Kinetics and Mass Transport in Plasma Catalysis
ORAL ยท Invited
Abstract
Coupling non-equilibrium plasma with heterogeneous catalysis offers a sustainable electrically driven route to produce a broad range of chemicals. Plasma catalysis leverages the highly selective nature of catalytic processes on surfaces and the activation of strong chemical bonds in, for example N2, by non-equilibrium electron-induced plasma reactions. In this presentation, we will report our work that probed mechanisms of coupling plasma- and catalytic-chemistry in plasma afterglows. The well-defined hydrodynamics in short contact time reactors equipped with a molecular beam mass spectrometry enabled us to determine the rates of plasma-driven and catalytic surface chemistry. These studies establish a quantitative description of plasma-catalyst interactions and elucidated selective routes for converting N2 in plasma-catalytic reactors. A key outcome of the work is the exceedingly important role of mass transport, of which we will highlight a few examples. The research provides critical insights for improving plasma catalytic reactor design which in the last decade has often been based on empirical reactor optimization.
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Publication: B.N. Bayer, P. Bruggeman and A. Bhan, Chem. Eng. J (2024) 482, 149041
B. N. Bayer, P. Bruggeman and A. Bhan, ACS Catal. 13 (2023) 2619โ2630
Presenters
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Peter Bruggeman
University of Minnesota
Authors
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Brian Bayer
University of Minnesota
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Aditya Bhan
University of Minnesota
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Peter Bruggeman
University of Minnesota