Provided is a red mud-based composite calcium ferrite and a preparation method and use thereof. The preparation method of the red mud-based composite calcium ferrite includes the following steps: mixing red mud and a calcium source, and roasting an obtained mixture in an oxygen-containing atmosphere to obtain the red mud-based composite calcium ferrite; where the calcium source is selected from the group consisting of lime and calcium carbonate. In the present disclosure, the composite calcium ferrite is prepared using a solid waste red mud, with a greatly reduced cost of raw materials; on the other hand, compared with traditional calcium ferrite, the composite calcium ferrite mainly has phase structures of CaFe.sub.2O.sub.4, Ca.sub.2FeAlO.sub.5, and Ca.sub.2Fe.sub.2O.sub.5. Therefore, the composite calcium ferrite has a lower melting point, a higher lime dissolution efficiency, and better fluxing and dephosphorization effects during primary smelting and refining of molten steel, and has broad prospects for use in industry.

A sol of inorganic oxide particles is stably dispersed in a hydrophilic organic solvent containing a hydrocarbon such as a paraffinic hydrocarbon or a naphthenic hydrocarbon. The sol contains a dispersion medium containing an organic solvent containing a C.sub.6-18 paraffinic hydrocarbon, a C.sub.6-18 naphthenic hydrocarbon, or a mixture of these, a C.sub.4-8 alcohol having a carbon chain with a carbon-carbon bond in the molecule in an amount of 0.1 to 5% by mass in the entire dispersion medium, and inorganic oxide particles having an average particle diameter of 5 to 200 nm as measured by dynamic light scattering as a dispersoid, wherein the inorganic oxide particles contain a C.sub.1-3 alkyl group bonded to a silicon atom and a C.sub.4-18 alkyl group. The paraffinic hydrocarbon is a normal paraffinic hydrocarbon or an isoparaffinic hydrocarbon. The naphthenic hydrocarbon is a saturated aliphatic cyclic hydrocarbon substitutable with a C.sub.1-10 alkyl group.

Electrode materials for electrochemical cells and batteries and methods of producing such materials are disclosed herein. The electrode materials comprise an active lithium metal oxide material prepared by: (a) contacting the lithium metal oxide material with an aqueous acidic solution containing one or more metal cations; and (b) heating the so-contacted lithium metal oxide from step (a) to dryness at a temperature below 200° C. The metal cations in the aqueous acidic solution comprise one or more metal cations selected from the group consisting of an alkaline earth metal ion, a transition metal ion, and a main group metal ion.

The present invention relates to a detoxified powder composition comprising a zinc-bearing compound selected from the group consisting of zinc carbonate, zinc hydroxide, zinc oxide, zinc sulphate and mixtures thereof, and at least one detoxification agent containing at least one oxide based on a cation, selected from the group consisting of calcium, barium, magnesium, strontium and beryllium.

Supplemental lithium can be used to stabilize lithium ion batteries with lithium rich metal oxides as the positive electrode active material. Dramatic improvements in the specific capacity at long cycling have been obtained. The supplemental lithium can be provided with the negative electrode, or alternatively as a sacrificial material that is subsequently driven into the negative electrode active material. The supplemental lithium can be provided to the negative electrode active material prior to assembly of the battery using electrochemical deposition. The positive electrode active materials can comprise a layered-layered structure comprising manganese as well as nickel and/or cobalt.

Electrode materials for electrochemical cells and batteries and methods of producing such materials are disclosed herein. The electrode materials comprise an active lithium metal oxide material prepared by: (a) contacting the lithium metal oxide material with an aqueous acidic solution containing one or more metal cations; and (b) heating the so-contacted lithium metal oxide from step (a) to dryness at a temperature below 200° C. The metal cations in the aqueous acidic solution comprise one or more metal cations selected from the group consisting of an alkaline earth metal ion, a transition metal ion, and a main group metal ion.

A positive active material for a rechargeable lithium battery includes a nickel-based lithium transition metal oxide including a secondary particle in which a plurality of primary particles are agglomerated, wherein the secondary particle includes a core and a surface layer surrounding the core, and the surface layer includes a plurality of primary particles and a nano-sized cobalt-based lithium transition metal oxide absorbed in the surface layer, between the primary particles.

A positive electrode active material contains a lithium transition metal oxide in the form of a secondary particle in which primary particles are aggregated, wherein a zirconium-containing coating film is formed on the surface of the lithium transition metal oxide secondary particle and at the interface between the primary particles present inside the secondary particle. A method of making the positive electrode active material is also provided.

A photocatalyst for air purification, a photocatalyst film including the photocatalyst, and an air purification device including the photocatalyst. The photocatalyst for air purification includes: a first metal oxide particle having ultraviolet absorptivity, and fluorine bound to a surface of the first metal oxide particle; second metal oxide particles present on the surface of the first metal oxide particle. The use of the photocatalyst for air purification to remove or degrade volatile organic compounds (VOCs) and viruses.

This zirconia powder contains 2.5 to 3.5 mol % of yttria; has a specific surface area of 5 to 20 m.sup.2/g; and has crystal phases that include a monoclinic crystal phase percentage of 20 to 40% and a tetragonal crystal phase percentage of 60 to 80%. When the zirconia powder is molded under a mold pressure of 0.8 t/cm.sup.2 and then sintered under a condition of 2 hours at 1450° C. to obtain a sintered body, the sintered body has crystal phases that include a monoclinic crystal phase percentage of 1 to 3%, a tetragonal crystal phase percentage of 77 to 94%, and a cubic crystal phase percentage of 5 to 20%.