JPS622640B2 - - Google Patents
Info
- Publication number
- JPS622640B2 JPS622640B2 JP57164415A JP16441582A JPS622640B2 JP S622640 B2 JPS622640 B2 JP S622640B2 JP 57164415 A JP57164415 A JP 57164415A JP 16441582 A JP16441582 A JP 16441582A JP S622640 B2 JPS622640 B2 JP S622640B2
- Authority
- JP
- Japan
- Prior art keywords
- powder
- water
- coating
- electrodeposition
- coating film
- 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 56
- 239000011248 coating agent Substances 0.000 claims description 46
- 238000004070 electrodeposition Methods 0.000 claims description 38
- 239000000843 powder Substances 0.000 claims description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 32
- 239000003973 paint Substances 0.000 claims description 22
- 238000001035 drying Methods 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 15
- 238000010422 painting Methods 0.000 claims description 11
- 238000005406 washing Methods 0.000 claims description 6
- 238000004132 cross linking Methods 0.000 claims description 3
- 125000002091 cationic group Chemical group 0.000 description 12
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000009472 formulation Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 3
- 230000007547 defect Effects 0.000 description 3
- 230000002209 hydrophobic effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 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
- 239000011230 binding agent Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000005342 ion exchange Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- KMOUUZVZFBCRAM-OLQVQODUSA-N (3as,7ar)-3a,4,7,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C=CC[C@@H]2C(=O)OC(=O)[C@@H]21 KMOUUZVZFBCRAM-OLQVQODUSA-N 0.000 description 1
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000036760 body temperature Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 238000007499 fusion processing Methods 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 238000007517 polishing process Methods 0.000 description 1
- 238000011176 pooling Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- -1 slurry coating Substances 0.000 description 1
- 238000007581 slurry coating method Methods 0.000 description 1
- NVKTUNLPFJHLCG-UHFFFAOYSA-N strontium chromate Chemical compound [Sr+2].[O-][Cr]([O-])(=O)=O NVKTUNLPFJHLCG-UHFFFAOYSA-N 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- DVKJHBMWWAPEIU-UHFFFAOYSA-N toluene 2,4-diisocyanate Chemical compound CC1=CC=C(N=C=O)C=C1N=C=O DVKJHBMWWAPEIU-UHFFFAOYSA-N 0.000 description 1
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
Description
【発明の詳細な説明】
本発明はリバース塗装方法、更に詳細には被塗
物の一部を合成樹脂粉体で塗装し、更に被塗物残
部を電着塗料するリバース塗装方法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a reverse coating method, and more particularly to a reverse coating method in which a part of an object to be coated is coated with synthetic resin powder, and the remaining part of the object to be coated is further coated with an electrodeposition coating.
リバース塗装方法は省力、省資源に有効な塗装
方法であり、かつ高防蝕塗装方法であるため、近
年特に自動車車体の塗装分野において注目されて
いる塗装方法である。 The reverse painting method is a painting method that is effective in saving labor and resources, and is a highly corrosion-resistant painting method, so it is a painting method that has been attracting attention in recent years, particularly in the field of painting automobile bodies.
ここにリバース塗装方法では、被塗物の一部を
一般に乾式(静電)粉体(ドライパウダー)、も
しくは湿式粉体(スラリー)塗装または粉体電着
(EPC)塗装をした後、塗膜をその軟化点以上で
かつ架橋硬化させない温度で熱融着させて、不動
性とし、次いで被塗物の他の部分を通常の電着塗
装する方法である。 In the reverse coating method, a part of the object to be coated is generally coated with dry (electrostatic) powder (dry powder), wet powder (slurry), or electrodeposited powder (EPC), and then the coating film is coated. This is a method in which the material is heat-sealed at a temperature above its softening point and at a temperature that does not cause crosslinking and hardening to make it immobile, and then the other parts of the object are coated by regular electrodeposition.
例を自動車車体の塗装にとつて述べれば、
(i) 車体外板部を予め上記粉体を含有する塗料で
厚塗塗装し、この塗膜を熱融着させて、不動性
にして特に防蝕性にすぐれた高性能塗膜を付着
させ、
(ii) その後通常の電着塗装により車体内板部を塗
装している。 For example, when painting an automobile body, (i) the outer panel of the automobile body is coated in advance with a thick coat of paint containing the above-mentioned powder, and this coating film is heat-fused to make it immobile and especially corrosion-resistant. A high-performance paint film with excellent properties is applied, and (ii) the interior of the vehicle is painted using regular electrodeposition coating.
この方法によれば、外板部に厚膜塗装を、容易
にうることができ、更に粉体等が使用できるため
自動車車体の最終塗装までの塗装回数を減じるこ
とができ、しかも良好な品質の塗膜が得られる。
また内板部の電着塗装におけるつきまわり性が良
好である等の利点を有する。 According to this method, it is possible to easily apply a thick film coating to the outer panel, and since powder etc. can be used, it is possible to reduce the number of times of painting up to the final painting of the automobile body, and it is possible to achieve good quality. A coating film is obtained.
It also has advantages such as good throwing power when electrodeposited on the inner plate.
かかるリバース塗装方法においては、被塗物の
一部を上述した粉体含有塗料で塗装した後、次の
電着塗装を行なう前に、上記粉体含有塗料による
塗装部の塗膜を不動性にする必要がある、このた
め通常塗膜を粉体の軟化点以上であるが架橋硬化
させない温度で被塗物に熱融着させる工程が必要
である。次に上記被塗物の他の部分を通常電着塗
装し、水洗工程を経た後、全塗膜を焼付けるため
の焼付乾燥工程に付している。 In such a reverse coating method, after a part of the object to be coated is coated with the above-mentioned powder-containing paint, the coating film on the area coated with the above-mentioned powder-containing paint is made immovable before the next electrodeposition coating. Therefore, a process is usually required to heat-fuse the coating film to the object to be coated at a temperature that is above the softening point of the powder but does not cause crosslinking and hardening. Next, other parts of the object to be coated are usually electrocoated, and after passing through a water washing process, a baking drying process is carried out to bake the entire coating film.
上述したリバース塗装方法において、前段の粉
体含有塗料での塗膜形成後、塗膜を熱融着させた
部分は、この段階で疎水性になつている。このた
め後段の通常電着塗装工程終了後、水洗した後の
水洗水が上記粉体含有塗料によつて形成された塗
膜上に大きな水滴または水溜り状に付着する。こ
のまま最終工程の焼付工程に付した場合、上記水
溜りによる塗膜性能の不具合を生ずることが判つ
た。即ち、水溜り部分が凹状の仕上りを現出し、
塗膜外観を損うこと、また性能的には耐湿性が悪
化することがあることが判つた。 In the reverse coating method described above, after the coating film is formed with the powder-containing paint in the first stage, the portion where the coating film is thermally fused has become hydrophobic at this stage. For this reason, after the subsequent ordinary electrodeposition coating process is completed, the washing water after rinsing adheres in the form of large water droplets or puddles on the coating film formed by the powder-containing coating material. It was found that if the film was subjected to the final baking step as it was, problems would occur in the coating film performance due to the water pooling. In other words, the water puddle area has a concave finish,
It has been found that the appearance of the coating film may be impaired, and that moisture resistance may deteriorate in terms of performance.
この理由は、上述したドライパウダー、スラリ
ー塗装またはEPC塗装では、塗装後熱融着工程
で、塗膜形成成分たる粉体が熱融着すると共に流
動して塗膜の均一平均化をもたらす。この結果塗
膜は被塗物に付着すると共に性能的には疎水性と
なる。この疎水性となつた塗膜に、次の通常電着
および水洗工程で付着した水は、最終焼付乾燥工
程で、その水付着部分の熱伝導を妨げ、塗膜の均
一平滑焼付を局部的に損う。また水分が沸とうし
た状態になつて、粘着化した塗膜の平滑化を妨害
するなどの理由により、最終的に塗膜の不具合を
生ずるものと考えられる。この水による塗膜不具
合は一般に水跡、水滴跡、ウオーターマーク等と
称されている。 The reason for this is that in the dry powder, slurry coating, or EPC coating described above, in the post-painting heat fusion process, the powder, which is a coating film forming component, is heat fused and flows, resulting in a uniform and even coating film. As a result, the coating film adheres to the object being coated and becomes hydrophobic in terms of performance. Water that adheres to this hydrophobic coating film during the next normal electrodeposition and water washing process will interfere with heat conduction in the areas where the water has adhered during the final baking drying process, causing localized areas that prevent uniform and smooth baking of the coating film. Lose. Furthermore, it is thought that the water becomes boiling and obstructs the smoothing of the sticky coating film, which ultimately causes defects in the coating film. This coating film defect caused by water is generally called a water mark, a water drop mark, a water mark, or the like.
リバース塗装方法における上述した水跡の問題
を解消する方法として、粉体含有塗料による塗膜
を焼付硬化させ、その後通常電着塗装する方法が
考えられる。しかしこの場合にも、後段の通常電
着塗装後の塗膜の焼付乾燥は必要であり、二度の
焼付乾燥実施は省エネルギーの点から大きなマイ
ナスである。またかかる中間焼付乾燥を行なうと
前段の粉体塗料による塗膜と、後段の電着塗装塗
膜の境界線が生ずる問題も生ずる。またこの方法
では水跡の解消はできても水分蒸沸による耐湿性
の問題は完全解決できないことが判つた。 As a method for solving the above-mentioned problem of water marks in the reverse coating method, a method can be considered in which a coating film made of a powder-containing paint is cured by baking, and then the coating film is usually subjected to electrodeposition coating. However, even in this case, it is necessary to bake and dry the coating film after the subsequent ordinary electrodeposition coating, and carrying out baking and drying twice is a big disadvantage from the point of view of energy saving. Further, when such intermediate baking drying is performed, a problem arises in that a boundary line is formed between the powder coating film in the first stage and the electrodeposition coating film in the second stage. It was also found that although this method could eliminate water marks, it could not completely solve the problem of moisture resistance caused by water evaporation.
上述した従来のリバース塗装方法の欠点を解消
するため本発明者等は被塗物の一部を粉体塗料に
よる塗膜形成後、粉体の軟点以上でかつ塗膜を硬
化させない温度で熱融着させ、次いで被塗物の他
の部分を通常の電着塗料により塗装し、水洗した
後、粉体の軟化点以下の温度で予備乾燥し、次い
で焼付けすることにより、前記水跡(ウオーター
マーク)の形成を防止しうることを見出したので
ある。 In order to eliminate the drawbacks of the conventional reverse coating method described above, the present inventors applied heat to a part of the object to be coated after forming a coating film using powder coating at a temperature that is above the soft point of the powder and does not harden the coating film. After fusing, the other parts of the object to be coated are painted with ordinary electrocoating paint, washed with water, pre-dried at a temperature below the softening point of the powder, and then baked to remove the water marks. They found that the formation of marks) can be prevented.
また本発明方法によれば、通常電着塗装後の焼
付乾燥炉内に打ち込まれる水分量が減少するた
め、該炉内で発生するヤニダレによる塗装不具合
の発生も防止しうる。 Furthermore, according to the method of the present invention, since the amount of water that is normally introduced into the baking drying oven after electrodeposition coating is reduced, it is possible to prevent coating defects due to tar sag that occurs in the oven.
なお本発明方法で使用しうる粉体電着塗料とし
ては例えば特公昭51―40585号、粉体塗料として
は特開昭48―29836号、湿式粉体塗料としては特
公昭55―50514号を参照しうる。また通常電着塗
料としては公知の任意のものを使用しうる。 For powder electrodeposition paints that can be used in the method of the present invention, see, for example, Japanese Patent Publication No. 51-40585, for powder paints see Japanese Patent Publication No. 48-29836, and for wet powder paints see Japanese Patent Publication No. 55-50514. I can do it. Further, any known electrodeposition paint can be used as the electrodeposition paint.
以下に実施例を記す。ここでいう部および%は
全て重量基準である。なお本発明はこれら実施例
に限定されるものではない。 Examples are described below. All parts and percentages herein are by weight. Note that the present invention is not limited to these Examples.
実施例 1
カチオン性水分散樹脂の調製:
エピコート#1001(シエル社製) 488部
イソプロピルアルコール 250〃
デイエタノールアミン 105〃
乳 酸 76.5〃
イオン交換水 1057〃
上記の配合によるアミン付加有機酸中和のエポ
キシ系カチオン性電着樹脂A固型分30%のバイン
ダーを得た。Example 1 Preparation of cationic water-dispersed resin: Epicote #1001 (manufactured by Ciel) 488 parts Isopropyl alcohol 250〃 Diethanolamine 105〃 Lactic acid 76.5〃 Ion exchange water 1057〃 Amine-added organic acid neutralization using the above formulation A binder with a solid content of epoxy cationic electrodeposition resin A of 30% was obtained.
粉体塗料の調製:
エピコート#1004(シエル社製) 40部
アダクトB―1065(ヒユルス社製) 30〃
酸化チタンR―550(石原産業社製) 19〃
カオリンASP―200(林化成社製) 10〃
カーボンブラツクMA―100(三菱化成社
製) 1〃
ベンゾイン 0.5〃
上記の配合によるイソシアネート硬化エポキシ
系熱硬化粉体塗料をプレミツクス、熱混練、冷
却、粗粉砕、微粉砕の工程をとる常法に従つて調
製した。 Preparation of powder coatings: Epicote #1004 (manufactured by Ciel) 40 parts Adduct B-1065 (manufactured by Hyurus) 30〃 Titanium oxide R-550 (manufactured by Ishihara Sangyo Co., Ltd.) 19〃 Kaolin ASP-200 (manufactured by Hayashi Kasei Co., Ltd.) 10〃 Carbon Black MA-100 (manufactured by Mitsubishi Kasei Corporation) 1〃 Benzoin 0.5〃 A conventional method that involves premixing the isocyanate-cured epoxy thermosetting powder coating with the above formulation, heat kneading, cooling, coarse pulverization, and fine pulverization. Prepared according to.
上記粉体塗料8.48トンと、上記カチオン性電着
樹脂Aのバインダー21.70トンと、イオン交換水
69.82トンとにより固型分濃度15%、PH5.3の粉体
電着塗料浴液100トンを調製、建浴した。 8.48 tons of the above powder coating, 21.70 tons of the above cationic electrodeposition resin A binder, and ion-exchanged water.
100 tons of powder electrodeposition paint bath liquid with solid content concentration of 15% and pH of 5.3 was prepared using 69.82 tons of liquid.
カチオン性電着塗料の調製:
エピコート#1001(シエル社製) 1000部
テトラヒドロ無水フタル酸 304〃
ヒドロキシエチルメタアクリレート 260〃
セロソルブアセテート 919.7〃
デイエチルエタノールアミン 234〃
トリレンデイイソシアネート 348〃
ハイドロキノン 10〃
トリエチルアミン 3〃
ギ 酸 49.4〃
上記の配合に基づいて、常法により調製された
固型分70%のカチオン性樹脂Bを得た。 Preparation of cationic electrodeposition paint: Epicote #1001 (manufactured by Ciel) 1000 parts Tetrahydrophthalic anhydride 304〃 Hydroxyethyl methacrylate 260〃 Cellosolve acetate 919.7〃 Diethylethanolamine 234〃 Tolylene diisocyanate 348〃 Hydroquinone 10〃 Triethylamine 3 Formic acid 49.4 Based on the above formulation, a cationic resin B having a solid content of 70% was prepared by a conventional method.
カチオン性樹脂B 50部
酸化チタン 7〃
カーボンブラツク 0.75〃
ストロンチウムクロメート 0.3〃
ケイ酸鉛 0.7〃
イオン交換水 87.1〃
上記の配合によつてプレミツクス、ボールミル
分散、レツトダウンなる常法工程のもとにカチオ
ン性電着塗料固型分30%を得た。 Cationic resin B 50 parts Titanium oxide 7〃 Carbon black 0.75〃 Strontium chromate 0.3〃 Lead silicate 0.7〃 Ion-exchanged water 87.1〃 Cationicity can be obtained by using the above-mentioned formulation under the conventional process of premix, ball mill dispersion, and letdown. An electrodeposition paint with a solid content of 30% was obtained.
上記カチオン性電着塗料90トンとイオン交換水
90トンとにより固型分濃度15%、PH6.0のカチオ
ン性電着塗料180トンを調製、建浴した。 90 tons of the above cationic electrodeposition paint and ion exchange water
180 tons of cationic electrodeposition paint with a solid content concentration of 15% and a pH of 6.0 were prepared using 90 tons of paint.
燐酸亜鉛処理を施した1800c.c.排気量、被塗面積
70m2の自動車車体をコンベアースピード4m、ボ
デイピツチ5.5mにて、上記粉体電着塗料浴液100
トン中にて、電着温度25℃、極間距離60cm、電着
時間15〜30秒電着電圧500Vなる条件により、カ
チオン性粉体電着塗装を行なつた。 1800 c.c. displacement with zinc phosphate treatment, coated area
A 70m2 car body was coated with the above powder electrodeposition paint bath solution at a conveyor speed of 4m and a body pitch of 5.5m.
Cationic powder electrodeposition coating was carried out in a vacuum chamber under the following conditions: electrodeposition temperature: 25° C., distance between electrodes: 60 cm, electrodeposition time: 15 to 30 seconds, and electrodeposition voltage: 500 V.
続いて、水洗し、3分間の水切セツテイングの
後、80〜85℃の雰囲気にて、約10分間の水切乾燥
炉を通過せしめた。外板部は不動体化しているこ
とが確認された。 Subsequently, the sample was washed with water, drained and set for 3 minutes, and then passed through a drain drying oven for about 10 minutes in an atmosphere of 80 to 85°C. It was confirmed that the outer panel was immobile.
次に、上記カチオン性電着塗料浴液180トン中
にて、電着温度25℃、極間距離50cm、全没電着時
間120秒、電着電圧250Vなる条件により、粉体電
着塗装されていない室内部、袋部、隙間部を通電
入槽方式でカチオン性電着塗装し、続いて水洗し
た。 Next, the powder was electrodeposited in 180 tons of the above cationic electrodeposition paint bath solution under the following conditions: electrodeposition temperature 25℃, electrode distance 50cm, total electrodeposition time 120 seconds, electrodeposition voltage 250V. The interior of the room, bags, and gaps that were not covered were coated with cationic electrodeposition using an energized tank method, and then washed with water.
上記の如くして粉体電着およびカチオン性電着
塗装された自動車車体を通過時間8分、1500m3/
分、60mmAq、50KWの循環フアン、150×
104Kcal/Hrのバーナー熱量、300m3/分、30mm
Aq、7.5KWの排気フアン、前後に各3mのエア
カーテンゾーンを持つ実効長35m、容積315m3、
炉温は70〜75゜の水切乾燥炉を通過させた。 Passage time 8 minutes, 1500m 3 /
min, 60mmAq, 50KW circulation fan, 150×
Burner heat capacity of 10 4 Kcal/Hr, 300m 3 /min, 30mm
Aq, 7.5KW exhaust fan, effective length 35m with 3m front and rear air curtain zones, volume 315m3 ,
It was passed through a drain drying oven with a furnace temperature of 70 to 75°.
水切乾燥炉から出炉させて後約1mの開放空間
を移動させた後、雰囲気温度185〜190℃、滞炉時
間25分の焼付乾燥炉に導入し、自動車車体の外板
に塗装された粉体電着塗膜および、内板に塗装さ
れたカチオン電着塗膜を同時に焼付硬化した。こ
の時の焼付乾燥炉の仕様は1000m3/分、70mm
Aq、25KWの循環フアン、110×104Kcal/Hrの
バーナー熱量、105m3/minのバーナーブロア、
60m3/分、30mmAq、1.5KWの排気フアンを3系
列具備するものであり、前後に各3mのエアカー
テンゾーンを持つ実効長90m、容積810m3であつ
た。 After being taken out of the drain drying oven and moved through an open space of approximately 1 m, the powder was introduced into a baking drying oven with an ambient temperature of 185 to 190°C and a residence time of 25 minutes. The electrodeposition coating film and the cationic electrodeposition coating film applied to the inner plate were simultaneously baked and cured. The specifications of the baking drying oven at this time are 1000m3 /min, 70mm
Aq, 25KW circulation fan, 110×10 4 Kcal/Hr burner heat, 105m 3 /min burner blower,
It was equipped with three sets of 60m 3 /min, 30mmAq, 1.5KW exhaust fans, and had an effective length of 90m and a volume of 810m 3 with air curtain zones of 3m each at the front and rear.
焼付塗装された粉体電着塗装塗膜表面に“水滴
あと”、“ウオーターマーク”等のトラブルは全く
認められなかつた。 No problems such as "water droplets" or "water marks" were observed on the surface of the baked powder electrodeposition coating.
比較例 1
実施例1に見る、通常電着水洗後の水切乾燥炉
を設置せず、他の条件はすべて実施例1と同様の
塗装工程を使用して、自動車塗装した。ボデー外
板部に多くのウオーターマークが認められ、良好
な外観を得るために研磨工程を要した。Comparative Example 1 An automobile was painted using the same painting process as in Example 1, except that the draining and drying oven after regular electrodeposition washing was not installed, and all other conditions were the same as in Example 1. Many water marks were observed on the exterior of the body, and a polishing process was required to obtain a good appearance.
実施例 2
実施例1に見る粉体塗料を平均粒径25μに粉砕
し、常法によりボデー外板部に50μになるように
静電塗装した。ボデーの大きさ、形状、コンベア
スピード、ボデーピツチ等は実施例1と同様であ
つた。外板部を不動体化するための乾燥は、ボデ
ー温度で170゜×10分であつた。この後ボデーは
実施例1と同条件で、電着、水洗、水切乾燥、本
焼付乾燥された。外板部仕上りは良好であつた。Example 2 The powder coating shown in Example 1 was pulverized to an average particle size of 25 μm, and electrostatically applied to the outer panel of a body to a particle size of 50 μm using a conventional method. The size, shape, conveyor speed, body pitch, etc. of the body were the same as in Example 1. Drying to make the outer panel part immobile was carried out at a body temperature of 170° for 10 minutes. Thereafter, the body was subjected to electrodeposition, washing with water, draining and drying, and final baking drying under the same conditions as in Example 1. The finish on the outer panel was good.
比較例 2
実施例2と、水切乾燥炉を使用しないこと以外
は、すべて同様にリバース塗装を実施した。ボデ
ー外板部に多くのウオーターマークが認めれら
た。Comparative Example 2 Reverse painting was carried out in the same manner as in Example 2, except that the drain drying oven was not used. Many water marks were observed on the outer panel of the body.
Claims (1)
体電着塗料により塗装した後、塗膜を粉体の軟化
点以上でかつ架橋硬化させない温度で熱融着さ
せ、次いで被塗物の他の部分を通常の電着塗料に
より塗装し、水洗し、次いで焼付けを行なうリバ
ース塗装方法において、上記水洗の後で焼付けを
行なう前に粉体の軟化点以下の温度で粉体塗膜を
予備乾燥することを特徴とするリバース塗装方
法。1 After coating a part of the object to be coated with powder, wet powder, or powder electrodeposition paint, the coating film is heat-fused at a temperature above the softening point of the powder but not crosslinking and hardening, and then the object to be coated is In the reverse coating method, in which other parts of the body are painted with ordinary electrodeposition paint, washed with water, and then baked, a powder coating film is applied at a temperature below the softening point of the powder after washing with water and before baking. A reverse painting method characterized by preliminary drying.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16441582A JPS5953694A (en) | 1982-09-21 | 1982-09-21 | Reverse coating method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP16441582A JPS5953694A (en) | 1982-09-21 | 1982-09-21 | Reverse coating method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5953694A JPS5953694A (en) | 1984-03-28 |
JPS622640B2 true JPS622640B2 (en) | 1987-01-21 |
Family
ID=15792707
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP16441582A Granted JPS5953694A (en) | 1982-09-21 | 1982-09-21 | Reverse coating method |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5953694A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6431919U (en) * | 1987-08-20 | 1989-02-28 | ||
JPH0546673Y2 (en) * | 1988-01-18 | 1993-12-07 |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS62263999A (en) * | 1986-05-09 | 1987-11-16 | Suzuki Motor Co Ltd | Painting method by electrodeposition |
WO2002002849A2 (en) * | 2000-06-29 | 2002-01-10 | Ppg Industries Ohio, Inc. | Methods for electrocoating a metallic substrate with a topcoat and articles produced thereby |
US6531043B1 (en) * | 2000-06-29 | 2003-03-11 | Ppg Industries Ohio, Inc. | Methods for electrocoating a metallic substrate with a primer-surfacer and articles produced thereby |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4860728A (en) * | 1971-12-03 | 1973-08-25 | ||
JPS49102748A (en) * | 1972-12-31 | 1974-09-27 | ||
JPS5597497A (en) * | 1979-01-19 | 1980-07-24 | Honda Motor Co Ltd | Drying and baking of paint film formed by powder electrodeposition coating method |
JPS5620359A (en) * | 1979-07-27 | 1981-02-25 | Fujitsu Ltd | Telegram relay system |
-
1982
- 1982-09-21 JP JP16441582A patent/JPS5953694A/en active Granted
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4860728A (en) * | 1971-12-03 | 1973-08-25 | ||
JPS49102748A (en) * | 1972-12-31 | 1974-09-27 | ||
JPS5597497A (en) * | 1979-01-19 | 1980-07-24 | Honda Motor Co Ltd | Drying and baking of paint film formed by powder electrodeposition coating method |
JPS5620359A (en) * | 1979-07-27 | 1981-02-25 | Fujitsu Ltd | Telegram relay system |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6431919U (en) * | 1987-08-20 | 1989-02-28 | ||
JPH0546673Y2 (en) * | 1988-01-18 | 1993-12-07 |
Also Published As
Publication number | Publication date |
---|---|
JPS5953694A (en) | 1984-03-28 |
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