摘要
Activation of hydrogen atoms of methyl in toluene and methanol is crucial for side-chain alkylation of toluene with methanol. Herein, two strategies were applied, introducing dehydrogenation component (Cu) and tailoring the catalyst acid-base property with NaOH. A series of Cu and NaOH dual-modified PAl-NaX catalysts were prepared by in-situ hydrothermal method, the synergistic effect of Cu and NaOH was investigated. It is revealed that the product of (medium base)* (weak acid) and surface Cu δ+ percentage is crucial in controlling the total yield of side chain alkylation products by enhancing ethyl benzene selectivity. Cat-3Cu-13Na exhibits the optimal catalytic performance with an average methanol conversion of 97.25 % and an average total yield of side chain alkylation products of 77.46 % without obvious deactivation occurs in 192 h, and Cat-3Cu-19Na shows a promising styrene selectivity of 44.06 %. The decrease of weak acid sites might result in the decline in selectivity of styrene.
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