Kinetics of Glycerol Selective Oxidation Over PtBi/C Catalyst

Wednesday, November 11, 2009: 1:20 PM
Lincoln C (Gaylord Opryland Hotel)

Wenbin Hu, School of Chemical Engineering, Purdue University, West Lafayette, IN
Daniel Knight, School of Chemical Engineering, Purdue University, West Lafayette, IN
Arvind Varma, School of Chemical Engineering, Purdue University, West Lafayette, IN

Identifying new uses of glycerol, a waste of biodiesel production from transesterification of vegetable oils, is of great current interest. Towards this end, catalytic oxidation of glycerol is a promising approach. The challenge, however, is the relatively complex oxidation reaction network. Our research is focused on maximizing the yield of a specific product, high-value chemical dihydroxyacetone (DHA). The selective oxidation of glycerol to DHA was conducted in a semi-batch reactor (Parr) in the presence of bismuth-promoted platinum catalyst, supported on activated carbon (PtBi/C). The experimental data, collected over a wide range of process conditions, including temperature, pressure and concentration, were fitted with a kinetic model. The obtained kinetics were used to identify the optimum reaction conditions for maximum DHA yield in a fixed-bed reactor.
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