Abstract
The H2/NO/O2 reaction under lean-burn conditions has been studied by means of in situ DRIFTS, reactor measurements and temperature-programmed desorption with the aim of understanding the very different behavior of Pd/TiO2 and Pd/Al2O3 catalysts. The former deliver very high NO x conversions (70-80%) with good N2 selectivity whereas the latter show very low activity. In addition, PdTiO2 exhibits two distinct NO x reduction pathways, thus greatly extending the useful temperature range. It is shown that the PdTiO2 low-temperature channel involves adsorption and subsequent dissociation of NO on reduced (Pd0) metal sites. The low activity of PdAl2O3 is a consequence of palladium remaining in an oxidized state under reaction conditions. The high-temperature NO reduction channel found with PdTiO2 is associated with the generation and subsequent reaction of NH x species.
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Macleod, N., Cropley, R. & Lambert, R.M. Efficient Reduction of NO x by H2 Under Oxygen-Rich Conditions over Pd/TiO2 Catalysts: An in situ DRIFTS Study. Catalysis Letters 86, 69–75 (2003). https://doi.org/10.1023/A:1022611109139
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DOI: https://doi.org/10.1023/A:1022611109139