期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 43, 期 14, 页码 5410-5415出版社
AMER CHEMICAL SOC
DOI: 10.1021/es801910w
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资金
- U.S. Department of Energy [DE-AC02-05CH11231]
- National Energy Technology Laboratory
- National High Technology Research and Development Program of China [2007AA06Z340]
Oxidation of Hg-0 with any oxidant or converting it to a particle-bound form can facilitate its removal. Two sulfur-chlorine compounds, sulfur dichloride (SCl2) and sulfur monochloride (S2Cl2), were investigated as oxidants for Hg-0 by gas-phase reaction and by surf ace-involved reactions in the presence of flyash or activated carbon. The gas-phase reaction between Hg-0 and SCl2 is shown to be more rapid than the gas-phase reaction with chlorine, and the second order rate constant was 9.1(+/- 0.5) x 10(-18) mL-molecules(-1).s(-1) at 373 K. The presence of flyash or powdered activated carbon in flue gas can substantially accelerate the reaction. The predicted Hg-0 removal is about 90% with 5 ppm SCl2 or S2Cl2 and 40 g/m(3) of flyash in flue gas. The combination of activated carbon and sulfur-chlorine compounds is an effective alternative. We estimate that co-injection of 3-5 ppm Of SCl2 (or S2Cl2) with 2-3 Lb/MMacf of untreated Darco-KB is comparable in efficiency to the injection of 2-3 Lb/MMacf Darco-Hg-LH. Extrapolation of kinetic results also indicates that 90% of Hg-0 can be removed if 3 Lb/MMacf of Darco-KB pretreated with 3% Of SCl2 or S2Cl2 is used. Mercuric sulfide was identified as one of the principal products of the Hg-0/SCl2 or Hg-0/S2Cl2 reactions. Additionally, about 8% Of SCl2 or S2Cl2 in aqueous solutions is converted to sulfide ions, which would precipitate mercuric ion from FGD solution.
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