Activity and SO2 deactivation mechanism of vanadium series catalyst containing cerium
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Graphical Abstract
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Abstract
The promotion effect of Ce modification on V2O5-WO3/TiO2 for the selective catalytic reduction (SCR) of NOx with NH3 and the SO2 deactivation mechanism were investigated. Compared with V1W5Ti catalyst, the advantage of V1W5Ce6Ti catalyst shows a good catalytic activity. These catalysts were investigated by means of XRD, BET, FT-IR, TG-DSC and XPS. The results demonstrate that the active components of V and W are well-dispersed, while a small cluster of cubic CeO2 appears over the V1W5Ce8Ti catalyst. The sulfation of V1W5Ti under reactive conditions can generate NH4HSO4 and (NH4)2SO4 at 250℃. The Ce additive to V1W5Ti could provide stronger Brønsted acid sites and more chemisorbed oxygen. The deposited ammonium sulfate on V1W5Ce6Ti catalyst is much smaller than that on V1W5Ti because the cerium sulfates species on the surface of V1W5Ce6Ti is formed and the deposition of ammonium sulfate is inhibited, which can disrupt the redox cycle between Ce3+ and Ce4+ and break the V-O-Ce structure, causing the deactivation of V1W5Ce6Ti catalyst.
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