HDO activity of carbon-supported Rh, Ni and Mo-Ni catalysts

Abstract

This work reports the performance of low metal loading (about 3wt.%) Rh, Ni and Mo-Ni catalysts supported on carbon in the hydrodeoxygenation (HDO) of phenol. The catalytic tests were carried out in a flow microreactor at 310°C and at a total hydrogen pressure of 3MPa. A commercial NiMoP/γ-Al2O3 sulfided catalyst was used as reference. The effect of catalyst pre-treatment (reduction against sulfidation) was investigated in the case of the noble metal catalyst. The thermally treated in inert atmosphere, fresh reduced and spent catalysts have been characterized by several physicochemical techniques: chemical analysis, N2 adsorption-desorption isotherms, Raman spectroscopy, Scanning Electron Microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and High Resolution Transmission Electron Microscopy (HRTEM).The HDO of phenol was found to be favored on the bifunctional Rh/C and Ni/AC catalysts which exhibit a large amount of well dispersed metallic species (from HRTEM). Contrary to a commercial sulfided NiMo/Al2O3 catalyst, the hydrogenation of aromatic ring of phenol was favored being the CO bond hydrogenolysis a minor reaction route. Catalytic HDO of phenol over Rh/C reveal that the catalyst activation by reduction is advantageous compared to that by sulfidation. The partial substitution of Ni by Mo in the Mo-Ni/AC catalyst led to enhance of the catalyst stability but decrease of overall activity occurs due to the decrease of amount of metallic nickel species. The role of the MoO3 species in the inhibition of deactivation by coke is discussed.