Deactivation performance and mechanism of alkali (earth) metals on V2O5–WO3/TiO2 catalyst for oxidation of gaseous elemental mercury in simulated coal-fired flue gas

Catalysis deactivation caused by alkali (earth) metals (Na, K, Mg and Ca) over V2O5–WO3/TiO2 catalyst for oxidation of Hg0 by hydrogen chloride was investigated in the presence of O2. Deactivation effects caused by alkali (earth) metals were well associated with alkalinity value and shown in sequence as: K > Na ∼ Ca > Mg. Results also indicated that the deactivation increased proportionately with alkali (earth) metal doping amounts. Further investigations on BET surface area, XRD, Hg-TPD, XPS and H2-TPR demonstrated that surface characteristics were not the dominant factor for the deactivation. However, surface coverage by alkali (earth) metals might cause decrease in the surface area and total pore volume. Hg-TPD results indicated that the doping of alkali (earth) metals would decrease surface Hg0 adsorption amount associated with alkalinity value. More decrease of surface adsorption and redox ability (Oα) in doped catalysts than the fresh one could lead to less active performance according to the H2-TPR and XPS of O 1s results. Consequently, the decrease of Hg0 adsorption and surface redox ability (Oα), and the formation of inactive metavanadate species such as KVO3 could be responsible for the deactivation performance caused by alkali (earth) metals over vanadium-based catalyst for oxidation of gaseous elemental mercury.

Deactivation performance and mechanism of alkali (earth) metals on V2O5–WO3/TiO2 catalyst for oxidation of gaseous elemental mercury in simulated coal-fired flue gas.Figure optionsDownload high-quality image (206 K)Download as PowerPoint slideHighlights
► An original research of deactivation performance and mechanism caused by alkali (earth) metals.
► Deactivation effects were ordered as K > Na ∼ Ca > Mg.
► Alkali (earth) metals would decrease surface Hg0 adsorption from original Hg-TPD results.
► Alkali (earth) metals migrated toward OV–OH or OV–OCl groups and changed to inactive metavanadate species.