Selenium Functionalized Metal-Organic Framework MIL-101 for Efficient and Permanent Sequestration of Mercury

被引:144
作者
Yang, Jianping [1 ]
Zhu, Wenbing [1 ]
Qu, Wenqi [1 ]
Yang, Zequn [2 ]
Wang, Jun [3 ]
Zhang, Mingguang [1 ]
Li, Hailong [1 ]
机构
[1] Cent S Univ, Sch Energy Sci & Engn, Changsha 410083, Hunan, Peoples R China
[2] Univ Hong Kong, Dept Civil Engn, Hong Kong, Peoples R China
[3] Univ Oklahoma, Hlth Sci Ctr, Hudson Coll Publ Hlth, Dept Occupat & Environm Hlth, Oklahoma City, OK 73126 USA
基金
中国国家自然科学基金;
关键词
COMBUSTION FLUE-GAS; ELEMENTAL MERCURY; COAL COMBUSTION; CATALYTIC-OXIDATION; FLY-ASH; MOS2; NANOSHEETS; REMOVAL; ADSORPTION; SORBENT; CAPTURE;
D O I
10.1021/acs.est.8b06321
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Abatement of mercury emission from coal-fired power plants remains a serious task for public health and environmental societies. Selenium functionalized metal-organic framework MIL-101 (Se/MIL-101) was prepared for mercury removal from power plants. The Se/MIL-101 exhibited a remarkable mercury adsorption capacity of 148.19 mg.g(-1), which was about 154 to 705 times larger than that of commercial activated carbons exclusively applied for mercury removal from power plants. The initial mercury adsorption rate for Se/MIL-101 reached up to 44.8 mu g.g(-1).min(-1), which was 89 to 1659-fold higher than those of mercury sorbents reported in the literature. The Se/MIL-101 maintained an excellent mercury adsorption stability under simulated flue gas atmosphere containing SO2, NO, and H2O. Gaseous elemental mercury (Hg-0) converted on the Se/MIL-101 to stable and water-insoluble mercury selenide (HgSe), which guaranteed minimum re-emission even sequestration of mercury. Moreover, the mercury-laden Se/MIL-101 could also immobilize mercury in gypsum and efficiently capture mercury ions from desulfurization effluent to an undetectable level (<0.0035 mu g.L-1). With these advantages, Se/MIL-101 appears to be a promising material for efficient and permanent sequestration of mercury from power plants.
引用
收藏
页码:2260 / 2268
页数:9
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