Kinetic study on reactive extraction of metoprolol enantiomers with cyclohexyl (D)-tartrate and boric acid as combined chiral selector

被引:3
|
作者
Zhang, Panliang [1 ,2 ]
Wang, Lujun [2 ]
Tang, Kewen [2 ]
Dai, Guilin [2 ]
Jiang, Pan [2 ]
Qiu, Yunren [1 ]
机构
[1] Cent S Univ, Sch Chem & Chem Engn, Changsha 410083, Hunan, Peoples R China
[2] Hunan Inst Sci & Technol, Dept Chem & Chem Engn, Yueyang 414006, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
Chiral separation; Extraction; Kinetics; Metoprolol; Tartrate; SUPPORTED LIQUID-MEMBRANE; BETA-CYCLODEXTRIN; AMINO-ALCOHOLS; SEPARATION; ENANTIOSEPARATION; CHROMATOGRAPHY; PHENYLALANINE; CRYSTALLIZATION; EQUILIBRIUM; DERIVATIVES;
D O I
10.1016/j.procbio.2016.10.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This paper reports on the kinetic study on reactive extraction of metoprolol (MT) enantiomers using cyclohexyl (D)-tartrate (DT) and boric acid (BA) as combined chiral selector in a modified Lewis cell. An interfacial reaction model is applied to understanding the experimental data. The MT enantiomers are extracted enantioselectively from aqueous phase through the interfacial reaction among BA, DT and MT. Important factors that influence the kinetics of extraction are investigated. The optimal conditions for kinetic study were as follows: agitation speed of 75 rpm, interfacial area of 12.56 cm(2), pH of 6, initial DT concentration of 0.075 mol/L, initial BA concentration of 0.1 mol/L, and initial MT concentration of 5 mmol/L at temperature of 5 degrees C. Important parameters concerning extraction kinetics are evaluated through multiple linear regression analysis of the experimental data. The interfacial reaction is 0.4, 0.6 and 1 order separately with respect to BA, MT and DT, and the total order of reaction is about 2. The forward rate constants have been found to be 5.24 x 10(-4) L/(mol s) for (R)-MT and 2.73 x 10(-4) L/(mol s) for (S)-MT. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:276 / 282
页数:7
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