A novel CNTs functionalized CeO2/CNTs-GAC catalyst with high NO conversion and SO2 tolerance for low temperature selective catalytic reduction of NO by NH3

被引:15
|
作者
Pu, Yijuan [1 ]
Wang, Pengchen [1 ]
Jiang, Wenju [1 ,2 ]
Dai, Zhongde [1 ,2 ]
Yang, Lin [1 ,2 ]
Jiang, Xia [1 ,2 ]
Jiang, Zhicheng [3 ]
Yao, Lu [1 ,2 ]
机构
[1] Sichuan Univ, Coll Architecture & Environm, Chengdu 610065, Peoples R China
[2] Natl Engn Res Ctr Flue Gas Desulfurizat, Chengdu 610065, Peoples R China
[3] Sichuan Univ, Dept Biomass Sci & Engn, Chengdu 610065, Peoples R China
基金
中国博士后科学基金;
关键词
CNTs; GAC; Nitrogen oxides; Low temperature NH3-SCR; SO2; poisoning; CARBON NANOTUBES; MIXED-OXIDE; ELECTRONIC-STRUCTURE; MN; NH3-SCR; CEO2; RESISTANCE; OXIDATION; TIO2/CEO2; WATER;
D O I
10.1016/j.chemosphere.2021.131377
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Low-temperature selective catalytic reduction of NOx by NH3 (NH3-SCR) for diminishing SO2 poisoning remains an issue in flue gas denitrification (DeNOx). Herein, A novel CNTs functionalized low temperature NH3-SCR catalyst CeO2/CNTs-GAC was prepared, which showed high NO conversion activity (100% at 150 degrees C) and SO2 resistance. The addition of CNTs restrained SO2 adsorption but improved the selective adsorption of NO, which restricted the deposition of (NH4)2SO4 and/or Ce2(SO4)3, and resulted in high SO2 resistance. The addition of CNTs facilitated the diffusion and transportation of NH3 and NO, and the electron transfer on CeO2/ CNTs-GAC, leading to higher content of Ce3+ and adsorbed O species on the CeO2/CNTs-GAC surface and promoted formation of surface-adsorbed oxygen OA. Therefore, CeO2/CNTs-GAC provided abundant NO adsorption and activation sites, facilitating "fast SCR" reaction and enhancing the NH3-SCR reaction. The proposed CeO2/CNTs-GAC catalyst exhibited higher NH3-SCR activity, N2 selectivity, catalytic durability and SO2 resistance than CeO2/GAC.
引用
收藏
页数:10
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