An aluminum alloy forging of the present invention includes 0.15 wt % to 1.0 wt % of Cu, 0.6 wt % to 1.3 wt % of Mg, 0.60 w t% to 1.45 wt % of Si, 0.03 wt % to 1.0 wt % of Mn, 0.2 wt % to 0.4 wt % of Fe, 0.03 wt % to 0.4 wt % of Cr, 0.012 wt % to 0.035 wt % of Ti, 0.0001 wt % to 0.03 wt % of B, 0.25 wt % or less of Zn, 0.05 wt % or less of Zr, the balance being Al and inevitable impurities. When integrated intensity of a diffraction peak of an AlFeMnSi phase in an X-ray diffraction pattern obtained by an X-ray diffraction measurement of a cross-section of the forging is “Q1” (cpd·deg) and integrated intensity of a diffraction peak of a (200) plane of an Al phase is “Q2” (cps·deg), a value of Q1/Q2 is 6×10−2 or less.
C22F 1/057 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with copper as the next major constituent
B21J 5/02 - Die forgingTrimming by making use of special dies
C22C 21/14 - Alloys based on aluminium with copper as the next major constituent with silicon
C22C 21/16 - Alloys based on aluminium with copper as the next major constituent with magnesium
2.
RADIATION CURABLE COMPOSITION FOR FORMING OPTICAL FIBER PRIMARY COAT LAYER, AND URETHANE (METH)ACRYLATE
The present invention pertains to a radiation curable composition which is for forming an optical fiber primary coat layer, and which is capable of forming a cured product having excellent flexibility and adequate mechanical strength. More specifically, the present invention pertains to a radiation curable composition which is for forming an optical fiber primary coat layer, and which comprises: (A) a urethane (meth)acrylate that is obtained by reacting at least (a) a polyether diol having a number average molecular weight of 2000-5000, (b) a diisocyanate compound, (c) a hydroxyl-containing (meth)acrylate compound, and (d) a diol having a molecular weight of 500 or less; (B) a (meth)acrylate compound other than component (A); and (C) a radiation polymerization initiator.
C08G 18/67 - Unsaturated compounds having active hydrogen
C09D 4/00 - Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond
Provided is a composition for forming a coating layer of an optical fiber, the composition comprising a compound having a structure represented by the following formula (I):
Provided is a composition for forming a coating layer of an optical fiber, the composition comprising a compound having a structure represented by the following formula (I):
*—NH—CO—N(R1)—R2—SiR3n—(OR4)3-n (I)
Provided is a composition for forming a coating layer of an optical fiber, the composition comprising a compound having a structure represented by the following formula (I):
*—NH—CO—N(R1)—R2—SiR3n—(OR4)3-n (I)
wherein, R1 is a hydrogen atom, an alkyl group, or an aryl group, R2 is a methylene group optionally substituted with a halogen, a C2-10 alkylene group that may have a heteroatom or an atomic group having a heteroatom between carbon atoms and may optionally be substituted with a halogen, or a phenylene group that may have a substituent, R3 is an alkyl group, and R4 is a C1-6 alkyl group, * being a bond and n indicating an integer of 0 or more and 2 or less.
An electrode binder for a nonaqueous secondary battery; and a nonaqueous secondary battery electrode. The electrode binder for a nonaqueous secondary battery contains a resin component and is water-soluble. The surface free energy γB at 23° C. is 70 mJ/m2 or less, and the dipole component γpB of the surface free energy is 26 mJ/m2 or less.
Provided is a transparent conducting film having a preferable optical property, a preferable electrical property, and further, a superior durability of folding. The transparent conducting film comprises a transparent substrate and a transparent conducting layer formed on at least one of main faces of the transparent substrate, wherein the transparent conducting layer contains a binder resin and a conducting fiber, a cut portion of the transparent conducting film has a straightness of 0.050 mm or less. Preferably, the transparent substrate is a resin film having an elongated resin film or cut out from an elongated film, and can be folded in with a folding axis in the direction perpendicular to the longitudinal direction of the elongated resin film.
An aluminum alloy member (1) for forming a fluoride film is used as a member of a semiconductor manufacturing device and has a composition containing 1.2-4.5 mass% of Mg and 0.2-1.0 mass% of Si, with the excess Mg concentration being 0.5 mass% or more.
C22C 21/06 - Alloys based on aluminium with magnesium as the next major constituent
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/047 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with magnesium as the next major constituent
C25D 11/04 - Anodisation of aluminium or alloys based thereon
LITHIUM ION CONDUCTIVE SOLID ELECTROLYTE MATERIAL, LITHIUM ION CONDUCTIVE SOLID ELECTROLYTE, METHOD FOR PRODUCING SAID LITHIUM ION CONDUCTIVE SOLID ELECTROLYTE MATERIAL, METHOD FOR PRODUCING SAID LITHIUM ION CONDUCTIVE SOLID ELECTROLYTE, AND ALL-SOLID-STATE BATTERY
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
H01B 1/08 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances oxides
H01M 4/48 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/58 - Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFySelection of substances as active materials, active masses, active liquids of polyanionic structures, e.g. phosphates, silicates or borates
H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
H01M 10/0585 - Construction or manufacture of accumulators having only flat construction elements, i.e. flat positive electrodes, flat negative electrodes and flat separators
9.
SOLID ELECTROLYTE, SOLID-STATE BATTERY, AND SOLID ELECTROLYTE MATERIAL
One embodiment of the present invention relates to a solid electrolyte, a solid-state battery, or a solid electrolyte material. The solid electrolyte contains: a lithium ion conducting phase including at least tantalum, phosphorus, and oxygen as constituent elements; and a chemical phase that has at least phosphorus and oxygen as constituent elements and does not include tantalum. In a scanning transmission electron microscopy energy dispersive X-ray spectroscopy (STEM-EDX) image of the solid electrolyte, the area ratio of the chemical phase relative to a total of 100% of the area of the lithium ion conducting phase, the area of the chemical phase, and the void area is at least 0.40%, and the solid electrolyte has at least lithium, tantalum, phosphorus, and oxygen as constituent elements.
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
C01B 25/45 - Phosphates containing plural metal, or metal and ammonium
H01B 1/08 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances oxides
H01M 4/48 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/58 - Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFySelection of substances as active materials, active masses, active liquids of polyanionic structures, e.g. phosphates, silicates or borates
H01M 4/587 - Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
Provided is a thermally conductive composition comprising a filler and a polymer component, wherein the filler includes at least one surface-treated filler selected from the group consisting of the following fillers (A) and (B). Filler (A): a filler which is surface-treated through chemical vapor deposition by using a siloxane having one SiH group. Filler (B): a filler which is surface-treated through chemical vapor deposition by using a siloxane having two or more SiH groups, and which has, on the surface thereof, silicon atoms to which at least one group selected from the group consisting of an unsubstituted C6-C20 alkyl group, a substituted C2-C20 alkyl group, and a group having a specific structure is bonded and introduced.
H01L 21/302 - Treatment of semiconductor bodies using processes or apparatus not provided for in groups to change the physical characteristics of their surfaces, or to change their shape, e.g. etching, polishing, cutting
Provided is a lining material containing a fiber base material including a resin composition, the resin composition comprising (A) a vinyl ester resin, (B) an ethylenically unsaturated group-containing monomer, (C) at least one compound selected from oxides and hydroxides of a Group 2 element, and (D) a photopolymerization initiator, wherein the vinyl ester resin (A) has an acid value of 1 to 35 KOHmg/g.
B29C 63/26 - Lining or sheathing of internal surfaces
C08F 283/01 - Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass on to unsaturated polyesters
C08F 290/00 - Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
A resin composition comprising (A) a vinyl ester resin, (B) a monomer containing an ethylenically unsaturated group, (C) at least one compound selected from an alkaline earth metal oxide and an alkaline earth metal hydroxide, and (D) at least one compound selected from water and a compound containing a hydroxy group, in which the vinyl ester resin (A) comprises a vinyl ester resin (A1), and the vinyl ester resin (A1) has a weight average molecular weight (Mw) of 1,500 or more and a molecular weight distribution (Mw/Mn) of 2.0 or more.
C08G 59/16 - Polycondensates modified by chemical after-treatment by monocarboxylic acids or by anhydrides, halides or low-molecular-weight esters thereof
C08J 5/24 - Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
This method for renovating a pipe includes: a step (I) for preparing a resin composition; a step (II) for impregnating a fiber base material (F) with the resin composition to obtain a resin composition-impregnated base material; a step (III) for obtaining a lining material containing the resin composition-impregnated base material; and a step (IV) for disposing the lining material in a pipe and photocuring the lining material. The resin composition contains: a resin (A); an ethylenically unsaturated group-containing monomer (B); a thickening agent (C); and a photopolymerization initiator (D). The resin composition has a viscosity of 0.1-3 Pa·s at 25°C in step (II). The resin composition has a viscosity of 400-3500 Pa·s at 25°C when the lining material is disposed in the pipe in step (IV).
B29C 63/34 - Lining or sheathing of internal surfaces using tubular layer or sheathings
C08F 283/01 - Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass on to unsaturated polyesters
C08F 290/00 - Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
A resin composition used for a lining material for pipe rehabilitation, the resin composition containing a resin (A), an ethylenic-unsaturated-group-containing monomer (B), a thickener (C), and a photopolymerization initiator (D), the resin composition having a viscosity at 25°C of 0.1-3 Pa∙s one hour after preparation, and the resin composition having a viscosity at 25°C of 400-3500 Pa∙s two days and/or five days after preparation.
Provided are: a resin composition which exhibits a low initial viscosity immediately after the production thereof, can be thickened at a proper speed, and has excellent handling properties; a method for producing the resin composition; and a composite material comprising the resin composition. The resin composition according to the present invention comprises (A) a vinyl ester resin, (B) a monomer containing an ethylenically unsaturated group, and (C) at least one metal compound selected from an oxide of a Group-2 element and a hydroxide of a Group-2 element, in which the vinyl ester resin (A) comprises a vinyl ester resin (A1) having a weight average molecular weight Mw of 1,500 or more and a ratio of an weight average molecular weight Mw to a number average molecular weight Mn, i.e., an Mw/Mn ratio, of 2.0 or more.
C08G 59/16 - Polycondensates modified by chemical after-treatment by monocarboxylic acids or by anhydrides, halides or low-molecular-weight esters thereof
C08J 5/24 - Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
17.
THERMALLY CONDUCTIVE RESIN COMPOSITION, CURED PRODUCT, HEAT TRANSFER MEMBER AND ELECTRONIC DEVICE
A thermally conductive resin composition which contains an epoxy resin and a thermally conductive powder, wherein: the thermally conductive powder contains aluminum nitride, which has a silicon-containing oxide coating film on the surface, and another thermally conductive powder; the content of the epoxy resin is from 1% by mass to 20% by mass relative to the total amount of the thermally conductive resin composition; the content of the thermally conductive powder is from 80% by mass to 99% by mass relative to the total amount of the thermally conductive resin composition; the content of the aluminum nitride, which has a silicon-containing oxide coating film on the surface, is from 10% by mass to 70% by mass relative to the total amount of the thermally conductive resin composition; and the content of the other thermally conductive powder is from 10% by mass to 89% by mass relative to the total amount of the thermally conductive resin composition.
An electrochemical device which is provided with a positive electrode, a negative electrode and an electrolyte solution, wherein: the negative electrode contains a silicon-based active material; and the electrolyte solution contains a compound represented by formula (1). In formula (1), each of R1to R3 independently represents a hydrogen atom or a methyl group; and X represents a divalent organic group.
Provided is a material design assistance device for assisting in optimizing the design conditions of a material, the material design assistance device having: a design condition setting unit for setting a range of design conditions of the material; a required characteristic setting unit for setting a range of required characteristics of the material; a covering prediction point generation unit for generating a plurality of covering prediction points within the range of design conditions; a prediction unit for inputting the plurality of covering prediction points to a trained model that is trained using a correspondence relation between the design conditions of the material and characteristic values of the material and predicting the characteristic values of the material; and a design condition adjustment unit for adjusting the range of design conditions of a material for which a plurality of covering prediction points is to be generated next, on the basis of range of required characteristics of the material and the characteristic values of the material for each of the predicted plurality of covering prediction points.
G06F 30/27 - Design optimisation, verification or simulation using machine learning, e.g. artificial intelligence, neural networks, support vector machines [SVM] or training a model
20.
THIOL-CONTAINING COMPOSITION, PHOTOCURABLE COMPOSITION, AND THERMOSETTING COMPOSITION
This thiol-containing composition contains a polyfunctional secondary thiol compound (A) and a disulfide dimer (B). The polyfunctional secondary thiol compound (A) is an ester of a carboxylic acid having a secondary mercapto group and a polyhydric alcohol. The disulfide dimer (B) is a disulfide dimer of the polyfunctional secondary thiol compound (A). The content of the disulfide dimer (B) is 0.001-1.5 parts by mass relative to 100 parts by mass of the polyfunctional secondary thiol compound (A).
C08F 2/44 - Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
C07C 323/52 - Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
Provided is a fluorine-containing ether compound that can form a lubricating layer with which it is possible to raise the chemical resistance of magnetic recording media even when the layer is thin and that can be used suitably as a material of a lubricant for magnetic recording media. Provided is a fluorine-containing ether compound represented by the following formula. R122-R2222-CHR3222-R422-R5(in the formula, R2and R4are perfluoropolyether chains. R1and R5are end groups that include two or three hydroxyl groups, each of the hydroxyl groups bonding to a mutually different carbon atom, and the carbon atoms to which the hydroxyl groups are bonded bonding to each other via linking groups that include carbon atoms to which no hydroxyl groups are bonded. R32aa-OH (a is an integer of 2-8.))
C07C 43/13 - Saturated ethers containing hydroxy or O-metal groups
C10N 30/00 - Specified physical or chemical property which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
C10N 40/18 - Electric or magnetic purposes in connection with recordings on magnetic tape or disc
G11B 5/70 - Record carriers characterised by the selection of the material comprising one or more layers of magnetisable particles homogeneously mixed with a bonding agent on a base layer
G11B 5/725 - Protective coatings, e.g. anti-static containing a lubricant
G11B 5/84 - Processes or apparatus specially adapted for manufacturing record carriers
C10M 105/54 - Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen containing carbon, hydrogen, halogen and oxygen
22.
TRANSPARENT CONDUCTIVE FILM LAMINATE AND METHOD FOR PRODUCING SAME
[Problem] To provide: a transparent conductive film laminate which is suppressed in curling of the transparent conductive film laminate during a heating process in cases where a polycarbonate resin is used as a base material for a transparent conductive film, and which is capable of ensuring the yield of the subsequent processes and capable of reducing the production cost; and a method for producing this transparent conductive film laminate. [Solution] A transparent conductive film laminate which comprises a transparent conductive film 10 and a carrier film 1 that is superposed on the transparent conductive film, wherein: the transparent conductive film 10 is obtained by sequentially superposing a transparent conductive layer 3 that comprises a metal thin wire and an overcoat layer 4 in this order on one main surface of a transparent resin film 2 that is formed of a polycarbonate film (having a thickness Ts of 30 to 100 µm); the transparent conductive film 10 is removably superposed on one adhesive main surface of the carrier film 1, which is formed of a polyolefin film and only one main surface of which is adhesive, so that the overcoat layer 4 serves as the outermost layer; and the ratio (Tc/Ts) of the thickness Tc of the carrier film 1 to the thickness Ts of the transparent resin film 2 satisfies 0.2 ≤ Tc/Ts ≤ 0.7.
B32B 15/09 - Layered products essentially comprising metal comprising metal as the main or only constituent of a layer, next to another layer of a specific substance of synthetic resin comprising polyesters
[Problem] To provide a transparent conductive film laminate and a method for manufacturing the same, whereby, when an amorphous cycloolefin-based resin is used in a base material of a transparent conductive film, curling of a transparent conductive film laminate during a heating process is suppressed, the yield of a subsequent process can be ensured, and manufacturing costs can be reduced. [Solution] Provided is a transparent conductive film laminate containing a transparent conductive film 10 and a carrier film 1 laminated thereto. The transparent conductive film 10 is obtained by laminating a transparent conductive layer 3, that contains a fine metal wire, and an overcoat layer 4, in this order, onto one main surface of a transparent resin film 2 comprising an amorphous cycloolefin-based resin (thickness Ts = 30 to 150 µm). The carrier film 1 comprises a polyolefin film, and only one main surface of the carrier film 1 is adhesive. The transparent conductive film 10 is releasably laminated to the one adhesive main surface of the carrier film 1 such that the overcoat layer 4 becomes the outermost layer. The ratio (Tc/Ts) of the thickness Tc of the carrier film 1 to the thickness Ts of the transparent resin film 2 satisfies 0.2 ≦ Tc/Ts ≦ 0.8.
B32B 15/085 - Layered products essentially comprising metal comprising metal as the main or only constituent of a layer, next to another layer of a specific substance of synthetic resin comprising polyolefins
Provided are an evaluation device, an evaluation method, and an evaluation program that make it possible to evaluate the quality of a sintered body. The evaluation device includes: an acquisition unit that acquires a cross-sectional image obtained by capturing an image of a cross section of a sintered body group dyed using a dyeing liquid; a generation unit that extracts a chroma component of each sintered body from the cross-sectional image and generates a chroma component image; and a visualization unit that visualizes the chroma component image.
24l36m24nn-H (In formula 1, l is an integer from 5 to 140, m is an integer from 15 to 75, and n is an integer from 5 to 140. The percentage of m in the total of l, m, and n is 5-85%.)
Provided is a method for producing an alcohol through an olefin hydration reaction using a heteropolyacid catalyst, the method enabling the catalyst to be stably used over a long period. In the olefin hydration reaction, in which the heteropolyacid catalyst is used, the pressure loss during the period of passing a feed-material gas through a catalyst layer is regulated to a certain value or less. Specifically, the method for producing an alcohol comprises using a solid-acid catalyst including a supported heteropolyacid or salt thereof, supplying water and a 2C-5C olefin to a reactor, and hydrating the olefin in a gas phase, wherein the pressure loss during the period of passing the feed-material gas through a layer of the catalyst is regulated to 350 kPa or less.
C07C 29/04 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
Provided is a method for producing alcohols by an olefin hydration reaction using a heteropolyacid catalyst, wherein the catalyst can be stably used on a long-term basis. The temperature difference within the catalyst layer in the olefin hydration reaction using a heteropolyacid catalyst is made less than or equal to a certain value. Specifically, in a method for producing alcohols in which a gas-phase hydration reaction is carried out using a solid acid catalyst that supports a heteropolyacid acid or salt thereof and supplying water and C2-C5 olefin to a reactor, the temperature difference within the catalyst layer in the reactor is established at less than or equal to 6°C.
C07C 29/04 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by addition of hydroxy groups to unsaturated carbon-to-carbon bonds, e.g. with the aid of H2O2 by hydration of carbon-to-carbon double bonds
Provided are: a filler for use in size exclusion chromatography which has high alkali resistance and in which non-specific adsorption is suppressed; and a method for producing the filler. The filler is characterized in that one end of at least one alkylene group selected from among linear alkylene groups, cycloalkylene groups, and linear alkylcycloalkylene groups with 4 to 9 carbon atoms is bonded by a glycidyl group derived from glycidyl methacrylate to a porous organic polymer carrier containing 60-95 mol% of a repeating unit derived from glycidyl methacrylate and 5-40 mol% of a repeating unit derived from a polyfunctional monomer, and the other end of the alkylene group is bonded with any one end of a polyol via an ether bond.
Provided is a pressure-sensitive adhesive composition which can give cured objects inhibited from changing in gel content even under high-temperature high-humidity conditions. This pressure-sensitive adhesive composition comprises a urethane polymer (A) containing an ethylenically unsaturated group, a monomer (B) containing an ethylenically unsaturated group, and a photopolymerization initiator (C). The urethane polymer (A) containing an ethylenically unsaturated group is a product of reaction among a polyoxyalkylene polyol (a1), polyisocyanates (a2), and either an ethylenically unsaturated hydroxylated compound (a3-1) or an ethylenically unsaturated compound (a3-2) containing an isocyanato group. The polyisocyanates (a2) comprise a polyisocyanate (a2-1) containing an ethylenically unsaturated group and a polyisocyanate (a2-2) containing no ethylenically unsaturated group.
Provided is a fluorine-containing ether compound that has excellent abrasion resistance even when the thickness thereof is low, and that can form a lubrication layer in which a reduction in film thickness caused by spin-off is unlikely to occur. This fluorine-containing ether compound is represented by the following formula: R1-R222-R322-O-R4-R5(R3represents a perfluoropolyether chain. R1and R5each represent either an alkyl group optionally having a substituent group, or a hydrocarbon group having a double bond or a triple bond. R2and R4each represent a divalent linkage group having one or more heteroatoms, each have one or more polar groups, and respectively have a heteroatom at the outermost terminal on the side where a bond is formed with R1and R5. At least one of R2or R4includes one or more secondary amine structures. At least one of R1-R2- or -R4-R5 has one or more cyano groups.)
C07C 255/24 - Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
G11B 5/725 - Protective coatings, e.g. anti-static containing a lubricant
C10M 105/54 - Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing halogen containing carbon, hydrogen, halogen and oxygen
C10M 107/38 - Lubricating compositions characterised by the base-material being a macromolecular compound containing halogen
31.
ETHYLENICALLY UNSATURATED GROUP-CONTAINING URETHANE POLYMER, METHOD FOR PRODUCING SAME, AND ADHESIVE COMPOSITION
Provided are: an ethylenically unsaturated group-containing urethane polymer able to suppress a change in the gel fraction of a cured product even under conditions of high temperature and high humidity; a method for producing same; and an adhesive composition obtained using the urethane polymer. This ethylenically unsaturated group-containing urethane polymer is a product of a reaction between: a urethane prepolymer, which is a product of a reaction between a polyoxyalkylene polyol (a1) and a polyisocyanate (a2); and a hydroxyl group-containing ethylenically unsaturated compound (a3-1) or an isocyanate group-containing ethylenically unsaturated compound (a3-2). The polyisocyanate (a2) contains a polyisocyanate (a2-1) that contains an ethylenically unsaturated group and a polyisocyanate (a2-2) that does not contain an ethylenically unsaturated group. A structure derived from the polyisocyanate (a2-1) that contains an ethylenically unsaturated group is present in at least the central region of the main chain of the ethylenically unsaturated group-containing urethane polymer.
A photosensitive resin composition comprising an alkali-soluble resin, an alkoxysilylated resin, a reactive diluent, a photo-radical polymerization initiator, and a solvent, wherein the alkali-soluble resin contains a constituent unit (a-1) derived from a compound having an ethylenically unsaturated group and containing an aromatic group, has an acid group and a (meth)acryloyloxy group, has an ethylenically-unsaturated-group equivalent of 400-2,500 g/mol, and contains the constituent unit (a-1) in an amount of 15-60 mol% with respect to all the repeating constituent units of the alkali-soluble resin and the alkoxysilylated resin includes a constituent unit derived from a compound having an ethylenically unsaturated group and containing an alkoxysilyl group.
A method for manufacturing a bonded body, having: a pre-bonding step in which a substrate A, a solid bonding agent, and a substrate B are positioned in this order to prepare a layered body, said solid bonding agent having, as the primary component thereof, an amorphous thermoplastic resin that is a thermoplastic epoxy resin and/or a phenoxy resin; and a bonding step in which the layered body is heated and pressurized to melt the solid bonding agent, and the substrate A and the substrate B are bonded, wherein the amorphous thermoplastic resin has an epoxy equivalent of 1,600 or greater or the amorphous thermoplastic resin does not include an epoxy group, and the heat of fusion of the amorphous thermoplastic resin is 15 J/g or less.
B29C 65/48 - Joining of preformed partsApparatus therefor using adhesives
C09J 5/06 - Adhesive processes in generalAdhesive processes not provided for elsewhere, e.g. relating to primers involving heating of the applied adhesive
C09J 163/00 - Adhesives based on epoxy resinsAdhesives based on derivatives of epoxy resins
A physical property prediction device for predicting a physical property of a compound. The physical property prediction device comprises: a creation unit which uses a first stage of synthesis information and synthesis result information as learning data to create a first stage of a trained model; a creation unit which uses an nth (n≧2) stage of synthesis information, an nth stage of synthesis result information, and an n-1th stage of synthesis result information as learning data to create a second stage to a final stage of trained models; an accepting unit for accepting a setting of synthesis information about a compound of which a physical property is to be predicted; a prediction unit for predicting a physical property value of a product synthesized by a first stage of chemical reaction of the compound; a prediction unit for repeating a process of predicting a physical property value of a product synthesized by an nth stage of chemical reaction of the compound from a second stage of the compound to a final stage of chemical reaction; and an output unit for outputting the predicted physical property value.
Provided are composite carbon particles with which it is possible to obtain a lithium ion secondary battery exhibiting improved cycle characteristics. The composite carbon particles each contain a porous carbon material and a silicon component. The silicon component is included in at least a portion of pores of the porous carbon material. The composite carbon particles contain phosphorus elements at an amount not less than 40 mass ppm but less than 8000 mass ppm.
The present invention is able to provide a radically polymerizable resin composition which is capable of suppressing change in the strength of a cured product thereof due to exposure to a high temperature environment. A radically polymerizable resin composition according to the present invention contains (A) a radically polymerizable resin, (B) an ethylenically unsaturated compound, (C) a hindered phenolic compound and (D) a hindered amine compound.
The present invention provides an aluminum alloy extrusion having a high tensile strength and a high offset yield strength at low cost. The aluminum alloy extrusion comprises 0.90 mass% to 2.00 mass% Si, 0.65 mass% to 0.90 mass% Mg, 0.25 mass% to 0.50 mass% Cu, 0.050 mass% to 0.49 mass% Fe, 0.10 mass% to 0.25 mass% Zr, 0.010 mass% to 0.10 mass% Ti, and an amount of B that, by mass, is 0.050 to 1.0 times the amount of Ti, with the remainder being made up of Al and unavoidable impurities. In a cross-section of aluminum alloy extrusion perpendicular to the extrusion direction, the area ratio occupied by crystal grains having an aspect ratio of 5.0 or below and a length in the long axis direction of 50 μm to 1000 μm is greater than or equal to 90.0%, and the electrical conductivity of the surface is less than or equal to 51.1 IACS%.
C22C 21/02 - Alloys based on aluminium with silicon as the next major constituent
C22F 1/00 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
C22F 1/043 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with silicon as the next major constituent
C22F 1/05 - Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys of the Al-Si-Mg type, i.e. containing silicon and magnesium in approximately equal proportions
38.
DRY ETCHING METHOD, METHOD FOR PRODUCING SEMICONDUCTOR ELEMENT, AND CLEANING METHOD
The present invention provides a dry etching method that is capable of selectively etching an etching object, which contains lanthanum, over a non-etching object at a sufficient etching rate without using a plasma. This dry etching method comprises a dry etching step in which an etching gas that contains nitrosyl fluoride is brought into contact with a member (12) to be etched, which comprises an etching object that is to be etched by the etching gas and a non-etching object that is not to be etched by the etching gas, and the etching object is selectively etched over the non-etching object without using a plasma. The etching object contains lanthanum.
H01L 21/302 - Treatment of semiconductor bodies using processes or apparatus not provided for in groups to change the physical characteristics of their surfaces, or to change their shape, e.g. etching, polishing, cutting
An information processing system including an annealing-type calculation device using an Ising model and a material composition searching device that converts a combination optimization problem of material compositions asymptotic to a target physical property value into the Ising model to make the calculation device solve the combination optimization problem, the information processing system further including: an input reception unit that receives input of a target value of at least one physical property; a conversion unit that converts a mathematical expression formulating the combination optimization problem of the material compositions asymptotic to the target value among mixed materials of materials having known physical property values into the Ising model of a data type that can be used by the calculation device; an optimized solution calculation unit that uses the Ising model to calculate an optimized solution of the material compositions asymptotic to the target value; and an output control unit that outputs the optimized solution of the material compositions asymptotic to the calculated target value, wherein the mathematical expression is formulated so that, of the material compositions asymptotic to the target value, a material composition containing a larger number of materials is less likely to be calculated as the optimized solution, and a material composition containing a smaller number of materials is more likely to be calculated as the optimized solution.
This information processing system, comprising an annealing-type computing device employing an Ising model, and a material composition search device which converts a material composition combinatorial optimization problem that asymptotically approaches a target physical property value into an Ising model, and causes the computing device to solve the same, includes: an input accepting unit for accepting input of a target value and an allowable variation range of a physical property; a converting unit for converting a formula formulating the material composition combinatorial optimization problem that asymptotically approaches the target value into an Ising model having a data format that can be used by the computing device; an optimal solution calculating unit for using the Ising model to calculate an optimal solution for the material composition that asymptotically approaches the target value; a post-processing unit for performing post-processing to exclude a material contained in a mixed material from the optimal solution of the material composition, within the allowable variation range of the target value; and an output control unit for outputting the post-processed material composition.
Provided is a highly sensitive chemical amplification photosensitive resin composition containing a metal complex dye. This positive photosensitive resin composition contains: (A) a first resin having multiple alkali-soluble functional groups in which at least a portion of the multiple alkali-soluble functional groups is protected by acid-decomposable groups, (B) a photoacid generator, and (C) a metal complex dye, wherein the metal complex dye (C) contains 50 to 94 mass% metal complex ions.
G03F 7/039 - Macromolecular compounds which are photodegradable, e.g. positive electron resists
H01L 27/32 - Devices consisting of a plurality of semiconductor or other solid-state components formed in or on a common substrate including components using organic materials as the active part, or using a combination of organic materials with other materials as the active part with components specially adapted for light emission, e.g. flat-panel displays using organic light-emitting diodes
H05B 33/12 - Light sources with substantially two-dimensional radiating surfaces
H01L 51/50 - Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes (OLED) or polymer light emitting devices (PLED)
H05B 33/22 - Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of auxiliary dielectric or reflective layers
42.
AQUEOUS RESIN COMPOSITION, COATING FILM, COATING FILM PRODUCTION METHOD, AND AQUEOUS RESIN COMPOSITION SET
An aqueous resin composition comprising an aqueous resin emulsion (α), a curing agent (β), and a curing accelerator (γ), wherein the aqueous resin emulsion (α) contains a copolymer (X), a polyepoxy compound (Y), and an aqueous medium (Z), the copolymer (X) includes structural units derived from a (meth)acrylic acid ester (A) and structural units derived from an ethylenically unsaturated carboxylic acid (B), the structural units derived from the (meth)acrylic acid ester (A) include a structural unit derived from a hydrophilic (meth)acrylic acid ester (A1), one or both of the copolymer (X) and the polyepoxy compound (Y) include a carboxy group, the curing agent (β) contains an aromatic polyamine (F) having active hydrogen, and the curing accelerator (γ) contains a tertiary amine not having active hydrogen.
C08L 33/00 - Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereofCompositions of derivatives of such polymers
Provided is a method for producing 1,2,3,4-tetrachloro-1-fluorobutane, which serves as a starting material that enables the production by a stable reaction of 1,2,3,4-tetrachloro-1,1,2,3,4,4-hexafluorobutane. The method for producing 1,2,3,4-tetrachloro-1-fluorobutane comprises a chlorination step of obtaining 1,1,2,3,4-pentachlorobutane by chlorinating 1,2,3,4-tetrachlorobutane by reacting 1,2,3,4-tetrachlorobutane with chlorine gas by a photoreaction in the liquid phase; and a fluorination step of obtaining 1,2,3,4-tetrachloro-1-fluorobutane by fluorinating the 1,1,2,3,4-pentachlorobutane yielded by the chlorination step.
Provided is a method for producing 1,2,3,4-tetrachloro-1,1,4,4-trifluorobutane as a raw material from which 1,2,3,4-tetrachloro-1,1,2,3,4,4-hexafluorobutane can be produced through a stable reaction. The method for producing 1,2,3,4-tetrachloro-1,1,4-trifluorobutane comprises: a chlorination step in which chlorine gas is reacted through photoreaction with 1,2,3,4-tetrachlorobutane in a liquid phase and 1,2,3,4-tetrachlorobutane is chlorinated to obtain 1,1,1,2,3,4,4-heptachlorobutane; and a fluorination step in which 1,1,1,2,3,4,4-heptachlorobutane obtained in the chlorination step is fluorinated to obtain 1,2,3,4-tetrachloro-1,1,4-trifluorobutane.
The present invention provides: a nonaqueous secondary battery electrode binder which enables a significant improvement of discharge capacity retention rate after charge and discharge cycles, while improving flexibility of an electrode active material layer that is formed on a collector; a composition of this nonaqueous secondary battery electrode binder; and a nonaqueous secondary battery electrode. This nonaqueous secondary battery electrode binder contains a copolymer (P). The copolymer (P) comprises: a main chain that is composed of carbon-carbon bonds; a substituent that has an amide bond and is bonded to the main chain; a substituent that has a salt of a carboxy group; and a substituent (c) that is represented by general formula (1). The amount of the amide bond contained per 1 g of the copolymer (P) is from 0.050 to 5.0 mmol/g; the amount of the substituent (b1) is from 5.0 to 12.0 mmol/g; and the amount of the substituent (c) is from 0.15 × 10-2to 8.0 × 10-2 mmol/g.
One embodiment of the present invention provides composite particles which contain silicon and carbon, while having the following characteristics. If the cross-sectional diameter and the silicon content ratio of each one of the composite particles are measured by means of cross-sectional SEM-EDS of the composite particles, and composite particles having a cross-sectional diameter that is not more than half the number average of the cross-sectional diameters are defined as small-diameter composite particles, the proportion of the number of small-diameter composite particles in the number of measured composite particles is from 5% to 50%, the ratio of the average silicon content ratio (% by mass) of particles other than the small-diameter composite particles to the average silicon content ratio (% by mass) of the small-diameter composite particles is 0.90 or less, and the silicon content ratio of the entire composite particles is 45% by mass or more.
The present invention addresses the problem of providing a negative electrode active material for lithium-ion secondary batteries that suppresses temporal oxidation and has excellent coulombic efficiency and cycle characteristics. Composite particles (A) according to the present invention, in which inorganic particles and a polymer are present in at least a portion of the surface of Si-C composite particles including silicon and a carbon material, have a polymer content of 0.1 to 10.0 mass% and a peak that is present in 450 to 495 cm-1SiSiGDGG) is 0.50 or more and less than 1.25. When an XRD pattern is subjected to powder XRD measurement using Cu-Kα radiation, (peak intensity of SiC111 surface)/(peak intensity of Si111 surface) is 0.01 or less.
This method for producing a silicon-carbon composite involves passing a silane-containing gas into a reactor filled with porous carbon particles, pyrolyzing the silane in the silane-containing gas and precipitating the silicon in the pores of the porous carbon particles, wherein the reactor is provided with a silane-containing gas passage that leads from a silane-containing gas inlet to an exhaust gas outlet, the porous carbon particles are filled in the silane-containing gas passage, the reaction temperature in the silane-containing gas passage is 330°C-450°C, and has a temperature distribution that rises from the silane-containing gas inlet towards the exhaust gas outlet; defining the reaction temperature of the porous carbon particles in the silane-containing gas passage at the silane-containing gas inlet end as Tup, the reaction temperature at the midpoint between the silane-containing gas inlet end and the exhaust gas outlet end as Tmid, and the reaction temperature at the exhaust gas outlet end as Tdown, it holds that 0°C < Tmid – Tup ≤ 70°C and 0°C ≤ Tdown – Tmid ≤ 50°C.
C01B 32/05 - Preparation or purification of carbon not covered by groups , , ,
C01B 33/029 - Preparation by decomposition or reduction of gaseous or vaporised silicon compounds other than silica or silica-containing material by decomposition of monosilane
H01M 4/36 - Selection of substances as active materials, active masses, active liquids
H01M 4/38 - Selection of substances as active materials, active masses, active liquids of elements or alloys
49.
PREDICTION DEVICE, LEARNING DEVICE, PREDICTION METHOD, LEARNING METHOD, PREDICTION PROGRAM, AND LEARNING PROGRAM
The present invention improves the prediction accuracy of a prediction device that uses a trained model. This prediction device includes: a first trained model and a second trained model to each of which is inputted input data to be predicted, and which thereby respectively output first output data and second output data; and an output unit which acquires the first and second output data, and outputs prediction data by calculating a weighted average value or by taking a weighted majority. The first trained model is configured so as to have higher prediction accuracy for input data of an interpolation area than the second trained model, and the second trained model is configured so as to have higher prediction accuracy for input data of an extrapolation area than the first trained model.
The present invention provides: titanium oxide particles which exhibits excellent uniformity and excellent dispersibility, while containing less coarse particles; a method for producing the titanium oxide particles; and a slurry, a dispersion, a composition and a dielectric starting material, each of which contains the titanium oxide particles. With respect to the titanium oxide particles according to the present invention, the D90(LD)/D50(LD) of the titanium oxide particles as determined by a laser diffraction/scattering method is more than 1.0 but not more than 2.0; and the concentration (on a number basis) of coarse particles relative to D50 (SEM) of primary particles as determined by the observation with a field-emission scanning electronic microscope is 20 ppm or less, the coarse particles having a size more than 16 times the D50 (SEM). During the production of the titanium oxide particles, when a starting material gas and an oxidizing gas are introduced into a reaction tube so as to be reacted with each other, the inner wall of the reaction tube is provided with a blow-off opening for a purge medium and the blow-off angle of the purge medium and the blow-off rate (B) of the purge medium from the inner wall of the reaction tube are set so that the purge medium whirls along the inner wall of the reaction tube.
Provided is a method for producing bromofluoromethane, the method making it possible to selectively synthesize tribromofluoromethane and/or dibromodifluoromethane. This method for producing bromofluoromethane has a fluorination step for reacting a fluorinating agent with a raw-material compound that is carbon tetrabromide and/or tribromofluoromethane in the presence of a simple substance or a salt of a metal belonging to period 3 or 4 of the periodic table and belonging to any of groups 3 through 13 to carry out fluorination and synthesize a target compound that is tribromofluoromethane and/or dibromodifluoromethane. However, the raw-material compound and the target compound are not the same.
Provided is an etching method by which an etching object containing silicon nitride can be selectively etched compared to a non-etching object, while suppressing the generation of particles and variations in etching rate. This etching method comprises an etching step in which an etching gas containing more than 20 vol% of nitrosyl fluoride is brought into contact with a member (12) to be etched, which has an etching object that is to be etched by the etching gas and a non-etching object that is not to be etched by the etching gas, and without using plasma, the etching object is selectively etched in comparison to the non-etching object. The etching object contains silicon nitride.
H01L 21/302 - Treatment of semiconductor bodies using processes or apparatus not provided for in groups to change the physical characteristics of their surfaces, or to change their shape, e.g. etching, polishing, cutting
53.
DECOMPOSING/CLEANING COMPOSITION, METHOD FOR PRODUCING SAME, AND METHOD FOR CLEANING ADHESIVE POLYMER
Provided is a decomposing/cleaning composition having a high etching speed. The decomposing/cleaning composition contains: (A) an N-substituted amide compound, in which 2 alkyl groups are bonded to an amide nitrogen atom, as an aprotic solvent; and (B) a quaternary ammonium alkyl fluoride or a hydrate thereof. The content of an N-substituted amide acid derivative, which is a compound in which 2 hydrogen atoms on a carbon atom at the α-position of the amide nitrogen atom of the N-substituted amide compound (A) are substituted with oxo groups, is 550 ppm by mass or less.
288, containing at least lithium, tantalum, boron, phosphorus, oxygen and fluorine as the constituent elements thereof, having a boron content represented by formula (1) of 4.0-15.0%, and having a fluorine content represented by formula (2) of 0.5-2.0%. (1): Number of B atoms/(number of B atoms + number of P atoms) × 100 (2): Number of F atoms/(number of O atoms + number of F atoms) × 100
H01M 4/58 - Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFySelection of substances as active materials, active masses, active liquids of polyanionic structures, e.g. phosphates, silicates or borates
H01B 1/08 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances oxides
C04B 35/495 - Shaped ceramic products characterised by their compositionCeramic compositionsProcessing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxides based on vanadium, niobium, tantalum, molybdenum or tungsten oxides or solid solutions thereof with other oxides, e.g. vanadates, niobates, tantalates, molybdates or tungstates
Provided are a recess filling material kit, a cured product of the recess filling material kit, and a recess filling method using the recess filling material kit, whereby it becomes possible to provide, for example, a technique for preventing defective working including a defect in initial adhesion to a concrete material and a steel iron material used in recesses. The recess filling material kit according to the present invention includes a first radical-polymerizable resin composition and a second radical-polymerizable resin composition. The first radical-polymerizable resin composition comprises a first radical-polymerizable compound (A-1), a first radical-polymerizable unsaturated monomer (B-1), an acidic compound (C) and a first radical-polymerization initiator (D-1), and the second radical-polymerizable resin composition comprises a second radical-polymerizable compound (A-2), a second radical-polymerizable unsaturated monomer (B-2), a second radical-polymerization initiator (D-2), an expansion material (J) and an aggregate (K).
Provided are: a recess filling material kit which is capable of providing a construction method and the like that eliminates construction defects such as initial adhesion to a concrete material or a steel material used in a recess; a cured product thereof; and a method for filling a recess using the recess filling material kit. The recess filling material kit according to the present invention has first and second radical polymerizable resin compositions. The first radical polymerizable resin composition contains a first radical polymerizable compound (A-1), a first radical polymerizable unsaturated monomer (B-1), an acidic compound (C), and a first radical polymerization initiator (D-1). The second radical polymerizable resin composition contains a second radical polymerizable compound (A-2), a second radical polymerizable unsaturated monomer (B-2), a second radical polymerization initiator (D-2), an expansion material (J), cement (P), and aggregate (K).
Provided is a high-sensitivity photosensitive resin composition which contains a black colorant and by which development and pattern formation are possible even at low amounts of light exposure. This photosensitive resin composition comprises: (A) a binder resin; (B1) a first quinone diazide adduct, which is a quinone diazide adduct to a first phenol compound; (B2) a second quinone diazide adduct, which is a quinone diazide adduct to a second phenol compound; and (C) a black colorant. The difference between the molecular weight of the first phenol compound and the molecular weight of the second phenol compound is 40-500. The molecular weight of the first phenol compound is smaller than the molecular weight of the second phenol compound.
H05B 33/12 - Light sources with substantially two-dimensional radiating surfaces
H01L 51/50 - Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes (OLED) or polymer light emitting devices (PLED)
H05B 33/22 - Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of auxiliary dielectric or reflective layers
58.
FLUOROETHER COMPOUND, LUBRICANT FOR MAGNETIC RECORDING MEDIUM, AND MAGNETIC RECORDING MEDIUM
A fluoroether compound represented by the formula R122- R222- R322-R422-R522-R622-R7(where R2, R4, and R6are each a perfluoropolyether chain, R3is formula (2), R5is formula (3), and R1and R7 are each independently a terminal group including two or three polar groups, wherein the polar groups have been bonded respectively to different carbon atoms and the carbon atoms having the polar groups bonded thereto have been bonded to each other by a linking group including a carbon atom having no polar group bonded thereto).
Provided is a fluorine-containing ether compound represented by the following formula. R122-R222-R322-R422-R522-R622-R7(R2, R4, and R6are perfluoropolyether chains having the same structure; R3and R5are each independently a connecting group including one or more hydroxyl groups; and R1and R72s22OH (2) (s is 0 or 1; [D] and [E] are each independently a chain-like structure constituted of a combination of 2-5 methylene groups and one oxygen atom or a chain-like structure constituted of 1-4 methylene groups, with the proviso that, when s is 0 and [E] includes an oxygen atom, the number of methylene groups included in [E] is 3 or more.)
C07C 43/13 - Saturated ethers containing hydroxy or O-metal groups
C08G 65/331 - Polymers modified by chemical after-treatment with organic compounds containing oxygen
C08G 67/00 - Macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing oxygen or oxygen and carbon, not provided for in groups
C10M 107/38 - Lubricating compositions characterised by the base-material being a macromolecular compound containing halogen
G11B 5/725 - Protective coatings, e.g. anti-static containing a lubricant
G11B 5/84 - Processes or apparatus specially adapted for manufacturing record carriers
C10N 30/06 - OilinessFilm-strengthAnti-wearResistance to extreme pressure
C10N 30/12 - Inhibition of corrosion, e.g. anti-rust agents, anti-corrosives
C10N 40/18 - Electric or magnetic purposes in connection with recordings on magnetic tape or disc
60.
HEAT CONDUCTIVE URETHANE RESIN COMPOSITION AND CURED PRODUCT
This heat conductive urethane resin composition contains a castor oil-based polyol, a polyisocyanate compound, and a filler, the heat conductive urethane resin composition being characterized in that: the equivalent ratio (NCO/OH) of the isocyanate group of the polyisocyanate compound to the hydroxyl group of the castor oil-based polyol is 0.8-1.6; the filler contains a filler (A) having an average particle diameter of 0.03-10 μm; and the filler (A) is surface-treated by using a specific surface treatment agent.
[Problem] To provide a silver nanowire manufacturing method by which silver nanoparticles can be efficiently removed from a coarse dispersion liquid containing silver nanowires and the silver nanoparticles. [Solution] A silver nanowire manufacturing method characterized by including a coarse dispersion liquid preparation step for preparing a coarse dispersion liquid containing silver nanowires and silver nanoparticles and a reprecipitation/cleaning step for refining the silver nanowires in the coarse dispersion liquid by means of a reprecipitation method, wherein in the reprecipitation/cleaning step, a series of operations, which comprise (a) a precipitation step for causing silver nanowire-containing precipitates to precipitate by adding a precipitation solvent to the coarse dispersion liquid or to a redispersion liquid described below, (b) a supernatant removal step for removing a supernatant containing at least some of the silver nanoparticles formed by the precipitation of the precipitates, and (c) a redispersion step for obtaining a redispersion liquid by redispersing the precipitates in water by adding water having a specific resistance value of 3.3 MΩ·cm or higher to the remaining precipitates, are repeated several times.
B22F 9/24 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
B82Y 40/00 - Manufacture or treatment of nanostructures
H01B 13/00 - Apparatus or processes specially adapted for manufacturing conductors or cables
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
[Problem] To provide a method for forming different transparent conductive patterns on both main surfaces of a transparent resin film using a pulse laser. [Solution] First and second transparent conductive films containing a nanostructure network having a metal nanowire intersecting part and a binder resin are formed on first and second main surfaces of a transparent resin film. The first and second transparent conductive films have an absorption peak based on the nanostructure network in a light transmittance spectrum. The transparent resin film has a thickness of 40 μm or more. After the formation of first and second protection films on the first and second transparent conductive films, only the first transparent conductive film is etched from the first protection film side by a pulse laser having a pulse width of one nanosecond or shorter and having an absorption peak maximum wavelength based on the nanostructure network of within ±30 nm, and a first transparent conductive pattern is formed on the first main surface from a first conductive region and a first non-conductive region formed from the first transparent conductive film.
[Problem] To provide a method for forming different transparent conductive patterns for both principal surfaces of a transparent resin film by using a pulse laser. [Solution] With respect to a transparent conductive film in which first and second transparent conductive layers and first and second protective layers are sequentially formed, each of the first and second transparent conductive layers including a binder resin and a nano-structured network that has intersection sections of metal nanowires on first and second respective principal surfaces of a resin film including a base resin and an ultraviolet absorber, and which, in a light transmission spectrum, has a light transmittance of 10% or smaller in a wavelength region of 350-370 nm and of 80% or larger in a wavelength region of 350-700 nm of a film of the base resin having the same thickness as the resin film, etching is performed only on the first transparent conductive layer from a first protective layer side by means of a pulse laser of which the wavelength is within a range of 350-370 nm and of which the pulse width is shorter than 1 nano second, and a first transparent conductive pattern is formed with a first conductive area and a first non-conductive area.
Provided is a spreading agent that has a high water solubility and can effectively enhance the adhesion force of a fertilizer component or an agricultural chemical to a plant. This spreading agent contains at least one oligosaccharide selected from the group consisting of a chitin oligosaccharide, a cello-oligosaccharide and a xylo-oligosaccharide.
C05G 3/70 - Mixtures of one or more fertilisers with additives not having a specifically fertilising activity for affecting wettability, e.g. drying agents
65.
MATERIAL CHARACTERISTICS PREDICTION METHOD AND MODEL GENERATION METHOD
The present invention includes: a model setting step for setting a trained model obtained by performing machine learning of the correspondence relationship between explanatory variables that each include information relating to a production condition or a material composition of a target material and response variables that each include information relating to material characteristics of the target material; and a prediction step for inputting, to the trained model that have been set in the model setting step, an explanatory variable relating to the target material for which material characteristics are to be predicted, outputting a response variable relating to information of the explanatory variable, and predicting the material characteristics of the target material to be predicted on the basis of the response variable. The explanatory variable further includes: a material characteristics evaluation temperature that is a temperature at the time of measurement of material characteristics and that is included in the response variable; and an evaluation temperature retention time in which the material characteristics evaluation temperature has been retained until measurement of the material characteristics.
G06F 30/27 - Design optimisation, verification or simulation using machine learning, e.g. artificial intelligence, neural networks, support vector machines [SVM] or training a model
The present invention provides an etching gas and an etching method, each of which is capable of selectively etching an etching object comprising silicon nitride over a non-etching object. The etching gas contains nitrosyl fluoride, while containing nitryl fluoride as an impurity; and the concentration of the nitryl fluoride is from 0.0001 ppm by mass to 100 ppm by mass. The etching method comprises an etching step in which this etching gas is brought into contact with a member (12) to be etched, which comprises an etching object that is to be etched by an etching gas and a non-etching object that is not to be etched by an etching gas, thereby selectively etching the etching object over the non-etching object. The etching object comprises silicon nitride.
Provided is a hydrogen fluoride gas removal device capable of continuously performing a removal process for removing hydrogen fluoride gas from a mixed gas containing hydrogen fluoride gas over an extended period of time without stopping. The hydrogen fluoride removal device can remove hydrogen fluoride gas from a mixed gas that contains hydrogen fluoride gas and other gases. This hydrogen fluoride removal device is equipped with a hydrogen fluoride gas removal processor (10) for performing a process to remove hydrogen fluoride gas from a mixed gas by bringing the mixed gas into contact with a removal agent for removing hydrogen fluoride gas from mixed gas, a removal agent supplier (20) for supplying the removal agent to the hydrogen fluoride gas removal processor (10), a removal agent regeneration processor (30) for subjecting used removal agent to a regeneration process to improve the hydrogen fluoride gas removal performance of the removal agent, and a regenerated removal agent transporter (40) for transporting the regenerated removal agent and supplying the regenerated removal agent to the removal agent supplier (20).
B01D 53/08 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by adsorption, e.g. preparative gas chromatography with moving adsorbents according to the "moving bed" method
B01J 20/04 - Solid sorbent compositions or filter aid compositionsSorbents for chromatographyProcesses for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
Provided is a hydrogen fluoride gas removal device which is insusceptible to adhesion of a removal agent when performing a removal process to remove hydrogen fluoride gas from a mixed gas containing hydrogen fluoride gas by using the removal agent. The hydrogen fluoride gas removal device can remove hydrogen fluoride gas from a mixed gas containing the hydrogen fluoride gas and another type of gas. This hydrogen fluoride gas removal device comprises: a hydrogen fluoride gas removal processing unit (10) which performs a process to remove hydrogen fluoride gas from a mixed gas by bringing the mixed gas into contact with a removal agent for removing the hydrogen fluoride gas from the mixed gas; a removal agent supplying unit (20) which supplies the removal agent to the hydrogen fluoride gas removal processing unit (10); a removal agent moving unit which moves the removal agent stored in the hydrogen fluoride gas removal processing unit (10) inside the hydrogen fluoride gas removal processing unit (10); and a removal agent discharging unit which discharges the used removal agent from the hydrogen fluoride gas removal processing unit (10).
B01D 53/08 - Separation of gases or vapoursRecovering vapours of volatile solvents from gasesChemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by adsorption, e.g. preparative gas chromatography with moving adsorbents according to the "moving bed" method
B01J 20/04 - Solid sorbent compositions or filter aid compositionsSorbents for chromatographyProcesses for preparing, regenerating or reactivating thereof comprising inorganic material comprising compounds of alkali metals, alkaline earth metals or magnesium
A composite laminate comprising a base material formed of a metal or a resin, and one or more resin primer layers laminated on a surface of the base material, wherein at least one of the resin primer layers is at least one polymer layer selected from the group consisting of polymer layers each formed of a polymer of an in-situ polymerization type thermoplastic resin composition that contains the following (A), polymer layers each formed of a polymer of an in-situ polymerization type thermoplastic resin composition that contains the following (B), polymer layers each formed of a polymer of an in-situ polymerization type thermoplastic resin composition that contains the following (C), polymer layers each formed of a polymer of an in-situ polymerization type thermoplastic resin composition that contains the following (D), and polymer layers each formed of a polymer of an in-situ polymerization type thermoplastic resin composition that contains the following (E) and any one of (A)-(D), and said polymer layer is disposed at the outermost surface. (A) A combination between a bifunctional thiol compound, and a phenol novolak-type epoxy resin and/or a cresol novolak-type epoxy resin. (B) A combination between a bifunctional amino compound, and a phenol novolak-type epoxy resin and/or a cresol novolak-type epoxy resin. (C) A combination between a bifunctional carboxy compound, and a phenol novolak-type epoxy resin and/or a cresol novolak-type epoxy resin. (D) A combination between a bifunctional isocyanate compound, and a phenol novolak resin and/or a cresol novolak resin. (E) A maleic anhydride-modified polyolefin and/or a chlorinated polyolefin.
A water- and oil-repellent composition that comprises copolymer (A) containing no structural unit having a siloxane bond, copolymer (B) containing a structural unit having a siloxane bond, a polyether-modified polydimethylsiloxane and an aqueous medium, wherein: copolymer (A) contains a structural unit derived from a compound having an ethylenically unsaturated bond and an ester bond and having no carboxy group and a structural unit derived from a compound having an ethylenically unsaturated bond and a carboxy group; and copolymer (B) contains a structural unit derived from a compound having an ethylenically unsaturated bond and an ester bond and having no carboxy group, a structural unit derived from a compound having an ethylenically unsaturated bond and a carboxy group, and a structural unit derived from a polydimethylsiloxane having an ethylenically unsaturated bond.
C09K 3/18 - Materials not provided for elsewhere for application to surface to minimize adherence of ice, mist or water theretoThawing or antifreeze materials for application to surfaces
D06M 15/263 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acidsSalts or esters thereof
D06M 15/647 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
71.
POLYMERIC DISPERSANT, PIGMENT DISPERSION COMPOSITION, AND PHOTOSENSITIVE COLORED COMPOSITION
Provided are a polymeric dispersant having satisfactory pigment-dispersing properties and storage stability and a pigment dispersion composition obtained using the polymeric dispersant. A photosensitive colored composition obtained using the pigment dispersion composition has satisfactory developability and gives cured objects having excellent solvent resistance. Also provided are a color filter including the cured object of the photosensitive colored composition and an image display element including the color filter. This polymeric dispersant has a quaternary ammonium cation group (g-1) having one or more groups selected from the group consisting of an ethylenically unsaturated group and groups each having a carbon-carbon triple bond.
A welding film comprising a phenoxy resin, wherein the Z‐average molecular weight of the phenoxy resin is 70,000 or more, and the ratio [Mz/Mn] of the Z‐average molecular weight with respect to the number average molecular weight of the phenoxy resin is 5.0 or more.
B29C 65/02 - Joining of preformed partsApparatus therefor by heating, with or without pressure
B29C 65/08 - Joining of preformed partsApparatus therefor by heating, with or without pressure using ultrasonic vibrations
B29C 65/20 - Joining of preformed partsApparatus therefor by heating, with or without pressure using heated tool with direct contact, e.g. using "mirror"
Provided is a vehicle on-board camera in which superior airtightness can be achieved, and a method by which such a vehicle on-board camera can be manufactured at low cost. A vehicle on-board camera (10) includes: a case (X) that has at least a first part (12) and a second part (14); and at least one module (Y) that is installed in the case. A first resin member is one of the first part and the second part, and a second resin member is the other of the first part and the second part. The first resin member and the second resin member are welded with a primer layer (3) interposed therebetween. At least one layer of the primer layer is an in situ polymerization type composition layer that is formed by polymerizing an in situ polymerization type composition on a thermoplastic resin material.
The present invention provides a bumper fascia that can achieve a desired rigidity even if the weight thereof is reduced and can achieve a favorable appearance, and a method that can be used to manufacture such a bumper fascia at a low cost. A first resin member (1) is a reinforcing rib and/or a bracket, a second resin member (4) is a bumper fascia main body, the first and second resin members are welded to each other, and at least one primer layer is an in-situ polymerization composition layer formed by polymerizing an in-situ polymerization composition over the thermoplastic resin material.
B60R 19/04 - Bumpers, i.e. impact receiving or absorbing members for protecting vehicles or fending off blows from other vehicles or objects formed from more than one section
75.
BACK DOOR OUTER PANEL AND PRODUCTION METHOD THEREFOR
The present invention provides: a back door outer panel that is capable of achieving a desired rigidity even in the case where weight reduction is pursued and that is also capable of achieving a favorable appearance; and a method with which it is possible to produce such a back door outer panel at low cost. A first resin member (1) serves as a reinforcement rib and/or a bracket. A second resin member (4) serves as a back door outer panel body. The first resin member and the second resin are welded together. At least one of primer layers is an in-situ polymerized-type composition layer that is formed by polymerizing an in-situ polymerizable composition on a thermoplastic resin material.
Provided are: a bumper fascia that achieves desired rigidity even if designed to be lighter and that can achieve a favorable appearance; and a method for enabling the low-cost production of said bumper fascia. A first resin member (1) is a reinforcing rib and/or a bracket. A second resin member (4) is a bumper fascia body. The first resin member and the second resin member are welded, and at least one layer of a primer layer is an in-situ polymerization-type composition layer, which is formed by polymerizing an in-situ polymerization-type composition on the thermoplastic resin material.
B60R 19/04 - Bumpers, i.e. impact receiving or absorbing members for protecting vehicles or fending off blows from other vehicles or objects formed from more than one section
A barrier function improver which contains methylhesperidin as an active ingredient, and a barrier function improver composition which contains said barrier function improver and a pharmaceutically acceptable carrier.
A61K 31/7034 - Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin
A61K 31/7048 - Compounds having saccharide radicals and heterocyclic rings having oxygen as a ring hetero atom, e.g. leucoglucosan, hesperidin, erythromycin, nystatin
A61P 17/16 - Emollients or protectives, e.g. against radiation
Provided are a backdoor outer panel which achieves desired rigidity even when the weight thereof is reduced and with which an excellent appearance can be achieved, and a method capable of manufacturing such a backdoor outer panel at a low cost. In this invention, a first resin member (1) is a reinforcing rib and/or a bracket. A second resin member (4) is a backdoor outer panel body. The first resin member and the second resin member are welded to each other. At least one layer of primer layers is an in-situ polymerization type composition layer formed by polymerizing an in-situ polymerization type composition on a thermoplastic resin material.
Provided are a radar device that can be easily manufactured with a reduced number of components, and a method for manufacturing the same. A first resin member (1) is a case, a second resin member (4) is a radome, the first resin member and the second resin member are welded through a primer layer, and at least one layer of the primer layer is an in-situ polymerized composition layer formed by polymerizing an in-situ polymerizable composition on a thermoplastic resin material.
The present invention provides a method for forming a pattern of a metal oxide, the method being capable of selectively etching an etching object that contains a metal oxide over a non-etching object, while being capable of forming a metal oxide pattern having the shape of the pattern of the non-etching object that serves as a template for the pattern formation of the metal oxide. According to the present invention, a pattern of a metal oxide is formed by etching a metal oxide, which contains an oxide of at least one of tin and indium, with use of an etching gas. According to the present invention, a predetermined pattern of a template layer (21) is transferred to a metal oxide layer (22) by bringing an etching gas that contains a halon into contact with a member to be etched in the presence of a plasma so as to etch the member to be etched, while applying a bias power to a lower electrode (2) that supports the member to be etched, thereby selectively etching the metal oxide layer (22) over a silicon substrate (24), the template layer (21) and a base layer (23).
Provided is a fluorine-containing ether compound represented by the following formula. R1－R222－R322－R4(wherein R1is a terminal group that includes an oxime group and is represented by formula (2), R2is a divalent linking group that has a polar group, R3is a perfluoropolyether chain, and R4 is a terminal group having at least two polar groups; in formula (2), X and Y are each a hydrogen atom, a C1 to C12 alkyl group that may have a substituent, or an organic group that has a double-bond or a triple bond).
C07C 251/54 - Oximes having oxygen atoms of oxyimino groups bound to carbon atoms of substituted hydrocarbon radicals of hydrocarbon radicals substituted by singly-bound oxygen atoms
C10M 107/44 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
G11B 5/725 - Protective coatings, e.g. anti-static containing a lubricant
G11B 5/84 - Processes or apparatus specially adapted for manufacturing record carriers
C10N 40/18 - Electric or magnetic purposes in connection with recordings on magnetic tape or disc
The present invention provides: a novel blocked isocyanate compound that can be produced at high yield; a compound having a low-temperature (at most 100ºC) crosslinkable double bond using said blocked isocyanate compound; and a resin obtained by curing said compound having a double bond. The present invention includes a blocked isocyanate compound (A) in which a compound (a1) having an isocyanate group and a compound (a2) represented by formula (1) and having a hydroxyl group are urethane-bonded via the isocyanate group and the hydroxyl group. (In formula (1), R1and R2are each independently a hydrogen atom or a C1-C20 hydrocarbon group. R3and R4 are each independently a hydrogen atom or a C1-C20 hydrocarbon group.)
C07C 271/16 - Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms
C07C 271/28 - Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring to a carbon atom of a non-condensed six-membered aromatic ring
C08F 8/00 - Chemical modification by after-treatment
C08F 299/00 - Macromolecular compounds obtained by interreacting polymers involving only carbon-to-carbon unsaturated bond reactions, in the absence of non-macromolecular monomers
C08F 220/18 - Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
[Problem] To provide a chlorinated-polyolefin composition, especially one excellent in terms of durability including acid resistance and heat resistance. [Solution] A chlorinated-polyolefin composition which comprises a chlorinated polyolefin and epoxidized polybutadiene.
C08L 23/28 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or halogen-containing compounds
A water- and oil-repellent composition that comprises copolymer (A) containing no structural unit having a siloxane bond, copolymer (B) containing a structural unit having a siloxane bond, a polyether-modified polydimethylsiloxane and an aqueous medium, wherein: copolymer (A) contains structural unit (a1) derived from a compound having an ethylenically unsaturated bond and an ester bond and having no amide bond and structural unit (a2) derived from a compound having an ethylenically unsaturated bond and an amide bond; and copolymer (B) contains structural unit (b1) derived from a compound having an ethylenically unsaturated bond and an ester bond and having no amide bond, structural unit (b2) derived from a compound having an ethylenically unsaturated bond and an amide bond, and structural unit (b3) derived from a polydimethylsiloxane having an ethylenically unsaturated bond.
C09K 3/18 - Materials not provided for elsewhere for application to surface to minimize adherence of ice, mist or water theretoThawing or antifreeze materials for application to surfaces
D06M 15/263 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acidsSalts or esters thereof
D06M 15/285 - Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acid amides or imides
D06M 15/647 - Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
85.
PHOTOSENSITIVE RESIN COMPOSITION AND ORGANIC EL ELEMENT PARTITION
The present invention provides a photosensitive resin composition that is highly sensitive and contains a black colorant, the composition making it possible to form a thick film pattern having a high optical density (OD value). Provided is a photosensitive resin composition containing (A) a first resin that has an epoxy group and a phenolic hydroxyl group, (B) a second resin that has a weight average molecular weight of 3,000 to 80,000, (D) a radiation-sensitive compound, and (E) a black colorant, wherein: the optical density (OD value) of a cured coating obtained from the photosensitive resin composition is 0.5 or higher per 1 μm of film thickness; and the alkaline dissolution rate of the second resin is no more than 5% of the alkaline dissolution rate of the first resin.
H05B 33/12 - Light sources with substantially two-dimensional radiating surfaces
H01L 51/50 - Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes (OLED) or polymer light emitting devices (PLED)
H05B 33/22 - Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of auxiliary dielectric or reflective layers
86.
PHOTOSENSITIVE RESIN COMPOSITION AND ORGANIC EL ELEMENT PARTITION
The present invention provides a photosensitive resin composition that is highly sensitive and contains a black colorant, the composition making it possible to form a thick film pattern having a high optical density (OD value) and limited surface roughness. Provided is a photosensitive resin composition containing (A) a first resin, (B) a second resin that differs from the first resin and has a phenolic hydroxyl group, (C) a third resin that differs from both the first resin and the second resin and has a phenolic hydroxyl group, (D) a radiation-sensitive compound, and (E) a black colorant, wherein: the optical density (OD value) of a cured coating obtained from the photosensitive resin composition is 0.5 or higher per 1 μm of film thickness; and the phenolic hydroxyl group equivalent of the second resin is 1.1 to 5.0 times the phenolic hydroxyl group equivalent of the third resin.
H05B 33/12 - Light sources with substantially two-dimensional radiating surfaces
H01L 51/50 - Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes (OLED) or polymer light emitting devices (PLED)
H05B 33/22 - Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of auxiliary dielectric or reflective layers
87.
PHOTOSENSITIVE RESIN COMPOSITION AND ORGANIC EL ELEMENT PARTITION
The present invention provides a photosensitive resin composition that is highly sensitive and contains a black colorant, the composition making it possible to form a thick film pattern having a high optical density (OD value). Provided is a photosensitive resin composition containing (A) a first resin that has an epoxy group and a phenolic hydroxyl group, (B) a second resin that has a weight average molecular weight of 3,000 to 80,000, a phenolic hydroxyl group equivalent of 250 to 700, and a carboxy group content of 0.0 to 0.5 mmol/g, (D) a radiation-sensitive compound, and (E) a black colorant, wherein the optical density (OD value) of a cured coating obtained from the photosensitive resin composition is 0.5 or higher per 1 μm of film thickness.
H05B 33/12 - Light sources with substantially two-dimensional radiating surfaces
H01L 51/50 - Solid state devices using organic materials as the active part, or using a combination of organic materials with other materials as the active part; Processes or apparatus specially adapted for the manufacture or treatment of such devices, or of parts thereof specially adapted for light emission, e.g. organic light emitting diodes (OLED) or polymer light emitting devices (PLED)
H05B 33/22 - Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of auxiliary dielectric or reflective layers
88.
AQUEOUS RESIN COMPOSITION, FILM, METHOD FOR PRODUCING COATING FILM, AQUEOUS RESIN COMPOSITION SET, AND METHOD FOR PROTECTING METAL
An aqueous resin composition which contains: an aqueous resin emulsion that comprises a copolymer, a polyepoxy compound and an aqueous medium; a curing agent; and a curing accelerator. With respect to this aqueous resin composition, the copolymer comprises a predetermined amount of a structural unit (a) which is derived from a (meth)acrylic acid alkyl ester, a predetermined amount of a structural unit (b) which is derived from an ethylenically unsaturated carboxylic acid, and a predetermined amount of a structural unit (c) which is derived from a compound having an epoxy group; the structural unit (a) comprises a predetermined amount of a structural unit (a1) which is derived from a hydrophilic (meth)acrylic acid alkyl ester; the polyepoxy compound (Y) comprises a predetermined amount of at least one compound that is selected from among bisphenol type epoxy compounds and hydrogenated bisphenol type epoxy compounds; the curing agent comprises a predetermined amount of a compound which has a functional group that is reactive with an epoxy group; and the curing accelerator comprises a predetermined amount of a tertiary amine.
C08F 283/10 - Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass on to polymers containing more than one epoxy radical per molecule
C08G 59/38 - Epoxy compounds containing three or more epoxy groups together with di-epoxy compounds
This aqueous resin composition contains: an aqueous resin emulsion including a copolymer, a polyepoxy compound, and an aqueous medium; a curing agent; and a curing accelerator. The carboxy group content and the epoxy group content within the copolymer are within a predetermined range. The polyepoxy compound does not include any ethylenically unsaturated bonds, includes two or more epoxy groups in the molecule thereof, and is at least one substance selected from among bisphenol-type epoxy compounds and hydrogenated bisphenol-type epoxy compounds. The epoxy group content within the polyepoxy compound is within a predetermined range. The curing agent includes a predetermined amount of a compound having a functional group that is reactive to epoxy groups. The curing accelerator includes a predetermined amount of a tertiary amine having no functional groups that are reactive to epoxy groups.
C08F 283/10 - Macromolecular compounds obtained by polymerising monomers on to polymers provided for in subclass on to polymers containing more than one epoxy radical per molecule
C08G 59/38 - Epoxy compounds containing three or more epoxy groups together with di-epoxy compounds
[Problem] The present invention relates to a chlorinated polyolefin composition, and more specifically relates to a chlorinated polyolefin composition having excellent durability properties such as acid resistance, alkali resistance, and heat resistance. [Solution] A chlorinated polyolefin composition comprising a chlorinated polyolefin and an acid acceptor, wherein the acid acceptor is at least one substance selected from among aliphatic glycidyl ether and epoxidized oil, and the molecular weight of the acid acceptor is not less than 200.
C08L 23/28 - Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bondCompositions of derivatives of such polymers modified by chemical after-treatment by reaction with halogens or halogen-containing compounds
C08L 63/00 - Compositions of epoxy resinsCompositions of derivatives of epoxy resins
The present invention relates to a polychloroprene latex composition, a dipped product, an adhesive, a bonding agent, and a bonded product. The polychloroprene latex composition includes a chloroprene (co)polymer (A) and an aromatic compound (B) having 7-10 carbon atoms. The ratio of the aromatic compound (B) having 7-10 carbon atoms is 0.0012-0.15 parts by mass when the solid content of the polychloroprene latex composition is defined as 100 parts by mass.
[Problem] To provide a silver nano-wire production method having high production capability and allowing for suppression of an increase in diameter during cooling that follows completion of reaction. [Solution] This silver nano-wire production method is characterized by comprising the step of synthesizing a silver nano-wire at a temperature of 120 to 170°C by the polyol reduction method, and the step of cooling, after the end of the silver nano wire synthesis, the reaction solution temperature from the temperature at the time of the end of the reaction to 80°C at a cooling speed of -0.50°C/minute or faster on average.
B22F 9/24 - Making metallic powder or suspensions thereofApparatus or devices specially adapted therefor using chemical processes with reduction of metal compounds starting from liquid metal compounds, e.g. solutions
B22F 1/00 - Metallic powderTreatment of metallic powder, e.g. to facilitate working or to improve properties
93.
ADHESIVE COMPOSITION, COPOLYMER DISPERSION, SET, ADHESIVE TAPE, AND ADHESION METHOD
This adhesive composition comprises a copolymer (A), a crosslinking agent (B), and an aqueous medium, wherein: the copolymer (A) has a structural unit derived from a monomer (a1), a structural unit derived from a monomer (a2) having a carboxy group, and a structural unit derived from a monomer (a3) having an epoxy group; the monomer (a1) is composed of one or both of alkyl (meth)acrylate having only one ethylenically unsaturated bond and hydrocarbon having only one ethylenically unsaturated bond; the content of the structural unit derived from the monomer (a2) with respect to 100 parts by mass of the structural unit derived from the monomer (a1) in the copolymer (A) is 1.0-12 parts by mass; the content of the structural unit derived from the monomer (a3) with respect to 100 parts by mass of the structural unit derived from the monomer (a1) in the copolymer (A) is 0.10-10 parts by mass; the crosslinking agent (B) contains at least one selected from the group consisting of a polycarbodiimide compound, a polyepoxy compound, and a polyisocyanate compound; and the content of the crosslinking agent (B) with respect to 100 parts by mass of the copolymer (A) is 0.010-10 parts by mass.
C09J 133/02 - Homopolymers or copolymers of acidsMetal or ammonium salts thereof
C09J 133/06 - Homopolymers or copolymers of esters of esters containing only carbon, hydrogen and oxygen, the oxygen atom being present only as part of the carboxyl radical
C09J 133/14 - Homopolymers or copolymers of esters of esters containing halogen, nitrogen, sulfur or oxygen atoms in addition to the carboxy oxygen
C09J 163/00 - Adhesives based on epoxy resinsAdhesives based on derivatives of epoxy resins
C09J 179/04 - Polycondensates having nitrogen-containing heterocyclic rings in the main chainPolyhydrazidesPolyamide acids or similar polyimide precursors
The purpose of the present invention is to provide: a resin composition which exhibits good developing performance when used as a photosensitive material, which has excellent storage stability, and which yields a cured product having excellent solvent resistance even if cured at a low temperature; a copolymer that is useful for preparing this resin composition; and a method for producing the copolymer. This copolymer contains a constituent unit (a) having a group represented by formula (1) or formula (2), a constituent unit (b) having a hydroxyl group and a constituent unit (c) having an acid group, and has a glass transition temperature of 30ºC or lower.
C08F 8/00 - Chemical modification by after-treatment
C08F 265/04 - Macromolecular compounds obtained by polymerising monomers on to polymers of unsaturated monocarboxylic acids or derivatives thereof as defined in group on to polymers of esters
C08F 220/36 - Esters containing nitrogen containing oxygen in addition to the carboxy oxygen
C08F 2/44 - Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
SEPARATOR BINDER FOR NONAQUEOUS SECONDARY BATTERIES, SEPARATOR FOR NONAQUEOUS SECONDARY BATTERIES, METHOD FOR PRODUCING SEPARATOR SLURRY FOR NONAQUEOUS SECONDARY BATTERIES, AND NONAQUEOUS SECONDARY BATTERY
The present invention provides a separator binder for nonaqueous secondary batteries and a separator binder composition for nonaqueous secondary batteries, each of which is capable of forming a slurry that has good wettability and coatability with respect to a base material, while enabling a coating layer to have high peel strength and suppressing thermal shrinkage of a separator. A separator binder composition for nonaqueous secondary batteries according to the present invention contains a polymer (A) and a polymer (B). The polymer (A) comprises a primary amide group and a hydroxyl group, while having a main chain that is composed of a bond of carbon atoms; the polymer (B) comprises a hydroxyl group, while having a main chain that is composed of a bond of carbon atoms; the amount of the primary amide group contained per 1 g of the polymer (A) is 7.5 × 10-3mol/g or more; the amount of the hydroxyl group contained per 1 g of the polymer (A) is from 0.50 × 10-3mol/g to 8.0 × 10-3mol/g; and the amount of the hydroxyl group contained per 1 g of the polymer (B) is 8.80 × 10-3 mol/g or more.
H01M 50/446 - Composite material consisting of a mixture of organic and inorganic materials
H01M 50/449 - Separators, membranes or diaphragms characterised by the material having a layered structure
H01M 50/489 - Separators, membranes, diaphragms or spacing elements inside the cells, characterised by their physical properties, e.g. swelling degree, hydrophilicity or shut down properties
Provided is a binder for non-aqueous secondary battery electrodes, that effectively improves peel strength from a current collector of an electrode active material layer and can contribute to a reduction in the internal resistance of a battery and an improvement in cycle characteristics. This binder for non-aqueous secondary battery electrodes includes a copolymer (A) and a copolymer (B). The copolymer (A) has 11th to 13th structural units that are derived from: monomers (a1), (a2) that have an ethylenically unsaturated bond; and an internal cross-linking agent (a3). The copolymer (B) has, among all structural units, 5.0–98 mol%, 0.30–90 mol%, and 0.30–10 mol%, respectively, of 21st to 23rd structural units indicated by formulas (1)–(3). Chemical formula 1 (In formula (2), R1indicates a C1–6 alkyl group that may be branched. In formula (3), R2 indicates a group having an ethylenically unsaturated bond.)
C08G 65/32 - Polymers modified by chemical after-treatment
C08L 25/04 - Homopolymers or copolymers of styrene
C08L 33/06 - Homopolymers or copolymers of esters of esters containing only carbon, hydrogen, and oxygen, the oxygen atom being present only as part of the carboxyl radical
[Problem] To provide a novel solid electrolyte having excellent lithium ion-conductivity. [Solution] A lithium ion-conductive solid electrolyte according to the present invention includes a chalcogenide having a monoclinic crystal structure, wherein the monoclinic crystal has an a-axis length of 9.690-9.711 Å, a b-axis length of 11.520-11.531 Å, and a c-axis length of 10.680-10.695 Å, and has an axis angle β in the range of 90.01-90.08°. An all-solid-state battery according to the present invention comprises: a positive electrode having a positive electrode active material; a negative electrode having a negative electrode active material; and a solid electrolyte layer disposed between the positive electrode and the negative electrode, wherein the solid electrolyte layer includes the lithium ion-conductive solid electrolyte.
H01M 12/06 - Hybrid cellsManufacture thereof composed of a half-cell of the fuel-cell type and of a half-cell of the primary-cell type with one metallic and one gaseous electrode
H01M 12/08 - Hybrid cellsManufacture thereof composed of a half-cell of a fuel-cell type and a half-cell of the secondary-cell type
H01M 4/13 - Electrodes for accumulators with non-aqueous electrolyte, e.g. for lithium-accumulatorsProcesses of manufacture thereof
H01M 4/48 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
H01M 4/485 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of mixed oxides or hydroxides for inserting or intercalating light metals, e.g. LiTi2O4 or LiTi2OxFy
H01M 4/505 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of manganese of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy
H01M 4/525 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides of nickel, cobalt or iron of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy
H01M 4/58 - Selection of substances as active materials, active masses, active liquids of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFySelection of substances as active materials, active masses, active liquids of polyanionic structures, e.g. phosphates, silicates or borates
H01M 4/587 - Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
H01M 4/62 - Selection of inactive substances as ingredients for active masses, e.g. binders, fillers
H01B 1/06 - Conductors or conductive bodies characterised by the conductive materialsSelection of materials as conductors mainly consisting of other non-metallic substances
The present invention easily provides a transparent electroconductive film laminate that is suitable for three-dimensional molding and that has a curved surface. A transparent electroconductive film laminate characterized by having a transparent substrate that is formed from a transparent thermoplastic resin film, a transparent electroconductive film that is formed on at least one principal surface of the transparent substrate and that is configured to include a binder resin and a metal nanowire, and a protective film that contains a resin component formed on the transparent electroconductive film, the transparent electroconductive film laminate moreover being characterized in that: the binder resin contains a copolymer including 70 mol% or more of poly-N-vinyl acetamide and N-vinylacetamide (NVA) as monomer units, and also contains at least one cellulose-based resin; and 94 mass% or more of the resin components constituting the protective film are derived from a thermoplastic resin.
Provided is a molding material which has a low specific gravity and exhibits good moldability. Provided is a molding material that contains: (A) a thermosetting resin; (B) a reactive diluent; (C) a thermoplastic resin; (D) hollow inorganic particles; and (E) a thermal polymerization initiator. The thermosetting resin (A) contains at least an unsaturated polyester resin. The content of the thermoplastic resin (C) is 5-15 mass%. The true density of the hollow inorganic particles (D) is 0.3-0.7 g/cm3. The pressure resistance strength of the hollow inorganic particles (D) is 10 MPa or more. The content of the hollow inorganic particles (D) is 35-70 vol%. If the specific gravity calculated from the blending quantity of the molding material is taken to be the theoretical specific gravity and the specific gravity measured using a test piece obtained by molding a contracted disk specified in JIS K 6911: 2006 by means of compression molding for a molding time of 3 minutes at a molding temperature of 150ºC and a molding pressure of 2 MPa and then cutting is taken to be the measured specific gravity, the difference between the measured specific gravity and the theoretical specific gravity (measured specific gravity minus theoretical specific gravity) is 0.03 or less.
B29C 70/02 - Shaping composites, i.e. plastics material comprising reinforcements, fillers or preformed parts, e.g. inserts comprising combinations of reinforcements and fillers incorporated in matrix material, forming one or more layers, with or without non-reinforced or non-filled layers
C08J 9/32 - Working-up of macromolecular substances to porous or cellular articles or materialsAfter-treatment thereof from compositions containing microballoons, e.g. syntactic foams
Provided is an unsaturated polyester resin composition which has satisfactory resin flowability during molding and can give molded objects excellent in terms of molded-article appearance, dimensional accuracy, and strength and having few burrs. The unsaturated polyester resin composition contains inorganic fillers in an amount in a specific range, the inorganic fillers comprising a specific proportion of three inorganic fillers having respective average particle diameters.
