Abstract

Fe-Mn/TiO2 catalysts were prepared through the wet impregnation process to selective catalytic reduction of NO by NH3 at low temperature, and series of experiments were conducted to investigate the effects of key precursors on their SCR performance. Ferric nitrate, ferrous sulfate, and ferrous chloride were chosen as Fe precursors while manganese nitrate, manganese acetate, and manganese chloride as Mn precursors. These precursors had been commonly used to prepare Fe-Mn/TiO2 catalysts by numerous researchers. The results showed that there were distinct differences in NO conversion efficiencies at low temperature of catalysts prepared with different precursors. Catalysts prepared with ferric nitrate and manganese nitrate precursors exhibited the best catalytic performance at low temperature, while three kinds of catalysts prepared with manganese chloride precursors exhibited significantly low catalytic activity. All catalysts were characterized by XRD, SEM, H2-TPR, NH3-TPD, and XPS. The results indicated that when the catalysts were prepared with manganese nitrate or manganese acetate as precursors, Mn4+ contents and Oβ/(Oβ+ Oα) ratios decreased in an order of ferric nitrate > ferrous sulfate > ferrous chloride, which was consistent with the change of catalytic activities of the corresponding catalysts at low temperature. It can be found that the excellent catalytic performance of Fe(A)-Mn(a)/TiO2 was ascribed to high redox property and enrichment of Mn4+species and surface chemical labile oxygen groups.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.