US2116400A - Hard substance alloy - Google Patents
Hard substance alloy Download PDFInfo
- Publication number
- US2116400A US2116400A US113741A US11374136A US2116400A US 2116400 A US2116400 A US 2116400A US 113741 A US113741 A US 113741A US 11374136 A US11374136 A US 11374136A US 2116400 A US2116400 A US 2116400A
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- US
- United States
- Prior art keywords
- metal
- hard
- alloy
- metals
- auxiliary
- 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.)
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Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C1/00—Making non-ferrous alloys
- C22C1/04—Making non-ferrous alloys by powder metallurgy
- C22C1/05—Mixtures of metal powder with non-metallic powder
- C22C1/051—Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor
- C22C1/053—Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor with in situ formation of hard compounds
- C22C1/056—Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor with in situ formation of hard compounds using gas
Definitions
- the hard-substance ingredient of the hard metal alloy is obtained by melting carbides, nitrides, silicides and borides of metals in the presence of atomic hydrogen and this hard substance produced under atomic-hydrogen is sintered in a powdered state with the auxiliary metals or metal alloys, for instance of the iron group. It is possible in this case to work with much higher additions of auxiliary metals without reducing the hardness, resistance and tenacity of this sintered hard metal alloy to an a 40 extent which would impair its fitness. for technical use. A metal alloy made of such components can be sintered without any special complicated equipments.
- the carbides, silicides, nitrides or borides of tungsten, molybdenum, titanium, vanadium, zirconium, cerium, silicium, boron, aluminium, beryllium, chromium formed under atomic hydrogen have proved particularly suitable for the formation of the hard metal alloy, while particularly the metals of the iron group are used, either by themselves or as alloys, as the auxiliary metals of the alloy
- Example-% of a pulverized low-carbon tungstencarbide with a carbon-content of about 3,7%, melted in the presence of atomic hydrogen, and 35% of powdered cobalt as auxiliary metal are sintered together.
- a sintered hard substance alloy of pulverized metal carbides, nitrides, silicides or borides and auxiliary metals in the production of which a metal carbide, silicide, nitride, or boride melted or formed in the presence of atomic hydrogen is sintered together with powdered auxiliary metals or metal alloys in the usual way.
- a sintered hard substance alloy according to claim 1 consisting of carbides, nitrides, silicides or borides of tungsten, molybdenum, titanium, vanadium, zirconium, cerium, silicium, boron, aluminium, beryllium or chromium, formed or melted in the presence of atomic hydrogen, and of metals of the iron group, either by themselves or alloyed with each other.
- a hard substance alloy comprising a pulverized compound chosen from the group of the carbides, nitrides, silicides and borides of a metal which compound has been melted in the presence
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Ceramic Products (AREA)
Description
: Patented May 3, 1938 UNITED STATES.
2,118,400 Hm SUBSTANCE ALLOY Paul Dusseldorf, Germany No Drawing.
rial No. 113,741.
Application December 1, 1936, Se-
In Germany December 2, I
4 Claims. .(Cl. 75-136) Up to the present it was only possible to make very hard sintered metal alloys-so-called hard metals, consisting mainly of tungsten-carbidewith a slight addition, about 5-6%, of auxiliary 5 metal. forinstance of the iron group, preferably. cobalt. If these hard metals contained more auxiliary metal their hardness was reduced to such an extent, that they no longer represented metal alloys flt for technical use. 20% of auidliary metal wastherefore taken as the maximum which should be added to the hard metal for sintering as far as hard metal alloys of tungstencarbide and auxiliary metals of the iron group are concerned. Though a. process for making sintered hard metal alloys, in which more than of auxiliary metals were added, has become known, it entailed operating at a gauge-pressure,
of about '10 kgs./sq. cm. It was only possible toincrease the content of auxiliary metal beyond 20 this figure in the case ofvdouble carbides, for instance with tungsten-chromium-double carbide, andwhen the auxiliary metal was not a pure metal of the iron group but was itself a hard metal-alloy, with an addition of tungsten and chromium, for instance. 7
' These disadvantages and difliculties are avoided and an extraordinarily hard, wear-resisting metal alloy with a high resistance and tenacity is surprisingly produced, it the hard-substance ingredient of the hard metal alloy is obtained by melting carbides, nitrides, silicides and borides of metals in the presence of atomic hydrogen and this hard substance produced under atomic-hydrogen is sintered in a powdered state with the auxiliary metals or metal alloys, for instance of the iron group. It is possible in this case to work with much higher additions of auxiliary metals without reducing the hardness, resistance and tenacity of this sintered hard metal alloy to an a 40 extent which would impair its fitness. for technical use. A metal alloy made of such components can be sintered without any special complicated equipments.
In case of the existence of various modifications of the metal carbides the use of the lower-carbon modification is advisable, thus, for instance, of the modification W2C or oi a lower carbon modification, in case of the use of tungsten-carbide melted in the presence of atomic hydrogen.
The carbides, silicides, nitrides or borides of tungsten, molybdenum, titanium, vanadium, zirconium, cerium, silicium, boron, aluminium, beryllium, chromium formed under atomic hydrogen have proved particularly suitable for the formation of the hard metal alloy, while particularly the metals of the iron group are used, either by themselves or as alloys, as the auxiliary metals of the alloy Example-% of a pulverized low-carbon tungstencarbide with a carbon-content of about 3,7%, melted in the presence of atomic hydrogen, and 35% of powdered cobalt as auxiliary metal are sintered together.
The tungsten carbide, melted in the presence of atomic hydrogen diflers considerably in structure 'and tenacity from the carbides obtained under the usual conditions, so that the alloy sintered from same also has dualities, which are. not present in the usual sintered hard-metal alloys. 1
I claim:
1. A sintered hard substance alloy of pulverized metal carbides, nitrides, silicides or borides and auxiliary metals, in the production of which a metal carbide, silicide, nitride, or boride melted or formed in the presence of atomic hydrogen is sintered together with powdered auxiliary metals or metal alloys in the usual way.
2. A sintered hard substance alloy according to claim 1, consisting of carbides, nitrides, silicides or borides of tungsten, molybdenum, titanium, vanadium, zirconium, cerium, silicium, boron, aluminium, beryllium or chromium, formed or melted in the presence of atomic hydrogen, and of metals of the iron group, either by themselves or alloyed with each other.
3. A hard substance alloy comprising a pulverized compound chosen from the group of the carbides, nitrides, silicides and borides of a metal which compound has been melted in the presence
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2116400X | 1935-12-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2116400A true US2116400A (en) | 1938-05-03 |
Family
ID=7985696
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US113741A Expired - Lifetime US2116400A (en) | 1935-12-02 | 1936-12-01 | Hard substance alloy |
Country Status (1)
Country | Link |
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US (1) | US2116400A (en) |
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2637890A (en) * | 1950-09-11 | 1953-05-12 | Stark Ceramics Inc | Method of making metallic and clay articles |
US2753621A (en) * | 1953-02-11 | 1956-07-10 | Firth Sterling Inc | Sintered carbide compositions and method of making the same |
US2779579A (en) * | 1954-07-26 | 1957-01-29 | Schwarzkopf Dev Co | Conveyor for high temperature furnaces |
US2779580A (en) * | 1954-07-26 | 1957-01-29 | Schwarzkopf Dev Co | High temperature furnaces and their production |
US2829061A (en) * | 1952-09-24 | 1958-04-01 | Jay E Comeforo | Machinable ceramic bonded material and method for producing same |
US2854736A (en) * | 1955-01-20 | 1958-10-07 | Carborundum Co | Boron nitride-metal silicide bodies and the manufacture thereof |
US2862828A (en) * | 1955-11-14 | 1958-12-02 | Borolite Corp | Hot strength corrosion resistant material and production thereof |
US2888738A (en) * | 1954-06-07 | 1959-06-02 | Carborundum Co | Sintered metal bodies containing boron nitride |
US2921861A (en) * | 1953-08-19 | 1960-01-19 | Fansteel Metallurgical Corp | Method of forming titanium silicide refractory articles |
US2982619A (en) * | 1957-04-12 | 1961-05-02 | Roger A Long | Metallic compounds for use in hightemperature applications |
US3110590A (en) * | 1961-10-06 | 1963-11-12 | Du Pont | Compositions of molybdenum, nitrogen and silicon and shaped objects therefrom |
WO1984004713A1 (en) * | 1983-05-27 | 1984-12-06 | Ford Werke Ag | Method of making and using a titanium diboride comprising body |
-
1936
- 1936-12-01 US US113741A patent/US2116400A/en not_active Expired - Lifetime
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2637890A (en) * | 1950-09-11 | 1953-05-12 | Stark Ceramics Inc | Method of making metallic and clay articles |
US2829061A (en) * | 1952-09-24 | 1958-04-01 | Jay E Comeforo | Machinable ceramic bonded material and method for producing same |
US2753621A (en) * | 1953-02-11 | 1956-07-10 | Firth Sterling Inc | Sintered carbide compositions and method of making the same |
US2921861A (en) * | 1953-08-19 | 1960-01-19 | Fansteel Metallurgical Corp | Method of forming titanium silicide refractory articles |
US2888738A (en) * | 1954-06-07 | 1959-06-02 | Carborundum Co | Sintered metal bodies containing boron nitride |
US2779579A (en) * | 1954-07-26 | 1957-01-29 | Schwarzkopf Dev Co | Conveyor for high temperature furnaces |
US2779580A (en) * | 1954-07-26 | 1957-01-29 | Schwarzkopf Dev Co | High temperature furnaces and their production |
US2854736A (en) * | 1955-01-20 | 1958-10-07 | Carborundum Co | Boron nitride-metal silicide bodies and the manufacture thereof |
US2862828A (en) * | 1955-11-14 | 1958-12-02 | Borolite Corp | Hot strength corrosion resistant material and production thereof |
US2982619A (en) * | 1957-04-12 | 1961-05-02 | Roger A Long | Metallic compounds for use in hightemperature applications |
US3110590A (en) * | 1961-10-06 | 1963-11-12 | Du Pont | Compositions of molybdenum, nitrogen and silicon and shaped objects therefrom |
WO1984004713A1 (en) * | 1983-05-27 | 1984-12-06 | Ford Werke Ag | Method of making and using a titanium diboride comprising body |
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