US3275537A - Process of anodizing aluminum - Google Patents

Process of anodizing aluminum Download PDF

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Publication number
US3275537A
US3275537A US275201A US27520163A US3275537A US 3275537 A US3275537 A US 3275537A US 275201 A US275201 A US 275201A US 27520163 A US27520163 A US 27520163A US 3275537 A US3275537 A US 3275537A
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Prior art keywords
aluminum
bath
citric acid
acid
bisulphate
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US275201A
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Petin Jean
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JJ Carnaud and Forges de Basse Indre SA
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JJ Carnaud and Forges de Basse Indre SA
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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
    • C25D11/06Anodisation of aluminium or alloys based thereon characterised by the electrolytes used

Definitions

  • the present invention relates to improvements in the processes for the anodic oxidation of aluminum or aluminum alloys.
  • the present invention has as its object the creation of an oxidising treatment allowing a reduction in the period of oxidation and equally in the amount of corrosion.
  • a method of anodising aluminum comprising the step of employing the aluminum to be treated as the anode in an aqueous bath comprising zinc sulphate, and an electrolyte selected from the group consisting of sulphuric acid and a bisulphate of an alkali metal with an organic acid selected from the group consisting of citric acid and tartaric acid.
  • a method of anodising aluminum comprising the step of employing the aluminum to be treated as the anode in an aqueous bath comprising zinc sulphate, a bisulphate of an alkali metal and an organic acid selected from the group consisting of citric acid and tartaric acid.
  • the bath comprises 250 g./ litre of sodium bisulphate, 200 g./litre of citric acid and between 10 and 50 g./litre of zinc sulphate.
  • the bath comprises between and g./litre of zinc sulphate.
  • the addition of an alkali metal bisulphate leads to a substantial reduction in the processing period, since it allows high current densities to be applied without appreciable corrosion. This addition is specially advantageous in the case of a sodium bisulphate/citric acid bath.
  • the zinc sulphate concentration preferably lies between 15 and 20 g./l., but good results are obtained with lower or higher concentrations, lying between 10 and 50 g./l.
  • citric acid and sodium bisulphate concentrations represent optimum values and satisfactory results are still obtained if citric acid concentration amounts to between 50 and 200 g./l., Whereas the concentration of sodium bisulphate may amount to between g./l. and the limit of solubility of this salt at 20 C.
  • the process according to the invention may be applied to the anodic treatment of aluminum in coils or rolls before glazing or varnishing, in order to obtain excellent protection against corrosion.
  • One may thus, quickly and economically obtain thick layers of oxide assuring the protection of aluminum alloy components, apart from those used in containers, against wear, the treated components frequently exhibiting low coefficients of friction. Many applications for such components can evidently be found in industry.
  • a method of anodizing aluminum comprising the step of employing the aluminum to be treated as the anode in a bath consisting essentially of an aqueous solution of a bisulfate of an alkali metal, of an organic acid selected from the group consisting of citric acid and tartaric acid, and of zinc sulfate.
  • a method according to claim 2 wherein the bath FOREIGN PATENTS comprises between about 15 and about 20 g./1iter of zinc 467,267 6/1937 Great Britain. sulfate. 245,379 7/ 1947 Switzerland.

Description

United States Patent 3,275,537 PROCESS OF ANODIZING ALUMINUM Jean Petin, Paris, France, assignor to Etablissements J. J. Carnaud & Forges de Basse-Indre, Paris, France, a corporation of the French Republic No Drawing. Filed Apr. 24, 1963, Ser. No. 275,201 Claims priority, application llirance, May 25, 1962,
3 Claims. (01. 204-58) The present invention relates to improvements in the processes for the anodic oxidation of aluminum or aluminum alloys.
It is known that these processes have many applications particularly in the manufacture of boxes. In this field of manufacture, the anodic oxidation not only, in the case of water containers, represents an optical treatment, but also a treatment preceding the glazing or varnishing of aluminum which renders it possible to secure excellent resistance against corrosion. The processes of anodic oxidation employed up to these past few years in which the electrolytic bath customarily contained sulphuric acid, had the main disadvantages of being slow and of requiring large-size plant.
More recently, new processes have been tried experimentally, which have recourse to electrolytes containing an alkali metal bisulphate and organic acids such as acetic, formic, citric, oxalic or tartaric acid. In particular, it was found that with the sodium bisulphate/ citric acid bath, use could be made of high current densities leading to a distinct reduction in the processing period. The densities were limited however by the appearance of extensive corrosion.
The present invention has as its object the creation of an oxidising treatment allowing a reduction in the period of oxidation and equally in the amount of corrosion.
According to the present invention there is provided a method of anodising aluminum comprising the step of employing the aluminum to be treated as the anode in an aqueous bath comprising zinc sulphate, and an electrolyte selected from the group consisting of sulphuric acid and a bisulphate of an alkali metal with an organic acid selected from the group consisting of citric acid and tartaric acid.
According to another aspect of the present invention there is provided a method of anodising aluminum comprising the step of employing the aluminum to be treated as the anode in an aqueous bath comprising zinc sulphate, a bisulphate of an alkali metal and an organic acid selected from the group consisting of citric acid and tartaric acid. Preferably, the bath comprises 250 g./ litre of sodium bisulphate, 200 g./litre of citric acid and between 10 and 50 g./litre of zinc sulphate. A particular advantage is gained if the bath comprises between and g./litre of zinc sulphate. The addition of an alkali metal bisulphate leads to a substantial reduction in the processing period, since it allows high current densities to be applied without appreciable corrosion. This addition is specially advantageous in the case of a sodium bisulphate/citric acid bath.
Example An electrolytic bath of the following composition has been used with excellent results:
G./l. Sodium bisulphate 250 Citric acid 200 Zinc sulphate 15 to 20 A bath of this nature renders it possible to operate with very high current densities, and above all to assure ex- Patented Sept. 27, 1966 ice G./l. Sodium bisulphate 250 Citric acid 50 to 200 The best results had been obtained with baths having a high citric acid concentration. These baths rendered it possible to use high current densities without involving the need to apply high voltages, and in addition operated very satisfactorily at high temperatures. Nevertheless, by using current densities of the order of 30 a./dm. corresponding to a processing period of 1 to 2 minutes instead of the 15 minutes usual in sulphuric acid baths, substantial corrosion was observed, so that in practice one could not count on exceeding a current density of 6 a./dm. At these high densities moreover, the layers obtained were not uniform and the projecting parts of the specimen were attacked. This led to losses of metal and to poor electrochemical efficiency.
By contrast, after the addition of a quantity of the order of 20 g. of zinc sulphate per litre to these baths, it was found that the components processed were anodised uniformly and that corrosion of the projecting parts had disappeared.
It is assumed that a film of zinc is deposited on the aluminum by chemical displacement from the time of the immersion of the component in the electrolyte, and thus protects the metal at the start of electrolysis. The electrochemical efficiency is increased considerably, so that a box or container may be treated in 30 seconds at the same current density as in the bath lacking zinc sulphate, and in this instance, without substantial corrosion.
Equally satisfactory results are obtained by adding zinc' sulphate to an electrolytic bath containing sulphuric acid or sodium bisulphate and tartaric acid. Likewise, the zinc sulphate concentration preferably lies between 15 and 20 g./l., but good results are obtained with lower or higher concentrations, lying between 10 and 50 g./l.
Moreover, the values specified for citric acid and sodium bisulphate concentrations represent optimum values and satisfactory results are still obtained if citric acid concentration amounts to between 50 and 200 g./l., Whereas the concentration of sodium bisulphate may amount to between g./l. and the limit of solubility of this salt at 20 C.
The process according to the invention may be applied to the anodic treatment of aluminum in coils or rolls before glazing or varnishing, in order to obtain excellent protection against corrosion. One may thus, quickly and economically obtain thick layers of oxide assuring the protection of aluminum alloy components, apart from those used in containers, against wear, the treated components frequently exhibiting low coefficients of friction. Many applications for such components can evidently be found in industry.
I claim:
1. A method of anodizing aluminum comprising the step of employing the aluminum to be treated as the anode in a bath consisting essentially of an aqueous solution of a bisulfate of an alkali metal, of an organic acid selected from the group consisting of citric acid and tartaric acid, and of zinc sulfate.
2. A method according to claim 1 wherein the bath contains about 250 g./liter of sodium bisulfate, about 200 g./liter of citric acid and between about 10 and about 50 g./ liter of zinc sulfate.
3. A method according to claim 2 wherein the bath FOREIGN PATENTS comprises between about 15 and about 20 g./1iter of zinc 467,267 6/1937 Great Britain. sulfate. 245,379 7/ 1947 Switzerland.
References Cited by the Examiner 5 HN MAC P i y Examiner. UNITED STATES PATENTS HOWARD S. WILLIAMS, Examiner.
' 1,965,682 7/1934 Work 20458 G. KAPLAN, Assistant Examiner.

Claims (1)

1. A METHOD OF ANODIZING ALUMINUM COMPRISING THE STEP OF EMPLOYING THE ALUMINUM TO BE TREATED AS THE ANODE IN A BATH CONSISTING ESSENTIALLY OF AN AQUEOUS SOLUTION OF A BISULFATE OF AN ALKALI METAL, OF AN ORGANIC ACID SELECTED FROM THE GROUP CONSISTING OF CITRIC ACID AND TARTARIC ACID, AND OF ZINC SULFATE.
US275201A 1962-05-25 1963-04-24 Process of anodizing aluminum Expired - Lifetime US3275537A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR898751A FR1331558A (en) 1962-05-25 1962-05-25 Improvements to the anodic oxidation of aluminum processes

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US3275537A true US3275537A (en) 1966-09-27

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US (1) US3275537A (en)
DE (1) DE1248416B (en)
FR (1) FR1331558A (en)
GB (1) GB962789A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4152221A (en) * 1977-09-12 1979-05-01 Nancy Lee Kaye Anodizing method
US4212685A (en) * 1978-12-11 1980-07-15 Lea Manufacturing Company Protective and color receptive coating for aluminum
US4448647A (en) * 1980-09-26 1984-05-15 American Hoechst Corporation Electrochemically treated metal plates
US4452674A (en) * 1980-09-26 1984-06-05 American Hoechst Corporation Electrolytes for electrochemically treated metal plates
US20090107848A1 (en) * 2007-10-29 2009-04-30 Pilar Ocon Esteban Procedure for anodising aluminium or aluminium alloys

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1965682A (en) * 1932-01-26 1934-07-10 Aluminum Colors Inc Coating aluminum
GB467267A (en) * 1935-11-14 1937-06-14 George Charles Jones Improvements in or relating to the production of protective coatings on aluminium and aluminium alloys
CH245379A (en) * 1945-05-31 1946-11-15 Magnetos Lucifer S A Process of anodic oxidation of the surface of objects made of aluminum or aluminum alloys.

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT144637B (en) * 1932-01-06 1936-02-10 Ernest Windsor-Bowen Process for anodic treatment of objects made of aluminum or aluminum alloys.

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1965682A (en) * 1932-01-26 1934-07-10 Aluminum Colors Inc Coating aluminum
GB467267A (en) * 1935-11-14 1937-06-14 George Charles Jones Improvements in or relating to the production of protective coatings on aluminium and aluminium alloys
CH245379A (en) * 1945-05-31 1946-11-15 Magnetos Lucifer S A Process of anodic oxidation of the surface of objects made of aluminum or aluminum alloys.

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4152221A (en) * 1977-09-12 1979-05-01 Nancy Lee Kaye Anodizing method
US4212685A (en) * 1978-12-11 1980-07-15 Lea Manufacturing Company Protective and color receptive coating for aluminum
US4448647A (en) * 1980-09-26 1984-05-15 American Hoechst Corporation Electrochemically treated metal plates
US4452674A (en) * 1980-09-26 1984-06-05 American Hoechst Corporation Electrolytes for electrochemically treated metal plates
US20090107848A1 (en) * 2007-10-29 2009-04-30 Pilar Ocon Esteban Procedure for anodising aluminium or aluminium alloys
ES2324850A1 (en) * 2007-10-29 2009-08-17 Airbus España, S.L. Procedure for anodising aluminium or aluminium alloys

Also Published As

Publication number Publication date
FR1331558A (en) 1963-07-05
DE1248416B (en) 1967-08-24
GB962789A (en) 1964-07-01

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