JPH0366030B2 - - Google Patents
Info
- Publication number
- JPH0366030B2 JPH0366030B2 JP15679183A JP15679183A JPH0366030B2 JP H0366030 B2 JPH0366030 B2 JP H0366030B2 JP 15679183 A JP15679183 A JP 15679183A JP 15679183 A JP15679183 A JP 15679183A JP H0366030 B2 JPH0366030 B2 JP H0366030B2
- Authority
- JP
- Japan
- Prior art keywords
- paint
- coating
- powder
- parts
- 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
- 239000003973 paint Substances 0.000 claims description 78
- 238000000576 coating method Methods 0.000 claims description 60
- 239000011248 coating agent Substances 0.000 claims description 48
- 239000000843 powder Substances 0.000 claims description 35
- 238000004070 electrodeposition Methods 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000007787 solid Substances 0.000 claims description 6
- 229920003002 synthetic resin Polymers 0.000 claims description 5
- 239000000057 synthetic resin Substances 0.000 claims description 5
- 238000004132 cross linking Methods 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 239000000155 melt Substances 0.000 claims description 3
- 239000002659 electrodeposit Substances 0.000 claims description 2
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 description 11
- 229920005989 resin Polymers 0.000 description 11
- 239000011347 resin Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 10
- 238000010422 painting Methods 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000006229 carbon black Substances 0.000 description 6
- 239000000428 dust Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 239000011230 binding agent Substances 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 4
- 238000007796 conventional method Methods 0.000 description 4
- 239000003822 epoxy resin Substances 0.000 description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 4
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 3
- 206010010904 Convulsion Diseases 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000004640 Melamine resin Substances 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 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 2
- 229910000165 zinc phosphate Inorganic materials 0.000 description 2
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229910002012 Aerosil® Inorganic materials 0.000 description 1
- 229910002016 Aerosil® 200 Inorganic materials 0.000 description 1
- 229920003270 Cymel® Polymers 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000002174 Styrene-butadiene Substances 0.000 description 1
- IBVAQQYNSHJXBV-UHFFFAOYSA-N adipic acid dihydrazide Chemical compound NNC(=O)CCCCC(=O)NN IBVAQQYNSHJXBV-UHFFFAOYSA-N 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000007664 blowing Methods 0.000 description 1
- MTAZNLWOLGHBHU-UHFFFAOYSA-N butadiene-styrene rubber Chemical compound C=CC=C.C=CC1=CC=CC=C1 MTAZNLWOLGHBHU-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- NCEXYHBECQHGNR-UHFFFAOYSA-N chembl421 Chemical compound C1=C(O)C(C(=O)O)=CC(N=NC=2C=CC(=CC=2)S(=O)(=O)NC=2N=CC=CC=2)=C1 NCEXYHBECQHGNR-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000012972 dimethylethanolamine Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000009503 electrostatic coating Methods 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 238000007591 painting process Methods 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 238000010298 pulverizing process Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000007581 slurry coating method Methods 0.000 description 1
- 238000007592 spray painting technique Methods 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
【発明の詳細な説明】
本発明の自動車車体の新規な下塗り塗装方法に
関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a novel method for undercoating an automobile body.
現在実用されている通常の自動車車体の塗装方
法は、まず(イ)車体全体を防錆を目的としたアニオ
ン系またはカチオン系のイオン性塗料による電着
塗装を施し、形成された塗膜を焼付硬化し、次に
(ロ)サイドシールの外側部あるいはドアの下部から
サイドシールまでの部位に耐チツピングを目的と
したいわゆるガードコート用塗料をスプレー塗装
し、形成された塗膜を焼付硬化後(ハ)車体の外板部
に上塗り塗装したときの仕上り美観を与えかつ膜
厚保持を目的とした中塗り塗料を塗装し、必要に
応じこれを風乾後(ニ)ドアサツシ部にデザインを目
的としたドアサツシ用塗料をスプレー塗装し、形
成された塗膜を前工程の中塗り塗膜と同時に焼付
硬化して下塗り塗装(中塗りを含む)をしてい
る。そして最後に(ホ)車体外板部に上塗り塗料を塗
装し形成された塗膜を焼付硬化する工程がとられ
ている。 The usual method of painting car bodies currently in use is (a) first applying electrodeposition coating to the entire car body with an anionic or cationic ionic paint for the purpose of rust prevention, and then baking the formed coating film. harden and then
(b) Spray a so-called guard coating paint for the purpose of chipping resistance on the outside of the side seal or the area from the bottom of the door to the side seal, and after hardening the formed coating film (c) Exterior of the vehicle body. Apply an intermediate coat of paint to give the board a beautiful finish and maintain the film thickness when the top coat is applied, and if necessary, after air-drying this, spray a door sash paint for design purposes on the (d) door sash area. The resulting coating film is baked and cured at the same time as the intermediate coating film in the previous step to form an undercoat (including intermediate coating). Finally, a step (e) of applying a top coat to the outer panel of the vehicle body and curing the formed coating film is performed.
このように従来の自動車車体の上塗り塗装前の
下塗り塗装(中塗り塗装を含む)では4回の塗装
工程と3回の焼付工程を経て行なわれており、塗
装回数および焼付回数が多い等工程が煩雑なう
え、さらに前記(ニ)のドアサツシ用塗料および前記
(ロ)のガードコート用塗料は前記(イ)の電着塗膜の焼
付後に塗装されるため、これらの塗装時のダスト
が焼付塗膜上に付着して、塗膜上に凹凸が生ぜし
め最終塗膜の外観に影響を与える欠点を有してい
た。このため上記ダストの付着をきらうその他の
部位をシールしてからこれらの塗料を塗装しなけ
ればならず生産性および経済性の点で問題があつ
た。 In this way, conventional undercoat painting (including intermediate coat painting) before topcoat painting of automobile bodies is done through four painting processes and three baking processes. In addition to being complicated, the above (d) door sash paint and the above
Since the guard coat paint in (b) is applied after baking the electrodeposited film in (a) above, the dust from these coatings adheres to the baked paint film, causing unevenness on the paint film. It had drawbacks that affected the appearance of the final coating. For this reason, it is necessary to apply these paints after sealing other parts where the dust should not adhere, which poses problems in terms of productivity and economy.
本発明者らは前記の如き実情に鑑み鋭意研究の
結果上塗り塗装以前の下塗り塗装工程において従
来の工程をきわめて簡素化できる塗装方法を見い
出し本発明を完成したものである。 In view of the above-mentioned circumstances, the inventors of the present invention have conducted extensive research and have found a coating method that can greatly simplify the conventional process in the undercoating process prior to topcoating, and have completed the present invention.
すなわち本発明は、自動車車体の下塗り塗装系
において、まず(1)車体全体を常温で固体であり、
加熱すると溶融する合成樹脂微粉体を含有する塗
料(粉体系塗料)を塗装し、形成された塗膜を該
塗膜の溶融を生ぜしめるが、架橋硬化を生ぜしめ
ない温度で加熱しあるいは加熱をせずに次に(2)上
記(1)の塗装で塗装されなかつた部分をイオン性塗
料(電着塗料)で電着塗装し、形成された塗膜を
水洗後エアブローあるいは水切乾燥しその後(3)ド
アサツシ部をドアサツシ用塗料でおよび/または
(4)サイドシール部をガードコート用塗料で塗装
し、しかる後(1)〜(4)で形成した各塗膜を同時に焼
付硬化する自動車車体の下塗り塗装方法を提供す
るものである。 In other words, the present invention provides an undercoat coating system for an automobile body, in which (1) the entire automobile body is solid at room temperature;
A coating containing synthetic resin fine powder that melts when heated (powder-based coating) is applied, and the coating film formed is heated at a temperature that causes the coating film to melt but does not cause crosslinking and hardening. (2) Electrodeposit the parts that were not painted in (1) above with ionic paint (electrodeposition paint), wash the formed coating film with water, then air blow or drain and dry. 3) Paint the door sash with door sash paint and/or
(4) The present invention provides a method for undercoating an automobile body, in which the side seal portion is coated with a guard coating paint, and then each coating film formed in (1) to (4) is baked and cured at the same time.
本発明において前記(1)の工程は主に車体の外板
部に下塗り塗料と中塗り塗料の性能を兼備した性
能の優れた粉体系塗料を適用するものであり、こ
れにより下塗りとしては1回でよく、2回以上の
重ね塗り、すなわち中塗りを必要としない。 In the present invention, the step (1) above is mainly to apply a powder-based paint with excellent performance that has both the performance of an undercoat and an intermediate paint to the outer panel of the car body, so that it can be applied once as an undercoat. It does not require two or more overcoatings, that is, intermediate coatings.
また粉体系塗料はその低公害性、厚膜に塗装し
うる作業性、すぐれた塗膜性能などから好ましい
塗料である。かかる粉体系塗料としては、静電粉
体塗装、流動浸漬塗装法などで使用される乾式粉
体塗料、イオン性バインダー樹脂水溶液中に合成
樹脂微粉体を分散した電着塗装方法で用いられる
粉体電着塗料および静電あるいはスプレー塗装方
法で用いられる湿式粉体塗料(スラリー塗料)な
ど公知の塗料を使用できる。これらの塗料および
塗装方法はそれぞれ一長一短を有するものである
が前記した粉体系塗料の特長は共有する。 Powder-based paints are preferred because of their low pollution properties, workability that allows thick film coating, and excellent coating performance. Examples of such powder coatings include dry powder coatings used in electrostatic powder coating and fluidized dipping coating methods, and powders used in electrodeposition coating methods in which fine synthetic resin powder is dispersed in an aqueous solution of an ionic binder resin. Known paints such as electrodeposition paints and wet powder paints (slurry paints) used in electrostatic or spray painting methods can be used. Although these paints and coating methods each have their own advantages and disadvantages, they share the characteristics of the powder-based paints described above.
上記の粉体系塗料はその種類により塗料の形
態、塗装方法において差異はあるが、いずれも常
温では固体であり、加熱すれば溶融する合成樹脂
微粉体を必須成分として含むものであり、それぞ
れ公知の適当な方法で塗装し、塗着された塗料は
塗膜の熱溶融を生ずる温度条件域で、しかも塗膜
に架橋反応を生じない温度条件(例えば70〜150
℃×5〜20分)で加熱するか、あるいは前記の如
き加熱を全く行なわずに次の(2)イオン性塗料によ
る電着塗装工程に移工する。 The above powder-based paints differ in their form and coating method depending on their type, but all of them contain as an essential component synthetic resin fine powder that is solid at room temperature and melts when heated, and each is a well-known method. It is applied by an appropriate method, and the applied paint is kept under temperature conditions that cause thermal melting of the coating film, but that do not cause crosslinking reactions in the coating film (for example, 70 to 150℃).
℃ x 5 to 20 minutes), or proceed to the next (2) electrodeposition coating step using an ionic paint without performing any heating as described above.
この工程は前工程において粉体系塗料が充分に
塗装されなかつた部分および塗り残した未塗装部
分(主に車体の内部)に下塗りとしてのイオン性
塗料を電着塗装する工程であり、使用されるイオ
ン性塗料としては公知のアニオン系、カチオン系
いずれの電着塗料も使用しうる。 This process is a process in which an ionic paint is electro-deposited as an undercoat on areas where the powder-based paint was not sufficiently applied in the previous process and unpainted areas (mainly inside the car body). As the ionic paint, any known anionic or cationic electrodeposition paint can be used.
ここで塗装された電着塗膜は水洗後エアブロー
あるいは水切乾燥(例えば50〜100℃×5〜15分)
し、その後(3)ドアサツシ部にメラミン−アルキド
樹脂系溶剤型塗料、アクリル−メラミン樹脂系水
溶性塗料、ポリエステル樹脂系スラリー塗料等か
らなる公知のドアサツシ用塗料で、および/また
は(4)サイドシールの外側部あるいはドアの下部か
らサイドシール部までの部位に公知のポリオール
樹脂系溶剤型塗料、エマルジヨン系塗料、エポキ
シ樹脂系スラリー塗料等のガードコート用塗料を
スプレー等にて塗装する。 The electrodeposited film applied here is washed with water and then air blown or drained and dried (e.g. 50-100℃ x 5-15 minutes)
Then, (3) coat the door sash with a known door sash paint such as melamine-alkyd resin solvent-based paint, acrylic-melamine resin water-soluble paint, polyester resin slurry paint, etc., and/or (4) apply side seals. Apply a guard coat paint such as a known polyol resin solvent-based paint, emulsion paint, or epoxy resin slurry paint to the outside part of the door or the area from the bottom of the door to the side seal part by spraying or the like.
しかる後(1)〜(4)で形成した粉体系塗料塗膜、電
着塗料塗膜、ドアサツシ用塗料塗膜、ガードコー
ト用塗料塗膜の各塗膜を同時に一つの炉で焼付硬
化し下塗り塗装を完了する。 After that, the powder-based paint film, electrodeposited paint film, door sill paint film, and guard coat paint film formed in steps (1) to (4) are baked and cured simultaneously in one oven to form an undercoat. Finish painting.
焼付硬化工程は使用する各塗料の種類、被塗物
の形状などにより異なるが、一般的には170〜200
℃で30分〜10分間熱風炉を通過させることにより
行なう。 The baking hardening process varies depending on the type of paint used and the shape of the object to be coated, but generally it is 170 to 200
This is done by passing through a hot air oven for 30 to 10 minutes at °C.
以上説明したように自動車車体の下塗り塗装系
において本発明の方法を採用した場合従来にくら
べ焼付回数はわずか1回でよく、さらにドアサツ
シ用塗料およびガードコート用塗料の塗装時にダ
ストを生じても、その前の(1)および(2)の塗装によ
る塗膜が焼付硬化していないため、これが凹凸を
生ぜしめることがないのでシールが不要となり生
産性および経済性が大幅に向上することが判つ
た。 As explained above, when the method of the present invention is adopted in the undercoat coating system of an automobile body, the number of baking steps is only one compared to the conventional method, and furthermore, even if dust is generated during the application of door sash paint and guard coat paint, Since the coating film from the previous coatings (1) and (2) has not been baked and hardened, it does not create any unevenness, making seals unnecessary and it has been found that productivity and economic efficiency are greatly improved. .
以下実施例により本発明を詳細に説明する。 The present invention will be explained in detail below with reference to Examples.
実施例 1 粉体電着塗装溶液は次の如くして作つた。Example 1 A powder electrodeposition coating solution was prepared as follows.
水稀釈性カチオン性樹脂は、エピコート#1001
(シエル社製エポキシ樹脂商品名)488部、ジエタ
ノールアミン105部、イソプロピルアルコール250
部を80〜85℃で3時間還流下に反応させて、液状
のアミノエポキシ樹脂を得た。 Water-dilutable cationic resin is Epicote #1001
(Product name of epoxy resin manufactured by Ciel) 488 parts, diethanolamine 105 parts, isopropyl alcohol 250 parts
A portion of the mixture was reacted under reflux at 80-85°C for 3 hours to obtain a liquid aminoepoxy resin.
また合成樹脂微粉体としてはエピコート#1004
(シエル社製エポキシ樹脂商品名)400部、アダク
トB−1065(フエバ社製ブロツクイソシアネート
商品名)300部、酸化チタンR−550(石原産業社
製)290部およびカーボンブラツクMA−100(三
菱化成社製)10部を粉体塗料製造の常法により、
エクストルーダーで溶融混練し、衝撃式粉砕機で
粉砕し平均粒径7μのエポキシ樹脂を主体とする
微粉体を得た。 Also, as a synthetic resin fine powder, Epicoat #1004
(epoxy resin trade name manufactured by Ciel Corporation) 400 parts, Adduct B-1065 (blocked isocyanate trade name manufactured by Fueva Corporation) 300 parts, titanium oxide R-550 (manufactured by Ishihara Sangyo Co., Ltd.) 290 parts, and Carbon Black MA-100 (Mitsubishi Kasei Co., Ltd.) Co., Ltd.) 10 parts by the conventional method of powder coating manufacturing.
The mixture was melted and kneaded using an extruder and pulverized using an impact pulverizer to obtain a fine powder mainly composed of epoxy resin with an average particle size of 7 μm.
バインダーとしての前記水稀釈性カチオン性樹
脂143部に氷酢酸6.2部および脱イオン水500部を
加えデイゾルバーで充分撹拌し、次いで前記微粉
体の280部を加えデイゾルバーで30分間撹拌混合
し、分散させた後固形分15重量%なるまで脱イオ
ン水で稀釈した。 Add 6.2 parts of glacial acetic acid and 500 parts of deionized water to 143 parts of the water-dilutable cationic resin as a binder, stir well with a dissolver, then add 280 parts of the fine powder and stir and mix with a dissolver for 30 minutes to disperse. It was then diluted with deionized water to a solids content of 15% by weight.
この浴液の特数はPH5.2、微粉体/バインダー
樹脂の比は2.8/1であつた。 This bath liquid had a pH of 5.2 and a fine powder/binder resin ratio of 2.8/1.
カチオン電着浴は次の如くして調製した。 A cationic electrodeposition bath was prepared as follows.
エピコート#1004 336部、エピコート#1001
143部、エチルセロソルブ140部を混合撹拌し完全
に溶解させる。50℃に昇温し、ジエタノールアミ
ン59部、イソプロピルアルコール20部の溶液を1
時間かけて撹拌下に投入した。投入後80〜85℃に
3時間保持した。アダクトB−1065 202部、エチ
ルセロソルブ100部を、上記に撹拌下に30分かけ
て投入し、更に1時間30分、80〜85℃に保持しア
ミノエポキシイソシアネート樹脂をえた。 Epicote #1004 336 copies, Epicote #1001
Mix and stir 143 parts of ethyl cellosolve and 140 parts of ethyl cellosolve to completely dissolve. Raise the temperature to 50℃ and add 1 part of a solution of 59 parts of diethanolamine and 20 parts of isopropyl alcohol.
The mixture was added to the mixture over a period of time with stirring. After charging, the temperature was maintained at 80-85°C for 3 hours. 202 parts of Adduct B-1065 and 100 parts of ethyl cellosolve were added to the above solution over 30 minutes with stirring, and the mixture was further maintained at 80 to 85°C for 1 hour and 30 minutes to obtain an aminoepoxy isocyanate resin.
前記カチオン性樹脂を用いて電着塗料製造の常
法により中和剤として酢酸、顔料として酸化チタ
ンおよびカーボンブラツクを使用して製造し純水
で所定濃度まで稀釈してカチオン性電着浴を得
た。その浴液の特数はPH5.4、灰分25重量%、中
和度7.5%、加熱残分13重量%であつた。 A cationic electrodeposition bath was obtained by using the above cationic resin and using acetic acid as a neutralizing agent and titanium oxide and carbon black as pigments by a conventional method for producing electrodeposition paints, and diluting it with pure water to a predetermined concentration. Ta. The bath liquid had a pH of 5.4, an ash content of 25% by weight, a degree of neutralization of 7.5%, and a heating residue of 13% by weight.
ドアサツシ用塗料は次の如くして調製した。 A paint for door sills was prepared as follows.
アクリル樹脂(日本解媒化学社製商品名アロン
#76)290部、メラミン樹脂(ユニオン・カーバ
イド・アンド・カーボン社製商品名サイメル
#300)30部、ジメチルエタノールアミン30部、
カーボンブラツク40部、体質顔料(日本アエロジ
ル社製商品名アエロジル200)15部、溶剤(ブチ
ルカービトール)5部、水155部を塗料製造の常
法により均一に混合分散しドアサツシ用塗料を得
た。 290 parts of acrylic resin (trade name Aron #76 manufactured by Nippon Kaihatsu Kagaku Co., Ltd.), 30 parts of melamine resin (trade name Cymel #300 manufactured by Union Carbide & Carbon Co., Ltd.), 30 parts of dimethylethanolamine,
40 parts of carbon black, 15 parts of extender pigment (trade name: Aerosil 200, manufactured by Nippon Aerosil Co., Ltd.), 5 parts of solvent (butyl carbitol), and 155 parts of water were uniformly mixed and dispersed using a conventional paint manufacturing method to obtain a paint for door sills. .
塗装する自動車車体はリン酸亜鉛化成処理後純
水で充分に洗浄し常法により水切乾燥を行なつ
た。この車体を前記粉体電着塗装浴中に浸漬し車
体を陰極として直流を通し粉体電着塗装を行なつ
た。 After the car body to be painted was subjected to zinc phosphate chemical conversion treatment, it was thoroughly washed with pure water and drained and dried in a conventional manner. This car body was immersed in the powder electrodeposition coating bath, and a direct current was passed through the car body using the car body as a cathode to perform powder electrodeposition coating.
塗装条件は電圧500V、通電時間17秒、浴液温
度25℃、極間距離(最小)60cmであた。 The coating conditions were a voltage of 500 V, a current application time of 17 seconds, a bath temperature of 25°C, and a minimum distance between electrodes of 60 cm.
粉体電着塗装終了後充分に水洗を行ない、80℃
〜100℃で10分間水切乾燥を行なつた後、前記カ
チオン電着塗装浴中に浸漬し電着塗装を行なつ
た。塗装条件は電圧250V、通電時間(通電開始
より出槽まで)180秒、浴液温度28℃、極間距離
60cmであつた。 After finishing powder electrodeposition coating, thoroughly rinse with water and heat to 80℃.
After draining and drying at ~100°C for 10 minutes, it was immersed in the cationic electrodeposition coating bath to perform electrodeposition coating. The painting conditions are voltage 250V, energization time (from the start of energization to tank removal) 180 seconds, bath temperature 28℃, distance between electrodes.
It was 60cm long.
出槽後充分水洗を行ないドアサツシ部の水分を
エアブローにより飛ばし、ドアサツシ用塗料をス
プレー塗装し、80〜100℃で水切乾燥を行なつた
後、形成された粉体電着塗膜、カチオン電着塗膜
およびドアサツシ用塗料塗膜の全塗膜を同時に同
一炉内で190℃で20分焼付けして架橋硬化させた。
以後は通常の方法で上塗りを行ない車体の塗装を
完了した。 After taking out the tank, thoroughly wash with water, remove moisture from the door sash by air blowing, spray paint for door sash, drain and dry at 80 to 100℃, then form powder electrodeposition coating and cationic electrodeposition. All the paint films and the door sash paint film were baked simultaneously in the same oven at 190°C for 20 minutes to crosslink and harden them.
After that, the car body was painted using the usual method.
この方法は従来の塗装方法にくらべ工数は約2
分の1となり、また焼付回数の減少による効果は
燃料に換算して約30〜40%減の省資源となつた。 This method requires approximately 2 man-hours compared to the conventional painting method.
The reduction in the number of seizures resulted in resource savings of about 30 to 40% in terms of fuel.
さらにドアサツシ用塗料の塗装時のダストによ
る仕上り面への影響もなく、防錆性、外観ともす
ぐれたものであつた。 Furthermore, there was no effect on the finished surface due to dust during application of the door sash paint, and the product had excellent rust prevention and appearance.
実施例 2 粉体塗料は次の如くして調製した。Example 2 The powder coating was prepared as follows.
エピコート#1004 100部、アジピン酸ジヒドラ
ジド5部、イミダゾール0.3部、ミキレベリング
(共栄社油脂製レベリング剤商品名)1.5部、酸化
チタン36部、カーボンブラツク4部を乾式粉体塗
料製造の常法により混合し熱混練し、冷却し、粉
砕する工程で製造した。平均粒径は50μであつ
た。 Mix 100 parts of Epicoat #1004, 5 parts of adipic acid dihydrazide, 0.3 parts of imidazole, 1.5 parts of Miki Leveling (trade name of leveling agent made by Kyoeisha Yushi Co., Ltd.), 36 parts of titanium oxide, and 4 parts of carbon black using a conventional method for manufacturing dry powder coatings. It was manufactured through a process of hot kneading, cooling, and pulverization. The average particle size was 50μ.
アニオン性電着塗装浴は次の如くして調製し
た。 An anionic electrodeposition coating bath was prepared as follows.
既知の処理によるポリブタジエン系樹脂よりな
るアニオン性樹脂、中和剤としてトリエチルアミ
ン、顔料として酸化チタンおよびカーボンブラツ
クよりなる電着浴を調製した。その浴液の特数は
PH7.8、灰分26重量%、加熱残分13重量%であつ
た。 An electrodeposition bath was prepared containing an anionic resin made of a polybutadiene resin by a known process, triethylamine as a neutralizing agent, and titanium oxide and carbon black as pigments. The special characteristics of the bath liquid are
The pH was 7.8, the ash content was 26% by weight, and the heating residue was 13% by weight.
ガードコート用塗料は次の如くして調製した。
スチレン−ブタジエンエマルジヨン樹脂(大日本
インキ社製商品名ラクスター4709A)400部、カ
ーポンブラツク10部、体質顔料(林化成社製商品
名ASP−200)220部、溶剤(エチレングリコー
ル)60部を塗料製造の常法により均一に混合分散
し更に水で吹付粘度に調整しガードコート用塗料
を得た。 The guard coating paint was prepared as follows.
Add 400 parts of styrene-butadiene emulsion resin (trade name Luxter 4709A, manufactured by Dainippon Ink Co., Ltd.), 10 parts of carbon black, 220 parts of extender pigment (trade name ASP-200, manufactured by Hayashi Kasei Co., Ltd.), and 60 parts of solvent (ethylene glycol) to the paint. The mixture was uniformly mixed and dispersed using a conventional manufacturing method, and the spraying viscosity was adjusted with water to obtain a guard coat paint.
塗装する自動車車体はリン酸亜鉛化成処理後純
水で充分に洗浄し常法により水切乾燥を行なつ
た。この車体の外板部に粉体塗料をサメス社製ス
タジエツトJR−50タイプ粉体静電塗装機により
−80KVで膜厚が50±5μになるように塗装を行な
つた。次に得られた塗膜を架橋硬化を生ぜしめな
い150℃で10分加熱後車体を室温まで冷却し、ア
ニオン電着塗装浴中に入れ、電圧200V、通電時
間180秒浴液温度28℃、極間距離40cmの条件で電
着を行なつた。水洗を充分に行なつた後80〜100
℃で10分間水切乾燥を行ない、車体のサイドシー
ルの外側部にガードコート用塗料をスプレー塗装
し、その後形成された粉体塗膜、アニオン電着塗
膜およびガードコート用塗料塗膜の全塗膜を同時
に同一炉内で200℃で20分焼付けして架橋硬化さ
せた。 After the car body to be painted was subjected to zinc phosphate chemical conversion treatment, it was thoroughly washed with pure water and drained and dried in a conventional manner. Powder coating was applied to the outer panel of this vehicle body using a Stadget JR-50 type powder electrostatic coating machine manufactured by Sames Co., Ltd. at -80 KV to a film thickness of 50±5 μm. Next, the obtained coating film was heated at 150℃ for 10 minutes without causing crosslinking and curing, and then the car body was cooled to room temperature and placed in an anionic electrodeposition coating bath at a voltage of 200V and a current application time of 180 seconds.The bath temperature was 28℃. Electrodeposition was carried out under the condition that the distance between the electrodes was 40 cm. 80-100 after thoroughly washing with water
After draining and drying at ℃ for 10 minutes, spray paint the guard coat paint on the outside of the side seal of the car body, and then apply the entire powder coat, anion electrodeposition coat, and guard coat paint that have been formed. The membranes were simultaneously baked in the same oven at 200°C for 20 minutes to crosslink and harden.
以後は通常の方法で上塗りを行ない車体の塗装
を完了した。 After that, the car body was painted using the usual method.
この方法は従来の塗装方法にくらべ工数は約2
分の1となり、また焼付回数の減少による効果は
燃料に換算して約20%減の省資源となつた。 This method requires approximately 2 man-hours compared to the conventional painting method.
The reduction in the number of seizures resulted in resource savings of about 20% in terms of fuel.
さらにガードコート用塗料の塗装時のダストに
よる仕上り面への影響もなく、防錆性、外観とも
すぐれたものであつた。 Furthermore, there was no effect on the finished surface due to dust during application of the guard coat paint, and the product had excellent rust prevention and appearance.
実施例 3
実施例1で使用したバインダーを固形分が15重
量%になるように水で稀釈し、これに実施例1で
使用した粉体を撹拌下に、バインダーと粉体の固
形分比が1:3になるまで、必要に応じて水を添
加して粘度を調整しながら添加した。かくして得
たスラリー塗料を水でフオードカツプ#4粘度で
30秒/25℃に調整して供試粉体塗料とした。Example 3 The binder used in Example 1 was diluted with water so that the solid content was 15% by weight, and the powder used in Example 1 was added to this with stirring until the solid content ratio of the binder and powder was adjusted. The mixture was added while adjusting the viscosity by adding water as needed until the ratio was 1:3. The slurry paint thus obtained was mixed with water to a food cup #4 viscosity.
The temperature was adjusted to 30 seconds/25°C and used as a test powder coating.
上記スラリー塗料をワインダー#61型スプレー
ガン(岩田塗装機社製)を使用して、実施例1と
同様に処理を施した車体外板部に乾燥膜厚が40〜
50μになるように塗装してから130℃雰囲気で10
分間乾燥した。次いでこの車体を実施例1と同じ
カチオン性電着浴で実施例1と同様に電着塗装し
てからよく水洗した。その後ドアサツシ部に実施
例1と同様のドアサツシ用塗料を、またサイドシ
ールの外側部に実施例2と同様のガードコート用
塗料を塗装し、しかる後形成されたスラリー塗
膜、カチオン性電着塗膜、ドアサツシ用塗料塗
膜、ガードコート用塗料塗膜の全塗膜を同時に同
一炉内で190℃で20分焼付けして架橋硬化した。 The above slurry paint was treated in the same manner as in Example 1 using a winder #61 type spray gun (manufactured by Iwata Paint Co., Ltd.) to a dry film thickness of 40~
Paint it to a thickness of 50μ and then apply it for 10 minutes in a 130℃ atmosphere.
Dry for a minute. Next, this car body was electrodeposited in the same cationic electrodeposition bath as in Example 1, and then thoroughly washed with water. After that, the same door sash paint as in Example 1 was applied to the door sash area, and the same guard coat paint as in Example 2 was applied to the outside of the side seal, and then the slurry coating film and cationic electrodeposition coating were applied. All coatings, including the membrane, door sash paint, and guard coat paint, were baked simultaneously in the same oven at 190°C for 20 minutes to crosslink and harden them.
以後は通常の方法で上塗りを行ない仕上げた。 After that, the final coat was applied in the usual manner.
この方法は従来の塗装方法にくらべ工数は約2
分の1となり、また焼付回数の減少による効果は
燃料に換算して約20%減の省資源となつた。 This method requires approximately 2 man-hours compared to the conventional painting method.
The reduction in the number of seizures resulted in resource savings of about 20% in terms of fuel.
さらにドアサツシ用塗料およびガードコート用
塗料の塗装時のダストによる仕上り面への影響も
なく、防錆性、外観ともすぐれたものであつた。 Furthermore, the finished surface was not affected by dust during the application of the door sash paint and the guard coat paint, and the rust prevention and appearance were excellent.
Claims (1)
車体全体を常温で固体であり、加熱すると溶融す
る合成樹脂微粉体を含有する塗料(粉体系塗料)
を塗装し、形成された塗膜を該塗膜の溶融を生ぜ
しめるが、架橋硬化を生ぜしめない温度で加熱し
あるいは加熱をせずに次に(2)上記(1)の塗装で塗装
されなかつた部分をイオン性塗料(電着塗料)で
電着塗装し、形成された塗膜を水洗後エアブロー
あるいは水切乾燥し、その後(3)ドアサツシ部をド
アサツシ用塗料でおよび/または(4)サイドシール
部をドアコート用塗料で塗装し、しかる後(1)〜(4)
で形成した各塗膜を同時に焼付硬化することを特
徴とする自動車車体の下塗り塗装方法。1. In the undercoat coating system for automobile bodies, first (1)
Paint for the entire car body that contains synthetic resin fine powder that is solid at room temperature and melts when heated (powder-based paint)
(2) The coating film formed is heated at a temperature that causes melting of the coating film but does not cause crosslinking hardening, or without heating, and then (2) is coated with the coating described in (1) above. Electrodeposit the missing parts with ionic paint (electrodeposition paint), wash the formed coating film with water, then air blow or drain and dry, then (3) paint the door sash area with door sash paint and/or (4) paint the sides. Paint the seal part with door coating paint, and then (1) to (4)
A method for undercoating an automobile body, characterized by simultaneously baking and curing each coating film formed in the step.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15679183A JPS6048173A (en) | 1983-08-26 | 1983-08-26 | Painting method of automotive body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15679183A JPS6048173A (en) | 1983-08-26 | 1983-08-26 | Painting method of automotive body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6048173A JPS6048173A (en) | 1985-03-15 |
| JPH0366030B2 true JPH0366030B2 (en) | 1991-10-15 |
Family
ID=15635381
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15679183A Granted JPS6048173A (en) | 1983-08-26 | 1983-08-26 | Painting method of automotive body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6048173A (en) |
-
1983
- 1983-08-26 JP JP15679183A patent/JPS6048173A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6048173A (en) | 1985-03-15 |
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