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Biocatalytic separation of (R, S)-1-phenylethanol enantiomers and fractionation of reaction products with supercritical carbon dioxide
Publikationstyp
Journal Article
Publikationsdatum
2011
Sprache
English
Author
Paiva, Alexandre
Vidinha, Pedro
Angelova, Maria
Rebocho, Sílvia
Barreiros, Susana
Enthalten in
Volume
55
Issue
3
Start Page
963
End Page
970
Citation
Journal of Supercritical Fluids 55 (3): 963-970 (2011)
Publisher DOI
Scopus ID
Publisher
Elsevier Science
The continuous kinetic resolution of (R, S)-1-phenylethanol via enzymatic transesterification was chosen as a benchmark reaction for the study of a complete reaction/separation process using supercritical carbon dioxide. Phase equilibrium data for binary and ternary systems was acquired as a starting point to determine the best conditions of operation. Total conversion of the (R)-isomer of the alcohol was achieved using a 10% molar excess of vinyl laurate. Three separators operating at given temperatures and pressures allowed the recovery of (S)-1-phenylethanol with a purity of 86%. The phase equilibrium data obtained indicates that an additional separation step should allow the recovery of both (S)-1-phenylethanol and (R)-1-phenylethylaurate with over 95% purity. Due to the low solubilities of the target compounds, CO2 from the outlet gas stream of the last separator must be recycled to ensure the technical viability of the integrated reaction/separation of (R, S)-1-phenylethanol.
Schlagworte
1-Phenylethanol
Enantioselectivity
Lipase
Phase equilibrium
Supercritical CO 2
DDC Class
620: Engineering