Significant Enhancement of Gaseous Elemental Mercury Recovery from Coal-Fired Flue Gas by Phosphomolybdic Acid Grafting on Sulfurated γ-Fe2O3: Performance and Mechanism

吸附 烟气 吸附剂 磷钼酸 Mercury(编程语言) 化学 嫁接 燃煤 环境化学 化学工程 催化作用 工程类 有机化学 计算机科学 聚合物 程序设计语言
作者
Jian Mei,Pengxiang Sun,Chang Wang,Qi Zhang,Qixing Hu,Shijian Yang
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:54 (3): 1992-2001 被引量:54
标识
DOI:10.1021/acs.est.9b06736
摘要

The existing technologies to control Hg emissions from coal-fired power plants can be improved to achieve the centralized control of Hg0 emissions, which continue to pose a risk of Hg exposure to human populations. In this work, MoSx@γ-Fe2O3, formed by the sulfuration of phosphomolybdic acid (HPMo)-grafted γ-Fe2O3, was developed as a magnetic and regenerable sorbent to recover gaseous Hg0 from coal-fired flue gas as a cobenefit to the use of wet electrostatic precipitators. The thermal stability of γ-Fe2O3 was notably enhanced by HPMo grafting; thus, the magnetization of MoSx@γ-Fe2O3 hardly decreased during the application. The kinetic analysis indicates that the chemical adsorption of gaseous Hg0 was mainly dependent on the amounts of surface S22- and surface adsorption sites. Although the amount of S22- on sulfurated γ-Fe2O3 decreased after HPMo grafting, the amount of surface adsorption sites significantly increased due to the formation of a layered MoSx structure on the surface. Therefore, the ability of sulfurated γ-Fe2O3 to capture Hg0 was improved considerably after HPMo grafting. Furthermore, low concentrations of gaseous Hg0 in coal-fired flue gas can be gradually enriched by at least 1000 times by MoSx@γ-Fe2O3, which facilitates the recovery and centralized control of gaseous Hg0 in flue gas.
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