Patent classifications
C01F17/32
METHOD OF PRODUCING METAL OXYHYDRIDE, METAL OXYHYDRIDE, AND METHOD OF SYNTHESIZING AMMONIA USING SAME
The invention provides a method of producing a metal oxyhydride, capable of synthesizing the metal oxyhydride under reaction conditions close to atmospheric pressure, and excellent in productivity and cost. The method of producing a metal oxyhydride of the present invention includes reacting an oxide with a metal hydride in a hydrogen atmosphere. A non-oxygen element constituting the oxide comprises only one kind of non-oxygen element. A pressure condition of the reaction is 0.1 to 0.9 MPa, and a temperature of the reaction is 500 to 1000° C.
FACILE CO2 SEQUESTRATION AND FUEL PRODUCTION FROM A HYDROCARBON
The present disclosure provide for methods of reforming a hydrocarbon such as methane. In an aspect, when the method is driven via renewable energy (e.g., use of solar energy, wind energy, or other renewable energy) and coupled with zero-energy input product gas separation, this enables the capture of pure CO.sub.2 (i.e., carbon sequestration) and carbon-neutral utilization of methane can be achieved. As a result, the present disclosure can provide for a method to reform methane with zero-energy input product gas separation.
FACILE CO2 SEQUESTRATION AND FUEL PRODUCTION FROM A HYDROCARBON
The present disclosure provide for methods of reforming a hydrocarbon such as methane. In an aspect, when the method is driven via renewable energy (e.g., use of solar energy, wind energy, or other renewable energy) and coupled with zero-energy input product gas separation, this enables the capture of pure CO.sub.2 (i.e., carbon sequestration) and carbon-neutral utilization of methane can be achieved. As a result, the present disclosure can provide for a method to reform methane with zero-energy input product gas separation.
Mixed oxide catalyst for the oxidative coupling of methane
A mixed oxide catalyst for the oxidative coupling of methane can include a catalyst with the formula A.sub.aB.sub.bC.sub.cD.sub.dO.sub.x, wherein: element A is selected from alkaline earth metals; elements B and C are selected from rare earth metals, and wherein elements B and C are different rare earth metals; the oxide of at least one of A, B, C, and D has basic properties; the oxide of at least one of A, B, C, and D has redox properties; and elements A, B, C, and D are selected to create a synergistic effect whereby the catalytic material provides a methane conversion of greater than or equal to 15% and a C.sub.2.sup.+ selectivity of greater than or equal to 70%. Systems and methods can include contacting the catalyst with methane and oxygen and purifying or collecting C.sub.2.sup.+ products.
Composite Oxide, Metal-Supported Material, and Ammonia Synthesis Catalyst
A composite oxide including a metal element represented by the composition of general formula:
A.sub.nX.sub.y,
represents an element selected from the group consisting of Sc, Y, and a trivalent lanthanoid; X represents an element selected from the group consisting of Ca, Sr, and Ba; n is 0<n<1; y is 0<y<1; and n+y=1. Also, a metal-supported material in which cobalt particles are supported on the composite oxide.
Composite Oxide, Metal-Supported Material, and Ammonia Synthesis Catalyst
A composite oxide including a metal element represented by the composition of general formula:
A.sub.nX.sub.y,
represents an element selected from the group consisting of Sc, Y, and a trivalent lanthanoid; X represents an element selected from the group consisting of Ca, Sr, and Ba; n is 0<n<1; y is 0<y<1; and n+y=1. Also, a metal-supported material in which cobalt particles are supported on the composite oxide.
THERMISTOR SINTERED BODY AND TEMPERATURE SENSOR ELEMENT
A thermistor sintered body stably provides a desired B constant even if a composition deviation of an additive element has occurred. The thermistor sintered body includes a Y.sub.2O.sub.3 phase and a Y(Cr, Mn)O.sub.3 phase, wherein a chemical composition of Cr, Mn, Ca, and Y excluding oxygen is Cr: 3 to 12 mol %, Mn: 5 to 15 mol %, Ca: 1 to 8 mol %, and Sr: 1 to 25 mol %, with the balance being unavoidable impurities and Y. In the thermistor sintered body, Ca and Sr may be dissolved in the Y(Cr, Mn)O.sub.3 phase.
Complex oxide, method for producing same, and exhaust gas purification catalyst
Provided are: a complex oxide that exhibits high redox ability even at low temperatures, has excellent heat resistance, and stably retains these characteristics even on repeated oxidation and reduction at high temperature; a method for producing the same; and an exhaust gas purification catalyst. The inventive complex oxide contains more than 0 but no more than 20 parts by mass of Si, calculated as SiO.sub.2, per total 100 parts by mass of rare earth metal elements including Ce, calculated as oxides; and has a characteristic such that when it is subjected to temperature-programmed reduction (TPR) measurement in a 10% hydrogen-90% argon atmosphere at from 50° C. to 900° C. with the temperature increasing at a rate of 10° C./min, followed by oxidation treatment at 500° C. for 0.5 hours, and then temperature-programmed reduction measurement is performed again, its calculated reduction rate at and below 400° C. is at least 1.5%.
Complex oxide, method for producing same, and exhaust gas purification catalyst
Provided are: a complex oxide that exhibits high redox ability even at low temperatures, has excellent heat resistance, and stably retains these characteristics even on repeated oxidation and reduction at high temperature; a method for producing the same; and an exhaust gas purification catalyst. The inventive complex oxide contains more than 0 but no more than 20 parts by mass of Si, calculated as SiO.sub.2, per total 100 parts by mass of rare earth metal elements including Ce, calculated as oxides; and has a characteristic such that when it is subjected to temperature-programmed reduction (TPR) measurement in a 10% hydrogen-90% argon atmosphere at from 50° C. to 900° C. with the temperature increasing at a rate of 10° C./min, followed by oxidation treatment at 500° C. for 0.5 hours, and then temperature-programmed reduction measurement is performed again, its calculated reduction rate at and below 400° C. is at least 1.5%.
POWDER FOR COATING AN ETCH CHAMBER
A powder of melted particles, more than 95% by number of the particles exhibiting a circularity of greater than or equal to 0.85. The powder including more than 99.8% of a rare earth metal oxide and/or of hafnium oxide and/or of an aluminum oxide, as percentage by mass based on the oxides. The powder has a median particle size D.sub.50 of less than 15 μm, a 90 percentile of the particle sizes, D.sub.90, of less than 30 μm, and a size dispersion index (D.sub.90−D.sub.10)/D.sub.10 of less than 2, and a relative density of greater than 90%. The D.sub.n percentiles of the powder are the particle sizes corresponding to the percentages, by number, of n%, on the cumulative distribution curve of the size of the particles in the powder and the particle sizes are classified by increasing order.