JPS6116438B2 - - Google Patents
Info
- Publication number
- JPS6116438B2 JPS6116438B2 JP16441682A JP16441682A JPS6116438B2 JP S6116438 B2 JPS6116438 B2 JP S6116438B2 JP 16441682 A JP16441682 A JP 16441682A JP 16441682 A JP16441682 A JP 16441682A JP S6116438 B2 JPS6116438 B2 JP S6116438B2
- Authority
- JP
- Japan
- Prior art keywords
- electrodeposition
- coating
- paint
- liquid
- tank
- 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
- 238000004070 electrodeposition Methods 0.000 claims description 43
- 238000000576 coating method Methods 0.000 claims description 34
- 239000007788 liquid Substances 0.000 claims description 30
- 239000003973 paint Substances 0.000 claims description 30
- 239000011248 coating agent Substances 0.000 claims description 29
- 238000000034 method Methods 0.000 claims description 26
- 239000000843 powder Substances 0.000 claims description 15
- 238000010422 painting Methods 0.000 claims description 10
- 238000004140 cleaning Methods 0.000 claims description 7
- 230000005611 electricity Effects 0.000 claims description 5
- 125000002091 cationic group Chemical group 0.000 description 11
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000003822 epoxy resin Substances 0.000 description 4
- 229920000647 polyepoxide Polymers 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 235000002639 sodium chloride Nutrition 0.000 description 3
- 238000000108 ultra-filtration Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 230000001788 irregular Effects 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000007798 antifreeze agent Substances 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 230000006866 deterioration Effects 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
- 238000001035 drying Methods 0.000 description 1
- 239000002659 electrodeposit Substances 0.000 description 1
- 238000009713 electroplating Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000003449 preventive effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Application Of Or Painting With Fluid Materials (AREA)
Description
本発明は自動車車体に経済的に強力な防錆塗膜
を付与する塗装方法に関する。
近時、高速道路の発達により走行速度が増加す
るに伴い走行中自車あるいは対向車が飛散させる
砂れきの衝撃による塗膜の損傷(所謂チツピング
現象)、更にはそれに加えて冬期の寒冷地におい
て凍結防止のため散布する岩塩などの腐食性凍結
防止剤に起因する腐蝕(所謂塩害)の問題が重大
になつているが、本発明はかかる損傷、腐蝕に対
して、強力な防御効果を与える防錆塗装方法に関
する。
自動車車体、特に車体の下回り部分の防錆は、
前述の如きチツピング現象および、塩害による塗
膜損傷の発生などの腐蝕性環境の悪化、必要耐要
年数の増大、高速走行により更に加えられた安全
性への要求などから、ますます強く求められてき
ており、防錆効果の向上は業界の重要課題の一つ
である。
自動車車体の防錆対策は種々研究されてきた。
例えば塗料および塗装面では、アニオン型電着塗
料の採用とそれに使用する塗料のその後の品質向
上、カチオン型電着塗装の採用、更には粉体塗装
および粉体電着塗装の開発および採用などがあ
る。
更には、粉体塗装、粉体電着塗装、厚膜型電着
塗装等を自動車車体の外板部、特に下回りに予め
施し、その後、内板部、袋構造部を通常電着塗料
特にカチオン電着塗料にて塗装する方法が検討実
施されつつある。この方法をリバース塗装方式と
呼ばれている。このリバース塗装方式を実用化す
るに当り、前工程を車体下回り部分を電着塗装で
厚塗塗装する方法として、特公昭56−2159号等が
挙げられるが、実用上、下記の不都合を生ずるこ
とがあることが判つた。
即ち、塗装方式として連続スリツパーデイツプ
方式を使用する場合、一般に自動車車体は棒状の
ハンガーに固定された形で懸垂され、コンベヤー
により移動せしめられる。この棒状ハンガーはコ
ンベヤーに対し大体直角に固定されている。これ
らハンガーとコンベヤーの連結固定は電着浴槽中
に車体に入槽する際生ずる浴液による浮力および
抵抗等により自動車車体が不安定に動くのを防止
し、また場合によつては通電中の短絡事故、さら
には車体がハンガーから落下するのを防止するた
め実施されているものである。
しかしながら、上記ハンガーで固定した自動車
車体特にその下回り部分をスリツパーデイツプ方
式で塗装する場合次の如き不都合を生ずる。
そもそも自動車車体の下回り部分を防錆塗膜す
る場合、車体の必要下回り部分のみを水平に塗装
するのが一般であり、またかくするのが塗膜外観
上好ましいことは明らかである。
しかるにスリツパーデイツプ方式で通電入槽お
よび通電出槽方法を使用した場合、自動車車体は
浴槽液面に対し傾斜した状態で入槽され、また出
槽される。このため自動車車体前部(入槽時)お
よび後部(出槽時)は、目的とする防錆塗膜下回
り水平部より上の部分(塗装不要部と称する)ま
で浴槽中に没入することは避けられない。入槽お
よび出槽の間には上記一度没入した塗装不要部は
浴液面上に現われ、車体は浴液中に水平に保た
れ、下回り部分のみを没入させた状態で電着塗装
される。このとき、上記方法では通電状態で車体
が入槽および出槽するため上記不要部も没入時に
電着されることはまぬかれない。また通電入槽お
よび無通電出槽方法または無通電入槽および通電
出槽方法でも、通電時の上記不要部の電着はまぬ
かれない。
上述した不要部電着は、目的とする車体下回り
部分の電着時間に比し、没入時のみの電着である
ため、電着時間が短く、塗膜の厚さは下回り部分
より薄くなり塗膜全体の外観を損うばかりでな
く、後工程で通常の電着塗装を施したとき、この
通常電着塗装が実施されず、膜厚的にも、塗膜美
観の上からも好ましからぬ不具合を生ずる。
このため、無通電入槽および無通電出槽法を採
用し、車体が完全に水平になつてから通電し、電
着する方法もあるが、この場合でも入槽時に没入
した車体前部の上部不要部には没入時に付着した
浴液がそのまま物理的に付着しており、完全に除
去されることはない。このため、車体を水平に保
つた後、目的とする電着塗装のため通電すると不
要部に残存付着していた塗料が電着され、この場
合は先の通電入槽および/または通電出槽法の場
合よりも塗量付着が不規則となり、斑を生じて、
塗膜美観をむしろ甚しく損う結果となる。またか
かる斑もしくは不規則塗膜を形成したまま該工程
での通常電着を行なうと、不連続塗膜を形成成し
て塗膜性能上も好ましくない。
本発明者等はかかる不都合を改良すべく検討し
た結果、自動車車体の下回り部位をスリツパーデ
イツプ方式でリバース塗装するにあたり、一度粉
体電着塗料または厚膜型電着塗料浴液中に没し、
再び該浴液面上に現われた自動車車体の下回り部
以外の浴液付着部位を洗浄した後に通電して電着
塗装し、次に通電の電着塗装を施すことを特徴と
する塗装方法が前記の如き不都合を改良できるこ
とを見い出したものである。
また、上記粉体電着塗装または厚膜型電着塗装
において、
(i) 洗浄完了後水平位置で通電を開始し、
(ii) 車体が水平移動するときのみ通電し、
(iii) 出槽時は無通電とする
ことにより、本発明の効果を最大限に発揮できる
ことを見い出したものである。
本発明の上記洗浄に用いる洗浄液としては、後
工程での通常の電着工程で電着されるような成分
を含有しないもの、すなわち塗膜有効成分となり
得ない水あるいは限外過(UF)液等が用い
られる。洗浄に当つては、車体が電着槽中で水平
になつた位置にノズルを設けて洗浄液を噴霧する
ことによつて行なうとよい。
以下、実施例および比較例により本発明を詳細
に説明する。
実施例 1
粉体電着塗料は以下の如くして作製した。
水稀釈性カチオン性樹脂は、エピコート#1001
(商標名:エポキシ樹脂、シエル社製品)488部、
ジエタノールアミン150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。
また合成樹脂微粉体としてはエピコート#1004
(シエル社製)40部、アダクトB−1065(フエバ
社製)30部、酸化チタンR−550(石原産業社
製)29部およびカーボンブラツクMA−100(三
菱化成社製)1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錬し、衝撃式粉砕機で
粉砕し平均粒型7μのエポキシ樹脂を主体とする
微粉体を得た。
上記の如くして得た液状のアミノエポキシ樹脂
(Bi)、微粉体(Po)および氷酢酸、脱イオン水
を加えて混合分散し、Po/Bi=2.8/1、PH52、
固型分15%の粉体電着塗料浴液を調製した。
また、カチオン電着塗料はウレタン変性エポキ
シ樹脂の末端グリシジル基をアルカノールアミン
で開環したアミノエポキシ樹脂にブロツクイソシ
アネートを付加反応させて得たカチオン型樹脂を
用い、酸化チタンとカーボンブラツク少量の溶剤
を通常の分散工程で分散し、酸性化合物で中和し
たもので、固形分15%、PH5.8、顔料分は23%で
あつた。
上記粉体電着塗料浴液を自動車車体のドア部で
下辺から20cmまでタンク中央部で浸漬するように
舟型電着槽に満たした。液量は約55tであつた。
陽極は車体の下回り部外板と1/1極間50cmとな
るように設置した。車体が電着槽中で水平になる
位置、即ち車体フエンダー部が入槽時一度没入し
た後再び液面上に現われる位置にノズルを設置
し、液比抵抗10万Ωcmの特数をもつ脱イオン水を
1台当り5噴霧し、この部位に付着した塗料を
浴液中に洗い流した後、通電を開始した。車体が
舟型タンクの出槽側勾配により、傾き始める以前
に通電を停止した。この時、通電条件は液温25
℃、電圧500V、時間30秒であつた。かくして形
成された電着塗膜を常法により水洗し、水切乾燥
後、後工程であるカチオン電着塗料を用いて塗装
を実施した。電着塗装条件は液温28℃、電圧
300Vとした。結果を第1表に示す。
比較例 1
粉体電着塗装前の脱イオン水による洗浄を行な
わない他は実施例1と同様にして塗装した。結果
を第1表に示す。
The present invention relates to a coating method for applying an economically strong anti-rust coating to an automobile body. In recent years, with the development of expressways, driving speeds have increased, resulting in paint film damage (so-called chipping phenomenon) due to the impact of flying debris from own vehicles or oncoming vehicles, and in addition to this, freezing in cold regions during the winter. The problem of corrosion (so-called salt damage) caused by corrosive antifreeze agents such as rock salt that are sprayed to prevent corrosion has become serious, but the present invention provides a rust preventive that provides a strong protective effect against such damage and corrosion. Regarding the painting method. Rust prevention for the car body, especially the lower part of the car body, is
Due to the above-mentioned chipping phenomenon, deterioration of the corrosive environment such as damage to the paint film due to salt damage, increased required lifespan, and increased safety requirements due to high-speed driving, there is an increasing demand for Therefore, improving the rust prevention effect is one of the important issues in the industry. Various rust prevention measures for automobile bodies have been studied.
For example, in the area of paints and painted surfaces, the adoption of anionic electrodeposition paints and the subsequent quality improvement of the paints used, the adoption of cationic electrodeposition coatings, and the development and adoption of powder coatings and powder electrodeposition coatings. be. Furthermore, powder coating, powder electrodeposition coating, thick-film electrodeposition coating, etc. are applied in advance to the outer panel of the automobile body, especially the underside, and then the inner panel and bag structure are coated with regular electrodeposition paint, especially cationic coating. A method of painting with electrodeposition paint is being studied and implemented. This method is called the reverse painting method. In order to put this reverse painting method into practical use, there is a method of applying a thick layer of electrodeposited paint to the lower part of the car body as a pre-process, such as in Japanese Patent Publication No. 56-2159, but in practice, it causes the following inconveniences. It turns out that there is. That is, when a continuous slipper dip method is used as a coating method, the automobile body is generally suspended fixedly on a rod-shaped hanger and moved by a conveyor. This rod-shaped hanger is fixed approximately at right angles to the conveyor. The connection and fixation of these hangers and conveyors prevents the car body from moving unstablely due to the buoyancy and resistance caused by the bath liquid that occurs when the car body is placed in the electroplating bath, and in some cases, short circuits may occur during energization. This is done to prevent accidents and even the vehicle falling from the hanger. However, when painting an automobile body fixed with the above-mentioned hanger, especially the lower part thereof, by the slipper dip method, the following disadvantages occur. In the first place, when applying a rust-preventing coating to the lower part of an automobile body, it is common to apply the coating horizontally to only the required lower part of the car body, and it is clear that this is preferable in terms of the appearance of the coating film. However, when using the energized entry and exit methods in the slipper dip system, the car body is entered and exited from the bathtub in an inclined state with respect to the liquid level of the bathtub. For this reason, avoid submerging the front part (when entering the tank) and rear part (when taking out the tank) of the car body into the bathtub up to the part above the horizontal part (referred to as the unpainted part) of the lower part of the target anti-rust coating. I can't. Between entering and exiting the tank, the unpainted parts that are once immersed appear on the surface of the bath liquid, and the car body is kept horizontally in the bath liquid, and only the lower part is immersed in the bath liquid for electrodeposition painting. At this time, in the above method, since the vehicle body enters and exits the tank while energized, it is inevitable that the above-mentioned unnecessary portions will also be electrodeposited during the insertion. Further, even with the method of energizing the tank and not energizing the tank, or the method of energizing the tank and the energizing tank, the electrodeposition on the unnecessary portions described above during energization cannot be avoided. Compared to the electrodeposition time for the target underbody part, the above-mentioned electrodeposition on unnecessary parts is performed only during immersion, so the electrodeposition time is shorter and the coating film is thinner than the underbody part. Not only does this damage the overall appearance of the film, but when regular electrodeposition coating is applied in the subsequent process, this regular electrodeposition coating is not carried out, resulting in problems that are undesirable from both the film thickness and the aesthetics of the coating film. will occur. For this reason, there is a method that uses non-energized entry and exit methods, and then applies electricity and electrodeposit after the vehicle body is completely horizontal. The bath liquid that adhered to the unnecessary parts during immersion physically adheres as it is, and is not completely removed. For this reason, after keeping the car body horizontal, when electricity is applied for the intended electrodeposition coating, the paint remaining on unnecessary parts will be electrodeposited, and in this case, the previous energization tank entry and/or energization exit method will be applied. The coating amount is more irregular than in the case of , causing spots,
The result is that the appearance of the paint film is seriously impaired. Furthermore, if ordinary electrodeposition is carried out in this step while such a patchy or irregular coating film is formed, a discontinuous coating film will be formed, which is unfavorable in terms of coating performance. The inventors of the present invention have studied to improve this inconvenience, and found that when reverse painting the lower part of an automobile body using the slipper dip method, it is necessary to first immerse it in powder electrocoating paint or thick film electrocoating paint bath liquid. died,
The above-mentioned painting method is characterized in that after cleaning the parts of the automobile body that have been exposed to the bath liquid other than the lower part of the car body that have appeared on the bath liquid surface again, the electrolytic coating is applied by applying an electric current. It has been discovered that such inconveniences can be improved. In addition, in the above-mentioned powder electrodeposition coating or thick film electrodeposition coating, (i) energization is started in the horizontal position after cleaning is completed, (ii) energization is applied only when the vehicle body moves horizontally, and (iii) when the vehicle is taken out of the tank. It has been discovered that the effects of the present invention can be maximized by not applying electricity. The cleaning liquid used in the above-mentioned cleaning of the present invention is one that does not contain components that would be electrodeposited in the normal electrodeposition process in the subsequent process, that is, water or ultrafiltration (UF) liquid that cannot become an active component of the coating film. etc. are used. Cleaning is preferably carried out by spraying a cleaning liquid by installing a nozzle at a position where the car body is horizontal in the electrodeposition tank. Hereinafter, the present invention will be explained in detail with reference to Examples and Comparative Examples. Example 1 A powder electrodeposition paint was prepared as follows. Water-dilutable cationic resin is Epicote #1001
(Trade name: epoxy resin, Ciel product) 488 parts,
150 parts of diethanolamine and 250 parts of isopropyl alcohol were reacted under reflux at 80°C to 85°C for 3 hours to obtain a liquid aminoepoxy resin. Also, as a synthetic resin fine powder, Epicoat #1004
(manufactured by Ciel Corporation) 40 parts, Adduct B-1065 (manufactured by Hueva Corporation) 30 parts, titanium oxide R-550 (manufactured by Ishihara Sangyo Co., Ltd.) 29 parts, and Carbon Black MA-100 (manufactured by Mitsubishi Kasei Corporation) 1 part as powder. By the conventional method of paint 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 7μ. The liquid aminoepoxy resin (Bi) obtained as above, fine powder (Po), glacial acetic acid, and deionized water were added and mixed and dispersed, Po/Bi=2.8/1, PH52,
A powder electrodeposition paint bath solution with a solid content of 15% was prepared. In addition, cationic electrodeposition paints use a cationic resin obtained by adding blocked isocyanate to an aminoepoxy resin in which the terminal glycidyl group of a urethane-modified epoxy resin is ring-opened with an alkanolamine. It was dispersed using a normal dispersion process and neutralized with an acidic compound, and had a solid content of 15%, a pH of 5.8, and a pigment content of 23%. A boat-shaped electrodeposition tank was filled with the powder electrodeposition paint bath solution so that the center of the tank was immersed up to 20 cm from the lower side of the door of an automobile body. The amount of liquid was approximately 55 tons.
The anode was installed with a distance of 50 cm between the lower part of the car body and the 1/1 pole. The nozzle is installed at a position where the car body is horizontal in the electrodeposition tank, that is, at a position where the fender of the car body immerses once in the tank and then reappears on the liquid surface. Water was sprayed 5 times per unit to wash away the paint adhering to this area into the bath liquid, and then electricity was started. The power was turned off before the vehicle began to tilt due to the slope on the outlet side of the boat-shaped tank. At this time, the energizing condition is liquid temperature 25
℃, voltage 500V, and time 30 seconds. The electrodeposited coating film thus formed was washed with water in a conventional manner, drained and dried, and then painted using a cationic electrodeposition paint as a subsequent step. Electrodeposition coating conditions are liquid temperature 28℃ and voltage.
It was set to 300V. The results are shown in Table 1. Comparative Example 1 Coating was carried out in the same manner as in Example 1, except that washing with deionized water before powder electrodeposition coating was not performed. The results are shown in Table 1.
【表】【table】
【表】
実施例 2
厚膜型電着塗料浴液の調製方法
下回り塗装用カチオン電着塗料は外観仕上り性
を重視せず膜厚確保を目的としてウレタン変性エ
ポキシ樹脂の末端グリシジル基をアルカノールア
ミンで開環したアミノエポキシ樹脂にブロツクイ
ソシアネートを付加反応させたカチオン樹脂を用
い、組成的には更に熱可塑性で室温で液状である
電着により解離せぬ成分を増量し、かつ、溶剤も
増量させた。固形分18%、PH=6.0、顔料分は20
%、クーロン効率は38mg/Cの特徴を持つ塗料で
あつた。
車体のドア部の下辺から10cmが浴液中に浸漬す
るように電着槽内に浴液を満たした。極間=30
cm、該当部/陽極=1/1とし、車体が水平に達
し、該当部外で一度、液面下に没し、再び液面上
に現われた部位に限界過(UF)により、本塗
料から常法で得られた液を噴霧し、付着した塗
料を洗い流した。なお、この液の固形分は0.5
%であつた。しかる後、電圧300V、28℃で1分
30秒通電した。通電終了時の車体位置は水平であ
つた。常法により水洗後50〜70℃の水切乾燥を実
施した後、通電入槽にてカチオン電着を実施し
た。カチオン電着塗料は実施例1と同様のものを
使用した。電着条件は浴温28℃、電圧300Vとし
た。通電時間は車体が浴中に全没している時間で
丁度3分であつた。結果を第2表に示す。
比較例 2
実施例2と同様のカチオン厚膜型電着塗料を使
用し、液中に一度没し、再び液面上に現れた部位
に付着した塗料を洗い落すことをせずに他の条件
は全く実施例2と同様に電着し、かつ、後工程を
も全て実施例2と同様にした。結果を第2表に示
す。[Table] Example 2 Method for preparing thick-film electrodeposition paint bath liquid For the cationic electrodeposition paint for underside coating, the terminal glycidyl group of the urethane-modified epoxy resin was replaced with alkanolamine in order to ensure film thickness without emphasizing the appearance finish. Using a cationic resin made by addition-reacting blocked isocyanate to a ring-opened aminoepoxy resin, the composition further increased the amount of components that are thermoplastic and liquid at room temperature that do not dissociate by electrodeposition, and also increased the amount of solvent. . Solid content 18%, PH=6.0, pigment content 20
%, and the coulombic efficiency was 38 mg/C. The electrodeposition bath was filled with bath liquid so that 10 cm from the bottom of the door of the car body was immersed in the bath liquid. Between poles = 30
cm, the relevant part/anode = 1/1, the car body reaches the horizontal level, once submerged below the liquid surface outside the relevant part, and the paint is removed from the paint due to limit excess (UF) at the part that reappears above the liquid surface. A liquid obtained in a conventional manner was sprayed to wash away the adhering paint. The solid content of this liquid is 0.5
It was %. After that, voltage 300V, 1 minute at 28℃
Power was applied for 30 seconds. The vehicle body position was horizontal at the end of energization. After washing with water and drying at 50 to 70°C using a conventional method, cationic electrodeposition was performed in an energized tank. The same cationic electrodeposition paint as in Example 1 was used. The electrodeposition conditions were a bath temperature of 28°C and a voltage of 300V. The energization time was exactly 3 minutes, which is the time when the car was fully immersed in the bath. The results are shown in Table 2. Comparative Example 2 Using the same cationic thick-film electrodeposition paint as in Example 2, the paint was submerged in the liquid and then resurfaced under other conditions without washing off the paint that had adhered to the area where it reappeared on the liquid surface. was electrodeposited in exactly the same manner as in Example 2, and all post-processes were performed in the same manner as in Example 2. The results are shown in Table 2.
【表】【table】
Claims (1)
プ方式でリバース塗装するにあたり、一度、粉体
電着塗料または厚膜型電着塗料浴液中に没し、再
び該溶液面上に現われた自動車車体の下回り部以
外の浴液付着部位を洗浄した後に通電して電着塗
装し、次に通常の電着塗装を施すことを特徴とす
る自動車車体下回りの塗装方法。1. When reverse painting the lower part of an automobile body using the slipper dip method, the automobile body is once immersed in a powder electrocoating paint or thick film electrocoating paint bath solution and reappears on the surface of the solution. 1. A method for painting the underside of an automobile body, which comprises cleaning the parts to which bath liquid is attached other than the underside of the car, applying electricity to apply electrodeposition coating, and then applying normal electrodeposition coating.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16441682A JPS5953695A (en) | 1982-09-21 | 1982-09-21 | Method for coating underpart of car body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16441682A JPS5953695A (en) | 1982-09-21 | 1982-09-21 | Method for coating underpart of car body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5953695A JPS5953695A (en) | 1984-03-28 |
| JPS6116438B2 true JPS6116438B2 (en) | 1986-04-30 |
Family
ID=15792727
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16441682A Granted JPS5953695A (en) | 1982-09-21 | 1982-09-21 | Method for coating underpart of car body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5953695A (en) |
-
1982
- 1982-09-21 JP JP16441682A patent/JPS5953695A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5953695A (en) | 1984-03-28 |
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