US3597338A - Method and electrolyte for anodic oxidation coating of aluminum - Google Patents
Method and electrolyte for anodic oxidation coating of aluminum Download PDFInfo
- Publication number
- US3597338A US3597338A US842030A US3597338DA US3597338A US 3597338 A US3597338 A US 3597338A US 842030 A US842030 A US 842030A US 3597338D A US3597338D A US 3597338DA US 3597338 A US3597338 A US 3597338A
- Authority
- US
- United States
- Prior art keywords
- electrolyte
- aluminum
- anodic oxidation
- coating
- acetamide
- 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
- 239000003792 electrolyte Substances 0.000 title abstract description 31
- 238000000576 coating method Methods 0.000 title abstract description 26
- 229910052782 aluminium Inorganic materials 0.000 title abstract description 25
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title abstract description 23
- 239000011248 coating agent Substances 0.000 title abstract description 22
- 230000003647 oxidation Effects 0.000 title abstract description 19
- 238000007254 oxidation reaction Methods 0.000 title abstract description 19
- 238000000034 method Methods 0.000 title description 18
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 abstract description 36
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract description 28
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 abstract description 20
- 235000006408 oxalic acid Nutrition 0.000 abstract description 12
- 239000007864 aqueous solution Substances 0.000 abstract description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 8
- 239000003086 colorant Substances 0.000 abstract description 7
- -1 SULPHATE COMPOUND Chemical class 0.000 abstract description 6
- 229910045601 alloy Inorganic materials 0.000 abstract description 6
- 239000000956 alloy Substances 0.000 abstract description 6
- 239000000243 solution Substances 0.000 abstract description 5
- 229910021653 sulphate ion Inorganic materials 0.000 abstract description 4
- 235000011149 sulphuric acid Nutrition 0.000 abstract description 2
- 239000001117 sulphuric acid Substances 0.000 abstract description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 10
- 239000000203 mixture Substances 0.000 description 10
- 238000007743 anodising Methods 0.000 description 6
- 238000005260 corrosion Methods 0.000 description 5
- 230000007797 corrosion Effects 0.000 description 5
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005299 abrasion Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000008151 electrolyte solution Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- DHROYPWJDYETPL-UHFFFAOYSA-N CC(N)=O.CC(N)=O Chemical compound CC(N)=O.CC(N)=O DHROYPWJDYETPL-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 240000007817 Olea europaea Species 0.000 description 1
- 241001417495 Serranidae Species 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000007799 cork Substances 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000007747 plating Methods 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D11/00—Electrolytic coating by surface reaction, i.e. forming conversion layers
- C25D11/02—Anodisation
- C25D11/04—Anodisation of aluminium or alloys based thereon
- C25D11/14—Producing integrally coloured layers
Definitions
- the present invention relates generally to improvements in metal treating and it relates particularly to an improved method for the production of integrally colored anodic oxidation coatings on articles of aluminum and alloys thereof and an improved electrolyte composition therefor.
- the conventional process for forming a colored anodic oxidized coating on articles of aluminum or aluminum alloys includes the step of immersing the aluminum article, which defines an anode, and a cathode defining electrode into an electrolyte, generally sulfuric acid, and applying a voltage between the article and cathode to effect the formation of an oxide coating on the article.
- the resulting coating is greatly deficient because of its high porosity a consequence of which is a low corrosion resistance.
- an additional separate dye treating step is required.
- the conventional aluminum anodizing procedure accordingly leaves much to be desired.
- Another object of the present invention is to provide an improved method and composition for the production of anodic oxidation coatings on surfaces of aluminum and alloys thereof.
- Still another object of the present invention is to provide an improved method and composition for producing on aluminum containing articles a hard highly corrosion resistant, colored, anodic oxidation coating.
- a further object of the present invention is to provide an improved single step method of the above nature characterized by a relatively low voltage requirement and power consumption, great versatility and adaptability, a wide range of colors and depths of color, and a superior resulting coating.
- the present invention is based on the discovery that the use, in the formation of an anodic oxidation coating on an aluminum containing surface, of an electrolyte comprising an aqueous solution containing, in addition to acetamide and oxalic acid, a small amount of sulfuric acid or a water soluble sulfate compound which provides sulfate ions in the aqueous solution, produces a hard, nonporous, highly corrosion resistant, deeply colored coating on the aluminum surface, and the voltage requirements between the aluminum surface and the cathode are greatly reduced with a corresponding reduction in power consumption.
- the present invention accordingly contemplates an electrolyte for the anodic oxidation of aluminum and alloys thereof comprising an aqueous solution of acetamide, oxalic acid, and sulfuric acid or a water soluble sulfate or a combination thereof, as well as the method of treating an aluminum containing work piece comprising immersing the work piece and another electrode in the improved electrolyte and applying a voltage between said work piece and said electrode of a value sufficient to form an oxidation coating on said work piece.
- the concentration of the sulfate ion in the aqueous electrolyte solution should be sufiicient to reduce the anodic oxidation coating voltage, advantageously to an initial voltage of less than 70 volts and a final voltage of less than volts, and advantageously constitutes by weight of the electrolyte of 0.01% and 0.5% sulfuric acid or its molar equivalent of a water soluble sulphate compound or a combination thereof with sulfuric acid, that is between about 0.01% and 0.5 of the sulfate ion.
- the electrolyte contains between 0.1 and 2.0 grams sulfuric acid per liter of electrolyte or the molar equivalent thereof of the sulfate compound or of said compound in combination with sulfuric acid.
- the electrolyte advantageously contains, by weight, 1% to 50% acetamide, preferably 30 to 200 grams acetamide per liter of electrolyte, and 0.1% to 10% oxalic acid, preferably 3 to 30 grams oxalic acid per liter of electrolyte.
- the temperature of the electrolyte in the anodizing procedure, the current density and the anodizing time may be greatly varied depending on the desired coating, and the optimum parameters are easily and readily determined by one skilled in the art. Thus an electrolyte temperature between 15 C. and 25 C. and a current density of the order of 2 a./dm. has been found to be highly satisfactory.
- the color of the anodic oxidation coating is dependent on the composition of the aluminum alloy of the article being treated.
- the present invention is characterized by an increased efficiency consequent to a reduction in the required anodizing voltage and in the power consumption and results in a significant reduction in equipment and costs.
- the improved process is capable of producing a very wide range and depth of colors without the need of separate dyeing steps.
- the color of the resulting coating is highly resistant to light and weathering and exhibits very little discoloration even when exposed for long periods to out-of-door infiuences and environments.
- articles coated by the present process posses such high wear and corrosion resistance properties that they are highly suitable for outdoor uses and applications.
- the coating obtained table, the voltage between the anode and cathode being with the use of the improved electrolyte is tough and regulated in known manner to maintaina constant current 1 high in wear resistance and is substantially free of any density: pores.
- Porhole test results in no deposition of copper Current Voltage range Temperature Time of density of solution anodizin N0. Material (aJdmfl) Starting Final 0 (min.
- an electrolyte similar to that ing in accordance with the present invention can 'be formed described above but without addition of sulfuric acid and in a wider range of colors which covers deeper colors as having the following composition was prepared: compared with the coating produced by anodic oxidation Grams/liter which utilizes an aqueous solution consisting of acetamide Acetamide 80 and oxalic acid. The higher the ratio of the amount of oxalic acid 10 acetamide to that of oxalic acid, the darker color of the Water 1 B a1 ance oxidized article is attained.
- the improved electrolyte set forth above may be 11 liter in total amounitmodified as earlier described by varying the concentra- Employing the above electrolyte Without sulfuric acid, tions of the acetamide, oxalic acid, and sulfuric acid or three aluminum plate work pieces were treated in the 40 sulfate ion in the manner earlier described.
- acid may be substituted in whole or in part by a water and parameters: soluble sulfate salt or compound which provides sulfate
- soluble sulfate salt or compound which provides sulfate The properties of the anodic oxidation coatings of the ions in aqueous solution whereby the sulfuric acid conlast treated samples are as follows: centration is as specified, preferably in the range of 0.1
- An electrolyte for the anodic oxidation of alumdensltles i c9nslderablii.less.wlth the Improved .electro inum and alloys thereof comprising an aqueous solution lyte resulting in a reduction in power consumption and containi b of S 1 t 01 t t 507 f equipment and installation costs.
- the electrolyte of claim 1 wherein said electrolyte performed but is preferably accomplished automatically Contains 30 to 200 grams P liter of Said acetamide, 3 by known electrical regulator networks so that the current to 30 grams per er of Said OXalic acid, and f0 2 density does not vary during the full treatment period grams per liter of said sulfuric acid or the molal equivalent thereof of a water soluble sulfate or a combiuation thereof with sulfuric acid.
Landscapes
- 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)
- Electrochemical Coating By Surface Reaction (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP44003522A JPS4924329B1 (enrdf_load_stackoverflow) | 1969-01-17 | 1969-01-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3597338A true US3597338A (en) | 1971-08-03 |
Family
ID=11559691
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US842030A Expired - Lifetime US3597338A (en) | 1969-01-17 | 1969-07-15 | Method and electrolyte for anodic oxidation coating of aluminum |
Country Status (2)
Country | Link |
---|---|
US (1) | US3597338A (enrdf_load_stackoverflow) |
JP (1) | JPS4924329B1 (enrdf_load_stackoverflow) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS55130881U (enrdf_load_stackoverflow) * | 1979-03-12 | 1980-09-16 | ||
JP6135062B2 (ja) | 2012-08-07 | 2017-05-31 | セイコーエプソン株式会社 | 発光装置、発光装置の製造方法、電子機器 |
-
1969
- 1969-01-17 JP JP44003522A patent/JPS4924329B1/ja active Pending
- 1969-07-15 US US842030A patent/US3597338A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPS4924329B1 (enrdf_load_stackoverflow) | 1974-06-21 |
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