NOX DECOMPOSITION AND REDUCTION BY METHANE OVER LA2O3

Nitric oxide reduction by methane was conducted in a quartz microreact or from 773 to 973 K over La2O3, a good methane oxidative coupling cat alyst. La2O3 is a better catalyst than MgO and Li/MgO for this reactio n because: (1) it has a much higher specific activity, (2) the presenc e of oxygen enhances the rate of reduction, and (3) it gives a selecti vity to nitrogen that is close to 100%. Both Li/MgO and La2O3 catalyst systems have rates that increase continuously with temperature and ex hibit no bend over. The apparent activation energy for nitric oxide re duction by methane over La2O3 was 24.4 kcal/mol (26.0 kcal/mol with ox ygen present), and the reaction orders in CH4, NO and O2 were 0.26, 0. 98 and 0.50, respectively. Unlike Li/MgO, La2O3 is also active for dir ect nitric oxide decomposition, but the activity is noticeably lower t han that for nitric oxide reduction by methane. Both the direct decomp osition of nitrous oxide and nitrogen dioxide and their reduction by m ethane were also studied on La2O3. The rate of direct nitrous oxide de composition was quite high and essentially unaltered by the presence o f methane; in contrast, the rate of nitrogen dioxide decomposition was very low. However, the rate of nitrogen dioxide reduction to nitrogen was greatly enhanced by methane, and the rate became comparable to th at for nitric oxide reduction by methane in the presence of 1.0% O2. M ethane oxidative coupling over this La2O3 catalyst was verified using oxygen and nitrous oxide as oxidants, whereas little or no coupling oc curred when nitric oxide or nitrogen dioxide was used. At this time, t he high NO(x) reductive activity of La2O3 and other coupling catalysts is attributed to the formation of surface methyl radicals.