The present invention addresses the problem of providing a pyrolysis device capable of sending a condensate liquid to an appropriate step according to the impurity concentration while stably operating the pyrolysis device. A pyrolysis device 1 according to the present invention comprises: a pyrolysis unit 20 that thermally decomposes a raw material resin; a condensation unit 30 that liquefies a pyrolysis gas; and a storage unit 40 that stores a condensate liquid. The storage unit 40 has two or more tanks 41, 42 connected in parallel or in series. At least one processing unit related to the subsequent step is connected to the discharge side of the tanks 41, 42. At least either the storage unit 40 or a secondary pipe P2 between the storage unit 40 and the processing unit is provided with a port S for taking out the condensate liquid.
C08J 11/12 - Récupération ou traitement des résidus des polymères par coupure des chaînes moléculaires des polymères ou rupture des liaisons de réticulation par voie chimique, p. ex. dévulcanisation uniquement par traitement à la chaleur sèche
The purpose of the present invention is to provide a method for efficiently producing an oligonucleotide by a solid-phase synthesis approach. The present invention provides a method for producing an oligonucleotide by a solid phase synthesis approach, the method comprising a step for reacting an oligonucleotide in which a hydroxyl group at a chain extendable end is protected with a protective group that can be removed under acidic conditions and a deblocking solution to remove a protective group for a hydroxyl group at the chain extendable end, wherein the deblocking solution is a deblocking solution containing a base, an acid, and an aprotic solvent, and the base is a base having an acid dissociation constant (pKa) of a conjugate acid of 5-12, and an oligonucleotide in which the content ratio of the 2', 3'transfer body is a certain amount or less.
C07H 21/02 - Composés contenant au moins deux unités mononucléotide comportant chacune des groupes phosphate ou polyphosphate distincts liés aux radicaux saccharide des groupes nucléoside, p. ex. acides nucléiques avec le ribosyle comme radical saccharide
C07H 21/04 - Composés contenant au moins deux unités mononucléotide comportant chacune des groupes phosphate ou polyphosphate distincts liés aux radicaux saccharide des groupes nucléoside, p. ex. acides nucléiques avec le désoxyribosyle comme radical saccharide
3.
PELLET, PELLET MANUFACTURING METHOD, COMPOSITION/MOLDED BODY MANUFACTURING METHOD USING PELLET, AND PELLET MANUFACTURING COMPOSITION
The pellet contains an olefin-based polymer A and a polymer B. The polymer B is a polyhydroxyalkanoate-based polymer having a melting point of 150° C. or higher. A scanning electron microscope observation image of a cross-section including the center of the pellet and is parallel to the axis of the pellet satisfies the following requirements (1) and (2).
Requirement (1): The olefin-based polymer A is a dispersed phase, and the polymer B is a continuous phase.
Requirement (2): In an observation area of 1200 μm2, three or more dispersed phases having a length of 5 μm or more in the direction of the axis of the pellet are observed.
A composition comprising: a phenol-based compound represented by formula (I) [in formula (I), R1and R2each independently represent a hydrogen atom, an alkyl group having 1-8 carbon atoms, or a cycloalkyl group having 5-8 carbon atoms, R3and R4 each independently represent a linear or branched, saturated or unsaturated hydrocarbon group having 2-20 carbon atoms, and X represents a linear or branched alkylene group having 1-3 carbon atoms]; and a phosphorus-based compound having a molecular weight of 550 or more.
C09K 15/08 - Compositions anti-oxydantesCompositions inhibant les modifications chimiques contenant des composés organiques contenant de l'oxygène contenant une fraction phénol ou quinone
C08K 5/52 - Phosphore lié à l'oxygène lié uniquement à l'oxygène
C08K 5/5393 - Composés phosphoneux, p. ex. R—P(OR')2
C08L 101/00 - Compositions contenant des composés macromoléculaires non spécifiés
C09K 15/32 - Compositions anti-oxydantesCompositions inhibant les modifications chimiques contenant des composés organiques contenant du bore, du silicium, du phosphore, du sélénium, du tellure ou un métal
5.
(METH)ACRYLIC POLYMER REGENERATION DEVICE, METHOD FOR REGENERATING (METH)ACRYLIC POLYMER, AND METHOD FOR PRODUCING MONOMER HAVING (METH)ACRYLIC GROUP
The present invention addresses the problem of providing a (meth)acrylic polymer regeneration device, a (meth)acrylic polymer regeneration treatment method, and a (meth)acrylic acid ester production method with which it is possible to effectively suppress water from being mixed into a thermal decomposition product of a (meth)acrylic polymer. The present invention relates to a (meth)acrylic polymer regeneration device 100 that includes: a dehydration unit 1 that removes water contained in a (meth)acrylic polymer; and a thermal decomposition unit 2 that thermally decomposes the (meth)acrylic polymer from which water has been removed by the dehydration unit 1.
C08J 11/12 - Récupération ou traitement des résidus des polymères par coupure des chaînes moléculaires des polymères ou rupture des liaisons de réticulation par voie chimique, p. ex. dévulcanisation uniquement par traitement à la chaleur sèche
The present invention addresses the problem of providing a method for producing propylene, with which propylene can be produced at a relatively excellent yield. A method for producing propylene according to the present invention has: a reaction step A for obtaining a crude product (A) from raw materials including ethanol in the presence of a catalyst (A); and a reaction step B for obtaining a crude product (B) from the crude product (A) in the presence of a catalyst (B). The composition of the catalyst (A) is different from that of the catalyst (B). The catalyst (A) contains a metal N and at least two types of metal M selected from the group consisting of zirconium and the like. The molar ratio of the metal M relative to the metal N is less than 100. The amount of acid centers in the catalyst (B) is 50 μmol/g or more.
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
B01J 23/02 - Catalyseurs contenant des métaux, oxydes ou hydroxydes métalliques non prévus dans le groupe des métaux alcalins ou alcalino-terreux ou du béryllium
Provided is a phenolic compound represented by formula (I). In formula (I), R1|and R2each independently represent a hydrogen atom, a C1-C8 alkyl group, or a C5-C8 cycloalkyl group, X represents a C1-C3, linear or branched alkylene group, Y represents *-C(=O)-O-**, *-O-C(=O)-**, *-O-**, or *-O-C(=O)-O-** (* indicates a bond with the X and ** indicates a bond with the Z), and Z represents a group (z1) represented by formula (z1) or a C9-C24, branched, (un)saturated hydrocarbon group (z2), with the proviso that when Y represents *-C(=O)-O-**, the hydrocarbon group (z2) is a group represented by formula (z2'). In formula (z1), A represents a C1-C20, linear or branched alkylene group, with the proviso that when Y represents *-C(=O)-O-**, the number of carbon atoms of the alkylene group is 4-20, B represents a C2 or C3, linear or branched alkylene group, n indicates an integer of 0-5, R3223232333)-, and *** indicates a bond with the Y.
C07C 69/732 - Esters d'acides carboxyliques dont le groupe carboxyle estérifié est lié à un atome de carbone acyclique et dont l'un des groupes OH, O-métal, —CHO, céto, éther, acyloxy, des groupes , des groupes ou des groupes se trouve dans la partie acide d'acides non saturés d'acides hydroxycarboxyliques non saturés
C07C 69/28 - Esters d'acides acycliques monocarboxyliques saturés dont le groupe carboxyle est lié à un atome de carbone acyclique ou à l'hydrogène avec au moins trois atomes de carbone dans la partie acide estérifiés par des composés dihydroxylés
C08L 23/00 - Compositions contenant des homopolymères ou des copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carboneCompositions contenant des dérivés de tels polymères
C08L 101/00 - Compositions contenant des composés macromoléculaires non spécifiés
C09K 15/08 - Compositions anti-oxydantesCompositions inhibant les modifications chimiques contenant des composés organiques contenant de l'oxygène contenant une fraction phénol ou quinone
A method for producing ethylene and propylene comprises: a reaction step (1) for bringing a raw material (1a) containing ethanol into contact with a catalyst to obtain a product (1b) containing ethylene and propylene; a gas-liquid separation step (2) for separating the product (1b) into a gas component (2a) containing ethylene and propylene and a liquid component (2b) containing acetone; a gas separation step (3) for separating carbon dioxide (3a), water (3b), and hydrogen (3c) from the gas component (2a) to obtain a gas component (3d) containing ethylene and propylene; and an olefin separation step (4) for separating the gas component (3d) into a low-boiling fraction (4a), ethylene (4b), propylene (4c), and a high-boiling fraction (4d).
C07C 7/04 - Purification, séparation ou stabilisation d'hydrocarburesEmploi d'additifs par distillation
C07C 1/20 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés organiques ne renfermant que des atomes d'oxygène en tant qu'hétéro-atomes
C07C 29/151 - Préparation de composés comportant des groupes hydroxyle ou O-métal liés à un atome de carbone ne faisant pas partie d'un cycle aromatique à six chaînons par réduction exclusivement des oxydes de carbone avec de l'hydrogène ou des gaz contenant de l'hydrogène
The present invention provides pest control compositions and control methods, and the pest control compositions containing natural pyrethrin can be used to control pests.
A01N 53/00 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des acides cyclopropane-carboxyliques ou leurs dérivés
A01N 43/90 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant plusieurs hétérocycles déterminants condensés entre eux ou avec un système carbocyclique commun
A composition contains a polymer B and a compound C. The polymer B is an aliphatic polyester, and a content of the compound C is 0.1 parts by mass or more and less than 100 parts by mass with respect to 100 parts by mass of a total of the polymer B and the compound C. The compound C has at least one functional group selected from the group consisting of a heterocyclic group having two or more heteroatoms, a cyclic ether group, an acid anhydride group, an isocyanate group, and a carbodiimide group.
Provided is a herbicidal composition comprising one or more uracil compounds represented by formula (I) and one or more compounds selected from the group consisting of the herbicide compound group B consisting of the following B-1 to B-12.
Provided is a herbicidal composition comprising one or more uracil compounds represented by formula (I) and one or more compounds selected from the group consisting of the herbicide compound group B consisting of the following B-1 to B-12.
A resist composition, a dry film resist, a method for producing a dry film resist, a method for forming a resist pattern, and a method for producing a plated object are described. The resist composition includes a resin (A1) having a group represented by formula (1), a resin (A2) including a structural unit represented by formula (a3), and an acid generator (B1).
A resist composition, a dry film resist, a method for producing a dry film resist, a method for forming a resist pattern, and a method for producing a plated object are described. The resist composition includes a resin (A1) having a group represented by formula (1), a resin (A2) including a structural unit represented by formula (a3), and an acid generator (B1).
G03F 7/038 - Composés macromoléculaires rendus insolubles ou sélectivement mouillables
C08L 29/08 - Copolymères de l'alcool allylique avec des monomères vinylaromatiques
G03F 7/00 - Production par voie photomécanique, p. ex. photolithographique, de surfaces texturées, p. ex. surfaces impriméesMatériaux à cet effet, p. ex. comportant des photoréservesAppareillages spécialement adaptés à cet effet
G03F 7/039 - Composés macromoléculaires photodégradables, p. ex. réserves positives sensibles aux électrons
G03F 7/16 - Procédés de couchageAppareillages à cet effet
The present disclosure is a metal organic framework containing a metal ion and a polyvalent carboxylic acid ligand, wherein: the polyvalent carboxylic acid ligand does not include elemental S element and elemental N; the metal organic framework includes elemental S and elemental N; the elemental S content and the elemental N content per 1 g of the metal organic framework are both 0.4 mmol/g or less; and the ratio (S/N) of the elemental S content (mmol/g) to the elemental N content (mmol/g) is 0.2-1.4.
Provided is a compound which has an excellent controlling effect on arthropod pests. A compound represented by the formula (wherein the symbols have the meanings set forth in the description) or an N-oxide thereof has an excellent controlling effect on arthropod pests.
A01N 43/90 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant plusieurs hétérocycles déterminants condensés entre eux ou avec un système carbocyclique commun
A01N 65/12 - Asteraceae ou Compositae [famille de l'aster ou du tournesol], p. ex. marguerite, pyrèthre, artichaut, laitue, tournesol, armoise ou estragon
C07D 491/048 - Systèmes condensés en ortho avec un seul atome d'oxygène comme hétéro-atome du cycle contenant de l'oxygène le cycle contenant de l'oxygène étant à cinq chaînons
C07D 519/00 - Composés hétérocycliques contenant plusieurs systèmes de plusieurs hétérocycles déterminants condensés entre eux ou condensés avec un système carbocyclique commun non prévus dans les groupes ou
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
09 - Appareils et instruments scientifiques et électriques
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
Produits et services
Industrial chemicals; carbon nanotubes Batteries; electrical cells; dry cells; wet cells; secondary batteries; lithium-ion batteries; electrodes Semi-processed plastics; semi-processed plastics containing carbon nanotubes; plastics in extruded form for use in further manufacturing; extruded plastics in the form of sheets for use in manufacture; extruded plastics in the form of tubes for use in manufacture; extruded plastics in the form of blocks for use in manufacture; extruded plastics in the form of pellets for use in manufacture
A composition comprising a polymer; diethylene glycol diethyl ether; and a compound of formula (I);
A composition comprising a polymer; diethylene glycol diethyl ether; and a compound of formula (I);
A composition comprising a polymer; diethylene glycol diethyl ether; and a compound of formula (I);
wherein: M+ is an alkali metal cation; X is Al or B; and R1 in each occurrence is independently a substituent wherein two R1 groups may optionally be linked to form a ring. A gel comprising the composition may be used as an electrolyte in a metal or metal ion battery.
H01M 10/0565 - Matériaux polymères, p. ex. du type gel ou du type solide
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p. ex. batteries à insertion ou intercalation de lithium dans les deux électrodesBatteries à l'ion lithium
A solution comprising a solvent, a fluorinated polymer and an alkali or alkali earth metal salt wherein the fluorinated polymer is a partially unsaturated poly(alkylene) polymer.
Provided is a filter in which a metal organic structure is supported on a base material, wherein a variation coefficient measured by fluorescent X-ray analysis of an amount (mol%) of a metal element M of the metal organic structure with respect to the total amount of target elements included in the filter is more than 0% but not more than 50%, and the target element is an element other than O and C, and has a peak intensity of 1 cps or more in fluorescent X-ray analysis.
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance organique
B01J 20/28 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation caractérisées par leur forme ou leurs propriétés physiques
The present invention provides a filter in which a metal–organic framework is supported on a base material, the filter satisfying the following requirements (R1) and (R2) when air of high temperature and low humidity is made to flow at a prescribed air velocity through the filter that has been subjected to a specific pretreatment (a) and a water adsorption treatment (b). Requirement (R1): A graph P, of which the horizontal axis is time (s) and the vertical axis is the cumulative amount (g) of water desorbed per gram of filter, and a graph Q, of which the horizontal axis is time (s) and the vertical axis is the temperature (°C) of the air downstream of the filter, are each acquired, the time t (s) to reach the point T at which the temperature of the air downstream of the filter is lowest in the graph Q is ascertained, and the absolute value of the linear slope connecting the origin and the point (t, P(t)) on the graph P at time t is 9 × 10-4 or more. Requirement (R2): The cumulative amount of water desorbed after 600 seconds is 0.133 g or more per gram of the filter.
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance organique
B01J 20/28 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation caractérisées par leur forme ou leurs propriétés physiques
24.
COMPOSITION, PHOTOELECTRIC CONVERSION ELEMENT, AND OPTICAL SENSOR
Provided are: a composition capable of absorbing light having a long wavelength and suppressing a dark current in a photoelectric conversion element; a photoelectric conversion element; and an optical sensor. This composition comprises a p-type semiconductor material and an n-type semiconductor material. The p-type semiconductor material includes a structural unit X represented by the following formula and a structural unit Y that is a divalent group and that has a chemical structure different from that of the structural unit X. The LUMO energy of the p-type semiconductor material is -3.35 eV to -2.75 eV. The n-type semiconductor material is a compound represented by formula (n1). The absolute value of the difference between the HOMO energy of a compound Ia and the HOMO energy of a compound II, and the absolute value of the difference between the HOMO energy of a compound Ib and the HOMO energy of the compound II are both 2.75-3.90 eV. The structural unit X, the structural unit Y, formula (n1), the compound Ia, and the compound II are as defined in the specification.
H10K 30/60 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire dans lesquels le rayonnement commande le flux de courant à travers les dispositifs, p. ex. photorésistances
H10K 30/30 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire comprenant des hétérojonctions de masse, p. ex. des réseaux interpénétrés de domaines de matériaux donneurs et accepteurs
H10K 85/60 - Composés organiques à faible poids moléculaire
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
The present disclosure provides a filter in which a metal organic structure is supported on a base material, wherein: the average value of the amount of an S element with respect to the total amount of a target element included in the filter, as measured by fluorescent X-ray analysis, is 8-30 mol%; the target element is an element other than O and C, said element having a peak intensity of 10 cps or greater in fluorescent X-ray analysis; the peak intensity (cps) of the S element at a plurality of locations of the filter and the peak intensity (cps) of a metal element M constituting the metal organic structure are each measured by fluorescent X-ray analysis; the peak intensities of the S element and the metal element M at each measurement point are plotted, with the peak intensity (cps) of the metal element M being on the horizontal axis and the peak intensity (cps) of the S element being on the vertical axis; and a determination coefficient R 2 of a linear one-dimensional approximation formula derived using the least-squares method is 0.70 or greater.
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance organique
B01J 20/28 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation caractérisées par leur forme ou leurs propriétés physiques
The purpose of the present invention is to provide a display device using a quantum dot organic EL panel, wherein is provided a laminate capable of achieving both suppression of reflective appearance caused by light reflection inside and outside the panel during black display and improvement of luminance during white display. Provided is a laminate including a low-reflection film and a functional layer, wherein the low reflection film has an average luminous reflectance of 0.05-5% and a total light transmittance of 93% or more, and the functional layer includes at least one type of dye and satisfies expression (I): (Tt50°/Tt0°) × 100 ≥ 60 (In the formula, Tt50° is the transmittance of light having a wavelength of 550 nm incident on the functional layer at an incident angle of 50°, and Tt0° is the transmittance of light having a wavelength of 550 nm incident on the functional layer at an incident angle of 0°.).
G09F 9/00 - Dispositifs d'affichage d'information variable, dans lesquels l'information est formée sur un support, par sélection ou combinaison d'éléments individuels
G09F 9/30 - Dispositifs d'affichage d'information variable, dans lesquels l'information est formée sur un support, par sélection ou combinaison d'éléments individuels dans lesquels le ou les caractères désirés sont formés par une combinaison d'éléments individuels
H10K 50/86 - Dispositions pour améliorer le contraste, p. ex. en empêchant la réflexion de la lumière ambiante
H10K 50/115 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des nanostructures inorganiques actives, p. ex. des points quantiques luminescents
H10K 50/856 - Dispositifs pour extraire la lumière des dispositifs comprenant des moyens réfléchissants
H10K 59/38 - Dispositifs spécialement adaptés à l'émission de lumière multicolore comprenant des filtres de couleur ou des supports changeant de couleur [CCM]
Provided is a laminate with which both suppression of reflection appearance caused by light reflection inside and outside a panel during black display and improvement of luminance during white display can be achieved in a display device using a quantum dot organic EL panel. This laminate includes a low reflection film and a functional layer. The low reflection film has a luminous average reflectance of 0.05%-5% inclusive and a total light transmittance of 93% or more. The functional layer is a cured film obtained by curing a liquid crystal compound and a dichroic dye in a state of being oriented in a direction perpendicular to a layer plane.
G09F 9/00 - Dispositifs d'affichage d'information variable, dans lesquels l'information est formée sur un support, par sélection ou combinaison d'éléments individuels
H10K 50/86 - Dispositions pour améliorer le contraste, p. ex. en empêchant la réflexion de la lumière ambiante
H10K 50/115 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des nanostructures inorganiques actives, p. ex. des points quantiques luminescents
To provide a carbon nanotube aggregate excellent in conductivity when used as a carbon nanotube dispersion, and the application thereof. The present invention provides a carbon nanotube aggregate, a carbon nanotube dispersion, a conductive material, an electrode, a secondary battery, a planar aggregate, a filter, an electromagnetic wave shield, and a pellicle for extreme ultraviolet rays that satisfy conditions (1), (2), and (3). (1) At least one of Fe atoms and Co atoms is contained, and the total content of Fe atoms and Co atoms is 2000-100,000 mass ppm with respect to the total mass of the carbon nanotube aggregate. (2) At least one of Na atoms and K atoms is contained, and the total content of Na atoms and K atoms is 50-1000 mass ppm with respect to the total mass of the carbon nanotube aggregate. (3) The ratio of the volume resistivity under 20 kN pressurization and the volume resistivity under 1 kN pressurization is 0.21 or more.
The present invention provides a carbon nanotube assembly excellent in conductivity when used to provide a carbon nanotube dispersion liquid, a carbon nanotube dispersion liquid, a conductive material, an electrode, a secondary battery, a planar assembly, a filter, an electromagnetic wave shield, and an extreme ultraviolet pellicle. The present invention provides the carbon nanotube assembly, carbon nanotube dispersion liquid, conductive material, electrode, secondary battery, planar assembly, filter, electromagnetic wave shield, and extreme ultraviolet pellicle satisfying the following conditions (1) and (2). (1) The pore volume is 0.60 cm3/g to 5.00 cm3/g. (2) The ratio between the volume resistivity under 20 kN pressurization and the volume resistivity under 1 kN pressurization is 0.18-0.30.
B01D 39/20 - Autres substances filtrantes autoportantes en substance inorganique, p. ex. papier d'amiante ou substance filtrante métallique faite de fils métalliques non-tissés
Provided are: a carbon nanotube assembly which has excellent dispersibility in a carbon nanotube dispersion and from which a carbon nanotube dispersion having an appropriate viscosity is obtained; and an application thereof. A carbon nanotube assembly, a carbon nanotube dispersion, a conductive material, an electrode, a secondary battery, a planar assembly, a filter, an electromagnetic wave shield, and an extreme-ultraviolet pellicle, which satisfy the conditions (1) and (2). (1) The peak intensity ratio G1/D1, which is the ratio of the peak intensity G1 of the G band to the peak intensity D1 of the D band in a Raman spectrum of carbon nanotubes, is 0.70-10.0, and the ratio of the peak area ratio G2/D2, which is the ratio of the peak area G2 of the G band to the peak area D2 of the D band, to the peak intensity ratio G1/D1 is 1.20-3.00. (2) The BET specific surface area of carbon nanotubes is 100 m2/g to 300 m2/g.
The present invention provides a carbon nanotube assembly which has excellent conductivity when used in the form of a carbon nanotube dispersion liquid, and applications thereof. The present invention provides a carbon nanotube assembly which satisfies the following conditions (1) and (2), and applications thereof. (1) The ratio of the pore volume to the BET specific surface area is 0.0100 μm to 0.0200 μm. (2) The ratio of the volume resistivity under the pressure of 20 kN to the volume resistivity under the pressure of 1 kN is 0.18 to 0.30 inclusive.
B01D 39/20 - Autres substances filtrantes autoportantes en substance inorganique, p. ex. papier d'amiante ou substance filtrante métallique faite de fils métalliques non-tissés
G03F 1/62 - Pellicules, p. ex. assemblage de pellicules ayant une membrane sur un cadre de supportLeur préparation
H01B 1/04 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement soit de compositions à base de carbone-silicium, soit de carbone soit de silicium
H01M 4/13 - Électrodes pour accumulateurs à électrolyte non aqueux, p. ex. pour accumulateurs au lithiumLeurs procédés de fabrication
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
H05K 9/00 - Blindage d'appareils ou de composants contre les champs électriques ou magnétiques
32.
METHOD FOR PRODUCING RECYCLED POSITIVE ELECTRODE ACTIVE MATERIAL
Provided is a method for producing a recycled positive electrode active material including the following steps. Step (1): a step for obtaining a mixture by mixing a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds; step (2): a step for heating the mixture to a temperature equal to or higher than the melting start temperature of the activation treatment agent in the presence of nitrogen and of oxygen having a flow rate of more than 0 L/min and at most 0.600 L/min per 1 L heating space to obtain a heated mixture; and step (3): a step for recovering the heated positive electrode active material from the heated mixture.
This production method for a recycled positive electrode active material includes the following steps: (1) a step in which a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds are mixed to obtain a mixture; (2) a step in which the mixture is heated at a temperature T °C and a heated mixture is obtained; and (3) a step in which the heated mixture is heated at a temperature (1.6×T) °C or higher and the heated positive electrode active material is recovered.
According to the present invention, a method for producing a recycled positive electrode active material includes the following steps. (1) A step of mixing a positive electrode mix containing a positive electrode active material and a carbon-containing material with an activation treatment agent containing one or more alkali metal compounds to obtain a mixture; (2) a step of carrying the mixture into a continuous furnace and heating the mixture by supplying air in a direction perpendicular to the advancing direction of the mixture to obtain a heated mixture; and (3) a step of recovering the heated positive electrode active material from the heated mixture.
A method for producing a recycled positive electrode active material including the following steps. Step (1): A step for obtaining a mixture by mixing a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds; Step (2): A step for heating the mixture to a temperature equal to or higher than the melting start temperature of the activation treatment agent in the presence of oxygen having a flow rate of more than 0 L/min and at most 0.120 L/min per 1 L heating space to obtain a heated mixture; Step (3): A step for recovering the heated positive electrode active material from the heated mixture.
C09D 11/037 - Encres d’imprimerie caractérisées par des particularités autres que la nature chimique du liant caractérisées par le pigment
H10K 30/30 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire comprenant des hétérojonctions de masse, p. ex. des réseaux interpénétrés de domaines de matériaux donneurs et accepteurs
H10K 30/60 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire dans lesquels le rayonnement commande le flux de courant à travers les dispositifs, p. ex. photorésistances
H10K 85/60 - Composés organiques à faible poids moléculaire
37.
ADHESIVE COMPOSITION AND OPTICAL FILM WITH ADHESIVE LAYER
Provided is an adhesive composition which is capable of forming an adhesive layer that has excellent heat resistance durability. This adhesive composition contains a (meth)acrylic resin, a crosslinking agent, a silane compound, and an ionic compound. The (meth)acrylic resin contains, as a monomer unit, an alkyl (meth)acrylate which has a homopolymer glass transition temperature of 30°C or higher. The ionic compound contains an anion that is represented by formula (1). (In formula (1), each of R1to R4 independently represents a hydrogen atom, a halogen atom, an alkyl group which may have a substituent, an alkenyl group which may have a substituent, an alkynyl group which may have a substituent, an aryl group which may have a substituent, or a heterocyclic group which may have a substituent.)
Provided is a method for producing a membrane element that includes a blocking rate adjustment step of adjusting a blocking rate by passing a chemical solution through a primary side channel of a membrane element. When the chemical solution is passed in the blocking rate adjustment step, a pressure difference added to both membrane surfaces of the membrane element is set to be smaller than an osmotic pressure of the chemical solution.
B01D 69/02 - Membranes semi-perméables destinées aux procédés ou aux appareils de séparation, caractérisées par leur forme, leur structure ou leurs propriétésProcédés spécialement adaptés à leur fabrication caractérisées par leurs propriétés
This method for producing an olefin includes a first thermal decomposition step (S12) for thermally decomposing a plastic and obtaining a first product and a second thermal decomposition step (S13) for further thermally decomposing at least a part of the first product. The hydrocarbons contained in the first product satisfy all the following conditions (i) to (iv): (i) the sum of the content of C3 or fewer alkanes and alkenes is 5≤X≤35 (wt%). (ii) The weight-average molecular weight calculated from C1-3 and C10-35 normal alkanes is 95≤Y≤240. (iii) The ratio of the sum of the content of C10-35 normal alkanes to the sum of the contents of C1-3 and C10-35 normal alkanes is 0.30≤Z≤0.93. (iv) The ratio of the content of C1-3 alkanes to the content of C35 normal alkanes is 5≤W≤205.
C08J 11/12 - Récupération ou traitement des résidus des polymères par coupure des chaînes moléculaires des polymères ou rupture des liaisons de réticulation par voie chimique, p. ex. dévulcanisation uniquement par traitement à la chaleur sèche
C10G 1/10 - Production de mélanges liquides d'hydrocarbures à partir de schiste bitumineux, de sable pétrolifère ou de matières carbonées solides non fusibles ou similaires, p. ex. bois, charbon à partir de caoutchouc ou de déchets de caoutchouc
40.
METHOD FOR KNOCKING-IN DESIRED NUCLEOTIDE SEQUENCE, METHOD FOR PRODUCING KNOCK-IN CELL, AND KIT
Provided is a method for inserting a donor sequence into a target region on target DNA, the method including a step in which donor DNA and a site-specific nicking system are brought into contact with the target DNA, wherein: the donor DNA is single-stranded DNA that comprises, from the 5' end, a 5'-end homology arm sequence, the donor sequence, and a 3'-end homology arm sequence in this order; and the site-specific nicking system includes a first fusion protein that includes a first DNA binding domain and an ND1 domain and a second fusion protein that includes a second DNA binding domain and a dND1 domain, wherein the ND1 domain and the dND1 domain together form a dimer to introduce a nick in the target region or in the vicinity of the target region.
The present invention provides: a novel method for producing a 3-phenylcyclohexenone compound having a substituent at the 6-position; and a novel method for producing, by using the same, a derivative of a 3-phenylcyclohexenone compound having a substituent at the 4-position. Provided is a method for producing a compound represented by formula (3), the method comprising a step for mixing a compound represented by formula (1) [in the formula, R1, R2, R3, R4, and R5are the same as or different from each other, and each represent a hydrogen atom or the like, R6represents a C1-C6 chain hydrocarbon group which may be substituted with one phenyl group, R7represents a hydrogen atom or the like, or R6and R7244- or the like] or a salt thereof, a compound represented by formula (2) [in the formula, R8represents a C1-C12 chain hydrocarbon group, and R9represents a hydrogen atom or the like], and an alkali metal carbonate, and reacting these components in the presence of pyrrolidone to obtain a compound represented by formula (3) [in the formula, R1, R2, R3, R4, R5, R8, and R9 have the same meanings as above].
C07C 45/61 - Préparation de composés comportant des groupes C=O liés uniquement à des atomes de carbone ou d'hydrogènePréparation des chélates de ces composés par des réactions ne créant pas de groupe C=O
C07C 49/683 - Composés non saturés comportant un groupe cétone faisant partie d'un cycle contenant des cycles aromatiques à six chaînons avec insaturation autre que celle des cycles aromatiques
C07C 67/30 - Préparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester
C07C 69/157 - Esters d'acide acétique de composés monohydroxylés d'alcools non saturés contenant des cycles aromatiques à six chaînons
C07C 69/736 - Éthers le groupe hydroxyle de l'ester étant éthérifié par un composé hydroxylé dont le groupe hydroxyle est lié à un atome de carbone d'un cycle aromatique à six chaînons
[Problem] The purpose of the present invention is to provide, in the field of foodstuffs, a composition effective for improving fatigue by using a component that can be eaten. [Solution] Provided is a composition for improving the feeling of fatigue, a composition for improving endurance, a composition for improving energy production, a composition for removing active oxygen species, and a composition for an exerciser that all contain Terminalia catappa L. and/or an extract thereof.
A composition having: a themophastic; a first chemical compound having the structure: wherein, each R1, R2, R4, and R51-85-86-127-126-146-14 aryl moiety; each R31-81-8 alkyl moiety; X is a single bond, a sulfur atom, or a CHR6moiety, wherein R61-85-8 2-82-8 alkylene moiety or an *COR7moiety, wherein R71-81-8 alkylene moiety, and wherein the "*" character is used to confirm the positional understanding that the "C" atom in the "*COR71-87-121-81-8 alkyl moiety, and a second chemical compound having the structure: wherein each R1, R2, R3, R4and R510-1812 2 is an integer ranging from 1-1000.
C08L 25/00 - Compositions contenant des homopolymères ou des copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et l'un au moins étant terminé par un cycle carbocyclique aromatiqueCompositions des dérivés de tels polymères
C08K 5/52 - Phosphore lié à l'oxygène lié uniquement à l'oxygène
A composition I contains a polymer B and a compound C. The polymer B is an aliphatic polyester-based polymer. A content of the compound C is 0.01 to 20 parts by mass with respect to 100 parts by mass of a total of the polymer B and the compound C. The compound C satisfies the following requirement 1:
requirement 1: when a melt mass flow rate of the polymer B as measured under conditions of a temperature of 210° C. and a load of 2.16 kgf is designated as MFR (B), and
a melt mass flow rate of a mixture X containing 0.5 parts by mass of the compound C with respect to 100 parts by mass of the total of the polymer B and the compound C as measured under conditions of a temperature of 210° C. and a load of 2.16 kgf is designated as MFR (X), MFR (X)/MFR (B) is 2.0 or less.
The present invention provides a method for controlling a plant disease which comprises applying a compound represented by formula (I) [wherein n is 0, 1, or 2, R1 represents a C1-C6 alkyl group etc., R2 and R3 are identical to or different from each other, and each represents a C1-C6 chain hydrocarbon group which may be optionally substituted with one or more halogen atoms, etc., R4 represents a C1-C6 chain hydrocarbon group, etc., q is 1, 2, or 3, and when q is 2 or 3, 2 or 3 of R4 are identical to or different from each other, a combination of X1, X2, X3, and X4 represents a combination wherein X1 represents CR5, X2 represents CR6, X3 represents CR7, and X4 represents a nitrogen atom, etc., and R5, R6, and R7 are identical to or different from each other, and each represents a C1-C6 chain hydrocarbon group which may be optionally substituted with one or more halogen atoms, etc.], or the N-oxide thereof, or the salt thereof to a plant or soil for cultivating the plant, which has excellent control efficacies against plant diseases.
The present invention provides a method for controlling a plant disease which comprises applying a compound represented by formula (I) [wherein n is 0, 1, or 2, R1 represents a C1-C6 alkyl group etc., R2 and R3 are identical to or different from each other, and each represents a C1-C6 chain hydrocarbon group which may be optionally substituted with one or more halogen atoms, etc., R4 represents a C1-C6 chain hydrocarbon group, etc., q is 1, 2, or 3, and when q is 2 or 3, 2 or 3 of R4 are identical to or different from each other, a combination of X1, X2, X3, and X4 represents a combination wherein X1 represents CR5, X2 represents CR6, X3 represents CR7, and X4 represents a nitrogen atom, etc., and R5, R6, and R7 are identical to or different from each other, and each represents a C1-C6 chain hydrocarbon group which may be optionally substituted with one or more halogen atoms, etc.], or the N-oxide thereof, or the salt thereof to a plant or soil for cultivating the plant, which has excellent control efficacies against plant diseases.
A01N 43/40 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec un atome d'azote comme unique hétéro-atome du cycle des cycles à six chaînons
This device comprises: an acquiring unit that acquires a spectroscopic image generated by causing an imaging signal obtained by imaging an object to spectrally diffract; a feature calculating unit that calculates a feature representing a texture on the basis of the spectroscopic image; and a predicting unit that inputs, into a trained model that has been trained using training data including the feature calculated for objects for learning and data representing the state of a microorganism included in the objects for learning, the feature calculated for an object for prediction, to predict data representing the state of a microorganism contained in the object for prediction.
G01N 21/27 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes en utilisant la détection photo-électrique
C12M 1/34 - Mesure ou test par des moyens de mesure ou de détection des conditions du milieu, p. ex. par des compteurs de colonies
According to the present invention, a method for producing a recycled positive electrode active material includes the following steps. (1) A step of mixing a positive electrode mix containing a positive electrode active material and a carbon-containing material with an activation treatment agent containing one or more alkali metal compounds to obtain a mixture; (2) a step of carrying the mixture into a continuous furnace and heating the mixture by supplying air in a direction opposite to the advancing direction of the mixture to obtain a heated mixture; and (3) a step of recovering the heated positive electrode active material from the heated mixture.
A method for producing a recycled positive electrode active material including the following steps. Step (1): A step for obtaining a mixture by mixing a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds; Step (2): A step for heating the mixture to a temperature equal to or higher than the melting start temperature of the activation treatment agent in the presence of nitrogen having a flow rate of more than 0 L/min and at most 0.400 L/min per 1 L heating space to obtain a heated mixture; Step (3): A step for recovering the heated positive electrode active material from the heated mixture.
This production method for a recycled positive electrode active material includes the following steps: (1) a step for mixing a positive electrode mixture that contains a positive electrode active material and a carbon-containing material, and an activation treatment agent that contains one type or two or more types of alkali compounds, thereby obtaining a mixture; (2) a step for bringing the mixture into a heating furnace, heating the mixture, and removing, from the heating furnace, carbon dioxide generated by heating the carbon-containing material, thereby obtaining a mixture after heating; and (3) a step for recovering, from the mixture after heating, a positive electrode active material after heating.
Provided is a method for producing a recycled positive electrode active material including the following steps. Step (1): a step for obtaining a mixture by mixing a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds; step (2): a step for heating the mixture to a temperature equal to or higher than the melting start temperature of the activation treatment agent in the presence of oxygen having a flow rate equal to or higher than 0.020 L/min per 1 L heating space to obtain a heated mixture; and step (3): a step for recovering the heated positive electrode active material from the heated mixture.
Provided is a method for producing a recycled positive electrode active material including the following steps. Step (1): a step for obtaining a mixture by mixing a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds; step (2): a step for heating the mixture to a temperature equal to or higher than the melting start temperature of the activation treatment agent in the presence of nitrogen having a flow rate equal to or higher than 0.070 L/min per 1 L heating space to obtain a heated mixture; and step (3): a step for recovering the heated positive electrode active material from the heated mixture.
This method of producing a recycled cathode active substance powder includes: a step (1) of mixing, into a cathode composite containing cathode active substance powder and a carbon-containing material, an activating agent to obtain a mixture; a step (2) of heating the mixture to obtain a post-heating mixture containing post-heating cathode active substance powder; and a step (3) of removing components apart from the post-heating cathode active substance powder from the post-heating mixture. The step (3) includes: a sub-step (A1) of bringing a liquid that contains water into contact with the post-heating mixture or the mixture resulting from the partial component removal, so as to obtain a slurry S1 containing the post-heating cathode active substance powder; a sub-step (A2) of wet-classifying, within the slurry S1, the post-heating cathode active substance powder so as to obtain a slurry S2 containing the post-heating cathode active substance powder having a relatively small average particle size, and a slurry S3 containing the post-heating cathode active substance powder having a relatively large average particle size; and a sub-step (A3) of subjecting the slurry S3 to solid/liquid separation.
This method for producing a recycled positive electrode active material involves the following steps: (1) a step for mixing a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds to obtain a mixture; (2) a step for heating the mixture to obtain a heated mixture; (3) a step for bringing the heated mixture into contact with a first liquid containing water and an alkali metal compound to obtain a first solid component and a first liquid component; (4) a step for bringing the first solid component into contact with a second liquid containing water and containing an alkali metal compound at an amount smaller than that in the first liquid to obtain a second solid component and a second liquid component; and (5) a step for recovering a recycled positive electrode active material from the second solid component.
According to the present invention, a method for producing a recycled positive electrode active material includes the following steps. (1) A step of mixing a positive electrode mix containing a positive electrode active material and a carbon-containing material with an activation treatment agent containing one or more alkali metal compounds to obtain a mixture; (2) a step of heating the mixture in a heating space having a high-temperature region and a low-temperature region having a temperature lower than that of the high-temperature region, and having a carbon dioxide concentration in the high-temperature region lower than the carbon dioxide concentration in the low-temperature region, to obtain a heated mixture; and (3) a step of recovering the heated positive electrode active material from the heated mixture.
A method for producing a recycled positive electrode active material including the following steps. Step (1): A step for obtaining a mixture by mixing a positive electrode mixture containing a positive electrode active material and an activation treatment agent containing one or more alkali metal compounds; Step (2): A step for heating the mixture to a temperature equal to or higher than the melting start temperature of the activation treatment agent in the presence of oxygen and nitrogen having a total flow rate of at least 0.100 L/min per 1 L heating space to obtain a heated mixture; Step (3): A step for recovering the heated positive electrode active material from the heated mixture.
This production method for a recycled positive electrode active material includes the following steps: (1) a step in which a positive electrode mixture containing a positive electrode active material and a carbon-containing material and an activation treatment agent containing one or more alkali metal compounds are mixed to obtain a mixture; (2) a step in which the mixture is heated at a temperature lower than the melting onset temperature of the activation treatment agent and a heated mixture is obtained; and (3) a step in which the heated positive electrode active material is recovered from the heated mixture.
The present disclosure provides a quasi-solid electrolyte composition comprising: an electrolytic solution that contains an alkali metal salt and an organic solvent; and a porous material. In a quasi-solid electrolyte, the content of the alkali metal salt is 11 mol% or more based on the sum of substance amounts of the alkali metal salt and the organic solvent. The pore size of the porous material is 7-13 Å. The content of the porous material is 20-33 mass% with respect to the total amount of the quasi-solid electrolyte composition.
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01M 10/054 - Accumulateurs à insertion ou intercalation de métaux autres que le lithium, p. ex. au magnésium ou à l'aluminium
H01M 10/056 - Accumulateurs à électrolyte non aqueux caractérisés par les matériaux utilisés comme électrolytes, p. ex. électrolytes mixtes inorganiques/organiques
[Problem] To provide an adhesive composition with which it is possible to form an adhesive layer that is excellent in terms of refractive index and high-temperature adhesiveness durability. [Solution] The present invention provides an adhesive composition which contains a (meth)acrylic polymer that has a constituent unit derived from a hydroxyl group-containing (meth)acrylic monomer and a constituent unit derived from a transition metal element-containing (meth)acrylic monomer. It is preferable that the content of the constituent unit derived from the hydroxyl group-containing (meth)acrylic monomer is 0.8 mass% to 15 mass% inclusive with respect to all constituent units that constitute the (meth)acrylic polymer. [Selected drawing] None
Provided is an adhesive composition from which an adhesive layer having excellent heat-resistant durability can be formed. This adhesive composition comprises a (meth)acrylic resin, a crosslinking agent, a silane compound, and an ionic compound, wherein: the (meth)acrylic resin contains, as monomer units, an alkyl (meth)acrylate having a homopolymer glass transition temperature of lower than 0ºC, an alkyl (meth)acrylate having a homopolymer glass transition temperature of at least 0ºC, and a monomer having a polar group; and the ionic compound contains a cyano group-containing anion.
The present invention provides an adhesive composition which is capable of forming an adhesive layer that is excellent in terms of both easy reworkability immediately after bonding and easy reworkability after being held in a high temperature environment after bonding. The present invention specifically provides an adhesive composition which contains a (meth)acrylic resin, a crosslinking agent, and a silane compound, wherein: the (meth)acrylic resin contains, as monomer units, an alkyl (meth)acrylate that has a homopolymer glass transition temperature of less than 0°C, an alkyl (meth)acrylate that has a homopolymer glass transition temperature of 0°C or higher, and a monomer that has a polar group; and the silane compound contains at least one of a compound represented by formula (1-1) and a compound represented by formula (1-2), and a compound represented by formula (2).
The present disclosure relates to the sufficient suppression of electrostatic charging of an adhesive layer, and to the suppression of corrosion of a metal layer when the adhesive layer is laminated onto the metal layer. The adhesive composition contains a (meth)acrylic resin and an ionic compound. The (meth)acrylic resin is a copolymer that contains a monomer unit derived from an alkoxyalkyl (meth)acrylate at a percentage of 1 mass% to 40 mass% with respect to the total amount of monomer units constituting the (meth)acrylic resin. The ionic compound has an anion having a pentafluorophenyl group and a cation.
C09J 133/00 - Adhésifs à base d'homopolymères ou de copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et l'un au moins étant terminé par un seul radical carboxyle, ou ses sels, anhydrides, esters, amides, imides ou nitrilesAdhésifs à base de dérivés de tels polymères
B32B 15/082 - Produits stratifiés composés essentiellement de métal comprenant un métal comme seul composant ou comme composant principal d'une couche adjacente à une autre couche d'une substance spécifique de résine synthétique comprenant des résines vinyliquesProduits stratifiés composés essentiellement de métal comprenant un métal comme seul composant ou comme composant principal d'une couche adjacente à une autre couche d'une substance spécifique de résine synthétique comprenant des résines acryliques
B32B 27/00 - Produits stratifiés composés essentiellement de résine synthétique
B32B 27/30 - Produits stratifiés composés essentiellement de résine synthétique comprenant une résine vinyliqueProduits stratifiés composés essentiellement de résine synthétique comprenant une résine acrylique
G09F 9/00 - Dispositifs d'affichage d'information variable, dans lesquels l'information est formée sur un support, par sélection ou combinaison d'éléments individuels
H10K 50/86 - Dispositions pour améliorer le contraste, p. ex. en empêchant la réflexion de la lumière ambiante
The present invention provides a technique for detecting chemical substances in a body fluid with higher sensitivity. This sample derived from a body fluid is characterized in that the concentration of free divalent cations is higher than the concentration in the body fluid.
The present invention provides a resin composition having excellent spinnability and dyeability. Provided is a resin composition comprising a propylene-based polymer A, an ester-based polymer B, and a compound C, wherein: the propylene-based polymer A has a Z-average molecular weight (Mz) of 600,000-750,000; the ester-based polymer B has (i) a heat of fusion of not less than 0 J/g but less than 35 J/g as obtained by differential scanning calorimetry and (ii) a limiting viscosity (IV) of 0.40-1.00 dl/g as measured in a liquid mixture of tetrachloroethane and phenol at 20°C; and the compound C has at least one group selected from the group consisting of heterocyclic groups having two or more heteroatoms, cyclic ether groups, acid anhydride groups, isocyanate groups, and carbodiimide groups.
C08L 23/10 - Homopolymères ou copolymères du propylène
C08L 67/00 - Compositions contenant des polyesters obtenus par des réactions créant une liaison ester carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
D01F 6/46 - Filaments, ou similaires, faits par l’homme, à un seul composant, formés de polymères synthétiquesLeur fabrication à partir de mélanges de polymères obtenus par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carbone comme constituant majeur avec d'autres polymères ou des composés de bas poids moléculaire de polyoléfines
A method of forming a product comprising a first component, a second component and a thermal transfer layer disposed between the first component and second component wherein the thermal transfer layer comprises a conjugated polymer; the thermal transfer layer is electrically insulating; and formation of the thermal transfer layer comprises application of a formulation comprising the conjugated polymer in dissolved form onto a surface of the first component or the second component.
C08G 69/32 - Polyamides dérivés, soit des acides amino-carboxyliques, soit de polyamines et d'acides polycarboxyliques dérivés de polyamines et d'acides polycarboxyliques à partir de diamines aromatiques et d'acides aromatiques dicarboxyliques avec des groupes amino et carboxylique liés tous deux aromatiquement
C09D 177/06 - Polyamides dérivés de polyamines et d'acides polycarboxyliques
H01L 23/29 - Encapsulations, p. ex. couches d’encapsulation, revêtements caractérisées par le matériau
H01L 23/373 - Refroidissement facilité par l'emploi de matériaux particuliers pour le dispositif
A composition contains 98.9 to 39.9 parts by mass of an olefin-based polymer A, 1 to 60 parts by mass of a fiber B, and 0.1 to 30 parts by mass of a polyhydroxyalkanoate-based polymer D. In the composition, the total amount of the olefin-based polymer A, the fiber B, and the polyhydroxyalkanoate-based polymer D is 100 parts by mass.
The present disclosure provides a battery comprising: a positive electrode having a porous structure; a negative electrode; and a quasi-solid electrolyte disposed between the positive electrode and the negative electrode, wherein the positive electrode contains a first polymer and a conductive auxiliary agent, the proportion of holes having a pore diameter of 0.1-100 μm to all holes, as measured by a mercury intrusion method, is at least 23%, and the quasi-solid electrolyte contains a second polymer having a polar functional group, an ionic compound, and particles.
The present disclosure provides a laminated separator for a nonaqueous electrolyte secondary battery which makes it possible to obtain a battery having an excellent rate characteristic and which has excellent heat resistance, the laminated separator including a polyolefin-based substrate, a heat-resistant layer that is provided on one surface or both surfaces of the polyolefin-based substrate, and a particle layer which is provided on at least one side of the laminated separator, a standard deviation of an IR peak intensity ratio (peak intensity which is of a resin contained in the particle layer and which is in an infrared absorption spectrum/peak intensity which is of a resin contained in the heat-resistant layer and which is in an infrared absorption spectrum) on a surface of the laminated separator which surface is located on the at least one side on which the particle layer is provided being not more than 0.025.
A compound of formula (I):
A compound of formula (I):
R1 in each occurrence is independently a substituent; R2 in each occurrence is H or substituent; R3-R6 are each independently in each occurrence H or a halogen; X in each occurrence is independently selected from is O, S and NR3 wherein R3 is H or a substituent; Y in each occurrence is independently O or S; B1 independently in each occurrence is a bridging group; and z in each occurrence is independently 0, 1, 2 or 3. The compound of formula (I) may be used as an electron-accepting material of an organic photoresponsive device.
C07D 495/22 - Composés hétérocycliques contenant dans le système condensé au moins un hétérocycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle dans lesquels le système condensé contient au moins quatre hétérocycles
H10K 50/814 - Anodes combinées à des électrodes auxiliaires, p. ex. une couche d'ITO combinée à des lignes métalliques
A heat medium storage apparatus 10 including a heat medium tank defining an airtight inside space 22 and a preheating device 30 including a temperature adjusting portion 32 capable of melting the heat medium in solid form, wherein the temperature adjusting portion has a first part 32a and a second part 32b, when the temperature adjusting portion is provided so as to extend in the inside space, the first part is in contact with the heat medium so as to be covered with the heat medium, and the second part is provided so as to protrude into a gap area in which the heat medium is absent in the inside space and thereby the second part is exposed, and when the temperature adjusting portion is provided so as to extend in contact with the outer surface of the heat medium tank, the temperature adjusting portion extends in a contact manner so as to stretch from a first area corresponding to an area in contact with the heat medium in the inside space to a second area corresponding to an area not in contact with the heat medium in the inside space, the areas forming the outer surface of the heat medium tank, the first part being in contact with the first area, the second part being in contact with the second area.
F28D 20/00 - Appareils ou ensembles fonctionnels d'accumulation de chaleur en généralAppareils échangeurs de chaleur de régénération non couverts par les groupes ou
F28D 1/06 - Appareils échangeurs de chaleur comportant des ensembles de canalisations fixes pour une seule des sources de potentiel calorifique, les deux sources étant en contact chacune avec un côté de la paroi de la canalisation, dans lesquels l'autre source de potentiel calorifique est une grande masse de fluide, p. ex. radiateurs domestiques ou de moteur de voiture avec canalisations d'échange de chaleur faisant partie du réservoir contenant la masse du fluide ou lui étant fixées
F28D 7/08 - Appareils échangeurs de chaleur comportant des ensembles de canalisations tubulaires fixes pour les deux sources de potentiel calorifique, ces sources étant en contact chacune avec un côté de la paroi d'une canalisation les canalisations ayant une autre courbure, p. ex. en serpentins ou en zigzag
A separation membrane element includes: a container; and a separation membrane including a region provided in a flat membrane shape in the container. The separation membrane includes a separation functional layer that selectively separates a specific fluid component contained in a raw material fluid. The container houses a laminate that includes (i) two permeate-side spacer members through which a permeate fluid that has permeated through the separation membrane flows, (ii) the separation membrane provided between the two permeate-side spacer members, and (iii) a feed-side spacer member through which the raw material fluid flows. The separation membrane element includes a sealing part for preventing a fluid flowing through the feed-side spacer member and a fluid flowing through the two permeate-side spacer members from being mixed with each other.
This aromatic polysulfone includes a repeating unit S1 derived from a compound represented by formula (S1), and a repeating unit S2 represented by formula (S2), wherein the repeating unit S1 content relative to all repeating units of the aromatic polysulfone is greater than or equal to 0.10 mol% and less than 1.50 mol%. (In formula (S1), R1, R2, and R3each independently represent a hydrogen atom or a methyl group. In formula (S2), R5and R6each independently represent a halogen atom, a phenyl group, a C1-6 alkyl group, or a C2-10 alkenyl group, m and n each independently represent an integer from 0 to 4, and when there are a plurality of R5or R6, these may be the same or different.)
C08G 65/40 - Composés macromoléculaires obtenus par des réactions créant une liaison éther dans la chaîne principale de la macromolécule à partir de composés hydroxylés ou de leurs dérivés métalliques dérivés des phénols à partir des phénols et d'autres composés
This aromatic polysulfone comprises a repeating unit S1 represented by formula (S1) and a repeating unit S2 represented by formula (S2). In formula (S1), R1and R2each independently represent a hydrogen atom or an alkyl group. In formula (S2): R5and R6each independently represent a halogen atom, a phenyl group, an alkyl group having 1-6 carbon atoms, or an alkenyl group having 2-10 carbon atoms; m and n each independently represent an integer of 0-4; and when there are multiple R5s or R6s, these moieties may be the same or different.
C08G 65/40 - Composés macromoléculaires obtenus par des réactions créant une liaison éther dans la chaîne principale de la macromolécule à partir de composés hydroxylés ou de leurs dérivés métalliques dérivés des phénols à partir des phénols et d'autres composés
73.
SOLID ELECTROLYTE MATERIAL, ELECTRODE, AND LITHIUM ION SECONDARY BATTERY
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/08 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques oxydes
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
The present invention provides a compound that has high heat resistance and can be used for processing of an organic material, which requires a high processing temperature. Disclosed is a diphosphite-based compound which is represented by formula (I) (wherein R1represents an alkyl group having 1-12 carbon atoms, a cycloalkyl group having 5-8 carbon atoms, an alkylcycloalkyl group having 6-12 carbon atoms, or an aralkyl group having 7-25 carbon atoms; R2represents an alkyl group having 1-12 carbon atoms, a cycloalkyl group having 5-8 carbon atoms, an alkylcycloalkyl group having 6-12 carbon atoms, or an aralkyl group having 7-12 carbon atoms; R3 represents a hydrogen atom, an alkyl group having 1-12 carbon atoms, a cycloalkyl group having 5-8 carbon atoms, an alkylcycloalkyl group having 6-12 carbon atoms, or an aralkyl group having 7-25 carbon atoms; and X represents a single bond, an alkylidene group having 1-4 carbon atoms, a sulfur atom, or an oxygen atom).
C07F 9/6578 - Composés hétérocycliques, p. ex. contenant du phosphore comme hétéro-atome du cycle comportant des atomes de phosphore, avec ou sans atomes d'azote, d'oxygène, de soufre, de sélénium ou de tellure, comme hétéro-atomes du cycle comportant des atomes de phosphore et de soufre, avec ou sans atomes d'oxygène, comme hétéro-atomes du cycle
C08K 5/524 - Esters des acides phosphoreux, p. ex. de H3PO3
C08L 23/00 - Compositions contenant des homopolymères ou des copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carboneCompositions contenant des dérivés de tels polymères
C08L 67/00 - Compositions contenant des polyesters obtenus par des réactions créant une liaison ester carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C08L 69/00 - Compositions contenant des polycarbonatesCompositions contenant des dérivés des polycarbonates
C08L 77/00 - Compositions contenant des polyamides obtenus par des réactions créant une liaison amide carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C08L 101/00 - Compositions contenant des composés macromoléculaires non spécifiés
A compound of formula (I) or (II), wherein: A1is a divalent heteroaromatic electron-accepting group; A2and A3independently in each occurrence is a monovalent electron-accepting group; D1, D2and D3independently in each occurrence is an electron-donating group; B1, B2, and B3independently in each occurrence is a bridging group; x1and x2are each independently 0, 1, 2 or 3; x3and x4are each independently 0, 1, 2 or 3; y1, y2and y3are each independently at least 1; z1and z2are each independently 0, 1, 2 or 3; and wherein at least one occurrence of D1of formula (I) or at least one occurrence of at least one of D2and D3of formula (II) is a group of formula (III), wherein: X1and X2are each independently selected from is O, S and NR1wherein R1is H or a substituent, with the proviso that at least one of X1and X2is NR1; Y is O or S; Ar1and Ar2are each independently is a monocyclic or fused aromatic or heteroaromatic group or is absent; R1is H or a substituent; and R2 in each occurrence is independently a substituent.
C07D 301/19 - Synthèse du cycle de l'oxirane par oxydation de composés non saturés, ou de mélanges de composés non saturés et de composés saturés par des hydroperoxydes organiques
KANAGAWA INSTITUTE OF INDUSTRIAL SCIENCE AND TECHNOLOGY (Japon)
SUMITOMO CHEMICAL COMPANY, LIMITED (Japon)
Inventeur(s)
Azuma Masaki
Shigematsu Kei
Yoshikawa Kota
Nakayama Hajime
Kaneko Satoru
Yasui Manabu
Kurouchi Masahito
Abrégé
This method for forming a composite oxide pattern includes: a first step of forming, on a substrate 10, a resist film 20 containing hydrogen silsesquioxane (HSQ); a second step of exposing the resist film 20 by using energy rays; a third step of developing the resist film 20 to form a mask 22; a fourth step of depositing a composite-oxide thin film 30 on the mask 22; and a fifth step of removing the mask 22.
H01L 21/363 - Dépôt de matériaux semi-conducteurs sur un substrat, p. ex. croissance épitaxiale en utilisant un dépôt physique, p. ex. dépôt sous vide, pulvérisation
222 selectivity without being combined with other components. A gas separation membrane according to the present disclosure comprises a separation function layer containing a copolymer, wherein either the copolymer contains an ethylene oxide structure and a propylene oxide structure, the weight-average molecular weight of the copolymer being 13,000 or greater, or the copolymer is a random copolymer.
B01D 53/22 - Séparation de gaz ou de vapeursRécupération de vapeurs de solvants volatils dans les gazÉpuration chimique ou biologique des gaz résiduaires, p. ex. gaz d'échappement des moteurs à combustion, fumées, vapeurs, gaz de combustion ou aérosols par diffusion
B01D 69/10 - Membranes sur supportSupports pour membranes
The present invention provides a negative electrode, for a lithium secondary battery, in which a negative electrode active material layer is formed on a current collector, wherein a negative electrode active material includes a phosphorus-carbon composite negative electrode material containing phosphorus atoms and carbon atoms, and the negative electrode active material layer has an area ratio of 0.05-12% of black portions with respect to the entirety of a binary image acquired through the following method. [Binary image acquisition method] A surface of the negative electrode active material layer is imaged by a scanning electron microscope at an imaging magnification of 40 times to obtain a negative electrode surface image. The negative electrode surface image is subjected to adaptive binarization processing to acquire a binary image.
H01M 4/58 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de composés inorganiques autres que les oxydes ou les hydroxydes, p. ex. sulfures, séléniures, tellurures, halogénures ou LiCoFyEmploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de structures polyanioniques, p. ex. phosphates, silicates ou borates
H01M 4/136 - Électrodes à base de composés inorganiques autres que les oxydes ou les hydroxydes, p. ex. sulfures, séléniures, tellurures, halogénures ou LiCoFy
H01M 4/36 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs
The present invention addresses the problem of providing a method for improving photocatalytic performance by using a ferrite material having an easily available element constitution. The problem is solved by using, as a photocatalyst, ferrite particles having a spinel-type crystal structure, a hexagonal crystal structure, or a garnet-type crystal structure in a magnetic field.
1−xx2212−y−δyδ2222. X is at least one element selected from the group consisting of Cr, Sb, In, and V. The relationship 0 ≤ x ≤ 1 is satisfied. The relationships 0 < y ≤ 2 and 0 ≤ δ ≤ 1, or 0 ≤ y ≤ 2 and 0 < δ ≤ 1, are satisfied. The film has a film thickness of at least 1.0 nm and less than 70 μm.
The present disclosure provides an electrolyte composition which contains a polymer, an organic solvent, and particles, wherein the polymer has a side group that comprises one or more groups selected from the group consisting of an alkali metallized phenolic group, an alkali metallized carboxylic acid group, an alkali metallized sulfonic acid group, and an alkali metallized sulfonyl imide group.
C08L 101/06 - Compositions contenant des composés macromoléculaires non spécifiés caractérisées par la présence de groupes déterminés contenant des atomes d'oxygène
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01M 4/13 - Électrodes pour accumulateurs à électrolyte non aqueux, p. ex. pour accumulateurs au lithiumLeurs procédés de fabrication
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
There is provided a diamond film-deposited substrate, including: a substrate comprising niobium metal; a niobium carbide layer on at least one main surface of the substrate; and a conductive diamond film on the niobium carbide layer,
There is provided a diamond film-deposited substrate, including: a substrate comprising niobium metal; a niobium carbide layer on at least one main surface of the substrate; and a conductive diamond film on the niobium carbide layer,
wherein when a surface of the conductive diamond film was observed using a scanning electron microscope, no pinholes reaching the substrate or the niobium carbide layer are present within a field of view of 20 μm×20 μm.
C23C 28/00 - Revêtement pour obtenir au moins deux couches superposées, soit par des procédés non prévus dans un seul des groupes principaux , soit par des combinaisons de procédés prévus dans les sous-classes et
C30B 28/14 - Production de matériaux polycristallins homogènes de structure déterminée directement à partir de l'état gazeux par réaction chimique de gaz réactifs
A composition having: a thermoplastic; a first chemical compound having the structure: (I) wherein, each R1, R2, R4, and R31-85-86-127-126- 146- 14 aryl moiety; each R31-81-8 alkyl moiety; X is a single bond, a sulfur atom, or a CHR6moiety, wherein R61-8 5-82-82-8 alkylene moiety or an *COR7moiety, wherein R71-81-8 alkylene moiety, and wherein the "*" character is used to confirm the positional understanding that the "C" atom in the "*COR71-87-121-812062062020 alkylaryl moiety, a methyl moiety, a tertiary butyl moiety, a cumyl moiety, or a hydrogen atom.
C08L 85/02 - Compositions contenant des composés macromoléculaires obtenus par des réactions créant dans la chaîne principale de la macromolécule une liaison contenant des atomes autres que le silicium, le soufre, l'azote, l'oxygène et le carboneCompositions contenant des dérivés de tels polymères contenant du phosphore
Provided is a propylene-based polymer composition which is capable of reducing odor that may occur when exposed to high temperatures in the interior of a vehicle. Specifically provided is a propylene-based polymer composition which contains a propylene-based polymer and talc, wherein: if the total of the content of the propylene-based polymer and the content of the talc is taken as 100 parts by mass, the content of the propylene-based polymer is 98.5 parts by mass to 55 parts by mass, and the content of the talc is 1.5 parts by mass to 45 parts by mass; the average particle diameter of the talc is 2 μm to 13 μm as measured by a wet laser diffraction method; and the first heating loss in the range of 450°C to 590°C in a differential curve obtained by differential thermogravimetric measurement (DTG) using 10 mg of the talc that is extracted from the propylene-based polymer composition is 60 μg or more and less than 230 μg, and the second heating loss in the range of 620°C to 730°C is more than 0 μg and less than 300 μg.
Disclosed is a kit for detecting a detection target substance, said kit comprising: a plasmon resonance chip; a first protein that specifically binds to the detection target substance; and a second protein that specifically binds to the detection target substance, wherein the plasmon resonance chip is provided with a substrate, a metallic particle aggregate layer that is formed on the substrate, and a protective layer that covers the metallic particle aggregate layer. Also disclosed is a detection method for a detection target substance which uses said kit.
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
This resin composition contains amorphous particles having an aspect ratio of less than 0.90, spherical particles having an aspect ratio of 0.90 or greater, and a resin. On an SEM image of a cross-section of the resin composition imaged at a magnification of 250x, three straight lines parallel to each other each having a length of 500 μm are drawn. In the amorphous particles overlapping at least one of the straight lines and having an overlapping length of 8 μm or greater, the total length X2 obtained by summing the overlapping lengths of 8 μm or greater exceeds 30.0% of the total length X1 of the straight lines.
This resin composition comprises inorganic particles and a resin, wherein the content of the inorganic particles is 55% by volume or more, with the total content of the inorganic particles and the resin taken as 100% by volume; the inorganic particles include amorphous particles, which are particles having an aspect ratio of less than 0.90, and spherical particles, which are particles having an aspect ratio of 0.90 or more; and the cumulative 50% particle diameter D50 from the fine particle side in the volume-based cumulative particle size distribution of the amorphous particles is more than 15 μm.
A photoelectric conversion element includes a pair of electrodes; an active layer provided between the pair of electrodes and including a p-type semiconductor (P); and a buffer layer provided between one of the pair of electrodes and the active layer and including a dielectric (D), in which the dielectric (D) has a band gap of 4 eV or more and a relative permittivity of 20 or more, and the photoelectric conversion element satisfies the following Expression (1).
A photoelectric conversion element includes a pair of electrodes; an active layer provided between the pair of electrodes and including a p-type semiconductor (P); and a buffer layer provided between one of the pair of electrodes and the active layer and including a dielectric (D), in which the dielectric (D) has a band gap of 4 eV or more and a relative permittivity of 20 or more, and the photoelectric conversion element satisfies the following Expression (1).
Ec
-
E
(
L
)
>
0.8
eV
(
1
)
A photoelectric conversion element includes a pair of electrodes; an active layer provided between the pair of electrodes and including a p-type semiconductor (P); and a buffer layer provided between one of the pair of electrodes and the active layer and including a dielectric (D), in which the dielectric (D) has a band gap of 4 eV or more and a relative permittivity of 20 or more, and the photoelectric conversion element satisfies the following Expression (1).
Ec
-
E
(
L
)
>
0.8
eV
(
1
)
In Expression (1), Ec represents an energy level at a lower end of a conduction band of the dielectric (D), and E(L) represents a LUMO energy level of the p-type semiconductor (P).
H10K 30/15 - Dispositifs à semi-conducteurs sensibilisés à large bande interdite, p. ex. TiO2sensibilisé aux colorants
H10K 30/60 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire dans lesquels le rayonnement commande le flux de courant à travers les dispositifs, p. ex. photorésistances
H10K 39/34 - Capteurs d'images organiques intégrés avec des diodes électroluminescentes organiques [OLED]
H10K 85/20 - Composés de carbone, p. ex. nanotubes de carbone ou fullerènes
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
The present disclosure relates to a molding raw material that contains a liquid crystal polyester and in which the full width at half maximum of a peak having a peak top at a diffraction angle 2θ=17° to 22° in the X-ray diffraction spectrum is from 5.00° to 9.00°. The present disclosure also relates to a film which is a molded article of the molding raw material.
C08G 63/60 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés dérivés de la réaction d'un mélange d'acides hydroxycarboxyliques, d'acides polycarboxyliques et de composés polyhydroxylés
A resin composition containing inorganic particles and a resin, wherein the ratio of the viscosity at a shear rate of 1/s with respect to the viscosity at a shear rate of 17.8/s at a temperature of 25°C is greater than 1.3.
This inorganic powder includes amorphous particles with an aspect ratio of less than 0.90, and spherical particles with an aspect ratio of 0.90 or more, and has an angle of repose of between 33° and 56° (non-inclusive).
Provided is an inorganic powder that contains amorphous particles having an aspect ratio of less than 0.90 and spherical particles having an aspect ratio of 0.90 or more, and that has a compressibility of more than 15.1% and no more than 60.0%.
A method for controlling weeds including a step of performing a spot treatment of at least one anionic herbicide selected from the group consisting of dicamba or salts thereof and 2,4-D or salts or esters in a cultivation area of soybean, corn, or cotton. The method provides an excellent control effect in weed control.
A01N 57/20 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques du phosphore comportant des liaisons phosphore-carbone contenant des radicaux acycliques ou cycloaliphatiques
A01N 37/40 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone possédant trois liaisons à des hétéro-atomes, avec au plus deux liaisons à un halogène, p. ex. acides carboxyliques contenant au moins un groupe carboxylique ou un thio-analogue, ou d'un de leurs dérivés, et un atome d'oxygène ou de soufre lié par une liaison simple, liés au même squelette carboné, cet atome d'oxygène ou de soufre ne faisant pas partie d'un groupe carboxylique ou d'un thio-analogue, ou d'une de leurs dérivés, p. ex. acides hydroxycarboxyliques contenant au moins un atome d'oxygène ou de soufre lié à un système cyclique aromatique contenant au moins un groupe carboxylique ou un thio-analogue, ou un de leurs dérivés, et un atome d'oxygène ou de soufre liés au même système cyclique aromatique
The present invention provides a new method for producing a 3-hydroxybiphenyl compound and a new method for producing a derivative of a 3-hydroxybiphenyl compound using the same. Specifically, the present invention provides a method for producing a compound represented by formula (3), the method comprising a step for obtaining the compound represented by formula (3) by reacting, in a solvent and under the presence of a base, a compound represented by formula (1) [in the formula, R1and R22a22222- through binding between R1and R2, and a represents 4 or 5] or a salt thereof with a compound represented by formula (2) [in the formula, R3represents a C1-C6 chain hydrocarbon group, a chlorine atom, or a hydrogen atom, and X1 represents a chlorine atom, a bromine atom, or an iodine atom].
C07C 37/20 - Préparation de composés comportant des groupes hydroxyle ou O-métal liés à un atome de carbone d'un cycle aromatique à six chaînons par des réactions augmentant le nombre d'atomes de carbone au moyen d'aldéhydes ou de cétones
C07C 39/15 - Composés comportant au moins un groupe hydroxyle ou O-métal lié à un atome de carbone d'un cycle aromatique à six chaînons polycycliques sans autre insaturation que celle des cycles aromatiques tous les groupes hydroxyle étant liés à des cycles non condensés
C07C 67/31 - Préparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par introduction de groupes fonctionnels avec de l'oxygène lié uniquement par liaison simple
C07C 67/343 - Préparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par isomérisationPréparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par modification de la taille du squelette carboné par augmentation du nombre d'atomes de carbone
C07C 69/712 - Éthers le groupe hydroxyle de l'ester étant éthérifié par un composé hydroxylé dont le groupe hydroxyle est lié à un atome de carbone d'un cycle aromatique à six chaînons
C07C 69/736 - Éthers le groupe hydroxyle de l'ester étant éthérifié par un composé hydroxylé dont le groupe hydroxyle est lié à un atome de carbone d'un cycle aromatique à six chaînons
98.
GALLIUM NITRIDE SINGLE CRYSTAL SUBSTRATE AND METHOD FOR PRODUCING THE SAME
There is provided a gallium nitride single crystal substrate, which is a gallium nitride single crystal substrate having a diameter of 50 mm or more, with a low-index crystal plane closest to a main surface being (0001), and in which an average density of etch pits during etching applied to the main surface using an alkaline etching solution is less than 1×106 cm−2; and in histograms of diameters of the etch pits in multiple different regions on the main surface, and among peaks appearing in the histograms, when a diameter of a first peak which is a smallest diameter is denoted as a, a diameter of a second peak which is a second smallest diameter is denoted as b, frequency of the first peak (the number of etch pits) is denoted as A, frequency of the second peak is denoted as B, the number of the etch pits constituting the first peak is denoted as α, and the number of the etch pits constituting the second peak is denoted as β, at least one of the following conditions (1), (2), and (3) is satisfied: (1) variation in a/b values in the multiple histograms is within ±5% of an average value. (2) variation in A/B values in the multiple histograms is within ±15% of an average value. (3) variation in α/β values in the multiple histograms is within ±30% of an average value.
There is provided a gallium nitride single crystal substrate, which is a gallium nitride single crystal substrate having a diameter of 50 mm or more, with a low-index crystal plane closest to a main surface being (0001), and in which Ge concentration in the substrate is 3×1018 cm−3 or more; and among peaks appearing in a histogram of diameters of etch pits during etching applied to the main surface with an alkaline etching solution, a first peak having a smallest diameter is a single peak having no shoulder.
There is provided a gallium nitride single crystal substrate, which is a gallium nitride single crystal substrate having a diameter of 50 mm or more, with a low-index crystal plane closest to a main surface being (0001), and in which a Mn concentration in the substrate is 5×1017 cm−3 or more; and secondary ion mass spectrometry at a plurality of arbitrary points on the main surface reveals that a variation in the Mn concentration is within ±20% from an average value.
C30B 31/06 - Procédés de diffusion ou de dopage des monocristaux ou des matériaux polycristallins homogènes de structure déterminéeAppareillages à cet effet par contact avec la substance de diffusion à l'état gazeux
