4.2 Article

Pd/activated carbon sorbents for mid-temperature capture of mercury from coal-derived fuel gas

Journal

JOURNAL OF ENVIRONMENTAL SCIENCES
Volume 26, Issue 7, Pages 1497-1504

Publisher

SCIENCE PRESS
DOI: 10.1016/j.jes.2014.05.016

Keywords

Coal-derived fuel gas; Hg removal; Pd/AC sorbents; H2S removal

Funding

  1. National Natural Science Foundation of China [21006067, 21276170]
  2. Shanxi Province Natural Science Foundation [2010021008-1, 201101008-4]
  3. National High-Tech Research and Development Program (863) of China [2013AA065404E]

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Higher concentrations of Hg can be emitted from coal pyrolysis or gasification than from coal combustion, especially elemental Hg. Highly efficient Hg removal technology from coal-derived fuel gas is thus of great importance. Based on the very excellent Hg removal ability of Pd and the high adsorption abilities of activated carbon (AC) for H2S and Hg, a series of Pd/AC sorbents was prepared by using pore volume impregnation, and their performance in capturing Hg and H2S from coal-derived fuel gas was investigated using a laboratory-scale fixed-bed reactor. The effects of loading amount, reaction temperature and reaction atmosphere on Hg removal from coal-derived fuel gas were studied. The sorbents were characterized by N-2 adsorption, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The results indicated that the efficiency of Hg removal increased with the increasing of Pd loading amount, but the effective utilization rate of the active component Pd decreased significantly at the same time. High temperature had a negative influence on the Hg removal. The efficiency of Hg removal in the N-2-H2S-H-2-CO-Hg atmosphere (simulated coal gas) was higher than that in N-2-H2S-Hg and N-2-Hg atmospheres, which showed that H-2 and CO, with their reducing capacity, could benefit promote the removal of Hg. The XPS results suggested that there were two different ways of capturing Hg over sorbents in N-2-H2S-Hg and N-2-Hg atmospheres. (C) 2014 The Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences. Published by Elsevier B.V.

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