A COMPARISON OF STEADY-STATE AND UNSTEADY-STATE REACTION-KINETICS OF N-BUTANE OXIDATION OVER VPO CATALYSTS USING A TAP-2 REACTOR SYSTEM

The reaction of n-butane with 'reactor-equilibrated' (VO)(2)P2O7 based catalysts has been investigated using a combination of low-pressure t ransient response experiments and atmospheric-pressure steady-flow rea ction experiments. The activation energy for n-butane conversion in bo th steady-flow and transient response experiments was a function of th e oxidation stare of the catalyst. Under steady-flow conditions an act ivation energy of 17 +/- 2 kcal/mol was obtained for 'reactor-equilibr ated' catalysts, and 13 +/- 2 kcal/mol for an oxygen-treated catalyst. The activation energy for n-butane conversion in transient-response e xperiments varied between 12 +/- 1 and 23 +/- 2 kcal/mol. An analysis of the transient response curves of the reaction products shows that t he rates of formation and desorption of products are strong functions of the catalyst oxidation state. Analysis of the kinetic results indic ated that the same sites are involved in the steady-state and unsteady -state conversion of n-butane.