Abstract
The local structure around Fe and Mn in Fe, Mn-promoted sulfated zirconia was investigated by means of m-situ XAFS. The Mn atoms are found to be present as MnSO4 on the surface. The first post-edge peak of the Mn K-edge XANES spectrum was sharpened in a working state, and restored by evacuation. Fe K-edge XANES spectra showed that Fe is in a trivalent state and located at a center of a distorted octahedron. Fe atoms were suggested to be interstitially located into ZrO2 to form a solid solution. Any procedure did not change the Fe K-edge EXAFS and the shape and edge-positions of the XANES spectra. The reaction gases are in contact with Mn atoms, but not with the Mn atoms of the catalyst.
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Yamamoto, T., Tanaka, T., Takenaka, S., Yoshida, S., Onari, T., Takahashi, Y., … Hasegawa, S. (1999). XAFS study of Fe- and Mn-promoted sulfated zirconia. Journal of Synchrotron Radiation, 6(3), 425–427. https://doi.org/10.1107/S0909049598017762
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