氯苯
催化作用
材料科学
选择性
傅里叶变换红外光谱
化学工程
核化学
化学
有机化学
工程类
作者
Junhua Li,Wenbo Shi,Kezhi Li,Jianjun Chen,Yue Peng
标识
DOI:10.1021/acsami.8b10636
摘要
Developing new technologies for the simultaneous removal of NO x and dioxins from metallurgical facility and waste incinerator emissions remains challenging. Here, we present a new synergistic improvement effects of NO x and chlorobenzene (CB) on the MnO x-CeO2 catalyst. CB promoted both the NO x conversion and N2 selectivity below 300 °C during the NO x reduction process, in which the MnO x-CeO2 catalyst caused the undesired side reactions due to the over-oxidation of NH3. Meanwhile, NO x and NH3 promoted the CB oxidation activity above 100 °C in the presence of O2. On the basis of the diffuse reflectance infrared Fourier transforms and kinetic studies, the promotion was due to the separation of the MnO x-CeO2 catalyst into different temperature windows: NO x reduction at 100-200 °C and CB oxidation at 200-300 °C. The side reactions mainly occurred above 200 °C, which is suppressed by the coverage and activation of CB on catalyst surface.
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