Issue 4, 2014

Off-line hyphenation of molecularly imprinted magnetic nanoparticle-based extraction with large volume sample stacking capillary electrophoresis for high-sensitivity detection of trace chloro-phenols

Abstract

The present work developed a sensitive and selective method for the determination of 4-chlorophenol (4-CP), 2,4-dichlorophenol (2,4-DCP) and 2,4,6-trichlorophenol (2,4,6-TCP) in an environmental water sample by molecularly imprinted magnetic nanoparticle (Fe3O4@MIP) based extraction coupled with capillary electrophoresis (CE). The highly selective, fast and effective sample pretreatment method with Fe3O4@MIPs can overcome the low sensitivity of the highly efficient capillary electrophoresis-ultraviolet detection method (CE-UV). In order to further improve the detection sensitivity, the analytes eluted from the Fe3O4@MIPs were analyzed by the on-line sample preconcentration large volume sample stacking (LVSS) technique with MEKC. Under optimal concentration conditions, signal enhancements of 781, 3276 and 8916-fold were achieved for 4-CP, 2,4-DCP and 2,4,6-TCP, respectively. The average recoveries of the three analytes in spiked water samples were 99.33–104.5% with a relative standard deviation (RSD) below 6.8%. The detection limits for 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol were 1.1 × 10−3, 2.13 × 10−4 and 6.68 × 10−5 μg mL−1, respectively.

Graphical abstract: Off-line hyphenation of molecularly imprinted magnetic nanoparticle-based extraction with large volume sample stacking capillary electrophoresis for high-sensitivity detection of trace chloro-phenols

Article information

Article type
Paper
Submitted
16 Sep 2013
Accepted
11 Dec 2013
First published
13 Dec 2013

Anal. Methods, 2014,6, 1219-1226

Off-line hyphenation of molecularly imprinted magnetic nanoparticle-based extraction with large volume sample stacking capillary electrophoresis for high-sensitivity detection of trace chloro-phenols

S. Qi, H. Zhang, Q. Zhu, H. Chen, Y. Dong, L. Zhou, C. Ren and X. Chen, Anal. Methods, 2014, 6, 1219 DOI: 10.1039/C3AY41606B

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