Field-amplified sample injection combined with capillary electrophoresis for the simultaneous determination of five chlorophenols in water samples

被引:26
作者
Gao, Fangfang [1 ,3 ]
Chen, Xiaoxia [2 ]
Li, Xiaobin [1 ]
Li, Jinhua [3 ]
Liu, Huitao [1 ]
Chen, Lingxin [3 ]
机构
[1] Yantai Univ, Coll Chem & Chem Engn, Yantai, Peoples R China
[2] Hebei Univ Sci & Technol, Hebei Res Ctr Anal & Testing, Shijiazhuang, Hebei, Peoples R China
[3] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Res Ctr Coastal Environm Engn & Technol, CAS Key Lab Coastal Environm Proc & Ecol Remediat, Yantai, Peoples R China
基金
中国国家自然科学基金;
关键词
Capillary electrophoresis; Chlorophenols; Field-amplified sample injection; Water samples; ASSISTED ELECTROKINETIC INJECTION; LIQUID-LIQUID MICROEXTRACTION; SOLID-PHASE EXTRACTION; ENVIRONMENTAL WATER; PHENOLIC-COMPOUNDS; IMPRINTED POLYMERS; TRACE ANALYSIS; CHROMATOGRAPHY; STACKING; OPTIMIZATION;
D O I
10.1002/elps.201800532
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive method of CZE-ultraviolet (UV) detection based on the on-line preconcentration strategy of field-amplified sample injection (FASI) was developed for the simultaneous determination of five kinds of chlorophenols (CPs) namely 4-chlorophenol (4-CP), 2-chlorophenol (2-CP), 2,4-dichlorophenol (2,4-DCP), 2,4,6-trichlorophenol (2,4,6-TCP), and 2,6-dichlorophenol (2,6-DCP) in water samples. Several parameters affecting CZE and FASI conditions were systematically investigated. Under the optimal conditions, sensitivity enhancement factors for 4-CP, 2-CP, 2,4-DCP, 2,4,6-TCP, and 2,6-DCP were 9, 27, 35, 43, and 43 folds, respectively, compared with the direct CZE, and the baseline separation was achieved within 5 min. Then, the developed FASI-CZE-UV method was applied to tap and lake water samples for the five CPs determination. The LODs (S/N = 3) were 0.0018-0.019 mu g/mL and 0.0089-0.029 mu g/mL in tap water and lake water, respectively. The values of LOQs in tap water (0.006-0.0074 mu g/mL) were much lower than the maximum permissible concentrations of 2,4,6-TCP, 2,4-DCP, and 2-CP in drinking water stipulated by World Health Organization (WHO) namely 0.3, 0.04, and 0.01 mu g/mL, respectively, and thereby the method was suitable to detect the CPs according to WHO guidelines. Furthermore, the method attained high recoveries in the range of 83.0-119.0% at three spiking levels of five CPs in the two types of water samples, with relative standard deviations of 0.37-8.58%. The developed method was proved to be a simple, sensitive, highly automated, and efficient alternative to CPs determination in real water samples.
引用
收藏
页码:1771 / 1778
页数:8
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