Abstract:The main products are toluene, ethylbenzene, iso-butylbenzene and hydrocarbon gases (C 1 , C 2 and C 3). Several organosulfur compounds are produced: mainly short thiols, phenylbutanethiols, and phenylthiophenes. H 2 S accelerates the pyrolysis of n-butylbenzene by a factor up to almost 4 depending on the experimental conditions.
“…Vitzthum et al determined that the pyrolysis rate of n -butylbenzene accelerated under high-pressure conditions during the pyrolysis of H 2 S with n -butylbenzene. 24 The apparent activation energy of the pyrolysis of n -butylbenzene decreased from 66.6 kcal mol −1 (pure n -butylbenzene) to 55.9 kcal mol −1 ( n -butylbenzene in a mixture with H 2 S). Nguyen et al reported on the pyrolysis properties of a mixture of n -octane and H 2 S. Many types of thiols and heavy hydrocarbons were formed in the presence of H 2 S, owing to the progress of the reaction between the hydrocarbon molecules and the radicals produced from H 2 S. 25 Zeng et al investigated the interaction of sulfanyl radicals (SH*) with aliphatic (C1–C4) hydrocarbons via calculations using CBS-QB3.…”
“…Vitzthum et al determined that the pyrolysis rate of n -butylbenzene accelerated under high-pressure conditions during the pyrolysis of H 2 S with n -butylbenzene. 24 The apparent activation energy of the pyrolysis of n -butylbenzene decreased from 66.6 kcal mol −1 (pure n -butylbenzene) to 55.9 kcal mol −1 ( n -butylbenzene in a mixture with H 2 S). Nguyen et al reported on the pyrolysis properties of a mixture of n -octane and H 2 S. Many types of thiols and heavy hydrocarbons were formed in the presence of H 2 S, owing to the progress of the reaction between the hydrocarbon molecules and the radicals produced from H 2 S. 25 Zeng et al investigated the interaction of sulfanyl radicals (SH*) with aliphatic (C1–C4) hydrocarbons via calculations using CBS-QB3.…”
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