Catalytic deep oxidation of toluene at low concentration in air, has been s
tudied over CuNaHY zeolites with different copper contents. The reaction ha
s been investigated in the course of time-on-stream, at temperatures betwee
n 150 and 500 degreesC. The effect of copper content on the conversion of t
oluene into CO2 and on the formation of carbonaceous deposits (coke) retain
ed inside the zeolite pores has been analyzed as a function of the reaction
temperature. The analysis of the coke extracted from the catalysts showed
that it is mainly composed of aromatic hydrocarbons and oxygenated aromatic
compounds, the latter being predominant at low temperature and preferentia
lly formed on the catalysts containing more copper. A bifunctional mechanis
m was proposed to explain the formation of coke over CuNaHY catalysts. Base
d on the differences of the nature of coke formed on NaHY and CuNaHY cataly
sts, and on a discussion about the coke formation and location, it was poss
ible to conclude that copper sites are involved in both toluene and coke ox
idation reactions. The increase of copper content from 1 to 8 wt.% promotes
the oxidation of toluene and facilitates the removal of coke formed in the
course of reaction. (C) 2001 Elsevier Science B.V. All rights reserved.