Abstract
Ag-modified vanadium silicate (EVS-Ag) has been regarded as a superior sorbent for elemental mercury (Hg0) capture from coal-fired flue gas. However, the atomic-level reaction mechanism which determines Hg0 adsorption capacity of EVS-Ag sorbent remains elusive. Reaction mechanism and active sites of Hg0 adsorption over EVS-Ag sorbent were studied using density functional theory (DFT) calculations systematically. DFT calculation results indicate that silver exchange shows little effects on the geometric structure of EVS-10 sorbent. Hg0 adsorption on EVS-10 and EVS-Ag surfaces is controlled by the physisorption and chemisorption mechanisms, respectively. Ag2 cluster is determined to be the most active site of Hg0 adsorption over Ag-modified EVS sorbent. The adsorption energy of Hg0 on Ag2 cluster is −51.93 kJ/mol. The orbital hybridization and electron sharing between Ag and Hg atoms are responsible for the strong interaction between EVS-Ag surface and Hg0. HgO prefers to adsorb on Ag2 cluster of EVS-Ag sorbent, and yields an energy release of 306.21 kJ/mol. HgO desorption from EVS-Ag sorbent surface needs a higher external energy, and occurs at the relatively higher temperatures. O2 molecule promotes Hg0 adsorption over EVS-Ag sorbent. HgO species can be easily formed during Hg0 adsorption over EVS-Ag sorbent in the presence of O2.
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