US2477841A - Method of coating metal surfaces comprising aluminum - Google Patents
Method of coating metal surfaces comprising aluminum Download PDFInfo
- Publication number
- US2477841A US2477841A US615501A US61550145A US2477841A US 2477841 A US2477841 A US 2477841A US 615501 A US615501 A US 615501A US 61550145 A US61550145 A US 61550145A US 2477841 A US2477841 A US 2477841A
- Authority
- US
- United States
- Prior art keywords
- solution
- boric acid
- fluoride
- fluoborate
- aluminum
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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Classifications
-
- 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
- C23C22/34—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 fluorides or complex fluorides
- C23C22/36—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 fluorides or complex fluorides containing also phosphates
Definitions
- This invention relates to the production of chemically formed coatings on aluminum and other metals, the coatings consisting essentially ofphosphates and fluorides.
- An object of the invention is to improve the prior processes, such as disclosed in the patent :to Thompson, 2,312,855, March 2nd, 1943, where fluoborate is employed in the solution.
- fluosilicate is specified in each of the formulas given, but it is stated that other double fluorides, including fluoborate, may be used. It has been found that fluoborate is more stable than fluosilicate, and less fluorine compounds are lost from the solution when fluoborate is used than when fluosilicate is used. This is especially true, and especially important, when the solution is applied to the metal surface by spraying.
- the coatin solution to which this invention relates comprises as its essential ingredients dihydrogen phosphate, an oxidizing agent, and a double fluoride.
- a phosphate solution is made up in any of the Ways described in said former patent, but instead of adding fluosilicate there is added boric acid and fluoborate, or boric acid and a single fluoride, such as sodium fluoride or bifiuoride, the proportion of boric acid to fluoride being greater than the amount necessary to form fluoborate with all of the fluoride present in the solution.
- This excess of boric acid aids in stabilizing the fluoride, and also results in a. somewhat thinner and harder coating than results where the only fluoborate is employed in making up the solution.
- the amount of excess boric acid is varied in accordance with the kind of coating desired, the more boric acid there is present-the thinner the resulting coating. Usually from 50% to 200% more boric acid is employed in making up the so- 4 Claims. (01. 148-615) lution than is required to form fluoborate with the fluoride used, but in any particular case the excess boric acid is adjusted to obtain the desired results.
- the fluorine is depleted much more rapidly than: the boric acid, both because the boric acid does not enter into the chemically formed coating and does not escape into the air as readily as some of the fluorine compounds formed in the solution. Accordingly, an excess of boric acid can be maintained without the addition of as much boric acidas would be required theoretically to form fluoborate With the fluoride added.
- While'other dihydrogen phosphates may be employedas'described in said patent, zinc dihydrogen phosphate is preferred, and nitrate is preferred as the oxidizing agent, though nitrite, iodate, periodate, peroxide, bromate, quinone, chlorate, perchlorate, sulphite and permanganate may be used, with proper control of acidity where iron is amongst the metals coated, as taught in the prior art.
- a quick approximation to the quantity of boric acid in the solution may be made by titration with phenolphthalein as an indicator first without and then with mannitol in the solution, the difference between the two titrations giving the amount of boric acid present as accurately as is usually necessary for proper control of the bath.
- the amount of fluorine present may be ascertained by known distillation methods not necessary to describe in detail.
- the free acid in the solution should be kept in proper proportion to the salts in the solution, as is well known. If the free acid tends to run too high, more of the fluorine can be added as sodium fluoride, while any tendency for the free acid to be low can be counteracted by addition of more of the fluorine as sodium bifluoride.
- fluoride in the solution is especially useful for producing a coatin on aluminum or alloys containing aluminum, it does not interfere with the production of phosphate coatings on iron, zinc or other metals which can be coated with phospates. Therefore it is a valuable addition to any solution which is to be used in whole or in part upon any surfaces rendered hard to coat by the presence of aluminum, even though most of the coating takes place upon readily coated surfaces.
- fluoride-containing solutions as described, are employed upon surfaces of iron or steel, there seems to be more etching of the surface than where the fluoride is not present, and therefore the use of fluoride may be desirable content of the solution by the-additlonpfra single fluoride and only the amoun'taofiboric acid-"t0 keep the excess boric acid in the solution within the desired Working range.
- a method of coating metal surfaces containing iron and aluminum and which can be coated by phosphate and fluoride solutions whichcomprises subjecting the surfaces to the action of a hotv aqueous solution containing as its-essential ingredients dihydrogen phosphate, an oxidizin regent,v fluoborate, .andexcess boric -acid,.-:and replenishing the fluoborate and 'boric acid content .of,: the solution by the-additionof a-single fluoride and: only the amount of-boric acid to-keep the excess boric' acid-in the "solution within the desiredworkingrange.
- Amethod of coating metal surfaces which can be coated by phosphate and fluoride solu- ,tions and some of which contain aluminum which comprises subjecting the surfaces to the faction of a-hot aqueous solution containing as its essential ingredients dihydrogen phosphate, an oxidizing agent, fluoborate, and excess boric acid, :and replenishing the fluoborate and boric acid content of'the solution by the addition of a single fluoride and only the amount of boric acid to "keepthe excess boric acid in the solution within the desired working range, the single fluoride being of the group consisting of sodium fluoride and sodium bifluoride, and the method comprising -;proportioning said two fluorides tomaintaingthe .desired-freeaoidity of thesolution.
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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 Aug. 2, 1 949 METHOD OF COATING METALQSURFACESJ 1 COMPRISING ALUMINUM Herbert K. Ward, Birmingham, Mich., assignor .to Parker Rust Proof Company, Detroit, Mich.,
a corporation of Michigan No Drawing. Application September 10, 1945, Serial No. 615,501
This invention relates to the production of chemically formed coatings on aluminum and other metals, the coatings consisting essentially ofphosphates and fluorides.
An object of the invention is to improve the prior processes, such as disclosed in the patent :to Thompson, 2,312,855, March 2nd, 1943, where fluoborate is employed in the solution. In said patent, fluosilicate is specified in each of the formulas given, but it is stated that other double fluorides, including fluoborate, may be used. It has been found that fluoborate is more stable than fluosilicate, and less fluorine compounds are lost from the solution when fluoborate is used than when fluosilicate is used. This is especially true, and especially important, when the solution is applied to the metal surface by spraying. The coatin solution to which this invention relates comprises as its essential ingredients dihydrogen phosphate, an oxidizing agent, and a double fluoride.
A solution made up in accordance with said patent, using fluoborate instead of fluosilicate, coats well when first made up, but it was found that continued use, with usual replenishment by the phosphates, oxidizing agent, and fluoborate, resulted in a solution which produced a much thinner coating than in the start, so that the initial coating action could not be continued without dumping the solution and making up a new one.
By the present invention, it is possible by varying the make up of the solution to produce a coating of the desired thickness throughout quite a wide range, and to replenish the solution so as to continue to obtain the desired coating indefinitely.
By this invention, a phosphate solution is made up in any of the Ways described in said former patent, but instead of adding fluosilicate there is added boric acid and fluoborate, or boric acid and a single fluoride, such as sodium fluoride or bifiuoride, the proportion of boric acid to fluoride being greater than the amount necessary to form fluoborate with all of the fluoride present in the solution. This excess of boric acid aids in stabilizing the fluoride, and also results in a. somewhat thinner and harder coating than results where the only fluoborate is employed in making up the solution.
The amount of excess boric acid is varied in accordance with the kind of coating desired, the more boric acid there is present-the thinner the resulting coating. Usually from 50% to 200% more boric acid is employed in making up the so- 4 Claims. (01. 148-615) lution than is required to form fluoborate with the fluoride used, but in any particular case the excess boric acid is adjusted to obtain the desired results.
Inuse-,the fluorine is depleted much more rapidly than: the boric acid, both because the boric acid does not enter into the chemically formed coating and does not escape into the air as readily as some of the fluorine compounds formed in the solution. Accordingly, an excess of boric acid can be maintained without the addition of as much boric acidas would be required theoretically to form fluoborate With the fluoride added. While'other dihydrogen phosphates may be employedas'described in said patent, zinc dihydrogen phosphate is preferred, and nitrate is preferred as the oxidizing agent, though nitrite, iodate, periodate, peroxide, bromate, quinone, chlorate, perchlorate, sulphite and permanganate may be used, with proper control of acidity where iron is amongst the metals coated, as taught in the prior art.
A quick approximation to the quantity of boric acid in the solution may be made by titration with phenolphthalein as an indicator first without and then with mannitol in the solution, the difference between the two titrations giving the amount of boric acid present as accurately as is usually necessary for proper control of the bath. The amount of fluorine present may be ascertained by known distillation methods not necessary to describe in detail.
The free acid in the solution should be kept in proper proportion to the salts in the solution, as is well known. If the free acid tends to run too high, more of the fluorine can be added as sodium fluoride, while any tendency for the free acid to be low can be counteracted by addition of more of the fluorine as sodium bifluoride.
While the fluoride in the solution is especially useful for producing a coatin on aluminum or alloys containing aluminum, it does not interfere with the production of phosphate coatings on iron, zinc or other metals which can be coated with phospates. Therefore it is a valuable addition to any solution which is to be used in whole or in part upon any surfaces rendered hard to coat by the presence of aluminum, even though most of the coating takes place upon readily coated surfaces.
When fluoride-containing solutions, as described, are employed upon surfaces of iron or steel, there seems to be more etching of the surface than where the fluoride is not present, and therefore the use of fluoride may be desirable content of the solution by the-additlonpfra single fluoride and only the amoun'taofiboric acid-"t0 keep the excess boric acid in the solution within the desired Working range.
2. A method of coating metal surfaces containing iron and aluminum and which can be coated by phosphate and fluoride solutions, Whichcomprises subjecting the surfaces to the action of a hotv aqueous solution containing as its-essential ingredients dihydrogen phosphate, an oxidizin regent,v fluoborate, .andexcess boric -acid,.-:and replenishing the fluoborate and 'boric acid content .of,: the solution by the-additionof a-single fluoride and: only the amount of-boric acid to-keep the excess boric' acid-in the "solution within the desiredworkingrange.
-31 -A-. method 101" t coating metal wear-resisting surfaces of thegroup comprising iron and alumi- ;-num and *Whichcan' be coatedby -phosphate and fluoride solutions, which -c0mprises subjecting theisurfaces to the (action 0fa'.hot aqueous solu- .,tion .-o ontaining as its essential ingredients dihy- "drogen phosphate, an 'oxidizinng agent, fluo- 4 borate, and excess boric acid, and replenishing the fluoborate and boric acid content of the solution by the addition of a single fluoride and only the amount of boric acid to keep the excess boric acid in the solution within the desired working range.
4. Amethod of coating metal surfaces which can be coated by phosphate and fluoride solu- ,tions and some of which contain aluminum, which comprises subjecting the surfaces to the faction of a-hot aqueous solution containing as its essential ingredients dihydrogen phosphate, an oxidizing agent, fluoborate, and excess boric acid, :and replenishing the fluoborate and boric acid content of'the solution by the addition of a single fluoride and only the amount of boric acid to "keepthe excess boric acid in the solution within the desired working range, the single fluoride being of the group consisting of sodium fluoride and sodium bifluoride, and the method comprising -;proportioning said two fluorides tomaintaingthe .desired-freeaoidity of thesolution.
HERBERT K. WARD.
REFERENCES CITED fI he following referenlces are of record in the file of thispatent:
UNITED STATES PATENTS Number Name Date 1,022,274- Strecker -Apr.;2, 1912 l;610;.-362 Coslett Dec. 14,1926 2,3125855 Thompson =,Mar;'2, 1943 *2;3'73;433 Tanner Apr. 10,11945
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US615501A US2477841A (en) | 1945-09-10 | 1945-09-10 | Method of coating metal surfaces comprising aluminum |
GB4662/48A GB655070A (en) | 1945-09-10 | 1948-02-17 | Improvements in or relating to the coating of metals with phosphates |
DEP4119A DE853697C (en) | 1945-09-10 | 1950-10-01 | Process for the formation of coatings on surfaces of aluminum |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US615501A US2477841A (en) | 1945-09-10 | 1945-09-10 | Method of coating metal surfaces comprising aluminum |
Publications (1)
Publication Number | Publication Date |
---|---|
US2477841A true US2477841A (en) | 1949-08-02 |
Family
ID=24465655
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US615501A Expired - Lifetime US2477841A (en) | 1945-09-10 | 1945-09-10 | Method of coating metal surfaces comprising aluminum |
Country Status (3)
Country | Link |
---|---|
US (1) | US2477841A (en) |
DE (1) | DE853697C (en) |
GB (1) | GB655070A (en) |
Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2609308A (en) * | 1947-11-22 | 1952-09-02 | Parker Rust Proof Co | Method and material for producing coatings on metal |
US2665231A (en) * | 1949-06-17 | 1954-01-05 | Parker Rust Proof Co | Coating process with alkali metal phosphate and added fluoride salt |
US2715083A (en) * | 1951-01-29 | 1955-08-09 | Parker Rust Proof Co | Method of applying sulfide coating on stainless steel and composition solution therefr |
US2843513A (en) * | 1954-07-28 | 1958-07-15 | Allied Res Products Inc | Mixture and method for imparting a corrosion-resistant surface to aluminum, aluminumalloys, and silver |
US2851386A (en) * | 1954-05-05 | 1958-09-09 | Allied Res Products Inc | Method for coating zinc and zinc alloy sheets |
US2859148A (en) * | 1954-12-16 | 1958-11-04 | Aluminium Walzwerke Singen | Method of producing a bohmite layer on etched aluminum foils |
DE1062519B (en) * | 1953-08-18 | 1959-07-30 | American Chem Paint Co | Agent for producing coatings on aluminum and aluminum alloys |
US2964434A (en) * | 1957-06-17 | 1960-12-13 | Victor Chemical Works | Pickling and rust-inhibiting bath for ferrous metals, and use of same |
US3076733A (en) * | 1960-05-03 | 1963-02-05 | Amchem Prod | Method of coating zirconium |
US3297494A (en) * | 1963-08-05 | 1967-01-10 | Amchem Prod | Concentrated material for use in preparing and preplenishing zinc phosphate coating solutions |
US3331710A (en) * | 1963-08-23 | 1967-07-18 | Hooker Chemical Corp | Method for coating aluminum |
US3454483A (en) * | 1964-04-30 | 1969-07-08 | Hooker Chemical Corp | Electrodeposition process with pretreatment in zinc phosphate solution containing fluoride |
US3676309A (en) * | 1970-02-04 | 1972-07-11 | Olin Mathieson | Aluminum welding wire electrode with an alumina coating containing phosphate |
US3819424A (en) * | 1971-06-17 | 1974-06-25 | Oxy Metal Finishing Corp | Method and composition for treating metal surfaces |
EP0399425A1 (en) * | 1989-05-20 | 1990-11-28 | KOLBENSCHMIDT Aktiengesellschaft | Process for applying a phosphate running layer on a bearing metal layer |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE525407A (en) * | 1952-06-18 | |||
DE1185037B (en) * | 1957-06-17 | 1965-01-07 | Budenheim Rud A Oetker Chemie | Aqueous acid solutions for pickling iron and steel |
DE1521877B1 (en) * | 1966-06-18 | 1970-07-02 | Metallgesellschaft Ag | Process for applying phosphate coatings to iron and steel |
DE1796218B1 (en) * | 1968-09-23 | 1971-10-07 | Metallgesellschaft Ag | METAL PHOSPHATING METHOD |
DE2342558C3 (en) * | 1973-08-23 | 1982-11-11 | Metallgesellschaft Ag, 6000 Frankfurt | Process for phosphating metals |
CA1132761A (en) * | 1978-09-19 | 1982-10-05 | Razmic S. Gregorian | Foam composition for treating textile materials |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1022274A (en) * | 1911-11-02 | 1912-04-02 | Otto Carl Strecker | Etching fluid for flat printing-plates of metal. |
US1610362A (en) * | 1925-06-26 | 1926-12-14 | Coslett Thomas Watts | Process for the treatment of iron or steel for preventing oxidation or rusting |
US2312855A (en) * | 1940-09-07 | 1943-03-02 | Parker Rust Proof Co | Method of coating aluminum |
US2373433A (en) * | 1944-10-13 | 1945-04-10 | Parker Rust Proof Co | Method of expediting chemical coatings on metal |
-
1945
- 1945-09-10 US US615501A patent/US2477841A/en not_active Expired - Lifetime
-
1948
- 1948-02-17 GB GB4662/48A patent/GB655070A/en not_active Expired
-
1950
- 1950-10-01 DE DEP4119A patent/DE853697C/en not_active Expired
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1022274A (en) * | 1911-11-02 | 1912-04-02 | Otto Carl Strecker | Etching fluid for flat printing-plates of metal. |
US1610362A (en) * | 1925-06-26 | 1926-12-14 | Coslett Thomas Watts | Process for the treatment of iron or steel for preventing oxidation or rusting |
US2312855A (en) * | 1940-09-07 | 1943-03-02 | Parker Rust Proof Co | Method of coating aluminum |
US2373433A (en) * | 1944-10-13 | 1945-04-10 | Parker Rust Proof Co | Method of expediting chemical coatings on metal |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2609308A (en) * | 1947-11-22 | 1952-09-02 | Parker Rust Proof Co | Method and material for producing coatings on metal |
US2665231A (en) * | 1949-06-17 | 1954-01-05 | Parker Rust Proof Co | Coating process with alkali metal phosphate and added fluoride salt |
US2715083A (en) * | 1951-01-29 | 1955-08-09 | Parker Rust Proof Co | Method of applying sulfide coating on stainless steel and composition solution therefr |
DE1062519B (en) * | 1953-08-18 | 1959-07-30 | American Chem Paint Co | Agent for producing coatings on aluminum and aluminum alloys |
US2851386A (en) * | 1954-05-05 | 1958-09-09 | Allied Res Products Inc | Method for coating zinc and zinc alloy sheets |
US2843513A (en) * | 1954-07-28 | 1958-07-15 | Allied Res Products Inc | Mixture and method for imparting a corrosion-resistant surface to aluminum, aluminumalloys, and silver |
US2859148A (en) * | 1954-12-16 | 1958-11-04 | Aluminium Walzwerke Singen | Method of producing a bohmite layer on etched aluminum foils |
US2964434A (en) * | 1957-06-17 | 1960-12-13 | Victor Chemical Works | Pickling and rust-inhibiting bath for ferrous metals, and use of same |
US3076733A (en) * | 1960-05-03 | 1963-02-05 | Amchem Prod | Method of coating zirconium |
US3297494A (en) * | 1963-08-05 | 1967-01-10 | Amchem Prod | Concentrated material for use in preparing and preplenishing zinc phosphate coating solutions |
US3331710A (en) * | 1963-08-23 | 1967-07-18 | Hooker Chemical Corp | Method for coating aluminum |
US3454483A (en) * | 1964-04-30 | 1969-07-08 | Hooker Chemical Corp | Electrodeposition process with pretreatment in zinc phosphate solution containing fluoride |
US3676309A (en) * | 1970-02-04 | 1972-07-11 | Olin Mathieson | Aluminum welding wire electrode with an alumina coating containing phosphate |
US3819424A (en) * | 1971-06-17 | 1974-06-25 | Oxy Metal Finishing Corp | Method and composition for treating metal surfaces |
EP0399425A1 (en) * | 1989-05-20 | 1990-11-28 | KOLBENSCHMIDT Aktiengesellschaft | Process for applying a phosphate running layer on a bearing metal layer |
US5073213A (en) * | 1989-05-20 | 1991-12-17 | Kolbenschmidt Aktiengesellschaft | Process for applying a phosphate sliding layer to a bearing metal layer |
Also Published As
Publication number | Publication date |
---|---|
GB655070A (en) | 1951-07-11 |
DE853697C (en) | 1952-10-27 |
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