US2559812A - Solution and method for coating zinc surfaces - Google Patents
Solution and method for coating zinc surfaces Download PDFInfo
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- US2559812A US2559812A US72751A US7275149A US2559812A US 2559812 A US2559812 A US 2559812A US 72751 A US72751 A US 72751A US 7275149 A US7275149 A US 7275149A US 2559812 A US2559812 A US 2559812A
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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
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/24—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing hexavalent chromium compounds
- C23C22/26—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing hexavalent chromium compounds containing also organic compounds
- C23C22/27—Acids
-
- 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
- C23C22/00—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
- C23C22/05—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions
- C23C22/06—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6
- C23C22/24—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing hexavalent chromium compounds
- C23C22/33—Chemical surface treatment of metallic material by reaction of the surface with a reactive liquid, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using aqueous solutions using aqueous acidic solutions with pH less than 6 containing hexavalent chromium compounds containing also phosphates
Definitions
- This invention relates to the production of a coating on zinc surfaces which is highly adherent, long-lived, attractive in appearance, resistant to corrosion and abrasion and affords a very satisfactory base for paint.
- Zinc surfaces such as those of galvanized sheets exhibit good corrosion resistance in certain locations but have only a limited life when subjected, for example, to industrial atmospheres containing carbon dioxide or sulphur, or to sea air. It has accordingly been proposed to form a protective coating on zinc surfaces by treating them with a solution of salts of chromic and formic acids. I have invented an improved solution and method for producing on zinc surfaces a coating which is not only corrosion resistant but is highly adherent, has a long life even under adverse conditions and imparts a coloration materially enhancing the appearance so that painting is unnecessary. A particular feature of the invention is that it afiords a choice in the color of the coating and a range of shades in each color.
- the solution contains chromic acid or a water-soluble salt thereof, or both, and an organic acid chosen from the group consisting of tartaric, succinic and citric acids.
- the solution preferably contains also a small amount of one or more mineral acids or salts thereof chosen from the group consisting of hydrochloric, sulphuric, nitric and phosphoric acids.
- the coating produced by the invention appears to be a durable film composed largely of insoluble chromate deposited by the interaction of the chromate ions of the solution and metal ions from the zinc surface.
- the organic acid determines the color of the coating or film formed and the shade thereof may be varied by changing the organic acid concentration.
- the mineral acid also modifies the color of the film.
- the solution may be applied at room temperature or may be heated to a moderate temperature, say 140 F.
- the length of contact of the solution with the surface varies inversely with the temperature, i. e., from about 60 seconds at room temperature to about 30 seconds at 140 F.
- I may use other nitrates such as sodium nitrate or nitrates of alkaline earth metals or nitric acid.
- I may use water-soluble salts of the mineral acids instead of the acids themselves, since it is the acid anion which forms the coating film.
- Mineral acid salts of sodium and potassium are specially suitable as substituents for the acids.
- Water-soluble chromates or dichromates such as those of sodium or potassium may be used to replace some or all the chromic acid.
- organic acids tartaric, succinic and citric
- salts of these acids such as those of potassium or sodium may be used instead of the acids but are not as desirable.
- the chromic acid content of the coating solutions should be preferably in the range of 2.5% to 18.0%, or the equivalent in chromium when using chromates. considered as forming chromic acid-chromate mixtures on going into solution.
- the organic acid additions, or respective anion additions from salts thereof, should 'be preferably in the range of 0.5% to 9.0% by weight depending to a great extent on the concentration of chromic acid in the coating solution and the shade of color desired.
- the mineral acid additions, or respective anion additions from salts thereof, should be preferably in the range of 0.1% to 8.0% by weight, the" amount depending on the amounts of chromic acid and organic acid anion present and the shade of color desired.
- Temperature and time of treatment are important. factors inemploying the invention for obtaining both desirable and adherent coatings. Room temperature of about 80 F. is preferable in most cases, but in some cases it is necessary to go to elevated temperatures of 160 to 180 F. to accomplish results. Fifteen seconds to two minutes immersion time is sufficient to promotedesirable coatings in allcases.
- the solution maybe: brushed or flowed thereon, or otherwise brought into contact with the zinc body.
- the resulting chromate coatings on the zinc are highly. resistant to atmospheric and salt" water corrosion. Adherence of the coatings to the zinc surface is good, as indicated by results of bend and abrasion tests. The adherence and appearance of the chromate coatings are enhanced' bythe presence of the additional cons'tituentspresent in the'solutions; namely'organic acid andmineral acid anions. the organic acid anion is, apparently, reduction or partial reduction of chromates at the metalsolution interface.
- a wide range of visible corrosion-resistant coatings varying from a light gold color through brown to a medium green are obtainable by the process of this invention. These coatings are especially suitable for galvanized steel products used in construction for roofing or siding.
- zinc as herein employed 1s mtendedto-include zinc coatingsrolled zinc sheets
- the compounds and amounts thereof may vary as indicated. However, close control is maintained to produce desiredqual'ities', espe- Dichromate's may be The function of v cially combinations of qualities. For instance, in the case of Example III, the solution described produces a medium green protective coating on zinc surfaces, but if the tartaric acid and phosphoric acid components are not controlled to specified amounts, the green coating will deteriorate rapidly under certain conditions such' as exposure to moisture condensates.
- the invention also afiords a greater range of adaptability to needs in coloration and corrosion resistance.
- the organic acid additions control, to a large extent, the color, adherence and corrosion-resisting qualities of the coatings and each acid imparts separate characteristics. These are not generally interchangeable for duplicating results.
- steps including subjecting. the surfacefon a period of from 15 seconds-to 2 minutes,-to contactwith a-solution, acid in character, composed of from l told% of a compound selected from the group consisting of chromic acid and sodium.
- A- solution adapted to form a corrosion-resistant and abrasion-resistant coating on a zinc"- surface composed of'from 4 to 18% of a compound selected from the group consisting of chromic acid and sodium and potassium salts thereof or mixtures but including at least 4% chromic' acid, from .5 to 9% of a compound selected from the'group consisting of tartaric acid, sue'cin'ic acid, citric acid and sodium and potas'- siuni salts thereof 'or mixtures, from .1 to 8% of a compound selected from the group consisting of hydrochloric, sulphuric, nitric and phosphoric acids and sodium and potassium salts thereof or mixtures and the remainder water, the salts in each case being used in anionic equivalent amounts of the amount of acid specified, and the solution being acid in character.
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- Chemical & Material Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Chemical Treatment Of Metals (AREA)
Description
Patented July IO, 1951.
SOLUTION AND METHOD FOR COATING ZINC SURFACES Charles T. Watson, Bessemer, Ala., assignor to Tennessee Coal, Iron and Railroad Company, a
corporation of Alabama No Drawing. Application January 25, 1949, Serial No. 72,751
2 Claims. 1
This invention relates to the production of a coating on zinc surfaces which is highly adherent, long-lived, attractive in appearance, resistant to corrosion and abrasion and affords a very satisfactory base for paint.
This is a continuation-in-part of my application Serial No. 648,025, filed February 15, 1946, now abandoned, for Coated Zinc and Process of Producing the Same.
Zinc surfaces such as those of galvanized sheets exhibit good corrosion resistance in certain locations but have only a limited life when subjected, for example, to industrial atmospheres containing carbon dioxide or sulphur, or to sea air. It has accordingly been proposed to form a protective coating on zinc surfaces by treating them with a solution of salts of chromic and formic acids. I have invented an improved solution and method for producing on zinc surfaces a coating which is not only corrosion resistant but is highly adherent, has a long life even under adverse conditions and imparts a coloration materially enhancing the appearance so that painting is unnecessary. A particular feature of the invention is that it afiords a choice in the color of the coating and a range of shades in each color.
In a preferred embodiment and practice of the invention, I subject the surfaces to be treated to contact with a novel film-forming solution by dipping, spraying or the like. The solution contains chromic acid or a water-soluble salt thereof, or both, and an organic acid chosen from the group consisting of tartaric, succinic and citric acids. The solution preferably contains also a small amount of one or more mineral acids or salts thereof chosen from the group consisting of hydrochloric, sulphuric, nitric and phosphoric acids. The coating produced by the invention appears to be a durable film composed largely of insoluble chromate deposited by the interaction of the chromate ions of the solution and metal ions from the zinc surface. The organic acid determines the color of the coating or film formed and the shade thereof may be varied by changing the organic acid concentration. The mineral acid also modifies the color of the film. The solution may be applied at room temperature or may be heated to a moderate temperature, say 140 F. The length of contact of the solution with the surface varies inversely with the temperature, i. e., from about 60 seconds at room temperature to about 30 seconds at 140 F.
In order to impart a more exact understanding of the invention, the following specific examples of solutions for forming a protective coating of attractive color on zinc surfaces are given. The percentages of the several components are by weight and, in each case, the balance of the solution is water.
EXAMPLES Per cent Chromic acid 5.0 Citric acid 1.0 Hydrochloric acid 0.5
Per centv Chromic acid 4.0 Sodium chromate 2.0 Succinic acid 1.0 to 5.0 Zinc nitrate 1.0
III
I Per cent Chromic acid 5.0 Tartaric acid 1.0 Hydrochloric acid 0.5 Phosphoric acid 3.0
Per cent Chromic acid 5.0 Tartaric acid 1.0 Sulphuric acid 2.0 Nitric acid 2.0
Per cent Chromic acid 5.0 Succinic acid"; 2.0 Hydrochloric acid 0.5 Phosphoric acid 3.0
Instead of zinc nitrate specified in Example II, I may use other nitrates such as sodium nitrate or nitrates of alkaline earth metals or nitric acid. Similarly I may use water-soluble salts of the mineral acids instead of the acids themselves, since it is the acid anion which forms the coating film. Mineral acid salts of sodium and potassium are specially suitable as substituents for the acids. Water-soluble chromates or dichromates such as those of sodium or potassium may be used to replace some or all the chromic acid.
The organic acids, tartaric, succinic and citric, may be used individually or a mixture of two or more may be employed. Salts of these acids such as those of potassium or sodium may be used instead of the acids but are not as desirable. 1,
The presence of all three acids, chromic, or
game and mineral, or their water-soluble salts;
is desirable in order to obtain adequate color and corrosion resistance.
In practice of the invention it has been found that the chromic acid content of the coating solutions should be preferably in the range of 2.5% to 18.0%, or the equivalent in chromium when using chromates. considered as forming chromic acid-chromate mixtures on going into solution.
The organic acid additions, or respective anion additions from salts thereof, should 'be preferably in the range of 0.5% to 9.0% by weight depending to a great extent on the concentration of chromic acid in the coating solution and the shade of color desired.
The mineral acid additions, or respective anion additions from salts thereof, should be preferably in the range of 0.1% to 8.0% by weight, the" amount depending on the amounts of chromic acid and organic acid anion present and the shade of color desired.
Temperature and time of treatment are important. factors inemploying the invention for obtaining both desirable and adherent coatings. Room temperature of about 80 F. is preferable in most cases, but in some cases it is necessary to go to elevated temperatures of 160 to 180 F. to accomplish results. Fifteen seconds to two minutes immersion time is sufficient to promotedesirable coatings in allcases.
Instead of" immersing or spraying the zinc body in the chromate producing solution, the solution maybe: brushed or flowed thereon, or otherwise brought into contact with the zinc body.
The resulting chromate coatings on the zinc are highly. resistant to atmospheric and salt" water corrosion. Adherence of the coatings to the zinc surface is good, as indicated by results of bend and abrasion tests. The adherence and appearance of the chromate coatings are enhanced' bythe presence of the additional cons'tituentspresent in the'solutions; namely'organic acid andmineral acid anions. the organic acid anion is, apparently, reduction or partial reduction of chromates at the metalsolution interface. A wide range of visible corrosion-resistant coatings varying from a light gold color through brown to a medium green are obtainable by the process of this invention. These coatings are especially suitable for galvanized steel products used in construction for roofing or siding.
The term zinc as herein employed 1s mtendedto-include zinc coatingsrolled zinc sheets,
galvanized material and zinc alloys.
Among the advantages of the invention; I may mention that it affords a wider range of" color inthe coatings and is more adaptable to producirig corrosionnesistant coatings to suit the need, such. as coatings to withstand high-moisture at mospheres, sulphur gases and other industrial fumes, expansion and contraction due to heating andcooling, salty seashore atmospheres and abrasion due to dust or other particles. Other qualities which can be imparted by the process include bright surfaces which will reflect light, dull surfaces which will absorb light, and sur faces which serve as good paint bases. The applied coating is found' to be an excellent base for aints-and the like,.should it be desired to paint, or similarly cover, the zinc surface after the treatment described.
The compounds and amounts thereof may vary as indicated. However, close control is maintained to produce desiredqual'ities', espe- Dichromate's may be The function of v cially combinations of qualities. For instance, in the case of Example III, the solution described produces a medium green protective coating on zinc surfaces, but if the tartaric acid and phosphoric acid components are not controlled to specified amounts, the green coating will deteriorate rapidly under certain conditions such' as exposure to moisture condensates.
The invention also afiords a greater range of adaptability to needs in coloration and corrosion resistance. The organic acid additions control, to a large extent, the color, adherence and corrosion-resisting qualities of the coatings and each acid imparts separate characteristics. These are not generally interchangeable for duplicating results.
Although I have illustrated and described but a preferred embodiment of the invention, changes therein may be made Without departing from the spirit of the invention or the scope of the appended claims.
I- claim:
1-. In a method of forming acorrosion-resistant and-abrasion-resistantcoating. on a zinc surface, steps including subjecting. the surfacefon a period of from 15 seconds-to 2 minutes,-to contactwith a-solution, acid in character, composed of from l told% of a compound selected from the group consisting of chromic acid and sodium. and potassium salts thereof or mixtures but including at least M chromic acid; from .5 to 9% of a compound selected from the group" con sisting of tartaric acid, succinic acid, citricacid and sodium and potassium salts thereof orm'ixtures, from .1 to 8% of a compound selectedfrom the group consisting of hydrochloric, s'u1- phuric, nitric and phosphoric acids and s'od'ium and potassium" salts thereof or mixtures; and tlie remainder water, the salts in each case being" used in anionic equivalent amounts of the amount of acid specified, and maintaining the temperature of said solution at a value between room temperature'and F.
2. A- solution adapted to form a corrosion-resistant and abrasion-resistant coating on a zinc"- surface composed of'from 4 to 18% of a compound selected from the group consisting of chromic acid and sodium and potassium salts thereof or mixtures but including at least 4% chromic' acid, from .5 to 9% of a compound selected from the'group consisting of tartaric acid, sue'cin'ic acid, citric acid and sodium and potas'- siuni salts thereof 'or mixtures, from .1 to 8% of a compound selected from the group consisting of hydrochloric, sulphuric, nitric and phosphoric acids and sodium and potassium salts thereof or mixtures and the remainder water, the salts in each case being used in anionic equivalent amounts of the amount of acid specified, and the solution being acid in character.
CHARLES T. WATSON.
REFERENCES CITED The following references are of record in" the file of this patent:
UNITED STATES PATENTS-
Claims (1)
1. IN A METHOD OF FORMING A CORROSION-RESISTANT AND ABRASION-RESISTANT COATING ON A ZINC SURFACE, STEPS INCLUDING SUBJECTING THE SURFACE FOR A PERIOD OF FROM 15 SECONDS TO 2 MINUTES, TO CONTACT WITH A SOLUTION, ACID IN CHARACTER, COMPOSED OF FROM 4 TO 18% OF A COMPOUND SELECTED FROM THE GROUP CONSISTING OF CHROMIC ACID AND SODIUM AND POTASSIUM SALTS THEREOF OR MIXTURES BUT INCLUDING AT LEAST 4% CHROMIC ACID, FROM .5 TO 9% OF A COMPOUND SELECTED FROM THE GROUP CONSISTING OF TARTARIC ACID, SUCCINIC ACID, CITRIC ACID AND SODIUM AND POTASSIUM SALTS THEREOF OR MIXTURES, FROM .1 TO 8% OF A COMPOUND SELECTED FROM THE GROUP CONSISTING OF HYDROCHLORIC, SULPHURIC, NITRIC AND PHOSPHORIC ACIDS AND SODIUM AND POTASSIUM SALTS THEREOF OR MIXTURES, AND THE REMAINDER WATER, THE SALTS IN EACH CASE BEING USED IN ANIONIC EQUIVALENT AMOUNTS OF THE AMOUNT OF ACID SPECIFIED, AND MAINTAINING THE TEMPERATURE OF SAID SOLUTION AT A VALUE BETWEEN ROOM TEMPERATURE AND 180* F.
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US72751A US2559812A (en) | 1949-01-25 | 1949-01-25 | Solution and method for coating zinc surfaces |
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US72751A US2559812A (en) | 1949-01-25 | 1949-01-25 | Solution and method for coating zinc surfaces |
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Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2768104A (en) * | 1952-03-25 | 1956-10-23 | Heintz Mfg Co | Method for coating iron |
US2777785A (en) * | 1953-07-30 | 1957-01-15 | Heintz Mfg Co | Composition for and method of treating metals as well as the treated product |
US2793932A (en) * | 1953-11-09 | 1957-05-28 | W H & L D Betz | Corrosion inhibiting |
US2855348A (en) * | 1955-08-25 | 1958-10-07 | Tiarco Corp | Chromium plating |
US2884350A (en) * | 1955-12-28 | 1959-04-28 | Sylvania Electric Prod | Solderable zinc alloy coating |
US2911332A (en) * | 1956-05-25 | 1959-11-03 | Kelsey Hayes Co | Process of coating metal and resulting articles |
DE1084103B (en) * | 1953-03-13 | 1960-06-23 | Armco Int Corp | Process for the production of corrosion-resistant, unpainted and shiny metal zinc or aluminum surfaces |
US2964433A (en) * | 1957-12-13 | 1960-12-13 | Nat Steel Corp | Process for inhibiting corrosion and product |
US3079288A (en) * | 1960-09-07 | 1963-02-26 | Amchem Prod | Method and composition for increasing the corrosion resistance of phosphatetype chemical conversion coatings on metal surfaces |
DE1208149B (en) * | 1958-12-11 | 1965-12-30 | United States Steel Corp | Process for the aftertreatment of a protective film on tin-coated steel |
US3382081A (en) * | 1965-09-02 | 1968-05-07 | Diamond Shamrock Corp | Chemical composition and method |
US3405014A (en) * | 1964-03-10 | 1968-10-08 | Mitsui Mining & Smelting Co | Process for producing dyed chromate films on zinc and zinc alloys |
US3519501A (en) * | 1968-04-16 | 1970-07-07 | Diamond Shamrock Corp | Chromic acid-organic coating compositions |
US3535166A (en) * | 1968-04-16 | 1970-10-20 | Diamond Shamrock Corp | Chromic acid-organic dibasic acid coating compositions for metals |
US3535167A (en) * | 1968-04-16 | 1970-10-20 | Diamond Shamrock Corp | Chromic acid-dimer acid coating composition for metals |
US3630789A (en) * | 1970-04-02 | 1971-12-28 | Du Pont | Hexavalent chromium/fumarate solutions and the treatment of metal substrates therewith |
US3942989A (en) * | 1970-10-22 | 1976-03-09 | Mayhew John T | White rust prevention for zinc coated surfaces |
US5368655A (en) * | 1992-10-23 | 1994-11-29 | Alchem Corp. | Process for chromating surfaces of zinc, cadmium and alloys thereof |
Citations (4)
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---|---|---|---|---|
FR731994A (en) * | 1930-12-17 | 1932-09-10 | Improvements in the surface treatment of aluminum and aluminum alloys | |
US2296884A (en) * | 1935-09-28 | 1942-09-29 | Parker Rust Proof Co | Method of coating |
US2393663A (en) * | 1943-03-22 | 1946-01-29 | Rheem Res Products Inc | Coating for cadmium and zinc |
US2477310A (en) * | 1947-07-23 | 1949-07-26 | Clark Thread Co | Process and composition for producing a dyeable corrosion resistant surface on zinc and high zinc alloys |
-
1949
- 1949-01-25 US US72751A patent/US2559812A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR731994A (en) * | 1930-12-17 | 1932-09-10 | Improvements in the surface treatment of aluminum and aluminum alloys | |
US2296884A (en) * | 1935-09-28 | 1942-09-29 | Parker Rust Proof Co | Method of coating |
US2393663A (en) * | 1943-03-22 | 1946-01-29 | Rheem Res Products Inc | Coating for cadmium and zinc |
US2477310A (en) * | 1947-07-23 | 1949-07-26 | Clark Thread Co | Process and composition for producing a dyeable corrosion resistant surface on zinc and high zinc alloys |
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2768104A (en) * | 1952-03-25 | 1956-10-23 | Heintz Mfg Co | Method for coating iron |
DE1084103B (en) * | 1953-03-13 | 1960-06-23 | Armco Int Corp | Process for the production of corrosion-resistant, unpainted and shiny metal zinc or aluminum surfaces |
US2777785A (en) * | 1953-07-30 | 1957-01-15 | Heintz Mfg Co | Composition for and method of treating metals as well as the treated product |
US2793932A (en) * | 1953-11-09 | 1957-05-28 | W H & L D Betz | Corrosion inhibiting |
US2855348A (en) * | 1955-08-25 | 1958-10-07 | Tiarco Corp | Chromium plating |
US2884350A (en) * | 1955-12-28 | 1959-04-28 | Sylvania Electric Prod | Solderable zinc alloy coating |
US2911332A (en) * | 1956-05-25 | 1959-11-03 | Kelsey Hayes Co | Process of coating metal and resulting articles |
US2964433A (en) * | 1957-12-13 | 1960-12-13 | Nat Steel Corp | Process for inhibiting corrosion and product |
DE1208149B (en) * | 1958-12-11 | 1965-12-30 | United States Steel Corp | Process for the aftertreatment of a protective film on tin-coated steel |
US3079288A (en) * | 1960-09-07 | 1963-02-26 | Amchem Prod | Method and composition for increasing the corrosion resistance of phosphatetype chemical conversion coatings on metal surfaces |
US3405014A (en) * | 1964-03-10 | 1968-10-08 | Mitsui Mining & Smelting Co | Process for producing dyed chromate films on zinc and zinc alloys |
US3382081A (en) * | 1965-09-02 | 1968-05-07 | Diamond Shamrock Corp | Chemical composition and method |
US3519501A (en) * | 1968-04-16 | 1970-07-07 | Diamond Shamrock Corp | Chromic acid-organic coating compositions |
US3535166A (en) * | 1968-04-16 | 1970-10-20 | Diamond Shamrock Corp | Chromic acid-organic dibasic acid coating compositions for metals |
US3535167A (en) * | 1968-04-16 | 1970-10-20 | Diamond Shamrock Corp | Chromic acid-dimer acid coating composition for metals |
US3630789A (en) * | 1970-04-02 | 1971-12-28 | Du Pont | Hexavalent chromium/fumarate solutions and the treatment of metal substrates therewith |
US3942989A (en) * | 1970-10-22 | 1976-03-09 | Mayhew John T | White rust prevention for zinc coated surfaces |
US5368655A (en) * | 1992-10-23 | 1994-11-29 | Alchem Corp. | Process for chromating surfaces of zinc, cadmium and alloys thereof |
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