C01P2006/37

CARBONACEOUS MATERIAL AND METHOD FOR PRODUCING SAME, ELECTRODE ACTIVE MATERIAL FOR ELECTROCHEMICAL DEVICES, ELECTRODE FOR ELECTROCHEMICAL DEVICES, AND ELECTROCHEMICAL DEVICE

A carbonaceous material may have a high capacitance per volume as well as a high durability, and/or may have a BET specific surface area is 1,500 to 1,900 m.sup.2/g, an average pore size is 1.84 to 2.05 nm at a nitrogen relative pressure P/P.sub.0 of 0.93 in a nitrogen adsorption isotherm measured at 77.4 K, a ratio of pore volume having a pore size of 3 nm or smaller, determined by the BJH method, is 65 to 90% relative to total pore volume calculated based on a nitrogen adsorption amount at a relative pressure P/P.sub.0 of 0.93 in the nitrogen adsorption isotherm, and a ratio of pore volume having a pore size of 1 to 2 nm, determined by the MP method, is 10 to 20% relative to total pore volume calculated based on the nitrogen adsorption amount at a relative pressure P/P.sub.0 of 0.93 in the nitrogen adsorption isotherm.

THERMAL BARRIER COATING MATERIAL AND ARTICLE

A thermal barrier coating material contains a compound X that is a cation-deficient-type defective perovskite complex oxide. Unit cells of the compound X each include six oxygen atoms and has a structure in which two octahedrons sharing one oxygen atom are aligned. In the compound X, central axes of two octahedrons that belong to adjacent unit cells, respectively, and are adjacent to each other are inclined relative to each other. A plurality of sets of the two octahedrons that belong to the adjacent unit cells, respectively, and are adjacent to each other are arranged to form a periodic structure in which octahedrons having different inclinations are alternately arranged, and the compound X has a boundary surface at which a periodicity of the periodic structure changes, in a crystal structure thereof.

NICKEL-BASED ACTIVE MATERIAL PRECURSOR FOR LITHIUM SECONDARY BATTERY, PREPARING METHOD THEREOF, NICKEL-BASED ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY FORMED THEREOF, AND LITHIUM SECONDARY BATTERY COMPRISING POSITIVE ELECTRODE INCLUDING THE NICKEL-BASED ACTIVE MATERIAL
20210202941 · 2021-07-01 ·

A nickel (Ni)-based active material for a lithium secondary battery, a preparing method thereof, and a lithium secondary battery including a positive electrode including the same. The Ni-based active material includes a secondary particle including a plurality of particulate structures, wherein each of the particulate structures includes a porous core portion and a shell portion including primary particles radially arranged on the porous core portion, and lithium phosphate is in the porous core portion, between the plurality of primary particles, and on the surface of the secondary particle. The Ni-based active material includes a porous inner portion including the porous core portion; and an outer portion comprising the the shell portion, and the Ni-based active material includes the porous inner portion having closed pores and the outer portion, wherein the porous inner portion has a density less than that of the outer portion, and the Ni-based active material has a net density of 4.7 g/cc or less.

PHOSPHOR AND PRODUCTION METHOD THEREOF PHOSPHOR-INCLUDING MEMBER, AND LIGHT EMITTING DEVICE OR PROJECTOR

Provided is a particulate phosphor including a single crystal having a composition represented by a compositional formula (Y.sub.1-x-y-zLu.sub.xGd.sub.yCe.sub.z).sub.3+aAl.sub.5−aO.sub.12 (0≤x≤0.9994, 0≤y≤0.0669, 0.001≤z≤0.004, −0.016≤a≤0.315) and a particle diameter (D50) of not less than 20 μm. Also provided is a light-emitting device including a phosphor-including member that includes the phosphor and a sealing member including a transparent inorganic material sealing the phosphor or a binder including an inorganic material binding particles of the phosphor, and a light-emitting element that emits a blue light for exciting the phosphor.

Positive Electrode Active Material for Secondary Battery, Method of Preparing the Same, and Lithium Secondary Battery Including the Same

The present invention relates to a positive electrode active material for a secondary battery which includes a lithium composite transition metal oxide including nickel (Ni), cobalt (Co), and manganese (Mn), wherein the lithium composite transition metal oxide includes the nickel (Ni) in an amount of 65 mol % or more and the manganese (Mn) in an amount of 5 mol % or more based on a total amount of transition metals, and wherein the electrode positive active material is composed of a single particle, having a crystallite size of 180 nm or more.

In-situ passivation and insulation layer for a flexible thermal protection system (FTPS)

A lightweight flexible BNNT mat or fabric provides improved thermal stability and shielding capabilities under a hypersonic thermal flux. The BNNT mat reduces the stagnation temperature and maintains a low regression rate. An in-situ passivation layer may be formed on the BNNT mat or fabric under high thermal flux. The passivation layer minimizes or prevents penetration of the atmosphere (air or gas) as well as heat and radiation through the thickness of the BNNT material, and it effectively diffuses heat throughout the mat or fabric laterally and radially to minimize localized excessive heat. A BNNT mat according to the present disclosure may also efficiently transfer heat from the BNNT material via radiation due to the high thermal emissivity (0.92) of the BNNT material.

Modified Y-type molecular sieve, preparation thereof and catalyst comprising the same

A modified Y-type molecular sieve has a rare earth oxide content of about 4% to about 12% by weight, a phosphorus content of about 0% to about 10% by weight, a sodium oxide content of no more than about 1.0% by weight, a total pore volume of about 0.36 to 0.48 mL/g, a percentage of the pore volume of secondary pores to the total pore volume of about 20% to about 40%, a lattice constant of about 2.440 nm to about 2.455 nm, a percentage of the non-framework aluminum content to the total aluminum content of no more than about 10%, a lattice collapse temperature of not lower than about 1060 C., and a ratio of Brnsted acid to Lewis acid of no less than about 3.50. The preparation of the molecular sieve includes ion-exchange with rare earth, hydrothermal roasting, gas phase ultra-stabilization, acid treatment, and an optional phosphorus modification.

Magnesium modified Y-type molecular sieve, preparation thereof and catalyst comprising the same

A magnesium modified Y-type molecular sieve has a rare earth oxide content of about 4% to about 11% by weight, a magnesium oxide content of about 0.1% to about 4% by weight, a sodium oxide content of about 0.3% to about 0.8% by weight, a total pore volume of about 0.33 mL/g to about 0.39 mL/g, a percentage of the pore volume of secondary pores having a pore size of 2-100 nm to the total pore volume of the modified Y-type molecular sieve of about 10% to about 30%, a lattice constant of about 2.440 nm to about 2.455 nm, a percentage of non-framework aluminum content to the total aluminum content of the modified Y-type molecular sieve of no more than about 20%, and a lattice collapse temperature of not lower than about 1045 C.

SINTERED METAL CARBIDE AND HEAT-RESISTANT MEMBER FOR SILICON CARBIDE SEMICONDUCTOR MANUFACTURING DEVICE COMPRISING SAME
20210024357 · 2021-01-28 ·

Out of sintered metal carbides having an extremely high melting point, there is provided a sintered metal carbide which can be produced without having to perform sintering under high pressure such as hot pressing or HIP, having a high relative density and excellent mechanical strength. A sintered metal carbide of at least one metal selected from the group consisting of elements of Groups 4 and 5 of the periodic table, wherein the sintered metal carbide contains Si element of 0.1 wtppm or more and 10,000 wtppm or less.

METAL COMPOSITE HYDROXIDE AND METHOD FOR PRODUCING SAME, POSITIVE ELECTRODE ACTIVE MATERIAL FOR NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY AND METHOD FOR PRODUCING SAME, AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY

A metal composite hydroxide represented by a general formula (1): Ni.sub.1xyCo.sub.xMn.sub.yM.sub.z(OH).sub.2+ (where 0.02x0.3, 0.02y0.3, 0z0.05, and 0.50.5 are satisfied and M is at least one element selected from the group consisting of Mg, Ca, Al, Si, Fe, Cr, V, Mo, W, Nb, Ti, and Zr), in which the metal composite hydroxide contains a first particle having a core portion inside the particle and a shell portion formed around the core portion and [(D90D10)/MV] is less than 0.80.