Article ID Journal Published Year Pages File Type
62763 Journal of Catalysis 2008 13 Pages PDF
Abstract

Propane epoxidation was carried out by sequential propane dehydrogenation–propylene epoxidation steps using a two-catalyst bed and H2 and O2 as the oxidant mixture. The propane dehydrogenation step used a Au/TiO2 catalyst that was active at the low temperature (443 K) used for the propylene epoxidation step; the latter used a Au/TS-1 catalyst. In situ Au L3-edge X-ray absorption near-edge structure and ultraviolet–visible measurements on Au/TiO2 under propane dehydrogenation conditions showed activation of oxygen on gold nanoparticles and evidence for the formation of adsorbed oxygen intermediate species responsible for the production of propylene. Propane epoxidation with H2 and O2 at 443 K and 0.1 MPa with the dual Au/TiO2 and Au/TS-1 catalysts resulted in an overall propane conversion of 2%, propylene selectivity of 57%, and propylene oxide selectivity of 8%, corresponding to a propylene oxide space-time yield of 4 gkgcat−1h−1. The catalysts showed little deactivation and maintained their conversion and selectivity levels for the 12 h duration of the measurements.

Related Topics
Physical Sciences and Engineering Chemical Engineering Catalysis
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