The influences of HCl, HNO3 and HF treatments of carbon on N2O and NO reduc
tion with 20 wt% Cu-loaded activated carbon were studied. The order of acti
vity in both N2O and NO is as follows: Cu20/AC-HNO3>Cu20/AC>Cu20/AC-HF>Cu20
/AC-HCl. The same sequence was also observed for the amount of CO2 evolved
during TPD experiments of supports acid for the catalyst dispersion. On the
other hand, N2O exhibited a higher reaction rate than NO and a higher sens
itivity to acid treatments, and the presence of gas-phase O-2 had opposite
effects in N2O and NO reduction. The key role of carbon surface chemistry i
s examined to rationalize these findings and the relevant mechanistic and p
ractical implications are discussed. The effects of oxygen surface groups o
n the pore structure of supports and catalysts are also analyzed, (C) 2000
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