US1727331A - Process of coating aluminum electrolytically - Google Patents
Process of coating aluminum electrolytically Download PDFInfo
- Publication number
- US1727331A US1727331A US161515A US16151527A US1727331A US 1727331 A US1727331 A US 1727331A US 161515 A US161515 A US 161515A US 16151527 A US16151527 A US 16151527A US 1727331 A US1727331 A US 1727331A
- Authority
- US
- United States
- Prior art keywords
- bath
- aluminum
- acid
- coating
- cathode
- 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.)
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- 229910052782 aluminium Inorganic materials 0.000 title description 13
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 title description 13
- 239000011248 coating agent Substances 0.000 title description 11
- 238000000576 coating method Methods 0.000 title description 11
- 238000000034 method Methods 0.000 title description 8
- 239000002253 acid Substances 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 239000012670 alkaline solution Substances 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
- 239000011260 aqueous acid Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000007747 plating Methods 0.000 description 3
- 239000001488 sodium phosphate Substances 0.000 description 3
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 3
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 3
- 235000019801 trisodium phosphate Nutrition 0.000 description 3
- 229910052725 zinc Inorganic materials 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-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
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 238000005868 electrolysis reaction Methods 0.000 description 2
- 238000009713 electroplating Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 101100165177 Caenorhabditis elegans bath-15 gene Proteins 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- -1 alkali metal salts Chemical class 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 238000011268 retreatment Methods 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25D—PROCESSES FOR THE ELECTROLYTIC OR ELECTROPHORETIC PRODUCTION OF COATINGS; ELECTROFORMING; APPARATUS THEREFOR
- C25D5/00—Electroplating characterised by the process; Pretreatment or after-treatment of workpieces
- C25D5/34—Pretreatment of metallic surfaces to be electroplated
- C25D5/42—Pretreatment of metallic surfaces to be electroplated of light metals
- C25D5/44—Aluminium
Definitions
- This invention relates to processes of coating aluminum and alloys containing the same, electrolyt-ically.
- One object of the invention is to provide a rocess in which an electrolytic coating o adequate density and adherence can be united to an aluminum surface in spite of the tendency of the latter to form a thin resistant film of oxide.
- Another object of the invention is to provide a process which will accomplish the above result at the minimum of trouble and expense. Other objects will hereinafter appear.
- Fig. 1 is a diagrammatic vertical section on a reduced scale of one form of apparatus in which the first be conveniently carried out;
- Fig. 2 is a similar view of one form of apparatus in which the second pretreatment step may conveniently be carried out;
- Fig. 3 is a similar view of one form of apparatus in which the electrodeposition may conveniently take place.
- a hydroxyl ion concentration of the same order of magnitude as that of a 5% solupretreatment step may tion of trisodium phosphate. Torking with such a solution at a temperature slightly below boiling, say 190 to 200 F. the surface to be treated requires only about a halfl minute immersion. Where it is undesirable to carry any of this alkaline bath into the bath for the second retreatment step, the aricle can be dipped or a few seconds in an acid bath, say 10% aqueous hydrochloric acid, but this is not indispensable, although desirable.
- the surface under treatment after undergoing the action of the alkaline solution in the first step, is then made a cathode in an aqueous acid solution.
- aqueous acid solution I
- it may be electrolyzed for about 3 to 5 minutes at a current density of 0.4' amperes per square inch with a. voltage of around 2.
- the acid solution can be, for example, a 5% aqueous sulfuric acid one, but the concentration can obviously be varied considerably, and any other acid can be substituted in an amount which will furnish a correspondingly sufcient hydrogen ion concentration.
- the final cleaning, or second pretreatment ste takes place in an electrolyte which contains substantially noy alkali metal salts. This is important because any considerable concentration of the ionsof such metal causes conditions in the cathode region,.which favor further filming of the aluminum 'surface which forms the l bi Icathode.
- the chief cations during the second pretreatment step are those of hydrogen (H*) and these'tend to dissolve the oxide and hydroxid that were previously formed or loosened during the first or alkaline pretreatment step.
- H* hydrogen
- the hydrogen polarization of the cathode surface prevents oxidation.
- IVhile I do not wish to be restricted to a particular theory of operation. since the above described pretreatment steps have been found in actual practice to be unexpectedly effective, nevertheless, I believe that hydrogen, in addition'95 to maintaining a non-oxidizing zone around the cathode, also mechanically eliminates some of the aluminum hydroxid coating, the
- the surface of the aluminum having undergone the pretreatment described above, can4 be lated in any well known acid-plating bat i, such as the standard acid-sulfate 5 zinc plating bath operating at a current density of 0.1 to 0.2 upon the treated surface.l As such bathsare well known, the lde-4 tails of them are omitted here.
- any well known acid-plating bat i such as the standard acid-sulfate 5 zinc plating bath operating at a current density of 0.1 to 0.2 upon the treated surface.l
- the lde-4 tails of them are omitted here.
- 1 represents any suitable container in which is the dilute aqueous alkaline solution inl which the article 3, having the surface of the readily oxidizable metal, is suspended in any suitable Way, say by rod 4 and hook. 5.
- any suitable vessel 6 contains the dilute acid solution 7 in which the artifcle to be treated 3 is immersed as the cathjode, say by electroconducting hook 7 from i cathode bar 8.
- Suitable anodes 9 are connected to anode bars 10.
- the bars 8 and .10 are connected to the poles of any suitable source of current 11..
- the anodes 9 are ...preferably of a material which does not foul the bath, such as carbon.
- any suitable vessel 12 has suspended in the bath, as 'the cathode, the treatedarticle 3 suspended by any suitable electroconducting hook 75 from cathode bar 8.
- the anodes 13 are connected to anode bars 14.
- Bars 8 and 14 are connected to any suitable source of current 11.
- ai standard electro-plating bath 15 of the type customarily used.
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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)
- Electroplating Methods And Accessories (AREA)
Description
sept. 1o, 1929. j C. L. BEM. 1,727,331
PROCESS QF COATING ALUMINUM ELECTROLYTICALLY Filed Jan. 1'?. 1927 .ilwe aqueous aad bath Subsantzay free #om aUfaZL lsalzsuchj as L 5% sulfuric 9 acid SOZzLOn/V//T/ he cathde.
ATTORNEY.
Patented Sept. 10, 1929.
vUNITED STATES PATENT OFFICE.
CARL L. BEAL, F ROCHESTER, NEW YORK, ASSIGNOR T0 EASTMA-N KODAK COMPANY,
OF ROCHESTER, NEW YORK, A CORPORATION OF NEW YORK.
.PROCESS OF' COATING ALUMINUM ELECTROLYTICALLY.
Application led January 17, 1927. Serial No. 161,515.
This invention relates to processes of coating aluminum and alloys containing the same, electrolyt-ically. One object of the invention is to provide a rocess in which an electrolytic coating o adequate density and adherence can be united to an aluminum surface in spite of the tendency of the latter to form a thin resistant film of oxide. Another object of the invention is to provide a process which will accomplish the above result at the minimum of trouble and expense. Other objects will hereinafter appear.
In the accompanying drawing,-
Fig. 1 is a diagrammatic vertical section on a reduced scale of one form of apparatus in which the first be conveniently carried out;
Fig. 2 is a similar view of one form of apparatus in which the second pretreatment step may conveniently be carried out;
Fig. 3 is a similar view of one form of apparatus in which the electrodeposition may conveniently take place.
It is well known that aluminum has been difficult to coat reliably, because its surface, inzcontact with the air, rapidlyv forms a tenacious film, which even when it is thin, resists the adherence of an electrodeposited coating over it. For instance, it has been difficult to )roduce a good reliable zinc coating electro ytically on aluminum.
I have found that this trouble can be avoided by first treating' the surface of. the aluminum in a dilute aqueous alkaline solution, preferably hot, and then making it a cathode in an acid bath, these successive pretreatment steps bringing the surface t0 a condition in which it can bereadily electroplated in a standard commercial bath, such as an acid-sulfate zinc plating bat i The first pretreatment step does not re'- quire any electrolysis, and is very rapid and economical. Various alkaline aqueous so-l lutions maybe employed, such as those of sodium hydroxid, sodium carbonate, or trisodium phosphate. The concentration of the solution may vary considerably. I have found it convenient to work with one having a hydroxyl ion concentration of the same order of magnitude as that of a 5% solupretreatment step may tion of trisodium phosphate. Torking with such a solution at a temperature slightly below boiling, say 190 to 200 F. the surface to be treated requires only about a halfl minute immersion. Where it is undesirable to carry any of this alkaline bath into the bath for the second retreatment step, the aricle can be dipped or a few seconds in an acid bath, say 10% aqueous hydrochloric acid, but this is not indispensable, although desirable.
The surface under treatment, after undergoing the action of the alkaline solution in the first step, is then made a cathode in an aqueous acid solution. I For example, it may be electrolyzed for about 3 to 5 minutes at a current density of 0.4' amperes per square inch with a. voltage of around 2. The acid solution can be, for example, a 5% aqueous sulfuric acid one, but the concentration can obviously be varied considerably, and any other acid can be substituted in an amount which will furnish a correspondingly sufcient hydrogen ion concentration.
It will be noted that the final cleaning, or second pretreatment ste takes place in an electrolyte which contains substantially noy alkali metal salts. This is important because any considerable concentration of the ionsof such metal causes conditions in the cathode region,.which favor further filming of the aluminum 'surface which forms the l bi Icathode. In my process the chief cations during the second pretreatment step are those of hydrogen (H*) and these'tend to dissolve the oxide and hydroxid that were previously formed or loosened during the first or alkaline pretreatment step. AIoreover, the hydrogen polarization of the cathode surface prevents oxidation. IVhile I do not wish to be restricted to a particular theory of operation. since the above described pretreatment steps have been found in actual practice to be unexpectedly effective, nevertheless, I believe that hydrogen, in addition'95 to maintaining a non-oxidizing zone around the cathode, also mechanically eliminates some of the aluminum hydroxid coating, the
bubbles acting on this coating. after the preliminary attack of the alkaline immersion.
The surface of the aluminum having undergone the pretreatment described above, can4 be lated in any well known acid-plating bat i, such as the standard acid-sulfate 5 zinc plating bath operating at a current density of 0.1 to 0.2 upon the treated surface.l As such bathsare well known, the lde-4 tails of them are omitted here.
In the drawing, 1 represents any suitable container in which is the dilute aqueous alkaline solution inl which the article 3, having the surface of the readily oxidizable metal, is suspended in any suitable Way, say by rod 4 and hook. 5. i
1'5 In Fig. 2 any suitable vessel 6 contains the dilute acid solution 7 in which the artifcle to be treated 3 is immersed as the cathjode, say by electroconducting hook 7 from i cathode bar 8. Suitable anodes 9 are connected to anode bars 10. The bars 8 and .10 are connected to the poles of any suitable source of current 11.. The anodes 9 are ...preferably of a material which does not foul the bath, such as carbon.
:l In Fig. 3 any suitable vessel 12 has suspended in the bath, as 'the cathode, the treatedarticle 3 suspended by any suitable electroconducting hook 75 from cathode bar 8. The anodes 13 are connected to anode bars 14. Bars 8 and 14 are connected to any suitable source of current 11. In the vesselis ai standard electro-plating bath 15 of the type customarily used. In fact, Fig. 3
is merely a diagrammatic representation of currentelectroplating practice.
Having thus described my invention, what I claim as new and desire to secure by Letters Patent is:
1. In the process of electroplatingl an aluminum surface, the steps of treating said surface in a dilute aqueous alkaline bath Wit-hout electrolysis, treating said surface as the cathode in an acid dilute aqueous bath under non-oxidizing conditions, and thereafter electrodepositing a coating upon said 'treated surface.
day of January 1927.
CARL L. BEAL.
Q. In the .process of electroplating upon an aluminum surface, the steps of immersing said surface 1n an aqueous alkaline solution to attack the film on said surface,
treating said surface as the cathode in a In-theprocess of electrodepositing al coating upon an aluminum surface, the steps 6.0 of immersng said surface in a hot aqueous f bath having an alkalinity of the orderof magnitude of a 5% solution of trisodium phosphate, dipping the' surface in a dilute Y aqueous acid solution, making said surface u a cathode in an aqueous acid bath, substan-
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US161515A US1727331A (en) | 1927-01-17 | 1927-01-17 | Process of coating aluminum electrolytically |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US161515A US1727331A (en) | 1927-01-17 | 1927-01-17 | Process of coating aluminum electrolytically |
Publications (1)
Publication Number | Publication Date |
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US1727331A true US1727331A (en) | 1929-09-10 |
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ID=22581482
Family Applications (1)
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US161515A Expired - Lifetime US1727331A (en) | 1927-01-17 | 1927-01-17 | Process of coating aluminum electrolytically |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2888387A (en) * | 1957-05-14 | 1959-05-26 | Tiarco Corp | Electroplating |
US4293617A (en) * | 1979-12-26 | 1981-10-06 | Gould Inc. | Process for producing strippable copper on an aluminum carrier and the article so obtained |
EP0624662A1 (en) * | 1993-05-12 | 1994-11-17 | Hughes Aircraft Company | Method for direct plating of iron on aluminium |
-
1927
- 1927-01-17 US US161515A patent/US1727331A/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2888387A (en) * | 1957-05-14 | 1959-05-26 | Tiarco Corp | Electroplating |
US4293617A (en) * | 1979-12-26 | 1981-10-06 | Gould Inc. | Process for producing strippable copper on an aluminum carrier and the article so obtained |
EP0624662A1 (en) * | 1993-05-12 | 1994-11-17 | Hughes Aircraft Company | Method for direct plating of iron on aluminium |
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