JPH10219494A - Chromate treated electrogalvanized steel sheet having excellent blackening resistance and its production - Google Patents
Chromate treated electrogalvanized steel sheet having excellent blackening resistance and its productionInfo
- Publication number
- JPH10219494A JPH10219494A JP32911797A JP32911797A JPH10219494A JP H10219494 A JPH10219494 A JP H10219494A JP 32911797 A JP32911797 A JP 32911797A JP 32911797 A JP32911797 A JP 32911797A JP H10219494 A JPH10219494 A JP H10219494A
- Authority
- JP
- Japan
- Prior art keywords
- steel sheet
- electrogalvanized
- chromate
- blackening
- electrogalvanized steel
- 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.)
- Granted
Links
Landscapes
- Electroplating And Plating Baths Therefor (AREA)
- Electroplating Methods And Accessories (AREA)
- Other Surface Treatments For Metallic Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】この発明は、耐黒変性に優れ
たクロメート処理電気亜鉛めっき鋼板およびその製造方
法に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a chromate-treated galvanized steel sheet having excellent resistance to blackening and a method for producing the same.
【0002】[0002]
【従来の技術】電気亜鉛めっき鋼板を無塗装で使用する
場合、通常、クロメート処理によって電気亜鉛めっき層
の上にクロメート被膜が形成される。このようなクロメ
ート被膜が形成されたクロメート処理電気亜鉛めっき鋼
板の耐食性は著しく改善されるが、これを、高温湿潤環
境下で保管中に、その表面の一部または全部が灰白色ま
たは褐色に変色する現象(以下、「黒変現象」という)
の生ずることがある。黒変現象の生じたクロメート処理
電気亜鉛めっき鋼板は、その商品価値を著しく低下させ
る。2. Description of the Related Art When an electrogalvanized steel sheet is used without painting, a chromate film is usually formed on the electrogalvanized layer by a chromate treatment. Although the corrosion resistance of the chromate-treated electrogalvanized steel sheet having such a chromate film formed thereon is remarkably improved, a part or all of the surface of the chromate-treated electrogalvanized steel sheet turns grayish brown or brown during storage in a high-temperature and humid environment. Phenomenon (hereinafter referred to as "blackening phenomenon")
May occur. A chromate-treated electrogalvanized steel sheet having a blackening phenomenon significantly reduces its commercial value.
【0003】黒変現象の詳細は必ずしも明らかではない
が、黒変は、亜鉛表面の腐食現象であり、めっき皮膜中
のPbが黒変を促進させ、Niは逆に黒変を抑制する作
用がある旨の報告がある。このような黒変現象の発生防
止手段に関しては、従来から種々研究がなされており、
例えば、特開昭60−77988号公報には、亜鉛めっ
き浴中のNiイオンを、不純物として含まれるPbイオ
ンの量の5〜500倍の範囲内、Znイオンの量の1/
25以下で且つ10g/l以下の量で含有する電気亜鉛め
っき浴を使用し、このような電気亜鉛めっき浴によって
鋼板を電気亜鉛めっきし、次いで、クロメート処理を施
すことにより耐黒変性を改善する方法(以下、先行技術
1という)が開示されている。Although the details of the blackening phenomenon are not always clear, blackening is a corrosion phenomenon on the zinc surface. Pb in the plating film promotes blackening, and Ni has the effect of suppressing blackening. There is a report that there is. Various studies have been made on the means for preventing the occurrence of such a blackening phenomenon.
For example, Japanese Patent Application Laid-Open No. 60-77988 discloses that Ni ions in a galvanizing bath are mixed in a range of 5 to 500 times the amount of Pb ions contained as impurities, and 1/100 of the amount of Zn ions.
Using an electrogalvanizing bath containing not more than 25 and not more than 10 g / l, the steel sheet is electrogalvanized by such an electrogalvanizing bath, and then subjected to chromate treatment to improve blackening resistance. A method (hereinafter referred to as Prior Art 1) is disclosed.
【0004】また、特開平2−8374号公報には、N
iイオンを、100〜300ppmの範囲内の量で含有
し、不純物として含まれるPbイオンの含有量が0.5
ppm以下で且つめっき浴中のNiイオン/Pbイオン
比が500超である電気亜鉛めっき浴を使用し、このよ
うな電気亜鉛めっき浴によって鋼板を電気亜鉛めっき
し、次いで、クロメート処理を施すことによって耐黒変
性を改善する方法(以下、先行技術2という)が開示さ
れている。[0004] Japanese Patent Application Laid-Open No. 2-8374 discloses N
i ions are contained in an amount within the range of 100 to 300 ppm, and the content of Pb ions contained as impurities is 0.5%.
By using an electrogalvanizing bath having a Ni ion / Pb ion ratio of 500 ppm or less and a Ni ion / Pb ion ratio in the plating bath exceeding 500, the steel sheet is electrogalvanized by such an electrogalvanizing bath, and then subjected to a chromate treatment. A method for improving blackening resistance (hereinafter referred to as Prior Art 2) is disclosed.
【0005】上述した先行技術1、2によれば、クロメ
ート処理電気亜鉛めっき鋼板の耐黒変性は改善される
が、めっき皮膜中にNiが含有されていることによっ
て、電気亜鉛めっき鋼板の表面外観、特に、白色度が低
下する。According to the prior arts 1 and 2 described above, although the blackening resistance of the chromate-treated electrogalvanized steel sheet is improved, the appearance of the surface of the electrogalvanized steel sheet is reduced due to the inclusion of Ni in the plating film. In particular, whiteness decreases.
【0006】このような問題に関して、特開昭63−4
099号公報には、亜鉛めっき浴中にNiイオンが30
0ppm以上存在すると、リン酸塩処理が施された亜鉛
めっき鋼板の白色度が50以下に低下するために、亜鉛
めっき浴中のNiイオン濃度をできるだけ低く維持する
必要があり、その対策として、亜鉛粉末を使用してNi
イオンを除去する方法(以下、先行技術3という)が開
示されている。Regarding such a problem, Japanese Patent Application Laid-Open No. 63-4 / 1988
No. 099 discloses that 30 ions of Ni are contained in a galvanizing bath.
If it is present in an amount of 0 ppm or more, the whiteness of the galvanized steel sheet subjected to the phosphate treatment is reduced to 50 or less. Therefore, it is necessary to maintain the Ni ion concentration in the galvanizing bath as low as possible. Ni using powder
A method for removing ions (hereinafter referred to as Prior Art 3) is disclosed.
【0007】また、特開平1−129991号公報に
は、電気亜鉛めっき鋼板のリン酸塩処理後の色調を白く
保持するためには、亜鉛めっき浴中のNiイオン濃度を
10ppm以下に管理する方法(以下、先行技術4とい
う)が開示されている。Japanese Patent Application Laid-Open No. 1-129991 discloses a method of controlling the concentration of Ni ions in a zinc plating bath to 10 ppm or less in order to keep the color tone of a galvanized steel sheet white after the phosphate treatment. (Hereinafter referred to as Prior Art 4).
【0008】[0008]
【発明が解決しようとする課題】一般に、電気亜鉛めっ
き鋼板の製造は、同一設備および同一めっき浴によりク
ロメート処理、リン酸塩処理、後処理無しの工程によっ
て行われる。従って、先行技術3および先行技術4のよ
うに、電気亜鉛めっき鋼板の耐黒変性を改善するため
に、めっき浴中にNiを添加すると、クロメート処理材
のみならず、それ以外のめっき鋼板の外観をも劣化させ
ることになる。従って、めっき浴中へのNi添加には従
来から問題があった。Generally, the production of an electrogalvanized steel sheet is carried out by the same equipment and the same plating bath without chromate treatment, phosphate treatment and post-treatment. Therefore, as in Prior Art 3 and Prior Art 4, when Ni is added to the plating bath in order to improve the blackening resistance of the electrogalvanized steel sheet, not only the chromate-treated material but also the appearance of other plated steel sheets Will also deteriorate. Therefore, there has conventionally been a problem with the addition of Ni to the plating bath.
【0009】一方、溶融亜鉛めっき鋼板の耐黒変性は、
電気亜鉛めっき鋼板よりも大きく劣ることが知られてい
る。その理由は、溶融亜鉛めっき鋼板の表面には、電気
亜鉛めっき鋼板に比較して、厚く不均一なZn酸化膜が
生成しており、且つ、めっき浴中のAlが酸化物として
めっき表面に存在しているので、黒変現象が進行しやす
いためである。On the other hand, blackening resistance of hot-dip galvanized steel sheet is as follows:
It is known to be significantly inferior to electrogalvanized steel sheets. The reason is that a thick and uneven Zn oxide film is generated on the surface of the hot-dip galvanized steel sheet compared to the electro-galvanized steel sheet, and Al in the plating bath exists as an oxide on the surface of the galvanized steel sheet. This is because the blackening phenomenon easily proceeds.
【0010】このような溶融亜鉛めっき鋼板の黒変対策
として、例えば、特公平3−49982号公報には、溶
融亜鉛めっき鋼板の表面に電気亜鉛めっきを施す技術
(以下、先行技術5という)が開示されており、電気亜
鉛めっき鋼板の耐黒変性は、溶融亜鉛めっき鋼板に比較
して良好であることが示唆されている。更に、先行技術
5には、溶融亜鉛めっき後の溶融亜鉛めっき鋼板を、N
iイオンまたはCoイオンを1〜20g/l含有するpH1
〜4またはpH11〜13.5の溶液に浸漬し、Niまた
はCoを0.3〜15mg/m2 付着させる方法が開示され
ている。As a countermeasure against blackening of the hot-dip galvanized steel sheet, for example, Japanese Patent Publication No. 3-49982 discloses a technique of electrogalvanizing the surface of a hot-dip galvanized steel sheet (hereinafter referred to as Prior Art 5). It is disclosed that the blackening resistance of the electrogalvanized steel sheet is better than that of the galvanized steel sheet. Further, in prior art 5, a hot-dip galvanized steel sheet after hot-dip galvanizing is
pH 1 containing 1 to 20 g / l of i ion or Co ion
A method is disclosed in which the substrate is immersed in a solution having a pH of 44 or pH 11 to 13.5 to deposit Ni or Co in an amount of 0.3 to 15 mg / m 2 .
【0011】また、特開平2−267279号公報に
は、同じく溶融亜鉛めっき鋼板を、グルコン酸NaとE
DTA、NTA,クエン酸塩等のような錯化剤を含有す
るNi、Co処理液に接触させることにより、耐黒変性
を改善する方法(以下、先行技術6という)が開示され
ている。Japanese Unexamined Patent Publication (Kokai) No. 2-267279 also discloses that a hot-dip galvanized steel sheet is made of Na gluconate and E
A method for improving the resistance to blackening by contacting with a Ni or Co treatment solution containing a complexing agent such as DTA, NTA, citrate (hereinafter referred to as Prior Art 6) is disclosed.
【0012】先行技術5および6によれば、溶融亜鉛め
っき鋼板の耐黒変性は改善される。しかしながら、電気
亜鉛めっき鋼板の耐黒変性は改善されない。その理由
は、前述したように、電気亜鉛めっき層の表面には、溶
融亜鉛めっき層のような厚い酸化膜やAl酸化物が存在し
ないために、Ni、Co処理液のような酸、アルカリ液
中ではめっき表面が過剰に侵食されて活性化しすぎる結
果、電気亜鉛めっき層の表面に不均一な酸化皮膜が生成
するためであると考えられる。According to the prior arts 5 and 6, the blackening resistance of a galvanized steel sheet is improved. However, the blackening resistance of the electrogalvanized steel sheet is not improved. The reason is that, as described above, since the surface of the electrogalvanized layer does not have a thick oxide film or Al oxide such as a hot-dip galvanized layer, an acid or alkaline solution such as a Ni or Co treatment solution is used. This is considered to be because a non-uniform oxide film is formed on the surface of the electrogalvanized layer as a result of excessive activation of the plating surface due to excessive erosion.
【0013】以上述べたように、電気亜鉛めっき鋼板と
溶融亜鉛めっき鋼板とでは、その表面状態特に酸化状態
が異なることから、黒変現象のような亜鉛めっき層表面
の軽微な酸化現象を抑制する手段は相違すると考えら
れ、電気亜鉛めっき鋼板に適した黒変防止対策が必要と
されている。しかしながら、未だ、電気亜鉛めっき鋼板
に適した黒変防止対策は確立されていない。As described above, since the electrogalvanized steel sheet and the hot-dip galvanized steel sheet have different surface states, particularly oxidation states, slight oxidation phenomena such as blackening on the surface of the galvanized layer are suppressed. The means are considered to be different, and there is a need for blackening prevention measures suitable for electrogalvanized steel sheets. However, blackening prevention measures suitable for electrogalvanized steel sheets have not yet been established.
【0014】従って、この発明の目的は、上述した問題
を解決し、電気亜鉛めっき鋼板に適した黒変防止対策が
施され、同一設備且つ同一めっき浴でクロメート処理、
リン酸塩処理、後処理無し等の電気亜鉛めっき鋼板を製
造する場合に、クロメート処理材の耐黒変性を著しく改
善すると共に、クロメート処理材以外のリン酸塩処理材
等に関しては外観の劣化することがない、耐黒変性に優
れた電気亜鉛めっき鋼板およびその製造方法を提供する
ことにある。[0014] Accordingly, an object of the present invention is to solve the above-mentioned problems, take measures to prevent blackening suitable for electrogalvanized steel sheets, and perform chromate treatment in the same equipment and the same plating bath.
When manufacturing electrogalvanized steel sheets without phosphating or post-treatment, the blackening resistance of chromate-treated material is remarkably improved, and the appearance of phosphate-treated materials other than chromate-treated material deteriorates. An object of the present invention is to provide an electrogalvanized steel sheet having excellent resistance to blackening and a method for producing the same.
【0015】[0015]
【課題を解決するための手段】請求項1に記載した発明
のクロメート処理電気亜鉛めっき鋼板は、鋼板と、前記
鋼板の表面上に形成された電気亜鉛めっき層と、前記電
気亜鉛めっき層の表面に、NiおよびCoの少なくとも
1つを、0.01mg/m2 以上、10mg/m2 以下の範囲内
の量で析出させることによって形成された金属層と、前
記金属層の上に形成されたクロメート皮膜とからなるこ
とに特徴を有するものである。A chromate-treated electrogalvanized steel sheet according to the first aspect of the present invention includes a steel sheet, an electrogalvanized layer formed on a surface of the steel sheet, and a surface of the electrogalvanized layer. A metal layer formed by depositing at least one of Ni and Co in an amount within a range of 0.01 mg / m 2 or more and 10 mg / m 2 or less, and a metal layer formed on the metal layer. It is characterized by being composed of a chromate film.
【0016】請求項2に記載した発明のクロメート処理
電気亜鉛めっき鋼板の製造方法は、鋼板に電気亜鉛めっ
きを施して、少なくとも一方の表面上に電気亜鉛めっき
層が形成された電気亜鉛めっき鋼板を調製し、前記電気
亜鉛めっき鋼板を、NiイオンおよびCoイオンの少な
くとも1つが、0.001g/l以上、10g/l以下の量
で添加され、pH値が8以上、11未満の弱アルカリ性溶
液に接触させることによって、前記電気亜鉛めっき層の
表面に、NiおよびCoの少なくとも1つを0.01mg
/m2 以上、10mg/m2 以下の範囲内の量で析出させて前
記電気亜鉛めっき層の表面に金属層を形成し、次いで、
クロメート処理を施すことに特徴を有するものである。According to a second aspect of the present invention, there is provided a method for producing a chromate-treated electrogalvanized steel sheet, comprising: applying an electrogalvanized steel sheet to an electrogalvanized steel sheet having an electrogalvanized layer formed on at least one surface. The electrogalvanized steel sheet is prepared by adding at least one of Ni ions and Co ions in an amount of not less than 0.001 g / l and not more than 10 g / l to a weak alkaline solution having a pH value of 8 or more and less than 11. By contacting, 0.01 mg of at least one of Ni and Co was applied to the surface of the electrogalvanized layer.
/ m 2 or more and 10 mg / m 2 to form a metal layer on the surface of the electrogalvanized layer by depositing in an amount within the range of
It is characterized by performing chromate treatment.
【0017】請求項3に記載の発明は、上記請求項2に
記載の方法における弱アルカリ性溶液が、ピロリン酸ナ
トリウム系溶液またはトリポリリン酸ナトリウム系溶
液、または、前記ピロリン酸ナトリウム系溶液と前記ト
リポリリン酸ナトリウム系溶液との混合液であることに
特徴を有するものである。According to a third aspect of the present invention, in the method according to the second aspect, the weak alkaline solution is a sodium pyrophosphate solution or a sodium tripolyphosphate solution, or the sodium pyrophosphate solution and the tripolyphosphate are combined. It is characterized by being a mixture with a sodium-based solution.
【0018】[0018]
【発明の実施の形態】次に、この発明の耐黒変性に優れ
た亜鉛めっき鋼板について、以下に説明する。この発明
の耐黒変性に優れた電気亜鉛めっき鋼板は、鋼板と、鋼
板の表面上に形成された電気亜鉛めっき層と、電気亜鉛
めっき層の上に形成された金属層と、金属層の上に形成
されたクロメート被膜とからなる基本構造を有してい
る。Next, a galvanized steel sheet having excellent blackening resistance according to the present invention will be described below. The electrogalvanized steel sheet having excellent blackening resistance according to the present invention includes a steel sheet, an electrogalvanized layer formed on the surface of the steel sheet, a metal layer formed on the electrogalvanized layer, and a metal layer formed on the electrogalvanized layer. And a chromate film formed on the substrate.
【0019】上述した基本構造において、この発明の特
徴は、電気亜鉛めっき層の表面にNiおよびCoの少な
くとも1つを0.01mg/m2 以上、10mg/m2 以下の範
囲内の量で析出させることによって、上記金属層が電気
亜鉛めっき層の表面上に形成されていることにある。In the basic structure described above, the present invention is characterized in that at least one of Ni and Co is deposited on the surface of the electrogalvanized layer in an amount of 0.01 mg / m 2 or more and 10 mg / m 2 or less. In this case, the metal layer is formed on the surface of the electrogalvanized layer.
【0020】即ち、電気亜鉛めっき層の表面に、Niお
よびCoの少なくとも1つを、0.01mg/m2 以上、1
0mg/m2 以下の範囲内の量で析出させ、電気亜鉛めっき
層の表面上に金属層を形成することによって、クロメー
ト処理材の耐黒変性を改善することができ、白色度に優
れた電気亜鉛めっき鋼板が得られる。That is, at least one of Ni and Co is applied on the surface of the electrogalvanized layer in an amount of 0.01 mg / m 2 or more,
By precipitating in an amount of 0 mg / m 2 or less and forming a metal layer on the surface of the electrogalvanized layer, the blackening resistance of the chromate-treated material can be improved, and the whiteness can be improved. A galvanized steel sheet is obtained.
【0021】NiおよびCoの少なくとも1つの析出量
が0.01mg/m2 未満では、クロメート処理材の耐黒変
性を顕著に改善することはできない。一方、Niおよび
Coの少なくとも1つの析出量が10mg/m2 を超える
と、白色度の低下、ムラの発生等の外観の劣化が生じ
る。従って、電気亜鉛めっき層の表面へのNiおよびC
oの少なくとも1つの析出量は0.01mg/m2 以上、1
0mg/m2 以下の範囲内に限定すべきであり、これによっ
て、クロメート処理材の耐黒変性を改善するというNi
および/またはCoの効果が十分に発揮されると共に、
上記成分に起因する外観の劣化を、実質的に無視できる
程度に抑制することができる。If the precipitation amount of at least one of Ni and Co is less than 0.01 mg / m 2 , the blackening resistance of the chromate-treated material cannot be remarkably improved. On the other hand, when the precipitation amount of at least one of Ni and Co exceeds 10 mg / m 2 , the appearance deteriorates such as a decrease in whiteness and unevenness. Therefore, Ni and C on the surface of the electrogalvanized layer
The amount of at least one of o is 0.01 mg / m 2 or more,
0 mg / m 2 or less, thereby improving the blackening resistance of the chromate-treated material.
And / or the effect of Co is fully exhibited,
Deterioration of appearance due to the above components can be suppressed to a substantially negligible degree.
【0022】電気亜鉛めっき層の表面へのNiおよびC
oの少なくとも1つの、より好ましい析出量は、0.0
1mg/m2 以上、1mg/m2 以下の範囲内であり、更に好ま
しくは、0.01mg/m2 以上、0.2mg/m2 以下の範囲
内である。Ni and C on the surface of electrogalvanized layer
At least one, more preferred deposition amount of o is 0.0
It is in the range of 1 mg / m 2 or more and 1 mg / m 2 or less, and more preferably in the range of 0.01 mg / m 2 or more and 0.2 mg / m 2 or less.
【0023】上述したように、この発明の耐黒変性に優
れた電気亜鉛めっき鋼板は、電気亜鉛めっき層の表面に
NiおよびCoの少なくとも1つが上述した所定量で析
出され、電気亜鉛めっき層の表面上に金属層が形成され
ていることを除き、従来の電気亜鉛めっき鋼板と同一で
ある。従って、その他の構成要素に関する説明を省略す
る。As described above, in the electrogalvanized steel sheet having excellent blackening resistance according to the present invention, at least one of Ni and Co is deposited on the surface of the electrogalvanized layer in the above-mentioned predetermined amounts, and It is the same as a conventional electrogalvanized steel sheet except that a metal layer is formed on the surface. Therefore, description of the other components will be omitted.
【0024】次に、この発明の、耐黒変性に優れた電気
亜鉛めっき鋼板の製造方法について以下に説明する。黒
変現象は、亜鉛表面の酸化によって生ずる現象であると
考えられており、従って、亜鉛めっき層の表面を改質す
ることによって、黒変現象を抑制することができると判
断される。即ち、亜鉛めっき被膜中へのNiの添加は耐
黒変性に好ましい影響を及ぼすことから、亜鉛めっき層
の表面にNiを析出させることによって、耐黒変性を改
善することができると判断される。Next, a method for producing an electrogalvanized steel sheet having excellent blackening resistance according to the present invention will be described below. The blackening phenomenon is considered to be a phenomenon caused by oxidation of the zinc surface. Therefore, it is determined that the blackening phenomenon can be suppressed by modifying the surface of the zinc plating layer. That is, since the addition of Ni to the galvanized coating has a favorable effect on the blackening resistance, it is determined that the blackening resistance can be improved by depositing Ni on the surface of the zinc plating layer.
【0025】何れの処理方法によっても、電気亜鉛めっ
き層の表面にNiを析出させて、耐黒変性を改善するこ
とができるわけではなく、限られた処理条件に従って、
電気亜鉛めっき層の表面にNiを析出させることによ
り、耐黒変性を改善することができる。その方法につい
て、以下に詳述する。According to any of the treatment methods, Ni cannot be precipitated on the surface of the electrogalvanized layer to improve the blackening resistance.
By depositing Ni on the surface of the electrogalvanized layer, blackening resistance can be improved. The method will be described in detail below.
【0026】本発明者等は、電気亜鉛めっき層の表面に
Niを析出させる方法に関して鋭意研究を重ねた結果、
黒変現象の防止に有効なNiの析出は、ピロリン酸ナト
リウム系溶液またはトリポリリン酸ナトリウム溶液また
は両者の混合液によってのみ可能であることを知見し
た。The present inventors have conducted intensive studies on a method of depositing Ni on the surface of an electrogalvanized layer, and as a result,
It has been found that precipitation of Ni effective for preventing the blackening phenomenon can be achieved only by a sodium pyrophosphate-based solution or a sodium tripolyphosphate solution or a mixture of both.
【0027】周知のように、Niは両性金属であり、N
iイオンは酸性溶液およびアルカリ性溶液中において、
より大きい溶解度を有する。そこで、酸性溶液およびア
ルカリ性溶液の双方を使用して、Niの析出処理を行っ
た。As is well known, Ni is an amphoteric metal and N
i-ions in acidic and alkaline solutions
Has greater solubility. Then, the precipitation treatment of Ni was performed using both the acidic solution and the alkaline solution.
【0028】先ず、酸性浴を使用し、電気亜鉛めっき層
の表面へのNiの析出を試みた結果、上記Niの析出は
可能であることが確認された。しかしながら、酸性浴を
使用してNiを析出させた場合には、その後のクロメー
ト処理におけるクロメート付着量が極端に低下し、ま
た、耐黒変性改善効果も不十分であった。一方、強アル
カリ浴、例えば、水酸化ナトリウム系溶液を用いて、電
気亜鉛めっき層の表面へのNiの析出を試みたが、同め
っき層の表面に十分な量のNiを析出させることはでき
なかった。First, Ni was deposited on the surface of the electrogalvanized layer using an acidic bath, and as a result, it was confirmed that the above-mentioned Ni deposition was possible. However, when Ni was precipitated using an acidic bath, the amount of chromate adhering in the subsequent chromate treatment was extremely reduced, and the effect of improving blackening resistance was insufficient. On the other hand, Ni was deposited on the surface of the electrogalvanized layer using a strong alkaline bath, for example, a sodium hydroxide solution, but a sufficient amount of Ni could be deposited on the surface of the galvanized layer. Did not.
【0029】そこで、本発明者等は、中性乃至弱アルカ
リ性の処理液を使用してNiを析出させる方法につき研
究を行った。前述したように、先行技術7(特開平2−
267279号公報)には、溶融亜鉛めっき鋼板を、グ
ルコン酸NaとEDTA、NTA,クエン酸塩等のよう
な錯化剤を含有するNi、Co処理液に接触させること
により耐黒変性を改善する方法が開示されているが、こ
の方法では、溶融亜鉛めっき鋼板の耐黒変性は改善され
ても、電気亜鉛めっき鋼板の耐黒変性を改善することは
できない。The present inventors have studied on a method for depositing Ni using a neutral or weakly alkaline processing solution. As described above, prior art 7 (Japanese Unexamined Patent Application Publication No.
No. 267279 discloses that a hot-dip galvanized steel sheet is contacted with a Ni or Co treatment liquid containing a complexing agent such as Na gluconate and EDTA, NTA, citrate, etc. to improve blackening resistance. Although a method is disclosed, this method cannot improve the blackening resistance of an electrogalvanized steel sheet even if the blackening resistance of a galvanized steel sheet is improved.
【0030】その理由は、電気亜鉛めっき鋼板に対して
は、使用した処理液の成分、および、それら成分の存在
状態に大きな影響を与えるpHが適切でなく、従って、析
出したNiおよび/またはCoの存在状態と電気亜鉛め
っき層の表面状態とが、電気亜鉛めっき鋼板の黒変防止
に不適切であったためであると考えられる。The reason is that for the electrogalvanized steel sheet, the components of the processing solution used and the pH which greatly affects the state of the presence of these components are not appropriate, and thus the deposited Ni and / or Co This is considered to be because the presence state and the surface state of the electrogalvanized layer were inappropriate for preventing blackening of the electrogalvanized steel sheet.
【0031】そこで、電気亜鉛めっき鋼板に対しもっと
も適切な、処理液の成分系とpH値の検討を進めた。その
結果、pH8以上11未満のピロリン酸ナトリウム系溶液
またはトリポリリン酸ナトリウム系溶液またはこれらの
混合液を使用した場合には、かなり高濃度のNiイオン
が溶解されることを見出した。Therefore, the study of the component system and the pH value of the treatment solution most suitable for the electrogalvanized steel sheet was advanced. As a result, it has been found that when a sodium pyrophosphate-based solution or a sodium tripolyphosphate-based solution having a pH of 8 or more and less than 11 or a mixture thereof is used, a considerably high concentration of Ni ions is dissolved.
【0032】電気亜鉛めっき鋼板にこのような溶液を接
触させたところ、電気亜鉛めっき層の表面に、十分な量
のNiおよび/またはCoを析出させることが可能であ
り、NiおよびCoが均一に析出していることが確認さ
れた。また、クロメート皮膜も均一に生成していた。こ
れによって、電気亜鉛めっき鋼板の場合でも、クロメー
ト処理後の耐黒変性が著しく改善されることが確認され
た。When such a solution is brought into contact with an electrogalvanized steel sheet, a sufficient amount of Ni and / or Co can be precipitated on the surface of the electrogalvanized layer, and Ni and Co are uniformly deposited. It was confirmed that they had precipitated. Further, the chromate film was also formed uniformly. Thereby, even in the case of the electrogalvanized steel sheet, it was confirmed that the blackening resistance after the chromate treatment was remarkably improved.
【0033】更に、Niと同様、Coイオンも、pH8以
上11未満の弱アルカリ性のピロリン酸ナトリウム系溶
液またはトリポリリン酸ナトリウム系溶液またはこれら
の混合液に溶解でき、この溶液に電気亜鉛めっき鋼板を
接触させることによって金属Coが析出し、クロメート
処理後の耐黒変性を大きく改善し得ることが確認され
た。Further, like Ni, Co ions can be dissolved in a weakly alkaline sodium pyrophosphate-based solution or a sodium tripolyphosphate-based solution having a pH of 8 or more and less than 11 or a mixture thereof, and an electrogalvanized steel sheet is brought into contact with this solution. By doing so, it was confirmed that metal Co was precipitated, and the blackening resistance after chromate treatment could be greatly improved.
【0034】前述したように、Niおよび/またはCo
の析出量は、0.01mg/m2 以上、10mg/m2 以下の範
囲内に維持しなければならないが、Niおよび/または
Coの析出量をこの範囲内に維持するためには、pH値が
8以上11未満の弱アルカリ性溶液であるピロリン酸ナ
トリウム系溶液またはトリポリリン酸ナトリウム系溶液
またはこれらの混合液中に、0.001g/l以上、10
g/l以下のNiイオンおよび/またはCoイオンを添加
すればよい。As described above, Ni and / or Co
Must be kept within the range of 0.01 mg / m 2 or more and 10 mg / m 2 or less. In order to maintain the precipitation amount of Ni and / or Co within this range, the pH value must be maintained. In a sodium pyrophosphate-based solution or sodium tripolyphosphate-based solution or a mixture thereof, which is a weakly alkaline solution having a pH of 8 to less than 11,
g / l or less of Ni ions and / or Co ions may be added.
【0035】弱アルカリ性溶液である、ピロリン酸ナト
リウム系溶液またはトリポリリン酸ナトリウム系溶液ま
たはこれらの混合液に対する、Niイオンおよび/また
はCoイオンの添加量が0.001g/l未満では、十分
な耐黒変性を発揮させることができず、一方、上記添加
量が10g/lを超えると鋼板の耐食性低下を招く。If the amount of Ni ions and / or Co ions added to the weakly alkaline solution, sodium pyrophosphate-based solution or sodium tripolyphosphate-based solution, or a mixture thereof, is less than 0.001 g / l, sufficient black resistance is obtained. On the other hand, when the amount of addition exceeds 10 g / l, the corrosion resistance of the steel sheet is reduced.
【0036】電気亜鉛めっき層の表面に対し、Niおよ
び/またはCoを、前述したより好ましい析出量であ
る、0.01mg/m2 以上、1mg/m2 以下の範囲内、更に
より好ましい析出量である、0.01mg/m2 以上、0.
2mg/m2 以下の範囲内で析出させるためには、pH値が8
以上11未満の弱アルカリ性溶液であるピロリン酸ナト
リウム系溶液またはトリポリリン酸ナトリウム系溶液ま
たはこれらの混合液に対するNiイオンおよび/または
Coイオンの添加量を、0.005g/l以上、0.2g/
l以下とすることが好ましい。[0036] Ni and / or Co are deposited on the surface of the electrogalvanized layer in the range of 0.01 mg / m 2 or more and 1 mg / m 2 or less, which is the more preferred amount of precipitation described above, and still more preferably. 0.01 mg / m 2 or more.
In order to precipitate within a range of 2 mg / m 2 or less, a pH value of 8
The addition amount of Ni ions and / or Co ions to a sodium pyrophosphate-based solution or a sodium tripolyphosphate-based solution or a mixed solution thereof, which is a weak alkaline solution of not less than 11, is 0.005 g / l or more,
It is preferably set to 1 or less.
【0037】上述したように、この発明の、耐黒変性に
優れた電気亜鉛めっき鋼板の製造方法は、電気亜鉛めっ
き層の表面にNiおよびCoの少なくとも1つを所定量
で析出させ、もって、電気亜鉛めっき層の表面上に金属
層を形成するステップを除き、従来の電気亜鉛めっき鋼
板の製造方法と同一である。従って、その他のステップ
の説明を省略する。As described above, the method for producing an electrogalvanized steel sheet having excellent resistance to blackening according to the present invention is characterized in that at least one of Ni and Co is deposited in a predetermined amount on the surface of the electrogalvanized layer. Except for the step of forming a metal layer on the surface of the electrogalvanized layer, it is the same as the conventional method for manufacturing an electrogalvanized steel sheet. Therefore, description of the other steps is omitted.
【0038】[0038]
【実施例】次に、この発明の耐黒変性に優れた電気亜鉛
めっき鋼板の製造方法を、実施例により、比較例と対比
しながら更に詳細に説明する。表1に示すめっき条件に
従って、鋼板に電気亜鉛めっきを施し、電気亜鉛めっき
鋼板を調製した。Next, the method for producing an electrogalvanized steel sheet having excellent resistance to blackening according to the present invention will be described in more detail with reference to examples and comparative examples. According to the plating conditions shown in Table 1, the steel sheet was electrogalvanized to prepare an electrogalvanized steel sheet.
【0039】[0039]
【表1】 [Table 1]
【0040】次いで、上記電気亜鉛めっき鋼板を本発明
の範囲内の成分組成およびpH値を有する処理液中に浸漬
させることによって金属析出処理を行い、かくして、電
気亜鉛めっき鋼板の亜鉛めっき層の表面に、Niおよび
Coの少なくとも1つを本発明の範囲内の量で析出さ
せ、もって、電気亜鉛めっき層の表面上に金属層を形成
した。上記金属析出処理における、処理液の成分組成、
pH値、処理時間、Niおよび/またはCoの析出量を
表2に記す。Next, the above galvanized steel sheet is subjected to a metal deposition treatment by immersing it in a treatment solution having a component composition and a pH value within the range of the present invention, and thus the surface of the galvanized layer of the galvanized steel sheet is obtained. Then, at least one of Ni and Co was deposited in an amount within the range of the present invention, thereby forming a metal layer on the surface of the electrogalvanized layer. In the metal deposition treatment, the component composition of the treatment liquid,
Table 2 shows the pH value, the treatment time, and the precipitation amount of Ni and / or Co.
【0041】[0041]
【表2】 [Table 2]
【0042】次いで、電気亜鉛めっき層の表面にNiお
よびCoの少なくとも1つからなる金属層が形成された
上記電気亜鉛めっき鋼板に、表4に示すクロメート条件
に従って、クロメート処理を行い、かくして、本発明の
範囲内の金属層を有する電気亜鉛めっき鋼板の供試体
(以下、「本発明供試体」という)No.1〜21を調
製した。適用されたクロメート処理の種類およびクロメ
ート付着量を表2に併せて記す。Next, the electrogalvanized steel sheet having a metal layer made of at least one of Ni and Co formed on the surface of the electrogalvanized layer is subjected to a chromate treatment in accordance with the chromate conditions shown in Table 4, and thus, Specimens of electrogalvanized steel sheets having a metal layer within the scope of the invention (hereinafter referred to as “specimens of the present invention”) Prepared 1-21. The type of chromate treatment applied and the amount of attached chromate are also shown in Table 2.
【0043】比較のために、上述した条件に従って調製
された電気亜鉛めっき鋼板を、成分組成およびpH値の少
なくとも1つが本発明の範囲を外れた処理液中に浸漬さ
せることによって金属析出処理を行い、電気亜鉛めっき
鋼板の亜鉛めっき層の表面に、NiおよびCoの少なく
とも1つを析出させることにより、電気亜鉛めっき層の
表面上に金属層を形成し、次いで、表4に示すクロメー
ト条件に従って、クロメート処理を行い、かくして、表
3に示す本発明の範囲外の電気亜鉛めっき鋼板の供試体
(以下、「比較用供試体」という)No.1〜6を調製
した。表4に、めっき条件、処理液の成分組成、pH
値、処理時間、Niおよび/またはCoの析出量、クロ
メート処理の種類およびクロメート付着量を併せて示
す。For comparison, a galvanized steel sheet prepared according to the above-described conditions was subjected to a metal deposition treatment by immersing it in a treatment solution in which at least one of the component composition and the pH value was out of the range of the present invention. A metal layer is formed on the surface of the electrogalvanized layer by depositing at least one of Ni and Co on the surface of the galvanized layer of the electrogalvanized steel sheet, and then according to the chromate conditions shown in Table 4, Chromate treatment was performed, and thus the specimens of the electrogalvanized steel sheet (hereinafter referred to as “comparative specimens”) No. 1-6 were prepared. Table 4 shows the plating conditions, the component composition of the treatment solution, and the pH.
The values, the treatment time, the amount of Ni and / or Co deposited, the type of chromate treatment and the amount of chromate adhering are also shown.
【0044】[0044]
【表3】 [Table 3]
【0045】[0045]
【表4】 [Table 4]
【0046】なお、表2および表3における処理液中の
NiおよびCoは、硫酸塩(6,7水塩)で添加した。
このように調製された本発明供試体No.1〜21およ
び比較用供試体No. 1〜6の各々について、下記方法に
より黒変試験および外観変化の検査を行った。Incidentally, Ni and Co in the treatment solutions in Tables 2 and 3 were added as sulfates (6,7 hydrate).
The thus-prepared specimen No. 1 of the present invention was prepared. For each of Sample Nos. 1 to 21 and Comparative Specimens Nos. 1 to 6, a blackening test and a change in appearance were inspected by the following methods.
【0047】(1) 黒変試験方法:供試体の白色度をJI
SZ8730に準拠したLab系で測定した。次いで、
供試体を積み重ねた状態で、50°Cの温度および95
%の相対湿度において、湿潤試験を60日間行い、当該
湿潤試験後に、供試体の白色度を上述した方法で再び測
定した。次いで、湿潤試験前後における測定された白色
度の変化量(ΔL)を求めた。このようにして求められ
た白色度の変化量(ΔL)に基づき、各供試体の耐黒変
性を、下記基準により評価した。評価結果を表2に併せ
て記す。(1) Black discoloration test method: The whiteness of the specimen was determined by JI
The measurement was performed using a Lab system based on SZ8730. Then
With the specimens stacked, a temperature of 50 ° C and 95
% Relative humidity, a wetness test was performed for 60 days, after which the whiteness of the specimen was measured again in the manner described above. Next, the amount of change (ΔL) in the measured whiteness before and after the wet test was determined. Based on the change in whiteness (ΔL) thus obtained, the blackening resistance of each specimen was evaluated according to the following criteria. The evaluation results are also shown in Table 2.
【0048】 ○:ΔL≧−2であって、耐黒変性に優れていた。 ×:ΔL<−2であって、耐黒変性に劣っていた。 (2) 外観判定基準:供試体の白色度を上記と同様にJI
SZ8730に準拠したLab系で測定した。次いで、
上述した金属析出処理を行っていない、基準供試体とし
ての電気亜鉛めっき鋼板の白色度を同様の方法で測定し
た。次いで、各供試体の各々の白色度の測定値と基準供
試体の白色度の測定値の差を求めた。このようにして求
められた差の値に基づいて、各供試体の外観を、下記に
より評価した。評価結果を、表2に併せて記す。○: ΔL ≧ −2, and excellent blackening resistance. ×: ΔL <−2, and poor blackening resistance. (2) Appearance criterion: The whiteness of the specimen was determined by JI in the same manner as above.
The measurement was performed using a Lab system based on SZ8730. Then
The whiteness of an electrogalvanized steel sheet as a reference specimen not subjected to the above-described metal deposition treatment was measured by the same method. Next, the difference between the measured value of whiteness of each specimen and the measured value of whiteness of the reference specimen was determined. Based on the difference value thus obtained, the appearance of each specimen was evaluated as follows. The evaluation results are also shown in Table 2.
【0049】 ◎:金属析出処理による白色度の低下が1未満であっ
た。 ○:金属析出処理による白色度の低下が1以上2未満で
あった。 △:金属析出処理による白色度の低下が2以上4未満で
あった。A: The decrease in whiteness due to the metal deposition treatment was less than 1. :: The decrease in whiteness due to the metal deposition treatment was 1 or more and less than 2. Δ: The decrease in whiteness due to the metal deposition treatment was 2 or more and less than 4.
【0050】 ×:金属析出処理による白色度の低下が4以上であっ
た。 表2から明らかなように、本発明供試体No.1〜21
の何れも、耐黒変性に優れており、しかも、十分なクロ
メート付着量が確保されていた。また、金属析出量が
0.01〜0.2mg/m2 の範囲内の本発明供試体No.
1〜4、9、11〜12、14〜16、18、20およ
び21においては、クロメート処理後の外観が優れてお
り、白色度の低下が1未満と著しく少なかった。金属析
出量が0.5〜1mg/m2 の範囲内の本発明供試体No.
5、6、10、13、17および19においては、クロ
メート処理後の外観が良好であり、白色度の低下が1以
上2未満と少なかった。金属析出量が4.5〜9.4mg
/m2 の範囲内の本発明供試体No.7および8において
は、クロメート処理後の外観が許容範囲内であり、白色
度の低下が2以上4未満であった。×: The decrease in whiteness due to the metal deposition treatment was 4 or more. As is clear from Table 2, the test sample No. of the present invention. 1-21
All of them were excellent in blackening resistance, and a sufficient amount of chromate was secured. In addition, the specimen No. of the present invention having a metal deposition amount in the range of 0.01 to 0.2 mg / m 2 .
In Examples 1-4, 9, 11-12, 14-16, 18, 20 and 21, the appearance after the chromate treatment was excellent, and the decrease in whiteness was extremely small at less than 1. The specimen No. of the present invention having a metal deposition amount in the range of 0.5 to 1 mg / m 2 .
In 5, 6, 10, 13, 17 and 19, the appearance after the chromate treatment was good, and the decrease in whiteness was as small as 1 or more and less than 2. 4.5-9.4 mg of metal deposition
/ m 2 within the range of the present invention. In Nos. 7 and 8, the appearance after chromate treatment was within the allowable range, and the decrease in whiteness was 2 or more and less than 4.
【0051】これに対し、処理液のpH値が本発明範囲を
超えて高く、Ni、Coの析出量が0の比較用供試体N
o.1においては、耐黒変性に劣っていた。処理液のpH
値が本発明範囲を外れて低い比較用供試体No.2およ
び3においては、耐黒変性および外観が共に劣ってい
た。処理液のpH値が本発明範囲を外れて低く、Ni、C
oの析出量が0または殆ど0の比較用供試体No.4お
よび5においは、耐黒変性に劣っていた。また、処理液
のNiイオン含有量が本発明の範囲を超えて多く、Ni
の析出量が本発明の範囲を超えて多い比較用供試体N
o.6においは、外観が劣っていた。On the other hand, when the pH value of the processing solution was higher than the range of the present invention and the precipitation amount of Ni and Co was 0,
o. In No. 1, the blackening resistance was inferior. PH of processing solution
The value of the comparative sample No. having a value outside the range of the present invention and low. In Nos. 2 and 3, both blackening resistance and appearance were inferior. The pH value of the processing solution is low outside the range of the present invention, and Ni, C
No. o for which the amount of precipitation was 0 or almost 0. 4 and 5 were inferior to blackening resistance. Further, the Ni ion content of the treatment liquid is large beyond the scope of the present invention,
Specimen N for comparison, in which the precipitation amount of N is larger than the range of the present invention.
o. In No. 6, the appearance was inferior.
【0052】[0052]
【発明の効果】以上説明したように、この発明によれ
ば、クロメート処理材に関しては、耐黒変性が改善さ
れ、クロメート処理材以外のリン酸塩処理材等に関して
は、外観の劣化がない、耐黒変性に優れた電気亜鉛めっ
き鋼板を得ることができ、また、鋼板に特定のめっき浴
を用いて亜鉛めっき処理を行い、次いで、クロメート処
理、リン酸塩処理等の後処理を行うことによって得られ
る亜鉛めっき鋼板の製造のみならず、鋼板に上述した同
一のめっき浴を用いて亜鉛めっき処理を行い、上述した
後処理を行わないことによって得られる、後処理なしの
電気亜鉛めっき鋼板の製造も可能な製造ラインにおい
て、クロメート処理材に関しては、耐黒変性を改善する
ことができ、クロメート処理材以外のリン酸塩処理材等
に関しては、外観の劣化を防止することが可能な、耐黒
変性に優れた亜鉛めっき鋼板およびその製造方法を提供
することができ、かくして、工業上有用な効果がもたら
される。As described above, according to the present invention, the blackening resistance of the chromate-treated material is improved, and the appearance of the phosphate-treated material other than the chromate-treated material is not deteriorated. An electrogalvanized steel sheet with excellent blackening resistance can be obtained, and the steel sheet is subjected to galvanization using a specific plating bath, and then subjected to post-treatments such as chromate treatment and phosphate treatment. Not only the production of the resulting galvanized steel sheet, but also the production of an electrogalvanized steel sheet without post-processing, which is obtained by performing galvanizing treatment on the steel sheet using the same plating bath described above and not performing the above-mentioned post-processing. In a production line where it is possible, the blackening resistance can be improved for chromate-treated materials, and the appearance of phosphate-treated materials other than chromate-treated materials deteriorates. Capable of preventing, it is possible to provide a galvanized steel sheet and a manufacturing method thereof having excellent blackening resistance, thus industrially useful effects are provided.
Claims (3)
電気亜鉛めっき層と、前記電気亜鉛めっき層の表面に、
NiおよびCoの少なくとも1つを、0.01mg/m2 以
上、10mg/m2 以下の範囲内の量で析出させることによ
って形成された金属層と、前記金属層の上に形成された
クロメート皮膜とからなることを特徴とする、耐黒変性
に優れたクロメート処理電気亜鉛めっき鋼板。A steel sheet, an electrogalvanized layer formed on a surface of the steel sheet, and a surface of the electrogalvanized layer,
A metal layer formed by depositing at least one of Ni and Co in an amount in the range of 0.01 mg / m 2 or more and 10 mg / m 2 or less, and a chromate film formed on the metal layer A chromate-treated electrogalvanized steel sheet having excellent resistance to blackening, characterized by comprising:
とも一方の表面上に電気亜鉛めっき層が形成された電気
亜鉛めっき鋼板を調製し、前記電気亜鉛めっき鋼板を、
NiイオンおよびCoイオンの少なくとも1つが、0.
001g/l以上、10g/l以下の量で添加され、pH値が
8以上、11未満の弱アルカリ性溶液に接触させること
によって、前記電気亜鉛めっき層の表面に、Niおよび
Coの少なくとも1つを0.01mg/m2 以上、10mg/m
2 以下の範囲内の量で析出させて前記電気亜鉛めっき層
の表面に金属層を形成し、次いで、クロメート処理を施
すことを特徴とする、耐黒変性に優れたクロメート処理
電気亜鉛めっき鋼板の製造方法。2. A steel sheet is electrogalvanized to prepare an electrogalvanized steel sheet having an electrogalvanized layer formed on at least one surface, and the electrogalvanized steel sheet is
When at least one of the Ni ion and the Co ion is in the range of 0.
At least one of Ni and Co is added to the surface of the electrogalvanized layer by contacting the electrogalvanized layer with a weak alkaline solution having a pH value of 8 or more and less than 11 which is added in an amount of 001 g / l or more and 10 g / l or less. 0.01 mg / m 2 or more, 10 mg / m
Forming a metal layer on the surface of the electrogalvanized layer by depositing in an amount within the range of 2 or less, and then performing a chromate treatment, the chromate-treated electrogalvanized steel sheet having excellent blackening resistance. Production method.
トリウム系溶液またはトリポリリン酸ナトリウム系溶
液、または、前記ピロリン酸ナトリウム系溶液と前記ト
リポリリン酸ナトリウム系溶液との混合液である、請求
項2に記載の方法。3. The method according to claim 2, wherein the weak alkaline solution is a sodium pyrophosphate-based solution or a sodium tripolyphosphate-based solution, or a mixed solution of the sodium pyrophosphate-based solution and the sodium tripolyphosphate-based solution. the method of.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32911797A JP3309788B2 (en) | 1996-12-02 | 1997-11-28 | Manufacturing method of chromate treated electrogalvanized steel sheet with excellent blackening resistance |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP32192096 | 1996-12-02 | ||
JP8-321920 | 1996-12-02 | ||
JP32911797A JP3309788B2 (en) | 1996-12-02 | 1997-11-28 | Manufacturing method of chromate treated electrogalvanized steel sheet with excellent blackening resistance |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH10219494A true JPH10219494A (en) | 1998-08-18 |
JP3309788B2 JP3309788B2 (en) | 2002-07-29 |
Family
ID=26570632
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Application Number | Title | Priority Date | Filing Date |
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JP32911797A Expired - Fee Related JP3309788B2 (en) | 1996-12-02 | 1997-11-28 | Manufacturing method of chromate treated electrogalvanized steel sheet with excellent blackening resistance |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3309788B2 (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20180118709A (en) | 2016-02-29 | 2018-10-31 | 가부시키가이샤 고베 세이코쇼 | Surface treated zinc plated steel sheet with excellent appearance |
KR20190039548A (en) | 2016-08-05 | 2019-04-12 | 가부시키가이샤 고베 세이코쇼 | Surface-treated metal plate, and method of manufacturing surface-treated metal plate |
-
1997
- 1997-11-28 JP JP32911797A patent/JP3309788B2/en not_active Expired - Fee Related
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20180118709A (en) | 2016-02-29 | 2018-10-31 | 가부시키가이샤 고베 세이코쇼 | Surface treated zinc plated steel sheet with excellent appearance |
KR20190039548A (en) | 2016-08-05 | 2019-04-12 | 가부시키가이샤 고베 세이코쇼 | Surface-treated metal plate, and method of manufacturing surface-treated metal plate |
Also Published As
Publication number | Publication date |
---|---|
JP3309788B2 (en) | 2002-07-29 |
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