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Boreskov Institute of Catalysis SB RAS, Novosibirsk, Russia

Boreskov Institute of Catalysis SB RAS, Novosibirsk, Russia

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OP-1-7DEOXYGENATION OF FATTY ACIDS AND THEIR ESTERSOVER PALLADIUM ON CARBON CATALYST: INVESTIGATIONOF REACTION MECHANISMBartosz Rozmysłowicz, Anton Tokarev, Päivi Mäki-Arvela, Dmitry Yu. MurzinProcess Chemistry Center, Åbo Akademi University, 20500 Turku, Finland,dmurzin@abo.fiProduction <strong>of</strong> biodiesel via deoxygenation <strong>of</strong> fatty acids and their esters havebeen <strong>of</strong> high interest over the last years [1]. It was shown that the bestdeoxygenation conversion and selectivity can be achieved over palladium on carboncatalyst at 300°C under hydrogen rich atmosphere, in which deoxygenation reactioncould proceed through three different pathways: decarboxylation, decarbonylationand hydrogenation <strong>of</strong> carboxylic group (Fig. 1). To investigate, which <strong>of</strong> thesemechanisms is predominant, depending on hydrogen presence, series <strong>of</strong>experiments with lauric acid, lauric aldehyde and dodecanol as well as with methyland ethyl esters <strong>of</strong> fatty acids, were carried out in hydrogen rich and in inertatmosphere.The experiments were performed in semibatch reactor at 300°C, over 5% Pd/Ccatalyst using hexadecane as a solvent. Catalyst was characterized by nitrogenadsorption and TEM leading to 380 m 2 /g <strong>of</strong> specific surface area and 2.4 nm <strong>of</strong>average palladium clusters size. Liquid phase products were analyzed by GC andGC-MS, while gas phase products were analyzed with micro-GC.In the final work the effect <strong>of</strong> gas atmosphere on catalytic deoxygenation as wellas the reaction network will be discussed.+ +H OH 3 CCH 2CO 2C H 3OOH+ H 2+ 3H 2H 3 CCH 3CO 2H 3 CCH 3CO H 2 OCH 3H 3 C2H 2 O++ ++Fig. 1. Simplified reaction network for the catalytic deoxygenation <strong>of</strong> fatty acids.References:[1]. Murzin, D.Yu., Kubickova, I., Snåre, M., Mäki-Arvela, P., Myllyoja, J., Method for the manufacture<strong>of</strong> hydrocarbons, WO 2006075057, 2006, pp. 21. US Patent 7, 491,858 2009.30

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