JPH0426745A - Colored alloy plating coating - Google Patents

Colored alloy plating coating

Info

Publication number
JPH0426745A
JPH0426745A JP2131207A JP13120790A JPH0426745A JP H0426745 A JPH0426745 A JP H0426745A JP 2131207 A JP2131207 A JP 2131207A JP 13120790 A JP13120790 A JP 13120790A JP H0426745 A JPH0426745 A JP H0426745A
Authority
JP
Japan
Prior art keywords
phase
coating
zinc alloy
cracks
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.)
Granted
Application number
JP2131207A
Other languages
Japanese (ja)
Other versions
JP2612954B2 (en
Inventor
Hiroshi Tazaki
博 田崎
Eiji Nishimura
栄二 西村
Yasunari Yamamoto
山本 泰然
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.)
Eneos Corp
Original Assignee
Nippon Mining Co Ltd
Nikko Kyodo 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
Priority claimed from JP1105819A external-priority patent/JPH07110962B2/en
Application filed by Nippon Mining Co Ltd, Nikko Kyodo Co Ltd filed Critical Nippon Mining Co Ltd
Priority to JP2131207A priority Critical patent/JP2612954B2/en
Priority to EP90119534A priority patent/EP0423624B1/en
Priority to DE69025022T priority patent/DE69025022T2/en
Priority to KR1019900016617A priority patent/KR930009988B1/en
Priority to AU86007/91A priority patent/AU645616B2/en
Priority claimed from AU86007/91A external-priority patent/AU645616B2/en
Publication of JPH0426745A publication Critical patent/JPH0426745A/en
Priority to US07/914,013 priority patent/US5200276A/en
Priority to US08/004,255 priority patent/US5364478A/en
Publication of JP2612954B2 publication Critical patent/JP2612954B2/en
Application granted granted Critical
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To form a colored alloy plating coating free from the generation of peeling and cracks on a steel, in a coated film of a zinc alloy constituted of Mn, Fe and the balance Zn, by forming a surface layer of a eta phase and a lower part layer of a zeta phase. CONSTITUTION:At the time of forming a coated film constituted of a zinc alloy on a steel by using a zinc alloy plating bath contg. Mn or the like, the temp. of the zinc alloy coating bath is controlled to the range of about 430 to 480 deg.C. In this way, the colored plating film in which the surface layer is formed of a eta phase (contg., by weight, 0.3wt.% Mn, about 0.003% Fe and the balance Zn) and the lower part layer is formed of a zeta phase (fundamentally consisting of FeZn13 and contg. about 0.2wt.% Mn or the like) and free from the generation of peeling and cracks can be obtd.

Description

【発明の詳細な説明】 竜−シ」二の利用ノ野 鋼材に着色溶融亜鉛めっきを施す際に、めっき後皮膜が
鋼材から剥離せず、しかも皮膜にクラックが発生しない
被覆物についての発明に関する。
[Detailed Description of the Invention] Utilization of Ryu-shi 2 This invention relates to a coating that does not peel off from the steel material after plating and does not cause cracks in the coating when colored hot-dip galvanizing is applied to steel material. .

且皿勿従来弦皿 従来、Mn等を添加した着色溶融亜鉛めっきにおいて、
好ましい茶色等の発色を得ていた。
In the conventional colored hot-dip galvanizing with addition of Mn, etc.,
A desirable color development such as brown was obtained.

鵞」1支歪1跣力。Goose” 1 branch strain, 1 leg strength.

しかしながら、例えば、Mn添加溶融亜鉛めっきの場合
、めっき後の冷却過程で皮膜が銅相から剥離したり、皮
膜にクラックが発生する場合があり、不良率が高い等の
問題点とめっき皮膜の耐衝撃性が弱いと云う問題点があ
った。そこで発明者等は鋭意検討した結果以下の発明を
なした。
However, in the case of Mn-added hot-dip galvanizing, for example, the film may peel off from the copper phase or cracks may occur in the film during the cooling process after plating, resulting in problems such as a high defect rate and the durability of the plating film. There was a problem that impact resistance was weak. Therefore, the inventors made the following invention as a result of intensive study.

且里豊豊底 即ち本発明は、 (1)亜鉛合金からなるめっき皮膜の表面層が、η相で
、該下部層が、ζ相であることを特徴とする着色めっき
被覆物。
The present invention is characterized in that: (1) the surface layer of the plating film made of a zinc alloy is an η phase, and the lower layer is a ζ phase;

(2)亜鉛合金がMn、Fe残部亜鉛からなる特許請求
範囲第1項記載の着色めっき被覆物に関する。
(2) The colored plating coating according to claim 1, wherein the zinc alloy is composed of Mn, Fe, and zinc.

】」[生民停止用 本発明において、めっき皮膜の表面層は、η相で、各該
下部層は、ζ相であることを要する。
In the present invention, the surface layer of the plating film is required to be in the η phase, and each of the lower layers is required to be in the ζ phase.

上記の相は、鉄製品に亜鉛合金からなる着色め寸きを行
う際に、めっき層として形成される相である。ここで用
いられる亜鉛は、蒸留亜鉛地金−種(純度98.5%以
」二)、最純亜鉛地金(純度99.995%以」二)並
びに電気亜鉛地金(純度99.99%以上)等である。
The above phase is a phase that is formed as a plating layer when coloring and sizing iron products made of zinc alloy. The zinc used here is distilled zinc ingot (purity of 98.5% or higher), purest zinc ingot (purity of 99.995% or higher), and electrolytic zinc ingot (purity of 99.99%). above) etc.

さらに着色させるための添加元素として、Mn等が添加
された合金を用いる。
Furthermore, an alloy to which Mn or the like is added as an additional element for coloring is used.

ここでη相はMn0,3wt%、Fed、003wt%
残部亜鉛で、ζ相はF e Z n、、を基本として、
これに着色添加元素のMn等0.2wt%を含むもので
ある。
Here, the η phase is Mn0,3wt%, Fed,003wt%
The balance is zinc, and the ζ phase is based on F e Z n,
This contains 0.2 wt % of coloring additive elements such as Mn.

発明者等は、」1記の層からなる被覆であると、被覆に
クラックが生ぜず、しかも機械的な外力に対して強度が
あることを見出したものである。上記の相を得る方法と
しては、例えば以下の方法がある。
The inventors have discovered that a coating consisting of the layer described in item 1 does not cause cracks in the coating and is strong against external mechanical forces. Examples of methods for obtaining the above phase include the following methods.

すなわち、亜鉛合金めっき浴温度を4.30〜480℃
の範囲・にコントロールすることにより、めっき後の冷
却過程及び皮膜特性を向]ニさせるための熱処理工程で
、鋼材からの皮膜の剥離及びクラックの発生を防止でき
る。430℃より低い温度では、めっきが良好に出来ず
、480℃より浴温度が高いと鋼材からの皮膜の剥離及
びクラックの発生する確率が高くなる。このような現象
は通常の溶融亜鉛めっきでは観察されず、Mnが含有さ
れている場合に始めて起こる。これはMnが鉄と亜鉛の
合金化を促進するために起こるものである。
That is, the zinc alloy plating bath temperature is 4.30 to 480°C.
By controlling the temperature within this range, peeling of the film from the steel material and generation of cracks can be prevented during the cooling process after plating and the heat treatment process to improve the film properties. If the bath temperature is lower than 430°C, plating cannot be performed well, and if the bath temperature is higher than 480°C, there is a high probability that the coating will peel off from the steel material and cracks will occur. Such a phenomenon is not observed in normal hot-dip galvanizing, but only occurs when Mn is contained. This occurs because Mn promotes alloying of iron and zinc.

すなわちMnが含有されている場合4.80℃を超える
浴温度では、通常存在するζ相(FeZn、)が消滅し
、鉄亜鉛の合金層は、殆どδ1相(FeZ n、)とな
る。発明者等は、鋭意検討の結果、このことが鋼材から
の皮膜の剥離及びクラックの発生の原因であることを見
出し、ζ相(F e Z n、)が消滅しない浴温度範
囲、すなわち430〜480℃でめっきを行なうことが
、鋼材からの剥離及びクラックを防止できる条件である
ことを見い出した。
That is, when Mn is contained, at a bath temperature exceeding 4.80° C., the normally existing ζ phase (FeZn,) disappears, and the iron-zinc alloy layer becomes almost the δ1 phase (FeZn,). As a result of intensive studies, the inventors found that this is the cause of peeling of the film from the steel material and the occurrence of cracks. It has been found that plating at 480° C. is a condition that can prevent peeling and cracking from the steel material.

実施例1 0.3重量%Mnを含有する亜鉛合金浴を460℃の温
度に固定し、鋼材を3分間浸漬後放冷した。このサンプ
ルについて皮膜の鋼材からの剥離及び皮膜のクラックの
有無と皮膜組織を調べた。
Example 1 A zinc alloy bath containing 0.3% by weight of Mn was fixed at a temperature of 460°C, and a steel material was immersed for 3 minutes and then allowed to cool. Regarding this sample, the presence or absence of peeling of the coating from the steel material, cracks in the coating, and coating structure were investigated.

その結果表面相は、η相であり該下部層は、ζ相rあっ
た。このため皮膜の鋼材からの剥離及び皮膜のクラック
の発生は観察されなかった。
As a result, the surface phase was η phase, and the lower layer was ζ phase r. Therefore, no peeling of the coating from the steel material or occurrence of cracks in the coating was observed.

実施例2 0.2重量%Mnを含有する亜鉛合金浴を450℃の温
度に固定し、銅相を3分間浸漬後、めっき皮膜の特性改
善のために500℃で10分間熱処理しその後放冷した
。このサンプルについて皮膜の鋼材からの剥離及び皮膜
のクラックの有無と皮膜組織を調べた。その結果表面相
はη相であり、下部層は、ζ相であった。このため皮膜
は、鋼材からの剥離及びのクラックの発生は生じてぃな
かった。
Example 2 A zinc alloy bath containing 0.2% by weight Mn was fixed at a temperature of 450°C, and the copper phase was immersed for 3 minutes, then heat treated at 500°C for 10 minutes to improve the properties of the plating film, and then allowed to cool. did. Regarding this sample, the presence or absence of peeling of the coating from the steel material, cracks in the coating, and coating structure were investigated. As a result, the surface phase was η phase, and the lower layer was ζ phase. Therefore, the coating did not peel off from the steel material and did not develop cracks.

比較例1 0.3重量%Mnを含有する亜鉛合金浴を500℃の温
度に固定し、鋼材を3分間浸漬後放冷した。このサンプ
ルについて皮膜の鋼材からの剥離及び皮膜のクラックの
有無と皮膜組織を調べた。
Comparative Example 1 A zinc alloy bath containing 0.3% by weight of Mn was fixed at a temperature of 500° C., and the steel material was immersed for 3 minutes and then allowed to cool. Regarding this sample, the presence or absence of peeling of the coating from the steel material, cracks in the coating, and coating structure were investigated.

その結果ζ相が観察されず、クラックの発生が観察され
た。
As a result, no ζ phase was observed, and the occurrence of cracks was observed.

°且里豊ガ末 本発明を実施することにより以下のような効果を有する
By implementing the present invention, the following effects can be obtained.

(1)溶融亜鉛めっきによる皮膜が、剥離及びクラック
を生じない好ましい皮膜を得ることができ(2)Mn等
を添加した溶融亜鉛めっきにより、茶色の強固な皮膜を
容易に得ることができる。
(1) Hot-dip galvanizing can provide a preferable coating that does not cause peeling or cracking. (2) Hot-dip galvanizing with Mn or the like can easily provide a strong brown coating.

Claims (2)

【特許請求の範囲】[Claims] (1)亜鉛合金からなるめっき皮膜の表面層が、η相で
、該下部層が、ζ相であることを特徴とする着色めっき
被覆物。
(1) A colored plating coating, characterized in that the surface layer of the plating film made of a zinc alloy is an η phase, and the lower layer is a ζ phase.
(2)亜鉛合金がMn、Fe残部亜鉛からなる特許請求
範囲第1項記載の着色めっき被覆物。
(2) The colored plating coating according to claim 1, wherein the zinc alloy is composed of Mn, Fe, and the balance is zinc.
JP2131207A 1989-04-27 1990-05-23 Brown colored plating coating Expired - Lifetime JP2612954B2 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP2131207A JP2612954B2 (en) 1989-04-27 1990-05-23 Brown colored plating coating
EP90119534A EP0423624B1 (en) 1989-04-27 1990-10-11 Color-coated article and method for producing the same
DE69025022T DE69025022T2 (en) 1989-04-27 1990-10-11 Colored coated article and process for its manufacture
KR1019900016617A KR930009988B1 (en) 1989-04-27 1990-10-18 Brown coated article and method for producing the same
AU86007/91A AU645616B2 (en) 1989-04-27 1991-10-18 Color-coated article and method for producing the same
US07/914,013 US5200276A (en) 1989-04-27 1992-07-15 Color-coated article and method for producing the same
US08/004,255 US5364478A (en) 1989-04-27 1993-01-14 Method for producing a color-coated article

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP1105819A JPH07110962B2 (en) 1989-04-27 1989-04-27 Colored zinc powder, method for producing the same, and method for producing a colored product
JP2131207A JP2612954B2 (en) 1989-04-27 1990-05-23 Brown colored plating coating
AU86007/91A AU645616B2 (en) 1989-04-27 1991-10-18 Color-coated article and method for producing the same

Publications (2)

Publication Number Publication Date
JPH0426745A true JPH0426745A (en) 1992-01-29
JP2612954B2 JP2612954B2 (en) 1997-05-21

Family

ID=27156663

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2131207A Expired - Lifetime JP2612954B2 (en) 1989-04-27 1990-05-23 Brown colored plating coating

Country Status (1)

Country Link
JP (1) JP2612954B2 (en)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5028900A (en) * 1973-07-13 1975-03-24

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5028900A (en) * 1973-07-13 1975-03-24

Also Published As

Publication number Publication date
JP2612954B2 (en) 1997-05-21

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