Study on the removal of elemental mercury from simulated flue gas by Fe2O3-CeO2/AC at low temperature

被引:67
|
作者
Wang, Yan [1 ,2 ]
Li, Caiting [1 ,2 ]
Zhao, Lingkui [1 ,2 ]
Xie, Yin'e [1 ,2 ]
Zhang, Xunan [1 ,2 ]
Zeng, Guangming [1 ,2 ]
Wu, Huiyu [1 ,2 ]
Zhang, Jie [1 ,2 ]
机构
[1] Hunan Univ, Coll Environm Sci & Engn, Changsha 410082, Hunan, Peoples R China
[2] Hunan Univ, Key Lab Environm Biol & Pollut Control, Minist Educ, Changsha 410082, Hunan, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划);
关键词
Elemental mercury; Activated coke; Adsorption; Catalytic oxidation; Flue gas; Low temperature; SELECTIVE CATALYTIC-REDUCTION; STRUCTURAL-CHARACTERIZATION; ACTIVATED CARBONS; UTILITY BOILER; HG-0; REMOVAL; OXIDATION; ADSORPTION; IRON; CEO2-TIO2; XPS;
D O I
10.1007/s11356-015-5717-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Fe2O3 and CeO2 modified activated coke (AC) synthesized by the equivalent-volume impregnation were employed to remove elemental mercury (Hg-0) from simulated flue gas at a low temperature. Effects of the mass ratio of Fe2O3 and CeO2, reaction temperature, and individual flue gas components including O-2, NO, SO2, and H2O (g) on Hg-0 removal efficiency of impregnated AC were investigated. The samples were characterized by Brunauer-Emmett-Teller (BET), X-ray diffraction (XRD), scanning electron microscopy (SEM), and X-ray photoelectron spectroscopy (XPS). Results showed that with optimal mass percentage of 3 % Fe2O3 and 3 % CeO2 on Fe3Ce3/AC, the Hg-0 removal efficiency could reach an average of 88.29 % at 110 A degrees C. Besides, it was observed that O-2 and NO exhibited a promotional effect on Hg-0 removal, H2O (g) exerted a suppressive effect, and SO2 showed an insignificant inhibition without O-2 to some extent. The analysis of XPS indicated that the main species of mercury on used Fe3Ce3/AC was HgO, which implied that adsorption and catalytic oxidation were both included in Hg-0 removal. Furthermore, the lattice oxygen, chemisorbed oxygen, and/or weakly bonded oxygen species made a contribution to Hg-0 oxidation.
引用
收藏
页码:5099 / 5110
页数:12
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