Non-thermal plasma catalysis for chlorobenzene removal over CoMn/TiO2 and CeMn/TiO2: Synergistic effect of chemical catalysis and dielectric constant

被引:82
作者
Song, Hua [1 ,2 ]
Hu, Fangyun [1 ]
Peng, Yue [1 ]
Li, Kezhi [1 ]
Bai, Shupei [2 ]
Li, Junhua [1 ]
机构
[1] Tsinghua Univ, Sch Environm, Beijing 100084, Peoples R China
[2] Res Inst Chem Def, Beijing 100191, Peoples R China
关键词
Non-thermal plasma; Catalysis; Dielectric constant; Chlorobenzene; BARRIER DISCHARGE REACTOR; ATMOSPHERIC-PRESSURE; MNOX/TIO2; CATALYSTS; OXIDATION; OXIDE; DECOMPOSITION; BENZENE; TOLUENE; DEGRADATION; PERFORMANCE;
D O I
10.1016/j.cej.2018.04.018
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The decomposition of chlorobenzene (CB) in a non-thermal plasma (NTP) catalysis combined reactor was investigated. CoMn/TiO2 and CeMn/TiO2 were prepared using a deposition-precipitation method. CB decomposition, carbon balance, selectivity of CO2, and the byproducts of NOx and O-3 were investigated. NTP catalysis provided significantly better CB removal efficiency and CO2 selectivity than did the plasma alone. CoMn/TiO2 exhibited better removal efficiency than CeMn/TiO2 in the NTP-catalysis reactor, but the performance of the catalysts during the thermal catalytic oxidation was reversed without the NTP. To reveal the activity difference with CB decomposition in the NTP-catalysis hybrid system, the dielectric constant and the physicochemical properties of CoMn/TiO2 and CeMn/TiO2 were analyzed. The plasma, which was affected by the dielectric constant, played a dominant role in this hybrid system. The reducibility of the catalysts promoted the CO2 selectivity and O-3 decomposition. The CoMn/TiO2 was remarkably stable in the NTP-catalysis hybrid system during extended testing.
引用
收藏
页码:447 / 454
页数:8
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