JP3368055B2 - Thermosetting powder coating method - Google Patents

Thermosetting powder coating method

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Publication number
JP3368055B2
JP3368055B2 JP17766194A JP17766194A JP3368055B2 JP 3368055 B2 JP3368055 B2 JP 3368055B2 JP 17766194 A JP17766194 A JP 17766194A JP 17766194 A JP17766194 A JP 17766194A JP 3368055 B2 JP3368055 B2 JP 3368055B2
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JP
Japan
Prior art keywords
powder coating
coating
thermosetting powder
powder
spread
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
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JP17766194A
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Japanese (ja)
Other versions
JPH0810686A (en
Inventor
利雄 大越
忠義 龍野
酉元 川本
利男 小笠原
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Kansai Paint Co Ltd
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Kansai Paint Co Ltd
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Publication date
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Priority to JP17766194A priority Critical patent/JP3368055B2/en
Publication of JPH0810686A publication Critical patent/JPH0810686A/en
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Description

【発明の詳細な説明】 【0001】 【産業上の利用分野】本発明は熱硬化性粉体塗膜形成方
法に関する。 【0002】 【従来の技術及びその課題】従来、エッジ部のある被塗
装面に通常の熱硬化性粉体塗料を塗装した場合には、粉
体塗料の静電反発によりエッジ部に付着し難いこと及び
加熱溶融物の表面張力によってエッジ部の塗装膜厚が薄
くなる。このためにエッジ部の防食性が劣るといった欠
点があった。 【0003】このエッジ部の防食性を改善するために熱
硬化性粉体塗料に顔料を多量に配合したり、ゲル化微粒
子を配合する等の種々の方法を試みたが平滑性とエッジ
部の塗膜形成とは両立せず、これらを満足するものが今
だに得られていないのが実情である。 【0004】 【課題を解決するための手段】本発明は、上記した問題
点を解消するために鋭意研究を重ねた結果、被塗装面に
熱硬化性粉体塗料を塗装し、次に該粉体塗料を加熱溶融
させずにこのものの上から更に別の熱硬化性粉体塗料を
塗装し、続いてこれらの熱硬化性粉体塗料を同時に加熱
し硬化させる塗装方法とし、かつ上記2種類の熱硬化性
粉体塗料を特定のフロー性に調製したものが平滑性及び
エッジ部に対する防食性に優れた硬化塗膜が形成できる
ことを見い出し、本発明を完成するに至った。 【0005】即ち、本発明は被塗装面に、1段目とし
て、熱硬化性粉体塗料約0.8gを直径13mm、高さ約
4mmの円柱状になるように30kg/mm2加圧成型したもの
を150℃−10分間加熱フローさせた時の広がりの長
さが平均直径13〜25mmであり、かつ熱硬化性樹脂1
00重量部に対して充填剤を1〜19.9重量部含有さ
せてなる熱硬化性粉体塗料(以下、このものを「粉体塗
料A」と略す。)を塗装し、次いで、2段目として、上
記と同様の方法で測定した加圧成型したものの広がりの
長さが平均直径20〜40mm、かつその広がり長さの差
が1段目よりも直径2mm以上大きい熱硬化性粉体塗料
(以下、このものを「粉体塗料B」と略す。)を塗装
し、続いてこれらの塗装膜を同時に焼付け硬化させるこ
とを特徴とする熱硬化性粉体塗膜形成方法に係る。 【0006】本発明方法で用いる粉体塗料Aは、粉体塗
料約0.8gを直径13mm、高さ約4mmの円柱状になる
ように30kg/mm2加圧成型したものを150℃−10分
間加熱フローさせた時の広がりの長さが平均直径13〜
25mmのものである。該加圧成型は例えば粉体塗料をK
Brデスクプレス(直径13mm)(日立製作所社製)に
入れ錠剤成型機(島津製作所社製)を用いておこなうこ
とができる。また、加圧成型したものは大きさ長さ15
cm×幅10cm×厚さ0.08cmのブライト鋼板(JIS
G−3141、SPCC、SB)の脱脂板の上に乗せ
たのち加熱される。 【0007】上記粉体塗料Aの広がりは平均直径13〜
25mmの範囲にあることが重要な要件である。その広が
りの長さが平均直径25mmを上回るとエッジ部を十分に
被覆することが難しく、そのために塗膜の防食性が劣る
ものとなる。 【0008】粉体塗料Aとしては、例えばエポキシ樹脂
系粉体塗料、ポリエステル樹脂系粉体塗料、アクリル樹
脂系粉体塗料及びこれらの混合物又はハイブリッド系の
ものが使用できる。 【0009】上記エポキシ樹脂系粉体塗料としては、例
えばビスフェノール−エピクロルヒドリン型、ノボラッ
ク型、脂環式などのエポキシ樹脂を基体樹脂とし、かつ
芳香族アミン、酸無水物、ジシアンジアミド又はその誘
導体、ジヒドラジド、フェノール樹脂などを硬化剤とし
て含有するものが好ましい。 【0010】ポリエステル樹脂系粉体塗料としては、例
えばテレフタル酸、イソフタル酸及びトリメリット酸な
どの飽和多塩基酸とエチレングリコール、グリセリン、
ネオペンチルグリコール、トリメチロールプロパンなど
の多価アルコールを原料とする水酸基及び/又はカルボ
キシル基含有オイルフリーポリエステルを基体樹脂と
し、かつブロックポリイソシアネート、アミノ樹脂、ト
リグリシジルイソシアヌレートなどを硬化剤として含有
するものが好ましい。 【0011】アクリル樹脂系粉体塗料としては、例えば
ヒドロキシエチル(メタ)アクリレートを共重合体成分
として含有する水酸基含有アクリル樹脂を基体樹脂及び
ブロックポリイソシアネート、アミノ樹脂を硬化剤とす
るものやグリシジル(メタ)アクリレートを共重合体成
分として含有するグリシジル基含有アクリル樹脂を基体
樹脂及びドデカン2酸などの多塩基酸を硬化剤とするも
のなどが好ましい。 【0012】また、粉体塗料Aには充填剤を粉体塗料の
硬化性樹脂(硬化剤成分も含む)100重量部に対して
1〜19.9重量部含有することが好ましい。充填剤の
含有量が1重量部を下回るとエッジ部に対する防食性が
十分でなく、一方、19.9重量部を上回ると仕上り性
が低下するので好ましくない。 【0013】上記充填剤としては、シリカ、アルミナ、
チタニア、ジルコニアなどの微粉末であり、該粉末の平
均粒子径が5〜50 mμ(0.005〜0.05μm
)、好ましくは5〜23 mμ(0.005〜0.02
3μm )の範囲のものを90重量%以上含有するもので
ある。これらの粉末の平均粒径が5 mμより小さくなる
と粘度およびチクソトロピック性が高すぎて、塗料の製
造作業性が著しく低下し、一方、50 mμより大きくな
るとチクソトロピック性が低下しエッジ部の被覆性が不
十分となるので、いずれも好ましくない。 【0014】粉体塗料Aの広がりの長さは、例えば基体
樹脂の分子量、Tg(ガラス転移温度)や充填剤配合割
合によって調製することができる。 【0015】本発明方法で用いる粉体塗料Bは、前記と
同様の方法で測定した加圧成型したものの加熱後の広が
りの長さが平均直径20〜40mm、好ましくは24〜4
0mmの範囲である。その広がりの長さが平均直径20mm
を下回るとユズ膚などによる仕上り外観が劣り、一方、
平均直径40mmを上回るとタレなどによる塗膜欠陥を生
じるといった欠点がある。また、粉体塗料Bは加圧成型
したものの加熱後の広がり長さの差が平均直径2mm以上
大きいものが使用される。この差が平均直径2mmを下回
るとユズ膚などによる仕上り外観が劣る。 【0016】粉体塗料Bとしては、前記と同様のエポキ
シ樹脂系粉体塗料、ポリエステル樹脂系粉体塗料、アク
リル樹脂系粉体塗料及びこれらの混合物又はハイブリッ
ド系のものが使用できる。 【0017】粉体塗料Bの広がりの長さは、例えば基体
樹脂の分子量、Tgによって調製することができる。ま
た、粉体塗料A及びBの平均粒子径は、約10〜150
μm のものが好ましい。 【0018】本発明方法において、粉体塗料A及びBと
してそれぞれアクリル樹脂系粉体塗料を用いることが仕
上り性の面から好ましい。上記粉体塗料A及びBには着
色顔料、ハジキ防止剤、紫外線吸収剤などの塗料用添加
剤を必要に応じて配合することができる。 【0019】本発明方法は、被塗装面に粉体塗料Aを静
電塗装し、次いで粉体塗料Bを静電塗装したのち、焼付
け硬化させることによって実施できる。 【0020】被塗装面としては、静電粉体塗装できるも
のであれば特に限定されず、例えばアルミニウム、鉄、
亜鉛などの金属やこのものに電着塗膜、中塗り塗膜及び
着色ベース塗膜(ソリッドカラー、メタリックカラーな
ど)などの下地塗膜を施したものが使用できる。また、
エッジ部を有する被塗装面としては例えば自動車用アル
ミニウムホイールなどがある。このものは例えばメタリ
ックベース(水性又は溶剤形)塗料を下塗りとして、ま
た粉体塗料A及びBを上塗りクリヤとして仕上げること
もできる。粉体塗料A及びBの塗装膜厚は焼付け硬化後
の膜厚で30〜150μm が好ましい。また、焼付けは
硬化剤の種類によって異なるが、通常、140℃〜26
0℃で10秒〜60分間で十分と思われる。 【0021】 【実施例】以下、実施例を掲げて本発明を詳しく説明す
る。 粉体塗料E、P、Aの製造例 表1に記載の成分をヘンシェルミキサー(三井三池社
製)で混合し、ブスコニーダーPR46(スイス:ブス
社製)混練機で吐出量30〜70kg/H、温度80〜12
0℃、スクリュー回転数100rpm の条件で混練する。
混練物を3〜6mm厚の平板状に取り出し速やかに冷却す
る。その後2〜3mm大に粗粉砕後アトマイザー(富士産
業(株)製)を用いて微粉砕する。そして150メッシ
ュ標準ふるいを用いてふるい分ける。粗粒を除去して粉
体塗料E、P、Aを得る。 【0022】表1中の各成分は次の通りである。 基体樹脂 エポキシ樹脂:エポン1004(油化シェルエポキシ社
製、ビスフェノールA−エピクロルヒドリン型エポキシ
樹脂、平均分子量約1400) ポリエステル樹脂:ファインデックM8010(大日本
インキ社製、水酸基含有ポリエステル樹脂) アクリル樹脂:アロマテックPD6300(三井東圧社
製、グリシジル基含有アクリル樹脂) 硬化剤 エポキシ用硬化剤:エピキュア108FF(油化シェル
エポキシ社製、アミン系) ポリエステル用硬化剤:IPD1−B1530(ダイセ
ルヒュルス社製、ε−カプロラクタムでブロック化され
たイソホロンジイソシアネート) アクリル用硬化剤:ドデカン2酸 充填剤:アエロジル#380(日本アエロジル(株)
製、商品名、微粉末シリカ、平均粒子径7 mμ) 添加剤 添加剤a:アクロナール4F(BASF社製) 添加剤b:ペインタッドM(ダウコーニング社製) 【0023】表1中の広がり長さは、粉体塗料約0.8
gを直径13mm高さ約4mmの円柱状になるように30kg
/mm2加圧成型したものを150℃−10分間加熱させた
時の平均直径を測定した数値である。 【0024】 【表1】【0025】実施例及び比較例 表2に記載の第1段目塗装用粉体塗料をパネルAに硬化
膜厚が30〜40μmになるように静電塗装し、次いで
表2に記載の第2段目塗装用粉体塗料を硬化膜厚が30
〜40μm になるように静電塗装したのち熱風乾燥機で
170℃−30分間加熱して塗膜を形成した。形成した
塗膜の仕上り性を評価した。 【0026】次にパネルBを用いて上記と同様の方法で
塗膜を形成した。形成した塗膜のエッジ防食性について
評価した。 パネルA:冷間圧延鋼板SPCC(幅100mm×長さ3
00mm×厚さ0.8mm)をトルエンで脱脂したもの。こ
のパネルを仕上り性用に用いた。 パネルB:ドリル(φ10mm刃)を用いて前記パネルA
の中央部に5mm間隔で5ケ所穴をあけて、裏面にエッジ
(バリ、突起)部のある穴を作成し、この裏面を被塗装
面として用いた。 結果を表2に示す。 【0027】 【表2】 【0028】表2中の塗膜性能は下記基準に従って評価
した。 仕上り性 パネルAに塗装した塗膜を目視で観察し、平滑性を調べ
た。 ◎ 平滑性に優れる。 ○ わずかに凹凸がある。 △ かなり凹凸がある × 凹凸がはげしい。 エッジ部防食性 パネルBに塗装した塗膜を塩水噴霧試験(JIS Z−
2371)で72Hおこなった。穴周辺のエッジ部(バ
リ、突起部)のサビの発生を調べた。 ◎ サビ発生なし。 ○ わずかにサビ発生。 △ かなりサビ発生。 × サビ発生著しい。 【0029】 【発明の効果】本発明方法は上記した方法であることか
ら下記した効果を発揮する。 (1)エッジ部に対する塗膜の防食性が良い。 (2)タレ、ユズ膚などの塗装欠陥がなく仕上り外観が
良い。 (3)従来、2種類の粉体塗料を塗り重ね同時に焼付け
硬化させる方法においては、塗料の表面張力を下層の塗
膜を形成する塗料よりも上層の塗膜を形成する塗料を小
さくすることによって仕上り外観を改善することが行な
われている。しかしながら、該方法ではエッジ部に対す
る防食性が十分でないこと及び2種類の塗料の表面張力
を調製するだけでは仕上り外観が十分でないために、通
常、有機溶剤系又は水性塗料などの溶液型塗料の上に粉
体塗料が塗装されるように、塗料系の異なったものの組
合わせが行なわれており、工程が煩わしいことなどの欠
点がある。本発明の方法は、例えば同一系態である粉体
塗料を用いしかも一方に充填剤を含有させるだけで防食
性及び仕上り性に優れた塗膜が形成できるといった特徴
がある。
Description: BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for forming a thermosetting powder coating film. 2. Description of the Related Art Conventionally, when a usual thermosetting powder coating is applied to a surface to be coated having an edge, it is difficult for the powder coating to adhere to the edge due to electrostatic repulsion of the powder coating. In addition, the coating thickness at the edge portion is reduced due to the fact and the surface tension of the heated melt. For this reason, there was a defect that the corrosion resistance of the edge portion was inferior. In order to improve the corrosion resistance of the edge portion, various methods have been tried, such as adding a large amount of a pigment to a thermosetting powder coating or compounding gelled fine particles. The fact is that it is incompatible with the formation of a coating film, and a product satisfying these has not yet been obtained. SUMMARY OF THE INVENTION The present invention has been made as a result of intensive studies to solve the above-mentioned problems, and as a result, a surface to be coated is coated with a thermosetting powder coating, and then the powder is coated. A coating method in which another thermosetting powder coating is applied from above without heating and melting the body coating, followed by simultaneously heating and curing these thermosetting powder coatings, and The present inventors have found that a thermosetting powder coating prepared to have a specific flow property can form a cured coating film having excellent smoothness and excellent anticorrosion properties on edge portions, and have completed the present invention. That is, according to the present invention, as a first step, about 0.8 g of a thermosetting powder coating is formed on a surface to be coated into a column having a diameter of 13 mm and a height of about 4 mm by a pressure of 30 kg / mm 2. The spread length when heated and flowed at 150 ° C. for 10 minutes has an average diameter of 13 to 25 mm, and the thermosetting resin 1
A thermosetting powder coating material containing 1 to 19.9 parts by weight of a filler with respect to 00 parts by weight (hereinafter referred to as “powder coating material A”) is applied, and then two steps. As an eye, the thermosetting powder coating has a spread length of 20 to 40 mm in average diameter and a difference in the spread length of 2 mm or more larger than that of the first stage measured by the same method as described above. (Hereinafter, this is abbreviated as “powder coating B”.) The present invention relates to a method for forming a thermosetting powder coating film, characterized in that these coating films are simultaneously baked and cured. The powder coating A used in the method of the present invention is obtained by pressing about 0.8 g of the powder coating into a column having a diameter of 13 mm and a height of about 4 mm at a pressure of 30 kg / mm 2 at 150 ° C.-10 The length of the spread when heated for a minute is 13 ~
It is 25mm. In the pressure molding, for example, the powder coating is
It can be carried out using a tablet molding machine (manufactured by Shimadzu Corporation) in a Br desk press (diameter: 13 mm) (manufactured by Hitachi, Ltd.). In addition, the one molded by pressure has a size of 15
Bright steel plate of cm × 10cm × 0.08cm thickness (JIS
G-3141, SPCC, SB) and then heated. [0007] The spread of the powder coating material A has an average diameter of 13 to
An important requirement is to be in the range of 25 mm. If the length of the spread exceeds 25 mm in average diameter, it is difficult to sufficiently cover the edge portion, so that the corrosion resistance of the coating film is inferior. As the powder coating A, for example, an epoxy resin powder coating, a polyester resin powder coating, an acrylic resin powder coating, a mixture thereof or a hybrid coating can be used. As the epoxy resin-based powder coating, for example, an epoxy resin of bisphenol-epichlorohydrin type, novolak type, alicyclic type or the like is used as a base resin, and aromatic amine, acid anhydride, dicyandiamide or a derivative thereof, dihydrazide, Those containing a phenol resin or the like as a curing agent are preferred. As the polyester resin powder coating, for example, saturated polybasic acids such as terephthalic acid, isophthalic acid and trimellitic acid and ethylene glycol, glycerin,
The base resin is a hydroxyl group- and / or carboxyl group-containing oil-free polyester made from a polyhydric alcohol such as neopentyl glycol or trimethylolpropane, and a block polyisocyanate, an amino resin, triglycidyl isocyanurate or the like is contained as a curing agent. Are preferred. As the acrylic resin-based powder coating, for example, a hydroxyl group-containing acrylic resin containing hydroxyethyl (meth) acrylate as a copolymer component is used as a base resin and a block polyisocyanate, an amino resin as a curing agent, or glycidyl ( A glycidyl group-containing acrylic resin containing (meth) acrylate as a copolymer component is preferably used as a base resin and a polybasic acid such as dodecane diacid as a curing agent. The powder coating material A preferably contains a filler in an amount of 1 to 19.9 parts by weight based on 100 parts by weight of the curable resin (including the hardener component) of the powder coating material. If the content of the filler is less than 1 part by weight, the anticorrosion property against the edge portion is not sufficient, while if it exceeds 19.9 parts by weight, the finish is undesirably deteriorated. As the filler, silica, alumina,
It is a fine powder such as titania and zirconia, and has an average particle diameter of 5 to 50 mμ (0.005 to 0.05 μm
), Preferably 5 to 23 mμ (0.005 to 0.02
3 μm) in an amount of 90% by weight or more. When the average particle size of these powders is smaller than 5 mμ, the viscosity and thixotropic properties are too high, and the workability of the coating material is significantly reduced. On the other hand, when the average particle size is larger than 50 mμ, the thixotropic properties are reduced and the coating of the edge portion is reduced. Any of these is not preferred because the properties are insufficient. The length of the spread of the powder coating A can be adjusted, for example, by the molecular weight of the base resin, Tg (glass transition temperature) and the proportion of the filler. The powder coating material B used in the method of the present invention has a spread length after heating of a molded article under pressure measured by the same method as described above and has an average diameter of 20 to 40 mm, preferably 24 to 4 mm.
The range is 0 mm. The average length of the spread is 20mm
If it is below, the finished appearance due to yuzu silk etc. will be inferior,
When the average diameter exceeds 40 mm, there is a disadvantage that a coating film defect due to sagging or the like occurs. As the powder coating material B, one obtained by molding under pressure and having a difference in spread length after heating of 2 mm or more in average diameter is used. If this difference is less than 2 mm in average diameter, the finished appearance due to yuzu skin etc. will be poor. As the powder coating B, the same epoxy resin powder coating, polyester resin powder coating, acrylic resin powder coating, and mixtures or hybrids thereof as described above can be used. The length of the spread of the powder coating material B can be adjusted, for example, by the molecular weight and Tg of the base resin. The average particle size of the powder coatings A and B is about 10 to 150.
μm is preferred. In the method of the present invention, it is preferable to use acrylic resin-based powder coatings as the powder coatings A and B, respectively, from the viewpoint of finishing properties. To the powder coatings A and B, coating additives such as a coloring pigment, an anti-cissing agent, and an ultraviolet absorber can be added as necessary. The method of the present invention can be carried out by electrostatically applying a powder coating A on a surface to be coated, electrostatically applying a powder coating B, and then baking and hardening. The surface to be coated is not particularly limited as long as it can be coated with an electrostatic powder. For example, aluminum, iron,
Metals such as zinc and those obtained by applying an undercoating film such as an electrodeposition coating film, an intermediate coating film and a colored base coating film (solid color, metallic color, etc.) to this can be used. Also,
The surface to be coated having the edge portion includes, for example, an aluminum wheel for an automobile. It can be finished, for example, with a metallic base (aqueous or solvent type) paint as an undercoat, and powder paints A and B as an overcoat clear. The coating thickness of the powder coatings A and B is preferably 30 to 150 μm after baking and curing. In addition, baking varies depending on the type of a curing agent, but is usually 140 ° C. to 26 ° C.
10 seconds to 60 minutes at 0 ° C. seems sufficient. Hereinafter, the present invention will be described in detail with reference to examples. Production Examples of Powder Coatings E, P, A The components listed in Table 1 were mixed with a Henschel mixer (manufactured by Mitsui Miike Co., Ltd.), and the mixture was kneaded with a Busconi Kneader PR46 (manufactured by Buss Co., Switzerland) at a discharge rate of 30-70 kg / H Temperature 80-12
Kneading is performed at 0 ° C. and a screw rotation speed of 100 rpm.
The kneaded material is taken out into a flat plate having a thickness of 3 to 6 mm and rapidly cooled. Thereafter, the mixture is roughly pulverized to a size of 2 to 3 mm and then finely pulverized using an atomizer (manufactured by Fuji Sangyo Co., Ltd.). Then, sieve using a 150 mesh standard sieve. The coarse particles are removed to obtain powder coatings E, P and A. The components in Table 1 are as follows. Base resin Epoxy resin: EPON 1004 (Bisphenol A-epichlorohydrin type epoxy resin, manufactured by Yuka Shell Epoxy Co., Ltd., average molecular weight: about 1400) Polyester resin: Finedec M8010 (hydroxyl-containing polyester resin manufactured by Dainippon Ink) Acrylic resin: Aroma TEC PD6300 (Mitsui Toatsu Co., Ltd., glycidyl group-containing acrylic resin) Curing agent Epoxy curing agent: Epicure 108FF (Yuika Shell Epoxy, amine type) Polyester curing agent: IPD1-B1530 (Daicel Huls Co., Ltd.) Isophorone diisocyanate blocked with ε-caprolactam) Acrylic curing agent: Dodecane diacid Filler: Aerosil # 380 (Nippon Aerosil Co., Ltd.)
Additive a: Acronal 4F (manufactured by BASF) Additive b: Paintad M (manufactured by Dow Corning) Additives a: Acronal 4F (manufactured by Dow Corning) Is about 0.8
g into a column with a diameter of 13mm and a height of about 4mm
/ mm 2 is a numerical value obtained by measuring the average diameter when the product molded under pressure was heated at 150 ° C. for 10 minutes. [Table 1] EXAMPLES AND COMPARATIVE EXAMPLES The powder coating for the first step coating shown in Table 2 was electrostatically coated on panel A so that the cured film thickness became 30 to 40 μm. Hardened film thickness of powder coating for stage coating is 30
After electrostatic coating to a thickness of 4040 μm, the coating was formed by heating at 170 ° C. for 30 minutes with a hot air drier. The finish of the formed coating film was evaluated. Next, using Panel B, a coating film was formed in the same manner as described above. The formed coating film was evaluated for edge corrosion resistance. Panel A: Cold-rolled steel plate SPCC (width 100 mm x length 3
(00 mm x 0.8 mm thick) degreased with toluene. This panel was used for finishing. Panel B: The panel A using a drill (φ10 mm blade)
5 holes were made at 5 mm intervals in the center of the sample, a hole having an edge (burr, projection) on the back surface was formed, and this back surface was used as a surface to be coated. Table 2 shows the results. [Table 2] The coating properties in Table 2 were evaluated according to the following criteria. The coating film applied to the finished panel A was visually observed to examine its smoothness. ◎ Excellent smoothness. ○ There are slight irregularities. △ There are considerable irregularities × Irregularities are severe. The coating applied to the edge anti-corrosion panel B is subjected to a salt spray test (JIS Z-
2371) for 72H. The occurrence of rust on the edge portion (burrs, protrusions) around the hole was examined. ◎ No rust occurred. ○ Slight rusting. △ Significant rust occurred. X: Rust is remarkable. The method of the present invention has the following effects because it is the method described above. (1) The corrosion resistance of the coating film on the edge portion is good. (2) Good finish appearance with no paint defects such as sagging and yuzu silk. (3) Conventionally, in a method in which two types of powder coatings are applied and baked and cured simultaneously, the surface tension of the coating is reduced by making the coating forming the upper coating film smaller than the coating forming the lower coating film. Improvements have been made to the finished appearance. However, in this method, the corrosion resistance against the edge portion is not sufficient, and the finished appearance is not sufficient just by adjusting the surface tension of the two types of paints. A combination of different paint systems is used so that the powder paint is applied to the varnish, and there is a drawback that the process is complicated. The method of the present invention is characterized in that, for example, a coating film having excellent anticorrosion properties and finish properties can be formed only by using powder coatings of the same system and by adding a filler to one of them.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 平5−115843(JP,A) 特開 昭62−269780(JP,A) (58)調査した分野(Int.Cl.7,DB名) B05D 1/06 B05D 7/24 301 C09D 5/03 ──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-5-115584 (JP, A) JP-A-62-269780 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) B05D 1/06 B05D 7/24 301 C09D 5/03

Claims (1)

(57)【特許請求の範囲】 【請求項1】 被塗装面に、1段目として、熱硬化性粉
体塗料約0.8gを直径13mm、高さ約4mmの円柱状に
なるように30kg/mm2加圧成型したものを150℃−1
0分間加熱フローさせた時の広がりの長さが平均直径1
3〜25mmであり、かつ熱硬化性樹脂100重量部に対
して充填剤を1〜19.9重量部含有させてなる熱硬化
性粉体塗料を塗装し、次いで、2段目として、上記と同
様の方法で測定した加圧成型したものの広がりの長さが
平均直径20〜40mm、かつその広がり長さの差が1段
目よりも直径2mm以上大きい熱硬化性粉体塗料を塗装
し、続いてこれらの塗装膜を同時に焼付け硬化させるこ
とを特徴とする熱硬化性粉体塗膜形成方法。
(57) [Claim 1] As a first step, about 0.8 g of a thermosetting powder coating is applied to a surface to be coated in a cylindrical shape having a diameter of 13 mm and a height of about 4 mm in a weight of 30 kg. / mm 2 Press molded at 150 ℃ -1
The average length of the spread when heated for 0 minutes is 1
A thermosetting powder coating material having a thickness of 3 to 25 mm and containing 1 to 19.9 parts by weight of a filler with respect to 100 parts by weight of the thermosetting resin is applied. The spread length of the pressure-molded product measured by the same method is coated with a thermosetting powder coating material having an average diameter of 20 to 40 mm and a difference in the spread length of 2 mm or more larger than the first stage, A thermosetting powder coating film forming method, wherein these coating films are simultaneously baked and cured.
JP17766194A 1994-07-04 1994-07-04 Thermosetting powder coating method Expired - Lifetime JP3368055B2 (en)

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Application Number Priority Date Filing Date Title
JP17766194A JP3368055B2 (en) 1994-07-04 1994-07-04 Thermosetting powder coating method

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JP3368055B2 true JP3368055B2 (en) 2003-01-20

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH11323202A (en) * 1998-05-15 1999-11-26 Nippon Kayaku Co Ltd Epoxy resin-based powder coating composition
JP2001115088A (en) * 1999-10-22 2001-04-24 Sanyo Electric Co Ltd Polyester powder coating
US7550176B2 (en) 2002-12-20 2009-06-23 Kansai Paint Co., Ltd. Method of forming coating film on aluminum substrate
JP4197164B2 (en) * 2004-02-09 2008-12-17 大日本塗料株式会社 Thermosetting powder paint, painted iron-based material, and method for producing painted iron-based material
PT2565240E (en) * 2009-04-03 2014-12-22 Akzo Nobel Coatings Int Bv Powder corrosion and chip-resistant coating
JP5757944B2 (en) 2009-07-29 2015-08-05 アクゾ ノーベル コーティングス インターナショナル ビー ヴィ Powder coating composition capable of having a substantially zinc-free primer
PL2828418T3 (en) 2012-03-21 2022-04-04 Swimc Llc Two-coat single cure powder coating
US9751107B2 (en) 2012-03-21 2017-09-05 Valspar Sourcing, Inc. Two-coat single cure powder coating

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