Kinetic Study of the Selective Hydrogenation of Acetylene over Supported Palladium under Tail-End Conditions

The kinetics of the selective hydrogenation of acetylene in the presence of an excess of ethylene has been studied over a 0.05 wt. % Pd/α-Al2O3 catalyst. The experimental reaction conditions were chosen to operate under intrinsic kinetic conditions, free from heat and mass transfer limitations. The data could be described adequately by a Langmuir⁻Hinshelwood rate-equation based on a series of sequential hydrogen additions according to the Horiuti⁻Polanyi mechanism. The mechanism involves a single active site on which both the conversion of acetylene and ethylene take place