Catalytic oxidation of light alkanes in presence of a base
Abstract
The presence of a base in the reaction mixture in a metal-ligand catalyzed partial oxidation of alkanes results in sustained catalyst activity, and in greater percent conversion as compared with oxidation in the absence of base, while maintaining satisfactory selectivity for the desired oxidation, for example the oxidation of isobutane to isobutanol.
- Inventors:
-
- Boothwyn, PA
- West Chester, PA
- Issue Date:
- Research Org.:
- Sun Refining and Marketing Co., Marcus Hook, PA (United States)
- OSTI Identifier:
- 871398
- Patent Number(s):
- 5723697
- Assignee:
- Sun Company, Inc. (R&M) (Philadelphia, PA)
- Patent Classifications (CPCs):
-
C - CHEMISTRY C07 - ORGANIC CHEMISTRY C07C - ACYCLIC OR CARBOCYCLIC COMPOUNDS
- DOE Contract Number:
- FC21-90MC26029
- Resource Type:
- Patent
- Country of Publication:
- United States
- Language:
- English
- Subject:
- catalytic; oxidation; light; alkanes; presence; base; reaction; mixture; metal-ligand; catalyzed; partial; results; sustained; catalyst; activity; percent; conversion; compared; absence; maintaining; satisfactory; selectivity; desired; example; isobutane; isobutanol; partial oxidation; reaction mixture; catalytic oxidation; light alkanes; /999/
Citation Formats
Bhinde, Manoj V, and Bierl, Thomas W. Catalytic oxidation of light alkanes in presence of a base. United States: N. p., 1998.
Web.
Bhinde, Manoj V, & Bierl, Thomas W. Catalytic oxidation of light alkanes in presence of a base. United States.
Bhinde, Manoj V, and Bierl, Thomas W. Thu .
"Catalytic oxidation of light alkanes in presence of a base". United States. https://www.osti.gov/servlets/purl/871398.
@article{osti_871398,
title = {Catalytic oxidation of light alkanes in presence of a base},
author = {Bhinde, Manoj V and Bierl, Thomas W},
abstractNote = {The presence of a base in the reaction mixture in a metal-ligand catalyzed partial oxidation of alkanes results in sustained catalyst activity, and in greater percent conversion as compared with oxidation in the absence of base, while maintaining satisfactory selectivity for the desired oxidation, for example the oxidation of isobutane to isobutanol.},
doi = {},
journal = {},
number = ,
volume = ,
place = {United States},
year = {1998},
month = {1}
}
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