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US2580773A - Method and composition for coating aluminum with zinc - Google Patents

Method and composition for coating aluminum with zinc Download PDF

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US2580773A
US2580773A US41891A US4189148A US2580773A US 2580773 A US2580773 A US 2580773A US 41891 A US41891 A US 41891A US 4189148 A US4189148 A US 4189148A US 2580773 A US2580773 A US 2580773A
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aluminum
zinc
fluoride
immersion
bath
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Heiman Samuel
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Philadelphia Rust-Proof Co
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    • C—CHEMISTRY; METALLURGY
    • C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23C—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C18/00—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating
    • C23C18/16—Chemical coating by decomposition of either liquid compounds or solutions of the coating forming compounds, without leaving reaction products of surface material in the coating; Contact plating by reduction or substitution, e.g. electroless plating
    • C23C18/31—Coating with metals

Definitions

  • This invention relates to a method of coating metals on articles of aluminum or alloys thereof by immersion of the articles in aqueous solutions More specifically the invention relates to a. method of producing smooth and adherent deposits of metals nobler than aluminum on aluminum surfaces by immersion in aqueous baths without the use of electric current.
  • the immersion deposits have a sound structure and such an unusually high degree of adhesion to the aluminum that they may be used as a base for the subsequent electrodeposition of other metals.
  • zinc, cadmium, tin, and other metals may be deposited on aluminum in accordance with the present invention which have a greater bond to the aluminum than the cohesive strength of the aluminum base metal itself.
  • Etching the surface.Aluminum may be etched in a mixture of nitric and hydrofluoric acids and then nickel plated.
  • the adhesion of the nickel to the aluminum depended to a large extent on the keying action of the nickel deposit in the pits in the aluminum surface.
  • the natural oxide coating on aluminum may be replaced by a relatively thick, porous, anodic oxide coating.
  • the electroplated metal adheres to the aluminum by virtue of filling the pores of the oxide coating.
  • I may also use suitable water-soluble salts of these metals with the addition of suitable amounts of hydrofluoric acid, sodium fluoride, ammonium fluoride, or ammonium acid fluoride, or ammonium bifiuoride to generate a fluoride anion in the bath.
  • the essential features of. my invention are illustrated by the following specific examples for producing smooth, uniform adherent coatings of zinc onaluminum articles.
  • My process is suit able for producing metallic deposits on aluminum articles or alloys thereof containing aluminum as the essential component.
  • the expression aluminu in the claims is intended to include articles made of commercially pure aluminum or aluminum alloys having aluminum as the 'essential component.
  • the aluminum article is first thoroughly degreased and cleaned so as to remove any grease, dirt or other undesirable foreign materials on the surface of the aluminum article.
  • the aluminum article is first immersed in an organic solvent, such as trichloroethylene.
  • the article is then treated toremove the surface oxide film in order 'to activate the surface.
  • the aluminum article may be immersed for about one to three minutes at room temperature in a bath containing 0.5.to 5.0 N hydrofluoric acid.
  • the articletreated is made of an aluminum alloy a film may 'remain on the surface of the article which consists of the metals-alloyed with the aluminum. It may be readily removed by dipping the article in 50% or more by volume of nitric acid at room temperature from ten to twenty seconds. This treatment is then followed by a cold water rinse. Warm or hot water should not be used to rinse the aluacid may be increased up to a maximum of 2.5 N with increase in the zinc sulfate concentration.
  • minum article because of the tendency to form an oxide film on the aluminum "surface which may interfere with the subsequent immersion process.
  • Aluminum articles may also be satisfactorily cleaned preparatory to my immersion'process by jusing suitably inhibited alkaline cleaners such as caustic soda or trisodium phosphate.
  • alkaline cleaners such as caustic soda or trisodium phosphate.
  • a solution of 50 g./l of sodium hydroxide at ,a temperature of 65 "C- is satisfactory.
  • the aluminum article after preliminary cleaning treatment previously described is then immersed in an aqueous bath containing "a zinc cation and a fluoride anion.
  • the bath for example may have zinc sulfate and hydrofluoric acid as its essential agents.
  • the aluminum article is immersedin this bam'rrom seconds to 5'minutes atab'out 20 C. room temperature or as high as 50 C. if desired to produce a clear, uniform gray color, strongly adherent zinc coating on the surface of the aluminum.
  • the hydrofluoric concentration is about 0.2 N.
  • the concentration of hydrofluoric Fromthe above" data it'is seen that the fluoride salts are just "as effective as hydrofiuoric'acid. Neither hydrofluoric acid nor the fluoride salts were effective below a concentration of 0.2 normal and the "plated coatings blistered in the furnace. While fthe zinc sulfate solutions and hydrofluoric acid were miscible in allproportions, there was a maximumsolubility of the fluoride salts in the 5 normalzinc sulfatesolu'tion.
  • the precipitate'which formed at the fluoride salt "concentrationsgiven in the table was probably the zinc alkali fluoride complex 0 POssibly zinc hydroxide'or basic zinc sulfate. This fixesan upper limit to the fluoride range at'which good deposits are obtained, and this is much narrower than that obtained withhydrofiuoric 'acid.
  • a convenient way of maintaining a 'fixe'd fluoride'concentration is available by keeping the solution saturated with the fluoride" salt.
  • the salt is easier to handle than the acid both for preparing the solution and making additions.
  • the concentration temperature and time in the hydrofluoric acid dip for activating the aluminum surface are not critical and the dip is effective under a wide range of conditions. The optimum conditions must be determined for each article plated depending on its alloy composition and surface condition.
  • the 0.5 N solution at room temperature is recommended and the time of dip should be sufiicient to activate the surface and permit maximum adhesion without removing too much metal and possibly etching the aluminum.
  • the eifect of variation in the time of immersion of the aluminum in the zinc immersion solution consisting of N zinc sulfate and 1 N hydrofluoric acid was studied. It was found that the immersion time was not critical and that satisfactory deposits were obtained when the time varied from ten seconds to two minutes. The zinc films had a uniform gray color. There was a slight amount of gassing, which increased in amount with time, but which was dislodged from the panel by the mild agitation during the immersion. On the basis of this work, the preferred time in the zinc immersion solution is 30 to 60 seconds. The thickness of coating thus produced is self-limiting as soon as the entire aluminum surface is coated.
  • the aluminum article may be connected as the cathode to a suitable source of direct current to produce excellent adherent deposits.
  • a fluoride salt to supply the fluoride anion rather than hydrofluoric acid so as not to develop too high acidity in the bath.
  • the temperature of the standard 5 N zinc sulfate-1 N hydrofluoric acid immersion solution was 25 C. in the previously noted work.
  • the effect of raising the temperature of this solution to 45 C., on the quality of the final copper electroplate was studied and evaluated by the Furnace Test.
  • the higher temperature had the effect of giving a heavier zinc coating and decreased the permissible immersion time from two minutes at 25 C. to 20 seconds.
  • the immersion solution should therefore be kept at room temperature, preferably between 20 and 25 C.
  • a suitable bath for such purpose consists of:
  • the hydrolyzed glue is prepared by adding one cc. of sodium hydroxide solution to 100 cc. of 10% bone glue solution and boiling under a reflux condenser for two hours. The excess alkali is neutralized with sulfuric acid and the solution then filtered to remove suspended matter.
  • Goulac is a concentrated sulfite paper pulp process waste and contains lignin sulfonates.
  • the optimum time of immersion of the aluminum in the tin solution is important for good results and is relatively critical.
  • the preferred time of immersion varies with the concentra- 1 tions of stannous sulfate and hydrofluoric acid.
  • the immersion time should not be longer than about ten seconds.
  • the amount of stannous sulfate in the bath may range from 0.5 to 2.5 N and the hydrofluoric acid from 0.25 to 5 N.
  • other metals nobler than aluminum can be successfully deposited on aluminum by immersion in a bath containing the cadmium cation and the fluoride anion.
  • satisfactory deposits can be obtained on aluminum articles which have been first pre-cleaned as previously described and then immersing the aluminum articles ina bath containing cadmium sulfate in amount 0.02 N to 0.055 N and hydrofluoric acid in amount 0.5 N to 12 N. It is advantageous to add a small amount of glue to improve the structure of the coating.
  • a preferred bath for general purposes contains 3 N hydrofluoric acid, 0.035 N cadmium sulfate and 2 g./l. hydrolyzed glue. Agitation of the aluminum article during immersion for about 5 to 15 seconds at roomtemperature is desirable to obtain deposits of uniform sound structure.
  • I may produce alloy coatings of metals on aluminum in accordance with my invention by utilizing a bath containing two or more metal cations.
  • a zinc-cadmium alloy coating on aluminum can be produced by immersing the aluminum article as cathode in a bath having 5 N zinc sulfate, 1 N cadmium sulfate, and 1 N hydrofluoric acid and passing direct current for about ten minutes using a current density 10 amps. per sq. ft. Satisfactory alloy coatings with or without the use of'current can be obtained particularly when the metals are close to each other in the electromotive series, such as zinc and cadmium, nickel and iron, nickel and cobalt, etc.
  • the present invention thus makes it possible to deposit metals on aluminum for any desired purpose, either for protecting the aluminum, for electrodeposition of other metals thereon. orfor receiving other coatings such as paint, lacquer, plastic films and the like.
  • the method. of coating aluminum articles Withanadherent smooth deposit of zinc which comprises cleaning the aluminum article to remove substantially all of the surface oxide film and immersing the cleaned aluminumarticle in an aqueous bath consisting essentially of water, a Water-soluble zinc salt and'a water-soluble; fluoride, the concentration-0f the zinc salt in said bath being in the range of 3 N to, 7 N and the concentration of the fluoride being in the range of 0.2 N to'2.5 N.
  • the method of coating aluminumarticles with an adherent, smooth deposit of zinc which comprises cleaning the aluminum article to remove substantially all of the surface oxide film and immersing the cleaned aluminum article in an-aqueous bath consisting essentially of water,
  • immersing the. cleaned aluminum article from- 301 seconds to aboutz5. minutesin. an aqueous bath.
  • said. bath consisting essentially; of water, .zincsulfate. and hydrofluoric acid the; concentration of.- zinc su1.- fate in said bath being: irrthe; range, of .3 N to? N:
  • an aqueous bath consisting essentially of. water. zinc sulfate and hydrofluoricacid, the concentration of zinc sulfate in saidbath: being about; 5. N andthe concentration. of hydrofluoric; acidbeing about 1'. N.
  • tion of the zinc salt in said bath being in the. range of 3N to 7 N and; the concentration of.
  • the fluoride being in the. range ofv 0.2 N to 2.5 N.
  • metallic zinc on a. clean aluminum surfacesubstantially free of surface oxide film. which consists essentially of water, zinc sulfate and hydro.- fiuoric acid, the concentration of the zinc sulfate in said bath being in the range of 3 N to 7 N and the concentration of thehydrofluoric acid being in therange of 0.2 N to 2.5 N. 1

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  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
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Description

.of suitable composition.
Patented Jan. 1, 1952 ME'IIHOD AND COMPOSITION FOR COATING ALUMINUM WITH ZINC Samuel Heiman, Philadelphia, Pa., assignor to Philadelphia Rust-Proof Co., Philadelphia, Pa.,
No Drawing. Application July 31, 1948,
Serial No. 41,891
6 Claims.
This invention relates to a method of coating metals on articles of aluminum or alloys thereof by immersion of the articles in aqueous solutions More specifically the invention relates to a. method of producing smooth and adherent deposits of metals nobler than aluminum on aluminum surfaces by immersion in aqueous baths without the use of electric current. The immersion deposits have a sound structure and such an unusually high degree of adhesion to the aluminum that they may be used as a base for the subsequent electrodeposition of other metals. For example, zinc, cadmium, tin, and other metals may be deposited on aluminum in accordance with the present invention which have a greater bond to the aluminum than the cohesive strength of the aluminum base metal itself.
Hitherto, electroplated coatings upon aluminum have assumed an important place among the finishes for this metal because the light weight and low cost of aluminum are combined with the specific desirable properties of. the plated coating. Thus, aluminum is plated with silver for increased surface conductivity on contacts and electronic parts, with cadmium .and nickel for improved solderability, brass for bonding to rubber, heavy chromium for wear resistance and decorative chromium on nickel for improved appearance and abrasion resistance." The applications are manifold and continually increasing. The difficulty in plating on aluminum results from the high potential of the metal which ordinarily tends to produce loosely adherent immersion deposits and the ever present surface oxide film. The problem has been attacked previously by five gen? eral methods:
1. Etching the surface.Aluminum may be etched in a mixture of nitric and hydrofluoric acids and then nickel plated. The adhesion of the nickel to the aluminum depended to a large extent on the keying action of the nickel deposit in the pits in the aluminum surface.
2. Deposition of a bonding metal by electrochemical displacement-The aluminum oxide film may be replaced by a metal deposited on the aluminum by electrochemical displacement. The immersion coating then serves as a base for the subsequent electrodeposition of other metals. Several processes have been proposed for depositing iron, manganese, nickel, and cadmium from hydrochloric acid solutions. In these processes, however, the aluminum was pitted by the hydrochloric acid and the adhesion attained was more the result of a mechanical keying action, in the pits in the aluminum than a true adhesion of the two metals. The process involving the deposition of zinc by immersion on the aluminum from a highly alkaline zincate solution has been much more successful in securing the highest degree of adhesion without pitting the base metal.
3. Anodz'c treatment.The natural oxide coating on aluminum may be replaced by a relatively thick, porous, anodic oxide coating. The electroplated metal adheres to the aluminum by virtue of filling the pores of the oxide coating.
4. Special plating solutions.--Various methods have been proposed for plating zinc, cadmium, copper and nickel directly on aluminum, usually from solutions of various compositions, but none of these coatings has the degree of adhesion'required.
5. Miscellaneous methods.-Copper has been deposited by' immersion on aluminum from molten cuprous chloride at 450 C. A high degree of adhesion is obtained but the physical properties resulting from heat treatment of the aluminum are adversely affected and the process, in generaL is more difiicult than those described'above.
Of all the methods which have been'devised and studied, only two produce smooth and adherent deposits and are used commercially today. They are the zinc immersion process and the anodic coating process. The former process is much more widely used because it is applicable to more alloys, requires less equipment and time, and the conditions are less critical. g
I have discovered that it is possible to produce smooth, extremely adherent and uniform coatings on aluminum surfaces of metals nobler than aluminum by immersion of the cleaned aluminum in aqueous baths containing water-soluble flue orides or fluoride complexes of the metal desired to be deposited, such as zinc, cadmium, tin, iron, nickel, cobalt or manganese, or alloys thereof. It is also possible to produce uniform coatings'of silver, gold, copper and antimony, or alloys thereof, on aluminum in accordance with my invention, although the coatings of these metals are not quite as adherent as in the case of the metals previously mentioned. I may also use suitable water-soluble salts of these metals with the addition of suitable amounts of hydrofluoric acid, sodium fluoride, ammonium fluoride, or ammonium acid fluoride, or ammonium bifiuoride to generate a fluoride anion in the bath.
The essential features of. my invention are illustrated by the following specific examples for producing smooth, uniform adherent coatings of zinc onaluminum articles. My process is suit able for producing metallic deposits on aluminum articles or alloys thereof containing aluminum as the essential component. The expression aluminu in the claims is intended to include articles made of commercially pure aluminum or aluminum alloys having aluminum as the 'essential component. The aluminum article is first thoroughly degreased and cleaned so as to remove any grease, dirt or other undesirable foreign materials on the surface of the aluminum article. For example, the aluminum article is first immersed in an organic solvent, such as trichloroethylene. The article is then treated toremove the surface oxide film in order 'to activate the surface. For this purpose the aluminum article may be immersed for about one to three minutes at room temperature in a bath containing 0.5.to 5.0 N hydrofluoric acid. In case the articletreated is made of an aluminum alloy a film may 'remain on the surface of the article which consists of the metals-alloyed with the aluminum. It may be readily removed by dipping the article in 50% or more by volume of nitric acid at room temperature from ten to twenty seconds. This treatment is then followed by a cold water rinse. Warm or hot water should not be used to rinse the aluacid may be increased up to a maximum of 2.5 N with increase in the zinc sulfate concentration.
For general plating purposes, a very satisfactory bath composition well within the preferred range is for example:
'in the'table. The zinc sulfate concentrationin all'cases was 5' normal. In the furnace test, the coated panel was heated in a furnace at 300 C. for 2 hours according to theprocedure given by Ferguson, Monthly Rev. Electroplaters Soc, vol. 33, 295 (1946).
Table Fluoride Salt Concentration of Fluoride Salt mixed with 5 N ZnSO4.7H2O at which- Precipitate Formed in ZnSO4.7H:O Fluoride Salt Copper Deposits on Zine Film passed Furnace 'lest Mixture Sodium Fluoride. NaF... earl-0.4 N 0.4 N Potassium Fluoride, KF.2HiO 0.2'N0.4 N 0.'4N Ammonium Fluoride, NH4F 0. 2 Nl.0 N 1.0 N Ammonium Acid Fluoride, NH F.HF 0.2 Nl.0 N 1.0 N
minum article because of the tendency to form an oxide film on the aluminum "surface which may interfere with the subsequent immersion process.
Aluminum articles may also be satisfactorily cleaned preparatory to my immersion'process by jusing suitably inhibited alkaline cleaners such as caustic soda or trisodium phosphate. For example, a solution of 50 g./l of sodium hydroxide at ,a temperature of 65 "C- is satisfactory.
The aluminum article after preliminary cleaning treatment previously described is then immersed in an aqueous bath containing "a zinc cation and a fluoride anion. The bath for example may have zinc sulfate and hydrofluoric acid as its essential agents. According'to my invention theranges of these ingredients in the bath'are 3Nto 7 N of fzinc'sulfate and 0.2 N to 2.5 N hydrdfiuoric acid. The aluminum article is immersedin this bam'rrom seconds to 5'minutes atab'out 20 C. room temperature or as high as 50 C. if desired to produce a clear, uniform gray color, strongly adherent zinc coating on the surface of the aluminum. v
The cohesion of thezinc coating "to the'aluminum thus produced has been 'found'to be greater than the cohesive strength of the aluminum base itself as determined by theOllard Test. Iron Age, vol. 146, 17-20 (1940),Trans. Faraday Soc.', vol. 21, 81 (1925).
There is a considerable range of concentrations of thetwo components of the immersion bath's'at whichexcellent'zinc deposits may be obtained. The hydrofluoric concentration. is about 0.2 N. The concentration of hydrofluoric Fromthe above" data, it'is seen that the fluoride salts are just "as effective as hydrofiuoric'acid. Neither hydrofluoric acid nor the fluoride salts were effective below a concentration of 0.2 normal and the "plated coatings blistered in the furnace. While fthe zinc sulfate solutions and hydrofluoric acid were miscible in allproportions, there was a maximumsolubility of the fluoride salts in the 5 normalzinc sulfatesolu'tion. The precipitate'which formed at the fluoride salt "concentrationsgiven in the table was probably the zinc alkali fluoride complex 0 POssibly zinc hydroxide'or basic zinc sulfate. This fixesan upper limit to the fluoride range at'which good deposits are obtained, and this is much narrower than that obtained withhydrofiuoric 'acid. On' the other hand, a convenient way of maintaining a 'fixe'd fluoride'concentration is available by keeping the solution saturated with the fluoride" salt. Furthermore, the salt is easier to handle than the acid both for preparing the solution and making additions.
The effect of varying the temperature and concentration of 'the hydrofluoric acid dip was studied for its effect "on" the "quality of the "zinc immersion coating as measuredby the Furnace Test on the "copper 'electrodeposits.
Tests we're made with 025 N h'ydrofluo'ric'a'cld at 40 C. and the results compared with those obtained at the-standard 25 C. It was found that, in general, "the activity'of the reaction'of hydrofluoric acid on aluminum "at 40 Cg-was approximately twice that at 25 Cyandtheminimum time in the acid dip therefore could be halved.
' The effect of acid concentration was studied with 0.5 N, 1.5N and 3.0 N hydrofluoric acid solutions at 25 C. There was a considerable increase in the activity of the acid with increase in strength. With a fifteen second'dip in 3.0 N acid, an aluminum pan'el plated according to the present method passed the Furnace Test.
The concentration temperature and time in the hydrofluoric acid dip for activating the aluminum surface are not critical and the dip is effective under a wide range of conditions. The optimum conditions must be determined for each article plated depending on its alloy composition and surface condition.
' In general, the 0.5 N solution at room temperature is recommended and the time of dip should be sufiicient to activate the surface and permit maximum adhesion without removing too much metal and possibly etching the aluminum.
The eifect of variation in the time of immersion of the aluminum in the zinc immersion solution consisting of N zinc sulfate and 1 N hydrofluoric acid was studied. It was found that the immersion time was not critical and that satisfactory deposits were obtained when the time varied from ten seconds to two minutes. The zinc films had a uniform gray color. There was a slight amount of gassing, which increased in amount with time, but which was dislodged from the panel by the mild agitation during the immersion. On the basis of this work, the preferred time in the zinc immersion solution is 30 to 60 seconds. The thickness of coating thus produced is self-limiting as soon as the entire aluminum surface is coated. However, if thicker zinc or other metal coatings are desired, the aluminum article may be connected as the cathode to a suitable source of direct current to produce excellent adherent deposits. When using current I prefer to use baths containing a fluoride salt to supply the fluoride anion rather than hydrofluoric acid so as not to develop too high acidity in the bath.
The temperature of the standard 5 N zinc sulfate-1 N hydrofluoric acid immersion solution was 25 C. in the previously noted work. The effect of raising the temperature of this solution to 45 C., on the quality of the final copper electroplate was studied and evaluated by the Furnace Test. The higher temperature had the effect of giving a heavier zinc coating and decreased the permissible immersion time from two minutes at 25 C. to 20 seconds. The immersion solution should therefore be kept at room temperature, preferably between 20 and 25 C. I prefer to use zinc sulfate in my baths but other zinc salts such as zinc chloride, zinc nitrate and zinc acetate may be used instead.
Excellent deposits of tin on aluminum surfaces can also be produced in accordance with the present invention. A suitable bath for such purpose consists of:
SnSC4=L5 N (161.1 g./l.) I
HF=2.0 N (70.0 ml./l. of 48% acid) Hydrolyzed glue: 1.0 g./l. Goulac=0.2 g./l. Purified residue acid: 1.3 ml./l.
The hydrolyzed glue is prepared by adding one cc. of sodium hydroxide solution to 100 cc. of 10% bone glue solution and boiling under a reflux condenser for two hours. The excess alkali is neutralized with sulfuric acid and the solution then filtered to remove suspended matter.
Goulac is a concentrated sulfite paper pulp process waste and contains lignin sulfonates.
Purified residue acid is a mixture of high boiling coal tar phenols and had the following distillation range: I. B. P.=102.; 5%:212"; 10%: 222; 30%:232; 50%:235"; '70%=238 C.; E. P.=%:276 C. V
Without the presence of addition agents, a heavy, block, pulverulent deposit of tin is precipitated on the aluminum which could be easily wiped off. The addition of glue and cresylic acid, to the stannous sulfate-hydrofluoric acid system results-in sound, homogeneous tin deposits. Further improvement is efiected by using a mixture of hydrolyzed glue, goulac and purified residue acid. These addition agents are added to the SnSOr-HF solution in the order given above and with vigorous stirring. The solution is then filtered through coarse filter paper to remove suspended matter and excess purified residue acid. The presence of small amounts of hydrophilic colloids in these solutions leads to smoother, brighter, and harder deposits of smaller grain size and less ductility.
Good agitation of the aluminum in the tin solution is essential for sound tin immersion deposits. Lack of agitation may result in dark streaks in the tin and subsequently poor adhesion of the copper plate.
The optimum time of immersion of the aluminum in the tin solution is important for good results and is relatively critical. The preferred time of immersion varies with the concentra- 1 tions of stannous sulfate and hydrofluoric acid.
The lower the SnSO4 and the higher the HF concentrations, the shorter the time for good tin deposits. In general, the immersion time should not be longer than about ten seconds.
The amount of stannous sulfate in the bath may range from 0.5 to 2.5 N and the hydrofluoric acid from 0.25 to 5 N. As previously stated, other metals nobler than aluminum can be successfully deposited on aluminum by immersion in a bath containing the cadmium cation and the fluoride anion. For example, satisfactory deposits can be obtained on aluminum articles which have been first pre-cleaned as previously described and then immersing the aluminum articles ina bath containing cadmium sulfate in amount 0.02 N to 0.055 N and hydrofluoric acid in amount 0.5 N to 12 N. It is advantageous to add a small amount of glue to improve the structure of the coating. A preferred bath for general purposes contains 3 N hydrofluoric acid, 0.035 N cadmium sulfate and 2 g./l. hydrolyzed glue. Agitation of the aluminum article during immersion for about 5 to 15 seconds at roomtemperature is desirable to obtain deposits of uniform sound structure.
I may produce alloy coatings of metals on aluminum in accordance with my invention by utilizing a bath containing two or more metal cations. For example, a zinc-cadmium alloy coating on aluminum can be produced by immersing the aluminum article as cathode in a bath having 5 N zinc sulfate, 1 N cadmium sulfate, and 1 N hydrofluoric acid and passing direct current for about ten minutes using a current density 10 amps. per sq. ft. Satisfactory alloy coatings with or without the use of'current can be obtained particularly when the metals are close to each other in the electromotive series, such as zinc and cadmium, nickel and iron, nickel and cobalt, etc.
- According:tothe-presentinvention it is. pos-.
sible to produce on aluminum articles depositsdesired to-be deposited and -a fluoride anion. The
scientific basis of my invention is not fully known to me but it appears that the fluoride anion has a. very high solvent action on, the surface oxide which. may be present on the aluminum, the pres? ence of which normally preventsadherent immersion coatings on aluminum. My immersion bath acts to remove-the. oxide film present and. permits. the metal to be deposited on the alumi-- num surface in metal to metal contact before any substantial formation of an intervening oxide film. The metal to metal contact of zinc and aluminum produced by my immersion bath is. so. intimate that the bond between the zinc de.--
positand the aluminum surface is greater than the cohesive strength of the aluminum base metal itself. The present invention thus makes it possible to deposit metals on aluminum for any desired purpose, either for protecting the aluminum, for electrodeposition of other metals thereon. orfor receiving other coatings such as paint, lacquer, plastic films and the like.
, It will be apparent that the novel and essential features-ofmy invention may be utilized to prepare a large number of immersion baths depending upon the metal desired to be coated. the aluminum article to be coated and the operating conditions under which the coating is to be carried out. The specific examples given herein are intended to be illustrative embodiments of the basic essential features of my invention as defined in the appended claims.
I claim:
1. The method. of coating aluminum articles Withanadherent smooth deposit of zinc which comprises cleaning the aluminum article to remove substantially all of the surface oxide film and immersing the cleaned aluminumarticle in an aqueous bath consisting essentially of water, a Water-soluble zinc salt and'a water-soluble; fluoride, the concentration-0f the zinc salt in said bath being in the range of 3 N to, 7 N and the concentration of the fluoride being in the range of 0.2 N to'2.5 N.
.2. The method of coating aluminumarticles with an adherent, smooth deposit of zinc which comprises cleaning the aluminum article to remove substantially all of the surface oxide film and immersing the cleaned aluminum article in an-aqueous bath consisting essentially of water,
81' sulfat and. hy rofluoric ac d; he concentrati noi: sulfate in said bath being. in the;
range; of-
to- 7 N and the-concentration ofvhydrofluon'c acid being in the range. of 0.2 N to 2.5.N.. 3. The method. of coating. aluminum articles with; an adherent; sm oth dep t. f zinc which.
comprisescleaningthe aluminum articleto re? move: substantially 'all. of the surface. oxide film,
immersing: the. cleaned aluminum article from- 301 seconds to aboutz5. minutesin. an aqueous bath.
aha-temperature.from20 to 50C.. said. bath consisting essentially; of water, .zincsulfate. and hydrofluoric acid the; concentration of.- zinc su1.- fate in said bath being: irrthe; range, of .3 N to? N:
and. theconcentration. of hydrofluoric acid being. in:.the.- range" of 0.2 N to 2.5118.
4.. The. method of coating aluminum articles. with an-adherent smooth depositof zinc which.
comprises cleaning the aluminum article-to re.- movesubstantially. all. of. the: surface oxidez'film and: immersing the cleaned aluminum article :in.
an aqueous bath. consisting essentially of. water. zinc sulfate and hydrofluoricacid, the concentration of zinc sulfate in saidbath: being about; 5. N andthe concentration. of hydrofluoric; acidbeing about 1'. N.
5. An immersion aqueousbath for depositing. metallic-zinc on :a clean aluminum surface-sub-.- stantially fr'ee of" surfacev oxide film which; com sists essentially of water, a. water-soluble; zinc.
salt and a water-soluble fluoride, the concentra:
tion of the zinc salt in said bath being in the. range of 3N to 7 N and; the concentration of.
the fluoride being in the. range ofv 0.2 N to 2.5 N.
6. An immersion aqueous bath for depositing:
metallic zinc on a. clean aluminum surfacesubstantially free of surface oxide film. which consists essentially of water, zinc sulfate and hydro.- fiuoric acid, the concentration of the zinc sulfate in said bath being in the range of 3 N to 7 N and the concentration of thehydrofluoric acid being in therange of 0.2 N to 2.5 N. 1
SAMUEL HEIMAN.
REFERENCES" CITED The following referencesare of record in the file of this patent:
PATENTS.

Claims (2)

1. THE METHO OF COATING ALUMINUM ARTICLES WITH AN ADHERENT SMOOTH DEPOSIT OF ZINC WHICH COMPRISES CLEANING THE ALUMINUM ARTICLE TO REMOVE SUBSTANTIALLY ALL OF THE SURFACE OXIDE FILM AND IMMERSING THE CLEANED ALUMINUM ARTICLE IN AN AQUEOUS BATH CONSISTING ESSENTIALLY OF WATER, A WATER-SOLUBLE ZINC SALT AND A WATER-SOLUBLE FLUORIDE, THE CONCENTRATION OF THE ZINC SALT IN SAID BATH BEING IN THE RANGE OF 3 N TO 7 N AND THE CONCENTRATION OF THE FLUORIDE BEING IN THE RANGE OF 0.2 N TO 2.5 N.
5. AN IMMERSION AQUEOUS BATH FOR DEPOSITING METALLIC ZINC ON A CLEAN ALUMINUM SURFACE SUBSTANTIALLY FREE OF SURFACE OXIDE FILM WHICH CONSISTS ESSENTIALLY OF WATER, A WATER-SOLUBLE ZINC SALT AND A WATER-SOLUBLE FLUORIDE, THE CONCENTRATION OF THE ZINC SALT IN SAID BATH BEING IN THE RANGE OF 3 N TO 7 N AND THE CONCENTRATION OF THE FLUORIDE BEING IN THE RANGE OF 0.2 N TO 2.5 N.
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Cited By (31)

* Cited by examiner, † Cited by third party
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US2624684A (en) * 1951-12-03 1953-01-06 Philadelphia Rust Proof Co Method and composition for coating aluminum with tin
US2662831A (en) * 1950-07-19 1953-12-15 Anderson Brass Works Method of bonding copper to aluminum or aluminum alloys
US2694017A (en) * 1952-09-16 1954-11-09 Gen American Transporation Cor Process of chemical nickel plating of aluminum and its alloys and baths therefor
US2694019A (en) * 1952-04-23 1954-11-09 Gen Am Transport Processes of chemical nickel plating and baths therefor
US2730490A (en) * 1951-11-13 1956-01-10 Wire Coating And Mfg Co Process of zinc coating magnesium articles
US2739932A (en) * 1952-09-05 1956-03-27 Clarence W Forestek Electrodepositing chromium on aluminum
US2811466A (en) * 1953-03-18 1957-10-29 Metal Diffusions Inc Process of chromizing
US2814589A (en) * 1955-08-02 1957-11-26 Bell Telephone Labor Inc Method of plating silicon
US2825682A (en) * 1953-08-31 1958-03-04 Menasco Mfg Company Process and composition for coating titanium surfaces
US2830881A (en) * 1954-01-25 1958-04-15 Kaiser Aluminium Chem Corp Treatment of material
US2850441A (en) * 1954-12-28 1958-09-02 Gen Motors Corp Chemical displacement process of plating cadmium on aluminum
US2932585A (en) * 1955-10-24 1960-04-12 Robertson Co H H Enameled aluminum products and methods of making the same
US2938841A (en) * 1956-04-13 1960-05-31 Olin Mathieson Preparation of zirconium for cold working
US2940867A (en) * 1958-12-24 1960-06-14 Du Pont Immersion tin plating and composition therefore
US2948643A (en) * 1958-01-22 1960-08-09 Turco Products Inc Process and compositions for producing aluminum surface conversion coatings
US3193474A (en) * 1959-07-13 1965-07-06 M & T Chemicals Inc Plating on aluminum
DE1203567B (en) * 1957-06-06 1965-10-21 Dow Chemical Co Bath for electroless nickel plating, especially of magnesium and its alloys
US3328271A (en) * 1964-09-22 1967-06-27 Nat Res Corp Method of electroplating copper on niobium-zirconium alloy superconductors for stabilization
US3472742A (en) * 1966-03-15 1969-10-14 Webb James E Plating nickel on aluminum castings
US3489657A (en) * 1968-09-30 1970-01-13 Sylvania Electric Prod Process for producing solderable aluminum materials
US3493474A (en) * 1966-04-29 1970-02-03 Gen Motors Corp Aluminum plating process
US3694899A (en) * 1969-10-22 1972-10-03 Chausson Usines Sa Process for brazing parts of aluminium and aluminium alloys
US3754970A (en) * 1970-10-29 1973-08-28 Fujitsu Ltd Method of plating beryllium article with zinc
EP0125832A1 (en) * 1983-05-09 1984-11-21 Alcan International Limited Deposition of zinc on aluminium
US5389453A (en) * 1991-09-05 1995-02-14 Kabushiki Kaisha Kobe Seiko Sho Aluminum alloy material having a surface of excellent zinc phosphate processability
WO1996041040A1 (en) * 1995-06-07 1996-12-19 Atotech Usa Inc. Etchant for aluminium alloys
US20050008788A1 (en) * 2003-06-26 2005-01-13 Joshi Nayan H. Aqueous acidic immersion plating solutions and methods for plating on aluminum and aluminum alloys
US9698283B2 (en) 2013-06-20 2017-07-04 PLANT PV, Inc. Core-shell nickel alloy composite particle metallization layers for silicon solar cells
US9741878B2 (en) 2015-11-24 2017-08-22 PLANT PV, Inc. Solar cells and modules with fired multilayer stacks
US10418497B2 (en) 2015-08-26 2019-09-17 Hitachi Chemical Co., Ltd. Silver-bismuth non-contact metallization pastes for silicon solar cells
US10550291B2 (en) 2015-08-25 2020-02-04 Hitachi Chemical Co., Ltd. Core-shell, oxidation-resistant, electrically conducting particles for low temperature conductive applications

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US1045718A (en) * 1912-04-29 1912-11-26 Quintin Marino Treatment of surfaces of aluminium or its alloys for the deposition of metals thereon.
US1607676A (en) * 1924-10-29 1926-11-23 Firm Dr Otto Sprenger Patentve Process for obtaining metal coatings on articles of aluminum and aluminum alloys
US1723067A (en) * 1926-04-16 1929-08-06 Pacz Aladar Method and composition of matter for coating and coloring metal articles
US1984624A (en) * 1931-06-15 1934-12-18 Bohn Aluminium & Brass Corp Method of forming connecting rods
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Cited By (38)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2662831A (en) * 1950-07-19 1953-12-15 Anderson Brass Works Method of bonding copper to aluminum or aluminum alloys
US2730490A (en) * 1951-11-13 1956-01-10 Wire Coating And Mfg Co Process of zinc coating magnesium articles
US2624684A (en) * 1951-12-03 1953-01-06 Philadelphia Rust Proof Co Method and composition for coating aluminum with tin
US2694019A (en) * 1952-04-23 1954-11-09 Gen Am Transport Processes of chemical nickel plating and baths therefor
US2739932A (en) * 1952-09-05 1956-03-27 Clarence W Forestek Electrodepositing chromium on aluminum
US2694017A (en) * 1952-09-16 1954-11-09 Gen American Transporation Cor Process of chemical nickel plating of aluminum and its alloys and baths therefor
US2811466A (en) * 1953-03-18 1957-10-29 Metal Diffusions Inc Process of chromizing
US2825682A (en) * 1953-08-31 1958-03-04 Menasco Mfg Company Process and composition for coating titanium surfaces
US2830881A (en) * 1954-01-25 1958-04-15 Kaiser Aluminium Chem Corp Treatment of material
US2850441A (en) * 1954-12-28 1958-09-02 Gen Motors Corp Chemical displacement process of plating cadmium on aluminum
US2814589A (en) * 1955-08-02 1957-11-26 Bell Telephone Labor Inc Method of plating silicon
US2932585A (en) * 1955-10-24 1960-04-12 Robertson Co H H Enameled aluminum products and methods of making the same
US2938841A (en) * 1956-04-13 1960-05-31 Olin Mathieson Preparation of zirconium for cold working
DE1203567B (en) * 1957-06-06 1965-10-21 Dow Chemical Co Bath for electroless nickel plating, especially of magnesium and its alloys
US2948643A (en) * 1958-01-22 1960-08-09 Turco Products Inc Process and compositions for producing aluminum surface conversion coatings
US2940867A (en) * 1958-12-24 1960-06-14 Du Pont Immersion tin plating and composition therefore
US3193474A (en) * 1959-07-13 1965-07-06 M & T Chemicals Inc Plating on aluminum
US3328271A (en) * 1964-09-22 1967-06-27 Nat Res Corp Method of electroplating copper on niobium-zirconium alloy superconductors for stabilization
US3472742A (en) * 1966-03-15 1969-10-14 Webb James E Plating nickel on aluminum castings
US3493474A (en) * 1966-04-29 1970-02-03 Gen Motors Corp Aluminum plating process
US3489657A (en) * 1968-09-30 1970-01-13 Sylvania Electric Prod Process for producing solderable aluminum materials
US3694899A (en) * 1969-10-22 1972-10-03 Chausson Usines Sa Process for brazing parts of aluminium and aluminium alloys
US3754970A (en) * 1970-10-29 1973-08-28 Fujitsu Ltd Method of plating beryllium article with zinc
EP0125832A1 (en) * 1983-05-09 1984-11-21 Alcan International Limited Deposition of zinc on aluminium
AU571871B2 (en) * 1983-05-09 1988-04-28 Alcan International Limited Deposition of zinc on aluminium
US5389453A (en) * 1991-09-05 1995-02-14 Kabushiki Kaisha Kobe Seiko Sho Aluminum alloy material having a surface of excellent zinc phosphate processability
US5601695A (en) * 1995-06-07 1997-02-11 Atotech U.S.A., Inc. Etchant for aluminum alloys
WO1996041040A1 (en) * 1995-06-07 1996-12-19 Atotech Usa Inc. Etchant for aluminium alloys
US20050008788A1 (en) * 2003-06-26 2005-01-13 Joshi Nayan H. Aqueous acidic immersion plating solutions and methods for plating on aluminum and aluminum alloys
WO2005010233A3 (en) * 2003-06-26 2005-02-24 Atotech Deutschland Gmbh Aqueous acidic immersion plating solutions and methods for plating on aluminum and aluminum alloys
US7407689B2 (en) * 2003-06-26 2008-08-05 Atotech Deutschland Gmbh Aqueous acidic immersion plating solutions and methods for plating on aluminum and aluminum alloys
US9698283B2 (en) 2013-06-20 2017-07-04 PLANT PV, Inc. Core-shell nickel alloy composite particle metallization layers for silicon solar cells
US10550291B2 (en) 2015-08-25 2020-02-04 Hitachi Chemical Co., Ltd. Core-shell, oxidation-resistant, electrically conducting particles for low temperature conductive applications
US10418497B2 (en) 2015-08-26 2019-09-17 Hitachi Chemical Co., Ltd. Silver-bismuth non-contact metallization pastes for silicon solar cells
US9741878B2 (en) 2015-11-24 2017-08-22 PLANT PV, Inc. Solar cells and modules with fired multilayer stacks
US10000645B2 (en) 2015-11-24 2018-06-19 PLANT PV, Inc. Methods of forming solar cells with fired multilayer film stacks
US10233338B2 (en) 2015-11-24 2019-03-19 PLANT PV, Inc. Fired multilayer stacks for use in integrated circuits and solar cells
US10696851B2 (en) 2015-11-24 2020-06-30 Hitachi Chemical Co., Ltd. Print-on pastes for modifying material properties of metal particle layers

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