High-resolution separation performance of poly(caprolactone)diol for challenging isomers of xylenes, phenols and anilines by capillary gas chromatography

被引:23
作者
Peng, Jianlin
Zhang, Yan
Yang, Xiaohong
Qi, Meiling [1 ]
机构
[1] Beijing Inst Technol, Key Lab Cluster Sci, Minist Educ China, Beijing Key Lab Photoelect Electrophoton Convers, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
Capillary gas chromatography; Stationary phase; Poly(caprolactone)diol; Selectivity; Positional isomers; LIQUID-LIQUID MICROEXTRACTION; MASS-SPECTROMETRY; SIMULTANEOUS DERIVATIZATION; STATIONARY PHASES; CHLOROPHENOLS; ETHYLBENZENE; OPTIMIZATION; EXTRACTION; COLUMNS; CRYSTAL;
D O I
10.1016/j.chroma.2016.09.005
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Efficient separation of xylenes., phenols and anilines is a big issue in chemical and petroleum industries. This work presents the first example of employing poly (caprolactone) diol (PCL-Diol) as stationary phase for high-resolution gas chromatographic (GC) separations of these tough isomer mixtures. It showed medium polarity and stronger H-bonding basicity than H-bonding acidity. Impressively, PCL-Diol column exhibited extremely high resolving capability for the isomer mixtures of xylenes, cresols/xylenols, and toluidines/xylidines with good peak shapes. Moreover, it exhibited preferential retention for analytes of a linear alkyl chain, suggesting its shape fitting selectivity for specific analytes. In addition, its separation performance has good repeatability with RSD values on retention times below 0.01% for run to run (n = 6), 0.67-0.80% for day to day (n =4) and 3.2-4.4% for column to column (n =4) repeatability, respectively. Furthermore, it was applied for the determination of isomer impurities in real samples, showing good potential for practical use. This work demonstrates the advantageous high-resolution separation performance for challenging isomers and shows its promising future of PCL-Diol-based materials in separation science. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:148 / 154
页数:7
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