The thermal dehydrochlorination has been studied CF ClCH : CF " CH ฯฉ HCl 2 3 2 2 in a static system between 597 and in the presence of CCl 4 , C 2 Cl 6 , CF 2 "CH 2 , HCl, and 664 K CF 3 CH 3 . A kinetic radical and molecular reaction model has been developed. In addition to describing earlier resul
Pyrolysis of 1-chloro-1,1-difluoroethane in the absence and in the presence of CCl4 and mixtures of CCl4 + HCl
โ Scribed by G. Huybrechts; Y. Hubin
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 354 KB
- Volume
- 17
- Category
- Article
- ISSN
- 0538-8066
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โฆ Synopsis
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 presence of CCl, and mixtures of CCl, and HCl between 585 and 662 K. It is then accelerated and the initial rate increase is given by with log,, (k', L1" /mo11'2 1 s) = -(41,650 t 180)/4.576T + (10.84 ? 0.06) and log,, k" = (7900 ? 180)/4.576T -(0.59 ? 0.06). A radical chain mechanism is shown to be consistent with these latter results.
Experimental
CF,ClCH, (Solvay), CCl, (Aldrich), and HC1 (Air Liquidle), 99.98%, 99.99%, and 99.995% pure, respectively, were used without further purification. * Predoctoral bursar of Belgian IWONL.
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