coating film, (d) on the top coat second layer coating film, in the colored top coat paint,
The present invention relates to a method for repairing a coating film, which comprises a step of applying a finish topcoat having a pigment content ratio of 0 to 90% of a resin solid content.
本発明方法によるとエナメル仕上げ、メタリック仕上
げのいずれの高級仕上げの塗膜も形成できる。According to the method of the present invention, it is possible to form a high-quality coating film of either enamel finish or metallic finish.
標準的な補修塗装の主要工程は、塗膜剥離、素地研
磨、フェザーエッジング、プライマー塗装、板金
パテやポリエステルパテ付けと研磨、プライマーサー
フェーサーの塗装、研磨、上塗塗装、磨き仕上げな
どであり、傷の程度などの状況に応じて省略される工程
もある。The main processes of standard repair painting are coating peeling, substrate polishing, feather edging, primer coating, sheet metal putty and polyester putty attaching and polishing, primer surfacer painting, polishing, top coat painting, polishing finish, etc. Some steps may be omitted depending on circumstances such as the degree.
本発明は、上記の補修塗装工程のうちの上塗塗装工程
に種々検討を加えて高級仕上げの補修方法としたもので
ある。The present invention provides a high-quality finishing repair method by conducting various studies on the topcoat painting step of the above-mentioned repair painting steps.
本発明における上塗塗装工程の第1の工程(a)は、
研磨されたプライマーサーフェーサー塗膜を介して、も
しくは介さずにアクリルウレタン塗料を塗装し、乾燥さ
せて上塗第1層塗膜を形成するものである。上記アクリ
ルウレタン塗料は水酸基含有アクリル樹脂、ポリイソシ
アネート化合物および顔料を主成分とするものである。The first step (a) of the overcoating step in the present invention comprises:
An acrylic urethane paint is applied with or without a polished primer surfacer coating film, and dried to form a top coat first layer coating film. The acrylic urethane paint contains a hydroxyl group-containing acrylic resin, a polyisocyanate compound and a pigment as main components.
上記水酸基含有アクリル樹脂とは、水酸基含有重合性
不飽和モノマーと、これと共重合可能なアクリル系モノ
マーとを主成分とするモノマー成分を共重合して得られ
る樹脂であり、水酸基含有重合性不飽和モノマーとして
は、ヒドロキシエチル(メタ)アクリレート、ヒドロキ
シプロピル(メタ)アクリレート等のヒドロキシ基含有
(メタ)アクリル酸アルキル(C2〜10)エステル;市
販品としてはダイセル化学工業(株)の製品であるプラ
クセルFA−1(アクリル酸2−ヒドロキシエチル1モル
にε−カプロラクトン1モルを付加したモノマー)、プ
ラクセルFM−1、プラクセルFM−3、プラクセルFM−5
(メタアクリル酸2−ヒドロキシエチル1モルにε−カ
プロラクトンをそれぞれ1モル、3モル、5モル付加し
たモノマー)、ユニオンカーバイド社(米)の商品であ
るTONE M−100(アクリル酸2−ヒドロキシエチル1
モルにε−カプロラクトン2モルを付加したモノマー)
などが挙げられる水酸基含有(メタ)アクリル酸エステ
ル1モルとラクトン類1〜5モルとの付加物などから選
ばれた1種もしくは2種以上を使用することができ、上
記水酸基含有重合性不飽和モノマーと共重合可能なアク
リル系モノマーとしては、例えばメチル(メタ)アクリ
レート、エチル(メタ)アクリレート、プロピル(メ
タ)アクリレート、ブチル(メタ)アクリレート、2−
エチルヘキシル(メタ)アクリレート等のアクリル酸も
しくはメタクリル酸と炭素数1〜20の1価アルコールと
のエステル化物などが挙げられ、これら以外にエチレン
グリコールジ(メタ)アクリレート、1,6−ヘキサンジ
(メタ)アクリレート、トリメチロールプロパンジ(メ
タ)アクリレート、アリル(メタ)アクリレート、トリ
(メタ)アクリル酸トリメチロールプロパン等のアクリ
ル酸もしくはメタクリル酸と炭素数2〜16の2価以上の
アルコールとを反応してなる1分子中に2個以上の重合
性二重結合を有する化合物;(メタ)アクリル酸等のモ
ノカルボン酸、マレイン酸、フマル酸、イタコン酸等の
ジカルボン酸又はジカルボン酸の半エステル化物等の
α,β−エチレン性不飽和カルボン酸;N−プロポキシメ
チル(メタ)アクリルアミド、N−ブトキシメチル(メ
タ)アクリルアミド、グリシジル(メタ)アクリレー
ト、ビニルトルエン、スチレン、ジメチルアミノエチル
アクリレート、アクリル酸アミド、酢酸ビニル等も用い
ることができる。The hydroxyl group-containing acrylic resin is a resin obtained by copolymerizing a monomer component mainly composed of a hydroxyl group-containing polymerizable unsaturated monomer and an acrylic monomer copolymerizable therewith, and is a hydroxyl group-containing polymerizable unsaturated resin. Examples of the saturated monomer include hydroxyethyl (meth) acrylate, hydroxypropyl (meth) acrylate, and other hydroxy group-containing alkyl (meth) acrylates ( C2-10 ) esters; commercially available products of Daicel Chemical Industries, Ltd. Certain Praxel FA-1 (a monomer obtained by adding 1 mol of ε-caprolactone to 1 mol of 2-hydroxyethyl acrylate), Praxel FM-1, Praxel FM-3, Praxel FM-5
(Monomer obtained by adding 1 mol, 3 mol, and 5 mol of ε-caprolactone to 1 mol of 2-hydroxyethyl methacrylate), TONE M-100 (2-hydroxyethyl acrylate), a product of Union Carbide (US) 1
Monomer in which 2 mol of ε-caprolactone is added to the mol)
One or two or more selected from adducts of 1 mol of a hydroxyl group-containing (meth) acrylate and 1 to 5 mol of a lactone can be used. Examples of the acrylic monomer copolymerizable with the monomer include methyl (meth) acrylate, ethyl (meth) acrylate, propyl (meth) acrylate, butyl (meth) acrylate, and 2- (meth) acrylate.
Examples thereof include esterified products of acrylic acid or methacrylic acid such as ethylhexyl (meth) acrylate and a monohydric alcohol having 1 to 20 carbon atoms. In addition to these, ethylene glycol di (meth) acrylate and 1,6-hexanedi (meth) acrylate By reacting acrylic acid or methacrylic acid such as acrylate, trimethylolpropane di (meth) acrylate, allyl (meth) acrylate, tri (meth) acrylate and trimethylolpropane with a dihydric or higher alcohol having 2 to 16 carbon atoms Compounds having two or more polymerizable double bonds in one molecule; monocarboxylic acids such as (meth) acrylic acid, dicarboxylic acids such as maleic acid, fumaric acid, and itaconic acid; and half-esterified products of dicarboxylic acids. α, β-ethylenically unsaturated carboxylic acid; N-propoxymethyl (meth) acrylamide , N-butoxymethyl (meth) acrylamide, glycidyl (meth) acrylate, vinyl toluene, styrene, dimethylaminoethyl acrylate, acrylamide, vinyl acetate and the like can also be used.
水酸基含有樹脂は、上記のモノマー成分をアゾ系重合
開始剤や過酸化物系重合開始剤の存在下で通常の方法に
よって共重合させることによって得られるが、その他、
モノマー成分として、例えば東亜合成化学(株)製品、
AA−2,AA−6,AB−2,AB−6などの、分子の片末端に重合
性不飽和基を有する分子量2000〜15000のアクリル系マ
クロモノマーを共重合させたり、セルロースアセテート
ブチレートを前記モノマー成分とともにグラフト共重合
させたものも使用できる。Hydroxyl group-containing resin is obtained by copolymerizing the above-mentioned monomer component by a usual method in the presence of an azo-based polymerization initiator or a peroxide-based polymerization initiator.
As a monomer component, for example, a product of Toa Gosei Chemical Co., Ltd.,
AA-2, AA-6, AB-2, AB-6 and other acrylic macromonomers having a molecular weight of 2000 to 15,000 having a polymerizable unsaturated group at one end of the molecule are copolymerized, or cellulose acetate butyrate is used. Those obtained by graft copolymerization with the monomer component can also be used.
これらの水酸基含有アクリル樹脂は、水酸基価20〜20
0、数平均分子量5000〜50000の範囲内にあることが好ま
しい。These hydroxyl-containing acrylic resins have a hydroxyl value of 20 to 20.
It is preferable that the number average molecular weight is in the range of 5,000 to 50,000.
また、前記ポリイソシアネート化合物は1分子中に2
個以上の遊離のイソシアネート基を有する化合物であっ
て、具体的には、トリレ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、キシリレンジイソ
シアネート、メタキシリレンジイソシアネート、ヘキサ
メチレンジイソシアネート、リジンジイソシアネート、
水素化4,4′−ジフェニルメタンジイソシアネート、水
素化トリレンジイソシアネート、イソホロンジイソシア
ネート、トリメチルヘキサメチレンジイソシアネート、
ダイマー酸ジイソシアネート、トリレンジイソシアネー
ト(3モル)とトリメチロールプロパン(1モル)との
付加物、トリレンジイソシアネートの重合体、ヘキサメ
チレンジイソシアネート(3モル)とトリメチロールプ
ロパン(1モル)との付加物、ヘキサメチレンジイソシ
アネートと水との反応物、キシリレンジイソシアネート
(3モル)とトリメチロールプロパン(1モル)との付
加物、トリレンジイソシアネート(3モル)とヘキサメ
チレンジイソシアネート(2モル)との付加物などから
選ばれた1種もしくは2種以上使用でき、このうち耐候
性などのすぐれたキシレンジイソシアネートと水との反
応物、キシリレンジイソシアネートとトリメチロールプ
ロパンとの付加物、トリレンジイソシアネートとヘキサ
メチレンジイソシアネートとの付加物、イソホロンジイ
ソシアネート、ヘキサメチレンジイソシアネート、リジ
ンジイソシアネートなどの無黄変タイプが好ましい。In addition, the polyisocyanate compound contains 2 per molecule.
A compound having at least one free isocyanate group, specifically, tolylene diisocyanate, 4,4′-
Diphenylmethane diisocyanate, xylylene diisocyanate, meta-xylylene diisocyanate, hexamethylene diisocyanate, lysine diisocyanate,
Hydrogenated 4,4'-diphenylmethane diisocyanate, hydrogenated tolylene diisocyanate, isophorone diisocyanate, trimethylhexamethylene diisocyanate,
Dimer acid diisocyanate, adduct of tolylene diisocyanate (3 mol) with trimethylolpropane (1 mol), polymer of tolylene diisocyanate, adduct of hexamethylene diisocyanate (3 mol) with trimethylolpropane (1 mol) Reaction product of hexamethylene diisocyanate and water, adduct of xylylene diisocyanate (3 mol) and trimethylolpropane (1 mol), adduct of tolylene diisocyanate (3 mol) and hexamethylene diisocyanate (2 mol) One or more selected from the group consisting of a reaction product of xylene diisocyanate and water, an adduct of xylylene diisocyanate and trimethylolpropane, and a tolylene diisocyanate and hexamethylene diisocyanate having excellent weather resistance. Soshi Adducts of sulfonates, isophorone diisocyanate, hexamethylene diisocyanate, are non-yellowing type, such as lysine diisocyanate preferable.
水酸基含有アクリル樹脂とポリイソシアネート化合物
との配合比は、これらに含まれている水酸基/イソシア
ネート基(モル比)にもとずいて0.5〜2.5、特に0.7〜
2.0の範囲が好ましい。また、該両成分は室温において
反応し架橋硬化するおそれがあるので、あらかじめ分離
しておき使用直前に混合することが好ましい。The compounding ratio of the hydroxyl group-containing acrylic resin to the polyisocyanate compound is 0.5 to 2.5, particularly 0.7 to 500, based on the hydroxyl group / isocyanate group (molar ratio) contained therein.
A range of 2.0 is preferred. Also, since both components may react at room temperature to cause crosslinking and curing, it is preferable to separate them in advance and mix them immediately before use.
また顔料としては、通常塗料の分野で用いられている
着色顔料および体質顔料を用いることができ、これらの
顔料は70〜170PHRの量含有され、さらには100〜150PHR
の範囲内にあることが好ましい。顔料が70PHR未満では
得られる上塗第1層塗膜の研磨性が劣り、一方、170PHR
を超えると、上塗第1層塗膜の吸い込みが大きくなり、
総合塗膜として高仕上りの塗膜が得られなくなる。また
顔料の分散程度はツブが50ミクロン以下、さらには30〜
50ミクロンの範囲内とすることが、研磨性および最終塗
膜のツヤ感の点から好ましい。As the pigment, coloring pigments and extenders commonly used in the field of paints can be used.These pigments are contained in an amount of 70 to 170 PHR, and more preferably 100 to 150 PHR.
Is preferably within the range. If the pigment is less than 70 PHR, the resulting top coat first layer coating film has poor abrasion properties, while 170 PHR
When it exceeds, the suction of the top coat first layer coating film becomes large,
A high-quality coating film cannot be obtained as an overall coating film. In addition, the degree of dispersion of the pigment is 50 microns or less, and 30 to
It is preferable that the thickness be within the range of 50 microns from the viewpoints of abrasion and glossiness of the final coating film.
第1層塗膜を形成するアクリルウレタン塗料は、前記
成分以外に硬化促進剤として、例えばジブチルスズ(2
−エチルヘキソエート)、オクテン酸スズ、ジラウリル
酸ジn−ブチルスズ、塩化トリn−ブチルスズ、テトラ
n−ブチルスズなどが好ましく、触媒の添加量は水酸基
含有アクリル樹脂固形分100重量部あたり、0.01〜10重
量部、特に0.05〜5重量部が好ましい。In addition to the above-mentioned components, the acrylic urethane coating material for forming the first-layer coating film may be, for example, dibutyltin (2
-Ethylhexoate), tin octenoate, di-n-butyltin dilaurylate, tri-n-butyltin chloride, tetra-n-butyltin, etc. are preferable, and the catalyst is added in an amount of 0.01 to 100 parts by weight of the hydroxyl group-containing acrylic resin solid content. 10 parts by weight, especially 0.05 to 5 parts by weight, is preferred.
また、アクリルウレタン塗料は、塗装作業性の点から
速乾型であること、すなわち20℃で3時間の乾燥、60℃
であれば20分間の乾燥によって、次工程である研磨が行
ない得るまでに硬化するものであることが好ましい。Also, acrylic urethane paint is a quick-drying type from the viewpoint of coating workability, that is, drying at 20 ° C for 3 hours, 60 ° C.
In that case, it is preferable that the resin be cured by the drying for 20 minutes before polishing in the next step can be performed.
本発明における工程(b)は、上記工程(a)によっ
て得られた塗膜を研磨する工程であり、工程(a)によ
って得られる、通常30〜80ミクロン、好ましくは40〜60
ミクロン程度の膜厚の塗膜をサンダー、手研ぎなどによ
って空研ぎおよび/または水研ぎするものである。研磨
用ペーパーとしては#600または#600より目の細かいペ
ーパーを使用し、平滑に研磨することが仕上り性の点で
好ましい。この研磨された上塗第1層塗膜を介在させる
ことによって、この上に塗装される塗料の吸い込みが抑
えられるため、ツヤ感のある仕上りが得られやすく、ま
た平滑な塗肌が得られやすくなる。The step (b) in the present invention is a step of polishing the coating film obtained in the step (a), and is usually 30 to 80 microns, preferably 40 to 60, obtained in the step (a).
A film having a film thickness of about a micron is ground and / or water-polished by sanding, hand polishing, or the like. As the polishing paper, # 600 or a finer paper than # 600 is used, and it is preferable to polish the surface smoothly in terms of finishability. By interposing this polished first-layer top coat, it is possible to prevent the paint to be applied onto the top coat, so that a glossy finish can be easily obtained, and a smooth coated skin can be easily obtained. .
本発明においては、(c)工程として(b)工程を経
た研磨された上塗第1層塗膜上に、色決めした着色上塗
塗料を塗装し、上塗第2層塗膜を形成する。上塗第2層
用塗料としては、アクリルラッカー、ニトロセルロース
又はセルロースアセテートブチレート変性アクリルラッ
カー、アクリルウレタンいずれも使用できるが、樹脂成
分としては、(a)工程で説明したアクリルウレタン塗
料の樹脂組成であることが、塗膜性能などの点から好ま
しい。In the present invention, a colored topcoat paint having a predetermined color is applied onto the polished topcoat first-layer paint film subjected to step (b) as step (c) to form a topcoat second-layer paint film. Acrylic lacquer, nitrocellulose or cellulose acetate butyrate-modified acrylic lacquer, or acrylic urethane can be used as the coating for the second layer of the top coat. As the resin component, the resin composition of the acrylic urethane paint described in the step (a) can be used. This is preferred from the viewpoint of coating film performance and the like.
また顔料分は所望の塗色に応じて適宜使用すればよ
く、通常、補修部周辺の塗色と同色ないしは近似色とな
る顔料組成である。The pigment component may be appropriately used according to the desired coating color, and is usually a pigment composition having the same or similar color as the coating color around the repaired part.
(c)工程は、特に限定されるものではないが、細か
くみると、通常、 上塗第1塗膜に塗料をなじませる捨て吹き工程、 スケのないように塗装する色決め工程、および 塗り肌を見ながら均一な肌に塗り込む塗面調整工程 の3工程からなり、−間は一般にウェット・オン・
ウェットで塗装され、−間はウェット・オン・ウェ
ット又は仕上り外観をさらに向上させるため工程後、
塗膜を硬化させ、ついで該硬化塗膜を研磨した後、の
工程を行なってもよく、また、工程後、硬化させ、研
磨することなしにの工程を行なってもよい。The step (c) is not particularly limited, but in detail, it is usually a waste blowing step in which the paint is applied to the first top coat, a color-determining step in which the paint is applied without scratches, and a coating surface. It consists of three steps, the process of adjusting the paint surface to apply it evenly to the skin while looking at it.
Painted wet, -between wet-on-wet or after the process to further improve the finished appearance,
The step of curing the coating film and then polishing the cured coating film may be performed, or the step of curing and polishing without polishing may be performed after the step.
〜の各工程で通常10〜30ミクロン程度、好ましく
は15〜30ミクロン程度、〜の和で30〜100ミクロ
ン、好ましくは45〜90ミクロン、エナメル仕上げの場
合、さらに好ましくは60〜75ミクロン(乾燥膜厚)とな
るよう塗装される。In each step of ~ 10 ~ 30 microns, preferably about 15 ~ 30 microns, the sum of ~ 30 ~ 100 microns, preferably 45 ~ 90 microns, in the case of enamel finish, more preferably 60 ~ 75 microns (dry The film thickness is applied.
本発明において、(d)工程としては(c)工程後、
未硬化もしくは硬化した上塗第2層塗膜上に仕上げ上塗
塗料を塗装する。In the present invention, as the step (d), after the step (c),
A finish topcoat is applied over the uncured or cured topcoat second layer coating.
仕上げ上塗塗料としては、アクリルラッカー、ニトロ
セルロース又はセルロースアセテートブチレート変性ア
クリルラッカー、アクリルウレタンいずれも使用できる
が、樹脂成分としては、(a)工程でのアクリルウレタ
ン塗料において説明した樹脂組成であることが塗膜性能
などの点から好ましい。また仕上げ上塗塗料の顔料分比
率は(c)工程で使用する第2層塗膜用塗料の顔料分比
率0〜90%、好ましくは0〜60%であって、すなわち、
クリヤ塗料であるか、低顔料濃度塗料であることが必要
である。低顔料濃度塗料の場合には、通常、第2層塗膜
用塗料と同色ないしは近似色の塗料をクリヤ塗料と混合
して顔料濃度を低下させたものを使用する。仕上げ上塗
塗料の顔料分比率が、第2層塗膜用顔料の顔料分比率の
90%を超えると最終的に得られる総合塗膜において肉持
ち感、ツヤ、深みの向上が十分でなくなるため好ましく
ない。仕上げ上塗塗料の膜厚(乾燥膜)はメタリック仕
上げの場合30〜90ミクロン、さらには50〜70ミクロンの
範囲内が好ましく、またエナメル仕上げの場合10〜90ミ
クロン、さらには15〜70ミクロンの範囲内が好ましい。As the finish topcoat, any of acrylic lacquer, nitrocellulose or cellulose acetate butyrate-modified acrylic lacquer, and acrylic urethane can be used. As the resin component, the resin composition described in the acrylic urethane paint in step (a) must be used. Is preferable from the viewpoint of coating film performance. In addition, the pigment content of the finish top coat is 0 to 90%, preferably 0 to 60%, of the pigment content of the second layer coating used in the step (c).
It must be a clear paint or a low pigment concentration paint. In the case of a low pigment concentration paint, a paint having the same or similar color as the paint for the second layer coating film is mixed with a clear paint to reduce the pigment concentration. The pigment ratio of the finish coating is the pigment ratio of the pigment for the second layer coating film.
If it exceeds 90%, it is not preferable because improvement in the feeling of stickiness, gloss and depth is not sufficiently achieved in the finally obtained total coating film. The film thickness (dry film) of the finish coat is preferably in the range of 30 to 90 microns, more preferably 50 to 70 microns in the case of metallic finish, and in the range of 10 to 90 microns, more preferably 15 to 70 microns in the case of enamel finish. Is preferred.
本発明においては、塗膜の補修方法における上塗り塗
装工程として、上記および前記の(a)〜(d)の工程
を有することによって、肉持ち感、ツヤ、深みのある高
仕上りの高級仕上げ塗膜を形成できる補修方法が提供さ
れ、特に自動車の高級塗膜の補修に適用できるものであ
る。In the present invention, by having the above-mentioned steps (a) to (d) as the top-coating step in the method for repairing a coating film, a high-quality finish coating film with a high finish having a feeling of meat retention, gloss, and depth. The present invention provides a repair method capable of forming a coating film, and is particularly applicable to repair of a high-grade coating film of an automobile.
[実施例] 以下、実施例を挙げて本発明をさらに具体的に説明す
る。なお、本発明は実施例のみに限定されるものではな
い。EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples. Note that the present invention is not limited to only the examples.
実施例1 ミガキ軟鋼板上にポリエステルパテを1000ミクロン塗
布し、室温(20℃)で1時間乾燥させた後、#120のサ
ンドペーパーにて研磨した。次いでこの上にラッカー系
のプライマーサーフェーサーを50ミクロン塗布し、室温
(20℃)で1時間乾燥させた後、#400のサンドペーパ
ーにて研磨して試験用素材とした。Example 1 Polyester putty was coated on a mild steel mild steel plate at 1000 μm, dried at room temperature (20 ° C.) for 1 hour, and polished with # 120 sandpaper. Next, a lacquer-based primer surfacer was applied thereon by 50 μm, dried at room temperature (20 ° C.) for 1 hour, and polished with # 400 sandpaper to obtain a test material.
上記試験用素材に上塗第1層塗料としてレタンPGファ
ーストコート(関西ペイント社製、アクリルウレタン塗
料、白色)を50ミクロン塗装し、60℃で20分間乾燥さ
せ、ついで#600のサンドペーパーにて研磨を行なっ
た。ついで研磨された上塗第1層塗膜上にレタンPG80メ
タリックカラー(関西ペイント社製、速乾性アクリルウ
レタン塗料、シルバーメタリック色)を50ミクロン(乾
燥膜厚)塗装し、3分間室温で静置した後、レタンPG−
80クオーツクリヤZ(関西ペイント社製、速乾型アクリ
ルウレタン塗料クリヤ)をウェット・オン・ウェットで
60ミクロン(乾燥膜厚)塗装し、60℃で30分間焼付けを
行ない試験用塗板を作成した。The test material is coated with 50 µm of urethane PG First Coat (Kansai Paint Co., Ltd., acrylic urethane paint, white) as the first coat of top coat, dried at 60 ° C for 20 minutes, and then polished with # 600 sandpaper. Was done. Then apply 50 μm (dry film thickness) of urethane PG80 metallic color (manufactured by Kansai Paint Co., Ltd., quick-drying acrylic urethane paint, silver metallic color) on the polished top coat first layer coating film, and leave it at room temperature for 3 minutes. , Retan PG-
80 Quartz Clear Z (Kansai Paint Co., Ltd., quick-drying acrylic urethane paint clear) wet-on-wet
60 micron (dry film thickness) was applied and baked at 60 ° C for 30 minutes to prepare a test coated plate.
実施例2 実施例1において使用したと同様の試験用素材に、上
塗第1層塗料としてレタンPGファーストコートを50ミク
ロン塗装し、室温(20℃)で3時間乾燥させ、ついで#
600のサンドペーパーにて研磨を行なった。ついで研磨
された上塗第1層塗膜上にレタンPG60ホワイト(関西ペ
イント社製、アクリルウレタン塗料エナメル、白色)を
70ミクロン(乾燥膜厚)塗装し、3分間室温で静置した
後、レタンPG−60ホワイトの樹脂固形分に対する顔料分
の比率Aに対して、50%の顔料分の比率、すなわち0.5A
になるように、レタンPGホワイトにレタンPG−60クリヤ
(関西ペイント社製、アクリルウレタン塗料クリヤ)を
混合した仕上げ上塗塗料をウェット・オン・ウェットで
25ミクロン塗装し70℃で30分間乾燥させて試験用塗板を
作成した。Example 2 A test material similar to that used in Example 1 was coated with 50 μm of Retan PG First Coat as a top coat first layer paint, dried at room temperature (20 ° C.) for 3 hours, and then #
Polishing was performed with 600 sandpapers. Then, on the polished top coat first layer coating, Retan PG60 White (Kansai Paint Co., Ltd., acrylic urethane paint enamel, white)
After painting 70 microns (dry film thickness) and leaving it to stand at room temperature for 3 minutes, the ratio of the pigment content of 50% to the ratio A of the pigment content to the resin solid content of the urethane PG-60 white, that is, 0.5A
As shown in the figure, Retan PG White is mixed with Retan PG-60 clear (Kansai Paint Co., Ltd., acrylic urethane paint clear), and the top finish paint is wet-on-wet.
It was coated with 25 microns and dried at 70 ° C. for 30 minutes to prepare a test coated plate.
実施例3 実施例2において、第1層塗膜上にレタンPG60ホワイ
トを70ミクロン塗装するかわりに、レタンPG60ホワイト
を50ミクロン(乾燥膜厚)塗装し60℃で30分間巻付けた
後、#1000のサンドペーパーにて研磨し、ついでその上
にレタンPG60ホワイトをスプレーにて25ミクロン(乾燥
膜厚)塗装する以外は実施例2と同様に行なった。Example 3 Instead of applying 70 μm of Retan PG60 White on the first layer coating film in Example 2, 50 μm of Retan PG60 White (dry film thickness) was applied and wound at 60 ° C. for 30 minutes. The same operation as in Example 2 was carried out except that the surface was polished with a sandpaper of 1000, and then, 25 μm (dry film thickness) of a urethane PG60 white was sprayed thereon.
実施例4 実施例1において、レタンPGファーストコート塗膜の
研磨を#400のサンドペーパーにて行なう以外は実施例
1と同様に行なった。Example 4 The same procedure was performed as in Example 1 except that the Rethane PG first coat coating film was polished with # 400 sandpaper.
比較例1 実施例1において、レタンPGファーストコートを塗装
しない以外は実施例1と同様に行なった。Comparative Example 1 The same procedure as in Example 1 was carried out except that the Retan PG first coat was not applied.
比較例2 実施例1において、レタンPGファーストコートのかわ
りにラッカー系プライマーサーフェーサーを50ミクロン
(乾燥膜厚)塗装する以外は実施例1と同様に行なっ
た。Comparative Example 2 The procedure of Example 1 was repeated, except that a lacquer-based primer surfacer was applied in 50 μm (dry film thickness) in place of the urethane PG first coat.
比較例3 実施例2において、レタンPGファーストコートを塗装
しない以外は実施例2と同様に行なった。Comparative Example 3 The procedure of Example 2 was repeated except that the Retan PG first coat was not applied.
上記実施例1〜4および比較例1〜3で得られた試験
用塗板について試験を行なった。その試験結果を下記第
1表に示す。A test was performed on the test coated plates obtained in Examples 1 to 4 and Comparative Examples 1 to 3 described above. The test results are shown in Table 1 below.
なお第1表における試験は下記方法に従って行なっ
た。 The tests in Table 1 were performed according to the following methods.
(*1)肉持ち感: 1000ルクスの照度の蛍光灯下で塗膜の肉持ち感の程度を
目視評価する。(* 1) Feeling of flesh: The degree of flesh of the coating film is visually evaluated under a fluorescent lamp with an illuminance of 1000 lux.
(*2)ツヤ: 1000ルクスの照度の蛍光灯下で塗膜のツヤ感を目視評価
する。また、光沢計にて20゜鏡面光沢反射率(20゜グロ
ス)も測定する。(* 2) Luster: The glossiness of the coating film is visually evaluated under a fluorescent lamp with an illuminance of 1000 lux. Also, measure the 20 ° specular gloss reflectance (20 ° gloss) with a gloss meter.
(*3)肌: 1000ルクスの照度の蛍光灯下で塗膜の平滑性を目視評価
する。また、日本色彩研究所販売の鮮明度光沢計PGD−I
Vにて塗膜の鮮映性の程度を測定する。(* 3) Skin: The smoothness of the coating film is visually evaluated under a fluorescent lamp with an illuminance of 1000 lux. Also, the PGD-I sharpness gloss meter sold by Japan Color Research Institute
Measure the degree of sharpness of the coating film with V.
なお、(*1)、(*2)、(*3)における目視評
価は下記の評価基準に従って行なった。In addition, the visual evaluation in (* 1), (* 2), and (* 3) was performed according to the following evaluation criteria.
Claims (4)
もしくは介さずに上塗り塗装を行なう塗膜の補修方法に
おいて、上塗り塗装工程として、 (a)顔料を70〜170PHRの量含有するアクリルウレタン
塗料を塗装し、乾燥させて上塗第1層塗膜を形成する工
程、 (b)該上塗第1層塗膜を研磨する工程、 (c)研磨された上塗第1層塗膜上に色決めした着色上
塗塗料を塗装し、上塗第2層塗膜を形成する工程、 (d)上塗第2層塗膜上に、該着色上塗塗料における、
樹脂固形分に対する顔料分比率の0〜90%の顔料分比率
を有する仕上げ上塗塗料を塗装する工程 を有する塗膜の補修方法。(1) through a primer surfacer coating film,
Alternatively, in a method of repairing a coating film in which a top coat is applied without intervening, as a top coat coating step, (a) an acrylic urethane paint containing a pigment in an amount of 70 to 170 PHR is applied and dried to form a top coat first layer coating film And (b) a step of polishing the first top coat film of the top coat, (c) a colored top coat paint that has been colored is applied onto the polished first coat film of the top coat to form a second top coat film of the top coat. (D) on the top coat second layer coating film,
A method for repairing a coating film, which comprises a step of applying a finish top coating having a pigment content ratio of 0 to 90% of a resin solid content.
上に色決めした着色上塗塗料を塗装し、硬化させ、つい
で該硬化塗膜を研磨した後、この塗膜上に該色決めした
着色上塗塗料を塗装する工程である請求項1記載の塗膜
の補修方法。2. The step (c) comprises applying a color-coded colored topcoat paint to the ground topcoat first layer coating film, curing the same, and then polishing the cured coating film. 2. The method for repairing a coating film according to claim 1, wherein the method is a step of applying the colored topcoat paint determined in color.
上塗第1層塗膜を研磨することを特徴とする請求項1又
は2記載の塗膜の補修方法。3. The method for repairing a coating film according to claim 1, wherein the top coat first layer coating film is polished with # 600 or a paper finer than # 600.
仕上げ上塗塗料がともにアクリルウレタン塗料であるこ
とを特徴とする請求項1、2又は3記載の塗膜の補修方
法。4. The method for repairing a coating film according to claim 1, wherein the colored top coating composition for forming the second coating film of the top coating and the finishing top coating composition are both acrylic urethane coating compositions.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63279977A JP2667886B2 (en) | 1988-11-05 | 1988-11-05 | Repair method of coating film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP63279977A JP2667886B2 (en) | 1988-11-05 | 1988-11-05 | Repair method of coating film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH02126972A JPH02126972A (en) | 1990-05-15 |
| JP2667886B2 true JP2667886B2 (en) | 1997-10-27 |
Family
ID=17618584
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63279977A Expired - Lifetime JP2667886B2 (en) | 1988-11-05 | 1988-11-05 | Repair method of coating film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2667886B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6534121B1 (en) * | 2000-06-22 | 2003-03-18 | Basf Corporation | Method of coating bare, untreated metal substrates |
| WO2014024315A1 (en) * | 2012-08-10 | 2014-02-13 | 株式会社 日立製作所 | Bogie for railway vehicle |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS609874A (en) * | 1983-06-29 | 1985-01-18 | Fujitsu Ltd | Sputtering device |
-
1988
- 1988-11-05 JP JP63279977A patent/JP2667886B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02126972A (en) | 1990-05-15 |
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