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  • Physics Chemistry  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 311-323 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A check of the data from comparative rate single-pulse shock tube experiments have been carried out through the use of a new standard reaction, the decyclization reaction of ethylcyclobutane. The rate expressions for cyclohexene and 2,2,3-trimethylbutane have been found to be \documentclass{article}\pagestyle{empty}\begin{document}$$ \begin{array}{l} k({\rm C}_{\rm 6} {\rm H}_{{\rm 10}} \to 1,3 - {\rm C}_4 {\rm H}_6 + {\rm C}_2 {\rm H}_4 ) = 10^{15.3} \exp ( - 33,690/T)\sec ^{ - 1} ,950^ \circ - 1100^ \circ {\rm K,2} - {\rm 6atm} \\ k(t{\rm C}_4 {\rm H}_9 - {\rm iC}_3 {\rm H}_7 \to t{\rm C}_{\rm 4} {\rm H}_{\rm 9} \cdot + {\rm iC}_{\rm 3} {\rm H}_7 \cdot ) = 10^{16.5} {{\exp ( - 36,830} \mathord{\left/ {\vphantom {{\exp ( - 36,830} T}} \right. \kern-\nulldelimiterspace} T})\sec ^{ - 1} ,1000^ \circ - 1100^ \circ {\rm K,2} - {\rm 6atm} \\ \end{array} $$\end{document} in excellent agreement with previously published results. Most of the small discrepancy that does exist is apparently due to the differences between the present and earlier (decomposition of isopropyl bromide) "standard" reaction. For the latter process, the present study yields \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm iC}_{\rm 3} {\rm H}_7 {\rm Br} \to {\rm C}_{\rm 3} {\rm H}_6 + {\rm HBr}) \to 10^{13.73} {\rm exp(}{{ - 23,970} \mathord{\left/ {\vphantom {{ - 23,970} {T\sec ^{ - 1} ,800^ \circ - 1000^ \circ {\rm K,2} - {\rm 6}}}} \right. \kern-\nulldelimiterspace} {T\sec ^{ - 1} ,800^ \circ - 1000^ \circ {\rm K,2} - {\rm 6}}}{\rm atm)} $$\end{document} These results confirm the correctness of previously published comparative rate single-pulse shock tube experiments. They demonstrate once again that for the decomposition of paraffin hydrocarbons, calculated preexponential factors are at least an order of magnitude higher than the directly measured number and that the accepted value of the heat of formation of t-butyl radicals ΔHf300(tC4H9·) = 29 kJ (6.8 kcals) is at least 10 kJ too low. Finally, attention is called to recent studies on neopentane decomposition in flow and static systems which are in complete agreement with the present conclusions.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 23-36 
    ISSN: 0538-8068
    Keywords: Chemistry ; Physics Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dilute mixtures of 4-methyl-l-pentyne have been pyrolyzed in a single-pulse shock tube. The decomposition process involves bond breaking: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm HC} \equiv {\rm C} - {\rm CH}_2 ({\rm i - C}_{\rm 3} {\rm H}_{\rm 7} )\stackrel{k_B}{\longrightarrow}{\rm HC} \equiv {\rm C} - {\rm CH}_2 \cdot ({\rm propynyl}) + {\rm i - C}_{\rm 3} {\rm H}_{\rm 7} \cdot $$\end{document} as well as a molecular reaction: \documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm HC}\equiv {\rm C} - {\rm CH}_{\rm 2} ({\rm \rm i - C}_{\rm 3} {\rm H}_{\rm 7} )\stackrel{k_M}{\rightarrow}{\rm C}_{\rm 3} {\rm H}_4 ({\rm allene}) + {\rm C}_3 {\rm H}_6 . $$\end{document} The rate parameters are: \documentclass{article}\pagestyle{empty}\begin{document}$$k_{\bf B} = 10^{15.56} \exp {\rm (} - 34,940/T){\rm (sec}^{ - {\rm 1}}) $$ $$\begin{array}{*{20}c} k_{\rm M} = 10^{13.1} \exp {\rm (} - {\rm 29,670/}T){\rm (sec}^{ - {\rm 1}})&{\rm 1100}^ \circ {\rm K, 1}{\rm .5} - 5{\rm atm}\end{array}$$\end{document} The heat of formation of propynyl radical is thus ΔHf300 = 338 kJ mol-1 (80.7 kcal mol-1)· This leads to a propynyl resonance energy of 40 kJ mol-1 (9.6 kcal mol-1).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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