EP0292798A2 - Procédé hydrométallurgique pour la préparation de poudre fine sphérique en métal - Google Patents

Procédé hydrométallurgique pour la préparation de poudre fine sphérique en métal Download PDF

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Publication number
EP0292798A2
EP0292798A2 EP88107645A EP88107645A EP0292798A2 EP 0292798 A2 EP0292798 A2 EP 0292798A2 EP 88107645 A EP88107645 A EP 88107645A EP 88107645 A EP88107645 A EP 88107645A EP 0292798 A2 EP0292798 A2 EP 0292798A2
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EP
European Patent Office
Prior art keywords
particles
process according
metal
droplets
metals
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.)
Withdrawn
Application number
EP88107645A
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German (de)
English (en)
Other versions
EP0292798A3 (fr
Inventor
Nelson E. Kopatz
Walter A. Johnson
Joseph E. Ritsko
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.)
Osram Sylvania Inc
Original Assignee
GTE Products Corp
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 GTE Products Corp filed Critical GTE Products Corp
Publication of EP0292798A2 publication Critical patent/EP0292798A2/fr
Publication of EP0292798A3 publication Critical patent/EP0292798A3/fr
Withdrawn legal-status Critical Current

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Classifications

    • 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
    • B22F1/00Metallic powder; Treatment of metallic powder, e.g. to facilitate working or to improve properties
    • B22F1/06Metallic powder characterised by the shape of the particles
    • B22F1/065Spherical particles

Definitions

  • This invention relates to the preparation of metal powders. More particularly it relates to the production of such powders having substantially spherical particles.
  • U.S. Patent 3,663,667 discloses a process for producing multimetal alloy powders.
  • multimetal alloy powders are produced by a process wherein an aqueous solution of at least two thermally reducible metallic compounds and water is formed, the solution is atomized into droplets having a droplet size below about 150 microns in a chamber that contains a heated gas whereby discrete solid particles are formed and the particles are thereafter heated in a reducing atmosphere and at temperatures from those sufficient to reduce said metallic compounds to temperatures below the melting point of any of the metals in said alloy.
  • U.S. Patent 3,909,241 relates to free flowing powders which are produced by feeding agglomerates through a high temperature plasma reactor to cause at least partial melting of the particles and collecting the particles in a cooling chamber containing a protective gaseous atmosphere where the particles are solidified.
  • the powders are used for plasma coating and the agglomerated raw materials are produced from slurries of metal powders and binders.
  • Both the 3,663,667 and the 3,909,241 patents are assigned to the same assignee as the present invention.
  • a process for producing metal spherical particles comprises forming an aqueous solution containing at least one metal value, evaporating sufficient water to form a reducible metal material selected from the group consisting of metal oxides, metallic salts and mixtures thereof, reducing the materials from the salt or oxide to form metallic particles. At least a portion of the metallic particles are entrained in a carrier gas and fed to a high temperature reaction zone. At least some of the particles are at least partially melted and upon solidification form spherical particles having an average particle size of less than about 20 micrometers. Particle size reduction can be performed on the reducible metal material or on the metallic particles prior to subsequent processing.
  • metal powders as starting materials in the practice of this invention because such materials dissolve more readily than other forms of metals, however, use of the powders is not essential.
  • Metallic salts that are soluble in water or in an aqueous mineral acid can be used.
  • the metallic ratio of the various metals in the subsequently formed solids of the salts, oxides or hydroxides can be calculated based upon the raw material input or the solid can be sampled and analyzed for the metal ratio in the case of alloys being produced.
  • the metal values can be dissolved in any water soluble acid.
  • the acids can include the mineral acids as well as the organic acids such as acetic, formic and the like. Hydrochloric is especially preferred because of cost and availability.
  • the resulting solution can be subjected to sufficient heat to evaporate water.
  • the metal compounds for example, the oxides, hydroxides, sulfates, nitrates, chlorides, and the like, will precipitate from the solution under certain pH conditions.
  • the solid materials can be separated from the resulting aqueous phase or the evaporation can be continued. Continued evaporation results in forming particles of a residue consisting of the metallic compounds.
  • the metal compounds may be the hydroxides, oxides or mixtures of the mineral acid salts of the metals and the metal hydroxides or oxides.
  • the residue may be agglomerated and contain oversized particles.
  • the average particle size of the materials can be reduced in size, generally below about 20 micrometers by milling, grinding or by other conventional methods of particle size reduction.
  • the particles are heated in a reducing atmosphere at a temperature above the reducing temperature of the salts but below the melting point of the metals in the particles.
  • the temperature is sufficient to evolve any water of hydration and the anion. If hydrochloric acid is used and there is water of hydration present the resulting wet hydrochloric acid evolution is very corrosive thus appropriate materials of construction must be used.
  • the temperatures employed are below the melting point of any of the metals therein but sufficiently high to reduce and leave only the cation portion of the original molecule. In most instances a temperature of at least about 500°C is required to reduce the compounds. Temperatures below about 500°C can cause insufficient reduction while temperatures above the melting point of the metal result in large fused agglomerates.
  • the metals in the resulting multimetal particles can either be combined as intermetallics or as solid solutions of the various metal components. In any event there is a homogenous distribution throughout each particle of each of the metals.
  • the particles are generally irregular in shape. If agglomeration has occurred during the reduction step, particle size reduction by conventional milling, grinding and the like can be done to achieve a desired average particle size for example less than about 20 micrometers with at least 50% being below about 20 micrometers.
  • a high velocity stream of at least partially molten metal droplets is formed.
  • a stream may be formed by any thermal spraying technique such as combustion spraying and plasma spraying.
  • Individual particles can be completely melted (which is the preferred process), however, in some instances surface melting sufficient to enable the subsequent formation of spherical particles from such partially melted particles is satisfactory.
  • the velocity of the droplets is greater than about 100 meters per second, more typically greater than 250 meters per second. Velocities on the order of 900 meters per second or greater may be achieved under certain conditions which favor these speeds which may include spraying in a vacuum.
  • a powder is fed through a thermal spray apparatus.
  • Feed powder is entrained in a carrier gas and then fed through a high temperature reactor.
  • the temperature in the reactor is preferably above the melting point of the highest melting component of the metal powder and even more preferably considerably above the melting point of the highest melting component of the material to enable a relatively short residence time in the reaction zone.
  • the stream of dispersed entrained molten metal droplets may be produced by plasma-jet torch or gun apparatus of conventional nature.
  • a source of metal powder is connected to a source of propellant gas.
  • a means is provided to mix the gas with the powder and propel the gas with entrained powder through a conduit communicating with a nozzle passage of the plasma spray apparatus.
  • the entrained powder may be fed into a vortex chamber which communicates with and is coaxial with the nozzle passage which is bored centrally through the nozzle.
  • an electric arc is maintained between an interior wall of the nozzle passage and an electrode present in the passage.
  • the electrode has a diameter smaller than the nozzle passage with which it is coaxial to so that the gas is discharged from the nozzle in the form of a plasma jet.
  • the current source is normally a DC source adapted to deliver very large currents at relatively low voltages.
  • torch temperatures can range from 5500 degrees centigrade up to about 15,000 degrees centigrade.
  • the apparatus generally must be adjusted in accordance with the melting point of the powders being sprayed and the gas employed.
  • the electrode may be retracted within the nozzle when lower melting powders are utilized with an inert gas such as nitrogen while the electrode may be more fully extended within the nozzle when higher melting powders are utilized with an inert gas such as argon.
  • metal powder entrained in an inert gas is passed at a high velocity through a strong magnetic field so as to cause a voltage to be generated in the gas stream.
  • the current source is adapted to deliver very high currents, on the order of 10,000 amperes, although the voltage may be relatively low such as 10 volts. Such currents are required to generate a very strong direct magnetic field and create a plasma.
  • Such plasma devices may include additional means for aiding in the initiation of a plasma generation, a cooling means for the torch in the form of annular chamber around the nozzle.
  • a gas which is ionized in the torch regains its heat of ionization on exiting the nozzle to create a highly intense flame.
  • the flow of gas through the plasma spray apparatus is effected at speeds at least approaching the speed of sound.
  • the typical torch comprises a conduit means having a convergent portion which converges in a downstream direction to a throat. The convergent portion communicates with an adjacent outlet opening so that the discharge of plasma is effected out the outlet opening.
  • torches may be used such as an oxy-acetylene type having high pressure fuel gas flowing through the nozzle.
  • the powder may be introduced into the gas by an aspirating effect.
  • the fuel is ignited at the nozzle outlet to provide a high temperature flame.
  • the powders utilized for the torch should be uniform in size and composition.
  • a relatively narrow size distribution is desirable because, under set flame conditions, the largest particles may not melt completely, and the smallest particles may be heated to the vaporization point. Incomplete melting is a detriment to the product uniformity, whereas vaporization and decomposition decreases process efficiency.
  • the size ranges for plasma feed powders of this invention are such that 80 percent of the particles fall within about a 15 micrometer diameter range.
  • the stream of entrained molten metal droplets which issues from the nozzle tends to expand outwardly so that the density of the droplets in the stream decreases as the distance from the nozzle increases.
  • the stream Prior to impacting a surface, the stream typically passes through a gaseous atmosphere which solidifies and decreases the velocity of the droplets. As the atmosphere approaches a vacuum, the cooling and velocity loss is diminished. It is desirable that the nozzle be positioned sufficiently distant from any surface so that the droplets remain in a droplet form during cooling and solidification. If the nozzle is too close, the droplets may solidify after impact.
  • the stream of molten particles may be directed into a cooling fluid.
  • the cooling fluid is typically disposed in a chamber which has an inlet to replenish the cooling fluid which is volatilized and heated by the molten particles and plasma gases.
  • the fluid may be provided in liquid form and volatilized to the gaseous state during the rapid solidification process.
  • the outlet is preferably in the form of a pressure relief valve.
  • the vented gas may be pumped to a collection tank and reliquified for reuse.
  • the choice of the particle cooling fluid depends on the desired results. If large cooling capacity is needed, it may be desirable to provide a cooling fluid having a high thermal capacity. An inert cooling fluid which is non-flammable and nonreactive may be desirable if contamination of the product is a problem. In other cases, a reactive atmosphere may be desirable to modify the powder. Argon and nitrogen are preferable nonreactive cooling fluids. Hydrogen may be preferable in certain cases to reduce oxides and protect from unwanted reactions. Liquid nitrogen may enhance nitride formation. If oxide formation is desired, air, under selective oxidizing conditions, is a suitable cooling fluid.
  • the melting system and cooling fluid may be selected to be compatible.
  • the cooling rate depends on the thermal conductivity of the cooling fluid and the molten particles to be cooled, the size of the stream to be cooled, the size of individual droplets, particle velocity and the temperature difference between the droplet and the cooling fluid.
  • the cooling rate of the droplets is controlled by adjusting the above mentioned variables.
  • the rate of cooling can be altered by adjusting the distance of the plasma from the liquid bath surface. The closer the nozzle to the surface of the bath, the more rapidly cooled the droplets.
  • Powder collection is conveniently accomplished by removing the collected powder from the bottom of the collection chamber.
  • the cooling fluid may be evaporated or retained if desired to provide protection against oxidation or unwanted reactions.
  • the particle size of the spherical powders will be largely dependent upon the size of the feed into the high temperature reactor. Some densification occurs and the surface area is reduced thus the apparent particle size is reduced.
  • the preferred form of particle size measurement is by micromergraphs, sedigraph or microtrac. A majority of the particles will be below about 20 micrometers or finer. The desired size will depend upon the use of the alloy. For example, in certain instances such as microcircuity applications extremely finely divided materials are desired such as less than about 3 micrometers.
  • the powdered materials of this invention are essentially spherical particles which are essentially free of elliptical shaped material and essentially free of elongated particles having rounded ends, is shown in European Patent Application WO8402864.
  • Spherical particles have an advantage over non-spherical particles in injection molding and pressing and sintering operations.
  • Ammonium hydroxide is added to a pH of about 6.5 - 7.5.
  • the iron, nickel and molybdenum are precipitated as an intimate mixture of hydroxides.
  • This mixture is then evaporated to dryness.
  • the mixture is then heated to about 350°C in air for about 3 hours to remove the excess ammonium chloride.
  • This mixture is then hammermilled to produce a powder having greater than 50% of the particles smaller than about 50 micrometers with no particles larger than about 100 micrometers. These milled particles are heated in a reducing atmosphere of H2 at a temperature of about 750°C for about 3 hours. Finely divided particles containing 78% iron and 18% nickel and 4% molybdenum are formed.
  • the Fe-Ni-Mo powder particles are entrained in an argon carrier gas.
  • the particles are fed to a Metco 9MB plasma gun at a rate of about 10 pounds per hour.
  • the gas is fed at the rate of about 6 cubic feet per hour.
  • the plasma gas (Ar +H2) is fed at the rate of about 70 cubic feet per hour.
  • the torch power is about 20 KW at about 50 volts and 400 amperes.
  • the molten droplets exit into a chamber containing inert gas.
  • the resulting powder contains two fractions, the major fraction consists of the spherical shaped resolidified particles.
  • the minor fraction consists of particles having surfaces which have been partially melted and resolidified.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nanotechnology (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)
  • Powder Metallurgy (AREA)
EP88107645A 1987-05-27 1988-05-11 Procédé hydrométallurgique pour la préparation de poudre fine sphérique en métal Withdrawn EP0292798A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US5455787A 1987-05-27 1987-05-27
US54557 1987-05-27

Publications (2)

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EP0292798A2 true EP0292798A2 (fr) 1988-11-30
EP0292798A3 EP0292798A3 (fr) 1989-08-30

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EP88107645A Withdrawn EP0292798A3 (fr) 1987-05-27 1988-05-11 Procédé hydrométallurgique pour la préparation de poudre fine sphérique en métal

Country Status (3)

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EP (1) EP0292798A3 (fr)
JP (1) JPS63307203A (fr)
CA (1) CA1330625C (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5173108A (en) * 1989-03-21 1992-12-22 Gte Products Corporation Method for controlling the oxygen content in agglomerated molybdenum powders

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0692601B2 (ja) * 1988-04-08 1994-11-16 新日本製鐵株式会社 鉄系球状粒子の製造方法
EP3710180A4 (fr) * 2017-11-14 2021-03-31 Pyrogenesis Canada Inc. Procédé et appareil de production de poudres sphériques fines à partir d'un matériau d'alimentation en poudre grossière et angulaire

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3663667A (en) * 1970-02-13 1972-05-16 Sylvania Electric Prod Process for producing metal powders
US3974245A (en) * 1973-12-17 1976-08-10 Gte Sylvania Incorporated Process for producing free flowing powder and product
GB2096176A (en) * 1981-04-01 1982-10-13 Nat Standard Co Process for producing controlled density metal bodies
JPS58224103A (ja) * 1982-06-21 1983-12-26 Mitsui Mining & Smelting Co Ltd 銅微粉の製造法
JPS5985804A (ja) * 1982-11-09 1984-05-17 Shintou Bureetaa Kk 球状鉄粉

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3663667A (en) * 1970-02-13 1972-05-16 Sylvania Electric Prod Process for producing metal powders
US3974245A (en) * 1973-12-17 1976-08-10 Gte Sylvania Incorporated Process for producing free flowing powder and product
GB2096176A (en) * 1981-04-01 1982-10-13 Nat Standard Co Process for producing controlled density metal bodies
JPS58224103A (ja) * 1982-06-21 1983-12-26 Mitsui Mining & Smelting Co Ltd 銅微粉の製造法
JPS5985804A (ja) * 1982-11-09 1984-05-17 Shintou Bureetaa Kk 球状鉄粉

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN, Vol. 8, No. 197 (M-324)[1634], 11th September 1984; & JP-A-59 085 804 (SHINTOU BUREETAA K.K.) (17-05-1984) *
PATENT ABSTRACTS OF JAPAN, Vol. 8, No. 80 (M-289)[1517], 12th April 1984; & JP-A-58 224 103 (MITSUI KINZOKU KOGYO K.K.) (26-12-1983) *
SOVIET POWDER METALLURGY AND METAL CERAMICS, Vol. 10, No. 5, May 1971, Pages 345-346, Plenum Publishing Corp., New York, US; V. Ya. BULANOV et al.: "Manufacture of alloyed iron powder by a chloride process". *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5173108A (en) * 1989-03-21 1992-12-22 Gte Products Corporation Method for controlling the oxygen content in agglomerated molybdenum powders

Also Published As

Publication number Publication date
EP0292798A3 (fr) 1989-08-30
JPS63307203A (ja) 1988-12-14
CA1330625C (fr) 1994-07-12

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