C-13 MAS NMR MECHANISTIC STUDY OF BENZENE ALKYLATION WITH PROPANE OVER GA-MODIFIED H-ZSM-5 CATALYST

C-13 MAS NMR has been performed in situ to investigate the mechanism o f benzene alkylation with propane over Ga/H-ZSM-5 catalyst. Propane 2- C-13 was used as a labelled reactant. In order to clarify the main rea ction pathways, conversions of the individual starting materials and s ome of the reaction intermediates such as cumene and n-propylbenzene w ere also studied under similar conditions. Benzene alkylation with pro pane begins at 573 K, toluene and ethylbenzene being the major primary products. The reaction is preceded by the induction period caused by stronger adsorption of benzene that prevents propane activation, The m ain reaction pathway includes bifunctional propane activation on Brons ted and Ga sites which leads to protonated pseudocyclopropane (PPCP) i ntermediate, which in turn decomposes preferentially to CH4 and C2H5+, or C2H6 and CH3+. The reaction of C2H5+ or CH3+ carbenium ions with b enzene leads to toluene or ethylbenzene, respectively. The less favour able reaction routes give propenium and cycloproponium ions upon PPCP decomposition, and result in observation of the traces of cumene and n -propylbenzene. These routes are reversible, the equilibrium being shi fted towards reactants at 573 K.