摘要:
A method of manufacturing a dispersion liquid for an electrode catalyst, the method comprising a step of supporting a precious metal on the surface of a carrier by an electrodeposition process using a raw material mixed solution in which a particulate carrier is dispersed in a solvent and a compound including the precious metal element is dissolved in the solvent, wherein the carrier has oxygen reduction capability and is free of precious metal elements.
摘要:
A method for producing an electrode catalyst, comprising a step of calcining a precursor of the electrode catalyst under conditions under which a second material defined below can change into a carbonaceous material, the precursor having been obtained by continuously hydrothermally reacting a mixture containing a first material defined below and the second material defined below in the presence of supercritical or subcritical water, wherein the first material is defined to be a metal compound composed of one or more metal elements selected from the group consisting of the elements of Group 4A and the elements of Group 5A group and one or more non-metal elements selected from the group consisting of hydrogen, nitrogen, chlorine, carbon, boron, sulfur, and oxygen, and the second material is defined to be a precursor of a carbonaceous material.
摘要:
An electrode catalyst, including: a metal compound which contains an oxygen atom and at least one metal element selected from a group consisting of Group 4 elements and Group 5 elements in the long-form periodic table, and a carbonaceous material which covers at least part of the metal compound; wherein an oxygen deficiency index, which is represented as an inverse number of a peak value of a first nearest neighbor element in a radial distribution function obtained by Fourier-transforming an EXAFS oscillation in EXAFS measurement of the metal element, is 0.125 to 0.170; and a crystallinity index, which is represented as a peak value of a second nearest neighbor element in the radial distribution function, is 4.5 to 8.0.
摘要:
A method for producing an electrode catalyst, comprising a step of calcining a precursor of the electrode catalyst under conditions under which a second material defined below can change into a carbonaceous material, the precursor having been obtained by hydrothermally reacting a mixture containing a first material defined below and the second material defined below in the presence of supercritical or subcritical water, or the precursor having been obtained by mixing a reaction product having been obtained by hydrothermally reacting a first material defined below in the presence of supercritical or subcritical water and the second material defined below, wherein the first material is defined to be a metal compound composed of one or more metal elements selected from the group consisting of the elements of Group 4A and the elements of Group 5A and one or more non-metal elements selected from the group consisting of hydrogen, nitrogen, chlorine, carbon, boron, sulfur, and oxygen, andthe second material is defined to be a precursor of a carbonaceous material.
摘要:
Disclosed are an electrode catalyst and a method for producing an electrode catalyst. The electrode catalyst is composed of: a metal compound comprising one or more metal elements selected from the group consisting of Groups 4A and 5A, and an oxygen atom; and a carbonaceous material covering at least part of the compound, wherein the electrode catalyst has a BET specific surface area of not less than 15 m2/g and not more than 500 m2/g and a carbon coverage of not less than 0.05 and not more than 0.5 as determined by the following equation (1): carbon coverage=carbon content (% by mass)/BET specific surface area (m2/g) (1). The method for producing an electrode catalyst comprises calcining a mixed material comprising a first material provided below and a second material provided below under conditions where the second material can be converted to a carbonaceous material: the first material that is a metal compound composed of one or more metal elements selected from the group consisting of Groups 4A and 5A, and one or more non-metal elements selected from the group consisting of a hydrogen atom, a nitrogen atom, a chlorine atom, a carbon atom, a boron atom and an oxygen atom; the second material that is a carbonaceous material precursor.
摘要:
A method for producing an α-alumina powder is described. The method for producing an α-alumina powder comprises a step of calcining an aluminum salt in the presence of a seed crystal at 600-890° C.
摘要:
A method for producing an α-alumina powder is provided. T method for producing an α-alumina powder comprising steps of: (1) pulverizing a metal compound having a full width at half maximum (Ho) of a main peak in XRD pattern to obtain a seed crystal having a full width at half maximum (H) of the main peak in XRD pattern in the presence of pulverizing agent, (2) mixing the obtained seed crystal with an aluminum salt, (3) calcining the mixture, and wherein a ratio of H/Ho is 1.06 or more.
摘要:
The present invention provides a fine α-alumina particle having a degree of α-transformation of not less than 95%, a BET specific surface area of not less than 10 m2/g, a degree of necking of not more than 30%, and a total content of Si, Fe, Cu, Na and Mg of not more than 500 ppm.
摘要:
The invention provides a process for producing a shaped body of aluminum titanate-based ceramic such as aluminum titanate or aluminum magnesium titanate having smaller shrinkage ratio relative to a shaped body of a starting material mixture, and having a smaller coefficient of thermal expansion. The invention is a process for producing an aluminum titanate-based ceramic, comprising firing a starting material mixture containing a titanium source material and an aluminum source material, wherein the BET specific surface area of the aluminum source material is 0.1 m2/g or more and 5 m2/g or less.
摘要:
The present invention provides a method of producing an α-alumina particle. The method of producing an α-alumina particle comprises steps of: (1) heating a mixture containing an amorphous alumina and a pyrolyzable salt at temperature of not less than the temperature at which the pyrolyzable salt is decomposed, and less than the temperature at which the amorphous alumina transforms to α-alumina; and (2) calcining the resultant under a partial pressure of water vapor of about 600 Pa or less.