2008 Annual Meeting
(316b) Supercritical Production of Biodiesel Using Methanol and Ethanol in Batch and Continuous Reactors
Authors
The evolution of the phase behavior with temperature, during the non-catalytic transesterification reaction, with and without propane as a co-solvent, was observed in a see-through, two window cylindrical reactor, at controlled reactor global densities and initial methanol / oil molar ratios. The reactor global density (ñg= defined as the total mass charged into the reactor divided by the reactor volume) is a key factor from a phase equilibrium engineering point of view. A high load global density (ñg > 0.7 g/cm3) produced a steep increase in pressure when the liquid phase completely filled the volume of the reactor. At smaller global densities (ñg < 0.5 g/cm3) the liquid-vapor (LV) equilibrium conditions prevailed up to 563K.
Different oils have been used in the batch transesterification studies: Raphanus sativus L. oil (Forage turnip oil) extracted by cold press, commercial soybean oil, and crude sunflower oil. The optimization of the process conditions was carried out based on a statistical design of experiments where the key process variables were studied over different ranges to obtain a reliable model for the efficiency of the reaction as a function of reactants residence time, temperature, pressure and molar ratio of alcohol/oil for the different oils and alcohols studied. The present results confirm preliminary studies that indicate that high conversions can be obtained at pressures of 10-15 Mpa at temperatures between 570 and 600 K using a molar ratio of 39. From direct observations and the modeling of the phase behavior, a better understanding of the supercritical alcohol transesterification process is obtained as well as the confirmation of the phase equilibrium predictions based on the GCA-EOS model. The optimum conditions obtained by statistical analysis in the batch reactors has been studied in a bench scale continuous reactor to obtain more reliable information between conversion and reactants residence time.
*Corresponding author, email: ebrignole@plapiqui.edu.ar