Contributions of theory to method development in solid-phase extraction

化学 色谱法 固相萃取 萃取(化学) 相(物质) 有机化学
作者
Colin F. Poole,Ajith D. Gunatilleka,Revathy Sethuraman
出处
期刊:Journal of Chromatography A [Elsevier BV]
卷期号:885 (1-2): 17-39 被引量:231
标识
DOI:10.1016/s0021-9673(00)00224-7
摘要

The kinetic and retention properties of solid-phase extraction devices are reviewed from the perspective of method development strategies. Models based on frontal analysis are used to correct retention properties of solid-phase extraction devices to account for the fact that too few theoretical plates are provided for retention to be independent of kinetic factors. The available pressure drop for the sampling device largely dictates the choice of useful particle sizes and maximum bed length. The use of octanol–water partition coefficients and extrapolated values of the retention factor obtained by liquid chromatography are poor empirical models for the estimation of breakthrough volumes with water as the sample solvent. The solvation parameter model provides an adequate description of sorbent retention for the estimation of breakthrough volumes, rinse solvent volume and composition, and elution solvent volume and composition. Combining the frontal analysis and solvation parameter models offers a comprehensive approach to computer-aided method development in solid-phase extraction. This is the first step in the development of a structure-driven approach to method development in solid-phase extraction that should be more reliable and less tedious than traditional trial and error approaches.
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