Selectivity equivalence of poly(ethylene glycol) stationary phases for gas chromatography

被引:44
|
作者
Poole, CF
Li, QL
Kiridena, W
Koziol, WW
机构
[1] Wayne State Univ, Dept Chem, Detroit, MI 48202 USA
[2] Flint Ink N Amer, Analyt Div, Ann Arbor, MI 48105 USA
关键词
stationary phases; GC; selectivity equivalence; poly(ethylene glycol);
D O I
10.1016/S0021-9673(00)00829-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The solvation parameter model is used to study differences in selectivity for poly(ethylene glycol) stationary phases for packed column (Carbowax 20M) and fused-silica, open-tubular column (HP-20M, AT-Wax, HP-INNOWax and DB-FFAP) gas chromatography. All phases are dipolar, strongly hydrogen-bond basic with no hydrogen-bond acidity and of moderate cohesion. No two phases are exactly alike, however, and selectivity differences identified with cavity formation and dispersion interactions, n- and pi -electron pair interactions, dipole-type interactions and hydrogen-bond interactions are quantified by differences in the system constants at a fixed temperature where retention occurs solely by gas-liquid partitioning. The system constants vary linearly with temperature over the range 60-140 degreesC (except for n- and pi -electron pair interactions which are temperature invariant) facilitating a general comparison of the importance of temperature on selectivity differences for compared phases. From a mechanistic point of view it is demonstrated that selectivity differences can result from chemical differences between the poly(ethylene glycol) stationary phases and from differences in the relative contribution of interfacial adsorption to the retention mechanism. The latter depends on both system properties and solute characteristics. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:211 / 226
页数:16
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