US3595484A - Reclamation of refractory carbides from carbide materials - Google Patents

Reclamation of refractory carbides from carbide materials Download PDF

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US3595484A
US3595484A US803323*A US3595484DA US3595484A US 3595484 A US3595484 A US 3595484A US 3595484D A US3595484D A US 3595484DA US 3595484 A US3595484 A US 3595484A
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zinc
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Paul G Barnard
Heine Kenworthy
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    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/56Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B32/00Carbon; Compounds thereof
    • C01B32/90Carbides
    • C01B32/914Carbides of single elements
    • C01B32/949Tungsten or molybdenum carbides

Definitions

  • tungsten car d carbides by treating the bide are reclaimed from cemente .1 nwfi b mmn u ua .wmm c ck rn mm mwma ey mm wmm wfltwmvm bnS a ua r mmwgm Dene fv W cemented carbide with molten zinc the zinc from the mass.
  • the zinc menting agent usually cobalt, the cementing agent bond and permit the carbide and the cementing reused in preparation of cemented carbides.
  • This invention relates to recovery of refractory carbides, such as tungsten, titanium, tantalum and niobium from cemented carbides.
  • the cemented carbides are conventionally prepared by mixing the carbide powder or powders with about to percent of cobalt or nickel powder which acts as a cementing agent when the product is sintered. The result is a cemented carbide that approaches the diamond for hardness.
  • tungsten carbide is widely used as a material for insert bits used in rock drilling, in tools for cutting cast iron, nonferrous metals, etc., and in dies for drawing wire, bar or sheet metal.
  • Highly alloyed steel cutting grades usually consist largely of tungsten carbide with additions of titanium or tantalum carbide.
  • the cemented carbides are made industrially by high-pressure compacting of refractory carbide powders with the binder (usually cobalt powder) and sintering the compact below 1,000 C. in a nonoxidizing atmosphere.
  • This compact is relatively soft and can be machined to required shape and dimensions before the compact is resinter ed at about 1,400" C. in hydrogen to produce optimum desirable properties.
  • Appreciable reject scrap is generated during the processing because of cracks, chips in too] cutting edges, or the tools not meeting desired dimensions or specifications, etc. Used carbide scrap also accumulates from industrial use and can be returned for reclamation. High expense is encountered in reclaiming the carbide scrap due to difficulty in either grinding or removing the cobalt binder to loose the carbide particles. Normally, in a carbide tool, a thin film of cobalt coats each carbide particle and also cements the particles together after fusion of these films. The carbide fraction of the reject scrap could be reused if thecobalt bond could be removed, but conventional methods of dissolving the cobalt will only slowly dissolve it over a period of many weeks.
  • the refractory carbides may be recovered from the scrap material by treatment of the scrap with molten zinc to form an alloy of the zinc and the cementing agent, e.g., cobalt. This alloy is then removed by dissolving in dilute acid.
  • This dissolution with acid constitutes a relatively expensive and time consuming operation since a large volume of acid and a leaching time of about 24-30 hours is required.
  • the resulting solution must be treated to recover the zinc and cobalt, and the remainder of the leach solution becomes a waste problem.
  • this method requires additional equipment for the leaching operation and also for filtering and drying the product carbides.
  • the mixture is, therefore, readily ground to a powder of a particle size similar to that of the original carbide and cementing agent, i.e., about to 1 micron, and reused in preparation of the cemented carbide without further processing or additives.
  • the zinc vapors are also readily recovered by condensation in a cooler zone of the furnace used in the distillation.
  • the process of the invention is, therefore, unique in that virtually all components are recovered and can be reused without any waste products.
  • the drawing illustrates, in cross section, one ,specific embodiment of an apparatus suitable for use in the method of the invention.
  • This apparatus comprises a quartz vacuum tube 1 containing carbon crucible 2 imbedded in dried Mg0 sand 3.
  • Crucible 2 in which the carbide is treated with the molten zinc, is covered by carbon plate 4 having hole 5 in the center thereof.
  • Carbon sleeves 6a, 6b and 6c are located-vertically above crucible 2 and plate 4 and are separated by carbon plates 7a and 7b.
  • Carbon plate 7c covers the top of sleeve 60. Plates 7a, 7b and 7c have holes 8a, 8b and 8c therethrough and located 05 center. These plates provide surfaces for condensation of the zinc vapor as it is distilled from crucible 2.
  • Quartz sleeve 9 surrounds the major portion of the combination of crucible, sleeves and plates and serves to prevent the zinc vapors from condensing on the inside of vacuum tube 1.
  • Stainless steel vacuum head 10 is fitted to the top of vacuum tube 1 via rubber gasket 11. Head 10 is provided with a vacuum line 12 and with water inlet and outlet lines 13 and 14 for watercooling of the head.
  • the apparatus employed is conventional distillation apparatus and many possible modifications will be apparent to those skilled in the art.
  • the furnace could be modified by attaching a condensing chamber on the side of the furnace and controlling the temperature of this chamber to permit the zinc vapors to condense to liquid zinc which could be tapped before the reclaimed carbides and cobalt were cooled to room temperature.
  • Heat required for the process of the invention is supplied to the apparatus by means of any conventional means such as resistance-heating using electrical energy.
  • the weight ratio of the zinc used in the process of the invention to cobalt or nickel in the cemented carbide will usually range from about 30:] to 10:1, with a range of about 20:1 to 15:1 being preferred.
  • the temperature employed in the treatment with molten zinc will range from about 750 to 850 C., with a temperature of about 800 C. usually being optimum.
  • Time required for the treatment with the molten zinc is dependent on the size and shape of the scrap objects and will range from about 2 to 4 hours, with about 2 hours usually being suf. ficient for smaller items.
  • the zinc treatment is preferably carried out in an inert atmosphere such as helium, nitrogen, or argon.
  • Removal of the zinc is then accomplished by distillation at a temperature of about 600 to 850 C., preferably about 800 C., under a pressure of about 1 to l00'microns, preferably about 10 to 50 microns. Removal of the zinc is usually complete in about 6 to 8 hours, about 6 hours usually being sufficient.
  • the resulting, usually spongy, product is then cooled to room temperature, preferably in an inert atmosphere such as helium to avoid any possibility of oxidation.
  • This product which contains virtually all of the refractory carbide and the cementing agent, is recovered in a mass which is brittle and can be readily ground to a powder of the original particle size of about /2 to 1 micron for reuse in preparation of cemented carbides.
  • EXAMPLE 1 The apparatus employed was of the type shown in the drawing and was heated by electrical resistance. 450 grams of cemented carbide reject scrap having a particle size of V2 to 1 micron and a composition of 94 percent tungsten carbide and 6 percent cobalt were treated with an equal weight of zinc at 800 C. for 2 hours in an atmosphere of helium (provided via vacuum line). The zinc was then distilled off in 6 hours at 800 C. under a pressure of l050 microns. The zinc vapors were collected in the cooler portion of the furnace, resulting in 99.9 percent recovery of the zinc.
  • the resulting spongy carbide-cobalt product was then cooled to room temperature in vacuo to yield a brittle mass containing substantially all of the original tungsten carbide and cobalt contents. This mass was readily ground to a particle size of as to 1 micron and all material could be reused directly in the preparation of a cemented carbide.
  • EXAMPLE 2 In this example the procedure and results were essentially the same as those of example 1, except that the cemented carbide reject scrap consisted of 72 percent tungsten carbide, 12 percent tantalum carbide, 8 percent titanium carbide and 8 percent cobalt.
  • a method for reclaiming refractory carbides from cemented carbides comprising treating the cemented carbide with molten zinc for a time and at a temperature sufficient to form an alloy of the zinc and the cementing agent, and subsequently distilling the zinc from the resulting mass.
  • the apparatus employed was of the type shown in the drawings and was heated by electrical resistance. 450 grams of cemented carbide reject scrap having a particle size of A to 1 micron and a composition of 94 percent tungsten carbide and 6 percent cobalt were treated with an equal weight of zinc at 800C. for 2 hours in an atmosphere of helium (provided via vacuum line). The zinc was then distilled off in 6 hours at 800C. under a pressure of l050 microns. The zinc vapors were collected in the cooler portion of the furnace, resulting in 99.9 percent recovery of the zinc.
  • a method for reclaiming refractory carbides from cemented carbides comprising treating the cemented carbide with molten zinc for a time and at a temperature sufficient to form an alloy of the zinc and the cementing agent, and subsequently distilling the zinc from the resulting mass.

Abstract

Refractory carbides, particularly tungsten carbide, are reclaimed from cemented carbides by treating the cemented carbide with molten zinc and subsequently distilling the zinc from the mass. The zinc forms an alloy with the cementing agent, usually cobalt, thereby dissolving the carbide-cementing agent bond and permitting recovery of a mixture of the carbide and the cementing agent in a form that can be reused in preparation of cemented carbides.

Description

United States Patent [56] References Cited UNITED STATES PATENTS [72] lnventors Paul G. Barnard;
' Aaron G. Starliper; Heine Kenworthy, all
of Rolla, Mo.
B m l W mmm mTmu n Ame MD- vh o G .OGM al 0 e E m m M G m 0 6 7 4 9 9" l l w a lm m w M .0 20 U m n 3 P. a M e m A m 91 6 8 9mm 11 391. 287 JJH 3ble oeuh 8F JT 0 06 e mm uw i DIN-13$ AFPA .1121] 253 2247 .llZlIl museum by the W of lntefior Attorneys- Ernest S. Cohen and William S. Brown [54] RECLAMATION 0F REFRACTORY CARBIDES v FROM CARBIDE MATERIALS A T A R 6 Claims 1 Drawing 8 BS R CT. efractory carbides,
particularly tungsten car d carbides by treating the bide, are reclaimed from cemente .1 nwfi b mmn u ua .wmm c ck rn mm mwma ey mm wmm wfltwmvm bnS a ua r mmwgm Dene fv W cemented carbide with molten zinc the zinc from the mass. The zinc menting agent, usually cobalt, the cementing agent bond and permit the carbide and the cementing reused in preparation of cemented carbides.
, 521 NW1 3 4 HN c 9 2 0 m =0 .0 .2 5 n m7 mm m M u n 5 a. "n n H "1 7 n ""114 u ""27 u ""1 m mm no u "h n a m mmw m m m fims u 2 w w 0 a & m U hi .I. ll. 2 0 5 55 l [.1
lllllf,
' 3.595484 PATENTEU JUL27 |97l INVENTORS PAUL 6'. BAR/VARD AARON 6. STARL/PER HE/NE KENWORTH) ATTORNEYS RECLAMATION OF REFRACTORY CARBIDES FROM CARBIDE MATERIALS This invention relates to recovery of refractory carbides, such as tungsten, titanium, tantalum and niobium from cemented carbides. The cemented carbides are conventionally prepared by mixing the carbide powder or powders with about to percent of cobalt or nickel powder which acts as a cementing agent when the product is sintered. The result is a cemented carbide that approaches the diamond for hardness. Because of this hardness tungsten carbide is widely used as a material for insert bits used in rock drilling, in tools for cutting cast iron, nonferrous metals, etc., and in dies for drawing wire, bar or sheet metal. Highly alloyed steel cutting grades usually consist largely of tungsten carbide with additions of titanium or tantalum carbide.
The cemented carbides are made industrially by high-pressure compacting of refractory carbide powders with the binder (usually cobalt powder) and sintering the compact below 1,000 C. in a nonoxidizing atmosphere. This compact is relatively soft and can be machined to required shape and dimensions before the compact is resinter ed at about 1,400" C. in hydrogen to produce optimum desirable properties.
Appreciable reject scrap is generated during the processing because of cracks, chips in too] cutting edges, or the tools not meeting desired dimensions or specifications, etc. Used carbide scrap also accumulates from industrial use and can be returned for reclamation. High expense is encountered in reclaiming the carbide scrap due to difficulty in either grinding or removing the cobalt binder to loose the carbide particles. Normally, in a carbide tool, a thin film of cobalt coats each carbide particle and also cements the particles together after fusion of these films. The carbide fraction of the reject scrap could be reused if thecobalt bond could be removed, but conventional methods of dissolving the cobalt will only slowly dissolve it over a period of many weeks.
It has previously been found, as disclosed in British Pat. No. 582,921, that the refractory carbides may be recovered from the scrap material by treatment of the scrap with molten zinc to form an alloy of the zinc and the cementing agent, e.g., cobalt. This alloy is then removed by dissolving in dilute acid. This dissolution with acid, however, constitutes a relatively expensive and time consuming operation since a large volume of acid and a leaching time of about 24-30 hours is required. Furthermore, the resulting solution must be treated to recover the zinc and cobalt, and the remainder of the leach solution becomes a waste problem. In addition, this method requires additional equipment for the leaching operation and also for filtering and drying the product carbides.
lt has now been found, according to the process of the invention, that recovery of the refractory carbide, as well as the cementing agent, from the cemented carbide may be accomplished rapidly and economically by treating the cemented carbide with molten zinc, followed by distillation of the zinc from the mixture at elevated temperature and under reduced pressure (vacuum). Treatment with the molten zinc, which results in formation of a molten alloy with the cementing agent, has been found to break the bond between the carbide and the cementing agent. Hence, when the zinc is removed from the mixture by distillation the resulting product consists of a mixture of the carbide and the cementing agent in which the bond between the twois broken. The mixture is, therefore, readily ground to a powder of a particle size similar to that of the original carbide and cementing agent, i.e., about to 1 micron, and reused in preparation of the cemented carbide without further processing or additives. The zinc vapors are also readily recovered by condensation in a cooler zone of the furnace used in the distillation. The process of the invention is, therefore, unique in that virtually all components are recovered and can be reused without any waste products.
The drawing illustrates, in cross section, one ,specific embodiment of an apparatus suitable for use in the method of the invention. This apparatus comprises a quartz vacuum tube 1 containing carbon crucible 2 imbedded in dried Mg0 sand 3. Crucible 2, in which the carbide is treated with the molten zinc, is covered by carbon plate 4 having hole 5 in the center thereof. Carbon sleeves 6a, 6b and 6c are located-vertically above crucible 2 and plate 4 and are separated by carbon plates 7a and 7b. Carbon plate 7c covers the top of sleeve 60. Plates 7a, 7b and 7c have holes 8a, 8b and 8c therethrough and located 05 center. These plates provide surfaces for condensation of the zinc vapor as it is distilled from crucible 2. Quartz sleeve 9 surrounds the major portion of the combination of crucible, sleeves and plates and serves to prevent the zinc vapors from condensing on the inside of vacuum tube 1. Stainless steel vacuum head 10 is fitted to the top of vacuum tube 1 via rubber gasket 11. Head 10 is provided with a vacuum line 12 and with water inlet and outlet lines 13 and 14 for watercooling of the head.
The apparatus employed is conventional distillation apparatus and many possible modifications will be apparent to those skilled in the art. For example, for large scale industrial application the furnace could be modified by attaching a condensing chamber on the side of the furnace and controlling the temperature of this chamber to permit the zinc vapors to condense to liquid zinc which could be tapped before the reclaimed carbides and cobalt were cooled to room temperature. Heat required for the process of the invention is supplied to the apparatus by means of any conventional means such as resistance-heating using electrical energy.
The weight ratio of the zinc used in the process of the invention to cobalt or nickel in the cemented carbide will usually range from about 30:] to 10:1, with a range of about 20:1 to 15:1 being preferred. The temperature employed in the treatment with molten zinc will range from about 750 to 850 C., with a temperature of about 800 C. usually being optimum. Time required for the treatment with the molten zinc is dependent on the size and shape of the scrap objects and will range from about 2 to 4 hours, with about 2 hours usually being suf. ficient for smaller items. The zinc treatment is preferably carried out in an inert atmosphere such as helium, nitrogen, or argon.
Removal of the zinc is then accomplished by distillation at a temperature of about 600 to 850 C., preferably about 800 C., under a pressure of about 1 to l00'microns, preferably about 10 to 50 microns. Removal of the zinc is usually complete in about 6 to 8 hours, about 6 hours usually being sufficient. The resulting, usually spongy, product is then cooled to room temperature, preferably in an inert atmosphere such as helium to avoid any possibility of oxidation. This product, which contains virtually all of the refractory carbide and the cementing agent, is recovered in a mass which is brittle and can be readily ground to a powder of the original particle size of about /2 to 1 micron for reuse in preparation of cemented carbides.
The following examples will illustrate the invention:
EXAMPLE 1 The apparatus employed was of the type shown in the drawing and was heated by electrical resistance. 450 grams of cemented carbide reject scrap having a particle size of V2 to 1 micron and a composition of 94 percent tungsten carbide and 6 percent cobalt were treated with an equal weight of zinc at 800 C. for 2 hours in an atmosphere of helium (provided via vacuum line). The zinc was then distilled off in 6 hours at 800 C. under a pressure of l050 microns. The zinc vapors were collected in the cooler portion of the furnace, resulting in 99.9 percent recovery of the zinc.
The resulting spongy carbide-cobalt product was then cooled to room temperature in vacuo to yield a brittle mass containing substantially all of the original tungsten carbide and cobalt contents. This mass was readily ground to a particle size of as to 1 micron and all material could be reused directly in the preparation of a cemented carbide.
EXAMPLE 2 In this example the procedure and results were essentially the same as those of example 1, except that the cemented carbide reject scrap consisted of 72 percent tungsten carbide, 12 percent tantalum carbide, 8 percent titanium carbide and 8 percent cobalt.
What we claim is:
l. A method for reclaiming refractory carbides from cemented carbides comprising treating the cemented carbide with molten zinc for a time and at a temperature sufficient to form an alloy of the zinc and the cementing agent, and subsequently distilling the zinc from the resulting mass.
2. The method of claim 1 in which the refractory carbide consists essentially of tungsten carbide.
3. The method of claim 1 in which the cementing agent is cobalt.
4. The method of claim 1 in which the temperature and time of the treatment with molten zinc are about 750 to 800 C. and 3 to 2 hours, respectively.
5. The method of claim 1 in which the distillation of the zinc is carried out at a temperature of about 700 to 800 C. and under a partial vacuum of about 10 to 50 microns.
6. The method of claim 1 in which the resulting mass is subsequently cooled to room temperature in an inert atmosphere or in a vacuum and then ground to a powder for reuse in preparation of a cemented carbide.
The apparatus employed was of the type shown in the drawings and was heated by electrical resistance. 450 grams of cemented carbide reject scrap having a particle size of A to 1 micron and a composition of 94 percent tungsten carbide and 6 percent cobalt were treated with an equal weight of zinc at 800C. for 2 hours in an atmosphere of helium (provided via vacuum line). The zinc was then distilled off in 6 hours at 800C. under a pressure of l050 microns. The zinc vapors were collected in the cooler portion of the furnace, resulting in 99.9 percent recovery of the zinc.
In this example the procedure and results were essentially the same as those of example 1, except that the cemented carbide reject scrap consisted of 72 percent tungsten carbide, 12 percent tantalum carbide, 8 percent titanium carbide and 8 percent cobalt.
What We claim is:
l. A method for reclaiming refractory carbides from cemented carbides comprising treating the cemented carbide with molten zinc for a time and at a temperature sufficient to form an alloy of the zinc and the cementing agent, and subsequently distilling the zinc from the resulting mass.
2. The method of claim 1 in which the refractory carbide consists essentially of tungsten carbide.
3. The method of claim 1 in which the cementing agent is cobalt.
6. The method of claim 1 in which the resulting mass is subsequently cooled to room temperature in an inert atmosphere or in a vacuum and then ground to a powder for reuse in preparation of a cemented carbide.

Claims (8)

  1. 2. The method of claim 1 in which the refractory carbide consists essentially of tungsten carbide.
  2. 2. The method of claim 1 in which the refractory carbide consists essentially of tungsten carbide.
  3. 3. The method of claim 1 in which the cementing agent is cobalt.
  4. 3. The method of claim 1 in which the cementing agent is cobalt.
  5. 4. The method of claim 1 in which the temperature and time of the treatment with molten zinc are about 750* to 800* C. and 3 to 2 hours, respectively.
  6. 5. The method of claim 1 in which the distillation of the zinc is carried out at a temperature of about 700* to 800* C. and under a partial vacuum of about 10 to 50 microns.
  7. 6. The method of claim 1 in which the resulting mass is subsequently cooled to room temperature in an inert atmosphere or in a vacuum and then ground to a powder for reuse in preparation of a cemented carbide.
  8. 6. The method of claim 1 in which the resulting mass is subsequently cooled to room temperature in an inert atmosphere or in a vacuum and then ground to a powder for reuse in preparation of a cemented carbide. The apparatus employed was of the type shown in the drawings and was heated by electrical resistance. 450 grams of cemented carbide reject scrap having a particle size of 1/2 to 1 micron and a composition of 94 percent tungsten carbide and 6 percent cobalt were treated with an equal weight of zinc at 800*C. for 2 hours in an atmosphere of helium (provided via vacuum line). The zinc was then distilled off in 6 hours at 800*C. under a pressure of 10-50 microns. The zinc vapors were collected in the cooler portion of the furnace, resulting in 99.9 percent recovery of the zinc. In this example the procedure and results were essentially the same as those of example 1, except that the cemented carbide reject scrap consisted of 72 percent tungsten carbide, 12 percent tantalum carbide, 8 percent titanium carbide and 8 percent cobalt. What We claim is:
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Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4879154A (en) * 1972-01-24 1973-10-24
US4227922A (en) * 1977-06-09 1980-10-14 Encomech Engineering Services Ltd. Material separation
DE3144284A1 (en) * 1981-11-07 1983-05-19 Leybold-Heraeus GmbH, 5000 Köln METHOD, DEVICE AND CONTROL ARRANGEMENT FOR WORKING UP HARD METAL SCRAP BY ALLOYS
US4466945A (en) * 1982-10-18 1984-08-21 Gte Products Corporation Method of recovering metal carbides
US4816069A (en) * 1988-05-23 1989-03-28 Gte Products Corporation Method for converting cobalt to cobalt metal powder
US5186892A (en) * 1991-01-17 1993-02-16 U.S. Synthetic Corporation Method of healing cracks and flaws in a previously sintered cemented carbide tools
US5384016A (en) * 1993-11-10 1995-01-24 National Science Council Process for recovering tungsten carbide from cemented tungsten carbide scraps by selective electrolysis
DE19521333C1 (en) * 1995-06-12 1996-12-05 Starck H C Gmbh Co Kg Process for the production of sodium tungstate
JP2013019019A (en) * 2011-07-11 2013-01-31 Toyota Motor Corp Method of recycling cemented carbide and device used in the method
EP2607512A1 (en) 2011-12-21 2013-06-26 Sandvik Intellectual Property AB Method of making a cemented carbide
EP2952260A1 (en) 2014-06-05 2015-12-09 Sandvik Intellectual Property AB A method for sorting a collection of bodies comprising cemented carbide bodies and non-cemented carbide bodies
RU2581690C1 (en) * 2014-12-10 2016-04-20 Федеральное государственное бюджетное образовательное учреждение высшего образования Северо-Кавказский горно-металлургический институт (государственный технологический университет) Reactor for decomposition of wastes of hard alloys with gaseous zinc
US9656873B2 (en) 2013-11-21 2017-05-23 Kennametal Inc. Purification of tungsten carbide compositions
WO2017132710A1 (en) 2016-02-04 2017-08-10 Ceratizit Austria Gesellschaft M.B.H. Method for producing a three-dimensional hard metal body in layers
RU2643291C1 (en) * 2017-04-12 2018-01-31 Федеральное государственное бюджетное образовательное учреждение высшего образования Северо-Кавказский горно-металлургический институт (государственный технологический университет) (СКГМИ (ГТУ) Method of processing lump wastes of solid alloys
DE102020129059A1 (en) 2020-11-04 2022-05-05 Betek Gmbh & Co. Kg Process for the preparation of cemented carbide

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GB582921A (en) * 1944-10-04 1946-12-02 Powderloys Ltd Process for separation and recovery of hard constituents from sintered hard metals
US3515540A (en) * 1964-12-16 1970-06-02 Du Pont Mixed cobalt/tungsten carbide powders

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB582921A (en) * 1944-10-04 1946-12-02 Powderloys Ltd Process for separation and recovery of hard constituents from sintered hard metals
US3515540A (en) * 1964-12-16 1970-06-02 Du Pont Mixed cobalt/tungsten carbide powders

Cited By (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS4879154A (en) * 1972-01-24 1973-10-24
JPS5120189B2 (en) * 1972-01-24 1976-06-23
US4227922A (en) * 1977-06-09 1980-10-14 Encomech Engineering Services Ltd. Material separation
DE3144284A1 (en) * 1981-11-07 1983-05-19 Leybold-Heraeus GmbH, 5000 Köln METHOD, DEVICE AND CONTROL ARRANGEMENT FOR WORKING UP HARD METAL SCRAP BY ALLOYS
US4466945A (en) * 1982-10-18 1984-08-21 Gte Products Corporation Method of recovering metal carbides
US4816069A (en) * 1988-05-23 1989-03-28 Gte Products Corporation Method for converting cobalt to cobalt metal powder
US5186892A (en) * 1991-01-17 1993-02-16 U.S. Synthetic Corporation Method of healing cracks and flaws in a previously sintered cemented carbide tools
US5384016A (en) * 1993-11-10 1995-01-24 National Science Council Process for recovering tungsten carbide from cemented tungsten carbide scraps by selective electrolysis
DE19521333C1 (en) * 1995-06-12 1996-12-05 Starck H C Gmbh Co Kg Process for the production of sodium tungstate
US5993756A (en) * 1995-06-12 1999-11-30 H.C. Starck, Gmbh & Co. Kg Sodium tungstate preparation process
JP2013019019A (en) * 2011-07-11 2013-01-31 Toyota Motor Corp Method of recycling cemented carbide and device used in the method
WO2013092733A1 (en) 2011-12-21 2013-06-27 Sandvik Intellectual Property Ab Method of making a cemented carbide
RU2618035C2 (en) * 2011-12-21 2017-05-02 Сандвик Интеллекчуал Проперти Аб Method for producing cemented carbide
CN104024447A (en) * 2011-12-21 2014-09-03 山特维克知识产权股份有限公司 Method of making a cemented carbide
US9827612B2 (en) 2011-12-21 2017-11-28 Sandvik Intellectual Property Ab Method of making a cemented carbide
EP2607512A1 (en) 2011-12-21 2013-06-26 Sandvik Intellectual Property AB Method of making a cemented carbide
CN104024447B (en) * 2011-12-21 2016-08-10 山特维克知识产权股份有限公司 The method preparing hard alloy
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