Abstract: Polyglycidyl ethers of the formula ##STR1## wherein: G represents hydrogen, ##STR2## R.sup.1 represents a hydrogen atom, an aliphatic, alicyclic, or aromatic hydrocarbon group, or a 5- or 6-membered oxygen or sulfur atom containing heterocyclic group which groups, other than hydrogen, may be substituted by halogen or the group --OG,R.sup.2 is hydrogen or ##STR3## n is a positive number up to 10, and at least two G groups in the molecule are other than hydrogen. The polyglycidyl ether is produced by condensing alpha-naphthol with an aldehyde, such as acetaldehyde, in the presence of an acid catalyst such as nitric acid, and optionally in the presence of an inert medium such as toluene, to form a novolak-type phenol which is thereafter condensed with an epihalohydrin. The polyglycidyl ethers may be cured with conventional curing agents. Composite materials containing a matrix formed from the cured polyglycidyl ether and a filler dispersed in the matrix have excellent heat resistance and low water absorption.

Abstract: A fiber- or film-forming wholly aromatic polyester having melt anisotropy, said polyester consisting essentially of(1) units (a) derived from an aromatic dicarboxylic acid at least 90 mole % of which consists of a p-oriented aromatic dicarboxylic acid and units (b) derived from an aromatic dihydroxy compound at least about 90 mole % of which consists of a mono-substituted hydroquinone ring-substituted by an alkyl group having at least 5 carbon atoms or an aralkyl group having at least 7 carbon atoms or a mixture of said mono-substituted hydroquinone and unsubstituted hydroquinone or a substituted hydroquinone other than said mono-substituted hydroquinone, the proportion of said mono-substituted hydroquinone being at least 80 mole %; or(2) said units (a) and (b), and units (c) derived from a p-oriented aromatic hydroxycarboxylic acid at least about 70 mole % of which consists of p-hydroxybenzoic acid and/or a mono-substituted p-hydroxybenzoic acid, the proportion of the units derived from the p-oriented aromat

Abstract: A wholly aromatic copolyester composed mainly of isophthalic acid units and hydroquinone units, the total proportion of said isophthalic acid units and hydroquinone units being at least about 80 mole % based on the entire units, said wholly aromatic copolyester having a terminal carboxyl group concentration, measured by the method described in the specification, of not more than about 90 eq/10.sup.6 g and a reduced viscosity, determined at 35.degree. C. in a mixed solvent of phenol and tetrachloroethane in a weight ratio of 4:6 in a concentration of 1.2 g/dl of at least about 0.6 and being substantially linear and melt-shapable and substantially free from a halogen atom bonded to the molecular chain, and a film prepared therefrom by melt shaping.

Abstract: A melt-molded film of a wholly aromatic polyester, said film having in its plane two perpendicularly crossing directions in each of which the Young's modulus and strength of the film at 25.degree. C. are at least about 200 kg/mm.sup.2 and at least about 5 kg/mm.sup.2 respectively, the product of the Young's moduli of the film in the two directions being at least 8.times.10.sup.4 (kg/mm.sup.2).sup.2, and said wholly aromatic polyester being substantially linear, having a melt viscosity at about its melting point of at least about 10000 poises, and being composed substantially of recurring units derived from p-hydroxybenzoic acid, recurring units derived from a m- or p-oriented aromatic dicarboxylic acid and recurring units derived from a m- or p-oriented aromatic dihydroxy compound, the proportion of said recurring units derived from p-hydroxybenzoic acid being about 30 to about 70 mole % based on the entire recurring units.

Abstract: The present invention provides a substantially linear aromatic polyester carbonate consisting essentially of hydroxybenzoic acid unit, hydroquinone unit, and carbonate unit as well as, depending on the circumstances, aromatic carboxylic acid unit, and having an inherent viscosity of at least 0.5. The present invention also provides an industrially advantageous method for producing such linear aromatic polyester carbonate through the process steps of melt-polycondensation, and, if necessary, followed by a further polycondensation in solid phase.Such aromatic polyester carbonate which the present invention provides exhibits excellent melt-forming property and melt anisotropy, hence any shaped article obtained by melt-forming of this aromatic polyester carbonate exhibits superior mechanical properties, in particular, excellent Young's modulus of longitudinal elasticity, and so on, which is highly useful as the material for industrial applications.

Abstract: A process for preparing diesters of carboxylic acids by oxidative carbonylation of C.sub.2 -C.sub.20 olefins, C.sub.1 -C.sub.20 monohydric aliphatic alcohols and carbon monoxide in an atmosphere containing molecular oxygen at a temperature of from room temperature to about 350.degree. C. in the presence of a carrier-supported catalyst containing a platinum group metal, wherein said catalyst comprises, supported on a carrier, a post-reduced compound of a platinum group metal and a post-reduced compound of a metal having an atomic number of not less than 22 selected from the group consisting of metals of Groups Ib, IIb, III, IV, V, VI and VIIb of the periodic table.

Abstract: According to this invention, during the formation of a fiber-forming polyester by the reaction of a dicarboxylic acid or its functional derivative with a glycol, an aromatic ortho-ester such as hexaphenyl ortho terephthalate is added to the molten polyester whereby a fiber-forming polyester of a low content of free carboxyl groups and diethylene glycol units is prepared. Moreover, the reaction rate of the polycondensation is greatly increased by selecting and using a suitable aromatic ortho-ester and thus there can be obtained a fiber-forming polyester of a very high molecular weight.

Abstract: A process for preparing 2,6-dimethylnaphthalene by the selective isomerization of an isomeric mixture of dimethylnaphthalenes(DMN), characterized in that1. the weight ratio of DMN of group A which includes 2,6-DMN, 1,6-DMN, and 1,5-DMN to other DMN (not belonging to group A) in the isomerization reactant is adjusted to not more than 12,2. the weight percent of 2,6-DMN in the reaction product is adjusted to at least 27 based on the DMN of group A contained therein,3. the disproportionation ratio D (weight percent) of other DMN (not belonging to group A) and the conversion G (weight percent) of DMN of group A to other DMN satisfy the relation expressed by D.ltoreq. -0.9G + 6.76, and4. the residue in the crystallization step is recycled to the isomerization step.

Abstract: A process for preparing alkenylbenzenes, which comprises reacting an alkylbenzene with 1,3-butadiene at elevated temperature in the presence of an alkali metal catalyst in the substantial absence of oxygen and moisture, characterized in that said catalyst is composed of1. 0.0005 to 0.03% by weight, based on the alkylbenzene, of metallic potassium, and2. metallic sodium in an amount expressed in percent by weight, based on the alkylbenzene, determined by the following relationship (i)-0.59x + 0.025 .gtoreq. Nawherein x is the amount expressed in percent by weight of the metallic potassium used.