Product sampling during transient continuous countercurrent hydrolysis of canola oil and development of a kinetic model
Type
ArticleKAUST Department
Clean Combustion Research CenterMechanical Engineering Program
Physical Science and Engineering (PSE) Division
high-pressure combustion (HPC) Research Group
Date
2013-11Permanent link to this record
http://hdl.handle.net/10754/563056
Metadata
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A chemical kinetic model has been developed for the transient stage of the continuous countercurrent hydrolysis of triglycerides to free fatty acids and glycerol. Departure functions and group contribution methods were applied to determine the equilibrium constants of the four reversible reactions in the kinetic model. Continuous countercurrent hydrolysis of canola oil in subcritical water was conducted experimentally in a lab-scale reactor over a range of temperatures and the concentrations of all neutral components were quantified. Several of the rate constants in the model were obtained by modeling this experimental data, with the remaining determined from calculated equilibrium constants. Some reactions not included in the present, or previous, hydrolysis modeling efforts were identified from glycerolysis kinetic studies and may explain the slight discrepancy between model and experiment. The rate constants determined in this paper indicate that diglycerides in the feedstock accelerate the transition from "emulsive hydrolysis" to "rapid hydrolysis". © 2013 Elsevier Ltd.Citation
Wang, W.-C., Natelson, R. H., Stikeleather, L. F., & Roberts, W. L. (2013). Product sampling during transient continuous countercurrent hydrolysis of canola oil and development of a kinetic model. Computers & Chemical Engineering, 58, 144–155. doi:10.1016/j.compchemeng.2013.06.003Sponsors
This material is based upon work supported by the National Science Foundation EFRI program under Grant EFRI-093772.Publisher
Elsevier BVJournal
Computers & Chemical Engineeringae974a485f413a2113503eed53cd6c53
10.1016/j.compchemeng.2013.06.003