Efficient catalytic oxidation of chlorinated volatile organic compounds over RuO2-WOx/Sn0.2Ti0.8O2 catalysts: Insight into the Cl poisoning mechanism of acid sites

Abstract

The development of catalysts with high activity, selectivity, and durability is crucial for the catalytic oxidation of chlorinated volatile organic compounds (CVOCs). Although acid-modified supports are widely used in catalysis to improve the catalytic activity at low temperature, the acid sites are easily deactivated by Cl poisoning, and the poisoning mechanism remains unclear. Here, a series of RuO2-WOx/Sn0.2Ti0.8O2 catalysts were synthesized for dichloromethane (DCM) catalytic oxidation. Spectroscopic characterizations revealed that the loading amount of tungsten oxide highly affects the structure of the surface species and, consequently, the low-temperature catalytic activity. SEM, XRD and DFT calculations elucidated that the loss of tungsten species in the form of WO2Cl2 is the main reason for the catalyst deactivation. By loading RuO2, the loss of tungsten species could be effectively avoided via the Deacon reaction. The cordierite catalyst exhibits excellent catalytic activity for the oxidation of different types of CVOCs.