Improved activity and SO2 tolerance of rare-earth elements modified CeTi catalyst for Hg0 and NO simultaneous removal from flue gas

被引:1
|
作者
Long, Yifei [1 ]
He, Zhong [4 ]
Liu, Shinian [2 ]
Zhou, Yongyan [3 ]
Liu, Wenjie [1 ]
Yin, Yajie [1 ]
Tong, Xin [1 ]
Li, Xiaoyi [1 ]
Hu, Kang [1 ]
Hu, Jiangjun [1 ]
机构
[1] Wuhan Univ, Sch Resource & Environm Sci, Wuhan 430079, Hubei, Peoples R China
[2] China Southern Power Grid Technol Co Ltd, Guangzhou, Peoples R China
[3] Guangdong Power Grid Co Ltd, Techn Management Elect Power Res Inst, Guangzhou, Peoples R China
[4] CCCC Second Highway Consultants Co Ltd, Green & Low Carbon Technol Ctr, Wuhan, Peoples R China
关键词
Rare-earth elements doping; Hg-0; oxidation; NO conversion; CeO2; TiO2; SO2; tolerance; MERCURY REMOVAL; REDUCTION; OXIDATION; ADSORPTION; OXIDES; NH3;
D O I
10.1080/15567036.2022.2067271
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
Six rare-earth elements (including La, Sm, Pr, Dy, Y, and Nd) were modified on the surface of the CeTi samples for Hg-0 oxidation and NO oxidation. The X-CeTi catalysts significantly improved the Hg-0 oxidation, NO oxidation, and SO2 tolerance compared with the CeTi catalyst. Moreover, O-2 and NO can facilitate the activities significantly. The BET results showed that the specific surface area could be increased by doping of rare-earth elements. In addition, XRD and FT-IR experiments indicated that the rare-earth elements can facilitate the formation of the amorphous structure of CeO2. The XPS curves of Ce 3d and O 1s showed that surface oxygen species and Ce4+/Ce3+ redox couples were responsible for the catalytic performance, confirming that the SO2 tolerance was improved via the electron transfer by Ce4++Dy2+Ce3++Dy3+ reactions. The H-2-TPR results suggested that the redox capacity of X-CeTi catalysts was enhanced, which could improve the activities of the catalysts. Moreover, Dy-CeTi had the highest NO and Hg-0 oxidation among these rare-earth elements on account of the largest specific surface, more surface-active oxygen and H-2-TPR reduction peak integral area. The catalyst can maintain the conversion efficiency of elemental mercury and NO at 67% and 76% even in flue gas containing 800 ppm SO2. Such work supplied new insights into modified Ce-Ti catalysts to simultaneously remove NO and elemental mercury from the flue gas with high efficiencies, which owned a promising prospect in the practical industrial application.
引用
收藏
页码:3575 / 3583
页数:9
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