Estimation of the phase ratio in reversed-phase high-performance liquid chromatography

被引:35
作者
Moldoveanu, Serban [1 ]
David, Victor [2 ]
机构
[1] RJ Reynolds Tobacco Co, Winston Salem, NC 27101 USA
[2] Univ Bucharest, Fac Chem, Bucharest, Romania
关键词
Phase ratio; Retention factor; Solvophobic theory; Van der Waals molecular surface area; Octanol/water partition coefficient; SOLVATION ENERGY RELATIONSHIPS; STATIONARY-PHASE; MOBILE-PHASE; EXCESS ADSORPTION; MODIFIED SILICA; VOID VOLUME; RP-HPLC; RETENTION; PARTITION; SOLVENT;
D O I
10.1016/j.chroma.2015.01.034
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phase ratio Phi for an HPLC column is a common parameter being defined as the ratio between the volume of the stationary phase V-st and the void volume of the column V-0. Although apparently simple, the evaluation of phase ratio presents difficulties because there is no sharp boundary between the mobile phase and the stationary phase, and different mobile phases lead to different "effective" phase ratios. A considerable number of studies have been dedicated to the evaluation of V-st and V-0 with the goal of obtaining the value for Phi. However, the parameter is seldom reported for common commercially available columns and key information for its calculation (e.g. the weight of column packing) is not typically reported by the vendors. Present study describes a novel procedure for the evaluation of phase ratio for a chromatographic column when used with a given mobile phase. The procedure allows the calculation of Phi only from the measurements of retention factors k' for two hydrocarbons i and j, for which the octanol/water partition coefficients log K-ow are known. A theoretical support for this procedure based on solvophobic theory of interactions in solution is presented, and several experimental results reported in the literature are used to demonstrate the validity of the procedure. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:194 / 201
页数:8
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