Journal
JOURNAL OF HAZARDOUS MATERIALS
Volume 172, Issue 2-3, Pages 1106-1110Publisher
ELSEVIER
DOI: 10.1016/j.jhazmat.2009.07.103
Keywords
Desulfurization solutions; Hg2+ reduction; Re-emission; Removal efficiency
Categories
Funding
- National High Technology Research and Development Program of China [2007AA06Z340]
- National Natural Science Foundation of China [20877066]
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In this study, considering that Hg2+ in wet flue gas desulfurization (FGD) systems can easily be reduced and then released into atmosphere, causing secondary pollution, the researches about Hg2+ reduction and Hg-0 re-emission mechanism were carried out. The effects of several experimental parameters on the reduction were studied, including initial pH, temperature, and concentrations of Cl- and S(IV). Our experimental results indicated that Cl- had a restraining effect on the Hg2+ reduction and Hg-0 re-emission, after 24 h reaction, only 20.5% of Hg2+ was reduced with 100 mM Cl- in simulated desulfurization solution. Cl- can slow Hg2+ reduction and Hg-0 re-emissions dramatically through changing reaction mechanism. with formation of new intermediate: ClHgSO3-, which can decompose to Hg-0, but much more slowly than Hg(SO3)(2)(2-) or HgO3. Simulating the conditions of the practical application (initial pH 5, T=50 degrees C, S(IV)=5 mM, Cl- = 100 mM), we also found that Ca2+, NO3-, F-, etc. all had obvious effects on reduction rates. Based on the material balance and characteristic of the reactants, the reduction emission mechanism of Hg2+ has been established, providing theoretical basis for industrial application of mercury control in wet FGD systems. (C) 2009 Elsevier B.V. All rights reserved.
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