摘要
The effect of K deactivation on V2OJWO3-TiO2 and Ce-doped V2O5/WO3-TiO2 catalysts in the selective catalytic reduction （SCR） of NOx by NH3 was studied. Ce-doped V2O5/WO3-TiO2 showed significantly higher resistance to K deactivation than V2O5/WO3-TiO2. Ce-doped V2O5/WO3-TiO2 with K/V = 4 （molar ratio） showed 90% NOx conversion at 350℃, whereas in this case V2O5/WO3-TiO2 showed no activity. The fresh and K-poisoned V2O5/WO3-TiO2 and Ce-doped V2O5/WO3-TiO2 catalysts were investigated by means of in situ diffuse reflectance infrared Fourier transform spectroscopy （DRIFTS）, NH3-temperature progress decomposition （NH3-TPD）, X-ray photoelectron spectroscopy （XPS） and H2-temperature program reduction （H2-TPR）. The effect of Ce doping on the improving resistance to K of V2O5/WO3- TiO2were discussed.
The effect of K deactivation on V2OJWO3-TiO2 and Ce-doped V2O5/WO3-TiO2 catalysts in the selective catalytic reduction （SCR） of NOx by NH3 was studied. Ce-doped V2O5/WO3-TiO2 showed significantly higher resistance to K deactivation than V2O5/WO3-TiO2. Ce-doped V2O5/WO3-TiO2 with K/V = 4 （molar ratio） showed 90% NOx conversion at 350℃, whereas in this case V2O5/WO3-TiO2 showed no activity. The fresh and K-poisoned V2O5/WO3-TiO2 and Ce-doped V2O5/WO3-TiO2 catalysts were investigated by means of in situ diffuse reflectance infrared Fourier transform spectroscopy （DRIFTS）, NH3-temperature progress decomposition （NH3-TPD）, X-ray photoelectron spectroscopy （XPS） and H2-temperature program reduction （H2-TPR）. The effect of Ce doping on the improving resistance to K of V2O5/WO3- TiO2were discussed.
基金
financially supported by the National Key research&development(R&D)Program of China(No.2017YFC0211101)
the Key Project of National Natural Science Foundation(No.21637005)
Science and Technology Program of Tianjin,China(No.16YFXTSF00290)
