A One-Step Conversion of Benzene to Phenol with a Palladium Membrane
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- 4 January 2002
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 295 (5552), 105-107
- https://doi.org/10.1126/science.1066527
Abstract
Existing phenol production processes tend to be energy-consuming and produce unwanted by-products. We report an efficient process using a shell-and-tube reactor, in which a gaseous mixture of benzene and oxygen is fed into a porous alumina tube coated with a palladium thin layer and hydrogen is fed into the shell. Hydrogen dissociated on the palladium layer surface permeates onto the back and reacts with oxygen to give active oxygen species, which attack benzene to produce phenol. This one-step process attained phenol formation selectivities of 80 to 97% at benzene conversions of 2 to 16% below 250°C (phenol yield: 1.5 kilograms per kilogram of catalyst per hour at 150°C).Keywords
This publication has 29 references indexed in Scilit:
- Catalytic hydroxylation of benzene over vanadium-containing molecular sievesCatalysis Today, 2000
- Oxidation reactions with in situ generated oxidantsCatalysis Today, 1998
- Reactivity of active oxygen species generated in the EuCl3 catalytic system for monooxygenation of hydrocarbonsJournal of the Chemical Society, Perkin Transactions 2, 1996
- Palladium Catalyzed Transformation of Benzene to Phenol with Molecular OxygenChemistry Letters, 1990
- Liquid-phase oxidation of benzene under ambient conditionsJournal of the Chemical Society, Perkin Transactions 2, 1990
- Heterogeneous Catalysts for the Continuous Oxidation of Benzene to PhenolsChemistry Letters, 1988
- Selectivity in catalysis by hydrogen-porous membranesFaraday Discussions of the Chemical Society, 1981
- Reaction of 3 P oxygen atoms with dimethyl ether and trans-but-2-eneJournal of the Chemical Society B: Physical Organic, 1970
- The role of adsorbed hydrogen in the catalytic hydrogenation of cyclohexeneJournal of Catalysis, 1966
- Electronic Structure and Reactivities of MonoölefinsJournal of the American Chemical Society, 1959