Abstract: A composition that enables a resist underlayer film to be formed, contains: a compound having at least one partial structure represented by formula (1); and a solvent. In the formula (1), for example, Ar1 represents a group obtained by removing (p+1) hydrogen atoms on an aromatic carbon ring from a substituted or unsubstituted arene having 6 to 30 ring atoms, or a group obtained by removing (p+1) hydrogen atoms on an aromatic heteroring from a substituted or unsubstituted heteroarene having 5 to 30 ring atoms; Ar2 represents a substituted or unsubstituted aryl group having 6 to 30 ring atoms, or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms, and R2 represents a hydrogen atom or a monovalent organic group having 1 to 20 carbon atoms, and R3 represents an ethynediyl group or a substituted or unsubstituted ethenediyl group.

Abstract: A hydrohaloolefin composition includes a hydrohaloolefin as a main component, further includes 1,1,2,3-tetrafluorobutane, in which a content of the 1,1,2,3-tetrafluorobutane is 0.001 to 0.1% by mass with respect to a total amount of organic compounds.

Abstract: The composition contains: a compound which has a group represented by formula (1); and a solvent. In the formula (1), R1 and R2 each independently represent a substituted or unsubstituted aryl group having 6 to 30 ring atoms or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms; R3 represents a hydrogen atom or a substituted or unsubstituted monovalent aliphatic hydrocarbon group having 1 to 10 carbon atoms; and * denotes a bonding site to a part other than the group represented by the following formula (1) in the compound.

Abstract: A composition that enables a resist underlayer film to be formed, contains: a compound having at least one partial structure represented by formula (1); and a solvent. In the formula (1), for example, Ar1 represents a group obtained by removing (p+1) hydrogen atoms on an aromatic carbon ring from a substituted or unsubstituted arene having 6 to 30 ring atoms, or a group obtained by removing (p+1) hydrogen atoms on an aromatic heteroring from a substituted or unsubstituted heteroarene having 5 to 30 ring atoms; Ar2 represents a substituted or unsubstituted aryl group having 6 to 30 ring atoms, or a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms, and R2 represents a hydrogen atom or a monovalent organic group having 1 to 20 carbon atoms, and R3 represents an ethynediyl group or a substituted or unsubstituted ethenediyl group.

Abstract: A composition contains: a compound including at least one group selected from the group consisting of a group represented by formula (1-1), a group represented by formula (1-2), and a group represented by formula (1-3); and a solvent. In formulae (1-1) to (1-3), * and ** each denote a site bonding to a part other than the group represented by the formulae (1-1) to (1-3) in the compound; and a and b are each independently an integer of 0 to 3. In a case in which a is 0, b is no less than 1, and in a case in which a is no less than 1, b is 0.

Abstract: A thermoelectric conversion module package includes: a thermoelectric conversion module including a first and a second substrate opposed to each other, a plurality of thermoelectric elements arranged between the first and second substrates, and a first and a second lead wire drawn out from one of the first and second substrates; and a package including a first metal foil covering the first substrate of the thermoelectric conversion module, a second metal foil covering the second substrate of the thermoelectric conversion module, a resin portion hermetically connecting the first metal foil and the second metal foil along an outer edge portion of the thermoelectric conversion module, and an insertion portion for hermetically passing the first and second lead wires through the resin portion.

Abstract: There is provided an economically advantageous manufacturing method capable of efficiently obtaining 1-chloro-2,3,3,3-tetrafluoropropene by using 1,2-dichloro-2,3,3,3-tetrafluoropropane as a raw material. A manufacturing method of 1-chloro-2,3,3,3-tetrafluoropropene is characterized in that it includes subjecting 1,2-dichloro-2,3,3,3-tetrafluoropropane to a dehydrochlorination reaction in a liquid phase in a presence of a base.

Abstract: There is provided a method of efficiently manufacturing purified 1224yd containing 1224yd at a high concentration from a mixture containing 1224yd and a compound that forms an azeotropic composition or an azeotropic-like composition with 1224yd. A manufacturing method of purified 1224yd, includes making a first mixture of 1224yd and a compound (X1) forming an azeotropic composition or an azeotropic-like composition with 1224yd to be brought into contact with a first extraction solvent to obtain purified 1224yd not substantially containing the compound (X1).

Abstract: A packaging material for electrical storage devices which includes a base layer, a metal foil layer arranged on the base layer, and a sealant layer arranged on the metal foil layer. In the packaging material for electrical storage devices, the base layer includes at least one of a stretched polyester resin and a stretched polyamide resin, and the metal foil layer is an aluminum foil containing iron in the range of about 0.5 mass % or more to about 5.0 mass % or less. The packaging material has a tensile elongation of about 50% or more both the MD and TD directions of the base layer.

Abstract: A thermoelectric conversion module package includes: a thermoelectric conversion module including a first and a second substrate opposed to each other, a plurality of thermoelectric elements arranged between the first and second substrates, and a first and a second lead wire drawn out from one of the first and second substrates; and a package including a first metal foil covering the first substrate of the thermoelectric conversion module, a second metal foil covering the second substrate of the thermoelectric conversion module, a resin portion hermetically connecting the first metal foil and the second metal foil along an outer edge portion of the thermoelectric conversion module, and an insertion portion for hermetically passing the first and second lead wires through the resin portion.

Abstract: There is provided a method of efficiently manufacturing purified 1224yd containing 1224yd at a high concentration from a mixture containing 1224yd and a compound that forms an azeotropic composition or an azeotropic-like composition with 1224yd. A manufacturing method of purified 1224yd, includes making a first mixture of 1224yd and a compound (X1) forming an azeotropic composition or an azeotropic-like composition with 1224yd to be brought into contact with a first extraction solvent to obtain purified 1224yd not substantially containing the compound (X1).

Abstract: A packaging material for lithium-ion battery comprises a substrate layer made of a plastic film, and a first adhesive layer, a metal foil layer, an anti-corrosion layer, a second adhesive layer and a sealant layer successively laminated on one surface of the substrate layer. The plastic film has a water absorption rate of not less than about 01% to not larger than about 3% when determined by a method described in JIS K 7209:2000 and when the plastic film is subjected to a tensile test (wherein the sample of the plastic film is stored for 24 hours in an environment of 23° C. and 40% R.H.

Abstract: There is provided an economically advantageous manufacturing method capable of efficiently obtaining 1-chloro-2,3,3,3-tetrafluoropropene by using 1,2-dichloro-2,3,3,3-tetrafluoropropane as a raw material. A manufacturing method of 1-chloro-2,3,3,3-tetrafluoropropene is characterized in that it includes subjecting 1,2-dichloro-2,3,3,3-tetrafluoropropane to a dehydrochlorination reaction in a liquid phase in a presence of a base.

Abstract: A composition is provided containing HFO-1123 having a low GWP, which is useful as a heat transfer composition, an aerosol sprayer, a foaming agent, a blowing agent, a solvent or the like. A composition containing HFO-1123, and at least one first compound selected from the group consisting of HFO-1132, HFO-1132a, CFO-1113, HCFO-1122, HCFO-1122a, HFC-143 and methane.

Abstract: To provide a working fluid for heat cycle, which has less influence over the ozone layer and has less influence over global warming, and which has favorable cycle performance. A working fluid for heat cycle, which contains trifluoroethylene and difluoroethylene, wherein the proportion of the content of difluoroethylene is less than 1.5 mass % based on the working fluid.

Abstract: A working fluid for heat cycle, which has less influence over the ozone layer, has less influence over global warming, and has favorable cycle performance, is provided. The working fluid contains trifluoroethylene and difluoroethylene and the proportion of the difluoroethylene is less than 1.5 mass % based on the working fluid.

Abstract: A power storage device packaging material includes: a base material layer; a metal foil layer formed on one surface of the base material layer via an adhesive layer; and a sealant layer arranged on a surface of the metal foil layer, the surface of the metal foil layer being on the opposite side to the base material layer, wherein the base material layer contains a polyester resin that contains a polyester elastomer and/or an amorphous polyester.

Abstract: A lithium-ion battery outer package material, provided with: a base layer, and a first adhesive layer, a metallic foil layer, a corrosion prevention treatment layer, a second adhesive layer, and a sealant layer sequentially layered on one of the surfaces of the base layer. When a tensile test (a sample of the substrate layer is stored for 24 hours in a 23° C. and 40% RH environment; a tensile test is subsequently performed in a 23° C. and 40% RH environment with the specimen width being 15 mm, the distance between gauge points being 50 mm, and the tensile speed being 100 mm/min; and the tensile elongation and tensile stress of the specimen are measured) is performed, the tensile elongation in a first direction, which is either the TD direction or the MD direction of the sample, relative to the length of the sample is from about not less than 50% to less than 80%, and the tensile stress in a second direction, which is perpendicular to the first direction, is from about not less than 150 to 230 MPa.

Abstract: A packaging material for lithium-ion battery comprises a substrate layer made of a plastic film, and a first adhesive layer, a metal foil layer, an anti-corrosion layer, a second adhesive layer and a sealant layer successively laminated on one surface of the substrate layer. The plastic film has a water absorption rate of not less than about 01% to not larger than about 3% when determined by a method described in JIS K 7209:2000 and when the plastic film is subjected to a tensile test (wherein the sample of the plastic film is stored for 24 hours in an environment of 23° C. and 40% R.H.

Abstract: A lithium-ion battery outer package material includes a base layer, a first adhesive layer, a metallic foil layer, a corrosion prevention treatment layer, a second adhesive layer, and a sealant layer sequentially layered on one of the surfaces of the base layer. When a tensile test is performed in a 23° C. and 40% RH environment, with the specimen width being 15 mm, the distance between gauge points being 50 mm, and the tensile speed being 100 mm/min, the tensile elongation and tensile stress of the specimen are measured. A ratio of tensile elongation measured in a first direction to tensile elongation measured in a second direction is from 135:85 to 140:75, and a ratio of tensile stress measured in the first direction to tensile stress measured in the second direction is from 195:225 to 200:229.