C08F290/046

Adhesive composition
11130884 · 2021-09-28 · ·

An adhesive composition may include 100 parts by weight of a (meth)acrylic polymer (A), 45 to 65 parts by weight of isoboronyl acrylate (B), and 0.1 to 10 parts by weight of a photoradical polymerization initiator (C). Each molecule of the (meth)acrylic polymer (A) may have at least one group represented by the general formula (1) at a molecular terminal: —OC(O)C(R.sup.1)═CH.sub.2 (1), where R.sup.1 is a hydrogen atom or an organic group containing 1 to 20 carbon atoms. The (meth)acrylic polymer (A) may have a number average molecular weight (Mn) of 3,000 to 100,000, and a ratio (Mw/Mn) of a weight average molecular weight (Mw) to a number average molecular weight (Mn) of less than 1.8.

SUBMICRONIC EMULSION
20210178350 · 2021-06-17 · ·

The invention relates to a process for preparing a dispersion of a lipophilic compound in a continuous hydrophilic phase, the morphology of which is submicronic. During the preparation of this dispersion, there is applied, by means of a device which produces a shearing gradient less than 5000 s.sup.−1, a shear stress from 100 to 5000 Pa during the addition of the lipophilic compound in the continuous phase which comprises a rheology-modifying compound selected from anionic copolymers, preferably an anionic polymer, in particular an ASE polymer or a HASE polymer. The dispersed particles of the lipophilic compound are nanometric particles whose size is less than 1 μm. The dispersion, particularly in the form of an emulsion, can be used in numerous fields.

ALL-ACRYLIC MULTIGRAFT COPOLYMER SUPERELASTOMERS
20210108018 · 2021-04-15 ·

Thermoplastic elastomer compositions comprising acrylic multigraft copolymers are described. The multigraft copolymers comprise a rubbery polyacrylate backbone and a plurality of randomly spaced glassy polyacrylate side chains. The multigraft copolymers can be prepared using a facile grafting through method that can provide copolymers with enhanced purity. The acrylic multigraft copolymers exhibit microphase separated morphologies and “superelastomeric” properties, including an elongation at break, strain at break, and/or strain recovery behavior that exceeds that of conventional triblock copolymer polyacrylate thermoplastic elastomers.

ALL-ACRYLIC MULTIGRAFT COPOLYMER SUPERELASTOMERS
20210108018 · 2021-04-15 ·

Thermoplastic elastomer compositions comprising acrylic multigraft copolymers are described. The multigraft copolymers comprise a rubbery polyacrylate backbone and a plurality of randomly spaced glassy polyacrylate side chains. The multigraft copolymers can be prepared using a facile grafting through method that can provide copolymers with enhanced purity. The acrylic multigraft copolymers exhibit microphase separated morphologies and “superelastomeric” properties, including an elongation at break, strain at break, and/or strain recovery behavior that exceeds that of conventional triblock copolymer polyacrylate thermoplastic elastomers.

SOLID ELECTROLYTE COMPOSITION, SOLID ELECTROLYTE-CONTAINING SHEET, ELECTRODE SHEET FOR ALL-SOLID STATE SECONDARY BATTERY, ALL-SOLID STATE SECONDARY BATTERY, METHOD OF MANUFACTURING SOLID ELECTROLYTE-CONTAINING SHEET, METHOD OF MANUFACTURING ALL-SOLID STATE SECONDARY BATTERY, AND METHOD OF MANUFACTURING PARTICLE BINDER
20210143472 · 2021-05-13 · ·

Provided is an a solid electrolyte composition including: an inorganic solid electrolyte; a particle binder that includes a polymer and has an average particle size of 5 nm to 10 μm, the polymer including a component that includes a binding site represented by Formula (H-1) or (H-2) at a side chain and has a C log P value of 4 or lower and a molecular weight of lower than 1000; and a dispersion medium. A solid electrolyte-containing sheet, an electrode sheet for an all-solid state secondary battery, and an all-solid state secondary battery that include layer formed of the solid electrolyte composition are also provided. In addition, method of manufacturing the particle binder, the solid electrolyte-containing sheet, and the all-solid state secondary battery are provided.

PHOTOCURABLE ADHESIVE SHEET, ADHESIVE SHEET LAMINATE, LAMINATE FOR IMAGE DISPLAY DEVICE, AND IMAGE DISPLAY DEVICE

Provided is a photocurable adhesive sheet having both step conformability and shape stability and also excellent in durability after attachment to an adherend member.

The photocurable adhesive sheet includes a first adhesive layer, a second adhesive layer, and an intermediate layer interposed between the first adhesive layer and the second adhesive layer, and is characterized in that the intermediate layer is a layer that is formed from a resin composition containing a (meth)acrylic copolymer as a main component resin and has a crosslinked structure, the first adhesive layer, the second adhesive layer, or both of these layers are photocurable resin layers each formed from a photocurable resin composition, and the fall time in the measurement of holding force at 40° C. under a load of 1 N/cm.sup.2 is 60 minutes or more, while the fall time in the measurement of holding force at 60° C. under a load of 1 N/cm.sup.2 is less than 60 minutes.

PHOTOCURABLE ADHESIVE SHEET, ADHESIVE SHEET LAMINATE, LAMINATE FOR IMAGE DISPLAY DEVICE, AND IMAGE DISPLAY DEVICE

Provided is a photocurable adhesive sheet having both step conformability and shape stability and also excellent in durability after attachment to an adherend member.

The photocurable adhesive sheet includes a first adhesive layer, a second adhesive layer, and an intermediate layer interposed between the first adhesive layer and the second adhesive layer, and is characterized in that the intermediate layer is a layer that is formed from a resin composition containing a (meth)acrylic copolymer as a main component resin and has a crosslinked structure, the first adhesive layer, the second adhesive layer, or both of these layers are photocurable resin layers each formed from a photocurable resin composition, and the fall time in the measurement of holding force at 40° C. under a load of 1 N/cm.sup.2 is 60 minutes or more, while the fall time in the measurement of holding force at 60° C. under a load of 1 N/cm.sup.2 is less than 60 minutes.

SOLID ELECTROLYTE COMPOSITION, SOLID ELECTROLYTE-CONTAINING SHEET, ALL-SOLID STATE SECONDARY BATTERY, METHOD OF MANUFACTURING SOLID ELECTROLYTE-CONTAINING SHEET, AND METHOD OF MANUFACTURING ALL-SOLID STATE SECONDARY BATTERY
20210083323 · 2021-03-18 · ·

Provided is a solid electrolyte composition including: an inorganic solid electrolyte having ion conductivity of a metal belonging to Group 1 or Group 2 in the periodic table; a binder including a polymer that includes a specific structural unit having 6 or more carbon atoms; and a dispersion medium. Provided are a solid electrolyte-containing sheet and an all-solid state secondary battery that include a layer formed of the composition, and method of manufacturing a solid electrolyte-containing sheet and an all-solid state secondary battery.

SOLID ELECTROLYTE COMPOSITION, SOLID ELECTROLYTE-CONTAINING SHEET, ALL-SOLID STATE SECONDARY BATTERY, METHOD OF MANUFACTURING SOLID ELECTROLYTE-CONTAINING SHEET, AND METHOD OF MANUFACTURING ALL-SOLID STATE SECONDARY BATTERY
20210083323 · 2021-03-18 · ·

Provided is a solid electrolyte composition including: an inorganic solid electrolyte having ion conductivity of a metal belonging to Group 1 or Group 2 in the periodic table; a binder including a polymer that includes a specific structural unit having 6 or more carbon atoms; and a dispersion medium. Provided are a solid electrolyte-containing sheet and an all-solid state secondary battery that include a layer formed of the composition, and method of manufacturing a solid electrolyte-containing sheet and an all-solid state secondary battery.

Block copolymer hydrogenate, resin composition, and applications thereof

A block copolymer hydrogenate, which is a hydrogenate of a block copolymer having a polymer block (A) containing a structural unit derived from an aromatic vinyl compound in an amount of more than 70 mol %, and a polymer block (B) containing a structural unit derived from a conjugated diene compound in an amount of 30 mol % or more, and further satisfies the following requirements: Requirement (1): The content of the polymer block (A) in the block copolymer hydrogenate is 1 to 30% by mass. Requirement (2): The conjugated diene compound contains isoprene. Requirement (3): A total content of the 1,2-bond unit and the 3,4-bond unit in the structural units derived from the conjugated diene compound is 60 mol % or more. Requirement (4): The hydrogenation rate of the polymer block (B) is 60 mol % or more. Requirement (5): The block copolymer hydrogenate has a serial temperature range where tan , as measured according to JIS K7244-10 (2005) and under the conditions of a strain of 0.1%, a frequency of 1 Hz, a measurement temperature of 70 to 100 C. and a rate of temperature increase of 3 C./min, is 1.0 or more, and the maximum width of the temperature range is 16 C. or more.