JPS6238440B2 - - Google Patents

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Publication number
JPS6238440B2
JPS6238440B2 JP1516881A JP1516881A JPS6238440B2 JP S6238440 B2 JPS6238440 B2 JP S6238440B2 JP 1516881 A JP1516881 A JP 1516881A JP 1516881 A JP1516881 A JP 1516881A JP S6238440 B2 JPS6238440 B2 JP S6238440B2
Authority
JP
Japan
Prior art keywords
voltage
aluminum
minutes
electrolysis
subjected
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
Application number
JP1516881A
Other languages
Japanese (ja)
Other versions
JPS57131390A (en
Inventor
Tatsuo Ootsuka
Akira Hashimoto
Eiji Yoshimoto
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.)
Altemira Co Ltd
Original Assignee
Showa Aluminum Corp
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 Showa Aluminum Corp filed Critical Showa Aluminum Corp
Priority to JP1516881A priority Critical patent/JPS57131390A/en
Publication of JPS57131390A publication Critical patent/JPS57131390A/en
Publication of JPS6238440B2 publication Critical patent/JPS6238440B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

この発明は、アルミニウム押出材に着色および
筋模様を施こす方法に関するものであつて、その
目的は、アルミニウム押出材の電解処理によつ
て、その表面に所望の着色を施こすとともに、柾
目様の筋模様を形成する方法を提供するにある。 すなわち、この発明によるアルミニウム押出材
に着色および筋模様を施こす方法は、銅を0.05〜
4.0%含むアルミニウム基合金製の押出材をシユ
ウ酸電解液中で陽極酸化処理して酸化皮膜を形成
する第1工程と、同一電解液中で電圧を第1工程
における値から5〜35Vに急激に降下させた後第
1工程の処理品を定電圧電解処理する第2工程
と、金属塩を含む電解液中で第2工程の処理品を
交流電解処理する第3工程とからなる。 銅含有アルミニウム基合金製の押出材をシウ酸
電解液中で陽極酸化処理する第1工程において、
アルミニウム基合金の銅含有量は、0.05%未満で
は、所望の着色が得られず、逆に4.0%を超える
と、形成された皮膜が柔らかくて耐食性に乏しい
ので、0.05〜4.0%の範囲に限定される。また、
シユウ酸の濃度は好ましくは1〜5重量%、特に
好ましくは2〜3重量%である。電解は交流、直
流または交流・直流の重畳流でなされ、定電流電
解であつても定電圧電解であつてもよい。 電圧を急激に降下させた後定電圧電解を行う第
2工程において、電圧降下後の電解の電流は即座
には通流せず、数秒〜数分経過後徐々に流れ始
め、さらにしばらくして定常状態に達する。この
現象は回復現象と呼ばれている。この現象によつ
て、陽極酸化皮膜が形成されるとともに、下地ア
ルミニウム面が一様に粗面化され、その結果この
粗面における乱反射によつて、第1工程で生成し
た陽極酸化皮膜が不透明なものとなる。ここで、
第1工程における電圧から第2工程における電圧
への電圧降下は、急激に行われることが好まし
く、実際の操作では、第1工程における通電を一
旦停止し、第2工程の初めに再び所定電圧に印加
する方法がよく行われる。 第2工程における電圧は、5V未満では、上記
の電流の回復効果が少ないため下地面の粗面化が
進まず、逆に35Vを超えると、皮膜が急速に生成
して下地粗面がなくなつてしまうので、5〜35V
の範囲に限定される。特に好ましい電圧は20〜
25Vである。またこの工程における電流も、交
流、直流または交流・直流の重畳流のいずれであ
つてもよい。 第2工程の処理時間は、特に限定されないが、
5分未満では、下地面の粗面化が進まず、逆に25
分を超えると、下地粗面がなくなるので、好まし
くは5〜25分間である。特に好ましくは10〜20分
間である。 金属塩含有電解液中で交流電解処理を行う第3
工程において、アルミニウム押出材の表面には着
色とともに、柾目様の筋模様が形成される。この
現象が生じる理由は、明確ではないが、つぎのよ
うに考えられる。アルミニウムの押出材において
は、常に押出方向に配向性を有した組織が表面に
現われるが、通常の陽極酸化処理や着色処理で
は、このような配向性に起因する模様は殆んど現
われない。しかしこの発明の場合には、前述した
ように、上記第1工程および第2工程の処理の結
果、下地アルミニウム面の粗面化によつて不透明
な乳白色が現われる。この状態では模様は全く生
じていないが、第2工程の定電圧電解処理によ
り、下地アルミニウム面の粗面化とともに同下地
面にごく薄い皮膜層が形成される。この皮膜層
は、下地アルミニウム面の配向性、結晶性の方位
に著しく影響された構造および厚さを有する。そ
のためこのようなアルミニウム押出材に、着色を
目的とした第3工程の電解処理を施こすと、上記
皮膜層の構造および厚さに起因して、皮膜中に沈
着する金属ないし金属酸化物の形態および沈着量
に差が生じ、この差によつて木材の柾目様の筋模
様が現われる。 第3工程の電解液の金属塩としては、ニツケ
ル、銅、銀、コバルト、クロム、カドミウム、チ
タン、マンガン、モリブデン、カルシウム、マグ
ネシウム、バナジウム、金、鉛、亜鉛等の金属の
硝酸、硫酸、塩酸、シユウ酸、酢酸、酒石酸、ク
ロム酸、燐酸等の塩が使用され、その代表例とし
ては硫酸ニツケル、硫酸銅および硫酸銀が挙げら
れる。また第3工程における交流は、極性が交互
に変換する波形をなすものであればよく、いわゆ
る正弦波交流に限定されない。第3工程における
電圧および通電時間は、5Vおよび5分未満で
は、着色および筋模様の形成が進まず、また35V
および25分を超えても効果の向上はさして認めら
れないので、好ましくは5〜35Vおよび5〜25分
である。 以上の次第で、この発明によれば、アルミニウ
ム材の表面に所望の着色を施こすとともに、柾目
様の筋模様を形成することができる。 以下、この発明の実施例を挙げる。 実施例 1 第1工程:供試料として下記表1に示す組成の銅
含有アルミニウム基合金製の板状押出材(75mm
×100mm×6mm)を用意し、これの片面を中磨
きして羽布で研磨仕上げした。ついでこれを5
%NaOHの水溶液に液温70℃にて30秒間浸漬し
てエツチング処理し、その後50%HNO3水溶液
で常温にて脱脂処理した。こうして前処理した
アルミニウム押出材を、全酸71.0g/、遊離
酸19.3g/および溶存アルミニウム10.3g/
を含む14のシユウ酸電解液中で、液温35℃
にて、電流密度1.5A/dm2で20分間直流にて
陽極酸化処理した。 第2工程:上記通電を一旦止めた後、同一電解液
中で同じく液温35℃で電圧25Vにて15分間、第
1工程の処理品を直流電解処理した。 第3工程:下記表2に示す組成の電解液のうちの
Ni含有液を用いて、電圧15Vで3分間、第2工
程の処理品を交流電解処理した。最後に純水の
沸騰液に電解処理品を20分間浸漬して、封孔処
理した。 以上の第1〜3工程の処理条件をまとめて表3
に示し、またこうして得られた色調および外観も
表3に示す。 実施例 2〜13 第2工程における電圧および通電時間を変化さ
せ、また第3工程における電解液としてNi含有
液のほかにCu含有液およびAg含有液を用い(表
2に示す)、やはり電圧および通電時間を変化さ
せて、実施例1の操作を繰返した。 処理条件、色調および外観を同じく表3に示
す。 比較例 実施例1の第1工程と第2工程の操作を繰返
し、第3工程を省略した。 この処理品についても処理条件、色調および外
観を表3に示す。
The present invention relates to a method for coloring and adding a striped pattern to an aluminum extrusion, and its purpose is to apply a desired color to the surface of the aluminum extrusion by electrolytic treatment, and to create a straight-grain pattern. The present invention provides a method for forming a striped pattern. That is, the method of coloring and streaking aluminum extrusions according to the present invention uses copper of 0.05 to
The first step is to anodize an extruded material made of aluminum-based alloy containing 4.0% in an oxalic acid electrolyte to form an oxide film, and the voltage is suddenly increased from the value in the first step to 5 to 35 V in the same electrolyte. The process consists of a second step in which the product treated in the first step is subjected to a constant voltage electrolytic treatment after being lowered to a temperature of 100.degree. In the first step of anodizing an extruded material made of a copper-containing aluminum-based alloy in an oxalic acid electrolyte,
If the copper content of the aluminum-based alloy is less than 0.05%, the desired coloration cannot be obtained, and if it exceeds 4.0%, the formed film will be soft and have poor corrosion resistance, so it should be limited to a range of 0.05 to 4.0%. be done. Also,
The concentration of oxalic acid is preferably 1 to 5% by weight, particularly preferably 2 to 3% by weight. Electrolysis is performed using alternating current, direct current, or a superimposed flow of alternating current and direct current, and may be constant current electrolysis or constant voltage electrolysis. In the second step of performing constant-voltage electrolysis after a sudden voltage drop, the electrolytic current does not flow immediately after the voltage drop, but begins to flow gradually after several seconds to several minutes, and after a while it returns to a steady state. reach. This phenomenon is called a recovery phenomenon. Due to this phenomenon, an anodic oxide film is formed and the base aluminum surface is uniformly roughened.As a result, the anodic oxide film formed in the first step becomes opaque due to diffuse reflection on this rough surface. Become something. here,
It is preferable that the voltage drop from the voltage in the first step to the voltage in the second step be performed rapidly.In actual operation, the energization in the first step is temporarily stopped, and then the voltage is reduced to the predetermined voltage again at the beginning of the second step. The method of applying it is often used. If the voltage in the second step is less than 5V, the above-mentioned current recovery effect will be small and the roughening of the underlying surface will not progress, and if it exceeds 35V, a film will rapidly form and the roughening of the underlying surface will disappear. 5 to 35V
limited to the range of Particularly preferred voltage is 20~
It is 25V. Further, the current in this step may be either an alternating current, a direct current, or a superimposed flow of alternating current and direct current. The processing time of the second step is not particularly limited, but
If the time is less than 5 minutes, the roughening of the underlying surface will not progress;
If the time exceeds 5 minutes, the rough surface of the base will disappear, so the time is preferably 5 to 25 minutes. Particularly preferably, the time is 10 to 20 minutes. The third step is to perform AC electrolytic treatment in an electrolytic solution containing metal salts.
In the process, the surface of the aluminum extrusion is colored and a straight-grained striped pattern is formed. The reason why this phenomenon occurs is not clear, but it is thought to be as follows. In extruded aluminum materials, a texture that is oriented in the extrusion direction always appears on the surface, but in normal anodizing or coloring treatments, patterns due to such orientation hardly appear. However, in the case of the present invention, as described above, as a result of the first and second steps, an opaque milky white color appears due to the roughening of the underlying aluminum surface. In this state, no pattern is formed at all, but due to the constant voltage electrolytic treatment in the second step, the underlying aluminum surface is roughened and a very thin film layer is formed on the underlying surface. This film layer has a structure and thickness that are significantly influenced by the orientation and crystalline direction of the underlying aluminum surface. Therefore, when such an aluminum extruded material is subjected to the third electrolytic treatment for the purpose of coloring, due to the structure and thickness of the above-mentioned film layer, the form of the metal or metal oxide deposited in the film changes. A difference occurs in the amount of deposited wood, and this difference causes the appearance of straight-grained streaks in the wood. Metal salts in the electrolyte in the third step include nitric acid, sulfuric acid, hydrochloric acid of metals such as nickel, copper, silver, cobalt, chromium, cadmium, titanium, manganese, molybdenum, calcium, magnesium, vanadium, gold, lead, and zinc. , oxalic acid, acetic acid, tartaric acid, chromic acid, phosphoric acid, etc., and representative examples thereof include nickel sulfate, copper sulfate, and silver sulfate. Further, the alternating current in the third step may have a waveform whose polarity changes alternately, and is not limited to a so-called sine wave alternating current. The voltage and energization time in the third step are 5V and less than 5 minutes, coloring and streak pattern formation will not progress, and 35V and less than 5 minutes.
Even if the heating time exceeds 25 minutes, no significant improvement in the effect is observed. Therefore, the heating time is preferably 5 to 35 V and 5 to 25 minutes. As described above, according to the present invention, it is possible to apply desired coloring to the surface of an aluminum material and to form a straight-grained striped pattern. Examples of this invention will be described below. Example 1 First step: As a test sample, a plate-shaped extruded material (75 mm
× 100 mm × 6 mm) was prepared, one side of this was medium polished and finished with a cloth. Then add this to 5
% NaOH aqueous solution at a temperature of 70° C. for 30 seconds, and then degreased with a 50% HNO 3 aqueous solution at room temperature. The thus pretreated aluminum extruded material was mixed with 71.0 g of total acid, 19.3 g of free acid, and 10.3 g of dissolved aluminum.
In 14 oxalic acid electrolytes containing
Anodization treatment was performed using direct current at a current density of 1.5 A/dm 2 for 20 minutes. Second step: After the electricity supply was once stopped, the product treated in the first step was subjected to direct current electrolysis treatment in the same electrolytic solution at a temperature of 35° C. and a voltage of 25 V for 15 minutes. Third step: Of the electrolyte solution with the composition shown in Table 2 below.
The product treated in the second step was subjected to AC electrolysis treatment using a Ni-containing solution at a voltage of 15 V for 3 minutes. Finally, the electrolytically treated product was immersed in boiling pure water for 20 minutes to seal the pores. Table 3 summarizes the processing conditions for the above 1st to 3rd steps.
The color tone and appearance thus obtained are also shown in Table 3. Examples 2 to 13 The voltage and energization time in the second step were varied, and the electrolyte in the third step was a Cu-containing solution and an Ag-containing solution in addition to the Ni-containing solution (shown in Table 2). The operation of Example 1 was repeated by changing the current application time. The processing conditions, color tone and appearance are also shown in Table 3. Comparative Example The operations of the first step and second step of Example 1 were repeated, but the third step was omitted. Table 3 also shows the treatment conditions, color tone, and appearance of this treated product.

【表】【table】

【表】【table】

【表】【table】

【表】 表3からわかるように、Ni含有液およびCu含
有液の場合には、処理品は淡い銀ネズミ色〜暗灰
色素の色調を呈し、またAg含有液の場合には、
ベージ色〜暗灰黄色系の色調を呈した。また各実
施例とも柾目様の筋模様が現われた。
[Table] As can be seen from Table 3, in the case of Ni-containing liquids and Cu-containing liquids, the treated products exhibit a pale silver gray to dark gray color tone, and in the case of Ag-containing liquids,
It had a beige to dark gray-yellow color tone. In addition, a straight grain pattern appeared in each of the examples.

Claims (1)

【特許請求の範囲】[Claims] 1 銅を0.05〜4.0%含むアルミニウム基合金製
の押出材をシユウ酸電解液中で陽極酸化処理して
酸化皮膜を形成する第1工程と、同一電解液中で
電圧を第1工程における値から5〜35Vに急激に
降下させた後第1工程の処理品を定電圧電解処理
する第2工程と、金属塩を含む電解液中で第2工
程の処理品を交流電解処理する第3工程とからな
る、アルミニウム押出材に着色および筋模様を施
こす方法。
1. A first step in which an extruded material made of aluminum-based alloy containing 0.05 to 4.0% copper is anodized in an oxalic acid electrolyte to form an oxide film, and a voltage is changed from the value in the first step in the same electrolyte. A second step in which the product treated in the first step is subjected to constant voltage electrolysis after the voltage is suddenly lowered to 5 to 35V, and a third step in which the product treated in the second step is subjected to AC electrolysis in an electrolytic solution containing a metal salt. A method for coloring and adding streaks to aluminum extrusions.
JP1516881A 1981-02-03 1981-02-03 Coloring and streaking method for aluminum material Granted JPS57131390A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1516881A JPS57131390A (en) 1981-02-03 1981-02-03 Coloring and streaking method for aluminum material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1516881A JPS57131390A (en) 1981-02-03 1981-02-03 Coloring and streaking method for aluminum material

Publications (2)

Publication Number Publication Date
JPS57131390A JPS57131390A (en) 1982-08-14
JPS6238440B2 true JPS6238440B2 (en) 1987-08-18

Family

ID=11881266

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1516881A Granted JPS57131390A (en) 1981-02-03 1981-02-03 Coloring and streaking method for aluminum material

Country Status (1)

Country Link
JP (1) JPS57131390A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0440125U (en) * 1990-08-03 1992-04-06

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2706681B2 (en) * 1992-05-29 1998-01-28 新日軽株式会社 Electrolytic coloring method of aluminum material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0440125U (en) * 1990-08-03 1992-04-06

Also Published As

Publication number Publication date
JPS57131390A (en) 1982-08-14

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