The invention relates to a process for the production of 1,3-butadiene from a feed comprising ethanol and acetaldehyde in the presence of a supported tantalum catalyst obtainable by aqueous impregnation of the support with a water-soluble tantalum precursor. Furthermore, the present invention relates to a process for the production of a supported tantalum catalyst, and the supported tantalum catalyst. Finally, the invention relates to the use of the supported tantalum catalyst for the production of 1,3-butadiene from a feed comprising ethanol and acetaldehyde to increase one or both of selectivity and yield of the reaction.

The invention relates to a process for the production of 1,3-butadiene from a feed comprising ethanol and acetaldehyde in the presence of a supported tantalum catalyst obtainable by aqueous impregnation of the support with a water-soluble tantalum precursor. Furthermore, the present invention relates to a process for the production of a supported tantalum catalyst, and the supported tantalum catalyst. Finally, the invention relates to the use of the supported tantalum catalyst for the production of 1,3-butadiene from a feed comprising ethanol and acetaldehyde to increase one or both of selectivity and yield of the reaction.

Provided is a composition for catalyst production which is used in the production of a catalyst for gas phase catalytic oxidation reaction or a catalyst for gas phase catalytic ammoxidation reaction, wherein the composition for catalyst production is an aqueous solution containing a niobium compound and hydrogen peroxide and optionally containing an organic acid, a molar ratio (organic acid/Nb) of a concentration of the organic acid to a Nb concentration is 0.00 or more and 2.00 or less, and a molar ratio (hydrogen peroxide/Nb) of a concentration of the hydrogen peroxide to a Nb concentration is 0.01 or more and 50 or less.

Provided is a composition for catalyst production which is used in the production of a catalyst for gas phase catalytic oxidation reaction or a catalyst for gas phase catalytic ammoxidation reaction, wherein the composition for catalyst production is an aqueous solution containing a niobium compound and hydrogen peroxide and optionally containing an organic acid, a molar ratio (organic acid/Nb) of a concentration of the organic acid to a Nb concentration is 0.00 or more and 2.00 or less, and a molar ratio (hydrogen peroxide/Nb) of a concentration of the hydrogen peroxide to a Nb concentration is 0.01 or more and 50 or less.

The present invention relates to a catalyst comprising at least one oxide of vanadium, at least one oxide of tungsten, at least one oxide of cerium, at least one oxide of titanium and at least one oxide of niobium, and an exhaust system containing said oxides.

The present invention relates to a catalyst comprising at least one oxide of vanadium, at least one oxide of tungsten, at least one oxide of cerium, at least one oxide of titanium and at least one oxide of niobium, and an exhaust system containing said oxides.

A method of turning a catalytic material by altering the charge state of a catalyst support. The catalyst support is intercalated with a metal ion, altering the charge state to alter and/or augment the catalytic activity of the catalyst material.

A cerium-zirconium based mixed oxide composition have: (a) a Ce:Zr molar ratio of 1 or less, and (b) a cerium oxide content of 10-50% by weight. The composition has (i) a surface area of at least 18 m.sup.2/g, and a total pore volume as measured by N.sub.2 physisorption of at least 0.11 cm.sup.3/g, after ageing at 1100° C. in an air atmosphere for 6 hours, (ii) a surface area of at least 42 m.sup.2/g, and a total pore volume as measured by N.sub.2 physisorption of at least 0.31 cm.sup.3/g, after ageing at 1000° C. in an air atmosphere for 4 hours, and (iii) Dynamic Oxygen Storage Capacity (D-OSC) value as measured by H.sub.2-TIR of greater than 500 μmol/g at 600° C. after aging at 800° C. in an air atmosphere for 2 hours. A process contacts the exhaust gas with the composition Another process is for preparing the composition.

The present invention provides a method for producing an oxide catalyst containing antimony, comprising a step (A) of obtaining the oxide catalyst using antimony particles containing a diantimony trioxide as a source of the antimony, wherein an abundance of a pentavalent antimony in a surface layer of the antimony particle to be measured in XPS analysis is less than 70 atom %, and the antimony particle has an average particle size of 1.2 μm or less.

The present invention provides a method for producing an oxide catalyst containing antimony, comprising a step (A) of obtaining the oxide catalyst using antimony particles containing a diantimony trioxide as a source of the antimony, wherein an abundance of a pentavalent antimony in a surface layer of the antimony particle to be measured in XPS analysis is less than 70 atom %, and the antimony particle has an average particle size of 1.2 μm or less.