Enantioselective extraction of phenylsuccinic acid in aqueous two-phase systems based on acetone and β -cyclodextrin derivative: Modeling and optimization through response surface methodology

2016 ◽  
Vol 1467 ◽  
pp. 490-496 ◽  
Author(s):  
Jun Wang ◽  
Qi Liu ◽  
Liya Rong ◽  
Hua Yang ◽  
Feipeng Jiao ◽  
...  
2009 ◽  
Vol 46 (3) ◽  
pp. 306-312 ◽  
Author(s):  
Radhouane Kammoun ◽  
Hichem Chouayekh ◽  
Hajeur Abid ◽  
Belgacem Naili ◽  
Samir Bejar

Processes ◽  
2018 ◽  
Vol 6 (11) ◽  
pp. 212 ◽  
Author(s):  
Danyu Sun ◽  
Runping Wang ◽  
Fenfang Li ◽  
Lianglei Liu ◽  
Zhijian Tan

(1) Background: The environmentally friendly choline-amino acid ionic liquids (ChAAILs) and deep eutectic solvents (DESs) have been used as excellent alternatives to volatile organic compounds (VOCs) and ionic liquids (ILs) in recent years; (2) Methods: Thus, ChAAILs/salt and DESs/salt aqueous two-phase systems (ATPSs) were developed for the chiral extraction of phenylalanine enantiomers. The optimum ATPS of [Ch][L-Pro]/K3PO4 was chosen, and the influencing parameters were investigated, including ChAAILs concentration, salt concentration, chiral selector concentration, extraction temperature, phenylalanine concentration, and system pH; (3) Results: The phenylalanine enantiomers were mainly extracted into the top phase (ChAAIL-rich phase), meanwhile, the (S)-phenylalanine [(S)-Phe)] was preferentially recognized by the chiral selector in the top phase. The maximum separation factor (α) of 2.05 was obtained under the optimal conditions; and (4) Conclusions: This ATPS that was used for the chiral extraction of enantiomers is much more environmentally friendly, simple, and rapid, and has the potential to be used in the enantioselective extraction of other enantiomers.


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