US1254263A - Rust-proofing iron and steel surfaces. - Google Patents
Rust-proofing iron and steel surfaces. Download PDFInfo
- Publication number
- US1254263A US1254263A US15001517A US15001517A US1254263A US 1254263 A US1254263 A US 1254263A US 15001517 A US15001517 A US 15001517A US 15001517 A US15001517 A US 15001517A US 1254263 A US1254263 A US 1254263A
- Authority
- US
- United States
- Prior art keywords
- iron
- acid
- rust
- phosphates
- water
- 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
- C23C22/40—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 molybdates, tungstates or vanadates
- C23C22/42—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 molybdates, tungstates or vanadates containing also phosphates
Definitions
- This invention relates to a process of forming non-corrodible protective surfaces on articles made from iron or steel, or alloys thereof, and to the production of the materials to be used in such process, and has for its object certain improvements in the method of treating said articles and in the compounds or materials used to produce permanent surfaces, which, while not injuriously affecting the ferrous masses, will retain their efficiency as a protective medium against the action of the elements of the atmosphere.
- the articles of iron and steel to be treated are placed in a bath which is usually kept at about the boiling point, but the exact temperature and the proportioning of the constituent elements of the bath are determined by the metallurgical character of the articles to be treated.
- the preferred composition of the bath is about 98 per cent. of water and less than two per cent. of a metallic phosphate such as the acid meta-phosphates of tungsten, molybdenum or of any of the metals of the third, fourth and fifth groups, according to the analytical classification (set forth by Prof. G. S. Newth, F. I. C., F. C. S., in the eighth edition of his Manual of (J'hemz'cal Analysis, published by Longmans, Green & Co., New York, in 1909), taken either singly or in combination with each other.
- tungsten is in the first group, molybdenum in the second group, while the third, fourth and fifth groups include aluminu rn, chromium, cobalt, iron, nickel, manganese, zinc, barium, strontium, calcium, sodium, potassium, magnesium and vanadium.
- the acid meta-phosphate of most general application is made by placing a quantity of iron oXid, preferably black iron scale, (Fe,O,) in a pot with sufficient phosphoric acid to form a soft paste.
- the iron oxid is preferably powdered in advance.
- the reactions may be expressed as follows :When heated And continued heating results in driving off the water of combination This is an acid meta-phosphate.
- the acid meta-phosphates thus produced are placed in water in the approximate proportions above set forth. It has been found that a percentage of phosphates as low as one-half of one per cent. will serve the purpose intended, butthat the action Will be slow. If more thantwo per cent. of phosphates are placed in the bath, the action is quite rapid and at times rather uneven.
- the preferred proportion of the acid meta-phosphates is about one and one-half per cent. The best action is secured when the bath is kept at about the boiling point.
- a new and useful process consistin of heating iron oxid with water and p osphoric acid and stirring while continuing the heat until a granular mass is obtained, placing this in an excess of Water, heating the bath and immersing articles of iron or steel until. a protective coating is formed thereon.
- a new and useful process consisting of placing the acid meta-phosphates of tungsten, molybdenum or any of the metals of the third, fourth and fifth groups in an excess of water, and immersin therein articles of iron and steel while the ath is kept at substantially the boilin point.
- a new and use ul process consisting in mixing iron oxid and phosphoric acid and heating them, adding water and stirring while the heat is continued, grinding the dry mass topowder, adding the powder to fifty times its Weight of water and two per cent. of'its Weight in meta-phosphate of another metal, then immersing articles of iron or steel to be treated.
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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
time :i sir WALTER I. OESCHGER, OF DETROIT, MICHIGAN, ASSIGNOR TO PARKER RUST PROOF COMPANY OF AMERICA, OF DETROIT, MICHIGAN, A CORPORATION OF MICHIGAN.
RUST-PROOFING IRON AND STEEL SURFACES.
No Drawing.
To all whom it may concern:
Be it known that I, WALTER I. Onsoncnn, a citizen of the United States, and residing at Detroit, in the county of Wayne and State of Michigan, have invented a new and Improved Process of Rust-Proofing Iron and Steel Surfaces, of which the following is a specification.
This invention relates to a process of forming non-corrodible protective surfaces on articles made from iron or steel, or alloys thereof, and to the production of the materials to be used in such process, and has for its object certain improvements in the method of treating said articles and in the compounds or materials used to produce permanent surfaces, which, while not injuriously affecting the ferrous masses, will retain their efficiency as a protective medium against the action of the elements of the atmosphere.
The articles of iron and steel to be treated are placed in a bath which is usually kept at about the boiling point, but the exact temperature and the proportioning of the constituent elements of the bath are determined by the metallurgical character of the articles to be treated. The preferred composition of the bath is about 98 per cent. of water and less than two per cent. of a metallic phosphate such as the acid meta-phosphates of tungsten, molybdenum or of any of the metals of the third, fourth and fifth groups, according to the analytical classification (set forth by Prof. G. S. Newth, F. I. C., F. C. S., in the eighth edition of his Manual of (J'hemz'cal Analysis, published by Longmans, Green & Co., New York, in 1909), taken either singly or in combination with each other.
In this classification, tungsten is in the first group, molybdenum in the second group, while the third, fourth and fifth groups include aluminu rn, chromium, cobalt, iron, nickel, manganese, zinc, barium, strontium, calcium, sodium, potassium, magnesium and vanadium.
The acid meta-phosphate of most general application is made by placing a quantity of iron oXid, preferably black iron scale, (Fe,O,) in a pot with sufficient phosphoric acid to form a soft paste. The iron oxid is preferably powdered in advance. An
Specification of Letters Patent.
amount of water equal to the acid is added to keep the mass from caking, after which heat 'is applied and the material is stirred until a dry granular mass is obtained,which isthen powdered. If desired, heat may be applied to the oxid and acid before water is added. To obtain the phosphates of the other metals, their oxide or carbonates may be similarly treated. Care must be taken to avoid heating these phosphates to a point where there is more than merely perceptible fuming.
The reactions may be expressed as follows :When heated And continued heating results in driving off the water of combination This is an acid meta-phosphate.
The acid meta-phosphates thus produced are placed in water in the approximate proportions above set forth. It has been found that a percentage of phosphates as low as one-half of one per cent. will serve the purpose intended, butthat the action Will be slow. If more thantwo per cent. of phosphates are placed in the bath, the action is quite rapid and at times rather uneven. The preferred proportion of the acid meta-phosphates is about one and one-half per cent. The best action is secured when the bath is kept at about the boiling point.
It has been found that the mixing of about two per cent. of strontium acid meta-phosphate with the iron compound above described gives a much more uniform and harder surface when high carbon steels are treated. Practically the same good result is attained by using the same percentage of molybdenum or tungsten acid meta-phosphates instead of the strontium acid metaphosphate in combination with the iron compound. There is little advantage in using any of these acid meta-phosphates alone or in any combination that does not include iron acid meta-phosphate as the cost is much higher and the addition of a large percentage of iron acid meta-phosphate seems to have no objectionable effect. Articles treated in this manner do not have Patented Jan. 22, 191.
. Application filed February 21, 1917. Serial No. 150,015.
the pickled appearance sometimes observed when ferric-acid-phosphates are used for this purpose.
I claim: v r
1. A new and useful process consistin of heating iron oxid with water and p osphoric acid and stirring while continuing the heat until a granular mass is obtained, placing this in an excess of Water, heating the bath and immersing articles of iron or steel until. a protective coating is formed thereon.
2. A new and useful process consisting of.
placing acid meta-phos hates of tungsten, molybdenum or any 0 the metals of the third,-fourth and fifth groups in an excess of water, and immersing therein articles of iron or steel.
3. A new and useful process consisting of placing the acid meta-phosphates of tungsten, molybdenum or any of the metals of the third, fourth and fifth groups in an excess of water, and immersin therein articles of iron and steel while the ath is kept at substantially the boilin point.
4. A new and use ul process consisting in mixing iron oxid and phosphoric acid and heating them, adding water and stirring while the heat is continued, grinding the dry mass topowder, adding the powder to fifty times its Weight of water and two per cent. of'its Weight in meta-phosphate of another metal, then immersing articles of iron or steel to be treated.
:WALTER 1. OESCI-IGER.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15001517A US1254263A (en) | 1917-02-21 | 1917-02-21 | Rust-proofing iron and steel surfaces. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US15001517A US1254263A (en) | 1917-02-21 | 1917-02-21 | Rust-proofing iron and steel surfaces. |
Publications (1)
Publication Number | Publication Date |
---|---|
US1254263A true US1254263A (en) | 1918-01-22 |
Family
ID=3321967
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US15001517A Expired - Lifetime US1254263A (en) | 1917-02-21 | 1917-02-21 | Rust-proofing iron and steel surfaces. |
Country Status (1)
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US (1) | US1254263A (en) |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2462196A (en) * | 1943-07-29 | 1949-02-22 | Westinghouse Electric Corp | Protective phosphate coatings for metal surfaces |
US2499261A (en) * | 1945-11-23 | 1950-02-28 | Hall Lab Inc | Compositions and methods for depositing amorphous metal-phosphate coatings on metal surfaces |
US2501349A (en) * | 1946-05-10 | 1950-03-21 | Westinghouse Electric Corp | Insulation for magnetic material |
US2502441A (en) * | 1946-11-22 | 1950-04-04 | Oakite Prod Inc | Phosphate coating of metals |
US2739114A (en) * | 1952-06-07 | 1956-03-20 | Pennsylvania Salt Mfg Co | Fluorine cell |
US2739115A (en) * | 1952-06-19 | 1956-03-20 | Pennsylvania Salt Mfg Co | Fluorine cell |
US2798015A (en) * | 1954-06-07 | 1957-07-02 | Hercules Powder Co Ltd | Coating composition for metals |
US2798017A (en) * | 1954-06-07 | 1957-07-02 | Hercules Powder Co Ltd | Coating composition for metals |
US2798016A (en) * | 1954-06-07 | 1957-07-02 | Hercules Powder Co Ltd | Coating composition for metals |
US2839439A (en) * | 1955-06-07 | 1958-06-17 | Detrex Chem Ind | Method and composition for producing phosphate coatings on metal |
DE974853C (en) * | 1945-11-23 | 1961-05-18 | Metallgesellschaft Ag | Process for the production of protective coatings on metals |
US5064468A (en) * | 1987-08-31 | 1991-11-12 | Nippon Paint Co., Ltd. | Corrosion preventive coating composition |
US5550006A (en) * | 1993-01-11 | 1996-08-27 | Macdermid, Incorporated | Phosphating compositions and processes, particularly for use in fabrication of printed circuits utilizing organic resists |
-
1917
- 1917-02-21 US US15001517A patent/US1254263A/en not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2462196A (en) * | 1943-07-29 | 1949-02-22 | Westinghouse Electric Corp | Protective phosphate coatings for metal surfaces |
DE974853C (en) * | 1945-11-23 | 1961-05-18 | Metallgesellschaft Ag | Process for the production of protective coatings on metals |
US2499261A (en) * | 1945-11-23 | 1950-02-28 | Hall Lab Inc | Compositions and methods for depositing amorphous metal-phosphate coatings on metal surfaces |
US2501349A (en) * | 1946-05-10 | 1950-03-21 | Westinghouse Electric Corp | Insulation for magnetic material |
US2502441A (en) * | 1946-11-22 | 1950-04-04 | Oakite Prod Inc | Phosphate coating of metals |
US2739114A (en) * | 1952-06-07 | 1956-03-20 | Pennsylvania Salt Mfg Co | Fluorine cell |
US2739115A (en) * | 1952-06-19 | 1956-03-20 | Pennsylvania Salt Mfg Co | Fluorine cell |
US2798015A (en) * | 1954-06-07 | 1957-07-02 | Hercules Powder Co Ltd | Coating composition for metals |
US2798016A (en) * | 1954-06-07 | 1957-07-02 | Hercules Powder Co Ltd | Coating composition for metals |
US2798017A (en) * | 1954-06-07 | 1957-07-02 | Hercules Powder Co Ltd | Coating composition for metals |
US2839439A (en) * | 1955-06-07 | 1958-06-17 | Detrex Chem Ind | Method and composition for producing phosphate coatings on metal |
US5064468A (en) * | 1987-08-31 | 1991-11-12 | Nippon Paint Co., Ltd. | Corrosion preventive coating composition |
US5550006A (en) * | 1993-01-11 | 1996-08-27 | Macdermid, Incorporated | Phosphating compositions and processes, particularly for use in fabrication of printed circuits utilizing organic resists |
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