Copper-zirconia catalysts have shown high activities and selectivities
for a NO-CO reaction at low temperature. Highly active Cu(L) species
are produced by replacing the terminal OH groups of the ZrO2 surface a
nd assigned to atomically dispersed Cu species. The deactivation of Cu
(L) species took place in two steps; relatively rapid activity loss an
d subsequent slow deterioration. Treatments with 1% NO regenerated the
deactivated Cu/ZrO2 at a much lower temperature than treatments with
5% O-2. The addition of Fe to Cu/ZrO2 was found to dramatically improv
e the catalytic performances; the activity and selectivity to N-2 at l
ow temperature and catalytic stability. The mechanisms of reaction, de
activation, and regeneration are proposed.