Dimerization of vinylarenes on zeolite catalysts

Григорьева, Н. Г.; Talipova, R. R.; Хазипова, А. Н.; Бубеннов, С. В.; Кутепов, Б. И.; Джемилев, У. М.

doi:10.1134/s0965544109010046

Cited by 4 publications

(1 citation statement)

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“…Thus, in both cases there are favorable condi tions for the formation of a strong protonic acid site, and this was indeed demonstrated experimentally [11,22]. It can be hypothesized that these protonic acid sites, which form in the course of the reaction, are the places where the olefin chain grows [23,24].…”

Section: Resultsmentioning

confidence: 82%

Mechanism of the reductive dehydration of ethanol into C3+ alkanes over the commercial alumina—platinum catalyst AP-64

et al. 2016

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The mechanism of the reductive dehydration of ethanol (RDE) into C 3+ alkanes over the com mercial alumina-platinum catalyst AP 64 has been investigated. The catalyst pre reduction time has an effect on the conversion of ethanol and on that of ethylene, a possible intermediate compound in the RDE reaction. Over the catalyst reduced for 12 h, ethanol turns into a C 3 -C 12 alkane fraction and ethylene turns into a C 3 -C 12 olefin fraction, whose yields are 39.0 and 31.4%, respectively. Energetic parameters of ethanol chemisorption and conversion on a Pt 6 Al 4 cluster have been determined by the density functional theory method using the PRIRODA 13 program. Ethanol dehydration into ethylene proceeds via the successive break ing of C-H and C-O bonds, and the rate determining step of the process depends on the atom (Pt or Al) to which the OH group of the alcohol is coordinated. Hydroxyl group transfer from the Pt atom to the nearest Al atom is energetically favorable here. It is hypothesized that the main role of the metal containing cluster is donation of chemisorbed ethylene to the nearest acid sites, on which the ethylene oligomerizes into a C 3 -C 10 hydrocarbon fraction.

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Section: Resultsmentioning

confidence: 82%