A phosphor including a crystal phase of an aluminate compound containing a metal element M constituting a luminescent center ion and aluminum, in which the crystal phase contains crystallites, and an average size of the crystallites is 2 to 100 μm.
The present disclosure provides a partition wall for an image display device, the partition wall which satisfies 0.8≤A/B<1.0 and 0.85≤C/B<1.0 when the line width at a thickness of 95% from the lowermost end portion of the partition wall is A, the maximum line width at a thickness of 50 to 90% from the lowermost end portion of the partition wall is B, and the line width at a thickness of 10% from the lowermost end portion of the partition wall is C, with respect to the total thickness of the partition wall, a manufacturing method thereof, and an image display device including the partition wall. The partition wall for an image display device according to the present disclosure can be effectively applied to the manufacture of the color conversion pixels through the inkjet process, and the image display device including the partition wall has excellent luminance and maintains high luminance even when observed from the side surface, thereby exhibiting an effect of excellent viewing angle properties.
The present invention provides: a liquid-crystal polyester solution composition which changes little in solution viscosity with the flow initiation temperature of the liquid-crystal polyester powder, and a liquid-crystal polyester powder useful for the liquid-crystal polyester solution composition. This liquid-crystal polyester powder is soluble in aprotic solvents and is characterized in that the proportion of particles having a particle diameter, as determined by dry sieving test according to JIS K 0069 (1992), of less than 250 μm is 23.5 mass % or less. The present invention further provides a method for producing the liquid-crystal polyester solution composition, the method comprising dissolving the liquid-crystal polyester powder in an aprotic solvent to obtain the liquid-crystal polyester solution composition.
A61K 31/167 - Amides, p.ex. acides hydroxamiques ayant des cycles aromatiques, p.ex. colchicine, aténolol, progabide ayant l'atome d'azote d'un groupe carboxamide lié directement au cycle aromatique, p.ex. lidocaïne, paracétamol
Provided is an inorganic fine particle dispersion which has excellent storage stability and from which it is possible to form a coating film having high light transmittance and high coating film strength (high adhesiveness with respect to a base material of the coating film). The inorganic fine particle dispersion contains inorganic fine particles, a liquid dispersion medium A (excluding water) having a boiling point not lower than 100° C. but lower than 190° C., and a liquid dispersion medium B having a boiling point lower than 100° C. The percentage content of the liquid dispersion medium A is not less than 0.5 mass % but less than 15 mass % with respect to 100 mass % of the total amount of the inorganic fine particle dispersion.
C03C 17/25 - Oxydes par dépôt à partir d'une phase liquide
C09D 1/00 - Compositions de revêtement, p.ex. peintures, vernis ou vernis-laques, à base de substances inorganiques
C09D 5/00 - Compositions de revêtement, p.ex. peintures, vernis ou vernis-laques, caractérisées par leur nature physique ou par les effets produits; Apprêts en pâte
The present invention provides: a type 1 crystal of 2-(5-cyclopropyl-3-(ethylsulfonyl)pyridin-2-yl)-5-((trifluoromethyl)sulfinyl)benzo[d]oxazole represented by formula (1) and having diffraction peaks at 2θ of 8.5 ± 0.2°, 12.0 ± 0.2°, 15.0 ± 0.2°, 16.6 ± 0.2°and 20.9 ± 0.2° in the powder X-ray diffractometry using a Cu-Kα ray, the crystal having excellent controlling effect on pests; a method for producing this crystal; a pest control composition which contains this crystal; and a pest control method using this crystal.
C07D 413/04 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes d'azote et d'oxygène comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une liaison directe de chaînon cyclique à chaînon cyclique
A01M 17/00 - Appareils pour la destruction de la vermine dans le sol ou dans les denrées alimentaires
A01N 47/02 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone ne faisant pas partie d'un cycle et ne comportant pas de liaison à un atome d l'atome de carbone ne comportant pas de liaison à un atome d'azote
The present invention provides: a type 1 crystal of 2-(5-cyclopropyl-3-(ethylsulfonyl)pyridin-2-yl)-5-((trifluoromethyl)sulfonyl)benzo[d]oxazole represented by formula (1) and having diffraction peaks at 2θ of 14.3 ± 0.2°, 15.6 ± 0.2°, 17.1 ± 0.2°, 18.7 ± 0.2°, 20.1 ± 0.2°, 22.4 ± 0.2°, 23.3 ± 0.2°, 24.8 ± 0.2°, 26.1 ± 0.2° and 28.5 ± 0.2° in the powder X-ray diffractometry using a Cu-Kα ray, the crystal having excellent controlling effect on pests; a method for producing this crystal; a pest control composition which contains this crystal; and a pest control method using this crystal.
C07D 413/04 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes d'azote et d'oxygène comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une liaison directe de chaînon cyclique à chaînon cyclique
A01M 17/00 - Appareils pour la destruction de la vermine dans le sol ou dans les denrées alimentaires
A01N 47/02 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone ne faisant pas partie d'un cycle et ne comportant pas de liaison à un atome d l'atome de carbone ne comportant pas de liaison à un atome d'azote
Provided is a curable composition that contains semiconductor particles (A), polymerizable compounds (B), a polymerization initiator (C), and an antioxidant (D). The polymerizable compounds (B) include, in an amount of 40 mass% or more with respect to the total amount of the polymerizable compounds (B), a polymerizable compound having a dipole moment in at least 3D.
H10K 50/125 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] spécialement adaptées à l'émission de lumière multicolore, p. ex. à l'émission de lumière blanche
H10K 50/854 - Dispositifs pour extraire la lumière des dispositifs comprenant des moyens de diffusion
H10K 59/38 - Dispositifs spécialement adaptés à l'émission de lumière multicolore comprenant des filtres de couleur ou des supports changeant de couleur [CCM]
8.
BOARD FOR ELECTRONIC PARTS, METHOD FOR MANUFACTURING BOARD FOR ELECTRONIC PARTS, AND DISPLAY DEVICE AND SEMICONDUCTOR DEVICE INCLUDING SAME
The present invention relates to a board for electronic parts, a method for manufacturing the board for electronic parts, and a display and a semiconductor device which include the board, the board comprising: a substrate including at least one through via; and a tight-adhesion enhancement layer on the surface of the substrate and in the through via, wherein the through via has, at at least one of the upper and lower surfaces, a hole diameter that is greater than the hole diameter at a site inside the hole. Due to the inclusion of the tight-adhesion enhancement layer, the tight adhesion of a metal plating layer is improved, thus preventing the occurrence of defects and also simplifying manufacturing processes as compared to conventional boards for electronic parts.
H05K 1/03 - Emploi de matériaux pour réaliser le substrat
H05K 3/18 - Appareils ou procédés pour la fabrication de circuits imprimés dans lesquels le matériau conducteur est appliqué au support isolant de manière à former le parcours conducteur recherché utilisant la technique de la précipitation pour appliquer le matériau conducteur
9.
NEGATIVE ELECTRODE FOR LITHIUM SECONDARY BATTERIES, NEGATIVE ELECTRODE PRECURSOR FOR LITHIUM SECONDARY BATTERIES, LITHIUM SECONDARY BATTERY, AND METHOD FOR PRODUCING NEGATIVE ELECTRODE FOR LITHIUM SECONDARY BATTERIES
This negative electrode for lithium secondary batteries is formed of a rolled material of aluminum or an aluminum alloy, the rolled material being capable of absorbing and desorbing lithium ions; and if two cycles of measurement at a heating rate of 10°C/minute for the range of 30°C to 500°C are performed in the differential scanning calorimetry of this negative electrode for lithium secondary batteries and ∆DSC is the value obtained by subtracting the amount of heat generation in the second cycle from the amount of heat generation in the first cycle, the integral value of the ∆DSC for the range from 100°C to 300°C is 0.5-8 mW/g or less.
H01M 4/134 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes composées d'un ou comprenant un matériau actif Électrodes pour accumulateurs à électrolyte non aqueux, p.ex. pour accumulateurs au lithium; Leurs procédés de fabrication Électrodes à base de métaux, de Si ou d'alliages
The present invention addresses the problem of providing a novel compound that can be used as a constituent material for printed wiring boards, has a low melting point and high solubility, and can be cured to provide a resin having high thermal conductivity and low dielectric loss. The present invention pertains to a vinyl compound represented by formula (1) or (2). (R is a (meth)acryloyl group or a vinylbenzyl group; A1is a chain-like saturated aliphatic hydrocarbon group, or a group containing at least one selected from the group consisting of an aromatic group and a cycloalkane group; A2is a group containing at least one selected from the group consisting of an aromatic group, a cycloalkane group, and a cycloalkene group; X1 is a single bond, an ester group, a carbonyl group, or an ether group; m is an integer of 3-6; and n is an integer of 1-20.)
C08F 12/34 - Monomères contenant plusieurs radicaux aliphatiques non saturés
B32B 27/30 - Produits stratifiés composés essentiellement de résine synthétique comprenant une résine acrylique
C07C 69/76 - Esters d'acides carboxyliques dont un groupe carboxyle estérifié est lié à un atome de carbone d'un cycle aromatique à six chaînons
C08J 5/24 - Imprégnation de matériaux avec des prépolymères pouvant être polymérisés en place, p.ex. fabrication des "prepregs"
H01B 3/44 - Isolateurs ou corps isolants caractérisés par le matériau isolant; Emploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques cires résines acryliques
11.
LED LIGHTING DEVICE AND METHOD FOR MANUFACTURING THE SAME
A method for manufacturing an LED lighting device includes forming a separation film on a substrate, patterning the separation film, forming LEDs on the separation film, bonding a stretch film to top surfaces of the LEDs and spacing between the LEDs, separating the separation film from the substrate, stretching the stretch film, exposing the top surfaces of the LEDs, and forming electrodes on the top surfaces of the LEDs, and a bottom surface of the separation film or bottom surfaces of the LEDs.
H01L 27/15 - Dispositifs consistant en une pluralité de composants semi-conducteurs ou d'autres composants à l'état solide formés dans ou sur un substrat commun comprenant des composants semi-conducteurs avec au moins une barrière de potentiel ou une barrière de surface, spécialement adaptés pour l'émission de lumière
A light-emitting composition containing first and second light-emitting markers. The first light-emitting marker comprises a first light-emitting material and a first binding group configured to bind to a first target analyte. The second light-emitting marker comprises a second light-emitting material which is different from the first light-emitting material and a second binding group which is different from the first binding group and which is configured to bind to a second target analyte. A luminescent lifetime of the first light-emitting material is shorter than a luminescent lifetime of the second light-emitting material. The difference in lifetimes of the first and second light-emitting materials may be used to distinguish between the first and second target analytes in a sample, e.g. by time-gated flow cytometry.
This composition includes an olefin polymer A, an aliphatic polyester polymer B, and an inorganic powder C. The pH of the inorganic powder C evaluated per JIS M 8016-1991 is 6.5-11.5.
C08L 23/00 - Compositions contenant des homopolymères ou des copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carbone; Compositions contenant des dérivés de tels polymères
C08L 67/02 - Polyesters dérivés des acides dicarboxyliques et des composés dihydroxylés
C08K 3/013 - Charges, pigments ou agents de renforcement
14.
PELLETS, METHOD FOR PRODUCING PELLETS, AND METHOD FOR PRODUCING INJECTION-MOLDED ARTICLE
The present invention relates to pellets comprising a liquid crystal polyester resin, wherein an average length (L) of the pellets is 3.2 to 12 mm, an average diameter (D) of the pellets is 3.2 to 6.0 mm, and a value of the average length (L)/the average diameter (D) of the pellets is 1 to 2.
C08G 63/664 - Polyesters contenant de l'oxygène sous forme de groupes éther dérivés d'acides hydroxycarboxyliques
B29C 45/00 - Moulage par injection, c. à d. en forçant un volume déterminé de matière à mouler par une buse d'injection dans un moule fermé; Appareils à cet effet
A composition comprising an electron-donating polymer and an electron acceptor wherein the electron-donating polymer comprises a benzo[1,2-b:4,5-b']dithiophene repeat unit and wherein a film of the electron-accepting material has a peak absorption wavelength greater than 1000 nm. The composition may be used as a photosensitive layer of an organic photodetector.
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
This method for producing a composition, which includes an olefin-based polymer A and a polyhydroxyalkanoate-based polymer B, and which contains 99.9-70 parts by mass of the olefin-based polymer A and 0.1-30 parts by mass of the polyhydroxyalkanoate-based polymer B with respect to the total 100 parts by mass of the olefin-based polymer A and the polyhydroxyalkanoate-based polymer B, comprises the steps of: supplying, to an extruder, a material 1 containing the olefin-based polymer A from a main feed port of the extruder and melting and kneading the material 1; and supplying, to the extruder, a material 2 containing the polyhydroxyalkanoate-based polymer B from a side feed port arranged on the downstream side of the main feed port in the extruder, and melting and kneading the material 2.
C08J 3/20 - Formation de mélanges de polymères avec des additifs, p.ex. coloration
B29B 7/24 - Mélange; Malaxage discontinu, avec dispositifs mécaniques de mélange ou de malaxage, c. à d. de type travaillant par charges - Eléments constitutifs, détails ou accessoires; Opérations auxiliaires pour alimentation
C08K 3/013 - Charges, pigments ou agents de renforcement
C08L 23/00 - Compositions contenant des homopolymères ou des copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carbone; Compositions contenant des dérivés de tels polymères
C08L 67/04 - Polyesters dérivés des acides hydroxycarboxyliques, p.ex. lactones
17.
SULFONAMIDE COMPOUND AND HARMFUL-ARTHROPOD CONTROLLING COMPOSITION CONTAINING SAME
The present invention provides a compound having an excellent control effect against harmful arthropods. A compound represented by formula (1) and an N oxide thereof have an excellent control effect against harmful arthropods. [In the formula, Q shown in the formula below (where # represents a site of bonding with a sulfur atom and ● represents a site of bonding with Het) is, for example, a group represented by formula Q1; R2aand R2bare the same or different from each other and represent, for example, a C1-C6 alkyl group that may be substituted with one or more halogen atoms; R3a, R3b, and R3dare the same or different from each other and represent, for example, a hydrogen atom; Het represents, for example, a group represented by formula Het1; A2represents a nitrogen atom or CR4a; W1represents an oxygen atom or a sulfur atom; R4arepresents, for example, a C1-C6 chain hydrocarbon group; the combination of B1, B2, B3, and B4represents, for example, a combination in which B1is a nitrogen atom or CR6a, B2is CR6e, B3is a nitrogen atom or CR6c, and B4is a nitrogen atom or CR6d; R6a, R6c, and R6dare the same or different from each other and represent, for example, a hydrogen atom; and R6e represents, for example, a C1-C6 chain hydrocarbon group that is substituted with one or more substituents selected from the group consisting of cyano groups and a halogen atom.]
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
A61K 31/437 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p.ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle condensés en ortho ou en péri avec des systèmes hétérocycliques le système hétérocyclique contenant un cycle à cinq chaînons ayant l'azote comme hétéro-atome du cycle, p.ex. indolizine, bêta-carboline
A61K 31/444 - Pyridines non condensées; Leurs dérivés hydrogénés contenant d'autres systèmes hétérocycliques contenant un cycle à six chaînons avec l'azote comme hétéro-atome du cycle, p.ex. amrinone
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
18.
SULFONAMIDE COMPOUND AND HARMFUL-ARTHROPOD-CONTROLLING COMPOSITION CONTAINING SAME
The present invention provides a compound, or an N-oxide thereof, which has an excellent controlling effect with respect to harmful arthropods and which is represented by formula (I) (in the formula: Q denotes a group represented by formula Q1, or the like; R2aand R2b, which may be the same or different, denote a C1-C6 alkyl group that may be substituted with one or more halogen atoms, or the like; and Het denotes a group represented by formula Het1, or the like).
A01M 1/20 - Capture ou destruction des insectes par les poisons, les narcotiques ou le feu
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
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 47/02 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone ne faisant pas partie d'un cycle et ne comportant pas de liaison à un atome d l'atome de carbone ne comportant pas de liaison à un atome d'azote
The present invention provides a compound represented by formula (I) [wherein, Q represented by the formula below (wherein # represents a binding site with a sulfur atom, and ● represents a binding site with Het) represents, inter alia, a group represented by formula Q1; R2aand R2bare identical with each other or different from each other and represent, inter alia, a C1-C6 alkyl group that may be substituted by one or more halogen atoms; R3a, R3b, and R3dare identical with each other or different from each other and represent, inter alai, a hydrogen atom; Het represents, inter alia, a group represented by the formula Het5; A2represents NR5aor CR4aR4d; A3represents CR4bR4e; W1represents an oxygen atom or a sulfur atom; when Het is a group represented by formula Het5, the combination of B1, B2, and B3represents, inter alia, a combination in which B1is CR6e, B2is a nitrogen atom or CR6b, and B3is a nitrogen atom or CR6c; R4a, R4b, R6a, R6b, and R6care identical with each other or different from each other and represent, inter alia, a hydrogen atom; R4dand R4eare identical with each other or different from each other and represent a hydrogen atom, etc.; R6erepresents, inter alia, a C1-C6 chain hydrocarbon group that has been substituted by one or more substituents selected from the group consisting of cyano groups and halogen atoms; and R5a represents a hydrogen atom, etc.] or an N-oxide thereof, said compound having an an excellent control effect against harmful arthropods.
C07D 401/04 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant deux hétérocycles liés par une liaison directe de chaînon cyclique à chaînon cyclique
A01M 1/20 - Capture ou destruction des insectes par les poisons, les narcotiques ou le feu
A01N 43/42 - 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 condensés avec des carbocycles
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 47/02 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés organiques comportant un atome de carbone ne faisant pas partie d'un cycle et ne comportant pas de liaison à un atome d l'atome de carbone ne comportant pas de liaison à un atome d'azote
A01N 53/12 - Composés contenant le groupe , X ou Y étant un atome d'azote, p.ex. amides des acides cyclopropane-carboxyliques
A method of treating a reaction mixture comprising light-emitting nanoparticles formed upon reaction of a silica-forming compound in the presence of a light-emitting material in a protic, water-miscible solvent. The method comprises forming a phase-separated system comprising: an aqueous phase comprising the protic, water miscible solvent, an organic phase comprising an organic solvent and a separating solvent; and separating the organic phase. The separating solvent is immiscible with water, miscible with the water-miscible protic solvent and miscible with the organic solvent.
The present invention addresses the problem of providing a polymer that suppresses dark current in a photoelectric conversion element. The present invention pertains to a polymer that has structural unit having a main chain and a side chain. The weighted average of the formula weight of the side chain weighted with the mole fraction of the structural unit included in the polymer is 160 or more. The absorption edge intensity of the polymer is 0.08 or less.
C08G 85/00 - Procédés généraux pour la préparation des composés prévus dans la présente sous-classe
C08G 61/12 - Composés macromoléculaires contenant d'autres atomes que le carbone dans la chaîne principale de la macromolécule
C08L 65/00 - Compositions contenant des composés macromoléculaires obtenus par des réactions créant une liaison carbone-carbone dans la chaîne principale; Compositions contenant des dérivés de tels polymères
C08L 101/12 - Compositions contenant des composés macromoléculaires non spécifiés caractérisées par des propriétés physiques, p.ex. anisotropie, viscosité ou conductivité électrique
C09D 11/102 - Encres d’imprimerie à base de résines artificielles contenant des composés macromoléculaires obtenus par des réactions autres que celles faisant intervenir uniquement des liaisons non saturées carbone-carbone
C09D 165/00 - Compositions de revêtement à base de composés macromoléculaires obtenus par des réactions créant une liaison carbone-carbone dans la chaîne principale; Compositions de revêtement à base de dérivés de tels polymères
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 39/00 - Dispositifs intégrés, ou ensembles de plusieurs dispositifs, comprenant au moins un composant organique sensible aux rayonnements couvert par le groupe
22.
LITHIUM-METAL COMPLEX OXIDE, POSITIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY, POSITIVE ELECTRODE FOR LITHIUM SECONDARY BATTERY, AND LITHIUM SECONDARY BATTERY
This lithium-metal complex oxide includes at least Li and Ni, and satisfies (1) and (2). (1) In a pore size distribution in the adsorption isotherm as determined using adsorption isotherm and desorption isotherm measurements of nitrogen gas and the Barrett-Joyner-Halenda method, the pore volume in the range in which the pore diameter is 2 to 10 nm is greater than 0.4×10–3cm3/g and less than or equal to 1.0×10–3cm35050 is 0.9×10–3to 3.4×10–3.
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
23.
STABILIZER, ORGANIC MATERIAL COMPOSITION, AND ORGANIC MATERIAL STABILIZING METHOD
The present invention pertains to a stabilizer which comprises: a compound (A) selected from the group consisting of compounds represented by formula (1) [in formula (1), R1, R2, R4, and R5each independently represent a hydrogen atom, an alkyl group having 1-8 carbon atoms, a cycloalkyl group having 5-8 carbon atoms, an alkyl cycloalkyl group having 6-12 carbon atoms, an aralkyl group having 7-12 carbon atoms, or a phenyl group, each R3independently represents a hydrogen atom or an alkyl group having 1-8 carbon atoms, X represents a single bond, a sulfur atom, or a -CH(-R13)-group (R13represents a hydrogen atom, an alkyl group having 1-8 carbon atoms, or a cycloalkyl group having 5-8 carbon atoms), A represents an alkylene group having 1-8 carbon atoms or a *-C(=O)-R14-group (R14represents a single bond or an alkylene group having 1-8 carbon atoms, and * represents an atomic bonding on the oxygen side), and one of Y and Z represents a hydroxyl group, an alkoxy group having 1-8 carbon atoms, or an aralkyloxy group having 7-12 carbon atoms, and the other of Y and Z represents a hydrogen atom or an alkyl group having 1-8 carbon atoms] and compounds represented by formula (2) [in formula (2), R6and R8each independently represent a hydrogen atom, a methyl group, or an alkyl group having 5-8 carbon atoms, each R7independently represents a hydrogen atom or a hydroxyl group, and each R91525-3125-31 group, but at least one of R6, R7, R8, or R9is not a hydrogen atom]; and a compound (B) represented by formula (3) [in formula (3), R10, R11, and R12each independently represent a hydrogen atom, an alkyl group having 1-12 carbon atoms, or an arylalkyl group having a total of 7-20 carbon atoms, but at least one of R10, R11, and R12 is not a hydrogen atom]. In the stabilizer, the contained amount of the compound (B) with respect to 100 parts by mass of the compound (A) is 0.01-50 parts by mass.
C09K 15/32 - Compositions anti-oxydantes; Compositions inhibant les modifications chimiques contenant des composés organiques contenant du bore, du silicium, du phosphore, du sélénium, du tellure ou un métal
The purpose of the present invention is to provide a pest control agent in which Bacillus bacteria are diluted in advance with water to a prescribed concentration range (especially a spray concentration range), the pest control agent having improved storage stability. The present invention provides a pH-adjusted stabilized pest control agent that contains Bacillus bacteria, a pH adjuster, and water.
Disclosed is a color filter comprising a glass substrate, a frit formed on the glass substrate, a pattern boundary unit formed inside the frit on the glass substrate, black matrix (BM) layers formed inside the pattern boundary unit on the glass substrate, a first colored layer formed between the BM layers, and a second colored layer formed between the pattern boundary unit and the BM layers.
H10K 59/38 - Dispositifs spécialement adaptés à l'émission de lumière multicolore comprenant des filtres de couleur ou des supports changeant de couleur [CCM]
H10K 50/85 - Dispositifs pour extraire la lumière des dispositifs
G03F 7/00 - Production par voie photomécanique, p.ex. photolithographique, de surfaces texturées, p.ex. surfaces imprimées; Matériaux à cet effet, p.ex. comportant des photoréserves; Appareillages spécialement adaptés à cet effet
A feed for livestock is provided that shows excellent weight gain and improved feed efficiency. A feed additive composition and a feed for livestock comprising abscisic acid and/or a salt thereof and glutamic acid; a method of feeding livestock, a method of improving the weight gain of livestock, and a method of increasing the feed efficiency in livestock, comprising letting livestock to take said feed; and a use of the feed for livestock for improving the weight gain of livestock, and a use of the feed for increasing the feed efficiency in livestock.
The present invention provides an efficient process for preparing a nucleic acid oligomer, in particular, a process for deprotecting efficiently a protecting group of hydroxy group of a ribose in a nucleic acid oligomer. Specifically, the present invention also provides a process for preparing a nucleic acid oligomer represented by formula (4), which comprises contacting a nucleic acid oligomer represented by formula (3) with a fluoride ion under an atmosphere of an inert gas or inert gases containing 15% or less of oxygen concentration (wherein the definitions of each groups described in formula (3) and formula (4) are the same as defined in the Description).
The present invention provides an efficient process for preparing a nucleic acid oligomer, in particular, a process for deprotecting efficiently a protecting group of hydroxy group of a ribose in a nucleic acid oligomer. Specifically, the present invention also provides a process for preparing a nucleic acid oligomer represented by formula (4), which comprises contacting a nucleic acid oligomer represented by formula (3) with a fluoride ion under an atmosphere of an inert gas or inert gases containing 15% or less of oxygen concentration (wherein the definitions of each groups described in formula (3) and formula (4) are the same as defined in the Description).
C07H 21/00 - 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
28.
METHOD FOR CONTROLLING SOYBEAN RUST FUNGUS HAVING RESISTANCE AGAINST Qo SITE INHIBITOR
The present invention provides a method for controlling a soybean rust fungus having an amino acid substitution of F129L on mitochondrial cytochrome b protein, by applying a compound represented by formula (I) [wherein Q represents a group represented by the following Q1, Q2, Q3, Q4 or Q5 (in the formulae, • represents a binding site to benzene ring); X represents an oxygen atom or NH; L represents CH2, an oxygen atom or NCH3; E represents a C6-C10 aryl group, etc.; R1 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R2 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R3 represents a C1-C3 alkoxy group or a C1-C3 chain hydrocarbon group, etc.; and n is 0, 1, 2, or 3] or its N oxide or an agriculturally acceptable salt thereof.
The present invention provides a method for controlling a soybean rust fungus having an amino acid substitution of F129L on mitochondrial cytochrome b protein, by applying a compound represented by formula (I) [wherein Q represents a group represented by the following Q1, Q2, Q3, Q4 or Q5 (in the formulae, • represents a binding site to benzene ring); X represents an oxygen atom or NH; L represents CH2, an oxygen atom or NCH3; E represents a C6-C10 aryl group, etc.; R1 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R2 represents a C1-C3 chain hydrocarbon group or a cyclopropyl group, etc.; R3 represents a C1-C3 alkoxy group or a C1-C3 chain hydrocarbon group, etc.; and n is 0, 1, 2, or 3] or its N oxide or an agriculturally acceptable salt thereof.
A01N 37/12 - 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 contenant le groupe , dans lequel Cn représente un squelette carboné ne comportant pas de cycle; Leurs thio-analogues
29.
REACTIVE COMPOUND, PRODUCTION METHOD FOR POLYMER COMPOUND, AND INTERMEDIATE
(Abstract) (Problem) To provide a (meth)acrylic resin composition which exhibits excellent heat resistance, a film formed from the same and a polarizing plate containing said film. (Solution) Provided are: a (meth)acrylic resin composition which contains a (meth)acrylic resin (A), an elastomer component (B) and an oxidation inhibitor (C), wherein the mass ratio of the content of the oxidation inhibitor (C) to the content of the elastomer component (B) is 0.006-0.2, inclusive; a film formed from the same; and a polarizing plate containing said film. [Selected drawing] None
C08L 33/04 - Homopolymères ou copolymères des esters
C08L 21/00 - Compositions contenant des caoutchoucs non spécifiés
C08L 57/00 - Compositions contenant des polymères non spécifiés obtenus par des réactions ne faisant intervenir que des liaisons non saturées carbone-carbone
G02B 5/30 - OPTIQUE ÉLÉMENTS, SYSTÈMES OU APPAREILS OPTIQUES Éléments optiques autres que les lentilles Éléments polarisants
Disclosed is a composition including a compound of formula (1), a compound of formula (2) having a maximum absorption wavelength of 550 nm or more and 650 nm or less, and a liquid crystalline compound. n and m are 1 or 2. R1 and R3 represent a substituent. R2 and R4 represent an alkylamino group, an alkoxy group, or an alkylthio group. P represents a single bond, —OC(═O)—, —C(═O)O—, —NHC(═O)—, —C(═O)NH—, —C≡C—, —CH═CH—, —CH═N—, —N═N—, and —N═CH—. Ar1, Ar2, and Ar3 represent a 1,4-phenylene group or a divalent sulfur-containing aromatic heterocyclic group, and at least one of Ar1 and Ar2 is substituted with fluorine. Ar4, Ar5, and Ar6 represent a 1,4-phenylene group, a naphthalenediyl group, or a divalent sulfur-containing aromatic heterocyclic group.
Disclosed is a composition including a compound of formula (1), a compound of formula (2) having a maximum absorption wavelength of 550 nm or more and 650 nm or less, and a liquid crystalline compound. n and m are 1 or 2. R1 and R3 represent a substituent. R2 and R4 represent an alkylamino group, an alkoxy group, or an alkylthio group. P represents a single bond, —OC(═O)—, —C(═O)O—, —NHC(═O)—, —C(═O)NH—, —C≡C—, —CH═CH—, —CH═N—, —N═N—, and —N═CH—. Ar1, Ar2, and Ar3 represent a 1,4-phenylene group or a divalent sulfur-containing aromatic heterocyclic group, and at least one of Ar1 and Ar2 is substituted with fluorine. Ar4, Ar5, and Ar6 represent a 1,4-phenylene group, a naphthalenediyl group, or a divalent sulfur-containing aromatic heterocyclic group.
H10K 85/40 - Composés organosiliciés, p. ex. pentacène TIPS
C09K 19/20 - Composés non stéroïdes formant des cristaux liquides contenant au moins deux cycles non condensés contenant au moins deux cycles benzéniques liés par une chaîne contenant des atomes de carbone et d'oxygène comme chaînons, p.ex. esters
C09K 19/30 - Composés non stéroïdes formant des cristaux liquides contenant au moins deux cycles non condensés contenant des cycles non aromatiques saturés ou insaturés, p.ex. cycle cyclohexanique
H10K 85/60 - Composés organiques à faible poids moléculaire
32.
POLARIZING PLATE FOR ANTIREFLECTION AND DISPLAY DEVICE COMPRISING THE SAME
Provided are a polarizing plate for antireflection including a polarizer, and a protective layer formed on at least one surface of the polarizer, wherein the polarizing plate has a single transmittance of 44.6% or more and a degree of polarization of 98% or more and satisfies 0≤[(orthogonal a*)2+(orthogonal b*)2]0.5≤16, and a display device including the polarizing plate. The polarizing plate for antireflection can exhibit high transmittance while preventing blue-shift phenomenon and having neutral reflection color. Further, the polarizing plate for antireflection can be made thinner.
G02B 5/30 - OPTIQUE ÉLÉMENTS, SYSTÈMES OU APPAREILS OPTIQUES Éléments optiques autres que les lentilles Éléments polarisants
B32B 37/12 - Procédés ou dispositifs pour la stratification, p.ex. par polymérisation ou par liaison à l'aide d'ultrasons caractérisés par l'usage d'adhésifs
The present invention addresses the problem of providing a composition capable of forming an optical filter that has fewer aggregates. The present invention relates to a composition comprising a near-infrared absorbing dye, an alkali-soluble resin, and a solvent, wherein the near-infrared absorbing dye comprises a compound represented by formula (I). (In formula (I), R1, R4, R5, and R8each independently represent a C1-20 hydrocarbon group or the like; R2, R3, R6, and R7each independently represent a hydrogen atom or the like; R9, R10, and R11each independently represent a C1-20 hydrocarbon group, and if two or more R11moieties are present, said moieties may be the same or different; X1-X4each independently represent a hydrogen atom or the like; Y1-Y8each independently represent a hydrogen atom or the like; and R12represents a C1-5 alkyl group, and if two or more R12 moieties are present, said moieties may be the same or different)
(Abstract) (Problem) To provide an optical laminate in which a release film can be satisfactorily released from an adhesive layer. (Solution) This optical laminate includes an optical film, an adhesive layer, and a release film in the stated order. The release film has a release treatment surface containing a siloxane compound on a side where the release film makes contact with the adhesive layer. The release treatment surface of the release film satisfies the relationship indicated by formula (1). (1): Ys/Xs × 100 ≤ 3.5 [In formula (1), Xs represents the intensity of the maximum peak Ps in a binding energy range of 96-108 eV of an XPS spectrum (Sr) of the release treatment surface, and Ys represents the intensity of the XPS spectrum (Sr) at a binding energy of (Es + 2) eV, when the binding energy at the peak PS is Es [eV].] (Selected figure) FIG. 1
The present invention provides a compound having excellent control efficacy against plant diseases. A compound represented by formula (I) has excellent control efficacy against plant diseases.
C07C 69/74 - Esters d'acides carboxyliques dont un groupe carboxyle est lié à un atome de carbone d'un cycle autre qu'un cycle aromatique à six chaînons
A01N 53/06 - Esters contenant le groupe , où l'atome de carbone marqué d'un astérisque est acyclique ou fait partie d'un cycle ou d'un système cyclique; Leurs thio-analogues l'atome de carbone marqué d'un astérisque étant acyclique et lié directement à un atome de carbone d'un cycle aromatique à six chaînons, p.ex. esters benzyliques; Leurs thio-analogues
The present invention addresses the problem of preventing the blockage of pipes and preventing combustion and explosion. The present invention relates to a regeneration system 1 that is for regenerating methyl (meth)acrylate from scraps of molded bodies obtained by molding a (meth)acrylic resin composition containing a (meth)acrylic polymer and comprises: a pyrolysis device 10 that has a loading section 12 and a gas removal section 14; a first capture tank 52 that has gas containing methyl (meth)acrylate introduced thereinto and serves to capture a residue containing undecomposed components included in the gas containing methyl (meth)acrylate and remove the residue containing undecomposed components; and a gas processing device 70 selected from the group consisting of a purifier for purifying gas containing methyl (meth)acrylate processed by the first capture tank and a cooler for cooling gas containing methyl (meth)acrylate.
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
C07C 67/475 - Préparation d'esters d'acides carboxyliques par ouverture de liaisons carbone-carbone suivie d'un réarrangement, p.ex. par dismutation ou migration de groupes entre différentes molécules
Provided is an inorganic fine particle dispersion capable of forming a layer having even higher light transmittance and exceptional antifouling properties. This inorganic fine particle dispersion contains inorganic fine particles, a liquid dispersion medium A having a boiling point higher than 121°C but lower than 190°C, a liquid dispersion medium B having a boiling point lower than 100°C, water, an alkoxysilane, and a pore-forming agent, wherein the percentage content of the liquid dispersion medium A is at least 0.5 mass% but less than 15.0 mass% per 100 mass% of the total amount of the inorganic fine particle dispersion.
C09D 17/00 - Pigments en pâtes, p.ex. pour pigmenter les peintures
B05D 7/24 - Procédés, autres que le flocage, spécialement adaptés pour appliquer des liquides ou d'autres matériaux fluides, à des surfaces particulières, ou pour appliquer des liquides ou d'autres matériaux fluides particuliers pour appliquer des liquides ou d'autres matériaux fluides particuliers
B32B 5/22 - Produits stratifiés caractérisés par l'hétérogénéité ou la structure physique d'une des couches caractérisés par la présence de plusieurs couches qui comportent des fibres, filaments, grains ou poudre, ou qui sont sous forme de mousse ou essentiellement poreuses
C09D 1/00 - Compositions de revêtement, p.ex. peintures, vernis ou vernis-laques, à base de substances inorganiques
According to the present invention, a compound represented by formula (I) (wherein, Q (# denotes a bonding site with a sulfur atom, and ● denotes a bonding site with Het) represented in the formula denotes a group or the like represented by formula Q1, R2aand R2bmay be the same or different and represent a C1-C6 alkyl group or the like that may be substituted with one or more halogen atoms, R3a, R3b, and R3dmay be the same or different and represent a hydrogen atom or the like, Het represents a group or the like represented by formula Het1, A2represents a nitrogen atom or CR4a, A3represents a nitrogen atom or CR4b, W1represents an oxygen atom or a sulfur atom, R4aand R4bmay be the same or different and represent a C1-C6 chain hydrocarbon group or the like, R6 represents a C1-C6 chain hydrocarbon group or the like, and T represents a C1-C10 chain hydrocarbon group {the C1-C10 chain hydrocarbon group having one or more substituents selected from the group consisting of a cyano group and a halogen atom} or the like) exhibits an excellent extermination effect against harmful arthropods.
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
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
A61K 31/444 - Pyridines non condensées; Leurs dérivés hydrogénés contenant d'autres systèmes hétérocycliques contenant un cycle à six chaînons avec l'azote comme hétéro-atome du cycle, p.ex. amrinone
A61K 31/506 - Pyrimidines; Pyrimidines hydrogénées, p.ex. triméthoprime non condensées et contenant d'autres hétérocycles
A61K 31/517 - Pyrimidines; Pyrimidines hydrogénées, p.ex. triméthoprime condensées en ortho ou en péri avec des systèmes carbocycliques, p.ex. quinazoline, périmidine
C07D 401/04 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant deux hétérocycles liés par une liaison directe de chaînon cyclique à chaînon cyclique
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
39.
CYCLOPROPANECARBOXYLIC ACID ESTER COMPOUND AND USE THEREOF
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases.
C07D 303/40 - Composés contenant des cycles oxirane avec des radicaux hydrocarbonés substitués par des atomes de carbone comportant trois liaisons à des hétéro-atomes, avec au plus une liaison à un halogène, p.ex. radicaux ester ou nitrile par des radicaux ester
A01N 53/06 - Esters contenant le groupe , où l'atome de carbone marqué d'un astérisque est acyclique ou fait partie d'un cycle ou d'un système cyclique; Leurs thio-analogues l'atome de carbone marqué d'un astérisque étant acyclique et lié directement à un atome de carbone d'un cycle aromatique à six chaînons, p.ex. esters benzyliques; Leurs thio-analogues
A01P 1/00 - Désinfectants; Composés antimicrobiens ou leurs mélanges
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a 2-hydroxypropan-2-yl group or a 1-propen-2-yl group).
41.
CYCLOPROPANECARBOXYLIC ACID ESTER COMPOUND AND USE THEREOF
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a chlorine atom or a hydroxy group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a 1-propen-2-yl group or a 2-hydroxypropan-2-yl group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a vinyl group or a 1-hydroxyethyl group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, R represents a 2-hydroxypropan-2-yl group or a 1-propen-2-yl group).
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases (in the formula, for R1and R2, R1represents a hydrogen atom and R2represents a 1-propen-2-yl group, or R1and R2 are united and represent an isopropylidene group).
The present invention relates to an infrared ray-transmitting photosensitive resin composition comprising a colorant, an alkali-soluble resin, a photopolymerizable compound, a photopolymerization initiator, and a solvent, wherein the infrared ray-transmitting photosensitive resin composition comprises at least one of a porphyrin compound and a chromatic colorant of a specific color. The infrared ray-transmitting photosensitive resin composition, according to the present invention, exhibits a high transmittance in the infrared region and a low transmittance in the visible light region, even in a thin film, and has excellent patterning properties.
G03F 7/031 - Composés organiques non couverts par le groupe
G03F 7/105 - Matériaux photosensibles - caractérisés par des détails de structure, p.ex. supports, couches auxiliaires avec des substances, p.ex. des indicateurs, pour obtenir des images visibles
G03F 7/00 - Production par voie photomécanique, p.ex. photolithographique, de surfaces texturées, p.ex. surfaces imprimées; Matériaux à cet effet, p.ex. comportant des photoréserves; Appareillages spécialement adaptés à cet effet
C08L 101/00 - Compositions contenant des composés macromoléculaires non spécifiés
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 pesticidal composition comprising a compound represented by the formula (I), a herbicidal active salt, an organic solvent having a water solubility at 25° C. of 10 mass % or less, a surfactant and water, wherein a weight ratio between the compound represented by the formula (I) and the surfactant is 1:10 or more and 1:50 or less.
Provided is a pesticidal composition comprising a compound represented by the formula (I), a herbicidal active salt, an organic solvent having a water solubility at 25° C. of 10 mass % or less, a surfactant and water, wherein a weight ratio between the compound represented by the formula (I) and the surfactant is 1:10 or more and 1:50 or less.
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 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 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
LIQUID CRYSTAL POLYESTER POWDER, METHOD FOR PRODUCING POWDER, COMPOSITION, METHOD FOR PRODUCING COMPOSITION, METHOD FOR PRODUCING FILM, AND METHOD FOR PRODUCING LAMINATED BODY
The present invention relates to a liquid crystal polyester powder comprising a liquid crystal polyester, wherein the liquid crystal polyester has a flow starting temperature of 255° C. or less and has a structural unit comprising a naphthalene structure, and, when a particle diameter at which a cumulative volume proportion from a small particle side in a volume-based cumulative particle diameter distribution curve by laser diffraction/scattering type particle diameter distribution measurement is 50% is defined as D50, D50 is 0.1 to 30 μm.
C08L 67/00 - Compositions contenant des polyesters obtenus par des réactions créant une liaison ester carboxylique dans la chaîne principale; Compositions contenant des dérivés de tels polymères
Provided is a method for producing elastomer pellets, the method comprising a step for hot-cutting an elastomer, in which the step for hot-cutting the elastomer includes cooling the elastomer extruded through the die hole with cooling water, and the value of a parameter A represented by general formula (I) is 1.8 or less. (I): A=-X0.41-Y0.36+Z0.71 (In general formula (I), X represents the weight average molecular weight (unit: ten-thousand) of the elastomer; Y represents the shear rate [1/sec] of the elastomer in the die hole; and Z represents the temperature [°C] of the cooling water for the elastomer.)
B29B 9/06 - Fabrication de granulés par division de matière préformée sous forme de filaments, p.ex. combinée avec l'extrusion
C08F 236/10 - Copolymères de composés contenant plusieurs radicaux aliphatiques non saturés et l'un au moins contenant plusieurs liaisons doubles carbone-carbone le radical ne contenant que deux doubles liaisons carbone-carbone conjuguées avec des monomères vinylaromatiques
50.
METHYL (METH)ACRYLATE RECYCLING SYSTEM, AND METHOD FOR RECYCLING METHYL (METH)ACRYLATE
The present invention addresses the problem of preventing the opening and closing of distribution channels and further preventing ignition and explosion. The present invention pertains to a recycling system comprising: a pyrolysis device 10 for pyrolyzing scrap to produce gas containing methyl (meth)acrylate and a residue containing undecomposed components; and a residue storage device 30 for storing the residue containing undecomposed components derived from the pyrolysis device, wherein the pyrolysis device has an input section 12, a gas extraction section 14 for extracting gas generated by the pyrolysis of a (meth)acrylic resin composition, and a residue discharge section 16 for discharging the residue containing undecomposed components to the residue storage device, and the residue storage device has a storage tank 32.
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
B29B 17/00 - Récupération de matières plastiques ou d'autres constituants des déchets contenant des matières plastiques
51.
SYSTEM FOR REGENERATING METHYL (METH)ACRYLATE AND METHOD FOR REGENERATING METHYL (METH)ACRYLATE
The present invention prevents ignition and explosion in a connecting pipe. A regeneration system 1 in the present invention comprises: a thermal decomposition apparatus 10 for thermally decomposing scraps of molded bodies obtained by molding a (meth)acrylic resin composition containing a (meth)acrylic polymer, the thermal decomposition apparatus comprising an introduction unit 12 for introducing scraps, and a gas discharge unit 14 for discharging a methyl (meth)acrylate-containing gas generated by the thermal decomposition of the (meth)acrylic resin composition; and a gas treatment apparatus 30 which is connected to the gas discharge unit 14 via a connecting pipe 20 and which includes at least one type selected from the group consisting of a refining unit for refining a gas discharged via the connecting pipe and a cooling unit for cooling the gas. The connecting pipe includes at least one pipe main body 22A, and at least a partial region of the pipe main body has a cooling unit 24 for cooling a gas that passes through the pipe main body.
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
C07C 67/475 - Préparation d'esters d'acides carboxyliques par ouverture de liaisons carbone-carbone suivie d'un réarrangement, p.ex. par dismutation ou migration de groupes entre différentes molécules
The present invention provides a compound having an excellent control effect on harmful arthropods. A compound represented by formula (I) [wherein the meaning of each symbol is as described in the description] or N-oxide thereof has an excellent control effect on harmful arthropods.
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
A61K 31/437 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p.ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle condensés en ortho ou en péri avec des systèmes hétérocycliques le système hétérocyclique contenant un cycle à cinq chaînons ayant l'azote comme hétéro-atome du cycle, p.ex. indolizine, bêta-carboline
The present invention provides an excellent control method against plant diseases. A compound represented by formula (I) or an N oxide thereof or salts thereof can be used for controlling plant diseases (in the formula, Z represents a C6-C10 aryl group, etc.; R1and R2are the same as or different from each other and each represents a C1-C6 chain hydrocarbon group, etc.; R3represents a C1-C6 chain hydrocarbon group or the like; adjacent R1and R3may be combined with a carbon atom to which they are bonded to form a C4-C7 alicyclic hydrocarbon; adjacent two R3and R3may be combined with a carbon atom to which they are bonded, to thereby form a C4-C7 alicyclic hydrocarbon; and p represents 0, 1, 2, or 3, and, when p is 2 or 3, two or three R3s may be the same as or different from each other.).
C07D 401/12 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
54.
CYCLOPROPANECARBOXYLIC ACID ESTER COMPOUND AND USE THEREOF
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula (I), has excellent control efficacy against plant diseases.
C07C 69/757 - Esters d'acides carboxyliques dont un groupe carboxyle est lié à un atome de carbone d'un cycle autre qu'un cycle aromatique à six chaînons 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
A01N 53/06 - Esters contenant le groupe , où l'atome de carbone marqué d'un astérisque est acyclique ou fait partie d'un cycle ou d'un système cyclique; Leurs thio-analogues l'atome de carbone marqué d'un astérisque étant acyclique et lié directement à un atome de carbone d'un cycle aromatique à six chaînons, p.ex. esters benzyliques; Leurs thio-analogues
A01P 1/00 - Désinfectants; Composés antimicrobiens ou leurs mélanges
The present invention provides a compound having excellent control efficacy against harmful arthropods. The compound, represented by formula (I), has excellent control efficacy against harmful arthropods.
The present invention provides a compound having excellent control efficacy against plant diseases. The compound, represented by formula 1, has excellent control efficacy against plant diseases (in the formula, for R1and R2, R1represents a hydrogen atom and R2represents a 1-propen-2-yl group or a 2-hydroxypropan-2-yl group, or R1and R2 are united and represent an isopropylidene group).
The present invention provides a method for producing elastomer pellets, the method comprising a step for hot cutting an elastomer that is extruded from a die hole of a die, wherein the value of parameter A that is expressed by general formula (I) is 3.5 or more. (I): A = 0.066 × X + 0.135 × Y (In general formula (I), X represents the shear rate (1/sec) of the elastomer in the die hole; Y represents the stress relaxation torque integral value (dNm∙sec) of the elastomer; and the stress relaxation torque integral value is obtained by integrating the torque values from 0.01 second to 10 seconds with respect to the torque curve that is obtained from a double logarithmic plot of stress relaxation times and torques, which are measured by performing a stress relaxation test of the elastomer at the temperature of 50°C and the strain rate of 13.95%.)
B29B 9/06 - Fabrication de granulés par division de matière préformée sous forme de filaments, p.ex. combinée avec l'extrusion
C08F 236/10 - Copolymères de composés contenant plusieurs radicaux aliphatiques non saturés et l'un au moins contenant plusieurs liaisons doubles carbone-carbone le radical ne contenant que deux doubles liaisons carbone-carbone conjuguées avec des monomères vinylaromatiques
58.
LIQUID-CRYSTAL POLYESTER COMPOSITION, METHOD FOR PRODUCING LIQUID-CRYSTAL POLYESTER COMPOSITION, AND MOLDED OBJECT
The present invention relates to a liquid-crystal polyester composition which comprises a liquid-crystal polyester and an olefin copolymer, wherein the olefin copolymer comprises repeating unit A derived from a C2-C8 olefin monomer and repeating unit B having a glycidyl group.
C08L 67/00 - Compositions contenant des polyesters obtenus par des réactions créant une liaison ester carboxylique dans la chaîne principale; Compositions contenant des dérivés de tels polymères
C08F 210/00 - Copolymères d'hydrocarbures aliphatiques non saturés contenant une seule liaison double carbone-carbone
C08G 63/02 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés
C08G 63/06 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés dérivés des acides hydroxycarboxyliques
C08L 23/02 - Compositions contenant des homopolymères ou des copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carbone; Compositions contenant des dérivés de tels polymères non modifiées par un post-traitement chimique
C08L 63/10 - Résines époxy modifiées par des composés non saturés
59.
HARD COATING FILM AND IMAGE DISPLAY DEVICE HAVING SAME
ITITIT) is controlled to a specific range, so that high hardness, excellent scratch resistance, and excellent bending resistance are exhibited, enabling repeated folding.
C09D 133/06 - Homopolymères ou copolymères d'esters d'esters ne contenant que du carbone, de l'hydrogène et de l'oxygène, l'atome d'oxygène faisant uniquement partie du radical carboxyle
G06F 3/041 - Numériseurs, p.ex. pour des écrans ou des pavés tactiles, caractérisés par les moyens de transduction
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
G02B 5/30 - OPTIQUE ÉLÉMENTS, SYSTÈMES OU APPAREILS OPTIQUES Éléments optiques autres que les lentilles Éléments polarisants
60.
LIQUID CRYSTAL POLYESTER POWDER, COMPOSITION, METHOD FOR PRODUCING COMPOSITION, METHOD FOR PRODUCING FILM, AND METHOD FOR PRODUCING LAMINATED BODY
The present invention relates to a liquid crystal polyester powder comprising a liquid crystal polyester, wherein, when a particle diameter at which a cumulative volume proportion from a small particle side in a volume-based cumulative particle diameter distribution curve by laser diffraction/scattering type particle diameter distribution measurement is 90% is defined as D90, D90 is 20 μm or less.
C09K 19/32 - Composés non stéroïdes formant des cristaux liquides contenant des systèmes cycliques condensés, c. à d. systèmes cycliques condensés en ortho ou en péri, pontés ou condensés en spiro
A method for producing a phosphor having a core-shell structure that includes: a core part formed of a crystal phase of an inorganic compound containing a metal element M constituting a luminescent center ion and aluminum; and a shell part containing at least one element selected from the group consisting of boron and silicon and formed on at least a portion of a surface of the core part, the method including: mixing a raw material of the crystal phase and a raw material of the shell part; and heating the obtained mixture at a temperature at which the raw material of the shell part is liquefied, but a host crystal of a phosphor to be obtained is maintained, in which the raw material of the crystal phase contains a raw material compound having D50 in a particle diameter distribution of 0.2 to 90 μm and containing aluminum.
The present invention pertains to, inter alia, a resin composition containing a liquid crystal polyester and a thermoplastic polyimide. The liquid crystal polyester has a repeating unit containing a naphthalene structure, and the number of the repeating units containing the naphthalene structure is 60% or more in relation to a total of 100% of all repeating units in the liquid crystal polyester. The content percentage of the liquid crystal polyester in relation to 100 mass% of the total content of the liquid crystal polyester and thermoplastic polyimide is 65 mass% or greater.
C08L 67/00 - Compositions contenant des polyesters obtenus par des réactions créant une liaison ester carboxylique dans la chaîne principale; Compositions contenant des dérivés de tels polymères
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
C08G 73/10 - Polyimides; Polyester-imides; Polyamide-imides; Polyamide-acides ou précurseurs similaires de polyimides
C08L 79/08 - Polyimides; Polyester-imides; Polyamide-imides; Polyamide-acides ou précurseurs similaires de polyimides
This electrolyte composition comprises: an ionically conductive inorganic solid electrolyte; a polymer having the ability to preferentially conduct metal ions; and an ionic liquid.
H01M 10/056 - Accumulateurs à électrolyte non aqueux caractérisés par les matériaux utilisés comme électrolytes, p.ex. électrolytes mixtes inorganiques/organiques
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/08 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques oxydes
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01G 11/56 - Condensateurs hybrides, c. à d. ayant des électrodes positive et négative différentes; Condensateurs électriques à double couche [EDL]; Procédés de fabrication desdits condensateurs ou de leurs composants Électrolytes Électrolytes solides, p.ex. gels; Additifs pour ceux-ci
H01M 10/056 - Accumulateurs à électrolyte non aqueux caractérisés par les matériaux utilisés comme électrolytes, p.ex. électrolytes mixtes inorganiques/organiques
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
An electrolyte composition comprising an ion-conductive inorganic solid electrolyte, a polymer having the ability to preferentially conduct metal ions, and an organic solvent, the electrolyte composition satisfying that the content of the ion-conductive inorganic solid electrolyte is (1) 50 mass% or greater with respect to the whole electrolyte composition and/or (2) 15 vol% or greater with respect to the whole electrolyte composition.
H01M 10/056 - Accumulateurs à électrolyte non aqueux caractérisés par les matériaux utilisés comme électrolytes, p.ex. électrolytes mixtes inorganiques/organiques
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/08 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques oxydes
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01G 11/56 - Condensateurs hybrides, c. à d. ayant des électrodes positive et négative différentes; Condensateurs électriques à double couche [EDL]; Procédés de fabrication desdits condensateurs ou de leurs composants Électrolytes Électrolytes solides, p.ex. gels; Additifs pour ceux-ci
A touch sensor includes a sensing part in which a plurality of sensing cells is arranged and connected and a wiring part connected to the sensing part and formed outside the sensing part. The wiring part includes a first divisional wiring part having a plurality of first divisional wires having a connecting protrusion with a width larger than that of the wiring at one end thereof and a second divisional wiring part having a plurality of second divisional wires having one end thereof with a width smaller than that of the connecting protrusion and coupled to and overlapped with the connecting protrusion. The first divisional wiring part and the second divisional wiring part are formed by divisional exposure.
There is provided a piezoelectric stack including: a substrate (1); a bottom electrode film (2) on the substrate; a piezoelectric film (3) on the bottom electrode film, having a planar area smaller than a planar area of the bottom electrode film; a top electrode film (4) on the piezoelectric film; and an insulating film (5) provided from the top electrode film to the bottom electrode film and covering at least a part of a side surface of the piezoelectric film, wherein the insulating film has a slope (9a) filling a step between a top surface of the top electrode film and a top surface of the bottom electrode film, and the slope has a shape alleviating the step.
H10N 30/03 - Assemblage de dispositifs incluant des parties piézo-électriques ou électrostrictives
H10N 30/00 - Dispositifs piézo-électriques ou électrostrictifs
H10N 30/063 - Formation d’interconnexions, p.ex. d’électrodes de connexion de parties piézo-électriques ou électrostrictives multicouches
H10N 30/076 - Formation de parties ou de corps piézo-électriques ou électrostrictifs sur un élément électrique ou sur un autre support par dépôt de couches piézo-électriques ou électrostrictives, p.ex. par impression par aérosol ou par sérigraphie par dépôt en phase vapeur
H10N 30/077 - Formation de parties ou de corps piézo-électriques ou électrostrictifs sur un élément électrique ou sur un autre support par dépôt de couches piézo-électriques ou électrostrictives, p.ex. par impression par aérosol ou par sérigraphie par dépôt en phase liquide
H10N 30/87 - Dispositifs piézo-électriques ou électrostrictifs - Détails de structure Électrodes ou interconnexions, p.ex. connexions électriques ou bornes
A herbicidal composition including ethyl [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxylacetate and a herbicide selected from the group consisting of bicyclopyrone, mesotrione, tembotrione, isoxaflutole, pyrasulfotole, topramezone, and tolpyralate. A weight ratio of ethyl [3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxylacetate to the herbicide is from 1:1 to 1:42.
C07D 401/12 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
69.
ION CONDUCTIVE SUBSTANCE, ELECTROLYTE, AND BATTERY
An ion conductive substance comprising: an alkali metal element; a tetravalent metal element M; a halogen element; a dopant element X; and an oxygen element, wherein the content of the dopant element X is 50 mol% or less with respect to the content of the metal element M, and, in an X-ray diffraction chart obtained by measuring the ion conductive substance using a CuKα ray at 25°C, a diffraction peak having a half width of 2.0-10° exists in a range of 10-20° for the 2θ angle.
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
C01B 25/45 - Phosphates contenant plusieurs métaux ou un métal et l'ammonium
The purpose of the present invention is to provide a colorant capable of producing a coating film having enhanced green spectral characteristics. The colorant of the present invention contains a compound represented by formula (I) and is characterized in that the ratio of the number of groups represented by formula (T-2) to the number of Al atoms in the compound represented by formula (I) in the colorant is from 0.1 to 3. [In formula (I), R1and R2each independently represent a hydrogen atom, a hydroxy group, -R13, or -O-R13. When at least one of R1and R2represents -R13or -O-R13, R1and R2may bond to each other to form a ring. Ring T1, ring T2, ring T3, and ring T4 each independently represent a group represented by formula (T-1) or formula (T-2).]
Provided is an ingredient for a feed for aquatic animals, the ingredient serving as an ingredient in fish-meal substitute. This ingredient for a feed for aquatic animals contains secretions from insects of the infraorder Muscomorpha.
A23K 10/20 - Produits alimentaires pour animaux à base de matières d’origine animale
A23K 10/26 - Produits alimentaires pour animaux à base de matières d’origine animale à base de matières résiduelles, p.ex. de plumes, d'os ou de peau
A23K 50/80 - Produits alimentaires spécialement conçus pour des animaux spécifiques pour les animaux aquatiques, p.ex. pour les poissons, les crustacés ou les mollusques
72.
METHOD FOR PRODUCING RESIN COMPOSITION, AND RESIN COMPOSITION
A method is provided for producing a resin composition including an olefin-based polymer; an inorganic filler; and a lubricant, in which the olefin-based polymer is at least one polymer selected from a propylene-based polymer and an ethylene-based polymer having a melt flow rate of 0.5 g/10 minutes or more measured at a temperature of 190° C. and a load of 2.16 kg. The method includes a step (1) of mixing the inorganic filler and a lubricant; a step (2) of mixing a mixture obtained in the step (1) and the olefin-based polymer; and a step (3) of kneading a mixture obtained in the step (2).
A propylene production method includes: a reaction step of supplying a fresh raw material and a recycled raw material to a reactor to obtain a crude product; a gas-liquid separation step of separating the crude product into a gas phase and a liquid phase; a propylene recovery step of recovering propylene from the gas phase; and a recycling step of recovering the recycled raw material from the liquid phase.
C07C 1/207 - 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 à partir de composés carbonylés
74.
ALKALI METAL ELEMENT-CONTAINING HALIDE, ELECTROLYTE, BATTERY, AND METHOD FOR PRODUCING HALIDE SOLID ELECTROLYTE
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisés; Emploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
C01F 17/36 - Composés contenant des métaux de terres rares et au moins un élément autre qu’un métal des terres rares, l'oxygène ou l'hydrogène, p.ex. La4S3Br6 le seul anion étant un halogénure, p.ex. NaYF4
H01G 11/56 - Condensateurs hybrides, c. à d. ayant des électrodes positive et négative différentes; Condensateurs électriques à double couche [EDL]; Procédés de fabrication desdits condensateurs ou de leurs composants Électrolytes Électrolytes solides, p.ex. gels; Additifs pour ceux-ci
H01M 4/13 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes composées d'un ou comprenant un matériau actif Électrodes pour accumulateurs à électrolyte non aqueux, p.ex. pour accumulateurs au lithium; Leurs procédés de fabrication
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p.ex. liants, charges
maxmax to the long wavelength side in the absorption spectrum thereof. A compound according to the present invention is characterized by being represented by formula (I). [In formula (I), R1represents a C2-20 unsaturated aliphatic hydrocarbon group that may have a substituent, and R2represents a hydrogen atom, a C1-20 hydrocarbon group that may have a substituent, or a single bond that joins Z2and R1. Z1and Z2 independently represent a single bond or an oxygen atom.]
NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (Japon)
AINO UNIVERSITY (Japon)
Inventeur(s)
Ozoe, Atsufumi
Kobayashi, Kentaro
Takahashi, Yasuhiko
Matsunaga, Kohei
Sato, Takaaki
Mizutani, Yoichi
Abrégé
The present invention provides a technology for performing a test for prostate cancer. This method is for testing the possibility of having prostate cancer, the method comprising (1) measuring the amount or concentration of a biomarker in a body fluid sample collected from a subject, the biomarker being at least one member selected from the group consisting of dimethyl glutarate, 2,6-xylidine, 2-hydroxy-2-methylpropiophenone, 2,6-di(propan-2-yl) phenol, dimethyl succinate, acetophenone, 2-phenyl-2-propanol, and 3,5,5-trimetyl-2-cyclohexenone.
A material comprising an electron-accepting unit of formula (I): Ar is an aromatic ring; Ar1 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring containing N and C ring atoms; when Ar1 is a substituted or unsubstituted 6-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 6-membered heteroaromatic ring wherein the ring atoms are selected from N and C; when Ar1 is a 5-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring; Ar3 is a 5-membered ring or a substituted or unsubstituted 6-membered ring; Ar4 is a 5-membered ring or a substituted or unsubstituted 6-membered ring or is absent; Ar5 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring; Ar6 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring or is absent; and each X is independently a substituent bound to a C atom of Ar3, and where present Ar4, with the proviso that at least one X is an electron withdrawing group; and wherein the material further comprises an electron-donating unit.
A material comprising an electron-accepting unit of formula (I): Ar is an aromatic ring; Ar1 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring containing N and C ring atoms; when Ar1 is a substituted or unsubstituted 6-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 6-membered heteroaromatic ring wherein the ring atoms are selected from N and C; when Ar1 is a 5-membered heteroaromatic ring, Ar2 is a substituted or unsubstituted 5- or 6-membered heteroaromatic ring; Ar3 is a 5-membered ring or a substituted or unsubstituted 6-membered ring; Ar4 is a 5-membered ring or a substituted or unsubstituted 6-membered ring or is absent; Ar5 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring; Ar6 is a substituted or unsubstituted monocyclic or polycyclic group containing at least one aromatic or heteroaromatic ring or is absent; and each X is independently a substituent bound to a C atom of Ar3, and where present Ar4, with the proviso that at least one X is an electron withdrawing group; and wherein the material further comprises an electron-donating unit.
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
H10K 71/15 - Dépôt d'une matière active organique en utilisant un dépôt liquide, p. ex. revêtement par centrifugation caractérisé par le solvant utilisé
The present invention addresses the problem of realizing a high recovery rate even when the raw material supply rate is particularly high. The present invention pertains to a regenerated methyl(meth)acrylate production method comprising: a thermal decomposition step for thermally decomposing a methyl(meth)acrylate-based polymer composition that contains one or more methyl(meth)acrylate-based polymers and includes a methyl(meth)acrylate-based polymer having a viscosity average molecular weight of 800000-5000000; and a recovery step for recovering a regenerated methyl(meth)acrylate generated in the thermal decomposition step.
C07C 67/475 - Préparation d'esters d'acides carboxyliques par ouverture de liaisons carbone-carbone suivie d'un réarrangement, p.ex. par dismutation ou migration de groupes entre différentes molécules
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
79.
POSITIVE ELECTRODE ACTIVE MATERIAL FOR LITHIUM SECONDARY BATTERY, ELECTRODE FOR LITHIUM SECONDARY BATTERY, AND LITHIUM SECONDARY BATTERY
This positive electrode active material for a lithium secondary battery has a layered structure that includes secondary particles that are an aggregate of primary particles, and includes an element M1 and an element M2, wherein the element M1 is at least one element selected from the group consisting of Nb, W, Mo, Ta, La, B, and P, the element M2 is at least one element M2 selected from the group consisting of Ni, Co, and Mn, and formulas (1) and (2) are satisfied.
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
H01M 4/36 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
A polymer comprising a repeating structure of formula (I) wherein Ar in each occurrence is an arylene or heteroarylene group; p is at least 2; one of Y1 and Y2 is CR1 wherein R1 is H or a substituent; and the other of Y1 and Y2 is N. The polymer may be formed by reaction of monomers containing reactive groups which react to form an imine. The polymer may be used as a thermally conductive polymer, e.g. a thermally conductive layer of an electronic device.
A polymer comprising a repeating structure of formula (I) wherein Ar in each occurrence is an arylene or heteroarylene group; p is at least 2; one of Y1 and Y2 is CR1 wherein R1 is H or a substituent; and the other of Y1 and Y2 is N. The polymer may be formed by reaction of monomers containing reactive groups which react to form an imine. The polymer may be used as a thermally conductive polymer, e.g. a thermally conductive layer of an electronic device.
A process or apparatus for producing polyethylene with improved film thinning and handleability involves polymerizing high-pressure ethylene using an autoclave-type reactor in the presence of a polymerization initiator. The reaction zone of the reactor has at least two different temperature sections; the polymerization initiator and the ethylene are supplied to the upstream temperature section in the reaction zone and the ethylene is polymerized to generate polyethylene; unreacted ethylene and the polyethylene generated at the upstream temperature section in the reactor flow into the downstream temperature section in communication with the upstream temperature section, so that additional polyethylene is generated at the downstream temperature section. A difference (ΔT [° C.]) between a temperature (T1 [° C.]) of the temperature section positioned upstream and a temperature (T2 [° C.]) of the temperature section positioned downstream in the reaction zone that receives the polymerization initiator and is in the autoclave-type reactor is 2.1° C. to 8.4° C.
This method for producing a positive electrode active material comprises the following steps. (1) a step in which an activation agent containing at least one compound that is selected from the group consisting of a potassium compound and a sodium compound is mixed into an electrode mixture which contains a positive electrode active material, a binder and an electrolyte, and from which at least some of the electrolyte is removed by means of a contact with an electrolyte cleaning solvent (2) a step in which the thus-obtained mixture is heated to a retention temperature that is not less than the melting initiation temperature of the activation agent, so that the positive electrode active material contained in the mixture is activated (3) a step in which the mixture after heating is brought into contact with a liquid that contains water, thereby obtaining a slurry that contains a solid component and a liquid component, and subsequently, the slurry is separated into the solid component and the liquid component, wherein the total content of potassium and sodium in the liquid component after the separation is 0.090 to 2.0% by mass, and the total content of potassium and sodium in the solid component after the separation is 1.2% by mass or less
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
C22B 7/00 - Mise en œuvre de matériaux autres que des minerais, p.ex. des rognures, pour produire des métaux non ferreux ou leurs composés
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
This positive electrode active material for a lithium secondary battery contains a composite oxide containing at least one element selected from the following element group 1, and at least one element selected from the following element group 2, and satisfies requirements (1)-(3). Element group 1: Ni, Co, Mn, Fe, Al, and P. Element group 2: Li, Na, K, Ca, Sr, Ba, and Mg. Requirement (1): The active material contains fluorine, sulfur, and potassium, and the total amount of fluorine, sulfur, and potassium is 0.12-10.0 mass%. Requirement (2): When the concentration of potassium in the active material is defined as CK (mass%) and the concentration of sulfur in the active material is defined as CS (mass%), CK/CS is 0.0001-2.0. Requirement (3): When the concentration of fluorine in the active material is defined as CF (mass%) and the concentration of sulfur in the active material is defined as CS (mass%), CF/CS is 0.0001-20.0.
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
The present invention addresses the problem of providing a new compound having excellent film formability and curability that can yield a cured product that exhibits a high refractive index. The present invention relates to a compound that is represented by formula (I). In the formula, L represents a divalent group; multiple L may be the same or different. m represents 0 or 1; multiple m may be the same or different. A represents an O atom or an S atom; multiple A may be the same or different. n represents any integer of 0 to 3; multiple n may be the same or different. R represents a monovalent substituent; when there are multiple R, the multiple R may be the same or different. R2represents a hydrogen atom or a monovalent substituent; multiple R2 may be the same or different. Two groups having S atoms bond to positions 1 and 6, positions 2 and 6, or positions 2 and 7 of the naphthalene ring.
C08G 59/02 - Polycondensats contenant plusieurs groupes époxyde par molécule
C08G 59/14 - Polycondensats modifiés par post-traitement chimique
C08G 59/30 - Composés diépoxydés contenant des atomes autres que le carbone, l'hydrogène, l'oxygène et l'azote
C08G 75/06 - Polythioéthers à partir de thioéthers cycliques
C08G 75/08 - Polythioéthers à partir de thioéthers cycliques à partir de thiiranes
G02B 1/04 - OPTIQUE ÉLÉMENTS, SYSTÈMES OU APPAREILS OPTIQUES Éléments optiques caractérisés par la substance dont ils sont faits; Revêtements optiques pour éléments optiques faits de substances organiques, p.ex. plastiques
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
H01L 21/301 - Traitement des corps semi-conducteurs en utilisant des procédés ou des appareils non couverts par les groupes pour subdiviser un corps semi-conducteur en parties distinctes, p.ex. cloisonnement en zones séparées
85.
COMPOSITION, CURED PRODUCT, DISPLAY DEVICE, AND SOLID-STATE IMAGING ELEMENT
The present invention provides a novel composition that has superior curability and can provide a cured product demonstrating a high refractive index. The present invention relates to a composition including a compound represented by formula (I), and an alkali-soluble resin. In formula (I), n represents an integer from 0 to 6, L represents a single bond or a divalent group, the plurality of Ls may be the same or different, R11represents a monovalent substituent, if there are a plurality of R11s then the plurality of R11s may be the same or different, R12is selected from the group consisting of a hydrogen atom, formula (1a), and formula (1b), and the plurality of R12s may be the same or different.
C08G 75/06 - Polythioéthers à partir de thioéthers cycliques
C08L 101/12 - Compositions contenant des composés macromoléculaires non spécifiés caractérisées par des propriétés physiques, p.ex. anisotropie, viscosité ou conductivité électrique
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
86.
SOLID CATALYST COMPONENT FOR OLEFIN POLYMERIZATION
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
A solid catalyst component for olefin polymerization containing a titanium atom, a magnesium atom, a halogen atom, and an internal electron donor, and having an envelope E1 calculated by the following Formula (1) in a range of 0.810 to 0.920.
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
A solid catalyst component for olefin polymerization containing a titanium atom, a magnesium atom, a halogen atom, and an internal electron donor, and having an envelope E1 calculated by the following Formula (1) in a range of 0.810 to 0.920.
E1=LE1/LS1 (1)
To produce an olefin-based polymer having a minor amount of decrease in bulk density due to heat.
A solid catalyst component for olefin polymerization containing a titanium atom, a magnesium atom, a halogen atom, and an internal electron donor, and having an envelope E1 calculated by the following Formula (1) in a range of 0.810 to 0.920.
E1=LE1/LS1 (1)
(In Formula, LE1 is a convex hull perimeter of the solid catalyst component for olefin polymerization obtained from an image of the solid catalyst component for olefin polymerization captured with a scanning electron microscope, and LS1 is an actual perimeter of the solid catalyst component for olefin polymerization obtained from the image of the solid catalyst component for olefin polymerization captured with the scanning electron microscope.)
C08F 4/16 - Composés métalliques autres que les hydrures et autres que les composés organiques de métal; Complexes d'halogénures de bore ou d'halogénures d'aluminium avec des composés organiques contenant de l'oxygène de silicium, de germanium, d'étain, de plomb, de titane, de zirconium ou de hafnium
C08F 4/12 - Composés métalliques autres que les hydrures et autres que les composés organiques de métal; Complexes d'halogénures de bore ou d'halogénures d'aluminium avec des composés organiques contenant de l'oxygène de bore, d'aluminium, de gallium, d'indium, de thallium ou des terres rares
87.
PHOTOELECTRIC CONVERSION ELEMENT, INK FOR PRODUCING PHOTOELECTRIC CONVERSION ELEMENT, METHOD FOR MANUFACTURING PHOTOELECTRIC CONVERSION ELEMENT, IMAGE SENSOR, AND FINGERPRINT AUTHENTICATION DEVICE
The present invention addresses the problem of providing a photoelectric conversion element in which an increase in dark current after heat treatment is suppressed. The present invention relates to a photoelectric conversion element having: an anode (12); a cathode (16); an active layer (14) provided between the anode (12) and the cathode (16); and intermediate layers (13, 15) provided between the anode (12) and the active layer (14) and/or between the cathode (16) and the active layer (14). The intermediate layers (13, 15) contain a non-ionic insulating polymer.
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 30/82 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire - Détails de structure Électrodes Électrodes transparentes, p. ex. électrodes en oxyde d'étain indium [ITO]
A sputtering target material made of a sintered object of an oxide comprising potassium, sodium, niobium, and oxygen, the sputtering target material having a density of 4.2 g/cm3 or less and a Vickers hardness of 30-200, wherein a plurality of crystal grains observed in the sputter surface have an area-average grain diameter of 3.0 μm or larger.
C04B 35/495 - Produits céramiques mis en forme, caractérisés par leur composition; Compositions céramiques; Traitement de poudres de composés inorganiques préalablement à la fabrication de produits céramiques à base d'oxydes à base d'oxydes de vanadium, de niobium, de tantale, de molybdène ou de tungstène ou de leurs solutions solides avec d'autres oxydes, p.ex. vanadates, niobates, tantalates, molybdates ou tungstates
H10N 30/076 - Formation de parties ou de corps piézo-électriques ou électrostrictifs sur un élément électrique ou sur un autre support par dépôt de couches piézo-électriques ou électrostrictives, p.ex. par impression par aérosol ou par sérigraphie par dépôt en phase vapeur
H10N 30/097 - Formation de matériaux inorganiques par frittage
This positive electrode active material for lithium secondary batteries comprises a plurality of secondary particles, in each of which a plurality of primary particles aggregate; and this positive electrode active material for lithium secondary batteries satisfies the requirements described below. (1) The secondary particles each internally comprise a plurality of voids, and the value at a cumulative frequency of 50% in the area-based cumulative frequency distribution of the circle-equivalent diameters of the voids on the basis of the cross-sectional images of the secondary particles is more than 0.2 µm but not more than 0.65 µm, while the value at a cumulative frequency of 50% in the area-based cumulative frequency distribution of the circularity of the voids on the basis of the cross-sectional images of the secondary particles is 2.2 to 6.5. (2) The primary particles are formed of an oxide which contains one or more elements that are selected from the element group 1 shown below and one or more elements that are selected from the element group 2 shown below. Element group 1: Ni, Co, Mn, Fe, Al and P Element group 2: Li, Na, K, Ca, Sr, Ba and Mg
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
90.
PRODUCTION METHOD FOR POSITIVE ELECTRODE ACTIVE MATERIAL
This production method for a positive electrode active material comprises the following steps. (1) A step for bringing an electrode mixture containing a positive electrode active material, a binder member, and an electrolyte into contact with an electrolyte cleaning solvent to obtain a slurry including solid components and liquid components, and thereafter, separating the slurry into the solid components and the liquid components, wherein, in the liquid components after the separation, the P amount is 0.0020-2.0 mass% and the F amount is 0.01-7.0 mass%, and, in the solid components after the separation, the P amount remaining therein is 0.7 mass% or less. (2) A step for mixing an activation agent containing one or more alkali metal compounds with the separated solid components. (3) A step for heating the obtained mixture to a retention temperature not less than the melting start temperature of the activation agent so as to activate the positive electrode active material contained in the mixture.
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
C22B 7/00 - Mise en œuvre de matériaux autres que des minerais, p.ex. des rognures, pour produire des métaux non ferreux ou leurs composés
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
91.
METHOD FOR PRODUCING POSITIVE ELECTRODE ACTIVE MATERIAL
This method for producing a positive electrode active material comprises the steps described below. (1) A mixture is obtained by mixing an activation agent which contains one or more alkali metal compounds into an electrode mixture which contains a positive electrode active material, a binder and an electrolyte, and from which at least some of the electrolyte is removed by means of a contact with an electrolyte cleaning solvent. (2) The mixture is heated to a retention temperature that is not less than the melting initiation temperature of the activation agent. (3) The mixture after the step (2) is brought into contact with a liquid that contains water, thereby obtaining a slurry that contains a solid component and a liquid component, and subsequently, the slurry is separated into the solid component and the liquid component. (4) The thus-obtained solid component is exposed to heat and/or a reduced pressure environment, thereby removing water from the solid component, and within 24 hours from the separation of the slurry into the solid component and the liquid component, the ambient pressure at which the solid component is present and/or the temperature of the solid component is changed so that the ratio of the saturated water vapor pressure at the temperature of the solid component to the ambient pressure is 80% or more. (5) The solid component after the step (4) is subjected to a heat treatment at less than 900°C.
H01M 10/54 - Récupération des parties utiles des accumulateurs usagés
C22B 7/00 - Mise en œuvre de matériaux autres que des minerais, p.ex. des rognures, pour produire des métaux non ferreux ou leurs composés
H01M 4/505 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de manganèse d'oxydes ou d'hydroxydes mixtes contenant du manganèse pour insérer ou intercaler des métaux légers, p.ex. LiMn2O4 ou LiMn2OxFy
H01M 4/525 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs d'oxydes ou d'hydroxydes inorganiques de nickel, de cobalt ou de fer d'oxydes ou d'hydroxydes mixtes contenant du fer, du cobalt ou du nickel pour insérer ou intercaler des métaux légers, p.ex. LiNiO2, LiCoO2 ou LiCoOxFy
The present invention addresses the problem of providing a novel compound which enables the production of a cured article having a high refraction index and which has excellent moldability and curability. The present invention relates to a compound that is represented by formula (I). In the formula, a plurality of L's each independently represents a bivalent group and may be the same as or different from each other; a plurality of m's each independently represent 0 or 1 and may be the same as or different from each other; n represents an integer of 0 to 6; R represents a monovalent substituent, and when there are a plurality of R's, the R's may be the same as or different from each other; and a plurality of R2's each represents a hydrogen atom or a monovalent substituent, and the R2's may be the same as or different from each other.
C08G 75/06 - Polythioéthers à partir de thioéthers cycliques
C08G 75/08 - Polythioéthers à partir de thioéthers cycliques à partir de thiiranes
G02B 1/04 - OPTIQUE ÉLÉMENTS, SYSTÈMES OU APPAREILS OPTIQUES Éléments optiques caractérisés par la substance dont ils sont faits; Revêtements optiques pour éléments optiques faits de substances organiques, p.ex. plastiques
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
H01L 21/301 - Traitement des corps semi-conducteurs en utilisant des procédés ou des appareils non couverts par les groupes pour subdiviser un corps semi-conducteur en parties distinctes, p.ex. cloisonnement en zones séparées
93.
COMPOSITION, CURED PRODUCT, DISPLAY DEVICE, AND SOLID-STATE IMAGING DEVICE
The present invention provides a novel composition that can yield a cured product having a high refractive index and has excellent curability. The present invention pertains to a composition comprising: a compound represented by formula (I); and a resin having a refractive index of at least 1.60 at a wavelength of 550 nm. In formula (I), n represents an integer of 0-6, L represents a single bond or a divalent group, a plurality of L's may be the same or different, R11represents a monovalent substituent (when there is a plurality of R11's, the plurality of R11may be the same or different), R12is selected from the group consisting of a hydrogen atom, formula (1a), and formula (1b), and a plurality of R12's may be the same or different.
C08G 75/06 - Polythioéthers à partir de thioéthers cycliques
C08L 101/12 - Compositions contenant des composés macromoléculaires non spécifiés caractérisées par des propriétés physiques, p.ex. anisotropie, viscosité ou conductivité électrique
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
The present invention addresses the problem of providing a novel compound that is capable of providing a cured product exhibiting a high refractive index, and has excellent curability. The present invention relates to a compound that is represented by formula (I). In the formula and in the compound represented by formula (I), R represents a monovalent hydrocarbon group, and if there are a plurality of Rs, the plurality of Rs may be may be the same or different. The symbol n represents an average value that is a number of 1 or greater. A represents an O atom or an S atom. The plurality of As may be the same or different, but at least one A is an S atom.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
Produits et services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
Produits et services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
Produits et services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
Produits et services
Industrial chemicals; adhesives and glues for industrial
purposes; plastics (raw materials); synthetic resins,
unprocessed; artificial resins, unprocessed; plastics,
unprocessed. Synthetic resins, semi-processed; artificial resins,
semi-processed; plastic film, other than for wrapping;
semi-finished plastic products; plastic semi-worked products
in the form of pellets, rods, bars, foils, foams, fibers,
films, boards, plates, profiles, hoses, tubes, tapes,
strips, blocks and sheets; plastic substances,
semi-processed; plastic sheet materials for use in
manufacture; plastic fibers, other than for textile use;
chemical fiber, not for textile use; gum, raw or
semi-worked; rubber, raw or semi-worked; synthetic rubber;
natural rubber; insulating materials; insulators; electrical
insulators; electrical insulating materials; insulating
varnish; soundproofing materials of rock wool, not for
building purposes; asbestos powder; asbestos boards.
Provided is a compound represented by formula (1). In formula (1), Ar11, Ar12, and Ar13represent a 1,4-phenylene group, a 1,4-naphthylene group, or a divalent aromatic condensed heterocyclic group having two five-membered rings, and at least one of Ar11, Ar12, and Ar13represents a divalent aromatic condensed heterocyclic group. k represents 1 or 2. R11, R12, R13, and R14represent a hydrogen atom, a linear or cyclic aliphatic group, or an aryl group. At least one set of: R11and R12; and R13and R14may be connected to each other to form a ring in which at least one of the methylene units constituting the ring may be substituted with an oxygen atom or a carbonyl group. At least one of R11, R12, R13, and R14 may be substituted with at least one of an organosilyloxy group or a polymerizable group.
H10K 50/10 - OLED ou diodes électroluminescentes polymères [PLED]
H10K 59/00 - Dispositifs intégrés, ou ensembles de plusieurs dispositifs, comprenant au moins un élément organique émetteur de lumière couvert par le groupe
