The Effect of Fe2O3 Modification on the CeO2-MnO2/TiO2 Catalyst for Selective Catalytic Reduction of NO with NH3

High denitration efficiency and strong adaptability to flue gas temperature fluctuations are the core properties of the NH₃-SCR catalyst. In this study, Fe₂O₃ modification is used as a means to explore the mechanism of adding Fe₂O₃ to broaden the temperature range of the 6CeO₂-40MnO₂/TiO₂ catalyst during the preparation process. The results show that the 6Fe₂O₃-6CeO₂-40MnO₂/TiO₂ catalyst exhibits excellent denitration performance, with a denitration efficiency higher than 90%. The temperature range is from 129 to 390 °C. N₂ selectivity and resistance to SO₂ and H₂O are good, and the denitration performance is significantly improved. When the Fe₂O₃ content is 6%, it promotes lattice shrinkage of TiO₂, improves its dispersion, refines the grain size, and increases the specific surface area of the catalyst. At the same time, Fe₂O₃ enhances the chemical adsorption of oxygen on the catalyst surface and increases the proportion of low-cost metal ions, thereby promoting electron transfer between active elements, generating more surface reactive oxygen species, increasing the oxygen vacancy content and adsorption sites for NO_x and NH₃, and significantly improving the redox performance of the catalyst. This effect is particularly conducive to the formation of strong acid sites on the catalyst surface. The NH₃-SCR reaction on the surface of the 6Fe₂O₃-6CeO₂-40MnO₂/TiO₂ catalyst follows both the L-H and E-R mechanisms, with the L-H mechanism being dominant.