Abstract

The formation of coke and the influence of the coke on selectivity were investigated during hydrogenation of acetylene on supported palladium catalysts. It was found that the total amount of coke was not directly related to the increase in formation of undesired ethane. Instead, the surface coverage of hydrogen during the deactivation was found to be a crucial parameter. A catalyst deactivated at low hydrogen surface coverage showed a higher ethane selectivity than a sample deactivated at higher surface coverage of hydrogen when compared under the same reaction conditions. In contrast, the coke formation rate was found to increase with increased hydrogen surface coverage. The role of carbon monoxide was also investigated, and the impact on selectivity and coke formation was explained by the reduced surface coverage of hydrogen in the presence of carbon monoxide. The coke was characterized by temperature-programmed oxidation, and deconvolution of the obtained peaks was carried out using a power-law model.

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