JP2756318B2 - Flux for hot-dip Zn-Al alloy plating - Google Patents
Flux for hot-dip Zn-Al alloy platingInfo
- Publication number
- JP2756318B2 JP2756318B2 JP23685589A JP23685589A JP2756318B2 JP 2756318 B2 JP2756318 B2 JP 2756318B2 JP 23685589 A JP23685589 A JP 23685589A JP 23685589 A JP23685589 A JP 23685589A JP 2756318 B2 JP2756318 B2 JP 2756318B2
- Authority
- JP
- Japan
- Prior art keywords
- plating
- flux
- hot
- dip
- alloy plating
- 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 - Fee Related
Links
Landscapes
- Coating With Molten Metal (AREA)
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 [Industrial Application Field] The present invention relates to a plating flux used for applying a hot-dip Zn-Al alloy plating process to a steel material or 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。BACKGROUND ART Conventionally, to prevent corrosion of steel materials and the like, it has been known to apply hot-dip galvanizing and electrogalvanizing to the surface thereof.
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
数多く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。In recent years, a number of new, high-value-added products have been introduced to the market by using zinc plating as a base and further adding surface treatments, such as painting and processing, to the base. The choices of users for such products are becoming more and more diversified.
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 requirements, with respect to the hot-dip galvanized product, it has been considerably attempted to improve the characteristics of the plating layer by selecting the added element and the added amount as the plating bath composition.
とりわけ、めっき層の耐食性を確保するために、Alを
3〜10重量%程度添加しためっき浴が知られている。こ
のめっき浴は、通常、鉄鋼部品等の被処理物にそれをZn
Cl2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。Particularly, a plating bath to which Al is added in an amount of about 3 to 10% by weight in order to ensure the corrosion resistance of the plating layer is known. This plating bath usually deposits Zn on the workpiece such as steel parts.
It is used after flux treatment such as immersion in Cl 2 aqueous 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 manner does not have a plated layer and is apt to cause non-plating.
そこで、一度、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−Al合金めっき浴で2次めっきを行なっている。Therefore, once, the primary plating is performed in a Zn plating bath containing no Al, and after performing the flux treatment as described above,
Secondary plating is performed in a Zn-Al alloy plating bath.
しかしながら、上記方法は、2回めっき工程を経るの
が煩雑であり、製造コストも高いという欠点があった。However, the above method has the drawback that it is complicated to perform the plating process twice and the production cost is 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−Al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-described conventional problems, and provides a flux for hot-dip Zn-Al alloy plating that does not cause non-plating even in a single plating operation on a workpiece such as a steel part. Aim.
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ZnCl2,NaClおよびCH2C
HCOOH(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ZnCl2,NaClおよび
CH2CHCOOHを付着させることにより被処理物へのZn−Al
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 as a result, as a flux, ZnCl 2 , NaCl and CH 2 C
Flux treatment of the object to be treated is performed using an aqueous solution containing HCOOH (acrylic acid), and ZnCl 2 , NaCl and
By attaching CH 2 CHCOOH, Zn-Al
It has been found that the adhesion of the alloy can be improved, and details thereof will be described below.
即ち、本発明は、溶融Zn−Al合金めっき用フラックス
としてZnCl2を150〜300g/、NaClを20〜40g/およびC
H2CHCOOHを10〜120g/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。That is, the present invention is a flux for hot-dip Zn-Al alloy plating ZnCl 2 150-300 g /, NaCl 20-40 g / and C
By using an aqueous solution of H 2 CHCOOH 10~120g / include those wherein the foregoing problems are eliminated.
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Al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。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
る効果が少なく、またAlの含有量が10重量%を越えても
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 reason for using the flux of the present invention as hot-dip Zn-Al alloy plating and containing Al in the zinc plating bath is to maintain the corrosion resistance of the plating layer. The Al content is preferably 3 to 10% by weight. If the content is less than 3% by weight, the effect of maintaining the above-mentioned corrosion resistance is small, and if the content of Al exceeds 10% by weight, it is difficult to further improve the corrosion resistance, and the melting point of the plating bath is increased. This is because the sex becomes worse.
また、本発明の水溶液フラックス中にZnCl2,NaClおよ
びCH2CHCOOHを含有せしめたのは、Zn−Al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。Further, the inclusion of ZnCl 2 , NaCl and CH 2 CHCOOH in the aqueous flux of the present invention improves the adhesion between the Zn-Al alloy plating layer and the object to be treated, and does not cause non-plating.
This is to form a smooth plating surface.
ZnCl2含有量、NaCl含有量およびCH2CHCOOH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ZnCl2含有量が300g/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/を超えると被処理物
に付着するZnCl2,NaClおよびCH2CHCOOH混合塩の融点が
増大し、フラックス性が低下する。更に、CH2CHCOOHは
不めっきを生ぜ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/
を超えてもこの作用は必ずしも増大しない。If at least one of the ZnCl 2 content, the NaCl content and the CH 2 CHCOOH content is less than the respective lower limits, the above effect is not sufficient, and if the ZnCl 2 content exceeds 300 g /
Not only the above effect cannot always be increased, but also the total amount becomes difficult to dissolve. In addition, NaCl acts to prevent non-plating, but when its content exceeds 40 g /, the melting point of ZnCl 2 , NaCl and CH 2 CHCOOH mixed salt attached to the workpiece increases, and the flux property decreases. I do. Furthermore, CH 2 CHCOOH not only does not cause non-plating, but also acts to form a smooth plating surface, but its content is 120 g /
This effect does not necessarily increase even if the pressure exceeds.
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 immersing the object to be treated therein or applying it to the surface thereof.
実施例、比較例、従来例 JIS H2107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、Al5
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, and Conventional Examples Using distilled zinc ingot (one kind) and aluminum ingot having a purity of 99.9% by weight or more according to JIS H2107, Al5
A hot-dip galvanizing bath having a composition of weight%, balance Zn and unavoidable impurities was placed in a graphite crucible No. 30 using an electric furnace at 520%.
Melted at ℃.
一方、板厚3mmの一般構造用圧延鋼板より板幅75mm、
板長150mm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, the width of 75mm,
A test piece with a plate length of 150 mm was cut out, the surface of the test piece was degreased with a heated 10% by weight aqueous solution of sodium orthosilicate, and then immersed in a 15% by weight sulfuric acid solution for 10 minutes to make the surface of the test piece acidic. Rinse, wash, and immerse in an aqueous solution of the composition shown in Table 1 heated to 70 ° C. for 3 minutes, pull up, and finally dry in a constant temperature bath maintained at 80 ° C. A test piece for evaluating the degree of non-plating on the hot-dip galvanized product was prepared.
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 previously melted as described above was adjusted to 440 ° C., and after sufficiently stirring the plating bath, dross on the plating bath surface was removed, and the test prepared as described above was performed. The specimen was immersed in the plating bath for 60 seconds, the dross on the plating bath surface was removed again, and the test piece was pulled up from the plating bath.Then, the specimen was kept in the air for 60 seconds, then put in water, and pulled up. A test piece subjected to a plating treatment was collected.
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. Table 1 shows the results.
〔発明の効果〕 以上から明らかなように、本発明の溶融Zn−Al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
−Al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。 [Effects of the Invention] As is clear from the above, according to the flux for hot-dip Zn-Al alloy plating of the present invention, the hot-dip Zn in which corrosion resistance is ensured
-An Al alloy plated product can be obtained in one plating operation.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.6,DB名) C23C 2/02 C23C 2/06 C23C 2/30──────────────────────────────────────────────────続 き Continued on front page (58) Field surveyed (Int. Cl. 6 , DB name) C23C 2/02 C23C 2/06 C23C 2/30
Claims (1)
およびCH2CHCOOHを10〜120g/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 is 150 to 300 g / NaCl is 20 to 40 g /
And CH 2 CHCOOH consisting of an aqueous solution 10~120G / containing molten
Flux for plating Zn-Al alloy.
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 JPH03100152A (en) | 1991-04-25 |
JP2756318B2 true 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) |
Families Citing this family (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
Also Published As
Publication number | Publication date |
---|---|
JPH03100152A (en) | 1991-04-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |