US2580273A - Refractory metal alloy castings and methods of making same - Google Patents
Refractory metal alloy castings and methods of making same Download PDFInfo
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- US2580273A US2580273A US776166A US77616647A US2580273A US 2580273 A US2580273 A US 2580273A US 776166 A US776166 A US 776166A US 77616647 A US77616647 A US 77616647A US 2580273 A US2580273 A US 2580273A
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C27/00—Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
- C22C27/04—Alloys based on tungsten or molybdenum
Definitions
- the present invention relates to improved refractory metal alloy castings and methods of preparing the same.
- a refractory metal in cast form which can be forged, swaged, rolled or drawn while hot.
- Another object of the present invention is to provide a process of producing such castings.
- refractory metals such as molybdenum and tungsten may be hot worked if they contain small quantities of carbon and the oxygen is reduced below an exceedingly minute quantity.
- an alloy containing carbon from 0.01 to 0.25 per cent, oxygen less than 0.005 per cent, and the balance molybdenum or tungsten or any alloy of both, may be forged.
- a metal is considerable forgeable if its cross-sectional area may be reduced at least fifty per cent while hot.
- the carbon content should lie between 0.03 and 0.10 per cent and the oxygen content should be less than 0.003 per cent.
- cast ingots which may be rolled into bars, rods, or sheet, and substantially reduced in cross-sectional area may be obtained.
- the preferred method is to mix the powdered refractory metal with powdered carbon in the necessary proportions and compact the mixture by pressure into a bar Or rod.
- This rod is then heated sufiiciently, preferably by electric resistance heating, to sinter the powdered ma terials into a bar of sufiicient strength to be used as an electrode in a vacuum arc melting furnace.
- This bar is then utilized as one electrode of the arc and consumed, the opposite electrode being preferably the bath of melted material.
- a water-cooled copper mold to collect the molten material.
- Any suitable means may be provided to support the consumable electrode in proper spaced relation to the bath of molten metal and maintain it in the spaced relation during the melting operation.
- a small piece of the same refractory metal may be placed in the mold to act as the starting electrode pending formation of the molten bath.
- the interior of the mold and the entire melting chamber is suitably enclosed and evacuated by conventional means.
- a cast alloy containing from 0.01 to 0.25 per cent carbon, not more than 0.005 per cent oxygen and the balance essentially all molybdenum.
- a cast alloy containing from 0.03 to 0.10 per cent carbon, not more than 0.003 per cent oxygen and the balance essentially all molybdenum.
- a cast alloy characterized by its forgeability and containing from .01 to .25 per cent carbon, not more than .005 per cent oxygen and the balance essentialh all of at least one metal selected from the group consisting of tungsten and molybdenum.
- a cast alloy characterized by its forgeability and containing from .03 to .1 per cent carbon, not more than .003 per cent oxygen and the balance essentially all of at least one metal selected from the group consisting of tungsten and molybdenum.
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- Chemical & Material Sciences (AREA)
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- Materials Engineering (AREA)
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- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Manufacture And Refinement Of Metals (AREA)
Description
Patented Dec. 25, 1951 REFRACTORY METAL ALLOY CASTIN GS AND METHODS OF MAKING SAME Frederick P. Bens, Detroit, and John L. Ham, Dearborn, Mich., and Robert M. Parke, Silver Spring, Md., assignors to Climax Molybdenum Company, New York, N. Y., a corporation of Delaware No Drawing. Application September 25, 1947, Serial No. 776,166
14 Claims. (Cl. 75-476) The present invention relates to improved refractory metal alloy castings and methods of preparing the same.
In the past it has not been possible to produce forgeable castings of refractory metals such as molybdenum and tungsten. Consequently, the only method of producing metals of this type which could be hot worked has been to form bars of sintered, powdered material. While this method has been used extensively, particularly in the production of tungsten wire, it isimpractical for the production of large forgings, because of the difliculty of making large bodies of sintered, powdered metal. Prior attempts to melt and cast such refractory metals have resulted in castings which were exceedingly brittle and which could not be hot worked.
Accordingly, it is the principal object of the present invention to provide a refractory metal in cast form which can be forged, swaged, rolled or drawn while hot.
Another object of the present invention is to provide a process of producing such castings.
In accordance with the present invention it is found that castings of refractory metals such as molybdenum and tungsten may be hot worked if they contain small quantities of carbon and the oxygen is reduced below an exceedingly minute quantity. Thus, an alloy containing carbon from 0.01 to 0.25 per cent, oxygen less than 0.005 per cent, and the balance molybdenum or tungsten or any alloy of both, may be forged. For this purpose a metal is considerable forgeable if its cross-sectional area may be reduced at least fifty per cent while hot. For best results the carbon content should lie between 0.03 and 0.10 per cent and the oxygen content should be less than 0.003 per cent. Within this preferred range, cast ingots which may be rolled into bars, rods, or sheet, and substantially reduced in cross-sectional area may be obtained.
At the present time so-called commercially pure refractory metals are obtainable as powders. It is found. however, that these metal powders contain small quantities of oxygen which must be removed in order to produce a forgeable casting. In accordance with the present invention, this oxygen is removed from the metal by the addition, at the time of melting or before, of calculated quantities of carbon and the melting operation is carried out under a high vacuum. For this purpose the pressure in the melting chamber must be less than 500 microns of mercury and preferably less than microns. The amount of carbon which is added must exceed the calculated amount necessary to combine with the quantity of oxygen present in the material by an amount sufficient to produce residual carbon within the limits specified above. In this connection it is found that as the pressures approach the higher limit it is necessary to employ carbon in quantities correspondingly approaching the higher carbon limit. Accordingly, the quantity of oxygen in the raw material must be accurately measured. For this purpose the wellknown vacuum fusion method of determining oxygen content may be employed.
While any suitable method of adding carbon to the metal and melting the mixture may be employed, the preferred method is to mix the powdered refractory metal with powdered carbon in the necessary proportions and compact the mixture by pressure into a bar Or rod. This rod is then heated sufiiciently, preferably by electric resistance heating, to sinter the powdered ma terials into a bar of sufiicient strength to be used as an electrode in a vacuum arc melting furnace. This bar is then utilized as one electrode of the arc and consumed, the opposite electrode being preferably the bath of melted material. For this purpose it is preferred to use a water-cooled copper mold to collect the molten material. Any suitable means may be provided to support the consumable electrode in proper spaced relation to the bath of molten metal and maintain it in the spaced relation during the melting operation. At the start of the melting operation a small piece of the same refractory metal may be placed in the mold to act as the starting electrode pending formation of the molten bath.
The interior of the mold and the entire melting chamber is suitably enclosed and evacuated by conventional means.
It will be apparent to those skilled in the art that variations in the method of producing forgeable refractory metal castings in accordance with the present invention may be indulged in without departing from the spirit of the invention or the scope of the appended claims.
We claim:
1. A cast alloy containing from 0.01 to 0.25 per cent carbon, not more than 0.005 per cent oxygen and the balance essentially all molybdenum.
2. A cast alloy containing from 0.03 to 0.10 per cent carbon, not more than 0.003 per cent oxygen and the balance essentially all molybdenum.
3. A cast alloy characterized by its forgeability and containing from .01 to .25 per cent carbon, not more than .005 per cent oxygen and the balance essentialh all of at least one metal selected from the group consisting of tungsten and molybdenum.
4. A cast alloy characterized by its forgeability and containing from .03 to .1 per cent carbon, not more than .003 per cent oxygen and the balance essentially all of at least one metal selected from the group consisting of tungsten and molybdenum.
5. The process of producing a casting consisting essentially of carbon and at least one metal selected from the group consisting of molybdenum and tungsten which consists in adding to the powdered metal a calculated quantity of carbon sufficiently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .01 and .25 per cent, sintering said powdered metal into a bar, melting said bar by utilizing it as an electrode in a vacuum arc furnace, and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 500 microns of mercury.
6. The process of producing a casting consisting essentially of carbon and at least one metal selected from the group consisting of molybdenum and tungsten which consists in adding to the powdered metal a calculated quantity of carbon sufficiently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .01 and .25 per cent, sintering said powdered metal into a bar, melting said bar by utilizing it as an electrode in a vacuum-arc furnace, and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 100 microns of mercury.
'7. The process of producing a casting consisting essentially of carbon and molybdenum which consists in adding to the powdered metal a calculated quantity of carbon suiiiciently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .01 and .25 per cent, sintering said powdered metal into a bar, melting said bar by utilizing it as an electrode in a vacuum arc furnace, and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 100 microns of mercury.
8. The process of producing a casting consisting essentially of carbon and molybdenum which consists in adding to the powdered metal a calculated quantity of carbon sufficiently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .03 and .10 per cent, sintering said powdered metal into a bar, melting said bar by 4 utilizing it as an electrode in a vacuum arc furnace, and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 100 microns of mercury.
9. The process of producing a casting consisting essentially of carbon and at least one metal selected from the group consisting of molybdenum and tungsten which consists in adding to the metal a calculated quantity of carbon sufficiently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .01 and .25 per cent and melting said mixture and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 500 microns of mercury.
10. The process of producing a casting consisting essentially of carbon and at least one metal selected from the group consisting of molybdenum and tungsten which consists in adding to the metal a calculated quantity of carbon sufliciently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .03 and .10 per cent and melting said mixture and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding microns of mercury.
11. The process of producing a casting consisting essentially of carbon and molybdenum which consists in adding to the metal a calculated quantity of carbon sufliciently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .01 and .25 per cent and melting said mixture and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 500 microns of mercury.
12. The process of producing a casting consisting essentially of carbon and molybdenum tungsten which consists in adding to the metal a calculated quantity of carbon sufiiciently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .03 and .10 per cent and melting said mixture and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 100 microns of mercury.
13. The process of producing a casting consisting essentially of carbon and molybdenum which consists in adding to the powdered metal a calculated quantity of carbon sufiiciently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .01 and .25 per cent, sintering said powdered metal into a bar, melting said bar by utilizing it as an electrode in a vacuum arc furnace, and collecting the molten metal in a mold, said melting and collecting operations being carried out at an absolute pressure not exceeding 500 microns of mercury.
14. The process of producing a casting consisting essentially of carbon and molybdenum which consists in adding to the powdered metal a calculated quantity of carbon sufliciently in excess of that required to combine with the oxygen in said metal to produce a residual carbon content of between .03 and .10 per cent, sintering said powdered metal into a bar, melting said bar by utilizing it as an electrode in a vacuum arc furnace, and collecting the molten metal in a mold,- said melting and collecting op- 5. 6 erations being carried out at an absolute pres- Number Name Date, sure not exceeding 500 microns of mercury. 1,658,712 Fonda Feb. 7, 1928 FREDERICK P. BENS. 1,731,267 Rich Oct. 15, 1929 JOHN L. HAM. 1,830,200 Hidnert Oct. 4, 1932 ROBERT M. PARKE. 5 2,040,566 Rohn May 12, 1936 2,277,211 Cooper Mar. 24, 1942 REFERENCES CITED N b FOREIGI: PATENTS t The following references are of record in the um er Conn ry 6 me of this, patent: m 338,409 Great Britain Nov. 20, 1930 UNITED STATES PATENTS OTHER REFERENCES Parke et a1.: Treatise in Metals Technology, Number Name Date Sept. 1946, Tech. Pub. No. 2052, 12 pages, pub.
1,365,091 Clement Jan. 11, 1921 b I t m 1 5 2 Lehmann 6' 1 7 15 y m 11$ M 11 8 Met- EngrS-. New YOlk-
Claims (1)
- 3. A CAST ALLOY CHARACTERIZED BY ITS FORGEABILITY AND CONTAINING FROM .01 TO .25 PER CENT CARBON, NOT MORE THEN .005 PER CENT OXYGEN AND THE BALANCE ESSENTIALLY ALL OF AT LEAST ONE METAL SELECTED FROM THE GROUP CONSISTING OF TUNGSTEN AND MOLYBDENUM.
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US776166A US2580273A (en) | 1947-09-25 | 1947-09-25 | Refractory metal alloy castings and methods of making same |
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US776166A US2580273A (en) | 1947-09-25 | 1947-09-25 | Refractory metal alloy castings and methods of making same |
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US2580273A true US2580273A (en) | 1951-12-25 |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2974033A (en) * | 1954-06-07 | 1961-03-07 | Titanium Metals Corp | Melting titanium metal |
US3116145A (en) * | 1962-04-30 | 1963-12-31 | American Metal Climax Inc | Tungsten-hafnium alloy casting |
US3169860A (en) * | 1962-04-30 | 1965-02-16 | American Metal Climax Inc | Molybdenum-hafnium alloy casting |
US3177076A (en) * | 1961-06-12 | 1965-04-06 | American Metal Climax Inc | Forgeable high temperature cast alloys |
US3508914A (en) * | 1965-10-07 | 1970-04-28 | Us Navy | Methods of forming and purifying nickel-titanium containing alloys |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1365091A (en) * | 1921-01-11 | Allot | ||
US1652027A (en) * | 1918-12-07 | 1927-12-06 | Lohmann Hugo | Process for the manufacture of very hard metallic alloys |
US1658712A (en) * | 1924-08-30 | 1928-02-07 | Gen Electric | Zirconium alloy |
US1731267A (en) * | 1927-03-01 | 1929-10-15 | Westinghouse Lamp Co | Resistance alloy |
GB338409A (en) * | 1929-01-18 | 1930-11-20 | Ass Elect Ind | Improved manufacture of iron and iron-nickel and iron-silicon alloys |
US1880200A (en) * | 1929-10-18 | 1932-10-04 | Us Government | Low expanding alloy |
US2040566A (en) * | 1933-11-20 | 1936-05-12 | Heraeus Vacuumschmelze Ag | Vacuum method of manufacturing steel |
US2277211A (en) * | 1940-10-11 | 1942-03-24 | Hugh S Cooper | Method of producing low carbon chromium-containing iron alloys |
-
1947
- 1947-09-25 US US776166A patent/US2580273A/en not_active Expired - Lifetime
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1365091A (en) * | 1921-01-11 | Allot | ||
US1652027A (en) * | 1918-12-07 | 1927-12-06 | Lohmann Hugo | Process for the manufacture of very hard metallic alloys |
US1658712A (en) * | 1924-08-30 | 1928-02-07 | Gen Electric | Zirconium alloy |
US1731267A (en) * | 1927-03-01 | 1929-10-15 | Westinghouse Lamp Co | Resistance alloy |
GB338409A (en) * | 1929-01-18 | 1930-11-20 | Ass Elect Ind | Improved manufacture of iron and iron-nickel and iron-silicon alloys |
US1880200A (en) * | 1929-10-18 | 1932-10-04 | Us Government | Low expanding alloy |
US2040566A (en) * | 1933-11-20 | 1936-05-12 | Heraeus Vacuumschmelze Ag | Vacuum method of manufacturing steel |
US2277211A (en) * | 1940-10-11 | 1942-03-24 | Hugh S Cooper | Method of producing low carbon chromium-containing iron alloys |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2974033A (en) * | 1954-06-07 | 1961-03-07 | Titanium Metals Corp | Melting titanium metal |
US3177076A (en) * | 1961-06-12 | 1965-04-06 | American Metal Climax Inc | Forgeable high temperature cast alloys |
US3116145A (en) * | 1962-04-30 | 1963-12-31 | American Metal Climax Inc | Tungsten-hafnium alloy casting |
US3169860A (en) * | 1962-04-30 | 1965-02-16 | American Metal Climax Inc | Molybdenum-hafnium alloy casting |
US3508914A (en) * | 1965-10-07 | 1970-04-28 | Us Navy | Methods of forming and purifying nickel-titanium containing alloys |
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