The results of studies on the creation of highly metalltceolitnyh systems and the study of their catalytic activities in the oxidation of lower olefin hydrocarbons (ethylene to acetaldehyde, acetone, propylene, butylene methyl ethyl ketone); aliphatic C 1 -C 5 alcohols to their corresponding aldehydes, ketones, carboxylic acids and carboxylic acid esters; oxidative dehydrogenation of naphthenes in the alicyclic diene hydrocarbons and the oxidative dimerization of methane to acetylene. It has been established that the selectivity of these catalysts determined optimal combination of metal components with the acidity and the structure of the zeolite. Selected highly effective catalysts for the reactions studied. Based on the results of experimental studies of the kinetics of the reactions of oxidation of lower olefin hydrocarbons and aliphatic alcohols, the oxidative dehydrogenation of naphthenes and oxidative coupling of methane on the synthesized catalysts are represented by their probable stepwise mechanism and kinetic models developed reactions.

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The catalytic activity of the modified zeolites in the reaction of selective oxidative dehydrogenation of cyclohexane to cyclohexadiene-1,3 has been investigated. It has been found that, the catalyst, Cu Zn Co Cr-clinoptilolite (Cu 2+-0.5%; Zn 2+-0.2%; Co 2+-0.1%; Cr 3+-0.1%) shows the most activity in this reaction. A kinetic scheme of the mechanism of the reaction has been suggested and on the basis of this scheme, kinetic model of the process has been developed. Numerical values of the kinetic parameters were calculated.