Au-ZSM-5 catalyses the selective oxidation of CH4 to CH3OH and CH3COOH using O2

The oxidation of methane, the main component of natural gas, to selectively form oxygenated chemical feedstocks using molecular oxygen has been a long-standing grand challenge in catalysis. Here, using gold nanoparticles supported on the zeolite ZSM-5, we introduce a method to oxidize methane to met...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature catalysis 2022-01, Vol.5 (1), p.45-54
Hauptverfasser: Qi, Guodong, Davies, Thomas E., Nasrallah, Ali, Sainna, Mala A., Howe, Alexander G. R., Lewis, Richard J., Quesne, Matthew, Catlow, C. Richard A., Willock, David J., He, Qian, Bethell, Donald, Howard, Mark J., Murrer, Barry A., Harrison, Brian, Kiely, Christopher J., Zhao, Xingling, Deng, Feng, Xu, Jun, Hutchings, Graham J.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The oxidation of methane, the main component of natural gas, to selectively form oxygenated chemical feedstocks using molecular oxygen has been a long-standing grand challenge in catalysis. Here, using gold nanoparticles supported on the zeolite ZSM-5, we introduce a method to oxidize methane to methanol and acetic acid in water at temperatures between 120 and 240 °C using molecular oxygen in the absence of any added coreductant. Electron microscopy reveals that the catalyst does not contain gold atoms or clusters, but rather gold nanoparticles are the active component, while a mechanism involving surface adsorbed species is proposed in which methanol and acetic acid are formed via parallel pathways. The conversion of methane to oxygenated molecules is a very challenging reaction that often requires the use of a coreductant or stoichiometric conditions. Here, the authors report the use of gold supported on ZSM-5 as a promising catalyst for this process in combination with oxygen in the absence of coreductants.
ISSN:2520-1158
2520-1158
DOI:10.1038/s41929-021-00725-8