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Pyrolysis of 1,1,1-Trichloroethane in the absence and the presence of added HCl and/or CCl4

✍ Scribed by G. Huybrechts; Y. Hubin; B. Van Mele


Publisher
John Wiley and Sons
Year
1989
Tongue
English
Weight
739 KB
Volume
21
Category
Article
ISSN
0538-8066

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✦ Synopsis


The title reaction has been studied in a static quartz reaction vessel between 587 and 658 K at pressures between 40 and 152 torr. The dehydrochlorination is the only significant reaction and is autoaccelerated by the produced HC1. Numerical modelling indicates that the Rice-Herzfeld mechanism, generally used for describing the pyrolysis of halogenated ethanes, has to be completed in the case of CC13CH3 with additional transfer reactions converting "dead' radicals into chain carriers and vice-versa. The numerical simulation fits the experimental results, in the absence as well as in the presence of different amounts of added HCI. The dehydrochlorination is also accelerated by the addition of CCl,,, which can be explained in terms of additional elementary steps involving . CC13 radicals.


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