Abstract: The instant invention relates to a process and plant for the transformation of dangerous wastes containing chromium six as contaminant into non dangerous wastes that can be stored without special care and will be degraded in the environment without time limit. The process basically consists of milling, extracting chromium six in liquid phase and under controlled conditions of stirring, time and temperature, proceeding then, through reduction, to transform the chromium six in chromium three and then precipitating as chromium trioxide, through gasification. The solid resulting from the transformation process can be used as raw material for the manufacturing of firebricks or eventually for the manufacturing of bricks used in the building industry through a process not included in the instant description.

Abstract: Provided is a roasting method capable of reducing both C and S components in minerals down to 0.5% or less, respectively, and securing a yield ratio of 90% or more for the Mo component. In a rotary kiln 7, a V, Mo and Ni containing material containing C and S components is subjected to oxidizing roasting to remove the C and S components from the material before reducing the material by means of a reducing agent in order to recover valuable metals composed of V, Mo and Ni. The rotary kiln is equipped with a burner 11 disposed on a material charge side 8a of the roasting furnace 8 to which the material is charged. In the roasting furnace, a direction along which the material moves and a flow of oxygen-containing gas introduced into the roasting furnace 8 are set to be parallel with each other.

Abstract: Process for recovering copper sulphide and optionally molybdenum sulphide from a copper bearing ore by froth flotation includes crushing said ore, mixing the obtained ground powder with at least a collector and water, aerating the slurry, and removing and concentrating the mineral froth formed at the surface of the bath, wherein the collector comprises a thioglycolic acid derivate having the following formula: wherein R1 is N or O, and R2 is an alkyl group having 2 to 12 carbon atoms.

Abstract: A method for detoxifying spent CCA (copper, chromium, arsenic) treated wood, from which CCA is efficiently removed from the wood, allowing both the CCA and the wood to be reused has been developed. The method comprises the steps of (1) microwave-enhanced acid extraction of CCA, (2) separation of the acid-containing CCA solution from the wood, (3) separation/precipitation of CCA from the acid extract, (4) recovery and regeneration of CCA-bearing precipitant for reuse in the wood preservation industry, (5) recycling recovered acid solution, (6) microwave-assisted liquefaction of the extracted wood, and (7) use of detoxified liquefied wood to form polymeric materials such as polyurethanes and phenolic resin adhesives. The recovered CCA may be used to treat wood. The recovered acids may be used to extract CCA from CCA-treated wood, and the liquefied wood may be used as phenolic or polyurethane resins.

Abstract: A method for producing a tungsten trioxide powder for a photocatalyst according to the present invention is characterized by comprising a sublimation step for obtaining a tungsten trioxide powder by subliming a tungsten metal powder or a tungsten compound powder by using inductively coupled plasma process in an oxygen atmosphere, and a heat treatment step for heat-treating the tungsten trioxide powder obtained in the sublimation step at 300° C. to 1000° C. for 10 minutes to 2 hours in an oxidizing atmosphere. A tungsten trioxide powder which is obtained by the method for producing a tungsten trioxide powder for a photocatalyst according to the present invention has excellent photocatalytic performance under visible light.

Abstract: According to various embodiments of the present teachings, there is a metal-carbon nanotubes composite and methods of making it. A method of forming a metal-carbon nanotube composite can include providing a plurality of carbon nanotubes and providing a molten metal. The method can also include mixing the plurality of carbon nanotubes with the molten metal to form a mixture of the carbon nanotubes and the molten metal and solidifying the mixture of the carbon nanotubes and the molten metal to form a metal-carbon nanotube composite.

Abstract: A method for recovering tungsten from a reaction mixture obtained by reacting an organic compound with hydrogen peroxide in the presence of a tungsten catalyst comprising blowing a gas into the reaction mixture to precipitate tungstic acid (WO3.H2O) and separating tungstic acid precipitated.

Abstract: A mineral processing facility is provided that includes a cogen plant to provide electrical energy and waste heat to the facility and an electrochemical acid generation plant to generate, from a salt, a mineral acid for use in recovering valuable metals.

Abstract: This invention relates to a method for producing chromates, especially for producing alkali metal chromates. The method comprises following steps: the obtaining of a mixture of alkali metal hydroxide, alkali metal chromate, and ferrous residue after the reaction of chromite ore with an oxidant in the reactor in the presence of molten salt or in aqueous solution of alkali metal hydroxide, the obtaining of a leaching slurry by leaching the reaction products with aqueous solution of alkali metal hydroxide, the separating of the primary chromate product from the leaching slurry, the obtaining of pure chromate crystal by purifying the primary chromate product. Both the primary chromate product and the pure chromate crystal can be used as the raw materials to manufacture other chromium compounds. Compared with the currently-used roasting method, the method has the advantages of decreasing the reaction temperature by about 700° C.

Abstract: A method for recovering high purity nickel, cobalt, molybdenum and vanadium from a waste catalyst in high yield by convenient means is provided. The method includes a step of heating a waste catalyst containing valuable metals in a non-oxidizing atmosphere, thereby deoiling an adhered oil content by thermal decomposition, a step of co-milling the deoiled waste catalyst and a chloride to form a chloride of nickel and/or cobalt, a step of water-leaching the co-milled waste catalyst to dissolve nickel and/or cobalt in water, a step of oxidizing leaching residue containing molybdenum and/or vanadium after water leaching to form an oxide of molybdenum and/or vanadium; and a step of subjecting the leaching residue containing the oxide of molybdenum and/or vanadium to alkali leaching to dissolve the molybdenum and/or vanadium in an alkali solution.

Abstract: A process for chlorinating ore, slag, mill scale, scrap, dust and other resources containing recoverable metals from the groups 4-6, 8-12, and 14 in the periodic table. The process comprises: a) forming a liquid fused salt melt consisting essentially of aluminum chloride and at least one other metal chloride selected from the group consisting of alkali metal chlorides and alkaline earth metal chlorides, wherein the aluminum chloride content in the liquid salt melt exceeds 10% by weight; b) introducing the recoverable metal resources into said liquid salt melt: c) reacting the aluminum chloride as chlorine donor with said recoverable metal resource to form metal chlorides, which are dissolved in the salt melt; and d) recovering the formed metal chlorides from the salt melt.

Abstract: Process for recovering copper sulphide and optionally molybdenum sulphide from a copper bearing ore by froth flotation includes crushing said ore, mixing the obtained ground powder with at least a collector and water, aerating the slurry, and removing and concentrating the mineral froth formed at the surface of the bath, wherein the collector comprises a thioglycolic acid derivate having the following formula: wherein R1 is N or O, and R2 is an alkyl group having 2 to 12 carbon atoms.

Abstract: A system and method for producing molybdenum oxide(s) from molybdenum sulfide are disclosed. The system includes a pressure leach vessel, a solid-liquid separation stage coupled to the pressure leach vessel, a solvent-extraction stage coupled to the solid-liquid separation stage, and a base stripping stage coupled to the solvent-extraction stage. The method includes providing a molybdenum sulfide feed, subjecting the feed to a pressure leach process, subjecting pressure leach process discharge to a solid-liquid separation process to produce a discharge liquid stream and a discharge solids stream, and subjecting the discharge liquid stream to a solvent extraction and a base strip process.

Abstract: Methods and systems for removing copper minerals from a molybdenite concentrate. One embodiment provides leaching copper from the molybdenite concentrate with a leaching solution comprising ferric chloride, removing molybdenite from the leaching solution, introducing an acid into the leaching solution and introducing O2, O3, or a combination of both, into the leaching solution. A method for regenerating ferric chloride in a leaching solution is also provided. One embodiment provides adding a leaching solution comprising Fe(II) ions, Fe(III) ions, or a combination of both, to a mixture of mineral sulfides, introducing an acid into the leaching solution, and introducing O2, O3, or a combination of both, into the leaching solution.

Abstract: The present invention relates to a process for the removal of metal catalyst degradation products from a bleed stream of a catalytic chemical reaction process, wherein the catalyst is based on a metal selected from those in group VIII of the periodic table, chromium, copper, molybdenum, tungsten, rhenium, vanadium, titanium and zirconium, said process comprising treatment of the bleed stream with an alkali metal carbonate or ammonium carbonate source to form a solid complex or an aqueous solution of said solid complex, and removal of the solid complex or the aqueous solution of said solid complex from the bleed stream.

Abstract: A process for producing metal compounds directly from underground mineral deposits including the steps of forming a borehole at a site into a mineral deposit containing metal compounds, inserting a slurry-forming device having a nozzle into the borehole adapted to direct pressurized water through the nozzle into the mineral deposit, supplying pressured water through the nozzle into the mineral deposit forming a mineral slurry containing metal compounds, extracting the mineral slurry containing metal compounds through the borehole, leaching the mineral slurry to convert the metal compounds to a soluble form in a leach solution, and removing metals and metal compounds by treating the leach solution with an extraction treatment adapted to remove the metal products. Steps of leaching the mineral slurry and removing metal products are performed at a location remote from the borehole site. Alternatively, the step of removing metal products from mineral slurry may be accomplished by pyrometallurgical processes.

Abstract: A process for converting fine catalyst slurried in heavy oil into a coke-like material from which catalytic metals can be recovered comprises mixing fine catalyst slurried in heavy oil with solvent, which causes asphaltenes in the heavy oil to precipitate from the heavy oil; separating fine catalyst and precipitated asphaltenes from the heavy oil and solvent; and converting precipitated asphaltenes to a coke-like material by pyrolizing fine catalyst and precipitated asphaltenes separated from the heavy oil.

Abstract: A process for recovering catalytic metals from fine catalyst slurried in heavy oil comprises pyrolizing fine catalyst slurried in heavy oil to provide one or more lighter oil products and a coke-like material and recovering catalytic metals from the coke-like material.

Abstract: A process is disclosed for separation and recovery of vanadium, molybdenum, iron, tungsten, cobalt and nickel from alumina-based materials, mattes, ores, manufacturing by-products and waste. These elements are oxidized. The oxides are reacted with gaseous HCl to form volatile chloride-bearing compounds that subsequently sublimate. The volatile compounds are condensed in a downward-stepped thermal gradient that allows collection of moderate to high purity compounds of individual elements with exception of a nickel-cobalt co-condensate. Nickel is separated from cobalt by precipitation of nickel chloride from concentrated HCl pressurized with gaseous HCl.

Abstract: Process for the production of hydrogen by the thermochemical route from water, based on the chlorine/cerium cycle, in which, according to a first reaction scheme, the following reactions are carried out: H2O+Cl2=2HCl+½O2;??(A) 8HCl+2CeO2=2CeCl3+Cl2+4H2O;??(B) 2CeCl3+4H2O=2CeO2+6HCl+H2;??(C) or in which, according to a second reaction scheme, the following reactions are carried out: H2O+Cl2=2HCl+½O2;??(A) 8HCl+2CeO2=2CeCl3+Cl2+4H2O;??(B) 2CeCl3+2H2O=2CeOCl+4HCl;??(B?) 2CeOCl+2H2O=2CeO2+2HCl+H2;??(C?) and in which the reaction (B) for the chlorination of cerium oxide is carried out in the liquid phase, the cerium chloride passing into solution.

Abstract: A method for increasing the chrome to iron ratio of a chromite product selected from the group consisting of ore and ore concentrate comprising the steps of mixing the chromite product with at least one salt so as to produce a mixture, whereby the concentration of salt in the mixture is selected to induce the selective chlorination of iron; and chlorinating the mixture in the presence of CO at a temperature sufficient to induce the formation of a thin film of a melt around the chromite product and at a temperature able to promote the selective chlorination of iron, whereby an iron impoverished chromite product is yielded having an increased chromite to iron ratio as compared to that of the chromite product.

Abstract: A metal sulfide nanocrystal manufactured by a method of reacting a metal precursor and an alkyl thiol in a solvent, wherein the alkyl thiol reacts with the metal precursor to form the metal sulfide nanocrystals, wherein the alkyl thiol is present on the surface of the metal sulfide nanocrystal, wherein the alkyl thiol is bonded to the sulfur crystal lattice. A metal sulfide nanocrystal manufactured with a core-shell structure by a method of reacting a metal precursor and an alkyl thiol in a solvent to form a metal sulfide layer on the surface of a core, wherein the alkyl thiol is present on the surface of the metal sulfide nanocrystal, wherein the alkyl thiol is bonded to the sulfur crystal lattice. These metal sulfide nanocrystals can have a uniform particle size at the nanometer-scale level, selective and desired crystal structures, and various shapes.

Abstract: A method of treating value bearing material comprising oxidised or surface oxidised mineral values includes the steps of crushing the value bearing material, contacting the crushed material! with a sulfide solution to sulfide the oxidised or surface oxidised mineral values, and adding ions of a selected base metal to the crushed value bearing material. The value bearing material may comprise oxidised or surface oxidised base metal or precious metal minerals. The crushed value bearing material is prepared as a slurry or pulp comprising from 15% to 40% solids and the remainder comprising water. The sulfide solution preferably comprises a soluble sulfidiser such as sodium hydrosulfide and the base-metal ion solution preferably comprises metal salt of base metals like copper or iron.

Abstract: Methods for the production of monometal carbides are disclosed. A metal source and a carbon source are reacted under conditions suitable to produce a reaction product. The reaction product may comprise fully carburized monometal carbide and excess carbon, or an intermediate product comprising partially carburized monometal carbide in the presence or absence of excess carbon. The carbon content in the reaction product may then be adjusted in a controlled removal or addition process to produce a product the fully carburized monometal carbide having near stoichiometric carbon.

Abstract: The present invention is to manufacture the organic silver solution by dissolving silver oxide in an organic solvent, and further provide an ink enabling a conductive circuit to be formed by applying it to an inkjet printer. Also, it is to provide a method for forming a conductive circuit on various substrates by printing it through the inkjet printer using the manufactured ink and further heat-treating it. The organic silver solution, a composition according to the present invention, can be manufactured by dissolving silver oxide in an amine-based compound and a lactone-based compound (or a lactam-based compound, a carbonate-based compound, a cyclic acid anhydride-based compound) by reacting the former an the latter, and in order to ensure the appropriate liquid fluidity for the inkjet printer, the ink was manufactured by adding an organic solvent, such as alcohol, a surfactant and the like thereto.

Abstract: A process is disclosed for separation and recovery of vanadium, molybdenum, iron, tungsten, cobalt and nickel from alumina-based materials, mattes, ores, manufacturing by-products and waste. These elements are oxidized. The oxides are reacted with gaseous HCl to form volatile chloride-bearing compounds that subsequently sublimate. The volatile compounds are condensed in a downward-stepped thermal gradient that allows collection of moderate to high purity compounds of individual elements with exception of a nickel-cobalt co-condensate. Nickel is separated from cobalt by precipitation of nickel chloride from concentrated HCl pressurized with gaseous HCl.

Abstract: Tungsten trioxide hydrate (WO3.H2O) was prepared from a precursor solution of ammonium paratungstate in concentrated aqueous hydrochloric acid. The precursor solution was rapidly added to water, resulting in the crash precipitation of a yellow white powder identified as WO3.H2O nanosized platelets by x-ray diffraction and scanning electron microscopy. Annealing of the powder at 200° C. provided cubic phase WO3 nanopowder, and at 400° C. provided WO3 nanopowder as a mixture of monoclinic and orthorhombic phases.

Abstract: The invention relates to a novel class of serine proteases of peptidase family S2A or S1E that are stable in the presence of copper (Cu2+) and/or inhibited by copper only to a limited extent. Structural features of potential relevance for this effect are also disclosed. This class of proteases includes proteases derived from Brachysporiella gayana, Nocardiopsis dassonvillei subsp. dassonvillei, Nocardiopsis prasina, and Nocardiopsis alba. The invention also relates to DNA encoding such proteases and the expression thereof in a host cell, animal and plant cells, as well as to the use thereof in animal feed and in detergents. In particular, the invention relates to animal feed and animal feed additives, such as premix, incorporating these proteases together with 1-500 ppm Cu (in-feed-concentration).

Abstract: Processes and systems for recovering promoter-containing compounds, for example, perrhenates, from promoter-containing catalyst substrates, for example, substrates containing precious metals, such as silver, are disclosed. The processes include contacting the substrates with a first solution adapted to remove at least some of the catalyst promoter from the substrates, for example, an oxidizing agent, to produce a second solution containing catalyst promoter, passing the second solution through a porous medium adapted to capture at least some of the catalyst promoter, for example, a ion exchange resin; and passing a third solution, for example, a base solution, through the porous medium to remove at least some of the catalyst promoter from the porous medium and produce a fourth solution containing compounds having a catalyst promoter. Systems adapted to practice these processes are also disclosed.

Abstract: A catalyst for the production of an oxygen-containing compound, comprising palladium, tungsten and zirconium, a production process thereof, and a production process of an oxygen-containing compound using the catalyst. The catalyst can provide an oxygen-containing compound from a lower olefin and oxygen with high productivity and high selectivity.

Abstract: A process is disclosed for separation and recovery of vanadium, molybdenum, iron, tungsten, cobalt and nickel from alumina-based materials, mattes, ores, manufacturing by-products and waste. These elements are oxidized. The oxides are reacted with gaseous HCl to form volatile chloride-bearing compounds that subsequently sublimate. The volatile compounds are condensed in a downward-stepped thermal gradient that allows collection of moderate to high purity compounds of individual elements with exception of a nickel-cobalt co-condensate. Nickel is separated from cobalt by precipitation of nickel chloride from concentrated HCl pressurized with gaseous HCl.

Abstract: A reactor for molybdenum sulphide (MoS2), wherein MoS2 is ionized by an electric field generated by a first set of magnetrons at a frequency in the range of 2500-3500 MHz and heated by a variable magnetic field of 2500 Hz produced by a winding coil, resulting in the exclusive evaporation of molybdenite. MoS2 in gas state is then stimulated by a second set of magnetrons and, with the injection of air, oxidized until trioxide is obtained. Hot gases essentially containing molybdenum trioxide, sulphur dioxide, and nitrogen are conducted from a first body towards a second body though a first duct. Cold air is added to the second body through a second duct to cool the gas, and crystals formed by liquefaction settle and are removed through a lower duct while gases at a temperature of 600° C. are conducted through a higher duct.

Abstract: Disclosed herein is a method for manufacturing metal sulfide nanocrystals using a thiol compound as a sulfur precursor. The method comprises reacting the thiol compound and a metal precursor in a solvent to grow metal sulfide crystals to the nanometer-scale level. Further disclosed is a method for manufacturing metal sulfide nanocrystals with a core-shell structure by reacting a metal precursor and a thiol compound in a solvent to grow a metal sulfide layer on the surface of a core. The metal sulfide nanocrystals prepared by these methods can have a uniform particle size at the nanometer-scale level, selective and desired crystal structures, and various shapes.

Abstract: A process for recovering nickel and cobalt values from nickel- and cobalt-containing laterite ores as an enriched mixed nickel and cobalt sulphide intermediate and for producing nickel and cobalt metal from the nickel and cobalt sulphide intermediate. The laterite ore is leached as a slurry in a pressure acid leach containing an excess of aqueous sulphuric acid at high pressure and temperature, excess free acid in the leach slurry is partially neutralized to a range of 5 to 10 g/L residual free H2SO4 and washed to yield a nickel- and cobalt-containing product liquor, the product liquor is subjected to a reductant to reduce any Cr(VI) in solution to Cr(III), the reduced product liquor is neutralized to precipitate ferric iron and silicon at a pH of about 3.5 to 4.0, and the neutralized and reduced product liquor is contacted with hydrogen sulphide gas to precipitate nickel and cobalt sulphides.

Abstract: The present invention relates generally to a process for recovering copper and other metal values from metal-containing materials using controlled, super-fine grinding and medium temperature pressure leaching. Processes embodying aspects of the present invention may be beneficial for recovering a variety of metals such as copper, gold, silver, nickel, cobalt, molybdenum, rhenium, zinc, uranium, and platinum group metals, from metal-bearing materials, and find particular utility in connection with the extraction of copper from copper sulfide ores and concentrates.

Abstract: A novel process for preparing chromium dioxide of substantially high purity as well as composites of CrO2/Cr2O3 and CrO2/Cr2O5 following a sequence of simple steps. The process does not require pressure as a control parameter during the process of synthesis. No chemical modifier has been used to bring down the working pressure during synthesis. Fairly hard sintered pellets of CrO2 can be obtained without introducing any detectable impurity phase that usually appears during the process of sintering. Further, CrO2/Cr2O3 and CrO2/Cr2O5 composites have also been prepared where the fraction of insulating Cr2O3 or Cr2O5 in metallic CrO2 can be easily controlled. Significant negative magnetoresistance is found in pure CrO2 (5% MR) as well as CrO2/Cr2O3 (33% MR) composites near room temperature. The MR studies on the CrO2/Cr2O5 composites have been done and significant negative MR (22%) has been found in CrO2/Cr2O5 composites near room temperature.

Abstract: The present invention relates to a process for simultaneous recovery of chromium and iron from Chromite Ore Processing Residue (COPR) and more particularly, the present invention relates to an economical and environment-friendly process for recovering chromium as a chromate salt and iron as an iron salt from non-leachable Chromite Ore Processing Residue and avoids landfilling of toxic metals.

Abstract: Granular secondary particles of a lithium-manganese composite oxide suitable for use in non-aqueous electrolyte secondary batteries showing high-output characteristics which are granular secondary particles made up of aggregated crystalline primary particles of a lithium-manganese composite oxide and have many micrometer-size open voids therein with a defined average diameter and total volume of open voids. A process for producing the granular secondary particles which includes spray-drying a slurry of at least a manganese oxide, a lithium source, and an agent for open-void formation to thereby granulate the slurry and then calcining the granules.

Abstract: A process for reducing the content of alkali metal impurities (e.g., potassium) in ammonium metallate solutions is described. The process involves subjecting a feed solution containing ammonium metallate and alkali metal impurities to membrane filtration. The membrane filtration results in the formation of a retentate having a reduced level alkali metal relative to the feed solution, and a permeate containing substantially the balance of alkali metal. The permeate may also be further treated, to remove alkali metal there from, by passage through a cation exchange column, thereby forming a cation exchange treated permeate that may be combined with the retentate of the membrane filtration step.

Abstract: Provided is a cathode composition for lithium secondary battery that includes a lithium-chromium-titanium-manganese oxide that has the formula Li[Li(1-x)/3CrxTi(2/3)yMn2(1-x-y)/3]O2 where 0?x?0.3, 0?y?0.3 and 0.1?x+y?0.3, and layered a-LiFeO2 structure. A method of synthesizing the lithium-chromium-titanium manganese oxide includes preparing a first mixed solution by dispersing titanium dioxide (TiO2) in a mixed solution of chrome acetate (Cr3(OH)2(CH3CO2)7) and manganese acetate ((CH3CO2)2Mn.4H2O), adding a lithium hydroxide (LiOH) solution to the first mixed solution to obtain homogeneous precipitates, forming precursor powder that has the formula Li[Li(1-x)/3CrxTi(2/3)yMn2(1-x-y)/3]O2 where 0?x?0.3, 0?y?0.3 and 0.1?x+y?0.3 by heating the homogeneous precipitates, and heating the precursor powder to form oxide powder having a layered structure.

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: Polyoxometalate compounds which exhibit anti-retroviral activity are disclosed. Compounds with anti-retroviral activity include those having the following general molecular formulas: M7PW11O39 M8SiW11O39 M9HSiW9O34 M8HPW9O34 M10(TM)4(PW9O34)2 M16(TM)4(P2W15O56)2 M14[NaP5W30O110] M12(TM)3(PW9O34)2 M6P2W18O62 wherein M is an alkali metal, NH4+ or other common monocation or soluble dication, or any combination of the above provided adequate water solubility is exhibited, or histidinium ion, argininium ion, or lysinium ion or any dication of a dipeptide or oligopeptide with 2 protonated basic amino acid residues, or any combination of these monocations or dications with each other or with any common inorganic cation, and TM is a divalent transition metal ion, such as Mn, Fe, Co, Ni, Cu and Zn.

Abstract: The process chemistry during the oxidation of molybdenite concentrates in an oxygen pressure leach can be controlled by regulating the amount of ferric iron and excess sulfuric acid recycled as autoclave discharge slurry or filtrate to the autoclave feed. A computer model capable of predicting the concentration of soluble molybdenum in the autoclave discharge and based on the concentrate and recycle analyses was developed.

Abstract: A novel molybdenum compound, ammonium dodecamolybdomolybdate (AMM), is described which may be used in the manufacture of molybdenum metal and molybdenum carbide powders. The molybdenum compound is a dodecaheteropoly acid salt having a Keggin-type structure wherein molybdenum resides in both the hetero as well as peripheral atomic positions. The novel compound has the general formula (NH4)2Mo12MoO40.6H2O. Because of its low solubility, the compound can be crystallized efficiently and at a high purity from ammonium molybdate solutions.

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 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: An environmentally benign process for remediating contaminated matter includes contact with a lixiviant. The lixiviant contains a chelating agent which chemically reacts with a selected contaminant, forming a chelate soluble within the lixiviant and thus extracting the selected contaminant from the matter. The lixiviant, including the chelate, is separated from the particulate matter, and chemically treated to demobilize the chelate. The selected contaminant is separated from the lixiviant and sent for disposal or further processing. The remidiated matter is also sent for disposal or further processing.

Abstract: A method for dissolving base metals and noble metals from ores having base metals and noble metals which comprises adding the ore to a solution of a non-acid oxidizing agent, then adding an aqueous solution of an acid forming halide and then adjusting the H+ concentration of the combined solutions to a minimum H+ concentration of 1 mol/l.