JPH0212748B2 - - Google Patents
Info
- Publication number
- JPH0212748B2 JPH0212748B2 JP58069793A JP6979383A JPH0212748B2 JP H0212748 B2 JPH0212748 B2 JP H0212748B2 JP 58069793 A JP58069793 A JP 58069793A JP 6979383 A JP6979383 A JP 6979383A JP H0212748 B2 JPH0212748 B2 JP H0212748B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- steel sheet
- coated steel
- polyethyleneimine
- sided coated
- 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
Links
- 229910000831 Steel Inorganic materials 0.000 claims description 21
- 239000010959 steel Substances 0.000 claims description 21
- 238000000576 coating method Methods 0.000 claims description 14
- 229920002873 Polyethylenimine Polymers 0.000 claims description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000011248 coating agent Substances 0.000 claims description 10
- 238000005260 corrosion Methods 0.000 claims description 9
- 230000007797 corrosion Effects 0.000 claims description 9
- 239000000377 silicon dioxide Substances 0.000 claims description 6
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical compound [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 claims description 3
- 239000004698 Polyethylene Substances 0.000 claims 1
- 150000002466 imines Chemical class 0.000 claims 1
- 229920000573 polyethylene Polymers 0.000 claims 1
- 238000003466 welding Methods 0.000 description 9
- 239000000843 powder Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 229910001335 Galvanized steel Inorganic materials 0.000 description 6
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 239000008397 galvanized steel Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 238000000034 method Methods 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 238000005476 soldering Methods 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 238000010422 painting Methods 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 241001163841 Albugo ipomoeae-panduratae Species 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910000576 Laminated steel Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 229910000611 Zinc aluminium Inorganic materials 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- HXFVOUUOTHJFPX-UHFFFAOYSA-N alumane;zinc Chemical compound [AlH3].[Zn] HXFVOUUOTHJFPX-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004566 building material Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000010960 cold rolled steel Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- KFZAUHNPPZCSCR-UHFFFAOYSA-N iron zinc Chemical compound [Fe].[Zn] KFZAUHNPPZCSCR-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 229910000679 solder Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Description
本発明は片面塗装鋼板において、未塗装面に溶
接性、ハンダ付け性などを損わない有機防錆皮膜
を形成して、未塗装面に耐食性を付与した片面塗
装鋼板に関する。
近年家庭電気製品や構造用建材などの分野にお
いては工程合理化のため必要部材の自家塗装を廃
止し、塗装鋼板を用いて部材に加工するプレコー
ト化が盛んに行われている。従来このプレコート
化は当初屋根や壁用の着色亜鉛鉄板などの如く表
側に耐食性、耐候性の着色皮膜を有し、裏側に防
錆的なサービス塗膜を有する両面塗装鋼板をその
まま使用できる部材の分野で行われたのである
が、最近は電気溶接やハンダ付け加工を行う部材
の分野にまで拡大されてきている。しかし上記の
ような両面塗装鋼板では塗膜が障害になつて電気
溶接やハンダ付け加工を行うことができない。こ
のためこれらの加工を行う部材の分野に使用する
塗装鋼板としては表側に耐食性、耐候性の着色塗
膜を有し、裏側が未塗装となつた片面塗装鋼板が
使用されている。
しかし従来の片面塗装鋼板はロールコート方式
の連続塗装ラインで裏側の塗装を中止し、表側の
み塗装する方法で製造していたため、裏側の未塗
装面は塗装前処理のリン酸塩処理とクロム酸シー
リング、ときにはクロム酸シーリングしか行われ
ていないものであつた。このため裏側の耐食性は
塩水噴霧試験で白錆の発生まで約48時間程度と悪
く、製品の横持ちや保管中に錆が発生するという
欠点があつた。またリン酸塩処理したものはリン
酸塩の結晶がコイルに巻取つた場合表側の塗膜に
転写したり、ロールフオーミングの際成型ロール
にビルドアツプして後に塗装面を成型するとき塗
膜を損傷するという欠点もあつた。このようなリ
ン酸塩処理の弊害を防止するため未塗装面の処理
を中止することも考えられるが、リン酸塩処理は
スプレー処理のため未塗装面にもまわり、その部
分の電気溶接性が劣つてしまう。
本発明は従来の片面塗装鋼板がこのような欠点
を有していた点に鑑み、それらを解消した片面塗
装鋼板を提供するもので、裏側の未塗装面にポリ
エチレンイミンまたはシリカゾル−ポリエチレン
イミンの通電性皮膜を形成したことを特徴として
いる。
従来一般に有機皮膜に通電性を付与する方法と
しては皮膜中に金属粉末や炭素粉末などの導電性
粉末を含有させる方法がある。しかしこの方法の
場合皮膜中に導電性粉末を約60%以上含有させな
いと皮膜に通電性が生じないものである。このた
め皮膜はバインダーとしての樹脂分が少いので加
工性が一般の塗料塗膜より劣るという欠点を有し
ている。また導電性粉末を配合した塗料は高価で
あるうえ、皮膜厚としては導電性粉末保持上厚く
しなければならないためかなりコスト高になる。
またロールフオーミングなどにおいては導電性粉
末が脱落して前記リン酸塩の場合と同様成型ロー
ルにビルドアツプするという問題もある。
そこで本発明者らはこのような問題のない通電
性皮膜の検討を行つた結果ポリエチレンイミンま
たはシリカゾル−ポリエチレンイミンの各単独皮
膜が適していることを見出したのである。
添付図面の第1図は板厚0.5mmの溶融亜鉛めつ
き鋼板片面にシリカゾル−ポリエチレンイミンの
皮膜を形成して、溶接電流7KA、加圧力150Kg、
通電時間10サイクルの条件でスポツト溶接を行つ
て溶接可能な皮膜厚さの限界を求めたもので、図
より明らかな如く2.5μが限界である。同様に第2
図に示すようにポリエチレンイミンの皮膜につい
てスポツト溶接を行つたところほぼ同一の結果が
得られた。一方ハンダ付け性について調査してみ
ると、いずれの皮膜も2μまでは可能であること
が判明した。しかし0.1μ未満にするといずれの皮
膜も耐食性が不十分であることが判明した。従つ
て皮膜厚は0.1〜2.5μにするのが好ましい。
通電性皮膜はこのように電気溶接性、ハンダ付
け性を確保する都合上薄くしなければならないの
で、腐食環境で使用する部材用には耐食性が不十
分な場合がある。このような場合にはクロメート
皮膜を鋼板素地と上記皮膜との間に介在させて耐
食性を向上させることも可能である。この場合の
クロメート皮膜は皮膜中の全クロム量で5〜150
mg/m2にするとよい。
通電性皮膜の形成はポリエチレンイミンまたは
シリカゾル−ポリエチレンイミンを溶解した水溶
液を鋼板表面に塗布して行う。この塗布方法とし
てはスクイズロール法、ロールコート法等公知の
方法でよい。水溶液濃度としてはシリカゾル−ポ
リエチレンイミンの場合シリカゾルを5〜10%、
ポリエチレンイミンを5〜40%含有したものが好
ましく、ポリエチレンイミンの場合それを5〜50
%含有したものが好ましい。塗布後の乾燥は40〜
250℃(到達板温)で行えばよい。
本発明の片面塗装鋼板の場合、素地原板として
は冷延鋼板であつてもよく、まためつき鋼板であ
つてもよい。例えばめつき鋼板の場合従来より使
用されている溶融亜鉛めつき鋼板、溶融亜鉛−ア
ルミニウムめつき鋼板、鉄−亜鉛合金化溶融亜鉛
めつき鋼板、電気亜鉛または亜鉛合金めつき鋼板
および溶融アルミニウムめつき鋼板などであつて
も問題はない。
次に本発明の効果を第1表に具体的に示す。板
厚はいずれも0.5mmである。
The present invention relates to a single-sided coated steel plate in which corrosion resistance is imparted to the unpainted surface by forming an organic rust-preventing film on the unpainted surface that does not impair weldability, solderability, etc. In recent years, in the fields of home appliances and structural building materials, in order to streamline processes, in-house painting of necessary parts has been abolished, and pre-coating, in which painted steel plates are used to process parts, has become popular. Conventionally, this pre-coating was initially applied to materials that can be used as is, such as colored galvanized iron sheets for roofs and walls, which have a corrosion-resistant and weather-resistant colored film on the front side and a rust-preventive service coating on the back side. It was originally practiced in the field, but recently it has been expanded to include parts that undergo electric welding and soldering. However, with the above-mentioned double-sided coated steel sheet, electric welding and soldering cannot be performed because the coating film becomes an obstacle. For this reason, the coated steel plates used in the field of parts that undergo these processes are single-sided coated steel plates that have a corrosion-resistant and weather-resistant colored coating on the front side and are left unpainted on the back side. However, conventional single-sided coated steel sheets were manufactured using a continuous roll-coat coating line that stopped painting the back side and painted only the front side, so the unpainted back side was treated with phosphate and chromic acid as a pre-painting treatment. Sealing, sometimes chromic acid sealing, was the only thing that had been done. For this reason, the corrosion resistance of the back side was poor, with white rust appearing in a salt spray test for about 48 hours, and the product had the disadvantage of rusting during horizontal handling or storage. In addition, for phosphate-treated products, when phosphate crystals are wound into a coil, they may be transferred to the coating on the front side, or they may be built up on a forming roll during roll forming, and the coating may be removed when forming the painted surface. It also had the disadvantage of being damaged. In order to prevent such adverse effects of phosphate treatment, it may be possible to discontinue treatment of unpainted surfaces, but since phosphate treatment is a spray treatment, it will also cover unpainted surfaces, and the electric weldability of that area may be affected. I become inferior. In view of the above-mentioned drawbacks of conventional single-sided coated steel plates, the present invention provides a single-sided coated steel plate that eliminates these drawbacks. It is characterized by the formation of a sexual film. A conventional method for imparting electrical conductivity to an organic film is to include a conductive powder such as metal powder or carbon powder in the film. However, in this method, the film does not have electrical conductivity unless the film contains about 60% or more of conductive powder. For this reason, the film has a disadvantage in that the processability is inferior to that of ordinary paint films because the resin content as a binder is small. Furthermore, paints containing conductive powder are expensive, and the coating must be thick in order to retain the conductive powder, resulting in a considerable increase in cost.
In addition, during roll forming, etc., there is a problem that the conductive powder falls off and builds up on the forming roll as in the case of the phosphate. The inventors of the present invention have investigated the development of electrically conductive coatings free of such problems and have found that polyethyleneimine or silica sol-polyethyleneimine coatings alone are suitable. Figure 1 of the attached drawings shows a silica sol-polyethyleneimine film formed on one side of a hot-dip galvanized steel plate with a thickness of 0.5 mm, welding current of 7 KA, pressure of 150 kg,
The limit of the weldable film thickness was determined by performing spot welding under the condition of 10 cycles of current application, and as is clear from the figure, the limit is 2.5μ. Similarly, the second
As shown in the figure, almost the same results were obtained when spot welding was performed on a polyethyleneimine film. On the other hand, when investigating the solderability, it was found that all films can be soldered up to 2μ. However, it was found that all films had insufficient corrosion resistance when the thickness was less than 0.1μ. Therefore, the film thickness is preferably 0.1 to 2.5 μm. Since the electrically conductive film must be made thin in order to ensure electrical weldability and solderability, it may not have sufficient corrosion resistance for parts used in corrosive environments. In such cases, it is also possible to interpose a chromate film between the steel sheet base and the above film to improve corrosion resistance. In this case, the chromate film has a total chromium content of 5 to 150.
It is best to use mg/ m2 . The conductive film is formed by applying an aqueous solution containing polyethyleneimine or silica sol-polyethyleneimine to the surface of the steel sheet. This coating method may be any known method such as a squeeze roll method or a roll coating method. In the case of silica sol-polyethyleneimine, the aqueous solution concentration is 5-10% of silica sol,
It is preferable to use polyethyleneimine containing 5 to 40%; in the case of polyethyleneimine, it should be 5 to 50%
% is preferable. Drying time after application is 40~
It can be done at 250℃ (achieved plate temperature). In the case of the single-sided coated steel sheet of the present invention, the base sheet may be a cold-rolled steel sheet or a laminated steel sheet. For example, in the case of galvanized steel sheets, conventionally used hot-dip galvanized steel sheets, hot-dip zinc-aluminum galvanized steel sheets, iron-zinc alloyed hot-dip galvanized steel sheets, electrolytic zinc or zinc alloy coated steel sheets, and hot-dip aluminum plated steel sheets. There is no problem even if it is made of steel plate or the like. Next, Table 1 specifically shows the effects of the present invention. The thickness of both plates is 0.5mm.
【表】
なお第1表における性能調査は次の要領で行つ
た。
(1) 塩水噴霧試験
JIS Z 2371に準じて720時間行い、錆の発生
面積率を下記基準で評価した。
評価点 錆の発生面積率(%)
5 0
4 1〜10
3 11〜30
2 31〜70
1 71〜99
0 100
(2) 湿潤試験
50℃、98%RHの湿潤試験機中で720時間行い、
塩水噴霧試験と同基準で評価した。
(3) 溶接性試験
35゜×4mmφの電極を用いて溶接電流7KA、加
圧力150Kg、通電時間10サイクルの条件でスポツ
ト溶接を行い、溶接後の引張強さが250Kg/1ス
ポツト以上のもの〇、250Kg/1スポツト未満の
もの×で評価した。
(4) ハンダ付け性試験
2mmφのSb−Pbハンダ線を5mmに切断して、
これを塩化物フラツクスを塗布した皮膜上に置い
た後ハンダゴテで溶融させて、その広がり面積を
下記基準で評価した。
評価記号 広がり面積
〇 6mmφ以上
△ 5mmφ
× 5mmφ未満
以上の如く本発明の片面塗装鋼板は未塗装面に
耐食性の通電性皮膜が形成されているので、横持
ちや保管中に錆が発生することがなく、電気溶接
も可能である。また皮膜はハンダ付け性を有する
ので電気機器部材などにおいてアース線接続など
をハンダ付け加工で行うことができる。さらに通
電性皮膜は導電性粉末を混合させたものでないの
で、加工性もよく、安価で、ロールフオーミング
のビルドアツプもない。[Table] The performance investigation in Table 1 was conducted in the following manner. (1) Salt spray test The test was conducted for 720 hours in accordance with JIS Z 2371, and the area ratio of rust was evaluated using the following criteria. Evaluation points Rust occurrence area ratio (%) 5 0 4 1~10 3 11~30 2 31~70 1 71~99 0 100 (2) Humidity test Conducted for 720 hours in a humidity tester at 50℃ and 98%RH ,
It was evaluated using the same criteria as the salt spray test. (3) Weldability test Spot welding is performed using a 35° x 4 mmφ electrode under the conditions of a welding current of 7 KA, a pressing force of 150 Kg, and energization time of 10 cycles, and the tensile strength after welding is 250 Kg/1 spot or more. , Less than 250Kg/1 spot was evaluated as ×. (4) Solderability test A 2mmφ Sb-Pb solder wire was cut into 5mm pieces.
This was placed on a film coated with chloride flux and melted with a soldering iron, and its spread area was evaluated using the following criteria. Evaluation symbol Spread area 〇 6 mmφ or more △ 5 mmφ × less than 5 mmφ As described above, since the single-sided coated steel sheet of the present invention has a corrosion-resistant conductive film formed on the unpainted surface, rust will not occur during horizontal handling or storage. Electric welding is also possible. Furthermore, since the film has solderability, it is possible to connect a ground wire to electrical equipment members by soldering. Furthermore, since the conductive film is not mixed with conductive powder, it has good processability, is inexpensive, and does not have build-up during roll forming.
第1図および第2図はそれぞれ片面にシリカゾ
ル−ポリエチレンイミン皮膜およびポリエチレン
イミン皮膜を形成した溶融亜鉛めつき鋼板をスポ
ツト溶接した場合の皮膜厚さと溶接部引張り強さ
および溶接不良率の関係を示すグラフである。
Figures 1 and 2 show the relationship between the film thickness, weld tensile strength, and weld failure rate when hot-dip galvanized steel sheets with a silica sol-polyethyleneimine film and a polyethyleneimine film formed on one side, respectively, are spot welded. It is a graph.
Claims (1)
成され、他方の面が未塗装となつた片面塗装鋼板
において、未塗装の他方の面にポリエチレンイミ
ンまたはシリカゾル−ポリエチレンイミンの通電
性皮膜を形成したことを特徴とする片面塗装鋼
板。 2 通電性皮膜の厚さが0.1〜2.5μであることを
特徴とする特許請求の範囲第1項に記載の片面塗
装鋼板。 3 鋼板と通電性皮膜との間にクロメート皮膜を
形成したことを特徴とする特許請求の範囲第1項
に記載の片面塗装鋼板。[Scope of Claims] 1. A single-sided coated steel plate in which a corrosion-resistant, weather-resistant colored coating is formed on one side of the steel plate and the other side is unpainted, and the other unpainted side is coated with polyethyleneimine or silica sol-polyethylene. A single-sided coated steel sheet characterized by forming an electrically conductive film of imine. 2. The single-sided coated steel sheet according to claim 1, wherein the conductive film has a thickness of 0.1 to 2.5μ. 3. The single-sided coated steel sheet according to claim 1, characterized in that a chromate film is formed between the steel sheet and the electrically conductive film.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6979383A JPS59194837A (en) | 1983-04-20 | 1983-04-20 | One-surface coated steel plate |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP6979383A JPS59194837A (en) | 1983-04-20 | 1983-04-20 | One-surface coated steel plate |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59194837A JPS59194837A (en) | 1984-11-05 |
JPH0212748B2 true JPH0212748B2 (en) | 1990-03-26 |
Family
ID=13412973
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP6979383A Granted JPS59194837A (en) | 1983-04-20 | 1983-04-20 | One-surface coated steel plate |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS59194837A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH074903B2 (en) * | 1986-11-01 | 1995-01-25 | 日新製鋼株式会社 | Conductive surface-treated steel sheet and method for producing the same |
BR112012012923A2 (en) * | 2009-12-03 | 2017-03-07 | Basf Se | use of oxide nanoparticles, process to protect metal surfaces from corrosion, metal surfaces, and anti-corrosion composition |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5161553A (en) * | 1974-11-26 | 1976-05-28 | Yamauchi Rubber Ind Co Ltd | YOSETSUNADONIOITESHOSERARERU DANNETSUSOSEIBUTSU |
JPS57156249A (en) * | 1981-03-23 | 1982-09-27 | Matsushita Electric Works Ltd | Corrosion-resisting steel material and its manufacture |
JPS5863442A (en) * | 1981-10-13 | 1983-04-15 | 三菱自動車工業株式会社 | Manufacture of metallic plate and processed article |
-
1983
- 1983-04-20 JP JP6979383A patent/JPS59194837A/en active Granted
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5161553A (en) * | 1974-11-26 | 1976-05-28 | Yamauchi Rubber Ind Co Ltd | YOSETSUNADONIOITESHOSERARERU DANNETSUSOSEIBUTSU |
JPS57156249A (en) * | 1981-03-23 | 1982-09-27 | Matsushita Electric Works Ltd | Corrosion-resisting steel material and its manufacture |
JPS5863442A (en) * | 1981-10-13 | 1983-04-15 | 三菱自動車工業株式会社 | Manufacture of metallic plate and processed article |
Also Published As
Publication number | Publication date |
---|---|
JPS59194837A (en) | 1984-11-05 |
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