In situ DRIFT study on NH3 selective catalytic reduction of NO over HBEA zeolite doped with CeO2

• DOI: 10.1016/j.apsusc.2019.144715
• Publication Date: 2019-11-28T17:55:23Z
• Authors: Yun Shi; Xiaoxiang Wang; Liang Chen; Sujing Li; Chao Wu; Shengdao Shan; Wei Li
• Keywords: Selective catalytic reduction

Abstract The reaction mechanism of selective catalytic reduction of NO with NH3 on Ce-doped HBEA catalysts was investigated using in-situ diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR). The results illustrated that the amide species adsorbed on Lewis acid sites (AlO)+ and NH4+ species adsorbed on Br o ¨ nsted acid sites (Al-OH-Si) were main intermediates on HBEA. Only Eley-Rideal (E-R) mechanism was presented over HBEA catalyst. By contrast, both E-R and Langmuir-Hinshelwood (L-H) mechanism were presented over Ce7.0HBEA and the E-R mechanism was the dominated reaction mechanism. NH4+ adspecies and nitrate adspecies were primary intermediates on Ce7.0HBEA. Meanwhile, the presence of Ce3+ could lead to the increase of surface oxygen concentration, which could actively take part in the activation process of ammonia adspecies and NOx adspecies and then facilitated the NH3-SCR reaction. Hence, the NOx conversion of Ce7.0HBEA was much higher than that of HBEA. In addition, the surface oxygen vacancy derived from ceria on Ce7.0HBEA could inhibit the formation of N2O. As a result, the N2 selectivity of Ce7.0HBEA is higher than that of HBEA. The above results are useful for guiding the way to develop Ce-containing SCR catalysts.