EP1543172A2 - Purification of electrochemically deoxidised refractory metal particles by heat processing - Google Patents

Purification of electrochemically deoxidised refractory metal particles by heat processing

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Publication number
EP1543172A2
EP1543172A2 EP03753690A EP03753690A EP1543172A2 EP 1543172 A2 EP1543172 A2 EP 1543172A2 EP 03753690 A EP03753690 A EP 03753690A EP 03753690 A EP03753690 A EP 03753690A EP 1543172 A2 EP1543172 A2 EP 1543172A2
Authority
EP
European Patent Office
Prior art keywords
metal
particles
impurities
powder
heat source
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.)
Granted
Application number
EP03753690A
Other languages
German (de)
French (fr)
Other versions
EP1543172B1 (en
Inventor
Charles Malcolm QinetiQ Limited WARD-CLOSE
Alastair Bryan QinetiQ Limited GODFREY
Paul Stephen Casting Technology Int. GOODWIN
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.)
Metalysis Ltd
Original Assignee
Qinetiq Ltd
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
Priority claimed from GB0222219A external-priority patent/GB0222219D0/en
Priority claimed from GB0222358A external-priority patent/GB2393451A/en
Priority claimed from GB0222348A external-priority patent/GB2393450A/en
Application filed by Qinetiq Ltd filed Critical Qinetiq Ltd
Publication of EP1543172A2 publication Critical patent/EP1543172A2/en
Application granted granted Critical
Publication of EP1543172B1 publication Critical patent/EP1543172B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B34/00Obtaining refractory metals
    • C22B34/10Obtaining titanium, zirconium or hafnium
    • C22B34/12Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08
    • C22B34/1295Refining, melting, remelting, working up of titanium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B34/00Obtaining refractory metals
    • C22B34/10Obtaining titanium, zirconium or hafnium
    • C22B34/12Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08
    • C22B34/129Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08 obtaining metallic titanium from titanium compounds by dissociation, e.g. thermic dissociation of titanium tetraiodide, or by electrolysis or with the use of an electric arc
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B9/00General processes of refining or remelting of metals; Apparatus for electroslag or arc remelting of metals
    • C22B9/14Refining in the solid state

Definitions

  • This invention relates to a method for the purification of metal particles, for example, metal powders and other finely sized metal samples, and, in particular, to ones that have been produced by the process of electrochemical reduction of metal compounds.
  • the invention is particularly suited to the purification of titanium powder formed from the electrolytic reduction of titanium oxide TiO 2 .
  • WO 99/64638 describes methods for the electrolytic reduction (or "electro- reduction") of metal compounds. Certain embodiments of those methods involve the electrolysis of metal oxides or other compounds in a cell containing a liquid (fused salt) electrolyte and an anode, the metal oxide forming or contacting the cathode. Conditions are controlled so as to bring about the selective dissolution of the oxygen of the cathode in preference to deposition of the metal cation of the fused electrolyte. The metals extracted by such methods, however, often require further purification.
  • GB2359564 is directed to improved methods for carrying out such processes, particularly to produce powdered titanium, and some of those methods are summarised below:-
  • Sintered granules or powders of metal oxide can be used as the feedstock for the electrolysis described in the above referenced method, as long as appropriate conditions are present.
  • powdered titanium dioxide in the form of granules or a powder is used, the powdered particles preferably having a size in the region of 200 ⁇ m.
  • the granules of titanium dioxide 1 are held in a basket 2 below a carbon anode 3 located in a crucible 4 having a molten salt 5 therein. These are prevented from sintering together by maintaining particle motion by any appropriate method e.g. in a fluidised bed arrangement.
  • Agitation is provided either by mechanical vibration or by the injection of gas underneath the basket. Mechanical vibration can, for example, be provided by ultrasonic transducers mounted on the outside of the crucible or on control rods.
  • the key variables to be adjusted are the frequency and amplitude of the vibrations in order to get an average particle contact time which is long enough to get reduction, but short enough to prevent diffusion bonding of the particles into a solid mass. Similar principles would apply to agitation by the injection of gas, except here the flow rate of the gas and size of the gas bubbles would be the variables controlling particle contact time.
  • a metal is deposited onto a cathode (based on the electrolytic process previously described) from a second source of the metal at a more positive potential, the resulting metal deposited thereon is dendritic in structure. This is particularly so where the metal is titanium.
  • This form of titanium is easy to break up in to a powder as individual particles are connected together only by a small surface area.
  • This method can be used to produce titanium powder from titania. In this method, illustrated in Figure 2, a second cathode 6 is provided which is maintained at a potential that is more negative than the first cathode 7.
  • Continuously feeding a fine powder of metal oxide into the electrochemical cell allows for a constant current and a higher reaction rate.
  • a carbon electrode is preferred for this method. This method permits the use of cheaper feedstock as a sintering and/or forming stage is no longer needed.
  • FIG. 3 shows a conducting crucible 1 which is made the cathode containing a molten salt 2 and inserted therein is an anode 3. Titanium dioxide powder 4 is fed into the crucible where it undergoes reduction and is deposited at the base of the crucible.
  • the thick arrow shows the increasing thickness of the reduced feedstock 5.
  • the purity of the metal powder may be affected by the starting materials and processing parameters used. For example, it has been found that some variations of the method when used to produce titanium powder result in powder that contains "contaminating impurities" resulting therefrom, including light metals such as magnesium or calcium, as well as salts such as calcium chloride (the latter being a preferred electrolyte). Such impurities are known to affect the mechanical properties of alloyed metal components, for example, salt inclusions are known to affect the fatigue performance and weldability of titanium alloys.
  • the present invention thus provides a method for purifying electrochemically reduced metal particles so as to reduce or remove the aforementioned "contaminating impurities" introduced by the reduction process, so as to enable, for example, direct use of the electrolytically reduced metals in lower temperature powder metallurgy processes.
  • the kinds of impurities introduced by such electro- reduction processes are usually more volatile than the metal Mi and may be conveniently removed by the present process.
  • Such impurities may comprise light metals, for example, calcium and magnesium, as well as salts from the electrolyte, such as calcium chloride.
  • the impurities should preferably be more volatile than the metal Mi by at least a factor often, or preferably 20, in terms of their respective vapour pressures at the processing temperature.
  • the processing temperature and/or heating time should be sufficient to remove substantially all the contaminating impurities, for example, so as to reduce their total level to less than 50 ppm, or less than 10% their initial total concentration.
  • the process is conducted so that there is little or no evaporation (for example, less than 5%) of the metal Mi .
  • metal powders produced by electrolytic reduction of oxide or oxides are desirable, and a fully dense spherical particle morphology is preferred, for example in order to impart good flowability.
  • the particles may only be partially melted in order to remove said impurities, in most cases the particles need to be fully melted to achieve dense, spherical particles.
  • the heat source is arranged such that the metal particles may be allowed to free fall through the heat source.
  • Suitable heat sources include but are not strictly limited to a hot plasma torch, a hot gas flame, a tube furnace, an induction coil, electric arcs and lasers.
  • the particles may be blown through a plasma torch into the flame and allowed to free fall into a collecting vessel.
  • the torch is preferably arranged at a sufficient height above the vessel such that any portion of the particles that is melted by the heat source is substantially solidified before collection. This prevents distortion of the shape of the particles.
  • the established method of levitation melting may be used to hold particles of powder in a surrounding heat source for a period sufficient to vaporise the impurities.
  • zero gravity processing may be used. The common purpose of these embodiments is to suspend the particles individually in mid-air, out of contact with any surfaces, so as to enable particles to be heated and melted and resolidified individually, without contact with each other, or a container.
  • the temperature of the heat source should be at or above the melting point of the metal Mi.
  • the desired point is about 1680°C and for titanium alloys approximately 1500-1800°C.
  • an argon or helium arc plasma torch can achieve temperatures sufficient to melt titanium powder particles entrained in the flame.
  • the process is conducted in a controlled atmosphere, for example, at low pressure/vacuum and/or in an inert atmosphere.
  • the powder particles are kept separate from oxygen or nitrogen while above a temperature of about 500°C. This is achieved in practice either by processing in a vacuum or in an atmosphere of Ar.
  • the method is applicable to all metals and alloys provided a temperature sufficient to melt the particles and volatise the contaminants can be achieved.
  • the step of removing the impurities may simply involve allowing them to be swept away by the gas flow from the flame of the heat source.
  • the step of removing the impurities involves condensing the vaporised impurities on cold collector plates positioned adjacent the hot gas flame and disposing of the condensed impurities. Additionally, if the contaminants re-condense onto the surfaces of the powder particles Mi, then they can be removed easily with a water or dilute acid wash.
  • the inventors have appreciated that by exposing small particles of a metal Mi to a heat source at around or above the melting point, but below the boiling point of Mi, and allowing them to fall freely through the heat source, the shape of the particles can be altered to a near spherical shape. Spherical particles provide improved bonding in powder metallurgy processes.
  • the temperature of the heat source used in the purification process of the method is substantially equal to or higher than the melting point of Mi but lower than the boiling point of Mi.
  • Powdered particles purified in accordance with the method of the invention may be used in the formation of alloy metal articles made by various powder metallurgy methods and will provide improved particle bonding and mechanical properties in the alloyed article.
  • the invention provides a method for the manufacture of a metal alloy article containing a metal Mi, comprising the steps of:
  • the temperature of the heat source will be substantially equal to or above the melting point of the metal Mi .
  • the electrochemical reduction method may comprise any suitable electro- reduction method for the production of metal particles, and includes the methods described herein or as described in WO 99/64638.
  • the powder metallurgy process used may be any conventional powder metallurgy process including but not limited to powder sintering and/or forging.
  • powder sintering and/or forging One example of such a process is hot isostatic pressing.
  • Purified powders made according to the first aspect of the invention may be used in various other processes for the manufacture of metal articles where powdered starting materials are desirable.
  • Mi may be construed to mean a single metal or a combination of different metals formed in a single method.
  • References to particles may be construed to mean a powder or other finely sized metal samples, for example, granules or pellets, that could be purified by the present method.
  • a powder may be construed to comprise small particles up to about 1mm in diameter.
  • sheets, or other shapes of metals produced by the previously described electrochemical reduction methods may also be purified through the application of heat at a temperature equal to or higher than the melting point of Mi for a period sufficient to cause vaporisation of a significant proportion of the one or more impurities.
  • the sheet or other shape of metal product Mi desirably has at least one dimension that is less than or equal to about 1mm in size.
  • a method for purifying metal Mi particles manufactured by an electrochemical reduction process comprising the steps of introducing the metal Mi particles into a heat source at a temperature substantially equal to or higher than the melting point of Mi so as to melt the particles and cause substantially all the contaminating impurities to separate out from the metal into a separate phase, cooling the metal Mi particles, and removing any impurities that are still in the vicinity of the particles.
  • the impurities may merely separate out into a separate liquid phase on the surface of the molten particles, rather than vaporise, and may subsequently be removed, for example, by a washing step.
  • Figure 1 shows a prior art electrolytic cell in which the metal oxide to be reduced is in the form of granules
  • Figure 2 shows a prior art electrolytic cell in which an additional cathode is provided in order to refine the metal to a dendritic form
  • Figure 3 shows a prior art electrolytic cell employing a continuous powder feed
  • Figure 4 shows a preferred purification apparatus according to the present invention
  • Figure 5 shows an alternative purification apparatus according to the present invention
  • Figure 6 shows a schematic illustration of an apparatus for the production of titanium metal or alloy sheet
  • Figure 7 shows a schematic illustration of an apparatus for the production of titanium metal or alloy bar stock.
  • Figures 1 to 3 show, by way of example, three suitable prior art arrangements for producing metal powders by electrolytic reduction, and are discussed in more detail above.
  • FIG 4 shows a preferred arrangement for purifying a powder in which the particles are blown through a plasma torch into a flame and allowed to free fall into a collecting means.
  • the reactor 10 comprises a large metal vessel 11, provided with an inert atmosphere 12, which is preferably argon dispensed from jets 9.
  • an inert atmosphere 12 which is preferably argon dispensed from jets 9.
  • the process should be entirely contained in a metal vessel in an inert gas atmosphere.
  • the metal particles (Mi) enter the vessel from a supply hopper 14 through the plasma torch 13, which is attached and sealed to the top of the vessel 11 so that it points downwards, and provides sufficient heat to melt and vaporise the metal particles and contaminants, respectively, as they pass through the upper section of the vessel 11.
  • the torch 13 is preferably arranged at a sufficient height above the collecting means that any portion of the particles that is melted by the heat source is substantially solidified before collection. This prevents distortion of the shape of the particles.
  • the re-solidified powder is collected and sealed into a metal collection hopper 15 via a funnel cyclone collector 16.
  • levitation melting is used to hold particles of powder in a surrounding heat source for a period sufficient to vaporise the impurities.
  • the apparatus comprises a supply hopper 14 through which metal particles (Mi) enter via a valve 24 into a large ceramic tube-like chamber 23.
  • the powder is allowed to fall through the ceramic tube under its own weight.
  • an external concentric electromagnetic induction coil 22 Around the mid-section of the chamber 23 is an external concentric electromagnetic induction coil 22, which both heats and levitates the metal powder particles such that they spend sufficient time at a suitable temperature for volatile contamination removal and spheroidisation to take place.
  • the purified powder then falls to the bottom of the chamber 23, cooling sufficiently to solidify, before exiting via valve 25 and being collected and sealed into a metal canister 15.
  • an inert gas flow is introduced counter to the direction of the metal powder flow via inlet 21 and outlet 20, and this both enhances the cooling of the powder particles at the lower end of the tube, and also helps to carry away volatile species.
  • An electro-reduction process also known as an electro-deoxidation (EDO) process, is less expensive and easier to perform than conventional metal extraction methods.
  • Metal particles produced by an EDO process may advantageously be used directly as feedstocks in manufacturing processes that incorporate the present purification process as an integral stage.
  • the present invention further provides a method for the manufacture of a metal alloy article of uniform cross section comprising the steps of: introducing a continuous source of metal alloy Mi pellets, manufactured by an electrochemical reduction process, to a processing means; heating the pellets as they approach the processing means, by free-fall through a heat source, to a temperature substantially equal to or higher than the melting point of Mi so as to cause vaporisation of some or substantially all of the contaminating impurities present; removing the vaporised impurities from the vicinity of the pellets; drawing the metal through the processing means so as to coalesce the pellets to form the desired article; and, cooling the cast stock.
  • Such a manufacturing process has, in particular, significant benefits over conventional processes for the production of titanium articles.
  • Conventional methods for the manufacture of titanium and titanium alloy stock involve hot working of large titanium alloy ingots. The high temperatures and pressures required for these processes contribute to the high cost of this stock compared to other metal products such as steel and aluminium alloys.
  • Titanium is conventionally obtained from its ore by the Kroll route, a complex chlorination and magnesium reduction method.
  • the purified metal granules, called sponge are then melted with the alloying additions and cast into large titanium alloy ingots.
  • the metal is melted at least twice and sometimes more, in order to ensure chemical homogeneity and freedom from defects.
  • the large titanium alloy ingots are then hot forged repeatedly to produce the semi-finished alloy stock shapes, such as bar, plate, sheet and wire, required for the manufacture of articles.
  • the present invention aims to provide novel methods for the manufacture of titanium or other metal alloy stock, which are less expensive and easier to perform.
  • the above-mentioned manufacturing process incorporating the purification stage may involve: introducing the continuous source of pellets of the metal alloy to a pair of cooled feed rollers; heating and simultaneously purifying the pellets in the above described manner as they approach the nip of the pair of feed rollers; drawing the metal through the nip of the rollers to form a sheet of metal alloy; and, cooling the sheet.
  • pellets should be heated sufficiently to allow them to coalesce to form a sheet when subjected to the pressure of the nip, and may be heated so that they soften, or, at least partly melt, or even fully melt.
  • pellet covers particles ranging from powders to granules.
  • either or both of the feed rollers are water cooled by passing a coolant through their centres.
  • a coolant is water, other suitable fluids will no doubt occur to the skilled addressee.
  • the above-mentioned manufacturing process incorporating the purification stage may involve: introducing the continuous source of pellets of the metal alloy to a shaped crucible; heating and simultaneously purifying the pellets in the above described manner as they approach the exposed surface of the crucible; drawing the at least partially molten metal from an opposing surface of the crucible through a die, the die having a cross section of near net shape and dimensions to the desired net shape and dimensions of the required stock; and cooling the cast stock.
  • the sheet or cast stock may be allowed to cool or may be actively cooled.
  • the alloy pellets may be obtained by an electro-deoxidation process such as that described in WO 99/64638, or, in the Applicant's co-pending applications GB2359564 or GB2362164. As is described in the above specifications, electrochemical reduction may be used to provide small pellets of alloy having high purity and good grain structure. Thus, heating and purification involving softening or partially melting the pellets is sufficient to bond the pellets and obtain a mass of alloy having good mechanical properties.
  • the step of heating the pellets is preferably carried out by means of an energy beam.
  • the energy beam may, optionally, be selected from an electron beam, a laser or a plasma torch.
  • the processing temperature and/or heating time should be sufficient to remove substantially all the contaminating impurities, for example, so as to reduce their total level to less than 50 ppm, or less than 10% their initial total concentration.
  • the process is conducted so that there is little or no evaporation (for example, less than 5%) of the metal.
  • the process is conducted in a controlled atmosphere, for example, at low pressure/vacuum and/or in an inert atmosphere.
  • a controlled atmosphere for example, at low pressure/vacuum and/or in an inert atmosphere.
  • Ti it is important that the powder particles are kept separate from oxygen or nitrogen while above a temperature of about 500°C. This is achieved in practice either by processing in a vacuum or in an atmosphere of Ar.
  • the use of argon or helium arc torches is particularly preferred.
  • the rolled or cast stock may be further processed, for example, by one or more additional intermediate steps such as further working or heat treatments of the stock, prior to final cooling.
  • Products of the methods are comprised of fully dense metal alloy.
  • the homogeneity of the final metal is improved considerably because the pellets are provided via an electrochemical reduction method, as compared to the alternative of using Kroll sponge and powder or particles of the alloy additions.
  • the present methods require considerably less cumbersome and costly apparatus compared to conventional methods where the starting materials are introduced to the casting or rolling apparatus fully molten and are particularly suited to the production of small quantities of stock where mechanical properties and metal homogeneity are of importance.
  • pellets of titanium metal or alloy 31 are delivered through a hopper 32 to a pair of counter-rotating feed rollers 33a, 33b.
  • the rollers are cooled by a water-cooling system (not shown).
  • An energy beam 34 is arranged to concentrate a beam of energy along a line just above the nip of rollers 33 a, 33b and causes at least partial melting of the pellets seated on and between the rollers.
  • the rollers 33 a, 33b rotate, the at least partially melted pellets are drawn into the nip and are squeezed together to form a solid mass of the titanium or titanium alloy in the form of a sheet 35.
  • the hot sheet falls to a conveyor 36 and is carried away for further processing and/or cooling.
  • Figure 7 illustrates a similar arrangement for the production of bar stock having a square cross-section.
  • a source of pellets 41 is delivered through a hopper 42 to a shallow crucible 47.
  • a laser 44 is mounted on a track 48 along which the energy beam sweeps back and forth.
  • the energy beam is aimed at the top surface of the crucible 47 and causes at least partial melting of the pellets 41 delivered thereto.
  • the metal is drawn through a square shaped die 49 communicating with a lower surface of the crucible 47 and bar stock 45 of the titanium or titanium alloy emerges.
  • the bar stock may be cut to length by a cutter (not shown).
  • the bar stock is collected by a conveyor system 46 and removed for cooling and/or further processing.
  • the feedstock in the form of pellets is stored inside a hopper that is an integral part of a vacuum chamber housing the roller and for example, E-beam (electron-beam) or a laser beam melting assembly.
  • E-beam electron-beam
  • the vacuum chamber is desirably at a pressure ranging from 1 x 10 "6 to 1 x 10 "5 mBar during the operation.
  • the energy beam directed at the pellets heats and at least partially melts the titanium feedstock between the roller gap, which either softens it sufficiently for it to be deformed and consolidated as it passes through the roll gap, or melts it then solidifies it instantaneously on contacting the rollers and also gets deformed into a strip subsequently.
  • the temperature of the solid strip coming out of the rollers is in the region of 600°C.
  • This method is not specific only to titanium feedstock, it has potential application for direct production of strips of any metallic powder, and especially those that are very sensitive to the absorption of impurities such as oxygen or nitrogen.
  • the method of manufacture of strip described above is ideally suited to feed stock of uniformly sized granules of less than about 1 mm dimensions. Larger granules may be optimal for production of thicker sheets by this method.
  • Rollers are desirably cooled through the centre.
  • the primary requirement is that the chamber housing the rollers should be in a vacuum (or very low pressure environment) to stop the molten titanium from picking up oxygen.
  • a water-cooled roller assembly has been developed by the applicants that lets the water flow through the rollers and bearings, while maintaining good vacuum tightness.
  • the heating is conducted so as simultaneously to remove all or part of any volatile contamination that may be present in the feed material, for example, EDO granules may contain contaminants such as calcium chloride, calcium oxide or calcium metal.

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Abstract

A method for purifying metal M1 particles manufactured by an electrochemical reduction process, the method comprising the steps of introducing the metal M1 particles into a heat source (13) at a temperature substantially equal to or higher than the melting point of M1 so as to cause vaporisation of some or substantially all of the contaminating impurities present, removing the vaporised impurities from the vicinity of the particles, and cooling the purified metal M1 particles. The purified particles can be used directly in lower temperature powder metallurgy processes and have a fully dense spherical particle morphology, imparting good flowability. The purification process can also be incorporated as an integral stage of sheet or stock production processes based on particle feedstocks that have been produced by electrochemical reduction.

Description

PURIFICATION PROCESS
This invention relates to a method for the purification of metal particles, for example, metal powders and other finely sized metal samples, and, in particular, to ones that have been produced by the process of electrochemical reduction of metal compounds. The invention is particularly suited to the purification of titanium powder formed from the electrolytic reduction of titanium oxide TiO2.
WO 99/64638 describes methods for the electrolytic reduction (or "electro- reduction") of metal compounds. Certain embodiments of those methods involve the electrolysis of metal oxides or other compounds in a cell containing a liquid (fused salt) electrolyte and an anode, the metal oxide forming or contacting the cathode. Conditions are controlled so as to bring about the selective dissolution of the oxygen of the cathode in preference to deposition of the metal cation of the fused electrolyte. The metals extracted by such methods, however, often require further purification.
GB2359564 is directed to improved methods for carrying out such processes, particularly to produce powdered titanium, and some of those methods are summarised below:-
Production of powder by reduction of sintered metal oxide granules
Sintered granules or powders of metal oxide can be used as the feedstock for the electrolysis described in the above referenced method, as long as appropriate conditions are present. In one example, powdered titanium dioxide in the form of granules or a powder is used, the powdered particles preferably having a size in the region of 200μm.
As illustrated in Figure 1, the granules of titanium dioxide 1 are held in a basket 2 below a carbon anode 3 located in a crucible 4 having a molten salt 5 therein. These are prevented from sintering together by maintaining particle motion by any appropriate method e.g. in a fluidised bed arrangement. Agitation is provided either by mechanical vibration or by the injection of gas underneath the basket. Mechanical vibration can, for example, be provided by ultrasonic transducers mounted on the outside of the crucible or on control rods. The key variables to be adjusted are the frequency and amplitude of the vibrations in order to get an average particle contact time which is long enough to get reduction, but short enough to prevent diffusion bonding of the particles into a solid mass. Similar principles would apply to agitation by the injection of gas, except here the flow rate of the gas and size of the gas bubbles would be the variables controlling particle contact time.
Production of powder by deposition of Mi onto the cathode
If a metal is deposited onto a cathode (based on the electrolytic process previously described) from a second source of the metal at a more positive potential, the resulting metal deposited thereon is dendritic in structure. This is particularly so where the metal is titanium. This form of titanium is easy to break up in to a powder as individual particles are connected together only by a small surface area. This method can be used to produce titanium powder from titania. In this method, illustrated in Figure 2, a second cathode 6 is provided which is maintained at a potential that is more negative than the first cathode 7. When the deposition of titanium on the first cathode has progressed sufficiently, the second electrode is switched on, leading to the dissolution of titanium from the first cathode and deposition 8 onto the second cathode 6 in dendritic form. The other reference numerals represent the same items as in Figure 1.
Use of continuous powder feed
Continuously feeding a fine powder of metal oxide into the electrochemical cell allows for a constant current and a higher reaction rate. A carbon electrode is preferred for this method. This method permits the use of cheaper feedstock as a sintering and/or forming stage is no longer needed.
This method is shown in Figure 3 which shows a conducting crucible 1 which is made the cathode containing a molten salt 2 and inserted therein is an anode 3. Titanium dioxide powder 4 is fed into the crucible where it undergoes reduction and is deposited at the base of the crucible. The thick arrow shows the increasing thickness of the reduced feedstock 5.
In electro-reduction methods such as those exemplified above, the purity of the metal powder may be affected by the starting materials and processing parameters used. For example, it has been found that some variations of the method when used to produce titanium powder result in powder that contains "contaminating impurities" resulting therefrom, including light metals such as magnesium or calcium, as well as salts such as calcium chloride (the latter being a preferred electrolyte). Such impurities are known to affect the mechanical properties of alloyed metal components, for example, salt inclusions are known to affect the fatigue performance and weldability of titanium alloys.
A consequence of the presence of those contaminating impurities in electrolytically reduced metal powders is that they are unsuitable for use in lower temperature powder metallurgy processes such as sintering or forging which are performed at temperatures below the alloy melting temperature.
In accordance with the present invention there is provided a method for purifying metal Mi particles manufactured by an electrochemical reduction process, the method comprising the steps of :
introducing the metal Mi particles into a heat source at a temperature substantially equal to or higher than the melting point of Mi so as to cause vaporisation of some or substantially all of the contaminating impurities present;
removing the vaporised impurities from the vicinity of the particles;
and cooling the purified metal Mi particles.
The present invention thus provides a method for purifying electrochemically reduced metal particles so as to reduce or remove the aforementioned "contaminating impurities" introduced by the reduction process, so as to enable, for example, direct use of the electrolytically reduced metals in lower temperature powder metallurgy processes.
It has been found that the kinds of impurities introduced by such electro- reduction processes are usually more volatile than the metal Mi and may be conveniently removed by the present process. Such impurities may comprise light metals, for example, calcium and magnesium, as well as salts from the electrolyte, such as calcium chloride. For effective removal of impurities without significant loss of metal Mi, the impurities should preferably be more volatile than the metal Mi by at least a factor often, or preferably 20, in terms of their respective vapour pressures at the processing temperature. Preferably, the processing temperature and/or heating time should be sufficient to remove substantially all the contaminating impurities, for example, so as to reduce their total level to less than 50 ppm, or less than 10% their initial total concentration. Preferably the process is conducted so that there is little or no evaporation (for example, less than 5%) of the metal Mi .
Another feature of metal powders produced by electrolytic reduction of oxide or oxides is that the powder particles tend to be irregular in shape, contain internal cavities and have a rough outer surface. For certain powder metallurgy processes these features are undesirable, and a fully dense spherical particle morphology is preferred, for example in order to impart good flowability. Hence, although the particles may only be partially melted in order to remove said impurities, in most cases the particles need to be fully melted to achieve dense, spherical particles.
Desirably, the heat source is arranged such that the metal particles may be allowed to free fall through the heat source. Suitable heat sources include but are not strictly limited to a hot plasma torch, a hot gas flame, a tube furnace, an induction coil, electric arcs and lasers.
In one embodiment of the invention, the particles may be blown through a plasma torch into the flame and allowed to free fall into a collecting vessel. The torch is preferably arranged at a sufficient height above the vessel such that any portion of the particles that is melted by the heat source is substantially solidified before collection. This prevents distortion of the shape of the particles.
In another embodiment the established method of levitation melting may be used to hold particles of powder in a surrounding heat source for a period sufficient to vaporise the impurities. In a further embodiment, zero gravity processing may be used. The common purpose of these embodiments is to suspend the particles individually in mid-air, out of contact with any surfaces, so as to enable particles to be heated and melted and resolidified individually, without contact with each other, or a container.
The temperature of the heat source should be at or above the melting point of the metal Mi. For titanium the desired point is about 1680°C and for titanium alloys approximately 1500-1800°C. It is known that an argon or helium arc plasma torch can achieve temperatures sufficient to melt titanium powder particles entrained in the flame. Ideally, the process is conducted in a controlled atmosphere, for example, at low pressure/vacuum and/or in an inert atmosphere. In the case of Ti it is important that the powder particles are kept separate from oxygen or nitrogen while above a temperature of about 500°C. This is achieved in practice either by processing in a vacuum or in an atmosphere of Ar.
The method is applicable to all metals and alloys provided a temperature sufficient to melt the particles and volatise the contaminants can be achieved.
The step of removing the impurities may simply involve allowing them to be swept away by the gas flow from the flame of the heat source. Preferably, the step of removing the impurities involves condensing the vaporised impurities on cold collector plates positioned adjacent the hot gas flame and disposing of the condensed impurities. Additionally, if the contaminants re-condense onto the surfaces of the powder particles Mi, then they can be removed easily with a water or dilute acid wash.
Aside from improving the purity of the metal powder, the inventors have appreciated that by exposing small particles of a metal Mi to a heat source at around or above the melting point, but below the boiling point of Mi, and allowing them to fall freely through the heat source, the shape of the particles can be altered to a near spherical shape. Spherical particles provide improved bonding in powder metallurgy processes. Thus it is preferred that the temperature of the heat source used in the purification process of the method is substantially equal to or higher than the melting point of Mi but lower than the boiling point of Mi.
Powdered particles purified in accordance with the method of the invention may be used in the formation of alloy metal articles made by various powder metallurgy methods and will provide improved particle bonding and mechanical properties in the alloyed article.
In another aspect, the invention provides a method for the manufacture of a metal alloy article containing a metal Mi, comprising the steps of:
electrochemically reducing a source of a compound of the general formula MiX to remove substantially all of element X and provide powder particles consisting substantially of metal Mi;
introducing the metal powder Mi into a heat source at a temperature substantially equal to or higher than melting point of Mi for a period of time sufficient to cause vaporisation of a significant proportion of the one or more impurities;
removing the vaporised impurities;
cooling the purified metal Mi powder; and
mixing the purified Mi powder with powder of other alloy components and, optionally, performing a powder metallurgy process on the mixture to form the alloyed article.
Preferably, the temperature of the heat source will be substantially equal to or above the melting point of the metal Mi . The electrochemical reduction method may comprise any suitable electro- reduction method for the production of metal particles, and includes the methods described herein or as described in WO 99/64638.
The powder metallurgy process used may be any conventional powder metallurgy process including but not limited to powder sintering and/or forging. One example of such a process is hot isostatic pressing.
Purified powders made according to the first aspect of the invention may be used in various other processes for the manufacture of metal articles where powdered starting materials are desirable.
For the purposes of this specification Mi may be construed to mean a single metal or a combination of different metals formed in a single method. References to particles may be construed to mean a powder or other finely sized metal samples, for example, granules or pellets, that could be purified by the present method. A powder may be construed to comprise small particles up to about 1mm in diameter.
In another aspect, the inventors have found that sheets, or other shapes of metals produced by the previously described electrochemical reduction methods, may also be purified through the application of heat at a temperature equal to or higher than the melting point of Mi for a period sufficient to cause vaporisation of a significant proportion of the one or more impurities. In order to benefit fully from this inventive method, the sheet or other shape of metal product Mi desirably has at least one dimension that is less than or equal to about 1mm in size.
In a further aspect, there is provided a method for purifying metal Mi particles manufactured by an electrochemical reduction process, the method comprising the steps of introducing the metal Mi particles into a heat source at a temperature substantially equal to or higher than the melting point of Mi so as to melt the particles and cause substantially all the contaminating impurities to separate out from the metal into a separate phase, cooling the metal Mi particles, and removing any impurities that are still in the vicinity of the particles. For example, where lower temperatures are employed the impurities may merely separate out into a separate liquid phase on the surface of the molten particles, rather than vaporise, and may subsequently be removed, for example, by a washing step.
Examples employing the present invention will now be described in more detail, by way of example only, with reference to the accompanying drawings of which:
Figure 1 shows a prior art electrolytic cell in which the metal oxide to be reduced is in the form of granules;
Figure 2 shows a prior art electrolytic cell in which an additional cathode is provided in order to refine the metal to a dendritic form;
Figure 3 shows a prior art electrolytic cell employing a continuous powder feed;
Figure 4 shows a preferred purification apparatus according to the present invention;
Figure 5 shows an alternative purification apparatus according to the present invention; Figure 6 shows a schematic illustration of an apparatus for the production of titanium metal or alloy sheet; and,
Figure 7 shows a schematic illustration of an apparatus for the production of titanium metal or alloy bar stock.
Figures 1 to 3 show, by way of example, three suitable prior art arrangements for producing metal powders by electrolytic reduction, and are discussed in more detail above.
Figure 4 shows a preferred arrangement for purifying a powder in which the particles are blown through a plasma torch into a flame and allowed to free fall into a collecting means. The reactor 10 comprises a large metal vessel 11, provided with an inert atmosphere 12, which is preferably argon dispensed from jets 9. For titanium, the process should be entirely contained in a metal vessel in an inert gas atmosphere. The metal particles (Mi) enter the vessel from a supply hopper 14 through the plasma torch 13, which is attached and sealed to the top of the vessel 11 so that it points downwards, and provides sufficient heat to melt and vaporise the metal particles and contaminants, respectively, as they pass through the upper section of the vessel 11. The torch 13 is preferably arranged at a sufficient height above the collecting means that any portion of the particles that is melted by the heat source is substantially solidified before collection. This prevents distortion of the shape of the particles. The re-solidified powder is collected and sealed into a metal collection hopper 15 via a funnel cyclone collector 16.
In the alternative embodiment shown in Figure 5, levitation melting is used to hold particles of powder in a surrounding heat source for a period sufficient to vaporise the impurities. The apparatus comprises a supply hopper 14 through which metal particles (Mi) enter via a valve 24 into a large ceramic tube-like chamber 23. The powder is allowed to fall through the ceramic tube under its own weight. Around the mid-section of the chamber 23 is an external concentric electromagnetic induction coil 22, which both heats and levitates the metal powder particles such that they spend sufficient time at a suitable temperature for volatile contamination removal and spheroidisation to take place. The purified powder then falls to the bottom of the chamber 23, cooling sufficiently to solidify, before exiting via valve 25 and being collected and sealed into a metal canister 15. In a further refinement, an inert gas flow is introduced counter to the direction of the metal powder flow via inlet 21 and outlet 20, and this both enhances the cooling of the powder particles at the lower end of the tube, and also helps to carry away volatile species.
An electro-reduction process, also known as an electro-deoxidation (EDO) process, is less expensive and easier to perform than conventional metal extraction methods. Metal particles produced by an EDO process may advantageously be used directly as feedstocks in manufacturing processes that incorporate the present purification process as an integral stage.
Thus, the present invention further provides a method for the manufacture of a metal alloy article of uniform cross section comprising the steps of: introducing a continuous source of metal alloy Mi pellets, manufactured by an electrochemical reduction process, to a processing means; heating the pellets as they approach the processing means, by free-fall through a heat source, to a temperature substantially equal to or higher than the melting point of Mi so as to cause vaporisation of some or substantially all of the contaminating impurities present; removing the vaporised impurities from the vicinity of the pellets; drawing the metal through the processing means so as to coalesce the pellets to form the desired article; and, cooling the cast stock.
Such a manufacturing process has, in particular, significant benefits over conventional processes for the production of titanium articles. Conventional methods for the manufacture of titanium and titanium alloy stock involve hot working of large titanium alloy ingots. The high temperatures and pressures required for these processes contribute to the high cost of this stock compared to other metal products such as steel and aluminium alloys. Titanium is conventionally obtained from its ore by the Kroll route, a complex chlorination and magnesium reduction method. The purified metal granules, called sponge, are then melted with the alloying additions and cast into large titanium alloy ingots. The metal is melted at least twice and sometimes more, in order to ensure chemical homogeneity and freedom from defects. The large titanium alloy ingots are then hot forged repeatedly to produce the semi-finished alloy stock shapes, such as bar, plate, sheet and wire, required for the manufacture of articles.
The present invention aims to provide novel methods for the manufacture of titanium or other metal alloy stock, which are less expensive and easier to perform.
For sheet production, the above-mentioned manufacturing process incorporating the purification stage may involve: introducing the continuous source of pellets of the metal alloy to a pair of cooled feed rollers; heating and simultaneously purifying the pellets in the above described manner as they approach the nip of the pair of feed rollers; drawing the metal through the nip of the rollers to form a sheet of metal alloy; and, cooling the sheet.
The pellets should be heated sufficiently to allow them to coalesce to form a sheet when subjected to the pressure of the nip, and may be heated so that they soften, or, at least partly melt, or even fully melt. The term "pellet" covers particles ranging from powders to granules.
Preferably either or both of the feed rollers are water cooled by passing a coolant through their centres. One suitable coolant is water, other suitable fluids will no doubt occur to the skilled addressee.
Alternatively, for stock production, the above-mentioned manufacturing process incorporating the purification stage may involve: introducing the continuous source of pellets of the metal alloy to a shaped crucible; heating and simultaneously purifying the pellets in the above described manner as they approach the exposed surface of the crucible; drawing the at least partially molten metal from an opposing surface of the crucible through a die, the die having a cross section of near net shape and dimensions to the desired net shape and dimensions of the required stock; and cooling the cast stock.
The sheet or cast stock may be allowed to cool or may be actively cooled.
The alloy pellets may be obtained by an electro-deoxidation process such as that described in WO 99/64638, or, in the Applicant's co-pending applications GB2359564 or GB2362164. As is described in the above specifications, electrochemical reduction may be used to provide small pellets of alloy having high purity and good grain structure. Thus, heating and purification involving softening or partially melting the pellets is sufficient to bond the pellets and obtain a mass of alloy having good mechanical properties.
The step of heating the pellets is preferably carried out by means of an energy beam. The energy beam may, optionally, be selected from an electron beam, a laser or a plasma torch.
Preferably, the processing temperature and/or heating time should be sufficient to remove substantially all the contaminating impurities, for example, so as to reduce their total level to less than 50 ppm, or less than 10% their initial total concentration. Preferably the process is conducted so that there is little or no evaporation (for example, less than 5%) of the metal. Ideally, the process is conducted in a controlled atmosphere, for example, at low pressure/vacuum and/or in an inert atmosphere. In the case of Ti it is important that the powder particles are kept separate from oxygen or nitrogen while above a temperature of about 500°C. This is achieved in practice either by processing in a vacuum or in an atmosphere of Ar. The use of argon or helium arc torches is particularly preferred.
In either method, the rolled or cast stock may be further processed, for example, by one or more additional intermediate steps such as further working or heat treatments of the stock, prior to final cooling. Products of the methods are comprised of fully dense metal alloy. The homogeneity of the final metal is improved considerably because the pellets are provided via an electrochemical reduction method, as compared to the alternative of using Kroll sponge and powder or particles of the alloy additions. The present methods require considerably less cumbersome and costly apparatus compared to conventional methods where the starting materials are introduced to the casting or rolling apparatus fully molten and are particularly suited to the production of small quantities of stock where mechanical properties and metal homogeneity are of importance.
The present methods are particularly suited to the manufacture of low volume or small size products, which could be prohibitively costly to produce by conventional methods. Two embodiments illustrating the roller and crucible based processes will now be further described with reference to Figures 6 and 7.
As can be seen from Figure 6, pellets of titanium metal or alloy 31 are delivered through a hopper 32 to a pair of counter-rotating feed rollers 33a, 33b. The rollers are cooled by a water-cooling system (not shown). An energy beam 34 is arranged to concentrate a beam of energy along a line just above the nip of rollers 33 a, 33b and causes at least partial melting of the pellets seated on and between the rollers. As the rollers 33 a, 33b rotate, the at least partially melted pellets are drawn into the nip and are squeezed together to form a solid mass of the titanium or titanium alloy in the form of a sheet 35. The hot sheet falls to a conveyor 36 and is carried away for further processing and/or cooling.
Figure 7 illustrates a similar arrangement for the production of bar stock having a square cross-section. A source of pellets 41 is delivered through a hopper 42 to a shallow crucible 47. A laser 44 is mounted on a track 48 along which the energy beam sweeps back and forth. The energy beam is aimed at the top surface of the crucible 47 and causes at least partial melting of the pellets 41 delivered thereto. The metal is drawn through a square shaped die 49 communicating with a lower surface of the crucible 47 and bar stock 45 of the titanium or titanium alloy emerges. The bar stock may be cut to length by a cutter (not shown). The bar stock is collected by a conveyor system 46 and removed for cooling and/or further processing.
The parameters for a method carried using either of the described apparatus are more generally described below.
The feedstock in the form of pellets (including powder or granules) is stored inside a hopper that is an integral part of a vacuum chamber housing the roller and for example, E-beam (electron-beam) or a laser beam melting assembly. During operation the feedstock is poured over the rollers at a controlled rate using a regulator valve attached to the feeder. The vacuum chamber is desirably at a pressure ranging from 1 x 10"6 to 1 x 10"5 mBar during the operation. The energy beam directed at the pellets heats and at least partially melts the titanium feedstock between the roller gap, which either softens it sufficiently for it to be deformed and consolidated as it passes through the roll gap, or melts it then solidifies it instantaneously on contacting the rollers and also gets deformed into a strip subsequently. The temperature of the solid strip coming out of the rollers is in the region of 600°C. Several titanium strips of dimensions in the range 300-900 mm (length) x 60-100 mm (width) x 3.0 mm (thickness) have been produced using this method.
This method is not specific only to titanium feedstock, it has potential application for direct production of strips of any metallic powder, and especially those that are very sensitive to the absorption of impurities such as oxygen or nitrogen.
The method of manufacture of strip described above is ideally suited to feed stock of uniformly sized granules of less than about 1 mm dimensions. Larger granules may be optimal for production of thicker sheets by this method.
Rollers are desirably cooled through the centre. The primary requirement is that the chamber housing the rollers should be in a vacuum (or very low pressure environment) to stop the molten titanium from picking up oxygen. A water-cooled roller assembly has been developed by the applicants that lets the water flow through the rollers and bearings, while maintaining good vacuum tightness.
For both variants of the invention described here for the production of metal alloy sheet and the production of shaped bar stock by energy beam heating of pellets or granular feed, the heating is conducted so as simultaneously to remove all or part of any volatile contamination that may be present in the feed material, for example, EDO granules may contain contaminants such as calcium chloride, calcium oxide or calcium metal.

Claims

1. A method for purifying metal Mi particles manufactured by an electrochemical reduction process, the method comprising the steps of :
introducing the metal Mi particles into a heat source at a temperature substantially equal to or higher than the melting point of Mi so as to cause vaporisation of some or substantially all of the contaminating impurities present;
removing the vaporised impurities from the vicinity of the particles;
and cooling the purified metal Mi particles.
2. A method for the manufacture of a metal alloy article containing a metal Mi , comprising the steps of:
electrochemically reducing a source of a compound of the general formula MiX to remove substantially all of element X and provide powder particles consisting substantially of metal Mi ;
introducing the metal powder Mi into a heat source at a temperature substantially equal to or higher than melting point of Mi for a period of time sufficient to cause vaporisation of a significant proportion of the one or more impurities;
removing the vaporised impurities;
cooling the purified metal Mi powder; and
mixing the purified Mi powder with powder of other alloy components and performing a powder metallurgy process on the mixture to form the alloyed article.
3. A method as claimed in claim 1 wherein the particles are in the form of a powder.
4. A method as claimed in claim 2 wherein the powder metallurgy process involves powder sintering.
5. A method as claimed in claim 2 wherein the powder metallurgy process involves powder pressing or forging.
6. A method as claimed in any preceding claim wherein the heat source is selected from any one of a plasma torch, a laser, an electric arc, an induction coil or a tube furnace.
7. A method as claimed in any preceding claim, wherein the method is conducted in a controlled atmosphere.
8. A method as claimed in any preceding claim, wherein a further purification step comprises water or acid washing and drying of the powder.
9. A method as claimed in any preceding claim conducted in apparatus comprising a heat source, collection means for collecting the purified particles, and separate collection means for collecting the impurities.
10. A method as claimed in any preceding claim wherein the particles are suspended in mid-air and/or permitted to free fall past or within the heat source.
11. A method as claimed in claim 10 wherein the free fall distance from the heat source is sufficiently long to allow any Mi melted by the heat source to resolidify before collection.
12. A method as claimed in claim 6 wherein the heat source is a plasma torch and the step of removing the vaporised impurities involves allowing the impurities to be swept away by the hot gas flow from the torch.
13. A method as claimed in any of claims 1 to 11 wherein the step of removing the, vaporised impurities involves condensing the vaporised impurities on cold collector plates positioned adjacent the heat source and disposing of the condensed impurities.
14. A method as claimed in any preceding claim wherein the temperature of the heat source is around or above the melting point, but below the boiling point ofMi.
15. A method for purifying a piece of metal Mi having at least one dimension of lmm or less in size and manufactured by an electrochemical reduction method, the metal Mi containing impurities with a boiling point below the boiling point of Mi comprising the steps of:
treating a planar surface of the piece of metal at a temperature substantially equal to or higher than the boiling point of the one or more impurities to be removed but below the boiling point of Mi for a period of time sufficient to cause vaporisation of a significant proportion of the one or more impurities present;
removing the vaporised impurities; and
cooling the purified metal piece.
16. A method as claimed in any preceding claim wherein Mi comprises titanium.
17. A method as claimed in any of claims 2 to 16 wherein MiX is titanium oxide TiO2.
18. A method as claimed in any preceding claim wherein the impurities comprise one or more of magnesium, calcium and calcium chloride.
19. A method for the manufacture of a metal alloy article of uniform cross section comprising the steps of: introducing a continuous source of metal alloy Mi pellets, manufactured by an electrochemical reduction process, to a processing means; heating the pellets as they approach the processing means, by free-fall through a heat source, to a temperature substantially equal to or higher than the melting point of Mi so as to cause vaporisation of some or substantially all of the contaminating impurities present; removing the vaporised impurities from the vicinity of the pellets; drawing the metal through the processing means so as to coalesce the pellets to form the desired article; and, cooling the cast stock.
20. A method as claimed in claim 19 for the manufacture of a metal alloy sheet comprising the steps of: introducing the continuous source of pellets to a pair of cooled feed rollers; heating the pellets as specified in claim 19 as they approach the nip of the pair of feed rollers; drawing the metal through the nip of the rollers to form a sheet of metal alloy; and, cooling the sheet.
21. A method as' claimed in claim 20, wherein either or both of the rollers are cooled.
22. A method as claimed in claim 21, wherein the rollers are cooled by a coolant continuously flowing through their centre.
23. A method as claimed in claim 22, wherein the coolant is water.
24. A method as claimed in claim 19 for the manufacture of a uniform cross- section metal alloy stock, comprising the steps of: introducing the continuous source of pellets of the metal alloy to a shaped crucible; heating the pellets as specified in claim 19 as they approach the exposed surface of the crucible; drawing the at least partially molten metal from an opposing surface of the crucible through a die, the die having a cross section of near net shape and dimensions to the desired net shape and dimensions of the required stock; and, cooling the cast stock.
25. A method as claimed in any of claims 19 to 24, wherein the step of heating the pellets is carried out by means of an energy beam selected from an electron beam, a laser or a plasma torch.
26. A method as claimed in any of claims 20 to 25, wherein the sheet or stock is submitted to additional metal working or heat treatment processes prior to cooling.
27. A method as claimed in any of claims 19 to 26, wherein the alloy substantially comprises titanium.
28. A method substantially as described herein and with reference to any one of Figures 1 to 7.
29. Metal particles or a metal alloy article manufactured according to the method of any preceding claim.
30. A metal alloy article substantially as described herein and with reference to Figures 1 to 7.
EP03753690A 2002-09-25 2003-09-24 Purification of metal particles by heat processing Expired - Lifetime EP1543172B1 (en)

Applications Claiming Priority (7)

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GB0222219A GB0222219D0 (en) 2002-09-25 2002-09-25 Purification process
GB0222219 2002-09-25
GB0222358A GB2393451A (en) 2002-09-26 2002-09-26 A Method of Manufacture of Metal Alloy Sheet
GB0222358 2002-09-26
GB0222348 2002-09-26
GB0222348A GB2393450A (en) 2002-09-26 2002-09-26 Method of Manufacture of Metal Alloy Stock
PCT/GB2003/004093 WO2004029332A2 (en) 2002-09-25 2003-09-24 Purification of electrochemically deoxidised refractory metal particles by heat processing

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Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100438965C (en) * 2003-08-28 2008-12-03 泰克纳等离子系统公司 Process for the synthesis, separation and purification of powder materials
US20070142693A1 (en) * 2003-10-09 2007-06-21 Ebara Corporation Clarification method and apparatus for material contaminated with heavy metals
CA2972974C (en) 2014-05-13 2021-07-13 University Of Utah Research Foundation Production of substantially spherical metal powders
JP2018502218A (en) 2014-12-02 2018-01-25 ザ ユニバーシティ オブ ユタ リサーチ ファウンデイション Deoxidation of powdered metal with molten salt
CN107208978B (en) * 2015-10-22 2019-08-23 株式会社Posco Raw material charging appliance, chill roll and the method for preventing adherency ore from generating
ES2964898T3 (en) 2015-12-16 2024-04-10 6K Inc Spheroidal dehydrogenated metals and metal alloy particles
US11077497B2 (en) 2017-06-07 2021-08-03 Global Titanium Inc. Deoxidation of metal powders
CA3134573A1 (en) 2019-04-30 2020-11-05 Sunil Bhalchandra BADWE Mechanically alloyed powder feedstock
AU2020266556A1 (en) 2019-04-30 2021-11-18 6K Inc. Lithium lanthanum zirconium oxide (LLZO) powder
CN114641462A (en) 2019-11-18 2022-06-17 6K有限公司 Unique raw material for spherical powder and manufacturing method
US11590568B2 (en) 2019-12-19 2023-02-28 6K Inc. Process for producing spheroidized powder from feedstock materials
US11181325B2 (en) * 2019-12-23 2021-11-23 Valgroup S.A. System for the production of molten salt used as a heat transfer medium for a pyrolysis system
AU2021297476A1 (en) 2020-06-25 2022-12-15 6K Inc. Microcomposite alloy structure
WO2022067303A1 (en) 2020-09-24 2022-03-31 6K Inc. Systems, devices, and methods for starting plasma
KR20230095080A (en) 2020-10-30 2023-06-28 6케이 인크. Systems and methods for synthesizing spheroidized metal powders
WO2022192394A1 (en) * 2021-03-10 2022-09-15 The Regents Of The University Of California Gas-phase production of aligned metal nanoparticles using external magnetic fields
US12042861B2 (en) 2021-03-31 2024-07-23 6K Inc. Systems and methods for additive manufacturing of metal nitride ceramics
US20220324022A1 (en) * 2021-03-31 2022-10-13 6K Inc. Microwave plasma processing of spheroidized copper or other metallic powders
CN113999981A (en) * 2021-11-02 2022-02-01 广东先导微电子科技有限公司 Impurity removal method for high-purity metal through vacuum sublimation
US12040162B2 (en) 2022-06-09 2024-07-16 6K Inc. Plasma apparatus and methods for processing feed material utilizing an upstream swirl module and composite gas flows
WO2024044498A1 (en) 2022-08-25 2024-02-29 6K Inc. Plasma apparatus and methods for processing feed material utilizing a powder ingress preventor (pip)
CN115846649B (en) * 2022-12-20 2024-08-16 江苏宇钛新材料有限公司 Preparation method of low-melting-point spherical metal powder

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2943032A (en) * 1951-06-23 1960-06-28 Nat Res Corp Electrolytic production of titanium
US2876094A (en) * 1956-02-17 1959-03-03 Du Pont Production of refractory metals
US3343944A (en) * 1963-09-06 1967-09-26 Pechiney Prod Chimiques Sa Electrolytic beryllium granules and method for manufacturing same
FR1445684A (en) * 1965-06-03 1966-07-15 Commissariat Energie Atomique Device for continuous casting of refractory materials
US3690635A (en) * 1969-05-16 1972-09-12 Air Reduction Condensate collection means
US4114251A (en) * 1975-09-22 1978-09-19 Allegheny Ludlum Industries, Inc. Process for producing elongated metal articles
JPS5779134A (en) * 1980-09-08 1982-05-18 Westinghouse Electric Corp Metal refining device and method
US4390368A (en) * 1981-04-01 1983-06-28 Gte Products Corporation Flame spray powder
AT380491B (en) * 1984-02-03 1986-05-26 Kos Bernd METHOD AND DEVICE FOR THE PREPARATION OF CHIPS FROM THE MACHINING OF TITANIUM WORKPIECES
US4602947A (en) * 1984-11-01 1986-07-29 Alti Corporation Process for producing titanium metal and titanium metal alloys
US4612179A (en) * 1985-03-13 1986-09-16 Sri International Process for purification of solid silicon
LU86090A1 (en) * 1985-09-23 1987-04-02 Metallurgie Hoboken PROCESS FOR PREPARING AFFINANT TANTALUM OR NIOBIUM
JPS63183145A (en) * 1987-01-22 1988-07-28 Sumitomo Electric Ind Ltd High hardness titanium-aluminum-vanadium alloy and its production
US5336378A (en) * 1989-02-15 1994-08-09 Japan Energy Corporation Method and apparatus for producing a high-purity titanium
DE69118069D1 (en) * 1990-09-20 1996-04-25 Fujitsu Ltd Josephson device with a overlay structure of improved thermal stability
US5147451A (en) * 1991-05-14 1992-09-15 Teledyne Industries, Inc. Method for refining reactive and refractory metals
US6309595B1 (en) * 1997-04-30 2001-10-30 The Altalgroup, Inc Titanium crystal and titanium
US6024847A (en) * 1997-04-30 2000-02-15 The Alta Group, Inc. Apparatus for producing titanium crystal and titanium
GB9812169D0 (en) * 1998-06-05 1998-08-05 Univ Cambridge Tech Purification method
JP2001020065A (en) * 1999-07-07 2001-01-23 Hitachi Metals Ltd Target for sputtering, its production and high melting point metal powder material
JP3053183B1 (en) * 1999-08-27 2000-06-19 科学技術振興事業団 Floating melting using pseudo-microgravity field by magnetic force
GB2359564B (en) * 2000-02-22 2004-09-29 Secr Defence Improvements in the electrolytic reduction of metal oxides

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2004029332A3 *

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