(138a) Highly Efficient SO2 Removal By Supported Manganese Sorbents for SOFCs Cathode Protection Conference: AIChE Annual MeetingYear: 2015Proceeding: 2015 AIChE Annual MeetingGroup: Catalysis and Reaction Engineering DivisionSession: Environmental Catalysis II: General Time: Monday, November 9, 2015 - 12:30pm-12:50pm Authors: Cheng, P., Auburn University Tatarchuk, B. J., Auburn University Chi, M., Auburn University Because of high energy efficiency and fuel flexibility, Solid Oxide Fuel Cells (SOFCs) are promising energy converting devices nowadays. However, researchers realized that SO2 can cause a rapid degradation by interacting with cathode side materials. In logistic solid oxide fuel cell systems, the sources of SO2 mainly arise from high sulfur-containing marine fuels, such as JP-5 and JP-8. Therefore, the cathode protection for SOFCs is a vital consideration for the power system. In this study, dispersed manganese oxides on supports such as ZrO2, SiO2, γ-Al2O3, and TiO2 were prepared by a method of incipient wetness impregnation (IWI). The breakthrough performance was evaluated in a conventional fixed-bed sorption system. Effects of precursor materials, supports, manganese loadings, and calcination temperature on the sorbent performance were investigated in details. A combination of various surface science techniques, including XRD, N2 physisorption, O2 chemisorption, H2-TPR, and XPS, were applied to characterize the chemical environment of the adsorbents. The highest saturation capacity was obtained by using 5 wt.% Mn supported on ZrO2. XRD and O2 chemisorption results demonstrated that MnO2 and Mn2O3 co-existed in well-dispersed forms at 5.0 wt.% of Mn on ZrO2. It was also found that the amount of manganese in sorbent has a remarkable influence on the oxidation state of manganese. In addition, XPS results revealed that the performance of Mn-doped adsorbent was strongly dependent on the population of surface terminal hydroxyl groups.