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Issue title: Mercury and Other Trace Elements in Fuel: Emissions and Control
Article type: Research Article
Authors: Li, Huixing; | Monnell, Jason D.; | Alvin, Maryanne | Vidic, Radisav D.;
Affiliations: National Energy Technology Laboratory, Pittsburgh, PA, USA | Department of Civil and Environmental Engineering, University of Pittsburgh, Pittsburgh, PA, USA
Note: [] Corresponding author. Email: jmonnell@pitt.edu
Note: [] Corresponding author. Email: vidic@pitt.edu
Abstract: The primary product of coal gasification processes is synthesis gas (syngas), a mixture of CO, H2, CO2, H2O and a number of minor components. Among the most significant minor components in syngas is hydrogen sulfide (H2S). In addition to its adverse environmental impact, H2S poisons the catalysts and hydrogen purification membranes, and causes severe corrosion in gas turbines. Technologies that can remove H2S from syngas and related process streams are, therefore, of considerable practical interest. To meet this need, we work towards understanding the mechanism by which prospective H2S catalysts perform in simulated fuel gas conditions. Specifically, we show that for low-temperature gas clean-up (˜40°C) using activated carbon fibers and water plays a significant role in H2S binding and helps to prolong the lifetime of the material. Basic surface functional groups were found to be imperative for significant conversion of H2S to daughter compounds, whereas metal oxides (La and Ce) did little to enhance this catalysis. We show that although thermal regeneration of the material is possible, the regenerated material has a substantially lower catalytic and sorption capacity.
Keywords: hydrogen sulfide, oxidation catalyst, activated carbon, IGCC, syngas clean-up, coal gasification
DOI: 10.1080/10241220802509796
Journal: Main Group Chemistry, vol. 7, no. 3, pp. 239-250, 2008
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