JPH0341225B2 - - Google Patents
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- Publication number
- JPH0341225B2 JPH0341225B2 JP24526183A JP24526183A JPH0341225B2 JP H0341225 B2 JPH0341225 B2 JP H0341225B2 JP 24526183 A JP24526183 A JP 24526183A JP 24526183 A JP24526183 A JP 24526183A JP H0341225 B2 JPH0341225 B2 JP H0341225B2
- Authority
- JP
- Japan
- Prior art keywords
- coating film
- film
- coat
- polishing
- coating
- 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
Links
- 238000000576 coating method Methods 0.000 claims description 63
- 239000011248 coating agent Substances 0.000 claims description 58
- 238000005498 polishing Methods 0.000 claims description 17
- 238000004070 electrodeposition Methods 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 239000000049 pigment Substances 0.000 claims description 14
- 125000002091 cationic group Chemical group 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 5
- 239000011164 primary particle Substances 0.000 claims description 2
- 239000003973 paint Substances 0.000 description 23
- 229920000877 Melamine resin Polymers 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229910000831 Steel Inorganic materials 0.000 description 3
- 229920000180 alkyd Polymers 0.000 description 3
- 239000011362 coarse particle Substances 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 239000000428 dust Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000002987 primer (paints) Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000010959 steel Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 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
- 230000007797 corrosion Effects 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000010445 mica Substances 0.000 description 2
- 229910052618 mica group Inorganic materials 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000013615 primer Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000002344 surface layer Substances 0.000 description 2
- 239000004593 Epoxy Substances 0.000 description 1
- 239000004640 Melamine resin Substances 0.000 description 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 1
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- 238000005537 brownian motion Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- -1 phosphomolybdates Chemical compound 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 235000019832 sodium triphosphate Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- 230000037303 wrinkles Effects 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
技術分野
本発明は積層塗膜の形成方法に関し、更に詳し
くは、被塗物に下塗り塗膜を塗装硬化せしめ、こ
の硬化した下塗り塗膜を研磨した後、次いで中塗
り塗膜及び上塗り塗膜を施し、該中塗り塗膜及び
上塗り塗膜を研磨することなく硬化せしめること
により、仕上り外観に優れた積層塗膜を形成する
方法に関する。
従来技術
自動車塗装に代表される積層塗膜の形成技術に
おいては、従来、防食性、耐チツピング性などの
機能及び量産適性、経済性等の追求が主体であつ
たが、防食性の点ではカチオン電着塗料の普及に
よつて、また耐チツピング性の点では特定のポリ
エステル系樹脂の採用や特定の粒径のタルクや雲
母を配合することによつて、それぞれ、改善さ
れ、例えば、特開昭58−74349号公報、特開昭57
−141459号公報及び特公昭52−43657号公報など
に提案されている。
しかしながら、これらの提案技術は被塗物の実
用性、大量生産に基づく経済性を達成しつつある
が、肉持ち感、鮮映性、艶などに優れた高級な外
観仕上げの面からは未だ不充分であつた。
乗用車については、皮膜化成、下塗り電着塗膜
−焼付硬化、一次中塗り及び二次中塗りを施して
焼付硬化後研磨し、次いでメタリツクベース、ト
ツプクリヤー又はソリツドコートを積層して仕上
げるのが、標準塗装系である。
又、特開昭58−70866号公報及び特開昭58−
3678号公報には電着塗膜と中塗り塗膜を研磨する
ことが開示されているが、中塗り工程で研磨した
場合には、上塗り塗料の吸込みが起るために肉持
ち感に優れた艶のある塗膜が得られなかつた。
一方、塗装過程における研磨工程なの必要性は
塗膜の不均一と共に素材自体に起因する場合も多
い。即ち、自動車の鋼板として用いられることの
多いダル鋼板はダル目(凹凸)が0.5〜0.8μmで
あつて、塗膜を単に積層するだけではこの凹凸を
解消することができないので、かかる理由からも
塗膜の研磨が必要となる。
発明の目的
従つて、本発明の目的は、前記した従来の技術
の問題点を排除し、仕上り外観に優れた積層塗膜
を形成する方法を提供することにある。
発明の構成
即ち、本発明に従えば、被塗物にカチオン電着
塗料を施して硬化せしめ、硬化したカチオン電着
塗膜の研磨を行い、次いで顔料容積濃度10〜50%
及び顔料容積濃度5〜40%の一次及び二次の2層
の中塗り塗膜を順次積層し、更に少なくとも一層
の上塗り塗膜を施し、該中塗り塗膜及び上塗り塗
膜を研磨することなく硬化せしめることを特徴と
する積層塗膜の形成方法が提供される。
発明の構成及び効果の具体的説明
本発明者らは、前記した積層塗膜の形成方法の
現状に鑑み、仕上り外観に優れた積層塗膜を形成
する方法を開発すべく鋭意検討を進めた結果、前
記したような構成をとることによつて従来の積層
塗膜の問題点を効果的に解決できることを見出し
本発明を完成するに至つた。
即ち、本発明に従えば、先づ、被塗物に、必要
に応じて皮膜化成処理などの前処理を施した後、
下塗り塗膜を施して硬化せしめ、硬化した下塗り
塗膜の研磨を行う。
下塗り塗膜の塗装に使用する塗料としては、従
来最も広く使用されているカチオン電着塗料をあ
げることができるが、本発明において使用する下
塗り用塗料としては、カチオン電着塗料に限ら
ず、溶剤型プライマー又は粉体塗料/カチオン又
はアニオン電着塗料のリバース工程後に研磨して
もよい。
下塗り塗膜の塗装膜厚は以下に説明する研磨に
より5μm程度減少すので、少なくとも20μm程度
の厚さを確保しないと防食性が低下したり、部分
的に素地まで研ぎ出す場合もある。塗装膜厚は
30μm以上であるのが好ましいが、電着塗膜は極
端に厚くつけることが難しいので、約50μm程度
が最大である。下塗り塗膜をそれ以上の膜厚に塗
布したい場合には、溶剤型プライマーや粉体塗料
などを用いるのも好ましいが、最近は、厚膜カチ
オン電着塗料も開発されているのでこれを使用す
ることもできる。
被塗物上に塗装された下塗り塗膜は常法に従つ
て焼付硬化する。カチオン電着塗料を使用した場
合の焼付硬化条件は標準的には165〜185℃×20分
であるが、研磨材に未硬化塗膜のからみのない半
硬化状態となる焼付硬化条件、例えば、140〜160
℃×20分程度としてもよい。
このようにして形成された下塗り塗膜はダル目
を反映しているので、サンドペーパーなどの研磨
材により、ダル目の角を落し、平滑にする必要が
ある。この研磨は下塗り塗膜の研磨であるため、
研き目が中塗りや上塗り塗膜に隠蔽されて目立た
ず、従つて280〜600番程度の粗いサンドペーパー
を用いて研磨することができる。下塗り塗膜の研
磨は水研ぎ、空研ぎのいずれでもよいが、平滑性
の高い研ぎ面を得るには水研ぎによるのが好まし
く、凹凸の少ない面の場合には作業の簡便性から
空研ぎとしてもよい。
このようにして、研磨された面は吸い込みの少
ない上層の樹脂層が削り取られているので上に塗
装される塗料の樹脂分を吸い込むが、本発明に従
えば、中塗り及び上塗り塗膜を塗装するので、仕
上り塗膜の肉持ち感と光沢を損ねることはない。
また研磨された面は非常に表面積が増大してお
り、毛ば立つているので、中塗り塗膜を研磨した
場合には上塗り塗膜が塗装された時に溶剤分と樹
脂分が毛管現象で吸われてしまうので、ウエツト
フイルム中での好ましいミクロブラウン運動が阻
害され、上塗り塗膜の表層に配列すべき樹脂分が
消耗されてしまうために前記したような問題が起
きるのであろうと考えられる。然るに、本発明に
従えば中塗り塗膜を研磨することなく上塗り塗膜
を施すのでかかる問題が効果的に解決されるもの
と思われる。
本発明に従つた積層塗膜の形成方法においては
中塗り塗膜を、サンドペーパーの目を消したり、
防食性を高める補助的機能を果したりする一次中
塗り塗膜と上塗り塗膜の仕上りを高める機能を持
つ二次中塗り塗膜とにその機能を分担させるのが
好ましい。
一次中塗り塗膜は研磨によるサンドペーパーの
目を消したり、防食性を高める補助的機能を果し
たりするのが主目的であるから顔料容積濃度(以
下、PVCと略す)10〜50%のものが適当であり、
15〜30%であるのが特に好ましい。PVCが10%
未満の場合にはサンドペーパー目の傷の隠蔽性が
充分でなく、逆に50%を超えると平滑な塗膜が得
られず、塗料の吸い込みが多くなり、肌荒れなど
の異常が起こりやすくなる。
一次中塗り塗膜用塗料に用いる顔料としては、
比較的粒径の粗い、一次粒子の90%以上が0.5〜
30μmの粒径を有するタルク、沈降性硫酸バリウ
ム、トリポリリン酸アルミニウム、炭酸カルシウ
ム、マイカ、リンモリブデン酸塩類、リン酸亜
鉛、亜鉛華、ケイ酸アルミニウム、亜鉛末粉及び
リン片状で最大径が30μmのアルミニウムフレー
クなどが好ましい。これちの顔料を適量配合する
ことによつて下地キズ隠蔽性とエツジ錆対策に効
果を現す。
これらの粒径の粗い顔料がキズ隠蔽力に有する
理由は定かでないが、下地の研ぎ面等に浸透する
ことなく(顔料粒子が研ぎ面などの間隙に入るこ
となく)、目止め効果を発揮しているからである
と考えられる。従つて、タルク、亜鉛末などの粒
子の粗いものの効果が大である反面、二次中塗り
塗膜のフラツト性が出しにくくなるので、これら
の点を適宜勘案して顔料の種類と使用量を選定す
るのが好ましい。
二次中塗り塗膜は通常一次中塗り塗膜の上にウ
エツトオンウエツト(以下、W/Wという)で塗
布され、上塗り塗膜の仕上りを向上せしめるため
に吸い込みの少ない塗膜を形成すののが好ましい
ことを見出した。このために、二次中塗り塗膜の
PVCは5〜40%であるのが適当であり、二次中
塗り塗膜のPVCが5%未満では一次中塗り塗膜
の肌の状態を反映しやすく、また40%を超えると
上塗り塗膜用塗料の吸い込みが発生しやすくな
る。
中塗り塗膜を一回塗りする場合には、前記した
期待性能を一層の塗膜で受け持つので、PVC及
び膜厚の制限範囲を更に限定して
PVC: 10〜30%
膜厚: 35〜50μm
とするのが好ましい。
従来の積層塗膜の形成技術においては中塗り塗
膜は、通常上塗り塗膜に鮮映性を与えるため、顔
料の量が制限され、最大30%程度のPVCが限界
となつている。しかしながら、本発明の好ましい
態様によれば、下塗り電着塗膜を形成せしめた
後、電着塗料を研磨し、中塗り塗膜は一次中塗り
及び二次中塗りで機能を分担できるため、かかる
制限を排除することができ、前記目的を達成する
ことができる。この場合には一次中塗り塗膜及び
二次中塗り塗膜が混ざり合つてしまうと外観向上
効果が低くなるので、場合によつては一次中塗り
塗膜と二次中塗り塗膜の塗装の間にプレヒート又
はフラツシユオフを行うことが必要となることが
ある。プレヒートまたはフラツシユオフは40〜80
℃×30秒〜5分の加温した条件で実施することが
できる。なお5分を超える加熱は保温設備が長く
なり、そのためにブース自体を長くする必要があ
り、好ましくない。また温度が80℃を超えると一
次中塗り塗膜の表面にワキが進行し過ぎてピンホ
ールなどが発生しやすくなり、好ましくない。な
お、保温設備としては、ホツトエアーのブロー装
置を使用することもできるが、ゴミ対策などを考
慮すると、パイプ内に温水を通す幅射方式が望ま
しい。
中塗り塗膜用塗料としては、従来の積層塗膜の
形成方法において一般に使用されているポリエス
テル−メラミン樹脂系を使用することができ、更
に必要に応じてアルキド樹脂、エポキシ樹脂など
を併用することができる。粉体中塗り塗膜などで
はポリエステル・エポキシ硬化型又はアクリル・
酸硬化型を使用することができ、更にアルキド・
メラミン型の水性中塗り塗膜を使用することもで
きる。
中塗り塗膜の焼付後、ゴミが付着する場合が多
く、そのまま上塗り塗膜を塗布すると、上塗り塗
膜面にゴミブツが発生する。この場合、中塗り塗
膜面はゴミの部分のみを360〜800番程度のサンド
ペーパーなどでスポツトサンデイングを行うのが
好まじい。全面研磨を実施すると、前述の如く上
塗りの吸い込みの原因となり、本発明の前記目的
の達成が損なわれる。
本発明の最大の効果が外観の大幅なレベルアツ
プであるが、更に別の効果として従来法に比べサ
ンデイングの工数を低減することができる点をあ
げることができる。これは従来中塗り塗膜面を研
磨する場合に研磨材として360〜800番程度のサン
ドペーパーを使用していたが、下塗り塗膜の研磨
では280〜600番程度の比較的粗いもので充分であ
り、従来のように水研ぎが必須条件でなくなるの
で、水研ぎ用の耐水サンドペーパーを使用する必
要性が減り、その使用量も大幅に減少できるし、
また従来は細かいサンドペーパーでの研磨のため
に長時間を要したが、この点でも著しく改良され
る。
例えば、従来ベンツなどの高級車が実施してい
るように、上塗り塗膜の顔料濃度を変えて4コー
ト4ベーク方式で上塗り塗膜を2回塗りする方法
もあるが、これらの方法は塗装工程を多く必要と
し、設備投資やランニングコストの点で非常にコ
ストアツプになるばかりでなく、その外観品質も
本発明のものの域には到達し得ない。更に、本発
明に従えば、エツジ防錆力が著しく向上するとい
う重要な効果も達成されるが、これは一次中塗り
塗膜用塗料に用いる粒径の大きい顔料の濃度を上
げることによつてコーナーの被覆力が増大し、従
来の系と比較してエツジ防錆力が上がり、エツジ
防錆対策に効果を発揮するものと想定される。
上塗り塗膜用塗膜としては、メタリツクカラー
系ではメタリツクベースコートとクリヤーコート
をウエツトオンウエツト系で塗装するのが一般的
で、ベース及びクリヤー共にアクリル・メラミン
型が主流であり、ウレタン型(2液)塗料、メタ
リツクベースとしてのポリエステル+セスロース
アセテートブチレート+メラミン塗料、トツプク
リヤーとしてのアクリルメラミンの使用が可能で
ある。ソリツドカラーは1コートでアルキドメラ
ミン型が主流であるが、アクリルメラミン系の2
コート1ベーク型ソリツドカラー及び2液ウレタ
ン型塗料も使用できる。
実施例
以下に本発明の実施例を説明するが、本発明の
範囲をこれらの実施例に限定するものでないこと
はいうまでもない。
例 11〜14
寸法0.8×100×300mmのダル鋼板試料に第1表
に記載の下塗り塗料を所定厚(乾時厚)に塗装
し、これを第1表に示す条件で研磨し、中塗り塗
料1を所定厚に塗装し、所定条件でプレヒート
し、次に中塗り塗料2を所定定圧に塗装し、その
後下記の上塗り塗料を所定厚(乾時厚)に塗装
し、焼付硬化して積層塗膜を形成した。
次にこの塗膜を、その外観、エツジ錆、設備費
用及びランニングコストについて試験評価した。
結果は第2表に示す通りであつた。
Technical Field The present invention relates to a method for forming a laminated coating film, and more specifically, the present invention relates to a method for forming a laminated coating film, and more specifically, after coating and curing an undercoat film on an object to be coated, and polishing the cured undercoat film, the intermediate coat film and top coat film are then applied. The present invention relates to a method for forming a laminated coating film with excellent finished appearance by applying the intermediate coating film and curing the intermediate coating film and the top coating film without polishing. Conventional technology Conventionally, the technology for forming laminated coatings, as typified by automobile coatings, has focused on the pursuit of functions such as corrosion resistance and chipping resistance, suitability for mass production, and economic efficiency. With the spread of electrodeposition paints, chipping resistance has been improved by using specific polyester resins and by incorporating talc and mica with specific particle sizes. Publication No. 58-74349, Japanese Unexamined Patent Publication No. 1983
It has been proposed in Japanese Patent Publication No. 141459 and Japanese Patent Publication No. 52-43657. However, although these proposed technologies are achieving practicality for the coated objects and economical efficiency based on mass production, they are still lacking in terms of providing a high-quality exterior finish with excellent durability, image clarity, and gloss. It was enough. For passenger cars, the standard method is to apply a chemical coating, an electrodeposited undercoat, bake harden, apply a first intermediate coat, and a second intermediate coat, polish after bake harden, and then finish by laminating a metallic base, top clear, or solid coat. It is a paint type. Also, JP-A-58-70866 and JP-A-58-
Publication No. 3678 discloses polishing the electrodeposition coating film and the intermediate coating film, but when polishing is done in the intermediate coating process, the top coating paint is sucked in, resulting in an excellent texture. A glossy coating film could not be obtained. On the other hand, the necessity of a polishing step during the painting process is often due to the unevenness of the paint film as well as the material itself. In other words, dull steel plates, which are often used as steel plates for automobiles, have dullness (unevenness) of 0.5 to 0.8 μm, and this unevenness cannot be eliminated simply by laminating a coating film. Polishing of the paint film is required. OBJECTS OF THE INVENTION Therefore, an object of the present invention is to eliminate the problems of the conventional techniques described above and to provide a method for forming a laminated coating film with excellent finished appearance. Structure of the Invention That is, according to the present invention, a cationic electrodeposition paint is applied to an object to be coated and cured, the cured cationic electrodeposition coating is polished, and then a pigment volume concentration of 10 to 50% is applied.
and two layers of primary and secondary intermediate coats having a pigment volume concentration of 5 to 40% are sequentially laminated, and at least one top coat is further applied, without polishing the intermediate coat and top coat. Provided is a method for forming a laminated coating film characterized by curing. Specific Description of the Structure and Effects of the Invention In view of the current status of the method for forming a laminated coating film as described above, the present inventors have conducted intensive studies to develop a method for forming a laminated coating film with an excellent finished appearance. The present inventors have discovered that the problems of conventional multilayer coatings can be effectively solved by adopting the configuration described above, and have completed the present invention. That is, according to the present invention, first, the object to be coated is subjected to pretreatment such as film conversion treatment as necessary, and then,
An undercoat film is applied and cured, and the cured undercoat film is polished. The paint used for the undercoat film is the cationic electrodeposition paint, which has been the most widely used conventionally.However, the undercoat used in the present invention is not limited to the cationic electrodeposition paint. Polishing may be performed after the reverse step of the mold primer or powder coating/cationic or anionic electrodeposition coating. The coating thickness of the undercoat film is reduced by about 5 μm by polishing as described below, so if the thickness is not maintained at least about 20 μm, the anticorrosion properties may deteriorate or the base layer may be partially polished. Paint film thickness is
The thickness is preferably 30 μm or more, but since it is difficult to apply an extremely thick electrodeposition coating, the maximum thickness is about 50 μm. If you want to apply an undercoat film to a thickness greater than that, it is preferable to use a solvent-based primer or powder paint, but recently, thick-film cationic electrodeposition paints have also been developed, so use these. You can also do that. The undercoat film applied to the object to be coated is cured by baking according to a conventional method. The standard bake-curing conditions when using cationic electrodeposition paints are 165 to 185°C x 20 minutes, but bake-curing conditions that give the abrasive a semi-cured state without entanglement of the uncured paint film, for example, 140-160
It may be heated at ℃ for about 20 minutes. Since the undercoat film formed in this manner reflects the dull grain, it is necessary to use an abrasive material such as sandpaper to smooth out the corners of the dull grain. This polishing is for polishing the undercoat film, so
The sharpening marks are hidden by the intermediate coat and top coat and are not noticeable, so they can be sanded using coarse sandpaper of about 280 to 600 grit. The undercoat film may be polished by either wet or dry sanding, but wet sanding is preferable to obtain a highly smooth polished surface, and dry sanding is preferable for surfaces with few irregularities due to the ease of work. Good too. In this way, the polished surface absorbs the resin of the paint applied on top because the upper resin layer, which has less suction, has been scraped off, but according to the present invention, the intermediate coat and top coat can be applied. Therefore, the texture and gloss of the finished coating will not be impaired.
In addition, the polished surface has a greatly increased surface area and is hairy, so if the intermediate coat is polished, the solvent and resin will be absorbed by capillary action when the top coat is applied. It is thought that the above-mentioned problems occur because the preferable micro-Brownian motion in the wet film is inhibited and the resin content that should be arranged on the surface layer of the top coat is consumed. However, according to the present invention, the top coat is applied without polishing the intermediate coat, so it seems that this problem can be effectively solved. In the method for forming a laminated coating film according to the present invention, the intermediate coating film is removed by removing the sandpaper marks,
It is preferable that the functions be shared between a primary intermediate coating film, which performs an auxiliary function to enhance corrosion resistance, and a secondary intermediate coating film, which functions to enhance the finish of the top coating film. The primary purpose of the primary intermediate coating is to erase the sandpaper marks caused by polishing and to perform an auxiliary function to increase anti-corrosion properties. things are appropriate,
Particularly preferred is 15-30%. 10% PVC
If it is less than 50%, the ability to hide the scratches caused by the sandpaper grains will not be sufficient, and if it exceeds 50%, a smooth coating film will not be obtained, and more paint will be absorbed, making abnormalities such as rough skin more likely to occur. Pigments used in primary intermediate coating paints include:
Relatively coarse particle size, more than 90% of primary particles are 0.5~
Talc, precipitated barium sulfate, aluminum tripolyphosphate, calcium carbonate, mica, phosphomolybdates, zinc phosphate, zinc white, aluminum silicate, zinc dust, and flakes with a maximum diameter of 30 μm. Aluminum flakes and the like are preferred. By blending appropriate amounts of these pigments, it is effective in hiding scratches on the base and preventing edge rust. It is not clear why these pigments with coarse particle sizes have good scratch-hiding ability, but they do not penetrate into the ground surface, etc. (pigment particles do not get into the gaps of the ground surface, etc.) and exhibit a sealing effect. This is thought to be because Therefore, while coarse particles such as talc and zinc dust are highly effective, they make it difficult to achieve flatness in the secondary intermediate coating, so these points should be taken into consideration when selecting the type and amount of pigment used. It is preferable to select The second intermediate coat is usually applied wet-on-wet (hereinafter referred to as W/W) on top of the first intermediate coat to form a coating with less suction to improve the finish of the top coat. I found that it was preferable. For this purpose, the second intermediate coating film is
A suitable PVC content is 5 to 40%; if the PVC content in the secondary intermediate coat is less than 5%, it will easily reflect the skin condition of the primary intermediate coat, and if it exceeds 40%, the top coat will paint is more likely to be sucked in. When applying the intermediate coating film once, the expected performance described above is achieved in one layer, so the limit range of PVC and film thickness is further limited to PVC: 10 to 30%, film thickness: 35 to 50 μm. It is preferable that In conventional laminated coating film formation technology, the amount of pigment in the intermediate coating film is usually limited to provide clarity to the topcoat film, and the maximum amount of PVC is about 30%. However, according to a preferred embodiment of the present invention, after forming the undercoating electrodeposition coating film, the electrocoating paint is polished, and the functions of the intermediate coating film can be shared between the primary intermediate coating and the second intermediate coating. The limitations can be eliminated and the above objectives can be achieved. In this case, if the primary intermediate coating film and the secondary intermediate coating film are mixed together, the appearance improvement effect will be reduced, so in some cases, the coating of the primary intermediate coating film and the secondary intermediate coating film may be mixed. It may be necessary to perform preheating or flash-off in between. Preheat or flash off is 40-80
It can be carried out under heated conditions of 30 seconds to 5 minutes at °C. It should be noted that heating for more than 5 minutes is not preferable because the heat retention equipment becomes longer and therefore the booth itself needs to be longer. Furthermore, if the temperature exceeds 80°C, the surface of the primary intermediate coat will develop too many wrinkles, making pinholes and the like more likely to occur, which is undesirable. Note that a hot air blowing device can be used as the heat insulation equipment, but in consideration of dust prevention, etc., it is preferable to use a radiant method in which hot water is passed through pipes. As the paint for the intermediate coating film, a polyester-melamine resin system that is generally used in the conventional method of forming a laminated coating film can be used, and if necessary, alkyd resin, epoxy resin, etc. can be used in combination. Can be done. For powder intermediate coatings, polyester/epoxy curing type or acrylic/
Acid curing type can be used, and alkyd type
It is also possible to use melamine-type water-based intermediate coats. After the intermediate coat is baked, dust often adheres to it, and if the top coat is applied as is, dust particles will be generated on the top coat surface. In this case, it is preferable to spot-sand only the dusty parts of the intermediate coating surface with sandpaper of about 360 to 800 grit. If the entire surface is polished, as described above, it causes suction of the top coat, which impairs the achievement of the above-mentioned object of the present invention. The greatest effect of the present invention is a significant improvement in the appearance, but another effect is that the number of steps required for sanding can be reduced compared to conventional methods. Conventionally, when sanding the intermediate coat surface, a sandpaper of about 360 to 800 grit was used as an abrasive, but for polishing the undercoat film, a relatively rough sandpaper of about 280 to 600 grit is sufficient. Yes, because wet sanding is no longer an essential condition as in the past, the need to use water-resistant sandpaper for wet sanding is reduced, and the amount used can be significantly reduced.
Additionally, polishing with fine sandpaper required a long time in the past, but this is also a significant improvement. For example, there is a method of applying the top coat twice in a 4-coat, 4-bake method by changing the pigment concentration of the top coat, as is conventionally done on luxury cars such as Mercedes-Benz, but these methods Not only is the cost extremely high in terms of equipment investment and running costs, but also the appearance quality cannot reach the level of that of the present invention. Furthermore, according to the present invention, the important effect of significantly improving the edge rust prevention ability is also achieved, which is achieved by increasing the concentration of the pigment with a large particle size used in the primary intermediate coating. It is expected that the corner coverage will be increased and the edge rust prevention will be improved compared to conventional systems, making it effective for edge rust prevention. As for the topcoat film, for metallic color systems, it is common to apply a metallic base coat and clear coat in a wet-on-wet system, and acrylic/melamine type is the mainstream for both the base and clear, while urethane type (2 It is possible to use liquid) paints, polyester + cellulose acetate butyrate + melamine paints as a metallic base, and acrylic melamine as a top clearer. Most solid colors are one-coat alkyd melamine type, but two-coat acrylic melamine type is the mainstream.
One-coat bake type solid color and two-component urethane type paints can also be used. Examples Examples of the present invention will be described below, but it goes without saying that the scope of the present invention is not limited to these examples. Examples 11 to 14 A dull steel plate sample with dimensions of 0.8 x 100 x 300 mm is coated with the primer coating listed in Table 1 to a specified thickness (dry thickness), and this is polished under the conditions listed in Table 1. 1 to a predetermined thickness, preheated under predetermined conditions, then apply intermediate coat 2 to a predetermined pressure, then apply the following top coat to a predetermined thickness (dry thickness), bake and harden to form a laminated coating. A film was formed. Next, this coating film was tested and evaluated for its appearance, edge rust, equipment cost, and running cost.
The results were as shown in Table 2.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】
以下の例から、本発明の実施例である例1〜7
は平滑性と艶が優れていると同時に、肉持感や、
エツジ錆等の各評価項目がバランスが良いのに対
して、比較例の例8〜14は研磨なし、又は研磨工
程が表層に近いため、研ぎ目が出る等を主体とす
る従来技術のレベルであつた。[Table] From the following examples, Examples 1 to 7 are examples of the present invention.
has excellent smoothness and gloss, and at the same time has a sense of fleshiness,
While each evaluation item such as edge rust was well balanced, Comparative Examples 8 to 14 did not require polishing or the polishing process was close to the surface layer, so the level of the conventional technology was mainly that the sharpness appeared. It was hot.
Claims (1)
め、硬化したカチオン電着塗膜の研磨を行い、次
いで顔料容積濃度10〜50%及び顔料容積濃度5〜
40%の一次及び二次の2層の中塗り塗膜を順次積
層し、更に少なくとも一層の上塗り塗膜を施し、
該中塗り塗膜及び上塗り塗膜を研磨することなく
硬化せしめることを特徴とする積層塗膜の形成方
法。 2 一次中塗り塗膜の顔料容積濃度が15〜30%で
あり、当該顔料の一次粒子の90%以上の粒径が
0.5〜30μmである特許請求の範囲第1項記載の方
法。[Claims] 1. A cationic electrodeposition coating is applied to an object to be coated and cured, the cured cationic electrodeposition coating is polished, and then a pigment volume concentration of 10 to 50% and a pigment volume concentration of 5 to 50% are applied.
Two layers of 40% primary and secondary intermediate coats are laminated in sequence, and at least one top coat is applied.
A method for forming a laminated coating film, which comprises curing the intermediate coating film and the top coating film without polishing. 2 The pigment volume concentration of the primary intermediate coating film is 15 to 30%, and the particle size of 90% or more of the primary particles of the pigment is
The method according to claim 1, wherein the thickness is 0.5 to 30 μm.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24526183A JPS60139366A (en) | 1983-12-28 | 1983-12-28 | Formation of laminated film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP24526183A JPS60139366A (en) | 1983-12-28 | 1983-12-28 | Formation of laminated film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60139366A JPS60139366A (en) | 1985-07-24 |
| JPH0341225B2 true JPH0341225B2 (en) | 1991-06-21 |
Family
ID=17131046
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP24526183A Granted JPS60139366A (en) | 1983-12-28 | 1983-12-28 | Formation of laminated film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60139366A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62289270A (en) * | 1986-06-09 | 1987-12-16 | Daihatsu Motor Co Ltd | Pearl mica coating method |
| JP5225058B2 (en) * | 2008-12-24 | 2013-07-03 | 日産自動車株式会社 | Method for painting automobile body and automobile body having coating film |
| JP6508758B1 (en) * | 2018-12-12 | 2019-05-08 | 株式会社フロント | Metal member subjected to polishing pattern and method for manufacturing the same |
-
1983
- 1983-12-28 JP JP24526183A patent/JPS60139366A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60139366A (en) | 1985-07-24 |
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