The low-temperature behavior of the selective catalytic reduction (SCR) process with feed gases containing both NO and NO 2 was investigated. The two main reactions are 4NH 3 + 2NO + 2NO 2 → 4N 2 + 6H 2 O and 2NH 3 + 2NO 2 → NH 4 NO 3 + N 2 + H 2 O. The “fast SCR reaction” exhibits a reaction rate at least 10 times higher than that of the well-known standard SCR reaction with pure NO and dominates at temperatures above 200 °C. At lower temperatures, the “ammonium nitrate route” becomes increasingly important. Under extreme conditions, e.g., a powder catalyst at T ≈ 140 °C, the ammonium nitrate route may be responsible for the whole NO x conversion observed. This reaction leads to the formation of ammonium nitrate within the pores of the catalyst and a temporary deactivation. For a typical monolithic sample, the lower threshold temperature at which no degradation of catalyst activity with time is observed is around 180 °C. The ammonium nitrate route is interesting from a standpoint of general DeNO x mechanisms: This reaction combines the features typical to the SCR catalyst with the features of the NO x storage−reduction catalyst, i.e., NO x adsorption to a basic site.
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Koebel et al. (2000) studied this question.
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