4.6 Article

Partial Hydrogenation of Soybean and Waste Cooking Oil Biodiesel over Recyclable-Polymer-Supported Pd and Ni Nanoparticles

Journal

CATALYSTS
Volume 12, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/catal12050506

Keywords

biodiesel; waste cooking oil; partial hydrogenation; palladium; nickel; nanoparticles; recyclable catalysts

Funding

  1. National Operational Programme 2014-2020 [1061]

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Biodiesel obtained from the transesterification of vegetable oils contains polyunsaturated fatty esters which negatively affect its oxidation stability. Catalytic partial hydrogenation can upgrade biodiesel by converting polyunsaturated fatty esters into monounsaturated methyl oleate. In this study, polymer-supported palladium and nickel nanoparticles were tested as catalysts for upgrading biodiesels under mild conditions. The palladium catalyst showed high activity but poor selectivity, while the nickel catalyst exhibited lower activity but higher selectivity. The recyclability tests demonstrated that the nickel-based system can retain its activity and selectivity for at least five subsequent runs, providing an opportunity for waste biomass valorization.
Biodiesel obtained through the transesterification in methanol of vegetable oils, such as soybean oil (SO) and waste cooking oil (WCO), cannot be used as a biofuel for automotive applications due to the presence of polyunsaturated fatty esters, which have a detrimental effect on oxidation stability (OS). A method of upgrading this material is the catalytic partial hydrogenation of the fatty acid methyl ester (FAME) mixture. The target molecule of the partial hydrogenation reaction is monounsaturated methyl oleate (C18:1), which represents a good compromise between OS and the cold filter plugging point (CFPP) value, which becomes too high if the biodiesel consists of unsaturated fatty esters only. In the present work, polymer-supported palladium (Pd-pol) and nickel (Ni-pol) nanoparticles were separately tested as catalysts for upgrading SO and WCO biodiesels under mild conditions (room temperature for Pd-pol and T = 100 degrees C for Ni-pol) using dihydrogen (p = 10 bar) as the reductant. Both catalysts were obtained through co-polymerization of the metal containing monomer M(AAEMA)(2) (M = Pd, Ni; AEEMA(-) = deprotonated form of 2-(acetoacetoxy)ethyl methacrylate)) with co-monomers (ethyl methacrylate for Pd and N,N-dimethylacrilamide for Ni) and cross-linkers (ethylene glycol dimethacrylate for Pd and N,N'-methylene bis-acrylamide for Ni), followed by reduction. The Pd-pol system became very active in the hydrogenation of C=C double bonds, but poorly selective towards the desirable C18:1 product. The Ni-pol catalyst was less active than Pd-pol, but very selective towards the mono-unsaturated product. Recyclability tests demonstrated that the Ni-based system retained its activity and selectivity with both the SO and WCO substrates for at least five subsequent runs, thus representing an opportunity for waste biomass valorization.

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