Determination of malachite green and crystal violet in environmental water using temperature-controlled ionic liquid dispersive liquid-liquid microextraction coupled with high performance liquid chromatography

被引:53
作者
Zhang, Zhen [1 ,3 ]
Zhou, Kai [1 ]
Bu, Yuan-qin [4 ]
Shan, Zheng-jun [4 ]
Liu, Jing-fu [3 ]
Wu, Xiang-yang [1 ]
Yang, Liu-qing [1 ]
Chen, Zhong-lin [2 ]
机构
[1] Jiangsu Univ, Sch Environm, Zhenjiang 212013, Peoples R China
[2] Harbin Inst Technol, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
[3] Chinese Acad Sci, State Key Lab Environm Chem & Ecotoxicol, Ecoenvironm Sci Res Ctr, Beijing 100085, Peoples R China
[4] Minist Environm Protect, Nanjing Inst Environm Sci, State Key Lab Pesticide Risk Assessment & Pollut, Nanjing 210042, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
TANDEM MASS-SPECTROMETRY; SOLID-PHASE EXTRACTION; LEUCOMALACHITE GREEN; MICRO-EXTRACTION; EXPERIMENTAL-DESIGN; ORGANIC-COMPOUNDS; GENTIAN-VIOLET; NATURAL-WATERS; SAMPLES; OPTIMIZATION;
D O I
10.1039/c2ay05665h
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Temperature-controlled ionic liquid dispersive liquid-liquid microextraction (TC-IL-DLLME) was introduced to analyze malachite green (MG) and crystal violet (CV) in environmental water by coupling with high performance liquid chromatography (HPLC). In the method, 1-octyl-3-methylimidazolium hexafluorophosphate ([C8MIM][PF6]) and methanol were selected as appropriate extraction and dispersive solvents, respectively. Target compounds were extracted into the IL phase (dispersed completely in the aqueous phase) at a proper temperature. Several other parameters that could affect extraction performance were optimized, such as IL volume, sample pH, salinity, extraction time, temperature and centrifuging velocity. Under the optimum conditions (IL volume, 80 mu L; sample pH, 4; salinity, 20% sodium chloride; extraction time, 50 min; temperature, 70 degrees C; centrifuging velocity, 1500 rpm), the established method offered: (i) good linear range (0.25-20 mu g L-1); (ii) low detection limits (MG, 0.086 mu g L-1; CV, 0.030 mu g L-1); (iii) good reproducibility (relative standard deviation, MG, 9.4%; CV, 7.6%; n = 5) and good recoveries (91.7% for MG and 97.2% for CV, respectively; n 5); (iv) high enrichment factor (254 for MG, 276 for CV), which makes the method suitable to monitor low concentrations of MG and CV in aqueous systems.
引用
收藏
页码:429 / 433
页数:5
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