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Boreskov Institute of Catalysis of the Siberian Branch of Russian ...

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PP-I-4Organic phase (n-hexane)OOHOH H 2 2+ +-- - - + - - ++ - ++ + - - + - + - - -+ + - + -PdPdPd - -+ + + +- ++ -- Pd+ - + + -- + - - + + - - - --+ - - +- + + - - + -+- + +- + + + - --- -+ + + + + - - - + -- - - ++ - + - + + - - ++ -Pd - -++ ++ -+-- + -++ + + +- - ---- +-Active Carbon SupportIonicLiquidLayerFigure 1. Picture <strong>of</strong> SILCA used in hydrogenation <strong>of</strong> cinnamaldehyde.Kinetic evaluation <strong>of</strong> catalysts with two different ionic liquids was performed with <strong>the</strong>results obtained from <strong>the</strong> hydrogenation experiments. Experiments showed that ionic liquidlayer on ACC can improve <strong>the</strong> hydrogenation reaction rate and tune <strong>the</strong> selectivity for variousproducts, depending on <strong>the</strong> ionic liquid applied. Kinetic modeling was based on <strong>the</strong> reactionscheme in Fig. 2. A classical Langmuir-Hinshelwood-Hougen-Watson type <strong>of</strong> kinetic modelwas applied in <strong>the</strong> estimation <strong>of</strong> rate and adsorption parameters.Ohydrocinnamaldehyde H 2H 2OOHcinnamaldehydeH 2hydrocinnamylalcoholOHH 2cinnamylalcoholFigure 2. A reaction scheme for cinnamaldehyde hydrogenation over SILCAReferences1. P. Bonhôte, A.-P. Dias, N. Papageorgiou, K. Kalyanasundaram, M. Grätzel, Inorg. Chem.,35 (1996) 1168.2. R.D. Rogers, K.R. Seddon, Science, 302 (2003) 792.3. J. Dupont, G.S. Fonseca, A.P. Umpierre, P.F.P. Fichtner, S.R. Teixeira, J. Am. Chem. Soc., 124 (2002)4228.4. R. Sheldon, Chem. Comm., (2001) 2399.5. J.-P. Mikkola, P. Virtanen, H. Karhu, T. Salmi, D.Y. Murzin, Green Chem., 8 (2006) 197.219

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