Determination of adsorption isotherms in supercritical fluid chromatography

被引:30
|
作者
Enmark, Martin [1 ]
Forssen, Patrik [1 ]
Samuelsson, Jorgen [1 ]
Fornstedt, Torgny [1 ]
机构
[1] Karlstad Univ, Dept Engn & Chem Sci, SE-65188 Karlstad, Sweden
基金
瑞典研究理事会;
关键词
Adsorption isotherms; Supercritical fluid chromatography; Perturbation Peak method; Elution by Characteristic Points; Retention Time Method; Inverse Method; PERTURBATION PEAK METHOD; CHIRAL STATIONARY-PHASE; HOLD-UP TIME; CARBON-DIOXIDE; ELUTION; PARAMETERS; SINGLE; ACCURACY; MIXTURES; BEHAVIOR;
D O I
10.1016/j.chroma.2013.09.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In this study we will demonstrate the potential of modern integrated commercial analytical SFC-systems for rapid and reliable acquisition of thermodynamic data. This will be done by transferring the following adsorption isotherm determination methods from liquid chromatography (LC) to supercritical fluid chromatography (SFC): Elution by Characteristic Points (ECP), the Retention Time Method (RTM), the Inverse Method (IM) and the Perturbation Peak (PP) method. In order to transfer these methods to SFC in a reliable, reproducible way we will demonstrate that careful system verification using external sensors of mass flow, temperature and pressure are needed first. The adsorption isotherm data generated by the different methods were analyzed and compared and the adsorption isotherms ability to predict new experimental elution profiles was verified by comparing experiments with simulations. It was found that adsorption isotherm data determined based on elution profiles, i.e., ECP, IM and RTM, were able to accurately predict overloaded experimental elution profiles while the more tedious and time-consuming PP method, based on small injections on concentration plateaus, failed in doing so. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:124 / 133
页数:10
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