Autor: |
V.A. Durante, J.E. Lyons, J. Biscardi, W.H. Seitzer, J. A. Hodge, W.A. Langdale, W.H. Tsao, S. N. Shaikh, R.C. Hayes, H.K. Myers, F.A. Moore, D. Messick, R.W. Wagner, T.P. Wijesekera, P.T. Bowden, M. E. Hughes, R.G. Gorbey, R.A. Merrill, H. B. Gray, P.E. Ellis, B. Marcus, R.W. Warren |
Rok vydání: |
1997 |
Předmět: |
|
DOI: |
10.2172/467133 |
Popis: |
The first Quarterly Report of 1992 on the Catalytic Conversion of Light Alkanes reviews the work done between January 1. 1992 and March 31, 1992 on the Cooperative Agreement. The mission of this work is to devise a new catalyst which can be used in a simple economic process to convert the light alkanes in natural gas to oxygenate products which can either be used as clean-burning, high octane liquid fuels, as fuel components or as precursors to liquid hydrocarbon transportation fuel. During the past quarter we have continued to design, prepare, characterize and test novel catalysts for the mild selective reaction of light hydrocarbons with air or oxygen to produce alcohols directly. These catalysts are designed to form active metal oxo (MO) species and to be uniquely active for the homolytic cleavage of the carbon-hydrogen bonds in light alkanes producing intermediates which can form alcohols. We continue to investigate three molecular environments for the active catalytic species that we are trying to generate: electron-deficient porphryinic macrocycles (PHASE I), polyoxometallates (PHASE II), and regular oxidic lattices including zeolites and related structures as well as other molecular surface structures having metal oxo groups (PHASE III). |
Databáze: |
OpenAIRE |
Externí odkaz: |
|