US3634208A - Coloring method of aluminum anodic oxide coating film - Google Patents

Coloring method of aluminum anodic oxide coating film Download PDF

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Publication number
US3634208A
US3634208A US861149A US3634208DA US3634208A US 3634208 A US3634208 A US 3634208A US 861149 A US861149 A US 861149A US 3634208D A US3634208D A US 3634208DA US 3634208 A US3634208 A US 3634208A
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Prior art keywords
alumite
effected
alternating current
electrolyzing
minutes
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Expired - Lifetime
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US861149A
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English (en)
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Koichi Kuroda
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Aiden KK
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Aiden KK
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    • CCHEMISTRY; METALLURGY
    • C25ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25DPROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
    • C25D11/00Electrolytic coating by surface reaction, i.e. forming conversion layers
    • C25D11/02Anodisation
    • C25D11/04Anodisation of aluminium or alloys based thereon
    • C25D11/18After-treatment, e.g. pore-sealing
    • C25D11/20Electrolytic after-treatment
    • C25D11/22Electrolytic after-treatment for colouring layers

Definitions

  • Alumite is colored by first subjecting same to an alternating current electrolyzing treatment in an electrolyte followed by a direct current electrolyzing treatment in a coloring solution in which the alumite is the cathode.
  • This invention relates to a method for coloring an aluminum anodic coating film which is hereinafter called alumite.
  • alumite coloring methods hitherto known there is a method of dyeing the same using a dyestuff; a method of coloring an aluminum alloy by electrolyzing; a method of coloring same by electrolyzing using an organic acid bath or the like and recently, there has been proposed an alternating current coloring method for alumite.
  • the dyeing method however is so defective that the product is poor in weather resistance, and all of the foregoing electrolyzing methods are defective in that they are of high cost and more importantly, uniformity of color is difficult to achieve.
  • the recently proposed alternating current method has overcome certain of these defects but still has a disadvantage regarding uniformity of color and the present invention is an improvement thereof.
  • the present invention is a method according to which an alumite produced by a conventional process is colored using an electrolyzing coloring solution with the use of a direct current after a pretreatment in which the alumite is subjected to an alternating current electrolyzing. This method gives excellent results in terms of uniformity of color when compared with the altematingcurrent method discussed above.
  • a sample of aluminum is anodized into alumite by a conventional method with an ordinary electrolyte such as sulfuric acid, oxalic acid, chromic acid or the like
  • an ordinary electrolyte such as sulfuric acid, oxalic acid, chromic acid or the like
  • the same is subjected to an alternating current for a short time within the same electrolyte, and then the alumite is electrolyzed in an electrolyte containing metallic ions while using the alumite as the cathode, ordinary carbon being used as the anode.
  • the metallic ions are attracted to the cathode and enter the pores of the alumite and thus the coloring of the alumite is brought about.
  • the present invention is especially characterized by this alternating current treatment after the anodizing; and by this alternating current treatment, any unevenness of the color can be eliminated and control of the coloring operation becomes very easy.
  • alumite is directly, that is, without being subjected to this alternating current treatment, electrolyzed within a metallic ion-containing electrolyte while using the alumite as the cathode, there is caused such trouble that the coating film breaks down, or the alumite is not colored but there is produced only hydrogen thereon, or the alumite, even if colored, has a coating film of uneven color and thus the uniformity of color is not achieved. If direct current coloring is effected after the alternating current electrolyzing treatment is effected, these defects are all overcome and a strong uniform coating is obtained.
  • the alternating current electrolyzing treatment is carried out within the anodizing electrolyzing bath, but any acid or alkali electrolyte, i.e., one which is separately prepared, can be used as well.
  • uniformity of color becomes possible by the length of coloring time regardless of the thickness of the coating film desired
  • the coloring solution in this method should be a strong electrolyte so that control of the solution is very easy and control of the electrolyzing condition, is also easy in comparison with that in the alternating current method.
  • the choice of the LII metallic ions in the coloring solution will naturally vary with and depend upon the desired color.
  • EXAMPLE I A piece of 99 percent pure aluminum (35x70x0.4 mm.) is used in this example. After this aluminum is anodized in an oxalic acid bath (5 percent. oxalic acid 20 C.) at a current density of 1.5 A/dm. for 30 minutes, the anodized aluminum is subjected to an alternating current electrolyzing (l A/dmf) for 2 minutes in a sulfuric acid bath, and then the same is electrolyzed, with the alumite being used as a cathode (the anode is carbon), for2 minutes at a current density of 0.6 A/dm.
  • oxalic acid bath 5 percent. oxalic acid 20 C.
  • l A/dmf alternating current electrolyzing
  • the alumite being used as a cathode (the anode is carbon), for2 minutes at a current density of 0.6 A/dm.
  • EXAMPLE II A piece of 99.99 percent pure aluminum (35X70X0.4 mm.) is used in this example. After this aluminum is anodized with a sulfuric acid bath (15 percent, 20 C.) for 30 minutes at a current density of 1.5 A/dmF, the anodized aluminum is subjected to an alternating current electrolyzing (l A/dm?) for 2 .minutes in the same sulfuric acid bath. Then, the same is electrolyzed, with the alumite being used as the cathode, (the anode is carbon) for 2 minutes at a current density of 0.6 A/dm.
  • a coloring solution comprising KAu (CN (3 g./l), citric acid (10 g./l) and sodium citrate (100 g./l) at room (i.e., about 20 C.) temperature whereby a purple-colored coating film is obtained.
  • a method of coloring an aluminum anodic oxide coating film comprising subjecting an article having said anodic aluminum oxide coating to an alternating current electrolyzing treatment in an electrolytic solution, position said article in said electrolytic solution to form a cathode, and then subjecting same to a direct current electrolyzing treatment in an electrolyte containing color producing metallic ions.
  • a method as claimed in claim 1 wherein the electrolyte containing color producing metallic ions comprises KAu(CN citric acid and sodium citrate.
  • a method as claimed in claim 1 wherein the electrolyte containing color producing metallic ions comprises NiSO.,, boric acid and NH CL.
  • a method as claimed in claim I wherein the anodic aluminum oxide is prepared by an oxidizing aluminum in a bath which is the same as the electrolytic solution in which the alternating current electrolyzing treatment is effected.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Chemical Treatment Of Metals (AREA)
  • Electroplating And Plating Baths Therefor (AREA)
US861149A 1968-09-26 1969-09-25 Coloring method of aluminum anodic oxide coating film Expired - Lifetime US3634208A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6909068 1968-09-26

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DE (1) DE1948552B2 (de)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3878056A (en) * 1973-08-24 1975-04-15 Sumitomo Chemical Co Process for electrolytic coloring of the anodic oxide film on a aluminum or aluminum base alloys
US3892636A (en) * 1972-06-06 1975-07-01 Riken Light Metal Ind Co Method for producing a colored oxide film on an aluminum or aluminum alloy
US3929612A (en) * 1973-10-20 1975-12-30 Sumitomo Chemical Co Process for electrolytically coloring the anodically oxidized coating on aluminum or aluminum base alloys
US4251330A (en) * 1978-01-17 1981-02-17 Alcan Research And Development Limited Electrolytic coloring of anodized aluminium by means of optical interference effects
US4310586A (en) * 1978-01-17 1982-01-12 Alcan Research And Development Limited Aluminium articles having anodic oxide coatings and methods of coloring them by means of optical interference effects
US4421610A (en) * 1981-01-16 1983-12-20 Dionisio Rodriguez Electrolytic coloring process
US4442829A (en) * 1977-06-14 1984-04-17 Sumitomo Aluminium Smelting Company, Ltd. Material for selective absorption of solar energy and production thereof
DE4034854A1 (de) * 1989-11-08 1991-05-16 Sandoz Ag Verfahren zum elektrolytischen faerben von aluminium und aluminiumlegierungen
US5288372A (en) * 1992-07-07 1994-02-22 Alumax Inc. Altering a metal body surface
US5674371A (en) * 1989-11-08 1997-10-07 Clariant Finance (Bvi) Limited Process for electrolytically treating aluminum and compositions therefor
US20060086479A1 (en) * 2004-10-26 2006-04-27 United Technologies Corporation Non-oxidizable coating
US20060086478A1 (en) * 2004-10-26 2006-04-27 Persky Joshua E Non-oxidizable coating

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3382160A (en) * 1960-03-31 1968-05-07 Asada Tahei Process for inorganically coloring aluminum

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3382160A (en) * 1960-03-31 1968-05-07 Asada Tahei Process for inorganically coloring aluminum

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3892636A (en) * 1972-06-06 1975-07-01 Riken Light Metal Ind Co Method for producing a colored oxide film on an aluminum or aluminum alloy
US3878056A (en) * 1973-08-24 1975-04-15 Sumitomo Chemical Co Process for electrolytic coloring of the anodic oxide film on a aluminum or aluminum base alloys
US3929612A (en) * 1973-10-20 1975-12-30 Sumitomo Chemical Co Process for electrolytically coloring the anodically oxidized coating on aluminum or aluminum base alloys
US4442829A (en) * 1977-06-14 1984-04-17 Sumitomo Aluminium Smelting Company, Ltd. Material for selective absorption of solar energy and production thereof
US4251330A (en) * 1978-01-17 1981-02-17 Alcan Research And Development Limited Electrolytic coloring of anodized aluminium by means of optical interference effects
US4310586A (en) * 1978-01-17 1982-01-12 Alcan Research And Development Limited Aluminium articles having anodic oxide coatings and methods of coloring them by means of optical interference effects
US4421610A (en) * 1981-01-16 1983-12-20 Dionisio Rodriguez Electrolytic coloring process
DE4034854C2 (de) * 1989-11-08 2000-08-17 Clariant Finance Bvi Ltd Verfahren zum elektrolytischen Färben von Aluminium und Aluminiumlegierungen
DE4034854A1 (de) * 1989-11-08 1991-05-16 Sandoz Ag Verfahren zum elektrolytischen faerben von aluminium und aluminiumlegierungen
US5674371A (en) * 1989-11-08 1997-10-07 Clariant Finance (Bvi) Limited Process for electrolytically treating aluminum and compositions therefor
US5288372A (en) * 1992-07-07 1994-02-22 Alumax Inc. Altering a metal body surface
US20060086479A1 (en) * 2004-10-26 2006-04-27 United Technologies Corporation Non-oxidizable coating
US20060086478A1 (en) * 2004-10-26 2006-04-27 Persky Joshua E Non-oxidizable coating
US7207373B2 (en) 2004-10-26 2007-04-24 United Technologies Corporation Non-oxidizable coating
US7207374B2 (en) 2004-10-26 2007-04-24 United Technologies Corporation Non-oxidizable coating
US20080023620A1 (en) * 2004-10-26 2008-01-31 United Technologies Corporation Non-oxidizable coating
US7967055B2 (en) 2004-10-26 2011-06-28 United Technologies Corporation Non-oxidizable coating

Also Published As

Publication number Publication date
DE1948552B2 (de) 1971-04-22
DE1948552A1 (de) 1970-04-23

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