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Studies on the hydrogenation of cinnamaldehyde over Pd/C catalysts
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1998
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Chemical EngineeringCatalytic ApplicationEngineeringPotassium AcetateIndustrial CatalysisReaction EngineeringTank ReactorOrganic ChemistryCatalysisPd/c CatalystsHydrogenChemistryCatalyst SelectivityCatalytic ProcessChemical KineticsCatalyst ActivationCatalytic SynthesisHydrothermal Processing
The hydrogenation of cinnamaldehyde was investigated using a 5% Pd/C catalyst in a 250 cm3 stirred tank reactor and 500 cm3 autoclave. The experiments were carried out at 273–343 K and 0·1–1·1 MPa. Non-polar solvents, e.g. toluene, decane, methylcyclohexane, decalin, ether and heptane, and polar solvents such as methanol, ethanol, propan-1-o1, propan-2-ol, butan-1-ol and butan-2-ol were used to study the selectivity with respect to hydrocinnamaldehyde formation, the reaction kinetics and mass transfer. The additives, such as potassium acetate, ferrous chloride, ferrous sulphate and quinoline were incorporated into the catalyst in order to improve the catalyst selectivity, which was observed especially in the case of potassium acetate. © 1998 SCI