Abstract

Catalytic reduction of nitric oxide with molecular hydrogen proceeded over metallo-tetraphenylporphyrins in the temperature range 200 – 350 °C in a circulating reactor. The activity order of the complexes was FeClTPP ≪ CoTPP ⩽ NiTPP ≫ CuTPP > ZnTPP, indicating the strong influence of central metal ions. CoTPP which adsorbed nitric oxide produced molecular nitrogen and nitrous oxide as well as ammonia, whereas Ni, Cu, and ZnTPP which do not stationarily adsorb nitric oxide, produced ammonia selectively. The reducing reactivities of carbon monoxide, ammonia, and methane were examined over CoTPP. The reactivities of these reducing agents were H 2 > CO > NH 3 > CH 4. Ammonia was found to enhance the adsorption of nitric oxide over CoTPP. The catalytic reaction is discussed in terms of the correlation between the electronic structure of the metalporphyrins and their activity for the adsorption and reduction of nitric oxide.

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