Reactive Distillation for Esterification of Bio-based Organic Acids

The following is the final report of the three year research program to convert organic acids to their ethyl esters using reactive distillation. This report details the complete technical activities of research completed at Michigan State University for the period of October 1, 2003 to September 30, 2006, covering both reactive distillation research and development and the underlying thermodynamic and kinetic data required for successful and rigorous design of reactive distillation esterification processes. Specifically, this project has led to the development of economical, technically viable processes for ethyl lactate, triethyl citrate and diethyl succinate production, and on a larger scale has added to the overall body of knowledge on applying fermentation based organic acids as platform chemicals in the emerging biorefinery. Organic acid esters constitute an attractive class of biorenewable chemicals that are made from corn or other renewable biomass carbohydrate feedstocks and replace analogous petroleum-based compounds, thus lessening U.S. dependence on foreign petroleum and enhancing overall biorefinery viability through production of value-added chemicals in parallel with biofuels production. Further, many of these ester products are candidates for fuel (particularly biodiesel) components, and thus will serve dual roles as both industrial chemicals and fuel enhancers in the emerging bioeconomy. The technical report from MSU is organized around the ethyl esters of four important biorenewables-based acids: lactic acid, citric acid, succinic acid, and propionic acid. Literature background on esterification and reactive distillation has been provided in Section One. Work on lactic acid is covered in Sections Two through Five, citric acid esterification in Sections Six and Seven, succinic acid in Section Eight, and propionic acid in Section Nine. Section Ten covers modeling of ester and organic acid vapor pressure properties using the SPEAD (Step Potential Equilibrium and Dynamics) method

Acetalization of formaldehyde with methanol in batch and continuous reactive distillation columns

Methylal, an important raw material and a solvent, is produced by acetalization of aqueous formaldehyde with methanol. This acetalization reaction was carried out in a closed system in the presence of a cation-exchange resin Indion 130 as catalyst and was found to be equilibrium limited. In order to increase the conversion for this reaction, reactive distillation was carried. Batch reactive distillation was performed in the presence of the cation-exchange resin Indion 130 as catalyst. Continuous reactive distillation was performed in a reactive distillation column (RDC) using three different types of catalyst packing. The first type of catalyst packing was coarse size macroporous cation-exchange resin Indion 130, which was directly packed along with Raschig rings. The second type of catalyst packing was Indion 130 tied in cloth bags. The third type of catalyst packing used was a silica-supported organic catalyst. Up to 99% conversion of formaldehyde was achieved by reactive distillation. Vapor-liquid equilibrium data for the quaternary system formaldehyde-methanol-methylal-water were experimentally obtained and correlated by the UNIFAC method. On the basis of the experimental results of the single-feed continuous reactive distillation column, preliminary modeling has been performed for the calculations of the minimum reflux ratio and the number of reactive equilibrium stages in the column used for synthesis