Influence of Co-Doped Metals On Mn/TiO2 Catalyst and Its Effect On Selective Reduction of NO with NH3 At Low-Temperatures

Monday, October 17, 2011: 9:10 AM
200 C (Minneapolis Convention Center)
Thirupathi Boningari, Krishna Reddy Gunugunuri and Panagiotis Smirniotis, Chemical Engineering Program, School of Energy, Environmental, Biological and Medicinal Engineering, University of Cincinnati, Cincinnati, OH

In recent years, there is an increasing interest in developing a novel low-temperature (353–523 K) SCR catalyst for the removal of NOx. In our earlier studies, manganese-based titania-supported catalysts have been established successfully for the low-temperature selective catalytic reduction (SCR) of NO. In continuation of our research in low-temperature SCR of NO, we prepared a series of Mn-Me/TiO2 (Me = Cr, Fe, Co, Ni, Cu, Zn, Ce, and Zr) catalysts by adopting wet-impregnation method and investigated for the low-temperature SCR of NO with NH3 by varying Me/Mn atomic ratio. The catalytic performance of these materials has been carried out with a high gas hourly space velocity (GHSV) 50,000 h-1, at the temperature range 433-523K. Physico-chemical techniques such as XRD, N2 physisorption, TPR, XPS, and in-situ FTIR were used to investigate the influence of co-doped metals. Our XPS results illustrated that the MnO2 phase is extremely dominant over the Mn2O3 phase (Mn4+/Mn3+=22.31, 96%) in our best catalyst Mn-Ni(0.4)/TiO2 anatase, whereas Mn2O3 phase is in competition with MnO2 in other catalysts (Mn4+/Mn3+=1.34-12.67). Increase in reducibility of manganese and absence of the high-temperature (736 K) peak in H2-TPR studies, suggested that the dominant phase is MnO2 in Mn-Ni/TiO2 catalyst. The catalytic performance and characterizations of optimized materials will be discussed in the presentation.

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