文摘
The reaction mechanism of the decomposition of ethoxy species to ethene and acidic OH groups on H-ZSM-5 was studied by IR spectroscopy using isotope-labeled ethanol. The concerted mechanism occurring on both the ethoxy (acid) site and the counterpart lattice oxygen was suggested by GC-MS analysis of evolved d2-ethene and IR observation of the recovery of OH s groups on acid sites from the decomposition of CH3CD2O鈥?ethoxy species. The concerted mechanism was further confirmed by the estimation of activation energy for decomposition of CH3CH2O鈥? CH3CD2O鈥? and CD3CD2O鈥?ethoxy species, 122 卤 3, 125 卤 3, and 140 卤 5 kJ mol鈥?, respectively, where the kinetic isotope effect was observed for the cleavage of the CH or CD bond of the methyl group of the ethoxy species.