C08G75/0231

POLYARYLENE SULFIDE PRODUCTION METHOD, POLYARYLENE SULFIDE COPOLYMER PRODUCTION METHOD, AND POLYARYLENE SULFIDE

A method of producing a polyarylene sulfide composed of amino groups, the method including allowing at least a dihalogenated aromatic compound, an inorganic sulfurizing agent and a compound (A) to react in an organic polar solvent and in the presence of an alkali metal hydroxide, wherein: said compound (A) is present in an amount of 0.04 moles or more and 0.5 moles or less with respect to 1 mole of said inorganic sulfurizing agent, in a reaction vessel; and said compound (A) is a compound comprising at least one aromatic ring, and having, on said one aromatic ring, an amino group, and at least one functional group selected from the group consisting of hydroxyl group, a salt of hydroxyl group, thiol group and a salt of thiol group.

Dual cure sealants

Compositions that are curable by free radical redox reactions are disclosed. Free radical curing reactions between polythiols and polyalkyenyls are initiated by the reaction of metal complexes and organic peroxides. The compositions are useful as sealants.

Dual cure sealants

Compositions that are curable by free radical redox reactions are disclosed. Free radical curing reactions between polythiols and polyalkyenyls are initiated by the reaction of metal complexes and organic peroxides. The compositions are useful as sealants.

POLY(ARYLENE SULFIDE) AND PRODUCTION METHOD THEREFOR

A polyarylene sulfide in which when the cumulative integral value from the molecular weight of 100 to the molecular weight of 10,000 in a molecular weight distribution curve is 100, the cumulative integrated value at the molecular weight of 4000 is 48 to 53, and when the melt flow rate of the polyarylene sulfide is defined as MFR1, and when the melt flow rate obtained after mixing the polyarylene sulfide with an epoxy silane coupling agent at a weight ratio of 100:1 and heating the resulting mixture at 315.5° C. for 5 minutes is defined as MFR2, the rate of change represented by MFR2/MFR1 is not more than 0.085.

POLYARYLENE SULFIDE PRODUCTION METHOD

A method for producing polyarylene sulfide that can have a high melt viscosity while suppressing ultra-fine powder generation. The method for producing polyarylene sulfide includes: (1) preparing a prepared mixture containing an organic polar solvent, a sulfur source, and a dihalo aromatic compound; (2) initiating a polymerization reaction by heating the prepared mixture to produce a prepolymer; (3) adding water as a phase separation agent to a reaction mixture in a reaction system to form a phase-separated state; and (4) continuing the polymerization reaction after phase separation. In the method, when a dihalo aromatic compound conversion ratio is 80 mass % or greater and 93 mass % or less and after the prepolymer reaches a weight average molecular weight of 10000 or greater in the first-stage polymerization step, an aromatic compound having 3 or more halogen atoms bonded to an aromatic ring is added to the reaction mixture.

POLYARYLENE SULFIDE PRODUCTION METHOD

A method for producing polyarylene sulfide that can have a high melt viscosity while suppressing ultra-fine powder generation. The method for producing polyarylene sulfide includes: (1) preparing a prepared mixture containing an organic polar solvent, a sulfur source, and a dihalo aromatic compound; (2) initiating a polymerization reaction by heating the prepared mixture to produce a prepolymer; (3) adding water as a phase separation agent to a reaction mixture in a reaction system to form a phase-separated state; and (4) continuing the polymerization reaction after phase separation. In the method, when a dihalo aromatic compound conversion ratio is 80 mass % or greater and 93 mass % or less and after the prepolymer reaches a weight average molecular weight of 10000 or greater in the first-stage polymerization step, an aromatic compound having 3 or more halogen atoms bonded to an aromatic ring is added to the reaction mixture.

Dual Cure Sealants

Compositions that are curable by free radical redox reactions are disclosed. Free radical curing reactions between polythiols and polyalkyenyls are initiated by the reaction of metal complexes and organic peroxides. The compositions are useful as sealants.

Dual Cure Sealants

Compositions that are curable by free radical redox reactions are disclosed. Free radical curing reactions between polythiols and polyalkyenyls are initiated by the reaction of metal complexes and organic peroxides. The compositions are useful as sealants.

HALOGENATED POLYPHENYLENE SULFIDE RESIN, RESIN COMPOSITION, MOLDED ARTICLE, AND VIBRATION-DAMPING AGENT FOR RESIN

Provided are: a halogenated polyphenylene sulfide resin that can make a resin vibration-damping without use of a filler when added to the resin; a resin composition containing the halogenated polyphenylene sulfide resin and another resin; a molded article formed of the resin composition; and a vibration-damping agent for a resin, the vibration-damping agent containing the halogenated polyphenylene sulfide resin. A halogenated polyphenylene sulfide resin is used as a component to make a resin vibration-damping in a resin composition. The halogenated polyphenylene sulfide resin is produced by polycondensation reaction of a halogenated benzene and an alkali metal sulfide. The halogenated benzene is a dihalobenzene and/or a trihalobenzene. A ratio of a mass of the trihalobenzene to a mass of the halogenated benzene being 50 mass % or greater.

Polyarylene sulfide resin and preparation method thereof
11390714 · 2022-07-19 · ·

The present invention relates to a polyarylene sulfide which has more improved compatibility with other polymer materials or fillers, and a method for preparing the same. The polyarylene sulfide is characterized in that at least part of end groups of the main chain of the polyarylene sulfide is hydroxyl group (—OH), the polyarylene sulfide contains iodine bonded to its main chain and free iodine, and the content of iodine bonded to the main chain and free iodine is 10 to 10,000 ppmw.