NO adsorption and reduction with NH3 over activated coke at low temperature
s were studied by temperature-programmed desoption (TPD) and step-response
experiments. NO adsorption is inhibited by competitive adsorption of NH3 in
the absence of oxygen, and is significantly increased in the presence of o
xygen. This phenomenon cannot be explained by either the oxidation of NO in
the gas phase, nor the creation of oxidized surface on the activated coke.
A hypothesis is proposed to interpret the phenomenon, which suggests that
on the surface of the activated coke there are at least two types of adsorp
tion sites, one of them adsorbs NO2 and/or the oxidized NO species rather t
han NO. NO-NH3-O-2 reaction proceeds via both the ED mechanism and the LH m
echanism. NO conversion decreases with increasing temperature in the range
of 30-250 degrees C, which suggests that the adsorption of reactants, espec
ially NH3, is the rate-limiting step. (C) 2000 Elsevier Science Ltd. All ri
ghts reserved.