Supported Co-Re Bimetallic Catalysts with Different Structures as Efficient Catalysts for Hydrogenation of Citral.

Abstract

Bimetallic Co-Re/TiO2 catalysts were developed for efficient citral hydrogenation. Bimetallic catalysts were prepared by co-impregnation (CI), successive-impregnation (SI), and surface redox method (SR). The arrangement between the Co and Re species on these systems was fully characterized using several techniques (TEM-energy-dispersive X-ray spectroscopy, H2 temperature-programmed reduction, temperature-programmed desorption, XRD, CO FTIR spectroscopy, model reaction of cyclohexane dehydrogenation), and their catalytic performances were evaluated for the selective hydrogenation of citral towards unsaturated alcohols. The Re and Co species are completely isolated in the CI sample, presenting a very limited Co-Re interaction. In SI samples, the metals coexist in a Janus-type structure with a concentration of Re around Co. Decoration/core-shell structures are observed for SR samples resulting from the redox exchange between the metallic surface of the parent Co/TiO2 catalyst and the Re7+ species of the modifier precursor salt. The contact degree between the two metals gradually increases as follows: Isolated structure (CI)<Janus-type structure(SI)<decoration/core-shell structure (SR). The unchanging structure of all SI samples independent of the Re loading leads to similar electron transfer, and the increase in Re content results in agglomeration of Re, thus decreasing the catalytic activity. Density-of-state (DOS) calculations prove that the high valence of Re is a disadvantage for the hydrogenation reaction. For SR samples, the increase of Re loading contributes to the electron transfer from Re to Co that is consistent with a change of structure from decoration to core-shell. The lack of directly accessible Co atoms for SR catalysts with fully coated structure decreases the efficiency of Re reduction. The presence of Co-Re interaction resulting from the close contact between metals plays a dominant role in the hydrogenation of citral. Nevertheless, an excessively high contact degree is unnecessary for citral hydrogenation once Co-Re interaction has formed.