JPH0311821B2 - - Google Patents
Info
- Publication number
- JPH0311821B2 JPH0311821B2 JP5651283A JP5651283A JPH0311821B2 JP H0311821 B2 JPH0311821 B2 JP H0311821B2 JP 5651283 A JP5651283 A JP 5651283A JP 5651283 A JP5651283 A JP 5651283A JP H0311821 B2 JPH0311821 B2 JP H0311821B2
- Authority
- JP
- Japan
- Prior art keywords
- pigment
- colored
- paint
- transparent
- parts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 239000000049 pigment Substances 0.000 claims description 76
- 238000000576 coating method Methods 0.000 claims description 43
- 239000011248 coating agent Substances 0.000 claims description 42
- 239000003973 paint Substances 0.000 claims description 39
- 238000004040 coloring Methods 0.000 claims description 18
- 238000000034 method Methods 0.000 claims description 18
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 14
- 229920003002 synthetic resin Polymers 0.000 claims description 9
- 239000000057 synthetic resin Substances 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 5
- 239000011164 primary particle Substances 0.000 claims description 3
- 239000000470 constituent Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 26
- 238000009472 formulation Methods 0.000 description 15
- 239000000243 solution Substances 0.000 description 10
- 229920000180 alkyd Polymers 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 239000007921 spray Substances 0.000 description 8
- 229920000877 Melamine resin Polymers 0.000 description 7
- 239000004640 Melamine resin Substances 0.000 description 7
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 6
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- 239000012860 organic pigment Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 238000002845 discoloration Methods 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 235000013305 food Nutrition 0.000 description 5
- 230000007774 longterm Effects 0.000 description 5
- 238000010422 painting Methods 0.000 description 5
- 239000004925 Acrylic resin Substances 0.000 description 3
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 229910001209 Low-carbon steel Inorganic materials 0.000 description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 3
- 229920003180 amino resin Polymers 0.000 description 3
- 125000002091 cationic group Chemical group 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 238000004070 electrodeposition Methods 0.000 description 3
- 238000005562 fading Methods 0.000 description 3
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 3
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 3
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004381 surface treatment Methods 0.000 description 2
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- OWYWGLHRNBIFJP-UHFFFAOYSA-N Ipazine Chemical compound CCN(CC)C1=NC(Cl)=NC(NC(C)C)=N1 OWYWGLHRNBIFJP-UHFFFAOYSA-N 0.000 description 1
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000980 acid dye Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 239000000981 basic dye Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
本発明は、長期耐久性に優れ、色落ちのない鮮
明性のある塗膜の形成方法に関するものである。
近年、自動車車体等の塗装は塗装工程の短縮化
のため、2コート、1ベーク方式が広く採用され
つつある。
また、塗膜の色相として、鮮やかでかつ深色な
ソリツドカラーが好んで使用されるようになり、
そのためレツド、オレンジ、イエロー、グリーン
あるいはブルー系の有機顔料が塗料用着色顔料と
して使用されるようになつてきた。
しかしながら、有機顔料は一般に隠蔽力が非常
に小さいことから、高濃度の有機顔料を使用する
ことで隠蔽力不足を補つているが、このように高
濃度の有機顔料を塗料に使用すると色落ちの危険
性が高くなるという問題点があつた。
そこで前記問題点を解決するため従来から有機
顔料を含む塗料(ベースコート)を塗布し、次い
で透明クリヤー塗料(トツプコート)を塗布する
という2コート1ベーク方式が知られている。し
かしながら、この方式では着色顔料の反転現象等
が生じやすく、それ故塗膜の仕上り外観、品質の
確保のためにはベースコートとトツプコートの合
成樹脂の組成や分子量等を変える必要があつた。
そのため両塗膜の膨張率、収縮率の差に帰因して
塗膜にクラツクやハクリ等が発生することが避け
られず長期耐久性に問題があつた。
また、前記色落ちの問題を解決するため、着色
ベースコート層上に着色半透明のトツプコート層
を2コート、1ベーク方式で形成するという方式
を提案されている。
しかしながら、この方式においても、ベースコ
ートとトツプコートの顔料濃度差に起因する反転
現象は、両層の合成樹脂の組成や分子量等をかえ
たり、あるいは表面調整剤を添加したりする等の
手段では完全には防止することが出来ず、そのた
めチリチリ肌等が屡々発生することがあり塗膜の
平滑性に問題があつた。
本発明者は、上記の如き現状に鑑み、長期耐久
性に優れ色落ちのない鮮明性のある塗膜を形成す
る方法につき鋭意検討の結果、本発明に到つたも
のである。
すなわち、本発明は、被塗物上に、必要に応じ
下地処理を施した後、有機着色顔料を主体とする
着色顔料の顔料重量濃度〔塗膜形成性固形分に対
する顔料の重量割合(以下PWCと略称する)〕が
約10〜30%の着色塗料Aを塗布し、該着色塗料A
の塗膜が末乾燥状態にある間に、着色半透明塗料
Bを塗り重ね、形成された両塗膜を同時に乾燥さ
せる塗膜の形成方法において、
着色塗料Aと着色半透明塗料Bの構成成分であ
る合成樹脂は同一であり、着色半透明塗料Bで使
用する顔料はPWCが約1〜10%の有機着色顔料
を主体とする着色顔料とPWCが約5〜50%の
透明顔料とからなり、かつ着色顔料と透明顔
料の合計PWCは着色塗料AのPWC以上である
ことを特徴とする塗膜の形成方法に関する。
本発明の方法により、従来の1コート1ベーク
方式のソリツド塗料に比べて塗膜表面部分の着色
顔料濃度を低くしているため塗膜の色落す性を著
しく向上させるという効果が得られる。加えて、
前記従来の2コート、1ベーク方式のベースコー
トとトツプコートに用いる合成樹脂の相違等に起
因するワレやハクリ等の、長期耐久性に悪影響を
及ぼす塗膜の破壊現象の防止、並びに着色顔料の
反転に起因する塗面のチリチリ肌等の如き、塗膜
の初期品質の改善に著しい効果が得られる。
本発明において使用される着色塗料Aは、従来
から一般に使用されている自動車用等の濃色ソリ
ツド塗膜が大略そのまま使用出来る。すなわち、
上記着色塗料Aはアクリル−ウレタン樹脂系、ア
クリル−アミノ樹脂系、アルキツド−アミノ樹脂
系、ポリエステル−アミノ樹脂系、ポリエステル
−ウレタン樹脂系等の合成樹脂;着色顔料;トル
オール、キシロール、エタノール、ブタノール、
セロソルブ、酢酸ブチル等の溶剤;及び紫外線吸
収剤、表面調整剤、可塑剤等の添加剤少量からな
るものである。
前記着色顔料としては、塗膜に鮮明性をもたせ
るため有機着色顔料をPWC約10〜30%使用する。
なお、着色顔料として酸化チタン、カーボンブラ
ツク、弁柄等の無機着色顔料を色相にもよるが半
分以下の量で有機着色顔料と置換えることも出来
る。なお、PWCが10%未満であると隠蔽力が十
分でなく、逆に30%を越えると塗料の粘度が高く
なり塗装作業性が悪くなるのでいずれも好ましく
ない。
前記有機着色顔料としては、アゾ系顔料、フタ
ロシアニン系顔料、塩基性染料系レーキ、酸性染
料系レーキ、アンスラキノン系顔料、ペリレン系
顔料、ペリノン系顔料、チオインジゴ系顔料、キ
ナクリドン系顔料、ジオキサジン系顔料、イソイ
ンドリノン系顔料、キノフタロン系顔料、アゾメ
チンアゾ系顔料等が挙げられる。
本発明において使用される着色半透明塗料Bに
施ては、着色塗料Aと同一の合成樹脂を使用す
る。このように同一の合成樹脂を使用することに
より、トツプコート、ベースコート間の相溶性が
良くなるため、従来の塗装方式で屡々生起してい
たような塗膜間の破壊現象が防止出来る。
上記着色半透明塗料Bに使用する着色顔料と
しては前記着色塗料Aと同様な有機着色顔料もし
くはそれを主体としたものが使用出来る。
該着色顔料は、色相にもよるがPWCが約1
〜10%が適当である。PWCが1%未満になると
膜厚差による色の濃淡が目立ちやすくなり、逆に
10%を越えると色落ちが発生しやすくなるのでい
ずれも好ましくない。
また、上記着色半透明塗料Bに使用する透明顔
料としては、粒径0.1μ以下の硫酸バリウム、炭
酸カルシウム等が使用出来るが、本発明において
は特に一次粒子の平均粒径が0.05μ以下の硫酸バ
リウム(以下これを超微粒子硫酸バリウムとい
う)が好適である。かかる超微粒子硫酸バリウム
は極めて透明であり、かつ着色顔料粒子間に存在
して着色顔料の凝集等を防止するため分散安定性
の向上に寄与し、鮮明で光沢ある塗膜を得ること
が出来る。
上記透明顔料はPWCが5〜50%が適当であ
る。PWCが5%未満になるとベースコートの着
色顔料の反転が生じやすくなり、逆に50%を越え
ると塗膜が脆くなるのでいずれも好ましくない。
また着色顔料と透明顔料の合計PWCは着
色顔料の反転を防止するため着色塗料AのPWC
以上にする必要がある。
本発明の方法に於ては、必要により表面処理、
プライマーを塗布する等の下地処理を施した被塗
物上にエアースプレー、エアレススプレー、静電
スプレー等の如き、通常の塗装手段により乾燥膜
厚が約15〜40μになるよう着色塗料Aを塗布す
る。
次いで1〜10分間程度静置し、塗膜が未乾燥状
態にある間に、半透明塗料Bを乾燥膜厚が約15〜
30μになるように塗布する。
次いで1〜20分間程度静置し、常温または加熱
により両塗膜を同時に乾燥させる。
以上の通り、本発明の方法により、色落ちのな
い鮮明な塗膜であつて、しかもトツプコートとベ
ースコート間の破壊現象の生じにくい長期耐久性
のある塗膜が得られる。
以下、本発明を実施例により、更に詳細に説明
する。なお、「部」、「%」はいずれも重量基準で
ある。
実施例 1
下記の配合のベースコート、透明顔料分散ベー
ス、半透明トツプコート、希釈シンナーの夫々
を、塗装前に予め調製した。
〈配合〉……ベースコート
チオインジゴマルーン 注1) 8部
弁柄 2部
アルキツド樹脂 注2) 36部
メラミン樹脂溶液 注3) 25部
キシロール 29部
(着色顔料のPWC=16.4%)
〈配合〉……透明顔料分散ベース
硫酸バリウム 注4) 40部
アルキツド樹脂 注2) 21部
メラミン樹脂溶液 注3) 15部
キシロール 24部
(着色顔料のPWC=57.1%)
〈配合〉……半透明トツプコート
配合 100部
配合 400部
アルキツド樹脂 注2) 120部
メラミン樹脂溶液 注3) 85部
キシロール 95部
(着色顔料のPWC=2.0%、
透明顔料のPWC=31.2%)
〈配合〉……希釈シンナー
ソルベツソ#100 80部
ブチルセロソルブ 15部
n−ブタノール 5部
注1)「クロモフタルボルド−RS」(チバガイ
ギー社製商品名)
注2)油長19、酸価7、数平均分子量3500のヤ
シ油変性アルキツド樹脂
注3)「ユーバン20SE」(三井東圧化学社製商
品名)〔固形分60%〕
注4)「BF−20」(小名浜堺化学社製商品名)
〔平均一次粒径0.05μ〕
配合を配合で希釈し、粘度25秒/20℃(フ
オードカツプ#4)とした塗料を、カチオン電着
塗膜(20μ)、アミノアルキツド樹脂系中塗塗膜
(30μ)を施した軟鋼板上に乾燥厚が20μになるよ
うエアースプレー塗装し、3分間セツテイング
後、配合を配合で希釈し、粘度25秒/20℃
(フオードカツプ#4)とした塗料を乾燥膜厚
20μになるようエアースプレーにて塗り重ね、7
分間セツテング後、150℃で20分間焼付けた。
比較例 1
配合において、硫酸バリウムを配合せず、ア
ルキツド樹脂を44部、メラミン樹脂溶液を32部と
する以外は実施例1と全く同一条件で塗膜を形成
させた。
比較例 2
配合において、配合の有機顔料をさらに
115部追加し、着色顔料のPWCを19.9%とする以
外は実施例1と全く同一条件で塗膜を形成させ
た。
実施例 2
下記の配合のベースコート、透明顔料分散ベー
ス、半透明トツプコート、希釈シンナーの夫々
を、塗装前に予め調製した。
〈配合〉……ベースコート
ペリレン系顔料 注5) 16部
弁柄 2部
酸化チタン 1部
アクリル樹脂溶液 注6) 51部
メラミン樹脂溶液 注7) 20部
キシロール 10部
(着色顔料のPWC=28.5%)
〈配合〉……透明顔料分散ベース
硫酸バリウム 注8) 35部
アクリル樹脂溶液 注6) 38部
メラミン樹脂溶液 注7) 15部
キシロール 12部
(着色顔料のPWC=49.6%)
〈配合〉……半透明トツプコート
配合 100部
配合 550部
アクリル樹脂溶液 注6) 285部
メラミン樹脂溶液 注7) 113部
(着色顔料のPWC=2.6%、
透明顔料のPWC=26.7%)
〈配合〉……希釈シンナー
ソルベツソ#100 80部
ブチルセロソルブ 15部
n−ブタノール 5部
注5) 「バリオゲンレツドL3910HD」
(BASF社製商品名)
注6)「コータツクスSB−302」(東レ社製商品
名)〔固形分70%〕
注7) 注3)と同じ
注8) 注4)と同じ
配合を配合で希釈し、粘度27秒/20℃(フ
オードカツプ#4)とした塗料を、カチオン電着
塗膜(20μ)、アミノアルキツド樹脂系中塗塗膜
(30μ)を施した軟鋼板上に乾燥膜厚が20μになる
ようエアースプレー塗装し、3分間セツテイング
後、配合を配合で希釈し、粘度27秒/20℃
(フオードカツプ#4)とした塗料を乾燥膜厚が
20μになるようエアースプレーにて塗り重ね、7
分間セツテング後、150℃で20分間焼付けた。
比較例 3
実施例2の配合を配合で希釈した塗料を乾
燥膜厚40μになるようにエアースプレー塗装し、
7分間セツテイング後、150℃で20分間焼付けた。
比較例 4
実施例2の配合においてペリレン系顔料16
部、弁柄2部、酸化チタン1部の代りにチオイン
ジゴマルーン16部、弁柄3部を使用する以外は同
様の塗料を配合で希釈し、粘度25秒/20℃(フ
オードカツプ#4)としたものを、カチオン電着
塗膜(20μ)、アミノアルキツド樹脂系中塗塗膜
(30μ)を施した軟鋼板上に乾燥膜厚が20μになる
ようエアースプレー塗装した。3分間セツテイン
グ後、実施例1の配合を配合で希釈し粘度25
秒/20℃(フオードカツプ#4)とした塗料を乾
燥膜厚が20μになるようエアースプレーにて塗り
重ね、7分間セツテイング後、150℃で20分間焼
付けた。
実施例1〜2及び比較例1〜4で得られた試験
板を、塗膜の光沢、平滑性、色落ち性及び耐久性
の夫々につき試験した結果を第1表に示した。
TECHNICAL FIELD The present invention relates to a method for forming a coating film that is excellent in long-term durability and has a clear color without fading. In recent years, a two-coat, one-bake method has been widely adopted for painting automobile bodies and the like in order to shorten the painting process. In addition, vivid and deep solid colors have come to be preferred as hues for paint films.
Therefore, red, orange, yellow, green, or blue organic pigments have come to be used as coloring pigments for paints. However, since organic pigments generally have very low hiding power, the lack of hiding power is compensated for by using organic pigments at high concentrations, but when such high concentrations of organic pigments are used in paints, color fading occurs. There was a problem with the increased risk. To solve this problem, a two-coat one-bake method has been known in which a paint containing an organic pigment (base coat) is applied and then a transparent clear paint (top coat) is applied. However, with this method, reversal of the colored pigments is likely to occur, and therefore, in order to ensure the finished appearance and quality of the coating film, it was necessary to change the composition and molecular weight of the synthetic resins used in the base coat and top coat.
Therefore, due to the difference in expansion rate and contraction rate between the two coating films, it was inevitable that cracks and peeling would occur in the coating film, resulting in problems in long-term durability. Furthermore, in order to solve the problem of discoloration, a method has been proposed in which a colored semitransparent top coat layer is formed on a colored base coat layer by a two-coat, one-bake method. However, even in this method, the reversal phenomenon caused by the difference in pigment concentration between the base coat and top coat cannot be completely resolved by changing the composition or molecular weight of the synthetic resin in both layers, or by adding a surface conditioning agent. It was not possible to prevent this, and as a result, scratchy skin often occurred, causing problems in the smoothness of the coating film. In view of the above-mentioned current situation, the inventors of the present invention have arrived at the present invention as a result of intensive studies on a method for forming a coating film with excellent long-term durability, no fading, and sharpness. That is, the present invention applies the pigment weight concentration [the weight ratio of the pigment to the film-forming solid content (hereinafter referred to as PWC Colored paint A containing approximately 10 to 30% of the coloring paint A is applied.
A method for forming a coating film in which a colored semi-transparent coating B is applied over and over while the coating film is in a semi-dry state, and both of the formed coating films are dried simultaneously, the constituent components of the colored coating A and the colored semi-transparent coating B are The synthetic resins are the same, and the pigments used in colored semi-transparent paint B consist of colored pigments mainly consisting of organic coloring pigments with a PWC of about 1 to 10% and transparent pigments with a PWC of about 5 to 50%. , and the total PWC of the colored pigment and the transparent pigment is greater than or equal to the PWC of the colored paint A. The method of the present invention has the effect of significantly improving the discoloration properties of the coating film, since the concentration of the coloring pigment on the surface of the coating film is lower than that of the conventional one-coat, one-bake solid paint. In addition,
To prevent paint film destruction such as cracking and peeling caused by the difference in synthetic resins used for the base coat and top coat of the conventional 2-coat, 1-bake method, which have a negative impact on long-term durability, and to reverse color pigments. A remarkable effect can be obtained in improving the initial quality of the coating film, such as the occurrence of scratchy skin on the coating surface. As the colored paint A used in the present invention, dark solid paint films commonly used for automobiles and the like can be used as they are. That is,
The colored paint A is a synthetic resin such as an acrylic-urethane resin system, an acrylic-amino resin system, an alkyd-amino resin system, a polyester-amino resin system, or a polyester-urethane resin system; a coloring pigment; toluol, xylol, ethanol, butanol,
It consists of a solvent such as cellosolve and butyl acetate; and a small amount of additives such as an ultraviolet absorber, a surface conditioner, and a plasticizer. As the coloring pigment, an organic coloring pigment is used in an amount of about 10 to 30% PWC in order to give the coating film clarity.
Incidentally, as a coloring pigment, an inorganic coloring pigment such as titanium oxide, carbon black, or Bengara may be substituted with an organic coloring pigment in an amount of less than half, depending on the hue. It should be noted that if the PWC is less than 10%, the hiding power will not be sufficient, and if it exceeds 30%, the viscosity of the paint will increase and the painting workability will deteriorate, so both are not preferred. The organic coloring pigments include azo pigments, phthalocyanine pigments, basic dye lakes, acid dye lakes, anthraquinone pigments, perylene pigments, perinone pigments, thioindigo pigments, quinacridone pigments, and dioxazine pigments. , isoindolinone pigments, quinophthalone pigments, azomethine azo pigments, and the like. The same synthetic resin as the colored paint A is used for the colored semi-transparent paint B used in the present invention. By using the same synthetic resin in this way, the compatibility between the top coat and the base coat is improved, so it is possible to prevent the phenomenon of destruction between the coating films that often occurs in conventional coating methods. As the colored pigment used in the above-mentioned colored translucent paint B, the same organic coloring pigment as the above-mentioned colored paint A or a material mainly composed of organic coloring pigments can be used. The color pigment has a PWC of about 1, depending on the hue.
~10% is appropriate. When the PWC is less than 1%, the color shading due to the difference in film thickness becomes more noticeable;
If it exceeds 10%, discoloration tends to occur, which is not preferable. In addition, as the transparent pigment used in the colored semi-transparent paint B, barium sulfate, calcium carbonate, etc. with a particle size of 0.1μ or less can be used, but in the present invention, sulfuric acid with an average primary particle size of 0.05μ or less can be used. Barium (hereinafter referred to as ultrafine barium sulfate) is preferred. Such ultrafine barium sulfate particles are extremely transparent and exist between colored pigment particles to prevent agglomeration of colored pigments, thereby contributing to improving dispersion stability and making it possible to obtain a clear and glossy coating film. The above transparent pigment suitably has a PWC of 5 to 50%. If the PWC is less than 5%, the color pigments in the base coat tend to reverse, while if it exceeds 50%, the coating film becomes brittle, so both are unfavorable. In addition, the total PWC of colored pigments and transparent pigments is the PWC of colored paint A to prevent reversal of colored pigments.
It is necessary to do more than that. In the method of the present invention, surface treatment,
Colored paint A is applied to the surface of the workpiece that has been subjected to surface treatment such as applying a primer using a normal painting method such as air spray, airless spray, electrostatic spray, etc. to a dry film thickness of approximately 15 to 40μ. do. Next, let it stand for about 1 to 10 minutes, and while the paint film is still in an undried state, apply semi-transparent paint B to a dry film thickness of about 15 to 100 ml.
Apply to a thickness of 30μ. Next, the coating is left to stand for about 1 to 20 minutes, and both coating films are simultaneously dried at room temperature or by heating. As described above, by the method of the present invention, it is possible to obtain a coating film that is clear and does not fade in color and has long-term durability and is resistant to destruction between the top coat and the base coat. Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that both "parts" and "%" are based on weight. Example 1 A base coat, transparent pigment dispersion base, translucent top coat, and diluent thinner having the following formulations were prepared in advance before painting. <Composition>...Base coat Thioindigo maroon Note 1) 8 parts Bengara 2 parts Alkyd resin Note 2) 36 parts Melamine resin solution Note 3) 25 parts Xylol 29 parts (PWC of color pigment = 16.4%) <Composition>... Transparent pigment dispersion base Barium sulfate Note 4) 40 parts Alkyd resin Note 2) 21 parts Melamine resin solution Note 3) 15 parts Xylol 24 parts (PWC of colored pigment = 57.1%) <Blend>... Translucent top coat Blend 100 parts Blend 400 parts Alkyd resin Note 2) 120 parts Melamine resin solution Note 3) 85 parts Xylene 95 parts (PWC of colored pigment = 2.0%, PWC of transparent pigment = 31.2%) <Formulation>... Diluting thinner Solbetsuso #100 80 parts Butyl cellosolve 15 parts n-butanol 5 parts Note 1) "Chromophthalbord-RS" (trade name manufactured by Ciba Geigy) Note 2) Coconut oil modified alkyd resin with oil length 19, acid value 7, number average molecular weight 3500 Note 3) "Yuban" 20SE” (trade name manufactured by Mitsui Toatsu Chemical Co., Ltd.) [Solid content 60%] Note 4) “BF-20” (trade name manufactured by Onahama Sakai Chemical Co., Ltd.)
[Average primary particle size 0.05μ] The formulation was diluted with a viscosity of 25 seconds/20℃ (Food Cup #4), and a cationic electrodeposition coating (20μ) and an amino alkyd resin intermediate coating (30μ) were applied. Air spray paint on the applied mild steel plate to a dry thickness of 20μ, and after setting for 3 minutes, dilute the formulation with a viscosity of 25 seconds / 20℃
(Food Cup #4) Dry film thickness
Repeat coating with air spray to make it 20μ, 7
After setting for a minute, it was baked at 150°C for 20 minutes. Comparative Example 1 A coating film was formed under exactly the same conditions as in Example 1, except that barium sulfate was not blended, the alkyd resin was 44 parts, and the melamine resin solution was 32 parts. Comparative Example 2 In the formulation, the organic pigment in the formulation was further added.
A coating film was formed under the same conditions as in Example 1, except that 115 parts of the pigment was added and the PWC of the colored pigment was 19.9%. Example 2 A base coat, a transparent pigment dispersion base, a translucent top coat, and a diluent thinner having the following formulations were each prepared in advance before painting. <Formulation> Base coat Perylene pigment Note 5) 16 parts Bengara 2 parts Titanium oxide 1 part Acrylic resin solution Note 6) 51 parts Melamine resin solution Note 7) 20 parts Xylol 10 parts (PWC of coloring pigment = 28.5%) <Blend>...Transparent pigment dispersion base Barium sulfate Note 8) 35 parts Acrylic resin solution Note 6) 38 parts Melamine resin solution Note 7) 15 parts Xylol 12 parts (PWC of colored pigment = 49.6%) <Blend>...Semi Transparent top coat Mixture 100 parts Mixture 550 parts Acrylic resin solution Note 6) 285 parts Melamine resin solution Note 7) 113 parts (PWC of colored pigment = 2.6%, PWC of transparent pigment = 26.7%) <Formulation>... Dilution thinner Solvetsuso # 100 80 parts Butyl cellosolve 15 parts n-butanol 5 parts Note 5) "Variogenredo L3910HD" (trade name manufactured by BASF) Note 6) "Kotakus SB-302" (trade name manufactured by Toray Industries) [Solid content 70%] Note 7) Same as note 3) Note 8) Same as note 4) Dilute the formulation and make the viscosity 27 seconds/20℃ (foed cup #4) with a cationic electrodeposition coating (20μ) and an amino alkyd resin intermediate coating. Air spray paint on a mild steel plate coated with a film (30μ) so that the dry film thickness is 20μ, and after setting for 3 minutes, dilute the formulation with a viscosity of 27 seconds/20℃.
The dry film thickness of the paint made with (Food Cup #4)
Repeat coating with air spray to make it 20μ, 7
After setting for a minute, it was baked at 150°C for 20 minutes. Comparative Example 3 A paint diluted with the formulation of Example 2 was air-sprayed to a dry film thickness of 40μ,
After setting for 7 minutes, it was baked at 150°C for 20 minutes. Comparative Example 4 Perylene pigment 16 in the formulation of Example 2
1 part, Bengara, 1 part of titanium oxide, 16 parts of Thioindigo Maroon, and 3 parts of Bengara were used, but the same paint was diluted with the same formulation, and the viscosity was 25 seconds/20°C (Food Cup #4). This was air-sprayed onto a mild steel plate that had been coated with a cationic electrodeposition coating (20μ) and an amino alkyd resin intermediate coating (30μ) to a dry film thickness of 20μ. After setting for 3 minutes, the formulation of Example 1 was diluted to a viscosity of 25.
The paint was coated with air spray at a temperature of 20°C/20°C (Food Cup #4) to a dry film thickness of 20μ, and after setting for 7 minutes, it was baked at 150°C for 20 minutes. The test plates obtained in Examples 1 to 2 and Comparative Examples 1 to 4 were tested for gloss, smoothness, discoloration, and durability of the coating film, and the results are shown in Table 1.
【表】【table】
【表】
第1表から明白な通り、本発明の方法によれば
優れた塗膜が得られることが判る。
一方、トツプコートの顔料分を少なくした比較
例1から得られた塗膜は、着色顔料が反転現象を
生じ、光沢、肌の平滑性が悪く、また耐久性も悪
かつた。またトツプコート着色顔料を過剰にした
比較例2、比較例3から得られた塗膜は色落ちが
著しかつた。またトツプコートとベースコートの
合成樹脂を変えた比較例4から得られた塗膜は耐
久性が悪かつた。[Table] As is clear from Table 1, it can be seen that excellent coating films can be obtained by the method of the present invention. On the other hand, in the coating film obtained from Comparative Example 1 in which the pigment content of the top coat was reduced, the colored pigments caused a reversal phenomenon, and the gloss and skin smoothness were poor, and the durability was also poor. Furthermore, the coating films obtained in Comparative Examples 2 and 3, in which the top coat coloring pigment was used in excess, showed significant discoloration. Furthermore, the coating film obtained in Comparative Example 4 in which the synthetic resins of the top coat and base coat were changed had poor durability.
Claims (1)
顔料の顔料重量濃度が約10〜30%の着色塗料Aを
塗布し、該着色塗料Aの塗膜が未乾燥状態にある
間に着色透明塗料Bを塗り重ね、形成された両塗
膜を同時に乾燥させる塗膜の形成方法において、 着色塗料Aと着色半透明塗料Bの構成成分であ
る合成樹脂は同一であり、着色半透明塗料Bで使
用する顔料は、顔料重量濃度が約1〜10%の有機
着色顔料を主体とする着色顔料と顔料重量濃度
が約5〜50%の透明顔料とからなり、かつ着色
顔料と透明顔料の合計顔料重量濃度は着色塗
料Aの顔料重量濃度以上であることを特徴とす
る、塗膜の形成方法。 2 上記透明顔料は、一次粒子の平均粒径が
0.05μ以下の硫酸バリウムであることを特徴とす
る特許請求の範囲第1項記載の塗膜の形成方法。[Scope of Claims] 1. A colored paint A having a pigment weight concentration of approximately 10 to 30% of a coloring pigment mainly composed of an organic coloring pigment is applied onto an object to be coated, and the coating film of the colored paint A is not dried. In the method of forming a paint film in which colored transparent paint B is applied over and over again while the paint is still in the state, and both coats are dried at the same time, the synthetic resins that are the constituent components of colored paint A and colored semi-transparent paint B are the same. The pigment used in the colored translucent paint B consists of a colored pigment mainly consisting of an organic coloring pigment with a pigment weight concentration of about 1 to 10%, and a transparent pigment with a pigment weight concentration of about 5 to 50%, and is colored. A method for forming a coating film, characterized in that the total pigment weight concentration of the pigment and the transparent pigment is greater than or equal to the pigment weight concentration of the colored paint A. 2 The above transparent pigment has an average particle size of primary particles.
2. The method for forming a coating film according to claim 1, wherein the coating material is barium sulfate having a particle size of 0.05μ or less.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5651283A JPS59183867A (en) | 1983-03-31 | 1983-03-31 | Formation of coating film |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5651283A JPS59183867A (en) | 1983-03-31 | 1983-03-31 | Formation of coating film |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59183867A JPS59183867A (en) | 1984-10-19 |
JPH0311821B2 true JPH0311821B2 (en) | 1991-02-18 |
Family
ID=13029173
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP5651283A Granted JPS59183867A (en) | 1983-03-31 | 1983-03-31 | Formation of coating film |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59183867A (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5867437B2 (en) * | 2013-03-28 | 2016-02-24 | マツダ株式会社 | Vehicle inner panel coating |
ES2849973T3 (en) * | 2015-07-21 | 2021-08-24 | Basf Coatings Gmbh | Procedure for producing a coating consisting of a filler layer and a cover lacquer layer |
JP6849655B2 (en) | 2015-07-21 | 2021-03-24 | ビーエーエスエフ コーティングス ゲゼルシャフト ミット ベシュレンクテル ハフツングBASF Coatings GmbH | Paint set, how to use paint set, how to use coating system |
-
1983
- 1983-03-31 JP JP5651283A patent/JPS59183867A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59183867A (en) | 1984-10-19 |
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