Mn-Cr mixed oxide adsorbents with high SO2 resistance for elemental mercury removal from coal-fired flue gas

被引:7
|
作者
Wang, Senyuan [1 ]
Ye, Dong [1 ]
Liu, Xin [1 ]
Wang, Haining [1 ]
Ma, Wei [2 ]
Liu, Hui [1 ]
机构
[1] China Jiliang Univ, Coll Qual & Safety Engn, Hangzhou 310018, Peoples R China
[2] Ganzhou Nonferrous Met Res Inst Co Ltd, Ganzhou 341000, Peoples R China
关键词
Elemental mercury; Adsorption; Mn-Cr mixed oxides; SO2; resistance; Synergistic interaction; HG-0; REMOVAL; AQUEOUS-SOLUTION; ISOTHERM DATA; ADSORPTION; NO; MECHANISM; OXIDATION; MIXTURE; REGENERATION; COMBUSTION;
D O I
10.1016/j.jiec.2023.03.041
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of Mn-Cr mixed oxide adsorbents were obtained using co-precipitation method. Then, an inves-tigation was conducted into the effects of Mn/Cr molar ratio, reaction temperature, calcination temper-ature, initial mercury concentration and flue gas constituents on the outcome of elemental mercury removal. Specifically, the MnCr1:3 with an optimal Mn/Cr molar ratio performed best in the efficiency of mercury removal (>95.4%) in a wide temperature range (100-250 degrees C). The physicochemical properties and the mechanism were characterized by N2 adsorption-desorption, SEM, XRD, NH3-TPD, H2-TPR, XPS and Hg-TPD in combination. According to the research results, mercury removal was facilitated by MnCr1:3 due to its larger surface area, smaller crystallite sizes, higher acidity and redox properties. Sulfur dioxide promoted elemental mercury capture for MnCr1:3 when different concentrations of SO2 existed in the flue gas. The relative activity over MnCr1:3 approached 100% after five regeneration cycles. Due to the combined effect of manganese and chromium, there was an increase in the concentration of high valence metal elements and surface adsorbed oxygen. MnCr1:3 had the highest content of Cr6+ and adsorbed oxygen species, for which they played a vital role in the outcome of mercury removal.(c) 2023 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:260 / 271
页数:12
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