Active sites in Fe/MFI catalysts for NOx reduction and oscillating N2O decomposition

Fe/MFI catalysts prepared either by sublimation of FeCl3 onto H-MFI or by s olid state ion exchange were characterized by XRD, FTIR, and ESR spectrosco py. Ligated Fe3+ ions, such as (Fe(OH)(2))(+) or (Fe=O)(+) in distorted tet rahedral coordination, multinuclear oxocations, such as (HO-Fe-O-FeOH)(2+), and Fe2O3 oxide particles have been identified. Their relative abundances depend on the Si/Al ratio and the Fe loading. Nitro and nitrate groups, ide ntified by their FTIR bands, are formed upon exposing Fe/MFI with high Fe l oading to N2O. These adsorption complexes are reduced with benzene at 200 d egreesC but not at room temperature. Their reduction with CO occurs at a lo wer temperature than that of the bridging oxygen. Exposure to N2O at 320 de greesC and 0.5 kPa pumps 30% more active oxygen into Fe/MFI than calcinatio n in O-2 of 100 kPa at 500 degreesC. Thermal decomposition releases NO and O-2 at the same temperature. The catalytic decomposition rate of N2O to N-2 + 1/2O(2) in diluted feed streams over Fe/MFI is first order in N2O. The r ate constant is very low for samples with low Fe loading, but jumps to a mu ch higher value for high Fe loadings, indicating the important role of mult inuclear Fe clusters in accordance with recent EXAFS results. Stable isothe rmal oscillations are observed with overexchanged Fe/MFI (Fe/Al = 1; Al/Si = 1/14), in the presence of H2O vapor, showing that two different states of catalytic activity exist. No oscillation is observed with a dry feed or ov er Fe/MFI with low loading. (C) 2000 Academic Press.