Abstract: Complex ceramic oxides of the general formula Mg2MM?O6+x where M=Rare metal ion or Yttrium or Lanthanum and M?=Sn, Sb, Zr, Hf, Ta, and Nb; and where ?0.5<x<0.5; having a defective pyrochlore structure are useful for active and passive electronic applications, as dielectrics, catalyst sensors, hosts for radioactive waste, etc. This process for the preparation of this class of compounds comprises: (i) mixing the compounds of magnesium, M and M? to get the molar ratio as 2:1:1 (ii) the mixture obtained in step (i) along with a wetting medium may be ball milled or mixed; (iii) the resultant slurry may be dried to obtain dry powder, (iv) the resultant mixture may be heated to a temperature in the range of 1000-1600° C. for the duration ranging from 3 hours to 50 hours, either in a single step or by taking out the reactant after heating, checking for the structure formation and heating again after grinding, if necessary.

Abstract: A method of producing a lithium-tantalate crystal, wherein at least a first material containing lithium tantalate, lithium niobate or hydrogen storage alloy storing hydrogen that is subjected to a heat treatment at a temperature of T1? that is Curie temperature or higher in a reducing atmosphere is superposed on a single-polarized lithium-tantalate crystal, and then the crystal is subjected to a heat treatment at a temperature of T2? that is lower than Curie temperature in a reducing atmosphere, thereby an electric conductivity of the single-polarized lithium-tantalate crystal is increased. There can be provided a method of producing a lithium-tantalate crystal wherein the surface charge generated by applying a temperature change to the lithium-tantalate crystal can be decayed quickly without accumulating by increasing the electric conductivity, and an effective piezoelectric property is exhibited by maintaining the single polarized structure.

Abstract: The method relates to a pyrometallurgical and hydrometallurgical process for the recovery and recycling of lithium and vanadium compounds from a material comprising spent rechargeable lithium batteries, particularly lithium metal gel and solid polymer electrolyte rechargeable batteries. The method involves providing a mass of the material, hardening it by cooling at a temperature below room temperature, comminuting the mass of cooled and hardened material, digesting with an acid its ashes obtained by incineration, or its solidified salts obtained by molten salt oxidation, or the comminuted mass itself, to give a mother liquor, extracting vanadium compounds from the mother liquor, separating heavy metals and aluminium therefrom, and precipitating lithium carbonate from the remaining solution.

Abstract: A method for the dissolution and purification of tantalum ore and synthetic concentrates is described. The method preferably uses ammonium bifluoride as the fluoride source in place of the hydrofluoric acid used in the conventional methods. Other fluoride compounds such as NaF, KF, and CaF2 may be used alone or in combination with ammonium bifluoride. The tantalum concentrate and fluoride source are combined with sulfuric acid to form a solution containing tantalum values and impurities. The tantalum values are then separated from the impurities by solvent extraction.

Abstract: The present invention relates to high-purity niobium monoxide powder (NbO) produced by a process of combining a mixture of higher niobium oxides and niobium metal powder or granules; heating and reacting the compacted mixture under controlled atmosphere to achieve temperatures greater than about 1800° C., at which temperature the NbO is liquid; solidifying the liquid NbO to form a body of material; and fragmenting the body to form NbO particles suitable for application as e.g., capacitor anodes. The NbO product is unusually pure in composition and crystallography, highly dense, and can be used for capacitors and for other electronic applications. The method of production of the NbO is robust, does not require high-purity feedstock, and can reclaim value from waste streams associated with the processing of NbO electronic components.

Abstract: This invention relates to a composition comprising nano-structured metal oxide particles (particularly, zirconia) and at least one stabilizing agent, a method to produce the composition, and a method to produce the thermally stable nano-structured particles. The method to produce the nano-structured particles comprises first preparing a base solution and a nanoparticle precursor solution, then combining these solutions at a final pH 7 or greater to precipitate a colloidal hydrous oxide. The colloidal hydrous oxide is then treated with at least one silicate, phosphate, or aluminum phosphate stabilizing agent and dried. These nano-structured particle products have high thermal stability and are particularly advantageous in applications as catalysts or catalyst supports that operate at high temperatures.

Abstract: In a metal oxide nanoparticle and a synthetic method thereof, and in particular to maghemite (?-Fe2O3) nanoparticles usable as a superhigh density magnetic recording substance by having good shape anisotropy and magnetic characteristics, hematite (?-Fe2O3) nanoparticles usable as a precursor to the maghemite or a catalyst, maghemite and hematite-mixed nanoparticles and a synthetic method thereof, the method for synthesizing metal oxide nanoparticles includes forming a reverse micelle solution by adding distilled water, a surfactant and a solvent to metallic salt not less than trivalent, precipitating and separating gel type amorphous metal oxide particles by adding proton scavenger to the reverse micelle solution; adjusting a molar ratio of metal oxide to the surfactant by washing the gel type amorphous metal oxide particles with a polar solvent; and crystallizing metal oxide nanoparticles through heating or reflux after dispersing the gel type amorphous metal oxide particles in a non-polar solvent having a h

Abstract: The present invention provides a process for producing particles, such as oxide nanoparticles, in a substantially water-free environment. The process involves mixing at least one metal compound of the formula MX(m?n) with at least one surfactant and at least one solvent, wherein M is an electropositive element of Groups 1–15; each X is independently selected from the group consisting of O1/2, F, Cl, Br, I, OR, O2CR, NR2, and R; each R is independently a hydrocarbyl group; n is equal to ½ the oxidation state of the metal M in the product particle; and m is equal to the oxidation state of the element M. The components are typically combined to form a mixture which is thermally treated for a time period sufficient to convert the metal compound into particles of the corresponding oxide, having sizes in a range between about 0.5 nanometer and about 1000 nanometers.

Abstract: A method of producing a single-phase composition Mn+1AzXn, primarily the production of the single-phase material Ti3SiC2, where n lies within a range of 0.8-3.2, where z lies within a range of 0.8-1.2, where M is at least one metal taken from the group of metals Ti (titanium), Sc (scandium), V (vanadium), Cr (chromium), Zr (zirconium), Nb (niobium) and Ta (tantalum), where X is at least one of the non-metals C (carbon) and N nitrogen), and where A is at least one of the chemical elements Si (silicon), Al (aluminum) and Sn (tin) or a compound of those elements, such that the final, desired compound will include the components Mn+1AzXn. A powder mixture of the components is formed and is ignited under an inert atmosphere to prevent promotion of dissociation and to cause the components to react.

Abstract: A method of recovering metal and/or oxide thereof from a slurry is described. The method involves magnetically separating at least a portion of any magnetic impurities from the slurry and then leaching or dissolving at least a portion of any remaining magnetic impurities in a slurry. At least one chelating agent can then be added to the slurry and the solids can be recovered from the slurry by various separation techniques. The methods of the present invention are particularly useful in the recovery of tantalum and/or oxide thereof especially tantalum and/or oxide thereof having a very fine size.

Abstract: The current invention relates to the preparation of an improved cathode active material for non-aqueous lithium electrochemical cell. In particular, the cathode active material comprises &egr;-phase silver vanadium oxide prepared by using a &ggr;-phase silver vanadium oxide starting material. The reaction of &ggr;-phase SVO with a silver salt produces the novel &egr;-phase SVO possessing a lower surface area than &egr;-phase SVO produced from vanadium oxide (V2O5) and a similar silver salt as starting materials. Consequently, the low surface area &egr;-phase SVO material provides an advantage in greater long term stability in pulse dischargeable cells.

Abstract: Methods to control hydrogen sulfide and/or arsine emissions are described. The method involves adding at least one copper compound (such as a copper(II) compound) to the material, such as material containing sulfur in a sufficient amount to control said emissions. The material that is treated with the copper compound(s) is preferably an ore, such as a valve metal containing ore.

Abstract: A process for preparing a reconstituted vanadyl sulphate/vanadous sulphate solution for use as an electrolyte in a vanadium redox battery is disclosed. The process includes preparing a starting material including a vanadyl sulphate/vanadous sulphate solution, evaporating the starting material by applying heat to form vanadyl sulphate/vanadous sulphate crystals, and re-dissolving the vanadyl sulphate/vanadous sulphate crystals with a volume of de-ionized water to form a reconstituted vanadyl sulphate/vanadous sulphate solution having substantially the same chemical composition at the starting material. A process for preparing a vanadyl sulphate/vanadous sulphate starting material from a vanadium bearing ore material, particularly a titaniferous magnetite ore material is also disclosed.

Abstract: The positive active material for secondary battery according to the invention comprises O, Fe in an amount of higher than 25% by weight, and V in an amount of from higher than 0% by weight to less than 35% by weight. The positive active material, when it is free of lithium, exhibits the following main peaks by the X-ray diffractometry using CuK&agr; rays: a peak within a 2&thgr; range of from greater than 26° to less than 29° and a peak within a 2&thgr; range of from greater than 29° to less than 32°. The non-aqueous secondary battery having a positive electrode comprising this positive active material exhibits a high capacity and good cycle life performance and is inexpensive and environmentally friendly.

Abstract: Methods to at least partially reduce a niobium oxide are described wherein the process includes heat treating the niobium oxide in the presence of a getter material and in an atmosphere which permits the transfer of oxygen atoms from the niobium oxide to the getter material, and for a sufficient time and at a sufficient temperature to form an oxygen reduced niobium oxide. Niobium oxides and/or suboxides are also described as well as capacitors containing anodes made from the niobium oxides and suboxides.

Abstract: A process for the production of a vanadium compound from carbonaceous residues containing vanadium, which includes the steps of: (a) combusting the carbonaceous residues at a temperature of 500-690° C. in an oxygen-containing gas to form vanadium-containing combustion residues; (b) heating the vanadium-containing combustion residues at a temperature T in ° C. under an oxygen partial pressure of at most T in kPa wherein T and P meet with the following conditions: log10(P)=−3.45×10−3×T+2.21 500≦T≦1300 to obtain a solid product containing less than 5% by weight of carbon and vanadium at least 80% of which is tetravalent vanadium oxide; (c) selectively leach tetravalent vanadium ion with sulfuring acid at pH in the range of 1.5-4; (d) separating a liquid phase from the leached mixture; (e) adding an alkaline substance to the liquid phase to adjust the pH thereof in the range of 4.5-7.

Abstract: An improved inclusive method for purifying a polar solvent such as water includes the re-suspension of finely divided layered materials within which contaminants have been captured, wherein the re-suspension is in a solvent selected primarily on the basis of its ability to re-suspend the finely divided layered materials and/or for its effect on the included contaminant material, and within which additional materials may or may not be intentionally dissolved, mixed, or suspended, in order to recover and reuse the finely divided layered material and/or to selectively recover a specific included contaminant or several specific included contaminants in series. The process is useful in the rapid and efficient recovery of the finely divided layered materials, and in the removal of suspended particles, dissolved materials, immiscible liquids, and living organisms from the polar solvent.

Abstract: The processes of the present invention include mineral acid leaching of a metal containing material, such as an ore residue, containing fluoridated metal values in the presence of a complexing agent which will complex fluoride ions. The processes of the present invention provide for the separation of valuable metal, fluoride and radionuclide values from a feed material of high mineral content wherein the metals and radionuclides are present as substantially water insoluble fluorides or are trapped within a metal fluorine matrix which is substantially insoluble in typical chemical reactant systems.

Abstract: Methods to control hydrogen sulfide and/or arsine emissions are described. The method involves adding at least one copper compound (such as a copper(II) compound) to the material, such as material containing sulfur in a sufficient amount to control said emissions. The material that is treated with the copper compound(s) is preferably an ore, such as a valve metal containing ore.

Abstract: The present invention provides method of producing a trivalent and tetravalent mixed vanadium compound having excellent solubility with sulfuric acid directly from a tetravalent or pentavalent vanadium compound by using a reducing agent,and a method of producing a vanadium electrolyte. For example, a vanadium compound mainly containing a pentavalent vanadium compound; sulfur and concentrated sulfuric acid in molar ratios with respect to (one mol of vanadium atom in the pentavalent vanadium compound) 0.35 to 0.4:1.2 to 1.9 are kneaded into paste form, and the paste-form mixture is calcined at a temperature of not less than 150° C. to less than 440° C. so that a trivalent and tetravalent mixed vanadium compound is obtained, and a redox flow battery-use vanadium electrolyte is obtained by dissolving the trivalent and tetravalent mixed vanadium compound in a sulfuric acid solution.

Abstract: This invention relates to an improved process for removing trace levels of Group IVb contaminants from a Group IVb metal tetrahalide of and particularly to a process for removing zirconium tetrachloride from titanium tetrachloride. The improvement resides in contacting a titanium tetrachloride feedstock containing trace impurities of zirconium tetrachloride or hafnium tetrachloride with a sufficient amount of titanium hydride to convert any zirconium tetrachloride or hafnium tetrachloride to a lower volatile compound. The resultant mixture is distilled and the titanium tetrachloride separated from the lower volatile zirconium or hafnium compounds.

Abstract: The invention encompasses methods of forming titanium-based mixed-metal materials and zirconium-based mixed-metal materials utilizing one or more of a reduction process, electrolysis process and iodide process. The invention also encompasses a sputtering target comprising zirconium and one or more elements selected from the group consisting of Al, B, Ba, Be, Ca, Ce, Co, Cs, Dy, Er, Fe, Gd, Hf, Ho, La, Mg, Mn, Mo, Nb, Nd, Ni, Pr, Sc, Sm, Sr, Ta, Ti, V, W, Y, and Yb. The invention also encompasses a sputtering target comprising titanium and boron.

Abstract: Rare earth-transition metal oxides are used as pigments. The rare earth-transition metal oxide pigments are preferably of the formula (RexTm)Oy, where Re is at least one rare earth element, Tm is at least one transition metal, x ranges from 0.08 to 12, and y ranges from x+1 to 2x+2. The pigments are useful as colorants, and possess good stability.

Abstract: Methods to at least partially reduce a niobium oxide are described wherein the process includes heat treating the niobium oxide in the presence of a getter material and in an atmosphere which permits the transfer of oxygen atoms from the niobium oxide to the getter material, and for a sufficient time and at a sufficient temperature to form an oxygen reduced niobium oxide. Niobium oxides and/or suboxides are also described as well as capacitors containing anodes made from the niobium oxides and suboxides. Anodes formed from niobium oxide powders using binders and/or lubricants are described as well as methods to form the anodes.

Abstract: A method of doping vanadium pentoxide with silver comprising the steps of: providing vanadium pentoxide gel providing stable colloidal silver and combining the vanadium pentoxide gel and the colloidal silver at room temperature for a period sufficient for vanadium (+5) to be electrochemically reduced to vanadium (+4) and for silver to be oxidized (+1).

Abstract: This invention concerns catalysts comprising a molybdenum compound of formula I, II, III, IV or V I VqMoAyOz II NiMoxByOz′ III VNiwMoxCy′Oz″ IV CoNiwMoxDyOz′″ V VNiwCorMoxEyOz″″ wherein: A is at least one cation selected from the group consisting of cations of: Cr, Sb, Co, Ce and Pb; B is at least one cation selected from the group consisting of cations of: Sb, Al and W; C is at least one cation selected from the group consisting of cations of: Fe, Zn, Al, Sb, Bi, W, Li, Ba, Nb and Sn; D is at least one cation selected from the group consisting of cations of: Ba, Mn, Al, Sb, Sn, and W; E is at least one cation selected from the group consisting of cations of: Fe, Ca, Mn, Sr, Eu, La, Zr, Ga, Sn and Pb; q, r, w, x and y are each independently a number from 0.1 to 10 and y′ is a number from 0 to 10, z, z′, z″, z′″, and z″″ are determined using the amounts and oxidation states of all cations present in each formula.

Abstract: The present invention provides a clathrate compound which can be used as a thermoelectric material, a hard material, or a semiconductor material. Silicon or carbon are formed into a clathrate lattice, and a clathrate compound is then formed in which specified doping atoms are encapsulated within the clathrate lattice, and a portion of the atoms of the clathrate lattice are substituted with specified substitution atoms. The clathrate lattice is, for example, a silicon clathrate 34 (Si34) mixed lattice of a Si20 cluster including a dodecahedron of Si atoms, and a Si28 cluster including a hexahedron of Si atoms. Suitable doping atoms are atoms from group 1A, group 2A, group 3A, group 1B, group 2B, group 3B, group 4A, group 5A, group 6A, and group 8, and suitable substitution atoms are atoms from group 1A, group 2A, group 3A, group 1B, group 2B, group 3B, group 5A, group 6A, group 7A, group 5B, group 6B, group 7B, and group 8 of the periodic table.

Abstract: Methods to at least partially reduce a niobium oxide are described wherein the process includes heat treating the niobium oxide in the presence of a getter material and in an atmosphere which permits the transfer of oxygen atoms from the niobium oxide to the getter material, and for a sufficient time and at a sufficient temperature to form an oxygen reduced niobium oxide. Niobium oxides and/or suboxides are also described as well as capacitors containing anodes made from the niobium oxides and suboxides.

Abstract: The process of the present invention relates to a process for recovering the carbide metal from metal carbide scrap wherein the metal is tungsten, titanium, vanadium, chromium or molybdenum, and this process comprises (A) providing a mixture comprising the metal carbide scrap and at least a stoichiometric amount, based on the amount of carbide metal present in the scrap, of an alkali metal hydroxide, (B) heating the mixture in the presence of oxygen at an elevated temperature and pressure for a period of time sufficient to form a water soluble alkali metal salt of the carbide metal, and (C) recovering the water soluble alkali metal salt.

Abstract: A piezoelectric single crystal wafer for SAW or LSAW devices has an x-ray rocking curve half width of up to 0.06° on the wafer surface on which electrodes are to be formed for transmitting and receiving SAW or LSAW.

Abstract: A process for recovering and purifying vanadium found in petroleum coke is disclosed. Coke containing V and other metals such as Ni is charged to a molten metal bath and dissolved to form a molten metal bath with dissolved carbon, dissolved V metal and dissolved Ni. Oxygen containing gas is added in an amount sufficient to heat balance the process and produce off gas. At least periodically the conditions in the bed are made more severely oxidizing so that a portion of the molten vanadium metal is oxidized to form slag. Oxidation is limited so that a majority of the Ni dissolved in the bath remains as dissolved elemental Ni metal. Oxidized vanadium species are continuously or intermittently withdrawn from the slag layer, by dust formation or by tapping the slag layer.

Abstract: An improved process for the beneficiation of mixtures of mineral particles (such as kaolin clays) containing minerals which chelate with hydroxamates. The use of a silicon-containing compound in combination with a hydroxamate results in a more effective separation of minerals which chelate with the hydroxamate.

Abstract: Besides a synthesis gas, a metallurgical raw material is to be produced from an oil containing heavy metals. To do this, the oil is partially oxidized and the heavy metal-containing soot is separated and burnt and the heavy metals thus occurring as ash can be taken to further processing, e.g. washing from the synthesis gas produced, using an aqueous washing solution.

Abstract: Niobium, Nb, is refined from FeNb by electron beam melt refining. The amount of the impurities in the FeNb which form suboxides with oxygen is optionally determined. Sufficient oxygen is added to form oxides with these impurities. The electron beam melt refining process is carried out at a sufficiently high temperature and under a sufficiently low vacuum so that the impurities are removed as oxides from the liquid Nb and the purified Nb is recovered. Preferably the oxygen is added as an oxygen-containing compound such as Nb.sub.2 O.sub.5. The recovered Nb can be subjected to additional electron beam melt refining cycles to obtain the desired purity.

Abstract: The stoichiometry and/or crystal structure of vanadium oxide particles are altered by heating initial particles of vanadium oxide under mild conditions. The temperature is generally at least about 300.degree. C. less than the melting point of both the initial vanadium oxide particle and the product vanadium oxide particles. Preferred initial particles are vanadium oxide nanoparticles. The heating can be performed under an oxidizing atmosphere or an inert atmosphere, depending on the particular initial particles and the desired product particles.

Abstract: Purification of tantalum by plasma arc melting. The level of oxygen and carbon impurities in tantalum was reduced by plasma arc melting the tantalum using a flowing plasma gas generated from a gas mixture of helium and hydrogen. The flowing plasma gases of the present invention were found to be superior to other known flowing plasma gases used for this purpose.

Abstract: A method for producing engineered materials from salt/polymer aqueous solutions in which an aqueous continuous phase having at least one metal cation salt is mixed with a hydrophilic organic polymeric disperse phase so as to form a metal cation/polymer gel. The metal cation/polymer gel is then treated to form a structural mass precursor, which structural mass precursor is heated, resulting in formation of a structural mass having predetermined characteristics based upon the intended application of the structural mass.

Abstract: A process for producing nano size powders comprising the steps of mixing an aqueous continuous phase comprising at least one metal cation salt with a hydrophilic organic polymeric disperse phase, forming a metal cation salt/polymer gel, and heat treating the gel at a temperature sufficient to drive off water and organics within the gel, leaving as a residue a nanometer particle-size powder.

Abstract: Process for the partial oxidation of a hydrocarbon feedstock, comprising the steps of gasification, partial oxidation and removal of the carbon by forming a soot water slurry containing the unburned carbon and ash and filtration of the soot water slurry to form a filtercake of carbon and ash, wherein the filter cake is dried by means of a fluid bed and the dried filtercake is burned at temperatures between 600.degree. C. and 1000.degree. C. Preferably The fluid bed is operated by means of a fluidizing gas at a temperature of at least 150.degree. C. The dried filtercake is burned under circumstances that carbon is left in the resulting ash.

Abstract: Photorefractive crystals having the formula K.sub.1-y Li.sub.y Ta.sub.1-x Nb.sub.x O.sub.3 wherein x is between 0 and 1 and y is between 0.0001 and 0.15. The crystals are useful as a photorefractive material for use in optical systems. The crystals may be doped with various first transition elements and lanthanides including copper, vanadium, chromium, iron, and manganese, nickel, europium and cerium.

Abstract: According to the invention there is now provided a simple method of preparing a powder containing WC and cobalt and/or nickel. APT-powder and a powder of a basic salt of cobalt and/or cobalt are mixed in water or in mixed solvents. The suspension is stirred to react at temperatures ranging from room temperature to the boiling point of the solution whereby a precipitate is formed, which precipitate is filtered off, dried and finally reduced to a metallic powder.

Abstract: A method for producing an electrolytic solution containing vanadium as positive and negative electrode active material, the electrolytic solutions being suitable for a redox battery which comprises: the steps of (1) a vanadium compound is dissolved in a solvent under an alkaline or neutral condition, a polyvanadate compound is precipitated and isolated by thermal polymerization of vanadium ions under an acidic condition; (2) a part of the polyvanadate compound is baked in an inert or oxidizing gas atmosphere so as to remove ammonium ions; (3) a trivalent vanadium compound is formed by treating another part of the polyvanadate compound under a reductive atmosphere; (4) a trivalent vanadium electrolytic solution is formed by dissolving the trivalent vanadium compound in an acid solution; and (5) vanadium pentoxide and a part of the trivalent vanadium compound are reacted by mixing so that mixed electrolytic solutions of V.sup.4+ and V.sup.3+ are formed.

Abstract: A method for preparing a cathode having as active material silver vanadium oxide formed by chemical addition, reaction or otherwise intimate contact of a silver-containing component and a vanadium-containing compound to form a mixed metal oxide bronze that is thermally treated and rapidly cooled to form an amorphous product. The method of the present invention provides an alternate preparation technique for improving chemical control in the formation of a cathode for incorporation into an electrochemical cell.

Abstract: A process for the low temperature, low pressure preparation of the hydride product of ferroalloys of Group IV and Group V metals including niobium, tantalum, vanadium, and silicon and the novel hydride product of ferroniobium.

Abstract: A process for the preparation of ceramic material Lithium stannate doped with a transition metal for a humidity sensor mixes a salt of Lithium with SnO.sub.2 in dry condition, thereafter mixes in wet conditions using an organic solvent, adds a transition metal compound to the resulting mixture, mixes the mixture thoroughly, drys and compacts the mixture in the range of 5000 to 8000 lbs and heats the pellets so formed at a temperature in the range of 600.degree. to 800.degree. C. for a period in the range of 6 to 12 hours followed by slow cooling to room temperature.

Abstract: A material for a magnetic head slider consists essentially of 0.1 to 20.0 vol % of at least one of oxides the group Va elements of the International Periodic Table (Ta, Nb, V) and 80.0 to 99.9 vol % of stabilized cubic ZrO.sub.2 containing a stabilizer (Y.sub.2 O.sub.3, MgO, CeO.sub.2). It has improved precision machinability, machining efficiency, high strength, densified structure, affinity with the recording medium or lubricity, besides wear resistance. It may be machined precisely into a thin film magnetic head slider with a reduced amount of chipping.

Abstract: The starting material is a vanadium-containing residue, which contains at least 5 weight percent carbon on an anhydrous basis. The residue is thermally treated in a furnace a) at temperatures from 400.degree. to 700.degree. C. under an oxidizing atmosphere and an O.sub.2 partial pressure of at least 10.sup.-4 bar, measured within the region which is occupied by the residue, and/or b) at temperatures from 500.degree. to 1300.degree. C. under an O.sub.2 partial pressure not in excess of 10.sup.-2 bar, measured within the region which is occupied by the residue. A solids mixture which contains at least 5 weight percent vanadium oxide is withdrawn from the furnace. A multiple-hearth furnace or a rotary kiln or a fluidized bed reactor containing a stationary or circulating fluidized bed may be used as a furnace for the thermal treatment.

Abstract: A method for preparing a cathode having as active material silver vanadium oxide formed by chemical addition, reaction or otherwise intimate contact of elemental silver and a vanadium-containing compound present in an anhydrous mixture, is described. The present invention provides alternate preparation techniques for improving chemical control in the formation of a cathode for incorporation into an electrochemical cell.

Abstract: Fine particles of vanadium oxide or lithiated vanadium oxide are less than 100 microns in size and on the order of 30 microns in size. Such fine particles are prepared by spray-drying a precursor mixture. Such oxide particles are also intermingled with fine particles of carbon by including carbon particles in the precursor mixture.

Abstract: Heavy metal compounds, particularly vanadium pentoxide, are recovered from petroleum coke by combusting the coke under conditions constraining the temperatures to within the range 680.degree. C. to 1400.degree. C., collecting the ash which is then subjected to a known process for the extraction of the metallic compounds.Whilst the combustion process may be achieved in a fluidised bed furnace, higher recovery rates are likely to be achieved utilising a tubular furnace chamber inclined at 10.degree. to horizontal. dried petroleum coke, ground to fine powder (ASTM 75 micron, or less) is entrained into a primary air flow injected tangentially into the chamber through ports together with secondary air sufficient to maintain an oxidising atmosphere. Molten slag is deposted on the chamber wall by centrifugal action and drained from the chamber to fall on a rotating steel drum immersed in a water trough. A scraper removes the slag from the drug as flakes which are removed from the water trough using a screw conveyor.