Rapid quantification of imidazolium-based ionic liquids by hydrophilic interaction liquid chromatography: Methodology and an investigation of the retention mechanisms

被引:30
作者
Hawkins, Cory A. [1 ]
Rud, Anna [1 ]
Guthrie, Margaret L. [1 ]
Dietz, Mark L. [1 ]
机构
[1] Univ Wisconsin, Dept Chem & Biochem, Milwaukee, WI 53211 USA
基金
美国能源部;
关键词
Ionic liquid determination; HPLC; Aqueous normal phase; Rapid separation; Mixed-mode retention; POLAR STATIONARY PHASES; REVERSED-PHASE; MOBILE-PHASE; TEMPERATURE; SEPARATION; CATIONS; SILICA; MODE; COLUMN; WATER;
D O I
10.1016/j.chroma.2015.04.047
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The separation of nine N,N'-dialkylimidazolium-based ionic liquids (ILs) by an isocratic hydrophilic interaction high-performance liquid chromatographic method using an unmodified silica column was investigated. The chosen analytical conditions using a 90:10 acetonitrile-ammonium formate buffer mobile phase on a high-purity, unmodified silica column were found to be efficient, robust, and sensitive for the determination of ILs in a variety of solutions. The retention window (k' = 2-11) was narrower than that of previous methods, resulting in a 7-min runtime for the nine IL homologues. The lower limit of quantification of the method, 2-3 mu mol L-1, was significantly lower than those reported previously for HPLC-UV methods. The effects of systematically modifying the IL cation alkyl chain length, column temperature, and mobile-phase water and buffer content on solute retention were examined. Cation exchange was identified as the dominant retention mechanism for most of the solutes, with a distinct (single methylene group) transition to a dominant partitioning mode at the highest solute polarity. (C) 2015 Elsevier RV. All rights reserved.
引用
收藏
页码:54 / 64
页数:11
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