Manganese oxide modified by various amounts of Ag was prepared and used for
CH4 deep oxidation. The most active catalysts are those with a Ag/Mn mol r
atio around 0.10. In these samples, XRD and TG-DTA showed the coexistence o
f alpha -Mn2O3 and Ag2Mn8O16. In the lattice of Ag2Mn8O16, the electron tra
nsfer between Mn3+ and Mn4+, the possible redox couple under reaction condi
tions, becomes easier since it can happen without changing the lattice stru
cture. alpha -Mn2O3 possibly functions as Mn3+ provider since in Ag2Mn8O16,
the Mn3+/Mn4+ atomic ratio is 2/6. Additional Mn3+ could be helpful for ef
fective electron transfer between Mn3+ and Mn4+. Moreover, CH4-TPR demonstr
ated the formation of bigger amounts of more active oxygen species in Ag-Mn
binary catalysts. Indeed, these factors are believed to be the main causes
leading to the enhanced CH4 oxidation activity of Ag-Mn binary oxide catal
ysts.