JPS5855593A - Multi-color electrolytic coloration of aluminum of aluminum alloy - Google Patents
Multi-color electrolytic coloration of aluminum of aluminum alloyInfo
- 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
Links
- 229910052782 aluminium Inorganic materials 0.000 title claims abstract description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims abstract description 10
- 229910000838 Al alloy Inorganic materials 0.000 title claims abstract description 6
- 238000000034 method Methods 0.000 claims abstract description 16
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000004040 coloring Methods 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 6
- 239000000956 alloy Substances 0.000 claims abstract description 5
- 239000003792 electrolyte Substances 0.000 claims abstract description 5
- 229910052751 metal Inorganic materials 0.000 claims abstract description 4
- 239000002184 metal Substances 0.000 claims abstract description 4
- LGQLOGILCSXPEA-UHFFFAOYSA-L nickel sulfate Chemical compound [Ni+2].[O-]S([O-])(=O)=O LGQLOGILCSXPEA-UHFFFAOYSA-L 0.000 claims abstract description 4
- 229910000363 nickel(II) sulfate Inorganic materials 0.000 claims abstract description 4
- 229910000906 Bronze Inorganic materials 0.000 claims abstract description 3
- 239000010974 bronze Substances 0.000 claims abstract description 3
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000010407 anodic oxide Substances 0.000 claims description 4
- 238000012986 modification Methods 0.000 claims description 3
- 230000004048 modification Effects 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 2
- 238000002845 discoloration Methods 0.000 claims 1
- RCIVOBGSMSSVTR-UHFFFAOYSA-L stannous sulfate Chemical compound [SnH2+2].[O-]S([O-])(=O)=O RCIVOBGSMSSVTR-UHFFFAOYSA-L 0.000 claims 1
- 229910000375 tin(II) sulfate Inorganic materials 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract description 9
- 230000002378 acidificating effect Effects 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 6
- 239000011248 coating agent Substances 0.000 abstract description 5
- 238000000576 coating method Methods 0.000 abstract description 5
- 239000011148 porous material Substances 0.000 abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 5
- 238000005406 washing Methods 0.000 abstract description 3
- 230000003647 oxidation Effects 0.000 abstract 3
- 238000007254 oxidation reaction Methods 0.000 abstract 3
- -1 NiSO4 by passing DC Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 7
- 238000003756 stirring Methods 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 238000007654 immersion Methods 0.000 description 4
- 229910045601 alloy Inorganic materials 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 239000006174 pH buffer Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-L Oxalate Chemical compound [O-]C(=O)C([O-])=O MUBZPKHOEPUJKR-UHFFFAOYSA-L 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229940085991 phosphate ion Drugs 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
Landscapes
- Electrochemical Coating By Surface Reaction (AREA)
Abstract
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12V9J2 process acidic bath composition 40171 bath temperature
30℃ Immersion time 1 minute Stirring 45KHz ultrasonic 3rd step electrolysis voltage AC 12V
Claims (1)
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.
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)
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 |
-
1981
- 1981-09-28 JP JP15440881A patent/JPS5855593A/en active Pending
Cited By (2)
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 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA1079680A (en) | Continuous electrolytical treatment of aluminum or its alloys | |
US3704209A (en) | Method for electrochemical coloring of aluminum and alloys | |
US3915813A (en) | Method for electrolytically coloring aluminum articles | |
US3704210A (en) | Process for coloring aluminum objects | |
JPS5855593A (en) | Multi-color electrolytic coloration of aluminum of aluminum alloy | |
JPS60110895A (en) | Electrolytic coloring method of aluminum and aluminum alloy | |
JPH0747836B2 (en) | Coloring method for aluminum or aluminum alloy materials | |
JP2000355795A (en) | Surface treatment of aluminum and aluminum alloy | |
JPH11256394A (en) | Production of colored product of anodized aluminum or aluminum alloy, and colored product produced by that | |
JPS59190389A (en) | Method for coloring aluminum or aluminum alloy | |
JPS61110797A (en) | Surface treatment of aluminum or aluminum alloy | |
JPS5831400B2 (en) | How to color aluminum or aluminum alloy | |
JPS60128288A (en) | Formation of black film on aluminum and aluminum alloy | |
JPS5920759B2 (en) | Coloring method for aluminum or aluminum alloy | |
JPS6020478B2 (en) | Aluminum surface treatment method | |
JPS63203795A (en) | Method for coloring aluminum or aluminum alloy | |
JPH02125896A (en) | Method for coloring aluminum-based metal having oxidized film | |
JPH0841684A (en) | Electrolytic pigmentation of anodic oxidation coating film of speeding-up of electrolytic pigmentation treatment | |
JPH01127696A (en) | Anodic oxidation method for colored titanium material | |
JPS58161795A (en) | Method for coloring anodic oxide film of aluminum or aluminum alloy | |
Tochi | Coloring of Anodic Oxide Layer on Aluminum or Its Alloys by Electrolytically Treating to Form Coating of Less Noble Metal and Then More-Noble Metal | |
JPS5913095A (en) | Electrolytic pigmentation method of aluminum or aluminum alloy | |
GB290901A (en) | An improved process for providing a resistant coating upon the surfaces of aluminiumor aluminium alloys | |
JPS59140397A (en) | Coloring method of aluminum or aluminum alloy | |
JPS5948878B2 (en) | Electrolytic coloring method for aluminum or its alloys |