The invention relates to a mixed oxide material comprising the elements molybdenum, vanadium, niobium and tellurium, which, when using the Cu-K radiation, has diffraction reflections h, i, k and l in the XRD spectrum, said diffraction reflexes having their apex points at the diffraction angles (2.Math.) 26.20.5 (h), 27.00.5 (i), 7.80.5 (k) and 28.00.5 (l), characterized in that the mixed oxide material has a pore volume of >0.1 cm.sup.3/g. The mixed oxide material according to the invention is produced by a method comprising the steps of: a) producing a mixture of starting compounds containing molybdenum, vanadium, niobium and tellurium dioxide as a tellurium-containing starting compound as well as oxalic acid and a further oxoligand selected from the group consisting of dicarboxylic acids and diols, b) hydrothermally treating the mixture of starting compounds at a temperature of 100 to 300 C., c) separating and drying the mixed oxide material which is contained in the suspension resulting from step b).

The invention relates to a mixed oxide material comprising the elements molybdenum, vanadium, niobium and tellurium, which, when using the Cu-K radiation, has diffraction reflections h, i, k and l in the XRD spectrum, said diffraction reflexes having their apex points at the diffraction angles (2.Math.) 26.20.5 (h), 27.00.5 (i), 7.80.5 (k) and 28.00.5 (l), characterized in that the mixed oxide material has a pore volume of >0.1 cm.sup.3/g. The mixed oxide material according to the invention is produced by a method comprising the steps of: a) producing a mixture of starting compounds containing molybdenum, vanadium, niobium and tellurium dioxide as a tellurium-containing starting compound as well as oxalic acid and a further oxoligand selected from the group consisting of dicarboxylic acids and diols, b) hydrothermally treating the mixture of starting compounds at a temperature of 100 to 300 C., c) separating and drying the mixed oxide material which is contained in the suspension resulting from step b).

A process for producing unsaturated nitrile, using a fluidized bed reactor having an internal space having a catalyst capable of being fluidized therein, a feed opening to feed a starting material gas comprising hydrocarbon to the internal space, and a discharge port to discharge a reaction product gas from the internal space, the process comprising a reaction step of subjecting the hydrocarbon to a vapor phase catalytic ammoxidation reaction in the presence of the catalyst in the internal space to produce the corresponding unsaturated nitrile, wherein when in the internal space, a space where an existing amount of the catalyst per unit volume is 150 kg/m.sup.3 or more is defined as a dense zone and a space where an existing amount of the catalyst per unit volume is less than 150 kg/m.sup.3 is defined as a sparse zone in the reaction step, a gas residence time in the sparse zone is 5 to 50 sec.

A process for producing unsaturated nitrile, using a fluidized bed reactor having an internal space having a catalyst capable of being fluidized therein, a feed opening to feed a starting material gas comprising hydrocarbon to the internal space, and a discharge port to discharge a reaction product gas from the internal space, the process comprising a reaction step of subjecting the hydrocarbon to a vapor phase catalytic ammoxidation reaction in the presence of the catalyst in the internal space to produce the corresponding unsaturated nitrile, wherein when in the internal space, a space where an existing amount of the catalyst per unit volume is 150 kg/m.sup.3 or more is defined as a dense zone and a space where an existing amount of the catalyst per unit volume is less than 150 kg/m.sup.3 is defined as a sparse zone in the reaction step, a gas residence time in the sparse zone is 5 to 50 sec.

There is described a hydroprocessing process of at least one gas oil cut having a weighted mean temperature (TMP) between 240 C. and 350 C. using a catalyst comprising at least one metal of the group VIB and/or at least one metal of the group VIII of the periodic classification and a support comprising an amorphous mesoporous alumina having a connectivity (Z) greater than 2.7, the hydroprocessing process operating at a temperature between 250 C. and 400 C., at a total pressure between 2 MPa and 10 MPa with a ratio of hydrogen volume to volume of hydrocarbon-containing feedstock between 100 and 800 litres per litre and at an Hourly Volume Rate (HVR) which is defined by the ratio of the volume flow rate of liquid hydrocarbon-containing feedstock to volume of catalyst fed into the reactor between 1 and 10 h.sup.1.

There is described a hydroprocessing process of at least one gas oil cut having a weighted mean temperature (TMP) between 240 C. and 350 C. using a catalyst comprising at least one metal of the group VIB and/or at least one metal of the group VIII of the periodic classification and a support comprising an amorphous mesoporous alumina having a connectivity (Z) greater than 2.7, the hydroprocessing process operating at a temperature between 250 C. and 400 C., at a total pressure between 2 MPa and 10 MPa with a ratio of hydrogen volume to volume of hydrocarbon-containing feedstock between 100 and 800 litres per litre and at an Hourly Volume Rate (HVR) which is defined by the ratio of the volume flow rate of liquid hydrocarbon-containing feedstock to volume of catalyst fed into the reactor between 1 and 10 h.sup.1.

A catalytic composition and process useful for the conversion of an olefin selected from the group consisting of propylene, isobutylene or mixtures thereof, to acrylonitrile, methacrylonitrile, hydrogen cyanide and acetonitrile and mixtures thereof, wherein the catalyst exhibiting increased selectivity to hydrogen cyanide compared to prior art catalysts.

A catalytic composition and process useful for the conversion of an olefin selected from the group consisting of propylene, isobutylene or mixtures thereof, to acrylonitrile, methacrylonitrile, hydrogen cyanide and acetonitrile and mixtures thereof, wherein the catalyst exhibiting increased selectivity to hydrogen cyanide compared to prior art catalysts.

This disclosure provides for routes of synthesis of acrylic acid and other ,-unsaturated carboxylic acids and their salts, including catalytic methods. For example, there is provided a process for producing an ,-unsaturated carboxylic acid or a salt thereof, the process comprising: (1) contacting in any order, a group 8-11 transition metal precursor, an olefin, carbon dioxide, a diluent, and a metal-treated chemically-modified solid oxide such as a sulfur oxoacid anion-modified solid oxide, a phosphorus oxoacid anion-modified solid oxide, or a halide ion-modified solid oxide, to provide a reaction mixture; and (2) applying reaction conditions to the reaction mixture suitable to produce the ,-unsaturated carboxylic acid or the salt thereof. Methods of regenerating the metal-treated chemically-modified solid oxide are described.

Articles comprising a catalyst film comprising VOx, MoO.sub.3 or WO.sub.3, and TiO.sub.2 deposited on a substrate are disclosed. The articles are useful for selective catalytic reduction (SCR) of NOx in exhaust gases. Methods for producing such articles deposit a catalyst film on the substrate to form a coated substrate, which is then calcined. When used in an SCR process, the coated articles have enhanced activity for NOx conversion, reduced activity for SOx conversion, or both. Light-weight, coated articles having high catalyst loads can be fabricated at the same or reduced dimensions when compared with laminated articles, and increased kNOx/kSOx ratios are available even from coated articles having relatively thin catalyst films. The articles should have particular value for power plant operations, where coal and high-sulfur fuels are commonly used and controlling sulfur trioxide generation is critical.