Effect of Mn and Ce oxides on low-temperature NH3-SCR performance over blast furnace slag-derived zeolite X supported catalysts

被引:97
作者
Chen, Lin [1 ]
Ren, Shan [1 ]
Jiang, Yanhua [1 ]
Liu, Lian [1 ]
Wang, Mingming [1 ]
Yang, Jie [1 ,2 ]
Chen, Zhichao [1 ]
Liu, Weizao [1 ]
Liu, Qingcai [1 ]
机构
[1] Chongqing Univ, Coll Mat Sci & Engn, Chongqing 400044, Peoples R China
[2] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
基金
中国国家自然科学基金;
关键词
BFS-derived zeolite X; Active sites; Low-temperature NH3-SCR; N2O generation; IN-SITU DRIFTS; SO2; TOLERANCE; NO REDUCTION; ACID SITES; NH3; MECHANISM; CO; TRANSIENT; REMOVAL; ZSM-5;
D O I
10.1016/j.fuel.2022.123969
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Several Mn and/or Ce oxides on blast furnace slag-derived (BFS-derived) zeolite X catalysts were prepared to investigate their low-temperature NH3-SCR performance. It was found that Mn-Ce/X catalyst had the highest NO conversion of nearly 98% at 250 ? and excellent N-2 selectivity of nearly 100% during 75-175 ?. The co addition of Ce and Mn could inhabit the growth of crystal grains, resulting in the increase of surface area and the generation of Mn-Ce double active sites. Besides, high concentration of Mn4+ and Mn3+ could promote oxidation of NO to NO2 accelerating the "fast-SCR " reaction and high concentration of Ce4+ could form more oxygen vacancies on Mn-Ce/X catalyst. In addition, the Mn-Ce/X catalyst had large acid amount and high redox ability owing to the co-existed Mn-Ce double active sites on zeolite catalyst and the co-effect of Mn-Ce oxides and zeolite X. Furthermore, the decomposition of NH4NO3 species on Mn/X catalyst led to the low N-2 selectivity at higher temperature. While NH2NO and NH4NO(2) intermediates on Mn-Ce/X catalyst played a vital part in NH3- SCR reaction and prevented the generation of N2O, and Mn-Ce/X catalyst provided more Mn-Ce active sites for the reaction between NO3- species and gaseous NO, accelerating SCR catalytic reaction.
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页数:13
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