Cl-Resistant Synergistic Removal of NO<sub><i>x</i></sub> and Chlorobenzene over SmMn<sub>2</sub>O<sub>5</sub>-Zeolite Composite Catalysts
Fuli Wang, Tianwei Lan, Xiaonan Hu, Aling Chen, Xin Chen, Xinrui Xu, Mengxue Wang, Ming Xie, Yongjie Shen, Penglu Wang, Dengsong Zhang
Abstract
Synergistic catalytic removal (SyCR) of NO x and chlorinated volatile organic compound (CVOCs) emission from nonelectric industries is effective to suppress PM 2.5 and ozone complex air pollution. Catalysts with balanced competence to reduce NO x and oxidize CVOCs, as well as the resistance to chlorine poisoning, are critical to SyCR. Here, neighboring effects over SmMn 2 O 5 mullite (SMO) modified by HZSM-5 composite catalysts (SMO-Z) were demonstrated in the Cl-resistant SyCR of NO x and chlorobenzene (CB, a representative CVOCs). Characterizations demonstrated that HZSM-5 modification did not alter the crystal structure of SMO and retained Mn–O–Mn–Mn active sites for the SyCR of NO x and CB. HZSM-5 regulated the redox ability of SMO-Z to reduce the formation of inert nitrate species and to promote the N 2 selectivity. Acidic HZSM-5 acted as dechlorination sites to promote the breakage of the C–Cl bond via the nucleophilic substitution reaction and accelerated the formation of HCl to avoid Cl poisoning on catalysts. The fine-tuned compensation of surface acidity by HZSM-5 suppressed the competitive adsorption of NH 3 and CB on SMO-Z, which promoted NO x reduction at high temperatures, whereupon neighboring effects between HZSM-5 acidic dechlorination sites and SMO active redox sites on SMO-Z capitally promoted the SyCR efficiency and antichlorination poisoning performance.