US2188405A - Molybdenum alloys - Google Patents
Molybdenum alloys Download PDFInfo
- Publication number
- US2188405A US2188405A US255871A US25587139A US2188405A US 2188405 A US2188405 A US 2188405A US 255871 A US255871 A US 255871A US 25587139 A US25587139 A US 25587139A US 2188405 A US2188405 A US 2188405A
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- molybdenum
- osmium
- alloys
- molybdenum alloys
- alloy
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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
- This invention relates to improvements in molybdenum base alloys.
- the present invention comprises a combination of elements, methods of manufacture and the product thereof brought out and exemplified in the disclosure hereinafter set forth, the scope of the invention being indicated in the appended claims.
- Per cent Molybdenum 60 to 99.75 Osmium .01 to 1 denum in solid solution and part of which exists as a free constituent, the bonded alloys showing increased hardness and considerable resistance to abrasion.
- Osmium is suitable as an alloy element for molybdenum because it has a melting point similarly high, the actual melting temperature being about 2700 centigrade while the boiling point is in the neighborhood of 5000 centigrade.
- Osmium in molybdenum can be sintered by heating to a temperature of about 2000 centigrade. Since the oxide of osmium can be readily reduced by hydrogen, the sintering can be carried out in a hydrogen atmosphere.
- molybdenum 01' high density by sintering only if small additions of osmium are being made.
- alloys up to approximately to l% of osmium in molybdenum can be manufactured by mixing the powders,,subjecting same to a high pressure to form an ingot.
- the ingot or special shapes then may be sintered and forged .or swaged, rolled or drawn to a convenient shape from which the various parts can be manufactured, forwlrrlch this alloy is particularly suitable. It is understood that one or more ofthe ingredients can be present originally in the form of chemical compounds and can be reduced a.
- our new alloying composition as a refractory base for a material composition consisting of molybdenum containing substantial quantities of osmium impregnated with low. melting point materials taken from the group copper, silver, gold, platinum and palladium and their alloys.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
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Description
Patented Jan. 30, 1940 UNITED STATES MOLYBDENUM ALLOYS Franz R. Hensel and Kenneth L. Emmert, Indianapolis, Ind., assignors to P. R. Mallory & 00., Inc., Indianapolis, Ind.,a corporation of Delaware No Drawing. Application February 11, 1939, Serial No. 255,871
2 Claims.
This invention relates to improvements in molybdenum base alloys.
It is the object of the invention to provide a material which possesses superior physical properties such as high specific gravity and satisfactory strength. Such a material is suitable for X-ray targets.
It is also an object of the present invention to provide a contact material of superior properties.
It is a further object of the invention to provide a material of high melting point and high recrystallization temperature.
Other objects of the invention will be apparent from the following description taken in connection with the appended claims.
The present invention comprises a combination of elements, methods of manufacture and the product thereof brought out and exemplified in the disclosure hereinafter set forth, the scope of the invention being indicated in the appended claims.
While a preferred embodiment of the invention is described herein, it is contemplated that considerable variation may be made in the meth od of procedure and the combination of elements without departing from the spirit of the invention.
According to the present invention an improved alloy is contemplated, having the following ingredients present in substantially theranges of proportion given below:
Per cent Molybdenum 60 to 99.75 Osmium .01 to 1 denum in solid solution and part of which exists as a free constituent, the bonded alloys showing increased hardness and considerable resistance to abrasion. Osmium is suitable as an alloy element for molybdenum because it has a melting point similarly high, the actual melting temperature being about 2700 centigrade while the boiling point is in the neighborhood of 5000 centigrade. Osmium in molybdenum can be sintered by heating to a temperature of about 2000 centigrade. Since the oxide of osmium can be readily reduced by hydrogen, the sintering can be carried out in a hydrogen atmosphere. It is also possible to produce molybdenum 01' high density by sintering only if small additions of osmium are being made. In our experiments we have found that alloys up to approximately to l% of osmium in molybdenum can be manufactured by mixing the powders,,subjecting same to a high pressure to form an ingot. The ingot or special shapes then may be sintered and forged .or swaged, rolled or drawn to a convenient shape from which the various parts can be manufactured, forwlrrlch this alloy is particularly suitable. It is understood that one or more ofthe ingredients can be present originally in the form of chemical compounds and can be reduced a. gether to the metallic state.- Binary alloys containing more than 1% of osmium are diflicult to swage and must be manufactured by sintered process only. This swaging difliculty, however, can be overcome if other elements of the tungsten group are added. The desirable characteristics described above will not be disturbed if small proportions of other ingredients are present from the iron group materials such as iron-cobalt and nickel or small percentages of tantalum, columbium, chromium and manganese.
We can use our new alloying composition as a refractory base for a material composition consisting of molybdenum containing substantial quantities of osmium impregnated with low. melting point materials taken from the group copper, silver, gold, platinum and palladium and their alloys.
' Since certain changes in producing the above alloy and certain modifications in the composition which embody the invention may be made, without departing from its scope, it is intended that all matter contained in the above description shall be interpreted as illustrative and not in a limited sense.
It is also to be understood that the following claims are intended to cover all of the generic 40 and specific features of the invention herein described and all statements of the scope of the invention, which as a matter of language might be said to fall therebetween.
What is claimed is:
1. An alloy formed of .01 to 1% osmium and the balance substantially all molybdenum.
2. An electric contact formed of an alloy of .01 to 1% osmium and the balance substantially all molybdenum. A
FRANZ R. HENSEL. 1
ENNETH L. EMMERT.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US255871A US2188405A (en) | 1939-02-11 | 1939-02-11 | Molybdenum alloys |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US255871A US2188405A (en) | 1939-02-11 | 1939-02-11 | Molybdenum alloys |
Publications (1)
Publication Number | Publication Date |
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US2188405A true US2188405A (en) | 1940-01-30 |
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Application Number | Title | Priority Date | Filing Date |
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US255871A Expired - Lifetime US2188405A (en) | 1939-02-11 | 1939-02-11 | Molybdenum alloys |
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Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2467675A (en) * | 1942-09-30 | 1949-04-19 | Callite Tungsten Corp | Alloy of high density |
US2678270A (en) * | 1951-10-06 | 1954-05-11 | Climax Molybdenum Co | Molybdenum-tantalum alloys |
US2678272A (en) * | 1951-10-06 | 1954-05-11 | Climax Molybdenum Co | Molybdenum-columbium alloys |
DE1135262B (en) * | 1954-03-01 | 1962-08-23 | Boehler & Co Ag Geb | Process for the production of wear-resistant surfaces on workpieces from non-magnetizable steels |
US3177076A (en) * | 1961-06-12 | 1965-04-06 | American Metal Climax Inc | Forgeable high temperature cast alloys |
US4370299A (en) * | 1980-07-08 | 1983-01-25 | Tokyo Shibaura Denki Kabushiki Kaisha | Molybdenum-based alloy |
-
1939
- 1939-02-11 US US255871A patent/US2188405A/en not_active Expired - Lifetime
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2467675A (en) * | 1942-09-30 | 1949-04-19 | Callite Tungsten Corp | Alloy of high density |
US2678270A (en) * | 1951-10-06 | 1954-05-11 | Climax Molybdenum Co | Molybdenum-tantalum alloys |
US2678272A (en) * | 1951-10-06 | 1954-05-11 | Climax Molybdenum Co | Molybdenum-columbium alloys |
DE1135262B (en) * | 1954-03-01 | 1962-08-23 | Boehler & Co Ag Geb | Process for the production of wear-resistant surfaces on workpieces from non-magnetizable steels |
US3177076A (en) * | 1961-06-12 | 1965-04-06 | American Metal Climax Inc | Forgeable high temperature cast alloys |
US4370299A (en) * | 1980-07-08 | 1983-01-25 | Tokyo Shibaura Denki Kabushiki Kaisha | Molybdenum-based alloy |
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