Modelling of retention behaviour of solutes in micellar liquid chromatography

被引:81
作者
GarciaAlvarezCoque, MC
TorresLapasio, JR
BaezaBaeza, JJ
机构
[1] Depto. de Quim. Analítica, Facultad de Química, Universidad de Valencia, 46100-Burjassot, Valencia
关键词
reviews; retention models; micellar liquid chromatography; mobile phase composition;
D O I
10.1016/S0021-9673(97)00051-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In micellar liquid chromatography (MLC), the resolution for a given multi-component mixture can be optimized by changing several variables, such as the concentrations of surfactant and organic modifier, the pH and temperature. However, this advantage can only be fully exploited with the development of mathematical models that describe the retention and the separation mechanisms. Several reports have appeared recently on the possibilities of accurately predicting the solute retention in MLC. Although the retention and selectivity may strongly change with varying concentrations of surfactant, organic modifier and/or pH, the observed changes are very regular, and are well described by simple models. This characteristic enables a successful prediction of retention times and compensates the negative effect of the broad and tailed chromatographic peaks obtained for some solutes when micellar eluents are used. An overview of the models proposed in the literature to describe the retention behaviour in pure micellar eluents and micellar eluents containing an organic modifier, at a fixed pH or at varying pH, is given. The equations derived permit the evaluation of the strength of micelle-solute and stationary phase-solute interactions. The prediction of the retention based on molecular properties and the use of neural networks, together with the factors affecting the prediction capability of the models (linearization of the equations, dead time, critical micellar concentration, ionic strength and temperature) are commented on. The strategies used for the optimization of resolution are also given. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:129 / 148
页数:20
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