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WO1988009391A1 - Procede de preparation de titane de valence nulle a partir d'un fluotitanate de metal alcalin - Google Patents

Procede de preparation de titane de valence nulle a partir d'un fluotitanate de metal alcalin Download PDF

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Publication number
WO1988009391A1
WO1988009391A1 PCT/US1987/001217 US8701217W WO8809391A1 WO 1988009391 A1 WO1988009391 A1 WO 1988009391A1 US 8701217 W US8701217 W US 8701217W WO 8809391 A1 WO8809391 A1 WO 8809391A1
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Prior art keywords
titanium
salt
aluminum
molten
stage
Prior art date
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PCT/US1987/001217
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English (en)
Inventor
Joseph A. Megy
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Occidental Research Corp
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Occidental Research Corp
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Priority to US06/745,591 priority Critical patent/US4668286A/en
Application filed by Occidental Research Corp filed Critical Occidental Research Corp
Priority to EP19870904997 priority patent/EP0360792A4/en
Priority to JP62504687A priority patent/JPH03500063A/ja
Priority to KR1019890700136A priority patent/KR890701782A/ko
Publication of WO1988009391A1 publication Critical patent/WO1988009391A1/fr
Priority to NO890315A priority patent/NO890315D0/no
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B34/00—Obtaining refractory metals
    • C22B34/10—Obtaining titanium, zirconium or hafnium
    • C22B34/12—Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08
    • C22B34/1263—Obtaining 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, e.g. by reduction
    • C22B34/1277—Obtaining 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, e.g. by reduction using other metals, e.g. Al, Si, Mn
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B34/00—Obtaining refractory metals
    • C22B34/10—Obtaining titanium, zirconium or hafnium
    • C22B34/12—Obtaining titanium or titanium compounds from ores or scrap by metallurgical processing; preparation of titanium compounds from other titanium compounds see C01G23/00 - C01G23/08
    • C22B34/129—Obtaining 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
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00—Technologies related to metal processing
    • Y02P10/20—Recycling

Definitions

  • the instant invention relates to a process for the reduction of an alkali metal fluotitanate salt to zero valent titanium and oxidation of aluminum to aluminum fluoride salts. Such reduction is carried out by contacting the alkali metal fluotitanate salt with a molten alloy
  • the zero valent titanium may be recovered as a titanium metal by subliming off the zinc.
  • the alkali metal fluotitanate salt may be
  • Titanium metal has been essential to the aerospace industry since the early fifties because it combines a high strength to weight ratio with the ability to perform at much higher temperatures than aluminum or magnesium. It also has growing usage in the chemical processing industries because of its excellent resistance to corrosion such as, chloride corrosion.
  • Titanium metal is also made by sodium reduction and electrowinning.
  • the product of the "Kroll Process” is a metallic sponge which is later consolidated by a high temperature arc melting process. ' The most important consideration for any process making titanium is to prevent contamination with either metallic or non-metallic impurities, because even small amounts of oxygen or nitrogen can make the product brittle and unworkable, although carefully controlled amounts of oxygen, nitrogen, and carbon may be added to strengthen titanium alloys.
  • Titanium may be produced by reducing volatile titanium halides such as the chloride, bromide or iodide with an aluminum-zinc alloy.
  • volatile titanium halides such as the chloride, bromide or iodide with an aluminum-zinc alloy.
  • the Olson patent describes a vapor-liquid reaction wherein the titanium compound that is being reduced is introduced to the process as a vapor. Therefore, relatively non-volatile titanium compounds, e.g. titanium fluoride, alkali metal fluotitanates, etc. are not mentioned as suitable for reduction to titanium.
  • the instant invention relates to a countercurrent process for reducing an alkali metal fluotitanate salt, e.g. Na2TiFs, comprising +4 valent titanium, to zero valent titanium, in a two-step reduction process, wherein said reduction process is carried out in an adiabatic mode, and which comprises: (a) contacting said alkali metal fluotitanate, as a crystalline salt, with a first molten alloy phase, comprising titanium, aluminum and zinc, to melt said
  • the above process is carried out in a countercurrent, two-stage, reduction process wherein said first molten alloy phase originates in the second stage (as said fourth molten alloy) and is passed to the first stage and utilized as said first molten alloy phase.
  • the instant invention preferably comprises a process for reducing an alkali metal fluotitanate, e.g. a2 iF6, comprising +4 valent titanium, to zero valent titanium, in a two-stage, countercurrent reduction process, which process is carried out in an adiabatic mode and comprises the steps of:
  • a molten salt phase comprising a mixture of an alkali metal fluoride, aluminum fluoride salts, and titanium as a +3 valent salt
  • a molten alloy phase comprising titanium and zinc and substantially depleted in aluminum
  • molten salt phase comprising a mixture of an alkali metal fluoride, and aluminum fluoride salts, which molten salt phase is substantially depleted in titanium
  • molten alloy phase comprising aluminum, titanium and .zinc
  • the process of the instant invention can be operated as a continuous, semi-continuous, or batch process.
  • the products of each stage flow to the next stage at completion of the reactions for further reduction or oxidation, as the case may be, as described herein.
  • the titanium in the alkali metal fluotitanate salt is reduced to zero valent titanium, i.e., titanium metal and the aluminum in the zinc-aluminum alloy is oxidized to aluminum fluoride salts.
  • the alkali metal fluotitanate salt stream and the zinc-aluminum alloy stream flow in opposing directions within the process, i.e., countercurrently.
  • the present process can produce up to about 25% excess heat energy over that required to carry out the process.
  • the surplus heat could be used for other purposes such as power production heating and for melting of the aluminum-zinc- alloy.
  • not all of the surplus heat energy is recoverable and a portion of such heat energy will be lost through convection, conduction and infra-red emissions.
  • the instant invention may be understood by reference to the preferred embodiment described in the following Figure 1 and accompanying description.
  • the numerals 1 through 12 refer to the various process streams and letters A through D refer to the various stages, zones (or reactors) of the preferred embodiment of the instant invention.
  • the reactions described below are carried out in a graphite vessel or other suitable material and under an inert atmosphere, e.g. argon, etc.
  • the molten alloy stream may be introduced into the process at any temperatures below the boiling point of the molten alloy, e.g. from about 400 to about 900°C, e.g. about 450°C.
  • the reactants in each stage are vigorously stirred to insure completion of the reactions.
  • a molten aluminum-zinc alloy 1 at about 450°C is passed into the stage C of a countercurrent contacting zone (said countercurrent contacting zone being represented by first stage B and said second stage C) and contacted therein with a molten salt phase 10 from first stage B at a temperature of about 900°C.
  • molten salt phase is the reaction product originating in said first stage B and comprises a mixture of an alkali metal fluoride, aluminum fluoride salts and titanium as a +3 valent salt.
  • Such contacting is effected by mixing the immiscible molten salt and molten alloy phases to disperse one phase as droplets within the other.
  • Sufficient agitation is provided to form droplets of sufficiently low or small diameter to maximize contact of such two immiscible phases at the interface of the droplets and the continuous phase and such agitation is continued until reaction is complete.
  • the reaction is rapid and therefore, residence time may be as low as 5 to 10 minutes in each stage in the semi-con inuous mode and 20 to 30 minutes in each stage for the continuous mode.
  • continuous process is meant a process wherein reactants and products are continuously introduced and removed, respectively, from the reactors.
  • the reactants will remain in the reactors for a predetermined residence time dependent upon the volume of the reactor, and the flow rates of the materials being introduced and removed from the reactor.
  • semi-continuous process is meant a process wherein reactants are added to a reactor and the resulting reaction between the reactants is permitted to approach, or go to, equilibrium. The resulting products if. intermediates, are passed to the next stage upon completion of the reaction; thus, each stage is in continuous use although there is not a continuous flow of material between stages.
  • the reactants in each stage are agitated or stirred to disperse droplets of molten salt into the molten alloy, separation of the molten salt and alloy in a continuous operation is easily obtained.
  • the salt and alloy are substantially immiscible in each other and readily separate because of their differences in surface tension and density (the salt has a specific gravity of about 3 and the alloy a specific gravity of about 7).
  • alloy free salt is withdrawn from the top of the reactants and salt free alloy is withdrawn from the bottom of the reactants.
  • the intimate mixing of salt and alloy is confined to the middle portion of the reactants with the salt, primarily, being dispersed into the alloy.
  • the +3 valent titanium salt reacts with the aluminum and is substantially converted to zero valent titanium.
  • the aluminum reactant reports to the salt phase as aluminum fluoride salts and the zero valent titanium reports to the alloy phase.
  • An excess of aluminum as aluminum-zinc alloy is provided in said second stage C to ensure substan ⁇ tially complete conversion of +3 valent titanium to zero valent titanium.
  • the heat of reaction in said second stage C is sufficient to heat the molten aluminum-zinc alloy 1 to about 900°C.
  • a molten salt phase 11 comprising a mixture of an alkali metal fluoride and aluminum fluoride salts, separates from a molten alloy phase 4 comprising aluminum, titanium and zinc. Such separation is quite easily effected by suitable design of the reactor due to the surface tension and density properties of the molten alloy phase 4 and the molten salt phase 11.
  • Said molten alloy phase 4 is passed to said first stage B of said countercurrent contacting zone at a temperature of about 900°C and therein contacted with a crystalline, alkali metal fluotitanate salt 7, e.g. Na2TiFg, comprising +4 valent titanium.
  • a crystalline, alkali metal fluotitanate salt 7, e.g. Na2TiFg, comprising +4 valent titanium is carried out in a manner similar to the contacting process of the second stage C described above.
  • the +4 valent titanium is reduced to +3 valent titanium and zero valent titanium by the aluminum in said molten alloy phase 4.
  • Substantially all of the aluminum in said molten alloy phase ' 4. is oxidized to aluminum fluoride salts.
  • the combination of the heat of said molten alloy phase 4 and the exothermic heat generated by reducing the +4 valent titanium to +3 valent titanium and zero valent titanium and oxidizing the aluminum is sufficient to melt said crystalline alkali metal fluotitanate salt 7 and raise the temperature thereof to about 900°C.
  • the aluminum present in molten alloy phase 4 is substantially converted to aluminum fluoride salts.
  • a molten alloy phase 5 substantially depleted in aluminum is separated from said molten salt phase 10.
  • the molten salt phase 10, including aluminum fluoride salt, alkali metal fluoride and titanium as a +3 valent titanium salt, is passed to the second stage C and utilized as described above.
  • the aluminum content of said molten alloy 5 may be less than 0.2% and the titanium content of said molten salt 11 may be less than 0.5%
  • the aluminum content of said molten alloy 6 or 5, reprectively may be less than 2 parts per million, by weight
  • the titanium content of said molten salt 12 or 11, respecti ely may be less than 100 parts per million, by weight.
  • the purity of said molten salt 11 is especially important if said salt is to be used for aluminum reduction cell feed; a well known use of the "psuedo cryolite" salt obtained from the instant process. Contamination of the titanium-zinc alloy 5 with aluminum may result in an inferior grade of titanium metal when the titanium-zinc alloy is used to prepare titanium metal as described below.
  • molten alloy phase 5 comprising less than about 0.2% by weight aluminum may be contacted in metal cleanup reactor A with a crystalline, alkali metal fluotitanate salt 8 to further deplete aluminum from the molten alloy phase 5 and provide a molten salt phase 9 wherein the +4 valent titanium is converted to +3 valent titanium.
  • the molten alloy phase 6 comprising less than about .005%, by weight, aluminum (less 50 parts per million, by weight) is separated from said molten salt phase 9 and said molten salt phase 9 may be passed to first stage B.
  • the contacting and separation is similar to that carried out in said first stage B except that the relative amounts of the molten salt phase 9 and the molten alloy phase 6 differ substantially from molten salt -phase 10 and molten alloy phase 5.
  • the relative amounts of the molten salt phase 9 and the molten alloy phase 6 differ substantially from molten salt -phase 10 and molten alloy phase 5.
  • from about 2 to about 5%, by weight, of the crystalline alkali metal fluotitanate, ultimately reduced to zero valent titanium may originate in the metal cleanup reactor A.
  • Molten salt phase 11 which typically comprises less than 0.5% titanium as +3 valent salt, may be passed to salt cleanup reactor D) and treated with a molten alloy phase 2, comprising an aluminum-zinc alloy at a temperature of about 450°C to reduce the titanium content of molten salt phase 11 to less than about 0.01% (less than 100 parts per million, by weight).
  • the molten salt is ultimately recovered as a very pure pseudocryolite 12 which is a mixture of a5Al3Fi4 and aAlF4 salts.
  • an aluminum-zinc alloy phase 3 including small amounts of zero valent titanium from said treatment in salt cleanup reactor D may be passed to the second stage C of the reduction zone. From about 5% to about 15%, by weight, of the aluminum-zinc alloy ultimately consumed in the reduction of the titanium salt to zero valent titanium may originate in said salt cleanup reactor D.
  • the process temperature in each of stages A through D may be from about 650°C to about 1000°C; preferably from about 850°C to about 950°C.
  • the zinc in the alloy will boil at atmospheric pressure. Accordingly, at process temperatures above about 925°C, the process is preferably conducted at above atmospheric pressures to minimize zinc losses.
  • the molten aluminum-zinc alloy introduced in stages C and D may have a temperature from the melting point temperature of the alloy to the boiling point temperature of the alloy; preferably the alloy temperature is from about 425°C to about 450°C for adiabatic operation.
  • the alloy can be heated to a higher temperature, such as 900°C, but this will require additional external energy.
  • the crystalline alkali metal fluotitanate is introduced into the process at ambient temperatures, i.e., 25°C.
  • the crystalline fluotitanate can be introduced into the process at a temperature between 0°C, or lower, and the melting point temperature of the fluotitanate. Conveniently the fluotitanate is introduced at ambient temperature for adiabatic operation.
  • stage B The proportions of aluminum in the aluminum-zinc alloy and the alkali metal fluotitanate salt in stages B and C are adjusted so that virtually all the +4 titanium salt in stage B will be reduced to +3 titanium salt and a portion of the +3 titanium salt to zero valent titanium and substantially all the remaining portion of +3 valent titanium salt (99% or more) in stage C will be reduced to zero valent titanium.
  • the aluminum-zinc alloy conveniently contains between about 5% and about 17%, by weight, aluminum, preferably between about .10% and about 12%, by weight, aluminum.
  • the alloy will preferably contain about 16 to about 18%, by weight, aluminum.
  • Aluminum-zinc alloys containing high loadings of aluminum will limit the amount of titanium metal recovery since titanium metal is less soluble in zinc than aluminum of the process temperatures of the present invention — at 900°C and at atmospheric pressure, about 14%, by weight, of titanium will dissolve in zinc. All elevated pressures, e.g. 2 to 3 atmospheres, about 22% to about 24%, by weight, of titanium is soluble in zinc.
  • Aluminum-zinc alloys containing low aluminum loadings are not preferred because the use of such alloys requires a higher mass of alloy to be introduced into the process to reduce all the alkali metal fluotitanate to zero valent 'titanium.
  • the reduction of the alkali metal fluotitanate must proceed in the step wise manner with partial reductions as described herein.
  • the reduction of alkali metal fluotitanate to zero valent titanium, i.e., titanium metal occurs in a stepwise manner in the present process.
  • the salt is first reduced to a +3 valent titanium salt.
  • the +3 valent titanium salt is then reduced to zero valent titanium, possibly through an unstable +2 valent titanium salt intermediate.
  • Zinc can reduce an alkali metal fluotitanate to a +3 valent titanium salt with the con ⁇ comitant production of a zinc fluoride salt or salt mixture and heat of reaction.
  • the aluminum preferentially reduces the +4 valent titanium to +3 valent titanium before reducing the +3 valent titanium to zero valent titanium.
  • the alkali metal fluotitanate is reduced to +3 valent titanium and a portion of the +3 valent titanium is reduced to zero valent titanium in the presence of less than a stiochiometric amount of aluminum to oxidize substantially all the aluminum.
  • the remaining +3 valent titanium is reduced in the presence of a greater than stiochiometric amount of aluminum to reduce substan- tially all of the +3 valent titanium to zero valent titanium.
  • the aluminum in the first stage B is oxidized to aluminum fluoride salts in the presence of a greater than stoichiometric amount of alkali metal fluotitanate.
  • the process is readily controlled by monitoring the temperature of each stage.
  • the temperature of each stage should be between about 650°C and about 1000°C, preferably between about 850°C and about 950°C. If the temperature of a given stage falls below the desired temperature, additional salt and/or alloy is added to the stage as described herein to maintain the desired temperature. If the temperature of a given stage rises above the desired temperature, agitation and/or addition of reactants may be diminished or stopped to slow down the reactions and production of exothermic heat of reaction.
  • the process can be controlled by temperature monitoring without the need to resort to chemical analysis of the products.
  • an alkali metal fluotitanate is reduced to zero valent titanium in accordance with the present process
  • the titanium-zinc alloy product will be substan ⁇ tially free of impurities, such as aluminum, alkali metal fluorine and salts thereof.
  • impurities such as aluminum, alkali metal fluorine and salts thereof.
  • the process will almost quantitatively reduce the fluotitanate salt to zero valent titanium (yields of 99% or more) .
  • 1.333 moles of aluminum are consumed, i.e., oxidized to aluminum fluoride salts.
  • 1.333 moles of aluminum as the molten alumi ⁇ num-zinc alloy are introduced into the process as described herein.
  • the +4 valent titanium salt is reduced completely to zero valent titanium and the balance of the +4 valent titanium salt is reduced to +3 valent titanium salt.
  • about 27% to about 40% of the reduction takes place in the first stage.
  • the reduction proceeds in at least two steps, first reduction of +4 valent titanium salt to +3 valent titanium salt and then the reduction of the +3 salt to zero valent titanium.
  • about 53% to about 80%, by weight, of the +3 va ⁇ ent titanium salt produced in the first stage B is transferred to the second stage c wherein it is reduced to zero valent titanium, the balance of the +3 salt being reduced in the first stage B.
  • the first stage B requires a large portion of the heat of reaction to heat and melt the solid alkali metal fluotitanate introduced into the first stage.
  • about 40 to about 60%, by weight, of the aluminum is oxidized to aluminum fluoride salts in the second stage C, preferably about 45% to about 55%, by weight, of the aluminum is oxidized to aluminum fluoride salts in the second stage.
  • stage B Sufficient solidalkali metal fluotitanate andmolten titanium-aluminum- zinc alloy from second stage C are added to stage B to supply sufficient heat from the .exothermic heat of reaction from the reduction of the +4 valent titanium to heat, and melt, the solid fluotitanate to the desired reaction temperature, e.g., about 900°C, and maintain the reactants and products in stage 3 at the desired reaction temperature.
  • desired reaction temperature e.g., about 900°C
  • the exothermic heat of reaction from the reduction of the +3 valent titanium salt in stage C is sufficient to raise the temperature of the molten aluminum-zinc alloy to the desired reaction temperature and maintain the reactants in stage C at the desired reaction temperature.
  • the reactors and piping in each stage are insulated with a conventional thermal insulation to minimize heat losses from conduction, convection and infra-red emissions.
  • the alkali metal fluotitanate may be substituted by any titanate . salt which is molten at the temperature conditions described above and comprises +4 valent titanium.
  • the chlortitanates are reduced with sodium or magnesium.
  • the instant invention further comprises an integral process for converting a titanium ore to titanium metal, by halogenating, e.g. fluorinating, a titanium oxide ore such as rutile, ilmenite, etc. to convert said titanium oxide to halides, e.g. fluorides, of titanium and then reducing said halides, e.g. fluorides, of . titanium to titanium metal in the multi-step, adiabatic, countercurrent reduction process.
  • halogenating e.g. fluorinating
  • a titanium oxide ore such as rutile, ilmenite, etc.
  • ilmenite which contains both iron and titanium in the oxide form, is fluorinated to convert said iron and titanium oxides to iron and titanium fluorides.
  • the fluorination is preferably carried out by contacting the ore with a fluosilicate salt such as an alkali metal fluosilicate, for example, K2SiF6, Na2SiFg, etc. at a temperature from about 600°C to 1000°C preferably 750°C to 950°C.
  • the iron and titanium fluorides may be leached from the fluorinated ore by an aqueous solution.
  • the aqueous solution may contain a strong acid (a mineral acid) to enhance the recovery of soluble titanium, i.e. alkali metal fluotitanate.
  • the corresponding fluotitante is the soluble titanium moiety.
  • a potassium fluotitanate salt will be dissolved in the leachate.
  • the leachate will also contain various other soluble fluorides such as, for example, potassium fluoride.
  • the leachate may be evaporated and cooled to precipitate out the alkali metal fluotitanate, for example, potassium fluotitanate.
  • the alkali metal fluotitanate precipitate may then be filtered and dried at a temperature of from about 110°C to 150°C and subsequently reduced to* titanium metal.
  • the method of reduction has been described above and comprises contacting the alkali metal fluotitanate salt with a molten zinc-aluminum alloy at a temperature of from about 650°C " to about 1000°C in an inert atmosphere.
  • the titanium present in the alkali metal fluotitanate salt will be converted into a titanium-zinc alloy by contacting with the aluminum-zinc alloy under such conditions and the aluminum will be converted into corresponding aluminum fluoride salts.
  • the aluminum fluoride salts will dissolve in the molten salt phase and may form a salt similar to cryolite, i.e. a pseudocryolite such as mixtures of a3 lFg, asAl3Fi4 and AIF3.
  • a pseudocryolite such as mixtures of a3 lFg, asAl3Fi4 and AIF3.
  • the molten zinc-titanium alloy is separated from the molten salt mixture and passed through a distillation zone wherein the zinc is sublimed from the titanium under an inert atmosphere.
  • the titanium may be recovered in the form of a titanium metal sponge.
  • Ilmenite which is an ore comprising titanium and iron oxides in admixture is available from various locations such as southern Georgia, northern Florida, and California.
  • the ore will typically comprise from 25 to 50% by weight, titanium and 8 to 36% by weight, iron.
  • a suitable ilmenite ore may be ground to a finely divided physical state to make it more susceptible to fluorination.
  • the ore may be ground to a particle size of from 30
  • the ore may be fluorinated by fluorination agents known in the art such as F2, SiF4, NH4F, NH4HF2. CIF3, etc.
  • fluorination agents known in the art such as F2, SiF4, NH4F, NH4HF2. CIF3, etc.
  • the fluorinating agent will be an alkali
  • Typical alkali metal fluosilicates include potassium
  • Sodium fluosilicates for example, may be blended with the ore at a weight ratio of from 0.5 to 5.0 and preferably from 1.0 to 2.5 to effect adequate fluorination.
  • the ore will be heated to a temperature of at least 600°C preferably from 750 to 950°C for a time sufficient to change the iron and titanium from oxides to the fluor-
  • the reactant mass may fuse and become difficult to remove from the reaction chamber; at lower temperatures, the reaction does not progress at a suitable rate.
  • iron acts to enhance the fluorination reaction of the alkali metal fluosilicates noted above, and an increased recovery of soluble titanium is thus obtained.
  • the ilmenite ores which are low in iron content may benefit from the addition of additional iron, for example, in the form of iron powder and/or iron oxide.
  • Other titanium ores such as rutile and anatase, which are substantially iron-free, have been found to be benefited greatly by the addition of iron.
  • the ilmenite -ores having at least from 14 to 36% iron are very easily fluorinated by the above alkali metal fluosilicates and may not require additional iron powder and/or iron oxide.
  • the fluorination reaction is benefited by being carried out under an atmosphere of a gaseous fluorinating agent such as silicon tetrafluoride. It is believed that the silicon tetrafluoride may be an active fluorinating -23-
  • the fluorination reaction may be carried out under an atmospheric pressure.
  • the reaction may be conducted at partial pressures or elevated pressures from about .1 to about 70 psig.
  • the fluorinated ore may be cooled and then ground prior to the recovery of the soluble titanium by leaching the ground mixture of the fluorinated ore and the residue
  • Leaching of the fluorinated ore may be carried out in an aqueous solution which may beneficially contain a strong acid such as hydrochloric, hydrofluoric or
  • the pH of said leaching solution is preferably less than about 5.0, more preferably less than about 1, e.g., 0.1.
  • the leaching may ta " Re place at a temperature of at least 25°C, preferably from 60°C to 95°C.
  • leaching 20 may be conducted at higher temperatures, e.g. 120°C. At elevated temperatures the leach is conducted in a pressure vessel. The leaching is carried out for a time sufficient to recover as much of the soluble fluorides of titanium as economically possible. Typically, leaching
  • 25 is carried out for about 0.1 to 3 hour with the ratio of leaching solution to the fluorinated ore varying from 15:1 to 5:1, e.g., 10:1 on a weight to weight basis.
  • the leaching is very rapid and typically is conducted in a matter of minutes.
  • the leachate is separated from
  • the filtrate will comprise soluble fluorides of titanium, for example, in the preferred embodiment K2TiF ⁇ or Na2TiFg.
  • various soluble fluorides may be present in the filtrate, such as the fluoride salt of the corresponding alkali metal fluosilicate, such as sodium fluoride or potassium fluoride. It has been found that it is easy to separate the fluorides of titanium from such other soluble fluorides since solubility characteristics are such that the fluorides of titanium precipitate as the temperature of the solution is lowered while other impurities are more or less soluble in lower temperature solutions comprising dissolved titanium fluorides. Thus, the solution may be evaporated to concentrate soluble fluorides and then the temperature decreased until the fluorides of titanium crystallize. The crystals of the fluorides of titanium may be separated and dried at a temperature of from 50 to 150°C to remove excess water. ⁇ ⁇
  • the dried crystals of the fluorides of titanium may be reduced as described above to provide a molten titanium-zinc alloy.
  • the molten titanium-zinc alloy will be passed to a distillation zone wherein the zinc may be sublimed off off, under an inert atmosphere, at a temperature of from about 800°C to 1000°C to leave behind a titanium sponge.
  • the zinc may be sublimed from the zinc-titanium alloy under a vacuum and at somewhat lower temperatures.
  • the titanium sponge may be sintered to reduce its surface area. After sintering and cooling, the sponge is passified by exposure to dilute O2 to give a thin (monomolecular) protective coating of titanium oxide thereon before the sponge is exposed to a non-inert atmosphere. The zinc will be recovered and recycled for use in subsequent reducing steps.
  • 38,000 lbs. of ilmenite having a composition of 31.6% titanium and 35% iron is mixed with 380 lbs. of carbon and the resulting mixture ground to a particle size of 100 mesh in grinding zone 10.
  • the ground ilmenite ° is then blended with 70,735 lbs. of sodium fluosilicate in blending zone 11.
  • the blended mixture is passed into calcining zone 12 wherein it is heated to a temperature of from 750 to 850°C, in the presence of one atmosphere of SiF4, for a time of about 1 hour whereby the titanium 5 oxides present in the ilmenite are converted to fluorides of titanium and the silicon fluorides present in the fluosilicate are converted to silicon dioxide.
  • some of the iron present- in the ilmenite is converted to ferric fluoride.
  • the fluorinated mixture is then ground in grinding zone 13 and leached with an aqueous hydrochloric acid solution containing 10% by weight hydrochloric acid at a ratio of 10 lbs. of solution/lb. fluorinated ore.
  • a leachate is separated from the silica- containing residue from fluorination of the ilmenite.
  • the silica-containing residue are removed from said grinding and leaching zone and may be dried and recovered as a mixture of silicon dioxide and ferric oxide in zone 14.
  • the leachate, after separation of the silica-containing residue is passed to a crystallizing and drying zone 15 wherein about 740,000 lbs. of water is removed by heat and/or vacuum and the dewatered solution is cooled to a temperature of about 4°C to crystallize sodium fluotitanate.
  • the crystallized sodium fluotitanate is reduced by contacting with an aluminum-zinc alloy comprising 11.71%, by weight, aluminum in reducing zone 16.
  • the operations occurring in reducing zone 16 may be understood by reference to Figure 1 and Table 1 wherein stages A through D represent reducing zone 16 and Table 1 gives the mass and heat balance for each stream of the above described multi-stage, continuous, countercurrent reduction process.
  • Table 2 demonstrates that the instant multi-stage, countercurrent reduction process may operate nearly adiabatically. This table is generated by summing the heat of reaction in each stage as well as the heat provided by the various streams entering such stage and subtracting the heat removed by the streams exiting each stage.
  • the crystallized sodium fluotitanate is divided and introduced into reducing zone 16 as feed streams 7 and 8 at the first stage B and the metal cleanup reactor A. Note again that no heat other than the heat necessary to heat molten alloy phases 1 and 2 to about 450°C is necessary to the process.
  • the titanium-zinc alloy is removed from reducing zone 16 and passed into distillation zone 17 wherein zinc is distilled off at a temperature of at least 800°C and at a vacuum of about 10 ⁇ 5 torr. The distilled zinc is recycled back to reduction zone 16 for subsequent reuse. Titanium metal is recovered from distillation zone 17 as a sponge 18.
  • the molten salt mixture which is a mixture of sodium and aluminum fluoride, i.e. a pseudo cryolite, is recovered from reduction zone 16 and sent to recovery zone 19. -27-
  • stage B 78.8% of the +4 valent titanium is reduced to zero valent titanium and 21.1% of the +4 valent titanium is reduced to +3 valent titanium ( a5Ti3F ⁇ _4 ) .
  • the product alloy contains .975 pound of titanium and 0.001 lbs of aluminum.
  • the salt product from stage C contains 0.025 pounds of titanium.
  • 97.5% of the titanium is recovered.
  • the heat balances for each stage show that sufficient heat is produced within the process to drive the process without the need for external heating, excluding the heat used to heat, and melt, the aluminum-zinc alloy to 450°C (stream 1) .
  • stage B 2680 BTU* s are required to heat and melt the sodium fluotitanate salt leaving a balance of about -400 BTU's in stage B .
  • stage C about 650 BTU 's are required to heat the molten aluminum-zinc alloy introduced via stream 1 from 450°C to 900°C leaving a heat balance of about -1000 BTU's in stage B.

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Abstract

Procédé continu à contre-courant, de réduction d'un fluotitanate de métal alcalin, par exemple Na2TiF6, comprenant du titane tétravalent, pour obtenir du titane de valeur nulle, comprenant deux phases de réduction, ledit procédé étant conduit en mode adiabatique, et consistant (a) à mettre en contact ledit fluotitanate de métal alcalin, sous forme de sel cristallin, avec un premier alliage en fusion à une température de réaction, cet alliage comprenant du titane, de l'aluminium et du zinc, afin de réduire une partie du titane tétravalent en titane trivalent et au moins 60% du reste en titane de valence nulle; ledit sel cristallin étant fondu et chauffé à la température de réaction, pour former une première phase de sel fondu comprenant un sel de titane trivalent et un fluorure d'aluminium et de métal alcalin, et une deuxième phase d'alliage fondu comprenant du titane et du zinc, cette deuxième phase n'étant pas miscible avec la première phase, (b) à séparer la première phase de sel fondu de la deuxième phase d'alliage fondu; (c) à réduire le titane trivalent à partir de la première phase de sel fondu en mettant en contact ladite première phase à la température de réaction, avec une troisième phase d'alliage fondu dont la température est inférieure à ladite température de réaction, cette troisième phase contenant de l'aluminium et du zinc, afin de réduire le titane trivalent en titane de valeur nulle, ladite troisième phase étant chauffée à la température de réaction, la première phase d'alliage fondu n'étant pas miscible avec la deuxième phase de sel fondu; (d) à séparer la deuxième phase de sel fondu de la première phase d'alliage fondu; et (e) à recycler ladite première phase d'alliage fondu vers l'étape (a).
PCT/US1987/001217 1982-05-14 1987-05-26 Procede de preparation de titane de valence nulle a partir d'un fluotitanate de metal alcalin Ceased WO1988009391A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US06/745,591 US4668286A (en) 1982-05-14 1985-06-17 Process for making zero valent titanium from an alkali metal fluotitanate
EP19870904997 EP0360792A4 (en) 1982-05-14 1987-05-26 Process for making zero valent titanium from an alkali metal fluotitanate
JP62504687A JPH03500063A (ja) 1982-05-14 1987-05-26 アルカリ金属フルオロチタン酸塩からゼロ価チタンの製法
KR1019890700136A KR890701782A (ko) 1985-07-01 1987-05-26 알칼리 금속 플루오티타네이트로 부터 0가의 티타늄을 제조하는 방법
NO890315A NO890315D0 (no) 1982-05-14 1989-01-25 Fremgangsmaate for fremstilling av nullverdig titan fra et alkalimetallfluortitanat.

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US37829282A 1982-05-14 1982-05-14

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2149199C1 (ru) * 1998-12-23 2000-05-20 Открытое акционерное общество "АВИСМА титано-магниевый комбинат" Устройство для вакуумной сепарации губчатого титана
WO2013107107A1 (fr) * 2012-01-18 2013-07-25 深圳市新星轻合金材料股份有限公司 Procédé de préparation d'une éponge de titane

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3000726A (en) * 1945-11-14 1961-09-19 Frank H Speeding Production of metals
US4127409A (en) * 1975-10-17 1978-11-28 Teledyne Industries, Inc. Method of reducing zirconium
US4359449A (en) * 1980-12-15 1982-11-16 Occidental Research Corporation Process for making titanium oxide from titanium ore

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3000726A (en) * 1945-11-14 1961-09-19 Frank H Speeding Production of metals
US4127409A (en) * 1975-10-17 1978-11-28 Teledyne Industries, Inc. Method of reducing zirconium
US4359449A (en) * 1980-12-15 1982-11-16 Occidental Research Corporation Process for making titanium oxide from titanium ore

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP0360792A4 *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2149199C1 (ru) * 1998-12-23 2000-05-20 Открытое акционерное общество "АВИСМА титано-магниевый комбинат" Устройство для вакуумной сепарации губчатого титана
WO2013107107A1 (fr) * 2012-01-18 2013-07-25 深圳市新星轻合金材料股份有限公司 Procédé de préparation d'une éponge de titane

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