hide
Free keywords:
-
Abstract:
The selective oxidation of methane to methanol is a highly challenging target, which is of considerable interest to gain value-added chemicals directly from fuel gas. Copper-containing zeolites, such as Cu/mordenite, have been currently reported to be the most efficient catalysts for this reaction. In this work, it is shown that solid-state ion-exchanged Cu/mordenites exhibit a significantly higher activity for the partial oxidation of methane to methanol than comparable reference catalysts, i.e., Cu/mordenites prepared by the conventional liquid-phase ion exchange procedure. The efficiency of these Cu/mordenites remained unchanged over several successive cycles. From temperature-programmed reduction (TPR) measurements, it can be concluded that the solid-state protocol accelerates Cu exchange at the small pores of mordenite: those are positions where the most active Cu species are presumably located. In situ ultraviolet–visible (UV-vis) spectroscopy furthermore indicates that different active clusters including dicopper- and tricopper-oxo complexes are formed in the catalyst upon oxygen treatment. Notably after activation of methane, different methoxy intermediates seem to be generated at the Cu sites from which one is preferably transformed to methanol by reaction with water. It is furthermore described that the applied reaction conditions have considerable influence on the finally observed methanol production from methane.
