The thermal dehydrochlorination CF,CICH, + CFFCH, + HCl has been studied in a static system between 637 and 758 K. It is a homogeneous, molecular first-order reaction and its rate constant is given by log,, (k, s-') = -(53,400 2 100)/4.576T + (12.21 ? 0.03) This reaction has also been studied in the
Pyrolysis of 1,1,1-Trichloroethane in the absence and the presence of added HCl and/or CCl4
β 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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β¦ 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.
π SIMILAR VOLUMES
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