US2580273A - Refractory metal alloy castings and methods of making same - Google Patents

Refractory metal alloy castings and methods of making same Download PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
metal
carbon
melting
per cent
oxygen
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
Application number
US776166A
Inventor
Frederick P Bens
John L Ham
Robert M Parke
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Climax Molybdenum Co
Original Assignee
Climax Molybdenum Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Climax Molybdenum Co filed Critical Climax Molybdenum Co
Priority to US776166A priority Critical patent/US2580273A/en
Application granted granted Critical
Publication of US2580273A publication Critical patent/US2580273A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C27/00Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
    • C22C27/04Alloys 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.

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)

  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.
US776166A 1947-09-25 1947-09-25 Refractory metal alloy castings and methods of making same Expired - Lifetime US2580273A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US776166A US2580273A (en) 1947-09-25 1947-09-25 Refractory metal alloy castings and methods of making same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US776166A US2580273A (en) 1947-09-25 1947-09-25 Refractory metal alloy castings and methods of making same

Publications (1)

Publication Number Publication Date
US2580273A true US2580273A (en) 1951-12-25

Family

ID=25106663

Family Applications (1)

Application Number Title Priority Date Filing Date
US776166A Expired - Lifetime US2580273A (en) 1947-09-25 1947-09-25 Refractory metal alloy castings and methods of making same

Country Status (1)

Country Link
US (1) US2580273A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (8)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Similar Documents

Publication Publication Date Title
US2548897A (en) Process for melting hafnium, zirconium, and titanium metals
US2467675A (en) Alloy of high density
CN109402428A (en) A kind of preparation method of high cleanliness powder metallurgy high-temperature alloy master alloy
US2678269A (en) Molybdenum-titanium alloys
US1437984A (en) Preparation of rare metals
US2580273A (en) Refractory metal alloy castings and methods of making same
US2678272A (en) Molybdenum-columbium alloys
US1906567A (en) Metal alloy
US3116145A (en) Tungsten-hafnium alloy casting
GB671171A (en) An improved process for forming ingots of refractory metal
US3054166A (en) Electrodes for melting refractory metals
US2675310A (en) Consolidation of metal powder
US3174853A (en) Chromium base alloys
US3194657A (en) Process for making workable ruthenium and product thereof
US3770392A (en) Molybdenum-base alloys
US3107165A (en) Purification of tantalum metal by reduction of the oxygen content by means of carbon
US2947624A (en) High temperature alloy
US1520794A (en) Refractory alloy for wires and rods
US1423338A (en) Alloy and the method of producing same
US3843358A (en) Master aluminum cobalt alloy
USRE26122E (en) Ductile niobium and tantalum alloys
US3372024A (en) Zone refinement of liquid-phase sintered tungsten alloys
Brace et al. Preparation and Properties of Titanium-Base Alloys
GB1496906A (en) Workable nickel material and the production thereof
US2169189A (en) Copper base alloy