Disclosed is method for removing carbonyl sulphide and/or carbon disulphide from a sour gas stream. The method comprises subjecting the gas stream to simultaneous contact with an absorption liquid, such as an aqueous amine solution, and with a catalyst suitable for hydrolyzing carbonyl sulphide and/or carbon disulphide. To this end, the invention also provides a reactor system wherein both an absorption liquid and a catalyst are present. In a preferred embodiment, the catalyst is a heterogeneous catalyst present on or in an absorption column, either coated on the trays of a column with trays, or contained in the packing of a packed column.

The invention relates to polyoxometalates represented by the formula (A.sub.n).sub.m+{[M.sub.6(O.sub.2).sub.9][(XM′.sub.10O.sub.37).sub.3]}.sup.m− or solvates thereof, corresponding supported polyoxometalates, and processes for their preparation, as well as their use in oxidative conversion of organic substrate.

Bulk catalysts comprised of nickel, molybdenum, tungsten and titanium and methods for synthesizing bulk catalysts are provided. The catalysts are useful for hydroprocessing, particularly hydrodesulfurization and hydrodenitrogenation, of hydrocarbon feedstocks.

The present disclosure relates to a process for stabilizing an antimony ammoxidation catalyst in an ammoxidation process. The process may comprise providing an antimony ammoxidation catalyst to a reactor; reacting propylene with ammonia and oxygen in the fluidized bed reactor in the presence of the antimony ammoxidation catalyst to form a crude acrylonitrile product; and adding an effective amount of an antimony-containing compound to the antimony ammoxidation catalyst to maintain catalyst conversion and selectivity; wherein the antimony-containing compound has a melting point less than 375° C. The present disclosure also relates to catalyst compositions and additional processes using the antimony ammoxidation catalyst stabilized by an antimony-containing compound.

The present disclosure relates to a process for stabilizing an antimony ammoxidation catalyst in an ammoxidation process. The process may comprise providing an antimony ammoxidation catalyst to a reactor; reacting propylene with ammonia and oxygen in the fluidized bed reactor in the presence of the antimony ammoxidation catalyst to form a crude acrylonitrile product; and adding an effective amount of an antimony-containing compound to the antimony ammoxidation catalyst to maintain catalyst conversion and selectivity; wherein the antimony-containing compound has a melting point less than 375° C. The present disclosure also relates to catalyst compositions and additional processes using the antimony ammoxidation catalyst stabilized by an antimony-containing compound.

Provided are titanium oxide fine particles capable of enhancing the photocatalytic activity of a photocatalyst when mixed with such photocatalyst. There are provided titanium oxide fine particles with at least an iron component and a silicon component solid-dissolved therein, in which the iron and silicon components are each contained in an amount of 1 to 1,000 in terms of a molar ratio to titanium (Ti/Fe or Ti/Si); and a titanium oxide fine particle dispersion liquid in which these titanium oxide fine particles are dispersed in an aqueous dispersion medium.

Provided are titanium oxide fine particles capable of enhancing the photocatalytic activity of a photocatalyst when mixed with such photocatalyst. There are provided titanium oxide fine particles with at least an iron component and a silicon component solid-dissolved therein, in which the iron and silicon components are each contained in an amount of 1 to 1,000 in terms of a molar ratio to titanium (Ti/Fe or Ti/Si); and a titanium oxide fine particle dispersion liquid in which these titanium oxide fine particles are dispersed in an aqueous dispersion medium.

The present invention relates to a hydrocarbon conversion catalyst, comprising: a first composition comprising a dehydrogenation active metal on a solid support, and a second composition comprising a transition metal and a doping agent, wherein the doping agent is selected from zinc, gallium, indium, lanthanum, and mixtures thereof, on an inorganic support.

The present invention relates to a hydrocarbon conversion catalyst, comprising: a first composition comprising a dehydrogenation active metal on a solid support, and a second composition comprising a transition metal and a doping agent, wherein the doping agent is selected from zinc, gallium, indium, lanthanum, and mixtures thereof, on an inorganic support.

A method of synthesizing a doped carbonaceous material includes mixing a carbon precursor material with at least one dopant to form a homogeneous/heterogeneous mixture; and subjecting the mixture to pyrolysis in an inert atmosphere to obtain the doped carbonaceous material. A method of purifying water includes providing an amount of the doped carbonaceous material in the water as a photocatalyst; and illuminating the water containing the doped carbonaceous material with visible light such that under visible light illumination, the doped carbonaceous material generates excitons (electron-hole pairs) and has high electron affinity, which react with oxygen and water adsorbed on its surface forming reactive oxygen species (ROS), such as hydroxyl radicals and superoxide radicals, singlet oxygen, hydrogen peroxide, that, in turn, decompose pollutants and micropollutants.