Abstract

The reduction of NO with CO over alumina supported iron oxide and chromium oxide is a relatively fast process. The reaction is strongly inhibited over both catalysts by small amounts (~0.7 mole %) of water. The reduction of NO by H 2 appears to be significantly slower than by CO, although this was shown to be due to inhibition by H 2O, which is a primary product of the NOH 2 reaction. The product distribution from competitive experiments with mixtures of CO and H 2, shows that H 2 reacts preferentially to CO, over iron oxide. The water-gas shift reaction occurs more readily over iron oxide than chromium oxide and the H 2 formed reduces NO to NH 3. The produet distribution from the NOH 2 reaction differs with the two catalysts. Over iron oxide the major product is NH 3, while with chromium oxide it is N 2. Since chromium oxide neither decomposes NH 3 nor promotes the NONH 3 reaction with any greater ease than Fe 2O 3, it is concluded that the reduction of NO with H 2 occurs by different mechanisms over the two catalysts.

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