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Hydrodenitrogenation of Simple Aromatic Amines on Molybdena Catalysts
Affiliation:1. Department of Physical Sciences, Landmark University, Omu-Aran, Nigeria;2. Department of Chemistry, University of Ilorin, P.M.B.1515, Ilorin, Kwara, Nigeria;3. Department of Chemistry, University of South Africa, Pretoria, South Africa;4. Department of Chemistry, College of Pure and Applied Sciences, Kwara State University, P.M. B 1530, Malete, Nigeria;5. Department of Biological Sciences, Afe Babalola University, PMB 5454, Ado-Ekiti, Nigeria;6. Department of Chemistry, Nelson Mandela University, P.O. Box 77000, Port Elizabeth 6031, South Africa;7. Department of Chemistry, University of Warwick, Coventry CV4 7AL, UK
Abstract:The hydrotreatment of some aromatic amines was studied at temperatures ranging from 400 to 450°C and PH2=1 atm under flow conditions. Hydrogenolysis of aromatic amines involves direct cleavage of the C(sp2)single bondN bond without saturation of the aromatic ring. The presence of hydrogen sulphide in the reaction stream has a promotional effect on the hydrogenolysis of C(sp3)single bondN bond and an inhibitive effect on the hydrogenolysis of C(sp2)single bondN bond. The use of a saturated hydrocarbon as diluent facilitates Csingle bondN bond hydrogenolysis in the presence of hydrogen, irrespective of the carbon being sp2 or sp3 hybridized.
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