Influence of calcination temperature on the plate-type V2O5–MoO3/TiO2 catalyst for selective catalytic reduction of NO
- 103 Downloads
A series of plate-type V2O5–MoO3/TiO2 catalysts for selective catalytic reduction (SCR) of NO from flue gas were prepared and calcined at different temperatures. XRD, XRF, N2-adsorption, Raman, H2-TPR, NH3-TPD and XPS were used to characterize the catalysts. From the experimental results, plate-type V2O5–MoO3/TiO2 catalyst calcined at 500 °C showed the best performance in the SCR of NO. Compared with the catalyst calcined at 440 °C, the calcination in the range of 500–620 °C resulted in an increase of polymeric vanadate and the augmentation of catalytic acidity. Furthermore, the V4/V5+, (V4+ + V3+)/V5+ and Oα/(Oα + Oβ) ratio of the catalysts also increased with the increase of calcination temperature, which resulted in the high catalytic efficiency in the SCR reaction. However, the higher calcination temperature would lead to the inevitable formation of N2O at high reaction temperatures (> 370 °C). Meanwhile, high calcination temperature resulted in decreased mechanical strength of the catalyst.
KeywordsNOx SCR Calcination temperature Plate-type
The authors are grateful to the financial supports of the Fund Project for Transformation of Scientific and Technological Achievements of Jiangsu Province of China (Grant No. BA2017095).
- 10.Chen L, Li JH, Ge MF (2009) Promotional Effect of Ce-doped V2O5–WO3/TiO2 with low vanadium loadings for selective catalytic reduction of NOx by NH3. J Phys Chem 113:21177–21184Google Scholar
- 11.Shi AJ, Wang XQ, Yu T, Shen MQ (2011) The effect of zirconia additive on the activity and structure stability of V2O5/WO3–TiO2 ammonia SCR catalysts. Appl Catal B 106(359–36):9Google Scholar
- 37.Magg N, Immaraporn B, Giorgi JB, Schroeder T, Bäumer M, Döbler J, Wu ZL, Kondratenko E, Cherian M, Baerns M, Stair PC, Sauer J, Freund HJ (2004) Vibrational spectra of alumina- and silica-supported vanadia revisited: an experimental and theoretical model catalyst study. J Catal 226:88–100CrossRefGoogle Scholar