Abstract: An oxygen absorption resin composition is provided that comprises a thermoplastic resin (A) having carbon-carbon double bonds substantially in its main chain and a transition metal salt (B). If necessary, the composition further comprises a gas barrier resin (C), a compatibilizer (D) and the like. The composition has excellent oxygen absorption properties, and when the composition is employed, generation of odorous substances derived from the decomposition of resins as a result of oxygen absorption can be suppressed.

Abstract: An oxygen absorber of the present invention includes at least one compound represented by Formula (1): and an oxidizable polymer. R1 and R2 each independently indicates a hydrogen atom or an organic group. R1 and R2 may form a ring together with carbon atoms to which they are bonded. R1 and/or R2 may form a carbon-carbon double bond with carbon atoms to which they are bonded.

Abstract: According to the present invention, a method of producing ethers, which includes subjecting a conjugated diene compound and an alcohol to a telomerization reaction in the presence of a composition containing a palladium compound, an isocyanide represented by the formula (I) R1R2R3CNC ??(I) and a base represented by the formula (II) M(OR4)n ??(II) as a catalyst is provided. According to the method of the present invention, by telomerization reaction of a conjugated diene compound and an alcohol, ethers can be produced industrially advantageously. (In the above-mentioned formulas, each symbol is as defined in the specification.

Abstract: In activated carbon obtained by subjecting a carbonaceous material to an activation treatment, the overall content of alkali metals is set at 100 ppm or less, or the overall content of heavy metals is set at 20 ppm or less and the overall content of alkali metals is set at 200 ppm or less. In cases where such activated carbon is used as a raw material in electronic devices, the formation of dendrites by the reductive deposition of alkali metals or heavy metals tends not to occur, so that problems such as short-circuiting or the like tend not to arise, and a good rate of self-discharge retention is shown.

Abstract: Activated carbon useful as polarizable electrode material for an electric double-layer capacitor can be obtained by mixing a carbonaceous material and an alkali metal hydroxide while maintaining a solid state, granulating the obtained mixture while maintaining its solid state, dehydrating the obtained granulated substance while maintaining its solid state, and subjecting the granulated dehydration product obtained in the dehydration step to an activation treatment. The preferred pressure of the granulation treatment in the granulation step is 0.01 to 300 Torr, and the preferred temperature of the granulation treatment is 90 to 140° C. The preferred pressure of the dehydration treatment in the dehydration step is 0.01 to 10 Torr, and the preferred temperature of the dehydration treatment is 200 to 400° C.

Abstract: An oxygen absorption resin composition is provided that comprises a thermoplastic resin (A) having carbon-carbon double bonds substantially in its main chain and a transition metal salt (B). If necessary, the composition further comprises a gas barrier resin (C), a compatibilizer (D) and the like. The composition has excellent oxygen absorption properties, and when the composition is employed, generation of odorous substances derived from the decomposition of resins as a result of oxygen absorption can be suppressed.

Abstract: An activated carbon which is prepared from granular isotropic pitch.

Abstract: The present invention provides an activated carbon produced by a process, which includes: activating a carbonaceous material, to obtain an activated carbonaceous material; and contacting the activated carbonaceous material with an acid. Another embodiment of the present invention provides an electrode for an electric double-layer capacitor, which includes the above-described activated carbon. Another embodiment of the present invention provides a filter, which includes the above-described activated carbon. Another embodiment of the present invention provides a shaped article, which includes the above-described activated carbon. Another embodiment of the present invention provides a method for producing activated carbon, which includes activating a carbonaceous material, to obtain an activated carbonaceous material; and contacting the activated carbonaceous material with an acid, to obtain the activated carbon.

Abstract: A hydrogenated polymer is prepared by a method comprising: hydrogenating a polymer having carbon—carbon double bonds and a hydroxy group and/or a functional group which is convertible into a hydroxy group or into a hydroxymethyl group in the presence of a catalyst of palladium on a base activated carbon and/or platinum on a base activated carbon.

Abstract: According to the present invention, provided is an industrially advantageous process for producing an epoxidized polymer, with safety and efficiency, wherein the epoxidation of a polymer having an olefinic carbon-carbon double bond is effected under the presence of substantially no alkali metal ion by adding an aqueous solution containing (i) ammonium tungstate and/or tungstophosphoric acid and (ii) phosphoric acid, in which the amount of (ii) phosphoric acid is not less than 0.25 moles relative to 1 gram atom of tungsten atom contained in the (i) ammonium tungstate and/or tungstophosphoric acid, and an aqueous hydrogen peroxide, separately to a solution of said polymer and a quaternary ammonium salt in an organic solvent immiscible with water.

Abstract: A hydrogenated polymer is prepared by a method comprising:

Abstract: According to the present invention, provided is an industrially advantageous process for producing an epoxidized polymer, with safety and efficiency, wherein the epoxidation of a polymer having an olefinic carbon-carbon double bond is effected under the presence of substantially no alkali metal ion by adding an aqueous solution containing (i) ammonium tungstate and/or tungstophosphoric acid and (ii) phosphoric acid, in which the amount of (ii) phosphoric acid is not less than 0.25 moles relative to 1 gram atom of tungsten atom contained in the (i) ammonium tungstate and/or tungstophosphoric acid, and an aqueous hydrogen peroxide, separately to a solution of said polymer and a quaternary ammonium salt in an organic solvent immiscible with water.

Abstract: An activated carbon which is prepared from granular isotropic pitch.

Abstract: A process for producing 3-methyltetrahydrofuran, and processes for producing 3-hydroxy-3-methyltetrahydrofuran and 3-methyldihydrofuran, which are intermediates thereof, are provided.

Abstract: Provided are a process for producing 6-methyl-3-hepten-2-one by cross aldol condensation carried out while each continuously adding to acetone, isovaleraldehyde and an aqueous alkali containing an alkaline substance; a process for producing a 6-methyl-2-heptanone analogue represented by Formula (1): wherein n is an integer of 0 or 1 or more; which comprises allowing hydrogen, acetone and an aldehyde represented by Formula (2): wherein n is as defined above; X and Y each represents a hydrogen atom or they are coupled together to form a carbon-carbon bond; and Z and W each represents a hydrogen atom or they are coupled together to form a carbon-carbon bond; to react in the presence of an aqueous alkali containing an alkaline substance, and a hydrogenation catalyst; and a process for producing phytone or isophytol using the 6-methyl-3-hepten-2-one or the 6-methyl-2-heptanone analogue.

Abstract: Provided are a process for producing 6-methyl-3-hepten-2-one by cross aldol condensation carried out while each continuously adding to acetone, isovaleraldehyde and an aqueous alkali containing an alkaline substance; a process for producing a 6-methyl-2-heptanone analogue represented by Formula (1): ##STR1## wherein n is an integer of 0 or 1 or more; which comprises allowing hydrogen, acetone and an aldehyde represented by Formula (2): ##STR2## wherein n is as defined above; X and Y each represents a hydrogen atom or they are coupled together to form a carbon-carbon bond; and Z and W each represents a hydrogen atom or they are coupled together to form a carbon-carbon bond;to react in the presence of an aqueous alkali containing an alkaline substance, and a hydrogenation catalyst; and a process for producing phyton or isophytol using the 6-methyl -3-hepten-2-one or the 6-methyl-2-heptanone analogue.

Abstract: In order to make it possible to produce 6-methylheptan-2-one, which is useful as a material for synthesizing isophytol or as a material for synthesizing fragrances such as tetrahydrolinalool and dihydrogeraniol, efficiently and in an industrially simple manner, isovaleral and acetone are subjected to aldol condensation in the presence of a basic substance to form a condensate which contains 4-hydroxy-6-methylheptan-2-one, and then the condensate is subjected to hydrogenation reaction under a dehydration condition to obtain the 6-methylheptan-2-one.

Abstract: A process is described for producing acetals comprising reacting an aldehyde or a ketone with an alcohol in the presence of a titanium compound having an acetylacetone as a ligand, or in the presence of a compound selected from the group consisting of stannous chloride dihydrate, cerium chloride hexahydrate and bismuth chloride. The process can be used in the synthesis of unstable acetals or when water exists in the reaction mixture, and therefore the process can be used for a wide variety of applications.

Abstract: Described is a process for producing a 4-substituted-2-butenal represented by the following formula (1); ##STR1## (wherein X represents an acyloxy group or halogen atom; R represents hydrogen atom, an aliphatic hydrocarbon group or an aromatic hydrocarbon group; and these hydrocarbon groups can be substituted with hydroxyl group, an alkoxy group, an aryloxy group, an acyl group or an alkoxycarbonyl group), which is useful as synthetic intermediates of phormaceutieals, agricultural chemicals and the like,comprising subjecting a substituted acetaldehyde represented by the following formula (2);X--CH.sub.2 --CHO (2)(wherein X has the same meaning as defined above), with an aldehyde represented by the following formula (3);R--CH.sub.2 --CHO (3)(wherein R has the same meaning as defined above) in the presence of an amino carboxylic acid.

Abstract: A compound that can be converted, at a low cost and in a simple way, into 2-aryl-1,3-propanediols serving as precursors for synthesizing felbamate acting as an antiepileptic has a structure represented by Formula (1): ##STR1## wherein Ar represents an aryl group; R.sup.1 represents a hydrogen atom or is R.sup.4 or R.sup.5, where R.sup.4 represents an alkoxy group having 1 to 10 carbon atoms and R.sup.5 represents a hydroxy group or an acyloxy group having 1 to 10 carbon atoms; and R.sup.2 and R.sup.3 are hydrogen atoms at the same time or R.sup.2 and R.sup.3 together form a group represented by Formula (2): ##STR2## wherein R.sup.6 and R.sup.7 each independently represent a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, or R.sup.6 and R.sup.7 together form an oligomethylene group having 2 to 10 carbon atoms.