JPS5947386A - Method for chromating plated steel sheet - Google Patents

Method for chromating plated steel sheet

Info

Publication number
JPS5947386A
JPS5947386A JP15521382A JP15521382A JPS5947386A JP S5947386 A JPS5947386 A JP S5947386A JP 15521382 A JP15521382 A JP 15521382A JP 15521382 A JP15521382 A JP 15521382A JP S5947386 A JPS5947386 A JP S5947386A
Authority
JP
Japan
Prior art keywords
additives
chromate treatment
plated steel
steel sheet
container
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
Application number
JP15521382A
Other languages
Japanese (ja)
Other versions
JPH0233790B2 (en
Inventor
Masaru Suzuki
優 鈴木
Takenori Deguchi
出口 武典
Kenji Koshiishi
興石 謙二
Takao Tomosue
友末 多賀夫
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.)
Nippon Steel Nisshin Co Ltd
Original Assignee
Nisshin Steel Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Nisshin Steel Co Ltd filed Critical Nisshin Steel Co Ltd
Priority to JP15521382A priority Critical patent/JPH0233790B2/en
Publication of JPS5947386A publication Critical patent/JPS5947386A/en
Publication of JPH0233790B2 publication Critical patent/JPH0233790B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/73Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals characterised by the process
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C22/00Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C22/05Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
    • C23C22/06Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
    • C23C22/34Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing fluorides or complex fluorides
    • C23C22/37Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing fluorides or complex fluorides containing also hexavalent chromium compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Treatment Of Metals (AREA)

Abstract

PURPOSE:To stabilize the quality, by filling hardly soluble additives into a container other than a chromating vessel and by gradually dissolving the additives at the outside of the vessel to prevent the suspension of undissolved solid matter and to keep the concn. of additives uniform. CONSTITUTION:Hardly soluble additives 5 such as barium silicofluoride as a reaction accelerator are filled into a container 4 communicating with a chromating vessel 1 in which a Zn or Al plated steel sheet is chromated. A chromating soln. 3 is circulated through the container 4 to dissolve the additives 5 in the container 4 up to the maximum solubility. The concn. of the additives 5 in the soln. 3 is kept uniform, and the suspension of the additives 5 in the vessel 1 is prevented.

Description

【発明の詳細な説明】 本発明は亜鉛2よびアルミニウムメッキ鋼板にクロメー
ト処理するに当り、その処理液’fl: j+11.、
lJに調整することによりクロメート処(41!製品の
本来の性能全発揮せしめる方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention uses a treatment solution 'fl: j+11. ,
This relates to a method for making full use of the original performance of a chromate treatment (41! product) by adjusting the chromate treatment to lJ.

従来、亜鉛メッキ、アルミニウムメッキ3% M vx
未塗装の伏、或いは塗装して、更には両者を組合わせて
使用されている。そこで夫々の用途に応じ防錆および塗
装後の塗膜の密着性、面]食性の向上を目的として主に
クロメート処理によりメンギ鋼板上にクロメート皮膜を
一形成させている。
Conventional, zinc plating, aluminum plating 3% M vx
It is used either unpainted, painted, or a combination of both. Accordingly, a chromate film is formed on the Mengi steel sheet by chromate treatment for the purpose of rust prevention, adhesion of the paint film after painting, and surface corrosion resistance depending on the respective application.

クロメート皮膜忙形成させるVこQコ、メッキ鋼板の表
面とクロメート処理液との間に起こるエノチンロムとが
共存する処理液をメッキ鋼板の表向に塗布する方法また
は酸がf処理による方法などが1f在している。
The method for forming a chromate film is to apply a treatment solution on the surface of the plated steel sheet in which enotinol coexists between the surface of the plated steel sheet and the chromate treatment solution, or a method using acid f treatment. There is.

このうち、メッキ鋼板の表面との化学反応によってクロ
メート皮膜全形成させる方法では該W4仮表面の金属(
亜鉛、アルミニラムノがクロメート処理液中に溶解して
金属イオンとなり同時に処理7f夕中の水素イオンが消
費される。その結果、被処理鋼板の処理紙に応じて処理
液中の遊離酸濃度が減少し目的とする化学反応が徐々に
低下して適正なりロノート皮膜が形成さ扛なくなり、処
理液は廃棄、更新せねばならなくなる。特に通常の化学
反応を利用する反応型クロメート処理液ではllllI
食性、塗膜密着性を向上させるため反応促進剤として、
例えば各種の酸や塩類若しくは無機高分子などを添加さ
せたものが使用されるが、之等の添加′吻を用いると耐
食性、塗j臭密屑性が同上する反面、必然的に処理液の
寿命が短くなる欠点がある。
Among these methods, a method in which the entire chromate film is formed by a chemical reaction with the surface of the plated steel sheet metal (
Zinc and aluminum are dissolved in the chromate treatment solution to become metal ions, and at the same time hydrogen ions from the treatment 7F are consumed. As a result, the concentration of free acid in the treatment solution decreases depending on the paper used to treat the steel sheet, and the desired chemical reaction gradually decreases until it becomes appropriate and no longer forms a Ronaut film, and the treatment solution must be discarded or renewed. It becomes necessary. In particular, in reactive chromate treatment solutions that utilize normal chemical reactions, llllI
As a reaction accelerator to improve edibility and paint film adhesion.
For example, products to which various acids, salts, or inorganic polymers have been added are used, but when these additives are used, corrosion resistance and odor-tightness of the coating are the same, but on the other hand, the processing solution is inevitably degraded. The disadvantage is that the lifespan is shortened.

そこで反応型クロメート処理液においてtよ処理液の老
化を防止する必要がある。このため反応促進剤の添加は
製品性能の安定化のため、反応で消費される祇に見付′
)厳t一定に補給しなければならない。従って添加物と
しての反応促進剤は効率の良いものが望1れ、一般には
各種のフッ素化合物が用いられる。
Therefore, it is necessary to prevent aging of the reactive chromate treatment solution. For this reason, the addition of reaction accelerators is necessary to stabilize the product performance by adding a reaction accelerator to the
) Must be supplied at a strict constant rate. Therefore, it is desirable that the reaction accelerator used as an additive be highly efficient, and various fluorine compounds are generally used.

例えばフッ素化合物としてケイフッ化バリウム(BaS
iF6Jはクロメート処理液中で飽和状態に溶解してい
てもエツチング縫は適(g−K /J−さく且つ耐食性
に優れた皮膜を得られるか、実際のクロメート処理にお
いては処理液中に飽第1]以上K 、1t=S剰に固形
状で含1せて置くとクロメート処理が進行−ノーるに従
って消費さ、fするり一イフソ化バリウムは逐次同形物
が溶解することにより絶えず補給され常に一定濃度に維
持されるけれ共、スプレ一方法でr1絶えず循環される
し、ディップ方法では撹拌されるため未溶解固形物がク
ロメート処理i&中に分散(昆在する。このことQよ決
して好ましい(−とではなく、上記の未溶1奸固形物か
分散7M: fl−懸濁することによってメッキ鋼板表
面に形成さitたクロメート皮膜に付着して接触腐食を
縛元させる。またCI −ル付着によってクロム酸汚れ
ケ訪兄するなどの影響、即ち製品外観を損ね製品価値が
1戊Fする。この現象の防1ににはフィルターVC,C
るp過去や別の槽による沈降法などが考えられるが、d
)来状の場合はフィルターの目詰りに伴うフィルターの
父照による作業の中断や繁雑さ、沈降徊設備の投・H7
1どの欠点もある。
For example, barium fluorosilicate (BaS) is a fluorine compound.
iF6J is suitable for etching even if it is saturated in the chromate treatment solution (g-K/J-Is it possible to obtain a film with excellent corrosion resistance? 1] Above K, 1t=S If a surplus of 1 is contained in solid form, the chromate treatment progresses and is consumed as time goes on. While a constant concentration is maintained, in the spray method r1 is constantly circulated and in the dip method undissolved solids are dispersed (inhabited) in the chromate treatment. This is definitely preferable ( By suspending the above-mentioned undissolved solids rather than with -, they adhere to the chromate film formed on the surface of the plated steel sheet and restrict contact corrosion. Due to this, the influence of chromic acid stains on the product, which impairs the appearance of the product and reduces the product value by 1F.To prevent this phenomenon, filters VC and C are used.
Possible methods include settling in the past or in a separate tank, but d
) In the case of the recent report, work interruptions and complexity due to filter clogging due to heat radiation, and the need for sedimentation equipment/H7
1.Everything has its drawbacks.

本発明者等に前記欠点全線くため鋭意研究の結果、製品
性能を向上させるための難溶性添加物〔以下、添加物と
云う〕全処理液槽とは別途の容器に充填させ、クロメー
ト処理液の循環にエリ溶Wlさせること、即ち処理液槽
外で逐次溶解させる方法全見出し本発明に到達した。
As a result of intensive research to eliminate all of the above-mentioned drawbacks, the inventors of the present invention have found that in order to improve product performance, a poorly soluble additive (hereinafter referred to as the additive) is filled in a separate container from the entire treatment liquid tank, and the chromate treatment solution is The present invention has been developed to solve the problem of dissolving the liquid Wl in circulation, that is, sequentially dissolving it outside the treatment liquid tank.

以下、本発明金図面にエリ詳細に説明する。Hereinafter, the present invention will be explained in detail with reference to the drawings.

第1図は本発明の基本的構成要件金成す別回路による溶
1管装置を示す側断面図であり図に2いて1tよりロノ
ート処理液槽であり、2.2’はクロメート処理液41
と容器4全連逃させるパイプでめり、5は添加物である
。クロメート処理液6は処理液槽1から連通バイグツ全
通り、容器4全通過する際に添加物5を溶解し、連>I
nnクイズ′盆辿ってクロメート処理液槽1に戻る様に
構成され王いる。第2図は本発明の別回路によ3るカラ
ム接触装置の一実施例全説明する側断面図でめり、図に
おいて容器4内には添加物の目詰り防止にプラスチツク
ポール6忙人扛た例でめり、更にフィルター7を設ける
ことにエリ未溶解固形物2工びクロメート処理液と化学
反応により処理液中に溶解するスラッチをも捕捉させる
こと’t 0]能ならしめた。
FIG. 1 is a side sectional view showing a molten tube apparatus with a separate circuit comprising the basic constituent elements of the present invention.
5 is the additive. The chromate treatment liquid 6 dissolves the additive 5 as it passes through the entire communication container 4 from the treatment liquid tank 1, and
nn Quiz' The tray is structured so that it returns to the chromate treatment liquid tank 1. FIG. 2 is a side cross-sectional view fully illustrating an embodiment of a column contacting device using a separate circuit according to the present invention. In addition, by providing the filter 7, it became possible to capture undissolved solids as well as slatch which dissolves in the treatment liquid due to a chemical reaction with the chromate treatment liquid.

なお図中8はポンプ、9は浮遊物ケ示す。」−記の如き
装置を用いることにエリ前)iドの製品性能の11υ上
を計り且つ処理液の老化金も防止するものである。
In the figure, 8 indicates a pump, and 9 indicates a floating object. The use of the above-mentioned apparatus achieves a product performance 11υ higher than that of the former) and also prevents aging of the processing solution.

次に本発明の実〃視に当ってはクロメート処理液1・1
−91内に所定濃度のクロメート処理rrJj、ろと入
れ、フィルター7を設けた容器4には添刈11勿5とし
てケイフッ化バリウム(BaSiF6)お工びプラスチ
ックボール6が入れてめる。ポンプ8の作動によりクロ
メート処理液ろは連通パイプ2τ経て容器4を通過する
際に被処理鋼板の金属表面で化学展j心に必要な鍍だけ
ケイフッ化バリウ11が溶1管さILフィルター7f:
経てクロメ−1・処理液酸に戻る。Elちクロメート処
理液が別に設けらI’した容器4を通過する度に化学脱
化、により消費ざJLる酬−に見合うフッ素イオンが供
給され連続してりaメート処理が可能となる。また、本
発明は易(6性添/)In物の場合V?−も適用されろ
。その方法としてはクロメ−(・処理液の循環流i+1
−を調整すればよい。葦た間歇的に循環させてもよい。
Next, in actually observing the present invention, chromate treatment solution 1.1
A chromate treatment rrJj of a predetermined concentration is poured into a container 91, and a plastic ball 6 made of barium fluorosilicate (BaSiF6) is placed in a container 4 provided with a filter 7 as a cutting material 11. When the chromate treatment liquid filters through the communication pipe 2τ and passes through the container 4 by the operation of the pump 8, only the amount of barium fluorosilicate 11 necessary for chemical development is melted on the metal surface of the steel plate to be treated.IL filter 7f:
After that, it returns to chromate-1/treated liquid acid. Each time the chromate treatment solution passes through a separately provided container 4, fluorine ions are supplied in an amount commensurate with the amount consumed due to chemical decomposition, making it possible to perform continuous amate treatment. In addition, the present invention is applicable to the case of easily (6-added/)In products. - also applies. The method is chrome (・circulation flow of treatment liquid i+1
- just adjust. It may be circulated intermittently.

以下実施例にエリ更に詳細に説明する。This will be explained in more detail in the following examples.

CrO3水m液K PVA (ホルピニルアルコール重
合+f500]でCr06(7)一部を還元し、cr+
6°とc r+ 6とノモル比(Cr  /Cr  )
(ro−3とした液にBa5iF65y、/l’f’加
えCr  とCr”との合計団、全Crus′a度に換
算した場合60 !/lで、更バ メート処理ラインで板厚1.0m、rn、、亜鉛付着量
片面9CVl/−2、幅914m、−のコイル2工び板
厚0.6m−、アルミニウム付着量片面40y/”−2
、幅914WLm、のコイル全容3QQ ton宛通板
して夫々のタロメート処理鋼板の耐食性、表面外観につ
いて調査した。
Part of Cr06 (7) is reduced with CrO3 water m solution K PVA (forpynyl alcohol polymerization + f500), and cr+
6° and cr+ 6 and nomolar ratio (Cr /Cr)
(The sum of Ba5iF65y, /l'f' and Cr and Cr'' to the ro-3 solution, when converted to total Crus'a degree, is 60!/l, and the plate thickness is 1.0 m in the bamate treatment line. ,rn,, Zinc coating amount 9CVl/-2 on one side, width 914m, -2 coils, plate thickness 0.6m-, aluminum coating amount 40y/''-2 on one side
The corrosion resistance and surface appearance of each talomete-treated steel sheet were investigated by threading a coil with a width of 914WLm and a total volume of 3QQ ton.

調査結果をF表に示す。The survey results are shown in Table F.

なお従来法として第6図に示す本発明によらない方法即
ち、クロメート処理槽に過剰なケイフッ化バリウム全添
加した状態で処理したものを用いた。
As a conventional method, a method not according to the present invention shown in FIG. 6 was used, that is, a method in which excess barium fluorosilicate was completely added to the chromate treatment tank.

調査の基@は次によって表示した。The basis of the investigation was indicated as follows.

製品外観は肉眼に工り クロム酸汚れの全く無いもの  ◎ 閉極く僅かに汚れ
たもの     (J 印はっきり汚れの判るもの  
  × 印耐食性は、 耐食1生試験は湿潤試験とスタック試験を行なった。湿
潤試験はJ工Sz  0236の6−1項に準拠した。
The appearance of the product is visible to the naked eye, and there is no chromic acid stain at all. ◎ It is extremely closed and has a slight stain (J mark indicates that the stain is clearly visible).
Corrosion resistance marked with × indicates Corrosion resistance 1 wet test and stack test were conducted. The wet test was conducted in accordance with Section 6-1 of J Engineering Sz 0236.

またスタック試験は70x150−島にカントした板1
0枚に霧吹で水滴を一様に散布し、檀み屯ねた後、ポリ
エチレンフィルムなどで梱包し悄7fl j口湿槽(温
IW49±1℃、相対湿度95%以上]内の一定条件ド
に2411時間放置後、湿潤試験と共に肉眼にエリ次の
様に評価した。
In addition, the stack test was carried out using a board 1 canted into 70x150-islands.
Sprinkle water droplets uniformly on the sheet with a sprayer, let it sit, then wrap it in polyethylene film, etc., and store it under certain conditions in a 7 fl J humidity tank (temperature IW 49 ± 1°C, relative humidity 95% or more). After being allowed to stand for 2411 hours, it was visually evaluated in addition to a wetness test as follows.

全く白ザビの無いもの    ◎ 閉 極く僅かの白サビの有るもの Q 印 出サビ発生が面績率1U%以上のもの × 即売に掲げ
た表において本発明における試験N011〜5の亜鉛メ
ッキ鋼板、N006〜10のアルミメッキ鋼板は共に耐
食性は良好な結果を示し、安定した製品性能であったの
に反し、従来法11〜20では白サビの発生が有り、製
品性能が不安定であることが判った。−万、表面外観は
本発明Vこおいては全くクロム酸汚れが無いのにに=J
 して従j17:法11〜20においては明らかにクロ
ム酸汚れが認められ製品外観を損ねていることが回る。
Items with no white rust at all ◎ Items with a very small amount of white rust Q Items with a surface grade rate of 1U% or more × Galvanized steel sheets with test Nos. The aluminized steel sheets of Nos. 1 to 10 all showed good corrosion resistance and stable product performance, whereas conventional methods Nos. 11 to 20 caused white rust and showed unstable product performance. Ta. - 10,000, even though the surface appearance of the present invention V has no chromic acid stains = J
Therefore, in J17: Methods 11 to 20, chromic acid stains were clearly observed, impairing the appearance of the product.

従って本発明に係る方法によればクロメ−1・処理液中
の未酵解固形吻の分数、混在、懸濁により誘発されるク
ロム酸汚れ全防止し、且つ処理?f中の硝力旧勿rlt
 l15j−を一定に保持されると共に製品性能の安定
化とクロメート処理液の老化をも防市出釆るものであり
工業的に1曲1直あるものと考える。
Therefore, according to the method of the present invention, chromic acid stains caused by the fraction, mixing, and suspension of unfermented solid proboscis in the chromate-1 treatment solution can be completely prevented, and the chromic acid stains can be completely prevented. Glass power former rlt in f
In addition to maintaining the l15j- constant, the product performance is stabilized and the aging of the chromate treatment solution is also prevented.Industrially, each piece is considered to have one shift.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の別回路IC,l:る浴ノqJ(装置で
ある。 第2図は本発明の別回路に裏るカラム接触座iべである
。第6図は従来法による補給力1ノテである。 1 ・・クロメート処理液僧 2.2′・・連通・畑プ ろ・・クロメート処理液 4・・容器 5・・添加物 6・・フラスチソク4ζ−ル ア・ ・フィルター 8・・ポンプ 9・・浮遊物 特許出願人  日新!!鋼株式会社 7]    ゝ 代 4 ノ゛  弁理士 野 間 ・懸 夫□・・ :
、・、・・弁理士野間忠之 ′・11 、(,, 1・1.−\゛パ N′)′12.′ 第1図 第2図 第3図
Figure 1 shows the separate circuit IC, l: bath noqJ (equipment) of the present invention. Figure 2 shows the column contact seat behind the separate circuit of the present invention. Figure 6 shows the replenishment by the conventional method. This is a power 1 note. 1... Chromate treatment liquid 2. 2'... Communication field filter... Chromate treatment liquid 4... Container 5... Additive 6... Flastisoku 4ζ-Lua... Filter 8.・Pump 9...Floating object patent applicant Nissin!! Steel Co., Ltd. 7] ゝ4゛Patent attorney Noma ・Kakeo□...:
,... Patent Attorney Tadayuki Noma'・11 , (,, 1・1.-\゛PaN')'12. ' Figure 1 Figure 2 Figure 3

Claims (1)

【特許請求の範囲】 1 クロメート処理液に難溶性添加物濃度給しながらメ
ッキ鋼板全処理する方法において、クロメート処理液槽
と連通ずる容器に難溶性添加物を充填し、クロメート処
理液を循環させながら該容器内の添加物を最太宕屏I度
まで溶解せしめ、クロメート処理液中の難溶性添加物濃
度を一定に保持ぜしめること勿竹徴とするメッキ鋼板の
クロメート処理方法。 2 メッキ鋼板が亜鉛メッキ鋼板でめる特許請求の範囲
第1項記載のメッキ鋼板のクロメート処理方法。 6 メッキ鋼板がアルミメッキ鋼板である特許請求の範
囲第1項記載のメッキ鋼板のクロメート処理方法。
[Claims] 1. In a method for completely treating a plated steel plate while supplying a concentration of a poorly soluble additive to a chromate treatment solution, a container communicating with a chromate treatment solution tank is filled with the hardly soluble additive, and the chromate treatment solution is circulated. A chromate treatment method for a plated steel sheet, in which the additives in the container are dissolved to a maximum degree and the concentration of the hardly soluble additives in the chromate treatment solution is kept constant. 2. The method for chromate treatment of a plated steel sheet according to claim 1, wherein the plated steel sheet is a galvanized steel sheet. 6. The method for chromate treatment of a plated steel plate according to claim 1, wherein the plated steel plate is an aluminized steel plate.
JP15521382A 1982-09-08 1982-09-08 METSUKIKOHANNOKUROMEETOSHORIHOHO Expired - Lifetime JPH0233790B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15521382A JPH0233790B2 (en) 1982-09-08 1982-09-08 METSUKIKOHANNOKUROMEETOSHORIHOHO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15521382A JPH0233790B2 (en) 1982-09-08 1982-09-08 METSUKIKOHANNOKUROMEETOSHORIHOHO

Publications (2)

Publication Number Publication Date
JPS5947386A true JPS5947386A (en) 1984-03-17
JPH0233790B2 JPH0233790B2 (en) 1990-07-30

Family

ID=15600977

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15521382A Expired - Lifetime JPH0233790B2 (en) 1982-09-08 1982-09-08 METSUKIKOHANNOKUROMEETOSHORIHOHO

Country Status (1)

Country Link
JP (1) JPH0233790B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0974682A1 (en) * 1998-07-18 2000-01-26 Henkel Kommanditgesellschaft auf Aktien Method and apparatus for the chemical treatment of metalsurfaces

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0974682A1 (en) * 1998-07-18 2000-01-26 Henkel Kommanditgesellschaft auf Aktien Method and apparatus for the chemical treatment of metalsurfaces

Also Published As

Publication number Publication date
JPH0233790B2 (en) 1990-07-30

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