Two different commercial SCR catalysts belonging to the V2O5-WO3-TiO2 syste
m, and different alternative catalysts based on Mn, Fe, Cr, Al and Ti oxide
s have been tested in the conversion of VOCs in excess oxygen in a temperat
ure range typical of the SCR process (500-700 K). Propane, propene, isoprop
anol, acetone, 2-chloropropane and 1,2-dichlorobenzene have been fed with e
xcess oxygen and helium. The industrial catalysts are poorly active in the
conversion of propane, giving mainly rise to propene by oxy-dehydrogenation
. The conversion of propene is higher with CO as the predominant product. I
n any case, the oxidation activity depends on the vanadium content of the c
atalyst. Isopropanol is mainly converted into acetone and propene, while ac
etone is burnt predominantly to CO. Mn- and Fe- containing systems are defi
nitely more active in the conversion of hydrocarbons and oxygenates, giving
rise almost exclusively to CO2. 2-Chloropropane is selectively dehydrochlo
rinated to propene and HCl starting from 350 K, propene being later burnt t
o CO on the industrial V2O5-WO3-TiO2 catalysts, whose combustion activity i
s, apparently, not affected by chlorine. On the contrary, chlorine strongly
affects the behavior of Mn-based catalysts, that are active in the dehydro
chlorination of 2-chloropropane, but are simultaneously deactivated with re
spect to their combustion catalytic activity. The conversion of 1,2-dichlor
obenzene gives rise to important amounts of heavy products in our experimen
tal conditions with relatively high reactant concentration. (C) 1999 Elsevi
er Science B.V. All rights reserved.