Reason for the deactivation of SnOx in acetylene hydrochlorination†
Abstract
To investigate the deactivation process of Sn-based catalysts and the transformation of their active sites during acetylene hydrochlorination, we synthesized a SnOx catalyst and subjected it to hydrochloric acid and water-washing treatments. Subsequent characterization showed that the active SnOx component was transformed into SnCl4 by hydrochloric acid treatment, and SnCl4 showed lower catalytic activity compared with SnOx components. Furthermore, SnOx reacted with the HCl reactant to form SnCl4 in the acetylene hydrochlorination, which led to a decline in catalytic performance and a loss of Sn components. Considering the influence of Sn valence states, we used ascorbic acid (C6H8O6) to regulate the valence in SnOx and found that Sn2+ was firstly oxidized to Sn4+ in the acetylene hydrochlorination, and then secondly Sn4+ reacted with HCl to form SnCl4, leading to the deactivation of the SnOx catalyst.