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US2698262A - Method of sealing anodized aluminum surfaces and article produced thereby - Google Patents

Method of sealing anodized aluminum surfaces and article produced thereby
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US2698262A
US2698262AUS21380951AUS2698262AUS 2698262 AUS2698262 AUS 2698262AUS 21380951 AUS21380951 AUS 21380951AUS 2698262 AUS2698262 AUS 2698262A
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aluminum
coating
oxide
sealing
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Balmas Frederic
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United States Patent METHOD OF SEALING ANODIZED ALUMINUM SURFACES AND ARTICLE PRODUCED THEREBY I Frdric Balmas, Versailles France No Drawing. Application March 3, 1951, Serial No. 213,809
7 Claims. (Cl. 117-135 This invention relates to the treatment of oxide layers formed on aluminum, magnesium, and aluminum or magnesium base alloys which will hereinafter be grouped and referred to by the term aluminum. It relates more specifically to the method for sealing oxide coatings formed on aluminum surfaces to improve the characteristics thereof.
For many purposes, an oxide layer is formed as a protective layer on the aluminum by making the aluminum the anode in an electrolytic cell having an electrolyte formed of about 2 to 70 percent by weight sulphuric acid or other acids or acid salts of the type chromic acid, oxalic acid, sulfamic acid and the like. Any suitable metal, such as lead, may form the cathode. A voltage of about to 20 volts is impressed upon the cell while the electrolyte is held at about 40 C. until an oxide coating of the desired thickness is formed.
in another method, the aluminum may be immersed in a solution, generally alkaline in nature, and the oxide film is formed thereon by chemical reaction. There are a number of other less commercial processes for producing oxide layers on aluminum.
The oxide layer formed under these conditions consists generally of anhydrous alumina (A1203). Especially when formed by anodic oxidation, the layer of aluminum oxide is considered to be relatively hard, porous, highly absorbent and of substantial thickness, depending upon the nature of the metal or alloy, the composition and character of the electrolyte, and the intensity of the electrical current. The oxide coating may contain other modifying components depending upon the process used and the base metal upon which the oxide layer is formed. The introduction of oxide coatings on the surfaces of aluminum is intended to improve resistance to corrosion, resistance to abrasion, and absorption of coloring when treated with suitable tinctorial agents, such as organic 1 dyes and inorganic pigments to provide permanent color in the surfaces of the aluminum.
It has been found that the characteristics of the oxide film can be markedly improved by a process, hereinafter referred to as scaling for rendering the film impervious and less porous. Sealing has been carried out commercially by immersing the anodized aluminum in water maintained between 80 C. and its boiling point. Sealing is believed to consist primarily in the conversion of the substantially porous and pervious oxide film of anhydrous alumina to a hydrated product, such as aluminum monohydrate AlzOsHzO with consequent swelling or volume increase of the oxide particles partially to close or seal the pores.
Sealing by the processes heretofore employed is superficial in nature. Measurements have shown that an oxide layer of 15 microns may be converted into the monohydrate to a depth of only 3 to 5 microns by the treatment with hot water depending upon the length of the sealing operation. Further to improve corrosion resistance, the sealing bath has been modified by additions of chromic acid, or boric acid, or metal salts such as sodium dichronate, zinc dichronate, ammonium dichronate, alone or in combination with organic acids, metal fluorides, metal borates and the like, or by the addition of nickel or cobalt sulfates and the like. The modified processes ofier some improvement but optimum conversion is not achieved and the sealed surface is ineffective for resistance against attack by strongly acidic or alkaline medium.
It is an object of this invention to provide a method of the formed aluminum oxide layer with a dilute solution of a halogenated phenyl or polyphenyl compound. It is preferred to make use of pentachlorodiphenyl as the halogenated compound but other substances such as partially chlorinated'phetfyl, diphenyl, terphenyls and the like may be used.
It has been found sufficient if the compound is present in solution in amounts ranging from 1 to 10 percent by Weight. It is preferred to carry out the treatment at room temperature, but it will be understood that elevated temperatures may be used depending upon the solvent system.
Dilution of the halogenated phenyl or polyphenyl compounds may be efiected in suitable organic solvents capable of fostering rapid and complete wetting out of the aluminum oxide surface layer so that full penetration may be achieved. It is preferred to make use of a solvent or solvent system which is non-inflammable, non-toxic, and has a slow evaporation rate, and for such purpose use may be made of the halogenated solvents such as perchloroethylene, trichloroethylene, dichloroethylene, ethylene, chlorohydrin, trichlorobenzine and the like. The solvent system may be further improved by the addition of small amounts of chlorinated paraffin such as in amounts ranging from 0.2 to 2.0 percent by Weight.
It has been found sufiicient to immerse the aluminum having the oxide surface thereon for 5 to 30 minutes in the bath, but it will be understood that substantial sealing can be effected in less time and that no harmful results will be secured if immersion exceeds 30 minutes. After immersion, the sealed aluminum oxide surfaces may be dried at room conditions but it is preferred to accelerate drying by exposure to elevate temperatures, such for example as drying in an air oven for 10 to 30 minutes at to C. depending upon the mass.
The following are specific examples given by way of illustration but not by way of limitation of the practice of this invention.
Example 1 A piece of anodically anodized aluminum is immersed for a few minutes in a bath formed of 1 to 5 percent by weight pentachlorodiphenyl dissolved in perchloroethylene maintained at room temperature. After immersion, the piece is dried by heating for about 30 minutes at a temperature of 100 to 120 C.
Example 2 A piece of aluminum having an anodized surface is immersed at room temperature into a bath formed of 2 percent by Weight hexochloroterphenyl and 0.5 percent by Weight chlorinated paraffin dissolved in trichloroethylene. After immersion for about 10 to 20 minutes, the piece is removed, rinsed, and then dried at elevated temperature of about 100 C.
Example 3 A piece of aluminum having an oxide layer formed thereon is immersed in a bath formed of 2 to 3 percent by weight pentachlorodiphenyl and 1.0 percent chlorinated paraffin dissolved in perchloroethylene. The bath is maintained at room temperature or slightly above. After immersion for about 10 minutes, the piece is allowed to dry.
It Will be understood that changes may be made in the details of composition, treatment and drying without departing from the spirit of the invention, especially as defined in the following claims.
I claim:
1. In the method of sealing an anodized oxide coating formed on aluminum, the step of coating the oxide coating with a dilute solution consisting essentially of chlorinated diphenyl as the substance which remains upon elimination of the diluent, and then drying the treated coating at elevated temperature up to about 120 C.
2. In the method of sealing an anodized oxide coating formed on aluminum, the step of coating the oxide coating with a solution the solids of which consist essentially of 1 to 10 percent of pentachlorodiphenyl.
' 3. In the method of sealing an anodized oxide coating on aluminum, the step of coating the oxide coating with a solution the solids of which consist essentially of 1 to 10 percent by weight of chlorinated diphenyl and 0.2 to 2.0 percent by weight of chlorinated parafiin.
4. In the method of sealing an anodized oxide coating on aluminum, the steps of coating the oxide coating with a solution the solids of which consist essentially of 1 to 10 percent by weight of chlorinated diphenyl and 0.2 to 2.0 percent by weight of chlorinated parafiin, and drying the treated coating at a temperature of about 100 C.-120 C.
-5. In the method of sealing an anodized oxide coating on aluminum, the steps of coating the oxide coating in a bath the solids of which consist essentially of 1 to 10 percent by weight pentachlorodiphenyl and 0.2 to 2.0 percent by weight chlorinated paraffin, maintaining the bath at a temperature corresponding to room conditions, and then drying the coating at elevated temperatures.
6. Aluminum having an anodized surface coated with a,
material consisting essentially of pentachlorodiphenyl thereon as a sealer.
7. Aluminum having an anodized surface coated with a material consisting essentially of pentachlorodiphenyl and chlorinated paraffin thereon as a sealer.
References Cited in the file of this patent OTHER REFERENCES Edwards, Iunius D., Anodic Coating of Aluminum, June 1939, pages 12 and 13.
Plasticizers and Resins, a publication of Monsanto Chemical Co., St. Louis,U. S. A., May 1940, pages 32-40.

Claims (1)

1. IN THE METHOD OF SEALING AN ANODIZED OXIDE COATING FORMED ON ALUMINUM, THE STEP OF COATING THE OXIDE COATING WITH A DILUTE SOLUTION CONSISTING ESSENTAILLY OF CHLORINATED DIPHENYL AS THE SUBSTANCE WITH REMAINS UPON ELIMINATION OF THE DILUENT, AND THEN DRYING THE TREATED COATING AT ELEVATED TEMPERATURE UP TO ABOUT 120* C.
US213809511951-03-031951-03-03Method of sealing anodized aluminum surfaces and article produced therebyExpired - LifetimeUS2698262A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3012917A (en)*1957-03-261961-12-12Pechiney Prod Chimiques SaMethod of protecting metal surfaces
US3303054A (en)*1963-01-301967-02-07Monsanto Res CorpDry cell having an electrolyte containing a poly-nitro-substituted aromatic polycarboylic acid
DE1301189B (en)*1965-08-031969-08-14Langbein Pfanhauser Werke Ag Process for re-densifying oxide layers produced by anodic oxidation on aluminum and aluminum alloys by steam treatment
US4046587A (en)*1975-12-231977-09-06Guglielmo Richard J SrPrimer composition, process for using same and product obtained thereby
WO1984003366A1 (en)*1983-02-221984-08-30Dennison Mfg CoAnodized electrostatic imaging surface
US4518468A (en)*1983-02-221985-05-21Dennison Manufacturing CompanyProcess for making electrostatic imaging surface
US8512872B2 (en)2010-05-192013-08-20Dupalectpa-CHN, LLCSealed anodic coatings
US8609254B2 (en)2010-05-192013-12-17Sanford Process CorporationMicrocrystalline anodic coatings and related methods therefor

Citations (5)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
GB488110A (en)*1936-12-311938-06-30Sydney Kerr SmithNew compositions of matter
US2294717A (en)*1940-01-241942-09-01Clifford R CarneyMethod of treating anodized aluminum surfaces
US2403179A (en)*1942-11-201946-07-02Standard Oil CoChlorination of hydrocarbon mixtures
US2424621A (en)*1945-07-061947-07-29Jr Marvin R McclatcheyShipping tags, labels, or the like and method of making the same
US2529188A (en)*1948-04-071950-11-07Gulf Research Development CoLubricating metal surfaces during cold-working

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
GB488110A (en)*1936-12-311938-06-30Sydney Kerr SmithNew compositions of matter
US2294717A (en)*1940-01-241942-09-01Clifford R CarneyMethod of treating anodized aluminum surfaces
US2403179A (en)*1942-11-201946-07-02Standard Oil CoChlorination of hydrocarbon mixtures
US2424621A (en)*1945-07-061947-07-29Jr Marvin R McclatcheyShipping tags, labels, or the like and method of making the same
US2529188A (en)*1948-04-071950-11-07Gulf Research Development CoLubricating metal surfaces during cold-working

Cited By (9)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
US3012917A (en)*1957-03-261961-12-12Pechiney Prod Chimiques SaMethod of protecting metal surfaces
US3303054A (en)*1963-01-301967-02-07Monsanto Res CorpDry cell having an electrolyte containing a poly-nitro-substituted aromatic polycarboylic acid
DE1301189B (en)*1965-08-031969-08-14Langbein Pfanhauser Werke Ag Process for re-densifying oxide layers produced by anodic oxidation on aluminum and aluminum alloys by steam treatment
US4046587A (en)*1975-12-231977-09-06Guglielmo Richard J SrPrimer composition, process for using same and product obtained thereby
US4129676A (en)*1975-12-231978-12-12Guglielmo Richard J SrPrimer composition, process for using same and product obtained thereby
WO1984003366A1 (en)*1983-02-221984-08-30Dennison Mfg CoAnodized electrostatic imaging surface
US4518468A (en)*1983-02-221985-05-21Dennison Manufacturing CompanyProcess for making electrostatic imaging surface
US8512872B2 (en)2010-05-192013-08-20Dupalectpa-CHN, LLCSealed anodic coatings
US8609254B2 (en)2010-05-192013-12-17Sanford Process CorporationMicrocrystalline anodic coatings and related methods therefor

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