Catalytic reduction of nitric oxide on copper. Part I

✍ Scribed by H. Lu; C-M. Pradier; A.S. Flodström

• Publisher: Elsevier Science
• Year: 1996
• Tongue: English
• Weight: 998 KB
• Volume: 112
• Category: Article
• ISSN: 1381-1169
• DOI: 10.1016/1381-1169(96)00244-0

✦ Synopsis

The mechanism of NO reduction on copper in the presence of oxygen and isobutene was studied at T = 770 K, under reducing conditions. Mass spectroscopy was used to identify gas-phase intermediates and reaction products. One interrnediate species resulting from the partial oxidation of isobutene was shown to be active in the NO conversion. X-ray photoelectron spectroscopy was used to analyze the copper surface at different stages of the reaction. Our conclusion is that oxygen first activates the surface, by forming coexisting phases of Cu,O and CuO. The copper surface is then reduced by the hydrocarbon, leading to Cu+ in majority, and to the formation of an active intermediate. At last, the reduction 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.