Abstract
In this work, the modified Mn-based NH3-SCR (NH3 low-temperature selective catalytic reduction) catalysts with excellent NO conversion and N2 selectivity be designed. N2 yield was hardly more than 75 % over MnOx/TiO2 for NH3-SCR reaction, whereas the NH3-SCR performance has been significantly improved by using 50 wt.% HPW (H3PW12O40)-MnOx/TiO2. 100 % NO conversion and more than 95 % N2 yield was obtained in wide operating temperature window (150–400°C), suggesting that the addition of HPW could effectively improve the NO reduction conversion. After that, the catalysts were further characterized by XRD, H2-TPR, XPS and in situ DRIFT. DRIFT analysis implied that the introduction of HPW significantly improve the capacity of NH4
+ species adsorbed on Brønsted acid sites accompanied with inhibiting the formation and consumption of nitrite species. It proved that the non-selective catalytic reduction reaction over HPW-MnOx/TiO2 catalysts are restrained. HPW could accelerate the formation and consumption of NH4
+ species adsorbed on Brønsted acid sites with deactivation of nitrate species. In addition, NH3(ad) could be hardly oxidized to NH species and then reacted with nitrate species (L-H mechanism) and gaseous NO (E-R mechanism). More importantly, the oxidation of NH3 was also suppressed, which plays a dominate role to form N2O above 300°C. Besides, the deactivation of potassium poisoning on the SCR activity significantly weakened for modified samples compared to parent catalyst.
In Situ DRIFTS Study of the Low Temperature Selective Catalytic Reduction of NO with NH3 over MnOx Supported on Multi-Walled Carbon Nanotubes Catalysts
