US2376082A - Surface treatment of aluminum and aluminum alloys - Google Patents
Surface treatment of aluminum and aluminum alloys Download PDFInfo
- Publication number
 - US2376082A US2376082A US378676A US37867641A US2376082A US 2376082 A US2376082 A US 2376082A US 378676 A US378676 A US 378676A US 37867641 A US37867641 A US 37867641A US 2376082 A US2376082 A US 2376082A
 - Authority
 - US
 - United States
 - Prior art keywords
 - aluminum
 - film
 - treatment
 - acid
 - brightening
 - 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 - Lifetime
 
Links
- 229910052782 aluminium Inorganic materials 0.000 title description 14
 - XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title description 14
 - 229910000838 Al alloy Inorganic materials 0.000 title description 11
 - 238000004381 surface treatment Methods 0.000 title description 4
 - 238000000034 method Methods 0.000 description 13
 - 238000005282 brightening Methods 0.000 description 12
 - XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
 - QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
 - 239000003792 electrolyte Substances 0.000 description 7
 - 239000002253 acid Substances 0.000 description 6
 - 230000000694 effects Effects 0.000 description 6
 - PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 6
 - MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 5
 - 238000007654 immersion Methods 0.000 description 5
 - 230000003014 reinforcing effect Effects 0.000 description 5
 - 239000000243 solution Substances 0.000 description 5
 - 239000001828 Gelatine Substances 0.000 description 4
 - 238000003776 cleavage reaction Methods 0.000 description 4
 - 229920000159 gelatin Polymers 0.000 description 4
 - 235000019322 gelatine Nutrition 0.000 description 4
 - 239000010410 layer Substances 0.000 description 4
 - 239000000203 mixture Substances 0.000 description 4
 - 230000007017 scission Effects 0.000 description 4
 - 239000002904 solvent Substances 0.000 description 4
 - BUACSMWVFUNQET-UHFFFAOYSA-H dialuminum;trisulfate;hydrate Chemical compound O.[Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O BUACSMWVFUNQET-UHFFFAOYSA-H 0.000 description 3
 - 239000012153 distilled water Substances 0.000 description 3
 - 229910052751 metal Inorganic materials 0.000 description 3
 - 239000002184 metal Substances 0.000 description 3
 - 239000011775 sodium fluoride Substances 0.000 description 3
 - 235000013024 sodium fluoride Nutrition 0.000 description 3
 - 239000001117 sulphuric acid Substances 0.000 description 3
 - KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 2
 - KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
 - VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
 - JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
 - SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
 - CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
 - 239000003513 alkali Substances 0.000 description 2
 - AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
 - 150000002222 fluorine compounds Chemical class 0.000 description 2
 - 238000010438 heat treatment Methods 0.000 description 2
 - 239000004615 ingredient Substances 0.000 description 2
 - 239000003112 inhibitor Substances 0.000 description 2
 - -1 oxalic acid Chemical class 0.000 description 2
 - 230000001590 oxidative effect Effects 0.000 description 2
 - TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
 - 239000000126 substance Substances 0.000 description 2
 - OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 2
 - 235000011149 sulphuric acid Nutrition 0.000 description 2
 - 238000005406 washing Methods 0.000 description 2
 - DDFHBQSCUXNBSA-UHFFFAOYSA-N 5-(5-carboxythiophen-2-yl)thiophene-2-carboxylic acid Chemical compound S1C(C(=O)O)=CC=C1C1=CC=C(C(O)=O)S1 DDFHBQSCUXNBSA-UHFFFAOYSA-N 0.000 description 1
 - 229920001353 Dextrin Polymers 0.000 description 1
 - GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
 - 238000010306 acid treatment Methods 0.000 description 1
 - 239000007864 aqueous solution Substances 0.000 description 1
 - 230000015572 biosynthetic process Effects 0.000 description 1
 - ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
 - KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 1
 - FYGDTMLNYKFZSV-MRCIVHHJSA-N dextrin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)OC1O[C@@H]1[C@@H](CO)OC(O[C@@H]2[C@H](O[C@H](O)[C@H](O)[C@H]2O)CO)[C@H](O)[C@H]1O FYGDTMLNYKFZSV-MRCIVHHJSA-N 0.000 description 1
 - 238000001035 drying Methods 0.000 description 1
 - AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 1
 - 235000011167 hydrochloric acid Nutrition 0.000 description 1
 - 229960000443 hydrochloric acid Drugs 0.000 description 1
 - 229910052500 inorganic mineral Inorganic materials 0.000 description 1
 - 238000011835 investigation Methods 0.000 description 1
 - 238000012423 maintenance Methods 0.000 description 1
 - 238000004519 manufacturing process Methods 0.000 description 1
 - 239000000463 material Substances 0.000 description 1
 - 239000011707 mineral Substances 0.000 description 1
 - 235000010755 mineral Nutrition 0.000 description 1
 - 229910017604 nitric acid Inorganic materials 0.000 description 1
 - 150000007524 organic acids Chemical class 0.000 description 1
 - 235000006408 oxalic acid Nutrition 0.000 description 1
 - 230000002085 persistent effect Effects 0.000 description 1
 - UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
 - 238000002310 reflectometry Methods 0.000 description 1
 - 238000000926 separation method Methods 0.000 description 1
 - 150000004760 silicates Chemical class 0.000 description 1
 - 229910000029 sodium carbonate Inorganic materials 0.000 description 1
 - 238000001179 sorption measurement Methods 0.000 description 1
 - 238000010186 staining Methods 0.000 description 1
 - 239000002344 surface layer Substances 0.000 description 1
 
Classifications
- 
        
- C—CHEMISTRY; METALLURGY
 - C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
 - C25F—PROCESSES FOR THE ELECTROLYTIC REMOVAL OF MATERIALS FROM OBJECTS; APPARATUS THEREFOR
 - C25F3/00—Electrolytic etching or polishing
 - C25F3/16—Polishing
 - C25F3/18—Polishing of light metals
 - C25F3/20—Polishing of light metals of aluminium
 
 
Definitions
- the invention relates to the surface treatment of aluminum and aluminum alloys. Although more particularly directed to treatment for maintaining the specular reflectivity of such surfaces, and the description below will be mainly applied to the maintenance of brightened surfaces, it is not limited thereto.
 - ment is to produce on the surface of the metal a film which has certain undesirable characteristics, the'main one being its softness giving rise to a white persistent smudge when fingered or rubbed. .
 - This film is more or less independent of the type of electrolyte employed. Its removal becomes essential if a surface free from a liability to smudge or finger-mark is to be produced.
 - the main object of the present invention is to provide a process for the removal of smudge film
 - the invention consists in a method having the object of the preceding paragraph, in which the undesired film formed on an aluminumor aluminum alloy surface is in effect split off from the desired surface by means of the formation of a cleavage plane or by separation of the smudge film at a cleavage plane incidentally formed, for instance, by aqueous treatment such as by immersion of the coated surface in aqueous solution, subject to the reservations regarding strong alkalies and solvents made above.
 - the invention also consists in a process according to the preceding paragraph, in which the aluminum or aluminum alloy is treated for the removal of undesired film by a solution containing the following ingredients substantially in the proportions stated,-namely,-su phuric acid 540%, aluminum sulphate 0.01-0.5%, sodium fluoride v 0.010.05%, gelatine 0.00-0.5%.
 - the invention also consists in processes for the surface treatment of aluminum and aluminum alloys substantially as hereinafter described, and in aluminum or aluminum alloy articles, the surfaces of which have been treated substantially as hereinafter described.
 - the ar ticle As soon as the ar ticle has regained a temperature of about 20 0., it is immersed in a solution at about that temperature containing about 7% sulphuric acid, 0.1% aluminum sulphate, 0.02% sodium fluoride After about one minute from the time of immersion the surface film will be seen to crack and start to peel off in small flakes, removal usually being complete in about five minutes or less. The film thus removed appears to consist of the whole of the soft smudge-forming film together with what appears to be the'soft outer layer of the reinforcing film. On removal from this solution washing in cold water and drying, it will be found that the surface is free or substantially free from the liability to smudge or finger-mark, and does not necessarily require any further treatment.
 - the surfacefllm after immersion, apparently first cracks, then curls at the edges and peels off, again suggesting that the efiect is mainly physical, and may be regarded as splitting along the cleavage plane, that is to say, a place of weakness along which splitting can occur under suitable conditions.
 - the sulphuric acid-fluoride mixture given above works well, but the ingredients may be replaced by others of like kind, for instance, the sulphuric acid by another strong mineral acid such as hydrochloric or nitric, or some organic acid such as oxalic acid, the aluminum sulphate by any other soluble aluminum salt, and the sodium fluoride by other soluble fluorides, fluoride complexes of hydrofluoric acid, such as ammonium fluoride, silico fluoride or fluoborates; the gelatine may also be replaced by dextrine, pyridine, quinoline or other inhibitors of a. similar nature, in which case some adjustment of the ranges may be required, according to the particular substance chosen.
 - the time of immersion in the aforesaid mixture may vary from about two to about twenty minutes, depending on temperature.
 
Landscapes
- Chemical & Material Sciences (AREA)
 - Engineering & Computer Science (AREA)
 - Chemical Kinetics & Catalysis (AREA)
 - Electrochemistry (AREA)
 - Materials Engineering (AREA)
 - Metallurgy (AREA)
 - Organic Chemistry (AREA)
 - ing And Chemical Polishing (AREA)
 - Chemical Treatment Of Metals (AREA)
 - Cleaning And De-Greasing Of Metallic Materials By Chemical Methods (AREA)
 
Description
Patented May 15, 1945 SURFACE TREATMENT or men AND ALUMINUM ALLOYS Alfred Norman Douglas Pullen, Shrewsbury, England, assignor, by 
mesne assignments, 
Aluminum Company of America, Pittsburgh, Pa., a corporation of Pennsylvania No Drawing. 
Application February 12, 1941, Se- 
rial No. 378,676. In Great Britain March 16, 1340 r 2 Claims. (01. 204-35) The invention relates to the surface treatment of aluminum and aluminum alloys. Although more particularly directed to treatment for maintaining the specular reflectivity of such surfaces, and the description below will be mainly applied to the maintenance of brightened surfaces, it is not limited thereto. 
 When a surface of aluminum or aluminum alloys is treated by an electrolytic brightening process for the purpose of producing a bright highly reflective surface, one effect of the first part of the process, i. e., the actual brightening treat-. 
ment, is to produce on the surface of the metal a film which has certain undesirable characteristics, the'main one being its softness giving rise to a white persistent smudge when fingered or rubbed. .This film is more or less independent of the type of electrolyte employed. Its removal becomes essential if a surface free from a liability to smudge or finger-mark is to be produced. 
 It has been proposed to effect this removal by chemicalsolvents such as sodium carbonate solutioncontaining chromates, silicates or other inhibitors applied either to an intermediate stage, i. e., between the brightening treatment and the subsequent reinforcing anodic treatment, or as a final treatment. Where the solvent is used at the aforesaid intermediate stage, an extension of the smudge film seems to be produced by the final washing in hot water, and when used at the final stage such strong alkaline solvents may attack the reinforcing film if carelessly applied. 
 It is known that when aluminum is subjected to electrical treatment in a suitable electrolyte such as sulphuric, oxalic or chromic acid, the aluminum being the anode, a film is formed on the surface of the metal which is not homogeneous, but consists of at least two and probably three layers, of which the outer layer is the softest and liable to become powdery. It is also known that, where a piece of aluminum is subjected to more than one anodic treatment, the film from the first treatment apparently remains on the outside, subsequent films forming under it next to the actual metal surface. 
In the case of the brightening process therefore, 
. the smudge film formed in the first treatment will moved. 
The main object of the present invention is to provide a process for the removal of smudge film, 
that is of the outer soft powdery or otherwise undesirable film. which method avoids the use of strong alkalies' or solvents as aforesaid, and also avoids the use of a frictional or dry rubbing method. 
 The invention consists in a method having the object of the preceding paragraph, in which the undesired film formed on an aluminumor aluminum alloy surface is in effect split off from the desired surface by means of the formation of a cleavage plane or by separation of the smudge film at a cleavage plane incidentally formed, for instance, by aqueous treatment such as by immersion of the coated surface in aqueous solution, subject to the reservations regarding strong alkalies and solvents made above. 
The invention also consists in a process according to the preceding paragraph, in which the aluminum or aluminum alloy is treated for the removal of undesired film by a solution containing the following ingredients substantially in the proportions stated,-namely,-su phuric acid 540%, aluminum sulphate 0.01-0.5%, sodium fluoride v 0.010.05%, gelatine 0.00-0.5%. 
 and 0.2% gelatine. 
 The invention also consists in processes for the surface treatment of aluminum and aluminum alloys substantially as hereinafter described, and in aluminum or aluminum alloy articles, the surfaces of which have been treated substantially as hereinafter described. 
 In carrying the invention into effect in one form by way of example, an aluminum article is given a brightening treatment, that is to say, it is first treated in a hot alkaline brightening bath, 
Q then given a second or acid treatment in which a reinforcing film is produced. It is then washed, the final traces of electrolyte being removed by immersion in distilled water, and heated to about C. for about ten minutes. 
 According to this example, as soon as the ar ticle has regained a temperature of about 20 0., it is immersed in a solution at about that temperature containing about 7% sulphuric acid, 0.1% aluminum sulphate, 0.02% sodium fluoride After about one minute from the time of immersion the surface film will be seen to crack and start to peel off in small flakes, removal usually being complete in about five minutes or less. The film thus removed appears to consist of the whole of the soft smudge-forming film together with what appears to be the'soft outer layer of the reinforcing film. On removal from this solution washing in cold water and drying, it will be found that the surface is free or substantially free from the liability to smudge or finger-mark, and does not necessarily require any further treatment. 
 The operation can be examined visually, and the flakes are seen to remain suspended in the solution for a considerable time after the article has been removed. The removal of the film thus appears to be effected by physical splitting off, and not by chemical solution. 
 In the sulphuric acid-fluoride mixture referred to above, the surfacefllm, after immersion, apparently first cracks, then curls at the edges and peels off, again suggesting that the efiect is mainly physical, and may be regarded as splitting along the cleavage plane, that is to say, a place of weakness along which splitting can occur under suitable conditions. 
 One of the effects of the hot water treatment appears to be the production of a cleavage plane somewhere near the surface of the reinforcing film at which splitting can readily occur, the optimum effect apparently being produced by distilled water at a temperature of 83 C., since both above and below this temperature splitting occurs less readily and seems to disappear if the water temperature is below 65 C. The speed and ease of stripping appear to be influenced by the temperature of the distilled water. 
General Although the process referred to above was arrived at during investigation of brightening surfaces of aluminum and aluminum alloys, it is not limited to use with brightened surfaces, for it is also found that a normal anodic film may be treated on similar lines for the removal of a surface layer by what may be termed a splitting process, this being useful because this layer appears to be that which causes most trouble in connection with finger-marking, adsorption of staining material and the like. 
 The sulphuric acid-fluoride mixture given above works well, but the ingredients may be replaced by others of like kind, for instance, the sulphuric acid by another strong mineral acid such as hydrochloric or nitric, or some organic acid such as oxalic acid, the aluminum sulphate by any other soluble aluminum salt, and the sodium fluoride by other soluble fluorides, fluoride complexes of hydrofluoric acid, such as ammonium fluoride, silico fluoride or fluoborates; the gelatine may also be replaced by dextrine, pyridine, quinoline or other inhibitors of a. similar nature, in which case some adjustment of the ranges may be required, according to the particular substance chosen. The time of immersion in the aforesaid mixture may vary from about two to about twenty minutes, depending on temperature. 
 The function of the gelatine seems to be to slow down the action of the mixture, and thereby enable control to be more easily effected. 
I claim: 
 1. The process of producing a highly reflective surface on aluminum and aluminum alloy articles which comprises brightening and oxidizing said surface by anodic treatment in a. hot alkaline brightening electrolyte, subjecting said brightened surface to further anodic treatment in an acid electrolyte adapted to produce an aluminum oxide film on the brightened surface, heating the article in water maintained at a temperature not substantially below 65 C., and thereafter immersing the article in an aqueous bath containing about 5-10 per cent of an acid selected from the group consisting of sulfuric acid, hydro chloric acid, and nitric acid, together with a soluble aluminum salt and a soluble fluoride, for a period of about 2 to 20 minutes, in order to selectively remove the oxide film produced in the brightening treatment. 
 2. The process of producing a highly reflective surface on aluminum and aluminum alloy articles which comprises brightening and oxidizing said surface by anodic treatment in a hot alkaline brightening electrolyte, subjecting said brightened surface to further anodic treatment in an acid electrolyte adapted to produce an aluminum oxide fllm on thebrightened surface, heating the article in water maintained at a temperature not substantially below 65 0., and thereafter immersing the article in an aqueous bath containing about 5-10 per cent of an acid selected from the group consisting of sulfuric acid, hydro- ALFRED NORMAN DOUGLAS PULLEN. 
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title | 
|---|---|---|---|
| GB2376082X | 1940-03-16 | 
Publications (1)
| Publication Number | Publication Date | 
|---|---|
| US2376082A true US2376082A (en) | 1945-05-15 | 
Family
ID=10905143
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date | 
|---|---|---|---|
| US378676A Expired - Lifetime US2376082A (en) | 1940-03-16 | 1941-02-12 | Surface treatment of aluminum and aluminum alloys | 
Country Status (1)
| Country | Link | 
|---|---|
| US (1) | US2376082A (en) | 
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US2550388A (en) * | 1945-05-12 | 1951-04-24 | Lockheed Aircraft Corp | Surface treatment of aluminum and aluminum alloys | 
| US3378669A (en) * | 1967-06-30 | 1968-04-16 | Olin Mathieson | Method of making non-porous weld beads | 
| US3378668A (en) * | 1964-01-24 | 1968-04-16 | Olin Mathieson | Method of making non-porous weld beads | 
| US3657077A (en) * | 1969-09-02 | 1972-04-18 | Henkel & Cie Gmbh | Process for the treatment of anodic oxidized aluminum surfaces | 
| US4116853A (en) * | 1974-02-14 | 1978-09-26 | Amchem Products, Inc. | Composition for cleaning aluminum at low temperatures | 
| US4124407A (en) * | 1975-08-25 | 1978-11-07 | Amchem Products, Inc. | Method for cleaning aluminum at low temperatures | 
| USRE31198E (en) * | 1974-02-14 | 1983-04-05 | Amchem Products, Inc. | Method for cleaning aluminum at low temperatures | 
| USRE32661E (en) * | 1974-02-14 | 1988-05-03 | Amchem Products, Inc. | Cleaning aluminum at low temperatures | 
| US4936957A (en) * | 1988-03-28 | 1990-06-26 | The United States Of America As Represented By The Secretary Of The Air Force | Thin film oxide dielectric structure and method | 
| US6320641B1 (en) | 1997-04-01 | 2001-11-20 | Agris-Schoen Vision Systems, Inc. | High-precision-resolution image acquisition apparatus and method | 
- 
        1941
        
- 1941-02-12 US US378676A patent/US2376082A/en not_active Expired - Lifetime
 
 
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title | 
|---|---|---|---|---|
| US2550388A (en) * | 1945-05-12 | 1951-04-24 | Lockheed Aircraft Corp | Surface treatment of aluminum and aluminum alloys | 
| US3378668A (en) * | 1964-01-24 | 1968-04-16 | Olin Mathieson | Method of making non-porous weld beads | 
| US3378669A (en) * | 1967-06-30 | 1968-04-16 | Olin Mathieson | Method of making non-porous weld beads | 
| US3519779A (en) * | 1967-06-30 | 1970-07-07 | Olin Corp | Method of making non-porous weld beads | 
| US3657077A (en) * | 1969-09-02 | 1972-04-18 | Henkel & Cie Gmbh | Process for the treatment of anodic oxidized aluminum surfaces | 
| US4116853A (en) * | 1974-02-14 | 1978-09-26 | Amchem Products, Inc. | Composition for cleaning aluminum at low temperatures | 
| USRE31198E (en) * | 1974-02-14 | 1983-04-05 | Amchem Products, Inc. | Method for cleaning aluminum at low temperatures | 
| USRE32661E (en) * | 1974-02-14 | 1988-05-03 | Amchem Products, Inc. | Cleaning aluminum at low temperatures | 
| US4124407A (en) * | 1975-08-25 | 1978-11-07 | Amchem Products, Inc. | Method for cleaning aluminum at low temperatures | 
| US4936957A (en) * | 1988-03-28 | 1990-06-26 | The United States Of America As Represented By The Secretary Of The Air Force | Thin film oxide dielectric structure and method | 
| US6320641B1 (en) | 1997-04-01 | 2001-11-20 | Agris-Schoen Vision Systems, Inc. | High-precision-resolution image acquisition apparatus and method | 
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