CATALYTIC REDUCTION OF NITRIC-OXIDE ON COPPER .1.

The mechanism of NO reduction on copper in the presence of oxygen and isobutene was studied at T = 770 K, under reducing conditions. Mass sp ectroscopy was used to identify gas-phase intermediates and reaction p roducts, One intermediate species resulting from the partial oxidation of isobutene was shown to be active in the NO conversion. X-ray photo electron spectroscopy was used to analyze the copper surface at differ ent stages of the reaction. Our conclusion is that oxygen first activa tes the surface, by forming coexisting phases of Cu2O and CuO. The cop per surface is then reduced by the hydrocarbon, leading to Cu+ in majo rity, and to the formation of an active intermediate. At last, the red uction of NO proceeds rapidly on a zero-valent copper surface together with consumption of the previously formed intermediate. At the end of the reaction, the surface is poisoned by carbon.