4.7 Article

Influence of bimetallic characteristics on the performance of MoCoP and MoFeP catalysts for methyl laurate hydrodeoxygenation

Journal

CATALYSIS TODAY
Volume 367, Issue -, Pages 43-50

Publisher

ELSEVIER
DOI: 10.1016/j.cattod.2020.09.034

Keywords

Hydrodeoxygenation; Methyl laurate; Bimetallic phosphide catalysts; Dispersion; Acidity

Funding

  1. Agencia Estatal de Investigacion (AEI) (Spain) [ENE2016-74889-C4-3-R]
  2. [BES-2017-079679]

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The study investigated the influence of bimetallic characteristics on catalytic activity and selectivity, finding that MoP/SiO2 exhibited the highest conversion rate for methyl laurate, MoCoP/SiO2 showed the highest hydrocarbon formation yield, and CoP/SiO2 had the highest C11 selectivity.
To study the influence of bimetallic characteristics on activity and selectivity, SiO2-supported monometallic (CoP, FeP and MoP) and bimetallic (MoxCo1-xP and MoxFe1-xP (x = 0.5)) phosphides were investigated for the deoxygenation of methyl laurate to C11-C12 hydrocarbons. Here, we aimed to modulate the catalytic properties using different metal compositions with equimolar amounts of total metal phosphide. The catalysts were characterized by X-ray diffraction, N2 adsorption-desorption at -196 ?C, transmission electron microscopy, CO chemisorption, NH3 temperature-programmed desorption and X-ray photoelectron spectroscopy; the conversion of methyl laurate, selectivity for hydrocarbons and C11/C12 ratio were related to the composition and physicochemical properties of the catalysts. The conversion (maximum of 85 % for MoP and minimum of 8 % for FeP) is mainly influenced by phosphide dispersion, which, in turn, is associated with acidity, and the same trend was found for both parameters (MoP/SiO2> MoCoP/SiO2 > MoFeP/SiO2 > FeP/SiO2 > CoP/SiO2). The yield of hydrocarbon formation follows the trend MoP/SiO2 > MoCoP/SiO2 > CoP/SiO2 > MoFeP/SiO2 > FeP/SiO2, with synergy between Mo and Co in the MoCoP catalyst. The C11/C12 ratio is influenced by the metal phosphide nature; the results indicate that Mo-based catalysts favor a hydrogenation (dehydration) pathway (C12 selectivity, 91 % in MoP/SiO2) and that Co-based catalysts favor oxygen elimination by decarbonylation/decarboxylation (C11 selectivity 75 % in CoP/SiO2). The activity results show synergy between Mo and Co in bimetallic phosphides by a kind of interaction that yields an enhancement in the catalytic activity of the MoCoP/SiO2 catalyst with respect to the sum of contributions from individual MoP/SiO2 and CoP/SiO2.

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