An object of the present invention is to provide a polyphenylene ether melt extrusion formed body which can be obtained by melt forming without mixing other resin components and has excellent properties such as mechanical strength, and a method for producing the same. The present invention relates to a polyphenylene ether melt extrusion formed body comprising a polyphenylene ether component which has a rearrangement structure having a continuous structure bonded at an ortho-position in a repeating unit continuously bonded at a para-position.

The present invention relates to a method for the manufacture of a poly(aryl ether) such as a poly(aryl ethersulfone) or a poly(aryl ether ketone) including the use of an organic base having a pKa of at least 10.

A novel polymer having high glass transition temperature and an excellent balance between heat resistance, high refractive index and mechanical properties, and a composition and molded article containing the polymer are provided. The polymer according to the invention has a first structural unit represented by at least one of formulae (1-1), (1-2) and (1-3) below and a second structural unit having either a secondary amino structure or a tertiary amino structure at two or more terminals. ##STR00001##

A novel polymer having high glass transition temperature and an excellent balance between heat resistance, high refractive index and mechanical properties, and a composition and molded article containing the polymer are provided. The polymer according to the invention has a first structural unit represented by at least one of formulae (1-1), (1-2) and (1-3) below and a second structural unit having either a secondary amino structure or a tertiary amino structure at two or more terminals.

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Provided are a continuous production method and a continuous production apparatus utilizing the solution polycondensation for aromatic cyclic oligomers, which achieve a good space-time yield and are inexpensive and simple. The continuous production method includes: (a) supplying a polymerization solvent and a reaction raw material to a continuous production apparatus; (b) performing a polymerization reaction in the reaction vessels to form a reaction mixture; (c) removing water in gas phase parts of the reaction vessels from the reaction vessels; and (d) successively moving the reaction mixture to each of the reaction vessels; the steps (a), (b), (c), and (d) being performed in parallel; wherein an amount of the polymerization solvent in the reaction vessel positioned furthest downstream in a movement direction of the reaction mixture is not less than 1 L and not greater than 50 L per 1 mol of arylene units in the reaction raw material.

A coated food or beverage contact article that has been or will be ibrmed into a food or beverage container or container component, a method for making such containers or container components, coating compositions and polymers for use in such article or method. The coating composition comprises a polymer derived from or derived from or derivable from a polyphenol having two or more phenylene rings linked to or through an aliphatic or cycloaliphatic group or groups, wherein the polyphenol is a reaction product of a monophenol with a polyolefinic terpene. The polyphenol may be a diphenol and a reaction product of a monophenol with a diolefinic terpene. The terpene may be a cyclic terpene.

A material for forming an organic film contains (A) a polymer having a repeating unit shown by the following general formula (1), and (B) an organic solvent. In the general formula (1), AR1, AR2, AR3, and AR4 each represent a benzene ring or a naphthalene ring; W1 represents a tetravalent organic group having 6 to 70 carbon atoms and at least one or more aromatic rings; and W2 represents a divalent organic group having 1 to 50 carbon atoms. An object of the present invention is to provide: a material for forming an organic film to enable high etching resistance and excellent twisting resistance without impairing the resin-derived carbon content; a patterning process using this material; and a polymer suitable for such a material for forming an organic film.

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Provided are a continuous production method and a continuous production apparatus utilizing the solution polycondensation for aromatic cyclic oligomers, which achieve a good space-time yield and are inexpensive and simple. The continuous production method includes: (a) supplying a polymerization solvent and a reaction raw material to a continuous production apparatus; (b) performing a polymerization reaction in the reaction vessels to form a reaction mixture; (c) removing water in gas phase parts of the reaction vessels from the reaction vessels; and (d) successively moving the reaction mixture to each of the reaction vessels; the steps (a), (b), (c), and (d) being performed in parallel; wherein an amount of the polymerization solvent in the reaction vessel positioned furthest downstream in a movement direction of the reaction mixture is not less than 1 L and not greater than 50 L per 1 mol of arylene units in the reaction raw material.

The present invention relates to a method for the manufacture of a poly(aryl ether) such as a poly(aryl ethersulfone) or a poly(aryl ether ketone) including the use of an organic base having a pKa of at least 10.

A method for preparing a poly(phenylene ether) includes oxidatively polymerizing a poly(phenylene ether) starting material having an initial intrinsic viscosity in the presence of an organic solvent and a copper-amine catalyst to form a reaction mixture including a poly(phenylene ether) having a final intrinsic viscosity that is at least 50% greater than the initial intrinsic viscosity. The method further includes terminating the oxidative polymerization to form a post-termination reaction mixture; combining an aqueous solution comprising a chelant with the post-termination reaction mixture to form a chelation mixture of an aqueous phase comprising chelated copper ion, and an organic phase comprising dissolved poly(phenylene ether); separating the aqueous phase and the organic phase; and isolating the poly(phenylene ether) from the organic phase. High molecular weight poly(phenylene ether)s prepared according to the method described herein are also disclosed.