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U.S. Department of Energy
Office of Scientific and Technical Information

Activation of methane by clean and chemically modified single crystal oxide surfaces. Annual report, September 1991-October 1992

Technical Report ·
OSTI ID:6933535

The oxidative coupling of methane to ethane over model MgO catalysts prepared under well-controlled, ultrahigh vacuum conditions has been studied using a combination of surface science techniques and reaction kinetic measurements. The utilization of electron energy loss spectroscopy has allowed the characterization of a variety of defects in the catalysts and the identification of the active sites which are responsible for the methane coupling reaction. A quantitative correlation between the density of specific defects and the ethane formation rate indicates that (Li(+1)O(-)) centers are not likely directly involved in the methane activation step as previously proposed. The (Li(+1)O(-)) centers, rather, promote the formation in the near-surface region of F-type centers which are responsible for the primary carbon-hydrogen bond scission reaction step. These results suggest new procedures to enhance the active site densities on Li/MgO catalysts, and thus offer a potential new approach to enhanced activities and selectivities for this class of materials.

Research Organization:
Texas A and M Univ., College Station, TX (United States). Dept. of Chemistry
OSTI ID:
6933535
Report Number(s):
PB-93-157295/XAB; RF--6888; CNN: GRI-5091-260-2182
Country of Publication:
United States
Language:
English