C08K5/353

THERMAL TRANSFER RECORDING SHEET
20240025197 · 2024-01-25 ·

A thermal transfer recording sheet includes a substrate, a yellow coloring material layer, a magenta coloring material layer, a cyan coloring material layer, and a protective layer. The yellow coloring material layer, the magenta coloring material layer, the cyan coloring material layer, and the protective layer are frame-sequentially arranged over the substrate. The protective layer contains a compound represented by formula (1):

##STR00001##

where each A is independently CH or CHC.sub.6H.sub.4, each Y is independently an oxygen atom or a sulfur atom, and R.sub.1 and R.sub.2 are each independently a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.

RUBBER COMPOSITION FOR DOWNHOLE TOOLS AND MEMBER FOR DOWNHOLE TOOLS
20200071486 · 2020-03-05 ·

A rubber composition for downhole tools having excellent degradability and storability is provided. The rubber composition for downhole tools includes degradable rubber, a degradation accelerator, and a degradation inhibitor. The degradation accelerator is at least one type of the compound represented by Formula (I) or Formula (II) below. The degradation inhibitor is at least one type selected from the group consisting of carbodiimide compounds, oxazoline compounds, oxazine compounds, and epoxy compounds. The content of the degradation accelerator is from 0.1 to 20 parts by mass relative to 100 parts by mass of the degradable rubber. The content of the degradation inhibitor is from 0.1 to 3 parts by mass relative to 100 parts by mass of the degradable rubber.

Prepreg, fiber-reinforced composite material, and resin composition containing particles

A prepreg 10 comprises: a reinforcing fiber layer 3 including reinforcing fibers 1 and a resin composition 2 with which the space between fibers of the reinforcing fibers is impregnated and which contains (A) a benzoxazine resin, (B) an epoxy resin, and (C) a curing agent having 2 or more phenolic hydroxy groups in a molecule; and surface layers 6a and 6b provided on the surfaces of the reinforcing fiber layer 3 and containing (A) a benzoxazine resin, (B) an epoxy resin, (C) a curing agent having 2 or more phenolic hydroxy groups in a molecule, and (D) polyamide resin particles 4 having an average particle size of 5 to 50 m, wherein the polyamide resin particles 4 include the polyamide 1010 resin particle.

Prepreg, fiber-reinforced composite material, and resin composition containing particles

A prepreg 10 comprises: a reinforcing fiber layer 3 including reinforcing fibers 1 and a resin composition 2 with which the space between fibers of the reinforcing fibers is impregnated and which contains (A) a benzoxazine resin, (B) an epoxy resin, and (C) a curing agent having 2 or more phenolic hydroxy groups in a molecule; and surface layers 6a and 6b provided on the surfaces of the reinforcing fiber layer 3 and containing (A) a benzoxazine resin, (B) an epoxy resin, (C) a curing agent having 2 or more phenolic hydroxy groups in a molecule, and (D) polyamide resin particles 4 having an average particle size of 5 to 50 m, wherein the polyamide resin particles 4 include the polyamide 1010 resin particle.

Prepreg, fiber-reinforced composite material, and resin composition containing particles

A prepreg 10 comprises: a reinforcing fiber layer 3 including reinforcing fibers 1 and a resin composition 2 with which the space between fibers of the reinforcing fibers is impregnated and which contains (A) a benzoxazine resin, (B) an epoxy resin, and (C) a curing agent having 2 or more phenolic hydroxy groups in a molecule; and surface layers 6a and 6b provided on the surfaces of the reinforcing fiber layer 3 and containing (A) a benzoxazine resin, (B) an epoxy resin, (C) a curing agent having 2 or more phenolic hydroxy groups in a molecule, and (D) polyamide resin particles 4 having an average particle size of 5 to 50 m, wherein the polyamide resin particles 4 include the polyamide 1010 resin particle.

Alternative methods to control crosslinking in high impact polystyrene

High impact polystyrene may be formed with increased swell index and reduced or eliminated discoloration. A process of forming high impact polystyrene may include providing a polymerization system including a polymerization reactor and a devolatilizer. High impact polystyrene may be formed in the polymerization reactor, and sent to the devolatilizer. A polar antioxidant having a hindered phenol structure and an aliphatic amine group, and with a phosphite antioxidant may be added to the polymerization system. In another process, a chemical retarder and a fluorescent whitening agent may be added to the polymerization system. In another process, a chemical retarder that inhibits free radical rubber crosslinking may be added to the polymerization system.

Alternative methods to control crosslinking in high impact polystyrene

High impact polystyrene may be formed with increased swell index and reduced or eliminated discoloration. A process of forming high impact polystyrene may include providing a polymerization system including a polymerization reactor and a devolatilizer. High impact polystyrene may be formed in the polymerization reactor, and sent to the devolatilizer. A polar antioxidant having a hindered phenol structure and an aliphatic amine group, and with a phosphite antioxidant may be added to the polymerization system. In another process, a chemical retarder and a fluorescent whitening agent may be added to the polymerization system. In another process, a chemical retarder that inhibits free radical rubber crosslinking may be added to the polymerization system.

Alternative methods to control crosslinking in high impact polystyrene

High impact polystyrene may be formed with increased swell index and reduced or eliminated discoloration. A process of forming high impact polystyrene may include providing a polymerization system including a polymerization reactor and a devolatilizer. High impact polystyrene may be formed in the polymerization reactor, and sent to the devolatilizer. A polar antioxidant having a hindered phenol structure and an aliphatic amine group, and with a phosphite antioxidant may be added to the polymerization system. In another process, a chemical retarder and a fluorescent whitening agent may be added to the polymerization system. In another process, a chemical retarder that inhibits free radical rubber crosslinking may be added to the polymerization system.

UV-LED COATING COMPOSITIONS
20200010687 · 2020-01-09 · ·

The present invention relates to UV-LED light curable coating compositions comprising a compound having at least one alpha, beta-ethylenically unsaturated polymerizable double bond, a type II photoinitiator system based on a thioxanthone and an amine, and a colorant. Optional inclusions are a type I photoinitiator and an optical brightener. The UV-LED curable composition provides good surface cure and low yellowing.

UV-LED COATING COMPOSITIONS
20200010687 · 2020-01-09 · ·

The present invention relates to UV-LED light curable coating compositions comprising a compound having at least one alpha, beta-ethylenically unsaturated polymerizable double bond, a type II photoinitiator system based on a thioxanthone and an amine, and a colorant. Optional inclusions are a type I photoinitiator and an optical brightener. The UV-LED curable composition provides good surface cure and low yellowing.