Processes for converting a hydrocarbon reactant into an alcohol compound and/or a carbonyl compound are disclosed, and these processes include the steps of forming a supported chromium catalyst comprising chromium in a hexavalent oxidation state, irradiating the hydrocarbon reactant and the supported chromium catalyst with a light beam at a wavelength in the UV-visible spectrum to reduce at least a portion of the supported chromium catalyst to form a reduced chromium catalyst, and hydrolyzing the reduced chromium catalyst to form a reaction product comprising the alcohol compound and/or the carbonyl compound. The supported chromium catalyst can be formed by heat treating a supported chromium precursor, contacting a chromium precursor with a solid support while heat treating, or heat treating a solid support and then contacting a chromium precursor with the solid support.

A composite material for photocatalytic hydrogen production and a photocatalytic hydrogen production catalyst are provided. The composite material includes a plurality of inorganic semiconductor particles and a linear conjugated polymer material. The conductive band of a material of the inorganic semiconductor particles is higher than the reduction potential of hydrogen, and the linear conjugated polymer material is compounded on a surface of each of the inorganic semiconductor particles, wherein the difference in the energy level of the lowest unoccupied molecular orbital (LUMO) of the linear conjugated polymer material and the conductive band of the material of the inorganic semiconductor particles is within 2 eV.

The disclosure provides a photocatalyst material and a method for fabricating the same. The photocatalyst material includes a zinc oxide material doped with metal, wherein the zinc oxide material has a lattice structure including a plurality of defects. A part of the defects are filled with a metal.

The inventive concepts disclosed and/or claimed herein relate generally to catalysts and, more particularly, but not by way of limitation, to a heterogeneous, metal-free hydrogenation catalyst containing frustrated Lewis pairs. In one non-limiting embodiment, the heterogeneous, metal-free catalyst comprises hexagonal boron nitride (h-BN) having frustrated Lewis pairs therein.

Supported chromium catalysts with an average valence less than +6 and having a hydrocarbon-containing or halogenated hydrocarbon-containing ligand attached to at least one bonding site on the chromium are disclosed, as well as ethylene-based polymers with terminal alkane, aromatic, or halogenated hydrocarbon chain ends. Another ethylene polymer characterized by at least 2 wt. % of the polymer having a molecular weight greater than 1,000,000 g/mol and at least 1.5 wt. % of the polymer having a molecular weight less than 1000 g/mol is provided, as well as an ethylene homopolymer with at least 3.5 methyl short chain branches and less than 0.6 butyl short chain branches per 1000 total carbon atoms.

The invention relates to polyoxometalates represented by the formula (A.sub.n).sup.m+{M′.sub.s[M″M.sub.12X.sub.8O.sub.yR.sub.zH.sub.q]}.sup.m− or solvates thereof, corresponding supported polyoxometalates, and processes for their preparation, as well as corresponding metal-clusters, optionally in the form of a dispersion in a liquid carrier medium or immobilized on a solid support, and processes for their preparation, as well as their use in reductive conversion of organic substrate.

The present invention refers to lightweight and settable photocatalytic compositions and solid composites; methods of preparing the compositions and solid composites; and their use in water purification. The compositions are comprised of photocatalysts such as titanium dioxide (TiO.sub.2) and zinc oxide (ZnO), lightweight glass bubbles, and a hydraulic cementing binder. The lightweight and settable photocatalytic compositions can be formed into lightweight photocatalytic solid composites and/or structures by mixing with water and moist curing. This invention also describes relatively simple, fast, and cost effective methodologies to photodope the TiO.sub.2—ZnO compositions and composites with silver (Ag), to enhance and extend the photocatalytic activity from the ultraviolet into the visible light spectrum. The lightweight and settable TiO.sub.2—ZnO and Ag—TiO.sub.2—ZnO compositions are used in making solids, structures, coatings, and continuous or semi-continuous water purification panels for purifying contaminated water.

The invention relates to a composition that contains a first semiconductor SC1, particles that comprise one or more element(s) M in the metal state selected from among an element of groups IVB, VB, VIB, VIIB, VIIIB, IB, IIB, IIIA, IVA and VA of the periodic table, and a second semiconductor SC2 that comprises cerium oxide, with said first semiconductor SC1 being in direct contact with said particles that comprise one or more element(s) M in the metal state, with said particles being in direct contact with said second semiconductor SC2 that comprises cerium oxide in such a way that the second semiconductor SC2 covers at least 50% of the surfaces of the particles that comprise one or more element(s) M in the metal state. The invention also relates to its preparation method as well as its application of photocatalysis.

The invention relates to the method of forming a platinum-based catalytic coating on electrodes for using in electrochemical devices such as fuel cells or electrolysis cells. According to the invention, to produce a platinum-based catalyst, the carrier is preliminary cleaned by ion etching and the catalytic coating is applied onto the cleaned surface from at least one target based on platinum in vacuum in the primary gas plasma with addition of reactive gas, sputtering being done at the power density on the magnetron sputtered target within (0.004-0.17)*10.sup.5 W/m.sup.2 and the ratio of concentrations of the primary and reaction gas of 75-99%. Technical result: increased specific catalytic activity of the electrode's catalytic coating for electrochemical devices (fuel cells and electrolysis cells). 2 primary claims, 8 depending claims, 5 figures.

Provided in the invention are a catalyst for preparing phosgene and a preparation method therefor, and a method for the preparation of phosgene and the comprehensive utilization of energy thereof. The preparation method comprises the following steps: 1) stirring and soaking activated carbon in a modifying solution, then adding dimethyltin dichloride and chromium oxide powders and carrying out a reaction, and then adding a nickel oxide fine powder and ultrasonically oscillating same to prepare a pre-modified activated carbon; 2) drying the pre-modified activated carbon; and 3) heating and calcinating the dried pre-modified activated carbon from step 2) to prepare the catalyst. Based on the preparation method, thin layers are formed on the surface of the catalyst by bonding chromium tin phosphate and chromium tin silicate with Ni by means of —O—Ni—O—, respectively, which can improve the high-temperature resistance and oxidation resistance of the activated carbon, and improve the safe and stable operation level of a device. The aim of integrated comprehensive utilization of energy is achieved by coupling phosgene production with an evaporation and concentration process of brine and using steam as a heat source for evaporation and concentration of the brine.