Enhancement of Mineralization Ability and Water Resistance of Vanadium-Based Catalysts for Catalytic Oxidation of Chlorobenzene by Platinum Loading

The design of a catalyst with multifunctional sites is one of the effective methods for low-temperature catalytic oxidation of chlorinated volatile organic compounds (CVOCs). The loss of redox sites and competitive adsorption of H 2 O prevalent in the treatment of industrial exhaust gases are the main reasons for the weak mineralization ability and poor water vapor resistance of V-based catalysts. In this work, platinum (Pt) is selected to combine with the V/CeO 2 catalyst, which provides more redox sites and H 2 O dissociative activation sites and further enhances its catalytic performance. The results show that PtV/CeO 2 achieves 90% of the CO 2 yield at 318 °C and maintains excellent catalytic activity rather than continuous deactivation within 15 h after water vapor injection. The formation of Pt–O–V bonds enhances the redox ability and promotes deep oxidation of polychlorinated intermediates, accounting for the significantly improved mineralization ability of PtV/CeO 2 . The dissociative activation effect of Pt on H 2 O molecules strengthens the migration and activation of V-adsorbed H 2 O, precluding V-poisoning and notably improving water resistance. This study lays a solid foundation for the efficient degradation of chlorobenzene under humid conditions.