Investigation of the temperature dependence of water adsorption on silica-based stationary phases in hydrophilic interaction liquid chromatography

被引:10
作者
Barto, Endre [1 ,2 ]
Felinger, Attila [1 ,2 ,3 ]
Jandera, Pavel [4 ]
机构
[1] Univ Pecs, Dept Analyt & Environm Chem, Ifjasag Utja 6, H-7624 Pecs, Hungary
[2] Univ Pecs, Szentdgothai Res Ctr, Ifjasag Utja 6, H-7624 Pecs, Hungary
[3] MTA PTE Mol Interact Separat Sci Res Grp, Ifjusag Utja 6, H-7624 Pecs, Hungary
[4] Univ Pardubice, Dept Analyt Chem, Studentska 573, CZ-53210 Pardubice, Czech Republic
关键词
Aqueous normal phase liquid chromatography; HILIC; Water adsorption; Karl Fischer titration; RETENTION BEHAVIOR; POLAR COMPOUNDS; SEPARATION; COLUMNS; INTERMEDIATE;
D O I
10.1016/j.chroma.2017.02.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the present work, the adsorption of water was investigated in aqueous normal-phase liquid chromatography on Cogent Silica C and Cogent Phenyl hydride stationary phases at different temperatures by frontal analysis - using coulometric Karl Fischer titration - to compare the temperature dependence of adsorption of water from aqueous acetonitrile. The Cogent Silica-C and Cogent Phenyl Hydride columns have a silicon hydride surface (silica hydride) with less than 2% free silanol group; therefore, they do not have a strong association with water. The adsorption behavior of water on the mentioned stationary phases was modeled by Langmuir isotherm. The preferentially adsorbed water was expressed in terms of a hypothetical monomolecular water layer equivalent in the inner pores. The uptake of water slightly depends on the temperature. The adsorbed water may fill four to eight percent of the pore volume over the studied temperature range, which approximately corresponds to the equivalent of 0.24-0.68 water layer coverage of the adsorbent surface. The phenyl hydride stationary phase shows decreased water uptake in comparison to the Silica C stationary phase. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 148
页数:6
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