论文部分内容阅读
Single-event microkinetic (SEMK) model of the catalytic cracking of methylcyclohexane admixed with 1-octene over REUSY zeolites at 693 K-753 K in the absence of coke formation is enhanced. To keep consistency with the well-known carbenium ion chemistry, hydride transfer forming and consuming allylic carbenium ions in the aromatization of cycloparafifns are further investigated and differentiated. The reversibility of endocyclicβ-scission and cyclization reactions is reifned by accounting explicitly for the reacting oleifns and resulting cycloparafifns in the corresponding thermodynam-ics. 24 activation energies for the reactions involved in the cracking of cycloparafifns are obtained by the regression of 15 sets of experimental data upon taking the resulting 37 main cracking products, i. e., responses into account. The enhanced SEMK model can adequately describe the catalytic behavior of 37 main products with conversion and temperature.