JPH0346188B2 - - Google Patents
Info
- Publication number
- JPH0346188B2 JPH0346188B2 JP8444587A JP8444587A JPH0346188B2 JP H0346188 B2 JPH0346188 B2 JP H0346188B2 JP 8444587 A JP8444587 A JP 8444587A JP 8444587 A JP8444587 A JP 8444587A JP H0346188 B2 JPH0346188 B2 JP H0346188B2
- Authority
- JP
- Japan
- Prior art keywords
- paint
- coating
- melamine resin
- film thickness
- weight
- 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 44
- 239000003973 paint Substances 0.000 claims description 42
- 239000011248 coating agent Substances 0.000 claims description 41
- 229920000877 Melamine resin Polymers 0.000 claims description 24
- 239000004640 Melamine resin Substances 0.000 claims description 24
- 150000007974 melamines Chemical class 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 16
- 239000000049 pigment Substances 0.000 claims description 13
- 239000002904 solvent Substances 0.000 claims description 12
- 238000009835 boiling Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- 239000012454 non-polar solvent Substances 0.000 claims 1
- 238000007665 sagging Methods 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 239000000428 dust Substances 0.000 description 7
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 6
- UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 description 6
- 229920000180 alkyd Polymers 0.000 description 5
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical group NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 230000037303 wrinkles Effects 0.000 description 4
- 230000007547 defect Effects 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 229920003270 Cymel® Polymers 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 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
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 229920001225 polyester resin Polymers 0.000 description 2
- 239000004645 polyester resin Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 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
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- QHIWVLPBUQWDMQ-UHFFFAOYSA-N butyl prop-2-enoate;methyl 2-methylprop-2-enoate;prop-2-enoic acid Chemical compound OC(=O)C=C.COC(=O)C(C)=C.CCCCOC(=O)C=C QHIWVLPBUQWDMQ-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 230000036632 reaction speed Effects 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000035936 sexual power Effects 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- -1 succinate ester Chemical class 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Paints Or Removers (AREA)
- Application Of Or Painting With Fluid Materials (AREA)
Description
[産業上の利用分野]
本発明は、車輛、化学プラント、建材用に好適
な2コート1ペーク塗装法用の高膜厚型チツピン
グ塗膜の形成方法に関する。
[従来の技術]
従来、樹脂および顔料とからなる高膜厚型塗料
としては、例えば顔料の種類、量、粒径等を特定
した塗料の開示がある(特開昭56−57855号公
報)。また高膜厚型塗料として焼付け工程を50〜
130℃の温度で5〜30分間さらに120〜180℃の温
度で10〜50分間と二段階焼付けする方法の開示が
ある(特開昭56−58564号公報)。他に塗料中にベ
ンゾインを添加した高膜厚塗料の開示がある(特
開昭56−167766号公報)。上記の手段により高膜
厚塗料の塗装により発生するタレ、ワキ(発泡)
性の向上を図つている。
従来この種のタイプの塗料は2コート2ベーク
用であり2コート1ベーク法の様にプレキユアー
(予備焼付)なしに高膜厚塗料の上に中塗り塗料
を塗装した後に焼付けした場合、塗面に細かい凹
凸が発生し塗面の外観を損う。
また2コート1ベーク法で良好な塗面外観を得
る方法は、高膜厚塗料を塗装した後アワ抜けや溶
剤を飛散させるため、塗料後のセツテイング時間
を30分以上設ける必要があり生産性に問題があ
る。また塗装時のアワの巻込み量を押えたり溶剤
を飛散をさせるため、塗装時に被塗物との距離を
50cm以上離して噴霧塗装を行わなければならな
い。さらに加熱残分を高くする方法もあるが塗料
の粘度が高くなり他の塗膜不良のワキ、フクレ、
ダスト性が現れて好ましくない。
[発明が解決しようとする問題点]
上記の高膜厚型塗料と中塗り塗料とを2コート
1ベーク法で塗装した場合、塗膜表面に生じる凹
凸等の外観不良を防止するとともに塗膜のレベリ
ング性を向上させた塗膜とすることを目的とす
る。
[問題点を解決するための手段]
本発明の高膜厚型チツピング塗膜の形成方法
は、硬化剤としてメチル化メラミン樹脂またはメ
チル化メラミン樹脂とブチル化メラミン樹脂の混
合物を含有し、顔料濃度(以下PWCと略す)が
60重量%以上70重量%未満であり、非極性の中沸
点溶剤を含有する高膜厚型塗料を塗布して第1ウ
エツト塗膜を形成する第1工程と、
該第1ウエツト塗膜の上に硬化剤としてブチル
化メラミン樹脂を含有する中塗り塗料を塗布して
第2ウエツト塗膜を形成する第2工程と、
該第1ウエツト塗膜と該第2ウエツト塗膜を一
体的に焼付け硬化させる第3工程と、からなるこ
とを特徴とする。
この高膜厚型チツピグ塗膜の形成方法は、高膜
厚型塗料を塗布する第1工程と、中塗り塗料を塗
布する第2工程とをウエツトオンウエツトで塗布
し、第3工程で焼付けして硬化塗膜とする。
このため高膜厚型塗料の硬化剤は、通常使用さ
れているブチル化メラミン樹脂より硬化反応速度
の速いメチル化メラミン樹脂を主体とする。すな
わち高膜厚塗料のチツプ材中のアワ、溶剤、反応
ガスが抜けた跡が、その塗膜の上面にウエツトオ
ンウエツトで塗布される中塗り塗面に残るのを防
ぐため、硬化反応速度の速いメチル化メラミン樹
脂を配合して中塗り塗膜が硬化しない前に高膜厚
塗膜を硬化させんとするものである。これにより
平滑な耐チツピング塗膜が形成できる。
顔料濃度(PWC)が60重量%未満の場合はワ
キ、タレ性が悪くなりPWCが70重量%を超える
と耐チツピング性および塗面が悪くなるので好ま
しくない。
非極性の中沸点の溶剤は、トリメチルベンゼ
ン、ジメチルエチルベンゼン、テトラメチルベン
ゼン等の単独または混合溶剤で沸点が160〜190℃
のものが使用できる。
高膜厚型塗料による塗装塗膜は膜厚が100〜
300μのものである。
第2工程で塗布される中塗り塗料は、硬化剤が
高膜厚型塗料に用いるメチル化メラミン樹脂より
反応性が遅いブチル化メラミン樹脂を用いたアル
キツド系塗料である。
このアルキツド系塗料は一般自動車中塗り塗料
で硬化剤が上記ブチル化メラミン樹脂であればど
んな塗色でも用いることができる。この中塗り塗
料によつて形成される塗膜は20〜50μの膜厚に形
成する。
高膜厚型塗料は樹脂、顔料、溶剤を主成分と
し、場合によつては必要な消泡剤、沈降防止剤及
びレベリング剤等を前記の成分に添加することが
できる。樹脂成分は周知の塗料用樹脂はいずれも
使用でき特に制限を設けないが好ましくはポリエ
ステル樹脂、オリルフリ−アルキツド樹脂及びウ
レタン樹脂、アクリル樹脂等である。顔料は必要
な体質顔料及び着色顔料を選択して使用し、具体
的には炭酸カルシウム、シリカ、酸化鉄、硫酸バ
リウム、ケイ酸アルミニウム、酸化チタン、酸化
亜鉛などが使用できる。
[発明の効果]
本発明の高膜厚型チツピング塗膜の形成方法で
は、高膜厚型塗料として硬化剤がメチル化メラミ
ン樹脂またはメチル化メラミン樹脂とブチル化メ
ラミン樹脂の混合物でPWCが60〜70重量%未満
で非極性の中沸点溶剤を含有する塗料を塗布し、
中塗り塗料として硬化剤がブチル化メラミン樹脂
であある塗料を2コート1ベーク法で塗装する。
高膜厚型塗料の硬化性が上面にウエツトオンウエ
ツトで塗布される中塗り塗膜よい速いので高膜厚
型塗膜の塗膜面の凹凸など欠陥が補えワキ、タ
レ、ダスト性等のない光沢度、鮮映性に優れた塗
面が形成される。
さらに塗装物のセツテイング時間も2分程度で
生産性が良くなり、塗装距離も30cmで良く既設設
備で使用できる利点を有する。
[実施例]
以下実施例により本発明を説明する。
実施例 1
ポリエステル樹脂(ベツコライトM−6205、大
日本インキ(株)製)85重量部と硬化剤のメチル化メ
ラミン樹脂(サイメル301、三井東圧化学(株)製)
20重量部、顔料のシリカ(トヤネ珪石、丸恵寿(株)
製)100重量部、顔料の酸化チタン(タイペーク、
R−680、石原産業(株)製)10重量部、顔料の炭酸
カルシウム(MC−S、丸尾カルシウム(株)製)
7重量部、添加剤BYK−052(ビツクマリンクロ
ツド社製)、ネーキユアー#3525(キング社製)各
1重量部、溶剤トリメチルベンゼン:ジメチルベ
ンゼン:テトラメチルベンゼン=1:2:7の容
量比品(丸善石油(株)製)45重量部をデイスパーで
15分間混合撹拌しサンドグラインダーで20分分散
し粘度調節後約70mmHgの減圧下で10分間脱泡し
高膜厚型塗料を作製した。この塗料のPWCは65
重量%であつた。
中塗り塗料は硬化剤にブチル化メラミン樹脂を
含有するオイルフリーアルキツド樹脂塗料(関西
ペイント(株)製)を使用した。
塗装方法
垂直に立てた鉄板上に上記の高膜厚型塗料をエ
アレス塗装して略100〜350μmの膜厚とし2分間
セツテイングした後、中塗り塗料をウエツトオン
ウエツトで塗装し略40μmの膜厚の中塗り塗面を
形成し10分間セツテイングした後140℃の温度で
30分焼付を行つた。
塗膜の評価
ワキ膜厚:焼付後の塗面でのワキ(フクレの状態
を含む)のない最大膜厚(単位μ)
タレ膜厚:焼付後の塗面でタレのない最大膜厚
(単位μ)
ダスト性:ダストが飛散した場合そのダストの目
立ちやすさ
光沢度:光沢計による60度の反射光沢(単位%)
鮮映性:鮮映性テスターによるPGD値
上記の5項目について評価した結果を第2表に
示す。ワキ膜厚、タレ膜厚はともに350μ、ダス
トは目立たず、光沢度は96%、鮮映性0.5と優れ
た高膜厚の塗面が得られた。
実施例 2〜5
実施例1と同様の方法により、第1表に示す割
合の配合で高膜厚型塗料を調合した。
[Industrial Application Field] The present invention relates to a method for forming a high-thickness chipping coating film for a two-coat one-paste coating method suitable for vehicles, chemical plants, and building materials. [Prior Art] Conventionally, as a high film thickness type paint made of a resin and a pigment, a paint in which the type, amount, particle size, etc. of the pigment is specified has been disclosed (Japanese Patent Laid-Open No. 57855/1983). In addition, as a high film thickness type paint, the baking process is
There is a method of baking in two stages: 5 to 30 minutes at a temperature of 130°C and a further 10 to 50 minutes at a temperature of 120 to 180°C (Japanese Patent Application Laid-open No. 58564/1983). There is also a disclosure of a paint with a high film thickness in which benzoin is added to the paint (Japanese Unexamined Patent Publication No. 167766/1983). Sagging and flaking (foaming) caused by applying high film thickness paint using the above methods.
We are trying to improve sexual performance. Traditionally, this type of paint was designed for two coats and two bakes, and when baked after applying an intermediate coat on top of a high film thickness paint without pre-curing (pre-baking) as in the two-coat, one-bake method, the painted surface Fine irregularities occur on the surface, damaging the appearance of the painted surface. In addition, the two-coat, one-bake method for obtaining a good painted surface appearance requires a setting time of at least 30 minutes after the paint is applied, which reduces productivity because it removes wrinkles and scatters the solvent after applying the high-film thickness paint. There's a problem. In addition, in order to reduce the amount of foxing that gets caught up during painting and to prevent the solvent from scattering, the distance from the object to be coated must be kept low during painting.
Spray painting must be done from a distance of at least 50 cm. There is also a method of increasing the heating residue, but this increases the viscosity of the paint and causes other paint film defects such as underarms, blistering, etc.
Dustiness appears, which is undesirable. [Problems to be Solved by the Invention] When the above-mentioned high film thickness paint and intermediate coating paint are applied using the two-coat, one-bake method, it is possible to prevent appearance defects such as unevenness on the surface of the paint film and improve the quality of the paint film. The purpose is to create a coating film with improved leveling properties. [Means for Solving the Problems] The method for forming a high-thickness chipping coating film of the present invention contains a methylated melamine resin or a mixture of a methylated melamine resin and a butylated melamine resin as a hardening agent, and the pigment concentration (hereinafter abbreviated as PWC)
A first step of forming a first wet coating film by applying a high film thickness paint containing a non-polar medium boiling point solvent that is 60% by weight or more and less than 70% by weight, and on the first wet coating film. a second step of applying an intermediate coating containing a butylated melamine resin as a hardening agent to form a second wet coating film, and integrally baking and curing the first wet coating film and the second wet coating film. and a third step of causing. The method for forming this high-thickness chippig coating consists of a first step of applying a high-thickness paint, a second step of applying an intermediate coat, wet-on-wet, and a third step of baking. to form a cured coating film. For this reason, the curing agent for high film thickness paints is mainly methylated melamine resin, which has a faster curing reaction rate than the commonly used butylated melamine resin. In other words, in order to prevent traces of bubbles, solvents, and reactive gases in the chip material of high film thickness paint from remaining on the intermediate coat surface that is applied wet-on-wet to the upper surface of the paint film, the curing reaction speed is increased. By blending a methylated melamine resin with a fast rate of oxidation, it is possible to cure a high-thickness coating film before the intermediate coating film has not yet cured. This allows a smooth chipping-resistant coating to be formed. If the pigment concentration (PWC) is less than 60% by weight, wrinkles and sagging properties will deteriorate, and if PWC exceeds 70% by weight, chipping resistance and painted surface will deteriorate, which is not preferable. Non-polar medium-boiling point solvents include trimethylbenzene, dimethylethylbenzene, tetramethylbenzene, etc. alone or in combination, with a boiling point of 160 to 190℃.
can be used. The coating film using high film thickness type paint has a film thickness of 100~
It is 300μ. The intermediate coating applied in the second step is an alkyd-based coating in which the curing agent is a butylated melamine resin, which has a slower reactivity than the methylated melamine resin used in high-film thickness coatings. This alkyd paint is a general automotive interior paint and can be used in any color as long as the curing agent is the above-mentioned butylated melamine resin. The coating film formed by this intermediate coating is formed to a thickness of 20 to 50 μm. The main components of high film thickness type paints are resins, pigments, and solvents, and if necessary, necessary antifoaming agents, antisettling agents, leveling agents, etc. may be added to the above components. As the resin component, any well-known coating resin can be used without any particular limitation, but polyester resins, oryl free-alkyd resins, urethane resins, acrylic resins, etc. are preferred. As the pigment, necessary extender pigments and coloring pigments are selected and used, and specifically, calcium carbonate, silica, iron oxide, barium sulfate, aluminum silicate, titanium oxide, zinc oxide, etc. can be used. [Effects of the Invention] In the method for forming a high-thickness chipping coating of the present invention, the curing agent is a methylated melamine resin or a mixture of a methylated melamine resin and a butylated melamine resin, and the PWC is 60 to 60. Applying a paint containing less than 70% by weight of a non-polar medium-boiling solvent;
A paint whose curing agent is a butylated melamine resin is applied as an intermediate paint by a two-coat, one-bake method.
The curing properties of high-thickness paints are very fast as the intermediate coat is applied wet-on-wet on the top surface, so it can compensate for defects such as unevenness on the surface of high-thickness paints, and eliminate wrinkles, sagging, dust, etc. A painted surface with excellent gloss and image clarity is formed. Furthermore, the setting time for the painted object is about 2 minutes, which improves productivity, and the coating distance is only 30 cm, which has the advantage of being able to be used with existing equipment. [Example] The present invention will be explained below with reference to Examples. Example 1 85 parts by weight of polyester resin (Betsucolite M-6205, manufactured by Dainippon Ink Co., Ltd.) and methylated melamine resin (Cymel 301, manufactured by Mitsui Toatsu Chemical Co., Ltd.) as a curing agent.
20 parts by weight, pigment silica (Toyane silica, Marueju Co., Ltd.)
) 100 parts by weight, pigment titanium oxide (Tipaque,
R-680, manufactured by Ishihara Sangyo Co., Ltd.) 10 parts by weight, pigment calcium carbonate (MC-S, manufactured by Maruo Calcium Co., Ltd.)
7 parts by weight, additive BYK-052 (manufactured by Bikkumarinckrodt), 1 part by weight each of Nakyur #3525 (manufactured by King), solvent volume ratio of trimethylbenzene: dimethylbenzene: tetramethylbenzene = 1:2:7 45 parts by weight of the product (manufactured by Maruzen Sekiyu Co., Ltd.) in a disper.
The mixture was mixed and stirred for 15 minutes, dispersed for 20 minutes using a sand grinder, and after adjusting the viscosity, defoamed for 10 minutes under reduced pressure of about 70 mmHg to produce a high film thickness type paint. The PWC of this paint is 65
It was in weight%. The intermediate paint used was an oil-free alkyd resin paint (manufactured by Kansai Paint Co., Ltd.) containing butylated melamine resin as a hardening agent. Painting method: Airless apply the high film thickness paint above on a vertical iron plate to a film thickness of approximately 100 to 350 μm. After setting for 2 minutes, apply wet-on-wet intermediate coating to create a film of approximately 40 μm. After forming a thick intermediate coat and setting for 10 minutes, apply at a temperature of 140℃.
I baked it for 30 minutes. Evaluation of paint film Flank film thickness: Maximum film thickness without flakes (including blistering) on the painted surface after baking (unit: μ) Sagging film thickness: Maximum film thickness without sagging on the painted surface after baking (unit: μ) Dust property: The conspicuousness of the dust when it is scattered.Glossiness: Reflective gloss at 60 degrees using a gloss meter (unit: %).Visibility: PGD value using a sharpness tester.Results of evaluating the above five items. are shown in Table 2. Both the armpit film thickness and the sagging film thickness were 350μ, dust was inconspicuous, the gloss was 96%, and the image clarity was 0.5, resulting in a high film thickness coating. Examples 2 to 5 High film thickness type paints were prepared in the same manner as in Example 1, with the proportions shown in Table 1.
【表】【table】
【表】
単位:重量部
【table】
Unit: parts by weight
【表】
* ○…ダストは目立たない ×…ダストが目立
つ
ただし実施例3は硬化剤をメチル化ブチル化メ
ラミン樹脂(サイメル1116、三井東圧(株)製)を、
実施例4では溶剤の組成比をトリメチルベンゼ
ン:ジメチルベンゼン:テトラメチルベンゼン=
1:6:3とした他は実施例1と同一物質を使用
した。
実施例1と同様に塗装し評価した結果を第2表
に示す。塗膜面はほぼ実施例1と同じであつた。
比較例
実施例1と同様の方法で塗料を調合し、塗装、
塗膜の評価を行つた。配合割合は第1表に、評価
結果は第2表に示す。
比較例1は高膜厚型塗料の硬化剤に従来のブチ
ル化メラミン樹脂、ユーバン20SF(三井東圧化学
(株)製)を用いた以外は実施例と同一である。実施
例1に比べて比較例1は光沢度が85%と低下して
いる。
比較例2は溶剤を極性溶剤のコハク酸エステル
を主成分とするDBE(デユポン化学(株)製)に代え
た以外は実施例1と同じ組成である。比較例2で
は光沢度が比較例1よりもさらに悪くなつてい
る。比較例3は、配合物質は実施例1と同じであ
るが顔料濃度のPWCが本発明より小さい値の55
重量%であるため塗膜、ワキ膜厚、タレ膜厚が小
さい、即ちワキ、タレがおきやすい。
比較例4は逆にPWC値が本発明より大きい場
合でありワキ、タレは良いがダスト性が悪く光沢
度も低くさらに鮮映性の値も小さい。
従つて高膜厚型チツピング塗料の硬化剤にメチ
ル化メラミン樹脂系を、溶剤に非極性の中沸点
(160〜190℃)のものを用い、PWCが60〜70重量
%の範囲の高膜厚型塗料とブチル化メラミン樹脂
系硬化剤を含むアルキツド系樹脂塗料を中塗り塗
料として2コート1ベーク塗装法で良好な高膜厚
チツピング塗面が得られることが示されている。[Table] *○...Dust is not noticeable ×...Dust is noticeable However, in Example 3, the curing agent was methylated butylated melamine resin (Cymel 1116, manufactured by Mitsui Toatsu Co., Ltd.).
In Example 4, the composition ratio of the solvent was trimethylbenzene:dimethylbenzene:tetramethylbenzene=
The same material as in Example 1 was used except that the ratio was 1:6:3. The results of coating and evaluation in the same manner as in Example 1 are shown in Table 2. The coating surface was almost the same as in Example 1. Comparative Example A paint was prepared in the same manner as in Example 1, and the paint was applied.
The coating film was evaluated. The blending ratios are shown in Table 1, and the evaluation results are shown in Table 2. Comparative Example 1 uses a conventional butylated melamine resin as a hardening agent for a high film thickness type paint.
The procedure was the same as in the example except that the material (manufactured by Co., Ltd.) was used. Compared to Example 1, Comparative Example 1 has a lower gloss level of 85%. Comparative Example 2 has the same composition as Example 1 except that the solvent was replaced with DBE (manufactured by DuPont Chemical Co., Ltd.) whose main component is a polar solvent succinate ester. In Comparative Example 2, the glossiness is even worse than in Comparative Example 1. In Comparative Example 3, the compounded substances were the same as in Example 1, but the pigment concentration PWC was 55, which was a smaller value than that of the present invention.
% by weight, the coating film, armpit film thickness, and sagging film thickness are small, that is, armpit and sagging easily occur. Comparative Example 4, on the other hand, has a PWC value larger than that of the present invention, and has good wrinkles and sagging, but poor dust properties, low gloss, and low image clarity. Therefore, by using a methylated melamine resin curing agent and a non-polar medium boiling point (160 to 190°C) solvent for high film thickness chipping paints, we have developed a high film thickness with a PWC of 60 to 70% by weight. It has been shown that a good chipping coating with a high film thickness can be obtained by a two-coat, one-bake coating method using an alkyd resin coating containing a mold coating and a butylated melamine resin curing agent as an intermediate coating.
Claims (1)
チル化メラミン樹脂とブチル化メラミン樹脂の混
合物を含有し、顔料濃度(以下PWCと略す)が
60重量%以上70重量%未満であり、非極性の中沸
点溶剤を含有する高膜厚型塗料を塗布して第1ウ
エツト塗膜を形成する第1工程と、 該第1ウエツト塗膜の上に硬化剤としてブチル
化メラミン樹脂を含有する中塗り塗料を塗布して
第2ウエツト塗膜を形成する第2工程と、 該第1ウエツト塗膜と第2ウエツト塗膜を一体
的に焼付け硬化させる第3工程と、からなること
を特徴とする高膜厚型チツピング塗膜の形成方
法。 2 非極性の溶剤は沸点が160〜190℃である特許
請求の範囲第1項記載の高膜厚型チツピング塗膜
の形成方法。[Claims] 1 Contains a methylated melamine resin or a mixture of a methylated melamine resin and a butylated melamine resin as a curing agent, and has a pigment concentration (hereinafter abbreviated as PWC).
A first step of forming a first wet coating film by applying a high film thickness paint containing a non-polar medium boiling point solvent that is 60% by weight or more and less than 70% by weight, and on the first wet coating film. a second step of applying an intermediate coating containing a butylated melamine resin as a hardening agent to form a second wet coating; and baking and curing the first wet coating and the second wet coating integrally. A method for forming a high thickness chipping coating film, comprising a third step. 2. The method for forming a high thickness chipping coating according to claim 1, wherein the non-polar solvent has a boiling point of 160 to 190°C.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8444587A JPS63248483A (en) | 1987-04-06 | 1987-04-06 | Thick film type chipping paint composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8444587A JPS63248483A (en) | 1987-04-06 | 1987-04-06 | Thick film type chipping paint composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63248483A JPS63248483A (en) | 1988-10-14 |
JPH0346188B2 true JPH0346188B2 (en) | 1991-07-15 |
Family
ID=13830801
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP8444587A Granted JPS63248483A (en) | 1987-04-06 | 1987-04-06 | Thick film type chipping paint composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63248483A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5150916B2 (en) * | 2006-12-12 | 2013-02-27 | 新日鐵住金株式会社 | Pre-coated metal plate and manufacturing method thereof |
-
1987
- 1987-04-06 JP JP8444587A patent/JPS63248483A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS63248483A (en) | 1988-10-14 |
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