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EN
A number of heterogeneous acid type catalysts of silica-alumina nature, which are proposed to be used for petrochemistry by-product oligomerization, have been investigated. Particularly, such key indicators as active site concentration and strength have been determined. These parameters have been determined by the method based on potentiometric titration that is relatively seldom used in heterogeneous catalysis. The number of active site types present in investigated catalysts, as well as concentrations of each type of site, has been determined by mathematical processing of potentiometric titration data. The sequence of mathematical processing of titration data is described. The relationship between the properties of the investigated catalysts and their effectiveness in heterogeneous catalytic cooligomerization of the C9 fraction of liquid products of diesel fuel pyrolysis has been analyzed. The relationships between yields achieved in the presence of various catalysts and the properties of these catalysts have been defined. Namely, it was determined that the product yield is almost proportional to the active site’s concentration of the catalysts (activated clay materials). The relationship between the strength of active sites and average molecular weight of the cooligomers has been found. The causes of obtained regularities have been analyzed and explained. [...]
EN
Cooligomerization of liquid products of the C9 fraction of diesel fuel pyrolysis to produce cooligomers of wide application is suggested to be carried out with silica-alumina catalysts, among which the activated bentonite clay seems to be optimal. Cooligomerization of the mixture simulating the C9 fraction composition was studied to compare the suggested heterogeneous catalytic method with other methods of cooligomers production. Different methods have been compared in terms of yield of cooligomers and their properties, namely molecular weight and its distribution, density, unsaturation and colour. The ratio of monomer units in cooligomer has been determined and the monomers conversion degrees have been calculated for different cooligomerization methods. Reasons of structure and composition differences of cooligomers obtained by different methods are suggested.
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