C09D133/24

Surface treatment liquid and surface treatment method

The purpose of the present invention is to provide: a surface treatment liquid that is capable of favorably hydrophilizing or hydrophobing surfaces of an object to be treated without having to include a film forming resin; and a surface treatment method using the surface treatment liquid. The present invention provides a surface treatment liquid which comprises (A) a resin and (C) a solvent, wherein as (A) the resin, a resin is used which has a weight average molecular weight of 100000 or more and contains a functional group I which comprises one group or more selected from the group consisting of a hydroxyl group, a cyano group, and a carboxyl group, and a functional group II which is a hydrophilic group or a hydrophobic group other than the functional group I.

SULFUR-CARBON COMPOSITE, POSITIVE ELECTRODE FOR LITHIUM-SULFUR BATTERY COMPRISING SAME, AND LITHIUM-SULFUR BATTERY COMPRISING POSITIVE ELECTRODE

Disclosed is a sulfur-carbon composite including a carbon material, a coating on the carbon material which comprises a copolymer containing a monomer unit containing a catechol group and a monomer unit containing a lithium ion conductor, and sulfur. Also disclosed is an electrode for lithium-sulfur battery including the same, and a lithium-sulfur battery including the electrode.

SULFUR-CARBON COMPOSITE, POSITIVE ELECTRODE FOR LITHIUM-SULFUR BATTERY COMPRISING SAME, AND LITHIUM-SULFUR BATTERY COMPRISING POSITIVE ELECTRODE

Disclosed is a sulfur-carbon composite including a carbon material, a coating on the carbon material which comprises a copolymer containing a monomer unit containing a catechol group and a monomer unit containing a lithium ion conductor, and sulfur. Also disclosed is an electrode for lithium-sulfur battery including the same, and a lithium-sulfur battery including the electrode.

RESIN COMPOSITION, RESIN SHEET, MULTILAYER PRINTED WIRING BOARD, AND SEMICONDUCTOR DEVICE

A resin composition of the present invention contains: a maleimide compound (A) having a transmittance of 5% or more at a wavelength of 405 nm (h-line); a particular carboxylic acid containing compound (B); and a photo initiator (C) having an absorbance of 0.1 or more at a wavelength of 405 nm (h-line).

Transparent laminate

A transparent laminate including a transparent substrate and structure layer, wherein the structure layer contains protrusion portions, depression portions, or both on a surface thereof, and an average distance between the adjacent protrusion portions or between the adjacent depression portions is equal to or less than a visible light wavelength, the structure layer includes a polymerized product of an active energy ray curable resin composition, the resin composition includes a composition of a (meth)acryloyl group-containing polymerizable compound, the compound composition includes one or more from each of (A), (B), and (C): (A) a monofunctional (meth)acryloyl group-containing polymerizable compound; (B) alkylene glycol di(meth)acrylate; and (C) trifunctional or higher (meth)acrylate,
the (A) satisfies certain conditions specifying a type and amount of a compound, and a ratio (E′.sub.150/E′.sub.50) of storage elastic modulus E′.sub.150 of the structure layer at 150° C. to storage elastic modulus E′.sub.50 thereof at 50° C. is 0.5 or less.

Transparent laminate

A transparent laminate including a transparent substrate and structure layer, wherein the structure layer contains protrusion portions, depression portions, or both on a surface thereof, and an average distance between the adjacent protrusion portions or between the adjacent depression portions is equal to or less than a visible light wavelength, the structure layer includes a polymerized product of an active energy ray curable resin composition, the resin composition includes a composition of a (meth)acryloyl group-containing polymerizable compound, the compound composition includes one or more from each of (A), (B), and (C): (A) a monofunctional (meth)acryloyl group-containing polymerizable compound; (B) alkylene glycol di(meth)acrylate; and (C) trifunctional or higher (meth)acrylate,
the (A) satisfies certain conditions specifying a type and amount of a compound, and a ratio (E′.sub.150/E′.sub.50) of storage elastic modulus E′.sub.150 of the structure layer at 150° C. to storage elastic modulus E′.sub.50 thereof at 50° C. is 0.5 or less.

ADHESIVE COMPOSITION
20210284879 · 2021-09-16 · ·

An adhesive composition having excellent adhesiveness to a cycloolefin resin or the like. The adhesive composition of the present invention includes a polymer having a repeating unit derived from a polymerizable compound represented by formula (I): Y—N(Ar)(R) Formula (I), in which Ar represents an unsubstituted or substituted C6 to C14 aryl group or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; R represents an unsubstituted or substituted C1 to C6 alkyl group, an unsubstituted or substituted C3 to C6 cycloalkyl group, an unsubstituted or substituted C6 to C14 aryl group, or an unsubstituted or substituted C6 to C10 aryl C1 to C3 alkyl group; and Y represents a polymerizable functional group. In Formula (I), a substituent on Ar and a substituent on R can bond to form a divalent organic group.

SYSTEMS AND METHODS FOR N-HALAMINE-DOPAMINE COPOLYMERS FOR HIGH-PERFORMANCE, LOW-COST, AND EASY-TO-APPLY ANTIMICROBIAL COATINGS
20210267200 · 2021-09-02 ·

The present application relates to copolymers of N-halamine (HA) and dopamine (DMA) and their method of formation. The HA and DMA are present in the copolymer in a ratio of 0.4:9.6 to 9.6:0.4 (HA: DMA). The copolymers can be used in novel antimicrobial compositions that can be coated, and covalently bonded to surfaces such as metal, plastic, glass, or paint surfaces. The coating provides a rechargeable antimicrobial surface with the treatment of a halogen. The coating thickness and halogen content can be tuned by adjusting the formulation and crosslinking the coating.

SYSTEMS AND METHODS FOR N-HALAMINE-DOPAMINE COPOLYMERS FOR HIGH-PERFORMANCE, LOW-COST, AND EASY-TO-APPLY ANTIMICROBIAL COATINGS
20210267200 · 2021-09-02 ·

The present application relates to copolymers of N-halamine (HA) and dopamine (DMA) and their method of formation. The HA and DMA are present in the copolymer in a ratio of 0.4:9.6 to 9.6:0.4 (HA: DMA). The copolymers can be used in novel antimicrobial compositions that can be coated, and covalently bonded to surfaces such as metal, plastic, glass, or paint surfaces. The coating provides a rechargeable antimicrobial surface with the treatment of a halogen. The coating thickness and halogen content can be tuned by adjusting the formulation and crosslinking the coating.

Barrier coating structure
11066561 · 2021-07-20 · ·

The present disclosure provides a barrier-coating structure that includes a polymer-matrix composite having a first surface and a second surface. The barrier-coating structure includes a flexible layer having a first surface and a second surface and a sol-gel layer having a first surface and a second surface. The first surface of the flexible layer contacts the second surface of the flexible layer. The barrier-coating structure includes a barrier layer having a first surface and a second surface. The sol-gel and/or the barrier layer may comprise one or more reactive substituents. The first surface of the barrier layer may be a laser-ablated surface.