Evaluation of the separation performance of polyvinylpyrrolidone as a virtual stationary phase for chromatographic NMR

被引:13
|
作者
Huang, Shaohua [1 ]
Wu, Rui [2 ]
Bai, Zhengwu [2 ]
Yang, Ying [1 ]
Li, Suying [1 ]
Dou, Xiaowei [1 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Key Lab Biobased Mat, Qingdao 266101, Peoples R China
[2] Wuhan Inst Technol, Sch Chem & Environm Engn, Wuhan 430073, Peoples R China
基金
中国国家自然科学基金;
关键词
NMR; H-1; chromatographic NMR; polyvinylpyrrolidone; virtual stationary phase; diffusion resolution; DIFFUSION-ORDERED SPECTROSCOPY; NUCLEAR-MAGNETIC-RESONANCE; LIQUID-CHROMATOGRAPHY; MIXTURE COMPONENTS; ORGANIC-SOLVENT; SMALL MOLECULES; RESOLUTION; MICELLES; RETENTION; SIZE;
D O I
10.1002/mrc.4102
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polyvinylpyrrolidone (PVP) was used as a virtual stationary phase to separate p-xylene, benzyl alcohol, and p-methylphenol by the chromatographic NMR technique. The effects of concentration and weight-average molecular weight (Mw) of PVP, solvent viscosity, solvent polarity, and sample temperature on the resolution of these components were investigated. It was found that both higher PVP concentration and higher PVP Mw caused the increase of diffusion resolution for the three components. Moreover, the diffusion resolution did not change at viscosity-higher solvents. Moreover, the three components showed different resolution at different solvents. As temperature increased, the diffusion resolution between p-xylene and benzyl alcohol gradually increased, and the one between p-xylene and p-methylphenol slightly increased from 278 to 298 K and then decreased above 298 K. It was also found that the polarity of the analytes played an important role for the separation by affecting the diffusion coefficient. Copyright (C) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:486 / 490
页数:5
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