A comparative study on the Mn/TiO2-M(M = Sn, Zr or Al) O-x catalysts for NH3-SCR reaction at low temperature

作者:Zhang, Yaping; Huang, Tianjiao; Xiao, Rui*; Xu, Haitao; Shen, Kai; Zhou, Changcheng
来源:Environmental Technology, 2018, 39(10): 1284-1294.
DOI:10.1080/21622515.2017.1329345

摘要

A series of TiO2-M(M = Sn, Zr or Al) O-x were prepared and manganese oxide (MnOx) was supported on the carrier by the traditional impregnation method for low-temperature selective catalytic reduction (SCR) of NOx with ammonia as a reductant. The obtained catalysts were characterized by XRD, BET, high-resolution transmission electron microscope (HRTEM), H-2-TPR, NH3-TPD, X-ray photoelectron spectroscopy (XPS) and in situ Fourier-transform infrared (FT-IR) and their catalytic activities for NOx reduction with NH3 in the presence of SO2 were investigated comparatively. The results showed that the highest NOx conversion of over 90% could be obtained with the Mn/Ti-Sn catalyst at a wide range of temperature window of 150-270 degrees C. The combination of characterization techniques, such as BET, XRD and HRTEM, revealed that manganese oxides were well dispersed on Ti-Sn. H-2-TPR suggested that Ti-Sn and Ti-Zr supports could enhance the reduction ability of catalysts. Accordingly, Mn/Ti-Al exhibited worse activity at low temperature. XPS results were in good agreement with H-2-TPR results, and Mn/Ti-Sn had more surface-reducible species of Mn4+ ions and more surface-adsorbed oxygen species, which was conducive to SCR reaction. The in situ FT-IR spectra of NH3 adsorption indicated that all the modified catalysts had more Lewis acid sites and the amide species at 1506cm(-1) had a certain influence on the catalytic reaction at low temperature. Mn/Ti-Zr showed a stronger resistance to SO2 but Mn/Ti-Al was affected more adversely and all the catalysts could not be restored to the initial catalytic activity after stopping feeding SO2. NH3-TPD revealed that the total acid amount of the Mn/Ti-Sn sample was larger than other samples, which indicated that the Ti-Sn solid solution could provide more surface acid sites over the catalyst.