Reequilibration time of superficially porous silica based columns in gradient elution reversed phase liquid chromatography

被引:11
作者
VanMiddlesworth, Bradley J. [1 ]
Dorsey, John G. [1 ]
机构
[1] Florida State Univ, Dept Chem & Biochem, Tallahassee, FL 32306 USA
基金
美国国家科学基金会;
关键词
Superficially porous silica; Fused core; Reequilibration time; Gradient elution; Reversed-phase; Aqueous-organic interface; AQUEOUS MOBILE PHASES; SHELL PARTICLES; PERFORMANCE; TEMPERATURE; ORIENTATION; MECHANISM;
D O I
10.1016/j.chroma.2011.08.030
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Between repetitive analyses using gradient elution liquid chromatography the column must be reequilibrated to the initial conditions, extending run times. We studied the reequilibration time of three superficially porous silica columns compared to one fully porous silica column on a chromatograph with a reduced flush-out volume. Post-gradient acetone injections made at the interface of the pure organic-highly aqueous phase show anomalous, pressure-related band focusing, and increased retention compared to injections on either side of the interface. These anomalies are explained by applying the Buckley-Leverett theory of oil displacement in sands to column reequilibration. Reequilibration was shown to occur quickly, with less than three column volumes of conditioning solvent, and depends on the reproducibility as required by the application. Offline LC-GC was used to quantitate the percent acetonitrile eluting from each column post-gradient. After an initial, large expulsion of acetonitrile, a steady small amount (similar to 0.03%) of acetonitrile is detected long after the column is considered equilibrated. The limiting variable with column equilibration is not the desorption of organic modifier from the stationary phase, but rather the pressure required to force the aqueous phase into the pores. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:7158 / 7165
页数:8
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