A catalyst containing, as an essential component, molybdenum; bismuth; and cobalt, in which, with respect to a peak intensity at 2θ=25.3°±0.2° in an X-ray diffraction pattern obtained by using CuKα rays as an X-ray source, a changing rate (Q1) per 1000 hours of reaction time represented by the following formulae (1) to (4) is 16 or less.

Q1={(U1/F1−1)×100}/T×1000  (1)

F1=(peak intensity of catalyst before oxidation reaction at 2θ=25.3°±)0.2°/(peak intensity of catalyst before oxidation reaction at 2θ=26.5°±0.2°)×100  (2)

U1=(peak intensity of catalyst after oxidation reaction at 2θ=25.3°±0.2°)/(peak intensity of catalyst after oxidation reaction at 2θ=26.5°±0.2°)×100  (3)

T=time (hr) during which oxidation reaction is carried out  (4)

The solid electrolyte material of the present disclosure includes Li, Ca, Y, Sm, X, and O, wherein X is at least one selected from the group consisting of F, Cl, Br, and I.

A solid electrolyte material is made of Li, Ca, Y, Gd, X, O, and H, where X is at least one selected from the group consisting of F, Cl, Br, and I; and the molar ratio of O to the sum of Y and Gd is greater than 0 and less than 0.82.

A method of forming an active material for a positive electrode of a lithium-ion battery includes quenching a powder of the active material in water. The active material may include layered lithium rich nickel manganese oxide.

A method of forming graphite includes carbonizing an upgraded coal, to form a carbonized upgraded coal. The method also includes graphitizing the carbonized upgraded coal, to form the graphite.

A method for crystallization of β-ammonium tetramolybdate includes: performing a stepwise pH-adjusting treatment of an ammonium molybdate solution via zoning to obtain the β-ammonium tetramolybdate. When feeding the ammonium molybdate solution into a reaction system from a first zone and then into second to sixth zones successively, pH.sup.1 of a resultant solution in the first zone is 7.0-6.0; pH.sup.2 of a resultant solution in the second zone is less than 6 and greater than or equal to 4; pH.sup.3 of a resultant solution in the third zone is less than 4 and greater than or equal to 2.5; pH.sup.4 of a crystallized slurry in the fourth zone is less than 2.5 and greater than or equal to 1; pH.sup.5 of a crystallized slurry in the fifth zone is 2.5-4.0; and pH.sup.6 of a crystallized slurry in the sixth zone is less than 2.5 and greater than or equal to 2.0.

Nano-structures of Aluminum Nitride and a method of producing nano-structures of Aluminum Nitride from nut shells comprising milling agricultural nuts into a fine nut powder, milling nanocrystalline Al.sub.2O.sub.3 into a powder, mixing, pressing the fine nut powder and the powder of nanocrystalline Al.sub.2O.sub.3, heating the pellet, maintaining the temperature of the pellet at about 1400° C., cooling the pellet, eliminating the residual carbon, and forming nano-structures of AlN. An Aluminum Nitride (AlN) product made from the steps of preparing powders of agricultural nuts using ball milling, preparing powders of nanocrystalline Al.sub.2O.sub.3, mixing the powders of agricultural nuts and the powders of nanocrystalline Al.sub.2O.sub.3 forming a homogenous sample powder of agricultural nuts and Al.sub.2O.sub.3, pressurizing, pyrolizing the disk, and reacting the disk and the nitrogen atmosphere and forming AlN.

The invention relates to a method for preparing a hierarchical porous zeolite membrane and an application thereof, comprising the following steps: a mesoporous structure-directing agent is added to limit the growth of zeolite crystals, and self-assembled in the crystallization process to generate a mesoporous structure. Based on a seed crystal induced secondary nucleation mechanism, this method can realize one-step hydrothermal synthesis of hierarchical porous zeolite membrane with the advantages of mild and controllable synthesis conditions, simple process, good repeatability, reduced energy consumption and cost savings. The hierarchical porous zeolite membrane prepared by the method has good cut-off performance, and the cut-off molecular weight is adjustable between 200 to 500,000 Da.

A sulfide solid electrolyte, which is able to adjust the morphology unavailable traditionally, or is readily adjusted so as to have a desired morphology, the sulfide solid electrolyte having a volume-based average particle diameter measured by laser diffraction particle size distribution measurement of 3 μm or more and a specific surface area measured by the BET method of 20 m.sup.2/g or more; and a method of treating a sulfide solid electrolyte including the sulfide solid electrolyte being subjected to at least one mechanical treatment selected from disintegration and granulation.

An ultraviolet light emitting phosphor for mercury-free lamps is a phosphor composed of a phosphate containing at least two metal elements selected from the group consisting of group 13 elements and lanthanoid series elements, and is excited to emit ultraviolet by irradiation with vacuum ultraviolet rays or an electron beam.