The catalytic reduction of NO by CH4 over Co/ZSM-5 zeolite is studied by me
ans of transient in situ DRIFT, SSITK and TAP analyses. Co ions located at
the interface of Co clusters and zeolite are found to react with NO in the
presence of oxygen to form anchored NO2delta+ species stabilized under reac
tion conditions. These species form the main active sites for activating me
thane molecule. Two ways of CO2 formation from the same intermediate includ
ing fragments of both NO2 and partially dehydrogenated CH4 molecule are pro
posed in the mechanistic scheme of the reaction. (C) 1999 Elsevier Science
Ltd. All rights reserved.