Add time:07/25/2019         Source:sciencedirect.com

The mechanism of the C-N bond cleavage in hydrodenitrogenation over NiMo/γ-Al2O3 and Mo(P)/γ-Al2O3 catalysts was studied. The major part of C-N cleavage of o-toluidine takes place via ring hydrogenation and β-Hofmann elimination. Direct conversions from o-toluidine to toluene and from methylcyclohexylamine to methylcyclohexane were observed as well. Some of these direct conversions were, however, only apparent. They were caused by diffusion limitation, because the intermediates could not diffuse out of the pores fast enough to be detected. The influence of diffusion was greater for the more active NiMo/γ-Al2O3 catalyst. Experiments with small catalyst particles at low conversions demonstrated that, even in the absence of diffusion limitation, direct C-N bond cleavage takes place. This is ascribed to C-N bond hydrogenolysis or to nucleophilic substitution of the NH2 group by a SH group, followed by C-S bond hydrogenolysis.

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