Abstract

The oxidation of propylene over a Pd(551) single crystal has been studied in the millibar pressure range using near-ambient pressure X-ray photoelectron spectroscopy and mass spectrometry. It has been shown that, irrespective of the O2/C3H6 molar ratio in the range 1–100, the total oxidation of propylene to CO2 and water and the partial oxidation of propylene to CO and H2 occur when the catalyst is heated above the light-off temperature; increasing the partial pressure of O2 leads to decreasing the catalytic activity. The selectivity toward CO2 is at least two times higher than the selectivity toward CO, indicating that the total oxidation is the main reaction route. The normal hysteresis with a light-off temperature higher than the extinction temperature is observed in the oxidation of propylene between 100 and 300 °C. According to NAP-XPS, the main reason for the hysteresis appearing is a competition between two surface processes: carbonization and oxidation of palladium. At low temperatures, the adsorp...

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