4.7 Article

Removal of mercury from flue gas using coal gasification slag

Journal

FUEL PROCESSING TECHNOLOGY
Volume 231, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.fuproc.2022.107258

Keywords

Mercury removal; Coal gasification fine slag; Ionic liquid; Sulfur dioxide; Oxidation reaction

Funding

  1. National Natural Science Foundation of Shangdong Province [ZR2017MB024]
  2. Foundation of State Key Laboratory of High-efficiency Utilization of Coal and Green Chemical Engineering [2021-K36]

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Coal combustion emits mercury, which can be removed using coal gasification fine slag (FS) immobilized with ionic liquids (IL-T and IL-B). The efficiency of mercury removal increased when supported by the ILs. The presence of SO2 had negligible impact on Hg0 capture. The total mercury removal efficiencies exceeded 90% for FS-T and FS-B in a specific atmosphere. The effective adsorption time for FS-T and FS-B was longer than FS, and Hg-0 and Hg2+ were detected in exhaust gas and solid phase.
Coal combustion often produces mercury emissions. Coal gasification fine slag (FS) was used to remove Hg0 from flue gas. To increase the removal efficiency, two ionic liquids (IL-T and IL-B) were immobilized on the surface of FS. The mercury removal performance was evaluated in a fixed-bed reactor in the presence of SO2 + O-2. The experimental results showed that the mercury removal efficiency increased when the adsorbents were supported by ionic liquids (FS-T and FS-B). The effect of 0.6% SO2 on the capture of Hg0 was negligible for all three ad-sorbents. The total mercury removal efficiencies exceeded 90% for FS-T and FS-B in the atmosphere of 0.6% SO2 + 6% O-2. When the initial mercury concentration was 60 mu g/m3, the effective adsorption time was about 80 min for FS and longer than 120 min for FS-T and FS-B. In the presence of 0.6% SO2 + 6% O-2, Hg-0 and Hg2+ were detected in exhaust gas using FS and FS-B and in solid phase using the three adsorbents. According to XPS analysis, an oxidation reaction occurred on the surface of FS and FS-T. For FS-B, the Br- anion of IL-B was the active site and oxidized Hg-0 to Hg2+ on the surface as well as in the gas phase.

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