US3017285A - Method of writing on anodized aluminum - Google Patents
Method of writing on anodized aluminum Download PDFInfo
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- US3017285A US3017285A US816664A US81666459A US3017285A US 3017285 A US3017285 A US 3017285A US 816664 A US816664 A US 816664A US 81666459 A US81666459 A US 81666459A US 3017285 A US3017285 A US 3017285A
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- pores
- solution
- writing
- alkali
- reducing agent
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- 238000000034 method Methods 0.000 title claims description 26
- 229910052782 aluminium Inorganic materials 0.000 title claims description 18
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title claims description 18
- 239000003638 chemical reducing agent Substances 0.000 claims description 20
- 150000003839 salts Chemical class 0.000 claims description 17
- 239000003513 alkali Substances 0.000 claims description 12
- 239000000203 mixture Substances 0.000 claims description 12
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims description 8
- 239000002344 surface layer Substances 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 5
- -1 AMMONIUM HYDROXIDES Chemical class 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 229910052751 metal Inorganic materials 0.000 description 15
- 239000002184 metal Substances 0.000 description 15
- 239000003518 caustics Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000011148 porous material Substances 0.000 description 11
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 6
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 5
- 235000011114 ammonium hydroxide Nutrition 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- 238000005530 etching Methods 0.000 description 5
- 239000003906 humectant Substances 0.000 description 5
- 239000000080 wetting agent Substances 0.000 description 5
- 239000004372 Polyvinyl alcohol Substances 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
- 239000000470 constituent Substances 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000004744 fabric Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 238000005470 impregnation Methods 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910001961 silver nitrate Inorganic materials 0.000 description 3
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 3
- 238000011282 treatment Methods 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- 229910000831 Steel Inorganic materials 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002250 absorbent Substances 0.000 description 2
- 230000002745 absorbent Effects 0.000 description 2
- 238000007605 air drying Methods 0.000 description 2
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000007598 dipping method Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 235000010981 methylcellulose Nutrition 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 241000416162 Astragalus gummifer Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical class [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical class [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 238000003486 chemical etching Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Chemical class 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical compound [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- WUWHPEZEVZLKEJ-UHFFFAOYSA-N hydrazine;sulfurous acid Chemical compound NN.OS(O)=O WUWHPEZEVZLKEJ-UHFFFAOYSA-N 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical class [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229940043349 potassium metabisulfite Drugs 0.000 description 1
- 235000010263 potassium metabisulphite Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- HADKRTWCOYPCPH-UHFFFAOYSA-M trimethylphenylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C1=CC=CC=C1 HADKRTWCOYPCPH-UHFFFAOYSA-M 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C25D11/18—After-treatment, e.g. pore-sealing
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
- Y10T428/24917—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including metal layer
Definitions
- One known procedure for treating aluminum surfaces to produce a more or less permanent image thereon involves the preparation of a porous oxidized surface on the aluminum, treatment of the resulting surface to incorporate a light sensitive medium therein and exposure of the resulting article in a manner resembling conventional photographic practice.
- This procedure taught in United States Patents 2,115,339, 2,126,017 and 2,766,119, represents a complex process in which particular care must be taken to. avoid exposure of sensitive chemicals to light and which therefore entails the use of a darkroom or its equivalent.
- This invention relates to permanent marking by writing or printing or both on the porous surface of an anodized layer of aluminum, by a simple procedure requiring neither the expensive chemicals nor the expensive apparatus of the foregoing prior art approaches and to the marked aluminum articles, so produced.
- Substrates which have been found to be amenable to this invention include aluminum and alloys in which the major component is aluminum, such as those described in Tables Ill and IV on page 793 of the 1948 Handbook published by the American Society of Metals. It will therefore be understood that the term aluminum as hereinafter employed, is intended to cover not only the metal but also any alloys in which it is the predominant constituent.
- an absorbent oxide or hydrated oxide film on such material is old and well known and may be accomplished by any of several techniques known to those skilled in the art.
- the oxide or hydrated oxide coating may be produced by treating the surface chemically, e.g. by contacting the surface with a solution of an alkali carbonate and a soluble dichromate, as described in T osterud Patent 1,946,150.
- the oxide or hydrated oxide may be produced by anodic oxidation of the surface in oxalic acid or sulfuric acid, or other appropriate liquid medium.
- chemical or electrochemical means are chosen to produce the absorbent film is immaterial, provided that a relatively thick film (about 0.5 mil) is formed.
- the thin aluminum oxide which forms naturally when the metal is exposed to air is not of sufiicient thickness to satisfactorily retain the image forming materials in the amounts found necessary to obtain the benefits of the present invention.
- the invention comprises the impregnation of a suitable porous surface of an anodized layer of aluminum even date herewith, there is disclosed a process of permanent writing and printing on unsealed anodized aluminum surfaces, i.e. surfaces prepared as above described, and merely rinsed with water prior to processing.
- One conventional finishing treatment applied to anodized aluminum surfaces is sealing wherein the pores are sealed for example by prolonged exposure to steam or boiling water.
- the pores be reopened and this is most readily accomplished by etching the sealed surface with a water or alcohol solution of a strong alkali such as NaOH, KOH or phenyl trimethylammonium hydroxide in which the concentration of alkali hydroxide is in the range of -25% for between seconds and 1 minute. Thereafter the surface is washed in running water for a few minutes and then thoroughly dried, preferably at an elevated temperature. The porous surface is then impregnated with a dilute solution of a strong reducing agent. Both inorganic and organic reducing agents have been found to be satisfactory as impregnants for the porous surface. By way of example, the following reducing agents have all been found suitab le when used in conjunction with the proper reducible salt, and generally concentrations of the order of l to 5% in water or organic solvents are found to be suitable.
- a strong alkali such as NaOH, KOH or phenyl trimethylammonium hydroxide in which the concentration of alkali hydroxide is in the
- Trivalent V compounds Divalent V compounds
- the solution of reducing agent may be in either an aqueous or nonaque'o'us solvent.
- Water, orlower alcohol, e.g. methanol and ethanol are preferred solvents, but any own sol'v'ent for the selected reducing agent may be used without any apparent detrimental effect on the process.
- One efef'red reducing agent is a 1% to 2% solution of hydrod't'unone in methyl alcohol. After impregnation the resulting article is air driedand may be stored with but decomposition, almost indefinitely. Printing or writing is thereafter accomplished by impressing the desired image on the treated surface with an ink containing a suitable reducible salt.
- the relative oxidation and reduction potentials of the reducing agent determine to some extent the reducible compound selected.
- organic and inorganic salts of silver, mercury, copper, the platinum metals, gold, zinc, cadmium, tin, lead, bismuth and antimony have been used with reducing agents of the proper reducing po 'tency.
- Concentrations of metal salts in the range of 3% to 25% by weight, in Water or in alcohol or similar Eehicles have been found to provide satisfactory writing ui'clh.
- the permanent marking is effected by Writing with a wooden stylus or steel nib dipped in the writing fluid or by transferring the desired image onto the impregnated surface by means of stencils, dies or other printing tech niques.
- the image appears almost immediately and is made permanent by the usual methods of sealing, e.g. by holding the image bearing surface for about to 30 minutes in boiling water. No bleeding or bleaching takes place.
- the sealed anodized surface may be treated with a fluid composed of the following (all percentages being by weight):
- alkali which may advantageously be a wateror alcohol-solution of a .NaOI-I, .KOH or phenyl trimethylam- 4 moniurn hydroxide in which the concentration of alkali hydroxide is in the range of 5% to 25%.
- the thickener, humectant and wetting agent are optional, albeit preferred constituents.
- the wetting agent if present, should be one which is compatible with alkali. Drying of the fluid is retarded by incorporation of suitable humectants such as glycerol and the glycols in the proportions stated above. Further, to improve ease of writing a thickener such as polyvinyl alcohol, methyl cellulose, modified polyvinyl acetate, gum tragacanth, gum arable or other wateror alcohol-soluble gums, or the like may be used.
- suitable humectants such as glycerol and the glycols in the proportions stated above.
- a thickener such as polyvinyl alcohol, methyl cellulose, modified polyvinyl acetate, gum tragacanth, gum arable or other wateror alcohol-soluble gums, or the like may be used.
- the caustic ink was applied to the surface with a steel pin when the writing was carried out by hand.
- a pen with a wooden nib may also be utilized.
- compositions containing humectants are used because of the thinness of layer of transfer.
- the ink or printing fluid was applied to the sealed surface and allowed to remain in contact for a period of 30 seconds to one minute, after which the caustic was washed or wiped off with a cloth. After air drying for one or two minutes, preferably under an infrared lamp, a 10% solution of silver nitrate was applied ei-ther by dipping or wiping. If dipping was utilized, an immersion time of five to twenty seconds is Slll'fiClBIlt.
- the black color was then developed by dipping in a 1% solution of hydroquinone in methyl alcohol or by wiping with a cloth dampened with the same solution. As soon as the black color develops fully, the surface of the place was then wiped with a damp cloth.
- the technique may be modified by incorporating the reducing agent such as hydroquinone in the caustic Writing fluid initially so that a concentration between 1 and 2% of hydroquinone is available. This may be added to the caustic solution in an alcohol medium. In this case, the black color is then developed by dipping or wiping with a 10% solution of silver nitrate or other reducible salt.
- the reducing agent such as hydroquinone
- a method of marking an aluminum substrate having a porous anodized surface layer wherein the pores in said surface layer have been sealed which comprises: opening the pores in said surface by contact with a solution of a strong alkali selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides; impregnating the opened pores of said surface with a dilute solution of a strong reducing agent and thereafter contacting portions of the impregnated surface with an ink composition consisting essentially of a salt of an easily reducible metal in a liquid vehicle.
- An alkaline composition useful in preparing an aluminum article having a porous oxide surface for subsequent impregnation thereof in a marking process and which comprises: a solution of a hydroxide from the group consisting of alkali metal hydroxides and organic ammonium hydroxides, in which the concentration of said hydroxide is between 5% and 25% by weight, and at least one of the following additional constituents: a thickener, selected from the group consisting of polyvinyl compounds, methyl cellulose and soluble gums; a humectant, selected from the group consisting of glycols and glycerol; and an alkali-compatible wetting agent.
- a hydroxide from the group consisting of alkali metal hydroxides and organic ammonium hydroxides, in which the concentration of said hydroxide is between 5% and 25% by weight, and at least one of the following additional constituents: a thickener, selected from the group consisting of polyvinyl compounds, methyl cellulose and soluble gums; a humec
- a method of marking an anodized aluminum-base material having a porous anodized surface layer, the pores of which are sealed which comprises: applying a caustic solution of an alkali selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides to selected portions of said surface for between about 10 seconds and 60 seconds; washing the so treated surface with water; drying the washed surface; applying a solution of an easily reducible salt to the surface; and thereafter developing a visible mark on said surface by application of a reducing agent thereto.
- reducible salt is silver nitrate and the reducing agent is a dilute solution of hydroquinone in methyl alcohol.
- a composition of matter comprising: between about 1% and 10% by weight of ethylene glycol; between about 0.5% and 5% by weight of polyvinyl alcohol; between 0.1% and 1% by weight of an alkali-compatible wetting agent; and the balance consisting essentially of a strong alkali, selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides, dissolved in a liquid vehicle the concentration of alkali in said composition being between 5% and 25% by Weight.
- composition of claim 7 wherein the vehicle is water.
- composition of claim 7 wherein the alkali is NaOH.
- a process of preparing an article having a porous anodized aluminum surface layer, the pores of which are sealed, for subsequent marking which comprises: etching the surface with a strong alkali, selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides, for between 10 seconds and 1 minute; washing the etched surface in running water; drying the washed surface; impregnating the pores in said dried surface with a reducing agent; air drying the resulting impregnated article and storing the so formed article.
- a strong alkali selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides
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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)
- ing And Chemical Polishing (AREA)
Description
3,017,285 NETHGD F WRK'EENG 6N ANQDIZED ALUMWUM Eugene Wainer, (Ileveland Heights, Ghio, assignor to Horizons Incorporated, Cleveland, Ohio, a corporation of New .lersey No Drawing. Filed May 29, 1959, Ser. No. 816,664 12 Qlaims. (Cl. 117-8) It is often desirable to produce a permanent light-fast marking on a permanent metal base for identification badges or the like.
One known procedure for treating aluminum surfaces to produce a more or less permanent image thereon involves the preparation of a porous oxidized surface on the aluminum, treatment of the resulting surface to incorporate a light sensitive medium therein and exposure of the resulting article in a manner resembling conventional photographic practice. This procedure, taught in United States Patents 2,115,339, 2,126,017 and 2,766,119, represents a complex process in which particular care must be taken to. avoid exposure of sensitive chemicals to light and which therefore entails the use of a darkroom or its equivalent.
Other methods are known for imparting permanent markings to aluminum, e.g. by mechanical means or by chemical etching, but the resulting images are not as readily legible as those in the above-mentioned photographic processes and in addition they require specialized apparatus which adds to the ultimate cost of the product.
This invention relates to permanent marking by writing or printing or both on the porous surface of an anodized layer of aluminum, by a simple procedure requiring neither the expensive chemicals nor the expensive apparatus of the foregoing prior art approaches and to the marked aluminum articles, so produced.
A schematic simplified flow diagram of the process is as follows:
3,017,235 Patented Jan. 16, 1962- with a dilute solution of a strong reducing agent and then writing or printing on the impregnated surface with a salt of an easily reducible metal, whereby an image prints out almost immediately. The procedure may be reversed, if desired by using a solution of the salt as the impregnant and writing or printing with the reducing agent. Because of the relative instability of the easily reducible metal salts suitable for the present process, it is preferred that they comprise the writing fluid.
Substrates which have been found to be amenable to this invention include aluminum and alloys in which the major component is aluminum, such as those described in Tables Ill and IV on page 793 of the 1948 Handbook published by the American Society of Metals. It will therefore be understood that the term aluminum as hereinafter employed, is intended to cover not only the metal but also any alloys in which it is the predominant constituent.
The formation of an absorbent oxide or hydrated oxide film on such material is old and well known and may be accomplished by any of several techniques known to those skilled in the art. For example, the oxide or hydrated oxide coating may be produced by treating the surface chemically, e.g. by contacting the surface with a solution of an alkali carbonate and a soluble dichromate, as described in T osterud Patent 1,946,150. Alternatively, as described in the same patent, the oxide or hydrated oxide may be produced by anodic oxidation of the surface in oxalic acid or sulfuric acid, or other appropriate liquid medium. Whether chemical or electrochemical means are chosen to produce the absorbent film is immaterial, provided that a relatively thick film (about 0.5 mil) is formed. The thin aluminum oxide which forms naturally when the metal is exposed to air is not of sufiicient thickness to satisfactorily retain the image forming materials in the amounts found necessary to obtain the benefits of the present invention.
In a co-pending application, Serial No. 816,701, filed of pores sealed, e.g. by boiling Anodized aluminum surface layer with 5 to 25% caustic Treatment with caustic to open pores 10 seconds to 1 minute Wash and thoroughly dry Impregnate with reducible metal salt Treat with caustic and reducing agent Impreguate with reducing agent (hydroquinone in CHQOH) Iii Air dry Store Write with ink containing Write with ink containing Write with ink containing reducible metal salt reducing agent reducible metal salt *Storage is optional.
Briefly the invention comprises the impregnation of a suitable porous surface of an anodized layer of aluminum even date herewith, there is disclosed a process of permanent writing and printing on unsealed anodized aluminum surfaces, i.e. surfaces prepared as above described, and merely rinsed with water prior to processing.
One conventional finishing treatment applied to anodized aluminum surfaces is sealing wherein the pores are sealed for example by prolonged exposure to steam or boiling water.
In order to practice the present invention it is necessary that the pores be reopened and this is most readily accomplished by etching the sealed surface with a water or alcohol solution of a strong alkali such as NaOH, KOH or phenyl trimethylammonium hydroxide in which the concentration of alkali hydroxide is in the range of -25% for between seconds and 1 minute. Thereafter the surface is washed in running water for a few minutes and then thoroughly dried, preferably at an elevated temperature. The porous surface is then impregnated with a dilute solution of a strong reducing agent. Both inorganic and organic reducing agents have been found to be satisfactory as impregnants for the porous surface. By way of example, the following reducing agents have all been found suitab le when used in conjunction with the proper reducible salt, and generally concentrations of the order of l to 5% in water or organic solvents are found to be suitable.
p-Phenylenediamine Potassium meta bisulfite Hydrazine Trivalent Ti compounds Trivalent V compounds Divalent V compounds The solution of reducing agent may be in either an aqueous or nonaque'o'us solvent. Water, orlower alcohol, e.g. methanol and ethanol are preferred solvents, but any own sol'v'ent for the selected reducing agent may be used without any apparent detrimental effect on the process. One efef'red reducing agent is a 1% to 2% solution of hydrod't'unone in methyl alcohol. After impregnation the resulting article is air driedand may be stored with but decomposition, almost indefinitely. Printing or writing is thereafter accomplished by impressing the desired image on the treated surface with an ink containing a suitable reducible salt.
The relative oxidation and reduction potentials of the reducing agent determine to some extent the reducible compound selected. In general organic and inorganic salts of silver, mercury, copper, the platinum metals, gold, zinc, cadmium, tin, lead, bismuth and antimony have been used with reducing agents of the proper reducing po 'tency. Concentrations of metal salts in the range of 3% to 25% by weight, in Water or in alcohol or similar Eehicles have been found to provide satisfactory writing ui'clh.
The permanent marking is effected by Writing with a wooden stylus or steel nib dipped in the writing fluid or by transferring the desired image onto the impregnated surface by means of stencils, dies or other printing tech niques.
The image appears almost immediately and is made permanent by the usual methods of sealing, e.g. by holding the image bearing surface for about to 30 minutes in boiling water. No bleeding or bleaching takes place.
Instead of etching and impregnating in the manner described above, the sealed anodized surface may be treated with a fluid composed of the following (all percentages being by weight):
Percent Thickener 0.55 Humectant 1-10 Wetting agent 0.1-1.0 Strong alkali and vehicle Balance The only essential constituent of the composition is the alkali which may advantageously be a wateror alcohol-solution of a .NaOI-I, .KOH or phenyl trimethylam- 4 moniurn hydroxide in which the concentration of alkali hydroxide is in the range of 5% to 25%.
The thickener, humectant and wetting agent are optional, albeit preferred constituents.
Thus the wetting agent, if present, should be one which is compatible with alkali. Drying of the fluid is retarded by incorporation of suitable humectants such as glycerol and the glycols in the proportions stated above. Further, to improve ease of writing a thickener such as polyvinyl alcohol, methyl cellulose, modified polyvinyl acetate, gum tragacanth, gum arable or other wateror alcohol-soluble gums, or the like may be used.
The following specific formulations are illustrative of suitable formulations. (All parts and percentages are by weight.)
(1) 10% solution NaOH containing 0.5% Aerosol OT.
(2) 10 parts NaOH, 3 parts ethylene glycol, 1 part polyvinyl alcohol, 0.5 part Aerosol OT, and parts water.
(3) 10 parts NaOH, 3 parts ethylene glycol, 1 part polyvinyl alcohol, 0.5 part Aerosol OT, and 100 parts methyl alcohol.
The caustic ink was applied to the surface with a steel pin when the writing was carried out by hand. A pen with a wooden nib may also be utilized. If printing or hand stamping is involved, compositions containing humectants are used because of the thinness of layer of transfer. In each case, the ink or printing fluid was applied to the sealed surface and allowed to remain in contact for a period of 30 seconds to one minute, after which the caustic was washed or wiped off with a cloth. After air drying for one or two minutes, preferably under an infrared lamp, a 10% solution of silver nitrate was applied ei-ther by dipping or wiping. If dipping was utilized, an immersion time of five to twenty seconds is Slll'fiClBIlt. The black color was then developed by dipping in a 1% solution of hydroquinone in methyl alcohol or by wiping with a cloth dampened with the same solution. As soon as the black color develops fully, the surface of the place was then wiped with a damp cloth.
The technique may be modified by incorporating the reducing agent such as hydroquinone in the caustic Writing fluid initially so that a concentration between 1 and 2% of hydroquinone is available. This may be added to the caustic solution in an alcohol medium. In this case, the black color is then developed by dipping or wiping with a 10% solution of silver nitrate or other reducible salt.
One chemical feature of the process should be especially noted. In etching the surface with a strong caustic solution, there is a good possibility that even with vigorous washing, some caustic may still remain in the pores especially when the writing is done almost immediately after the caustic etching. By using a metal salt which on decomposition to the metal produces some acid, as for example nitric acid, this caustic is neutralized and stability and permanency of the surface is thereby improved.
I claim:
1. A method of marking an aluminum substrate having a porous anodized surface layer wherein the pores in said surface layer have been sealed, which comprises: opening the pores in said surface by contact with a solution of a strong alkali selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides; impregnating the opened pores of said surface with a dilute solution of a strong reducing agent and thereafter contacting portions of the impregnated surface with an ink composition consisting essentially of a salt of an easily reducible metal in a liquid vehicle.
2. An aluminum plate marked by the process of claim 1.
3. An alkaline composition useful in preparing an aluminum article having a porous oxide surface for subsequent impregnation thereof in a marking process and which comprises: a solution of a hydroxide from the group consisting of alkali metal hydroxides and organic ammonium hydroxides, in which the concentration of said hydroxide is between 5% and 25% by weight, and at least one of the following additional constituents: a thickener, selected from the group consisting of polyvinyl compounds, methyl cellulose and soluble gums; a humectant, selected from the group consisting of glycols and glycerol; and an alkali-compatible wetting agent.
4. A method of marking an anodized aluminum-base material having a porous anodized surface layer, the pores of which are sealed, which comprises: applying a caustic solution of an alkali selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides to selected portions of said surface for between about 10 seconds and 60 seconds; washing the so treated surface with water; drying the washed surface; applying a solution of an easily reducible salt to the surface; and thereafter developing a visible mark on said surface by application of a reducing agent thereto.
5. The process of claim 4 wherein the reducible salt is silver nitrate and the reducing agent is a dilute solution of hydroquinone in methyl alcohol.
6. The process of claim 4 wherein the reducing agent is included in the caustic solution used in the initial treatment of the surface.
7. A composition of matter comprising: between about 1% and 10% by weight of ethylene glycol; between about 0.5% and 5% by weight of polyvinyl alcohol; between 0.1% and 1% by weight of an alkali-compatible wetting agent; and the balance consisting essentially of a strong alkali, selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides, dissolved in a liquid vehicle the concentration of alkali in said composition being between 5% and 25% by Weight.
8. The composition of claim 7 wherein the vehicle is water.
9. The composition of claim 7 wherein the vehicle is a lower alcohol.
10. The composition of claim 7 wherein the alkali is NaOH.
11. A process of preparing an article having a porous anodized aluminum surface layer, the pores of which are sealed, for subsequent marking which comprises: etching the surface with a strong alkali, selected from the group consisting of alkali metal hydroxides and organic ammonium hydroxides, for between 10 seconds and 1 minute; washing the etched surface in running water; drying the washed surface; impregnating the pores in said dried surface with a reducing agent; air drying the resulting impregnated article and storing the so formed article.
12. The process of claim 11 which comprises in addition impressing on the air-dried resulting impregnated article the desired image by means of an ink consisting essentially of between 3% and 25% by weight of an easily reducible metal salt in a suitable liquid vehicle.
References Cited in the file of this patent UNITED STATES PATENTS 1,988,012 Mason Jan. 15, 1935 2,019,229 Leahy Oct. 29, 1935 2,710,804 Shenk June 14, 1955 2,930,106 Wrotnowski Mar. 29, 1960
Claims (1)
1. A METHOD OF MARKING AN ALUMINUM SUBSTRATE HAVING A POROUS ANODIZED SURFACE LAYER WHEREIN THE PORES IN SAID SURFACE LAYER HAVE BEEN SEALED, WHICH COMPRISES: OPENING THE PORES IN SAID SURFACE BY CONTACT WITH A SOLUTION OF A STRONG ALKALI SELECTED FRM THE GROUP CONSISTING OF ALKALI METAL HYDROXIDES AND ORGANIC AMMONIUM HYDROXIDES; IMPREGNATING THE OPENED PORES OF SAID SURFACE WITH A DILUTE SOLUTION OF A STRONG REDUCING AGENT AND THEREAFTER CONTACTING PORTIONS OF THE IMPREGNATED SURFACE WITH AN INK COMPOSITION CONSISTING ESSENTIALLY OF A SALT OF AN EASILY REDUCIBLE METAL IN A LIQUID VEHICLE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US816664A US3017285A (en) | 1959-05-29 | 1959-05-29 | Method of writing on anodized aluminum |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US816664A US3017285A (en) | 1959-05-29 | 1959-05-29 | Method of writing on anodized aluminum |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3017285A true US3017285A (en) | 1962-01-16 |
Family
ID=25221301
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US816664A Expired - Lifetime US3017285A (en) | 1959-05-29 | 1959-05-29 | Method of writing on anodized aluminum |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3017285A (en) |
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3257244A (en) * | 1964-10-14 | 1966-06-21 | Reynolds Metals Co | Sealing and inhibiting corrosion of anodized aluminum |
| US3374155A (en) * | 1965-02-19 | 1968-03-19 | Ludwig J. Weber | Modified oxide-coated aluminum and the method of modifying |
| US3742602A (en) * | 1970-03-31 | 1973-07-03 | Spear & Jackson Ashberry Ltd | Cutlery and flatware |
| US3953625A (en) * | 1971-12-07 | 1976-04-27 | Horizons Incorporated | Process for making indicia bearing anodized article |
| US4209569A (en) * | 1977-07-20 | 1980-06-24 | Langbein-Pfanhauser Werke Ag | Baking form and method of making same |
| EP0042715A1 (en) * | 1980-06-16 | 1981-12-30 | The Fujikura Cable Works, Ltd. | Method of surface treatment of porous material |
| US4624752A (en) * | 1983-06-02 | 1986-11-25 | The Secretary Of State For Defence In Her Brittanic Majesty's Government Of The United Kingdom Of Great Britian And Northern Ireland | Surface pretreatment of aluminium and aluminium alloys prior to adhesive bonding, electroplating or painting |
| US20060001726A1 (en) * | 2001-10-05 | 2006-01-05 | Cabot Corporation | Printable conductive features and processes for making same |
| US20190208646A1 (en) * | 2017-10-03 | 2019-07-04 | Tengyuan Zhang | React-on-demand (rod) fabrication method for high performance printed electronics |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1988012A (en) * | 1932-10-27 | 1935-01-15 | Aluminum Co Of America | Metal deposites in oxide coatings |
| US2019229A (en) * | 1931-11-16 | 1935-10-29 | Atlas Tack Corp | Coloration of aluminum articles |
| US2710804A (en) * | 1949-08-08 | 1955-06-14 | Von Glutz & Muller Ag Dr | Process for the production of photographic reproduction surfaces on aluminium and its alloys |
| US2930106A (en) * | 1957-03-14 | 1960-03-29 | American Felt Co | Gaskets |
-
1959
- 1959-05-29 US US816664A patent/US3017285A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2019229A (en) * | 1931-11-16 | 1935-10-29 | Atlas Tack Corp | Coloration of aluminum articles |
| US1988012A (en) * | 1932-10-27 | 1935-01-15 | Aluminum Co Of America | Metal deposites in oxide coatings |
| US2710804A (en) * | 1949-08-08 | 1955-06-14 | Von Glutz & Muller Ag Dr | Process for the production of photographic reproduction surfaces on aluminium and its alloys |
| US2930106A (en) * | 1957-03-14 | 1960-03-29 | American Felt Co | Gaskets |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3257244A (en) * | 1964-10-14 | 1966-06-21 | Reynolds Metals Co | Sealing and inhibiting corrosion of anodized aluminum |
| US3374155A (en) * | 1965-02-19 | 1968-03-19 | Ludwig J. Weber | Modified oxide-coated aluminum and the method of modifying |
| US3742602A (en) * | 1970-03-31 | 1973-07-03 | Spear & Jackson Ashberry Ltd | Cutlery and flatware |
| US3953625A (en) * | 1971-12-07 | 1976-04-27 | Horizons Incorporated | Process for making indicia bearing anodized article |
| US4209569A (en) * | 1977-07-20 | 1980-06-24 | Langbein-Pfanhauser Werke Ag | Baking form and method of making same |
| EP0042715A1 (en) * | 1980-06-16 | 1981-12-30 | The Fujikura Cable Works, Ltd. | Method of surface treatment of porous material |
| US4624752A (en) * | 1983-06-02 | 1986-11-25 | The Secretary Of State For Defence In Her Brittanic Majesty's Government Of The United Kingdom Of Great Britian And Northern Ireland | Surface pretreatment of aluminium and aluminium alloys prior to adhesive bonding, electroplating or painting |
| US20060001726A1 (en) * | 2001-10-05 | 2006-01-05 | Cabot Corporation | Printable conductive features and processes for making same |
| US20190208646A1 (en) * | 2017-10-03 | 2019-07-04 | Tengyuan Zhang | React-on-demand (rod) fabrication method for high performance printed electronics |
| US10772218B2 (en) * | 2017-10-03 | 2020-09-08 | The University Of Western Ontario | React-on-demand (ROD) fabrication method for high performance printed electronics |
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