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Investigation of elemental mercury removal from coal-fired flue gas over MIL101-Cr

Dong, Lu; Huang, Yaji; Liu, Lingqin; Liu, Changqi; Xu, Ligang; Zha, Jianrui; Chen, Hao; Liu, Hao

Investigation of elemental mercury removal from coal-fired flue gas over MIL101-Cr Thumbnail


Authors

Lu Dong

Yaji Huang

Lingqin Liu

Changqi Liu

Ligang Xu

Jianrui Zha

Hao Chen

HAO LIU LIU.HAO@NOTTINGHAM.AC.UK
Professor of Energy Engineering



Abstract

In this work, the MIL101-Cr sorbent with a large BET surface area was prepared and used to remove Hg0 from the simulated coal-fired boiler flue gas. The chemical and physical properties of the prepared sorbent were characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) and X-ray photoelectron spectroscopy (XPS). A range of experiments was conducted in a fixed-bed reactor to investigate the effects of reaction temperature, Hg0 inlet concentration, gas hourly space velocity (GHSV) and flue gas composition on the Hg0 removal for the prepared sorbent. The mechanisms and kinetics of the Hg0 adsorption were also studied. The results showed that the MIL101-Cr sorbent achieved the Hg0 removal efficiency of more than 85% for 4 h at 200 oC under the condition of a relatively high Hg0 inlet concentration (203 ?g/m3) and large GHSV (8 ? 105 h-1). The O2 in the flue gas was found to be beneficial to Hg0 removal. The NO in the flue gas favoured Hg0 removal both in the presence and absence of O2. The SO2 in the flue gas notably inhibited Hg0 adsorption in the absence of O2, whereas a low concentration of SO2 slightly inhibited Hg0 removal in the presence of O2. However, high concentrations of SO2 in the flue gas still significantly weakened the Hg0 removal ability even in the presence of O2 due to the competitive adsorption of SO2 with Hg0 on the sorbent and the sulfation of the sorbent. A simultaneous presence of O2 and NO in the flue gas could overcome the adverse impact of SO2 on the Hg0 adsorption. The H2O in the flue gas could have a minor influence on Hg0 removal as a result of the competitive adsorptions between Hg0 and H2O. The XPS analysis indicated that the surface Cr3+, oxygen species and C=O group in MIL101-Cr acted as the active adsorption/oxidation sites for Hg0. The Hg0 removal by MIL101-Cr belonged to chemisorption and could be described by the pseudo-second-order model. The equilibrium adsorption capacity calculated for the sorbent amounted to 25656 ?g/g at 200 oC, which indicated that MIL101-Cr could be used as a promising sorbent to remove Hg0 from coal-fired boiler flue gases.

Journal Article Type Article
Acceptance Date Aug 6, 2019
Online Publication Date Aug 6, 2019
Publication Date Aug 6, 2019
Deposit Date Aug 13, 2019
Publicly Available Date Aug 7, 2020
Journal Energy & Fuels
Print ISSN 0887-0624
Electronic ISSN 1520-5029
Publisher American Chemical Society
Peer Reviewed Peer Reviewed
Volume 33
Issue 9
Pages 8864-8875
DOI https://doi.org/10.1021/acs.energyfuels.9b01355
Keywords Fuel Technology; Energy Engineering and Power Technology; General Chemical Engineering
Public URL https://nottingham-repository.worktribe.com/output/2422847
Publisher URL https://pubs.acs.org/doi/10.1021/acs.energyfuels.9b01355
Additional Information This document is the Accepted Manuscript of a published work that appeared in final form in Energy and Fuels, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://pubs.acs.org/doi/10.1021/acs.energyfuels.9b01355

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