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Abstract
Among various electrochemical reactions to produce fuels and chemicals, glycerol electrolysis to co-produce hydrogen and lactic acid has received great attention. However, studies have shown the benchmark Pt based catalysts are insufficient in selectively catalysing the glycerol to lactic acid transformation, resulting in a low yield of lactic acid. Here we report a study on glycerol electrolysis with anion-exchange membrane electrode assembly electrolyser. The reaction conditions including mass transport, temperature, current density and KOH concentration were optimised, among which temperature played a significant role in facilitating the reaction rate and thermodynamics. With the optimised condition a multicomponent Pt/C-zeolite electrocatalyst system (Pt/C-CBV600) was developed and tested, which is capable to increase the lactic acid selectivity to 57.3% from the 33.8% with standalone Pt/C. Although the detailed mechanism required further investigation, it is hypothesised that the CBV600 zeolite with abundant Lewis acid surface sites can effectively bind the dihydroxyacetone intermediate, and drive the reaction towards pyruvaldehyde heterogeneously, the key step to form lactic acid.
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Details
1 Department of Chemical Engineering, Imperial College London, South Kensington Campus , SW7 2AZ London, United Kingdom
2 Materials Science Institute and Inorganic Chemistry Department, University of Alicante , Ap. 99, E-03080 Alicante, Spain
3 Department of Chemical Engineering, Imperial College London, South Kensington Campus , SW7 2AZ London, United Kingdom; School of Mechanical Engineering Sciences, University of Surrey, Stag Hill Campus , GU2 7XH Guildford, United Kingdom




