The present invention relates to a bismuth tungstate/bismuth sulfide/molybdenum disulfide heterojunction ternary composite material and a preparation method and application thereof. The composite material is composed of bismuth tungstate, bismuth sulfide and molybdenum disulfide in an ordered layered way, Bi.sub.2WO.sub.6 is an orthorhombic system, Bi.sub.2S.sub.3 is a p-type semiconductor located on a (130) crystal face, MoS.sub.2 is a layered transition metal sulfide located on a (002) crystal face, the whole composite material is of a spherical structure with an unsmooth surface, and a layer of nanosheets uniformly grow on an outer layer. The average particle size of composite materials is in the range of 2.4-2.6 m. The spherical Bi.sub.2WO.sub.6/Bi.sub.2S.sub.3/MoS.sub.2 heterojunction ternary composite material prepared in the present invention has good adsorption of Cr(VI) and high catalytic reduction ability under visible light.

The present invention relates to a bismuth tungstate/bismuth sulfide/molybdenum disulfide heterojunction ternary composite material and a preparation method and application thereof. The composite material is composed of bismuth tungstate, bismuth sulfide and molybdenum disulfide in an ordered layered way, Bi.sub.2WO.sub.6 is an orthorhombic system, Bi.sub.2S.sub.3 is a p-type semiconductor located on a (130) crystal face, MoS.sub.2 is a layered transition metal sulfide located on a (002) crystal face, the whole composite material is of a spherical structure with an unsmooth surface, and a layer of nanosheets uniformly grow on an outer layer. The average particle size of composite materials is in the range of 2.4-2.6 m. The spherical Bi.sub.2WO.sub.6/Bi.sub.2S.sub.3/MoS.sub.2 heterojunction ternary composite material prepared in the present invention has good adsorption of Cr(VI) and high catalytic reduction ability under visible light.

An ammoxidation catalyst includes a metal oxide represented by Chemical Formula 1 supported on a silica carrier, wherein the catalyst has pores having a diameter of 5 to 200 nm, a pore volume of 0.1 to 3.0 cm.sup.3/g, and a BET surface area of 50 m2/g to 1,000 m2/g:
Mo.sub.12Bi.sub.aFe.sub.bA.sub.cB.sub.dC.sub.eO.sub.xChemical Formula 1 wherein in Chemical Formula 1, A is one or more elements of Ni, Mn, Co, Zn, Mg, Ca, and Ba, B is one or more elements of Li, Na, K, Rb, and Cs, C is one or more elements of Cr, W, B, Al, Ca, and V, and a to e, and x are respectively fractions of each atom or atomic group, wherein a is 0.1 to 5, b is 0.1 to 5, c is 0.1 to 10, d is 0.1 to 2, e is 0 to 10, and x is 24 to 48.

An ammoxidation catalyst includes a metal oxide represented by Chemical Formula 1, wherein a first peak having intensity of A appears in the 2 range of 26.3=0.5, and a second peak having intensity of B appears in the 2 range of 28.30.5 in X ray diffraction analysis by CuK, and an intensity ratio (A/B) of the first peak to the second peak is 1.5 or more:
Mo.sub.xBi.sub.aFe.sub.bA.sub.cB.sub.dC.sub.eD.sub.fO.sub.yChemical Formula 1 wherein in Chemical Formula 1, A and B are different from each other, and each independently, are one or more elements of Ni, Mn, Co, Zn, Mg, Ca, and Ba, C is one or more elements of Li, Na, K, Rb, and Cs, D is one or more elements of Cr, W, B, Al, Ca, and V, a to f, x, and y are respectively mole fractions of each atom or atomic group, a is 0.1 to 7, b is 0.1 to 7, provided that the sum of a and b is 0.1 to 7, c is 0.1 to 10, d is 0.01 to 5, e is 0.1 to 10, f is 0 to 10, x is 11 to 14, y is a value determined by each oxidation number of Mo, Bi, Fe, A, B, C, and D.

Melamine is calcined to obtain melem; melem, perylene tetracarboxylic dianhydride and a solvent are mixed to obtain a mixture, and the mixture is subjected to a solvothermal reaction in an inert atmosphere to obtain perylene imide; and the perylene imide is dispersed in an aqueous solution containing a bismuth source and a tungsten source, and is subjected to a hydrothermal reaction to obtain a perylene imide/bismuth tungstate composite photocatalytic material. By means of constructing an organic-inorganic composite photocatalytic material, the introduction of the organic photocatalytic material that responds to visible light may enable the composite material to have a wider spectral response range; and the introduction of an inorganic semiconductor catalyst enables the composite material to produce more oxidizing active free radicals, thereby enhancing the photocatalytic degradation performance of the composite material on organic pollutants. The constructed organic-inorganic composite photocatalytic material has an excellent catalytic performance.

Disclosed are a catalyst composition for oxidative dehydrogenation and a method of preparing the same. More particularly, disclosed is a catalyst composition comprising a multi-ingredient-based metal oxide catalyst and a mixed metal hydroxide. The catalyst composition and the method of preparing the same according to the present disclosure may prevent loss occurring in a filling process due to superior mechanical durability and wear according to long-term use, may inhibit polymer formation and carbon deposition during reaction, and may provide a superior conversion rate and superior selectivity.

Disclosed are a catalyst composition for oxidative dehydrogenation and a method of preparing the same. More particularly, disclosed is a catalyst composition comprising a multi-ingredient-based metal oxide catalyst and a mixed metal hydroxide. The catalyst composition and the method of preparing the same according to the present disclosure may prevent loss occurring in a filling process due to superior mechanical durability and wear according to long-term use, may inhibit polymer formation and carbon deposition during reaction, and may provide a superior conversion rate and superior selectivity.

To provide a novel visible light-responsive photocatalyst or tungsten oxide visible light-responsive semiconductor improved in environmental resistance under an alkaline condition. The tungsten oxide visible light-responsive semiconductor unstable under an alkaline condition is improved in environmental resistance without losing photocatalytic function thereof by adding thereto at least one element selected from the group consisting of copper, tantalum, niobium, lanthanum, bismuth, calcium, chromium, manganese and zinc. The obtained environmental resistant visible light-responsive photocatalyst is subjected to an alkaline treatment to thereby be improved in photocatalytic activity.

To provide a novel visible light-responsive photocatalyst or tungsten oxide visible light-responsive semiconductor improved in environmental resistance under an alkaline condition. The tungsten oxide visible light-responsive semiconductor unstable under an alkaline condition is improved in environmental resistance without losing photocatalytic function thereof by adding thereto at least one element selected from the group consisting of copper, tantalum, niobium, lanthanum, bismuth, calcium, chromium, manganese and zinc. The obtained environmental resistant visible light-responsive photocatalyst is subjected to an alkaline treatment to thereby be improved in photocatalytic activity.

An electrode assembly includes a first electrode and a dielectric layer on the first electrode. The dielectric layer includes a bismuth compound of the formula Bi.sub.2(CrO.sub.4).sub.2Cr.sub.2O.sub.7, Pb.sub.4(BiO.sub.4)(PO.sub.4), Ag.sub.3BiO.sub.3, Bi.sub.2CdO.sub.2(GeO.sub.4), Bi.sub.2Te.sub.4O.sub.11, Cs.sub.6Bi.sub.4O.sub.9, Na.sub.3Bi(PO.sub.4).sub.2, Bi.sub.2(SeO.sub.3).sub.3, or a combination thereof. The electrode assembly can be particularly useful in various electronic devices.