Inherent thermal regeneration performance of different MnO2 crystallographic structures for mercury removal

[Display omitted] •Different crystallographic MnOx were tested for Hg0 removal.•α-MnO2 exhibits a better regeneration performance for Hg0 removal than γ-MnO2.•Regeneration mechanisms of α- and γ-MnO2 are proposed. Manganese oxides with different crystallographic structures were investigated for gas-...

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Published inJournal of hazardous materials Vol. 374; pp. 267 - 275
Main Authors Yao, Ting, Duan, Yufeng, Bisson, Teresa M., Gupta, Rajender, Pudasainee, Deepak, Zhu, Chun, Xu, Zhenghe
Format Journal Article
LanguageEnglish
Published Elsevier B.V 15.07.2019
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Summary:[Display omitted] •Different crystallographic MnOx were tested for Hg0 removal.•α-MnO2 exhibits a better regeneration performance for Hg0 removal than γ-MnO2.•Regeneration mechanisms of α- and γ-MnO2 are proposed. Manganese oxides with different crystallographic structures were investigated for gas-phase elemental mercury removal. The inherent thermal regeneration performance and mechanism of α- and γ-MnO2 were studied. The manganese dioxides were found to possess a mercury removal efficiency of higher than 96% even after 120 min mercury exposure except for β-MnO2 which removed much less mercury than Mn2O3. The α-MnO2 was found to have a higher recyclability of mercury capture and better durability for regeneration than γ-MnO2. During the first 1 h of exposure, α-MnO2 showed an excellent mercury capacity of 128 μg/g over 5 regeneration cycles. While for γ-MnO2, the mercury capacity of the fifth cycle was reduced to 68.74 μg/g, which is much lower than 131.42 μg/g for the first cycle. The microstructure of α-MnO2 was maintained throughout regeneration cycles due to its capability to retain lattice oxygen. In comparison, γ-MnO2 experienced reconstruction and phase transformation induced by oxygen vacancies due to lattice oxygen loss during regeneration process, leading to a degradation in mercury capture. The α-MnO2 oriented composite was found to be better developed into a regenerable catalytic sorbent for mercury removal from flue gases of coal-fired power plants.
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ISSN:0304-3894
1873-3336
DOI:10.1016/j.jhazmat.2019.04.006