CH4 deep oxidation on Ag promoted manganese oxide catalysts

Authors
Citation
X. Wang et Yc. Xie, CH4 deep oxidation on Ag promoted manganese oxide catalysts, Z PHYS CHEM, 215, 2001, pp. 1151-1164
Citations number
31
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
ZEITSCHRIFT FUR PHYSIKALISCHE CHEMIE-INTERNATIONAL JOURNAL OF RESEARCH IN PHYSICAL CHEMISTRY & CHEMICAL PHYSICS
ISSN journal
09429352 → ACNP
Volume
215
Year of publication
2001
Part
9
Pages
1151 - 1164
Database
ISI
SICI code
0942-9352(2001)215:<1151:CDOOAP>2.0.ZU;2-3
Abstract
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.