Patent classifications
C04B35/6268
ZIRCONIA-BASED POROUS BODY
The purpose of the present invention is to provide a zirconia-based porous body which can be pulverized in a relatively short time and in which performance deterioration caused by pulverization is suppressed. The present invention pertains to a zirconia-based porous body in which the total pore volume is at least 1.0 ml/g, the pore volume of pores having a diameter of 20-100 nm (exclusive of 100) is at most 0.3 ml/g, and the pore volume of pores having a diameter of 100-1000 nm is at least 0.5 ml/g.
GARNET-MGO COMPOSITE THIN MEMBRANE AND METHOD OF MAKING
A sintered composite ceramic, including: a lithium-garnet major phase; and a grain growth inhibitor minor phase, such that the grain growth inhibitor minor phase has a metal oxide in a range of 0.1 wt. % to 10 wt. % based on the total weight of the sintered composite ceramic.
SILICON-CONTAINING OXIDE-COATED ALUMINUM NITRIDE PARTICLE AND METHOD OF MANUFACTURING THE SAME
A method of manufacturing a silicon-containing oxide-coated aluminum nitride particle; a method of manufacturing a heat dispersing resin composition containing the silicon-containing oxide-coated aluminum nitride particle; and the silicon-containing oxide-coated aluminum nitride particle. The method of manufacturing includes: a first step of covering the surface of the aluminum nitride particle with an organic silicone compound including a specific structure; and a second step of heating the aluminum nitride particle covered with the organic silicone compound at a temperature of 300° C. or more and less than 1000° C., wherein the content of carbon atoms in the silicon-containing oxide-coated aluminum nitride particle is less than 1000 ppm by mass.
METHOD FOR PREPARING ALUMINA-BASED SOLID SOLUTION CERAMIC POWDER BY USING ALUMINUM OXYGEN COMBUSTION SYNTHESIS WATER MIST PROCESS
Disclosed is a method for preparing an alumina-based solid solution ceramic powder by using an aluminum oxygen combustion synthesis water mist process, which comprises: drying raw materials and then mixing same until uniform to obtain a mixed material; loading the mixed material into a high-pressure reactor, igniting same in an oxygen-containing atmosphere, carrying out a high-temperature combustion synthesis reaction to form a high-temperature melt and then carrying out heat preservation for 1-60 s; and then opening a nozzle, ejecting the high-temperature melt through the nozzle and rapidly cooling same through a liquid phase, thus obtaining the alumina-based solid solution ceramic powder.
CUBIC BORON NITRIDE SINTERED MATERIAL
A cubic boron nitride sintered material comprises 30% by volume or more and 80% by volume or less of cubic boron nitride grains and 20% by volume or more and 70% by volume or less of a binder phase, the cubic boron nitride grains having a dislocation density of 3×10.sup.17/m.sup.2 or more and 1×10.sup.20/m.sup.2 or less.
CUBIC BORON NITRIDE SINTERED MATERIAL
The cubic boron nitride sintered material comprises 30% by volume or more and 80% by volume or less of cubic boron nitride grains and 20% by volume or more and 70% by volume or less of a binder phase, the cubic boron nitride grains having a dislocation density of 1×10.sup.15/m.sup.2 or more and 1×10.sup.17/m.sup.2 or less.
SILICON-CARBON-GRAPHENE COMPOSITE AND MANUFACTURING METHOD THEREOF, AND LITHIUM ION SECONDARY BATTERY USING THE SAME
The present disclosure provides a method for manufacturing a silicon-carbon-graphene composite comprising, preparing a suspension in which silicon, carbon source and graphene oxide are dispersed, subjecting the suspension to an aerosol process to form a silicon-carbon source-graphene oxide composite and heat-treating the silicon-carbon source-graphene oxide composite to form a silicon-carbon-graphene composite, and prevents direct contact of the electrolyte, so it can exhibit excellent cycling performance and stability.
COMPOSITE FORMED OF CUBIC BORON NITRIDE WITHOUT TI-BASED CERAMIDE AND METHOD OF MAKING THEREOF
A cubic boron nitride (cBN)-based composite including about 30-65 vol. % cBN, about 3-30 vol. % zirconium (Zr)-containing compounds, about 0-10 vol. % cobalt-tungsten-borides (Co.sub.xW.sub.yB.sub.z), about 2-30 vol. % aluminum oxide (Al.sub.2O.sub.3), about 0.5-10 vol. % tungsten borides, and less than or equal to about 5 vol. % aluminum nitride (AlN).
Z-TYPE HEXAFERRITE HAVING A NANOCRYSTALLINE STRUCTURE
In an aspect, a Co.sub.2Z ferrite has the formula: (Ba.sub.1−xSr.sub.x).sub.3Co.sub.2+yM.sub.yFe.sub.24−2y−zO.sub.41. M is at least one of Mo, Ir, or Ru. The variable x can be 0 to 0.8, or 0.1 to 0.8. The variable y can be 0 to 0.8, or 0.01 to 0.8. The variable z can be −2 to 2. The Co.sub.2Z ferrite can have an average grain size of 5 to 100 nanometers, or 30 to 80, or 10 to 40 nanometers as measured using at least one of transmission electron microscopy, field emission scanning electron microscopy, or x-ray diffraction.
Method for Producing Non-Oxide Ceramic Powders
The invention relates to a method for producing a non-oxide ceramic powder comprising a nitride, a carbide, a boride or at least one MAX phase with the general composition Mn+1AXn, where M=at least one element from the group of transition elements (Sc, Ti, V, Cr, Zr, Nb, Mo, Hf and Ta), A=at least one A group element from the group (Si, Al, Ga, Ge, As, Cd, In, Sn, Tl and Pb), X=carbon (C) and/or nitrogen (N) and/or boron (B), and n=1, 2 or 3. According to the invention, corresponding quantities of elementary starting materials or other precursors are mixed with at least one metal halide salt (NZ), compressed (pellet), and heated for synthesis with a metal halide salt (NZ). The compressed pellet is first enveloped with another metal halide salt, compressed again, arranged in a salt bath and heated therewith until the melting temperature of the salt is exceeded. Optionally, melted silicate can be added, which prevents the salt from evaporating at high temperatures. Advantageously, the method can be carried out in the presence of air.