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 heap leach process for the recovery of nickel and cobalt from a lateritic ore, said process including the steps of leaching and/or agglomerating the ore with a lixiviant that includes ferrous ions, wherein the lixiviant is able to liberate cobalt from the cobalt containing minerals within the ore in preference to nickel, to produce a cobalt rich pregnant leach solution relatively free of nickel.

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: The present invention provides a method for extraction of metals selected from Cr, Mo, Pd, Tc, W, Re, and Pu using a new extractant of methyliminobisalkylacetamide represented by a formula (I): CH3—N—(CH2CONR2)2??(I) wherein R represents an alkyl group having 8-12 carbon atoms.

Abstract: A method for preparing manganese sulfate and zinc sulfate from waste batteries containing manganese and zinc, and more particularly to a method for preparing manganese sulfate and zinc sulfate from waste batteries containing manganese and zinc. Zinc powder and activated carbon are added to a leached solution obtained from a continuous leaching process so as to remove heavy metals and organic materials from the leached solution, and then the leached solution is spray-dried to simultaneously obtain manganese sulfate and zinc sulfate at high-purity by a simple process without generating wastewater. An environmentally friendly waste battery recycling process is thereby provided, because it is not required to use additional chemical substances for neutralization titration or impurity removal in recovering manganese sulfate and zinc sulfate by leaching a waste battery powder.

Abstract: The present application relates to novel gel-type or macroporous picolylamine resins which are based on at least one monovinylaromatic compound and at least one polyvinylaromatic compound and/or a (meth)acrylic compound and contain tertiary nitrogen atoms in structures of the general formula (I) as functional group, where R1 is an optionally substituted radical from the group consisting of picolyl, methylquinoline and methylpiperidine, R2 is —CH2—S—CH2COOR3 or —CH2—S—C1-C4-alkyl or —CH2—S—CH2CH(NH2)COOR3 or —CH2—S—CH2—CH(OH)—CH2(OH) or or derivatives thereof or —C?S(NH2), R3 is a radical from the group consisting of H, Na and K, m is an integer from 1 to 4, n and p are each, independently of one another, a number in the range from 0.1 to 1.9 and the sum of n and p is 2 and M is the polymer matrix, a process for preparing them and their uses, in particular the use in hydrometallurgy and electroplating.

Abstract: A heap leach process for the recovery of nickel and cobalt from a lateritic ore, said process including the steps of leaching and/or agglomerating the ore with a lixiviant that includes ferrous ions, wherein the lixiviant is able to liberate cobalt from the cobalt containing minerals within the ore in preference to nickel, to produce a cobalt rich pregnant leach solution relatively free of nickel.

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 method for preparing lithium transitional metal oxides, comprises the steps of: preparing a carbonate precursor using the following substeps: forming a first aqueous solution containing a mixture of at least two of the ions of the following metal elements (“Men+”): cobalt (Co), nickel (Ni), and manganese (Mn); forming a second aqueous solution containing ions of CO32?; and mixing and reacting the first solution and the second solution to produce the carbonate precursor, Ni1-x-yCoxMnyCO3; and preparing the lithium transition metals oxide from the carbonate precursors using the following substeps: evenly mixing Li2CO3 and the carbonate precursor; calcinating the mixed material in high temperature; and cooling and pulverizing the calcinated material to obtain the lithium transition metal oxide, Li Ni1-x-yCoxMnyO2.

Abstract: The invention provides a lithium-manganese-based composite oxide containing Ti and Ni, which is represented by the compositional formula: Li1+x(Mn1?n?mNimTin)1?xO2, wherein 0<x?0.33, 0.05<m<0.3, and 0.3<n<0.5, and includes a crystal phase of layered rock-salt type structure. The composite oxide is a novel material that is capable of maintaining an average discharge voltage of 3 V or more over long charge/discharge cycles, while providing a discharge capacity equal to or higher than those of lithium-cobalt-oxide-based positive electrode materials, and that can be prepared using starting materials that are inexpensive and less limited as natural resources, while exhibiting improved charge/discharge characteristics over known low-cost positive electrode materials.

Abstract: A method of isolating 186Re according to example embodiments may include vaporizing a source compound containing 185Re and 186Re. The vaporized source compound may be ionized to form negatively-charged molecules containing 185Re and 186Re. The negatively-charged molecules may be separated to isolate the negatively-charged molecules containing 186Re. The isolated negatively-charged molecules containing 186Re may be collected with a positively-charged collector. Accordingly, the isolated 186Re may be used to produce therapeutic and/or diagnostic radiopharmaceuticals having higher specific activity.

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: Sorbents for removal of mercury and other pollutants from gas streams, such as a flue gas stream from coal-fired utility plants, and methods for their manufacture and use are disclosed. The methods include mixing fly ash particles with a sulfide salt and a metal salt to form a metal sulfide on the outer surface of the fly ash particles.

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: Disclosed is a process that relates to the recovery of a metal catalyst from an oxidizer purge stream produced in the synthesis of carboxylic acid, typically terephthalic acid. The process involves the addition of a wash solution to a high temperature molten dispersion to recover the metal catalyst and then subjecting an aqueous mixture or purified aqueous mixture so formed to a single stage extraction to remove organic impurities to produce an extract stream and a raffinate stream comprising the metal catalyst.

Abstract: The present application relates to granules of powdery mineral particles produced by spray granulation of a liquid slurry comprising powdery minerals particles having particle size below 10 m, at least one water-reducing agent and/or at least one binder agent and/or at least one dispersing agent. The application further relates to a method for producing such granules.

Abstract: Methods and systems for regenerating and pretreating oxides of manganese and precipitation of oxides of manganese from manganese salt solutions. Oxides of manganese, a slurry containing oxides of manganese or manganese salt solutions are mixed with heated aqueous oxidizing solutions and processed in a continuous process reactor. Temperature, pressure, Eh value, and pH value of the mixed solution are monitored and adjusted so as to maintain solution conditions within the MnO2 stability area during processing. This results in regenerated, pretreated and precipitated oxides of manganese having high or increased pollutant loading capacities and/or oxidation states. Oxides of manganese thus produced are, amongst other uses; suitable for use as a sorbent for capturing or removing target pollutants from industrial gas streams. Filtrate process streams containing useful and recoverable value present as spectator ions may be further processed to produce useful and marketable by-products.

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 method of isolating 186Re according to example embodiments may include vaporizing a source compound containing 185Re and 186Re. The vaporized source compound may be ionized to form negatively-charged molecules containing 185Re and 186Re. The negatively-charged molecules may be separated to isolate the negatively-charged molecules containing 186Re. The isolated negatively-charged molecules containing 186Re may be collected with a positively-charged collector. Accordingly, the isolated 186Re may be used to produce therapeutic and/or diagnostic radiopharmaceuticals having higher specific activity.

Abstract: A method for removing impurities from a mother liquor comprising a carboxylic acid, a metal catalyst, impurities by (a) evaporating the mother liquor comprising a carboxylic acid, a metal catalyst, impurities and a solvent in a first evaporator zone to produce a vapor stream and a concentrated mother liquor stream; (b) evaporating the concentrated mother liquor stream in a second evaporator zone to form a solvent rich stream and a super concentrated mother liquor stream; (c) mixing in a mixing zone a water-solvent solution and optionally an extraction solvent with the super concentrated mother liquor stream to form an aqueous mixture; (d) optionally separating organic impurities from the aqueous mixture in a solid-liquid separation zone to form a purified aqueous mixture; and (e) extracting the aqueous mixture or purified aqueous mixture with an extraction solvent in an extraction zone to form an extract stream and the raffinate stream.

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 process for the separation of cobalt and/or manganese from impurity elements selected from one or more of calcium and magnesium contained in a leach solution, the process comprising the step of subjecting the leach solution to solvent extraction using an organic solution of a carboxylic acid such as Versatic 10 and a hydroxyoxime such as LIX 63, optionally together with a stabilzer.

Abstract: A solvent extraction composition is comprised of one or more orthohydroxyarylaldoximes and one or more othohydroxyarylketoximes, and one or more equilibrium modifiers in an amount providing a degree of modification of the orthohydroxyarylaldoximes from about 0.2 to 0.

Abstract: A lithium-containing complex oxide exhibits a high performance as a cathode active material of a lithium secondary cell or the like and having a high tap density. A granular lithium-containing complex oxide, such as lithium manganese complex oxide, is made up of “complex oxide grains produced by integrating lithium-rich material grains abnormally grown during a firing reaction with the surfaces of the base grains by sintering.” The number of complex oxide grains is not more than 50 per gram of the complex grains. A metal oxide such as manganese oxide and lithium carbonate not more than 5 ?m in average grain size are mixed by means of a mixer which grinds and mixes particles by using a shearing force and heated and fired at a warming rate of not more than 50° C./h., thus producing the lithium-containing complex oxide.

Abstract: A method for recovering and recycling catalyst coated fuel cell membranes includes dissolving the used membranes in water and solvent, heating the dissolved membranes under pressure and separating the components. Active membranes are produced from the recycled materials.

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: 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: Single-phase lithium-transition metal oxide compounds containing cobalt, manganese and nickel can be prepared by wet milling cobalt-, manganese-, nickel- and lithium-containing oxides or oxide precursors to form a finely-divided slurry containing well-distributed cobalt, manganese, nickel and lithium, and heating the slurry to provide a lithium-transition metal oxide compound containing cobalt, manganese and nickel and having a substantially single-phase O3 crystal structure. Wet milling provides significantly shorter milling times than dry milling and appears to promote formation of single-phase lithium-transition metal oxide compounds. The time savings in the wet milling step more than offsets the time that may be required to dry the slurry during the heating 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: An efficient process for forming anhydrous metal halides includes the reaction of a metal powder with a hydrogen halide under anhydrous conditions. In one example, manganese powder is reacted with hydrogen chloride under anhydrous reaction conditions.

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: The present invention relates to the macroporous manganese oxide material having ferromagnetic property and a method of preparing the same, more particularly to the macroporous ferromagnetic manganese oxide having three-dimensionally ordered nanopores, which is prepared by aligning colloidal polymer particles with an average diameter of a few hundred nanometers in 3D, infiltrating a solution of the precursor compound capable of forming manganese oxide represented by the following Chemical Formula 1 into interstices of the colloidal template and heating in an oxygen atmosphere to decompose and remove the polymer template, and a method for preparing the same: La1-xCax-ySryMnO3 ??(1) wherein 0.25<x<0.35 and 0<y?0.35.

Abstract: The electrode material for positive electrodes of rechargeable lithium batteries is based on a lithium transition metal oxide. Said lithium transition metal oxide is a lithium transmission metal mixed oxide with at least two transition metals (for example nickel and/or manganese), has a layer structure and is doped (for example, with aluminium and/or boron). This inventive electrode material is characterized by a high cycle stability, yet is still economical to produce.

Abstract: A process for elution of rhenium adsorbed on strongly basic ion-exchange resins by means of highly concentrated aqueous hydrochloric acid solution is described, in which the ion-exchange resin is treated with aqueous solution containing an oxidizing agent.

Abstract: Stabilized lithiated manganese oxide (LMO) is prepared by reacting cubic spinel lithium manganese oxide particles and particles of an alkali metal compound in air for a time and at a temperature sufficient to decompose at least a portion of the alkali metal compound, providing a treated lithium manganese oxide. The reaction product is characterized as particles having a core or bulk structure of cubic spinel lithium manganese oxide and a surface region which is enriched in Mn+4 relative to the bulk. X-ray diffraction data and x-ray photoelectron spectroscopy data are consistent with the structure of the stabilized LMO being a central bulk of cubic spinel lithium manganese oxide with a surface layer or region comprising A2MnO3, where A is an alkali metal. Electrochemical cells containing the stabilized LMO of the invention have improved charging and discharging characteristics and maintain integrity over a prolonged life cycle.

Abstract: A solvent extraction composition is comprised of one or more orthohydroxyarylaldoximes and one or more othohydroxyarylketoximes, and one or more equilibrium modifiers in an amount providing a degree of modification of the orthohydroxyarylaldoximes from about 0.2 to 0.

Abstract: The present invention allows the determination of trace levels of ionic substances in a sample solution (ions, metal ions, and other electrically charged molecules) by coupling a separation method, such as liquid chromatography, with ion selective electrodes (ISE) prepared so as to allow detection at activities below 10−6M. The separation method distributes constituent molecules into fractions due to unique chemical and physical properties, such as charge, hydrophobicity, specific binding interactions, or movement in an electrical field. The separated fractions are detected by means of the ISE(s). These ISEs can be used singly or in an array. Accordingly, modifications in the ISEs are used to permit detection of low activities, specifically, below 10−6M, by using low activities of the primary analyte (the molecular species which is specifically detected) in the inner filling solution of the ISE. Arrays constructed in various ways allow flow-through sensing for multiple ions.

Abstract: The invention relates to a method of extracting anions based on metals of groups IV B to VIII of the periodic table from aqueous solutions thereof, wherein compounds of general formula are used as extractants, in which a maximum of two of the R1, R2, R3 and R4 substituents represent hydrogen atoms and the remaining substituents represent identical or different alkyl or aminoakyl groups, which are optionally branched and which contain on average at least 5 C atoms.

Abstract: The invention provides a lithium manganese oxide spinel suited as a cathode active material for lithium ion secondary batteries showing excellent high-temperature cycling behavior. The lithium manganese oxide is represented by the following general formula (1): Li1+&agr;Mn2−&agr;−yMyO4−&dgr; wherein O≦&agr;≦0.5, 0.005≦y≦0.5, −0.1≦&dgr;÷0.1, and M represents a metal element other than Li and Mn, and which shows the ratio of a main peak intensity at 5±40 ppm to a main peak intensity at 525+40 ppm (I0ppm/I500ppm), each intensity being obtained by 7Li-NMR measurement according to the following measuring method, falling within the following range: I0ppm/I500ppm≦0.65y+0.02.

Abstract: A process of manufacturing a positive active material for a lithium secondary battery includes adding a metal source to a doping element-containing coating liquid to surface-treat the metal source, wherein the metal source is selected from the group consisting of cobalt, manganese, nickel, and combination thereof; drying the surface-treated metal source material to prepare a positive active material precursor; mixing the positive active material precursor with a lithium source; and subjecting the mixture to heat-treatment. Alternatively, the above drying step during preparation of the positive active material precursor is substituted by preheat-treatment or drying followed by preheat-treatment.

Abstract: The present invention relates to a method for labelling a sulfide compound with technetium or rhenium, comprising the reaction of a disulfide compound with pertechnetate or perrhenate in the presence of borohydride exchange resin to obtain a complex of technetium or rhenium with the sulfide compound. The method can directly label disulfide compounds with technetium or rhenium, can skip the synthetic step of thiol-protected S-precursor, and is useful for high value-added radiopharmaceuticals.

Abstract: Disclosed is a positive active material of for a rechargeable lithium battery and a method of preparing the same. The positive active material is represented by formula 1: LixMn2-a-bCraMbO4+z  [formula 1] where x≧2; 0.25<a<2; 0<b≦0.3; z≧0; M is an alkali earth metal, a transition metal or a mixture thereof. The method includes the steps of dissolving a chromium salt, a manganese salt, and a metal salt(s) in a solvent to produce a solution; performing a first heat-treatment step on the obtained solution at 400 to 500° C. to produce a chromium manganese metal oxide; mixing the chromium manganese metal oxide with a lithium salt; and performing a second heat-treatment step at 600 to 800° C.

Abstract: Novel stable forms of technetium and methods for their production are provided. These methods have particular application for the removal of technetium from industrial waste compositions.

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: A process for recovering components of a catalyst from a mother liquor of liquid phase oxidation in production of aromatic carboxylic acids by liquid phase oxidation of aromatic hydrocarbons having substituents with a gas containing oxygen in a presence of a catalyst comprising cobalt, manganese and bromine in acetic acid or acetic acid containing water as a solvent, which process comprises adding a compound generating an ion of an alkali metal to the mother liquor of liquid phase oxidation obtained after separating crystals of the aromatic carboxylic acid from a reaction fluid of the liquid phase oxidation, bringing the mother liquor containing the compound into contact with an ion exchange resin so that the components of the catalyst are adsorbed to the ion exchange resin and recovering the components of the catalyst comprising cobalt, manganese and bromine ion by passing an elution liquid through the ion exchange resin.

Abstract: This invention provides a method for recovering rhenium oxide from a material containing rhenium by itself or rhenium in combination with some other element, such as an element catalytically active for a catalytic process, such as hydrogenation, oxidation, reforming, and hydrocracking. The method includes conversion of rhenium to a sublimable oxide via oxidation, heating in an oxidizing atmosphere to sublime the oxide as a volatized oxide, and then isolation of rhenium from the volatized oxide.

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: The present invention provides a lithium manganese oxide, wherein a content of sulfur is not more than 0.32% by weight, and an averaged diameter of pores is not less than 120 nanometers, and the lithium manganese oxide is represented by Li1+xMn2−x−yMyO4, where “M” is at least one of metals and 0.032≦x≦0.182; 0≦y≦0.2, and also provides a non-aqueous electrolyte secondary battery using the above lithium manganese compound oxide as a positive electrode active material.

Abstract: A method of treating metal-contaminated spent foundry sand, or other industrial waste, by combining the sand with a sulfite to produce insoluble metal sulfur oxide complexes that do not leach from the sand. The treated waste may also be processed to reducing “clumping,” thereby rendering the treated waste appropriate for use in another industrial process.