Location: Online
Add to Calendar 2020-10-29T11:00:00 2020-10-29T12:00:00 America/New_York Chemical Engineering Seminar: Dr Magnus Skoglundh Professor Magnus Skoglundh Chemistry and Chemical Engineering, Applied Surface Chemistry Competence Centre for Catalysis Chalmers Operando X-ray Absorption Spectroscopy Studies of Methane Oxidation Catalysts Online

Professor Magnus Skoglundh
Chemistry and Chemical Engineering, Applied Surface Chemistry
Competence Centre for Catalysis
Chalmers

Operando X-ray Absorption Spectroscopy Studies of Methane Oxidation Catalysts

Operando spectroscopy is an experimental method in catalysis that combines measurements of catalytic activity and selectivity with simultaneous in situ spectroscopic characterization of the catalyst. Since the structure and composition of the catalyst are probed under reaction conditions, the method can provide valuable information to elucidate the mechanism of the studied reaction. Here, operando spectroscopy has been performed using X-ray absorption fine structure (XAFS) as an in situ characterization technique to study catalysts during the total oxidation of methane. Methane is a strong greenhouse gas and catalytic oxidation can be used, for example, to remove un-combusted methane from the exhausts of vehicles fueled with natural gas or biogas.

Palladium is the most active metal for the total oxidation of methane, but the oxidation state of palladium can change rapidly during reaction conditions, which influences the catalytic activity. Time-resolved XAFS was used to investigate Pd/Al2O3 catalysts under transiently changing reaction conditions for methane oxidation, by performing oxygen pulse-response experiments, so the conditions periodically change from net-reducing to net-oxidizing. Simultaneously, the outlet concentrations of reactants and products were monitored with mass spectrometry. The XAFS data show that palladium in the catalyst is readily reduced and oxidized when the feed gas composition is changed from reducing to oxidizing. The highest activity for methane oxidation is found over bulk-oxidized palladium (PdO), while surface oxidized palladium in comparison is less active. Similar experiments were also performed for Pd/CeO2. Compared to the alumina supported catalyst, palladium supported on CeO2 is oxidized more rapidly in an oxidizing atmosphere and is reduced at a slower rate in a reducing atmosphere. This shows that CeO2 can stabilize Pd in the oxidized state which, could be beneficial for the activity for methane oxidation.

Although XAFS is only available at synchrotron light sources, the ability to investigate the active phase of catalysts with high time resolution, under reaction conditions, makes it a highly useful technique in catalysis research.

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