H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
C01B 25/14 - Sulfur, selenium, or tellurium compounds of phosphorus
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (Japan)
Inventor
Kobayashi, Keigo
Kato, Jun
Hirayama, Yusuke
Liu, Zheng
Takagi, Kenta
Abstract
Provided is an aluminum alloy powder comprising 0.1-2.0 mass% or one or more metal elements from among rare earth metal elements comprising the lanthanide elements and yttrium, wherein the iron content is suppressed to not more than 2.0 mass%. The rare earth metal element is preferably one of praseodymium, neodymium, europium, samarium, terbium, gadolinium, dysprosium, holmium, erbium, thulium, ytterbium, and lutetium.
This copper alloy deposition model is formed of a Cu-Cr-Ni-Si-based alloy, the Cu-Cr-Ni-Si-based alloy having a Cr content within the range of 0.1-0.8 mass%, a Si content within the range of 0.4-0.8 mass%, and a Ni content within the range of 1.8-3.0 mass%. The model density is 99.5% or more, and the area ratio of a crystal having a plane orientation of (101) ± 15° in a specific direction is 51% or more as determined by crystal orientation measurement by means of electron backscattered diffraction.
C22C 9/06 - Alloys based on copper with nickel or cobalt as the next major constituent
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 1/16 - Metallic particles coated with a non-metal
B22F 10/28 - Powder bed fusion, e.g. selective laser melting [SLM] or electron beam melting [EBM]
B22F 10/38 - Process control to achieve specific product aspects, e.g. surface smoothness, density, porosity or hollow structures
B33Y 80/00 - Products made by additive manufacturing
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
4.
LITHIUM SULFIDE AND SULFIDE SOLID ELECTROLYTE PRODUCTION METHOD
This lithium sulfide is characterized in that the 50% diameter on a volume basis is in the range of 0.1-600 μm, inclusive, and the half-value width of a peak at 2θ= 27°±0.03° as measured using X-ray diffraction is in the range of 0.10-0.50°, inclusive. This sulfide solid electrolyte production method is characterized by using said lithium sulfide as a starting material.
Provided is a method for producing a sulfide-based solid electrolyte, the method having: a raw material preparation step for preparing an electrolyte raw material containing an element other than sulfur among elements constituting the sulfide-based solid electrolyte, and elemental sulfur and forming a raw material aggregate; and a synthesis step for heating the raw material aggregate to synthesize the sulfide-based solid electrolyte, wherein in the raw material preparation step, a molar ratio of the elemental sulfur to a lithium element in the raw material aggregate is set to be 1.5 to 6.5.
H01B 13/00 - Apparatus or processes specially adapted for manufacturing conductors or cables
H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
This additively manufactured copper alloy object comprises a Cu-Cr-Zr-based alloy, and is characterized in that: the Cu-Cr-Zr-based alloy has a Cr content within a range of 0.5-1.5 mass% and a Zr content within a range of 0.02-0.2 mass%; the density of the manufactured object is not less than 99.1%; and, as a result of measuring the crystal orientation of the same by electron backscatter diffraction, the area ratio of crystals having a plane orientation of {101}±15° in a specific direction is not less than 50%.
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 1/16 - Metallic particles coated with a non-metal
B22F 10/28 - Powder bed fusion, e.g. selective laser melting [SLM] or electron beam melting [EBM]
B22F 10/36 - Process control of energy beam parameters
B22F 10/38 - Process control to achieve specific product aspects, e.g. surface smoothness, density, porosity or hollow structures
B33Y 70/00 - Materials specially adapted for additive manufacturing
B33Y 80/00 - Products made by additive manufacturing
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
This Au-Sn alloy has an Sn content of 15.0–25.0 mass%, the remainder being Au and impurities, and an α-ray emission amount of no more than 0.010 cph/cm2. The amount of Cu, Pb, As, Sb, and Ag included as impurities is no more than 10 mass ppm each.
H01L 21/52 - Mounting semiconductor bodies in containers
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
B22F 9/00 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor
B23K 35/22 - Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
B23K 35/30 - Selection of soldering or welding materials proper with the principal constituent melting at less than 1550°C
A silicon member is characterized by comprising a polycrystalline region, having a percentage of coincidence grain boundary in the crystal grain boundary of the polycrystalline region of 80% or greater, and having a recess depth from the surface of 0.5 μm or less. The percentage of the Σ3 grain boundary in the coincidence grain boundary is preferably 80% or greater. The percentage of the Σ9 grain boundary in the coincidence grain boundary is preferably from 3% to 20%. The percentage of random grain boundaries in the crystal grain boundary of the polycrystalline region is preferably 15% or less.
C30B 11/14 - Single-crystal-growth by normal freezing or freezing under temperature gradient, e.g. Bridgman- Stockbarger method characterised by the seed, e.g. its crystallographic orientation
In an aspect of metal oxide fine particles, with regard to a transmission spectrum measured under conditions where the metal oxide fine particles are dispersed in a dispersion medium at a concentration of 0.7 mass % to prepare a dispersion and the dispersion is put into a 1 mm cell, an inclination k1 obtained by linearly approximating the transmission spectrum in a wavelength range of 290 nm to 330 nm by a least squares method is in a range of 0.90 or more and 1.60 or less.
This thermally conductive resin material (10) includes a resin (11) and a particulate filler (12) that is dispersed in the resin (11). A graph that represents the particle size distribution of the filler (12) of the thermally conductive resin material (10) has a first peak, a second peak, and a third peak. The first peak is at at least 20 μm but no more than 80 μm, the second peak is at at least 1 μm but no more than 10 μm, and the third peak is at at least 0.1 μm but less than 1 μm. The filler (12) includes first particles (21) that have a particle size of at least 10 μm, second particles (22) that have a particle size of at least 1 μm but less than 10 μm, and third particles (23) that have a particle size of at least 0.1 μm but less than 1 μm. The average circularity of a random sample of 30 of the third particles (23) that have a circle equivalent diameter of less than 1 μm is no more than 0.7.
A surface-coated cutting tool characterized in that: a substrate includes a binder phase containing Co and/or Ni as a main component, a hard phase containing W carbide as a main component, and a γ phase having an FCC structure and containing Zr as an optional component, V as an optional component, and a composite carbide of at least one element selected from the group consisting of Ti, Ta, Nb, and Hf as a main component; the substrate does not include unreacted carbon or free carbon, and has C00 porosity; and in the case where the Vickers hardness is measured under a load of 500 g every 4 μm toward the substrate interior from a substrate-interior position 2 μm from the interface between the substrate and a coating layer, the substrate has a reference hardness average value of A (HV0.5) at a depth of 2-450 μm, the substrate has a relative hardness average value of 0.70A-0.78A (HV0.5) at a depth of 2-14 μm, and the substrate has a relative hardness average value of 1.04A-1.10A (HV0.5) at a depth of 2-150 μm.
B23B 27/14 - Cutting tools of which the bits or tips are of special material
B23P 15/28 - Making specific metal objects by operations not covered by a single other subclass or a group in this subclass cutting tools
C22C 1/051 - Making hard metals based on borides, carbides, nitrides, oxides or silicidesPreparation of the powder mixture used as the starting material therefor
C22C 27/04 - Alloys based on tungsten or molybdenum
C22C 29/08 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
A surface-coated cutting tool characterized in that: a substrate includes a binder phase containing Co and/or Ni as a main component, a hard phase containing W carbide as a main component, and a γ phase having an FCC structure and containing Zr as an optional component, V as an optional component, and a composite carbide of at least one element selected from the group consisting of Ti, Ta, Nb, and Hf as a main component; the substrate does not include unreacted carbon or free carbon, and has C00 porosity; and in the case where the Vickers hardness is measured under a load of 500 g every 4 μm toward the substrate interior from a substrate-interior position 2 μm from the interface between the substrate and a coating layer, the substrate has a reference hardness average value of A (HV0.5) at a depth of 2-450 μm, the substrate has a relative hardness average value of 0.80A-0.86A (HV0.5) at a depth of 2-14 μm, and the substrate has a relative hardness average value of 1.11A-1.17A (HV0.5) at a depth of 2-150 μm.
B23B 27/14 - Cutting tools of which the bits or tips are of special material
B23P 15/28 - Making specific metal objects by operations not covered by a single other subclass or a group in this subclass cutting tools
C22C 1/051 - Making hard metals based on borides, carbides, nitrides, oxides or silicidesPreparation of the powder mixture used as the starting material therefor
C22C 29/08 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
This cutting tool made of cermet is characterized by comprising a hard phase, a binder phase, and a carbonitride phase, wherein: the hard phase contains TiCN and TiMCN (M is at least one element selected from the group consisting of Zr, Hf, V, Nb, Ta, Cr, Mo, and W) as a main component; the binder phase contains Co as a main component; and the carbonitride phase is dispersed within the binder phase and contains a carbonitride of the element M as a main component.
C22C 29/04 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides based on carbides or carbonitrides based on carbonitrides
B23B 27/14 - Cutting tools of which the bits or tips are of special material
C22C 1/051 - Making hard metals based on borides, carbides, nitrides, oxides or silicidesPreparation of the powder mixture used as the starting material therefor
A cutting tool having a substrate comprising a first hard phase, a second hard phase, and a binder phase, wherein the first hard phase is a composite carbonitride containing 3.0 mass% or less of at least one selected from Zr, V, Nb, Ta, Mo, and W, less than 0.2 mass% of Cr, and 18.0-22.0 mass% in total of C and N, with the remainder comprising Ti and inevitable impurities, the second hard phase is a composite carbonitride containing 10.0-25.0 mass% of at least one selected from Zr, V, Nb, Ta, Mo, and W, more than 0.0 and less than 1.0 mass% of Cr (higher content than the first hard phase), and 15.0-20.0 mass% in total of C and N, with the remainder comprising Ti and inevitable impurities, the binder phaser contains less than 5.0 mass% in total of Ni and Fe, and 1.0-8.0% of Cr in terms of mass ratio with respect to the Co content, with the remainder comprising Co and inevitable impurities, and the Vickers hardness of the substrate monotonically decreases from the flank face toward the inside to 100 μm, with 1700-2100 Hv up to 40 μm and 1600-1780 Hv at a position of 600 μm inside.
C22C 29/04 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides based on carbides or carbonitrides based on carbonitrides
B23B 27/14 - Cutting tools of which the bits or tips are of special material
C22C 1/051 - Making hard metals based on borides, carbides, nitrides, oxides or silicidesPreparation of the powder mixture used as the starting material therefor
This thermally conductive resin composition has an organo-polysiloxane blended therein in an amount in a range of 0.1-10.0 parts by mass with respect to 100 parts by mass of a filler. A polysiloxane compound having, at one terminal of a main chain, an ester functional group having a terminal modified by a hydroxyl group is blended in an amount in a range of 0.4-5.0 parts by mass with respect to 100 parts by mass of the filler. With respect to 100 parts by mass of the filler, an alkoxy silane compound is blended in an amount in a range of 1.2X to 10.0X parts by mass, where X represents a value obtained by dividing, by the minimum coated area (m2/g) of the alkoxy silane compound, a value obtained by multiplying the specific surface area (m2/g) of the filler with 100 parts by mass indicating the amount of the filler.
Provided is a temperature sensor which is inserted into an object to be measured and is reliably prevented from falling out. A temperature sensor 1 according to the present invention is inserted into a sensor hole of a socket section provided in an object to be measured. The temperature sensor 1 comprises: a belt-shaped insulating substrate 3; a heat-sensitive element 4 which is provided on one end side of the insulating substrate; a pair of pattern wires 5 which are formed on the insulating substrate and one end of which is connected to the heat-sensitive element; and a leaf spring member 6 which is attached to one end side of the insulating substrate. The leaf spring member comprises: a bottom plate part 6a to the upper surface of which one end side of the insulating substrate is fixed; and an upper plate part 6b which is connected to one end of the bottom plate part, extends gradually away from the bottom plate part toward the other end side of the bottom plate part, and has a biasing force in a direction away from the bottom plate part. The socket section has a through-hole penetrating from the inside of the sensor hole to the upper surface. The upper plate part comprises a locking part 6c that protrudes upward and is fitted into the through-hole when inserted into the sensor hole.
G01K 1/14 - SupportsFastening devicesArrangements for mounting thermometers in particular locations
G01K 7/22 - Measuring temperature based on the use of electric or magnetic elements directly sensitive to heat using resistive elements the element being a non-linear resistance, e.g. thermistor
Provided is a surface coated cutting tool including a substrate and a coating layer, wherein: the substrate contains 4.0 to 16.0 mass% of Co and/or Ni in total, 0.0 to 0.5 mass% of Cr, 4.0 to 12.0 mass% of at least one of Ti, Ta, Nb, Zr, Hf and V, and 6.0 to 7.5 mass% of C, with the remainder comprising W and unavoidable impurities; and in crystal grains constituting a hard phase, a ratio (d99/d50) of the cumulative equivalent circle diameter area proportion 99% grain size to the cumulative equivalent circle diameter area proportion 50% grain size is 2.0 to 2.4 in an internal cross-sectional region 300 μm or more toward the inside of the substrate from an interface between the substrate and the coating layer, and 3.0 to 4.0 in a cross-sectional region from the interface to 20 μm toward the inside of the substrate.
B23B 27/14 - Cutting tools of which the bits or tips are of special material
C22C 1/051 - Making hard metals based on borides, carbides, nitrides, oxides or silicidesPreparation of the powder mixture used as the starting material therefor
C22C 27/04 - Alloys based on tungsten or molybdenum
C22C 29/08 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
19.
METHOD FOR PRODUCING METAL SULFATE CRYSTAL AND METAL SULFATE
The present invention provides a method for producing a metal sulfate crystal, in which a metal sulfate crystal is crystallized and recovered from a metal sulfate solution that contains a metal sulfate and has a pH of less than 4.0. This method for producing a metal sulfate crystal is characterized by including: an alkaline metal compound addition step in which an alkaline metal compound of the metal that constitutes the metal sulfate is added to the metal sulfate solution that has a pH of less than 4.0 to so as to increase the pH to 4.5 or more; a crystallization step in which the metal sulfate crystal is crystallized from the metal sulfate solution that has a pH of 4.5 or more so as to obtain a metal sulfate crystal-containing slurry that contains the metal sulfate crystal; and a solid-liquid separation step in which the metal sulfate crystal-containing slurry is separated into the metal sulfate crystal and the residual liquid.
This solder paste contains solder powder and a spacer. The spacer content is 1 mass% or less. The spacer does not dissolve in the solder even if the melting temperature is higher than the melting temperature of the solder powder and the spacer is heated for 5 minutes at a temperature that is 20°C higher than the melting point of the solder powder. The spacer has a columnar shape or a tube shape, and the diameter variation σ/Da of the spacer calculated from the average diameter Da of the spacer and the standard deviation σ is 6.0% or less.
B23K 35/22 - Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
NATIONAL UNIVERSITY CORPORATION YOKOHAMA NATIONAL UNIVERSITY (Japan)
Inventor
Arai Koya
Oya Takahide
Abstract
A liquid detecting sensor element (20) according to the present invention detects a change of state of a target substance between a solid and a liquid, or a change of state of a target substance between dry and wet, the liquid detecting sensor element being characterized by including a liquid holding portion (25) into which the target substance in a liquid state is impregnated and held, and a first electrode portion (21) and a second electrode portion (22) which are arranged with the liquid holding portion (25) interposed therebetween, wherein the liquid holding portion (25) consists of an electrically conductive fiber body or an electrical-conductor-containing fiber body obtained by dispersing an electrical conductor in an insulating fiber body.
G01N 27/04 - Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
G01N 27/06 - Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a liquid
22.
COPPER TERMINAL MATERIAL WITH PLATING FILM AND METHOD FOR MANUFACTURING SAME
65655 alloy layer is an ally layer having a compound in which a part of the copper is substituted with nickel, and a part of the alloy layer is exposed on the surface of the tin layer. The exposed area ratio of the copper-tin alloy layer exposed on the surface of the tin layer is 1-60%. The tin layer has an average thickness of 0.20-1.20 μm, and the nickel layer has an average thickness of 0.05-2.00 μm. The arithmetic average curve Spc of the crest point on the surface of the coating film exceeds 70 mm-1but does not exceed 200 mm-1, and the standard deviation/average value of Spc found when visual field measurement is performed 10 times is 30% or less.
231-yy1-xx3233 (wherein Ma represents at least one trivalent metal element having an ion radius greater than that of Y, Mb represents at least one of Mg, Ca, Sr, and Ba, and 0.0≤x≤1.0, 0.0
H01C 7/04 - Non-adjustable resistors formed as one or more layers or coatingsNon-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material having negative temperature coefficient
C04B 35/01 - Shaped ceramic products characterised by their compositionCeramic compositionsProcessing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxides
C04B 35/50 - Shaped ceramic products characterised by their compositionCeramic compositionsProcessing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on rare earth compounds
H01C 17/00 - Apparatus or processes specially adapted for manufacturing resistors
24.
THERMISTOR ELEMENT, TEMPERATURE SENSOR PROVIDED WITH SAME, AND THERMISTOR ELEMENT MANUFACTURING METHOD
Provided are a thermistor element with minimal characteristic variation over time in a high temperature environment and during a heat resistance test, a temperature sensor including the thermistor element, and a thermistor element manufacturing method. This thermistor element comprises: a thermistor element body 2 having a crystal structure which includes a perovskite-type oxide thermistor material; and a pair of electrodes 3 on which the thermistor element body is formed. The electrodes comprise a Pt electrode layer 3a formed on the surface of the thermistor element body, and an intermetallic compound layer 3b including Pt, Sn, and M formed on the outside of the Pt electrode layer, wherein M is at least one of Ag, Ni, Co, and Mn, and the thickness of the intermetallic compound layer is 50 nm or more.
H01C 7/04 - Non-adjustable resistors formed as one or more layers or coatingsNon-adjustable resistors made from powdered conducting material or powdered semi-conducting material with or without insulating material having negative temperature coefficient
G01K 7/22 - Measuring temperature based on the use of electric or magnetic elements directly sensitive to heat using resistive elements the element being a non-linear resistance, e.g. thermistor
H01C 17/28 - Apparatus or processes specially adapted for manufacturing resistors adapted for applying terminals
25.
MELTING/SOLIDIFICATION SENSOR ELEMENT AND MELTING/SOLIDIFICATION SENSOR
A melting/solidification sensor element (20) according to the present invention detects a state change between solid and liquid in a target substance having electroconductivity in a liquid state, the melting/solidification sensor element (20) being characterized by including a liquid-holding part (25) in which the target substance in a liquid state is impregnated and held, and a first electrode part (21) and a second electrode part (22) that are arranged with the liquid-holding part (25) interposed therebetween, a state change between solid and liquid of the target substance held by the liquid-holding part (25) being detected according to an electric signal generated between the first electrode part (21) and the second electrode part (22).
G01N 27/06 - Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a liquid
G01N 27/00 - Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
G01N 27/04 - Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
26.
ATOMIZATION AGENT REPLENISHING LIQUID FOR PLATING SOLUTION AND METHOD FOR MANUFACTURING TIN-BASED PLATING MATERIAL
This atomization agent replenishing liquid for a plating solution replenishes a tin-based plating solution with an atomization agent containing one or more compounds selected from the group consisting of benzaldehyde, 1-naphthaldehyde, 1-naphthoic acid, 1-acetonaphthone, DL-1-(1-naphthyl)ethylamine, and benzylideneacetone. This atomization agent replenishing liquid for a plating solution comprises a phenyl glycol-based surfactant, the atomization agent, and water, where the atomization agent content is in the range from 0.1 g/L to 10.0 g/L, the phenyl glycol-based surfactant content is in the range from 5 g/L to 50 g/L, and the alcohol content is less than 1 mass%.
This silicon member includes a plurality of plate-shaped members consisting of a Si-containing material, the plate-shaped members are bonded in a thickness direction, a bonding layer is formed between the plate-shaped members, and an area ratio of Si phases in the bonding layer is 12% or less. An aspect ratio of the Si phase in the bonding layer is preferably 3.0 or less.
B32B 9/04 - Layered products essentially comprising a particular substance not covered by groups comprising such substance as the main or only constituent of a layer, next to another layer of a specific substance
C22C 21/02 - Alloys based on aluminium with silicon as the next major constituent
28.
METHOD FOR BONDING CU PILLARS, AND METHOD FOR MANUFACTURING CU PILLAR BONDED BODY
This method for bonding Cu pillars includes a Cu particle layer forming step for forming a Cu particle layer composed of a plurality of Cu particles on one or both of a bonding surface of a first Cu pillar and a bonding surface of a second Cu pillar, a stacking step for stacking the first Cu pillar and the second Cu pillar on one another with the Cu particle layer interposed therebetween, and a bonding step for heating the stacked first Cu pillar and second Cu pillar while applying pressure thereto in the stacking direction, to perform solid phase diffusion bonding of the first Cu pillar and the second Cu pillar, wherein, in the bonding step, a deformation amount L (μm), in the stacking direction, before and after bonding satisfies the relationship L≥1.4 μm, and the deformation amount L and a bonding surface area A (μm2) of the first Cu pillar and the second Cu pillar satisfy the relationship L/A≥0.0025.
Provided is a drill (10) having a body (1) extending in the axial direction around a central axis (O). The body (1) includes: chip discharge grooves (4) that open in a leading end face (3) and an outer peripheral surface (8) of the body (1) and that extend from the leading end face (3) to the trailing end side; recessed thinnings (5) that are disposed at the distal end of the body (1) and that are continuous with the chip discharge grooves (4) and the leading end face (3); and cutting edges (7) that are disposed at the distal end of the body (1). The cutting edges (7) have thinning edges (70) that are disposed at the radially inner ends of the cutting edges (7). The thinning edges (70) have curved concave-curved edges (71) that are continuous with ridge lines (6) at which the thinnings (5) and the leading end face (3) meet and that are recessed toward the side opposite to the drill rotation direction (T) about the central axis (O).
This acidic electrolytic copper plating solution is characterized by comprising a soluble copper salt, an azole compound, a carboxylic acid, water, and an acid, the azole compound content being 5-100 mmol/L, and the carboxylic acid content being 5-500 mg/L.
This drill (10) is provided with a body (1) extending axially centered on the center axis (O) of the body. The body (1) has: chip discharge grooves (4) that opens onto a tip-end face (3) and an outer peripheral surface (8) of the body (1), and that extends from the tip-end face (3) toward the rear end; thinnings (5) in the form of recesses disposed at the tip-end portion of the body (1) and connected to the chip discharge grooves (4) and the tip-end face (3); and cutting edges (7) disposed at the tip-end portion of the body (1). The cutting edges (7) have a thinning edge (70) disposed at a radially inner end portion of the cutting edges (7). Ridge lines (6) connecting the thinnings (5) and the tip-end face (3) have a curved section (60) stretching to the thinning edge (70) and concave in the drill rotation direction (T) about the center axis (O), the curved section (60) having a radius of curvature that grows larger as heading radially outward.
In this valuable-metal-recovery method, a valuable metal composed of cobalt and/or nickel is recovered from a raw solution that contains cobalt and/or nickel and also contains copper, wherein an ion adsorption step S01 for bringing the raw solution into contact with a chelate resin having a bispicolylamine group to adsorb metals in the raw solution onto the chelate resin, and a cobalt and nickel elution step S02 for eluting the cobalt andand/or nickel adsorbed onto the chelate resin by using a sulfuric acid solution, said method further comprising a copper elution step S04 for eluting the copper adsorbed onto the chelate resin by using an aqueous ammonia solution according to the amount of copper adsorbed onto the chelate resin.
C22B 3/14 - Extraction of metal compounds from ores or concentrates by wet processes by leaching in inorganic alkaline solutions containing ammonia or ammonium salts
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
This base with a bonding bump is characterized in that a bonding bump having a structure in which a seed layer and a nanoporous Cu layer are laminated is formed on the surface of a base, and the seed layer is composed of a metal that is less electropositive than Cu.
H01L 21/60 - Attaching leads or other conductive members, to be used for carrying current to or from the device in operation
C23C 28/02 - Coating for obtaining at least two superposed coatings either by methods not provided for in a single one of main groups , or by combinations of methods provided for in subclasses and only coatings of metallic material
C25D 3/12 - ElectroplatingBaths therefor from solutions of nickel or cobalt
C25D 3/38 - ElectroplatingBaths therefor from solutions of copper
C25D 5/02 - Electroplating of selected surface areas
C25D 7/00 - Electroplating characterised by the article coated
H05K 3/18 - Apparatus or processes for manufacturing printed circuits in which conductive material is applied to the insulating support in such a manner as to form the desired conductive pattern using precipitation techniques to apply the conductive material
A wafer-holding ring member (10) for use in a polishing device is characterized by being provided with a polishing surface (12) and by being made from a silicon material. The wafer-holding ring member is preferably made from a silicon material having a purity of 99.9999 mass % or more. The contact angle of water on the polishing surface (12) is preferably 30° or less.
Provided is a charging plug in which it is not necessary to open a hole and onto which a temperature sensor has been attached in a high heat-joining state. This charging plug is provided with: a pin-like plug body (2); a temperature sensor (3); and a metal clip member (4) having been attached to the plug body in a state in which the temperature sensor is in contact with the plug body. The plug body is provided with a pin section (2a) that is inserted into a counterpart connector and plug-in connected thereto, and a plug basal-end section (2b) provided on the basal end-side of the pin section. The clip member, with the temperature sensor being in contact with the plug basal-end section, clasps the temperature sensor between the clip member itself and the plug basal-end section, and is anchored to the plug basal-end section.
H01R 13/66 - Structural association with built-in electrical component
B60L 53/16 - Connectors, e.g. plugs or sockets, specially adapted for charging electric vehicles
G01K 1/14 - SupportsFastening devicesArrangements for mounting thermometers in particular locations
G01K 7/22 - Measuring temperature based on the use of electric or magnetic elements directly sensitive to heat using resistive elements the element being a non-linear resistance, e.g. thermistor
H01R 13/04 - Pins or blades for co-operation with sockets
H02J 7/00 - Circuit arrangements for charging or depolarising batteries or for supplying loads from batteries
37.
COPPER ALLOY POWDER FOR METAL AM AND METHOD FOR MANUFACTURING ADDITIVE MANUFACTURING PRODUCT
This copper alloy powder for a metal AM is used in the metal AM and includes a copper alloy containing Cr and Zr, and a Cr compound layer including a Cr-containing compound is formed on a surface of a copper alloy particle constituting the copper alloy powder.
A copper alloy powder for a metal AM includes a copper alloy containing Cr, Si, and Ni, and any one or both of a CrSi-based compound containing Cr and Si and a NiSi-based compound containing Ni and Si are precipitated on a copper crystal grain boundary of a surface of a copper alloy particle constituting the copper alloy powder.
Provided is a surge protection element capable of reducing damage caused by surges and suppressing fluctuation in discharge start voltage. A surge protection element according to the present invention comprises: an insulating tube (2); a pair of sealing electrodes (3) that close off both end openings of the insulating tube and seal a discharge control gas in the interior thereof; a pair of discharge electrodes (4) in which base ends are in contact with inner surfaces of the sealing electrodes and tip ends protrude into the insulating tube and face each other; and an insulating member (5) sandwiched between tip end surfaces of the pair of discharge electrodes and accommodated inside the insulating tube. The insulating member has a columnar shape having an axial line orthogonal to an axial line of the insulating tube, and is such that groove portions (5a) extending along the axial line of the insulating member are formed in an outer circumferential surface exposed between the pair of discharge electrodes.
x1−xy1−yz1−z−mmmN (where: M is at least one selected from the group consisting of Cr, Mo, Ta, B, Si, W, and lanthanoids; on average, 0.45 ≤ z ≤ 0.65; on average, 0.01 ≤ m ≤ 0.20; and x < z < y).
This copper alloy powder for a metal AM is formed of a copper alloy containing Cr, and a Cr compound layer including a Cr-containing compound is formed on a surface of a copper alloy particle constituting the copper alloy powder.
B22F 1/16 - Metallic particles coated with a non-metal
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
B22F 10/28 - Powder bed fusion, e.g. selective laser melting [SLM] or electron beam melting [EBM]
B22F 10/64 - Treatment of workpieces or articles after build-up by thermal means
A method for manufacturing an insulated circuit board with a heat sink, the circuit board comprising a heat sink including a flat, plate-shaped top plate portion and a heat-dissipating fin, an insulation layer provided on the top plate portion side of the heat sink, and a circuit layer provided on the insulation layer, the method comprising: a material formation step for fabricating the top plate portion separately from the fin; a first bonding step in which the top plate portion is laminated on one surface side of the insulation layer, and a metal plate for the circuit layer is laminated on the other surface side of the insulation layer, followed by bonding the laminated members together; and a second bonding step in which, after the first bonding step, the fin is bonded to a surface of the top plate portion opposite to the surface bonded to the insulation layer.
The present invention is provided with: a substrate (11); a silicon oxide layer (12) formed on at least the front surface of the substrate (11); an electrode layer (13) laminated on the silicon oxide layer (12); and a PZT-based ferroelectric layer (14) laminated on the electrode layer (13). The Pb content in the silicon oxide layer (12) is 1 atom% or less. Preferably, an insulating oxide layer (15) is formed between the silicon oxide layer (12) and the electrode layer (13). Preferably, a conductive oxide layer (16) is formed between the electrode layer (13) and the PZT-based ferroelectric layer (14).
In the present invention, a coating film is formed on a surface of a substrate made of copper or a copper alloy. The coating film comprises: a nickel layer that is composed of nickel or a nickel alloy and is formed on the surface of the substrate; a copper-tin alloy layer that is composed of an alloy of copper and tin and is formed on the nickel layer; and a tin layer that is composed of tin or a tin alloy and is formed on the copper-tin alloy layer. The average thickness of the nickel layer is 0.05 μm to 3.00 μm, the arithmetic mean peak curvature Spc of the surface of the copper-tin alloy layer is 700 mm-1to 2200 mm-1, the average thickness of the tin layer is 0.05 μm to 2.00 μm, and the average thickness of the copper-tin alloy layer is 0.15 μm to 1.55 μm.
A heat-storing thermally conductive material characterized by comprising: a heat storage material; a thermally conductive filler; and an oil-gelling agent or a two-component curable base resin.
22 gas is blown into the lithium carbonate slurry so as to produce lithium bicarbonate, thereby obtaining a lithium bicarbonate solution; a first solid-liquid separation step (S53) in which calcium carbonate suspended in the lithium bicarbonate solution is separated; a purified lithium carbonate crystallization step (S54) in which the lithium bicarbonate solution after the removal of the calcium carbonate is warmed so as to decompose the lithium bicarbonate, thereby precipitating purified lithium carbonate; a second solid-liquid separation step (S55) in which the precipitated purified lithium carbonate is separated from the mother liquid; and a mother liquid returning step (S56) in which the mother liquid obtained in the second solid-liquid separation step (S55) is returned to the slurrying step (S51).
This method for producing lithium carbonate (S04) comprises: a first carbonation reaction step (S41) for adding a soluble carbonate compound to a lithium-containing liquid in which calcium ions are also present and heating to produce calcium carbonate; a first solid-liquid separation step (S42) for separating the calcium carbonate generated in the first carbonation reaction step (S41) and the lithium-containing liquid; a second carbonation reaction step (S43) for adding a soluble carbonate compound to the lithium-containing liquid separated in the first solid-liquid separation step (S42) and heating to produce lithium carbonate; and a second solid-liquid separation step (S44) for separating the lithium carbonate generated in the second carbonation reaction step (S43) and the mother liquor.
This lithium-concentrated liquid production method (S03) is characterized by comprising: a carbonation reaction step (S31) in which a soluble carbonic acid compound is added to a lithium-containing liquid having calcium ions coexisting therein to produce calcium carbonate; a solid-liquid separation step (S32) in which the calcium carbonate produced in the carbonation reaction step (S31) and the lithium-containing liquid are separated; a decarbonation step (S33) in which an inorganic acid is added to the lithium-containing liquid separated in the solid-liquid separation step (S32) and the dissolved carbonic acid compound is removed from the lithium-containing liquid as carbon dioxide gas; and a membrane separation step (S34) in which, after the decarbonation step (S33), a reverse osmosis membrane is used to obtain a lithium-concentrated liquid in which lithium ions in the lithium-containing liquid are concentrated.
This aluminum powder product has powder particle bodies made of aluminum or an aluminum alloy, and barrier layers formed on surfaces of the powder particle bodies. An oxygen content in the aluminum powder product is 0.5 mass % or less, and in a case where a test, in which a mixture obtained by mixing the aluminum powder product and pure water at a mass ratio of 1:100 is held at 80° C. for 12 hours, is performed, no aluminum hydroxide phase is formed on a surface of the aluminum powder product after the test.
42 - Scientific, technological and industrial services, research and design
Goods & Services
Providing technical advice relating to the selection of
cutting tools; providing technical advice relating to the
selection of metalworking machines and tools; technological
consultancy services relating to the selection and usage of
metalworking machines and tools; providing on-line
non-downloadable computer software for the selection of
tools and power tools for machine tools; providing on-line
non-downloadable computer software for the selection of
cutting tools for machine tools; software as a service
[SaaS]; providing online non-downloadable computer software.
51.
THERMALLY CONDUCTIVE POLYMER COMPOSITION, MATERIAL FOR FORMING THERMALLY CONDUCTIVE POLYMER COMPOSITION, AND THERMALLY CONDUCTIVE POLYMER
The thermally conductive polymer composition contains a liquid rubber having two or more hydroxyl groups in one molecule, a solvent having one or more hydroxyl groups in one molecule, a curing agent having, in one molecule, two or more functional groups which are reactive with both the hydroxyl groups of the liquid rubber and the hydroxyl groups of the solvent, and a filler having thermal conductivity.
C08G 18/28 - Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
This method for leaching an electrode material is a method for subjecting an electrode material of a lithium ion secondary battery to acid leaching, the method including a leaching step of reacting the electrode material of a lithium ion secondary battery with sulfuric acid to obtain a leachate in which metals contained in the electrode material are leached, in which the leaching step includes a sulfuric acid adding step of adding the sulfuric acid to the electrode material to obtain a sulfuric acid-added electrode material, a kneading step of kneading the sulfuric acid-added electrode material to form a leaching paste, and a diluting step of diluting the leaching paste with water.
A thermally conductive filler includes: coarse inorganic particles; and the small inorganic particles, wherein the coarse inorganic particles includes large fused alumina particles having an average particle size in the range of 20 μm or more and 50 μm or less and the medium inorganic particles having an average particle size in the range of 1.0 μm or more and 10 μm or less, in a mass ratio of 60:40 to 100:0, the small inorganic particles have an average particle size of 0.1 μm or more and less than 1.0 μm, and a content of the small inorganic particles is in a range of 15% by mass or more and 30% by mass or less.
A turning tool according to the present invention includes a tool main body that extends along a tool axis (J) and that has a base at a tip portion on one side in an axial direction (Dj) along the tool axis (J), a cutting insert detachably attached to the base, and a camera provided in the tool main body and configured to image a machined surface of a work material cut by the cutting insert, in which the camera is disposed to image an outer side in a radial direction (Dr) of the tool main body intersecting with the axial direction (Dj).
A cutting tool includes a lower layer having an average thickness At from 0.3 μm to 6.0 μm and an upper layer having an average thickness Bt from 0.1 to 3.0 μm, and 2.0≤At/Bt≤5.0; the lower layer includes an alternating laminate of A1α sublayers with an average thickness αt and A1β sublayers with an average thickness βt, and 0.5 nm≤αt≤4.0 nm, 0.5 nm≤βt≤4.0 nm, and 0.7≤βt/αt≤1.3; the A1α sublayers each have a composition AlxTi1-xN (the average xavg of x is 0.35≤xavg≤0.55); the A1β sublayers each have a composition AlyTi1-yN (average yavg of y is 0.60≤yavg≤0.80); 1.2≤yavg/xavg; and the upper layer has a composition AlaTi1-a-bSibN (average values of aavg and bavg are represented by 0.35≤aavg≤0.60 and 0.00
B23B 27/14 - Cutting tools of which the bits or tips are of special material
C22C 29/00 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides
C22C 29/08 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
C25D 9/12 - Electrolytic coating other than with metals with inorganic materials by cathodic processes on light metals
56.
RESIN COMPOSITION, RESIN MOLDED BODY, AND METHOD FOR PRODUCING RESIN COMPOSITION
A resin composition includes a thermoplastic resin; a carbon fiber; and a silane coupling agent, in which a content of the thermoplastic resin is within a range of 59 parts by mass or more and 88 parts by mass or less, a content of the carbon fiber is within a range of 1 part by mass or more and 18 parts by mass or less, and a content of the silane coupling agent is within a range of 0.3 parts by mass or more and 7 parts by mass or less, with respect to a total of 100 parts by mass of the resin composition, and the carbon fiber is an isotropic pitch-based carbon fiber.
This heat transfer member is a heat transfer member constituted of a fired body of a molded object including a fluorine-based resin or a fluorine-based elastomer, in which a hardness measured using a type AM durometer conforming to JIS K 6253-3:2012 is lower by 7 or greater than a hardness of the molded object. This heat transfer member has a high plasma resistance and can maintain a high state of adhesion with respect to various members over a long period of time.
A surface coated cutting tool includes a substrate and a coating layer. The coating layer includes a complex carbonitride layer. The complex carbonitride layer has an average thickness of 1.0 μm or more and 20.0 μm or less. The complex carbonitride layer includes NaCl-type face-centered cubic crystal grains, each containing: metal components Ti, V, Zr, and Nb in atomic fractions a1, a2, a3, and a4, respectively, where the total atomic fraction of the metal components in the layer is 1; non-metallic components C and N in atomic fractions b1 and b2, respectively, where the total atomic fraction of the non-metallic components is 1; and inevitable impurities. The atomic fractions a1, a2, a3, a4, b1, and b2 satisfy the relations:
A surface coated cutting tool includes a substrate and a coating layer. The coating layer includes a complex carbonitride layer. The complex carbonitride layer has an average thickness of 1.0 μm or more and 20.0 μm or less. The complex carbonitride layer includes NaCl-type face-centered cubic crystal grains, each containing: metal components Ti, V, Zr, and Nb in atomic fractions a1, a2, a3, and a4, respectively, where the total atomic fraction of the metal components in the layer is 1; non-metallic components C and N in atomic fractions b1 and b2, respectively, where the total atomic fraction of the non-metallic components is 1; and inevitable impurities. The atomic fractions a1, a2, a3, a4, b1, and b2 satisfy the relations:
0.01
≤
a
1
≤
0.6
,
0.01
≤
a
2
≤
0.6
,
0.01
≤
a
3
≤
0.6
,
0.01
≤
a
4
≤
0.6
,
0.2
≤
b
1
≤
0.8
,
and
0.2
≤
b
2
≤
0.8
.
A copper alloy catalyst according to the present invention is characterized by being composed of a bulk material of a copper alloy which contains one or more kinds of alloy elements that are selected from among Zn, Al, Ca, Mg, Ni, Si, Mn, In, Fe, Co, Ag, and Sn, and which has a Cu content of 50 atom% or more. The copper alloy catalyst is also characterized in that if a droplet of ion exchange water is dropped on the surface of the bulk material, the contact angle measured by a θ/2 method is 95° or more.
B01J 23/80 - 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 with zinc, cadmium or mercury
B01J 23/78 - 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 with alkali- or alkaline earth metals or beryllium
B01J 23/89 - Catalysts comprising metals or metal oxides or hydroxides, not provided for in group of the iron group metals or copper combined with noble metals
B01J 23/825 - 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 with gallium, indium or thallium
B01J 23/835 - 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 with germanium, tin or lead
C07C 29/154 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing copper, silver, gold, or compounds thereof
C07C 29/156 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively with hydrogen or hydrogen-containing gases characterised by the catalyst used containing iron group metals, platinum group metals, or compounds thereof
C22C 9/01 - Alloys based on copper with aluminium as the next major constituent
C22C 9/02 - Alloys based on copper with tin as the next major constituent
C22C 9/04 - Alloys based on copper with zinc as the next major constituent
C22C 9/05 - Alloys based on copper with manganese as the next major constituent
C22C 9/06 - Alloys based on copper with nickel or cobalt as the next major constituent
C22C 9/10 - Alloys based on copper with silicon as the next major constituent
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
C25B 9/00 - Cells or assemblies of cellsConstructional parts of cellsAssemblies of constructional parts, e.g. electrode-diaphragm assembliesProcess-related cell features
NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (Japan)
Inventor
Kobayashi Keigo
Kato Jun
Hirayama Yusuke
Liu Zheng
Takagi Kenta
Abstract
This powder for sintering contains: a primary powder composed of aluminum or an aluminum alloy; and an oxide of at least one rare earth metal element selected from scandium, yttrium, and lanthanoid elements. This powder (1) for sintering is composed of a mixed powder having: particles (2) of a primary powder composed of aluminum or an aluminum alloy; and additive particles (3) composed of an oxide of at least one rare earth metal element selected from scandium, yttrium, and lanthanoid elements, wherein at least some of the additive particles (3) may adhere to the surface of the particles (2) of the primary powder.
B22F 1/16 - Metallic particles coated with a non-metal
B22F 1/052 - Metallic powder characterised by the size or surface area of the particles characterised by a mixture of particles of different sizes or by the particle size distribution
C22C 1/04 - Making non-ferrous alloys by powder metallurgy
61.
THERMALLY CONDUCTIVE POLYMER COMPOSITION, MATERIAL FOR FORMING THERMALLY CONDUCTIVE POLYMER COMPOSITION, THERMALLY CONDUCTIVE POLYMER
The thermally conductive polymer composition includes: a liquid rubber having two or more hydroxyl groups in one molecule; a solvent having one or more hydroxyl groups per molecule; a curing agent having two or more functional groups capable of reacting with both the hydroxyl groups of the liquid rubber and the hydroxyl groups of the solvent in one molecule; and a filler, wherein a compression modulus of a cured thermally conductive polymer at room temperature is 4.5N/mm2 or more and 5.5N/mm2 or less, the cured thermally conductive polymer being obtained after mixing the thermally conductive polymer composition and then allowing the thermally conductive polymer composition that is mixed to stand in an atmosphere at 25° C. for 24 hours or more.
In an aluminum powder product for metal additive manufacturing, a purity of aluminum in the entire powder is 98 mass % or more, 0.01 mass % or more and 0.5 mass % or less of Mg is contained, and a ratio Mg amount/oxygen amount of a contained amount of Mg (mass %) to a contained amount of oxygen (mass %) is 0.1 or more and 2.0 or less.
A tin alloy plating solution of the present invention includes (A) a soluble salt or oxide including at least a stannous salt, (B) a soluble salt of a metal nobler than tin, (C) a tin complexing agent formed of a sugar alcohol having 4 or more and 6 or less carbon atoms, (D) a free acid, and (E) an antioxidant. In addition, a content of the tin complexing agent is 0.1 g/L or more and 5 g/L or less, and a concentration of divalent tin ions (Sn2+) is 30 g/L or more.
Provided is a porous Cu member which comprises: a member main body (11) that is formed of Cu or a Cu alloy and has a porous structure; and a nano-Cu structure layer (16) that is formed on at least a part of the surface of the member main body (11). The member main body (11) has a porosity in the range of 38% to 95% inclusive and a thickness in the range of 0.1 mm to 1.0 mm inclusive. The nano-Cu structure layer (16) is configured as a layer by laminating Cu particles, which have an average length of 20 µm to 1 nm, on the surface.
A heatsink-integrated insulated circuit board includes a heatsink, an insulation layer formed on a top plate part of the heatsink, and a circuit layer formed on a surface of the insulation layer opposite to the heatsink, in which an electronic component is mounted on a mounting surface of the circuit layer. The circuit layer is made of copper or a copper alloy, and when a component occupancy ratio, which is a ratio of an occupied area of the electronic component to an area of the mounting surface of the circuit layer, is defined as X and a ratio λR/tR of a thermal conductivity λR of the insulation layer to a thickness tR of the insulation layer is defined as Y, in a range in which the component occupancy ratio X is 0.6 or less, a thickness tC of the circuit layer is set within a range of 0.7×(−5X−0.005Y+4.5)≤tC≤1.3×(−5X−0.005Y+4.5).
A method for processing a lithium ion secondary battery includes: a crushing and sorting step (S02) of crushing and classifying a lithium ion secondary battery to obtain an electrode material containing at least lithium; a leaching step (S03) of immersing the electrode material in an acid to obtain a leachate; a pH adjustment step (S04) of adding lithium hydroxide to the leachate to adjust a pH; a metal recovery step (S05) of recovering a metal other than lithium in the leachate to obtain a lithium-containing liquid; and a lithium hydroxide recovery step (S06) of recovering lithium in the lithium-containing liquid as lithium hydroxide, in which the lithium hydroxide recovered in the lithium hydroxide recovery step (S06) is used in the pH adjustment step (S04).
The surface coated cutting tool has the same multiple cutting edges. The coating layer of the flank face has a composition represented by (AlxTi1-x) (CyN1-y) (the average content xavg of x is 0.60 to 0.95 and the average content yavg of y's is 0.0000 to 0.0050); the crystal grains in each flank face have an average value I(200) of 200 diffraction intensities and a standard deviation σI(200), where the σI(200)/I(200) is 0.00 to 0.20; the average value Lavg and standard deviation σL of the thicknesses Lm's of the coating layer on a line 100 μm away from the ridge of each cutting edge in the direction of the flank face is within a σL/Lavg of 0.00 to 0.20; and the coating layer on each flank face has a region containing variable amounts of Al and Ti, and the difference between the maximum xmax and the minimum xmin is 0.02 to 0.40.
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
69.
THERMOPLASTIC ELASTOMER COMPOSITION, THERMALLY CONDUCTIVE SHEET, AND HEAT-DISSIPATING STRUCTURE
The thermoplastic elastomer composition contains a base polymer containing a styrene-based thermoplastic elastomer and an ethylene-propylene-based rubber, and a thermally conductive filler, in which the thermoplastic elastomer composition contains 200 parts by mass or more and 4,000 parts by mass or less of the thermally conductive filler with respect to 100 parts by mass of the base polymer.
Provided is a catalyst for hydrogen generation comprising a mixture of tungsten carbide and cobalt, the catalyst for hydrogen generation being characterized in that the absolute value of the cathode current per mg of the catalyst is 0.10 mA/mg or more when the catalyst for hydrogen generation is loaded on a glassy carbon electrode and subjected to potential scanning at -1.2 V with respect to a silver/silver chloride reference electrode under nitrogen bubbling in a 1 mol/L sodium hydroxide aqueous solution.
B01J 35/70 - Catalysts, in general, characterised by their form or physical properties characterised by their crystalline properties, e.g. semi-crystalline
C25B 11/091 - Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalysts material consisting of at least one catalytic element and at least one catalytic compoundElectrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalysts material consisting of two or more catalytic elements or catalytic compounds
71.
LITHIUM SULFIDE AND METHOD FOR MANUFACTURING SULFIDE SOLID ELECTROLYTE
The purpose of the present invention is to provide: lithium sulfide that has sufficiently high purity and is particularly suitable as a feedstock for a sulfide solid electrolyte; and a method, for manufacturing a sulfide solid electrolyte, that uses this lithium sulfide. The present invention pertains to: lithium sulfide characterized in that the L*value (brightness) as defined in the L*a*b* color space is 85 or more; and a method for manufacturing a sulfide solid electrolyte, the method being characterized in that the aforementioned lithium sulfide is used as a feedstock.
Provided is a sulfide solid electrolyte that is characterized by having an LGPS type crystal structure belonging to the space group P42/nmc, and is characterized in that the half value width of a peak of 2θ=29.58°±1.0° is 0.1 or less in an X-ray diffraction measurement using CuKα rays.
H01B 1/10 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances sulfides
C01B 25/14 - Sulfur, selenium, or tellurium compounds of phosphorus
H01B 13/00 - Apparatus or processes specially adapted for manufacturing conductors or cables
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
73.
DIMENSION MEASUREMENT DEVICE, CUTTING TOOL SYSTEM, AND DIMENSION MEASUREMENT METHOD
This dimension measurement device comprises a sensor unit (3) and a measurement device body (100). The sensor unit (3) includes a first distance sensor (31) that uses an eddy current sensor, and a signal conversion unit (35A, 35B) that outputs, as a detection value, an output signal from the distance sensor for each preset time interval. The measurement device body (100) is provided with: a detection control unit (101) that causes the sensor unit (3) to detect the distance to a material being cut while rotating the material being cut; an acquisition unit (103) that acquires a plurality of detection values outputted from the sensor unit (3) for each time interval within a preset stipulated time; a calculation unit (105) that calculates the average value of the plurality of detection values acquired by the acquisition unit (103); and a result output unit (107) that outputs a measurement result for the material being cut, the measurement result being based on the average value of the detection values that was calculated by the calculation unit (105).
B23Q 17/20 - Arrangements for indicating or measuring on machine tools for indicating or measuring workpiece characteristics, e.g. contour, dimension, hardness
Provided is a copper-clad laminate (10) in which a base material (11) containing a fluororesin and a metal copper layer (12) are laminated, the copper-clad laminate (10) being characterized in that: an alloy layer (13) is formed between the base material (11) and the metal copper layer (12), the alloy layer (13) being composed of 25.0-75.0 at% Co, with the balance being Mo and unavoidable impurities; and the metal copper layer (12) has a copper plating layer.
B32B 15/08 - Layered products essentially comprising metal comprising metal as the main or only constituent of a layer, next to another layer of a specific substance of synthetic resin
A method for manufacturing a copper alloy powder for a metal AM includes a casting step of manufacturing a copper alloy ingot with a casting apparatus including a molten copper supply unit which melts a copper raw material consisting of high-purity copper having a purity of 99.99 mass % or more to obtain molten copper, an addition unit which adds alloy elements of a copper alloy to the molten copper, and a mold to which the molten copper alloy is supplied, and an atomizing treatment step of powdering the copper alloy ingot by performing melting and decomposing by an atomizing treatment in an inert gas or a vacuum atmosphere using the copper alloy ingot, in which the O concentration of the copper alloy ingot is set to 10 mass ppm or less, and the H concentration of the copper alloy ingot is set to 5 mass ppm or less.
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
B22F 1/05 - Metallic powder characterised by the size or surface area of the particles
B33Y 70/00 - Materials specially adapted for additive manufacturing
COPPER ALLOY, COPPER ALLOY PLASTIC PROCESSING MATERIAL, COMPONENT FOR ELECTRONIC/ELECTRICAL APPARATUS, COMPONENT FOR FLEXIBLE DEVICE, COMPONENT FOR HEAT DISSIPATION, AND METAL SEALING MATERIAL
Provided is a copper alloy having a composition containing 15 to 57 mass% of Zn, containing 12 mass% or less of Al, and having a Zn content of A mass% and an Al content of B mass% where A + 5 × B ≥ 30 and A + 3.5 × B ≤ 57 are satisfied, with the balance being Cu and unavoidable impurities. The copper alloy has a β-phase volume fraction of 50% or greater, the average value of Kernel average misorientation (KAM) values of the β phase is 2.0° or less, said average value having been obtained by measuring a measurement area of 1 mm2 or greater using an EBSD method at measurement intervals of 1-μm steps and excluding measurement points at which a CI value obtained by being analyzed using data analysis software OIM is 0.1 or less. The copper alloy has excellent conductivity, a low Young's modulus, and a sufficiently large elastic deformation amount, and is not likely to plastically deform even when subjected to significant deformation.
C22C 9/04 - Alloys based on copper with zinc as the next major constituent
C22C 18/02 - Alloys based on zinc with copper as the next major constituent
H01B 1/02 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of metals or alloys
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
C22F 1/16 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of other metals or alloys based thereon
77.
COPPER ALLOY, COPPER ALLOY PLASTIC PROCESSING MATERIAL, COMPONENT FOR ELECTRONIC AND ELECTRICAL EQUIPMENT, COMPONENT FOR FLEXIBLE DEVICE, HEAT DISSIPATION COMPONENT, AND METAL SEALING MATERIAL
A copper alloy according to the present invention has a composition comprising 15-57 mass% of Zn and 12 mass% or less of Al, with the remainder being Cu and inevitable impurities, and when the content of Zn is denoted by A mass% and the content of Al is denoted by B mass%, the composition satisfies A+5×B ≥ 30 and A+3.5×B ≤ 57. A volume fraction of a β-phase is 50% or more, and when a measurement area of 8 mm2 or more is measured at a measurement interval of 8 μm steps by an EBSD method and analyzed except at measurement points at which an CI value analyzed by data analysis software OIM is 0.1 or less, and a boundary between measurement points at which an orientation difference between adjacent measurement points is 5º or greater is defined as a crystal grain boundary, the ratio of each corresponding grain boundary length of 3 ≤ Σ ≤ 29 to all crystal grain boundary lengths L where the measured β-phases contact each other is 4% or more. The copper alloy has excellent conductivity, has a low Young's modulus and a sufficiently large elastic deformation amount, and does not easily undergo plastic deformation even when subjected to large deformation.
C22C 9/04 - Alloys based on copper with zinc as the next major constituent
C22C 18/02 - Alloys based on zinc with copper as the next major constituent
H01B 1/02 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of metals or alloys
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
C22F 1/16 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of other metals or alloys based thereon
In this drill, a cutting blade (7) has a thinning blade (70) that is disposed at a radial inner end part of the cutting blade (7), and a main cutting blade (71) that is disposed on the radially outer side of the thinning blade (70) and that is connected to a leading edge (12) via an outer peripheral corner (15), the main cutting blade (71) and the leading edge (12) having honing in which a cross section perpendicular to ridge line parts has a convex curve shape, the honing curvature radius at a position within 1.5 mm from the outer peripheral corner (15) toward the rear end side of the leading edge (12) being 25-80 μm, and being smaller than the honing curvature radius of a radial outer end part connected to the outer peripheral corner (15) of the main cutting blade (71).
In a drill according to the present invention, a thinning blade, a main cutting blade, and a leading edge each have honing (H) where a cross section perpendicular to each ridge line part is formed in a convex curved shape. In this cross section, among both end parts (h1) and (h2) of the honing H, a surface connected to the first end part (h1) is defined as a first surface (101), a surface connected to the second end part (h2) is defined as a second surface (102), the distance to the first end part h1 from an intersection point P of an extension line of the first surface (101) and an extension line of the second surface (102) is defined as a first width dimension (L1), the distance to the second end part h2 from the intersection point P is defined as a second width dimension (L2), and [L1/L2] is defined as a width ratio. The thinning blade and the main cutting blade each have the first surface (101) as a rake face, and the second surface (102) as a flank face, and the width ratio of the thinning blade is larger than the width ratio of a radial outer end part connected to an outer peripheral corner of the main cutting blade.
This Cu-Zn-Si-Pb-P-based alloy continuous cast wire rod material comprises more than 60.0 mass% but less than 65.0 mass% of Cu, Si in the range of 0.40 mass% to 1.20 mass% inclusive, Pb in the range of 0.002 mass% to 0.250 mass% inclusive, and P in the range of 0.040 mass% to 0.190 mass% inclusive, and comprises, as an optional element, 0.001 mass% to 0.100 mass% inclusive of Bi, with the balance being Zn and impurities, wherein: the total content of Fe, Mn, Co, and Cr, which are impurities, is 0.450 mass% or less; the total content of Sn and Al is 0.30 mass% or less; and in a cross section perpendicular to the casting direction, the area ratio between the α phase and the β phase is α:β = 40 to 70:60 to 30, the area ratio of the γ phase is 0.1% or less, and the area ratio of a fine α phase in which the particle diameter is 10 μm or less is 30% to 60% inclusive.
C22C 9/04 - Alloys based on copper with zinc as the next major constituent
B22D 11/00 - Continuous casting of metals, i.e. casting in indefinite lengths
B22D 11/04 - Continuous casting of metals, i.e. casting in indefinite lengths into open-ended moulds
B23B 1/00 - Methods for turning or working essentially requiring the use of turning-machinesUse of auxiliary equipment in connection with such methods
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
42 - Scientific, technological and industrial services, research and design
Goods & Services
Providing technical advice relating to the selection of cutting tools; providing technical advice relating to the selection of metalworking machines and tools; technological consultancy services relating to the selection and usage of metalworking machines and tools; providing on-line non-downloadable computer software for the selection of tools and power tools for machine tools; providing on-line non-downloadable computer software for the selection of cutting tools for machine tools; software as a service [SaaS]; providing online non-downloadable computer software.
This WC-based cemented carbide, which is suitable for a substrate of a surface-coated cutting tool or the like, contains 6.0-10.0 mass% of Co, 0.08-0.90 mass% of Cr (where the ratio Cr content (mass%)/Co content (mass%) is 10% or lower), 0.0-3.8 mass% of M (where M is one or more of V, Ta, Nb, Ti, and Zr), and 4.5-7.5 mass% of C, the balance being W and unavoidable impurities. The WC-based cemented carbide has a binder phase, a hard phase, and a γ phase, the binder phase containing Co as the main component, the hard phase containing a carbide of W as the main component, and the γ phase containing a carbide of M as the main component. In crystal particles constituting the hard phase, the grain diameter C99 (μm) for 99% cumulative particle count is 3.30 or lower, and the ratio C99/C50 (grain diameter C99 (μm) for 99% cumulative particle count to grain diameter C50 (μm) for 50% cumulative particle count) is 4.80-6.50. The proportion (L) of the phase interface length along which the hard phase and the binder phase are in contact with respect to the total phase interface length of the hard phase is 35% or greater.
C22C 29/08 - Alloys based on carbides, oxides, borides, nitrides or silicides, e.g. cermets, or other metal compounds, e. g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
C22C 1/051 - Making hard metals based on borides, carbides, nitrides, oxides or silicidesPreparation of the powder mixture used as the starting material therefor
C22C 27/04 - Alloys based on tungsten or molybdenum
A surface-coated cutting tool includes a substrate and a coating layer provided on the substrate, wherein
1) the coating layer includes an alternating layer of A sublayers and B sublayers,
2) the A sublayers are each A Al1-aTiaN (where 0.30≤a≤0.70),
3) the B sublayers are each Cr1-cM2cN (where M2 is B and/or Si, where 0.01≤c≤0.40),
4) the A and B sublayers each have an average thickness of 1 nm or more and 500 nm or less, and
5) the alternating layer has an average thickness of 0.3 μm or more and 7.0 μm or less,
6) the adjoining A and B sublayers satisfy the relation: 0.1≤TA/TB≤0.8 or 1.2≤TA/TB≤10.0, where TA is the average thickness of the A sublayers and TB is the average thicknesses of the B sublayers.
Performance is improved. There is provided a negative electrode material for a battery, in which the negative electrode material includes carbon, sodium tungstate, and silicon particles 33 including silicon, and in the silicon particle 33, a ratio of the amount of Si in Si2p derived from elemental silicon to the amount of Si in Si2p derived from SiO2 in a surface layer when measured by X-ray photoelectron spectroscopy is 3 or more on an atomic concentration basis.
A copper/ceramic bonded body (10) formed by bonding copper member (12, 13) and a ceramic member (11), wherein the copper member has a Cu content of at least 99.96 mass%, and the ratio C/D is 0.93-1.05, where C is the proportion of KAM values of 0.25° or less in a measurement field of view arranged around a grain boundary triple point, and D is the proportion of KAM values of 0.25° or less within grains on the basis of the observation of a cross section of the copper member along a thickness direction after 3000 cycles of a thermal cycle test including holding at -65°C for 5 minutes and then holding at 150°C for 5 minutes in a liquid bath per cycle.
C04B 37/02 - Joining burned ceramic articles with other burned ceramic articles or other articles by heating with metallic articles
B32B 15/04 - Layered products essentially comprising metal comprising metal as the main or only constituent of a layer, next to another layer of a specific substance
C22F 1/08 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
H01L 23/12 - Mountings, e.g. non-detachable insulating substrates
H01L 23/13 - Mountings, e.g. non-detachable insulating substrates characterised by the shape
This copper/ceramic joined body is obtained by joining a copper member and a ceramic member. The copper member has a Cu content of at least 99.96 mass%, and has, in a cross section along the thickness direction of the copper member, an average crystal grain size of at most 100 μm after performing 3000 cycles of a heat cycle test in which the copper member is, in a liquid tank, held at -65°C for 5 minutes and then held at 150°C for 5 minutes in a single cycle.
A hafnium compound-containing sol-gel liquid contains an alcohol as a solvent and a hafnium compound as a hafnia source, in which the hafnium compound-containing sol-gel liquid contains one or two or more elements M selected from the group consisting of Zr, Ti, and Nb, a mass ratio WM/WHf of a content WM of the elements M to a content WHf of Hf as a metal component is within a range of 0.2% or more and 5.0% or less. A hafnia-containing film containing hafnia (HfO2) and one or two or more elements M selected from the group consisting of Zr, Ti, and Nb, and in which a mass ratio WM/WHfO2 of a content WM of the elements M to a content WHfO2 of the HfO2 is within a range of 0.05% or more and 5.0% or less.
B01J 13/00 - Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided forMaking microcapsules or microballoons
This method for separating cobalt and nickel includes a step (S3) of immersing an electrode material of a lithium ion secondary battery in a treatment liquid containing sulfuric acid and hydrogen peroxide to obtain a leachate, a step (S4) of adding a hydrogen sulfide compound to the leachate to precipitate copper, either one of a first treatment step (S5A) or a second treatment step (S5B), a step (S6) of obtaining a precipitate substance containing cobalt sulfide and nickel sulfide and a residual liquid containing lithium, and a re-dissolution step (S7) of dissolving cobalt and nickel in a suspension obtained by suspending the precipitate substance in distilled water or dilute sulfuric acid, in which, in the re-dissolution step (S7), the suspension is bubbled with an oxidizing gas containing oxygen using a fine-bubble generation apparatus.
Provided are: a tin oxide particle dispersion in which tin oxide particles are dispersed in a solvent, from which it is possible to form a tin oxide particle laminated film having excellent conductivity as a result of the tin oxide particles being arranged uniformly, and which is characterized by having a zeta potential of -35 mV or less at pH 10; and a method for producing a tin oxide particle laminated film. The tin oxide particles may be doped with a different element. The different element is preferably one or more selected from antimony, fluorine, and phosphorus. The primary particle size of the tin oxide particles is preferably in the range of 1.5-100 nm.
In the present invention, the following steps are carried out: a leaching step S01 in which a lithium-containing substance is immersed in an acidic solution to leach lithium into the acidic solution, thereby obtaining a lithium leachate; a heavy metal and first fluorine precipitation step S02 in which a first calcium compound is added to the lithium leachate to produce a metal hydroxide precipitate and a fluorine-containing precipitate; a first solid-liquid separation step S03 in which the precipitated metal hydroxide precipitate and fluorine-containing precipitate are removed from the lithium leachate; a second fluorine precipitation step S04 in which a second calcium compound is added to the lithium leachate from which the precipitates have been removed, to precipitate dissolved fluorine; and a second solid-liquid separation step S05 in which the precipitated dissolved fluorine and unreacted second calcium compound are removed from the lithium leachate.
2 or more is measured by an EBSD method at a measurement interval of 1 μm, measurement points at which a CI value obtained by an analysis using data analysis software OIM is 0.1 or less are excluded, and boundaries between adjacent pixels with a misorientation of 5° or more are regarded as crystal grain boundaries, an average of local orientation spread (LOS) is 2.00° or less.
B32B 15/04 - Layered products essentially comprising metal comprising metal as the main or only constituent of a layer, next to another layer of a specific substance
B32B 15/20 - Layered products essentially comprising metal comprising aluminium or copper
In a cutting insert and an edge replaceable end mill according to the present invention, a cutting blade (14) has: a main cutting blade (17) that is disposed on a first side of four sides of a quadrangular surface (11); a sub-cutting blade (18) that is disposed on a second side; and a corner blade (19). The sub-cutting blade (18) has a curved blade part (18a) that is connected to the corner blade (19), and forms a curved shape protruding toward a front side; and a linear blade part (18b) that is connected to the curved blade part (18a), and linearly extends toward a rear side as extending toward the side opposite to the curved blade part (18a) in the left-right direction. A flank (16) has: a first sub-flank (16b) that is connected to the curved blade part (18a), and forms a curved surface shape protruding toward the front side; and a planar second sub-flank (16c) that is connected to the linear blade part (18b).
Provided is an insulated circuit board in which a metal layer formed from pure aluminum is bonded to at least one surface of a ceramic substrate. In this circuit board: the pure aluminum is aluminum having a purity of 99.9%mass or more; a slip plane of metal crystal in the metal layer and the bonding interface with the ceramic substrate form an angle of 40° or less; and a second metal layer formed from any of aluminum, an aluminum alloy, copper, or a copper alloy may be bonded on the metal layer.
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/04 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
H01L 23/13 - Mountings, e.g. non-detachable insulating substrates characterised by the shape
94.
Pure copper material, insulating substrate, and electronic device
This pure copper material includes Cu in an amount of 99.96 mass % or more, either one or both of one or more A-group elements selected from Ca, Ba, Sr, Zr, Hf, Y, Sc, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu, and one or more B-group elements selected from O, S, Se, and Te are included in a total amount of 10 mass ppm or more and 300 mass ppm or less, an average crystal grain size in a rolled surface is 15 μm or more, and a high-temperature Vickers hardness at 850° C. is 4.0 HV or more and 10.0 HV or less.
An adhesive structure according to the present invention is characterized in that a tube array structure (20) formed by erecting a plurality of tube bodies (21) formed from a metal oxide is formed on at least a portion of the surface of a base material that comprises an inorganic material. The adhesive structure can be stably used even in high-temperature environments and clean environments and makes it possible to achieve sufficient adhesive force. The metal oxide is preferably an aluminum oxide or a titanium oxide. The tube bodies (21) preferably have an average outer diameter D of at least 40 nm and an average height H of at least 300 nm.
Provided is a program for instructing a processor of a map creation device, which communicates with a monitoring device that includes one or more sensors and moves together with a user being monitored, to execute: a process for acquiring an output value of the sensor of the monitoring device and the location of the user of the monitoring device; a process for determining that a prescribed event has occurred to the user of the monitoring device on the basis of information acquired from the monitoring device; a process for creating map information for displaying a map image representing the number or frequency of the events for each place where the prescribed event has occurred; and a process for outputting the map information to another terminal device.
G08G 1/13 - Traffic control systems for road vehicles indicating the position of vehicles, e.g. scheduled vehicles to a central station the indicator being in the form of a map
G09B 29/00 - MapsPlansChartsDiagrams, e.g. route diagrams
G09B 29/10 - Map spot or co-ordinate position indicatorsMap-reading aids
Provided is an adhesive structure in which a fiber structure layer configured from a plurality of fiber bodies composed of an inorganic material is formed on at least a portion of the surface of a base material composed of an inorganic material, the equivalent circle diameter D of a cross-section orthogonal to the extension direction of a fiber body (21) constituting the fiber structure layer is within the range of 15-400 nm, an aspect ratio H/D calculated from the height H and the equivalent circle diameter D of the fiber body (21) is 3 or greater, and the adhesive structure can be stably used even in a high-temperature environment and a clean environment and can achieve sufficient adhesive force.
B32B 5/02 - Layered products characterised by the non-homogeneity or physical structure of a layer characterised by structural features of a layer comprising fibres or filaments
B32B 9/00 - Layered products essentially comprising a particular substance not covered by groups
H01L 21/304 - Mechanical treatment, e.g. grinding, polishing, cutting
98.
MONITORING DEVICE, MONITORING MANAGEMENT DEVICE, AND MONITORING SYSTEM
This monitoring device is incorporated into or accommodated in a shoe and is detachably attached thereto, the monitoring device comprising: one or more left-foot pressure sensors; one or more right-foot pressure sensors; and a determination unit that acquires output values from the one or more left-foot pressure sensors and the one or more right-foot pressure sensors, and determines that the user has fallen when all of the output values indicate values lower than a threshold value.
G08B 25/04 - Alarm systems in which the location of the alarm condition is signalled to a central station, e.g. fire or police telegraphic systems characterised by the transmission medium using a single signalling line, e.g. in a closed loop
A43B 3/44 - Footwear characterised by the shape or the use with electrical or electronic arrangements with sensors, e.g. for detecting contact or position
A43B 3/48 - Footwear characterised by the shape or the use with electrical or electronic arrangements with transmitting devices, e.g. GSM or Wi-Fi®
A61B 5/00 - Measuring for diagnostic purposes Identification of persons
A61B 5/11 - Measuring movement of the entire body or parts thereof, e.g. head or hand tremor or mobility of a limb
A61B 5/022 - Measuring pressure in heart or blood vessels by applying pressure to close blood vessels, e.g. against the skinOphthaldynamometers
A61B 5/0245 - Measuring pulse rate or heart rate using sensing means generating electric signals
G01S 1/68 - Marker, boundary, call-sign, or like beacons transmitting signals not carrying directional information
G01S 5/14 - Determining absolute distances from a plurality of spaced points of known location
G08B 21/02 - Alarms for ensuring the safety of persons
G08B 25/08 - Alarm systems in which the location of the alarm condition is signalled to a central station, e.g. fire or police telegraphic systems characterised by the transmission medium using communication transmission lines
G08B 25/10 - Alarm systems in which the location of the alarm condition is signalled to a central station, e.g. fire or police telegraphic systems characterised by the transmission medium using wireless transmission systems
This drill (1) comprises a shaft-shaped tool body (10) that is rotated about a central axis, the drill having a chip discharge groove (14) formed on the outer periphery of the tool body (10), and a cutting blade (15) formed at an intersecting ridge portion between the chip discharge groove (14) and a tip flank (13) of the tool body (10)). The tool body (10) has a base material and a hard coating (17) formed in a region of a prescribed length from the tip of the base material. The chip discharge groove (14) has, in the central axis direction, in order from the tip of the tool body (10), a first section (S1) having a first surface roughness and a second section (S2) positioned closer to the rear end side than the first section (S1) and having a second surface roughness less than the first surface roughness. The first section (S1) has a length of at least 0.5 times a tool diameter (D). The hard coating (17) is formed in the first section (S1), and a hard coating (S17) is not formed in the second section (S2).
A titanium substrate material includes: a substrate main body made of a sintered titanium particle body; and a titanium oxide film formed on the substrate main body, wherein a proportion of anatase titanium oxide among titanium oxide constituting the titanium oxide film is 90% or more. It may have a porosity of the substrate main body is within a range of 30% or more and 92% or less. It may have a compressive strength of the titanium substrate is 0.5 MPa or more.
C25B 11/077 - Electrodes formed of electrocatalysts on a substrate or carrier characterised by the electrocatalysts material consisting of a single catalytic element or catalytic compound the compound being a non-noble metal oxide
