Promoters state and catalyst activation during ammonia synthesis over Ru/C

Higher H 2 and O 2 uptakes have been observed during reduction and chemisorption, respectively, on Cs- and K-promoted samples supported on graphitised carbon, at difference with samples promoted with Ba or supported on active carbon. This indicates that alkaline promoters reduction under the ammonia synthesis conditions is favoured by the formation of graphite intercalation compounds. The efficacy of catalyst activation depends on the nature of Ru precursor. ▪ Carbon-supported, promoted Ru-based catalysts for ammonia synthesis proved to be interesting substitutes for the traditional Fe-based ones. A debate recently arose on the active state of promoters, mainly Cs and Ba, and on the effect of the latter on Ru active sites. In the present work a set of Ba-, Cs- and K-promoted samples has been characterised by various techniques. Higher H 2 and O 2 uptakes have been observed during reduction and chemisorption, respectively, on Cs- and K-promoted samples supported on graphitised carbon. No evidence of this has been observed with samples supported on active carbon. This is in line with the hypothesis of alkaline promoters partial reduction under the ammonia synthesis conditions, favoured by the formation of graphite intercalation compounds. Furthermore, some suggestions are here introduced on the beneficial role of Ba, especially in increasing the support resistance to methanation. Finally, the efficacy of catalyst activation was found to depend on the nature of Ru precursor. Indeed, a prolonged activation at relatively high temperature is usually needed with chloride precursors, to remove the counterion, a poison for the catalyst, whereas less dramatic conditions are required for different precursors, such as nitrosylnitrate.