Temperature dependence of the kinetics for the complete oxidation of methane on palladium and palladium oxide

The kinetics for the complete combustion of methane was studied on a Pd foil in the regions where the oxide and then the metal were the bulk stable phases. The use of a model catalyst allowed the kinetics to be studied at higher temperatures than are possible on supported catalysts since heat and mass transport limitations could be avoided for this nonporous model catalyst. For all reaction conditions, CH4 and O-2 reaction orders remained the same at about 0.7 and 0, respectively. With PdO as the stable phase, the water reaction order increased from -1 to 0 and the apparent activation energy (Ea) decreased from 125 to 30 kJ mol(-1) as the reaction temperature increased from 600 to 880 K. We propose that as the temperature is increased water desorbs from the sites responsible for combustion and as a result water inhibition and Ea decrease. To investigate the rate of reaction on Pd versus PdO, the rates were measured around the Pd-PdO transition temperature. The turnover rate decreased from 3.0 s(-1) to 0.3 s(-1) at the transition temperature (907 K with 1.5 Torr O-2 and 0.30 Torr CH4) when PdO decomposed to Pd metal, showing that PdO was more active than Pd metal for methane oxidation at this temperature. The reaction orders for Pd metal in the range of 933-1003 K were 0.7, 0, and 0 for methane, water, and O-2, respectively, with an apparent activation energy of 125 kJ mol(-1). Thus, the turnover rate and Ea changes suggest that the reaction mechanism for methane oxidation on Pd is different from the one on PdO.