Patent classifications
C08G75/0254
Preparation method of polyarylene sulfide
The present disclosure relates to a preparation method of a polyarylene sulfide, and this method may produce a polyarylene sulfide having properties equal to or higher than those of the conventional method at a high yield by adding an aliphatic amino acid hydrochloride in addition to existing materials for dehydration.
Preparation method of polyarylene sulfide
The present disclosure relates to a preparation method of a polyarylene sulfide, and this method may produce a polyarylene sulfide having properties equal to or higher than those of the conventional method at a high yield by adding an aliphatic amino acid hydrochloride in addition to existing materials for dehydration.
CATALYST FOR HYDROGENATION REACTION AND METHOD FOR PRODUCING SAME
A catalyst for a hydrogenation reaction including: a polymer support; and a catalytic component supported on the polymer support. The polymer support comprises a repeating unit represented by Formula 1.
CATALYST FOR HYDROGENATION REACTION AND METHOD FOR PRODUCING SAME
A catalyst for a hydrogenation reaction including: a polymer support; and a catalytic component supported on the polymer support. The polymer support comprises a repeating unit represented by Formula 1.
Method for producing polyarylene sulphide resin
Provided is a method for producing a polyarylene sulfide resin, the method including subjecting a dihaloaromatic compound and a sulfidizing agent to a polymerization reaction in the presence of an aliphatic cyclic compound having a ring openable by hydrolysis, in which corrosion of a production apparatus is suppressed. More particularly, provided is a method for producing a polyarylene sulfide resin, the method including a dehydration step (1) in which a water-containing sulfidizing agent and an aliphatic cyclic compound having a ring openable by hydrolysis are heated in the presence of a dihaloaromatic compound to a liquid temperature in the range of 90° C. or higher and 170° C. or lower under the atmospheric pressure, and then dehydration is performed while maintaining the liquid temperature and reducing the pressure to a pressure in the range of 30 [kPa abs] or higher and 80 [kPa abs] or lower to thus obtain a mixture.
Method for producing polyarylene sulphide resin
Provided is a method for producing a polyarylene sulfide resin, the method including subjecting a dihaloaromatic compound and a sulfidizing agent to a polymerization reaction in the presence of an aliphatic cyclic compound having a ring openable by hydrolysis, in which corrosion of a production apparatus is suppressed. More particularly, provided is a method for producing a polyarylene sulfide resin, the method including a dehydration step (1) in which a water-containing sulfidizing agent and an aliphatic cyclic compound having a ring openable by hydrolysis are heated in the presence of a dihaloaromatic compound to a liquid temperature in the range of 90° C. or higher and 170° C. or lower under the atmospheric pressure, and then dehydration is performed while maintaining the liquid temperature and reducing the pressure to a pressure in the range of 30 [kPa abs] or higher and 80 [kPa abs] or lower to thus obtain a mixture.
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.
Method for producing polyarylene sulfide
A method for producing PAS having an average particle size of 50 μm or greater and 550 μm or less is provided. The method can include: (1) a preparation step of preparing a prepared mixture containing an organic polar solvent, a sulfur source, and a dihalo aromatic compound; (2) a pre-stage polymerization step of initiating a polymerization reaction by heating the prepared mixture to produce a prepolymer; (3) a phase separation step of adding water as a phase separation agent to a reaction mixture in a reaction system to form a phase separation state; and (4) a post-stage polymerization step of continuing the polymerization reaction after the phase separation step, in which an organic sulfonic acid metal salt having a specific solubility in water is contained in the prepared mixture or the reaction mixture.
Method for producing polyarylene sulfide
A method for producing PAS having an average particle size of 50 μm or greater and 550 μm or less is provided. The method can include: (1) a preparation step of preparing a prepared mixture containing an organic polar solvent, a sulfur source, and a dihalo aromatic compound; (2) a pre-stage polymerization step of initiating a polymerization reaction by heating the prepared mixture to produce a prepolymer; (3) a phase separation step of adding water as a phase separation agent to a reaction mixture in a reaction system to form a phase separation state; and (4) a post-stage polymerization step of continuing the polymerization reaction after the phase separation step, in which an organic sulfonic acid metal salt having a specific solubility in water is contained in the prepared mixture or the reaction mixture.
POLYTHIOL COMPOSITION AND OPTICAL COMPOSITION COMPRISING SAME
A polythiol composition according to exemplary embodiments includes at least two different polythiol-based compounds, wherein a peak area (%) of the polythiol compound represented by C8H18S6, which is measured through a high performance liquid chromatographic (HPLC) analysis graph obtained at a wavelength of 230 nm, ranges from 0.90% to 1.30%. By controlling the sub-polythiol compound, an optical product having excellent transmittance and optical properties can be manufactured.