The reaction behaviors of acetonitrile and ethyl acetate simultaneous degradation over Cu-Ce/ZSM-5 catalyst

被引:5
|
作者
Zhang, Yaoyu [1 ]
Wang, Yuxiong [1 ]
Liu, Yue [1 ]
Xu, Huimin [1 ]
Wu, Zhongbiao [1 ,2 ]
机构
[1] Zhejiang Univ, Dept Environm Engn, 866 Yuhangtang Rd, Hangzhou 310058, Peoples R China
[2] Zhejiang Prov Engn Res Ctr Ind Boiler & Furnace Fl, 866 Yuhangtang Rd, Hangzhou 310058, Peoples R China
关键词
Acetonitrile; Ethyl acetate; Simultaneous removal; Cu-Ce; ZSM-5; catalyst; Mutual inhibition mechanism; N2; selectivity; VOLATILE ORGANIC-COMPOUNDS; IN-SITU FTIR; ACETIC-ACID; COMBUSTION; ACRYLONITRILE; ADSORPTION; OXIDATION; MECHANISM; IR; DECOMPOSITION;
D O I
10.1016/j.apsusc.2022.155190
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Aiming at the coexistence of pollutants in the actual industrial process, the catalytic oxidation of acetonitrile and ethyl acetate mixture on the Cu-Ce/ZSM-5 catalyst was studied. The mutual inhibition effect during catalytic removal of acetonitrile and ethyl acetate mixture was observed. Acetonitrile showed a more obvious inhibitory effect on the conversion of ethyl acetate, and the introduction of ethyl acetate reduced the N2 selectivity of acetonitrile oxidation. The simulation results demonstrated acetonitrile could be preferentially adsorbed on Cu center of the catalyst surface, leading to significant inhibition of the initial conversion of ethyl acetate. In addition, the coexistence of ethyl acetate would weaken the hydrolysis of acetonitrile to generate carboxylic acid and -NHx species. As such, no enough adsorbed NHx species could be used to reduce the NOx produced by excessive oxidation of acetonitrile, resulting in a decreased in N2 selectivity. This study could provide reference on the application of catalysts for cyanide-containing waste gas degradation.
引用
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页数:10
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