JPH03100152A - Flux for hot dip zn-al alloy plating - Google Patents
Flux for hot dip zn-al alloy platingInfo
- Publication number
- JPH03100152A JPH03100152A JP23685589A JP23685589A JPH03100152A JP H03100152 A JPH03100152 A JP H03100152A JP 23685589 A JP23685589 A JP 23685589A JP 23685589 A JP23685589 A JP 23685589A JP H03100152 A JPH03100152 A JP H03100152A
- Authority
- JP
- Japan
- Prior art keywords
- plating
- flux
- hot dip
- nacl
- alloy
- 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
- Coating With Molten Metal (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、鉄鋼材料等に溶融Zn−Al合金めっき処理
を施す際に用いるめっき用フラックスに関する。DETAILED DESCRIPTION OF THE INVENTION [Field of Industrial Application] The present invention relates to a plating flux used when hot-dip Zn-Al alloy plating is applied to steel materials and the like.
従来、鉄鋼材料等の腐食を防止することを目的として、
その表面に溶融亜鉛めっき並びに電気亜鉛めっきを施す
ことが知られている。Traditionally, for the purpose of preventing corrosion of steel materials,
It is known to apply hot-dip galvanizing and electrogalvanizing to the surface.
また最近では、亜鉛めっき処理を下地として、更にその
上に表面処理、例えば塗装・加工等の後処理を加味する
ことによって、市場には新しく付加価値の高い商品が数
多(進出するようになり、これ等の商品に対する利用者
の選択も益々多様化してきている。Recently, a large number of new, high value-added products have entered the market by using zinc plating as a base and adding surface treatments such as painting and finishing. , and the choices of users regarding these products are becoming increasingly diverse.
これらの要求を満足させるため溶融亜鉛めっき処理品に
ついても、そのめっき浴組成としての添加元素と添加量
の選択により、めっき層の特性向上を図ることがかなり
行われてきた。In order to satisfy these demands, considerable efforts have been made to improve the properties of the galvanized layer by selecting the additive elements and amounts added in the plating bath composition for hot-dip galvanized products.
とりわけ、めっき層の耐食性を確保するために、^iを
3〜10重量%程度添加しためっき浴が知られている。In particular, a plating bath containing about 3 to 10% by weight of ^i is known in order to ensure the corrosion resistance of the plating layer.
このめっき浴は、通常、鉄鋼部品等の被処理物にそれを
ZnCl2水溶液中に浸漬するなどによりフラックス処
理をした後、使用されている。This plating bath is usually used after subjecting an object to be treated, such as a steel part, to a flux treatment by immersing it in an aqueous ZnCl2 solution.
ところが、このようにして製造されるめっき処理品には
、めっき層がのらず不めっきを生じ易い。However, the plated product manufactured in this way does not have a plating layer and is likely to be unplated.
そこで、−度、Alを含まないZnめっき浴で1次めっ
きを行ない、前記のようなフラックス処理をした後、前
記Zn−A 1合金めっき浴で2次めっきを行なってい
る。Therefore, primary plating is performed in a Zn plating bath that does not contain Al, and after the above-described flux treatment, secondary plating is performed in the Zn-A 1 alloy plating bath.
しかしながら、上記方法は、2回のめっき工程を経るの
で煩雑であり、製造コストも高いという欠点があった。However, the above method has the disadvantage that it is complicated because it requires two plating steps, and the manufacturing cost is also high.
本発明は、上記従来の問題点に鑑みてなされたもので、
鉄鋼部品等の被処理物に、1度のめっき作業でも不めっ
きを生じない溶融Zn−A1合金めっき用フラックスを
提供することを目的とする。The present invention has been made in view of the above-mentioned conventional problems.
The purpose of the present invention is to provide a flux for hot-dip Zn-A1 alloy plating that does not cause unplated surfaces on objects to be treated such as steel parts even in a single plating operation.
上記の目的を達成するために、本発明者等は種々研究を
重ねた結果、フラックスとしてZnCl t+NaCl
およびCH2CHCOOH(アクリル酸)を含む水溶液
を用いて被処理物のフラックス処理を行ない、被処理物
にZnCl g、 NaClおよびCI(zcHcOO
Hを付着させることにより被処理物へのZn−A1合金
の密着性を向上させ得ることを見出したものであり、そ
の詳細を以下に述べる。In order to achieve the above object, the present inventors have conducted various studies and found that ZnCl t+NaCl t+NaCl as a flux.
The workpiece is subjected to flux treatment using an aqueous solution containing CH2CHCOOH (acrylic acid) and ZnCl g, NaCl and CI (zcHcOO
It has been discovered that the adhesion of Zn-A1 alloy to the workpiece can be improved by attaching H, and the details thereof will be described below.
即ち、本発明は、溶融Zn−A1合金めっき用フラック
スとしてZnC1,を150〜300 g/l。That is, the present invention uses 150 to 300 g/l of ZnC1 as a flux for hot-dip Zn-A1 alloy plating.
NaClを20〜40g/lおよびCH2CHCOOH
を10〜120g/l含む水溶液を用いることにより上
記の課題を解決したものである。20-40 g/l of NaCl and CH2CHCOOH
The above problem was solved by using an aqueous solution containing 10 to 120 g/l of.
この水溶液に塩酸、硫酸などの少量の酸を加えてもよい
。A small amount of acid such as hydrochloric acid or sulfuric acid may be added to this aqueous solution.
本発明のフラックスの用途を溶融Zn−Al合金めっき
とし、亜鉛めっき浴中にA1を含有せしめたのは、めっ
き層の耐食性を維持するためである。The reason why the flux of the present invention is used for hot-dip Zn-Al alloy plating and A1 is contained in the galvanizing bath is to maintain the corrosion resistance of the plating layer.
そのAl量は3〜10重量%が好ましい。3重量%未満
では上記の耐食性を維持する効果が少な(、またAlの
含有量が10重量%を超えても耐食性のより一層の向上
が得られ難くなると共に、めっき浴の融点が上昇するた
め作業性が悪くなるからである。The amount of Al is preferably 3 to 10% by weight. If the Al content is less than 3% by weight, the effect of maintaining the above-mentioned corrosion resistance is small (Also, if the Al content exceeds 10% by weight, it becomes difficult to obtain further improvement in corrosion resistance, and the melting point of the plating bath increases. This is because workability deteriorates.
また、本発明の水溶液フラックス中にZnCI Z+N
aClおよびCH2CHCOOHを含有せしめたのは、
ZnA1合金めっき層と被処理物との密着性を改善して
、不めっきを生じず、かつ平滑なめっき表面を形成させ
るためである。In addition, ZnCI Z+N is added to the aqueous flux of the present invention.
The reason for containing aCl and CH2CHCOOH is
This is to improve the adhesion between the ZnA1 alloy plating layer and the object to be treated, thereby preventing unplatedness and forming a smooth plating surface.
ZnCf、含有量、NaCIl含有量およびC)lzc
HcOOR含有量のうちの少くとも1つが前記夫々の下
限未満では、上記効果が充分でなく、またZnC1,含
有量が300 g/lを超えると、上記効果を必ずしも
増大できないばかりでなく、全量溶解し難くなる。また
NaClは不めっきを生ぜしめないように作用するが、
その含有量が40g/lを超えると被処理物に付着する
ZnC1、、NaC1およびCHICHCOOH混合塩
の融点が増大し、フラックス性が低下する。ZnCf, content, NaCIl content and C)lzc
If at least one of the HcOOR contents is below the respective lower limits, the above effects will not be sufficient, and if the ZnC1 content exceeds 300 g/l, not only will the above effects not necessarily be increased, but the entire amount will dissolve. It becomes difficult to do. Also, NaCl acts to prevent unplating, but
When the content exceeds 40 g/l, the melting point of the mixed salt of ZnC1, NaC1 and CHICHCOOH that adheres to the object to be treated increases, and the flux property decreases.
更に、CH2CHCOOHは不めっきを生ゼしめないの
みならず、めっき表面を平滑に形成させるように作用す
るが、その含有量が120g/lを超えてもこの作用は
必ずしも増大しない。Furthermore, CH2CHCOOH not only does not cause unplatedness but also acts to form a smooth plated surface, but this effect does not necessarily increase even if its content exceeds 120 g/l.
本発明のフラックスは、被処理物をその中に浸漬したり
、その表面に塗布したりなどして用いればよい。The flux of the present invention may be used by dipping the object to be treated therein or by applying it to the surface of the object.
実施例、比較例、従来例
JIS 82107の規定による蒸溜亜鉛地金(一種)
および純度99.9重量%以上のアルミニウム地金を用
いて、A15重量%、残部Znおよび不可避不純物から
なる組成の溶融亜鉛めっき浴を30番の黒鉛坩堝中で電
気炉を用いて520℃にて溶製した。Examples, Comparative Examples, Conventional Examples Distilled zinc ingot (class 1) according to JIS 82107
Using an aluminum ingot with a purity of 99.9% by weight or more, a hot-dip galvanizing bath with a composition of 15% by weight of A, the balance being Zn and unavoidable impurities was heated at 520°C in a No. 30 graphite crucible using an electric furnace. Melted.
一方、板厚3謳の一般構造用圧延鋼板より板幅75璽鳳
、板長150fiの試験片を切り出し、その試験片の表
面を加熱したオルト珪酸ソーダの10重量%水溶液で脱
脂した後、15重量%の硫酸溶液中に10分間浸漬する
ことにより試験片の表面を酸洗し、更に、70℃に加熱
した、第1表に示す組成の水溶液中に3分間浸漬して引
上げることによってフラックス処理を施し、最後に80
℃に保持された恒温槽中で乾燥することによって溶融亜
鉛めっき処理品に対する不めっきの度合を評価するため
の試験片を準備した。On the other hand, a test piece with a width of 75 mm and a length of 150 mm was cut from a general structural rolled steel plate with a thickness of 3 mm, and the surface of the test piece was degreased with a heated 10% by weight aqueous solution of sodium orthosilicate. The surface of the test piece was pickled by immersing it in a sulfuric acid solution of 10% by weight for 10 minutes, and then it was immersed in an aqueous solution heated to 70°C with the composition shown in Table 1 for 3 minutes and pulled up to obtain a flux. Processed and finally 80
A test piece was prepared for evaluating the degree of non-plating on a hot-dip galvanized product by drying it in a constant temperature bath maintained at ℃.
次いで、上記のようにあらかじめ溶製された溶融亜鉛め
っき浴の温度を440℃に調整し、充分にめっき浴を撹
拌した後、めっき浴表面のドロスを除去し、上記のよう
に調製された試験片を60秒間めっき浴中に浸漬し、再
びめっき浴表面のドロスを除去して上記試験片をめっき
浴より引上げ、60秒間空気中に保持したのち水中に投
入し、これを引上げることにより、めっき処理の施され
た試験片を採取した。Next, the temperature of the hot-dip galvanizing bath prepared in advance as described above was adjusted to 440°C, the plating bath was sufficiently stirred, and the dross on the surface of the plating bath was removed. By immersing the piece in the plating bath for 60 seconds, removing the dross on the surface of the plating bath again, lifting the test piece from the plating bath, holding it in the air for 60 seconds, putting it into water, and pulling it up, A test piece that had been subjected to plating treatment was taken.
これらの試験片の不めっきの度合を目視により観察した
。その結果を第1表に示す。The degree of non-plating of these test pieces was visually observed. The results are shown in Table 1.
以上から明らかなように、本発明の溶融Zn−A R合
金めっき用フラックスによれば、耐食性の確保された溶
融Zn−A 1合金めっき処理品を1度のめっき作業で
得ることができる。As is clear from the above, according to the flux for hot-dip Zn-A R alloy plating of the present invention, a hot-dip Zn-A 1 alloy plated product with ensured corrosion resistance can be obtained in a single plating operation.
Claims (1)
を20〜40g/lおよびCH_2CHCOOHを10
〜120g/l含む水溶液からなる溶融Zn−Al合金
めっき用フラックス。1. ZnCl_2 150-300g/l, NaCl
20-40 g/l and CH_2CHCOOH 10
A flux for hot-dip Zn-Al alloy plating consisting of an aqueous solution containing ~120 g/l.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23685589A JP2756318B2 (en) | 1989-09-14 | 1989-09-14 | Flux for hot-dip Zn-Al alloy plating |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23685589A JP2756318B2 (en) | 1989-09-14 | 1989-09-14 | Flux for hot-dip Zn-Al alloy plating |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03100152A true JPH03100152A (en) | 1991-04-25 |
| JP2756318B2 JP2756318B2 (en) | 1998-05-25 |
Family
ID=17006803
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23685589A Expired - Fee Related JP2756318B2 (en) | 1989-09-14 | 1989-09-14 | Flux for hot-dip Zn-Al alloy plating |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP2756318B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006224583A (en) * | 2005-02-21 | 2006-08-31 | Konica Minolta Holdings Inc | Adhesion recovering method for transfer member, transfer apparatus, and image recording apparatus |
-
1989
- 1989-09-14 JP JP23685589A patent/JP2756318B2/en not_active Expired - Fee Related
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2006224583A (en) * | 2005-02-21 | 2006-08-31 | Konica Minolta Holdings Inc | Adhesion recovering method for transfer member, transfer apparatus, and image recording apparatus |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2756318B2 (en) | 1998-05-25 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |