Abstract: Provided is a method for producing fluorenone comprising an oxidation step of oxidizing fluorene in the presence of an aliphatic carboxylic acid having 2 to 3 carbon atoms, a metal catalyst, a bromine compound, and oxygen, and a phosphoric acid treatment step of bringing an oxidation reaction mixture into contact with phosphoric acid in the order indicated.

Abstract: Provided is a work machine that allows assisting a loading work without giving uncomfortable feeling to an operator. The control device 40 of the work machine 1 includes an allowable range calculation section 46 that calculates an allowable range indicating a range in which the front work device 2 is movable in a height direction allowed in a swing operation; an operation determining section 45 that determines whether the work machine 1 is under a convey operation; and an operation control section 4 that controls a turn operation of a boom 8 such that the position of the front work device 2 in the height direction remains within the allowable range when the work machine 1 is determined to be under the convey operation.

Abstract: The patch of the present invention comprises a backing layer and an adhesive layer laminated on the backing layer, wherein a water vapor transmission rate of the backing layer is 400 g/m2·24 hours or more, and the adhesive layer comprises a drug, dimethylsulfoxide and an adhesive. Such a patch does not fall off easily even after long wear.

Abstract: This aluminum-plated steel sheet has a steel sheet and a plating layer formed on a surface of the steel sheet, the plating layer contains one or more A group elements selected from a group consisting of Be, Mg, Ca, Sr, Ba, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, and Zn, a remainder of Al, Fe, and impurities, a thickness t of the plating layer is 10 to 60 ?m, and an average grain size is 2t/3 or less and 15 ?m or less in a thickness range from an outermost surface of the plating layer to a ? thickness t position.

Abstract: The present disclosure relates to a non-aqueous electrolyte secondary battery comprising a wound-type electrode assembly and an electrolyte solution. In the non-aqueous electrolyte secondary battery according to the present disclosure, a dimension of at least one of a positive electrode active material layer and a negative electrode active material layer in a direction of an axis of winding of the electrode assembly is 150 mm or more, the electrolyte solution includes an electrolyte salt and LiFSO3, the electrolyte salt includes at least one of LiPF6 and LiBF4, a ratio of a total concentration A (mol/L) of LiPF6 and LiBF4 to a concentration B (mol/L) of LiFSO3 in the electrolyte solution, which is expressed as an A/B ratio, is from 5 to 12, and a pressure of 0.5 MPa or more is applied to the electrode assembly in an electrode plate stacking direction.

Abstract: A non-aqueous electrolyte secondary battery comprises an electrode assembly and an electrolyte solution. The electrode assembly is a wound-type electrode assembly or a stack-type electrode assembly each of which comprises a positive electrode plate having an active material layer. To the non-aqueous electrolyte secondary battery, a restraining pressure of 0.5 MPa or more is applied in a stacking direction of the positive electrode plates. The electrolyte solution includes LiFSO3, and the electrolyte solution has an electrical conductivity of 0.86 S/m or more at 25° C.

Abstract: A non-aqueous secondary battery includes a positive electrode composite material layer. In a cross-section in a direction of thickness of the positive electrode composite material layer, the positive electrode composite material layer includes a first region including one end portion in a direction intersecting with the direction of thickness, a second region including the other end portion, and a third region lying between the first region and the second region. The first region is composed of a first composite material containing lithium iron phosphate and lithium nickel cobalt manganese composite oxide, and the second region is composed of a second composite material containing lithium iron phosphate and lithium nickel cobalt manganese composite oxide. The third region is composed of a third composite material containing lithium nickel cobalt manganese composite oxide.

Abstract: The present disclosure relates to a non-aqueous electrolyte secondary battery, wherein an electrolyte solution includes a solvent, a lithium salt, and an additive agent, the additive agent includes at least one selected from a group consisting of a boron compound having an oxalate group and a compound having a fluorosulfonyl group, a BET specific surface area of a negative electrode active material layer is 1.8 m2/g or more and 3.0 m2/g or less, the negative electrode active material layer includes a particle group consisting of a negative electrode active material particle, an average sphericity of the particle group is 0.87 or more.

Abstract: The present disclosure relates to a non-aqueous electrolyte secondary battery including an electrode assembly and an electrolyte solution, wherein the electrode assembly includes a positive electrode plate, a separator, and a negative electrode plate, the electrolyte solution contains a Li salt, a solvent, and an additive agent, the positive electrode plate includes a positive electrode core body and a positive electrode active material layer, the negative electrode plate includes a negative electrode core body and a negative electrode active material layer, and in at least one of the positive electrode active material layer and the negative electrode active material layer, a ratio A/B is 1.4 or more and 2.6 or less.

Abstract: A method for producing fluorenone including a pretreatment step of heating fluorene in the presence of a lower aliphatic carboxylic acid, a bromine compound, and a metal catalyst, and an oxidation step of continuously supplying fluorene and oxygen to perform an oxidation reaction, in the order indicated.

Abstract: Provided is a method for producing fluorenone comprising an oxidation step of oxidizing fluorene in the presence of an aliphatic carboxylic acid having 2 to 3 carbon atoms, a metal catalyst, a bromine compound, and oxygen, a solvent removal step of removing the aliphatic carboxylic acid, a heating step at 120 to 350° C., and a distillation step in the order indicated.

Abstract: A non-aqueous electrolyte secondary battery includes at least a positive electrode active material layer, a porous film, and a negative electrode active material layer. The negative electrode active material layer contains at least a graphite-based carbon material and silicon oxide. The porous film is interposed between the positive electrode active material layer and the negative electrode active material layer. The porous film contains at least a ceramic material. The negative electrode active material layer has a first spring constant. The porous film has a second spring constant. A ratio of the second spring constant to the first spring constant is higher than 1.

Abstract: A valve device includes: valves configured to control a flow of processing gases supplied to a process vessel; a housing in which first flow paths through which the processing gases flow are formed; a heat diffuser configured to cover the housing and diffuse heat of the housing; a heating part configured to cover the housing covered with the heat diffuser and heat the housing via the heat diffuser; a supply configured to supply a coolant to a second flow path formed between the housing and the heat diffuser; and a controller configure to control the heating part to heat the housing to a first temperature when a predetermined process is performed on a target substrate, and before a start of a cleaning process of the process vessel, control the heating part to stop heating of the housing and control the supply to supply the coolant to the second flow path.

Abstract: A non-aqueous electrolyte secondary battery includes: a pressure-type current interrupt device arranged in a conductive path, for interrupting the conductive path when an internal pressure exceeds a working pressure; a non-aqueous electrolyte; and a positive electrode composite material layer. The non-aqueous electrolyte contains a gas generation agent that generates a gas in an overcharge region, and the positive electrode composite material layer contains a first positive electrode active material particle including lithium iron phosphate, and a second positive electrode active material particle including lithium-nickel composite oxide. A ratio of the first positive electrode active material particle to a total mass of the first positive electrode active material particle and the second positive electrode active material particle is 5% by mass or more and 20% by mass or less.

Abstract: A nonaqueous electrolyte secondary battery according to the present invention includes: an electrode body including a positive electrode including a positive-electrode active material layer; an external terminal connected to the electrode body; a nonaqueous electrolyte including a gas generant, and a current interrupt device. A content of the gas generant is at least 4 mass %. The positive-electrode active material layer includes, as a positive-electrode active material, a complex oxide containing at least zirconium (Zr) and calcium (Ca) as constituent elements. When a sum total of metal elements, except metal that becomes a charge carrier, in the complex oxide is 100 mol % in terms of a mole percentage, the complex oxide contains Zr from 0.1 mol % to 0.5 mol % inclusive and Ca from 0.1 mol % to 0.3 mol % inclusive.

Abstract: A method of producing a lithium ion secondary battery includes preparing a case in which an electrode group including at least a positive electrode and a negative electrode is accommodated; impregnating a first electrolyte solution into the electrode group, lowering a potential of the negative electrode to a first potential, injecting FEC into a case, and lowering a potential of the negative electrode to a second potential. The negative electrode contains at least graphite and silicon oxide. The first electrolyte solution does not contain FEC. An additive has a reductive decomposition potential of 0.5 V (vs. Li+/Li) or more and 1.5 V (vs. Li+/Li) or less. The first potential is higher than 0.2 V (vs. Li+/Li) and is equal to or lower than the reductive decomposition potential. The second potential is 0.2 V (vs. Li+/Li) or less.

Abstract: Disclosed herein is a method for producing high-purity terephthalic acid, including steps of dissolving crude terephthalic acid crystal in water and performing catalytic hydrogenation treatment, depressurizing and cooling a reaction liquid after the catalytic hydrogenation treatment in stages with two or more stages of crystallization vessels, to crystallize terephthalic acid to obtain a terephthalic acid slurry, introducing the terephthalic acid slurry into an upper portion of a mother liquor replacement tower, bringing the terephthalic acid crystal into contact with an upward flow of replacement water introduced from a tower lower compartment of the mother liquor replacement tower while making the terephthalic acid crystal settled down in the tower, withdrawing the terephthalic acid crystal as slurry with the replacement water from the tower lower compartment, subjecting the slurry withdrawn from the tower lower compartment to solid-liquid separation into water and the terephthalic acid crystal, and drying

Abstract: A valve device includes: valves configured to control a flow of processing gases supplied to a process vessel; a housing in which first flow paths through which the processing gases flow are formed; a heat diffuser configured to cover the housing and diffuse heat of the housing; a heating part configured to cover the housing covered with the heat diffuser and heat the housing via the heat diffuser; a supply configured to supply a coolant to a second flow path formed between the housing and the heat diffuser; and a controller configure to control the heating part to heat the housing to a first temperature when a predetermined process is performed on a target substrate, and before a start of a cleaning process of the process vessel, control the heating part to stop heating of the housing and control the supply to supply the coolant to the second flow path.

Abstract: A method of manufacturing a non-aqueous electrolyte secondary battery includes: (A) constructing an electrode group including a positive electrode and a negative electrode; (B) impregnating the electrode group with a first electrolyte solution; (C) charging the electrode group impregnated with the first electrolyte solution to a voltage of 4.3 V or more; and (E) manufacturing the non-aqueous electrolyte secondary battery by impregnating the electrode group with a second electrolyte solution after the charging. The first electrolyte solution includes a first solvent, a first lithium salt, and biphenyl. The first solvent does not include 1,2-dimethoxyethane. The second electrolyte solution includes a second solvent and a second lithium salt. The second solvent includes 1,2-dimethoxyethane.

Abstract: In an electrode body for use in non-aqueous electrolyte secondary battery, a first end of a separator is located more interiorly than one positive electrode end of a positive electrode plate in a width direction, located more exteriorly than one end of a coated positive electrode portion of the positive electrode plate, and located more exteriorly than one end of a coated negative electrode portion of a negative electrode plate. The first end of the separator is thicker than an intermediate portion. A second end of the separator is located more interiorly than an other negative electrode end of the negative electrode plate in the width direction, located more exteriorly than the other end of the coated positive electrode portion of the positive electrode plate, and located more exteriorly than an other end of the coated negative electrode portion of the negative electrode plate. The second end of the separator is thicker than the intermediate portion.