Deoxygenation of oleic acid: Influence of the synthesis route of Pd/mesoporous carbon nanocatalysts onto their activity and selectivity

Abstract

Abstract Supported Pd nanocatalysts were prepared by deposition of Pd nanoparticles (NPs) onto spherical mesoporous carbon beads (MB) functionalized by thermal or acidic treatement. The Pd NPs were synthesized by decomposition of [Pd 2 (dba) 3 ] (dba: dibenzylideneacetone) under dihydrogen either directly on the carbon supports without stabilizer leading to naked Pd NPs (Pd/MB series) or in solution in the presence of a stabilizer (polymer (PVP series) or triphenylphosphine (TPP series)) to obtain stable colloidal solutions that were further used to impregnate the carbon materials to have carbon-deposited Pd NPs. The NPs deposited on carbon displayed a Pd loading from 0.5 to 14.8 wt.% and were characterized by different techniques (nitrogen physisorption at 77 K, H 2 -chemissorption and TPD, XRD, XPS and HRTEM). Their catalytic performance in deoxygenation of oleic acid was evaluated in batch and flow reaction conditions. Flow conditions led to superior results compared to batch. No aromatic compounds were detected as side products, but in the case of the Pd/MB series, octadecanol and octadecane were significantly formed suggesting the involvement of a deoxygenation mechanism in which the hydrocarbons were produced via both decarbonylation/decarboxylation and dehydration steps. Further experiments carried out in H 2 /N 2 mixture or in pure N 2 highlighted the key role of hydrogen. For a N 2 /H 2 of 2.5:1 the dehydration route was crossing out and even no traces of octadecanol nor octadecane were detected. Then, complete removal of H 2 produced heptadecene in a high excess compared to heptadecane (almost 7–1) thus suggesting the decarbonylation/decarboxylation steps as the main route. ICP-OES measurements indicated no leaching of palladium and simple washing of catalysts with mesitylene allowed recycling without any change in conversion or product distribution.