Natural ferruginous manganese ore for efficient immobilization of elemental mercury from coal combustion flue gas

被引:47
|
作者
Xu, Yang [1 ]
Luo, Guangqian [2 ,3 ]
Zhou, Mengli [1 ,2 ]
Zhang, Qingzhu [1 ]
Li, Zehua [2 ,4 ]
Zhang, Shibo [1 ]
机构
[1] Shandong Univ, Environm Res Inst, Qingdao 266237, Peoples R China
[2] Huazhong Univ Sci & Technol, State Key Lab Coal Combust, Sch Energy & Power Engn, Wuhan 430074, Peoples R China
[3] Huazhong Univ Sci & Technol, Shenzhen Inst, Shenzhen 518000, Peoples R China
[4] Karlsruhe Inst Technol, Inst Quantum Mat & Technol, Hermann von Helmholtz Pl 1, D-76344 Eggenstein Leopoldshafen, Germany
基金
中国国家自然科学基金;
关键词
Elemental mercury; Flue gas; Ferruginous manganese ore; Sorbent; Calcination; CATALYTIC-OXIDATION; SIMULTANEOUS REMOVAL; POLYVINYL-CHLORIDE; ACTIVATED CARBON; FLY-ASH; ADSORPTION; FE; MN; REDUCTION; SORBENTS;
D O I
10.1016/j.fuel.2020.118946
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
Mercury emission from industrial activities poses a serious threat to the ecosystem. The development of cost-effective sorbents for mercury removal is a feasible method to alleviate this problem. In this study, natural ferruginous manganese ore (NFM) was adopted as a cost-effective sorbent for elemental mercury (Hg-0) removal from flue gas. Samples characterization indicated that the pore stricture of NFM was deteriorated after calcination procedure. The secondary recrystallization of manganese oxides and decomposition of MnO2 into Mn2O3 also happened during calcination process. Raw NFM exhibited high Hg-0 removal efficiency (E-T > 80%) over a broad temperature range (100 degrees C-200 degrees C), whereas calcination procedure had negative effects on Hg-0 removal performance. The effects of calcination temperature (450 degrees C-650 degrees C) and reaction temperature (100 degrees C-400 degrees C) on Hg-0 removal performance were also explored. Under the simulated flue gas condition, both equilibrium mercury adsorption capacity and adsorption rate were superior to those of a commercial activated carbon specifically used for mercury emission reduction. The Hg-0 removal mechanism was revealed by combining with Hg-0 adsorption/oxidization behavior and XPS analysis. It was demonstrated that chemisorption dominated Hg-0 removal process, where MnO2 could serve as active components for Hg-0 capture. The results were affirmed by the mercury temperature programmed desorption experiments.
引用
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页数:9
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