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In-Situ Investigation of Gas Phase Radical Chemistry in the Catalytic Partial Oxidation of Methane on Pt

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Geske,  Michael
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Pelzer,  Katrin
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Horn,  Raimund
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Jentoft,  Friederike C.
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Schlögl,  Robert
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

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Citation

Geske, M., Pelzer, K., Horn, R., Jentoft, F. C., & Schlögl, R. (2009). In-Situ Investigation of Gas Phase Radical Chemistry in the Catalytic Partial Oxidation of Methane on Pt. Catalysis Today, 142(1-2), 61-69. doi:10.1016/j.cattod.2009.01.005.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-FA87-8
Abstract
The catalytic partial oxidation of methane on platinum was studied in situ under atmospheric pressure and temperatures between 1000 and 1300 °C. By combining radical measurements using a molecular beam mass spectrometer and threshold ionization with GC, GC-MS and temperature profile measurements it was demonstrated that a homogeneous reaction pathway is opened at temperatures above 1100 °C, in parallel to hetero-geneous reactions which start already at 600 °C. Before ignition of gas phase chemistry, only CO, H2, CO2 and H2O are formed at the catalyst surface. Upon ignition of gas chemistry, CH3⋅ radicals, C2 coupling products and traces of C3 and C4 hydrocarbons are observed. Because the formation of CH3⋅ radicals correlates with the formation of C2 products it can be concluded that C2 products are formed by coupling of methyl radicals in the gas phase followed by dehydrogenation reactions. This formation pathway was predicted by numerical simulations and this work presents an experimental confirmation under high temperature atmospheric pressure conditions.