JP2011026543A - Paint composition and method of forming paint film - Google Patents

Paint composition and method of forming paint film Download PDF

Info

Publication number
JP2011026543A
JP2011026543A JP2010065329A JP2010065329A JP2011026543A JP 2011026543 A JP2011026543 A JP 2011026543A JP 2010065329 A JP2010065329 A JP 2010065329A JP 2010065329 A JP2010065329 A JP 2010065329A JP 2011026543 A JP2011026543 A JP 2011026543A
Authority
JP
Japan
Prior art keywords
coating
pigment
paint
brightness
color
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2010065329A
Other languages
Japanese (ja)
Inventor
Tatsuo Kuramochi
竜生 倉持
Masaki Yamada
正樹 山田
Toru Iwamoto
亨 岩本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kansai Paint Co Ltd
Original Assignee
Kansai Paint Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Kansai Paint Co Ltd filed Critical Kansai Paint Co Ltd
Priority to JP2010065329A priority Critical patent/JP2011026543A/en
Publication of JP2011026543A publication Critical patent/JP2011026543A/en
Pending legal-status Critical Current

Links

Landscapes

  • Application Of Or Painting With Fluid Materials (AREA)
  • Paints Or Removers (AREA)

Abstract

<P>PROBLEM TO BE SOLVED: To provide a paint composition capable of forming a paint film showing particle feeling with high brightness and high color saturation at highlight (near the regular reflection) and no particle feeling with low brightness and low color saturation at shade (concave direction), and having a design of smoky texture with smooth brightness variation in between highlight and shade to various industrial products such as an exterior panel of a car body and having a heat shielding property, and a method of forming a paint film. <P>SOLUTION: This paint composition is one containing a coloring pigment reflecting and/or transmitting infrared rays and a scale-like bright pigment and whose paint film obtained by painting has a brightness of not greater than 10 in L*a*b* color system and whose brightness and color saturation varies from highlight to shade, and a method of forming a paint film is disclosed. A paint composition and a method of forming a paint film where the color pigment which reflects and/or transmits the infrared rays is perylene and/or a composite metal oxide are also disclosed. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

本発明は、ハイライト(正反射光近傍)では高明度且つ高彩度で粒子感があり、シェード(スカシ方向)では粒子感がなく彩度と明度が低く、ハイライトとシェードの中間において明度変化が緩やかなスモーキーな質感の意匠及び遮熱性を有する塗膜を形成可能な塗料組成物及び塗膜形成方法に関するものである。 In the present invention, the highlight (near the specular reflection light) has high brightness and high saturation, and there is no grain feeling in the shade (squash direction), and the saturation and lightness are low, and the brightness changes between the highlight and the shade. The present invention relates to a coating composition and a coating film forming method capable of forming a coating film having a mild smoky texture design and heat shielding properties.

自動車等の工業製品には、商品力を高めるために、観察角度によって明度が変化するフリップフロップ感を有するメタリック塗色が適用される場合がある。その中でもハイライトでは明度が高く、シェードで明度が低いメタリック塗色は落ち着きがあり高級感を有する塗色として着目されている。 For industrial products such as automobiles, a metallic paint color having a flip-flop feeling in which the brightness changes depending on the observation angle may be applied in order to increase the product power. Among them, metallic paint colors having high brightness at highlights and low brightness at shades are attracting attention as paint colors having a calm and high-class feeling.

特許文献1は、メタリック塗料着色用カーボンブラック分散体、メタリック塗料組成物および塗膜形成方法に関するものであり、セルロース誘導体及びカーボンブラック顔料を含むカーボンブラック分散体と光輝性顔料を含むメタリック塗料組成物が開示されている。特許文献1に開示されたメタリック塗料組成物を塗装して得られた塗膜は、フリップフロップ感を有するものではあるが、ハイライトからシェードに明度が大きく下がる単調な意匠であることや、塗膜中のカーボンブラックが赤外線を吸収することによって塗装された基材の温度が上昇してしまう等の問題点があった。   Patent Document 1 relates to a carbon black dispersion for coloring a metallic paint, a metallic paint composition, and a coating film forming method, and a metallic paint composition containing a carbon black dispersion containing a cellulose derivative and a carbon black pigment and a bright pigment. Is disclosed. Although the coating film obtained by applying the metallic paint composition disclosed in Patent Document 1 has a flip-flop feeling, it is a monotonous design whose brightness is greatly reduced from highlight to shade, There has been a problem that the temperature of the coated substrate is increased by the carbon black in the film absorbing infrared rays.

特開2002−146243号公報JP 2002-146243 A

本発明の目的は、ハイライト(正反射光近傍)では高明度且つ高彩度で粒子感があり、シェード(スカシ方向)では粒子感がなく彩度と明度が低く、ハイライトとシェードの中間において明度変化が緩やかなスモーキーな質感の意匠及び遮熱性を有する塗膜を形成可能な塗料組成物及び塗膜形成方法を提供することである。 The object of the present invention is that the highlight (in the vicinity of specular reflection light) has high brightness and high saturation and has a grain feeling, and the shade (in the direction of the shadow) has no grain feeling and has low saturation and brightness, and the brightness between the highlight and the shade. It is an object to provide a coating composition and a method of forming a coating film capable of forming a smoky textured design with a gentle change and a coating film having a heat shielding property.

本発明は、
1.赤外線を反射及び/又は透過する着色顔料及び鱗片状光輝性顔料を含む塗料組成物であって、塗装して得られる塗膜のL*a*b*表色系における明度が10以下であって且つハイライトからシェードに明度及び彩度が変化する塗料組成物、
2.赤外線を反射及び/又は透過する着色顔料が、ペリレン及び/又は複合金属酸化物である1項に記載の塗料組成物、
3.鱗片状光輝性顔料が、ガラスフレーク又は酸化アルミニウム表面に金属酸化物を被覆した干渉性光輝性顔料である1項又は2項に記載の塗料組成物、
4.基材に1〜3項のいずれか1項に記載の塗料組成物を塗装して得られた塗膜上に、さらにトップクリヤー塗料を塗装する塗膜形成方法
に関する。
The present invention
1. A coating composition containing a colored pigment that reflects and / or transmits infrared rays and a scaly glittering pigment, and a coating film obtained by coating has a brightness in an L * a * b * color system of 10 or less And a paint composition whose brightness and saturation change from highlight to shade,
2. The coating composition according to 1, wherein the color pigment that reflects and / or transmits infrared rays is perylene and / or a composite metal oxide,
3. 3. The coating composition according to item 1 or 2, wherein the scaly glitter pigment is an interference glitter pigment in which a metal oxide is coated on the surface of glass flakes or aluminum oxide.
4). It is related with the coating-film formation method which coats a top clear coating material further on the coating film obtained by apply | coating the coating composition of any one of 1-3 to a base material.

本発明の塗料組成物は、ハイライト(正反射光近傍)では高明度且つ高彩度で粒子感があり、シェード(スカシ方向)では粒子感がなく彩度と明度が低く、ハイライトとシェードの中間において明度変化が緩やかなスモーキーな質感の意匠及び遮熱性を有する塗膜を形成可能なものであって、特に自動車外板、家電製品等の高級外観を求められている分野に有用なものである。 The coating composition of the present invention has high brightness and high saturation in the highlight (near the specular reflection light) and has a particle feeling, and there is no particle feeling in the shade (squash direction), and the saturation and brightness are low. Can be used to form a smoky textured design with a moderate change in brightness and a heat-shielding coating film, and is particularly useful in fields requiring a high-grade appearance such as automobile outer panels and home appliances. .

本発明の塗料組成物は、赤外線を反射及び/又は透過する着色顔料を含む。本明細書において、赤外線を反射及び/又は透過する着色顔料とは、波長780nm〜2500nmの領域において、JIS K5101 4隠ぺい率試験紙法に記載された隠ぺい率試験紙に該着色顔料のみを着色材として含む塗料を塗装して得られた塗膜の白素地上のJIS K5602に定義された日射反射率が50%以上又は黒素地上の日射反射率が10%以上の顔料を意味する。 The coating composition of the present invention includes a color pigment that reflects and / or transmits infrared rays. In the present specification, a colored pigment that reflects and / or transmits infrared rays is a colorant in which only the colored pigment is applied to a cover rate test paper described in JIS K51014 Coverage Rate Test Paper Method in a wavelength range of 780 nm to 2500 nm. Means a pigment having a solar reflectance of 50% or more defined on JIS K5602 on a white substrate or a solar reflectance of 10% or more on a black substrate.

本明細書における具体的な試験方法を以下に説明する。水酸基含有アクリル樹脂(水酸基価100、数平均分子量20000)及びメラミン樹脂からなる樹脂成分100固形分質量部あたり、該着色顔料を15質量部配合して攪拌混合し、適当な溶媒を用いて希釈して固形分約25%の有機溶剤型塗料を調製する。隠ぺい率試験紙を平らなガラス板の上に水平に固定し、その上にドクターブレードを使用して、硬化塗膜厚が30μmとなるように塗装し、室温約20℃の実験室に15分間放置し、その後に熱風乾燥機を使用して140℃で30分間加熱して硬化せしめた塗膜の白素地部分及び黒素地部分の日射反射率を、積分球ISR−3100を搭載した分光光度計UV−3100PC(共に島津製作所社製)を使用して入射角度を8°としたときの日射反射率として定義するものとする。   Specific test methods in this specification will be described below. 15 parts by mass of the colored pigment is mixed per 100 parts by mass of a resin component comprising a hydroxyl group-containing acrylic resin (hydroxyl value 100, number average molecular weight 20000) and melamine resin, and the mixture is stirred and mixed, and diluted with an appropriate solvent. An organic solvent-type paint having a solid content of about 25% is prepared. Cover the opacity test paper horizontally on a flat glass plate, apply it on it using a doctor blade so that the cured coating thickness is 30 μm, and place it in a laboratory at room temperature of about 20 ° C. for 15 minutes. A spectrophotometer equipped with an integrating sphere ISR-3100 is used to measure the solar reflectance of the white base and black base portions of the coating film which has been allowed to stand and then heated and cured at 140 ° C. for 30 minutes using a hot air dryer. It is defined as the solar reflectance when UV-3100PC (both manufactured by Shimadzu Corporation) is used and the incident angle is 8 °.

赤外線を反射及び/又は透過する着色顔料としては具体的には、アゾ系顔料、アニリンブラック、ペリレンブラック等の有機顔料や複合酸化物顔料等を挙げることができる。   Specific examples of the colored pigment that reflects and / or transmits infrared rays include azo pigments, organic pigments such as aniline black and perylene black, composite oxide pigments, and the like.

ペリレン系の顔料としては、特開2003−41144号公報及び特関2003−41145号公報に開示のペリレンテトラカルボン酸の酸無水物、特開2006−328238号に開示の2−メチル−2,4−ペンタンジオール及び硝酸を加熱反応して得られる黒色顔料、ペリレンテトラカルボン酸のジイミド誘導体、ペリレンジイミノジカルボン酸のジイミド誘導体を焼成処理して得られた黒色ペリレン系顔料や、特開2007−522297号公報に開示の式1a又は1bで表される異性体の1種又は2つの異性体の混合物を含有する黒色顔料を使用することができる。   Examples of perylene pigments include perylene tetracarboxylic acid anhydrides disclosed in JP-A Nos. 2003-411144 and 2003-411145, and 2-methyl-2,4 disclosed in JP-A-2006-328238. A black pigment obtained by heating reaction of pentanediol and nitric acid, a diimide derivative of perylenetetracarboxylic acid, a black perylene pigment obtained by baking a diimide derivative of perylene diiminodicarboxylic acid, and JP2007-522297 Black pigments containing one or a mixture of two isomers of the isomers represented by formula 1a or 1b disclosed in US Pat.

Figure 2011026543
Figure 2011026543

(式中、R1、R2は互いに独立にフェニレン、ナフチレンまたはピリジレンであり、これらはそれぞれC1〜C12−アルキル、C1〜C6−アルコキシ、ヒドロキシル、ニトロおよび/またはハロゲンにより一置換または多置換されていてもよく、Xはハロゲンであり、nは0〜4である)。 Wherein R 1 and R 2 are independently of each other phenylene, naphthylene or pyridylene, which are mono- or polysubstituted by C 1 -C 12 -alkyl, C 1 -C 6 -alkoxy, hydroxyl, nitro and / or halogen, respectively. X is halogen and n is 0-4).

無機顔料としては、Cu−Fe−Mn系、Cu−Cr系、Cu−Cr―Mn系、Cu−Cr―Mn―Ni系、Cu−Cr―Fe系、Co―Cr―Fe系、Mn−Bi系、Mn−Y系、等の複合酸化物顔料を挙げることができる。   Inorganic pigments include Cu-Fe-Mn, Cu-Cr, Cu-Cr-Mn, Cu-Cr-Mn-Ni, Cu-Cr-Fe, Co-Cr-Fe, and Mn-Bi. And composite oxide pigments such as Mn-Y and Mn-Y.

本発明において、赤外線を反射及び/又は透過する着色顔料は、塗装して得られる塗膜の色調によって、上記から1種類又は複数を選択して使用することができる。   In the present invention, the color pigment that reflects and / or transmits infrared rays can be used by selecting one or more kinds from the above depending on the color tone of the coating film obtained by coating.

本発明の塗料組成物における赤外線を反射及び/又は透過する着色顔料の量は、塗装して得られる塗膜の色調や、仕上がり性の点から、塗料組成物中の樹脂固形分100質量部に対して、合計で1〜20質量部の範囲内が好ましく、より好ましくは2〜18質量部の範囲内、特に好ましくは3〜15質量部の範囲内である。   The amount of the color pigment that reflects and / or transmits infrared rays in the coating composition of the present invention is 100 parts by mass of the resin solid content in the coating composition from the viewpoint of the color tone and finish of the coating film obtained by coating. On the other hand, the total is preferably in the range of 1 to 20 parts by mass, more preferably in the range of 2 to 18 parts by mass, and particularly preferably in the range of 3 to 15 parts by mass.

本発明の塗料組成物は鱗片状光輝性顔料を含む。   The coating composition of the present invention contains a scaly glittering pigment.

鱗片状光輝性顔料とは、マイカ、人工マイカ、ガラス、酸化鉄、酸化アルミニウムや各種金属等鱗片状基材の表面に、二酸化チタンや酸化鉄等の基材と屈折率が異なる金属酸化物を被覆された光干渉性顔料や、アルミニウム、銅、ニッケル合金、ステンレス等の鱗片状金属顔料を意味する。   The scaly glitter pigment is a surface of a scaly substrate such as mica, artificial mica, glass, iron oxide, aluminum oxide or various metals, and a metal oxide having a refractive index different from that of the substrate such as titanium dioxide or iron oxide. It means a coated optical interference pigment or a scale-like metal pigment such as aluminum, copper, nickel alloy, stainless steel.

本発明においては、塗装して得られる塗膜のハイライトにおける明度や粒子感の点から、鱗片状光輝性顔料として前記光干渉性顔料を用いることが好ましい。特に干渉色が鮮やかに発色し、粒子感に優れる光干渉性顔料であるガラスフレーク又は酸化アルミニウムを金属酸化物で被覆した光干渉性顔料を用いることが特に好ましい。   In the present invention, it is preferable to use the light-interfering pigment as the scaly glittering pigment from the viewpoint of brightness and particle feeling in the highlight of the coating film obtained by coating. In particular, it is particularly preferable to use a light interference pigment obtained by coating a glass flake or aluminum oxide with a metal oxide, which is a light interference pigment having a bright interference color and excellent particle feeling.

光干渉性顔料を用いる場合、塗装して得られる塗膜の観察角度による彩度変化を顕著なものとし、スモーキーな意匠を発現させる点から、ハイライトにおける干渉色のL*C*h表色系における色相角度hが、60°〜270°範囲内のものを使用することが好ましく、より好ましくは90°〜180°の範囲内である。L*C*h表色系とは、1976年に国際照明委員会で規定され、JIS Z 8729にも採用されているL*a*b*表色系をベースに考案された表色系であって、hは色相角度を表わし、色度図において赤方向の軸を0°として、反時計方向に移動した角度である。   When light interference pigment is used, L * C * h color of the interference color in highlights from the point that the change in saturation depending on the observation angle of the coating film obtained by painting is remarkable and a smoky design is expressed. The hue angle h in the system is preferably in the range of 60 ° to 270 °, more preferably in the range of 90 ° to 180 °. The L * C * h color system is a color system designed based on the L * a * b * color system specified by the International Commission on Illumination in 1976 and adopted in JIS Z 8729. H represents a hue angle, and is an angle moved counterclockwise with the red axis as 0 ° in the chromaticity diagram.

光干渉性顔料のハイライトにおける干渉色の色相角度とは具体的には、塗料組成物中に、光干渉性顔料のみを着色材として含む塗料を塗装して得られた塗膜に45°の角度から光を照射して、正反射光に対して15°の方向において測色して得られた分光反射率に基づいて計算した数値を意味する。   Specifically, the hue angle of the interference color in the highlight of the light interference pigment is 45 ° on the coating film obtained by applying a paint containing only the light interference pigment as a colorant in the coating composition. It means a numerical value calculated based on the spectral reflectance obtained by irradiating light from an angle and measuring the color in the direction of 15 ° with respect to the regular reflection light.

本明細書において、光干渉性顔料のハイライトにおける干渉色とは、水酸基含有アクリル樹脂(水酸基価100、数平均分子量20000)及びメラミン樹脂からなる樹脂成分100固形分質量部あたり、光干渉性顔料を15質量部配合して攪拌混合し、溶媒を添加して塗装に適正な粘度に希釈して得られた固形分約25%の有機溶剤型塗料を、予め黒色(N−2)の塗膜を形成した塗板上に硬化塗膜として18μmの膜厚となるようにエアスプレー塗装し、室温にて15分間放置し、ついで、未硬化塗面にクリヤー塗料(ル−ガベ−ククリヤ−、関西ペイント製、商品名、アクリル樹脂・アミノ樹脂系、有機溶剤型)を硬化塗膜として、35μmとなるようにエアスプレー塗装し、さらに室温にて15分間放置し、その後に熱風乾燥機を使用して140℃で30分加熱して硬化乾燥せしめて得られた塗膜をX−Rite社製のMA−68II(商品名、多角度分光光度計)を使用して、正反射光に対して15°で受光した分光反射率に基づいて測定した測色値で定義するものとする。   In this specification, the interference color in the highlight of a light interference pigment is a light interference pigment per 100 parts by mass of a resin component consisting of a hydroxyl group-containing acrylic resin (hydroxyl value 100, number average molecular weight 20000) and a melamine resin. An organic solvent-type paint having a solid content of about 25% obtained by adding a solvent and diluting to an appropriate viscosity for coating is added in advance to a black (N-2) coating film. The sprayed coating is coated with air spray to a film thickness of 18 μm as a cured coating film, left at room temperature for 15 minutes, and then the clear coating (Lugabe Kuku Clear, Kansai Paint) is applied to the uncured coating surface. (Product name, Acrylic resin / Amino resin type, Organic solvent type) is used as a cured coating film, air-sprayed to a thickness of 35 μm, and allowed to stand at room temperature for 15 minutes, after which a hot air dryer is used. Then, the coating film obtained by heating at 140 ° C. for 30 minutes and curing and drying was applied to specularly reflected light using MA-68II (trade name, multi-angle spectrophotometer) manufactured by X-Rite. The colorimetric value measured based on the spectral reflectance received at 15 ° is defined.

本発明の塗料組成物において、鱗片状光輝性顔料の大きさは、平均粒径が5〜25μmの範囲内のものを使用することが、塗装された塗膜の仕上がり性やハイライトにおける粒子感の点から好ましく、より好ましくは粒径が7〜20μmの範囲内もの、特に好ましくは8〜18μmの範囲内ものである。厚さは0.05〜0.5μmの範囲内のものを使用することが好ましい。ここでいう粒径及び厚さは、光学顕微鏡又は電子顕微鏡で該鱗片状光輝性顔料を観察して得られた数値を意味する。   In the coating composition of the present invention, the scale-like glitter pigment has an average particle size in the range of 5 to 25 μm. In view of the above, it is preferable that the particle diameter is in the range of 7 to 20 μm, particularly preferably in the range of 8 to 18 μm. It is preferable to use a thickness in the range of 0.05 to 0.5 μm. The particle diameter and thickness here mean numerical values obtained by observing the scaly glittering pigment with an optical microscope or an electron microscope.

本発明における鱗片状光輝性顔料の塗料組成物中への含有量は、塗装して得られる塗膜のハイライトにおける粒子感から、塗料組成物中の樹脂固形分100質量部に対して、合計で1〜20質量部の範囲内が好ましく、より好ましくは2〜18質量部の範囲内、特に好ましくは3〜15質量部の範囲内である。   The content of the scaly glittering pigment in the coating composition of the present invention is the sum of the particle feeling in the highlight of the coating film obtained by coating, with respect to 100 parts by mass of the resin solid content in the coating composition. Is preferably in the range of 1 to 20 parts by mass, more preferably in the range of 2 to 18 parts by mass, and particularly preferably in the range of 3 to 15 parts by mass.

本発明の塗料組成物は、さらに赤外線を反射及び/又は透過する着色顔料以外の着色顔料を配合せしめることができる。特に鱗片状光輝性顔料として光干渉性顔料を用いる場合、光干渉性顔料のハイライトにおける干渉色と同系色の着色顔料を配合せしめることができる。この組み合わせによって、塗装して形成された塗膜のハイライトの彩度を高くすることができ、さらに干渉色を際立たせる効果を奏する。   The coating composition of the present invention may further contain a color pigment other than a color pigment that reflects and / or transmits infrared rays. In particular, when a light interference pigment is used as the scaly glitter pigment, a color pigment having the same color as the interference color in the highlight of the light interference pigment can be blended. By this combination, it is possible to increase the saturation of the highlight of the coating film formed by painting, and to produce an effect of making the interference color stand out.

本発明における着色顔料は、特に制限されるものではないが、具体的には、透明性酸化鉄顔料、チタンイエロー等の複合酸化金属顔料、アゾ系顔料、キナクリドン系顔料、ジケトピロロピロール系顔料、ペリレン系顔料、ペリノン系顔料、ベンズイミダゾロン系顔料、イソインドリン系顔料、イソインドリノン系顔料、金属キレートアゾ系顔料、フタロシアニン系顔料、インダンスロン系顔料、ジオキサン系顔料、スレン系顔料、インジゴ系顔料等の中から任意のものを1種もしくはそれ以上を組み合わせて使用することができる。   The color pigment in the present invention is not particularly limited, but specifically, a transparent iron oxide pigment, a composite metal oxide pigment such as titanium yellow, an azo pigment, a quinacridone pigment, a diketopyrrolopyrrole pigment. Perylene pigment, perinone pigment, benzimidazolone pigment, isoindoline pigment, isoindolinone pigment, metal chelate azo pigment, phthalocyanine pigment, indanthrone pigment, dioxane pigment, selenium pigment, indigo Arbitrary pigments and the like can be used alone or in combination.

本発明においては特に、上記着色顔料の中から、透明性着色顔料を用いることが、塗装して得られる塗膜の深み感や透明感の点から好ましい。透明性着色顔料とは具体的には、塗料中の樹脂固形分100質量部に基づいて顔料量が20質量部となるように配合して塗料化し、硬化塗膜厚が30μmとなるように平滑なPTFE板に塗装し、硬化、剥離した塗膜を分光光度計MPS−2450(商品名、島津製作所製)にて測定した可視光領域(波長400nm〜700nm)における光線透過率が90%以上となるような顔料を意味し、平均一次粒子径が100nm以下である顔料を意味する。   In the present invention, it is particularly preferable to use a transparent color pigment among the above-mentioned color pigments from the viewpoint of the depth and transparency of the coating film obtained by coating. Specifically, the transparent coloring pigment is blended so that the pigment amount is 20 parts by mass based on 100 parts by mass of the resin solid content in the paint, and the paint is smoothed so that the cured coating thickness is 30 μm. The coated film that was coated on a hard PTFE plate, cured, and peeled was measured with a spectrophotometer MPS-2450 (trade name, manufactured by Shimadzu Corporation), and the light transmittance in the visible light region (wavelength 400 nm to 700 nm) was 90% or more. The average primary particle diameter is 100 nm or less.

本発明において、上記着色顔料の塗料組成物中への含有量は、塗装して得られる塗膜のハイライトの彩度を高める効果や仕上がり性の点から、塗料組成物中の樹脂固形分100質量部に対し0.01〜20質量部の範囲内であることが好ましく、より好ましくは0.1〜10質量部の範囲内、特に好ましくは、0.5〜3質量部の範囲内である。   In the present invention, the content of the color pigment in the coating composition is such that the resin solid content in the coating composition is 100 in terms of the effect of increasing the highlight saturation of the coating film obtained by coating and the finish. It is preferably within a range of 0.01 to 20 parts by mass, more preferably within a range of 0.1 to 10 parts by mass, and particularly preferably within a range of 0.5 to 3 parts by mass with respect to parts by mass. .

本発明の塗料組成物には、通常、ビヒクルとして、樹脂成分を含有することができる。樹脂成分としては、具体的には、水酸基などの架橋性官能基を有する、アクリル樹脂、ポリエステル樹脂、アルキド樹脂、ウレタン樹脂などの基体樹脂と、必要に応じてメラミン樹脂、尿素樹脂、ポリイソシアネ−ト化合物(ブロック体も含む)などの架橋剤とを併用したものが挙げられ、これらは有機溶剤及び/又は水などの溶媒に溶解または分散して使用される。   The coating composition of the present invention can usually contain a resin component as a vehicle. Specifically, the resin component includes a base resin such as an acrylic resin, a polyester resin, an alkyd resin, or a urethane resin having a crosslinkable functional group such as a hydroxyl group, and a melamine resin, a urea resin, or a polyisocyanate as necessary. A combination of a crosslinking agent such as a compound (including a block body) is used, and these are used by being dissolved or dispersed in a solvent such as an organic solvent and / or water.

さらに、本発明の塗料組成物には、必要に応じて、水あるいは有機溶剤等の溶媒、顔料分散剤、沈降防止剤、硬化触媒、消泡剤、酸化防止剤、紫外線吸収剤等の各種添加剤、体質顔料などを適宜配合することができる。   Furthermore, various additives such as a solvent such as water or an organic solvent, a pigment dispersant, an antisettling agent, a curing catalyst, an antifoaming agent, an antioxidant, and an ultraviolet absorber are added to the coating composition of the present invention as necessary. An agent, extender, etc. can be appropriately blended.

本発明の塗料組成物は、前述の成分を混合分散せしめることによって調製される。塗装時の固形分含有率を、塗料組成物に基づいて、12〜50質量%、好ましくは15〜30質量%に、また、20℃における粘度を15〜20秒/フォ−ドカップ#3に調整しておくことが好ましい。   The coating composition of the present invention is prepared by mixing and dispersing the aforementioned components. The solid content at the time of painting is adjusted to 12 to 50% by mass, preferably 15 to 30% by mass based on the coating composition, and the viscosity at 20 ° C. is adjusted to 15 to 20 seconds / ford cup # 3. It is preferable to keep it.

本発明の塗料組成物は、静電塗装、エア−スプレ−、エアレススプレ−などの方法で塗装することができ、その膜厚は硬化塗膜に基づいて10〜45μmの範囲内とするのが、塗膜の平滑性の点から好ましい。本発明の塗料組成物の塗膜は通常、約70〜約150℃の温度で架橋硬化させることができる。   The coating composition of the present invention can be applied by a method such as electrostatic coating, air spray, airless spray, etc., and its film thickness should be in the range of 10 to 45 μm based on the cured coating film. From the viewpoint of the smoothness of the coating film. The coating film of the coating composition of the present invention can usually be crosslinked and cured at a temperature of about 70 to about 150 ° C.

本明細書の塗料組成物は、塗装して得られる塗膜のL*a*b*表色系における明度L*が10以下である。本明細書において塗料組成物を塗装して得られる塗膜の明度とは、予めグレー色(N−6)の塗膜を形成した塗板上に、該塗料組成物を塗装に適正な粘度に希釈して、硬化塗膜として18μmの膜厚となるようにエアスプレー塗装し、室温にて15分間放置し、ついで、未硬化塗面にクリヤー塗料(ル−ガベ−ククリヤ−、関西ペイント製、商品名、アクリル樹脂・アミノ樹脂系、有機溶剤型)を硬化塗膜として、35μmとなるようにエアスプレー塗装し、さらに室温にて15分間放置し、その後に熱風乾燥機を使用して140℃で30分加熱して硬化乾燥せしめて得られた塗膜をX−Rite社製のMA−68II(商品名、多角度分光光度計)を使用して、正反射光に対して45°で受光した分光反射率に基づいて計算した数値で定義するものとする。   In the coating composition of the present specification, the lightness L * in the L * a * b * color system of the coating film obtained by painting is 10 or less. In the present specification, the lightness of the coating film obtained by applying the coating composition refers to diluting the coating composition to a viscosity suitable for coating on a coating plate on which a gray (N-6) coating film has been formed in advance. Then, it was air spray coated to a film thickness of 18 μm as a cured coating film, left at room temperature for 15 minutes, and then a clear paint (Lugabe Kukuriya, manufactured by Kansai Paint, product) Name, acrylic resin / amino resin type, organic solvent type) as a cured coating film, air sprayed to 35 μm, left at room temperature for 15 minutes, and then at 140 ° C. using a hot air dryer The coating film obtained by heating and drying for 30 minutes was received at 45 ° with respect to specular reflection light using MA-68II (trade name, multi-angle spectrophotometer) manufactured by X-Rite. Defined with numerical values calculated based on spectral reflectance And things.

本発明の塗膜形成方法は、基材上に上記塗料組成物を塗装し、硬化乾燥せしめる方法に関するものである。   The coating film forming method of the present invention relates to a method of coating the coating composition on a substrate and curing and drying the coating composition.

本発明の塗膜形成方法において、基材としては、鉄、亜鉛、アルミニウム等の金属やこれらを含む合金、及びこれらの金属によるメッキまたは蒸着が施された成型物、コンクリートやスレート等の建材ならびに、ガラス、プラスチックや発泡体などによる成型物等を挙げることができる。これら素材に応じて適宜、脱脂処理や表面処理して基材とすることができる。さらに、上記基材に下塗り塗膜や中塗り塗膜を形成させて基材とすることもでき、これらのものが特に好ましい。   In the coating film forming method of the present invention, the base material is a metal such as iron, zinc or aluminum, an alloy containing these, a molded product plated or vapor-deposited with these metals, a building material such as concrete or slate, and And a molded product made of glass, plastic, foam or the like. Depending on these materials, it can be appropriately degreased or surface treated to form a substrate. Furthermore, an undercoat film or an intermediate coat film can be formed on the substrate to form a substrate, and these are particularly preferable.

上記下塗り塗膜とは、素材表面を隠蔽したり、素材に防食性及び防錆性などを付与するために形成されるものであり、下塗り塗料を塗装し、乾燥、硬化することによって得ることができる。この下塗り塗料種としては特に限定されるものではなく、例えば、電着塗料、溶剤型プライマー等を挙げることができる。   The undercoat film is formed to conceal the surface of the material or impart anticorrosion and rustproofness to the material, and can be obtained by applying an undercoat paint, drying and curing. it can. The type of the undercoat paint is not particularly limited, and examples thereof include an electrodeposition paint and a solvent-type primer.

また、上記中塗り塗膜とは、下塗り塗膜を隠蔽したり、付着性や耐チッピング性などを付与するために形成されるものであり、乾燥硬化した下塗り塗膜又は未硬化の下塗り塗膜上に、中塗り塗料を塗装し、乾燥、硬化することによって得ることができる。中塗り塗料種は、特に限定されるものではなく、既知のものを使用でき、例えば、熱硬化性樹脂組成物及び着色顔料を必須成分とする有機溶剤系又は水系の中塗り塗料を好ましく使用できる。   The intermediate coating film is formed to conceal the undercoat film or impart adhesion, chipping resistance, etc., and is a dry-cured undercoat film or an uncured undercoat film. It can be obtained by applying an intermediate coating on top, drying and curing. The type of intermediate coating is not particularly limited, and known ones can be used. For example, an organic solvent-based or water-based intermediate coating containing a thermosetting resin composition and a color pigment as essential components can be preferably used. .

本発明の塗膜形成方法においては、適用される鋼板等の日射による温度上昇を低減する点から反射率が高い中塗り塗膜を形成可能な中塗塗料を適用することが好ましい。具体的には、明度が高い塗膜を形成可能なものであり、カーボンブラック顔料の含有率が塗料中の樹脂固形分100質量部に対して0.5質量部以下の塗料が好ましい。また中塗塗料に白色酸化チタン顔料以外の着色顔料を配合する場合には、赤外線を反射及び/又は透過する着色顔料を用いることが好ましい。   In the method for forming a coating film of the present invention, it is preferable to apply an intermediate coating material capable of forming an intermediate coating film having a high reflectivity from the viewpoint of reducing temperature rise due to solar radiation of the applied steel sheet or the like. Specifically, it is possible to form a coating film with high brightness, and a coating material having a carbon black pigment content of 0.5 parts by mass or less with respect to 100 parts by mass of resin solid content in the coating is preferable. Moreover, when mix | blending coloring pigments other than a white titanium oxide pigment with an intermediate coating, it is preferable to use the coloring pigment which reflects and / or permeate | transmits infrared rays.

また、基材として、下塗り塗膜あるいは中塗り塗膜を形成させる場合においては、下塗り塗膜あるいは中塗り塗膜を加熱し、架橋硬化後に本発明の塗料組成物を塗装することができる。あるいは、下塗り塗膜及び/又は中塗り塗膜が未硬化の状態で、塗装することもできる。   In the case where an undercoat film or an intermediate coat film is formed as a substrate, the undercoat film or the intermediate coat film can be heated, and the coating composition of the present invention can be applied after crosslinking and curing. Alternatively, the undercoating film and / or the intermediate coating film can be applied in an uncured state.

本発明の塗膜形成方法においては、基材上に上記塗料組成物を塗装して得られた塗膜上にさらにトップクリヤー塗料を1層もしくは2層以上塗装して、トップクリヤー塗膜を形成させる。   In the coating film forming method of the present invention, a top clear coating film is formed by further coating one or more top clear coatings on the coating film obtained by coating the above coating composition on a substrate. Let

本発明の塗膜形成方法におけるトップクリヤー塗料は、樹脂成分および溶剤を主成分とし、さらに必要に応じてその他の塗料用添加剤などを配合してなる無色もしくは有色の透明塗膜を形成する液状塗料である。   The top clear coating in the method for forming a coating film of the present invention is a liquid that forms a colorless or colored transparent coating film comprising a resin component and a solvent as main components, and further blending with other coating additives as required. It is a paint.

本発明方法におけるトップクリヤー塗料としては、従来公知のものを制限なく使用することができる。例えば、基体樹脂及び架橋剤を含有する液状もしくは粉体状の塗料組成物が適用できる。基体樹脂の例としては、水酸基、カルボキシル基、シラノ−ル基、エポキシ基などの架橋性官能基を含有する、アクリル樹脂、ポリエステル樹脂、アルキド樹脂、フッ素樹脂、ウレタン樹脂、シリコン含有樹脂などが挙げられる。架橋剤としては、前記基体樹脂の官能基と反応しうるメラミン樹脂、尿素樹脂、ポリイソシアネ−ト化合物、ブロックポリイソシアネ−ト化合物、エポキシ化合物又は樹脂、カルボキシル基含有化合物又は樹脂、酸無水物、アルコキシシラン基含有化合物又は樹脂等が挙げられる。また、必要に応じて、水や有機溶剤等の溶媒、硬化触媒、消泡剤、紫外線吸収剤、レオロジーコントロール剤、酸化防止剤、表面調整剤等の添加剤を適宜配合することができる。   As the top clear paint in the method of the present invention, a conventionally known one can be used without limitation. For example, a liquid or powdery coating composition containing a base resin and a crosslinking agent can be applied. Examples of the base resin include acrylic resin, polyester resin, alkyd resin, fluororesin, urethane resin, and silicon-containing resin containing a crosslinkable functional group such as a hydroxyl group, a carboxyl group, a silanol group, and an epoxy group. It is done. As a crosslinking agent, a melamine resin capable of reacting with the functional group of the base resin, urea resin, polyisocyanate compound, block polyisocyanate compound, epoxy compound or resin, carboxyl group-containing compound or resin, acid anhydride, Examples thereof include alkoxysilane group-containing compounds or resins. Further, if necessary, additives such as a solvent such as water and an organic solvent, a curing catalyst, an antifoaming agent, an ultraviolet absorber, a rheology control agent, an antioxidant, and a surface conditioner can be appropriately blended.

上記トップクリヤー塗料には、透明性を損なわない範囲内において、着色顔料や染料を適時配合することができる。着色顔料や染料としては、インク用、塗料用として従来公知の顔料や染料を1種あるいは2種以上を組み合わせて配合することができる。その添加量は、適宜決定されて良いが、クリヤー塗膜中の樹脂固形分100質量部に対して、30質量部以下、好ましくは0.1〜10質量部である。   In the top clear coating, a color pigment or a dye can be blended in a timely manner within a range not impairing transparency. As the color pigments and dyes, conventionally known pigments and dyes for inks and paints can be used alone or in combination of two or more. The amount of addition may be determined as appropriate, but is 30 parts by mass or less, preferably 0.1 to 10 parts by mass with respect to 100 parts by mass of the resin solid content in the clear coating film.

上記トップクリヤー塗料は、静電塗装、エア−スプレ−、エアレススプレ−などの方法で塗装することができ、その膜厚は硬化塗膜に基づいて5〜40μmの範囲内とするのが好ましい。トップクリヤー塗料の塗膜それ自体は約70〜150℃の温度で架橋硬化させることができる。   The top clear coating can be applied by methods such as electrostatic coating, air spray, airless spray, etc., and the film thickness is preferably in the range of 5 to 40 μm based on the cured coating film. The top clear coating itself can be crosslinked and cured at a temperature of about 70-150 ° C.

本発明の塗膜形成方法においては、本発明の塗料組成物を塗装後、加熱し、乾燥硬化後に、その塗膜上にトップクリヤー塗料を塗装して加熱し、乾燥硬化させるいわゆる2C2B工程であっても良いが、該塗料組成物を塗装後にその未硬化の状態でトップクリヤー塗料を塗装して、その後に加熱し、これらを同時に硬化せしめるいわゆる2C1B工程で、複層塗膜を得ることもできる。   The coating film forming method of the present invention is a so-called 2C2B process in which the coating composition of the present invention is applied, heated, dried and cured, and then the top clear coating is applied on the coated film, heated, and dried and cured. However, a multi-layer coating film can also be obtained by the so-called 2C1B process in which the top clear paint is applied in an uncured state after the coating composition is applied, and then heated to cure them simultaneously. .

以下、実施例及び比較例を挙げて本発明をさらに具体的に説明する。ただし、本発明はこれらの実施例のみに限定されるものではない。なお、「部」及び「%」はいずれも質量基準によるものである。
次に、実施例を挙げて、本発明をより具体的に説明する。
(製造例1)水酸基含有アクリル樹脂の製造
温度計、サーモスタット、撹拌器、還流冷却器及び滴下装置を備えた反応容器にエチレングリコールモノエチルエーテルアセテート50部を仕込み、撹拌混合し、135℃に昇温した。次いで下記のモノマー/重合開始剤の混合物を3時間かけて、同温度に保持した反応容器内に滴下し、滴下終了後1時間熟成を行なった。その後、エチレングリコールモノエチルエーテルアセテート10部、2,2‘−アゾビス(2−メチルプロピオニトリル)0.6部からなる混合物を同温度に保持した1時間30分かけて滴下し、さらに2時間熟成した。次にエチレングリコールモノエチルエーテルアセテートを減圧下で留去し、水酸基価54mgKOH/g、数平均分子量20,000、樹脂固形分65質量%の水酸基含有アクリル樹脂を得た。ここで数平均分子量とは、ゲル浸透クロマトグラフィー(GPC)によって標準ポリスチレンの検量線を用いて測定したものを意味する。
モノマー/重合開始剤の混合物:
メチルメタクリレ−ト38部、エチルアクリレ−ト17部、n−ブチルアクリレ−ト17部、ヒドロキシエチルメタクリレ−ト7部、ラウリルメタクリレ−ト20部及びアクリル酸1部及び2,2'−アゾビス(2−メチルプロピオニトリル)2部からなる混合物。
(鱗片状光輝性顔料の干渉色測定)
実施例及び比較例に使用する鱗片状光輝性顔料の干渉色を以下の要領で測定し、結果を表1に示した。
Hereinafter, the present invention will be described more specifically with reference to examples and comparative examples. However, the present invention is not limited to only these examples. “Part” and “%” are based on mass.
Next, an Example is given and this invention is demonstrated more concretely.
(Production Example 1) Production of hydroxyl group-containing acrylic resin 50 parts of ethylene glycol monoethyl ether acetate was charged in a reaction vessel equipped with a thermometer, thermostat, stirrer, reflux condenser and dropping device, stirred and mixed, and the temperature was raised to 135 ° C. Warm up. Subsequently, the following monomer / polymerization initiator mixture was dropped into a reaction vessel maintained at the same temperature over 3 hours, and aging was performed for 1 hour after the completion of the dropping. Thereafter, a mixture of 10 parts of ethylene glycol monoethyl ether acetate and 0.6 parts of 2,2′-azobis (2-methylpropionitrile) was added dropwise over 1 hour 30 minutes maintained at the same temperature, and further 2 hours. Aged. Next, ethylene glycol monoethyl ether acetate was distilled off under reduced pressure to obtain a hydroxyl group-containing acrylic resin having a hydroxyl value of 54 mgKOH / g, a number average molecular weight of 20,000, and a resin solid content of 65% by mass. Here, the number average molecular weight means that measured by gel permeation chromatography (GPC) using a standard polystyrene calibration curve.
Monomer / polymerization initiator mixture:
38 parts of methyl methacrylate, 17 parts of ethyl acrylate, 17 parts of n-butyl acrylate, 7 parts of hydroxyethyl methacrylate, 20 parts of lauryl methacrylate and 1 part of acrylic acid and 2,2′-azobis A mixture consisting of 2 parts of (2-methylpropionitrile).
(Measurement of interference color of scaly glitter pigment)
The interference color of the scaly glitter pigment used in Examples and Comparative Examples was measured in the following manner, and the results are shown in Table 1.

Figure 2011026543
Figure 2011026543

鱗片状光輝性顔料のハイライトにおける干渉色は、製造例1で得られた水酸基含有アクリル樹脂75部、ユーバン28−60(商品名、ブチルエーテル化メラミン樹脂、三井化学社製)25部からなる樹脂成分100部(固形分)あたり、鱗片状光輝性顔料を15部配合して攪拌混合し、溶剤を添加して塗装に適正な粘度に希釈して得られた塗料を、予め黒色(N−2)の塗膜を形成した塗板上に硬化塗膜として18μmの膜厚となるようにエアスプレー塗装し、室温にて15分間放置し、ついで、未硬化塗面にクリヤー塗料(ル−ガベ−ククリヤ−、関西ペイント製、商品名、アクリル樹脂・アミノ樹脂系、有機溶剤型)を硬化塗膜として、35μmとなるようにエアスプレー塗装し、さらに室温にて15分間放置し、その後に熱風乾燥機を使用して140℃で30分加熱して硬化乾燥せしめて得られた塗膜をX−Rite社製のMA−68II(商品名、多角度分光光度計)を使用して、正反射光に対して15°で受光した分光反射率に基づいて測定したL*C*h表色系における色相角度hで示した。
(着色顔料の白素地上と黒素地上の日射反射率測定)
実施例及び比較例に使用する着色顔料各々の白素地及び黒素地上の日射反射率を以下の要領で測定し、結果を表1に示した。
The interference color in the highlight of the scaly glittering pigment is a resin comprising 75 parts of the hydroxyl group-containing acrylic resin obtained in Production Example 1 and 25 parts of Uban 28-60 (trade name, butyl etherified melamine resin, manufactured by Mitsui Chemicals). For 100 parts (solid content) of the component, 15 parts of a scaly glittering pigment are blended, mixed by stirring, and a paint obtained by adding a solvent and diluting to an appropriate viscosity for coating is prepared in advance with a black (N-2 ) Is applied by air spray so that the film thickness becomes 18 μm as a cured coating film, and left at room temperature for 15 minutes, and then a clear paint (Lube-Club clear) is applied to the uncured coating surface. -Kansai Paint Co., Ltd., trade name, acrylic resin / amino resin type, organic solvent type) as a cured coating film, air sprayed to 35 μm and left at room temperature for 15 minutes, then hot air dryer The Using the coating film obtained by heating and drying at 140 ° C. for 30 minutes using MA-68II (trade name, multi-angle spectrophotometer) manufactured by X-Rite, The hue angle h in the L * C * h color system measured based on the spectral reflectance received at 15 °.
(Measurement of solar reflectance of colored pigments on white and black surfaces)
The solar reflectance of each of the color pigments used in Examples and Comparative Examples was measured in the following manner, and the results are shown in Table 1.

水酸基含有アクリル樹脂(水酸基価100、数平均分子量20000)及びメラミン樹脂からなる樹脂成分100固形分質量部あたり、該着色顔料を15質量部配合して攪拌混合し、塗装に適正な粘度に希釈して固形分約25%の有機溶剤型塗料を調製する。JIS K5101 4隠ぺい率試験紙法に記載された隠ぺい率試験紙を平らなガラス板の上に水平に固定し、その上にドクターブレードを使用して、硬化塗膜厚が30μmとなるように塗装し、室温約20℃の実験室に15分間放置し、その後に熱風乾燥機を使用して140℃で30分間加熱して硬化せしめた塗膜の白素地部分及び黒素地部分の日射反射率として、積分球ISR−3100を搭載した分光光度計UV−3100PC(共に島津製作所社製)を使用して入射角度を8°としたときのJIS K5602に定義された反射率を測定した。   15 parts by mass of the coloring pigment is mixed per 100 parts by mass of a resin component comprising a hydroxyl group-containing acrylic resin (hydroxyl value 100, number average molecular weight 20000) and melamine resin, and the mixture is stirred and mixed. An organic solvent-type paint having a solid content of about 25% is prepared. Cover the opacity test paper described in JIS K5101 4 Coverage Test Paper Method horizontally on a flat glass plate, and apply a doctor blade on it so that the cured coating thickness is 30 μm. The solar reflectance of the white base and black base portions of the coating that was left in a laboratory at room temperature of about 20 ° C. for 15 minutes, and then cured by heating at 140 ° C. for 30 minutes using a hot air dryer. Using a spectrophotometer UV-3100PC (both manufactured by Shimadzu Corporation) equipped with an integrating sphere ISR-3100, the reflectance defined in JIS K5602 was measured when the incident angle was 8 °.

実施例1〜7、比較例1、2
製造例1で得られた水酸基含有アクリル樹脂75部、ユーバン28−60(商品名、ブチルエーテル化メラミン樹脂、三井化学社製)25部からなる樹脂成分100部(固形分)あたり、鱗片状光輝性顔料及び着色顔料を表2に示す比率で配合して攪拌混合し、塗装に適正な粘度に希釈して、固形分約25%の有機溶剤型塗料を調製し、実施例1〜7及び比較例1、2に使用する塗料組成物を作成した。
(試験板の作成)
基材の調整
脱脂及びりん酸亜鉛処理した鋼板(JISG3141、大きさ150×75×0.8mm)にカチオン電着塗料「エレクロン9400HB」(商品名:関西ペイント株式会社製、エポキシ樹脂ポリアミン系カチオン樹脂に硬化剤としてブロックポリイソシアネ−ト化合物を使用したもの)を硬化塗膜に基づいて膜厚20μmになるように電着塗装し、170℃で20分加熱して架橋硬化させて電着塗膜を得た。
Examples 1 to 7, Comparative Examples 1 and 2
Scale-like glitter per 100 parts (solid content) of a resin component comprising 75 parts of a hydroxyl group-containing acrylic resin obtained in Production Example 1 and 25 parts of Uban 28-60 (trade name, butyl etherified melamine resin, manufactured by Mitsui Chemicals, Inc.) Pigments and colored pigments were blended in the ratios shown in Table 2, mixed with stirring, diluted to an appropriate viscosity for coating, and organic solvent-type paints having a solid content of about 25% were prepared. Examples 1 to 7 and Comparative Examples The coating composition used for 1 and 2 was created.
(Creation of test plate)
Cationic electrodeposition paint “ELECRON 9400HB” (trade name: manufactured by Kansai Paint Co., Ltd., epoxy resin polyamine-based cation resin) on steel plate (JISG3141, size 150 × 75 × 0.8 mm) subjected to adjustment degreasing and zinc phosphate treatment of the base material (Using a block polyisocyanate compound as a curing agent) is electrodeposited so as to have a film thickness of 20 μm based on the cured coating film, and heated at 170 ° C. for 20 minutes to be crosslinked and cured to be electrodeposited. A membrane was obtained.

得られた電着塗面に、中塗塗料「ル−ガベ−ク中塗り白N−9」(商品名:関西ペイント株式会社製、ポリエステル樹脂・メラミン樹脂系、有機溶剤型)をエアスプレーにて硬化塗膜に基づいて膜厚30μmになるように塗装し、140℃で30分加熱して架橋硬化させて、中塗塗膜を形成した塗板を基材とした。
塗装
(1)で調整した基材に実施例及び比較例で調製した塗料組成物をそれぞれREAガンを用いて、ブ−ス温度25℃、湿度75%の条件で、硬化塗膜として、25μmとなるように塗装し、室温にて15分間放置し、ついで、これらの未硬化塗面にクリヤー塗料(ル−ガベ−ククリヤ−、関西ペイント製、商品名、アクリル樹脂・アミノ樹脂系、有機溶剤型)をミニベル型回転式静電塗装機を用いて、ブ−ス温度25℃、湿度75%の条件で硬化塗膜として、25〜35μmとなるように塗装した。塗装後、室温にて15分間放置した後に、熱風循環式乾燥炉内を使用して、140℃で30分間加熱し、複層塗膜を同時に乾燥硬化せしめて試験板を得た。
(3)明度の測定
(2)で作成した塗板の明度を測定した。測定は、X−Rite社製のMA−68II(商品名、多角度分光光度計)を使用して行ない、正反射光に対して45°で受光した分光反射率に基づいて計算したL*a*b*表色系における明度L*を表2に示した。
On the obtained electrodeposited surface, an intermediate coating “Lugabek intermediate coating white N-9” (trade name: manufactured by Kansai Paint Co., Ltd., polyester resin / melamine resin type, organic solvent type) is applied by air spray. Based on the cured coating film, it was applied to a film thickness of 30 μm, heated at 140 ° C. for 30 minutes to be crosslinked and cured, and a coated plate on which an intermediate coating film was formed was used as a substrate.
The coating composition prepared in Examples and Comparative Examples was applied to the base material prepared in the coating (1), using a REA gun, respectively, at 25 ° C. and 75% humidity as a cured coating film at 25 μm. Then, leave it at room temperature for 15 minutes, and then apply a clear paint (Lugabe Clear, manufactured by Kansai Paint, trade name, acrylic resin / amino resin, organic solvent type) to these uncured coating surfaces. ) Was coated as a cured coating film at 25-35 [mu] m under the conditions of a boot temperature of 25 [deg.] C. and a humidity of 75% using a mini-bell type rotary electrostatic coating machine. After coating, the sample was allowed to stand at room temperature for 15 minutes, and then heated in a hot-air circulating drying oven at 140 ° C. for 30 minutes to simultaneously dry and cure the multilayer coating film to obtain a test plate.
(3) Measurement of brightness The brightness of the coated plate prepared in (2) was measured. The measurement was performed using MA-68II (trade name, multi-angle spectrophotometer) manufactured by X-Rite, and L * a calculated based on the spectral reflectance received at 45 ° with respect to the regular reflection light. The lightness L * in the * b * color system is shown in Table 2.

Figure 2011026543
Figure 2011026543

(4)目視による意匠性評価
作成した塗板を、人工太陽灯(セリック社製、色温度6500K)で照明し、試験板の照明に対する角度を変えて観察して、ハイライト(正反射光近傍)やシェード(スカシ)の意匠性を目視にて評価し、結果を表2に示した。
・ハイライトの粒子感
◎:粒子感に優れる。
○:粒子感がある。
△:粒子感がほとんどない。
×:粒子感がない。
・ハイライトの彩度感
◎:干渉色が強く発現して彩度感に優れる。
○:干渉色が発現して彩度感がある。
△:干渉色が弱く彩度感が少ない。
×:彩度感がない。
・シェードのスモーキー感(シェードの明度が低く、ハイライトとシェードの中間において明度変化が緩やかな質感をスモーキー感として定義する。)
◎:スモーキー感に優れる。
○:スモーキー感がある。
△:スモーキー感が少ない。
×:スモーキー感がない。
(5)遮熱性評価
1辺が40cmのダンボール箱上部に70mm四方の正方形の穴をあけたものを、室温約20℃の実験室に30分間静置した。意匠性評価に使用した試験板を、75mm×75mmの大きさに切断して、裏に熱電対のセンサーをセロハンテープで固定した塗板を、
前記穴をふさぐように静置した。40cmの距離から、HALOGEN LIGHT(LPL1500)を照射し、15分後の塗板温度を測定した。
(4) Evaluation of design properties by visual observation The prepared coated plate is illuminated with an artificial sun lamp (manufactured by Celic, color temperature 6500K), and observed at different angles with respect to the illumination of the test plate to highlight (near specular reflection light) The design properties of the shade and the shade were visually evaluated, and the results are shown in Table 2.
-Highlight particle feeling A: Excellent particle feeling.
○: Particle feeling
Δ: There is almost no particle feeling.
X: There is no particle feeling.
-Highlight saturation ◎: The interference color is strongly expressed and the saturation is excellent.
○: Interference color appears and there is a sense of saturation.
Δ: The interference color is weak and the saturation is low.
X: There is no feeling of saturation.
-Shade smoky feeling (Definition of a smoky feeling is a texture with low shade brightness and a moderate change in brightness between highlight and shade.)
A: Excellent smoky feeling.
○: There is a smoky feeling.
Δ: Little smoky feeling.
X: There is no smoky feeling.
(5) Evaluation of heat shielding properties A 70 mm square hole formed in the upper part of a corrugated cardboard box having a side of 40 cm was left in a laboratory at room temperature of about 20 ° C. for 30 minutes. A test plate used for design evaluation was cut into a size of 75 mm × 75 mm, and a coated plate with a thermocouple sensor fixed on the back with a cellophane tape,
It left still so that the said hole might be plugged up. HALOGEN LIGHT (LPL1500) was irradiated from a distance of 40 cm, and the coating plate temperature after 15 minutes was measured.

本発明の塗料組成物、塗膜形成方法は、各種工業製品、特に自動車車体の外板に適用できる。 The coating composition and the coating film forming method of the present invention can be applied to various industrial products, particularly to the outer plate of an automobile body.

Claims (4)

赤外線を反射及び/又は透過する着色顔料及び鱗片状光輝性顔料を含む塗料組成物であって、塗装して得られる塗膜のL*a*b*表色系における明度が10以下であって且つハイライトからシェードに明度及び彩度が変化する塗料組成物。 A coating composition containing a colored pigment that reflects and / or transmits infrared rays and a scaly glittering pigment, and a coating film obtained by coating has a brightness in an L * a * b * color system of 10 or less A paint composition whose brightness and saturation change from highlight to shade. 赤外線を反射及び/又は透過する着色顔料が、ペリレン及び/又は複合金属酸化物である請求項1に記載の塗料組成物。 The coating composition according to claim 1, wherein the color pigment that reflects and / or transmits infrared rays is perylene and / or a composite metal oxide. 鱗片状光輝性顔料が、ガラスフレーク又は酸化アルミニウム表面に金属酸化物を被覆した干渉性光輝性顔料である請求項1又は2に記載の塗料組成物。 The coating composition according to claim 1 or 2, wherein the scaly glittering pigment is a coherent glittering pigment having a glass flake or aluminum oxide surface coated with a metal oxide. 基材に1〜3項のいずれか1項に記載の塗料組成物を塗装して得られた塗膜上に、さらにトップクリヤー塗料を塗装する塗膜形成方法。 The coating-film formation method which coats a top clear coating material further on the coating film obtained by apply | coating the coating composition of any one of 1-3 to a base material.
JP2010065329A 2009-06-22 2010-03-22 Paint composition and method of forming paint film Pending JP2011026543A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2010065329A JP2011026543A (en) 2009-06-22 2010-03-22 Paint composition and method of forming paint film

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2009147153 2009-06-22
JP2010065329A JP2011026543A (en) 2009-06-22 2010-03-22 Paint composition and method of forming paint film

Publications (1)

Publication Number Publication Date
JP2011026543A true JP2011026543A (en) 2011-02-10

Family

ID=43635652

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2010065329A Pending JP2011026543A (en) 2009-06-22 2010-03-22 Paint composition and method of forming paint film

Country Status (1)

Country Link
JP (1) JP2011026543A (en)

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011225652A (en) * 2010-04-16 2011-11-10 Kansai Paint Co Ltd Coating composition and coating film forming method
JP2013040257A (en) * 2011-08-12 2013-02-28 Kansai Paint Co Ltd Coating material composition and method for forming coating film
JP2013230440A (en) * 2012-04-27 2013-11-14 Kansai Paint Co Ltd Coating film forming method
JP2014098056A (en) * 2012-11-13 2014-05-29 Kansai Paint Co Ltd Coating material composition and coating film formation method
WO2014155930A1 (en) * 2013-03-28 2014-10-02 マツダ株式会社 Internal plate part coating for vehicle
JP2014210856A (en) * 2013-04-18 2014-11-13 関西ペイント株式会社 Coating composition and coating film forming method
WO2018155362A1 (en) * 2017-02-21 2018-08-30 日本ペイント・オートモーティブコーティングス株式会社 Water-based coating composition, and multi-layer coating film
US10174213B2 (en) 2011-09-16 2019-01-08 Basf Se Coating system
US11808833B2 (en) 2016-10-28 2023-11-07 Ppg Industries Ohio, Inc. Coatings for increasing near-infrared detection distances
US11809933B2 (en) 2018-11-13 2023-11-07 Ppg Industries Ohio, Inc. Method of detecting a concealed pattern
US12001034B2 (en) 2022-11-04 2024-06-04 Ppg Industries Ohio, Inc. Near infrared control coating, articles formed therefrom, and methods of making the same

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6485173A (en) * 1986-07-29 1989-03-30 Nippon Paint Co Ltd Method for formation of coating film
JPH05112735A (en) * 1990-01-22 1993-05-07 Basf Corp Pigment composition containing laminar graphite
JPH07224235A (en) * 1994-02-07 1995-08-22 Dainichiseika Color & Chem Mfg Co Ltd Coating composition and coating film composition
JPH111641A (en) * 1997-06-13 1999-01-06 Kansai Paint Co Ltd Process for forming double-layer coating film
JP2002060698A (en) * 2000-08-15 2002-02-26 Origin Electric Co Ltd Infrared transmitting layer-forming composition, infrared reflector and treated matter
JP2002273335A (en) * 2001-03-16 2002-09-24 Nippon Paint Co Ltd Method for forming pearl gloss coating film and coated article
JP2008132436A (en) * 2006-11-28 2008-06-12 Kansai Paint Co Ltd Coating formation method and coating structure
JP2010094575A (en) * 2008-10-14 2010-04-30 Denso Corp Method of manufacturing catalyst-supported material

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6485173A (en) * 1986-07-29 1989-03-30 Nippon Paint Co Ltd Method for formation of coating film
JPH05112735A (en) * 1990-01-22 1993-05-07 Basf Corp Pigment composition containing laminar graphite
JPH07224235A (en) * 1994-02-07 1995-08-22 Dainichiseika Color & Chem Mfg Co Ltd Coating composition and coating film composition
JPH111641A (en) * 1997-06-13 1999-01-06 Kansai Paint Co Ltd Process for forming double-layer coating film
JP2002060698A (en) * 2000-08-15 2002-02-26 Origin Electric Co Ltd Infrared transmitting layer-forming composition, infrared reflector and treated matter
JP2002273335A (en) * 2001-03-16 2002-09-24 Nippon Paint Co Ltd Method for forming pearl gloss coating film and coated article
JP2008132436A (en) * 2006-11-28 2008-06-12 Kansai Paint Co Ltd Coating formation method and coating structure
JP2010094575A (en) * 2008-10-14 2010-04-30 Denso Corp Method of manufacturing catalyst-supported material

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011225652A (en) * 2010-04-16 2011-11-10 Kansai Paint Co Ltd Coating composition and coating film forming method
JP2013040257A (en) * 2011-08-12 2013-02-28 Kansai Paint Co Ltd Coating material composition and method for forming coating film
US10174213B2 (en) 2011-09-16 2019-01-08 Basf Se Coating system
JP2013230440A (en) * 2012-04-27 2013-11-14 Kansai Paint Co Ltd Coating film forming method
JP2014098056A (en) * 2012-11-13 2014-05-29 Kansai Paint Co Ltd Coating material composition and coating film formation method
US11254800B2 (en) 2013-03-28 2022-02-22 Mazda Motor Corporation Coating of inner plate part of vehicle
WO2014155930A1 (en) * 2013-03-28 2014-10-02 マツダ株式会社 Internal plate part coating for vehicle
JP2014193938A (en) * 2013-03-28 2014-10-09 Mazda Motor Corp Inner plate portion coating film of vehicle
JP2014210856A (en) * 2013-04-18 2014-11-13 関西ペイント株式会社 Coating composition and coating film forming method
US11977154B2 (en) 2016-10-28 2024-05-07 Ppg Industries Ohio, Inc. Coatings for increasing near-infrared detection distances
US11808833B2 (en) 2016-10-28 2023-11-07 Ppg Industries Ohio, Inc. Coatings for increasing near-infrared detection distances
CN110291163A (en) * 2017-02-21 2019-09-27 日涂汽车涂料有限公司 Water-based paint compositions and multilayer film
JP2022075758A (en) * 2017-02-21 2022-05-18 日本ペイント・オートモーティブコーティングス株式会社 Water-based coating composition and multi-layer coating film
JP7090399B2 (en) 2017-02-21 2022-06-24 日本ペイント・オートモーティブコーティングス株式会社 Water-based paint composition and multi-layer coating
US11518890B2 (en) 2017-02-21 2022-12-06 Nippon Paint Automotive Coatings Co., Ltd. Water-based coating composition, and multi-layer coating film
JP7360490B2 (en) 2017-02-21 2023-10-12 日本ペイント・オートモーティブコーティングス株式会社 Water-based paint compositions and multilayer coatings
JP2018135439A (en) * 2017-02-21 2018-08-30 日本ペイント・オートモーティブコーティングス株式会社 Aqueous coating material composition and multilayer coating film
WO2018155362A1 (en) * 2017-02-21 2018-08-30 日本ペイント・オートモーティブコーティングス株式会社 Water-based coating composition, and multi-layer coating film
US11809933B2 (en) 2018-11-13 2023-11-07 Ppg Industries Ohio, Inc. Method of detecting a concealed pattern
US12001034B2 (en) 2022-11-04 2024-06-04 Ppg Industries Ohio, Inc. Near infrared control coating, articles formed therefrom, and methods of making the same

Similar Documents

Publication Publication Date Title
JP5567297B2 (en) Coating method
JP2011026543A (en) Paint composition and method of forming paint film
JP6323932B2 (en) Coating composition and coating film forming method
JP6195559B2 (en) Coating method
JP2011162732A (en) Metallic paint composition and method of forming paint film
JP2012232236A (en) Method for forming multilayer coated film
JP5547526B2 (en) Coating composition, coating film forming method and coating film structure
JP5421028B2 (en) Coating method
JP2012036331A (en) Coating composition and method for forming coating film
JP4958090B2 (en) MULTILAYER COATING FORMATION METHOD AND COATED ARTICLE
JP2011225652A (en) Coating composition and coating film forming method
JP2012170910A (en) Multi-layered coating film forming method
JP5939604B2 (en) Coating composition and coating film forming method
JP2012050938A (en) Coating composition and coating film-forming method
JP5936433B2 (en) Coating method
JPWO2015056715A1 (en) Coating composition and coating film forming method
JP5368967B2 (en) Multi-layer coating formation method
JP4971611B2 (en) Metallic coating composition, multilayer coating film forming method, coating film structure and coated article
JP5611629B2 (en) Coating method
JP4751043B2 (en) MULTILAYER COATING FORMATION METHOD AND COATED ARTICLE
JP2012017364A (en) Metallic coating composition and method for forming coating film
JP6026930B2 (en) Coating method
JP2012170909A (en) Multi-layered coating film forming method
JP2012021089A (en) Coating composition and method for forming coated film
JP2013040257A (en) Coating material composition and method for forming coating film

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20121011

A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20130807

A131 Notification of reasons for refusal

Free format text: JAPANESE INTERMEDIATE CODE: A131

Effective date: 20131022

A02 Decision of refusal

Free format text: JAPANESE INTERMEDIATE CODE: A02

Effective date: 20140828

A521 Written amendment

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20141127

A911 Transfer to examiner for re-examination before appeal (zenchi)

Free format text: JAPANESE INTERMEDIATE CODE: A911

Effective date: 20141205

A912 Re-examination (zenchi) completed and case transferred to appeal board

Free format text: JAPANESE INTERMEDIATE CODE: A912

Effective date: 20150306