To provide a functional structural body that can realize ong life time by suppressing the decline in function of the functional substance and that can attempt to save resources without requiring a complicated replacement operation, and to provide a method for making the functional structural body. The functional structural body (1) includes a skeletal body (10) of a porous structure composed of a zeolite-type compound, and at least one functional substance (20) present in the skeletal body (10), the skeletal body (10) has channels (11) connecting with each other, and the functional substance is present at least the channels (11) of the skeletal body (10).

The present invention relates to a catalyst for oxidative dehydrogenation of butene and a method for producing the same. The catalyst for oxidative dehydrogenation of butene has a large amount of Mo—Bi phase acting as a reaction active phase on the surface, and therefore, can exhibit high catalytic activity, high conversion rate and high butadiene selectivity in the oxidative dehydrogenation of butene.

The present invention relates to a catalyst for oxidative dehydrogenation of butene and a method for producing the same. The catalyst for oxidative dehydrogenation of butene has a large amount of Mo—Bi phase acting as a reaction active phase on the surface, and therefore, can exhibit high catalytic activity, high conversion rate and high butadiene selectivity in the oxidative dehydrogenation of butene.

The present disclosure relates to a catalyst that removes an organic compound by using a metal oxide catalyst and a preparation method thereof and a method for degradation of an organic compound using the same. Particularly, the present disclosure relates to a copper-iron oxide (Cu—Fe.sub.2O.sub.3) catalyst composition that is prepared by following steps of: adding a mixed solution of an iron (Fe) precursor and a copper (Cu) precursor to a precipitator solution (S1); obtaining precipitates by heating a solution prepared in the step S1 (S2); obtaining a metal oxalate by filtering the precipitates obtained in the step S2 (S3); drying the metal oxalate obtained in the step S3 (S4); and obtaining a copper-iron oxide catalyst by calcinating the metal oxalate subjected to the step S4 (S5) and a method for removal of an organic compound using the same.

Proposed are a photocatalyst, including titanium dioxide particles including titanium dioxide (TiO.sub.2), a carbon material located on all or part of the surface of the titanium dioxide particles and including at least one selected from the group consisting of graphene, reduced graphene oxide (rGO), and carbon nanotubes (CNTs), and bimetallic nanoparticles supported on the carbon material and including first metal nanoparticles and second metal nanoparticles, and a water treatment method using the same. In the photocatalyst and the water treatment method using the same, the photocatalyst including bimetallic nanoparticles and graphene oxide is prepared, thereby exhibiting high reduction efficiency and high selectivity to nitrogen gas even without the use of an external electron donor.

A process for the preparation of transition metal nanoparticles, the process comprising: (a) providing a mixture comprising one or more salts of one or more transition metals M, one or more complexing agents C, and a solvent system S; (b) optionally adjusting the pH of the mixture provided in (a) to a pH comprised in the range of from 4 to 8; (c) heating the mixture provided in (a) or obtained in (b) for obtaining a colloidal suspension of transition metal nanoparticles; (d) optionally isolating the transition metal nanoparticles obtained in (c), preferably by centrifugation and/or evaporation to dryness of the colloidal suspension obtained in (c) wherein the mixture provided in (a) and heated in (c) or obtained in (b) and heated in (c) does not comprise polyvinyl sulfate and/or polyvinylpyrrolidone.

The present disclosure provides a preparation method of a doped ZnO catalyst. The preparation method includes the following steps: mixing a precipitant and a first solvent to form a first solution having 1 mol/L to 5 mol/L of the precipitant by concentration; mixing one of a Cu salt or a Ga salt, a Zn salt, and a second solvent to form a second solution having Cu and Zn at a molar ratio of less than 0.05:1 and Ga and Zn at a molar ratio of less than 0.1:1; subjecting the first solution and the second solution to precipitation or hydrolysis at 50° C. to 90° C. to obtain a precipitate, and washing and drying the precipitate to obtain a precursor sample; and conducting calcination on the precursor sample at 300° C. to 500° C. for 3 h to 5 h to obtain a Cu-doped ZnO catalyst or a Ga-doped ZnO catalyst.

To provide a functional structural body that can realize a long life time by suppressing the decline in function of the functional substance and that can attempt to save resources without requiring a complicated replacement operation, and to provide a method for making the functional structural body. The functional structural body (1) includes a skeletal body (10) of a porous structure composed of a zeolite-type compound, and at least one functional substance (20) present in the skeletal body (10), the skeletal body (10) has channels (11) connecting with each other, and the functional substance is present at least in the channels (11) of the skeletal body (10).

The present invention relates to a new chiral zeolite material of composition a SiO.sub.2:b GeO.sub.2:c X.sub.2O.sub.3:d YO.sub.2, with an ITV structure, prepared with a specific chiral organic structure-directing agent, (1S,2S)—N-ethyl-N-methyl-pseudoephedrine or its enantiomer, (1R,2R)—N-ethyl-N-methyl-pseudoephedrine, which means that the material is rich in one of the crystalline forms; a method whereby said material is obtained, and the use thereof in adsorption and catalysis processes.

A process for the production of an ester product from a mixture of at least two different ester compounds includes the steps of mixing together at least two different starting ester compounds to form a first ester mixture; and contacting the first ester mixture with a catalyst including from 30-60% of calcium oxide and at least one second metal oxide at a temperature of at least 180° C., for a duration of at least one hour, with mixing, to form a second ester mixture having a melting point which is lower than the melting point of the first ester mixture.