The present invention is a catalyst comprising:
(i) a compound comprising at least one first metal element selected from boron, magnesium, zirconium, and hafnium, and
(ii) an alkali metal element,
wherein the compound and the alkali metal element are supported on a carrier having silanol groups,
an average particle size of the compound of the first metal element is 0.4 nm or more and 50 nm or less,
the catalyst satisfies the following formula (1):
The present invention is a catalyst comprising:
(i) a compound comprising at least one first metal element selected from boron, magnesium, zirconium, and hafnium, and
(ii) an alkali metal element,
wherein the compound and the alkali metal element are supported on a carrier having silanol groups,
an average particle size of the compound of the first metal element is 0.4 nm or more and 50 nm or less,
the catalyst satisfies the following formula (1):
0.9
×
10
-
21
(
g
/
number
)
≦
X
/
(
Y
×
Z
)
<
10.8
×
10
-
21
(
g
/
number
)
,
formula
(
1
)
in which X is a molar ratio of the alkali metal element to the at least one first metal element in the catalyst, Y is a BET specific surface area of the catalyst (m2/g), and Z is a number of the silanol groups per unit area (number/nm2).
B01J 37/02 - Impregnation, coating or precipitation
C07C 67/347 - Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
In a partitioning member that is accommodated in a battery assembly to partition single cells and in which a liquid is sealed, an opening position of the partitioning member that opens upon receiving heat generated from the single cells is defined at a specific spot at a peripheral edge portion or a surface of the partitioning member. A partitioning member 1 includes a sealing portion 32 formed by sealing edge portions of multilayer sheets 31, 31 each including a resin layer and a metal layer in a band-like manner, a liquid and a heat insulation material 2 are sealed in an internal space surrounded by the sealing portion 32, and a weak seal strength portion 4A protruding from a side facing the internal space to an edge portion side of the sealing portion 32 is provided in the sealing portion 32.
H01M 10/647 - Prismatic or flat cells, e.g. pouch cells
H01M 50/209 - Racks, modules or packs for multiple batteries or multiple cells characterised by their shape adapted for prismatic or rectangular cells
H01M 50/211 - Racks, modules or packs for multiple batteries or multiple cells characterised by their shape adapted for pouch cells
H01M 50/293 - Mountings; Secondary casings or frames; Racks, modules or packs; Suspension devices; Shock absorbers; Transport or carrying devices; Holders characterised by spacing elements or positioning means within frames, racks or packs characterised by the material
H01M 50/358 - External gas exhaust passages located on the battery cover or case
H01M 50/682 - Containers for storing liquids; Delivery conduits therefor accommodated in battery or cell casings
3.
RESIN COMPOSITION, MULTILAYER STRUCTURE, MOLDED ARTICLE, AND METHOD FOR PRODUCING RESIN COMPOSITION
A resin composition having excellent thermal stability is provided. The resin composition contains an ethylene-vinyl alcohol copolymer (A) and lycopene (B).
A toner comprising at least a binder resin,
the binder resin including at least a polyester resin,
wherein a content of the polyester resin is 2.5% by mass or more of a total mass of the toner, and
when a total length of a portion of a cross section of a printed article produced by fixing the toner to a PET coated paper sheet under printing conditions including a printing temperature of 175° C., a printing speed of 16 ppm, and a printing density of 0.8 mg/cm2, the portion in which the polyester resin is in contact with the PET coated paper sheet, is defined as A, and a total length of a portion of the cross section, the portion in which the toner is in contact with the PET coated paper sheet, is defined as B, A and B satisfy Formula (1) below.
A toner comprising at least a binder resin,
the binder resin including at least a polyester resin,
wherein a content of the polyester resin is 2.5% by mass or more of a total mass of the toner, and
when a total length of a portion of a cross section of a printed article produced by fixing the toner to a PET coated paper sheet under printing conditions including a printing temperature of 175° C., a printing speed of 16 ppm, and a printing density of 0.8 mg/cm2, the portion in which the polyester resin is in contact with the PET coated paper sheet, is defined as A, and a total length of a portion of the cross section, the portion in which the toner is in contact with the PET coated paper sheet, is defined as B, A and B satisfy Formula (1) below.
0.05
≤
A
/
B
≤
0
.55
(
1
)
A method for producing tert-butyl alcohol, including (i) a step of feeding a raw material liquid including isobutylene and water, to a reactor having a cation exchange resin, and (ii) a step of producing a reaction product including tert-butyl alcohol, by hydration reaction of isobutylene in the reactor, in which, in step (ii), the average superficial linear velocity of the raw material liquid, as calculated in the following expression (I), is 5 m/hour or more,
A method for producing tert-butyl alcohol, including (i) a step of feeding a raw material liquid including isobutylene and water, to a reactor having a cation exchange resin, and (ii) a step of producing a reaction product including tert-butyl alcohol, by hydration reaction of isobutylene in the reactor, in which, in step (ii), the average superficial linear velocity of the raw material liquid, as calculated in the following expression (I), is 5 m/hour or more,
Average linear velocity of raw material liquid (m/hour)=Volume flow rate of raw material liquid (m3/hour)/Cross-sectional area of reactor (m2) (I), and
A method for producing tert-butyl alcohol, including (i) a step of feeding a raw material liquid including isobutylene and water, to a reactor having a cation exchange resin, and (ii) a step of producing a reaction product including tert-butyl alcohol, by hydration reaction of isobutylene in the reactor, in which, in step (ii), the average superficial linear velocity of the raw material liquid, as calculated in the following expression (I), is 5 m/hour or more,
Average linear velocity of raw material liquid (m/hour)=Volume flow rate of raw material liquid (m3/hour)/Cross-sectional area of reactor (m2) (I), and
the volume of an aqueous phase (Vw) in a fluid (fluid A) to the total volume of the fluid A in the reactor is 4 to 12% by volume.
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
C07C 29/80 - Separation; Purification; Stabilisation; Use of additives by physical treatment by distillation
6.
THERMOSETTING RESIN COMPOSITION, THERMALLY CONDUCTIVE RESIN SHEET, HEAT-DISSIPATING LAYERED PRODUCT, HEAT-DISSIPATING CIRCUIT BOARD, SEMICONDUCTOR DEVICE AND POWER MODULE
A thermosetting resin composition containing a thermosetting resin, an inorganic filler, and a polymer having a mass average molecular weight of 10,000 or more, wherein the thermosetting resin composition includes boron nitride agglomerated particles as the inorganic filler, and includes an epoxy compound and a benzoxazine compound as the thermosetting resin, and a ratio of a mass content of the boron nitride agglomerated particles to a mass content of the benzoxazine compound (boron nitride agglomerated particles/benzoxazine) is 5 or more and 50 or less, a thermally conductive sheet having thermal conductivity and heat resistance can be formed. In addition, the thermosetting resin composition can be formed into a film without any problem when forming a sheet, and sufficient adhesive strength can be obtained when cured.
C08G 59/68 - Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups characterised by the catalysts used
C08J 3/24 - Crosslinking, e.g. vulcanising, of macromolecules
An aspect of the present invention relates to an acid-modified polyester-based resin in which an α,β-unsaturated carboxylic acid and/or an anhydride thereof (X) is grafted to an aliphatic-aromatic polyester-based resin containing an aliphatic diol unit, an aliphatic dicarboxylic acid unit, an aromatic dicarboxylic acid unit, the acid-modified polyester-based resin has a melt flow rate (210° C., load: 2160 g) of 1.4 g/10 min to 15 g/10 min, and a content of the α,β-unsaturated carboxylic acid and/or an anhydride thereof (X) is 0.0001 to 0.8 parts by mass with respect to 100 parts by mass of the aliphatic-aromatic polyester-based resin.
B32B 37/12 - Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by using adhesives
C09J 167/03 - Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the hydroxy and the carboxyl groups directly linked to aromatic rings
8.
ORGANIC-INORGANIC HYBRID MEMBRANE, ORGANIC-INORGANIC HYBRID MEMBRANE COMPOSITE, GAS SEPARATION AND CONCENTRATION METHOD, GAS SEPARATION MEMBRANE MODULE, METHOD FOR PRODUCING ORGANIC-INORGANIC HYBRID MEMBRANE, AND METHOD FOR PRODUCING ORGANIC-INORGANIC HYBRID MEMBRANE COMPOSITE
An object of an aspect of the present invention is to provide a new organic-inorganic hybrid membrane composite excellent in permeance and a relevant technique thereof. An organic-inorganic hybrid membrane composite in an aspect of the present invention includes a porous support layer and an organic-inorganic hybrid membrane formed on the porous support layer, an air permeation amount is 10000 L/(m2·h) or less, the organic-inorganic hybrid membrane contains a matrix polymer and a gas-selective inorganic filler, a contained amount of the gas-selective inorganic filler relative to the organic-inorganic hybrid membrane is 35% by mass or more, the gas-selective inorganic filler contains zeolite, a framework density in a case where all T elements of the zeolite are silicon is 16.0 T/1000 Å3 or less, and a membrane thickness of the organic-inorganic hybrid membrane is 0.05 μm or more and 50 μm or less.
B01D 53/22 - Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by diffusion
B01D 67/00 - Processes specially adapted for manufacturing semi-permeable membranes for separation processes or apparatus
B01D 69/02 - Semi-permeable membranes for separation processes or apparatus characterised by their form, structure or properties; Manufacturing processes specially adapted therefor characterised by their properties
The present invention provides a modified polyester-based resin, an adhesive resin composition having a high biodegradation rate and excellent adhesiveness, and a laminate using the same. The modified polyester-based resin composition according to the present invention is a copolymer in which an aliphatic-aromatic polyester-based resin is graft-modified with at least one selected from the group consisting of an α,β-unsaturated carboxylic acid and an anhydride thereof, and contains a succinic acid unit as an aliphatic dicarboxylic acid unit constituting the aliphatic-aromatic polyester-based resin.
Provided is an oil-in-water emulsion composition comprising water, an oil-and-fat, a pea protein and/or a fava protein, and a sucrose fatty acid ester, wherein the sucrose fatty acid ester has a ratio of a sucrose fatty acid monoester with respect to the total sucrose fatty acid ester of 3 to 45% by mass, and an amount of the sucrose fatty acid ester is 1 to 30 parts by mass with respect to 1 part by mass of a total amount of the pea protein and the fava protein.
A23C 11/10 - Milk substitutes, e.g. coffee whitener compositions containing at least one non-milk component as source of fats or proteins containing or not lactose but no other milk components as source of fats, carbohydrates or proteins
One problem addressed by the present invention is to provide an emulsion composition that maintains its quality even when stored frozen. The problem is solved by a protein that satisfies one of the following conditions (A) to (C) and is partially in the state of particles when made into an aqueous dispersion: (A): having at least one peak in a region of a molecular weight of 66,000 or more in terms of polyethylene glycol in a gel filtration chromatography elution curve; (B): having a weight-average molecular weight of more than 27,000 in terms of polyethylene glycol as measured by gel filtration chromatography; and (C): having a number-average molecular weight of more than 3,500 in terms of polyethylene glycol as measured by gel filtration chromatography.
A23J 1/14 - Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from press-cake or oil-bearing seeds
A23C 11/10 - Milk substitutes, e.g. coffee whitener compositions containing at least one non-milk component as source of fats or proteins containing or not lactose but no other milk components as source of fats, carbohydrates or proteins
A23F 3/30 - Further treatment of dried tea extract; Preparations produced thereby, e.g. instant tea
A23F 5/40 - Further treatment of dried coffee extract; Preparations produced thereby, e.g. instant coffee using organic additives, e.g. milk, sugar
A23L 23/00 - Soups; Sauces ; Preparation or treatment thereof
A23L 35/00 - Food or foodstuffs not provided for in groups ; Preparation or treatment thereof
C07K 14/415 - Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
12.
RESIN COMPOSITION, FILM, METHOD FOR PRODUCING FILM, AND LAMINATE
Provided is a colored resin product which contains a fluorescent dye and in which color fading over time is suppressed. A resin composition includes: a polycarbonate resin (A) containing a structural unit (a) derived from a specific dihydroxy compound represented by formula (1); and a fluorescent dye (B). A laminate (10) is configured in which the film (11) composed of the resin composition, the retroreflective element layer (12), and the substrate (13) are layered in this order.
C08L 101/02 - Compositions of unspecified macromolecular compounds characterised by the presence of specified groups
13.
CATALYST FOR METHACRYLIC ACID PRODUCTION, METHOD FOR PRODUCING SAME, AND METHOD FOR PRODUCING METHACRYLIC ACID AND METHACRYLIC ACID ESTERS USING CATALYST
An object is to provide a catalyst which has high heat resistance and which can allow for production of methacrylic acid at a high yield, and to provide methods for producing methacrylic acid and methacrylic acid ester with the catalyst, and the object is achieved by use of a catalyst having a specified 31P-NMR spectrum.
C01B 25/45 - Phosphates containing plural metal, or metal and ammonium
C07C 51/235 - Preparation of carboxylic acids or their salts, halides, or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups
14.
AQUEOUS DISPERSION, AND FILM AND LAMINATED BODY USING THE SAME
An aqueous dispersion including a binder resin, a nonionic surfactant, and a wax component, wherein the content of the nonionic surfactant is 0.1 to 200 parts by mass based on 100 parts by mass of the binder resin, and 2 parts by mass or more based on 100 parts by mass of the wax component.
C09D 135/06 - Copolymers with vinyl aromatic monomers
C09D 167/00 - Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
D21H 19/18 - Coatings without pigments applied in a form other than the aqueous solution defined in group comprising waxes
D21H 19/20 - Coatings without pigments applied in a form other than the aqueous solution defined in group comprising macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
D21H 19/34 - Coatings without pigments applied in a form other than the aqueous solution defined in group comprising cellulose or derivatives thereof
The present invention provides a double-sided adhesive sheet having a laminate structure with an intermediate layer (α layer) and a surface layer (β layer), wherein the intermediate layer (α layer) is formed from a resin composition containing a (meth)acrylic polymer, a crosslinking agent, and a photopolymerization initiator; the surface layer (β layer) is formed from an adhesive composition containing a (meth)acrylic polymer, a crosslinking agent, a photopolymerization initiator that can be activated by light having a wavelength of 405 nm or more, and an ultraviolet absorber; and the double-sided adhesive sheet has a stress relaxation rate of 30% or more. The double-sided adhesive sheet has curability, prevents ultraviolet degradation of the adhesive sheet, and has excellent discoloration resistance and step absorbability.
The present invention provides a microbial carrier in which denitrification efficiency is stabilized and improved, and a water treatment method using the same. The microbial carrier of the present invention is a microbial carrier which carries a microorganism having denitrification ability, the microbial carrier comprising an iron-containing carrier which comprises a biodegradable resin and iron, in which, when the iron-containing carrier comprises phosphorus, a molar ratio (phosphorus/iron) X of the phosphorus to the iron in the iron-containing carrier is 0
Provided is a prepreg in which gas barrier properties in a case of being molded into a molded product are improved. In the prepreg of the present invention, a thermoplastic resin with which a carbon fiber base material is impregnated, and the thermoplastic resin comprises a vinyl alcohol-based polymer.
F17C 1/06 - Protecting sheatings built-up from wound-on bands or filamentary material, e.g. wires
B32B 5/02 - Layered products characterised by the non-homogeneity or physical structure of a layer characterised by structural features of a layer comprising fibres or filaments
B32B 5/26 - Layered products characterised by the non-homogeneity or physical structure of a layer characterised by the presence of two or more layers which comprise fibres, filaments, granules, or powder, or are foamed or specifically porous one layer being a fibrous or filamentary layer another layer also being fibrous or filamentary
B32B 37/20 - Methods or apparatus for laminating, e.g. by curing or by ultrasonic bonding characterised by the properties of the layers with all layers existing as coherent layers before laminating involving the assembly of continuous webs only
Particles may include graphite (A) and a particle (B) containing at least one selected from the group consisting of a tantalum compound and a cerium compound. The particle (B) may be encapsulated in the graphite (A). Particles including a particle (B) may contain a cerium compound. The particle (B) may be a particle (B1) containing a silicon element, and the particle (B1) may have a surface coated with a cerium compound.
H01M 4/48 - Selection of substances as active materials, active masses, active liquids of inorganic oxides or hydroxides
H01M 4/587 - Carbonaceous material, e.g. graphite-intercalation compounds or CFx for inserting or intercalating light metals
19.
CATALYST FOR METHACRYLIC ACID PRODUCTION, METHOD FOR PRODUCING SAME, AND METHOD FOR PRODUCING METHACRYLIC ACID AND METHACRYLIC ACID ESTERS USING CATALYST
An object is to provide a catalyst which has high heat resistance and which can allow for production of methacrylic acid at a high yield and to provide methods for producing methacrylic acid and methacrylic acid ester with the catalyst, and the object is achieved by use of a catalyst having a specified peak in powder X-ray measurement.
A carbon material composition may easily increase a density of a negative electrode plate and provide a secondary battery that is excellent in all of an initial efficiency, rate characteristics, and remaining capacity retention rate after high-temperature storage, and as a result, to provide a high-performance secondary battery. Such a carbon material composition may include a carbon material (A) and a carbon material (B), wherein the carbon material (A) has a cumulative pore volume of 0.02 mL/g or more in a range of pore diameters of 0.01 μm or more and 1 μm or less, and a ratio of a pore diameter to a volume-based average particle diameter, PD/d50 (%), expressed by formula (1) of 1.8 or less:
A carbon material composition may easily increase a density of a negative electrode plate and provide a secondary battery that is excellent in all of an initial efficiency, rate characteristics, and remaining capacity retention rate after high-temperature storage, and as a result, to provide a high-performance secondary battery. Such a carbon material composition may include a carbon material (A) and a carbon material (B), wherein the carbon material (A) has a cumulative pore volume of 0.02 mL/g or more in a range of pore diameters of 0.01 μm or more and 1 μm or less, and a ratio of a pore diameter to a volume-based average particle diameter, PD/d50 (%), expressed by formula (1) of 1.8 or less:
PD
/
d
50
(
%
)
=
(
[
mode
pore
diameter
(
PD
)
in
a
range
of
pore
diameters
of
0.01
μm
or
more
and
1
μm
or
less
in
a
pore
distribution
obtained
by
a
mercury
intrusion
porosimetry
]
/
[
volume
-
based
average
particle
diameter
(
d
50
)
]
)
×
100
,
and
(
1
)
the
carbon
material
(
B
)
is
an
organic
compound
-
coated
carbon
material
.
An ethylene-vinyl alcohol copolymer composition which suppresses coloring change due to thermal degradation during melt molding is provided. An ethylene-vinyl alcohol copolymer composition contains an ethylene-vinyl alcohol copolymer and a titanium compound, wherein the amount of the titanium compound on a metal basis is 0.001 ppm or more and less than 5 ppm per mass of the ethylene-vinyl alcohol copolymer composition.
A resin composition containing, per 100 parts by mass of a thermoplastic resin, 0.1 to 10.0 parts by mass of a carbon nanotube, and 10 to 100 parts by mass of a glass fiber, with a mass proportion of the carbon nanotube and the glass fiber (carbon nanotube/glass fiber) being 0.01 to 0.30.
C08K 13/00 - Use of mixtures of ingredients not covered by any single one of main groups , each of these compounds being essential
G01N 22/00 - Investigating or analysing materials by the use of microwaves or radio waves, i.e. electromagnetic waves with a wavelength of one millimetre or more
23.
METHOD FOR PRODUCING CARBON FIBER BUNDLE COMPOSITE, AND CARBON FIBER BUNDLE COMPOSITE
Provided are a method for producing a carbon fiber bundle composite and a carbon fiber bundle composite. The method contains a step of mixing carbon fiber fluff made of short carbon fibers and a molten resin containing an epoxy resin component to obtain a carbon fiber bundle containing the molten resin, a step of solidifying the molten resin, and a step of mixing at least one type of epoxy curing agent into the molten resin. The carbon fiber bundle composite contains a plurality of short carbon fibers forming the bundle and an uncured solid epoxy resin composition. The positions of the tips of the short carbon fibers are uneven at each end of the bundle; and the uncured solid epoxy resin composition contains at least one type of epoxy curing agent.
D04H 1/60 - Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in dry state, e.g. thermo-activatable agents in solid or molten state, and heat being applied subsequently
C08J 5/04 - Reinforcing macromolecular compounds with loose or coherent fibrous material
C08J 5/24 - Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
D04H 1/4382 - Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
D04H 1/54 - Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by welding together the fibres, e.g. by partially melting or dissolving
D04H 1/587 - Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives characterised by the bonding agents used
24.
POLYESTER PRESSURE-SENSITIVE ADHESIVE COMPOSITION, POLYESTER PRESSURE-SENSITIVE ADHESIVE, PRESSURE-SENSITIVE ADHESIVE SHEET, DECORATIVE FILM, FILM FOR ELECTRONIC MEMBER, AND DECORATIVE MOLDED OBJECT
Provided is a polyester adhesive composition containing a polyester resin (A) and a polyepoxy compound (B), wherein the polyester resin (A) contains structural units derived from a polyvalent carboxylic acid, structural units derived from a polyhydric alcohol, and wherein the structural units derived from the polyvalent carboxylic acid contain a specific amount of structural units derived from a cyclic structure, and the structural units derived from the polyhydric alcohol contain structural units derived from an aliphatic polyhydric alcohol. The polyester resin (A) also has a specific acid value and a specific glass transition temperature.
What is provided is an adhesive sheet in which a high level of both unevenness followability during bonding and shape holding power when not bonded is achieved and flexibility especially in a low-temperature environment is excellent. The adhesive sheet includes an adhesive layer formed from an adhesive composition containing a (meth)acrylic copolymer, in which (1) when the thickness is set to 0.7 to 1.0 mm, a strain (creep strain) by applying a pressure of 2 kPa at a temperature of 60° C. for 600 seconds is 1000% or more and 100000% or less, (2) in a holding power measurement in accordance with JIS-Z-0237 (ISO29863), a falling time when the adhesive sheet is adhered to a SUS plate with an area of 20 mm×20 mm and a load of 500 gf is applied in an atmosphere of 40° C. is 60 seconds or more, and (3) when the thickness is set to 0.7 to 1.0 mm, a storage shear modulus at −20° C. (G′ (−20° C.)) obtained by a dynamic viscoelasticity measurement in a shear mode at a frequency of 1 Hz is 10 kPa or more and 1000 kPa or less are satisfied.
A thermoplastic resin composition pellet may include 30 to 100 parts by mass of a polybutylene terephthalate resin (A) having an intrinsic viscosity of 0.3 to 1.3 dl/g and 0 to 70 parts by mass of a polystyrene or a rubber-reinforced polystyrene resin (B), and 0.5 to 20 parts by mass of heat-expandable microsphere (C) having a maximum expansion temperature in a range of 250 to 320° C. and an average particle diameter in a range of 10 to 50 μm, relative to 100 parts by mass of the total (A) and (B). A method may produce the thermoplastic resin composition pellet including melt kneading a master batch including the heat-expandable microsphere (C) and a thermoplastic resin with the polybutylene terephthalate resin (A) and the polystyrene or rubber-reinforced polystyrene resin (B).
C08L 67/02 - Polyesters derived from dicarboxylic acids and dihydroxy compounds
27.
METHOD FOR PRODUCING CATALYST MOLDED ARTICLE USED WHEN PRODUCING alpha,beta-UNSATURATED CARBOXYLIC ACID, AND METHOD FOR PRODUCING alpha,beta-UNSATURATED CARBOXYLIC ACID AND alpha,beta-UNSATURATED CARBOXYLIC ACID ESTER USING SAME
An object is to provide a method capable of stably producing a catalyst molded article which is favorable in moldability in a step of molding a dried catalyst product and which provides a high yield of α,β-unsaturated carboxylic acid, and methods for producing α,β-unsaturated carboxylic acid and α,β-unsaturated carboxylic acid ester with the catalyst molded article. The object is achieved by a method for producing a catalyst molded article by preparing a catalyst raw material-containing slurry with a catalyst production apparatus washed under specified conditions, and methods for producing α,β-unsaturated carboxylic acid and α,β-unsaturated carboxylic acid ester with the catalyst molded article.
B30B 11/02 - Presses specially adapted for forming shaped articles from material in particulate or plastic state, e.g. briquetting presses or tabletting presses using a ram exerting pressure on the material in a moulding space
C07C 51/16 - Preparation of carboxylic acids or their salts, halides, or anhydrides by oxidation
C07C 67/04 - Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
A GaN substrate doped with manganese, in which an activation energy of a carrier is 0.7 eV or more when a carrier concentration is represented by the formula (I): carrier concentration (atoms/cm3)=A×EXP(−Ea/kT). In the formula (I), A represents a proportional constant, EXP represents an exponential function, Ea represents a carrier activation energy (eV), k represents a Boltzmann constant (8.617×10−5 eV/K), and T represents a temperature (K) in Kelvin units.
H01L 29/20 - Semiconductor bodies characterised by the materials of which they are formed including, apart from doping materials or other impurities, only AIIIBV compounds
C30B 25/20 - Epitaxial-layer growth characterised by the substrate the substrate being of the same materials as the epitaxial layer
H01L 29/778 - Field-effect transistors with two-dimensional charge carrier gas channel, e.g. HEMT
29.
METHOD FOR PRODUCING CATALYST COMPACT FOR USE IN PRODUCING UNSATURATED CARBOXYLIC ACID, AND METHOD FOR PRODUCING UNSATURATED CARBOXYLIC ACID AND UNSATURATED CARBOXYLIC ESTER USING SAME
An object is to provide a method for producing a catalyst molded article which is high in mechanical strength and which enables unsaturated aldehyde and/or unsaturated carboxylic acid to be produced at high yield(s). The object is achieved by a method for producing a catalyst molded article, the method including (1) a step of adding an ammonium radical to a slurry (liquid A) including molybdenum and phosphorus, at a rate satisfying the following expression (I), to prepare a slurry (liquid B), 0.1≤v/M≤3 (I), in which v represents the rate of addition of the ammonium radical [mol/hour], and M represents the mass of the liquid A [kg], (2) a step of adjusting the pH of the liquid B, to prepare a slurry (liquid C) having a pH lower than that of the liquid B by 0.2 or more and having a pH of 4 or less, (3) a step of drying the liquid C, to obtain a catalyst powder, (4) a step of mixing the catalyst powder and a liquid, to produce a catalyst powder mixture, and (5) a step of molding the catalyst powder mixture, to produce a catalyst molded article, in which the penetration rate coefficient of the liquid to the catalyst powder in step (4) is 0.07 g2/s or more.
A GaN epitaxial substrate contains a GaN substrate and a GaN buffer layer epitaxially grown on the GaN substrate. The GaN epitaxial substrate includes a point A and a point B positioned on a straight line parallel to a [0001] axis passing through the point A, the point B being present in a [0001] axis direction relative to the point A. The point A is present in the GaN substrate or the GaN buffer layer, the point B is present in the GaN buffer layer, a ratio ([Mn]B/[Mn]A) is 1/100, and a distance between the point A and the point B is 0.7 μm or less.
H01L 29/20 - Semiconductor bodies characterised by the materials of which they are formed including, apart from doping materials or other impurities, only AIIIBV compounds
C30B 25/20 - Epitaxial-layer growth characterised by the substrate the substrate being of the same materials as the epitaxial layer
A modified ethylene-vinyl alcohol copolymer composition that allows thermal degradation to be suppressed during heating in melt kneading, melt molding, or the like is provided as follows. A modified ethylene-vinyl alcohol copolymer composition contains a modified ethylene-vinyl alcohol copolymer having a primary hydroxyl group structural unit in a side chain, and a titanium compound. The amount of the titanium compound on a metal basis is 0.001 ppm or more and less than 5 ppm per mass of the modified ethylene-vinyl alcohol copolymer composition.
An object is to provide a method for producing methacrolein and/or methacrylic acid from isobutanol, in which methacrolein and/or methacrylic acid are/is obtained at high selectivity with suppressed generation of a by-product, and a method for producing methacrylic acid ester from the methacrylic acid obtained. The object is achieved by a method for producing methacrolein and/or methacrylic acid, including (i) a step of feeding an isobutanol-containing gas to a dehydration catalyst layer, to produce an isobutylene-containing gas 1 by dehydration reaction of isobutanol, and (ii) a step of feeding an isobutylene-containing gas 2 containing at least one portion of the isobutylene-containing gas 1, and an oxygen-containing gas to an oxidation catalyst layer, to produce methacrolein and/or methacrylic acid by oxidation reaction of isobutylene, in which x1/x2 is 0.4 or more when the content rate of isobutylene in the isobutylene-containing gas 1 is x1 (% by mol) and the content rate of isobutylene in the isobutylene-containing gas 2 is x2 (% by mol).
C07C 51/235 - Preparation of carboxylic acids or their salts, halides, or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of —CHO groups or primary alcohol groups
C07C 45/29 - Preparation of compounds having C=O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
33.
COMPOSITION FOR ORGANIC ELECTROLUMINESCENT ELEMENT, METHOD FOR PRODUCING ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, DISPLAY DEVICE, AND ILLUMINATOR
An object of the present invention is to provide a composition for an organic electroluminescent element, which is used for forming an emission layer in an organic electroluminescent element by wet-process film formation, and which has favorable stability of liquid physical properties, in particular, favorable surface tension stability of ink. The present invention relates to a composition for an organic electroluminescent element including a functional material, a specific compound, alkylated naphthalene or diphenyl alkane as a first solvent, and at least one of an aromatic ether and an aromatic ester as a second solvent.
A silica particle in which, in an image obtained by taking a scanning transmission electron image in a bright field mode using an ultra-high resolution electron microscope, a ratio of an area of a white portion within the silica particle to a total area of the silica particle is 2% to 12%. The ratio of the area of the white portion within the silica particle to the total area of the silica particle may be 7% to 10%.
An ethylene-vinyl alcohol copolymer composition having excellent long-run workability and allowing suppression of coloring change due to thermal degradation during melt molding is provided as follows. An ethylene-vinyl alcohol copolymer composition contains an ethylene-vinyl alcohol copolymer (A) having two or more kinds of ethylene-vinyl alcohol copolymers with different ethylene structural unit contents, and a titanium compound (B). The amount of the titanium compound (B) on a metal basis is 0.001 to 5 ppm per mass of the ethylene-vinyl alcohol copolymer composition.
A resin composition contains a polyester resin and a polycarbonate resin, wherein a mass ratio between the polyester resin and the polycarbonate resin is 10/90 to 90/10, wherein a total of the polyester resin and the polycarbonate resin is 100 parts by mass, and a content of aluminum element contained in the polycarbonate resin is 0.50 to 1000.00 ppm by mass per 100 parts by mass of the polycarbonate resin.
An ethylene-vinyl alcohol copolymer composition that allows suppression of thermal degradation during melt molding is provided as follows. A modified ethylene-vinyl alcohol copolymer composition contains a modified ethylene-vinyl alcohol copolymer including an aliphatic polyester unit, and a titanium compound. The amount of the titanium compound on a metal basis is 0.001 ppm or more and less than 5 ppm per mass of the modified ethylene-vinyl alcohol copolymer composition.
A resin composition contains a polybutylene terephthalate resin; and a polystyrene-based resin having a weight average molecular weight (Mw) of 2.00×105 or more and a molecular weight distribution (Mw/Mn) of 3.20 or more, wherein the polystyrene-based resin contains elemental iron in a proportion of from 0.1 to 160.0 ppm by mass with respect to 100 parts by mass of the polystyrene-based resin.
A uniaxially stretched multilayer structure with excellent transparency is provided, which is stretched in a uniaxial direction and has a resin composition (A) layer containing an ethylene-vinyl alcohol copolymer. A multilayer structure having layers stretched in a uniaxial direction includes a resin composition (A) layer containing an ethylene-vinyl alcohol copolymer, in which the ethylene-vinyl alcohol copolymer in the resin composition (A) layer has an ethylene unit content of less than 32 mol %, and the ethylene-vinyl alcohol copolymer has a single ethylene unit content.
B29C 48/22 - Articles comprising two or more components, e.g. co-extruded layers the components being layers with means connecting the layers, e.g. tie layers or undercuts
B29C 48/21 - Articles comprising two or more components, e.g. co-extruded layers the components being layers the layers being joined at their surfaces
B29K 23/00 - Use of polyalkenes as moulding material
B29K 105/00 - Condition, form or state of moulded material
40.
ETHYLENE-VINYL ALCOHOL COPOLYMER COMPOSITION AND METHOD FOR PRODUCING SAME, MELT-FORMING MATERIAL AND PELLETS USING SAME, AND MULTILAYER STRUCTURE AND PRODUCTION METHOD THEREOF
An ethylene-vinyl alcohol copolymer composition which suppresses thermal degradation during melt molding is provided as follows. An ethylene-vinyl alcohol copolymer composition contains: an ethylene-vinyl alcohol copolymer (A); at least one compound (B) selected from a group consisting of a metal compound belonging to period 4 d-block of along Periodic Table (other than a titanium compound) (B1), a specific polyolefin resin (B2), an olefin polymer (B3), a polyamide resin (B4), and a styrene derivative having a substituent at an α-position (B5); and a titanium compound (C), wherein the amount of the titanium compound (C) on a metal basis is 0.00005 ppm or more and less than 5 ppm per mass of the ethylene-vinyl alcohol copolymer composition.
A phosphor contains a crystal phase having a composition represented by RexMAaMBbMCcDdXe, and an element Z, in which a content of the element Z is 1,000 mass ppm or less, and the element Z includes at least one of Mo, W, Nb, Ta, Ni, Pt, or Ir. Regarding the composition, MA includes at least one of Ca, Sr, Ba, Na, K, Y, Gd, or La, MB includes at least one of Li, Mg, or Zn, MC includes at least one of Al, Si, Ga, In, or Sc, D is N (nitrogen) and/or O (oxygen), X includes at least one of F, Cl, Br, or I, and Re includes at least one of Eu, Ce, Pr, Tb, or Dy, and a, b, c, d, e, and x satisfy the specific expressions, respectively.
Provided is a resin composition which can be molded into a product with excellent transparency, as a recycled composition of a multilayer structure using a polyolefin resin and an ethylene-vinyl alcohol copolymer. The resin composition comprises a polyolefin resin (A), an ethylene-vinyl alcohol copolymer (B), and an amine-modified resin (C), wherein the content of the amine-modified resin (C) is 0.1 to 20 parts by mass per 100 parts by mass of the polyolefin resin (A).
A phosphor includes a crystal phase having a composition represented by RexMAaMBbMCcDdXe, in which MA includes at least one of Ca, Sr, Ba, Na, K, Y, Gd, or La, MB includes at least one of Li, Mg, or Zn, MC includes at least one of Al, Si, Ga, In, or Sc, D is N (nitrogen) and/or O (oxygen), X includes at least one of F, Cl, Br, or I, Re includes at least one of Eu, Ce, Pr, Tb, or Dy, and a, b, c, d, e, and x satisfy the specific expressions, respectively. In the phosphor, when a content of B (boron) is designated as b (mass ppm), a value of Log10(b) is 3.5 or less.
A uniaxially stretched multilayer structure with excellent transparency is provided that is stretched in a uniaxial direction and has a resin composition (A) layer containing an ethylene-vinyl alcohol copolymer. A multilayer structure having layers stretched in a uniaxial direction includes a resin composition (A) layer containing an ethylene-vinyl alcohol copolymer. The ethylene-vinyl alcohol copolymer in the resin composition (A) layer has an ethylene unit content of less than 32 mol %. The resin composition (A) layer is provided in a layer other than an outermost layer of the multilayer structure.
Provided is an adhesive sheet including an adhesive layer formed from an adhesive composition containing: a (meth)acrylic copolymer (A); a photocurable compound (B); and a photopolymerization initiator (C), wherein the (meth)acrylic copolymer (A) has: a structural unit derived from an alkyl (meth)acrylate (a1) having a linear and/or branched alkyl group having 3 to 6 carbon atoms; and a structural unit derived from a (meth)acrylate (a2) having a glass transition temperature lower than that of the alkyl (meth)acrylate (a1), the structural unit derived from the alkyl (meth)acrylate (a1) is contained by not less than 20 mass % and not greater than 60 mass %, a content mass ratio (W(a2)/W(a1)) of the structural unit derived from the (meth)acrylate (a2) relative to the structural unit derived from the alkyl (meth)acrylate (a1) is 0.3 to 3.0, and the adhesive sheet has a storage shearing elastic modulus (G′) at −20° C. of not greater than 800 kPa.
Monoorgano tin trialkoxide compounds having chemical formula R′Sn(OR)3 and containing less than about 5 mol % tin tetraalkoxide are described. R′ is a linear or branched, unsaturated hydrocarbon group having about 2 to about 4 carbon atoms and each R is independently trimethylsilyl, phenyl, or a linear or branched, optionally fluorinated, alkyl group having about 1 to about 5 carbon atoms. Methods for synthesizing and purifying these compounds are also provided. The monoorgano tin compounds may be used for the formation of high-resolution EUV lithography patterning precursors and are attractive due to their high purity and minimal concentration of diorgano tin impurities.
Provided is an adhesive sheet having good flexibility and recovering ability, and excellent adhesiveness. An adhesive sheet having a storage shearing elastic modulus at −20° C. [G′(−20° C.)] of not greater than 700 kPa, wherein the adhesive sheet is formed from an adhesive composition [I] including an acrylic polymer (A) and a radically polymerizable compound (B), the acrylic polymer (A) includes: a structural portion derived from an alkyl (meth)acrylate (a1) with an alkyl group having 5 to 20 carbon atoms; and a structural portion derived from a hydroxy-group-containing (meth)acrylate (a2), and the radically polymerizable compound (B) includes a di(meth)acrylate (B1) having an alkylene group having 2 to 4 carbon atoms.
C09J 7/30 - Adhesives in the form of films or foils characterised by the adhesive composition
C09J 4/06 - Adhesives based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups
C09J 133/08 - Homopolymers or copolymers of acrylic acid esters
A polycarbonate resin composition containing a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), and a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), wherein the content of the carbonate structural unit (X) in 100 mol % of all carbonate structural units of the polycarbonate resin composition is 31.6 mol % or more. Alternatively, a polycarbonate resin composition containing a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), and a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), wherein a molar ratio (Y)/(X) of the content of the carbonate structural unit (Y) to the carbonate structural unit (X) is 0.33 or more and 2.95 or less.
A polycarbonate resin composition containing a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), and a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), wherein the content of the carbonate structural unit (X) in 100 mol % of all carbonate structural units of the polycarbonate resin composition is 31.6 mol % or more. Alternatively, a polycarbonate resin composition containing a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), and a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), wherein a molar ratio (Y)/(X) of the content of the carbonate structural unit (Y) to the carbonate structural unit (X) is 0.33 or more and 2.95 or less.
A multilayer structure easily recyclable and having excellent transparency and impact resistance is provided as follows. A multilayer structure includes: a polar group-containing resin layer (A) including a polar group-containing resin (a) including an ethylene-vinyl alcohol copolymer and/or a polyamide; a polyolefin resin layer (B) including a polyolefin resin (b1) and a compatibilizer (b2); and an adhesive resin layer (C), wherein the compatibilizer (b2) has a melt flow rate of 600 or less g/10 minutes (at 190° C. with a load of 2160 g), and the compatibilizer (b2) has a content of 10 to 200 parts by mass per 100 parts by mass of the polar group-containing resin (a).
B32B 27/08 - Layered products essentially comprising synthetic resin as the main or only constituent of a layer next to another layer of a specific substance of synthetic resin of a different kind
B32B 27/20 - Layered products essentially comprising synthetic resin characterised by the use of special additives using fillers, pigments, thixotroping agents
JAPAN TECHNOLOGICAL RESEARCH ASSOCIATION OF ARTIFICIAL PHOTOSYNTHETIC CHEMICAL PROCESS (Japan)
Inventor
Satou, Kiminori
Horie, Hideyoshi
Kikuchi, Tomohisa
Miyagi, Hidekazu
Hayashi, Mikio
Takewaki, Takahiko
Abstract
A composite separation structure may include a substrate section, a first separation section disposed in contact with the substrate section, and a second separation section disposed not in contact with the substrate section but in contact with the first separation section. The second separation section may be amorphous and have a thickness from an end portion in contact with the first separation section to the opposite end portion of 5 nm or more and 200 nm or less. Such a composite separation structure may be capable of separating gases having various small kinetic diameters (kinetic diameters) with high separability, and particularly capable of realizing the separation or concentration of a gas mixture containing a gas having a kinetic diameter of 4 Å or less.
B01D 53/22 - Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases or aerosols by diffusion
51.
CATALYST, PRODUCTION METHOD FOR CATALYST, AND PRODUCTION METHOD FOR alpha,beta-UNSATURATED ALDEHYDE AND/OR alpha,beta-UNSATURATED CARBOXYLIC ACID USING SAME
An object of the present invention is mainly to provide a catalyst with which an α,β-unsaturated aldehyde and/or an α,β-unsaturated carboxylic acid can be produced with a high selectivity. Provided is a catalyst used for producing, by an oxidation reaction of a hydrocarbon, a corresponding α,β-unsaturated aldehyde and/or α,β-unsaturated carboxylic acid, and the catalyst contains molybdenum, bismuth, and cobalt, and satisfies the following Formula (I-1): (x2−x1)/σ1≤1.5 (I-1) In Formula (I-1), x1, x2, and σ1 are values obtained by binarizing a reflected electron image of the catalyst, which is obtained using a scanning electron microscope (SEM) at an accelerating voltage of 15 kV, into black and white and subsequently performing an energy dispersive X-ray spectroscopy (EDS) analysis; x1 represents a bismuth concentration [% by mass] in black parts; x2 represents a bismuth concentration [% by mass] in white parts; and σ1 represents a standard deviation of the bismuth concentration in the black parts.
C07C 45/34 - Preparation of compounds having C=O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with molecular oxygen of CHx-moieties in unsaturated compounds
C07C 51/25 - Preparation of carboxylic acids or their salts, halides, or anhydrides by oxidation with molecular oxygen of unsaturated compounds containing no six-membered aromatic ring
A conductive composition which contains a conductive polymer (A) comprising a polyaniline and a basic compound (E2), which is a quaternary ammonium salt in which at least one of four groups bonded to a nitrogen atom is an alkyl group having 3 or more carbon atoms, is provided. A conductive composition, containing a polyaniline comprising a monomer unit having an acidic group; and a basic compound (E3) having a basic group and two or more hydroxyl groups in the molecule, and having a melting point of 30° C. or more, is also provided.
H01B 1/12 - Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors mainly consisting of other non-metallic substances organic substances
C08F 26/06 - Homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containin by a heterocyclic ring containing nitrogen
The present invention provides a modified epoxy resin including a structural unit derived from an epoxy compound, and a structural unit derived from an acid-terminated polyester, wherein the modified epoxy resin has a weight average molecular weight of from 1,500 to 50,000, and an epoxy equivalent of from 500 to 10,000 g/eq, and wherein the modified epoxy resin is represented by the following formula (1) (wherein, in the formula (1), n represents a number from 1 to 30, X is a structural unit derived from an epoxy compound, and Y is a structural unit derived from an acid-terminated polyester).
The present invention provides a modified epoxy resin including a structural unit derived from an epoxy compound, and a structural unit derived from an acid-terminated polyester, wherein the modified epoxy resin has a weight average molecular weight of from 1,500 to 50,000, and an epoxy equivalent of from 500 to 10,000 g/eq, and wherein the modified epoxy resin is represented by the following formula (1) (wherein, in the formula (1), n represents a number from 1 to 30, X is a structural unit derived from an epoxy compound, and Y is a structural unit derived from an acid-terminated polyester).
A thermoplastic resin composition containing a compound (F) which is at least one selected from the group consisting of a macromonomer (A) represented by Formula (1) and a copolymer (C) containing a structural unit derived from the macromonomer (A), and a compound (G) represented by Formula (2). (In Formula (1), R0 to Rn each independently represent a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, or a heterocyclic group, X1 to Xn each independently represent a hydrogen atom or a methyl group, Z represents a terminal group, and n represents a natural number of 1 to 10,000.) (In Formula (2), R1 to R4 each independently represent an alkyl group having 1 to 5 carbon atoms, and R5 represents an alkyl group having 1 to 5 carbon atoms, or a hydrogen atom.)
A thermoplastic resin composition containing a compound (F) which is at least one selected from the group consisting of a macromonomer (A) represented by Formula (1) and a copolymer (C) containing a structural unit derived from the macromonomer (A), and a compound (G) represented by Formula (2). (In Formula (1), R0 to Rn each independently represent a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group, or a heterocyclic group, X1 to Xn each independently represent a hydrogen atom or a methyl group, Z represents a terminal group, and n represents a natural number of 1 to 10,000.) (In Formula (2), R1 to R4 each independently represent an alkyl group having 1 to 5 carbon atoms, and R5 represents an alkyl group having 1 to 5 carbon atoms, or a hydrogen atom.)
C08L 53/00 - Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
C08F 2/26 - Emulsion polymerisation with the aid of emulsifying agents anionic
C08F 2/44 - Polymerisation in the presence of compounding ingredients, e.g. plasticisers, dyestuffs, fillers
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
C08F 228/02 - Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur by a bond to sulfur
A method for producing a polyhydric alcohol includes: subjecting a crude reaction solution obtained by performing a reduction reaction in the presence of a hydrogenation catalyst and hydrogen using a polyhydric aldehyde having an alicyclic structure as a starting material to distillation purification. The distillation purification is performed after a content of a metal element in the crude reaction solution is 30 ppm by mass or less, and preferably 10 mass ppm or less.
C07C 29/145 - Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen-containing functional group of C=O containing groups, e.g. —COOH of ketones with hydrogen or hydrogen-containing gases
C07C 29/80 - Separation; Purification; Stabilisation; Use of additives by physical treatment by distillation
C07C 29/88 - Separation; Purification; Stabilisation; Use of additives by treatment giving rise to a chemical modification of at least one compound
56.
IRIDIUM COMPLEX COMPOUND, COMPOSITION FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT, METHOD FOR PRODUCING SAME, AND DISPLAY DEVICE
An iridium complex compound represented by formula (1′) below.
An iridium complex compound represented by formula (1′) below.
R2 to R5 are each selected from a [substituent group W]; R1, R6 to R10, and R14 are a hydrogen atom, F, a methyl group, a trifluoromethyl group, an ethyl group, a vinyl group, or an ethynyl group; R15 and R16 are a linear, branched, or cyclic alkyl group having 1 to 30 carbon atoms, an aralkyl group having 5 to 60 carbon atoms, or a heteroaralkyl group having 5 to 60 carbon atoms; one of R11 to R13 has a structure represented by formula (2) below; and the remaining two are selected from a [substituent group Z].
An iridium complex compound represented by formula (1′) below.
R2 to R5 are each selected from a [substituent group W]; R1, R6 to R10, and R14 are a hydrogen atom, F, a methyl group, a trifluoromethyl group, an ethyl group, a vinyl group, or an ethynyl group; R15 and R16 are a linear, branched, or cyclic alkyl group having 1 to 30 carbon atoms, an aralkyl group having 5 to 60 carbon atoms, or a heteroaralkyl group having 5 to 60 carbon atoms; one of R11 to R13 has a structure represented by formula (2) below; and the remaining two are selected from a [substituent group Z].
An aqueous resin composition including at least: a polyurethane resin that contains a carboxylate group; a crosslinking agent that contains at least two or more carbodiimide groups in one molecule; and a surfactant, wherein a molar ratio of the carbodiimide groups contained in the crosslinking agent to the carboxylate group contained in the polyurethane resin is 0.1 or greater and 5.0 or less, and the aqueous resin composition further contains an amine compound having a pkb of 3.5 or greater and 4.7 or less.
The present invention provides a curable composition which provides a coating film having excellent hot water-resistant adhesiveness, a cured product of the curable composition, a laminate using the curable composition, and production methods thereof.
The present invention provides a curable composition which provides a coating film having excellent hot water-resistant adhesiveness, a cured product of the curable composition, a laminate using the curable composition, and production methods thereof.
The curable composition of the present invention comprises the following compound A and the following compound B.
Compound A: a compound in which (TI) 2 calculated by the following expression (L) is 3.65 to 9.17 (excluding the compound B)
Compound B: a polyfunctional (meth)acrylate monomer having three or more (meth)acryloyl groups
The present invention provides a curable composition which provides a coating film having excellent hot water-resistant adhesiveness, a cured product of the curable composition, a laminate using the curable composition, and production methods thereof.
The curable composition of the present invention comprises the following compound A and the following compound B.
Compound A: a compound in which (TI) 2 calculated by the following expression (L) is 3.65 to 9.17 (excluding the compound B)
Compound B: a polyfunctional (meth)acrylate monomer having three or more (meth)acryloyl groups
(TI)2=4/(N×χ2) Expression (L)
N: a number of atoms in a skeleton of the compound A, excluding hydrogen atoms
χ2: a second smallest value among eigenvalues of a Laplacian matrix representing a molecular structure of the compound A
An adhesive tape includes a substrate [I] and an adhesive agent layer of a polyester adhesive agent provided on at least one of opposite surfaces of the substrate [I]. The substrate [I] is one selected from a polyolefin resin foam substrate, a urethane resin foam substrate, and an acrylic resin foam substrate. The polyester adhesive agent is made from a polyester adhesive agent composition [II] which contains a polyester resin (A) having a weight average molecular weight of 5,000 to 300,000, and having a structural unit derived from a polyol and a structural unit derived from a polyvalent carboxylic acid compound containing an aromatic structure-containing compound in a proportion of not greater than 80 mol %. The adhesive tape is excellent in adherence between a polyester adhesive agent layer and a polyolefin resin foam substrate, a urethane resin foam substrate, or an acrylic resin foam substrate.
C08G 63/52 - Polycarboxylic acids or polyhydroxy compounds in which at least one of the two components contains aliphatic unsaturation
C09J 7/25 - Plastics; Metallised plastics based on macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
A compound represented by the formula (1) below is proposed as a novel compound having electron-transporting property which dissolves sufficiently in an organic solvent.
A compound represented by the formula (1) below is proposed as a novel compound having electron-transporting property which dissolves sufficiently in an organic solvent.
one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents one or more substituents
G03G 5/047 - Photoconductive layers characterised by having two or more layers or characterised by their composite structure characterised by the charge-generation layers or charge-transporting layers
G03G 15/00 - Apparatus for electrographic processes using a charge pattern
61.
ELECTROPHOTOGRAPHIC PHOTORECEPTOR, ELECTROPHOTOGRAPHIC PHOTORECEPTOR CARTRIDGE, IMAGE FORMATION DEVICE, COATING LIQUID FOR FORMING ELECTROPHOTOGRAPHIC PHOTORECEPTOR PROTECTIVE LAYER, AND COMPOUND
A resin composition may exhibit excellent low warpage and heat resistance, and may include, based on a total of 100 parts by mass of (A) to (C): (A) 25 to 48 parts by mass of a polyphenylene +-sulfide resin having an MVR, measured at 295° C. under a 1.00 kgf load, of 60 to 500 cm3/10 min; (B) an amorphous rubber-reinforced polystyrene or polystyrene having an MVR, measured at 200° C. under a 5 kgf load, of 0.3 to 16 cm3/10 min and/or (C) a polyphenylene ether resin, a total content of (B) and (C) being 52 to 75 parts by mass; and (D) 5 to 150 parts by mass of a fibrous filler.
Provided is a colored resin composition which can be applied as a color filter of a solid-state imaging device capable of performing high-level imaging by not only spectrally splitting light in a visible region into three colors but also spectrally splitting infrared rays. The colored resin composition includes a colorant (A), a solvent (B), and a binder resin (C), and has a maximum transmittance in a specific wavelength region in a wavelength range of 400 to 900 nm. The colorant (A) includes a colorant having specific light absorbing characteristics and a near-infrared absorbing compound.
C09D 4/06 - Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond in combination with a macromolecular compound other than an unsaturated polymer of groups
C09D 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
C09D 135/02 - Homopolymers or copolymers of esters
BONDING STRUCTURE, AND CONTAINER, PIPE FOR TRANSFERRING HIGHLY PURE ORGANOTIN COMPOUND, AND HIGHLY PURE ORGANOTIN COMPOUND MANUFACTURING APPARATUS HAVING THE SAME
A bonding structure used for forming a sealed space (for example, a container) for containing or transferring an organotin compound, wherein the bonding structure is a structure in which a first member is connected with a second member via a gasket or an O-ring, and the gasket or the O-ring is formed with a fluororesin derived from monomers of at least tetrafluoroethylene and perfluoromethyl vinyl ether.
Provided is a methacrylic resin molding material containing methacrylic resin pellets to which a fatty acid is externally added, in which an externally added amount of the fatty acid is 0.002 parts by mass or more with respect to 100 parts by mass of the methacrylic resin pellets.
An aqueous dispersion including a nonionic surfactant, an anionic surfactant, and a wax dispersed in water, where the wax includes an ester compound having a fatty acid-derived structural moiety and an aliphatic alcohol-derived structural moiety, and the content of the nonionic surfactant is 40 to 99 parts by mass based on 100 parts by mass of the total of the nonionic surfactant, the anionic surfactant, and the wax, and is 5 to 50 parts by mass based on 100 parts by mass of the total of the nonionic surfactant, the anionic surfactant, the wax, and the water.
The disclosure provides an electrophotographic photoconductor comprises a photosensitive layer and a protective layer in sequence on a conductive support, wherein the protective layer contains a polymer having a structure represented by the following formula (1) or (2):
The disclosure provides an electrophotographic photoconductor comprises a photosensitive layer and a protective layer in sequence on a conductive support, wherein the protective layer contains a polymer having a structure represented by the following formula (1) or (2):
A method for producing a fiber assembly, including: putting a plurality of fibers and a fiber treatment agent into a stirring tank; and stirring a mixture of the fibers and the fiber treatment agent with a stirring blade to granulate the mixture, wherein the fibers include carbon fibers, and the mixture is granulated such that the fibers are aligned. A method for producing a fiber assembly, wherein a plurality of fibers containing carbon fibers and a liquid are put into a stirring tank and the mixture of the fibers and the liquid is stirred with a stirring blade, thereby obtaining a fiber assembly which has a spheroidal shape or a strand shape.
B29K 105/12 - Condition, form or state of moulded material containing reinforcements, fillers or inserts of short lengths, e.g. chopped filaments, staple fibres or bristles
A method for producing an aldehyde includes: subjecting an olefin to a hydroformylation reaction with a gas containing hydrogen and carbon monoxide in the presence of a catalyst; withdrawing part or all of a reaction solution having accumulated therein a high-boiling-point byproduct from a reaction zone; mixing the withdrawn reaction solution with a poor solvent for the catalyst in a mixing tank to precipitate an aggregate containing the catalyst and the high-boiling-point byproduct; and adhering the precipitated aggregate to an inner surface of the mixing tank to recover the aggregate.
C07C 45/50 - Preparation of compounds having C=O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
B01J 31/18 - Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony
70.
PHOTOCATALYST PRODUCTION METHOD, AND HYDROGEN AND OXYGEN PRODUCTION METHOD USING SAID PHOTOCATALYST
JAPAN TECHNOLOGICAL RESEARCH ASSOCIATION OF ARTIFICIAL PHOTOSYNTHETIC CHEMICAL PROCESS (Japan)
Inventor
Yoshida, Hiroaki
Tsutsuminai, Susumu
Kariya, Nobuko
Domen, Kazunari
Hisatomi, Takashi
Lin, Lihua
Tao, Xiaoping
Liang, Xizhuang
Abstract
Provided is a photocatalyst with significantly enhanced water splitting performance in YTOS or in a composition in which the yttrium element of YTOS has been replaced with another element. Also provided is a method for producing a photocatalyst that has a composition represented by the following general formula (I), the method including mixing, with a raw material of the photocatalyst, a flux component at a mass ratio of 0.01 times to 50 times, the flux component being composed of one or more chlorides and/or iodides of at least one selected from Li, Na, K, Rb, Mg, Ca, Sr, and Ba, and calcining a resultant product at 450° C. to 1050° C.:
Provided is a photocatalyst with significantly enhanced water splitting performance in YTOS or in a composition in which the yttrium element of YTOS has been replaced with another element. Also provided is a method for producing a photocatalyst that has a composition represented by the following general formula (I), the method including mixing, with a raw material of the photocatalyst, a flux component at a mass ratio of 0.01 times to 50 times, the flux component being composed of one or more chlorides and/or iodides of at least one selected from Li, Na, K, Rb, Mg, Ca, Sr, and Ba, and calcining a resultant product at 450° C. to 1050° C.:
MaTibOcSd (I)
Provided is a photocatalyst with significantly enhanced water splitting performance in YTOS or in a composition in which the yttrium element of YTOS has been replaced with another element. Also provided is a method for producing a photocatalyst that has a composition represented by the following general formula (I), the method including mixing, with a raw material of the photocatalyst, a flux component at a mass ratio of 0.01 times to 50 times, the flux component being composed of one or more chlorides and/or iodides of at least one selected from Li, Na, K, Rb, Mg, Ca, Sr, and Ba, and calcining a resultant product at 450° C. to 1050° C.:
MaTibOcSd (I)
(where M is a combination of one or more selected from Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, and Y, a is a number of 1.7 to 2.3, b is a number of 2, c is a number of 4.7 to 5.3, and d is a number of 1.7 to 2.3).
B01J 19/12 - Processes employing the direct application of electric or wave energy, or particle radiation; Apparatus therefor employing electromagnetic waves
C25B 1/04 - Hydrogen or oxygen by electrolysis of water
To provide a novel resin composition that contains a polyethylene terephthalate resin and a polybutylene terephthalate resin, as well as a resin composition, a molded article, a composite, and a metal-resin composite formed from such resin composition. The resin composition contains an inorganic filler with respect to a total of 100 parts by mass of a polybutylene erephthalate resin and a polyethylene terephthalate resin, wherein a mass ratio of the polybutylene terephthalate resin and the polyethylene terephthalate resin with respect to a total of 100 parts by mass of the polybutylene terephthalate resin and the polyethylene terephthalate resin is from 10/90 to 90/10, and the polyethylene terephthalate resin comprises from 1.0 to 100 μg/g of elemental iron.
A laminate film having at least a base layer and a sealant layer in which: the sealant layer is composed of a resin composition containing a thermoplastic elastomer (B) as the main component; the thermoplastic elastomer (B) contains a styrene unit; and the sealant layer further contains a crosslinker (C). According to the present invention, a laminate film having excellent suitability for thermal lamination and excellent humidity and heat resistance can be provided.
B32B 27/08 - Layered products essentially comprising synthetic resin as the main or only constituent of a layer next to another layer of a specific substance of synthetic resin of a different kind
B32B 33/00 - Layered products characterised by particular properties or particular surface features, e.g. particular surface coatings; Layered products designed for particular purposes not covered by another single class
73.
CURABLE COMPOSITION, MOLDED BODY, SILICONE HYDROGEL, METHOD FOR PRODUCING SILICONE HYDROGEL, AND MACROMONOMER
A curable composition includes a macromonomer (A) having a structural unit (a1) of formula (1):
A curable composition includes a macromonomer (A) having a structural unit (a1) of formula (1):
A curable composition includes a macromonomer (A) having a structural unit (a1) of formula (1):
R1 being a hydrogen atom or a methyl group, R2 being an alkylene group having 1 to 4 carbon atoms, R3 being a hydrocarbon group having 1 to 6 carbon atoms, and h being a natural number of 1 to 20; a silicone-based (meth)acrylate (B); and a hydrophilic monomer (C).
A resin composition contains a polybutylene terephthalate resin and a polyethylene terephthalate resin, wherein a mass ratio of the polybutylene terephthalate resin and the polyethylene terephthalate resin with respect to a total of 100 parts by mass of the polybutylene terephthalate resin and the polyethylene terephthalate resin is from 10/90 to 90/10, and wherein, when one cycle is defined as an operation in which, based on JIS K7121, a temperature is increased by DSC from 40° C. to 300° C. at a rate of temperature increase of 20° C./min and then the temperature is reduced to 40° C. at a rate of temperature cooling of −20° C./min, the polyethylene terephthalate resin has an absolute value of a heat of crystallization during a heating phase in a first cycle (ΔHTc1-1st) and/or an absolute value of a heat of crystallization during the heating phase in a second cycle (ΔHTc1-2nd) of the operation of less than 3 J/g.
F21S 41/37 - Illuminating devices specially adapted for vehicle exteriors, e.g. headlamps characterised by reflectors characterised by their material, surface treatment or coatings
F21S 43/33 - Signalling devices specially adapted for vehicle exteriors, e.g. brake lamps, direction indicator lights or reversing lights characterised by reflectors characterised by their material, surface treatment or coatings
To provide a resin composition containing a polyethylene terephthalate resin and an inorganic filler, wherein when one cycle is defined as an operation in which, based on JIS K7121, a temperature is increased by DSC from 40° C. to 300° C. at a rate of temperature increase of 20° C./min and then the temperature is reduced to 40° C. at a rate of temperature cooling of −20° C./min, the polyethylene terephthalate resin has an absolute value of a heat of crystallization during a heating phase in a first cycle (ΔHTc1-1st) of the operation and/or an absolute value of a heat of crystallization during the heating phase in a second cycle (ΔHTc1-2nd) of less than 3 J/g, and a content of the inorganic filler in the resin composition is 40% by mass or more.
C08L 67/03 - Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the hydroxy and the carboxyl groups directly linked to aromatic rings
The present invention relates to a method for producing a cardiomyocyte. In more detail, the present invention relates to a method for producing a cell population containing cardiomyocytes, including differentiation process from cells capable of differentiating into cardiomyocytes to cardiomyocytes, and the differentiation process includes culturing the cells in a serum-free medium containing α fetoprotein to obtain the cardiomyocytes.
A methacrylic resin composition for injection molding or extrusion molding comprising a component (A), a component (B), and a component (C) below, wherein a ratio denoted by [mass of component (C)]/[mass of component (B)] is 0.01 to 50,
component (A): an acrylic resin having a mass average molecular weight of less than 200,000
component (B): at least one selected from a fatty acid, a fatty acid derivative, and a fatty alcohol
component (C): a methacrylic polymer having a mass average molecular weight of 200,000 or more.
A method for producing an aldehyde includes the following steps (1) to (3): (1) withdrawing part or all of a reaction solution from a hydroformylation reaction zone while performing the hydroformylation reaction; (2) oxidizing by bringing the withdrawn reaction solution into contact with an oxygen-containing gas in an atmosphere having a total pressure of 0.8 MPaA or less and an oxygen partial pressure ratio of 10% or less; and (3) feeding the oxidized reaction solution to the hydroformylation reaction zone while maintaining a state in which the catalyst is dissolved or dispersed in the reaction solution.
C07C 45/50 - Preparation of compounds having C=O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with carbon monoxide by oxo-reactions
According to the present disclosure, there is provided a resin composition containing a vinyl chloride-based polymer (A1), a plasticizer (A2), and a (meth)acrylic copolymer (B), in which the (meth)acrylic copolymer (B) is a block copolymer or a graft copolymer, which contains a monomer unit (b1) represented by Formula (1).
According to the present disclosure, there is provided a resin composition containing a vinyl chloride-based polymer (A1), a plasticizer (A2), and a (meth)acrylic copolymer (B), in which the (meth)acrylic copolymer (B) is a block copolymer or a graft copolymer, which contains a monomer unit (b1) represented by Formula (1).
The present invention provides: a carbon fiber that gives a carbon fiber bundle having a high strand strength and a high strand elastic modulus and has reduced defects; a carbon fiber bundle including the carbon fiber; and a production method for a carbon fiber bundle having a high strand strength and a high strand elastic modulus and having reduced defects in single fibers. The carbon fiber of the present invention is such that the number of voids in a cross-section of a single fiber is 8 or less; the carbon fiber bundle of the present invention includes the carbon fiber of the present invention; and in the production method for a carbon fiber bundle of the present invention, a temperature increase rate in a case of raising a heating temperature from 1,800° C. to 2,200° C. is 300° C./min to 600° C./min.
D01F 9/22 - Carbon filaments; Apparatus specially adapted for the manufacture thereof by decomposition of organic filaments from polyaddition, polycondensation or polymerisation products from macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from polyacrylonitriles
G01N 23/04 - Investigating or analysing materials by the use of wave or particle radiation, e.g. X-rays or neutrons, not covered by groups , or by transmitting the radiation through the material and forming images of the material
A structure and a solid-state imaging device, each of which enables high-level imaging by infrared rays. The structure is provided with a plurality of color filters positioned on a support, in which the color filters include a first infrared color filter and a second infrared color filter. When a near-infrared region is divided into two parts, a short wavelength side is defined as a specific wavelength band 1, and a long wavelength side is defined as a specific wavelength band 2, the first infrared color filter shields light in a visible region, transmits at least a part of light in the specific wavelength band 1, and shields light in the specific wavelength band 2, and the second infrared color filter shields light in the visible region, shields light in the specific wavelength band 1, and transmits at least a part of light in the specific wavelength band 2.
An object of the present invention is to provide a resonator that is relatively lightweight, has high sound-blocking performance overwhelming the law of mass action, and is excellent in terms of manufacturability and durability. The resonator includes at least a sheet and at least one resonance portion. The resonance portion is provided in contact with a sheet surface of the sheet, and the resonance portion includes a weight portion and a base portion. The weight portion is supported by the base portion and has a larger mass than the base portion, and the weight portion has a penetration portion. The base portion is in contact with a surface on a resonance portion front end side of the weight portion and covers the weight portion.
G10K 11/172 - Methods or devices for protecting against, or for damping, noise or other acoustic waves in general using resonance effects
B29C 39/10 - Shaping by casting, i.e. introducing the moulding material into a mould or between confining surfaces without significant moulding pressure; Apparatus therefor for making articles of definite length, i.e. discrete articles incorporating preformed parts or layers, e.g. casting around inserts or for coating articles
B29L 31/30 - Vehicles, e.g. ships or aircraft, or body parts thereof
B32B 3/26 - Layered products essentially comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products essentially having particular features of form characterised by a layer with cavities or internal voids
B32B 3/30 - Layered products essentially comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products essentially having particular features of form characterised by a layer with cavities or internal voids characterised by a layer formed with recesses or projections, e.g. grooved, ribbed
B32B 25/04 - Layered products essentially comprising natural or synthetic rubber comprising rubber as the main or only constituent of a layer, next to another layer of a specific substance
B60R 13/08 - Insulating elements, e.g. for sound insulation
The present invention provides a novel polycarbonate diol and a polyurethane using the polycarbonate diol as raw materials. The novel polycarbonate diol produces polycarbonate diol-based polyurethane which has a high degree of hardness, superior abrasion resistance, and superior hydrophilicity, and is usable for an application such as a paint, a coating agent, a synthetic leather, an artificial leather, and a highly-functional elastomers, or the like. The present invention also provides an active-energy radiation curable polymer composition giving a cured film having a superior contamination resistance and high degree of hardness. The present invention is obtained, for example, by reacting specific two types of diols with diester carbonate in the presence of a transesterification catalyst being a compound using a metal of Group 1 or 2 on the periodic table. The present invention provides a polycarbonate diol wherein the metal content of the transesterification catalyst is 100 weight ppm or less, a polyurethane obtainable by using this polycarbonate diol and an active-energy radiation curable polymer composition containing the urethane(meth)acrylate oligomer which is obtained from the polycarbonate diol.
A nonaqueous electrolyte secondary battery having excellent discharge load characteristics and are excellent in high-temperature storability, cycle characteristics, high capacity, continuous-charge characteristics, storability, gas evolution inhibition during continuous charge, high-current-density charge/discharge characteristics, discharge load characteristics is provided. The battery contains a negative electrode having an active material comprising Si or a Si alloy; a positive electrode; and a nonaqueous electrolyte solution, containing an electrolyte; a nonaqueous solvent including an acyclic carbonate having a halogen atom; and at least one compound selected from the group consisting of a monofluorophosphate and a difluorophosphate. A nonaqueous electrolyte in contact with a negative electrode having an active material comprising Si or a Si alloy is also provided.
A cleaning liquid for removing a cerium compound contains (A) a six-membered ring compound having two or more hydroxy groups, and (B) an inorganic acid compound, and a mass ratio of the component (B) to the component (A) is 0.05 to 0.6. The component (A) may contain at least one selected from the group consisting of catechol, resorcinol, hydroquinone, pyrogallol, and methylcatechol.
A modified ethylene-vinyl alcohol resin composition including: a modified ethylene-vinyl alcohol resin having 1 to 16.5 mol % of a primary hydroxy group structural unit at a side chain; and a conjugated polyene, wherein the resin composition exhibits not less than five melting peaks when subjected to differential scanning calorimetry (DSC) according to specific analysis conditions.
The present disclosure provides an adhesive sheet formed from an adhesive composition containing a (meth)acrylic acid ester copolymer and a crosslinker, in which the (meth)acrylic acid ester copolymer contains, as components that constitute the copolymer, (A) a branched or linear C1 to C20 alkyl (meth)acrylic acid ester monomer, (B) a monomer having an alkylene glycol group in a molecule and having a (meth)acryloyl group, and (C) a nitrogen-containing vinyl monomer, and the adhesive sheet has a storage shear modulus at −30° C. (G′ (−30° C.)) of not greater than 250 kPa obtained by dynamic viscoelasticity measurement with a shearing mode at a frequency of 1 Hz, and has a strain recovery rate (400%, 1 minute) of not less than 70%.
A bonding structure used for forming a sealed space (for example, a container) for containing or transferring an organotin compound, wherein the bonding structure is a structure in which a first metal member (for example, a lid of the container) is connected to a second metal member (for example, a container body of the container) via a metal gasket or a metal O-ring, and the metal gasket or the metal O-ring has a surface having a Vickers hardness set to be not less than lower than a Vickers hardness of a surface of a portion of the metal member, the portion being contacted with the metal gasket or the metal O-ring.
A method for producing a prepreg according an aspect of the present invention includes: obtaining an impregnated fiber reinforcement by impregnating a fiber reinforcement with a liquid epoxy resin composition which is a precursor material of a matrix; and thickening the liquid epoxy resin composition in the impregnated fiber reinforcement. An epoxy resin, an epoxy curing agent, a thickening agent, and a radically polymerizable liquid monomer are mixed in the liquid epoxy resin composition, and the thickening is performed so that the epoxy curing agent and the radically polymerizable liquid monomer remain in the matrix.
Provided is an n-type GaN crystal, in which a donor impurity contained at the highest concentration is Ge, and which has a room-temperature resistivity of lower than 0.03 Ω·cm and a (004) XRD rocking curve FWHM of less than 20 arcsec. The n-type GaN crystal has two main surfaces, each having an area of 3 cm2 or larger. One of the two main surfaces can have a Ga polarity and can be inclined at an angle of 0° to 10° with respect to a (0001) crystal plane. Further, the n-type GaN crystal can have a diameter of 20 mm or larger.
C30B 25/20 - Epitaxial-layer growth characterised by the substrate the substrate being of the same materials as the epitaxial layer
H01L 21/02 - Manufacture or treatment of semiconductor devices or of parts thereof
H01L 29/04 - Semiconductor bodies characterised by their crystalline structure, e.g. polycrystalline, cubic or particular orientation of crystalline planes
H01L 29/20 - Semiconductor bodies characterised by the materials of which they are formed including, apart from doping materials or other impurities, only AIIIBV compounds
H01L 29/36 - Semiconductor bodies characterised by the concentration or distribution of impurities
H01L 33/00 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof
H01L 33/02 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies
H01L 33/16 - SEMICONDUCTOR DEVICES NOT COVERED BY CLASS - Details thereof characterised by the semiconductor bodies with a particular crystal structure or orientation, e.g. polycrystalline, amorphous or porous
H01L 33/32 - Materials of the light emitting region containing only elements of group III and group V of the periodic system containing nitrogen
91.
BIODEGRADABLE RESIN COMPOSITION, MOLDED ARTICLE, AND BIOLOGICAL DEGRADATION METHOD
A biodegradable resin composition may include a polyester resin and one or more nitrogen compounds of formula (I):
A biodegradable resin composition may include a polyester resin and one or more nitrogen compounds of formula (I):
A biodegradable resin composition may include a polyester resin and one or more nitrogen compounds of formula (I):
R, R″, and R″″ each independently being H or a monovalent organic group which may have a substituent group which does not form a ring structure with each other, optionally in salt form (excluding (RS)-1-methyl-2-nitro-3-[(3-tetrahydrofuryl)methyl]guanidine, and/or compounds of formula NH2—CHR—COOH, with R being H or a monovalent aliphatic hydrocarbon group, and phenylalanine). The polyester resin may be a resin having dicarboxylic acid unit and a diol unit. The content of the compound of formula (I) may be in a range of from 0.1 to 70 wt. %. The concentration of nitrogen atom in the compound of formula (I) may be 6 wt. % or more. The molecular weight of the compound of formula (I) may be less than 10000.
A polycarbonate resin composition including a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), and a carbonate structural unit (Z) derived from an aromatic dihydroxy compound represented by the following formula (3). A molar ratio of the content of the carbonate structural unit (Y) to the carbonate structural unit (X) is 0.65 or more, and the content of the carbonate structural units (Y) in 100 mol % of all carbonate structural units of the polycarbonate resin composition is 49 mol % or less.
A polycarbonate resin composition including a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), and a carbonate structural unit (Z) derived from an aromatic dihydroxy compound represented by the following formula (3). A molar ratio of the content of the carbonate structural unit (Y) to the carbonate structural unit (X) is 0.65 or more, and the content of the carbonate structural units (Y) in 100 mol % of all carbonate structural units of the polycarbonate resin composition is 49 mol % or less.
A polycarbonate resin composition including a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), and a carbonate structural unit (Z) derived from an aromatic dihydroxy compound represented by the following formula (3). A molar ratio of the content of the carbonate structural unit (Y) to the carbonate structural unit (X) is 0.65 or more, and the content of the carbonate structural units (Y) in 100 mol % of all carbonate structural units of the polycarbonate resin composition is 49 mol % or less.
(R1 and R2 represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted aryl group. R1 and R2 may be bonded to each other to form a ring)
A polycarbonate resin composition including a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), and a carbonate structural unit (Z) derived from an aromatic dihydroxy compound represented by the following formula (3). A molar ratio of the content of the carbonate structural unit (Y) to the carbonate structural unit (X) is 0.65 or more, and the content of the carbonate structural units (Y) in 100 mol % of all carbonate structural units of the polycarbonate resin composition is 49 mol % or less.
(R1 and R2 represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted aryl group. R1 and R2 may be bonded to each other to form a ring)
A polycarbonate resin composition including a carbonate structural unit (X) derived from an aromatic dihydroxy compound represented by the following formula (1), a carbonate structural unit (Y) derived from an aromatic dihydroxy compound represented by the following formula (2), and a carbonate structural unit (Z) derived from an aromatic dihydroxy compound represented by the following formula (3). A molar ratio of the content of the carbonate structural unit (Y) to the carbonate structural unit (X) is 0.65 or more, and the content of the carbonate structural units (Y) in 100 mol % of all carbonate structural units of the polycarbonate resin composition is 49 mol % or less.
(R1 and R2 represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted aryl group. R1 and R2 may be bonded to each other to form a ring)
(W represents —O—, —S—, —SO2—, or —CR3R4—. R3 and R4 represent a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 20 carbon atoms, or a substituted or unsubstituted aryl group. R3 and R4 may be bonded to each other to form a ring)
Particles may have a chromaticity b* of 2.0 or less. Such particles may include graphite (A) and particles (B) containing a silicon element. The chromaticity b* of the particles is preferably 0.2 or more and 1.1 or less, and the chromaticity a* of the particles is preferably 0.2 or more and 1.2 or less. A method can manufacture a secondary battery including a positive electrode, a negative electrode, and an electrolyte, wherein the negative electrode includes a current collector and a negative electrode active material layer disposed on the current collector, and the negative electrode active material layer contains such graphite.
A method for purifying a tin compound, including: making an inert gas pass through in, or on a surface of, a liquid containing a tin compound represented by a chemical formula RSnX3, where R represents a hydrocarbon group having 1 to 30 carbon atoms optionally substituted with a halogen atom, and X represents a hydrolysable substituent, to perform stripping, before or after a distillation step of the tin compound.
An ethylene-vinyl alcohol copolymer containing 1 to 16.5 mol % of an ethylene structural unit and has a yellowness of 80 or less, wherein the yellowness is determined by a reflection measuring method in accordance with JIS K7373 after heating a particle of the ethylene-vinyl alcohol copolymer at 170° C. for 5 hours in air.
To provide a pellet which is formed from a composition comprising 5 to 65 parts by mass of recycled carbon fibers as a heated product of carbon fiber reinforced resin, and 0.05 to 25 parts by mass of a nonmetal salt-based flame retardant, relative to 100 parts by mass of a polycarbonate resin having a terminal hydroxyl group content of 150 to 800 ppm.
B29C 48/285 - Feeding the extrusion material to the extruder
B29C 48/88 - Thermal treatment of the stream of extruded material, e.g. cooling
B29K 69/00 - Use of polycarbonates as moulding material
B29K 105/12 - Condition, form or state of moulded material containing reinforcements, fillers or inserts of short lengths, e.g. chopped filaments, staple fibres or bristles
CARBON MATERIAL, METHOD FOR PRODUCING CARBON MATERIAL, METHOD FOR PRODUCING SPHERICAL CARBON MATERIAL, METHOD FOR PRODUCING COMPOSITE CARBON MATERIAL, AND METHOD FOR MANUFACTURING SECONDARY BATTERY
A carbon material comprising natural graphite, wherein the carbon material satisfies the following formulas (1) and (2),
A carbon material comprising natural graphite, wherein the carbon material satisfies the following formulas (1) and (2),
y≥0.23x+3.1 (1)
A carbon material comprising natural graphite, wherein the carbon material satisfies the following formulas (1) and (2),
y≥0.23x+3.1 (1)
z≥0.43 (2)
wherein x is d50 (μm) of the carbon material, y is d90/d10 of the carbon material, and z is the tap density (g/cm3).
An information generation method includes: a manufacturing step; an input step; a generation step; and a registration step. In the manufacturing step, a product including a plastic article to which a chemical tag is attached is manufactured. In the input step, product information related to recycling of the product is input. In the generation step, tag product information with which the product information is associated in a wavelength spectral profile of the chemical tag readable from the product is generated. In the registration step, the tag product information is registered.
A method for producing an olefin polymer includes polymerizing an olefin in the presence of a catalyst composition including a compound represented by the general formula (A) or (B) and a transition metal compound represented by the general formula (C), or in the presence of a metal complex represented by the general formula (D) (the general formulas are defined in the specification). The olefin polymerization catalyst is capable of catalyzing copolymerization of an olefin and a vinyl monomer with high activity and high comonomer incorporation efficiency to achieve a high molecular weight. The olefin polymer production method uses the catalyst.
NEGATIVE ELECTRODE MATERIAL FOR NONAQUEOUS SECONDARY BATTERIES, NEGATIVE ELECTRODE FOR NONAQUEOUS SECONDARY BATTERIES, AND NONAQUEOUS SECONDARY BATTERY
Provided are: a negative electrode material for nonaqueous secondary batteries, which can yield a high-capacity nonaqueous secondary battery having excellent discharge rate characteristics; and a negative electrode for nonaqueous secondary batteries and a nonaqueous secondary battery. Also provided is a nonaqueous secondary battery having excellent charge-discharge efficiency. The negative electrode material for nonaqueous secondary batteries includes carbonaceous particles (A) and silicon oxide particles (B), and satisfies the followings: a) the average particle size (50% cumulative particle size from the smaller particle side; d50) is 3 μm to 30 μm, and the 10% cumulative particle size from the smaller particle side (d10) is 0.1 μm to 10 μm; b) the ratio (R1=d90/d10) between the 90% cumulative particle size from the smaller particle side (d90) and the d10 is 3 to 20; and c) the ratio (R2=d50/d10) between the d50 and the d10 is 1.7 to 5.