US1111698A - Process for the manufacture of ductile bodies of high-fusing metals and alloys of the same. - Google Patents

Process for the manufacture of ductile bodies of high-fusing metals and alloys of the same. Download PDF

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US1111698A
US1111698A US84258814A US1914842588A US1111698A US 1111698 A US1111698 A US 1111698A US 84258814 A US84258814 A US 84258814A US 1914842588 A US1914842588 A US 1914842588A US 1111698 A US1111698 A US 1111698A
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tungsten
oxid
ductile
particles
powdered
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US84258814A
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Alfred J Liebmann
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NATHAN HOFHEIMER
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NATHAN HOFHEIMER
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F3/00Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
    • B22F3/18Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces by using pressure rollers

Description

, UNITED STATES PATENT OFFICE.
ALFRED J. LIEBHANN, OF NEW YORK, N. Y., ASSIGNOR TO NATHAN HOFHEIMEB, OF
NEW YORK, N. Y.
PROCESS FOR THE MANUFACTURE OF DUC'IILE BODIES OF HIGH-FUSING METALS ALLOYS OF THE SAME.
Ho Drawing.
- To all whom it may concern:
Be it known that I, ALFRED J LIEBMANN, a citizen of Switzerland, residin at No. West Ninety-fifth street, in the city, county, and State of New York, have invented certain new and useful Improvements in the Process for the Manufacture of Ductile Bodics of High-Fusing Metals and Alloys of the Same, of which the following is a specification.
This invention relates to the production of ductile bodies, masses, rods or ingots of tungsten, molybdenum, titanium, uranium and similar high-fusing metals or alloys thereof. The products'resulting from the operation of my invention are designed to be ultimately used in the manufacture of metallic bodies consisting of the above mentioned metals or their alloys for the purposes which the physical and chemical properties of these metals obviously predestine them, as for instance, filaments for incandescent lamps, :upporting hooks for such 'filaments, heating appliances, all sorts of wires and cables which have to stand a very high tension, targets for X-ray tubes or similar apparatus, contacts for magnetos and similar devices when there is-a frequent making and breaking of an electric circuit, wire cable, netting and other similar appliances where a high resistivity against chemicals of all kinds, especially acids is required.
- My invention consists in the process, more particularly herein described and claimed.
In the following description I shall refer particularly to the metal tungsten, but I wish it to be distinctly understood that it is not to be inferred that tungsten is the only metal to which this invention relates, for it also relates to the metals mentioned above and in general to all high-fusing metals and their alloys.
By means of the present invention, 1- obtain a compact massof pure tungsten metal which is ductile without any further treatment and which may thereafter, within certain limits, be treated mechanically the same as steel may be treated mechanically and can .be worked in the same manner as steel can beworked, mto any required shape or form.
Under certain precautions it can even be worked down into exceedingly fine wires which can be used for incandescent lamp Specification of Letters Patent.
Application filed J mm 3, 1914. Serial No. 842,588.
Patented Sept. 22, 1914.
filaments. It has been known quite generally 55 that the final success depends to the largest extent upon the preparation of an ingot or in which the crystalline structure of the tungsten body has been prevented from becoming coarse and the body at the same time becoming brittle.
In carrying out my invention, I take a quantity of metallic tungsten powder and intimately mix it with tungsten tri-oxid WO or some lower oxid of tungsten. It will thus be made possible to obtain a coherent body of tungsten from a tungsten powder of almost any structure whatsoever, thus gaining a distinct advantageover the previous methods known to the art,for as a rule previous investigators have had to confine themselves to material within narrow limits, with regard to its physical or molecular condition.
I have discovered that I can use a tungsten metal powder of almost any size of grain by simply choosing a simllar sized grain of tungsten oxid powder which is to be mixed withthe metal owder. A further wide possibility of varlation is given by a still further possibility is given in the free choice of a higher or lower oxid of tungsten.
which is to be mixed with the metalpowder inasmuch as the larger the size of the grain of the tungsten metal, the higher the oxid which is to be used therewith and vice-versa. By the expression higher or lower oxid 1 means that the chemical composition of the oxide used may be between W0, and W,().
In carrying out my invention, it is possible to transform tungsten powders of different structures into such bodies'as ingots or rods by simply using a sufiicient amount and a sufiicient kind of tungsten oxid particles which will be scattered among the particles of powdered tungsten. It is obvious that the dense structure which is desirable in the nnal ingot suggests in itself the use of a material of not too coarse a grain.
I wish it to be clearly understood, how- 25 Y of it are tapped in a measuring'cylinder,
over, that I have succeeded in roduc' ingots which may be quite easi y works even from the coarser powder by simply using the proper amount of tungsten oxid of similar gram. As a general rule, I refer to use a material of fine grain of big specific gravit In order to destroy the original crystal ine character, it is necessary to favor the formation of aggregates of crystals.- I have observed that the closer the contact of the single particles, the easierthis formation of crystal .aggregates will take place. Another means to this end, most naturally is, that the material should be pressed to other as closely as possible, therefore I submit the powdered mlxture to a very high pressure before treatment.
In the carrying out of my invention, as one of the initial materials essential thereto, I select a tungsten metal powder which has been obtained by one of the various methods that are well known, but which preferably should not be of too coarse a grain. The volume should be such that if 10 grams subjecting it to further its minimum volume will not be less than one cubic centimeter and its maximum vol ume not more than two cubic centimeters. I wish it to be clearly understood, however, that it is within the purview of my present invention to use either metallic powders of greater or smaller molecular volume which can be brought into a workable ingot by simply selecting a suitable powdered oxid to be mixed with it.-
When a very fine powdered metal tungsten is used, as above described, I mix therewith a tungsten oxid of as fine a grain as can possibly be obtained. The reason for this, is to distribute the particles of powdered oxid as much as possible among the particles of powdered tungsten metal, so that the oxid can be of the greatest help in the formation of crystal aggregates in as many places as possible. Such tungsten oxid is obtained by dissolving commercial pure tungsten oxid first in ammonia water, diluting the solution and thenprecipitating the tungsten oxid out again by administering hydrochloric acid while at the same time steam is blown through the solution, which should not be very concentrated in order to allow the oxid to reeipitate out in as fine a grain as possib e. In no case should the size of the grain permit 10 grams of it, when tapped in a measurin cylinder, to amount to more than 3.5 cubic centimeters in volume. If-the grain should be too large, these oxid particles would shrink so much in size, that their desired action would be impossible or they might even be detrimental.
to the structure of the ingot, for the reason that there would be the-possibility of the formatiorm of infinitely small holes therein.
mately heat resistingmaterial,
I have found by experiment that if the grain is too large, the formation of crystal aggregates is impaired and destruction of the originally coarse crystalline structure is' not obtaine For the best result I have found that about 1% of this fine powdered tungsten oxid should be mixed into the pure powdered tungsten metal, and to insure that it is properly distributed the two materials should be passed together through a ver fine mesh sieve and thoroughly and intimixed together. When coarser particles are used not more than 5% of powdered tungsten oxid should be mixed with the metallic tungsten powder, as I have found that more than this amount of oxid not only is of no advantage but even has a tendency to make the resultin body or ingot brittle. The mixture thus ormed is then brought into a steel mold which is capable of withstanding a very high pressure without any of its parts moving one upon the other. This .high pressureis necessa to bring the particles of powdered metal and the particles of powdered oxid in as close a contact with each other as possible, in order to facilitate their combined action during the subsequent treatment of the same. The coarser the grain of material used, the higher the pressure should be, but as a rule, I have found that a pressure of about 40-to 50 tons per square inch is sufficient. The mold to be used should be composed of several parts which can be separated from each other very gently and in such a way that the compressed mass or body when exposed by the removal of the parts of the mold does not show any cracks or splits whatsoever. This coherent mass' or body is now gently pushed from the sup- 105 porting plate on to another plate of some as for instance, tungsten molybdenum, nickel or some composition of high-fusin oxids and is then simultaneously expose to what I term a 110 combined reducing and sintering operation.
In the carrying out of my invention, I have found that this combined operation takes place in such a way that smgle' articles of the powdered metallic tungsten gin to 1 5 sinter, while at the same time, the particles of powdered tungsten oxid (which are intimatelly distributed in between and are surroun ed by the particles of owdered metallic tungsten) are being reduced. After 2 the oxid particles are completely reduced to metallic tungsten, these particles will also sinter together with the surrounding tungsten particles into an absolutely uniform body of pure tun desired quality 0 being ductile.- The particles of tungsten oxid act during the combined reducing and sintering operation as some sort of a flux for the other particles of metallic'tungsten'and gently assist in 0 n..met al which has the the formation of the uniform body of pure tungsten metal having the essential quality of ductility.
The combined process of reducing and sintering must be carried out most carefully but it gives an unlimited number of ways to obtain the final tungsten body in which the original crystalline character has been destroyed.
The combined action naturally will have to be carried on in a reducing agent. The reducing action starts at a comparatively low temperature, that is at dark red, while the sintering process actually starts later and does not progress very far until a very high temperature, even a temperature very near the melting point of tungsten is obtained. According to the invention, it is therefore quite easy to regulate the forming of the ductile body by simply carrying on the combined reducing and sintering operation either at a lower temperature or at a higher temperature depending upon the structure of the original material. If held for a long time, at a relatively low temperature, the reduction of the tungsten oxid will be carried very far, and may even be carried to the complete reduction of the oxid into the tungsten metal before the actual sintering process sets in. On the other hand, by quickly bringing up the tungsten body to a very high temperature, the sintering will set in before the reduction of the tungsten oxid has progressed very far. It can easily be seen therefore, that between these two extremes there is covered every possibility and it is only a question of skill and experience that will determine for each and every material the necessary amount and condition of the powdered tungsten oxid which is to be mixed in with the powdered tungsten metal and the regulation of temperature and other variable facts as hereinafter described, during the combined reducing and sintering process, in order to obtain a compact body of ductile tungsten.
As I have previously stated, the combined reducing and sintering operation can be carried out in any reducing agent, but as a rule I prefer hydrogen. here pure metal, without oxid is used it is not necessary to employ a reducing agent, as any inert atmosphere or even a vacuum will be sufficient to allow the sintering operation to take place;
while in the present invention, the presence of a reducing agent is absolutely necessary.
There is still, however, a possibility of delaying the reducing action as against the sintering action, or to precipitate the reducing as against the sintering operation. If the first should be desirable, the reducing agent, for instance hydrogen, can be, diluted by some inert gas, for instance nitrogen, or there might even be added a gas or vapor of oxidizing power, for instance water vapor.
- the rapidity of the reduction.
On the other hand, if the reducing action should be precipitated and the sintering action delayed, this can be very easily accomplished by not carrying out the combined operation in a quiet atmosphere of hydrogen, but in a moving current of the same. By this means, the water vapor pressure in the parts directly surrounding the coherent mass will be kept very low and therefore the reduction, which naturally is a reversible operation, takes place much more quickly than if the treatment took place merely in a quiet atmosphere 0f hydrogen. At the same time the stream of hydrogen which is a gas of very high thermal conductivity will delay the obtaining of a high temperature and thereby work in the desired direction. It has been found desirable in most cases to have a slow speed of the sintering process and at the same time a high rate of reduction, as it is found that thereby the formation of the crystal aggregates is favored and the finally resulting ingot is more ductile than if an opposite procedure is followed.
I therefore carry on the combined operation as a rule in an atmosphere of pure hydrogen which is flowing in a constant stream over the coherent tungsten body. This results in the quick removal of all reaction products, which if left in the immediate vicinity of the material would tend to reverse the action and considerably decrease I have found that it is quite necessary to carry on the reduction process to the very end in every case, for whatever purpose the final product is to be used, while the sintering process is not quite so material. It is quite sufiicient for some purposes to completely reduce the tungsteiroxid in the body and sinter it at a temperature of about 1600 to 2000 C. It is necessary, however, to carry the sinter ing process much farther, if the final product in view is to undergo great physical tests; as for instance, when it is ultimately desired to produce a filament for incandescent lamps, or a contact for magnetos or other like devices. In these cases, the temperature of the body is brought up as close as possible to the fusingpoint of the metal itself.
The step of the combined reducing and sintering operation will now be more particularly described.
The plates or boats containing the compressed bodies are pushed into a tube of a suitable material which may be heated by an electric current. I prefer to use tubes for lie purpose which are of a non-conducting material such as magnesia, alumina or .quartz which are wound with some suitable resistance material as for instance, tungsten or molybdenum wire, nickel wire, platinum foil or other wires of similar nature and a constant stream of hydrogen is maintained during the entire operation which can be carried out at any temperature between red and a bright white heat, according to the proportion which is desirable between the reducing and sintering operations. As a rule this furnace is kept at a temperature of about 800 to 1000 C. for a period of 15 to 30 minutes for each charge. The furnace structure as above described-is similar to that illustrated and described by R. Winne and C, Dantsizen in their article published in the T ransactiom American Electra-Chemical Society, vol. XX, 1911, pages 28990. Such a furnace is shown by the authors in Fig. 2. in vertical length section. The boat with the compressed body is then gently pushed into a cooling chamber at the end of the heating tube and when cooled the body is clamped at both ends into contacts of an electric circuit over which a bell is placed and through this bell a hydrogen stream is passed. In this apparatus an electric current is passed through the body and the combined operation of reducing and sintering is continued and completed by bringing the body up to the required temperature which is predetermined by the ultimate use to which the article is to be put as previously mentioned. In some instances, I bring the temperature up to as high as about 2700 to 2800 C. This temperature should be reached in progressive steps which are slower when the reducing action is .to be completed before the sintering is completed, or quicker when "the reduction is to be delayed. As a rule the maximum temperaature is reached within about 15 minutes, and upheld for about the same length .of time. The cooling 0E is conducted sufiiciently slow to prevent the. air from being sucked in by contraction of the heated atmosphere inside the bell.
The size of the body which I most commonly use is about'8" in length and 5:" square in its cross sectional dimensions. To fully sinter a body or rod of this size, as a rule a current of about 1600 amperes at about 11 volts is required, while a hydrogen stream of 300 to 500 liters per hour is passed through the covering bell. The hydrogen gas before entering the vessel in which the reducing and sintering operation takes place, should be absolutely pure and free of oxygen and at least towardthe' end of the operation perfectly dry. To this end, I pass it through a series of cleansing and drying devices. The resulting ingot of metallic tungsten is ductile and of an exceedingly fine crystalline structure. No coarse crystals willbe found in it, which if present would tend to impair the ductility. Therefore these ingots can be rolled, or drawn by any of the well known methods commonly employed by those skilled in the art in the manufacture of steel, nickel, copof drawn wire for filaments in incandescent lamps, I have observed that the filaments after burning in the lamp for some time show a tendency to develop a coarse crystalline structure and become brittle, especially if such lamps are being burned on an alternating current circuit. In order to prevent this-brittleness, I add to the tungsten powder at the same time as it is being mixed with the tungsten oxid, some oxid or mixture of oxids which will tend to lower the vapor pressure of the tungsten and thereby prevent, or at least retard the formation of coarse crystals which are the cause of the extreme brittleness of the wire. It is not necessary to use large amounts of these admixtures of oxids, and as a rule I use no more than 1 3% of the combined weight of the mixture of tungsten metal and tungsten oxid.
I have found that titanium or chromium oxid or mixtures of the same give good results, but I donot want to limit myself to these as almost any oxid which has the same tendencies will produce the same beneficial result.
Instead of adding oxide as such, I have found it convenient to add them in the form of another compound of the same metal or metals which will ultimately, especially after being heated, result in the desired oxids. To this end, I preferably use the nitrates which are as a rule easily soluble in water and can be mixed into the tungsten inetal and tungsten oxid mixture very conveniently in their watery solution and which when heated dlssociate into the oxid and nitrogen oxids Y which latter are given off as gases.
Having now described my invention, what I claim as new and desire to obtain by United States Letters Patent is:
1. The recess for the manufacture of ductile b0 ies of high-fusing metals, which metallic powder with 9.-
consists in mixin powdered oxid o the same metal sub'ectmg the mixture to a hi h pressure to one a compact mass and t en submitting the formed mass to a combined reducing and sintering operation.
'2. The process for the manufacture of ductile bodies of high-fusing metals, such as tungsten which consists in mixing into the metallic tungsten owder, about 1% of powdered tungsten oxid, subjecting the mixture to high compression thereby forming a mass of suitable dimensions and then submitting the formed mass to a combined reducing and sintering operation as and for the purpose described.
3. The process for the manufacture of i with bodies of ductile tungsten which consists in intimately mixing metallic tungsten powder powdered tungsten tri-oxidforming the mixture into a body of'suitable dimensions by compression and then simultaneously subjecting the same to a combined reducing and sinterin operation.
4. The process or the manufacture of bodies of ductile tungsten which consists in intimately mixing into metallic tungsten powder approximately 1% of pow ered tungsten oxid so that the particles of tungsten oxid are strewn in between the particles of powdered metallic tungsten, forming the mixture into a compressed mass of suitable dimensions and then submittingit to a combined reducing and sintering operation which results n thesintering 'of the particles of metallic tungsten and the complete reduction of the particles of powdered tungsten oxid to metallic tungsten and subsequently sintering the particles of metallic tungsten so reduced to the surrounding tungsten particles, thereby formform body of ductile tungste 40 mg a uniform bod of ductile tungsten. 5. The process or the manufacture of ductile bodies of tungsten which consists in intimately mixing tungsten metal powder of substantially uniform grain, with tlmgsten oxid powder of substantially the same size ofgrain so that the particles of tungsten oxi-d are strewn in between the articles of owdered metallic tungsten t en formingbt e mixture into a compressed mass of suita le dimensions and then submittin the said'mass to a combined reducing sintering operation, thereby forming a uni- 6. The rocess for the manufacture of ductile bodies of tungsten which consists in mixing with metallic tungsten owder, the grains of which are substantia y uniform in size, powdered oxid of tungsten, the chemical com osition of which is between W0 and-W then formin the mixture into a pressed mass of suitab e dimensions and then submitting the pressed mass to a combined reducing and sintering operation.
7, The process for the manufacture ofbodies of ductile tungsten which consists in intimately mixing the metallic tungsten powder of comparatlvely small sizegrain ture by compression-into a compact mass.
and then submitting the mass to a combined reducing and sintering operation.
'9. The process for the manufacture of bodies of high-fusing metals or their alloys, which process consists in mixin mto powdered metal, powdered oxid o the same metal compressing the' mixture thus ob--' tained into a suitable mold and then submitting the formed piece to a combined reducin and sintering operation.
10. Ihe process for the manufacture of ductile tungsten which consists in reducing and sintering a compact mass of powders tungsten metal and powdered tungsten oxidintimately mixed together so that the particles of tungsten oxid. will be completely surrounded by the particles of tungsten metal, the oxid acting as a flux during the reducing and sintering operation.
' In witness whereof I have hereunto set my hand at the boron h of Manhattan, city and State of New ork, this second day of June, 1914.
. ALFRED J. LIEBMANN.- In presence of ISABEL R. Thomas,
Acme 0. 0 0mm
US84258814A 1914-06-03 1914-06-03 Process for the manufacture of ductile bodies of high-fusing metals and alloys of the same. Expired - Lifetime US1111698A (en)

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2489912A (en) * 1941-12-13 1949-11-29 Westinghouse Electric Corp Method of producing tungsten alloys
US2598796A (en) * 1947-02-08 1952-06-03 Husqvarna Vapenfabriks Ab Methods for the reduction and sintering of bodies containing reducible metal compounds
US2652623A (en) * 1945-03-10 1953-09-22 Westinghouse Electric Corp Manufacture of refractory metal tubes
US2743174A (en) * 1946-04-25 1956-04-24 John R Keeler Uranium-titanium alloys
US2755925A (en) * 1952-02-26 1956-07-24 Pechiney Prod Chimiques Sa Extrusion of metals
US2877149A (en) * 1946-05-21 1959-03-10 Albert R Kaufmann Method of hot rolling uranium metal
US2977220A (en) * 1944-09-28 1961-03-28 Wood Cissie Process of producing uranium
US3185652A (en) * 1960-04-29 1965-05-25 Nuclear Corp Of America Refractory rare earth material

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2489912A (en) * 1941-12-13 1949-11-29 Westinghouse Electric Corp Method of producing tungsten alloys
US2977220A (en) * 1944-09-28 1961-03-28 Wood Cissie Process of producing uranium
US2652623A (en) * 1945-03-10 1953-09-22 Westinghouse Electric Corp Manufacture of refractory metal tubes
US2743174A (en) * 1946-04-25 1956-04-24 John R Keeler Uranium-titanium alloys
US2877149A (en) * 1946-05-21 1959-03-10 Albert R Kaufmann Method of hot rolling uranium metal
US2598796A (en) * 1947-02-08 1952-06-03 Husqvarna Vapenfabriks Ab Methods for the reduction and sintering of bodies containing reducible metal compounds
US2755925A (en) * 1952-02-26 1956-07-24 Pechiney Prod Chimiques Sa Extrusion of metals
US3185652A (en) * 1960-04-29 1965-05-25 Nuclear Corp Of America Refractory rare earth material

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