Removal mechanism of elemental mercury by using non-thermal plasma

► The removal mechanism of the elemental mercury (Hg 0) has been investigated within the atmosphere of non-thermal plasma. ► A sudden increase in the removal efficiency is observed after several minutes of the reaction time. ► The formation of HgO 3(s) species deposited on the reactor surface accele...

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Veröffentlicht in:Chemosphere (Oxford) 2011-03, Vol.83 (1), p.69-75
Hauptverfasser: Byun, Youngchul, Koh, Dong Jun, Shin, Dong Nam
Format: Artikel
Sprache:eng
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Zusammenfassung:► The removal mechanism of the elemental mercury (Hg 0) has been investigated within the atmosphere of non-thermal plasma. ► A sudden increase in the removal efficiency is observed after several minutes of the reaction time. ► The formation of HgO 3(s) species deposited on the reactor surface accelerates the removal rate of Hg 0. The removal mechanism of elementary mercury (Hg 0) by non-thermal plasma (NTP) has been investigated, where dielectric barrier discharge and O 3 injection methods as oxidation techniques are employed, together with the analysis of mercury species deposited on the reactor surface using temperature-programmed desorption and dissociation (TPDD) and scanning electron microscopy–energy dispersive spectroscopy. The removal of Hg 0 by NTP is found to be time-dependent and proceed through three domains; the Hg 0 concentration just slightly decreases as soon as NTP is initiated and then becomes constant for several minutes (Region 1), thereafter starts to decrease rapidly for 1 h (Region 2) and, after passing fall-off region, very slowly decreases for about 4 h (Region 3). The deposited mercury species on the reactor surface were conglomerated like islands, rather than dispersed uniformly, and their ratio of Hg 0 to O composition is observed to be 1:2. Additionally, the new peak in TPDD spectra observed in the region of 260–380 °C is proposed as HgO 3. These results lead us to conclude that the deposited mercury species by NTP have extra O atoms to oxidize the adsorbed Hg 0, resulting in the acceleration of removal rate as the oxidation of Hg 0 proceeds.
ISSN:0045-6535
1879-1298
DOI:10.1016/j.chemosphere.2010.12.003