Abstract
Hydrotreatment of 4-chloronitrobenzene in aqueous phase has been carried out under ambient-like operating conditions (25°C and 1atm) with H2 using an own-prepared catalyst based on Pd (1wt%) supported on Al-pillared clay. Nitrobenzene, 4-chloroaniline, aniline and cyclohexanone were identified as reaction byproducts and trace amounts of different azobenzenes were also detected. Complete dechlorination was achieved in around 1.5h reaction time. Experiments with the aforementioned nitrogenated byproducts were performed to elucidate the reaction pathway. Nitrobenzene was completely converted in short reaction time leading to aniline as main product. Disappearance of 4-chloroaniline was complete after 1h giving rise to aniline as primary product. An unstable imine/enamine was obtained from aniline, yielding cyclohexanone upon reaction with water. Hydrodenitrogenation of aniline was favored at acidic pH, being released more than 85% N after 10h. A kinetic analysis is included and values of activation energy are given.
Published Version
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