Provided is a cyclic olefin copolymer production method that can produce, with high efficiency, a cyclic olefin copolymer that is a copolymer of a cyclic olefin monomer and an α-olefin monomer having 3-20 carbon atoms and that has excellent toughness. According to the present invention, a copolymer of a cyclic olefin monomer and an α-olefin monomer having 3-20 carbon atoms is produced using a method comprising: a first polymerization for polymerizing monomers including the cyclic olefin monomer and the α-olefin monomer in a polymerization vessel in the presence of a titanocene catalyst, an alkyl aluminum compound, and a borate compound; addition of an alkyl aluminum compound solely to the polymerization vessel after the first polymerization; and a second polymerization for further adding the monomers into the polymerization vessel after the addition of the alkyl aluminum compound, and continuously polymerizing the monomers.
C08F 232/00 - Copolymères de composés cycliques ne contenant pas de radicaux aliphatiques non saturés dans une chaîne latérale et contenant une ou plusieurs liaisons doubles carbone-carbone dans un système carbocyclique
C08F 4/6592 - Composant couvert par le groupe contenant une liaison métal de transition-carbone contenant au moins un cycle cyclopentadiényle, condensé ou non, p. ex. un cycle indényle ou fluorényle
C08F 210/00 - Copolymères d'hydrocarbures aliphatiques non saturés contenant une seule liaison double carbone-carbone
Provided is a cyclic olefin copolymer production method with which it is possible to efficiently produce a cyclic olefin copolymer that has excellent toughness and comprises a cyclic olefin monomer and a C3-20 α-olefin monomer. This copolymer comprising a cyclic olefin monomer and a C3-20 α-olefin monomer is produced by means of a method comprising: a first polymerization in which monomers including the cyclic olefin monomer and the α-olefin monomer are polymerized in a polymerization vessel in the presence of a titanocene catalyst, an alkylaluminum compound, and a borate compound; an addition of the monomers and the alkylaluminum compound into the polymerization vessel after the first polymerization; and a second polymerization in which the monomers are continually polymerized after the addition of the monomers and the alkylaluminum compound.
C08F 232/00 - Copolymères de composés cycliques ne contenant pas de radicaux aliphatiques non saturés dans une chaîne latérale et contenant une ou plusieurs liaisons doubles carbone-carbone dans un système carbocyclique
C08F 4/6592 - Composant couvert par le groupe contenant une liaison métal de transition-carbone contenant au moins un cycle cyclopentadiényle, condensé ou non, p. ex. un cycle indényle ou fluorényle
C08F 210/00 - Copolymères d'hydrocarbures aliphatiques non saturés contenant une seule liaison double carbone-carbone
The present invention addresses the problem of providing a filter medium which can be used for a pleated filter, has low pressure loss and is highly efficient. This problem is solved by a laminate in which a collection layer and a support layer are laminated in this order, said collection layer containing a plurality of first fibres and a plurality of second fibres that have an outer diameter smaller than that of the first fibres and are supported by the first fibres in a dispersed state, and in which the bending resistance as measured by the Gurley method is 1 to 14 mN.
B32B 5/26 - Produits stratifiés caractérisés par l'hétérogénéité ou la structure physique d'une des couches caractérisés par la présence de plusieurs couches qui comportent des fibres, filaments, grains ou poudre, ou qui sont sous forme de mousse ou essentiellement poreuses une des couches étant fibreuse ou filamenteuse un autre couche également étant fibreuse ou filamenteuse
B01D 39/16 - Autres substances filtrantes autoportantes en substance organique, p. ex. fibres synthétiques
B32B 27/34 - Produits stratifiés composés essentiellement de résine synthétique comprenant des polyamides
B32B 27/36 - Produits stratifiés composés essentiellement de résine synthétique comprenant des polyesters
D04H 1/4382 - Fibres obtenues par étirage de film réticuléFibres compositesFibres mixtesFibres ultrafinesFibres pour cuir artificiel
This cellulose acylate composition contains a cellulose acylate, a plasticizer, and a coloring material. The cellulose acylate has a degree of substitution with an acetyl group of 2.0-2.6. The content of the plasticizer is 30.0 wt.% or more. When the cellulose acylate composition has a thickness of 3.0 mm, the b*value in the L*a*b* color system measured by a reflection method is 5.0 or less.
The present invention addresses the problem of providing a fiber layered body in which a pre-collection layer and a collection layer have been unified without using an adhesive, and which has a low pressure loss and a high dust retention quantity. This problem is solved by a fiber layered body that has a pre-collection layer and a collection layer layered in order therein, wherein the pre-collection layer includes a plurality of fibers, and the collection layer includes a plurality of first fibers and a plurality of second fibers, said plurality of second fibers having a smaller outer diameter than the first fibers and being supported by the first fibers in a dispersed condition.
B01D 39/16 - Autres substances filtrantes autoportantes en substance organique, p. ex. fibres synthétiques
B01D 46/10 - Séparateurs de particules utilisant des plaques, des feuilles ou des tampons filtrants à surface plane, p. ex. appareils de précipitation de poussières
B32B 5/26 - Produits stratifiés caractérisés par l'hétérogénéité ou la structure physique d'une des couches caractérisés par la présence de plusieurs couches qui comportent des fibres, filaments, grains ou poudre, ou qui sont sous forme de mousse ou essentiellement poreuses une des couches étant fibreuse ou filamenteuse un autre couche également étant fibreuse ou filamenteuse
D04H 1/498 - Non-tissés formés uniquement ou principalement de fibres coupées ou autres fibres similaires relativement courtes à partir de voiles ou couches composés de fibres ne possédant pas des propriétés cohésives réelles ou potentielles les voiles ou couches étant renforcées par des moyens mécaniques, p. ex. par roulage par aiguilletage ou opérations similaires pour provoquer l'enchevêtrement des fibres enchevêtrement des couches de non-tissés
D04H 1/593 - Non-tissés formés uniquement ou principalement de fibres coupées ou autres fibres similaires relativement courtes à partir de voiles ou couches composés de fibres ne possédant pas des propriétés cohésives réelles ou potentielles par application, incorporation ou activation de liages chimiques ou thermoplastiques, p. ex. adhésifs à des couches superposées
D04H 5/04 - Non-tissés formés de mélanges de fibres relativement courtes et de fils ou de matériaux filamenteux similaires de bonne longueur renforcés ou consolidés par application ou incorporation d'agents de liage chimiques ou thermo-activables sous une forme solide ou liquide
A water electrolyzer that has an anode including a nanodiamond and a light irradiator that irradiates the anode with light is provided. A water electrolysis method in which water is electrolyzed while an anode including a nanodiamond is irradiated with light is also provided.
Biodegradable spherical particles contain a biodegradable polymer as a main component. The biodegradable spherical particles have a particle size variation coefficient CV of 40% or less, and a biodegradation degree on the fifth day in a biodegradability test in accordance with OECD TG301F of 40% or less. A cosmetic composition contains the biodegradable spherical particles. A method for producing the biodegradable spherical particles includes preparing a mixture by mixing a biodegradable polymer, a plasticizer, and a water-soluble polymer; melt-kneading the mixture at 200° C. or higher and 280° C. or lower to yield a kneaded product; and removing the water-soluble polymer from the kneaded product.
12 - Véhicules; appareils de locomotion par terre, par air ou par eau; parties de véhicules
13 - Armes à feu; explosifs
Produits et services
Gas generators for airbags in automobiles and aircraft; gas generators for seat belt pretensioners in automobiles and aircraft; gas generators for safety devices in automobiles and aircraft; inflators for airbags in automobiles and aircraft; inflators for seat belt pretensioners in automobiles and aircraft; inflators for safety devices in automobiles and aircraft; igniters for airbags in automobiles and aircraft; igniters for seat belt pretensioners in automobiles and aircraft; igniters for safety devices in automobiles and aircraft; parts and fittings for automobiles; parts and fittings for aircraft Pyrotechnic products; pyrotechnic gas generators; gunpowder; explosives; explosives for use in airbags for automobiles and aircraft; explosives for use in seat belt pretensioners for automobiles and aircraft; detonators; gas igniters for pyrotechnic devices
9.
AMYLOID FIBRIL FORMATION METHOD, AMYLOID FIBRIL FORMATION DEVICE, AND AMYLOID FIBRIL ANALYSIS SYSTEM
Provided is a novel amyloid fibril formation method that makes it possible to form amyloid fibrils more easily than in the past. According to the present invention, an amyloid fibril formation method for forming amyloid fibrils from an amyloid fibril formation protein involves allowing a fluid that includes the amyloid fibril formation protein to flow into a fluid tube and forming the amyloid fibrils from the amyloid fibril formation protein by transporting the fluid using a means that gradually compresses the fluid tube in one direction to pressurize and depressurize the fluid and thereby move the fluid through the fluid tube.
D01F 4/00 - Filaments, ou similaires, artificiels, à un seul composant, formés de protéinesLeur fabrication
C07K 14/47 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains provenant de vertébrés provenant de mammifères
The present disclosure provides a 1,3-butylene glycol product, having, according to a gas chromatographic analysis performed under predetermined conditions, a peak ratio of 2000 ppm or lower appearing in a relative retention time ranging from 1.6 to 1.8, provided that the relative retention time for a peak of 1,3-butylene glycol is 1.0. The present disclosure also provides a 1,3-butylene glycol product, having, according to a gas chromatographic analysis performed under predetermined conditions, a peak area ratio of 100 ppm or lower appearing in a relative retention time ranging from 1.35 to 1.45, provided that the relative retention time for a peak of 1,3-butylene glycol is 1.0. The present disclosure also provides a 1,3-butylene glycol product, having, according to a gas chromatographic analysis performed under predetermined conditions, a peak area ratio of 1000 ppm or lower appearing in a relative retention time ranging from 2.3 to 2.4, provided that the relative retention time for a peak of 1,3-butylene glycol is 1.0.
A61Q 5/02 - Préparations pour le lavage des cheveux
A61Q 5/12 - Préparations contenant des agents de conditionnement des cheveux
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
A61Q 19/00 - Préparations pour les soins de la peau
C07C 29/141 - Préparation de composés comportant des groupes hydroxyle ou O-métal liés à un atome de carbone ne faisant pas partie d'un cycle aromatique à six chaînons par réduction d'un groupe fonctionnel contenant de l'oxygène de groupes contenant C=O, p. ex. —COOH d'un groupe —CHO avec de l'hydrogène ou des gaz contenant de l'hydrogène
C07C 29/156 - Préparation de composés comportant des groupes hydroxyle ou O-métal liés à un atome de carbone ne faisant pas partie d'un cycle aromatique à six chaînons par réduction exclusivement des oxydes de carbone avec de l'hydrogène ou des gaz contenant de l'hydrogène caractérisée par le catalyseur utilisé contenant des métaux du groupe du fer, des métaux du groupe du platine, ou leurs composés
The purpose of the present disclosure is to provide a technique capable of easily rupturing a burst plate. This rupture device includes: a burst plate that has a first surface and a second surface on the opposite side from the first surface, and closes the opening of a container filled with pressurized gas, the burst plate having a fragile part on at least one surface of the first surface and the second surface of the burst plate, the fragile part having a start point and an end point that are located at different positions and having an extension region between the start point and the end point, the extension region having an annular shape including a curved part or a straight line part or a curved part and a straight line part; and an igniter that includes an ignition part on the tip side, the ignition part facing a rupture starting point region that is a part of the extension region of the fragile part excluding the start point and the end point so that rupture starts from the rupture starting point region and the distance from the extension region becomes indefinite over the outer peripheral part of the ignition part.
B60R 21/274 - Moyens gonflables de retenue ou d'immobilisation des occupants prévus pour se gonfler lors d'un choc ou en cas de choc imminent, p. ex. sacs gonflables caractérisés par la source de fluide de gonflage ou par les moyens de commande de l'écoulement du fluide de gonflage utilisant l'émission instantanée de gaz comprimé stocké caractérisés par des moyens de rupture ou d'ouverture de la source de fluide
12.
LAMINATED MATERIAL, METHOD FOR PRODUCING SAME, AND USE APPLICATION OF SAME
A laminated material includes a first base material, and a sheet material laminated on and integrated with a surface of this first base material. The first base material is made of a material selected from the group consisting of a biomass material, a plastic, a metal, a ceramic, a glass, a molded pulp, and a paper. The sheet material is substantially made of a plant-derived component. The sheet material has an absorption peak in a region of 1715 to 1725 cm−1 in an infrared absorption spectrum. The sheet material can be produced by removing a liquid component from a lignocellulose solution produced by dissolving a plant raw material in an organic acid. A laminated material is produced by laminating the sheet material on a surface of the first base material, and thermocompression-bonding the sheet material and the first base material.
B32B 23/04 - Produits stratifiés composés essentiellement de substances cellulosiques plastiques comprenant de telles substances comme seul composant ou comme composant principal d'une couche adjacente à une autre couche d'une substance spécifique
B32B 21/04 - Produits stratifiés composés essentiellement de bois, p. ex. une planche de bois, une feuille de placage, une feuille de bois aggloméré comprenant du bois comme seul composant ou composant principal d'une couche adjacente à une autre couche d'une substance spécifique
B32B 37/06 - Procédés ou dispositifs pour la stratification, p. ex. par polymérisation ou par liaison à l'aide d'ultrasons caractérisés par le procédé de chauffage
B32B 37/10 - Procédés ou dispositifs pour la stratification, p. ex. par polymérisation ou par liaison à l'aide d'ultrasons caractérisés par la technique de pressage, p. ex. faisant usage de l'action directe du vide ou d'un fluide sous pression
B32B 38/00 - Opérations auxiliaires liées aux procédés de stratification
The purpose of the present invention is to provide a water-in-oil emulsion composition having improved dispersibility of polysaccharide-based particles. This water-in-oil emulsion composition is obtained by a water-in-oil emulsion composition production method comprising: a step A for preparing a base-use water-in-oil emulsion composition from an oil-phase composition and a water-phase composition; and a step B for mixing the base-use water-in-oil emulsion composition with particles mainly composed of a polysaccharide-based polymer selected from the group consisting of polysaccharides and polysaccharide esters. The water-in-oil emulsion composition excels in dispersibility with respect to particles containing a polysaccharide-based polymer as a main component.
NATIONAL UNIVERSITY CORPORATION SAITAMA UNIVERSITY (Japon)
Inventeur(s)
Inada, Yuki
Yamano, Yasushi
Nakanishi, Yoshiaki
Abrégé
This electric circuit protection device comprises: a current interruption device including a conductor piece forming a part of an electric circuit and an igniter for cutting the conductor piece; and a current limiting element that is connected in series with the conductor piece of the current interruption device to form a part of the electric circuit, and that is connected in parallel with the igniter to exhibit a current limiting operation when an abnormal current flows, wherein the igniter has impedance higher than that of the current limiting element at a normal time, and when the current limiting element exhibits the current limiting operation, a current flows through the igniter, whereby the igniter is operated to interrupt a current flowing in the electric circuit.
The purpose of the present invention is to provide a thermosetting epoxy resin composition which is capable of preventing deterioration of reliability due to long-term storage while improving durability against heat generation and vibration after curing. A thermosetting epoxy resin composition according to the present disclosure is characterized by: containing an epoxy compound (A), an acid anhydride-based curing agent (B), a curing accelerator (C), a silane coupling agent (D), a defoaming agent (E), and an inorganic filler (F), wherein the inorganic filler (F) is a resin composition that contains spherical silica and amorphous calcium carbonate, and the content of the spherical silica is 50-90 mass% and the content of the amorphous calcium carbonate is 5-50 mass% with respect to the total amount of the resin composition; and being in liquid state at 25°C.
Provided are: a liquid crystalline resin composition which has good fluidity and provides a molded article having excellent low warpage and reduced blisters; and a connector using same. A liquid crystalline resin composition according to the present invention contains (A) a wholly aromatic polyester, (B) a plate-like filler, and (C) a fibrous filler, wherein the wholly aromatic polyester (A) contains predetermined amounts of constituent units (I)-(V) as essential constituent components, the weight average fiber length of the fibrous filler (C) is 500 μm or less, and the content of the wholly aromatic polyester (A) is 70-85 mass%, the content of the plate-like filler (B) is 10-25 mass%, the content of the fibrous filler (C) is 1.5-8.5 mass%, and the total content of the plate-like filler (B) and the fibrous filler (C) is 15-30 mass%, with respect to the entirety of the liquid crystalline resin composition. A connector according to the present invention includes a molded article of the liquid crystalline resin composition.
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
C08G 63/60 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés dérivés de la réaction d'un mélange d'acides hydroxycarboxyliques, d'acides polycarboxyliques et de composés polyhydroxylés
C08K 7/00 - Emploi d'ingrédients caractérisés par leur forme
H05K 1/03 - Emploi de matériaux pour réaliser le substrat
17.
LIQUID CRYSTALLINE RESIN COMPOSITION AND FILM USING SAME
The present invention provides: a liquid crystalline resin composition which is capable of providing a film that has excellent dielectric characteristics, film forming properties, and mechanical strength in a well-balanced manner; and a film using the same. A liquid crystalline resin pellet according to the present invention contains (A) a liquid crystalline resin and (B) an amorphous polyarylate. The liquid crystalline resin (A) contains the following constituent units (I) and (II) as essential constituent components, and with respect to all constituent units in the liquid crystalline resin (A), the content of the constituent unit (I) is 60-85 mol% and the content of the constituent unit (II) is 12-40 mol%. With respect to the entire liquid crystalline resin composition, the content of the liquid crystalline resin (A) is 95.5-99.9 mass% and the content of the amorphous polyarylate (B) is 0.1-4.5 mass%.
C08L 67/04 - Polyesters dérivés des acides hydroxycarboxyliques, p. ex. lactones
C08G 63/06 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés dérivés des acides hydroxycarboxyliques
C08L 67/03 - Les acides dicarboxyliques et les composés dihydroxylés ayant les groupes hydroxy et carboxyliques liés directement à des cycles aromatiques
Provided is a method for safely producing zeta-positive hydrogenated nanodiamond particles. The method for producing hydrogenated nanodiamond particles according to the present disclosure is a method for obtaining hydrogenated nanodiamond particles with a zeta potential of +35 mV or more in water with a pH of 5-8 by subjecting diamond particles with a zeta potential of +30 mV or less in water with a pH of 5-8 to a hydrogenation treatment step in which the diamond particles are heated at a temperature of 300°C-850°C in a gas atmosphere with a hydrogen gas concentration of less than 1%. The hydrogen gas concentration in the gas atmosphere is preferably 0.01% or more and less than 1%, and the gas atmosphere preferably contains hydrogen gas and nitrogen gas.
G03F 7/11 - Matériaux photosensibles caractérisés par des détails de structure, p. ex. supports, couches auxiliaires avec des couches de recouvrement ou des couches intermédiaires, p. ex. couches d'ancrage
H01L 21/027 - Fabrication de masques sur des corps semi-conducteurs pour traitement photolithographique ultérieur, non prévue dans le groupe ou
The present disclosure relates to a composition containing cancer cells that express damage-associated molecular patterns (DAMPs) and a method of administering the composition to a subject with a needleless injector.
A61K 39/00 - Préparations médicinales contenant des antigènes ou des anticorps
A61K 41/17 - Inactivation ou décontamination d'une préparation médicinale avant son administration à un animal ou une personne par lumière ultraviolette [UV] ou infrarouge [IR], rayons X ou rayons gamma
Provided is a surface-modified nanodiamond having excellent dispersibility in an organic solvent, and a method capable of introducing various surface-modifying groups and easily producing surface-modified nanocarbon particles with little zirconia contamination. The surface-modified nanodiamond includes nanodiamond particles and a group that surface-modifies the nanodiamond particles and is represented by Formula (1): —X—R1 (1) [where X represents —NH—, —O—, —O—C(═O)—, —C(═O)—O—, —NH—C(═O)—, —C(═O)—NH—, or —S—; the bond extending left from X is bonded to a nanodiamond particle; R1 represents a monovalent organic group that does not have a hydroxy group, carboxy group, amino group, mono-substituted amino group, terminal alkenyl group, and terminal epoxy group; an atom bound to X is a carbon atom; and a molar ratio of carbon atoms to the total amount of heteroatoms selected from the group consisting of nitrogen atoms, oxygen atoms, sulfur atoms, and silicon atoms is 4.5 or greater.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
40 - Traitement de matériaux; recyclage, purification de l'air et traitement de l'eau
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
Unprocessed plastics; artificial resins, unprocessed;
unprocessed plastics for industrial use; unprocessed
plastics in primary form; chemicals used in industry;
unprocessed plastic in the form of pellet, powder, flake or
grain; synthetic resins, unprocessed; thermoplastic resins,
unprocessed; unprocessed polymer resins in the form of
pellet; polymer resins, unprocessed; unprocessed artificial
resins for industrial purposes; unprocessed synthetic resins
for use in the manufacture of plastic molding compounds;
recycled unprocessed plastic in the form of pellet, powder,
flake or grain for use in further manufacturing; recycled
unprocessed plastics in extruded form for use in further
manufacturing. Plastic semi-worked products; plastic substances,
semi-processed; semi-processed plastics; semi-processed
synthetic resins; artificial resins, semi-processed;
semi-processed polymers in pellet form; semi-processed
thermoplastics in pellet form; recycled semi-processed
plastic in the form of pellet, powder, flake or grain for
use in further manufacturing; recycled semi-processed
plastics in extruded form for use in further manufacturing;
recycled thermoplastic compounds in pellet form for use in
further manufacture; semi-worked synthetic plastic and
synthetic resins as semi-finished products in form of
pellets, rods, foils, foams, fibers, films and sheets. Recycling of plastic; processing of plastics; recycling of
waste; providing information relating to material treatment;
sorting of waste and recyclable material; upcycling in the
nature of waste recycling; waste transformation; waste
processing; recycling of waste materials; recycling of
chemicals. Scientific research in the field of environmental
protection; providing scientific information, advice and
consultancy relating to carbon offsetting; providing
scientific information, advice and consultancy relating to
net zero emissions; biological research.
Provided is a 1,3-butylene glycol product unlikely to generate apple odor and pungent odor even when blended in a cosmetic composition. The 1,3-butylene glycol product has an area ratio represented by the following formula of from 54 to 130. Area ratio=peak X area/area obtained by subtracting peak area of diethylene glycol dimethyl ether from total peak area×106. Peak X area: area of a peak having a peak top in the retention time 6.2-6.32 range in gas chromatographic analysis under specific conditions when the retention time of diethylene glycol dimethyl ether, the internal standard, is taken to be 1.0.
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
40 - Traitement de matériaux; recyclage, purification de l'air et traitement de l'eau
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
Unprocessed plastics; artificial resins, unprocessed;
unprocessed plastics for industrial use; unprocessed
plastics in primary form; chemicals used in industry;
unprocessed plastic in the form of pellet, powder, flake or
grain; synthetic resins, unprocessed; thermoplastic resins,
unprocessed; unprocessed polymer resins in the form of
pellet; polymer resins, unprocessed; unprocessed artificial
resins for industrial purposes; unprocessed synthetic resins
for use in the manufacture of plastic molding compounds;
recycled unprocessed plastic in the form of pellet, powder,
flake or grain for use in further manufacturing; recycled
unprocessed plastics in extruded form for use in further
manufacturing. Plastic semi-worked products; plastic substances,
semi-processed; semi-processed plastics; semi-processed
synthetic resins; artificial resins, semi-processed;
semi-processed polymers in pellet form; semi-processed
thermoplastics in pellet form; recycled semi-processed
plastic in the form of pellet, powder, flake or grain for
use in further manufacturing; recycled semi-processed
plastics in extruded form for use in further manufacturing;
recycled thermoplastic compounds in pellet form for use in
further manufacture; semi-worked synthetic plastic and
synthetic resins as semi-finished products in form of
pellets, rods, foils, foams, fibers, films and sheets. Recycling of plastic; processing of plastics; recycling of
waste; providing information relating to material treatment;
sorting of waste and recyclable material; upcycling in the
nature of waste recycling; waste transformation; waste
processing; recycling of waste materials; recycling of
chemicals. Scientific research in the field of environmental
protection; providing scientific information, advice and
consultancy relating to carbon offsetting; providing
scientific information, advice and consultancy relating to
net zero emissions; biological research.
The purpose of the present disclosure is to provide a 1,3-butylene glycol product which is less likely to produce an apple odor or an irritating odor even if blended in a cosmetic composition. Provided is a 1,3-butylene glycol product which has an area ratio represented by the following formula of 10 to 280 inclusive. Area ratio = (peak X area)/(1,3 BG peak area) × 106 Peak X area: the area of peak X in an m/z101 ion chromatogram in SIM mode, the peak X having a relative retention time within the range of 0.59 to 0.65 when the relative retention time of the peak of diethylene glycol dimethyl ether, which is an internal standard substance, is taken as 1.0 in a gas chromatography analysis under specific conditions. 1,3 BG peak area: the area of a peak of 1,3-butylene glycol in an m/z72 ion chromatogram in Scan mode, the peak of 1,3-butylene glycol having a relative retention time within the range of 0.72 to 0.88 when the relative retention time of the peak of diethylene glycol dimethyl ether, which is an internal standard substance, is taken as 1.0 in a gas chromatography analysis under specific conditions.
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 19/00 - Préparations pour les soins de la peau
The present invention provides a 1,3-butylene glycol product which is less likely to produce an apple odor or an irritating odor even if blended in a cosmetic composition. Provided is a 1,3-butylene glycol product which has an area ratio represented by the following formula of 20 to 260 inclusive. Area ratio = (peak X area)/(1,3 BG peak area) × 106 Peak X area: the area of peak X in an m/z145 ion chromatogram in Scan mode, the peak X having a relative retention time within the range of 6.6 to 6.7 when the relative retention time of the peak of diethylene glycol dimethyl ether, which is an internal standard substance, is taken as 1.0 in a gas chromatography analysis under specific conditions. 1,3 BG peak area: the area of a peak of 1,3-butylene glycol in an m/z72 ion chromatogram in Scan mode, the peak of 1,3-butylene glycol having a relative retention time within the range of 5.23 to 6.27 when the relative retention time of the peak of diethylene glycol dimethyl ether, which is an internal standard substance, is taken as 1.0 in a gas chromatography analysis under specific conditions.
The purpose of the present invention is to provide a technology capable of limiting deterioration of slidability of a projectile in a sliding structure. The sliding structure comprises: a housing that encloses an accommodation space extending in one direction; an igniter that is provided to the housing; a projectile that is disposed in the accommodation space, is fired from one end side of the accommodation space by means of energy received from the igniter, and slides along the extending direction of the accommodation space; and a relief space that is provided in at least a portion of a site where an inner wall defining the accommodation space and the projectile are fitted, and releases an expanding portion when the volume of at least one among the projectile and the housing has expanded with respect to the other among the projectile and the housing.
Provided is a method for producing a concentrated liquid of a minute useful substance. The method for producing a concentrated liquid containing a minute useful substance involves: adding an oxyethylene adduct of a sorbitan unsaturated fatty acid ester to a primary liquid raw material containing a minute useful substance to obtain a secondary liquid raw material; and applying the secondary liquid raw material to a hollow fiber membrane to concentrate the secondary liquid raw material.
C12P 1/00 - Préparation de composés ou de compositions, non prévue dans les groupes , utilisant des micro-organismes ou des enzymesProcédés généraux de préparation de composés ou de compositions utilisant des micro-organismes ou des enzymes
29.
PHARMACEUTICAL COMPOSITION FOR INTRAVASCULAR ADMINISTRATION
NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY (Japon)
Inventeur(s)
Uchimura, Seiichi
Nakatsuka, Shuji
Kawabori, Masahito
Abrégé
The purpose of the present disclosure is to provide a pharmaceutical composition having excellent therapeutic effects in the treatment of central nervous system diseases. This pharmaceutical composition for intravascular administration is used for treating central nervous system diseases and contains a purified extracellular vesicle product. The purified extracellular vesicle product is obtained by a method for producing a purified extracellular vesicle product, the method comprising: (i) a purification step for bringing a solution to be treated containing extracellular vesicles and foreign substances into contact with size-exclusion and anion-exchange carriers to obtain a treated solution containing the extracellular vesicles; and (ii) a membrane filtration step for subjecting the treated solution to membrane filtration to obtain a concentrated solution of the extracellular vesicles. The pharmaceutical composition has excellent therapeutic effects in the treatment of central nervous system diseases.
A61K 35/12 - Substances provenant de mammifèresCompositions comprenant des tissus ou des cellules non spécifiésCompositions comprenant des cellules souches non embryonnairesCellules génétiquement modifiées
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p. ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénale
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
A composition contains an acetylated wood flour. This acetylated wood flour is substantially free of an inorganic acid ester bound to a cellulose main chain. A method of manufacturing the composition includes: treating a wood flour under reduced pressure; subjecting the wood flour treated under reduced pressure to pressurization treatment at an absolute pressure of 10 bar or more in an immersed state in a solvent containing an acetylating agent; and after the pressurization treatment, subjecting the wood flour to acetylation treatment by maintaining the solvent containing the wood flour and the acetylating agent at a temperature of 60 to 130° C. in a pressurized state at an absolute pressure of 1.1 to 1.9 bar in an inert gas atmosphere.
Provided is a macromolecular compound that, when used in a photoresist resin composition, has high sensitivity and excellent resolution, can accurately form a fine pattern, and can reduce the occurrence of development defects. Also provided is a photoresist resin composition that has high sensitivity and excellent resolution, can accurately form a fine pattern, and can reduce the occurrence of development defects. The macromolecular compound contains at least a monomer unit a represented by formula (a) and a monomer unit b having an alicyclic skeleton that has a polar group (however, this does not include a monomer unit c represented by formula (c)). The monomer unit c content is less than 5 mol% relative to all of the monomer units constituting the macromolecular compound.
A protection device including an inflating strap having flexibility and configured to be disposed in contact with a skin of a wearer along at least a part of a boundary region between the neck and a head of the wearer in a state before the protection device is operated, the inflating strap including an inflating portion configured to be inflated when an inflation source is supplied at a time of operation of the protection device, an inflation source supply unit configured to supply the inflation source to the inflating portion, and an activation unit configured to inflate the inflating portion by activating the inflation source supply unit, a movement of the neck of the wearer is restricted by inflating the inflating portion at a time of operation.
22-free regenerated cellulose fibers having a monofilament tensile elongation at break measured according to JIS L1015 of 10% or more and a toughness of 35 MPa or more.
C08L 23/00 - Compositions contenant des homopolymères ou des copolymères d'hydrocarbures aliphatiques non saturés ne possédant qu'une seule liaison double carbone-carboneCompositions contenant des dérivés de tels polymères
C08L 59/00 - Compositions contenant des polyacétalsCompositions contenant des dérivés des polyacétals
C08L 77/00 - Compositions contenant des polyamides obtenus par des réactions créant une liaison amide carboxylique dans la chaîne principaleCompositions contenant des dérivés de tels polymères
C08L 101/00 - Compositions contenant des composés macromoléculaires non spécifiés
B29B 15/08 - Prétraitement de la matière à façonner non couvert par les groupes d'agents de renforcement ou des charges
B29K 105/12 - Présentation, forme ou état de la matière moulée contenant des agents de renforcement, charges ou inserts de longueur réduite, p. ex. filaments coupés, fibres coupées ou crins
34.
METHOD FOR CALCULATING ACTUAL CONTACT RATIO OF THERMOPLASTIC RESIN GEAR, METHOD FOR DERIVING COEFFICIENT OF FRICTION OF THERMOPLASTIC RESIN GEAR, METHOD FOR PREDICTING TOOTH ROOT TEMPERATURE OF THERMOPLASTIC RESIN GEAR, AND METHOD FOR PREDICTING SERVICE LIFE OF THERMOPLASTIC RESIN GEAR
A method for calculating an actual contact ratio of thermoplastic resin gears, including: measuring a temperature distribution of a pair of gears; calculating a temperature distribution of a structural analysis model A identical in geometry to the pair of gears by CAE structural analysis; preparing data on temperature dependency of an elastic modulus a of thermoplastic resin; correcting the elastic modulus a in accordance with a strain rate dependency and correcting the elastic modulus a in accordance with an actual amount of deformation of the gears; using a corrected elastic modulus a′ to calculate a contact stress distribution by the CAE structural analysis; calculating an angular difference between a meshing start point and a meshing end point of the pair of gears based on the contact stress distribution; and calculating the actual contact ratio of the pair of gears from the angular difference.
G01N 3/32 - Recherche des propriétés mécaniques des matériaux solides par application d'une contrainte mécanique en appliquant des efforts répétés ou pulsatoires
G01N 19/02 - Mesure du coefficient de frottement entre matériaux
A protection device including: a wearable structure to be worn by an user; an airbag configured to be attached to the wearable structure in a contracted state during standby, and configured to inflate to surround a protection target portion in a spiral and cylindrical form at completion of expansion, the airbag including one end fixed to the wearable structure, and the other end located on an opposite side to the one end, the airbag being configured to inflate with the other end separated from the wearable structure when the airbag is expanded; and a fluid supplier connected to the airbag and configured to supply fluid into the airbag.
The purpose of the present invention is to provide a urethane composition which is excellent in terms of handleability at normal temperature, has flexibility when cured, and is capable of maintaining high mechanical properties. A urethane composition according to the present disclosure contains an ester-based polyol and a polyisocyanate, the ester-based polyol contains at least two or more kinds of diol compounds, the difference in SP value between a diol compound (A) that has the lowest SP value among the diol compounds and the other diol compounds (B) is 1.3 or less, and the content of the diol compound (A) is 1-55 mass% of the total amount of the ester-based polyol.
(i)(i)(i)(i)(i) measured by a differential scanning calorimeter of 15°C to 105°C inclusive, and a melt flow rate of 0.8 g/10 min to 1,000 g/10 min inclusive as measured at a temperature higher than the melting point by 10°C under a load of 2.16 kg, a second modeling material which is different from the first modeling material in the composition and/or the physical properties by means of a fused deposition modeling method. The first modeling material and the second modeling material contain a thermoplastic resin.
B29C 64/118 - Procédés de fabrication additive n’utilisant que des matériaux liquides ou visqueux, p. ex. dépôt d’un cordon continu de matériau visqueux utilisant un matériau filamentaire mis en fusion, p. ex. modélisation par dépôt de fil en fusion [FDM]
Provided is a separation agent having a carrier and a ligand that is supported on the surface of the carrier by means of physical adsorption or chemical bonding, wherein the ratio of the particle diameter d90 to the particle diameter d10 of the separation agent is 1.00-1.38, the carrier is core-shell particles having an inorganic non-porous core and a porous shell, the porous shell contains silica gel, and the ligand is one or more selected from the group consisting of optically active polymers, optically inactive polyesters, proteins, and nucleic acids. The separation agent has good separation performance.
B01J 20/281 - Absorbants ou adsorbants spécialement adaptés pour la chromatographie préparative, analytique ou de recherche
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance organique
B01J 20/28 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation caractérisées par leur forme ou leurs propriétés physiques
Provided is a separation agent having a carrier and a ligand that is supported on the surface of the carrier by means of physical adsorption or chemical bonding, wherein the carrier is core-shell particles having an inorganic non-porous core and a porous shell, the inorganic non-porous core contains glass, the porous shell contains silica gel, the ratio of the average particle size of the core to the average thickness of the shell in the core-shell particles is 4.0-12.0, and the ligand is one or more selected from the group consisting of optically active polymers, optically inactive polyesters, proteins, and nucleic acids. The separation agent has good separation performance.
B01J 20/281 - Absorbants ou adsorbants spécialement adaptés pour la chromatographie préparative, analytique ou de recherche
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance organique
B01J 20/28 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation caractérisées par leur forme ou leurs propriétés physiques
Provided is a separation agent having a carrier and a ligand that is supported on the surface of the carrier by means of physical adsorption or chemical bonding, wherein the carrier is core-shell particles composed of an inorganic non-porous core and a porous shell, the shell contains silica gel, the ligand is at least one selected from the group consisting of optically active polymers, optically inactive polyesters, proteins, and nucleic acids, and the maximum pore diameter is 15 nm or more. The separation agent achieves high resolution.
B01J 20/281 - Absorbants ou adsorbants spécialement adaptés pour la chromatographie préparative, analytique ou de recherche
B01J 20/22 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation contenant une substance organique
B01J 20/28 - Compositions absorbantes ou adsorbantes solides ou compositions facilitant la filtrationAbsorbants ou adsorbants pour la chromatographieProcédés pour leur préparation, régénération ou réactivation caractérisées par leur forme ou leurs propriétés physiques
An object of the present invention is to provide an effective and highly safe agent for inhibiting osteoclast differentiation, and a food or drink, pharmaceutical, supplement, and cosmetic that produce an osteoclast differentiation-inhibiting effect; and the object is fulfilled by an agent for inhibiting osteoclast differentiation, comprising a urolithin.
A23L 33/00 - Modification de la qualité nutritive des alimentsProduits diététiquesLeur préparation ou leur traitement
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61K 9/00 - Préparations médicinales caractérisées par un aspect particulier
A61P 19/10 - Médicaments pour le traitement des troubles du squelette des maladies osseuses, p. ex. rachitisme, maladie de Paget de l'ostéoporose
42.
METHOD FOR MANUFACTURING CORE-SHELL POROUS SILICA PARTICLES
The present invention provides a method for manufacturing core-shell porous silica particles, the method involving using steps a1) and a2) to produce core-shell silica particles having a core and a shell precursor, and using step b) to convert the shell precursor into a porous material. Step a1) is a first reaction initiation step for adding a silica source-containing liquid to a first aqueous suspension containing nonporous silica particles, a cationic surfactant, a basic catalyst, an electrolyte, and an alcohol, or is a second reaction initiation step for adding a silica source-containing liquid and an electrolyte to a second aqueous suspension containing nonporous silica particles, a cationic surfactant, a basic catalyst, and an alcohol. Step a2) is a first silica source continuous addition step for adding a cationic surfactant and continuously adding a silica source-containing liquid to the reaction system after the first reaction initiation step or the second reaction initiation step. Step b) is a shell porosity forming step for removing the cationic surfactant from the shell precursor.
Provided is a stationary phase for chromatography, the stationary phase being made of inorganic carrier particles to which is bonded a polymer having a hydrophilic group on repeating units of a main chain thereof, and being produced by a particular production method.
B01J 20/285 - Absorbants ou adsorbants poreux à base de polymères
B01D 15/40 - Adsorption sélective, p. ex. chromatographie caractérisée par le mécanisme de séparation utilisant un fluide supercritique comme phase mobile ou comme éluant
B01J 20/30 - Procédés de préparation, de régénération ou de réactivation
C08F 2/44 - Polymérisation en présence d'additifs, p. ex. plastifiants, matières colorantes, charges
A23L 11/50 - Légumes secs ou légumineuses fermentésFermentation de légumes secs ou de légumineuses par l’entremise de micro-organismes ajoutés
A23L 11/00 - Légumes secs, c.-à-d. fruits de plantes légumineuses, pour l'obtention d'alimentsProduits dérivés de légumineusesLeur préparation ou leur traitement
A23L 11/30 - Élimination des substances indésirables, p. ex. des substances amères
A23L 11/70 - Produits à base de légumes secs germés, p. ex. à base de germes de fèves de soja
A61K 31/353 - 3,4-Dihydrobenzopyranes, p. ex. chromane, catéchine
This pressure container is provided with: a pressure chamber that can accommodate a sample; a pressure application device that emits a pressure wave to the pressure chamber during operation; a pressure sensor that measures the pressure wave emitted from the pressure application device; and a pressure wave transmission medium liquid that fills the pressure chamber so that there is no gap between the chamber and an inner wall surface that defines the chamber.
This pressure vessel comprises: a pressure chamber that is defined by an inner wall surface made of metal and that can accommodate a sample; a pyrotechnic pressurization device that has an explosive container which is made of metal and which accommodates an explosive, that performs ignition control with respect to the explosive by receiving supply of operating electric power, and that emits a pressure wave to the pressure chamber; a pressure sensor that measures the pressure wave emitted from the pressurization device; and an insulation structure that maintains an insulated state between the wall surface which is made of metal inner and a ruptured piece of the explosive container which ruptures due to combustion energy of the explosive occurring along with ignition control of the explosive.
B01J 3/04 - Récipients sous pression, p. ex. autoclaves
B01J 3/00 - Procédés utilisant une pression supérieure ou inférieure à la pression atmosphérique pour obtenir des modifications chimiques ou physiques de la matièreAppareils à cet effet
The purpose of the present invention is to provide a novel enzyme for dehydroxylating a hydroxyl group at a specific position in a urolithin compound that has the hydroxyl group at the specific position. This novel enzyme is derived from a microorganism belonging to the genus Enterocloster or a microorganism belonging to the genus Clostridium, and has an activity to catalyze a dihydroxylation reaction for a hydroxyl group at position-10 in a urolithin compound.
C12N 9/04 - Oxydoréductases (1.), p. ex. luciférase agissant sur des groupes CHOH comme donneurs, p. ex. oxydase de glucose, déshydrogénase lactique (1.1)
C12N 1/15 - ChampignonsLeurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 1/19 - LevuresLeurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 1/21 - BactériesLeurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 5/10 - Cellules modifiées par l'introduction de matériel génétique étranger, p. ex. cellules transformées par des virus
C12N 15/31 - Gènes codant pour des protéines microbiennes, p. ex. entérotoxines
C12N 15/63 - Introduction de matériel génétique étranger utilisant des vecteursVecteurs Utilisation d'hôtes pour ceux-ciRégulation de l'expression
C12P 17/06 - Préparation de composés hétérocycliques comportant O, N, S, Se ou Te comme uniques hétéro-atomes du cycle l'oxygène comme unique hétéro-atome du cycle contenant un hétérocycle à six chaînons, p. ex. fluorescéine
C12P 21/02 - Préparation de peptides ou de protéines comportant une séquence connue de plusieurs amino-acides, p. ex. glutathion
Provided is a release film that comprises a base material layer and a release layer that is layered on at least one surface of the base material layer, the surface free energy of the release layer being no more than 35 mN/m, and the release layer including a resin that has at least one glass transition temperature in the range of 150°C–350°C as measured by viscoelasticity measurement.
B32B 27/00 - Produits stratifiés composés essentiellement de résine synthétique
B32B 27/32 - Produits stratifiés composés essentiellement de résine synthétique comprenant des polyoléfines
B32B 27/36 - Produits stratifiés composés essentiellement de résine synthétique comprenant des polyesters
C08F 232/08 - Copolymères de composés cycliques ne contenant pas de radicaux aliphatiques non saturés dans une chaîne latérale et contenant une ou plusieurs liaisons doubles carbone-carbone dans un système carbocyclique contenant des cycles condensés
C08J 7/043 - Amélioration de l'adhésivité des revêtements en soi, p. ex. par formation d'apprêts
H01M 8/10 - Éléments à combustible avec électrolytes solides
H01M 8/1004 - Éléments à combustible avec électrolytes solides caractérisés par les ensembles membrane-électrodes [MEA]
H01M 8/1067 - Matériaux d’électrolyte polymère caractérisés par leurs propriétés physiques, p. ex. la porosité, la conductivité ionique ou l’épaisseur
A gas generator includes a gas generating agent that generates gas by combustion, a housing made of metal and accommodating the gas generating agent therein, the housing having a gas discharge port formed therein, through which the gas is emitted to an exterior of the housing, an ignition device configured to ignite the gas generating agent by actuation; and a temperature rise suppressing member provided in contact with an outer surface of a housing to cover at least a part of the outer surface. The temperature rise suppressing member includes an endothermic agent that absorbs heat of the housing by undergoing a chemical change or a state change by the heat of the housing when a temperature of the housing rises due to combustion of a gas generating agent, and a binder agent present together with the endothermic agent such that the temperature rise suppressing member has flexibility.
B60R 21/264 - Moyens gonflables de retenue ou d'immobilisation des occupants prévus pour se gonfler lors d'un choc ou en cas de choc imminent, p. ex. sacs gonflables caractérisés par la source de fluide de gonflage ou par les moyens de commande de l'écoulement du fluide de gonflage utilisant une génération instantanée de gaz, p. ex. pyrotechnique
B60R 21/26 - Moyens gonflables de retenue ou d'immobilisation des occupants prévus pour se gonfler lors d'un choc ou en cas de choc imminent, p. ex. sacs gonflables caractérisés par la source de fluide de gonflage ou par les moyens de commande de l'écoulement du fluide de gonflage
Provided is a method for producing a film that contains a liquid-crystalline resin and that has a small anisotropy. A method for producing a film, the method comprising forming a film by layering m sets of n layer units each including x layers formed in the same print direction (x represents an integer of 1-3, n represents an integer of 3 or more, m represents an integer of 1 or more, x may be the same or different in each of the layer units, and n may be the same or different in each of the sets) by a filament-melting method using a filament containing a thermoplastic resin, wherein the thermoplastic resin contains 55-100 mass% of a liquid-crystalline resin with respect to the entirety of the thermoplastic resin, and the layer units forming any one of the sets each have a print direction that is different by at least 180/n (±10)° or more from the print direction of any one of the other layer units.
B29C 64/118 - Procédés de fabrication additive n’utilisant que des matériaux liquides ou visqueux, p. ex. dépôt d’un cordon continu de matériau visqueux utilisant un matériau filamentaire mis en fusion, p. ex. modélisation par dépôt de fil en fusion [FDM]
B29C 64/393 - Acquisition ou traitement de données pour la fabrication additive pour la commande ou la régulation de procédés de fabrication additive
The present disclosure provides a liquid pharmaceutical composition containing a biofunctional substance, an injector to inject the same, and a method of injecting the same.
A61K 47/26 - Hydrates de carbone, p. ex. polyols ou sucres alcoolisés, sucres aminés, acides nucléiques, mono-, di- ou oligosaccharidesLeurs dérivés, p. ex. polysorbates, esters d’acide gras de sorbitan ou glycyrrhizine
A61M 5/155 - Perfusion sous pression, p. ex. utilisant des pompes utilisant des réservoirs sous pression, p. ex. au moyen de pistons mis sous pression par un gaz
Provided is a composition that is easy to swallow, has a good texture, has a good filling property, has low dispersibility, and/or demonstrates high transportability when contained in tablets. This composition has a specific range for a particle parameter, such as the particle area, the Feret diameter, and/or the aspect ratio, for a composition parameter, such as the BS ratio at a height of 30 mm, the BS ratio 60 minutes after the start of measurement, the powder water absorption ratio, the angle of repose, the difference angle, the weight residual ratio, and/or the electromotive force, and/or for a tablet parameter, such as the disintegration time in water and/or the disintegrability in water.
NATIONAL UNIVERSITY CORPORATION KANAZAWA UNIVERSITY (Japon)
DAICEL CORPORATION (Japon)
Inventeur(s)
Hasegawa, Hiroshi
Nakakubo, Keisuke
Taka, Shunsuke
Mashio, Asami
Wong, Kuo Hong
Maeda, Katsuhiro
Taniguchi, Tsuyoshi
Nishimura, Tatsuya
Ito, Yuma
Arai, Takashi
Endo, Masaru
Abrégé
To provide a new cellulose derivative capable of easily being incorporated into an aqueous solution in which a noble metal is dissolved and selectively and efficiently adsorbing and recovering the noble metal dissolved in the aqueous solution. The cellulose derivative according to the present disclosure has a repeating unit represented by formula (I). In formula (I), Rais a hydrogen atom or a group represented by formula (a-1). In formula (a-1), R1is a single bond or a C1-10 alkylene group. R2-R4are a hydrogen atom or a C1-10 alkyl group. n represents 1 or 2. R1and R2may bond with each other to form a ring together with adjacent nitrogen atoms. R3and R4 may also bond with each other to form a ring together with adjacent nitrogen atoms.
To provide a composition that is easy to swallow, has good texture, has good filling properties, has low dispersibility, and/or has high portability of tablets containing the composition. This composition has specific ranges: in particle parameters including particle area, Feret diameter, and/or aspect ratio; in composition parameters including BS ratio at a height of 30 mm, BS ratio 60 minutes after the start of measurement, powder water absorption rate, angle of repose, difference angle, weight residual ratio, and/or electromotive force; and/or in tableting parameters including disintegration time in water and/or disintegrability in water.
The present invention improves the structure of a gas generator capable of taking in and sending out external air. This gas generator comprises: a housing that accommodates a gas source for generating gas through an operation of an igniter and is provided with a gas discharge hole for discharging the gas; and a cover that covers a part of the housing and forms a flow passage for gas, between the cover and the housing, along the housing. The gas discharge hole is formed to communicate the inside of the housing and the inside of the flow passage and discharge the gas toward one end side of the flow passage. When the gas is discharged from the gas discharge hole of the housing, an outlet for the gas is formed on one end side of the flow passage, and an intake port for taking in the external air is formed on the other end side of the flow passage.
B60R 21/264 - Moyens gonflables de retenue ou d'immobilisation des occupants prévus pour se gonfler lors d'un choc ou en cas de choc imminent, p. ex. sacs gonflables caractérisés par la source de fluide de gonflage ou par les moyens de commande de l'écoulement du fluide de gonflage utilisant une génération instantanée de gaz, p. ex. pyrotechnique
B60R 21/30 - Moyens gonflables de retenue ou d'immobilisation des occupants prévus pour se gonfler lors d'un choc ou en cas de choc imminent, p. ex. sacs gonflables caractérisés par la source de fluide de gonflage ou par les moyens de commande de l'écoulement du fluide de gonflage avec des moyens pour introduire l'air ambiant dans le circuit et mélanger cet air avec le fluide de gonflage
56.
SOLVENT COMPOSITION FOR ELECTRODE-FORMING PASTE, ELECTRODE-FORMING PASTE, METHOD FOR MANUFACTURING ELECTRODE, AND METHOD FOR MANUFACTURING SECONDARY BATTERY
Provided is a solvent composition for an electrode-forming paste, the solvent composition having excellent crack resistance during manufacture of an electrode and being capable of reducing the solvent residue in the electrode. The solvent composition for an electrode-forming paste comprises a solvent (A) having a boiling point of 180°C to 240°C, and has a Hansen solubility parameter hydrogen bond term δH of 4-11 (J/cm3) 0.5. The solvent (A) preferably has a solubility in water of 5 g/100 g or more. The solvent (A) preferably comprises an ether skeleton and/or an ester skeleton.
The impact absorption device includes an impact absorbing member and an auxiliary member. The impact absorbing member is attached to an installation surface of a base portion rotatably about a first pivoting axis extending in a first direction and is reversibly switched between a retracted state and a protruding state, and the auxiliary member is attached rotatably about a second pivoting axis and is reversibly switched between a retracted state and a protruding state. A height of the impact absorbing member from the base portion in the protruding state is higher than that of the auxiliary member. In the protruding state, at least a portion of the impact absorbing member and at least a portion of the auxiliary member face each other, and the impact absorbing member deforms when receiving a load including a component in a direction opposite to the base portion, thereby engaging with the auxiliary member.
The purpose of the technology disclosed herein is to provide a human body protection device that can be easily maintained. This human body protection device comprises: a gas generator that supplies gas; a base part that can be attached to a human body; an airbag that is disposed on the base part and expands due to gas supplied from the gas generator; and a supply pipe that supplies gas from the gas generator to the airbag. The supply pipe includes a connection part which is provided between the gas generator and the airbag, and in which a first connection part on a side of the gas generator and a second connection part on a side of the airbag can be repeatedly attached to and detached from each other in a state before operation.
A41D 13/018 - Vêtements protecteurs de travail ou de sport, p. ex. blouses de chirurgien ou vêtements protégeant des coups ou des chocs avec des moyens absorbeurs de chocs se gonflant automatiquement
B60R 21/261 - Moyens gonflables de retenue ou d'immobilisation des occupants prévus pour se gonfler lors d'un choc ou en cas de choc imminent, p. ex. sacs gonflables caractérisés par la source de fluide de gonflage ou par les moyens de commande de l'écoulement du fluide de gonflage avec des moyens autres que la structure du coussin pour diffuser ou guider le fluide de gonflage
59.
METHOD FOR MANUFACTURING 3D PRINTED ARTICLE BY MEANS OF FUSED FILAMENT FABRICATION, AND FILAMENT FOR METHOD FOR MANUFACTURING 3D PRINTED ARTICLE BY MEANS OF FUSED FILAMENT FABRICATION
The present invention provides a method for manufacturing a 3D printed article, whereby a 3D printed article having higher rigidity and a smaller variation in mechanical properties can be manufactured. Provided is a method for manufacturing a 3D printed article by means of fused filament fabrication using a filament containing a thermoplastic resin, wherein: the thermoplastic resin contains 55 to 100 mass% of a liquid crystalline resin in the thermoplastic resin as a whole; the difference (Tm2 - Tc) between the melting point Tm2 of the filament measured by differential scanning calorimetry and the crystallization temperature Tc is 25°C to 60°C; and the printing speed, which is the relative movement speed between a stage and a nozzle part of a 3D printing device, is controlled to be faster than 35 mm/sec and slower than 1000 mm/sec.
B29C 64/118 - Procédés de fabrication additive n’utilisant que des matériaux liquides ou visqueux, p. ex. dépôt d’un cordon continu de matériau visqueux utilisant un matériau filamentaire mis en fusion, p. ex. modélisation par dépôt de fil en fusion [FDM]
Provided are: a three-dimensional shaped article having a controlled molecular orientation; and a method for manufacturing same. The three-dimensional shaped article contains a thermoplastic resin, wherein the thermoplastic resin contains 55-100 mass% of a liquid crystalline resin in the entirety of the thermoplastic resin. The three-dimensional shaped article is used in an environment where an electric field and/or heat is applied. The thermoplastic resin is molecularly oriented in at least a portion of the three-dimensional shaped article. At least one of the directions of the molecular orientation is a direction of an electric field applied to the three-dimensional shaped article and/or a direction in which heat applied to the three-dimensional shaped article is dissipated.
B29C 64/393 - Acquisition ou traitement de données pour la fabrication additive pour la commande ou la régulation de procédés de fabrication additive
B29C 64/118 - Procédés de fabrication additive n’utilisant que des matériaux liquides ou visqueux, p. ex. dépôt d’un cordon continu de matériau visqueux utilisant un matériau filamentaire mis en fusion, p. ex. modélisation par dépôt de fil en fusion [FDM]
B29C 64/236 - Moyens d’entraînement pour un mouvement dans une direction dans le plan d’une couche
The present disclosure provides a humidification including a laminate with a porous reinforcing material and a moisture-permeable membrane laminated on at least one surface of the porous reinforcing material, and a frame.
F24F 6/04 - Humidification de l'air par évaporation d'eau dans l'air en utilisant des éléments humides fixes non chauffés
B32B 3/26 - Produits stratifiés comprenant une couche ayant des discontinuités ou des rugosités externes ou internes, ou une couche de forme non planeProduits stratifiés comprenant une couche ayant des particularités au niveau de sa forme caractérisés par une couche continue dont le périmètre de la section droite a une allure particulièreProduits stratifiés comprenant une couche ayant des discontinuités ou des rugosités externes ou internes, ou une couche de forme non planeProduits stratifiés comprenant une couche ayant des particularités au niveau de sa forme caractérisés par une couche comportant des cavités ou des vides internes
B32B 7/02 - Propriétés physiques, chimiques ou physicochimiques
B32B 7/12 - Liaison entre couches utilisant des adhésifs interposés ou des matériaux interposés ayant des propriétés adhésives
B32B 27/08 - Produits stratifiés composés essentiellement de résine synthétique comme seul composant ou composant principal d'une couche adjacente à une autre couche d'une substance spécifique d'une résine synthétique d'une sorte différente
B32B 27/30 - Produits stratifiés composés essentiellement de résine synthétique comprenant une résine vinyliqueProduits stratifiés composés essentiellement de résine synthétique comprenant une résine acrylique
B32B 27/32 - Produits stratifiés composés essentiellement de résine synthétique comprenant des polyoléfines
62.
RECOMMENDED AMOUNT OUTPUT SYSTEM, RECOMMENDED AMOUNT OUTPUT METHOD, AND PROGRAM
The present invention improves the amount of equol intake of each individual user. This recommended amount output system comprises one or more computers that execute: calculating the amount of equol deficiency of a user by using a predicted value of the amount of equol production of the user and a predetermined target amount; calculating a recommended amount of equol or isoflavone to be ingested by the user on the basis of the calculated amount of equol deficiency and an index value indicating the level of equol production ability of the user; and outputting the calculated recommended amount.
G16H 20/60 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p. ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant le contrôle de l’alimentation, p. ex. les régimes
The present disclosure provides a laminate for humidification including a porous reinforcing material, and a non-porous membrane that is laminated on at least one surface of the porous reinforcing material.
The present disclosure relates to an agricultural composition with a granular material containing acetic acid, a biodegradable polymer miscible with acetic acid, and an inorganic additive. The agricultural composition may have a coating film that coats the granular material.
A01N 43/32 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des composés hétérocycliques comportant des cycles avec un ou plusieurs atomes d'oxygène ou de soufre comme uniques hétéro-atomes du cycle avec plusieurs hétéro-atomes des cycles à six chaînons
A01N 59/00 - Biocides, produits repoussant ou attirant les animaux nuisibles, ou régulateurs de croissance des végétaux, contenant des éléments ou des composés inorganiques
Provided are a novel chitosan compound represented by Formula (I) and a separating agent for optical isomers. In Formula (I), each R is independently a group represented by Formula (II) or a group represented by Formula (III); Ra is an alkyl group having from 1 to 5 carbons or an alkyl group having from 3 to 5 carbons and having a branched chain; and n is an integer of 5 or greater; and in Formulas (II) and (III), each Rb is independently an unsubstituted phenyl group, a phenyl group having a substituent, an unsubstituted cyclohexyl group, or a cyclohexyl group having a substituent, and each of the substituent is independently an alkyl group having from 1 to 5 carbons, or a halogen.
C08B 37/08 - ChitineSulfate de chondroïtineAcide hyaluroniqueLeurs dérivés
B01D 15/20 - Adsorption sélective, p. ex. chromatographie caractérisée par des caractéristiques de structure ou de fonctionnement relatives au conditionnement de la matière adsorbante ou absorbante
B01J 20/24 - Composés macromoléculaires d'origine naturelle, p. ex. acides humiques ou leurs dérivés
This airbag module comprises: an airbag having a gas introduction port; a module case which has a gas supply port connected to the gas introduction port of the airbag and in which an accommodation space accommodating internal gas is formed; a gas generator which is attached to the module case and supplies gas generated upon activation into the accommodation space of the module case; and a pusher which is disposed so as to be movable in the accommodation space by the pressure of the gas supplied from the gas generator due to activation of the gas generator, and which pushes, due to movement accompanying the activation of the gas generator, the internal gas that had been accommodated in the accommodation space even before the activation of the gas generator to the airbag.
B60R 21/261 - Moyens gonflables de retenue ou d'immobilisation des occupants prévus pour se gonfler lors d'un choc ou en cas de choc imminent, p. ex. sacs gonflables caractérisés par la source de fluide de gonflage ou par les moyens de commande de l'écoulement du fluide de gonflage avec des moyens autres que la structure du coussin pour diffuser ou guider le fluide de gonflage
67.
GAS GENERATOR AND FIXING STRUCTURE OF GAS GENERATOR
The gas generator includes an ignition device and a case, the case including a side wall portion, an opening portion, and a closing portion closing a tip end side of the side wall portion, the opening portion being connected to the ignition device, closing portion includes, an annular inclination portion connected to the tip end side of the side wall portion, and formed in a funnel shape inclined to radially converge to an inner side of the case from a base end side toward a tip end side, and a lid portion connected to the tip end side of the annular inclination portion, the annular inclination portion and the lid portion are integrally formed, and the lid portion is formed to have a thickness smaller than a thickness of the annular inclination portion, except for an end portion of the lid portion connected to the annular inclination portion.
An object of the present invention is to provide a method for selectively producing a hydroxycarboxylic acid ester, the method including reducing a dicarboxylic acid monoester by means of a heterogeneous reaction. According to a method for producing a hydroxycarboxylic acid ester in an embodiment of the present invention, a hydroxycarboxylic acid ester represented by Formula (2) is produced by reducing a substrate dicarboxylic acid monoester represented by Formula (1) in the presence of a catalyst.
An object of the present invention is to provide a method for selectively producing a hydroxycarboxylic acid ester, the method including reducing a dicarboxylic acid monoester by means of a heterogeneous reaction. According to a method for producing a hydroxycarboxylic acid ester in an embodiment of the present invention, a hydroxycarboxylic acid ester represented by Formula (2) is produced by reducing a substrate dicarboxylic acid monoester represented by Formula (1) in the presence of a catalyst.
The catalyst comprises:
metal species including M1 and M2; and
a support supporting the metal species, and
wherein
M1 is rhodium, platinum, ruthenium, iridium or palladium;
M2 is tin, vanadium, molybdenum, tungsten or rhenium; and
the support is hydroxyapatite, fluorapatite, or hydrotalcite.
An object of the present invention is to provide a method for selectively producing a hydroxycarboxylic acid ester, the method including reducing a dicarboxylic acid monoester by means of a heterogeneous reaction. According to a method for producing a hydroxycarboxylic acid ester in an embodiment of the present invention, a hydroxycarboxylic acid ester represented by Formula (2) is produced by reducing a substrate dicarboxylic acid monoester represented by Formula (1) in the presence of a catalyst.
The catalyst comprises:
metal species including M1 and M2; and
a support supporting the metal species, and
wherein
M1 is rhodium, platinum, ruthenium, iridium or palladium;
M2 is tin, vanadium, molybdenum, tungsten or rhenium; and
the support is hydroxyapatite, fluorapatite, or hydrotalcite.
C07C 67/317 - Préparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par élimination d'hydrogène ou de groupes fonctionnelsPréparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par hydrogénolyse de groupes fonctionnels
C08L 101/00 - Compositions contenant des composés macromoléculaires non spécifiés
B29C 64/141 - Procédés de fabrication additive n’utilisant que des matériaux solides
B33Y 70/00 - Matériaux spécialement adaptés à la fabrication additive
70.
FUNCTIONAL MATERIAL CONTAINING 8-PRENYLNARINGENIN, ORAL COMPOSITION, FOOD AND DRINK, ATROGIN-1 EXPRESSION INHIBITOR, AND FUNCTIONAL MATERIAL COMPOSITION
The purposes of the present invention are: to provide a functional material having improved bioavailability of 8-prenylnaringenin (8PN); to provide a novel application of 8PN; to provide a formulation for improving muscle atrophy inhibitory effect by 8PN; and to provide a technique for suppressing odor of an 8PN-producing culture of a Blautia microorganism. A functional material containing an amorphous body having a predetermined average particle diameter and containing 8PN can improve the bioavailability of 8PN. When a bitter amino acid and 8PN are present together, bitterness can be reduced. When a protein and 8PN are present together, the flavor peculiar to the protein can be reduced. When 8PN is blended in protein-containing food and drink, a long-lasting feeling of satiety due to the food and drink is improved. When 8PN and leucine are combined, the atrogin-1 expression can be inhibited. When calcium hydroxide and an 8PN-producing culture of a Blautia microorganism are present together, the odor peculiar to the culture can be suppressed.
C12P 17/06 - Préparation de composés hétérocycliques comportant O, N, S, Se ou Te comme uniques hétéro-atomes du cycle l'oxygène comme unique hétéro-atome du cycle contenant un hétérocycle à six chaînons, p. ex. fluorescéine
A23L 33/10 - Modification de la qualité nutritive des alimentsProduits diététiquesLeur préparation ou leur traitement en utilisant des additifs
The present disclosure provides a technique for producing a composition in which at least urolithins are solubilized, and a method for producing an emulsified composition.
The purpose of the present disclosure is to provide a protective agent excellent in a protective effect of a phospholipid membrane. This liquid composition for protecting a phospholipid membrane comprises (A) a magnesium salt, (B) an acetate buffer solution, a citrate buffer solution, a carbonate buffer solution, and/or a succinate buffer solution, and preferably further contains at least any of (C) a polyhydric alcohol, (D) a saccharide and/or a sugar alcohol, (E) polyethylene glycol, and (F) an amino acid. The liquid composition for protecting the phospholipid membrane is excellent in the protective effect of the phospholipid membrane.
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
A61K 9/19 - Préparations médicinales caractérisées par un aspect particulier à l'état particulaire, p. ex. poudres lyophilisées
A61K 9/127 - Vecteurs à bicouches synthétiques, p. ex. liposomes ou liposomes comportant du cholestérol en tant qu’unique agent tensioactif non phosphatidylique
A61K 35/12 - Substances provenant de mammifèresCompositions comprenant des tissus ou des cellules non spécifiésCompositions comprenant des cellules souches non embryonnairesCellules génétiquement modifiées
This underwater sliding member is obtained by molding a resin composition which contains a thermoplastic resin that has water absorption resistance, and a granular inorganic filler and/or a plate-shaped inorganic filler, wherein the Mohs hardness of the inorganic filler is 5 or less.
Provided is a new method for producing liquid crystalline resin microparticles. A method for producing liquid crystalline resin microparticles according to the present invention includes subjecting a raw material compound containing one or more selected from the group consisting of aromatic hydroxycarboxylic acids and polymerizable derivatives thereof to a polycondensation reaction in an organic solvent in the presence of a vinylpyrrolidone copolymer. The blending amount of the raw material compound is 0.5-40 mass% of the total amount (100 mass%) of the raw material compound, the organic solvent, and the vinylpyrrolidone copolymer.
C08G 63/81 - Procédés de préparation utilisant des solvants
C08G 63/06 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés dérivés des acides hydroxycarboxyliques
The purpose of the present invention is to provide a method for producing a polyacetal resin composition that is excellent in terms of rigidity and creep resistance characteristics. A method for producing a polyacetal resin composition according to the present invention includes: a step (I) for producing a polyacetal copolymer (A) by copolymerizing trioxane (a), a cyclic acetal compound (b), and an aliphatic glycidyl ether compound (c) that has a chlorine content of 4% or more in the presence of a linear formal compound (d); a step (II) for producing a linear polyacetal resin (B) by copolymerizing trioxane (a') and a cyclic acetal compound (b'); and a step (III) for mixing and melt-kneading the linear polyacetal resin (B) and the polyacetal copolymer (A).
488 alpha olefin comonomers. The present invention is, furthermore, directed to a film comprising the polypropylene composition. Apart from that, a biaxially oriented film comprising the polypropylene composition and a capacitor are provided.
The present invention provides a novel graft polymer composition which contains a graft polymer of cellulose acetate and a lactone and which achieves both excellent thermoplasticity and suppression of bleed out. Provided is a polymer composition which contains a graft polymer of cellulose acetate and a lactone, wherein the proportion of a methanol-soluble material of the polymer composition as measured via the method below is in the range of 13-33 mass%. (Method for measuring proportion of methanol-soluble material) Under atmospheric pressure, in a 20°C environment, acetone is dissolved in 144 ml with respect to 24 g of the polymer composition, 1.5 L of methanol is added, and stirring is carried out for 12 hours. A mixture thus obtained is filtered with a PTFE membrane filter having a pore diameter of 1 μm, and a filter residue is collected. The obtained filter residue is put into 0.5 L of methanol again, and stirring is carried out for 1 hour. A mixture thus obtained is filtered with a PTFE membrane filter having a pore diameter of 1 μm, and a filter residue and a filtrate are collected. The obtained filter residue is put into 0.5 L of methanol again, and stirring is carried out for 1 hour. A mixture thus obtained is filtered with a PTFE membrane filter having a pore diameter of 1 μm, and a filter residue and a filtrate are collected. After the pH of the filtrate is confirmed to be 7, the filter residue is added to 1 L of methanol, and stirring is carried out for 12 hours. A mixture thus obtained is filtered with a PTFE membrane filter having a pore diameter of 1μm, and a filter residue is collected. The obtained filter residue is dried at 40°C for 12 hours in a vacuum, and a dry mass is thus obtained. From the dry mass of the polymer composition before purification and the dry mass of the polymer composition after the purification, the proportion of the methanol-soluble material contained in the polymer composition is calculated. Methanol-soluble component of polymer composition = dry mass of polymer composition before purification - dry mass of polymer composition after purification Proportion of methanol-soluble material contained in polymer composition = (mass of methanol-soluble component of polymer composition) / dry mass of polymer composition after purification × 100 (mass%)
01 - Produits chimiques destinés à l'industrie, aux sciences ainsi qu'à l'agriculture
17 - Produits en caoutchouc ou en matières plastiques; matières à calfeutrer et à isoler
22 - Cordes; filets; tentes, auvents, voiles et sacs; matières de rembourrage
Produits et services
Chemicals for use in industry; unprocessed plastics for
industrial purposes; unprocessed synthetic resins for use in
the manufacture of plastic molding compounds; unprocessed
biodegradable plastics; chemicals, namely, cellulose
derivatives for use in industry; cellulose esters for
industrial purposes; unprocessed cellulose acetate plastics;
acetate of cellulose, unprocessed; unprocessed biodegradable
cellulose acetate. Semi-worked plastic substances, biodegradable; biodegradable
plastic film for use in commercial or industrial
manufacturing; plastic films for electrical insulation;
chemical fiber, not for textile use; semi-synthetic fibers,
not for textile use; cellulose acetate, semi-processed;
biodegradable cellulose acetate, semi-processed; plastic
substances, semi-processed; semi-processed plastic in the
form of sheet; semi-processed biodegradable plastic in the
form of sheet; filtering materials of semi-processed foams
of plastic; chemical fibers for use in making cigarette
filters, not for textile use; chemical fibers made of
cellulose acetate for use in making cigarette filters, not
for textile use; chemical fibers made of cellulose acetate
in the form of tow for use in making cigarette filters, not
for textile use; chemical fiber for use in making wadding
for filtering, not for textile use. Chemical fiber netting; chemical fiber rope; chemical fibers
for textile use; chemical textile fibers for use in making
cigarette filters; chemical textile fibers made of cellulose
acetate for use in making cigarette filters; chemical
textile fibers made of cellulose acetate in the form of tow
for use in making cigarette filters; chemical textile fiber
for use in making wadding for filtering.
This laminated film comprises a substrate layer and a resin layer that is formed on the substrate layer and that has a surface with projections and recesses, which is on the side away from the substrate layer. The average projection area occupancy of the surface with projections and recesses is 6% or more. B1/A1 is 0.80 or more, B2/A2 is 0.60 or more, B3/A3 is 0.60 or more, and B4/A4 is 0.60 or more (A1, A2, A3, and A4 are, respectively, Ra, Rz, Rc, and Rzjis of the surface with projections and recesses before an abrasion resistance test; and B1, B2, B3, and B4 are, respectively, Ra, Rz, Rc, and Rzjis of the surface with projections and recesses after the abrasion resistance test).
B32B 27/00 - Produits stratifiés composés essentiellement de résine synthétique
B32B 3/30 - Produits stratifiés comprenant une couche ayant des discontinuités ou des rugosités externes ou internes, ou une couche de forme non planeProduits stratifiés comprenant une couche ayant des particularités au niveau de sa forme caractérisés par une couche continue dont le périmètre de la section droite a une allure particulièreProduits stratifiés comprenant une couche ayant des discontinuités ou des rugosités externes ou internes, ou une couche de forme non planeProduits stratifiés comprenant une couche ayant des particularités au niveau de sa forme caractérisés par une couche comportant des cavités ou des vides internes caractérisés par une couche comportant des retraits ou des saillies, p. ex. des gorges, des nervures
C08J 7/046 - Formation de revêtements résistants à l'abrasionFormation de revêtements de durcissement de surface
G02B 1/10 - Revêtements optiques obtenus par application sur les éléments optiques ou par traitement de la surface de ceux-ci
G02B 1/14 - Revêtements protecteurs, p. ex. revêtements durs
The present disclosure provides a laminate for humidification including a porous reinforcing material and a non-porous membrane laminated on at least one surface of the porous reinforcing material.
F24F 3/14 - Systèmes de conditionnement d'air dans lesquels l'air conditionné primaire est fourni par une ou plusieurs stations centrales aux blocs de distribution situés dans les pièces ou enceintes, blocs dans lesquels il peut subir un traitement secondaireAppareillage spécialement conçu pour de tels systèmes caractérisés par le traitement de l'air autrement que par chauffage et refroidissement par humidificationSystèmes de conditionnement d'air dans lesquels l'air conditionné primaire est fourni par une ou plusieurs stations centrales aux blocs de distribution situés dans les pièces ou enceintes, blocs dans lesquels il peut subir un traitement secondaireAppareillage spécialement conçu pour de tels systèmes caractérisés par le traitement de l'air autrement que par chauffage et refroidissement par déshumidification
B32B 5/18 - Produits stratifiés caractérisés par l'hétérogénéité ou la structure physique d'une des couches caractérisés par le fait qu'une des couches contient un matériau sous forme de mousse ou essentiellement poreux
82.
COMPOSITE PARTICLES AND METHOD FOR PRODUCING COMPOSITE PARTICLES
The present invention provides composite particles which can be sintered at a low temperature when used for sintering bonding, and are still capable of forming a sintered body that has excellent heat resistance. Composite particles according to the present disclosure are characterized by comprising base material particles and Ag and/or Cu that is supported by the base material particles. The composite particles are also characterized in that: the linear expansion coefficient of the base material particles is 8 ppm/K or less; and the average value of the numbers of particle aggregates A in images captured at any given five locations in a cross-section with use of an SEM at a magnification of 1,000 times is two or less. Particle aggregate A: A plurality of base material particles and Ag and/or Cu are contained therein, the area ratio of the supported Ag and/or Cu is 70 area% or more with respect to the base material particles, and the diameter of the longest part of the aggregate is 5 μm or more.
B22F 1/18 - Particules non métalliques revêtues de métal
B22F 1/107 - Poudres métalliques contenant des agents lubrifiants ou liantsPoudres métalliques contenant des matières organiques contenant des matériaux organiques comportant des solvants, p. ex. pour la coulée en moule poreux ou absorbant
B22F 7/08 - Fabrication de couches composites, de pièces ou d'objets à base de poudres métalliques, par frittage avec ou sans compactage de pièces ou objets composés de parties différentes, p. ex. pour former des outils à embouts rapportés avec une ou plusieurs parties non faites à partir de poudre
B22F 9/24 - Fabrication des poudres métalliques ou de leurs suspensionsAppareils ou dispositifs spécialement adaptés à cet effet par un procédé chimique avec réduction de mélanges métalliques à partir de mélanges métalliques liquides, p. ex. de solutions
H01L 21/52 - Montage des corps semi-conducteurs dans les conteneurs
To provide a composition that, when used for sinter bonding, can be sintered at a low temperature, can be firmly bonded, and can form a sintered body having excellent heat resistance. A composition according to the present disclosure includes composite particles, an organic material, and particles containing Ag and/or Cu other than the composite particles. The composite particles include base material particles and Ag and/or Cu supported on the base material particles. The linear expansion coefficient of the base material particles is 8 ppm/K or less. The particle sintering rate represented by formula (1) is 30% or more. Formula (1): Particle sintering rate = (total number of base material particles bonded to the object to be bonded that have a length of 100 nm or more in at least one direction in an image obtained by photographing a cross section of a sintered body after the sintering step at 20,000× using FE-SEM)/(total number of base material particles having a length of 100 nm or more in at least one direction in an image obtained by photographing a cross section of the sintered body after the sintering step at 20,000× using FE-SEM)
B22F 1/107 - Poudres métalliques contenant des agents lubrifiants ou liantsPoudres métalliques contenant des matières organiques contenant des matériaux organiques comportant des solvants, p. ex. pour la coulée en moule poreux ou absorbant
B22F 7/08 - Fabrication de couches composites, de pièces ou d'objets à base de poudres métalliques, par frittage avec ou sans compactage de pièces ou objets composés de parties différentes, p. ex. pour former des outils à embouts rapportés avec une ou plusieurs parties non faites à partir de poudre
B22F 9/00 - Fabrication des poudres métalliques ou de leurs suspensionsAppareils ou dispositifs spécialement adaptés à cet effet
B22F 9/24 - Fabrication des poudres métalliques ou de leurs suspensionsAppareils ou dispositifs spécialement adaptés à cet effet par un procédé chimique avec réduction de mélanges métalliques à partir de mélanges métalliques liquides, p. ex. de solutions
H01L 21/52 - Montage des corps semi-conducteurs dans les conteneurs
84.
POLY(ARYLENE SULFIDE) RESIN COMPOSITION FOR RECYCLE MATERIALS
Provided is a poly(arylene sulfide) resin composition which, during recycling, can be inhibited from forming burrs. The poly(arylene sulfide) resin composition (X) for recycle materials comprises (A) 100 parts by mass of a linear poly(arylene sulfide) resin having a carboxy group and (B) 0.3-10 parts by mass of an alkoxysilane compound.
B29C 45/00 - Moulage par injection, c.-à-d. en forçant un volume déterminé de matière à mouler par une buse d'injection dans un moule ferméAppareils à cet effet
C08K 3/013 - Charges, pigments ou agents de renforcement
C08K 5/5415 - Composés contenant du silicium contenant de l'oxygène contenant au moins une liaison Si—O
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
C08G 63/60 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés dérivés de la réaction d'un mélange d'acides hydroxycarboxyliques, d'acides polycarboxyliques et de composés polyhydroxylés
C08K 7/24 - Particules expansibles, poreuses ou creuses inorganiques
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
C08G 63/60 - Polyesters dérivés soit d'acides hydroxycarboxyliques, soit d'acides polycarboxyliques et de composés polyhydroxylés dérivés de la réaction d'un mélange d'acides hydroxycarboxyliques, d'acides polycarboxyliques et de composés polyhydroxylés
Provided are an equol determination kit that selectively determines equol with high sensitivity by surface-enhanced Raman scattering, and a method for selectively determining equol with high sensitivity by surface-enhanced Raman scattering. The equol determination kit of the present disclosure determines equol by the surface-enhanced Raman scattering spectroscopy. The method for determination of equol of the present disclosure is a method for determination of equol by the surface-enhanced Raman scattering spectroscopy. In the method, equol is preferably determined by analyzing a peak found in at least one wavelength region selected from the group consisting of 1530 to 1630 cm−1, 1230 to 1330 cm−1, 1140 to 1240 cm−1, and 535 to 635 cm−1.
Provided is a method for producing acylated cellulose by conducting delignification and acylation in a one-stage reaction. This method for producing acylated cellulose according to the present disclosure includes a step (I) in which plant-derived biomass (A) is reacted with a carboxylic acid (B) represented by formula (b): R1mm (wherein R1represents a hydrocarbon group and m indicates an integer of 1 or larger), in such a proportion that the amount of the (B) is 1.3-30 parts by weight per part by weight of the (A) (in terms of dry weight), thereby obtaining acylated cellulose having repeated units represented by formula (1) and having a total degree of R1CO-group substitution of 0.1-3.
An electric circuit breaker device (1) comprises: a housing (10) which has a metal outer shell container (120) that defines at least a portion of an accommodation space (13); an igniter (20) which is provided in the housing (10); a projectile (40) which is disposed in the accommodation space (13); a conductor strip (50) which forms part of an electric circuit, wherein the conductor strip (50) has a cutout target portion (53) that is to be cut out by the projectile (40), and the conductor strip (50) is disposed such that the cutout target portion (53) crosses the accommodation space (13); a conductive coolant material (60) which is disposed in an arc extinguishing region (R2) for receiving the cutout target portion (53) that has been cut, by the projectile (40), out of the accommodation space (13); and an insulating cover member (70) which is disposed between the outer shell container (120) inside the accommodation space (13) and the coolant material (60) and which covers the outside of the arc extinguishing region (R2).
The present invention provides a method for obtaining an acylated cellulose by performing a delignification treatment and an acylation treatment in a single-step reaction. A method for producing an acylated cellulose according to the present disclosure enables the achievement of an acylated cellulose that has a repeating unit represented by formula (1), a total degree of substitution of R1CO groups of 0.1 to 3, and a structure of a cellulose crystal and/or a cellulose triester crystal through a step (I) in which lignocellulose (A) and a carboxylic acid (B) that is represented by formula (b) R1mm (wherein R1 represents a hydrocarbon group and m represents an integer of 1 or more) are reacted with each other.
Provided is a method for efficiently separating and recovering, from plant-derived biomass, a biomass composition containing highly pure mono- and/or polycarboxylic acid that is highly useful industrially. This method obtains a biomass composition containing a mono- and/or polycarboxylic acid that has a molecular weight of 200 or less, and a polycarboxylic acid that has a molecular weight cut-off using ultrafiltration of 3,000 or more, and having a combined neutral sugar component content and lignin content of 70 wt% or less, by performing step 1 and step 2-1, or step 1 and step 2-2. Step 1: In a reaction system, plant-derived biomass, a solvent containing water in at least a portion thereof, and peroxide and/or peroxy acid are combined and reacted. Step 2-1: Separate out the aqueous phase from the reaction solution after step 1. Step 2-2: Add water and/or a non-water soluble organic solvent to the reaction solution after step 1 to separate the liquid, and separate out the aqueous phase.
Provided are a poly(arylene sulfide) resin composition for plate-shaped electroconductive members which has excellent high- and low-temperature impact resistance, an electroconductive member, and a production method therefor. The poly(arylene sulfide) resin composition for plate-shaped electroconductive members comprises (A) a poly(arylene sulfide) resin, (B) a fibrous inorganic filler, and (C) an alkoxysilane compound, wherein the poly(arylene sulfide) resin (A) has a crystallization temperature (Tc) during cooling of 215°C or higher, the fibrous inorganic filler (B) includes a fibrous inorganic filler (b1) having an aspect ratio of 3.0 or higher, the content of the fibrous inorganic filler (b1) is 50-100 mass% in the fibrous inorganic filler (B), and the content of the fibrous inorganic filler (B) and the content of the alkoxysilane compound (C) are 55-250 parts by mass and 0.3-10 parts by mass, respectively, per 100 parts by mass of the poly(arylene sulfide) resin (A).
B32B 27/00 - Produits stratifiés composés essentiellement de résine synthétique
B32B 27/20 - Produits stratifiés composés essentiellement de résine synthétique caractérisée par l'emploi d'additifs particuliers utilisant des charges, des pigments, des agents thixotropiques
C08K 13/04 - Ingrédients caractérisés par leur forme et ingrédients organiques ou inorganiques
H01B 3/30 - Isolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques matières plastiquesIsolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques résinesIsolateurs ou corps isolants caractérisés par le matériau isolantEmploi de matériaux spécifiés pour leurs propriétés isolantes ou diélectriques composés principalement de substances organiques cires
H01B 7/00 - Conducteurs ou câbles isolés caractérisés par la forme
The present disclosure relates to a laminate for humidification including a porous reinforcing material, and a non-porous membrane that is laminated on at least one surface of the porous reinforcing material and functions as a moisture-permeable membrane.
F24F 1/037 - Climatiseurs individuels monoblocs pour le conditionnement de l'air, c.-à-d. avec tout l'appareillage nécessaire au traitement placé dans une enveloppe comportant des moyens d’humidification
F24F 3/14 - Systèmes de conditionnement d'air dans lesquels l'air conditionné primaire est fourni par une ou plusieurs stations centrales aux blocs de distribution situés dans les pièces ou enceintes, blocs dans lesquels il peut subir un traitement secondaireAppareillage spécialement conçu pour de tels systèmes caractérisés par le traitement de l'air autrement que par chauffage et refroidissement par humidificationSystèmes de conditionnement d'air dans lesquels l'air conditionné primaire est fourni par une ou plusieurs stations centrales aux blocs de distribution situés dans les pièces ou enceintes, blocs dans lesquels il peut subir un traitement secondaireAppareillage spécialement conçu pour de tels systèmes caractérisés par le traitement de l'air autrement que par chauffage et refroidissement par déshumidification
Provided is a method for producing equol and 5-hydroxyequol using a microorganism having a capability of producing equol from a daidzein compound and a capability of producing 5-hydroxyequol from a genistein compound, wherein the daidzein compound and the genistein compound are present at the start of the culture of the microorganism, the molar conversion efficiency of the genistein compound to 5-hydroxyequol is 0.200%/h or more, the molar concentration ratio of the genistein compound to the daidzein compound at the start of the culture is 1.500 or more or 0.500 or less, the daidzein compound is selected from daidzin, malonyldaidzin, acetyldaidzin, daidzein, dihydrodaidzein, and combinations thereof, and the genistein compound is selected from genistin, malonylgenistin, acetylgenistin, genistein, dihydrogenistein, and combinations thereof.
C12P 17/06 - Préparation de composés hétérocycliques comportant O, N, S, Se ou Te comme uniques hétéro-atomes du cycle l'oxygène comme unique hétéro-atome du cycle contenant un hétérocycle à six chaînons, p. ex. fluorescéine
The present invention provides a method for efficiently separating and recovering, from plant-derived biomass, a biomass composition containing, at high purity, mono- and/or poly-carboxylic acids that are highly valuable in industrial applications. The method according to the present disclosure is a method for producing a biomass composition through steps 1 and 2-1 or steps 1 and 2-2 mentioned below, the biomass composition containing mono- and/or poly-carboxylic acids and having a total content of neutral sugar components and lignin of 70 wt% or less. Step 1: Plant-derived biomass, a solvent at least partially containing water, and a peroxide and/or a peracid are fed into a reaction system and reacted. Step 2-1: The aqueous phase is separated from the post-reaction mixture in step 1. Step 2-2: Water and/or a water-immiscible organic solvent is added to the post-reaction mixture in step 1 for liquid-liquid phase separation, and the aqueous phase is separated.
The present invention provides a plant bark solution capable of imparting water repellency to the surface of an article. Provided is a plant bark solution containing plant bark and an organic acid.
This method for producing equol and 5-hydroxyequol uses a microorganism capable of producing the equol from a daidzein and producing the 5-hydroxyequol from a genistein. The daidzein and the genistein are present at the start of culturing the microorganism. The molar transformation efficiency from the genistein into the 5-hydroxyequol is 0.150%/h or more. The molar concentration ratio of the genistein with respect to the daidzein at the start of the culturing is not less than 1.300 or not more than 0.700. The daidzein is daidzin, malonyldaidzin, acetyldaidzin, daidzein, dihydrodaidzein, or a combination thereof. The genistein is genistein, malonyldaidzin, acetyldaidzin, genistein, dihydrogenistein, or a combination thereof.
C12P 17/06 - Préparation de composés hétérocycliques comportant O, N, S, Se ou Te comme uniques hétéro-atomes du cycle l'oxygène comme unique hétéro-atome du cycle contenant un hétérocycle à six chaînons, p. ex. fluorescéine
A23L 21/00 - Marmelades, confitures, gelées ou similairesProduits de l’apicultureLeur préparation ou leur traitement
A23L 33/10 - Modification de la qualité nutritive des alimentsProduits diététiquesLeur préparation ou leur traitement en utilisant des additifs
The present invention provides a tree bark solution capable of imparting water repellency to a surface of an article. The tree bark solution contains tree bark and an organic acid.
C09K 3/18 - Substances non couvertes ailleurs à appliquer sur des surfaces pour y minimiser l'adhérence de la glace, du brouillard ou de l'eauSubstances antigel ou provoquant le dégel pour application sur des surfaces
99.
CURABLE COMPOUND, CURABLE COMPOSITION, AND METHOD FOR PRODUCING CURABLE COMPOUND
Provided is a curable compound which can be cured at a low temperature in the presence of oxygen. The present disclosure provides a curable compound represented by formula (1). [In the formula, R1denotes a curable functional group having a cyclic imide structure, and R2denotes a functional group which has a succinimide structure and promotes curing of the curable functional group. D1and D2 may be the same as, or different from, each other, and are each a single bond or a linking group. L denotes a divalent group having a repeating unit that contains a structure represented by formula (I) and a structure represented by formula (II).]
C08G 65/48 - Polymères modifiés par post-traitement chimique
C08F 299/02 - Composés macromoléculaires obtenus par des interréactions de polymères impliquant uniquement des réactions entre des liaisons non saturées carbone-carbone, en l'absence de monomères non macromoléculaires à partir de polycondensats non saturés
100.
REMOVAL OF CELLULOSE-DERIVED IMPURITIES FROM IONIC LIQUID
NATIONAL UNIVERSITY CORPORATION KOBE UNIVERSITY (Japon)
DAICEL CORPORATION (Japon)
Inventeur(s)
Kato, Noriaki
Matsuyama, Hideto
Matsuoka, Atsushi
Hamada, Toyozo
Okabe, Shinsuke
Abrégé
Provided is a method for removing cellulose-derived impurities from an ionic liquid and effectively recovering the ionic liquid. This method is for recovering a liquid comprising an ionic liquid and a cosolvent from an impurity-containing liquid comprising the ionic liquid, the cosolvent, and cellulose-derived impurities, the method including treating the impurity-containing liquid with an ultrafiltration membrane and thereby separating the liquid comprising the ionic liquid and the cosolvent from the cellulose-derived impurities.