JP2662841B2 - Cast structural parts - Google Patents

Cast structural parts

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Publication number
JP2662841B2
JP2662841B2 JP30015492A JP30015492A JP2662841B2 JP 2662841 B2 JP2662841 B2 JP 2662841B2 JP 30015492 A JP30015492 A JP 30015492A JP 30015492 A JP30015492 A JP 30015492A JP 2662841 B2 JP2662841 B2 JP 2662841B2
Authority
JP
Japan
Prior art keywords
casting
chromic acid
cast
electroplating
galvanized layer
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
Application number
JP30015492A
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Japanese (ja)
Other versions
JPH06146000A (en
Inventor
敏道 鈴木
昌 川本
猛雄 沖
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Yuken Kogyo Co Ltd
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Yuken Kogyo Co Ltd
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Priority to JP30015492A priority Critical patent/JP2662841B2/en
Publication of JPH06146000A publication Critical patent/JPH06146000A/en
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は、鋳物製構造部品の基材
表面に、電気めっき又は溶融めっきにより亜鉛めっき層
が形成され、さらに、クロム酸系皮膜が形成されてなる
鋳物製構造部品に関する。特に多くの鉄系鋳物の如く錆
が発生し易い鋳物製構造部品に好適な発明である。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a structural part made of a casting, in which a galvanized layer is formed by electroplating or hot-dip coating on the surface of a base material of the structural part made of a casting, and a chromic acid-based film is formed. . In particular, the present invention is suitable for casting structural parts in which rust is likely to occur, such as many iron-based castings.

【0002】ここで、鋳物とは、鋳鉄(普通鋳鉄、及
び、Ni、Cr、Mo、Mn等を添加した合金鋳鉄)鋳
物、球状黒鉛鋳鉄(ダクタイル鋳鉄)鋳物、チル鋳物、
可鍛鋳鉄鋳物、鋼鋳物、等の鉄系鋳物の他に、非鉄合金
鋳物も含む概念である。
[0002] Here, castings include cast iron (plain cast iron and alloy cast iron to which Ni, Cr, Mo, Mn, etc. are added), spheroidal graphite cast iron (ductile cast iron) casting, chill casting,
This concept includes non-ferrous alloy castings in addition to iron-based castings such as malleable iron castings and steel castings.

【0003】また、亜鉛とは、亜鉛ばかりでなく、亜鉛
と、鉄、ニッケル、アルミニウム、銅、マグネシウム、
マンガン等との合金を指す。
[0003] Zinc means not only zinc but also zinc, iron, nickel, aluminum, copper, magnesium,
Refers to an alloy with manganese or the like.

【0004】さらに、鋳物製構造部品とは、ピストンシ
リンダ、ホースニップル、バルブケーシング、クランプ
等の機械部品、及び、建築用の各種金具等を含む概念で
ある。
[0004] Further, the cast structural component is a concept including mechanical parts such as a piston cylinder, a hose nipple, a valve casing, and a clamp, and various fittings for construction.

【0005】[0005]

【従来の技術及び発明が解決しようとする課題】以下、
鉄系鋳物を例に採り説明をするが、非鉄系であっても錆
の発生し易い鋳物の場合は、本発明を適用可能である。
BACKGROUND OF THE INVENTION Problems to be Solved by the Invention
The description will be made by taking an iron-based casting as an example, but the present invention can be applied to a casting that is likely to generate rust even if it is non-ferrous.

【0006】鉄系鋳物の防錆処理方法として、電気めっ
き又は溶融めっきにより亜鉛めっき層を形成し、さら
に、該亜鉛めっき層上に焼成クロメート被膜を形成する
ことが、一般に行なわれている。
[0006] As a method of rust-preventing treatment of iron-based castings, it is common practice to form a galvanized layer by electroplating or hot-dip plating, and further form a calcined chromate film on the galvanized layer.

【0007】しかし、当該防錆処理方法では、鉄系鋳物
の場合、通常の鋼板に同様の防錆処理をした場合に比し
て、格段に防錆性に劣る。鋳物は多孔性(多数の微細空
孔を有する)であり、微細空孔中に電気めっき又は溶融
めっきによる亜鉛めっきが浸透せず、亜鉛めっき層自体
もポーラスになると推定される。
[0007] However, in the rust-preventive treatment method, in the case of an iron-based casting, the rust-preventive property is remarkably inferior to that in a case where the same rust-preventive treatment is applied to a normal steel plate. It is presumed that the casting is porous (having a large number of fine holes), the zinc plating by electroplating or hot-dip plating does not penetrate into the fine holes, and the zinc plating layer itself becomes porous.

【0008】本発明は、上記にかんがみて、電気めっき
又は溶融めっきにより亜鉛めっき層が形成され、さら
に、クロム酸系皮膜が形成されてなる鋳物製構造部品に
おいて、格段に耐食性の向上した鋳物製構造部品を提供
することを目的とする。
[0008] In view of the above, the present invention provides a cast structural part having a galvanized layer formed by electroplating or hot-dip galvanizing and further having a chromic acid-based film formed thereon. It is intended to provide structural parts.

【0009】[0009]

【課題を解決するための手段】本発明は、上記課題を下
記構成により、解決するものである。
According to the present invention, the above-mentioned object is achieved by the following constitution.

【0010】鋳物製の基材表面に、電気めっき又は溶融
めっきにより亜鉛めっき層が形成され、さらに、該亜鉛
めっき層上にクロム酸系皮膜が形成されてなる鋳物製構
造部品において、前記クロム酸系皮膜が、三酸化クロム
及び燐酸二水素金属塩を必須配合成分とし、両者の配合
比を前者/後者=9/1〜4/6とする水系皮膜剤で形
成されていることを特徴とする。
[0010] In the cast structural component, a zinc plating layer is formed on the surface of a casting base material by electroplating or hot-dip plating, and a chromic acid-based film is further formed on the zinc plating layer. The chromium trioxide and the metal salt of dihydrogen phosphate are essential components, and the lacquer is formed of an aqueous coating agent in which the ratio of the former and the latter is 9/1 to 4/6. .

【0011】[0011]

【手段の詳細な説明】以下、本発明の手段について、詳
細に説明する。なお、配合単位は、特に断らない限り重
量単位である。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS The means of the present invention will be described in detail below. The blending units are weight units unless otherwise specified.

【0012】(1) 本発明の鋳物製構造部品は、鋳物製構
造部品の基材表面に、電気めっき又は溶融めっきにより
亜鉛めっき層が形成され、さらに、亜鉛めっき層上にク
ロム酸系皮膜が形成されてなることを前提とする。
(1) In the cast structural component of the present invention, a galvanized layer is formed on the surface of the base material of the cast structural component by electroplating or hot-dip plating, and a chromic acid-based film is further formed on the zinc plated layer. It is assumed that it is formed.

【0013】ここで、電気めっきで亜鉛めっき層の形成
する場合は、通常、酸性亜鉛めっき浴を使用して行な
う。酸性亜鉛めっき浴を使用するのは、水素過電圧が高
く、亜鉛が優先析出するためである。
Here, when a zinc plating layer is formed by electroplating, it is usually performed using an acidic zinc plating bath. The acidic zinc plating bath is used because the hydrogen overvoltage is high and zinc is preferentially deposited.

【0014】また、亜鉛めっき層の厚みは、電気めっき
の場合、通常1〜10μmとし、溶融めっきの場合、通
常、10〜100μmとする。
The thickness of the galvanized layer is usually 1 to 10 μm in the case of electroplating, and usually 10 to 100 μm in the case of hot dip plating.

【0015】なお、この亜鉛めっき層の形成に先立ち、
基材表面は、常法により清浄化しておく。即ち、トリク
ロロエチレン、トリクロロエタン等の有機溶剤、または
アルカリ洗浄剤等の水性洗浄剤を用いて油脂類の除去を
行って、表面を活性化しておく。または、ショットブラ
スト等の物理的方法によって表面を清浄化してもよい。
Prior to the formation of the galvanized layer,
The surface of the substrate is cleaned by a conventional method. That is, the surface is activated by removing oils and fats using an organic solvent such as trichloroethylene and trichloroethane or an aqueous detergent such as an alkaline detergent. Alternatively, the surface may be cleaned by a physical method such as shot blasting.

【0016】(2) そして、本発明は、上記構成の鋳物製
構造部品において、三酸化クロム及び燐酸二水素金属塩
(第一燐酸金属塩)を必須配合成分とし、両者の配合比
を前者/後者=9/1〜4/6(望ましくは7/1〜1
/1)とする水系皮膜剤で、前記クロム酸系皮膜が形成
されてなることを特徴とする。
(2) The present invention relates to a cast structural part having the above-mentioned structure, in which chromium trioxide and metal dihydrogen phosphate (metal first phosphate) are essential components, and the mixing ratio of both is the former / The latter = 9/1 to 4/6 (preferably 7/1 to 1
/ 1), wherein the chromic acid-based coating is formed with an aqueous coating agent.

【0017】燐酸二水素金属塩の比率が過少であると、
防錆性向上の作用を奏しがたく、燐酸二水素金属塩の比
率が過多であると、硬化皮膜の耐水性が劣化する。
If the proportion of the metal dihydrogen phosphate is too small,
It is difficult to achieve the effect of improving the rust resistance, and if the ratio of the metal dihydrogen phosphate is excessive, the water resistance of the cured film deteriorates.

【0018】また、必須配合成分の配合量(三酸化クロ
ムと燐酸二水素金属塩の合計量)で、10〜70%(望
ましくは40〜60%)とする。10%未満では、所定
の皮膜厚(通常、0.1 μm)を得がたく、70%を越え
ると両成分の飽和溶解度を越え沈殿が発生し易くなる。
The amount of the essential components (total amount of chromium trioxide and metal dihydrogen phosphate) is 10 to 70% (preferably 40 to 60%). If it is less than 10%, it is difficult to obtain a predetermined film thickness (usually 0.1 μm), and if it exceeds 70%, the saturation solubility of both components is exceeded and precipitation is liable to occur.

【0019】上記燐酸二水素金属塩の金属としては、カ
ルシウム・アルミニウム・マグネシウム・亜鉛等を挙げ
ることができる。なお、燐酸二水素塩の一部を、燐酸一
水素金属塩・燐酸正金属塩に置換してもよい(水溶性の
場合は約1/2以下、難溶性の場合は約1/9以下)。
Examples of the metal of the above-mentioned metal dihydrogen phosphate include calcium, aluminum, magnesium, and zinc. In addition, a part of dihydrogen phosphate may be replaced by metal monohydrogen phosphate / metal phosphate normal (about 1/2 or less in the case of water solubility, and about 1/9 or less in the case of poor solubility). .

【0020】また、三酸化クロムの一部を、クロム酸塩
・重クロム酸金属塩(カリウム・ナトリウム・マグネシ
ウム・亜鉛等の)または、三酸化二クロムと置換しても
よい(水溶性の場合は約1/2以下、難溶性の場合は約
1/9以下)。
Further, a part of the chromium trioxide may be replaced with a chromate / metal dichromate salt (such as potassium, sodium, magnesium, zinc, etc.) or dichromium trioxide (in the case of water solubility). Is about 1/2 or less, and when it is hardly soluble, about 1/9 or less).

【0021】また、他の配合成分として、一価・二価の
アルコール類及び界面活性剤を、通常使用する。
As other components, monohydric / dihydric alcohols and surfactants are usually used.

【0022】アルコール類は、クロム酸を還元重合させ
る作用を奏すると推定され、具体的には、エチルアルコ
ール、イソプロピルアルコール、イソブチルアルコー
ル、セロソルブ(以上一価)、エチレングリコール、ジ
エチレングリコール、ポリエチレングリコール(分子量
200〜600)等を使用可能である。アルコール類の
配合量は、必須配合成分の種類及び配合量により異なる
が、通常、1〜10%とする。
Alcohols are presumed to have an effect of reducing and polymerizing chromic acid. Specifically, alcohols include ethyl alcohol, isopropyl alcohol, isobutyl alcohol, cellosolve (monovalent), ethylene glycol, diethylene glycol, and polyethylene glycol (molecular weight). 200 to 600) can be used. The blending amount of the alcohol varies depending on the kind and blending amount of the essential blending component, but is usually 1 to 10%.

【0023】界面活性剤は、コーテイング膜のレベリン
グ性を高める作用を奏し、好ましくは、フッ素系界面活
性剤を使用する。その配合量は、通常、0.01〜0.1 %と
する。
The surfactant has an effect of improving the leveling property of the coating film, and a fluorine-based surfactant is preferably used. The amount is usually 0.01 to 0.1%.

【0024】(3) 上記要件の水系皮膜剤を前記亜鉛めっ
き層上に塗布し、加熱硬化させてが、クロム酸系皮膜を
形成する。
(3) The chromic acid-based film is formed by applying the water-based film agent of the above requirements on the galvanized layer and curing by heating.

【0025】塗布方法は、特に限定されないが、浸漬含
浸法またはスプレー法により行なう。また、必要によ
り、重ね塗りしてもよい。
The coating method is not particularly limited, but is performed by a dipping impregnation method or a spray method. Moreover, you may apply repeatedly, if needed.

【0026】加熱硬化の条件は、通常、100〜400
℃×5〜120min とする。加熱温度100℃未満で
は、耐水性が劣り、400℃を越えると皮膜にクラック
の発生が増加、膜特性が低下するおそれがある。
The conditions for heat curing are usually from 100 to 400
C. x 5-120 min. If the heating temperature is lower than 100 ° C., the water resistance is inferior. If the heating temperature is higher than 400 ° C., the occurrence of cracks in the film increases, and the film properties may be deteriorated.

【0027】上記クロム酸系皮膜の膜厚は、通常、0.05
〜10μm(望ましくは 0.1〜5μm)とする。0.05μ
m未満では耐熱性・硬度・耐食性等に対する効果が十分
に得られず、10μmを越えると皮膜の内部応力の蓄積
による膜質の低下及び着膜のための時間を要し、皮膜の
均一性に問題が生じ易い。
The thickness of the chromic acid-based coating is usually 0.05
To 10 μm (preferably 0.1 to 5 μm). 0.05μ
If it is less than m, the effects on heat resistance, hardness, corrosion resistance, etc. cannot be sufficiently obtained. If it exceeds 10 μm, deterioration of the film quality due to accumulation of internal stress of the film and time for film deposition are required, and uniformity of the film is problematic. Tends to occur.

【0028】[0028]

【発明の作用・効果】本発明の鋳物製構造部品は、基材
表面に、電気めっき又は溶融めっきにより亜鉛めっき層
が形成され、さらに、該亜鉛めっき層上にクロム酸系皮
膜が形成されてなるものにおいて、クロム酸系皮膜が、
三酸化クロム及び燐酸二水素金属塩を必須配合成分と
し、両者の配合比を前者/後者=9/1〜4/6とする
水系水系皮膜剤で形成されてなることを特徴とすること
により、後述の実施例で支持される如く、耐食性が著し
く向上した鋳物製構造部品を得ることができる。
The cast structural part of the present invention is characterized in that a galvanized layer is formed on the surface of a base material by electroplating or hot-dip plating, and a chromic acid-based film is formed on the galvanized layer. In the following, the chromic acid-based film is
It is characterized by being formed of an aqueous coating agent in which chromium trioxide and metal dihydrogen phosphate are essential components and the mixing ratio of the two is former / latter = 9/1 to 4/6. As supported by the examples described below, it is possible to obtain a structural part made of a casting with significantly improved corrosion resistance.

【0029】その理由は、下記の如くであると推定され
る。
The reason is presumed to be as follows.

【0030】鋳物上に電気科学的に犠牲陽極となるべく
亜鉛層を電気めっき又は溶融めっきで形成し電気化学防
食を行い、さらに鋳物(多孔性)自体及びそれに起因す
る亜鉛めっき層の多孔性を活用し、微溶解性のリン酸・
クロム酸複合化合物で浸透・充填させることによってク
ロムの不働態化による電気化学防食を呈していると考え
られる。
A zinc layer is formed on a casting by electroplating or hot-dip galvanizing to become a sacrificial anode electrochemically, electrochemical corrosion protection is performed, and the porosity of the casting (porosity) itself and the zinc plating layer resulting therefrom are utilized. And slightly soluble phosphoric acid
It is thought that the permeation and filling with the chromic acid complex compound results in electrochemical corrosion protection due to passivation of chromium.

【0031】クロム酸系皮膜の耐食性は、生成する皮
膜はガラス状で密着良く被覆するため、下地金属と空気
及び水分との接触を断ち、酸素の供給を遮蔽する、皮
膜中には6価クロムが残存しており加熱硬化によって微
溶解性になっているため、長時間に渡って経時的に6価
クロムを金属表面に補給し、6価クロムによる不働態化
を促進させる、の各作用が相乗して得られると考えられ
る。
The corrosion resistance of the chromic acid-based coating is such that the resulting coating is glassy and is coated with good adhesion, so that the contact between the base metal and air and moisture is cut off and the supply of oxygen is blocked. Remains and is slightly soluble by heat curing, so that hexavalent chromium is replenished to the metal surface over time over a long period of time to promote the passivation by hexavalent chromium. It is thought that they can be obtained in a synergistic manner.

【0032】[0032]

【実施例】以下、本発明の効果を確認するために、比較
例とともに行なった実施例について説明をする。
EXAMPLES Hereinafter, examples performed together with comparative examples to confirm the effects of the present invention will be described.

【0033】(1) 亜鉛めっき層が形成された各鋳物製構
造部品(被塗布物:20cm×5cmφピストンシリンダ、
ねずみ鋳鉄製)を、予め調製しておいた表1・2に示す
組成の水系皮膜剤に浸漬塗布して、引き上げ後、遠心乾
燥(800rpm×30秒)し、さらに、表示の条件で
塗膜を加熱硬化させた。
(1) Casting structural parts on which a galvanized layer is formed (object to be coated: 20 cm × 5 cm φ piston cylinder,
(Made of gray cast iron) is immersed and coated in a water-based coating agent having the composition shown in Tables 1 and 2 prepared in advance, and after lifting, centrifugal drying (800 rpm × 30 seconds), and coating under the conditions shown. Was cured by heating.

【0034】なお、実施例1〜7及び比較例1〜7につ
いては、下記亜鉛めっき浴(塩化浴)及び条件で電気め
っきを行なった。
In Examples 1 to 7 and Comparative Examples 1 to 7, electroplating was performed in the following zinc plating bath (chloride bath) and conditions.

【0035】 ZnCl2 ・7H2 O 30g/L NH4 Cl 200g/L 光沢剤 31.5ml/
L pH 5 温度 25℃ 電流密度 2A/dm2 めっき層厚み 5μm また、実施例8については、浸漬温度450℃で、めっ
き厚み30μmとなるように溶融めっきを行なった。
ZnCl 2 .7H 2 O 30 g / L NH 4 Cl 200 g / L Brightener 31.5 ml /
L pH 5 Temperature 25 ° C. Current Density 2 A / dm 2 Plating Layer Thickness 5 μm Further, in Example 8, hot-dip plating was performed at an immersion temperature of 450 ° C. to a plating thickness of 30 μm.

【0036】(2) こうして得た各構造部品について、下
記項目の試験を行なった。表1・2に示す試験結果か
ら、本発明の鋳物製構造部品である各実施例は、比較例
に比して、格段に耐食性及び表面硬度が向上しているこ
とが判る。
(2) The following items were tested for each of the structural parts thus obtained. From the test results shown in Tables 1 and 2, it can be seen that the respective examples which are the cast structural parts of the present invention have significantly improved corrosion resistance and surface hardness as compared with the comparative examples.

【0037】塩水噴霧試験…耐熱試験(200度×5
h)後、 JIS Z 2371 に準じて行なった。
Salt spray test: heat resistance test (200 degrees × 5)
h) Thereafter, the measurement was performed according to JIS Z 2371.

【0038】[0038]

【表1】 [Table 1]

【0039】*1)「フロラード FC−95」住友3
M社製
* 1) "Floraldo FC-95" Sumitomo 3
M company

【0040】[0040]

【表2】 [Table 2]

【0041】*1)「フロラード FC−95」住友3
M社製 *2)日本油脂(株)製非イオン界面活性剤 *3)ダイヤモンドシャムロック社製非イオン界面活性
* 1) "Floraldo FC-95" Sumitomo 3
* 2) Nonionic surfactant manufactured by NOF Corporation * 3) Nonionic surfactant manufactured by Diamond Shamrock

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 鋳物製の基材表面に、電気めっき又は溶
融めっきにより亜鉛めっき層が形成され、さらに、該亜
鉛めっき層上にクロム酸系皮膜が形成されてなる鋳物製
構造部品において、 前記クロム酸系皮膜が、三酸化クロム及び燐酸二水素金
属塩を必須配合成分とし、両者の配合比を前者/後者=
9/1〜4/6とする水系皮膜剤で形成されていること
を特徴とする鋳物製構造部品。
1. A cast structural component comprising: a galvanized layer formed by electroplating or hot-dip plating on a surface of a cast base material; and a chromic acid-based film formed on the galvanized layer. The chromic acid-based film contains chromium trioxide and metal dihydrogen phosphate as essential components, and the mixing ratio of both is the former / the latter =
A casting-made structural part characterized by being formed of an aqueous coating agent of 9/1 to 4/6.
JP30015492A 1992-11-10 1992-11-10 Cast structural parts Expired - Lifetime JP2662841B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP30015492A JP2662841B2 (en) 1992-11-10 1992-11-10 Cast structural parts

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30015492A JP2662841B2 (en) 1992-11-10 1992-11-10 Cast structural parts

Publications (2)

Publication Number Publication Date
JPH06146000A JPH06146000A (en) 1994-05-27
JP2662841B2 true JP2662841B2 (en) 1997-10-15

Family

ID=17881400

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30015492A Expired - Lifetime JP2662841B2 (en) 1992-11-10 1992-11-10 Cast structural parts

Country Status (1)

Country Link
JP (1) JP2662841B2 (en)

Also Published As

Publication number Publication date
JPH06146000A (en) 1994-05-27

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