Selective oxidation of glycerol over carbon-supported AuPd catalysts

Carbon-supported AuPd bimetallic nanoparticles were synthesized, characterized, and evaluated as catalysts in the aqueous-phase selective oxidation of glycerol. The bimetallic catalysts were synthesized by two different methods. The first method involved the deposition of Au onto the surface of 3-nm supported Pd particles by catalytic reduction of HAuCl4 in aqueous solution by H-2. The second method used the formation of a AuPd sol that was subsequently deposited onto a carbon support. Characterization of the catalysts using analytical transmission electron microscopy, H-2 titration, and X-ray absorption spectroscopy at the Au L-III and I'd K-edges confirmed that the first synthesis method successfully deposited Au onto the Pd particles. Results from the AuPd sol catalyst also revealed that Au was preferentially located on the surface. Measurement of glycerol oxidation rates (0.3 M glycerol, 0.6 M NaOH, 10 atm 02, 333 K) in a sernibatch reactor gave a turnover frequency (TOF) of 17 s(-1) for monometallic An and 1 s(-1) for monometallic Pd, with Pd exhibiting a higher selectivity to glyceric acid. Although the activity of the bimetallic AuPd catalysts depended on the amount of Au present, none of them had a TOF greater than that of the monometallic Au catalyst. However, the AuPd catalysts had higher selectivity to glyceric acid compared with the monometallic An. Because a physical mixture of monometallic An and Pd catalysts also gave higher selectivity to glyceric acid, the Pd is proposed to catalyze the decomposition of the side product H2O2 that is also formed over the Au but is detrimental to the selectivity toward glyceric acid. (c) 2007 Elsevier Inc. All fights reserved.