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Water Inhibition in Methane Oxidation over Alumina Supported Palladium Catalysts

2019; American Chemical Society; Volume: 123; Issue: 42 Linguagem: Inglês

10.1021/acs.jpcc.9b07606

1932-7455

Peter Velin, Martin Ek, Magnus Skoglundh, Andreas Schaefer, Agnes Raj, David Thompsett, Gudmund Smedler, Per‐Anders Carlsson,

Catalysts for Methane Reforming

In situ diffuse reflectance infrared Fourier transform spectroscopy has been used to distinguish surface hydroxyl groups on Al2O3 and PdO/Al2O3 model catalysts calcined at 500–900 °C. Employing the operando approach, the formation of surface hydroxyl groups has been correlated to the methane oxidation activity for PdO/Al2O3 catalysts using a PdO powder sample as reference. The results show that the alumina support stabilizes active PdO particles leading to enhanced apparent methane turnover frequency (TOF), which decreases slowly in dry conditions due to alumina hydroxylation. Wet conditions cause severe hydroxylation that is detrimental for the methane TOF. The hydroxylation follows two different routes, i.e., spillover of hydrogen-containing species to the PdO-Al2O3 boundary and/or the close proximity of the supported PdO particles and under wet conditions also dissociation of gas phase water on the entire alumina surface. Both hydroxylation routes obey varying kinetics such that near saturation is reached quickly (minutes) followed by a continuous slow growth for prolonged exposure times (hours). At low temperatures, inhibition of palladium active sites on the rim of the PdO particles close to alumina seems to be of particular importance for the observed detrimental effect of water, whereas water induced morphological changes (no sintering observed) of the PdO particles play a minor role.