A method according to an embodiment is for recovering a valuable metal from a waste electrode material of a lithium secondary battery by using lithium carbonate. An anode-cathode mixed electrode material that has been separated by draining, crushing, screening, and sorting a waste lithium secondary battery is preprocessed. A precipitation operation performed by adding lithium carbonate (Li2CO3) to a metal melt acquired by performing sulfuric acid dissolution using sulfuric acid. A valuable metal such as nickel, cobalt, manganese, aluminum, and copper is recovered as a residue in the form of a carbonate composite, and a lithium sulfate (Li2SO4) aqueous solution including lithium is recovered as a filtrate.

Aspects of the present disclosure generally relate to battery technology, and more specifically relate to manganese oxides and cathode active materials. In an aspect, a cathode active material is provided. The cathode active material includes a composition comprising a manganese oxide represented by Formula (I): Li.sub.aNa.sub.b(M.sup.1).sub.cMn.sub.dO.sub.e, a manganese oxide represented by Formula (II): Na.sub.w(M.sup.2).sub.xMn.sub.yO.sub.z (II), or combinations thereof, wherein: each of M.sup.1 and M.sup.2 is, individually, Ni, Cu, Zn, Mg, Fe, Co, Li, Al, Cr, LiAl, LiCr, LiCo, or combinations thereof, a, b, c, d, and e represent molar ratios of respective elements in Formula (I); and w, x, y, and z represent molar ratios of respective elements in Formula (II). Batteries and articles comprising a manganese oxide described herein are provided. Processes for forming manganese oxides are also provided.

Disclosed are a precursor for preparation of a lithium composite transition metal oxide, a method for preparing the same and a lithium composite transition metal oxide obtained from the same. More particularly, the transition metal precursor which has a composition represented by Formula 1 below and is prepared in an aqueous transition metal solution, mixed with a transition metal-containing salt, including an alkaline material, the method for preparing the same and the lithium composite transition metal oxide obtained from the same are disclosed.

Mn.sub.aM.sub.b(OH.sub.1-x).sub.2-yA.sub.y (1) wherein M is at least one selected form the group consisting of Ni, Ti, Co, Al, Cu, Fe, Mg, B, Cr, Zr, Zn and Period II transition metals; A is at least one selected form the group consisting of anions of PO.sub.4, BO.sub.3, CO.sub.3, F and NO.sub.3, and 0.5a1.0; 0b0.5; a+b=1; 0<x<1.0; and 0y0.02.

An object is to reduce variation in shape of crystals that are to be formed. Solutions containing respective raw materials are made in an environment where an oxygen concentration is lower than that in air, the solutions containing the respective raw materials are mixed in an environment where an oxygen concentration is lower than that in air to form a mixture solution, and with use of the mixture solution, a composite oxide is formed by a hydrothermal method.

A method of recovering metal compounds from solid oxide fuel cell scrap includes processing the solid oxide fuel cell scrap to form a powder, digesting the processed scrap, extracting lanthanum oxide and cerium oxide from a solution containing the digested processed scrap, extracting a zirconium compound from the solution after extracting the lanthanum oxide and cerium oxide, and extracting scandium compound from the solution extracting the zirconium compound from the solution.

Disclosed are a precursor for preparation of a lithium composite transition metal oxide, a method for preparing the same and a lithium composite transition metal oxide obtained from the same. More particularly, the transition metal precursor which has a composition represented by Formula 1 below and is prepared in an aqueous transition metal solution, mixed with a transition metal-containing salt, including an alkaline material, the method for preparing the same and the lithium composite transition metal oxide obtained from the same are disclosed.
Mn.sub.aM.sub.b(OH.sub.1-x).sub.2-yA.sub.y(1) wherein M is at least one selected form the group consisting of Ni, Ti, Co, Al, Cu, Fe, Mg, B, Cr, Zr, Zn and Period II transition metals; A is at least one selected form the group consisting of anions of PO.sub.4, BO.sub.3, CO.sub.3, F and NO.sub.3, and 0.5a1.0; 0b0.5; a+b=1; 0<x<1.0; and 0y0.02.

The present invention relates to a process for conversion of a hydrocarbon feed comprising saturated hydrocarbon compounds to olefin products comprising contacting a hydrocarbon feed stream with a catalyst in an oxidic form of the formula M1M2M3M4O comprising metals M1, M2, M3 and M4, wherein: M1 is selected from Si, Al, Zr, and mixtures thereof; M2 is selected from Pt, Cr, and mixtures thereof; M3 is selected from W, Mo, Re, and mixtures thereof; and M4 is selected from Sn, K, Y, Yb and mixtures thereof; wherein: mass fraction of M1 is in the range of 0.1 to 0.8; mass fraction of M2 is in the range of 0.001 to 0.2; mass fraction of M3 is in the range of 0.001 to 0.2; mass fraction of M4 is in the range of 0.0001 to 0.2; and mass fraction of oxygen is in the range of 0.1 to 0.8.

A positive-electrode active material contains a compound represented by the following composition formula (1):

Li.sub.xMe.sub.yO.sub.X.sub.(1) where Me denotes one or more elements selected from the group consisting of Mn, Ni, Co, Fe, Al, Sn, Cu, Nb, Mo, Bi, Ti, V, Cr, Y, Zr, Zn, Na, K, Ca, Mg, Pt, Au, Ag, Ru, Ta, W, La, Ce, Pr, Sm, Eu, Dy, and Er, X denotes two or more elements selected from the group consisting of F, Cl, Br, I, N, and S, and x, y, , and satisfy 0.75x2.25, 0.75y1.50, 1<3, and 0<2, respectively. A crystal structure of the compound belongs to a space group Fm-3m.

The present invention relates to a method for producing a hexafluoromanganate(IV), said method being characterized by comprising: inserting an anode and a cathode into a reaction solution that contains a compound containing manganese having an atomic valence of less than 4 and/or manganese having an atomic valence of more than 4 and hydrogen fluoride; and then applying an electric current having an electric current density of 100 to 1000 A/m.sup.2 between the anode and the cathode. According to the present invention, it becomes possible to produce a hexafluoromanganate(IV) in which the content ratio of manganese having an atomic valence of 4 is high and the contamination with oxygen is reduced and which has high purity. When a complex fluoride red phosphor is produced using the hexafluoromanganate(IV) as a raw material, the phosphor produced has high luminescence properties, particularly high internal quantum efficiency.

A process for water removal and/or recycling of sodium sulphate and/or sodium dithionate containing liquors derived from processing a cobalt resource derived from components of lithium ion batteries comprising steps of deriving from the cobalt resource a solution containing cobalt sulphate and cobalt dithionate, precipitation of cobalt as cobaltous carbonate or cobaltous hydroxide followed by removal thereof from the liquor, crystallization of sodium sulphate and sodium dithionate and removal of the resulting crystals, followed by heating of the crystals to anhydrous sodium sulphate, sulphur dioxide and water and then separating the anhydrous sodium sulphate.