Metal-organic framework MIL-100(Fe) as the stationary phase for both normal-phase and reverse-phase high performance liquid chromatography

被引:110
|
作者
Fu, Yan-Yan [1 ,2 ]
Yang, Cheng-Xiong [1 ,2 ]
Yan, Xiu-Ping [1 ,2 ]
机构
[1] Nankai Univ, State Key Lab Med Chem Biol, Coll Chem, Tianjin 300071, Peoples R China
[2] Nankai Univ, Res Ctr Analyt Sci, Coll Chem, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Metal-organic frameworks; Stationary phase; High performance liquid chromatography; Normal phase; Reverse phase; Isomers; COATED CAPILLARY COLUMNS; SELECTIVE ADSORPTION; XYLENE ISOMERS; MOBILE-PHASE; SEPARATION; ALKYLAROMATICS; ETHYLBENZENE; MIL-101(CR); AROMATICS; ALKANES;
D O I
10.1016/j.chroma.2012.12.015
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metal-organic framework MIL-100(Fe) was explored as a novel stationary phase for both normal-phase and reverse-phase high performance liquid chromatography. Two groups of analytes (benzene, toluene, ethylbenzene, naphthalene and 1-chloronaphthalene; aniline, acetanilide, 2-nitroaniline and 1-naphthylamine) were used to test the separation performance of MIL-100(Fe) in the reverse-phase mode, while the isomers of chloroaniline or toluidine were employed to evaluate its performance in the normal-phase mode. The MIL-100(Fe) packed column gave a baseline separation of all the tested analytes with good precision. The separation was controlled by negative enthalpy change and entropy change in the reverse-phase mode, but positive enthalpy change and entropy change in the normal-phase mode. The relative standard deviations of retention time, peak area, peak height, and half peak width for eleven replicate separations of the tested analytes were 0.2-0.7%, 0.5-3.6%, 0.6-2.3% and 0.8-1.7%, respectively. The mesoporous cages, accessible windows, excellent chemical and solvent stability, metal active sites and aromatic pore walls make MIL-100(Fe) a good candidate as a novel stationary phase for both normal-phase and reverse-phase high performance liquid chromatography. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:137 / 144
页数:8
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