JPS5855593A - Multi-color electrolytic coloration of aluminum of aluminum alloy - Google Patents

Multi-color electrolytic coloration of aluminum of aluminum alloy

Info

Publication number
JPS5855593A
JPS5855593A JP15440881A JP15440881A JPS5855593A JP S5855593 A JPS5855593 A JP S5855593A JP 15440881 A JP15440881 A JP 15440881A JP 15440881 A JP15440881 A JP 15440881A JP S5855593 A JPS5855593 A JP S5855593A
Authority
JP
Japan
Prior art keywords
color
aluminum
electrolytic
anodic oxidation
coating
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.)
Pending
Application number
JP15440881A
Other languages
Japanese (ja)
Inventor
Shinichi Ishida
石田 愼一
Jitsuo Mizuno
水野 実夫
Takashi Onaka
大中 隆
Yuji Sakaguchi
坂口 雄二
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 Aluminium Co Ltd
Original Assignee
Nippon Aluminium 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 Nippon Aluminium Co Ltd filed Critical Nippon Aluminium Co Ltd
Priority to JP15440881A priority Critical patent/JPS5855593A/en
Publication of JPS5855593A publication Critical patent/JPS5855593A/en
Pending legal-status Critical Current

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  • Electrochemical Coating By Surface Reaction (AREA)

Abstract

PURPOSE:To color aluminum or an aluminum allou optional color such as red, blue or green, by a method wherein an anodic oxidation film is formed in an electrolite based on sulfuric acid in a first process and modified in a acidic bath in a second process and the modified coating is electrolyzed in an electrolytic coloring liquid containing a metal salt such as NiSO4 in a third process. CONSTITUTION:An Al material or an Al alloy material is subjected to electrolytic treatment in an electrolyte based on sulfuric acid in a first process to chemically form an anodic oxidation coating having plural fine pores on the ground material. After washing by water, the anodic oxidation material is immersed in an acidic liquid in a second process to increase the diameter of each fine pore as well as to form plural further finer pores to each pore bottom part in a branched form. Subsequently, in a third process, electrolytic coloring treatment is applied in an electrolytic coloring liquid based on a metal salt such as NiSO4 by passing DC, AC or pulse current to develop a gray color, a bronze color, a blue color, a green color or a reddish purple color on the coating.

Description

【発明の詳細な説明】 本発明はアルミニウムやその合金を着色するための電解
着色法に関し、従来ブロンズ色や黒楓以外の色に着色す
ることが困難とされている上記材料を赤、青、緑等の任
意色に着色できるようにし、それによりアルミニウムや
その合金を建材等に使用した場合の外観を向上させると
共に、それらの材料の用途を拡張できるようにすること
を目的としている。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an electrolytic coloring method for coloring aluminum and its alloys, and the present invention relates to an electrolytic coloring method for coloring aluminum and its alloys. The purpose is to make it possible to color any color such as green, thereby improving the appearance of aluminum and its alloys when used in building materials, etc., as well as expanding the uses of these materials.

本発明によると、アルミニウム又はアルミニウム合金の
素地は前処理を施された後に第1工程において硫酸を主
体とする電解液中で電解処理され、多数の微細孔を有す
る陽極酸化皮膜か素地の表面に化成される′。
According to the present invention, the aluminum or aluminum alloy substrate is pretreated and then electrolytically treated in an electrolyte mainly containing sulfuric acid in the first step, and an anodic oxide film having many micropores is formed on the surface of the substrate. to be chemically formed.

次&:、酸化皮膜は水洗後、!J2工程において酸性浴
に浸漬され、第1工程で生成した陽極酸化皮膜は改質さ
れる。すなわち9J2工程で使用される上記酸性浴はり
ん酸を主体とするもの、あるいはりん酸、硝酸、硫酸、
有機酸をそれぞれ単独で使用するか、又はそれらのい(
つかを組み合わせたものである。上記の酸性浴に浸漬す
ることにより微細孔の直径は第1工程終了時の直径より
も増大し、また微細孔の底部は更に細い多数の微細孔に
枝分れする。更に第1工程において御飯酸化皮膜中に混
入したりあるいは微細孔の孔壁に吸着した硫酸イオン(
804”−)が第2工程における酸性浴のアニオン種(
例えばリン酸イオン、硝酸イオン、しゆう酸イオン等]
と置換される。以上のようにして皮膜構造あるいは皮膜
組成を改質する。
Next &:, After washing the oxide film with water,! In the J2 step, it is immersed in an acid bath, and the anodic oxide film produced in the first step is modified. That is, the acidic bath used in the 9J2 process is one mainly composed of phosphoric acid, or one containing phosphoric acid, nitric acid, sulfuric acid,
Each organic acid may be used alone or in combination with
It is a combination of two things. By immersing it in the above acidic bath, the diameter of the micropore becomes larger than the diameter at the end of the first step, and the bottom of the micropore branches into a large number of even smaller micropores. Furthermore, in the first step, sulfate ions (
804”-) is the anionic species (
For example, phosphate ion, nitrate ion, oxalate ion, etc.]
will be replaced with The film structure or film composition is modified as described above.

9J2工程を完了した素地及び皮膜は水洗後、第3工程
において金属塩を含む電解液中で電解着色処理が施され
、電解液の金属塩から析出した金属が微細孔及び枝孔内
に付着又は充填され、皮膜全体が外部から見た場合に着
色された状態になる。
After completing the 9J2 process, the substrate and coating are washed with water, and then electrolytically colored in an electrolytic solution containing metal salts in the third step. The entire coating becomes colored when viewed from the outside.

この第3工程における電解液としては、錫、マンガン、
ニッケル、銅、セレン、銀等の硫i!!塩又は酢ram
<例えば硫酸ニッケル、硫rII9I61錫】を単独で
使用するか、あるいは上記塩のい(つかの混合水浴液が
使用され、又必要に一応じてそれらの液にpH緩衝剤、
酸化防止剤又は安定剤を添加した浴が使用される。電解
波形としては直流、交流、パルス電流等が使用される。
The electrolyte in this third step includes tin, manganese,
Sulfuric acid such as nickel, copper, selenium, silver, etc. ! salt or vinegar ram
[For example, nickel sulfate, rII9I61tin sulfur] is used alone, or a mixed water bath solution of the above salts is used, and if necessary, a pH buffer, a pH buffer,
Baths with added antioxidants or stabilizers are used. Direct current, alternating current, pulsed current, etc. are used as the electrolytic waveform.

又処理後の皮膜はグレー色、ブロンズ色、ブルー系色、
緑色、赤紫系色等に発色し、又これらの色調は電解液の
組成や電解条件を変えることにより任意に選ぶことがで
きる。jl!3工程を終えた皮膜には好ましくは煮沸水
や蒸気等により封孔処理が施されるか、又は必要に応じ
て塗装が施される。
The film after treatment is gray, bronze, blue,
It develops a color such as green or reddish-purple, and these colors can be arbitrarily selected by changing the composition of the electrolytic solution and the electrolytic conditions. jl! After completing the three steps, the film is preferably subjected to a pore sealing treatment using boiled water, steam, etc., or painted as necessary.

このように本発明においてはアルミニウムやアルミニウ
ム合金を青、緑、赤等の任意の色に着色することができ
るので、アルミニウムやその合金を建材等に使用した場
合に外観を向上させることができ、又それらの材料の用
途を拡げることができる。第2工程の皮膜改質時に本発
明では単に浸漬処理だけが施されているが、本発明とは
別に皮膜改質時に電解処理を施すことも考えられている
In this way, in the present invention, aluminum and aluminum alloys can be colored in any color such as blue, green, red, etc., so when aluminum or aluminum alloys are used as building materials, the appearance can be improved. Moreover, the uses of those materials can be expanded. In the present invention, only a dipping treatment is performed during film modification in the second step, but it is also contemplated that an electrolytic treatment may be performed during film modification separately from the present invention.

ところが電解処理法を採用すると、電気設備が必要にな
ると共に電力費用も当然必要になり、製造コストが高(
なる。又電極に近い部分と遠い部分との間で改質状態に
差が生じ、第3工程終了後の着色状態にむらが生じて商
品価値が損われる恐れがある。これに対して本発明では
改質時に電解処理を施さないので、設備費および製造コ
ストが安くなる。すなわち、例えば、処理工程として@
1工程終了後の水洗浴を第2工程の酸性浴として建浴す
れば従来の処理工程をそのまま利用する(々ができる。
However, when the electrolytic treatment method is adopted, electrical equipment is required, and of course electricity costs are also required, resulting in high manufacturing costs (
Become. Furthermore, there is a possibility that there will be a difference in the modified state between the part close to the electrode and the part far away, and the coloring state after the third step will be uneven, resulting in loss of commercial value. On the other hand, in the present invention, since electrolytic treatment is not performed during reforming, equipment costs and manufacturing costs are reduced. That is, for example, as a processing step @
If the washing bath after the completion of the first step is used as an acidic bath for the second step, the conventional treatment steps can be used as is.

又、電解処理における極間距離の差により生じる色むら
などは浸漬処理では生じにくい。
In addition, color unevenness caused by a difference in distance between electrodes during electrolytic treatment is less likely to occur in dipping treatment.

さらに複雑な形状の材料の処理においても有効な攪拌を
採用することで均一な色調の仕上げが可能である。
Furthermore, even when processing materials with complex shapes, it is possible to achieve a finish with a uniform color tone by using effective stirring.

実施例1 第1工程 電解液組成     硫II? 15W(重量)/V(
体積)%液温  −20℃ 電流密度・時間    I A/dm” X 30分膜
厚   9μ 第2工程 酸性浴組成    りん$501711液温   20
℃ 浸漬時間     5分間 攪 拌      液循環攪拌 電圧   直流−15V 電解時間と各電解時間に対応する着色状態実施例2 1J1工程、第2工程・・・実施例1と同じ。
Example 1 First step electrolyte composition Sulfur II? 15W (weight)/V(
Volume) % Liquid temperature -20°C Current density/time I A/dm" x 30 minutes Film thickness 9μ 2nd step acidic bath composition Phosphorus $501711 Liquid temperature 20
°C Immersion time 5 minutes Stirring Liquid circulation Stirring voltage DC -15V Electrolysis time and coloring state corresponding to each electrolysis time Example 2 1J1 step, 2nd step...Same as Example 1.

第3工程 電 圧      交流10V 実施例3 gJ1工程・・・実施例1と同じ。Third step Voltage AC 10V Example 3 gJ1 step: Same as Example 1.

1J2工程 液温   20℃ 浸漬時間     3分 攪 拌      空気攪拌 第3工程 通電条件     直流、+10VX3秒と一15VX
lO秒の交互通電 通電繰返し数と着色状態 実施例4 液温   20℃ 電流密度・時間    1.5 A/dm’X30分膜
厚   12μ 第2工程 酸性浴組成    硝酸 so fil液温   20
°C 浸漬時間     10分 第3工程 電解着色液組成   実施例2と同−液電 圧    
 交流12V 実施例5 第1工程・・一実施例1と同じ。
1J2 process liquid temperature 20℃ Immersion time 3 minutes Stirring Air stirring 3rd process energizing conditions DC, +10VX for 3 seconds and -15VX
Number of alternating energization repetitions of 10 seconds and coloring state Example 4 Liquid temperature 20°C Current density/time 1.5 A/dm'X30 film thickness 12μ 2nd step acidic bath composition Nitric acid so fil liquid temperature 20
°C Immersion time 10 minutes Third step electrolytic coloring solution composition Same as Example 2 - Solution voltage
AC 12V Example 5 First step: Same as Example 1.

9J2工程 酸性浴組成    しゆうm  40171浴温   
30℃ 浸漬時間     1分 攪 拌      45KHzの超音波第3工程 電解電圧     交流12V
9J2 process acidic bath composition 40171 bath temperature
30℃ Immersion time 1 minute Stirring 45KHz ultrasonic 3rd step electrolysis voltage AC 12V

Claims (1)

【特許請求の範囲】[Claims] アルミニウム又はアルミニウム合金材に、第1工程とし
て硫酸を主体とする電解液中で陽極酸化皮膜を化成して
から、第2〒程として酸性浴に浸漬して第1工程で生成
した陽極酸化皮膜の改質を合い、続いて第3工程どして
硫酸ニッケル、硫酸第1錫等の金属塩を主体とする電解
着色液にて直流、交流あるいはパルス電流等にて電解着
色処理を施して上記皮膜をグレー色、ブロンズ色、プル
解着色法。
In the first step, an anodic oxide film is formed on the aluminum or aluminum alloy material in an electrolyte mainly containing sulfuric acid, and then in the second step, it is immersed in an acid bath to remove the anodic oxide film formed in the first step. After the modification, in the third step, the film is electrolytically colored with an electrolytic coloring solution mainly containing metal salts such as nickel sulfate and stannous sulfate using direct current, alternating current, or pulsed current. The gray color, bronze color, pull discoloration method.
JP15440881A 1981-09-28 1981-09-28 Multi-color electrolytic coloration of aluminum of aluminum alloy Pending JPS5855593A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15440881A JPS5855593A (en) 1981-09-28 1981-09-28 Multi-color electrolytic coloration of aluminum of aluminum alloy

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15440881A JPS5855593A (en) 1981-09-28 1981-09-28 Multi-color electrolytic coloration of aluminum of aluminum alloy

Publications (1)

Publication Number Publication Date
JPS5855593A true JPS5855593A (en) 1983-04-01

Family

ID=15583491

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15440881A Pending JPS5855593A (en) 1981-09-28 1981-09-28 Multi-color electrolytic coloration of aluminum of aluminum alloy

Country Status (1)

Country Link
JP (1) JPS5855593A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4563397A (en) * 1983-09-19 1986-01-07 Pilot Man-Nen-Hitsu Kabushiki Kaisha Process for producing a magnetic recording material and article produced
JPH01168892A (en) * 1987-12-23 1989-07-04 Fujisash Co Production of colored aluminum building material

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4563397A (en) * 1983-09-19 1986-01-07 Pilot Man-Nen-Hitsu Kabushiki Kaisha Process for producing a magnetic recording material and article produced
JPH01168892A (en) * 1987-12-23 1989-07-04 Fujisash Co Production of colored aluminum building material

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