The UV-induced photo-oxidation of propene, propane, ethene, ethane, n-butan
e and n-hexane were studied over a TiO2 photo-catalyst at 150 degreesC with
hydrocarbon concentrations up to 4000 ppm and O-2 concentrations up to 20%
. In the absence of O-2, very little reaction was observed and rapid cataly
st deactivation occurred. Increasing the O-2 concentration led to increased
hydrocarbon conversion. Under most conditions, the selectivity of hydrocar
bon conversion to CO2 was at least 95% for propene, propane, ethene and eth
ane. The only exception was 50% selectivity observed for the highest propen
e concentration studied (4000 ppm) in the presence of 12% O-2.
For propene and propane, the extent of photo-conversion depended on the gas
-phase hydrocarbon concentration, and had maxima at 500 and 1000 ppm, respe
ctively. The observed decrease at higher concentrations was attributed to h
ydrocarbon blocking oxygen adsorption sites, and thereby inhibiting the pro
duction of the photo-generated reactive oxygen species responsible for hydr
ocarbon oxidation. Durability of the photo-oxidation reaction without catal
yst deactivation was demonstrated for propene, propane, ethene and ethane.
In contrast with n-butane and to a greater extent n-hexane, the deposition
of stable carbonaceous species on the TiO2 surface led to catalyst deactiva
tion. (C) 2001 Published by Elsevier Science B,V.