METHOD FOR PRODUCING REGENERATED POSITIVE ELECTRODE MATERIAL PRECURSOR AND REGENERATED POSITIVE ELECTRODE MATERIAL, AND METHOD FOR USING REGENERATED POSITIVE ELECTRODE MATERIAL
Provided is a method for producing a regenerated positive electrode material precursor from a lithium-ion secondary cell that is an object to be processed, the method comprising performing a heat treatment step, a crushing step, a classification and sorting step, a magnetic separation step, an acid leaching step, an iron removal step, an ion exchange step, an alkali treatment step, and a washing step on the lithium-ion secondary cell that is the object to be processed.
C22B 3/06 - Extraction of metal compounds from ores or concentrates by wet processes by leaching in inorganic acid solutions
C22B 3/24 - Treatment or purification of solutions, e.g. obtained by leaching by physical processes, e.g. by filtration, by magnetic means by adsorption on solid substances, e.g. by extraction with solid resins
C22B 3/44 - Treatment or purification of solutions, e.g. obtained by leaching by chemical processes
H01M 10/54 - Reclaiming serviceable parts of waste accumulators
NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (Japan)
Inventor
Yamada Tomoya
Michiaki Yoshiyuki
Kumon Shoichi
Sato Kimitaka
Yamaguchi Wataru
Hosokawa Akihide
Takagi Kenta
Abstract
5050 in the volume-based particle size distribution by the laser diffraction scattering method of, for example, 0.5-5.0 μm (inclusive). As the alkaline earth metal element Ae, for example, one or more elements selected from Mg and Ca can be employed. The coating layer can be formed by performing co-sputtering of Al and Ae using, for example, a sputtering film forming device.
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 1/05 - Metallic powder characterised by the size or surface area of the particles
B22F 9/08 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
C22C 21/06 - Alloys based on aluminium with magnesium as the next major constituent
C22C 23/02 - Alloys based on magnesium with aluminium as the next major constituent
H01F 1/06 - Magnets or magnetic bodies characterised by the magnetic materials thereforSelection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys in the form of particles, e.g. powder
H01F 1/059 - Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and Va elements, e.g. Sm2Fe17N2
01 - Chemical and biological materials for industrial, scientific and agricultural use
09 - Scientific and electric apparatus and instruments
Goods & Services
Battery material, namely silver oxide, silver powder, silver oxide powder, zinc powder, nickel powder, metal powder, ferrite powder,and compositions thereof. Laboratory apparatus and instruments; photographic machines and apparatus; cinematographic machines and apparatus; optical machines and apparatus; measuring or testing machines and instruments; power distribution or control machines and apparatus; rotary converters; phase modifiers; solar batteries; batteries and cells; electric or magnetic meters and testers; electric wires and cables; telecommunication machines and apparatus; personal digital assistants; electronic machines, apparatus and their parts; semi-conductor elements; electronic circuits, not including those recorded with computer programs; magnetic cores; resistance wires; electrodes, other than welding electrodes or medical electrodes; circuit board for power modules.
6.
METHOD FOR TREATING LITHIUM-ION-CONTAINING AQUEOUS SOLUTION
[Problem] To efficiently obtain, from a lithium-ion-containing aqueous solution containing anions, a lithium-ion-containing aqueous solution which has a reduced content of anions other than hydroxide ions. [Solution] This method for treating lithium-ion-containing aqueous solution uses an electrodialyzer equipped with a raw-solution tank separated from adjacent tanks on both sides by a cation-exchange membrane and an anion-exchange membrane respectively, a first adjoining tank which adjoins the raw-solution tank with the cation-exchange membrane interposed therebetween, and a second adjoining tank which adjoins the raw-solution tank with the anion-exchange membrane interposed therebetween, wherein: a lithium-ion-containing aqueous solution which contains lithium ions, cations other than lithium ions, and anions is put in the raw-solution tank; water or an aqueous solution is put in the first adjoining tank and the second adjoining tank; a voltage is applied between a cathode inside the first adjoining tank and an anode inside the second adjoining tank; and, while the pH of the liquid inside the raw-solution tank is kept at 10.5 or higher, lithium ions inside the raw-solution tank are caused to move into the first adjoining tank through the cation-exchange membrane.
C02F 1/469 - Treatment of water, waste water, or sewage by electrochemical methods by electrochemical separation, e.g. by electro-osmosis, electrodialysis, electrophoresis
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 1/05 - Metallic powder characterised by the size or surface area of the particles
B22F 9/04 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from solid material, e.g. by crushing, grinding or milling
Provided are a method of producing single crystal AlN, single crystal AlN, and a single crystal AlN production apparatus with which single crystal AlN can be cheaply and continuously produced. The method of producing single crystal AlN includes a melt formation step of heating and melting an alloy to form a melt of the alloy and a deposition step of cooling a portion of the melt and providing a temperature gradient in the melt while causing deposition of single crystal AlN. In the deposition step, a nitrogen-containing gas is brought into contact with a high-temperature portion of the melt and a single crystal AlN seed crystal or a substrate for crystal growth is held in a low-temperature portion of the melt so as to continue to take nitrogen into the melt in the high-temperature portion while causing deposition of single crystal AlN.
C30B 35/00 - Apparatus not otherwise provided for, specially adapted for the growth, production or after-treatment of single crystals or of a homogeneous polycrystalline material with defined structure
9.
ALL-SOLID-STATE BATTERY CELL, SOLID ELECTROLYTE POWDER, METHOD FOR PRODUCING SOLID ELECTROLYTE POWDER, AND METHOD FOR PRODUCING COVERED BODY
Provided are: a solid electrolyte powder which contains 0.7% by mass to 5% by mass of Li, 8% by mass to 60% by mass of Nb, and 1.0% by mass to 30% by mass of P with respect to the solid electrolyte powder, with the content of the non-oxygen remainder, which is the remainder excluding oxygen (O), being 10% by mass or less with respect to the solid electrolyte powder, and which has a crystallite diameter of 100 nm or less; and related art thereof.
H01M 10/0585 - Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
C01B 25/45 - Phosphates containing plural metal, or metal and ammonium
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
H01M 4/13 - Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulatorsProcesses of manufacture thereof
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
44SiO (lithium orthosilicate) having good Li ion conductivity and a method for producing the aqueous solution, and a method for producing a positive electrode active material for a lithium secondary battery having a coating layer containing lithium orthosilicate using the aqueous solution. [Solution] An aqueous solution containing lithium and silicon that contains 0.1-3.0 mass% of lithium and 0.1-3.0 mass% of silicon and has a molar ratio Li/Si of lithium and silicon of 3.70-5.20 and an absorbance at a wavelength of 660 nm of 0.10 or less.
An Sm—Fe—N-based magnetic powder includes particles containing Sm, Fe, and N as main components. The powder has a composition wherein a molar ratio of Sm to Fe (Sm/Fe) is 0.09 or more and 0.25 or less, a molar ratio of N to Fe (N/Fe) is 0.06 or more and 0.30 or less, and a Ca content in the powder is 0.002 mass % or less. When a cumulative 10% particle diameter is represented by D10, a cumulative 50% particle diameter is represented by D50, and a cumulative 90% particle diameter is represented by D90 in a volume-based particle size distribution according to a laser diffraction/scattering method, D50 is 2.0 to 11.0 μm, and D10, D50, and D90 satisfy a relationship of the following formula: (D90−D10)/D50<1.10. The Sm—Fe—N-based magnetic powder is advantageous in improving coercive force, containing few impurities, and improving the performance and manufacturability of a bonded magnet.
H01F 1/059 - Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and Va elements, e.g. Sm2Fe17N2
B22F 9/08 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
12.
AQUEOUS SOLUTION CONTAINING NIOBIUM POLYACID IONS, LITHIUM IONS, AND PHOSPHATE IONS, PRODUCTION METHOD THEREFOR, AND METHOD FOR PRODUCING ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY
[Problem] To provide an aqueous solution and a production method therefor, the aqueous solution containing niobium polyacid ions, lithium ions, and phosphate ions, suppressing an increase in the specific surface area of a coated positive electrode active material when the surfaces of positive electrode active material particles of a lithium-ion secondary battery are coated with a coating layer containing niobium, lithium, and phosphorus, which are solid electrolytes, and having excellent storage stability. [Solution] This aqueous solution contains niobium polyacid ions, lithium ions, and phosphate ions, wherein: the ratio P/(Nb+Li+P) of the molar number of the phosphorus to the sum of the molar numbers of the niobium, lithium, and phosphorus contained in the aqueous solution is at least 0.04 and less than 0.5; the molar ratio Li/Nb of the lithium and the niobium is greater than 0.6 and at most 2.0; and 0.01-10 mass% of hydrogen peroxide is preferably further contained.
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
13.
ARRANGEMENT STRUCTURE OF SOLID ELECTROLYTE IN ALL-SOLID-STATE CELL, AND BATTERY
36x3+x3+x, where x is 2.0-5.0, and the second solid electrolyte includes sulfide or oxide as a main component. The first solid electrolyte is interposed between the electroconductive material on the high potential side and the second solid electrolyte, and a contact part is provided between the electroconductive material on the high potential side and the first solid electrolyte, and a contact part is provided between the first solid electrolyte and the second solid electrolyte.
C01F 7/54 - Double compounds containing both aluminium and alkali metals or alkaline earth metals
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
H01M 10/0585 - Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
09 - Scientific and electric apparatus and instruments
11 - Environmental control apparatus
Goods & Services
(1) Semi-conductors; semiconductor wafers; semiconductor chips; semiconductor power elements; LED (light emitting diode) chips; Sensors
(2) Furnaces; Industrial furnaces; incinerator, furnaces, other than for laboratory use; Heat treatment furnaces; fittings, shaped, for furnaces; heat treatment equipment for treating metal parts, namely, furnaces and gas generators; Gas burner, heating furnace, non-experimental furnace, incinerator, sintering furnace, blunting furnace, hot air furnace, mobile metal heating furnace, electric furnace.
[Problem] To directly bond a metal layer in the shape of a thin line to a surface of a ceramic substrate. [Solution] A method for producing a ceramic/metal bonded object which comprises: causing laser beams to strike on a surface of a ceramic substrate while sweeping the laser beams; simultaneously therewith, feeding a solid metallic material toward a region (hereinafter, referred to as "irradiated area") in the ceramic-substrate surface, the region being irradiated with the laser beams, so that the metallic material being supplied is also in the state of being irradiated with the laser beams, thereby melting the metallic material while heating the ceramic-substrate surface located in the irradiated area; and causing the molten metallic material to adhere to the ceramic-substrate surface and then solidifying the metallic material.
C23C 24/10 - Coating starting from inorganic powder by application of heat or pressure and heat with intermediate formation of a liquid phase in the layer
Provided are: a method for producing AlN single crystals, the method capable of producing AIN single crystals at low cost and in a continuous manner; AlN single crystals; and a device for producing AlN single crystals. The method for produing AlN single crystals includes: a melt formation step for heating and melting an alloy containing Al to form a melt of the alloy; and a deposition step for depositing AlN single crystals while providing a temperature gradient to the melt by cooling a part of the melt. In the deposition step, by bringing a nitrogen-containing gas into contact with a high-temperature section of the melt and holding AlN seed crystals or a crystal growth substrate for single crystals in a low-temperature section in the melt, with nitrogen being taken into the melt in the high-temperature section, AlN single crystals are deposited on the AlN seed crystals or on the substrate in the low-temperature section, and thereby AlN single crystals continuously grow.
[Problem] To provide an Sm-Fe-N-based magnetic powder that is configured from fine-sized particles advantageous for improving coercivity, that contains minimal impurities, and that is useful for improving the productivity and performance of bond magnets. [Solution] A powder composed of particles having Sm, Fe, and N as main components, the powder having a composition in which the molar ratio Sm/Fe of Sm to Fe is 0.09-0.25, the molar ratio N/Fe of N to Fe is 0.06-0.30, and the Ca content of the powder is 0.002 mass% or less, and, in a volume-based grain size distribution measured by laser diffraction/scattering, D50 being 2.0-11.0 μm, and D10, D50, and D90 satisfying the following relationship (1), where D10 is the cumulative 10% particle diameter, D50 is the cumulative 50% particle diameter, and D90 is the cumulative 90% particle diameter. Relationship (1): (D90−D10)/D50≤1.10
B22F 9/08 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from liquid material by casting, e.g. through sieves or in water, by atomising or spraying
C22C 1/04 - Making non-ferrous alloys by powder metallurgy
H01F 1/059 - Alloys characterised by their composition containing rare earth metals and magnetic transition metals, e.g. SmCo5 and Va elements, e.g. Sm2Fe17N2
H01F 1/06 - Magnets or magnetic bodies characterised by the magnetic materials thereforSelection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials metals or alloys in the form of particles, e.g. powder
H01F 41/02 - Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformersApparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils or magnets
Provided is an ultraviolet light receiving device having photosensitivity effective to target wavelengths in the ultraviolet region. A Schottky junction ultraviolet light receiving device has the photosensitivity peak wavelength in an ultraviolet region of 230 nm or more and 320 nm or less, and exhibits a rejection ratio of 105 or more, the rejection ratio being the ratio of the responsivity Rp to the peak photosensitivity wavelength to the average of the responsivity Rv to a visible region of 400 nm or more and 680 nm or less (Rp/Rv).
H01L 31/108 - Devices sensitive to infrared, visible or ultraviolet radiation characterised by only one potential barrier or surface barrier the potential barrier being of the Schottky type
H01L 31/0304 - Inorganic materials including, apart from doping materials or other impurities, only AIIIBV compounds
A raw material solution containing trivalent iron ions, or trivalent iron ions and ions of a metal element that partially substitutes Fe sites, and an alkaline aqueous solution for neutralizing the raw material solution are added to a reaction system to adjust the pH of the reaction system from 1.0 to 3.0 or lower. Hydroxycarboxylic acid is added to the obtained reaction solution and the pH of the reaction system is then neutralized from 7.0 to 10.0 or lower. The obtained precipitate of a substituent metal element-containing iron oxyhydroxide is coated with silicon oxide, followed by heating so as to form particles of ε-iron oxide in which Fe sites are partially substituted by other metal elements, and then, a slurry containing the particles is classified. The iron-based oxide magnetic powder has a particle shape close to a perfect sphere and is suitable for use in a magnetic recording medium.
H01F 1/11 - Magnets or magnetic bodies characterised by the magnetic materials thereforSelection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials non-metallic substances, e.g. ferrites in the form of particles
Provided is a metal negative electrode used for a secondary battery. The metal negative electrode includes an active material portion, a current collector, and a non-electronically conductive reaction space divider. The active material portion forms metal during charging and forms an oxidation product of the metal during discharging. The metal is used as a negative-electrode active material. The current collector is electrically connected to the active material portion. The non-electronically conductive reaction space divider is integrally formed with or connected to the current collector and/or the active material portion. The reaction space divider has a plurality of electrolyte holder portions configured to hold a liquid electrolyte.
01 - Chemical and biological materials for industrial, scientific and agricultural use
Goods & Services
Metallic oxides; metal oxide powders for industrial purposes; silver oxides; oxides; magnetic fluid for industrial purposes; chemical compositions for metal plating; catalysts for oxidation processes
24.
ZINC NEGATIVE ELECTRODE AND MANUFACTURING METHOD THEREFOR, AND SECONDARY CELL COMPRISING SAID ZINC NEGATIVE ELECTRODE AND MANUFACTURING METHOD THEREFOR
Provided are: a zinc negative electrode having exceptional repeating resistance, and excellent charge/discharge cycling characteristics even at a high charge/discharge rate; a manufacturing method therefor; a secondary cell using the zinc negative electrode; and a manufacturing method therefor. A zinc negative electrode used in a secondary cell, wherein the zinc negative electrode comprises: an active material part in which zinc is generated during charging, and oxidized zinc is generated during discharging, the zinc being used as a negative electrode active material; a collector that is electrically connected to the active material part; and a non-electron-conductive reaction space restriction part that is integrally formed with or connected to the collector and/or the active material part. The reaction space restriction part has a plurality of electrolyte-holding parts comprising a space that can hold a liquid electrolyte.
Provided is an ultraviolet-light-receiving element that has light-receiving sensitivity effective for a target wavelength in the ultraviolet region. A Schottky-junction-type ultraviolet-light-receiving element, wherein: there is a light-receiving sensitivity peak wavelength in the ultraviolet ray region of 230-320 nm (inclusive); and the rejection rate, which is the ratio (Rp/Rv) of a responsivity Rp at the light-receiving sensitivity peak wavelength to an average value Rv of the responsivity of the visible region of 400-680 nm (inclusive), is 105 or greater.
H01L 31/108 - Devices sensitive to infrared, visible or ultraviolet radiation characterised by only one potential barrier or surface barrier the potential barrier being of the Schottky type
C22C 27/04 - Alloys based on tungsten or molybdenum
B32B 5/16 - Layered products characterised by the non-homogeneity or physical structure of a layer characterised by features of a layer formed of particles, e.g. chips, chopped fibres, powder
B32B 15/16 - Layered products essentially comprising metal next to a particulate layer
B32B 15/20 - Layered products essentially comprising metal comprising aluminium or copper
H01L 23/373 - Cooling facilitated by selection of materials for the device
H01L 21/48 - Manufacture or treatment of parts, e.g. containers, prior to assembly of the devices, using processes not provided for in a single one of the groups or
H01L 23/00 - Details of semiconductor or other solid state devices
27.
IRON-BASED OXIDE MAGNETIC POWDER AND METHOD FOR MANUFACTURING SAME
[Problem] To provide an iron-based oxide magnetic powder which has a sufficiently reduced amount of fine particles and coarse particles, has a powder shape that is close to a perfect sphere, and is suitable for magnetic recording medium applications. [Solution] A source solution containing ferric ions or ferric ions and metal element ions which substitute a portion of the Fe site and an alkali aqueous solution for neutralizing the source solution are added to a reaction system so that the reaction system has a pH of 1.0 to 3.0; a hydroxy carboxylic acid is added to the obtained reaction solution and thereafter the pH of the reaction system is neutralized to 7.0 to 10.0; a deposit of the obtained substituted metal element-containing iron oxyhydroxide is coated with a silicon oxide and heated to form particles of ε-iron oxide in which a portion of the Fe site is substituted with another metal element; and the slurry containing the particles is classified.
G11B 5/706 - Record carriers characterised by the selection of the material comprising one or more layers of magnetisable particles homogeneously mixed with a bonding agent on a base layer characterised by the composition of the magnetic material
G11B 5/714 - Record carriers characterised by the selection of the material comprising one or more layers of magnetisable particles homogeneously mixed with a bonding agent on a base layer characterised by the dimension of the magnetic particles
G11B 5/84 - Processes or apparatus specially adapted for manufacturing record carriers
H01F 1/11 - Magnets or magnetic bodies characterised by the magnetic materials thereforSelection of materials for their magnetic properties of inorganic materials characterised by their coercivity of hard-magnetic materials non-metallic substances, e.g. ferrites in the form of particles
28.
METAL NEGATIVE ELECTRODE, METHOD FOR FABRICATING THE SAME AND SECONDARY BATTERY INCLUDING THE SAME
Provided are: a metal negative electrode having exceptional repeating resistance, and excellent charge/discharge cycling characteristics even at a high charge/discharge rate; a method for manufacturing same; and a secondary cell in which the metal negative electrode is used. A metal negative electrode used in a secondary cell, wherein the metal negative electrode comprises: an active material part in which a metal is produced during charging and an oxidation product of the metal is produced during discharging, the metal being used as a negative electrode active material; a collector electrically connected to the active material part; and a non-electron-conductive reaction space restriction part integrally formed with or connected to the collector and/or the active material part. The reaction space restriction part has a plurality of electrolyte-holding parts capable of holding a liquid electrolyte.
H01M 12/08 - Hybrid cellsManufacture thereof composed of a half-cell of a fuel-cell type and a half-cell of the secondary-cell type
H01M 50/474 - Spacing elements inside cells other than separators, membranes or diaphragmsManufacturing processes thereof characterised by their position inside the cells
H01M 50/477 - Spacing elements inside cells other than separators, membranes or diaphragmsManufacturing processes thereof characterised by their shape
29.
METAL NEGATIVE ELECTRODE, METHOD FOR MANUFACTURING METAL NEGATIVE ELECTRODE, AND SECONDARY CELL COMPRISING METAL NEGATIVE ELECTRODE
Provided are: a metal negative electrode having exceptional repeating resistance, and excellent charge/discharge cycling characteristics even at a high charge/discharge rate; a method for manufacturing same; and a secondary cell in which the metal negative electrode is used. A metal negative electrode used in a secondary cell, wherein the metal negative electrode comprises: an active material part in which a metal is produced during charging and an oxidation product of the metal is produced during discharging, the metal being used as a negative electrode active material; a collector electrically connected to the active material part; and a non-electron-conductive reaction space restriction part integrally formed with or connected to the collector and/or the active material part. The reaction space restriction part has a plurality of electrolyte-holding parts capable of holding a liquid electrolyte.
2Deff is the effective refractive index of two-dimensional photonic crystals, and a is the period of the two-dimensional photonic crystals) satisfies 2≤m≤4, and the radius of each void is R, R/a satisfies 0.30≤R/a≤0.40.
H01L 33/10 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a light reflecting structure, e.g. semiconductor Bragg reflector
H01L 33/00 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof
H01L 33/06 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a quantum effect structure or superlattice, e.g. tunnel junction within the light emitting region, e.g. quantum confinement structure or tunnel barrier
H01L 33/32 - Materials of the light emitting region containing only elements of group III and group V of the periodic system containing nitrogen
1Dneff2Deff2Deff2Deff being the effective refractive index of the two-dimensional photonic crystal, and a being the period of the two-dimensional photonic crystal) satisfies 2≤m≤4, and in that, when the radius of the holes is R, 0.30≤R/a≤0.40.
H01L 33/10 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a light reflecting structure, e.g. semiconductor Bragg reflector
H01L 33/32 - Materials of the light emitting region containing only elements of group III and group V of the periodic system containing nitrogen
Provided are a cladding and a method for producing the same with which it is possible to prevent cracking and peeling from occurring even in the case of punching out (application of shear that is greater than thermal shock) due to press-machining. An Mo-Cu layer 10 on which a metal film 10a is formed on at least one surface thereof, the metal layer 10a comprising one metal selected from the group consisting of Co, Ti, Pd, Pt, and Ni, is disposed on each surface of a Cu-graphite layer 12 obtained by sintering a graphite powder having a Cu film formed on the surface thereof, the Mo-Cu layer 10 being disposed such that the metal film 10a contacts the surface of the Cu-graphite layer 12, and then the Cu-graphite layer 12 and the Mo-Cu layer 10 are heated while pressure is applied therebetween.
01 - Chemical and biological materials for industrial, scientific and agricultural use
09 - Scientific and electric apparatus and instruments
Goods & Services
Magnetic metal oxides for industrial purposes Soft magnetic powders for industrial purposes; soft magnetic powders for industrial purpose for use in the manufacturing of electric wave-absorbing materials, sensors, and injectors
34.
Silver nanowires, method for producing same, and ink
Silver nanowires having a thin and long shape that exhibit excellent dispersibility in an aqueous solvent having an alcohol added thereto are provided by silver nanowires having an average diameter of 50 nm or less and an average length of 10 μm or more, covered with a copolymer of a maleimide-based monomer and vinylpyrrolidone. The silver nanowires can be produced by a method for producing silver nanowires, containing reductively depositing silver in a wire form in an alcohol solvent having dissolved therein a silver compound, the deposition being performed in the solvent having dissolved therein a copolymer of a maleimide-based monomer and vinylpyrrolidone.
H01B 1/02 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of metals or alloys
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 9/24 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
H01B 1/22 - Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
C09D 11/037 - Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
C09D 11/106 - Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
C08K 7/24 - Expanded, porous or hollow particles inorganic
C08K 9/04 - Ingredients treated with organic substances
01 - Chemical and biological materials for industrial, scientific and agricultural use
06 - Common metals and ores; objects made of metal
09 - Scientific and electric apparatus and instruments
Goods & Services
(1) Electrically conductive paste for soldering electronic components; industrial chemicals, namely carrier particles for use with electrostatic image development toner; electrically conductive paste mixed with metal powder for printing the conductive pattern of electronic circuits and electrodes.
(2) Electronic chips for the manufacture of integrated circuits; gallium arsenide semiconductor wafer; LED (light emitting diode) chips; Laser diodes; Light-emitting diodes (LED); Semiconductors; electronic semiconductors; infrared sensors, biochip sensors, pressure sensors, proximity sensors, sensors for determining temperature; Silicon wafers; Semiconductor wafers; electronic tags for goods; LED's (light emitting diodes), electrical conductors for transformers, for fuel cells, for integrated circuits.
36.
Method for producing negative electrode active material for lithium ion secondary battery
A method for producing a negative electrode active material for a lithium ion secondary battery, comprising a step of charging either silicon and copper (II) oxide or silicon and copper metal in a pulverization device, pulverizing either the silicon and copper (II) oxide or silicon and copper metal, and simultaneously mixing either silicon and copper (II) oxide or silicon and copper metal thus pulverized. A negative electrode active material for a lithium ion secondary battery is produced by the method.
H01M 4/82 - Multi-step processes for manufacturing carriers for lead-acid accumulators
H01M 4/38 - Selection of substances as active materials, active masses, active liquids of elements or alloys
C04B 35/626 - Preparing or treating the powders individually or as batches
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodesLithium-ion batteries
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
C04B 35/58 - Shaped ceramic products characterised by their compositionCeramic compositionsProcessing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxides based on borides, nitrides or silicides
x) measured by an X-ray diffractometry of 50 nm or less, and having elemental ratios, expressed by molar ratios, Cu/(Si+Cu+O) and O/(Si+Cu+O) of from 0.02 to 0.30, wherein the negative electrode active material contains an intermetallic compound of silicon and copper.
H01M 4/38 - Selection of substances as active materials, active masses, active liquids of elements or alloys
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodesLithium-ion batteries
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/02 - Electrodes composed of, or comprising, active material
38.
Method for producing silver nanowires, silver nanowires, and ink using same
A method for producing silver nanowires, containing reduction-precipitating silver in the form of wire in an alcohol solvent having dissolved therein a silver compound, the deposition being performed in the alcohol solvent having dissolved therein a chloride, a bromide, an alkali metal hydroxide, an aluminum salt, and an organic protective agent, the molar ratio Al/OH of the total Al amount of the aluminum salt dissolved in the solvent and the total hydroxide ion amount of the alkali metal hydroxide dissolved therein being from 0.01 to 0.40, the molar ratio OH/Ag of the total hydroxide ion amount of the alkali metal hydroxide dissolved in the solvent and the total Ag amount of the silver compound dissolved therein being from 0.005 to 0.50.
H01B 1/02 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of metals or alloys
B22F 1/02 - Special treatment of metallic powder, e.g. to facilitate working, to improve properties; Metallic powders per se, e.g. mixtures of particles of different composition comprising coating of the powder
B22F 9/24 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
H01B 1/22 - Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
39.
Active material composite powder, lithium battery, and method for manufacturing the same
H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
Provided is a silver nanowire having a long, thin shape that demonstrates excellent dispersibility in an aqueous medium to which alcohol has been added, the silver nanowire being coated with a copolymer of a maleimide monomer and vinylpyrrolidone and having an average diameter of 50 nm or less and an average length of 10 μm or less. A method for manufacturing a silver nanowire in which silver has been reduced and precipitated into a wire shape in an alcohol solvent in which a silver compound has been dissolved, wherein the silver nanowire is manufactured using a technique that promotes the precipitation with the copolymer of a maleimide monomer and vinylpyrrolidone having been dissolved in the solvent.
B22F 1/02 - Special treatment of metallic powder, e.g. to facilitate working, to improve properties; Metallic powders per se, e.g. mixtures of particles of different composition comprising coating of the powder
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 9/24 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
3, wherein 0 £ X £ 0.5. An average proportion of a total atom number of Al, Ti and P in a total atom number of Al, Ti, M and P within an etching depth of 1 nm from the outermost surface determined by analysis in a depth direction with XPS is 50% or more. The transition metal M is, for example, at least one kind of Co, Ni and Mn.
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/1391 - Processes of manufacture of electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
C01B 25/45 - Phosphates containing plural metal, or metal and ammonium
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodesLithium-ion batteries
H01M 4/02 - Electrodes composed of, or comprising, active material
H01M 4/58 - Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFySelection of substances as active materials, active masses, active liquids of polyanionic structures, e.g. phosphates, silicates or borates
42.
Negative electrode active material for lithium ion secondary battery, method for producing the same, negative electrode, and battery
In the case where a silicon substance having a high theoretical capacity as a negative electrode active material for a lithium ion secondary battery is used as a negative electrode active material, such a negative electrode active material is provided that has a high initial battery capacity and suffers less deterioration in performance even when many cycles of charge and discharge are repeated. A lithium ion secondary battery using the negative electrode active material is provided. Silicon and copper (II) oxide, or silicon, metallic copper and water are pulverized and simultaneously mixed in a pulverization device, thereby providing a negative electrode active material that has good cycle characteristics and a large battery capacity.
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/38 - Selection of substances as active materials, active masses, active liquids of elements or alloys
C04B 35/626 - Preparing or treating the powders individually or as batches
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodesLithium-ion batteries
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
C04B 35/58 - Shaped ceramic products characterised by their compositionCeramic compositionsProcessing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxides based on borides, nitrides or silicides
H01M 4/02 - Electrodes composed of, or comprising, active material
A method for producing silver nanowires, wherein silver is precipitated in the form of wires by reduction in an alcohol solvent into which a silver compound is dissolved. The precipitation is carried out in an alcohol solvent into which a chloride, a bromide, an alkali metal hydroxide, an aluminum salt and an organic protection agent, which is a copolymer having a polymer composition of vinyl pyrrolidone and a diallyldimethylammonium salt monomer, are dissolved. The molar ratio of the total amount of Al in the aluminum slat to be dissolved in the solvent to the total amount of hydroxide ions in the alkali metal hydroxide to be dissolved in the solvent, namely Al/OH is set to 0.01-0.40. The molar ratio of the amount of hydroxide ions in the alkali metal hydroxide to be dissolved in the solvent to the total amount of Ag in the silver compound to be dissolved in the solvent, namely OH/Ag is set to 0.005-0.50. Consequently, thin and long silver nanowires, which have an average diameter of 50 nm or less and an average length of 10 μm or more and are suitable for the production of a transparent conductor, are stably produced by this method for producing silver nanowires.
B22F 9/24 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 1/02 - Special treatment of metallic powder, e.g. to facilitate working, to improve properties; Metallic powders per se, e.g. mixtures of particles of different composition comprising coating of the powder
B22F 9/00 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor
H01B 1/00 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors
H01B 1/22 - Conductive material dispersed in non-conductive organic material the conductive material comprising metals or alloys
H01B 5/00 - Non-insulated conductors or conductive bodies characterised by their form
H01B 13/00 - Apparatus or processes specially adapted for manufacturing conductors or cables
44.
Radioactive cesium decontaminator and method of producing the same, and method of removing the radioactive cesium
50 is less than 6. The decontaminator is made by adding a ferrocyanide aqueous solution and an aqueous solution containing at least one transition metal into a suspension liquid containing a precursor formed by magnetic particles coated with organic monomer or polymer while applying a strong shear force.
B01J 20/02 - Solid sorbent compositions or filter aid compositionsSorbents for chromatographyProcesses for preparing, regenerating or reactivating thereof comprising inorganic material
B01J 20/28 - Solid sorbent compositions or filter aid compositionsSorbents for chromatographyProcesses for preparing, regenerating or reactivating thereof characterised by their form or physical properties
2 on a surface of the film, and carbon nanotubes are exposed on a wall surface of the grooves. After forming an ITO film containing carbon nanotubes on a substrate, grooves are formed on a surface of the ITO film, and the end portions of the carbon nanotubes exposed to the wall surface of the grooves are designated as an emitter.
H01J 9/02 - Manufacture of electrodes or electrode systems
H01J 31/12 - Image or pattern display tubes, i.e. having electrical input and optical outputFlying-spot tubes for scanning purposes with luminescent screen
H01J 63/02 - Details, e.g. electrode, gas filling, shape of vessel
Provided is a silver nanowire production method which also exhibits a yield improving effect for protective agents other than PVP. When precipitating silver nanowires in an alcohol solvent in which a silver compound, a halogen compound and an organic protective agent are dissolved, the silver precipitation reaction is advanced in a state in which aluminum nitrate is also dissolved in the solvent. Relative to the total amount of the silver compound, the total amount of aluminum nitrate dissolved in the solvent is 0.01-0.50, expressed as the molar ratio Al/Ag, and the organic protective agent comprises, for example, alkylated PVP and/or a PVP/PVA graft copolymer.
B22F 9/24 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 1/02 - Special treatment of metallic powder, e.g. to facilitate working, to improve properties; Metallic powders per se, e.g. mixtures of particles of different composition comprising coating of the powder
47.
Catalyst, method for producing catalyst, and method for producing hydrogen-containing gas using catalyst, and hydrogen generating device, fuel cell system, and silicon-supported CeZr-based oxide
B01J 23/63 - Platinum group metals with rare earths or actinides
B01J 23/76 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups
H01M 8/12 - Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
C01B 3/40 - Production of hydrogen or of gaseous mixtures containing hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts characterised by the catalyst
H01M 8/06 - Combination of fuel cells with means for production of reactants or for treatment of residues
H01M 8/0612 - Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
C01B 3/32 - Production of hydrogen or of gaseous mixtures containing hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
B01J 23/00 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group
B01J 23/10 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group of rare earths
B01J 35/00 - Catalysts, in general, characterised by their form or physical properties
B01J 8/08 - Chemical or physical processes in general, conducted in the presence of fluids and solid particlesApparatus for such processes with moving particles
B01J 21/06 - Silicon, titanium, zirconium or hafniumOxides or hydroxides thereof
B01J 23/46 - Ruthenium, rhodium, osmium or iridium
H01M 8/124 - Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte characterised by the process of manufacturing or by the material of the electrolyte
48.
ACTIVE MATERIAL COMPOSITE POWDER, LITHIUM BATTERY, METHOD FOR PRODUCING ACTIVE MATERIAL COMPOSITE POWDER, AND METHOD FOR MANUFACTURING LITHIUM BATTERY
Provided are: an active material composite powder which is capable of reducing resistance; and a method for producing the active material composite powder. This active material composite powder contains an active material and lithium niobate adhered to the surface of the active material, and has a BET specific surface area (S [m2/g]) satisfying 0.93 < S < 1.44. This method for producing an active material composite powder comprises: a spray drying step wherein a solution containing lithium and a peroxo complex of niobium is sprayed onto an active material and dried thereon in parallel; and a heat treatment step wherein a heat treatment is carried out after the spray drying step. The temperature of the heat treatment is more than 123°C but less than 350°C.
There is provided an aggregate of radioactive material removing particles in which two or more radioactive material removing particles having magnetic particles and a radioactive material adsorption component are assembled, wherein a pore volume in the aggregate is 0.5 mL/g or more and 5.0 mL/g or less, and the pore volume means a cumulative value obtained by a mercury press-in method.
B01J 20/28 - Solid sorbent compositions or filter aid compositionsSorbents for chromatographyProcesses for preparing, regenerating or reactivating thereof characterised by their form or physical properties
[Problem] To provide a lithium-ion secondary-battery positive-electrode active material with drastically reduced transition-metal content near the outermost surfaces thereof. [Solution] A solid-electrolyte-coated positive-electrode active-material powder comprising particles having solid-electrolyte coating layers that can be represented by Li1+XAlXTi2−X(PO4)3, with 0 ≤ X ≤ 0.5, on the surfaces of particles of a lithium-ion secondary-battery positive-electrode active material comprising a compound oxide of lithium and one or more transition metals (M). An XPS depth profile shows that up to a depth of 1 nm from the outermost surfaces of the abovementioned particles, the total number of atoms of aluminum, titanium, and phosphorus is, on average, at least 50% of the total number of atoms of aluminum, titanium, the transition metal(s) (M), and phosphorus. The transition metal(s) (M) could be, for example, one or more of cobalt, nickel, and manganese.
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
51.
NEGATIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM ION SECONDARY BATTERIES, METHOD FOR PRODUCING SAME, NEGATIVE ELECTRODE, AND BATTERY
[Problem] To obtain a negative electrode active material which is composed of a silicon-based substance having a high theoretical capacity in terms of a negative electrode active material for lithium ion secondary batteries, and which has a high initial battery capacity and is suppressed in deterioration of the performance even after a plurality of charge/discharge cycles if used as a negative electrode active material for a lithium ion secondary battery. To provide a lithium ion secondary battery which uses this negative electrode active material. [Solution] A negative electrode active material having good cycle characteristics and a high battery capacity is able to be obtained by pulverizing silicon and copper (II) oxide, or alternatively silicon, copper metal and water, using a pulverization means and mixing these materials at the same time.
Provided is a method for producing a decontaminating agent particle, which enables the easy and high-productivity production of a decontaminating agent particle that can decontaminate a radioactive substance with high efficiency, has high environmental resistance, is suitable for the treatment of a large amount of the radioactive substance, and can be used in a radioactive substance decontamination system or the like. Provided is a method for producing a radioactive cesium decontaminating agent, which comprises: a step of suspending a magnetic particle in a solvent and coating the magnetic particle with a monomer or polymer of an organic substance to form a precursor; a step of adding an aqueous ferrocyanide solution and an aqueous solution containing at least one transition metal to a suspension containing the coated precursor while applying strong shear force to the suspension to produce a radioactive cesium decontaminating agent; and a step of removing water from a slurry containing the radioactive cesium decontaminating agent.
B01J 20/02 - Solid sorbent compositions or filter aid compositionsSorbents for chromatographyProcesses for preparing, regenerating or reactivating thereof comprising inorganic material
B01J 20/28 - Solid sorbent compositions or filter aid compositionsSorbents for chromatographyProcesses for preparing, regenerating or reactivating thereof characterised by their form or physical properties
B01J 20/30 - Processes for preparing, regenerating or reactivating
[Problem] Provided are a field electron emission film that can operate with a small electric power and has high uniformity of brightness in a light emission surface, a field electron emission element and a light emitting element using the field electron emission film, and a method for producing the same. [Solution] Provided is a field electron emission film that contains 60 to 99.9 mass% of tin-doped indium oxide and 0.1 to 20 mass% of carbon nanotubes, wherein grooves having a width in a range of 0.1 to 50 μm each and having a total length of 2 mm or more per 1 mm2 are formed on a surface of the film, and the carbon nanotubes are exposed on walls of the grooves. After an ITO film containing carbon nanotubes is formed on a substrate, grooves are formed on a surface of the ITO film, and ends of carbon nanotubes that are exposed on walls of the grooves are used as emitters.
H01J 9/02 - Manufacture of electrodes or electrode systems
H01J 31/12 - Image or pattern display tubes, i.e. having electrical input and optical outputFlying-spot tubes for scanning purposes with luminescent screen
H01J 63/06 - Lamps with luminescent screen excited by the ray or stream
54.
CATALYST, METHOD FOR PRODUCING CATALYST, AND METHOD FOR PRODUCING HYDROGEN-CONTAINING GAS USING CATALYST, AND HYDROGEN GENERATING DEVICE, FUEL CELL SYSTEM, AND SILICON-SUPPORTED CeZr-BASED OXIDE
The purpose of the present invention is to provide a catalyst, etc. having a low reaction start temperature at which a self-heating function appears, and whereby carbon accumulation is suppressed even when reaction is repeated. This catalyst comprises a CeZr-based oxide, silicon, and a catalytically active metal, and is characterized in that the CeZr-based oxide satisfies the formula CexZryO2 (x + y = 1), and the silicon satisfies the mole ratios 0.02 ≤ Si/Zr and 0.01 < Si/(Ce + Zr + Si) < 0.2. This catalyst is capable of lowering the initial reduction temperature for causing oxygen vacancies, and, according to the catalytically active metal, enables reductive activation even at approximately 20°C, at which there is no need for heating. In repeated hydrogen generation reactions, since deposition of generated carbon on the catalyst surface can also be suppressed, and catalytic activity can be prevented from decreasing, the performance of the catalyst can be maintained for a long time.
B01J 23/76 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups
B01J 23/63 - Platinum group metals with rare earths or actinides
C01B 3/40 - Production of hydrogen or of gaseous mixtures containing hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts characterised by the catalyst
H01M 8/06 - Combination of fuel cells with means for production of reactants or for treatment of residues
H01M 8/12 - Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
55.
Lithium—transition metal oxide powder and method of producing the same, positive electrode active material for lithium ion battery, and lithium ion secondary battery
There is provided a lithium-transition metal oxide powder with a coating layer containing lithium niobate formed on a part or the whole part of a surface of a lithium-transition metal oxide particle and having a low powder compact resistance, and a positive electrode active material for a lithium ion battery containing the lithium-transition metal oxide powder. Specifically, there is provided the lithium-transition metal oxide powder composed of a lithium-transition metal oxide particle with a part or the whole part of a surface coated with a coating layer containing lithium niobate, wherein a carbon-content is 0.03 mass % or less.
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/131 - Electrodes based on mixed oxides or hydroxides, or on mixtures of oxides or hydroxides, e.g. LiCoOx
H01M 10/0525 - Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodesLithium-ion batteries
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
37 - Construction and mining; installation and repair services
Goods & Services
Waste crushing machines; waste compacting machines; washing machines for industrial use; high pressure washers; shredders [machines] for industrial use. Installation, maintenance and repair of contaminated soil purifying apparatus; installation, maintenance and repair of industrial furnaces; installation, maintenance and repair of air pollution control apparatus; installation, maintenance and repair of waste treatment apparatus; installation, maintenance and repair of effluent treatment apparatus; installation, maintenance and repair of sludge treatment apparatus; installation, maintenance and repair of sewage treatment apparatus; repair information.
Foil (Silver -) [leaf]; Powders (Silvering -); Foil (Metal -) for use in the manufacture of paints; Multilayer foils of aluminium alloys for use in the manufacture of paints; Paste (Silver -); Silver emulsions [pigments]; Printing ink.
A method wherein a metal film composed of Cu, In and Ga is formed and then the metal film is selenized is known as a method for obtaining a film-like crystal of a chalcogen compound. This method, however, involves problems of film uniformity and productivity. Although a film-like crystal of a chalcogen compound with high uniformity can be obtained by a low-cost method for obtaining nanoparticles containing Cu, In, Ga and Se, the resistivity of the film-like crystal of a chalcogen compound is high since a large amount of carbon is contained in the chalcogen compound and thus the film-like crystal of the chalcogen compound does not have characteristics sufficient for applications such as solar cells. Specifically disclosed is a chalcogen compound powder which contains Cu, In, Se and optionally Ga, has an average particle diameter (D50) of less than 0.5 μm, and has a carbon content in the powder of 0.2% or less. The chalcogen compound powder is obtained by heating a metal hydroxide powder having an average primary particle diameter of 0.3 μm or less and one or more substances selected from among selenium and selenium compounds to a temperature not less than 220˚C in a reducing gas.
A method wherein a metal film composed of Cu, In and Ga is formed and then the metal film is selenized is known as a method for obtaining a film-like crystal of a chalcogen compound. This method, however, involves problems of film uniformity and productivity. Although a film-like crystal of a chalcogen compound with high uniformity can be obtained by a low-cost method for obtaining nanoparticles containing Cu, In, Ga and Se, the resistivity of the film-like crystal of a chalcogen compound is high and thus the film-like crystal of the chalcogen compound does not have characteristics sufficient for applications such as solar cells. The disclosed low-carbon chalcogen compound powder containing Cu, In, Ga and Se, and having an average particle diameter (DSEM) of 80nm or less is obtained by generating a mixed solvent formed by mixing selenium or a selenium compound, a solvent with a boiling point of 250°C or less, and at least one of a mixture of copper salt and indium salt, a complex hydroxide of copper and indium, and a complex oxide of copper and indium, and heating the mixed solvent at a temperature of 220°C-500°C. By means of a paste of the chalcogen compound powder, a low-resistance thin film is obtained containing Cu, In, Ga and Se.
[Problem] To obtain a solder powder having an average particle diameter of 0.05 µm or more but less than 3 µm. [Solution] A solder powder having an average particle diameter of, for example, 0.05 µm or more but less than 3 µm is obtained by using a process for solder powder production which comprises a step in which a solid or liquid metal, a nonaqueous solvent, and balls for pulverization which have a diameter of 0.05-5 mm are introduced into a vessel to obtain a mixture, a step in which the mixture is heated to 150ºC or higher and stirred, a step in which the balls for pulverization are separated from the stirred mixture to obtain a mixture of a solder powder and the nonaqueous solvent, and a step in which the solder powder/nonaqueous-solvent mixture is subjected to solid/liquid separation to obtain the solder powder.
B22F 9/06 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from liquid material
There is provided a high-purity carbon nanotube, which can be produced with simple purification by causing graphite to be hardly contained in crude soot obtained immediately after being synthesized by arc-discharge, and a method for producing the same. Soot containing carbon nanotubes produced by arc-discharge using an anode which contains amorphous carbon as a main component is heated at a temperature of not lower than 350° C. to be burned and oxidized, immersed in an acid, heated at a temperature, which is not lower than the heating temperature in the previous burning and oxidation and which is not lower than 500° C., to be burned and oxidized, and immersed in an acid again.
H01B 1/04 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of carbon-silicon compounds, carbon, or silicon
B82Y 30/00 - Nanotechnology for materials or surface science, e.g. nanocomposites
B82Y 40/00 - Manufacture or treatment of nanostructures
63.
LITHIUM-TRANSITION METAL OXIDE POWDER, METHOD FOR PRODUCING SAME, POSITIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM ION BATTERY, AND LITHIUM ION SECONDARY BATTERY
Provided are: a lithium-transition metal oxide powder, which has low powder compact resistance, and wherein a coating layer that contains lithium niobate is formed on a part or the entire of the surface of each lithium-transition metal oxide particle; and a positive electrode active material for a lithium ion battery, which contains the lithium-transition metal oxide powder. Specifically provided is a lithium-transition metal oxide powder that is composed of lithium-transition metal oxide particles each of which has a surface that is partially or entirely covered with a coating layer that contains lithium niobate. The lithium-transition metal oxide powder has a carbon content of not more than 0.03% by mass.
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
64.
METHOD FOR PRODUCING SUBSTRATE FOR GROUP III NITRIDE SEMICONDUCTOR ELEMENT FABRICATION, METHOD FOR PRODUCING GROUP III NITRIDE SEMICONDUCTOR FREE-STANDING SUBSTRATE OR GROUP III NITRIDE SEMICONDUCTOR ELEMENT, AND GROUP III NITRIDE GROWTH SUBSTRATE
Provided is a method for producing a substrate for group III nitride semiconductor element fabrication with an improved area ratio of chromium nitride microcrystals with a triangular pyramid shape in a chromium nitride layer surface. That is, there is provided a method for producing a substrate for group III nitride semiconductor element fabrication comprising a depositing step of forming a chromium layer on a base substrate for growth, a nitriding step of nitriding the chromium layer under prescribed conditions to form a chromium nitride layer, and a crystalline layer growth step of epitaxially growing at least one layer of a group III nitride semiconductor layer on the chromium nitride layer, characterized in that the chromium layer is deposited by a sputtering method such that the deposition rate is in the range of 7 to 65 Å/sec in the sputtering particle range and the thickness is in the range of 50 to 300 Å, the chromium nitride layer is formed in a MOCVD growth furnace with a furnace pressure of 6.666-66.66 kPa and a temperature of 1,000°C or more in a gas atmosphere containing ammonia gas, the gas component other than the ammonia gas in the gas atmosphere is a carrier gas comprising a nitrogen gas and a hydrogen gas, and the content ratio of the nitrogen gas in the carrier gas is in the range of 60 to 100 volume%.
C30B 25/18 - Epitaxial-layer growth characterised by the substrate
H01L 33/32 - Materials of the light emitting region containing only elements of group III and group V of the periodic system containing nitrogen
65.
Group III nitride semiconductor growth substrate, group III nitride semiconductor epitaxial substrate, group III nitride semiconductor element and group III nitride semiconductor free-standing substrate, and method of producing the same
1-xN having a high Al composition, the growth temperature of which is high; a Group III nitride semiconductor growth substrate used for producing these, and a method for efficiently producing those. The present invention provides a Group III nitride semiconductor growth substrate comprising a crystal growth substrate including a surface portion composed of a Group III nitride semiconductor which contains at least Al, and a scandium nitride film formed on the surface portion are provided.
1-xN, the growth temperature of which is high and which has a high Al composition, as well as a III-nitride semiconductor growth substrate for fabricating these and a method for efficiently fabricating these. The invention is characterized by being equipped with: a crystal growth substrate, at least the surface portion of which substrate includes a III-nitride semiconductor containing Al; and a single metallic layer formed on the surface portion, the single metallic layer being made from Zr or Hf.
H01L 29/20 - Semiconductor bodies characterised by the materials of which they are formed including, apart from doping materials or other impurities, only AIIIBV compounds
67.
METHOD FOR PRODUCING LOW-MELTING-POINT METAL NANOPARTICLES
Provided is a method for producing low-melting-point metal nanoparticles, which can produce low-melting-point metal nanoparticles without using a high-vacuum container and which can produce alloy nanoparticles having a stable metal composition ratio. Specifically, provided is a method for producing low-melting-point metal nanoparticles, which involves: a step for obtaining a mixture by placing a solid or liquid low-melting-point metal, a non-water-based solvent, and pulverization balls having a diameter of 0.015mm to 5mm in a container; a step for stirring and heating the aforementioned mixture between the temperatures of -5°C to +20°C of the melting point of the aforementioned low-melting-point metal; a step for separating the aforementioned pulverization balls from the stirred mixture, and for obtaining a mixture of low-melting-point metal nanoparticles and the non-water-based solvent; and a step for performing solid-liquid separation on the mixture of the low-melting-point nanoparticles and the non-water-based solvent, and for obtaining low-melting-point nanoparticles.
B22F 9/06 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from liquid material
B22F 9/04 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from solid material, e.g. by crushing, grinding or milling
A process for producing a solder powder is provided by which it is possible to efficiently obtain a solder powder having an average particle diameter of 0.05 µm or larger but less than 3 µm in a stable yield. The process for producing a solder powder comprises: a step in which a solid or liquid metal, a nonaqueous solvent, and balls for pulverization that have a diameter of 0.05-5 mm are introduced into a vessel to obtain a mixture; a step in which the mixture is heated to a temperature between (melting point of the metal)-5ºC and (melting point of the metal)+20ºC and stirred; a step in which the balls for pulverization are separated from the stirred mixture to obtain a mixture of a solder powder and the nonaqueous solvent; and a step in which the mixture of a solder powder and the nonaqueous solvent is subjected to solid-liquid separation to obtain the solder powder.
B22F 9/06 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from liquid material
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 9/04 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using physical processes starting from solid material, e.g. by crushing, grinding or milling
B23K 35/40 - Making wire or rods for soldering or welding
B23K 35/26 - Selection of soldering or welding materials proper with the principal constituent melting at less than 400°C
A method wherein a metal film composed of Cu, In and Ga is formed and then the metal film is selenized is known as a method for obtaining a film-like crystal of a chalcogen compound. This method, however, involves a problem of film uniformity, a problem of productivity and the like. Although a film-like crystal of a chalcogen compound with high uniformity can be obtained by a low-cost method for obtaining nanoparticles containing Cu, In, Ga and Se, the resistivity of the film-like crystal of a chalcogen compound is high since a large amount of carbon is contained in the chalcogen compound and thus the film-like crystal of the chalcogen compound does not have characteristics sufficient for applications such as solar cells. Specifically disclosed is a chalcogen compound powder which contains Cu, In, Se and optionally Ga, has an average particle diameter (D50) of less than 0.5 μm, and has a carbon content in the powder of 0.2% or less. The chalcogen compound powder is obtained by heating a metal hydroxide powder having an average primary particle diameter of 0.3 μm or less and one or more substances selected from among selenium, selenium compounds, sulfur and sulfur compounds, to a temperature not less than 220˚C in a reducing gas.
Provided are high-purity carbon nanotubes which can be produced through simple purification by conducting synthesis by arc discharge so that substantially no graphite is contained in the crude soot obtained immediately after the synthesis. Also provided is a process for producing the carbon nanotubes. Soot containing carbon nanotubes which was produced by arc discharge using an anode comprising amorphous carbon as a main component is burned and oxidized by heating the soot in the air at a temperature of 350ºC or higher, thereafter treated by immersion in an acid, subsequently burned and oxidized by heating the soot in the air at a temperature which is not lower than the heating temperature used in the preceding combustion/oxidation and is 500ºC or higher, and then treated by immersion in an acid again.
Disclosed is a method for metal recovery using plants. The aforementioned metal recovery method involves bringing protonemata from moss plants belonging to the family Funariaceae into contact with a metal-containing solution in which is dissolved metal having an ionization tendency less than that of silver.
C22B 3/24 - Treatment or purification of solutions, e.g. obtained by leaching by physical processes, e.g. by filtration, by magnetic means by adsorption on solid substances, e.g. by extraction with solid resins
C02F 3/32 - Biological treatment of water, waste water, or sewage characterised by the animals or plants used, e.g. algae
C22B 7/00 - Working-up raw materials other than ores, e.g. scrap, to produce non-ferrous metals or compounds thereof
A01G 1/00 - Horticulture; Cultivation of vegetables (labels or name-plates G09F 3/00, G09F 7/00)
72.
SUBSTRATE FOR GROWING GROUP-III NITRIDE SEMICONDUCTORS, EPITAXIAL SUBSTRATE FOR GROUP-III NITRIDE SEMICONDUCTORS, GROUP-III NITRIDE SEMICONDUCTOR ELEMENT, STAND-ALONE SUBSTRATE FOR GROUP-III NITRIDE SEMICONDUCTORS, AND METHODS FOR MANUFACTURING THE PRECEDING
Provided are an epitaxial substrate for group-III nitride semiconductors, a group-III nitride semiconductor element, and a stand-alone substrate for group-III nitride semiconductors, which produce good crystallinity not only for materials having growth temperatures at or below 1050°C, such as AlGaN, GaN, and GaInN, but also for high-aluminum AlxGa1-xN compositions having high growth temperatures. Also provided are a stand-alone substrate for group-III nitride semiconductors, for fabricating the above, and a method for efficient fabrication thereof. These are characterized by being provided with a crystal growth substrate, at least the surface region of which comprises an aluminum-containing group-III nitride semiconductor, and a scandium nitride film formed on top of said surface region.
H01L 21/205 - Deposition of semiconductor materials on a substrate, e.g. epitaxial growth using reduction or decomposition of a gaseous compound yielding a solid condensate, i.e. chemical deposition
H01L 33/02 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies
73.
III-NITRIDE SEMICONDUCTOR GROWTH SUBSTRATE, III-NITRIDE SEMICONDUCTOR EPITAXIAL SUBSTRATE, III-NITRIDE SEMICONDUCTOR ELEMENT, III-NITRIDE SEMICONDUCTOR FREESTANDING SUBSTRATE, AND METHOD FOR FABRICATING THESE
Disclosed are a III-nitride semiconductor epitaxial substrate, a III-nitride semiconductor element, and a III-nitride semiconductor freestanding substrate, which have good crystallinity, not only with AlGaN, GaN, or GaInN, the growth temperature of which is at or below 1050°C, but also with AlxGa1-xN, the growth temperature of which is high and which has a high Al composition, a III-nitride semiconductor growth substrate for fabricating these, and a method to efficiently fabricate these, which is characterized by being equipped with a crystal growth substrate, at least the surface portion of which is made from a III-nitride semiconductor containing Al, and a single metallic layer that is made from Zr or Hf and is formed on the aforementioned surface portion.
H01L 21/205 - Deposition of semiconductor materials on a substrate, e.g. epitaxial growth using reduction or decomposition of a gaseous compound yielding a solid condensate, i.e. chemical deposition
74.
WATER PURIFICATION METHOD AND PURIFICATION APPARATUS
A method of water purification that is capable of efficiently reducing the contents of organic matter and nitrogen in various treatment object waters, such as wastewater and polluted water, and that is advantageous from the viewpoint of cost. There are provided a method of water purification, and water purification apparatus, characterized in that treatment object waters are brought into contact with plant materials, such as wood splinters, so as to attain purification thereof. The above method and apparatus are based upon noting of, for example, the availability of organic matter dissolved out from plant materials, such as wood splinters,as a supply source for organic matter needed for nitrogen elimination. The method and apparatus excel in the feasibility of easy, efficient water purification with the use of wood splinters procurable at low cost, etc.
A semiconductor substrate fabrication method according to the first aspect of this invention is characterized by including a preparation step of preparing an underlying substrate, a stacking step of stacking, on the underlying substrate, at least two multilayered films each including a peeling layer and a semiconductor layer, and a separation step of separating the semiconductor layer.
01 - Chemical and biological materials for industrial, scientific and agricultural use
06 - Common metals and ores; objects made of metal
09 - Scientific and electric apparatus and instruments
11 - Environmental control apparatus
40 - Treatment of materials; recycling, air and water treatment,
42 - Scientific, technological and industrial services, research and design
Goods & Services
Battery material, namely silver oxide, silver powder, silver oxide powder, zinc powder, nickel powder, metal powder, ferrite powder. Copper alloy and its coil; high purity metal. Measurement equipment; carrier for use of electrostatic image development; LED (light emitting diode) chips; GaAs wafer. Heat treatment furnaces; environmental equipment, namely waste water treatment unit, incinerators. Heat treatment; waste treatment; recycling; soil remediation, namely purification of soil, treatment of soil for the purpose of prevention of contamination. Site assessment, namely analysis of environment and soil, particularly evaluation of soil substance for the purpose of analyzing contaminated substances in the soil, evaluation of the compatibility of environment and the soil.
01 - Chemical and biological materials for industrial, scientific and agricultural use
06 - Common metals and ores; objects made of metal
09 - Scientific and electric apparatus and instruments
11 - Environmental control apparatus
Goods & Services
SILVER OXIDE POWDERS FOR USE IN MANUFACTURING DRY BATTERY OR CELL ELECTRODES METALS, NAMELY, SILVER POWDERS FOR USE IN THE MANUFACTURE OF CONDUCTIVE PASTES, IRON POWDERS FOR USE IN MANUFACTURING VIDEOTAPES, FERRITE POWDERS FOR USE IN MANUFACTURING MAGNETS, COPPER ALLOYS FOR USE IN MANUFACTURING SPRINGS AND REED FRAMES, COPPER ALLOY WIRES, AND HIGH PURITY METALS INCLUDING GALLIUM, INDIUM, COPPER, ANTIMONY, CADMIUM, ZINC, TELLURIUM, GERMANIUM, SILVER, SELENIUM, BISMUTH AND MAGNESIUM MEASURING EQUIPMENTS FOR MEASURING CARBON DIOXIDE DENSITY WITHIN A FURNACE, LIGHT EMITTING DIODE CHIPS, GALLIUM/ARSENITE WAFERS FOR USE IN MANUFACTURING SEMICONDUCTORS AND BATTERY MATERIALS INCLUDING ZINC POWDERS, SILVER OXIDE POWDERS, LITHIUM-COBALT ALLOY POWDERS, AND LITHIUM-NICKEL ALLOY POWDERS INDUSTRIAL FURNACES
09 - Scientific and electric apparatus and instruments
11 - Environmental control apparatus
40 - Treatment of materials; recycling, air and water treatment,
Goods & Services
[ TONER CARRIERS FOR ELECTRO PHOTOGRAPHING APPARATUS ] LED'S (LIGHT EMITTING DIODES), ELECTRICAL CONDUCTORS HAVING SUPERCONDUCTIVE PROPERTIES; CONTROLS AND MEASURING APPARATUS FOR USE IN CONNECTION WITH HEAT TREATMENT EQUIPMENT, NAMELY, FURNACES AND WASTE INCINERATORS EQUIPMENT, NAMELY, ENVIRONMENTAL EQUIPMENT, NAMELY, INCINERATORS, FURNACES, RESERVOIRS, PUMPS, FILTERS AND CLEANERS FOR TREATING SOLID WASTE, CONTAMINATED SOIL, WASTE WATER AND GAS AND FOR RECOVERING BYPRODUCTS FROM WASTE MATERIALS AND INCINERATING WASTE; HEAT TREATMENT EQUIPMENT FOR TREATING METAL PARTS, NAMELY, FURNACES AND GAS GENERATORS HEAT TREATMENT OF METALLIC PARTS, NAMELY, HARDENING, TEMPERING, CARBURIZING AND SHOT PEENING OF AUTOMOTIVE AND CONSTRUCTION MACHINERY METALLIC PARTS; METAL RECYCLING; ENVIRONMENTAL REMEDIATION, NAMELY, SOLID WASTE, WATER, SOIL AND GAS TREATMENT