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Bifunctional mechanism of pyridine hydrodenitrogenation

Journal Article · · Journal of Catalysis
; ;  [1]
  1. Univ. of Louisville, KY (United States)
The role of Mo coordinatively unsaturated sites (CUS) and Broensted acidic sites in the hydrodenitrogenation of pyridine was investigated in an atmospheric-pressure microreactor. The test catalysts consisted of nonsulfided Mo oxide supported on Al{sub 2}O{sub 3}, SiO{sub 2}, and silica-aluminas, containing different concentrations of Mo CUS and Broensted acidic sites. The kinetic study revealed that Mo loading and support composition affect the specific activity of Mo and selectivity of the catalysts. For the range of conditions used in this study (360-420{degrees}C, 1 atm H{sub 2}, 0.2 mol% pyridine concentration, differential conversion), the most abundant reaction intermediate was trans-2-pentene, and the rate-limiting step was the hydrogenation of the ring. Thus, the overall activity was correlated with the concentration of Mo CUS, which are the hydrogenation sites. The yield of denitrogenated product was also correlated with concentration of CUS. The Broensted acidic sites determined the selectivity towards the observed cracking, isomerization, and alkylation products. 55 refs., 11 figs., 4 tabs.
OSTI ID:
191959
Journal Information:
Journal of Catalysis, Journal Name: Journal of Catalysis Journal Issue: 2 Vol. 156; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English