Provided is a crystalline oxide thin film including In as a main component, wherein 50% or more of Fourier transform images obtained by subjecting each of lattice images in a plurality of image regions extracted from a transmission electron microscope (TEM) image of a cross-section of the crystalline oxide thin film to two-dimensional Fourier transform (FFT) processing exhibit any one of plane orientations selected from (100), (110), (111), (211), (411), (125), (210), (310), and (320).
A lubricating oil composition may contain a base oil (A), a phosphorous acid ester (B) having at least one sulfur atom-containing group having 2 to 20 carbon atoms, the sulfur atom-containing group having at least one —(S)x— group (x is an integer of 1 or more) between two adjacent carbon atoms in a structure of an alkyl group, a thiadiazole-based compound (C), and a benzotriazole-based compound (D). A content of the component (C) may be 0.01 mass % or more and less than 0.60 mass %, based on the total mass of the lubricating oil composition. A content of the component (D) is 0.02 mass % or more and less than 0.20 mass %, based on the total mass of the lubricating oil composition.
C10M 141/10 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'au moins deux composés couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé organique contenant du phosphore
C10M 133/44 - Cycle à cinq chaînons ne contenant que du carbone et de l'azote
C10M 135/36 - Composés hétérocycliques contenant du soufre, du sélénium ou du tellure le cycle contenant du soufre et du carbone ainsi que de l'azote ou de l'oxygène
C10N 40/00 - Utilisation ou application particulière de la composition lubrifiante
C10N 40/04 - Bains d'huileBoîtes de vitessesTransmissions automatiquesMécanismes de traction
F16H 57/04 - Caractéristiques relatives à la lubrification ou au refroidissement
H02K 7/116 - Association structurelle avec des embrayages, des freins, des engrenages, des poulies ou des démarreurs mécaniques avec des engrenages
H02K 9/19 - Dispositions de refroidissement ou de ventilation pour machines avec enveloppe fermée et circuit fermé de refroidissement utilisant un agent de refroidissement liquide, p. ex. de l'huile
Provided is a lubricating oil composition that maintains excellent defoaming properties over a long period of time. The lubricating oil composition contains a hydrocarbon synthetic oil (X1), an ester synthetic oil (X2), and a phosphorus-containing copolymer (Y). The phosphorus-containing copolymer (Y) includes a structural unit (a) derived from a specific alkyl (meth)acrylate (A), a structural unit (b) derived from a specific hydroxyl group–containing (meth)acrylate (B), and a structural unit (c) derived from a specific phosphorus-containing (meth)acrylate (C).
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 50/13 - 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 comprenant des couches EL empilées dans une unité EL
The present invention provides a polycarbonate-based resin composition including a polycarbonate-based resin (S) containing a polycarbonate-polyorganosiloxane copolymer (S-1), which contains a polycarbonate block (A-1) containing a repeating unit having a specific structure and a polyorganosiloxane block (A-2) containing a specific amount of a repeating unit having a specific structure, and having a specific average chain length, and an aromatic polycarbonate-based resin (S-2) except the polycarbonate-polyorganosiloxane copolymer (S-1), the polycarbonate-based resin (S) having a specific viscosity-average molecular weight MvPC, wherein a difference MvSi-MvPC between the viscosity-average molecular weight MvPC of the polycarbonate-based resin (S) and the viscosity-average molecular weight MvSi of the polycarbonate-polyorganosiloxane copolymer (S-1) is from −3,100 or more to 6,000 or less.
A catalyst that has a high electrolytic activity and a high CO2 reduction reaction rate and a method of producing the same, a cathode, an ion exchange membrane-electrode assembly, and a solid electrolyte electrolysis apparatus are provided. The catalyst includes a metal ion selected from the group consisting of a copper ion, a nickel ion, an iron ion, a cobalt ion, a zinc ion, a manganese ion, a molybdenum ion, and an aluminum ion, a nitrogen-containing compound, and a carrier containing carbon having a primary particle diameter of 5 to 200 nm, the metal ion is coordinated to the nitrogen atom on the nitrogen-containing compound, the catalyst has a content of the metal ion coordinated to the nitrogen atom of 0.7% by mass or more, and the catalyst has a particle diameter of 10 nm to 50 μm.
C25B 9/23 - Cellules comprenant des électrodes fixes de dimensions stablesAssemblages de leurs éléments de structure avec des diaphragmes comprenant des membranes échangeuses d'ions dans ou sur lesquelles est incrusté du matériau pour électrode
C25B 11/091 - Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé d’au moins un élément catalytique et d’au moins un composé catalytiqueÉlectrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé de plusieurs éléments catalytiques ou composés catalytiques
C25B 13/05 - DiaphragmesÉléments d'espacement caractérisés par le matériau à base de matériaux inorganiques
7.
RESIN COMPOSITION, COMPOSITE MATERIAL, AND MOLDED BODY
This resin composition comprises: an aromatic polyether (A) having a radical amount at 25 °C of 6.5×1015-9.0×1017 spin/g, as measured using TEMPOL as a standard substance and benzene as a solvent for the standard substance; and an amorphous resin (B) in an amount of 10-300 parts by mass with respect to 100 parts by mass of the aromatic polyether (A), wherein the glass transition temperature of the amorphous resin (B) is 180°C or higher.
C08L 71/00 - Compositions contenant des polyéthers obtenus par des réactions créant une liaison éther dans la chaîne principaleCompositions contenant des dérivés de tels polymères
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
C10M 171/00 - Compositions lubrifiantes caractérisées par des critères purement physiques, p. ex. contenant comme matériau de base, épaississant ou additif des ingrédients exclusivement caractérisés par des valeurs numériques particulières de leurs propriétés physiques, c.-à-d. contenant des ingrédients physiquement bien définis mais dont la nature chimique n'est pas précisée ou n'est que très vaguement indiquée
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
C10N 30/02 - Point d'écoulementIndice de viscosité
C10N 40/00 - Utilisation ou application particulière de la composition lubrifiante
C10N 40/04 - Bains d'huileBoîtes de vitessesTransmissions automatiquesMécanismes de traction
To provide a compound for further improving the performance of an organic EL device, a material for an organic electroluminescent device, an organic electroluminescent device having further improved device capability, and an electronic device including such an organic electroluminescent device, and the compound is represented by formula (1). (Each symbol in the formula is as defined in the description.) In addition, the organic electroluminescent device contains the compound or has a highest occupied molecular orbital energy level HOMO, a triplet energy T1, and an 80% attenuation time t of a photoluminescence intensity PL within a predetermined range.
C07D 405/04 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une liaison directe de chaînon cyclique à chaînon cyclique
C07D 407/04 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant deux hétérocycles liés par une liaison directe de chaînon cyclique à chaînon cyclique
C07D 409/04 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une liaison directe de chaînon cyclique à chaînon cyclique
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
11.
COMPOUND, LIGHT-EMITTING ELEMENT MATERIAL, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
Provided is a compound having a structure represented by general formula (1). In general formula (1), R101to R121are each independently a hydrogen atom or a substituent, provided that R101to R121are each not a substituted or unsubstituted N-carbazolyl group. The structure represented by general formula (1) has at least one group represented by general formula (2). In general formula (2), at least one of X1to X5 represents a nitrogen atom.
The purpose of the present invention is to provide a method for producing an asphalt mixture, the method having: a step for mixing 100 parts by mass of an aggregate with 0.03-4 parts by mass of an asphalt masterbatch at 100-200ºC; and a step for further adding and mixing asphalt (c). The asphalt masterbatch contains: 10-50 mass% of a modified hydrogenated petroleum resin (a) that satisfies conditions (1) to (3); and straight asphalt (b). By using this method, it is possible to obtain an asphalt mixture which can efficiently bring out a water resistance-improving effect of an additive and which exhibits excellent water resistance. (1) Silicon element is contained at a quantity of 0.5-20 mass% in terms of silicon atoms; (2) The weight average molecular weight is 500-5000; (3) The molecular weight distribution (Mw/Mn) is 1.1-3.5.
C08L 23/20 - Homopolymères ou copolymères d'hydrocarbures contenant au moins quatre atomes de carbone contenant de quatre à neuf atomes de carbone
C08L 23/26 - Compositions contenant des homopolymères ou des copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carboneCompositions contenant des dérivés de tels polymères modifiées par post-traitement chimique
C08L 25/16 - Homopolymères ou copolymères de styrènes substitués par un radical alkyle
C08L 45/00 - Compositions contenant des homopolymères ou des copolymères de composés ne possédant pas de radicaux aliphatiques non saturés dans une chaîne latérale et contenant une ou plusieurs liaisons doubles carbone-carbone dans un système carbocyclique ou hétérocycliqueCompositions contenant des dérivés de tels polymères
E01C 7/22 - Liant introduit à chaud, p. ex. bitume chauffé
13.
CATALYST, CATHODE, ION EXCHANGE MEMBRANE-ELECTRODE ASSEMBLY AND SOLID ELECTROLYTE ELECTROLYSIS APPARATUS
A catalyst having a high production efficiency of a synthetic gas, including CO, a cathode, an ion exchange membrane-electrode assembly, and a solid electrolyte electrolysis apparatus. The catalyst includes fine particles selected from gold, silver, copper, nickel, iron, cobalt, zinc, chromium, palladium, tin, manganese, aluminum, indium, bismuth, molybdenum, and carbon nitride, a metal complex including a metal selected from copper, nickel, iron, cobalt, zinc, manganese, molybdenum, and aluminum, or an ion of the metal, having a ligand coordinated to the metal, and a carrier including carbon the carrier having a nitrogen-containing heteroaryl group having a primary amino group on a surface.
C25B 11/069 - Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau du substrat ou du support formé d’un élément et d’au moins un composéÉlectrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau du substrat ou du support formé de plusieurs composés
C25B 9/23 - Cellules comprenant des électrodes fixes de dimensions stablesAssemblages de leurs éléments de structure avec des diaphragmes comprenant des membranes échangeuses d'ions dans ou sur lesquelles est incrusté du matériau pour électrode
Provided is an aromatic polyether having a radical amount of 6.5×1015 spin/g or more at 25 °C, as measured with TEMPOL as a standard substance and benzene as a solvent of the standard substance, and having a number average molecular weight (Mn) of 14,000 or more, and a molecular weight distribution (Mw/Mn) of 6.0 or less.
C08G 65/40 - Composés macromoléculaires obtenus par des réactions créant une liaison éther dans la chaîne principale de la macromolécule à partir de composés hydroxylés ou de leurs dérivés métalliques dérivés des phénols à partir des phénols et d'autres composés
C08K 3/013 - Charges, pigments ou agents de renforcement
This aromatic polyether includes structural units represented by formula (1) and structural units represented by formula (2). The radical amount at 25°C is 6.5 × 1015to 9.0 × 1017 spin/g, as measured using TEMPOL as a standard substance and using benzene as a solvent of the standard substance, and the potassium atom (K) content is not less than 0 ppm but less than 110 ppm.
C08G 65/40 - Composés macromoléculaires obtenus par des réactions créant une liaison éther dans la chaîne principale de la macromolécule à partir de composés hydroxylés ou de leurs dérivés métalliques dérivés des phénols à partir des phénols et d'autres composés
16.
NOVEL COMPOUND, ORGANIC ELECTROLUMINESCENCE DEVICE AND ELECTRONIC APPARATUS
A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.
A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.
Provided is an ammonia production apparatus comprising: a first electrolytic cell in which at least a portion of a first electrolytic medium is housed; a first electrode disposed in the first electrolytic cell; a second electrolytic cell in which at least a portion of a second electrolytic medium is housed; a second electrode disposed in the second electrolytic cell; a separator provided between the first electrolytic cell and the second electrolytic cell; and a first separation part separating ammonia from the second electrolytic medium. The first electrolytic cell is configured such that a proton source contained in the first electrolytic medium is oxidized at the first electrode, protons are generated, and, in the second electrolytic medium, ammonia and hydrogen are generated from nitrogen, protons, and electrons in the presence of a nitrogen activation catalyst. The first separation part is configured such that nitrogen and hydrogen that have been separated from the ammonia are supplied to the first electrolytic medium.
C25B 9/00 - Cellules ou assemblages de cellulesÉléments de structure des cellulesAssemblages d'éléments de structure, p. ex. assemblages d'électrode-diaphragmeCaractéristiques des cellules relatives aux procédés
C25B 9/19 - Cellules comprenant des électrodes fixes de dimensions stablesAssemblages de leurs éléments de structure avec des diaphragmes
C25B 11/075 - Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé d’un seul élément catalytique ou composé catalytique
C25B 15/08 - Alimentation ou vidange des réactifs ou des électrolytesRégénération des électrolytes
Provided is an ammonia production device comprising: a first electrolytic cell in which at least some of a first electrolytic medium is stored; a first electrode that is disposed in the first electrolytic cell; a second electrolytic cell in which at least some of a second electrolytic solution is stored; a second electrode that is disposed in the second electrolytic cell; a separator provided between the first electrolytic cell and the second electrolytic cell; and a solvent separation part for separating nitrogen, hydrogen, and ammonia from the second electrolytic solution discharged from the second electrolytic cell. In the ammonia production device, the first electrolytic cell is configured such that a proton source contained in the first electrolytic medium is oxidized at the first electrode to generate protons, and ammonia and hydrogen are generated from nitrogen, protons, and electrons in the presence of a nitrogen activation catalyst in the second electrolytic solution.
C25B 9/00 - Cellules ou assemblages de cellulesÉléments de structure des cellulesAssemblages d'éléments de structure, p. ex. assemblages d'électrode-diaphragmeCaractéristiques des cellules relatives aux procédés
C25B 9/19 - Cellules comprenant des électrodes fixes de dimensions stablesAssemblages de leurs éléments de structure avec des diaphragmes
C25B 11/075 - Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé d’un seul élément catalytique ou composé catalytique
C25B 15/08 - Alimentation ou vidange des réactifs ou des électrolytesRégénération des électrolytes
19.
LITHIUM-ION-SELECTIVE PERMEABLE MEMBRANE, LITHIUM-ION RECOVERY DEVICE, AND SENSOR
Provided are: a lithium-ion-selective permeable membrane containing an oxide solid electrolyte and a resin, the lithium-ion-selective permeable membrane including either a single film, in which a film having at least one of the below-mentioned properties (1) to (4) is provided independently, or a laminated film, in which a plurality of such films are provided; a lithium-ion recovery device comprising the lithium-ion-selective permeable membrane; and a sensor. (1) The volume-based particle size distribution of the oxide solid electrolyte has a peak within a particle diameter range of at least 0.1 μm or higher to less than 2 μm. (2) The oxide solid electrolyte has a bimodal or higher volume-based particle size distribution. (3) The oxide solid electrolyte has a bimodal volume-based particle size distribution, said distribution having one peak within a particle diameter range of 0.1 μm or higher to less than 2 μm and one peak within a particle diameter range of 10 μm or higher to less than 50 μm. (4) The oxide solid electrolyte has a trimodal volume-based particle size distribution, said distribution having one peak within a particle diameter range of 0.1 μm or higher to less than 2 μm, one peak within a particle diameter range of 2 μm or higher to less than 10 μm, and one peak within a particle diameter range of 10 μm or higher to less than 50 μm.
B01D 69/02 - Membranes semi-perméables destinées aux procédés ou aux appareils de séparation, caractérisées par leur forme, leur structure ou leurs propriétésProcédés spécialement adaptés à leur fabrication caractérisées par leurs propriétés
B01D 69/00 - Membranes semi-perméables destinées aux procédés ou aux appareils de séparation, caractérisées par leur forme, leur structure ou leurs propriétésProcédés spécialement adaptés à leur fabrication
B01D 71/40 - Polymères d'acides non saturés ou de leurs dérivés, p. ex. sels, amides, imides, nitriles, anhydrides, esters
G01N 27/06 - Recherche ou analyse des matériaux par l'emploi de moyens électriques, électrochimiques ou magnétiques en recherchant l'impédance en recherchant la résistance d'un liquide
G01N 27/333 - Électrodes ou membranes sélectives à l'égard des ions
Provided is a compound which is represented by formula (A) or (B). (Symbols in the formulae are as defined in the description.) Also provided are: a material for organic electroluminescent elements and an organic electroluminescent element, each of which contains the compound; and an electronic device which includes such an organic electroluminescent element.
C07C 211/54 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à deux ou trois cycles aromatiques à six chaînons
2p4-p4-p [in general formula (I), the R moieties each independently represent a hydrogen atom, a chlorine atom, a bromine atom, or an iodine atom and p is an integer of 1-3]. The refrigerating-machine oil composition comprises a base oil (A), an aliphatic epoxy compound (B1), an alicyclic epoxy compound (B2), and a terpene compound (C).
C10M 141/02 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'au moins deux composés couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé organique contenant de l'oxygène
C09K 5/04 - Substances qui subissent un changement d'état physique lors de leur utilisation le changement d'état se faisant par passage de l'état liquide à l'état vapeur ou vice versa
C10M 127/02 - Compositions lubrifiantes caractérisées en ce que l'additif est un hydrocarbure non macromoléculaire aliphatique défini
The present invention provides: a compound represented by formula (1), (2), or (3) (where each symbol in formulas (1), (2), and (3) is as defined in the description); a material that contains this compound and that is for an organic electroluminescent element; an organic electroluminescent element containing this compound; and an electronic device comprising such an organic electroluminescent element.
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/10 - OLED ou diodes électroluminescentes polymères [PLED]
This method for conveying a sulfide solid electrolyte comprises: a step for obtaining a green compact by compressing a pulverulent sulfide solid electrolyte containing a lithium atom, a sulfur atom and a phosphorus atom; a step for filling a packaging container with the green compact to obtain packaged article; a step for conveying the packaged article; and a step of taking out the green compact from the packaged article and crushing the green compact to obtain a crushed product.
2p4-p4-p … (I) [In general formula (I), R each independently represent a hydrogen atom, a chlorine atom, a bromine atom, or an iodine atom, and p is an integer of 1-3.], wherein the refrigerator oil composition contains a base oil (A), an epoxy compound (B), and a terpene compound (C), the epoxy compound (B) is an aliphatic epoxy compound (B1) or an alicyclic epoxy compound (B2), and the total content of the epoxy compound (B) and the terpene compound (C) is 4.0 mass% or more in terms of the total amount of the refrigerator oil composition.
C10M 141/02 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'au moins deux composés couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé organique contenant de l'oxygène
C09K 5/04 - Substances qui subissent un changement d'état physique lors de leur utilisation le changement d'état se faisant par passage de l'état liquide à l'état vapeur ou vice versa
C10M 127/02 - Compositions lubrifiantes caractérisées en ce que l'additif est un hydrocarbure non macromoléculaire aliphatique défini
Provided is an oxide semiconductor film having crystallinity, said oxide semiconductor film comprising indium (In) and a first metal element selected from the group consisting of aluminum (Al), gallium (Ga), yttrium (Y), scandium (Sc), and lanthanoid-based elements. The oxide semiconductor film contains a plurality of crystal grains which each include at least one of the <101> crystal orientation, the <111> crystal orientation, and the <001> crystal orientation that are measured by an electron backscatter diffraction method. The occupancy ratio of a first region in which the <101> crystal orientation is oriented within 15° with respect to the normal direction of the surface of the oxide semiconductor film is not less than 20%.
A refrigerator oil composition may have an appropriate dissolution viscosity when a hydrocarbon-based refrigerant is dissolved and having a low solubility of the hydrocarbon-based refrigerant. A mixed composition for a refrigerator may include such a refrigerator oil composition. Such a refrigerator oil composition used for a refrigerant may include a hydrocarbon-based refrigerant, and one or more aromatic ester-based compounds (A) of formula (1):
A refrigerator oil composition may have an appropriate dissolution viscosity when a hydrocarbon-based refrigerant is dissolved and having a low solubility of the hydrocarbon-based refrigerant. A mixed composition for a refrigerator may include such a refrigerator oil composition. Such a refrigerator oil composition used for a refrigerant may include a hydrocarbon-based refrigerant, and one or more aromatic ester-based compounds (A) of formula (1):
A refrigerator oil composition may have an appropriate dissolution viscosity when a hydrocarbon-based refrigerant is dissolved and having a low solubility of the hydrocarbon-based refrigerant. A mixed composition for a refrigerator may include such a refrigerator oil composition. Such a refrigerator oil composition used for a refrigerant may include a hydrocarbon-based refrigerant, and one or more aromatic ester-based compounds (A) of formula (1):
in which R1 is a linear or branched alkyl group having 5 or more and 24 or less carbon atoms or a linear or branched alkenyl group having 5 or more and 24 or less carbon atoms; m is an integer of 2 or more and 4 or less; and a plurality of R1's may be the same or different.
C09K 5/04 - Substances qui subissent un changement d'état physique lors de leur utilisation le changement d'état se faisant par passage de l'état liquide à l'état vapeur ou vice versa
C10N 40/30 - Lubrifiants pour machines frigorifiques
27.
METHOD FOR PRODUCING SULFIDE SOLID ELECTROLYTE HAVING ARGYRODITE CRYSTAL STRUCTURE
This method for producing a sulfide solid electrolyte having an argyrodite crystal structure includes: mixing a raw material-containing substance in a solvent to obtain an intermediate-containing substance; drying the intermediate-containing substance through fluidized drying using medium particles as media to obtain an intermediate; and firing the intermediate.
This thin-film transistor includes: an oxide semiconductor layer having crystallinity; a metal oxide layer in contact with the oxide semiconductor layer; a gate electrode provided to be superimposed on the oxide semiconductor layer; and a gate insulating layer provided between the oxide semiconductor layer and the gate electrode. The oxide semiconductor layer includes a plurality of crystal grains each including at least one of a crystal orientation <101>, a crystal orientation <111>, and a crystal orientation <001> as measured by an electron backscatter diffraction method. The occupancy rate of a first region in which the crystal orientation <101> is oriented within 15° with respect to the normal direction of the surface of the oxide semiconductor layer is 20% or more.
Provided is a method for producing a sulfide solid electrolyte having an argyrodite-type crystal structure in a liquid phase, the method having a production efficiency enhanced by efficiently using a raw material-containing substance and enabling easy production of a high-quality sulfide solid electrolyte, the method including mixing a raw material-containing substance and a first solvent to prepare a mixture, mixing the mixture and a second solvent to prepare a solution containing a solid electrolyte precursor, subjecting the solid electrolyte precursor to a heat treatment while supplying hydrogen sulfide to produce a heated solid electrolyte precursor, and firing the heated solid electrolyte precursor.
A polycarbonate-based resin composition including: an aromatic polycarbonate resin; inorganic particles; and a liquid oil component. The inorganic particles have an average particle diameter of from 0.1 μm to 1 μm. A content of the inorganic particles is from 0.00001 part by mass to 0.001 part by mass with respect to 100 parts by mass of the aromatic polycarbonate resin. When a part by mass of the inorganic particles with respect to 100 parts by mass of the aromatic polycarbonate resin is represented by mB, a specific surface area of the inorganic particles is represented by SB (m2/g), and a part by mass of the liquid oil component with respect to 100 parts by mass of the aromatic polycarbonate resin is represented by mC, α determined by the following equation 1 is more than 0.005 and less than 0.1: Equation 1: α=(mB×SB)/mC.
A method for producing a sulfide solid electrolyte, which includes obtaining a mixture by mixing a raw material inclusion containing a lithium atom, a phosphorus atom, a sulfur atom, and a halogen atom in an organic solvent; and performing microwave irradiation on the mixture, is provided, and thereby a sulfide solid electrolyte can be efficiently produced while maintaining a particle diameter by reducing a heating temperature and suppressing granulation due to heating by employing a liquid phase method.
A lubricating oil composition for two-wheeled motor vehicles including a base oil and a metal phenate and having a coefficient of friction measured of less than 0.0900. The lubricating oil composition in which a performance required for lubricating oil for engines is satisfied, and a good shift feeling is achieved while a high coefficient of friction is kept in a wet clutch.
C10M 129/02 - Compositions lubrifiantes caractérisées en ce que l'additif est un composé organique non macromoléculaire contenant de l'oxygène comportant une chaîne carbonée de moins de 30 atomes
C10M 159/00 - Compositions lubrifiantes caractérisées en ce que l'additif est de constitution indéterminée ou incomplètement déterminée
C10M 169/04 - Mélanges de matériaux de base et d'additifs
A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.
A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.
MAXMAXMAX (EM) of the organic luminescent material are different from each other; the minimum excitation triplet energy of each of the two or more triplet sensitizers is not lower than the minimum excitation triplet energy of the organic luminescent material; and the minimum excitation singlet energy of each of the two or more triplet sensitizers is lower than the minimum excitation singlet energy of the organic luminescent material.
A sulfide solid electrolyte may be able to adjust the morphology unavailable traditionally, or readily adjust so as to have a desired morphology. Such a sulfide solid electrolyte may include a substance including a lithium element, a sulfur element, and a phosphorus element; and an amine compound. The solid electrolyte may have a volume-based average particle diameter of 10 μm or less, measured by laser diffraction particle size distribution measurement, and/or a BET specific surface area of 40 m2/g or less.
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01M 10/42 - Procédés ou dispositions pour assurer le fonctionnement ou l'entretien des éléments secondaires ou des demi-éléments secondaires
36.
COMPOUND, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
A compound represented by a formula (1C-A) below.
A compound represented by a formula (1C-A) below.
A compound represented by a formula (1C-A) below.
One of R4 to R8 and R10 to R12 is a group represented by a formula (1D-A) above; R1 to R3, R9, and R4 to R8 and R10 to R12 not being the group represented by the formula (1D-A) are each a hydrogen atom, a substituent, or the like; at least one of R21 to R30 is other than a hydrogen atom; when R11 is a group represented by a formula (1D), R12 is a hydrogen atom or a phenyl group; when R12 is a group represented by the formula (1D), R11 is a hydrogen atom or a phenyl group; in the formula (1D), one of R21 to R30 represents a bonding position to a benz[a]anthracene ring in the formula (1C), and R21 to R30 not being the bonding position are each a hydrogen atom, a substituent, or the like.
A compound is represented by a formula (1A-A). One of R4 to R8 and R10 to R12 is a group represented by a formula (1B-A1), (1B-A2), or (1B-A3) above; R1 to R3, R9, and R4 to R8 and R10 to R12 other than the above are each a hydrogen atom, a substituent, or the like; when R11 or R12 is a group represented by the formula (1B-A1), (1B-A2), or (1B-A3), R12 or R11 is a hydrogen atom or a phenyl group; and in the formulae (1B-A1) to (1B-A3), R51 to R57, R61 to R64, R71 to R74, and R81 to R84 forming no ring in the formulae (1B-A1) to (1B-A3) are each a hydrogen atom, a substituent, or the like; and * represents a bonding position to a benz[a]anthracene ring in the formula (1A-A).
A compound is represented by a formula (1A-A). One of R4 to R8 and R10 to R12 is a group represented by a formula (1B-A1), (1B-A2), or (1B-A3) above; R1 to R3, R9, and R4 to R8 and R10 to R12 other than the above are each a hydrogen atom, a substituent, or the like; when R11 or R12 is a group represented by the formula (1B-A1), (1B-A2), or (1B-A3), R12 or R11 is a hydrogen atom or a phenyl group; and in the formulae (1B-A1) to (1B-A3), R51 to R57, R61 to R64, R71 to R74, and R81 to R84 forming no ring in the formulae (1B-A1) to (1B-A3) are each a hydrogen atom, a substituent, or the like; and * represents a bonding position to a benz[a]anthracene ring in the formula (1A-A).
C09K 11/02 - Emploi de substances particulières comme liants, revêtements de particules ou milieux de suspension
H10K 50/13 - 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 comprenant des couches EL empilées dans une unité EL
38.
CRYSTALLINE SULFIDE SOLID ELECTROLYTE AND METHOD FOR MANUFACTURING SAME
The present invention provides: a crystalline sulfide solid electrolyte which contains lithium atoms, phosphorus atoms, sulfur atoms, and halogen atoms, is excellent in battery lifetime characteristics and voltage resistance, also has excellent coatability, and has an elastic dissipation energy, calculated from a focus curve measured by an atomic force microscopy, of 5.0×10-18 J or more; and a method for manufacturing the same.
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 13/00 - Appareils ou procédés spécialement adaptés à la fabrication de conducteurs ou câbles
A sulfide solid electrolyte that contains lithium, phosphorus, sulfur, chlorine and bromine, wherein in powder X-ray diffraction analysis using CuKα rays, it has a diffraction peak A at 2θ=25.2±0.5 deg and a diffraction peak B at 2θ=29.7±0.5 deg, the diffraction peak A and the diffraction peak B satisfy the following formula (A), and a molar ratio of the chlorine to the phosphorus “c (Cl/P)” and a molar ratio of the bromine to the phosphorus “d (Br/P)” satisfies the following formula (1):
A sulfide solid electrolyte that contains lithium, phosphorus, sulfur, chlorine and bromine, wherein in powder X-ray diffraction analysis using CuKα rays, it has a diffraction peak A at 2θ=25.2±0.5 deg and a diffraction peak B at 2θ=29.7±0.5 deg, the diffraction peak A and the diffraction peak B satisfy the following formula (A), and a molar ratio of the chlorine to the phosphorus “c (Cl/P)” and a molar ratio of the bromine to the phosphorus “d (Br/P)” satisfies the following formula (1):
1.2
<
c
+
d
<
1.9
(
1
)
0.845
<
S
A
/
S
B
<
1.2
(
A
)
A sulfide solid electrolyte that contains lithium, phosphorus, sulfur, chlorine and bromine, wherein in powder X-ray diffraction analysis using CuKα rays, it has a diffraction peak A at 2θ=25.2±0.5 deg and a diffraction peak B at 2θ=29.7±0.5 deg, the diffraction peak A and the diffraction peak B satisfy the following formula (A), and a molar ratio of the chlorine to the phosphorus “c (Cl/P)” and a molar ratio of the bromine to the phosphorus “d (Br/P)” satisfies the following formula (1):
1.2
<
c
+
d
<
1.9
(
1
)
0.845
<
S
A
/
S
B
<
1.2
(
A
)
where SA is an area of the diffraction peak A and SB is an area of the diffraction peak B.
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01M 4/136 - Électrodes à base de composés inorganiques autres que les oxydes ou les hydroxydes, p. ex. sulfures, séléniures, tellurures, halogénures ou LiCoFy
H01M 4/58 - Emploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de composés inorganiques autres que les oxydes ou les hydroxydes, p. ex. sulfures, séléniures, tellurures, halogénures ou LiCoFyEmploi de substances spécifiées comme matériaux actifs, masses actives, liquides actifs de structures polyanioniques, p. ex. phosphates, silicates ou borates
H01M 10/0525 - Batteries du type "rocking chair" ou "fauteuil à bascule", p. ex. batteries à insertion ou intercalation de lithium dans les deux électrodesBatteries à l'ion lithium
An organic electroluminescence device includes an anode, a cathode, and an emitting region disposed between the anode and the cathode, in which the emitting region includes a first emitting layer and a second emitting layer, the first emitting layer contains a first compound represented by a formula below, and the second emitting layer contains a second compound.
An organic electroluminescence device includes an anode, a cathode, and an emitting region disposed between the anode and the cathode, in which the emitting region includes a first emitting layer and a second emitting layer, the first emitting layer contains a first compound represented by a formula below, and the second emitting layer contains a second compound.
An organic electroluminescence device includes an anode, a cathode, and an emitting region disposed between the anode and the cathode, in which the emitting region includes a first emitting layer and a second emitting layer, the first emitting layer contains a first compound represented by a formula below, and the second emitting layer contains a second compound.
At least one of R101 to R112 in the formula (100A), L101 or Ar101 in the formula (100B) has at least one deuterium atom. When only L101 has at least one deuterium atom, the at least one deuterium atom is bonded to a ring that is of rings forming L1 and directly bonded to a benz[a]anthracene ring in the formula (100A).
C07B 59/00 - Introduction d'isotopes d'éléments dans les composés organiques
C07C 13/547 - Hydrocarbures polycycliques ou leurs dérivés hydrocarbonés acycliques à cycles condensés à trois cycles condensés un cycle au moins n'étant pas un cycle à six chaînons, les autres cycles étant au plus des cycles à six chaînons
C07C 15/38 - Hydrocarbures polycycliques condensés contenant quatre cycles
A refrigerator oil composition used in a refrigerant containing one or more unsaturated fluorinated hydrocarbon compounds selected from compounds represented by the following general formula (1): CxFyHz (1), wherein x is an integer of 2 to 6, y is an integer of 1 to 11, z is an integer of 1 to 11, and there are one or more carbon-carbon unsaturated bonds in the molecule, the refrigerator oil composition containing a base oil (A) that includes polyvinyl ether, a modified silicone compound (B), and a specific epoxy compound (C).
C09K 5/04 - Substances qui subissent un changement d'état physique lors de leur utilisation le changement d'état se faisant par passage de l'état liquide à l'état vapeur ou vice versa
A lubricating oil composition may have excellent fuel economy and high shear stability. Such a lubricating oil composition may include: a comb-like polymer (A1) having a weight average molecular weight (Mw) of less than 300,000; and a comb-like polymer (A2) having a Mw of at least 400,000. The (A1)/(A2) mass content ratio of the comb-like polymer (A1) to the comb-like polymer (A2) in terms of resin content may be at least 0.25.
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
Provided is a compound that improves the performance of an organic EL element, the compound being represented by formula (1) and containing at least one deuterium atom in a molecule. (The symbols in the formula are as defined in the specification.)
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
A thin film transistor includes an oxide semiconductor layer having a polycrystalline structure over a substrate, a gate electrode over the oxide semiconductor layer, and a gate insulating layer between the oxide semiconductor layer and the gate electrode. The oxide semiconductor layer includes a first region having a first carrier concentration and overlapping the gate electrode, a second region having a second carrier concentration and not overlapping the gate electrode, and a third region between the first region and the second region and overlapping the gate electrode. The second carrier concentration is larger than the first carrier concentration. A carrier concentration of the third region decreases from the second region to the first region in a channel length direction. A length of the third region is greater than or equal to 0.00 μm and less than or equal to 0.60 μm in the channel length direction.
H01L 29/04 - Corps semi-conducteurs caractérisés par leur structure cristalline, p.ex. polycristalline, cubique ou à orientation particulière des plans cristallins
H01L 29/06 - Corps semi-conducteurs caractérisés par les formes, les dimensions relatives, ou les dispositions des régions semi-conductrices
H01L 29/49 - Electrodes du type métal-isolant-semi-conducteur
Provided is a method for producing sulfide solid electrolyte having an argyrodite-type crystal structure, the method including mixing lithium sulfide, a phosphorus sulfide, and an ammonium halide to produce a solid electrolyte precursor, and firing the solid electrolyte precursor. The method for producing a sulfide solid electrolyte having an argyrodite-type crystal structure provides a method for easily producing a high-quality sulfide solid electrolyte without using an elemental halogen which complicates the handling or a lithium halide which has a considerably high hygroscopicity.
The present invention provides a sulfide solid electrolyte mixture which contains: a sulfide solid electrolyte that contains lithium atoms, sulfur atoms, and phosphorus atoms, the sulfide solid electrolyte having a high ion conductivity and being easily densified when compressed; and an electrolyte solution that contains a lithium salt and an ionic liquid. With respect to this sulfide solid electrolyte mixture, the product of (A) the number of moles of the lithium salt in 1 liter of the electrolyte solution and (B) the content (mass%) of the electrolyte solution based on the total amount of the sulfide solid electrolyte mixture is 11 or more.
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01M 4/13 - Électrodes pour accumulateurs à électrolyte non aqueux, p. ex. pour accumulateurs au lithiumLeurs procédés de fabrication
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
H01M 10/056 - Accumulateurs à électrolyte non aqueux caractérisés par les matériaux utilisés comme électrolytes, p. ex. électrolytes mixtes inorganiques/organiques
47.
RADIO WAVE ABSORBER, RADIO WAVE ABSORPTION STRUCTURE INCLUDING RADIO WAVE ABSORBER, AND COMPOSITION FOR RADIO WAVE ABSORBER
A radio wave absorber comprising a resin and a carbon filler, wherein 60 to 90% by volume of the total carbon filler is present in a region from the first surface of the radio wave absorber to half of the total thickness of the radio wave absorber.
H01Q 17/00 - Dispositifs pour absorber les ondes rayonnées par une antenneCombinaisons de tels dispositifs avec des éléments ou systèmes d'antennes actives
48.
ELECTRODE, LITHIUM ION BATTERY POSITIVE ELECTRODE, AND LITHIUM ION BATTERY
An electrode having a structure in which a plurality of layers including a sulfur-based active material, a conductive assistant, and a solid electrolyte are laminated, wherein: the conductive assistant is a carbon material; and, in the plurality of layers, the ratio of the content of the solid electrolyte with respect to the content of the conductive assistant becomes higher from a layer of one end side toward a layer of the other end side in the lamination direction, and the content of the conductive assistant throughout the entirety of the plurality of layers is 10-30 mass%.
H01M 10/0585 - Structure ou fabrication d'accumulateurs ayant uniquement des éléments de structure plats, c.-à-d. des électrodes positives plates, des électrodes négatives plates et des séparateurs plats
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
04 - Huiles et graisses industrielles; lubrifiants; combustibles
Produits et services
Coolants; dielectric fluids as a chemical preparation for
cooling computer servers, except oils. Cooling lubricants; dielectric oils for cooling computer
servers.
50.
ORGANIC ELECTROLUMINESCENCE ELEMENT, ELECTRONIC DEVICE, COMPOSITION, AND MIXTURE POWDER
An organic EL device includes an emitting region and a first anode side organic layer. The first anode side organic layer contains a first material. The emitting region includes a first emitting layer containing first and second host materials and a second emitting layer containing a third host material. Energy levels of highest occupied molecular orbitals of the first material, the first host material, and the second host material HOMO(HT1), HOMO(H1), and HOMO(H2) satisfy a relationship of a numerical formula (Numerical Formula A1) below, and triplet energies of the first host material, the second host material, and the third host material T1(H1), T1(H2), and T1(H3) satisfy relationships of numerical formulae (Numerical Formula A2 and Numerical Formula A3) below,
An organic EL device includes an emitting region and a first anode side organic layer. The first anode side organic layer contains a first material. The emitting region includes a first emitting layer containing first and second host materials and a second emitting layer containing a third host material. Energy levels of highest occupied molecular orbitals of the first material, the first host material, and the second host material HOMO(HT1), HOMO(H1), and HOMO(H2) satisfy a relationship of a numerical formula (Numerical Formula A1) below, and triplet energies of the first host material, the second host material, and the third host material T1(H1), T1(H2), and T1(H3) satisfy relationships of numerical formulae (Numerical Formula A2 and Numerical Formula A3) below,
HOMO
(
HT
1
)
>
HOMO
(
H
2
)
>
HOMO
(
H
1
)
(
Numerical
Formula
A1
)
T
1
(
H
1
)
>
T
1
(
H
3
)
(
Numerical
Formula
A2
)
T
1
(
H
2
)
>
T
1
(
H
3
)
.
(
Numerical
Formula
A3
)
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 50/13 - 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 comprenant des couches EL empilées dans une unité EL
H10K 85/60 - Composés organiques à faible poids moléculaire
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
54.
COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
A viscosity index improver composition which has an excellent viscosity index improving effect. A viscosity index improver composition which includes a poly(meth)acrylate (A) including a constituent unit (Y) derived from a monomer (y) having a diol functional group, and a poly(meth)acrylate (B) including a constituent unit (Z) derived from a monomer (z) having a boronic acid ester.
C10M 157/10 - Compositions lubrifiantes caractérisées en ce que l'additif est un mélange d'au moins deux composés macromoléculaires couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé contenant des atomes d'éléments non prévus par les groupes
C10N 20/04 - Poids moléculaireRépartition du poids moléculaire
C10N 30/02 - Point d'écoulementIndice de viscosité
H01B 1/10 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques sulfures
H01B 1/06 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques
H01B 1/08 - Conducteurs ou corps conducteurs caractérisés par les matériaux conducteurs utilisésEmploi de matériaux spécifiés comme conducteurs composés principalement d'autres substances non métalliques oxydes
H01M 4/62 - Emploi de substances spécifiées inactives comme ingrédients pour les masses actives, p. ex. liants, charges
A compound represented by a formula (1).
A compound represented by a formula (1).
A compound represented by a formula (1).
In the formula (1): X1 to X4 are each independently a nitrogen atom or CRx; at least one of X1 to X4 is a nitrogen atom; a ring A, a ring B, and a ring C are each independently an aromatic hydrocarbon ring or a heterocycle; Ar1 is a hydrogen atom, an aryl group, or a group represented by a formula (2); and Ar2 is an aryl group or a group represented by a formula (3).
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
59.
PRODUCTION METHOD FOR SULFIDE SOLID ELECTROLYTE AND SULFIDE SOLID ELECTROLYTE
A method of producing a sulfide solid electrolyte having high ionic conductivity and high thermal stability without complicating the production process is provided, by a method of producing a sulfide solid electrolyte containing: mixing a raw material inclusion containing at least one type selected from a lithium atom, a sulfur atom, and a phosphorus atom, and a complexing agent having 2 or more of hetero atoms in the molecule to obtain an electrolyte precursor; mixing the electrolyte precursor in a solvent containing an oxygen atom-containing compound having a relative permittivity of 3.2 or higher at 25° C.; obtaining a grinding treatment product by performing grinding treatment of the mixture; and removing the solvent from the grinding treatment product to obtain a sulfide solid electrolyte.
Provided are: a compound represented by formula (1) (the symbols in the formula being as defined in the specification); a material, comprising the compound, for an organic electroluminescent element; an organic electroluminescent element comprising the compound; and an electronic device comprising the organic electroluminescent element.
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C07D 405/12 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device.
The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device.
The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device.
wherein
at least one of R1, R2, R3 and R4 represents an alkyl group having from 1 to 20 carbon atoms which is unsubstituted or substituted or an amino group NR84R85, and
at least one of R5, R6, R7 and R8 represents an aryl group having from 6 to 30 ring carbon atoms which is unsubstituted or substituted; or a heteroaryl group having from 5 to 30 ring atoms which is unsubstituted or substituted, whereby the aryl group or the heteroaryl group may bind back to an adjacent residue and form a ring structure;
Y1 and Y2 each independently represents RY or a group of formula (II)
The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device.
wherein
at least one of R1, R2, R3 and R4 represents an alkyl group having from 1 to 20 carbon atoms which is unsubstituted or substituted or an amino group NR84R85, and
at least one of R5, R6, R7 and R8 represents an aryl group having from 6 to 30 ring carbon atoms which is unsubstituted or substituted; or a heteroaryl group having from 5 to 30 ring atoms which is unsubstituted or substituted, whereby the aryl group or the heteroaryl group may bind back to an adjacent residue and form a ring structure;
Y1 and Y2 each independently represents RY or a group of formula (II)
The present invention relates to specific compounds, a material, preferably an emitter material, for an organic electroluminescence device comprising said specific compounds, an organic electroluminescence device comprising said specific compounds, an electronic equipment comprising said organic electroluminescence device, a light emitting layer comprising at least one host and at least one dopant, wherein the dopant comprises at least one of said specific compounds, and the use of said compounds in an organic electroluminescence device.
wherein
at least one of R1, R2, R3 and R4 represents an alkyl group having from 1 to 20 carbon atoms which is unsubstituted or substituted or an amino group NR84R85, and
at least one of R5, R6, R7 and R8 represents an aryl group having from 6 to 30 ring carbon atoms which is unsubstituted or substituted; or a heteroaryl group having from 5 to 30 ring atoms which is unsubstituted or substituted, whereby the aryl group or the heteroaryl group may bind back to an adjacent residue and form a ring structure;
Y1 and Y2 each independently represents RY or a group of formula (II)
wherein at least one of Y1 and Y2 is a group of formula (II).
A lubricating oil composition, including: a base oil including an ester base oil and a hindered amine compound, where a content of the hindered amine compound is from 0.60 mass % to 10.0 mass % based on a total amount of the lubricating oil composition. An internal combustion engine installed in a hybrid system, the internal combustion engine filled with the lubricating oil composition. A method of lubricating an internal combustion engine installed a hybrid system, including: applying the lubricating oil composition to the internal combustion engine.
C10M 111/02 - Compositions lubrifiantes caractérisées en ce que le matériau de base est un mélange d'au moins deux composés couverts par plus d'un des groupes principaux , chacun de ces composés étant un composé essentiel l'un d'eux, au moins, étant un composé organique non macromoléculaire
C10M 133/40 - Cycle à six chaînons ne contenant que du carbone et de l'azote
C10N 30/04 - Propriétés détergentes ou dispersantes
C10N 30/10 - Inhibition de l'oxydation, p. ex. anti-oxydants
A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.
A compound having structures represented by the following formulas (1) or (2): wherein in the formulas (1) and (2), at least one of R1 to R8 is a deuterium atom.
H10K 85/60 - Composés organiques à faible poids moléculaire
C07D 239/26 - Composés hétérocycliques contenant des cycles diazine-1, 3 ou diazine-1, 3 hydrogéné non condensés avec d'autres cycles comportant au moins trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle
C07D 251/24 - Composés hétérocycliques contenant des cycles triazine-1, 3, 5 non condensés avec d'autres cycles comportant trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des atomes d'hydrogène ou de carbone liés directement à au moins un atome de carbone du cycle à trois atomes de carbone du cycle
C07D 403/10 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 405/10 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
A photoelectric conversion element includes a light absorbing layer, a hole transport layer that transports holes generated by photoexcitation of the light absorbing layer, and a transparent conductive layer that is in contact with the hole transport layer and receives holes from the hole transport layer. The carrier density of the transparent conductive layer is more than 1×1016 cm−3 and 1×1020 cm−3 or less.
H10K 30/40 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire comprenant une structure p-i-n, ayant p. ex. un absorbeur pérovskite entre des couches de transport de charge de type p et de type n
H10K 30/57 - Dispositifs photovoltaïques [PV] comprenant des jonctions multiples, p. ex. des cellules PV en tandem
H10K 30/86 - Couches à haute mobilité des trous, p. ex. de transport des trous ou couches de blocage des électrons
177K177K77K(M2) < 0.3eV. (In general formula (1): each of X1to X4independently is a nitrogen atom or CRx, provided that at least one of X1to X4is a nitrogen atom; and Ar1 is a hydrogen atom, a substituted or unsubstituted aryl group, or a group represented by general formula (2)).
Provided is a thermosetting composition which contains components (A), (B) and (C) and also contains one or more components selected from the group consisting of components (D) to (F). The content of components having a melting point of -5°C or higher among components (A) and (D) to (F) is 40 mass% or more relative to the total amount of components (A) and (D) to (F). (A) A substituted or unsubstituted monofunctional or polyfunctional (meth)acrylate compound which has a group having an alicyclic hydrocarbon group with 6 or more ring-forming carbon atoms as an ester substituent group and which has a viscosity at 25°C of 1 to 300 mPa·s. (B) Spherical silica. (C) A pigment or dye. (D) (Meth)acrylic acid or a monofunctional (meth)acrylate compound having a polar group as an ester substituent group. (E) A monofunctional (meth)acrylate compound having a group other than the ester substituent group in component (A) and the ester substituent group in component (D) as an ester substituent group. (F) A polyfunctional (meth)acrylate compound having a group other than the ester substituent group in component (A) as an ester substituent group
C08F 2/44 - Polymérisation en présence d'additifs, p. ex. plastifiants, matières colorantes, charges
C08F 20/00 - Homopolymères ou copolymères de composés contenant un ou plusieurs radicaux aliphatiques non saturés, chaque radical ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle ou un sel, anhydride, ester, amide, imide ou nitrile
C08F 292/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des substances inorganiques
C08F 293/00 - Composés macromoléculaires obtenus par polymérisation sur une macromolécule contenant des groupes capables d'amorcer la formation de nouvelles chaînes polymères rattachées exclusivement à une ou aux deux extrémités de la macromolécule de départ
C08K 3/013 - Charges, pigments ou agents de renforcement
C08K 7/00 - Emploi d'ingrédients caractérisés par leur forme
C08K 9/06 - Ingrédients traités par des substances organiques par des composés contenant du silicium
C08L 33/00 - Compositions contenant des homopolymères ou des copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle, ou ses sels, anhydrides, esters, amides, imides ou nitrilesCompositions contenant des dérivés de tels polymères
C08L 51/10 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères greffés sur des substances inorganiques
C08L 53/00 - Compositions contenant des copolymères séquencés possédant au moins une séquence d'un polymère obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères
68.
PHOTOELECTRIC CONVERSION ELEMENT, SOLAR CELL MODULE, AND PADDLE
Provided is a photoelectric conversion element capable of maintaining photoelectric conversion element performance under a high-temperature and high-humidity environment. A photoelectric conversion element (10) comprises: at least one photoelectric conversion layer (26); a conductive layer (24) electrically connected to the photoelectric conversion layer; a first sealing layer (40) on the conductive layer; and a second sealing layer (41) on the first sealing layer. The first sealing layer (40) contains at least one from among an inorganic metal oxide, an inorganic metal nitride, an inorganic metal oxynitride, and an inorganic metal fluoride. The second sealing layer (41) includes a polymer layer or a nitride coating layer.
C25B 9/00 - Cellules ou assemblages de cellulesÉléments de structure des cellulesAssemblages d'éléments de structure, p. ex. assemblages d'électrode-diaphragmeCaractéristiques des cellules relatives aux procédés
C25B 9/21 - Cellules comprenant des électrodes fixes de dimensions stablesAssemblages de leurs éléments de structure avec des diaphragmes avec plusieurs diaphragmes
C25B 13/08 - DiaphragmesÉléments d'espacement caractérisés par le matériau à base de matériaux organiques
70.
THERMOSETTING COMPOSITION, METHOD FOR PRODUCING MOLDED ARTICLE USING SAME, AND CURED PRODUCT
Provided is a thermosetting composition containing components (A) to (C) below, a component (G) below, and one or more compounds selected from the group consisting of components (D) to (F) below. (A) a monofunctional or polyfunctional (meth)acrylate compound that has, as an ester substituent, a group having a substituted or unsubstituted alicyclic hydrocarbon group having 6 or more ring-forming carbon atoms, and that has a viscosity of 1-300 mPa·s at 25°C; (B) a spherical silica; (C) a black pigment or a black dye; (D) a monofunctional (meth)acrylate compound having, as an ester substituent, a group having a (meth)acrylic acid or a polar group; (E) a monofunctional (meth)acrylate compound having, as an ester substituent, a group other than the ester substituent of the component (A) and the ester substituent of the component (D); (F) a polyfunctional (meth)acrylate compound having, as an ester substituent, a group other than the ester substituent of the component (A); and (G) a block copolymer containing at least one each of a block comprising a repeating unit represented by formula (G1) and a block comprising a repeating unit represented by formula (G2)
C08F 2/44 - Polymérisation en présence d'additifs, p. ex. plastifiants, matières colorantes, charges
C08F 20/00 - Homopolymères ou copolymères de composés contenant un ou plusieurs radicaux aliphatiques non saturés, chaque radical ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle ou un sel, anhydride, ester, amide, imide ou nitrile
C08F 287/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des polymères séquencés
C08F 292/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des substances inorganiques
C08F 293/00 - Composés macromoléculaires obtenus par polymérisation sur une macromolécule contenant des groupes capables d'amorcer la formation de nouvelles chaînes polymères rattachées exclusivement à une ou aux deux extrémités de la macromolécule de départ
C08K 3/013 - Charges, pigments ou agents de renforcement
C08K 9/06 - Ingrédients traités par des substances organiques par des composés contenant du silicium
C08L 33/00 - Compositions contenant des homopolymères ou des copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle, ou ses sels, anhydrides, esters, amides, imides ou nitrilesCompositions contenant des dérivés de tels polymères
C08L 51/10 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères greffés sur des substances inorganiques
C08L 53/00 - Compositions contenant des copolymères séquencés possédant au moins une séquence d'un polymère obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères
71.
THERMOSETTING COMPOSITION, METHOD FOR PRODUCING MOLDED ARTICLE USING SAME, AND CURED PRODUCT
Disclosed is a thermosetting composition which contains the components (A) to (C) described below, the component (G) described below, and one or more components selected from the group consisting of the components (D) to (F) described below. (A) a monofunctional or polyfunctional (meth)acrylate compound which has, as an ester substituent, a group having a substituted or unsubstituted alicyclic hydrocarbon group having 6 or more ring carbon atoms, and which has a viscosity of 1-300 mPa∙s at 25°C (B) a spherical silica (C) a white pigment (D) a (meth)acrylic acid or a monofunctional (meth)acrylate compound which has, as an ester substituent, a group having a polar group (E) a monofunctional (meth)acrylate compound which has, as an ester substituent, a group other than the ester substituent of the component (A) and the ester substituent of the component (D) (F) a polyfunctional (meth)acrylate compound which has, as an ester substituent, a group other than the ester substituent of the component (A) (G) a block copolymer which contains at least one block composed of repeating units represented by formula (G1) and at least one block composed of repeating units represented by formula (G2)
C08F 2/44 - Polymérisation en présence d'additifs, p. ex. plastifiants, matières colorantes, charges
C08F 20/00 - Homopolymères ou copolymères de composés contenant un ou plusieurs radicaux aliphatiques non saturés, chaque radical ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle ou un sel, anhydride, ester, amide, imide ou nitrile
C08F 287/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des polymères séquencés
C08F 292/00 - Composés macromoléculaires obtenus par polymérisation de monomères sur des substances inorganiques
C08F 293/00 - Composés macromoléculaires obtenus par polymérisation sur une macromolécule contenant des groupes capables d'amorcer la formation de nouvelles chaînes polymères rattachées exclusivement à une ou aux deux extrémités de la macromolécule de départ
C08K 3/013 - Charges, pigments ou agents de renforcement
C08K 9/06 - Ingrédients traités par des substances organiques par des composés contenant du silicium
C08L 33/00 - Compositions contenant des homopolymères ou des copolymères de composés possédant un ou plusieurs radicaux aliphatiques non saturés, chacun ne contenant qu'une seule liaison double carbone-carbone et un seul étant terminé par un seul radical carboxyle, ou ses sels, anhydrides, esters, amides, imides ou nitrilesCompositions contenant des dérivés de tels polymères
C08L 51/10 - Compositions contenant des polymères greffés dans lesquels le composant greffé est obtenu par des réactions faisant intervenir uniquement des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères greffés sur des substances inorganiques
C08L 53/00 - Compositions contenant des copolymères séquencés possédant au moins une séquence d'un polymère obtenu par des réactions ne faisant intervenir que des liaisons non saturées carbone-carboneCompositions contenant des dérivés de tels polymères
A continuous organic matter pyrolysis device includes: a charging section that continuously charges an organic matter; a vertical vessel for accommodating the organic matter charged from the charging section, a stirring means that is provided in the vertical vessel and that stirs the organic matter, a first heating means that heats the vertical vessel to pyrolyze and gasify the organic matter, a lead-out section connected to an upper portion of the vertical vessel and including a lead-out path through which the pyrolysis gas of the organic matter is led out, and a discharging section connected to a lower portion of the vertical vessel and including a discharge path through which an organic matter residue is continuously discharged.
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
C10B 53/07 - Distillation destructive spécialement conçue pour des matières premières solides particulières ou sous forme spéciale de matières polymères synthétiques, p. ex. pneumatiques
C10G 1/10 - Production de mélanges liquides d'hydrocarbures à partir de schiste bitumineux, de sable pétrolifère ou de matières carbonées solides non fusibles ou similaires, p. ex. bois, charbon à partir de caoutchouc ou de déchets de caoutchouc
A lubricant base oil for use in the preparation of a cooling lubricant composition, may have a % CP of 60 or more, and the dynamic viscosity at 40° C. is less than 3 mm2/s. Such a lubricant base oil may include a base oil (A) having % Cp of 60 or more and a kinematic viscosity at 40° C. of less than 3 mm2/s, the base oil (A) being 80% by mass or more of the total lubricant base oil mass. Such a lubricant base oil may further include a base oil (B) that is different from the base oil (A), in a range of from 1 to 20% by mass of the total lubricant base oil mass. The base oil (A) may be an isoparaffin-based base oil. Such a lubricant base oil may have a % CN of 21 or less. A cooling lubricant composition may include such a lubricant base oil.
An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.
An organic EL device includes an anode, an emitting layer, an electron transporting zone and a cathode in this sequence, in which the electron transporting zone contains an aromatic heterocyclic derivative represented by a formula (1) below. In the formula (1), X1 to X3 are a nitrogen atom or CR1, and A is represented by a formula (2) below. In the formula (2), L1 is s single bond or a linking group, and HAr is represented by a formula (3) below. In the formula (3), Y1 is an oxygen atom, a sulfur atom or the like, and one of X11 to X18 is a carbon atom bonded to L1 by a single bond and the rest of X11 to X18 are a nitrogen atom or CR13.
H10K 85/60 - Composés organiques à faible poids moléculaire
C07D 405/10 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 405/14 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07D 409/10 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 409/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C09K 11/02 - Emploi de substances particulières comme liants, revêtements de particules ou milieux de suspension
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 101/30 - Valeurs d'énergie de la plus haute orbitale moléculaire occupée [HOMO], de la plus basse orbitale moléculaire inoccupée [LUMO] ou de Fermi
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
H10K 102/00 - Détails de structure relatifs aux dispositifs organiques couverts par la présente sous-classe
H10K 102/10 - Électrodes transparentes, p. ex. utilisant du graphène
75.
POLYCARBONATE-POLYARYLATE RESIN, COATING COMPOSITION, MOLDED BODY, AND ELECTROPHOTOGRAPHIC PHOTORECEPTOR
Provided is a polycarbonate-polyarylate resin including at least one of structural units represented by general formulae (A1) and (A2), a structural unit represented by general formula (B1), and a structural unit represented by general formula (C1), the polycarbonate-polyarylate resin being such that the molar fraction ax of structural units represented by general formula (A1), the molar fraction ay of structural units represented by general formula (A2), and the molar fraction c of structural units represented by general formula (C1) satisfy the following mathematical formula (formula 1). (Formula 1) 0.1 ≤ {(ax_ay)/(ax+ay+c)} ×100 < 50
C08G 63/64 - Polyesters contenant à la fois des groupes ester carboxylique et des groupes carbonate
C08L 67/00 - Compositions contenant des polyesters obtenus par des réactions créant une liaison ester carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C08L 69/00 - Compositions contenant des polycarbonatesCompositions contenant des dérivés des polycarbonates
G03G 5/05 - Matériaux de liaison organiquesMéthodes d'enduction d'un substrat avec une couche photoconductriceAdditifs inertes utilisables dans des couches photoconductrices
C07D 403/14 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant au moins trois hétérocycles
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
A compound may include partial structures of formula (3-11B) and (31a) in one molecule:
A compound may include partial structures of formula (3-11B) and (31a) in one molecule:
A compound may include partial structures of formula (3-11B) and (31a) in one molecule:
R314 being a single bond bonded to * in formula (31a), R300 being independently H or a substituent, or at least one of adjacent pairs of R300 are mutually bonded to form a ring, or R300 is a single bond bonded to another atom/structure in the molecule, one or more R300 is H, at least one of H being D, Y12 to Y16 being independently N, CR31, or C bonded to another atom/structure in the molecule, 1 to 3 of Y12 to Y16 being N, and R31 independently being H or a substituent.
H10K 85/60 - Composés organiques à faible poids moléculaire
C07D 209/86 - CarbazolesCarbazoles hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du système cyclique
C07D 405/10 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 405/14 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07D 491/048 - Systèmes condensés en ortho avec un seul atome d'oxygène comme hétéro-atome du cycle contenant de l'oxygène le cycle contenant de l'oxygène étant à cinq chaînons
An organic electroluminescence device including: a cathode, an anode, and an organic layer disposed between the cathode and the anode, wherein the organic layer comprises an emitting layer and a first layer, the first layer is disposed between the cathode and the emitting layer, the emitting layer comprises one or both of a compound represented by the following formula (1A) and a compound represented by the following formula (1B), and the first layer comprises a compound represented by the following formula (BE1):
An organic electroluminescence device including: a cathode, an anode, and an organic layer disposed between the cathode and the anode, wherein the organic layer comprises an emitting layer and a first layer, the first layer is disposed between the cathode and the emitting layer, the emitting layer comprises one or both of a compound represented by the following formula (1A) and a compound represented by the following formula (1B), and the first layer comprises a compound represented by the following formula (BE1):
A water-soluble metalworking fluid that includes a base oil (A) and an ether carboxylic acid (B) represented by general formula (b-1), where A is a C1-4 alkylene group, when multiple A are present, each A may be the same group or may be a different group, B is a single bond or a C1-4 alkylene group, n is an integer of 1-100, and R is a hydrocarbon group. The ether carboxylic acid (B) content is 0.1-10 mass % based on the total amount of the water-soluble metalworking fluid.
A water-soluble metalworking fluid that includes a base oil (A) and an ether carboxylic acid (B) represented by general formula (b-1), where A is a C1-4 alkylene group, when multiple A are present, each A may be the same group or may be a different group, B is a single bond or a C1-4 alkylene group, n is an integer of 1-100, and R is a hydrocarbon group. The ether carboxylic acid (B) content is 0.1-10 mass % based on the total amount of the water-soluble metalworking fluid.
This information processing device (PC 100) is capable of outputting information relating to a key management method for a vehicle key of a vehicle that is rented out in a vehicle rental business, said information processing device comprising: an input means 11 for inputting information relating to the vehicle (specific information that can identify the movement mode of the vehicle); a calculation means 13 for calculating respective costs of a plurality of key management methods (on-vehicle device type, locker type, etc.) on the basis of the information relating to the vehicle; and an output means 14 for outputting, on the basis of the calculation results of the calculation means 13, information about a key management method to be selected. As the respective costs, the calculation means 13 calculates the results of calculation, for each of the plurality of key management methods, of the subtraction result (net cost) obtained by subtracting an information value (for example, an advertisement fee) calculated for a case where one key management method is used, from a cost (gross cost) calculated for the case where said key management method is used.
Provided is a zipper tape comprising a first base part and a first engagement part formed on the first base part, wherein: the first base part is folded back or can be folded back on a first side in the width direction of the zipper tape; and the first engagement part is formed on a surface which serves as an outer side when the first base part is folded back.
A44B 19/16 - Élément d'accrochage à section constante tout le long de la bande
B65D 33/00 - Parties constitutives ou accessoires pour sacs ou sachets
B65D 33/25 - RivetageAssemblage à queue-d'arondeVissageDispositifs de fermeture de l'extrémité ou de l'ouverture utilisant des boutons-pression ou des fermetures à glissières
B65D 75/66 - Cordons de déchirure ou éléments flexibles analogues incorporés ou ajoutés
82.
CHALCOGENIDE PEROVSKITE AND METHOD FOR PRODUCING CHALCOGENIDE PEROVSKITE BY LIQUID PHASE SYNTHESIS
A chalcogenide perovskite, having a crystallite size T1 of less than 40 nm, calculated by Scherrer equation based on the diffraction peak having the largest peak height in the X-ray diffraction spectrum obtained by X-ray diffraction measurement, and a proportion of a total area occupied by particles having a particle diameter of 10 μm or more measured by microscopy to a total area occupied by particles existing in a captured image range in an image range captured by a microscope of 10% or less.
C07D 235/08 - Radicaux ne contenant que des atomes d'hydrogène et de carbone
C07D 401/10 - 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 carbonée contenant des cycles aromatiques
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
Disclosed is a grease composition which contains a base oil (A) and a thickening agent (B), wherein: the base oil (A) includes one or more components selected from the group consisting of the component (A1) and the component (A2) described below; and the thickening agent (B) includes one or more components selected from the group consisting of the component (B1) and the component (B2) described below. Component (A1): an ester of a polyol (A11) having 3 to 6 hydroxyl groups and a branched fatty acid (A12) having 14 to 20 carbon atoms Component (A2): an alkylnaphthalene that has a 3% mass loss temperature of 450°C or higher in gas chromatography distillation in accordance with ASTM-D7500 Component (B1): melamine cyanurate Component (B2): pre-made urea
C10M 115/08 - Compositions lubrifiantes caractérisées en ce que l'épaississant est un composé organique non macromoléculaire, autre qu'un acide carboxylique ou ses sels contenant de l'azote
C10N 30/06 - OnctuositéRésistance du filmAnti-usureRésistance aux pressions extrêmes
C10N 40/04 - Bains d'huileBoîtes de vitessesTransmissions automatiquesMécanismes de traction
C10N 50/10 - Forme sous laquelle est appliqué le lubrifiant au matériau à lubrifier semi-solideForme sous laquelle est appliqué le lubrifiant au matériau à lubrifier huileuse
A problem to be solved is to provide a refrigerator oil composition that has an appropriate dissolution viscosity in the case where a hydrocarbon based refrigerant is dissolved therein, and has a low solubility of a hydrocarbon based refrigerant, and a mixed composition for a refrigerator containing the refrigerator oil composition. The problem is solved by a refrigerator oil composition that is used with a refrigerant containing a hydrocarbon based refrigerant, the refrigerator oil composition containing one or more kind selected from a polyalkylene glycol based compound (A) having a number average molecular weight of 1,100 or more represented by the following general formula (1):
A problem to be solved is to provide a refrigerator oil composition that has an appropriate dissolution viscosity in the case where a hydrocarbon based refrigerant is dissolved therein, and has a low solubility of a hydrocarbon based refrigerant, and a mixed composition for a refrigerator containing the refrigerator oil composition. The problem is solved by a refrigerator oil composition that is used with a refrigerant containing a hydrocarbon based refrigerant, the refrigerator oil composition containing one or more kind selected from a polyalkylene glycol based compound (A) having a number average molecular weight of 1,100 or more represented by the following general formula (1):
A problem to be solved is to provide a refrigerator oil composition that has an appropriate dissolution viscosity in the case where a hydrocarbon based refrigerant is dissolved therein, and has a low solubility of a hydrocarbon based refrigerant, and a mixed composition for a refrigerator containing the refrigerator oil composition. The problem is solved by a refrigerator oil composition that is used with a refrigerant containing a hydrocarbon based refrigerant, the refrigerator oil composition containing one or more kind selected from a polyalkylene glycol based compound (A) having a number average molecular weight of 1,100 or more represented by the following general formula (1):
wherein in the general formula (1), one of R1 and R2 represents a hydrogen atom, and the other thereof represents a linear or branched alkyl group having 1 or more and 16 or less carbon atoms, E represents an ethylene group, P represents a propylene group, and m and n each represent a number of 0 or more, provided that m+n is 1 or more and 50 or less.
C08G 65/26 - Composés macromoléculaires obtenus par des réactions créant une liaison éther dans la chaîne principale de la macromolécule à partir d'éthers cycliques par ouverture d'un hétérocycle à partir d'éthers cycliques et d'autres composés
C09K 5/04 - Substances qui subissent un changement d'état physique lors de leur utilisation le changement d'état se faisant par passage de l'état liquide à l'état vapeur ou vice versa
C10N 20/04 - Poids moléculaireRépartition du poids moléculaire
C10N 40/30 - Lubrifiants pour machines frigorifiques
86.
ZIPPER TAPE, ZIPPER-TAPE-EQUIPPED CONTAINER, AND METHOD FOR PREVENTING FALSIFICATION
A zipper tape is provided including: a first base; a male engagement portion protruding from the first base; a second base; and a female engagement portion protruding from the second base, in which the male engagement portion includes first and second hooks protruding outward, the female engagement portion includes third and fourth hooks protruding inward, the first hook is engaged with the third hook and the second hook is engaged with the fourth hook when the male engagement portion fits inside the female engagement portion, and a force required for causing the male engagement portion to fit inside the female engagement portion is in a range from 30 N/15 mm to 100 N/15 mm.
B65D 33/25 - RivetageAssemblage à queue-d'arondeVissageDispositifs de fermeture de l'extrémité ou de l'ouverture utilisant des boutons-pression ou des fermetures à glissières
87.
COMPOUND, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
Provided is a compound represented by formula (A), (B), (C) or (D). (Symbols in the formulas are as defined in the Description.) Also provided are: an organic electroluminescent element comprising the compound; and an electronic device comprising the organic electroluminescent element.
C07C 211/54 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à deux ou trois cycles aromatiques à six chaînons
C07C 211/57 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons faisant partie de systèmes cycliques condensés du squelette carboné
C07C 211/61 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons du squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles aromatiques à six chaînons faisant partie de systèmes cycliques condensés du squelette carboné avec au moins un des systèmes cycliques condensés formé par trois cycles ou plus
C07D 209/86 - CarbazolesCarbazoles hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du système cyclique
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C07D 405/12 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
C07D 405/14 - Composés hétérocycliques contenant à la fois un ou plusieurs hétérocycles comportant des atomes d'oxygène comme uniques hétéro-atomes du cycle et un ou plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C07D 409/12 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
C07D 409/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant au moins trois hétérocycles
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
Provided is a photoelectric conversion module capable of connecting photoelectric conversion elements with stable connection strength. The photoelectric conversion module (100) comprises a first photoelectric conversion element (10a), a second photoelectric conversion element (10b) and a connector (200). The first photoelectric conversion element (10a) and the second photoelectric conversion element (10b) are arranged side by side so as to partially overlap each other. The connector (200) is connected to the first photoelectric conversion element (10a) at a first connection portion (210). The connector (200) is connected to the second photoelectric conversion element (10b) at a second connection portion (10b) away from the first connection portion (10a).
An oxide semiconductor film having crystallinity over a substrate contains indium (In) and a first metal element (M1). The oxide semiconductor film includes a plurality of crystal grains. Each of the plurality of crystal grains includes at least one of a crystal orientation <001>, a crystal orientation <101>, and a crystal orientation <111> obtained by an electron backscatter diffraction (EBSD) method. In occupancy rates of crystal orientations calculated based on measurement points having crystal orientations with a crystal orientation difference greater than or equal to 0 degrees and less than or equal to 15 degrees with respect to a normal direction of a surface of the substrate, an occupancy rate of the crystal orientation <111> is greater than an occupancy rate of the crystal orientation <001> and an occupancy rate of the crystal orientation <101>.
C07D 307/77 - Composés hétérocycliques contenant des cycles à cinq chaînons comportant un atome d'oxygène comme unique hétéro-atome du cycle condensés en ortho ou en péri avec des carbocycles ou avec des systèmes carbocycliques
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 59/32 - Dispositifs empilés comportant plusieurs couches, chacune émettant à des longueurs d'onde différentes
H10K 59/95 - Ensembles de plusieurs dispositifs comprenant au moins un élément organique émetteur de lumière dans lesquels tous les éléments émetteurs de lumière sont organiques, p. ex. ensembles d'affichages à OLED
H10K 85/60 - Composés organiques à faible poids moléculaire
H10K 101/40 - Interrelation des paramètres entre plusieurs couches ou sous-couches actives constitutives, p. ex. valeurs HOMO dans des couches adjacentes
91.
COMPOUND, ORGANIC ELECTROLUMINESCENT ELEMENT MATERIAL, ORGANIC ELECTROLUMINESCENT ELEMENT, AND ELECTRONIC DEVICE
111212 are each independently a group represented by general formula (11), (12), or (13), R is a hydrogen atom or a substituent of an aryl group or same, k is 1, 2, or 3, m is 0, 1, or 2, n is 1, 2, or 3, and k + m + n is 4.
C07D 495/22 - Composés hétérocycliques contenant dans le système condensé au moins un hétérocycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle dans lesquels le système condensé contient au moins quatre hétérocycles
C07D 209/86 - CarbazolesCarbazoles hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du système cyclique
C07D 251/24 - Composés hétérocycliques contenant des cycles triazine-1, 3, 5 non condensés avec d'autres cycles comportant trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des atomes d'hydrogène ou de carbone liés directement à au moins un atome de carbone du cycle à trois atomes de carbone du cycle
C07D 403/10 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant deux hétérocycles liés par une chaîne carbonée contenant des cycles aromatiques
C07D 491/048 - Systèmes condensés en ortho avec un seul atome d'oxygène comme hétéro-atome du cycle contenant de l'oxygène le cycle contenant de l'oxygène étant à cinq chaînons
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
H10K 50/11 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL]
H10K 50/12 - OLED ou diodes électroluminescentes polymères [PLED] caractérisées par les couches électroluminescentes [EL] comprenant des dopants
H10K 59/00 - Dispositifs intégrés, ou ensembles de plusieurs dispositifs, comprenant au moins un élément organique émetteur de lumière couvert par le groupe
H10K 85/60 - Composés organiques à faible poids moléculaire
Provided is a method for producing calcium carbonate particles, whereby calcium carbonate particles having high whiteness (high purity) can be produced in a few steps. Specifically, the method for producing calcium carbonate particles comprises mixing a Ca-containing waste, a carbonate ion-containing compound, and an organic acid.
A thin film transistor includes a metal oxide layer over the substrate, an oxide semiconductor layer having crystallinity in contact with the metal oxide layer, a gate electrode overlapping the oxide semiconductor layer, and an insulating layer between the oxide semiconductor layer and the gate electrode. The oxide semiconductor layer includes a plurality of crystal grains. Each of the plurality of crystal grains includes at least one of a crystal orientation <001>, a crystal orientation <101>, and a crystal orientation <111> obtained by an EBSD method. In occupancy rates of crystal orientations calculated based on measurement points having crystal orientations with a crystal orientation difference greater than or equal to 0 degrees and less than or equal to 15 degrees with respect to a normal direction of a surface of the substrate, an occupancy rate of the crystal orientation <001> is less than or equal to 5%.
Provided is a method for producing calcium carbonate particles with which it is possible to continuously produce calcium carbonate particles of high whiteness (high purity) in few steps. Specifically, the method for producing calcium carbonate particles uses a reaction vessel 10 that is provided with a filter medium 2 compatible with crossflow filtration and is capable of circulating a suspension and circulates a suspension containing Ca-containing waste and carbonate ion-containing aqueous solution through the filter medium 2.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
04 - Huiles et graisses industrielles; lubrifiants; combustibles
Produits et services
Coolants; dielectric fluids as a chemical preparation for cooling computer servers, except oils. Cooling lubricants; dielectric oils for cooling computer servers.
There has been a need for development of a lubricating oil composition which is reduced in the oil evaporation amount at lower temperatures, and is capable of improving the fuel consumption saving. Disclosed is a lubricating oil composition which includes a base oil (A) in which the content of a fraction containing hydrocarbon groups having not less than 14 but less than 16 carbon atoms is within the range of 0.10% by mass to 0.60% by mass based on the total amount of the base oil (A), and the content of a fraction containing hydrocarbon groups having not less than 16 but less than 18 carbon atoms is within the range of 0.35% by mass to 1.85% by mass based on the total amount of the base oil (A).
C10M 171/00 - Compositions lubrifiantes caractérisées par des critères purement physiques, p. ex. contenant comme matériau de base, épaississant ou additif des ingrédients exclusivement caractérisés par des valeurs numériques particulières de leurs propriétés physiques, c.-à-d. contenant des ingrédients physiquement bien définis mais dont la nature chimique n'est pas précisée ou n'est que très vaguement indiquée
C10N 30/00 - Propriétés physiques ou chimiques particulières améliorées par l'additif caractérisant la composition lubrifiante, p. ex. additifs multifonctionnels
C07D 209/88 - CarbazolesCarbazoles hydrogénés avec des hétéro-atomes ou 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, liés directement aux atomes de carbone du système cyclique
C07D 239/26 - Composés hétérocycliques contenant des cycles diazine-1, 3 ou diazine-1, 3 hydrogéné non condensés avec d'autres cycles comportant au moins trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle
C07D 251/24 - Composés hétérocycliques contenant des cycles triazine-1, 3, 5 non condensés avec d'autres cycles comportant trois liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des atomes d'hydrogène ou de carbone liés directement à au moins un atome de carbone du cycle à trois atomes de carbone du cycle
C09K 11/06 - Substances luminescentes, p. ex. électroluminescentes, chimiluminescentes contenant des substances organiques luminescentes
Disclosed is a compound which has a structure represented by general formula (1). In the general formula (1), R101to R121are each independently a hydrogen atom or a substituent, provided that at least one of R101to R111and R115to R118 is a substituted or unsubstituted N-carbazolyl group.
A lubricant base oil having a natural origin content (ISO 16128) of 100%, may contain a monoester compound having one or more branched structures and 18 or more carbon atoms. The monoester compound may a compound of formula (1):
A lubricant base oil having a natural origin content (ISO 16128) of 100%, may contain a monoester compound having one or more branched structures and 18 or more carbon atoms. The monoester compound may a compound of formula (1):
A lubricant base oil having a natural origin content (ISO 16128) of 100%, may contain a monoester compound having one or more branched structures and 18 or more carbon atoms. The monoester compound may a compound of formula (1):
wherein R1 and R2 are each independently a hydrocarbon group, at least one of R1 and R2 is a branched hydrocarbon group, and a total number of carbon atoms of R1 and R2 is 17 or more. In the compound of formula (1), R1 may be an alkyl group or alkenyl group having 8 or more carbon atoms, R2 may be an alkyl group or alkenyl group having 5 or more carbon atoms, and at least one of R1 and R2 may be a branched alkyl group or a branched alkenyl group
Provided is a zipper tape-equipped container including: a container body; and a zipper tape including a first base part and a second base part attached to the container body, and a first engagement part and a second engagement part which are respectively formed on the first base part and the second base part and can engage with each other. A first engagement strength between the first engagement part and the second engagement part in a first section which is a part of 40% or less of an effective section in a length direction of the zipper tape is lower than a second engagement strength between the first engagement part and the second engagement part in a second section which is the remaining part of the effective section.
B65D 33/25 - RivetageAssemblage à queue-d'arondeVissageDispositifs de fermeture de l'extrémité ou de l'ouverture utilisant des boutons-pression ou des fermetures à glissières
A44B 19/16 - Élément d'accrochage à section constante tout le long de la bande
B31B 70/81 - Formation ou fixation d’accessoires, p. ex. de dispositifs d’ouverture ou de fermeture, de cordons de déchirure
B31B 160/20 - Forme des réceptacles flexibles avec une configuration particulière pour tenir compte de l’épaisseur du contenu
