Oxidative esterification of furfural over Au-Pd/HAP-T and Au-Ag/HAP-T bimetallic catalysts supported on mesoporous hydroxyapatite nanorodsElectronic supplementary information (ESI) available. See DOI: 10.1039/c6ra07614a

The conversion of furfural, a lignocellulose biomass, into fuels and value-added fine chemicals has attracted many researchers. In this study, structurally uniform and porous hydroxyapatite nanorods (HAP-T) with the gel composition 1Ca 2+ : 0.66PO 4 3− : 0.3 CTAB : 120H 2 O were synthesized using a hydrothermal method. The synthesized HAP-T was impregnated with Au, Pd or Ag so as to obtain either monometallic (Au/HAP-T, Pd/HAP-T and Ag/HAP-T) or bimetallic (Au 1− x Pd x /HAP-T and Au 1− x Ag x /HAP-T) catalysts. The obtained hydroxyapatite catalysts were thoroughly characterized by using various analytical techniques such as FT-IR, XRD, BET, UV-DRS, XPS, HR-SEM & HR-TEM. A thorough characterization of the catalysts led to the valid information that bimetallic Au 1− x Pd x /HAP-T catalysts have a core-shell bimetallic morphology, whereas the Au 1− x Ag x /HAP-T catalysts have an alloy morphology. The catalytic activities of the bare HAP-T, monometallic (Au/HAP-T, Pd/HAP-T and Ag/HAP-T) and bimetallic (Au 1− x Pd x /HAP-T and Au 1− x Ag x /HAP-T) catalysts were evaluated at atmospheric pressure towards the oxidative esterification of furfural to methyl 2-furoate using TBHP as oxidant and methanol as solvent. Among the various synthesized catalysts, the Au 0.8 Pd 0.2 /HAP-T catalyst with a core-shell structure showed the maximum conversion of furfural (94.2%) with very high selectivity towards methyl-2-furoate (99%). In addition, the efficiency of the Au 0.8 Pd 0.2 /HAP-T catalyst was maintained even after 5 cycles, supporting its reusability and stability. Core-shell (Au-Pd) and alloy (Au-Ag) architectured bimetallic mesoporous hydroxyapatite nano rods in the oxidative esterification of furfural.