SO2-tolerant selective catalytic reduction (SCR) of NOx at low temperature is still challenging. Traditional metal oxide catalysts are prone to be sulfated and the as-formed sulfates are difficult to decompose.… Click to show full abstract
SO2-tolerant selective catalytic reduction (SCR) of NOx at low temperature is still challenging. Traditional metal oxide catalysts are prone to be sulfated and the as-formed sulfates are difficult to decompose. In this study, we discovered that SO2 adsorption could be largely restrained over FeδCe1-δVO4 catalysts, which effectively restrained the deposition of sulfate species and endowed catalysts with strong SO2 tolerance at an extremely low temperature of 240 °C. The increasing oxygen vacancies, enhanced redox properties, and improved acidity contributed to the SCR activity of the FeδCe1-δVO4 catalyst. The reaction pathway changed from the reaction between bidentate nitrate and the NH3 species over CeVO4 catalysts via the Langmuir-Hinshelwood mechanism to that between gaseous NOx and the NH4+/NH3 species over FeδCe1-δVO4 catalysts via the Eley-Rideal mechanism. The effective suppression of SO2 adsorption allowed FeδCe1-δVO4 catalysts to maintain the Eley-Rideal pathways on account of the reduced formation of sulfate species. This work demonstrated an effective route to improve SO2 tolerance via modulating SO2 adsorption on Ce-based vanadate catalysts, which presented a new point for the development of high-performance SO2-tolerant SCR catalysts.
               
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