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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18554
Title: Sequence Studies in Liquid Phase Hydrocarbon Oxidation Part 4: Hydroperoxide-Alcohol and Hydroperoxide-Ketone Transitions in the Oxidation of Ethylbenzene
Authors: Danoczy, Eva
Nemes, Istvan
Gal, Dezso
Keywords: Chemistry
Hydrocarbon
Oxidation
Journal of the Chemical Society : Faraday Transaction - I
Issue Date: 1977
Publisher: Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (1)
Abstract: The rates of consumption of a-phcnylcthyihydroperoxide molecules during the oxidation of ethylbenzene at 120°C have been measured using radioactive tracer procedures; balance equations for the total activities and concentrations were used for the calculations. In order to obtain a coherent set of rates a hydrogen transfer reaction between hydroperoxide molecules and peroxy radicals had to be taken into account. It was established that ketone and alcohol molecules were formed mainly as a result of the induced decomposition of the hydroperoxide and the contribution to their formation by termination processes was <10 % of their total formation rates. The formation rates of alcohol and ketone via hydroperoxide molecules were very similar. The relative reactivity of hydroperoxide and ethylbenzene molecules toward peroxy radicals was found to be two. Further kinetic data, such as ease of oxidation and kinetic chain length both for the oxidation of the parent hydrocarbon and its main intermediate, have been determined.
URI: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18554
Appears in Collections:Journal Articles (before-1995)

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