Vanadium-based catalysts have been commercially used
in selective
catalytic reduction (SCR), owing to their high catalytic activity
and effectiveness across a wide temperature range; however, their
catalytic efficiency decreases at lower temperatures under exposure
to SO
X
. This decrease is largely due to
ammonium sulfate generation on the catalyst surface. To overcome this
limitation, we added ammonium nitrate to the V2O5-WO3/TiO2 catalyst, producing a V2O5-WO3/TiO2 catalyst with nitrate
functional groups. With this approach, we found that it was possible
to adjust the amount of these functional groups by varying the amount
of ammonium nitrate. Overall, the resultant nitrate V2O5-WO3/TiO2 catalyst has large quantities
of NO3
– and chemisorbed oxygen, which
improves the density of Brønsted and Lewis acid sites on the
catalyst surface. Furthermore, the nitrated V2O5-WO3/TiO2 catalyst has a high NO
X
removal efficiency and N2 selectivity
at low temperatures (i.e., 300 °C); this is because NO3
– and chemisorbed oxygen, generated by nitrate
treatment, facilitated the occurrence of a fast SCR reaction. The
approach outlined in this study can be applied to a wide range of
SCR catalysts, allowing for the development of more, low-temperature
SCR catalysts.