Synergistic removal of NOx and CB by Co-MnOx catalysts in a low-temperature window

被引:13
作者
Kang, Dongrui [1 ]
Shi, Qiqi [1 ]
Zhang, Chenguang [1 ]
Zhao, Peng [1 ]
Lyu, Honghong [1 ]
Yang, Mingtao [1 ]
Bian, Yao [1 ]
Shen, Boxiong [1 ,2 ]
机构
[1] Hebei Univ Technol, Sch Energy & Environm Engn, Tianjin Key Lab Clean Energy & Pollut Control, Tianjin 300401, Peoples R China
[2] Hebei Univ Technol, Sch Chem Engn & Technol, Tianjin 300401, Peoples R China
基金
中国国家自然科学基金;
关键词
CVOCs; CB; Flue gas; Synergistic removal; OXIDE CATALYSTS; CHLOROBENZENE; SCR; REDUCTION; NI; COMBUSTION; OXIDATION; EXHAUST; STATES; NH3;
D O I
10.1016/j.cej.2023.146369
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The simultaneous removal of NOx and CVOCs in a deNOx unit has gained significant attention in recent years. However, efficient co-removal of NOx and CVOCs is still a challenge due to the low tail gas emission temperatures in the non-electric industry. To address this, m-MnOx (m = Sn or Co) catalysts were prepared based on the Mnbased catalyst to investigate their catalytic performance in removing NOx and CB. The results demonstrated that the Co-MnOx catalyst exhibited the best catalytic activity, achieving over 90 % NOx conversion within the temperature window of 105-275 degrees C, while CB conversion rates surpassed 90 % above 180 degrees C. The characterization results revealed that Co doping formed MnCo2O4 adding additional Lewis acid sites and promoted the conversion of Mn2+ to Mn3+ and Mn4+, thereby improving the redox ability and surface acidity of the Co-MnOx catalyst. DFT simulations revealed that Co addition improved the adsorption of NH3 and CB on the Co-MnOx catalyst and effectively reduced the energy barriers for N-H cleavage and oxygen vacancy formation. This work is hoped to provide an important reference for the further design and optimization of efficient low-temperature NOx/CB synergistic removal catalysts.
引用
收藏
页数:9
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