Mechanism-Imposed Limitations on the Yield of Higher Hydrocarbons from the Oxidative Coupling of Methane, and Alternate Approaches to Methane Conversion

Abstract

The conversion of methane to higher hydrocarbons via oxidative coupling over metal oxide catalysts is the subject of intense study as a route for natural gas upgrading. Detailed study on the reaction of methane over a mixed manganese-magnesium oxide implicates a mechanism involving generation of methyl radicals at the surface, followed by radical coupling as well as other radical reactions in the gas phase as the predominant mode of carbon-carbon bond formation. Analysis of the consequences of this mechanisms suggests that there is an inherent limit on yield, including a major adverse pressure effect, that may severely impact the potential utility of this route. Among several possible approaches to circumventing this limitation, a novel class of catalyst - transition metal-exchanged P -alumina -- has been found to be highly active for complete oxidation of methane. Results of catalytic and characterization studies will be presented.

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Document Details

Document Type
Technical Report
Publication Date
Apr 01, 1991
Accession Number
ADA258801

Entities

People

  • J. A. Labinger

Organizations

  • California Institute of Technology

Tags

Communities of Interest

  • Energy and Power Technologies

DTIC Thesaurus Topics

  • Alcohols
  • Catalysts
  • Chemical Engineering
  • Chemical Synthesis
  • Chemistry
  • Conversion
  • Couplings
  • Engineering
  • Hydrocarbons
  • Magnesium Compounds
  • Materials
  • Metal Oxides
  • Metals
  • Oxidation
  • Oxides
  • Transition Metals
  • Transitions

Fields of Study

  • Chemistry
  • Environmental science

Readers

  • Microwave Engineering.
  • Organic Chemistry
  • Systems Analysis and Design