The role of hydrogen bronzes in the hydrogenation of polyfunctional reagents: cinnamaldehyde, furfural and 5-hydroxymethylfurfural over Pd/HxWO3 and Pd/HxMoO3 catalysts

Abstract

Differences in the activity of Pd/WO3 and Pd/MoO3 (Pd loading 0.4–4 wt%) catalysts in competitive hydrogenations of the CC and CO groups in polyfunctional reagents have been studied as a function of two effects: (1) the in situ formation of hydrogen bronzes, HxWO3 and HxMoO3, and (2) the electronic interaction between the supports and the metallic Pd. The cinnamaldehyde (CAL), furfural (FU) and 5-hydroxymethylfurfural (HMF) were hydrogenated under mild reaction conditions. The formation of hydrogen bronzes in Pd/WO3 and physical mixture of Pd/WO3 with supporting WO3 oxide upon exposure to H2 was also studied using the gas flow-through microcalorimetry. In both Pd/MoO3 and Pd/WO3 catalysts, the electronic interactions contributed to the promotion of selectivity toward the CO hydrogenation in CAL and FU, yet in Pd/MoO3 this effect was much more pronounced. On the other hand, apart from increasing the overall reaction rate, the formation of hydrogen bronzes remarkably enhances the CC hydrogenation in CAL, as well as the decarbonylation of FU to furan and hydrogenolysis of C–OH in HMF to 5-methylfurfural. The bronze effects are significantly stronger in HxWO3, compared to HxMoO3, which may be related to higher H-species mobility and weaker H-bonding in the W–O–H (54 kJ/mol H2) than in the Mo–O–H (100 kJ/mol H2). This may also explain very high tendency of Pd/WO3 to furan ring hydrogenation in FU and HMF as well as almost selective (>98%) hydrogenation of furfuryl alcohol to tetrahydrofurfuryl alcohol.