Application of dispersive liquid-liquid microextraction and high-performance liquid chromatography for the determination of three phthalate esters in water samples

被引:258
作者
Liang, Pei [1 ]
Xu, Jing [1 ]
Li, Qian [1 ]
机构
[1] Cent China Normal Univ, Coll Chem, Key Lab Pesticide & Chem Biol, Minist Educ, Wuhan 430079, Peoples R China
关键词
dispersive liquid-liquid microextraction; high-performance liquid chromatography; phthalate esters; water samples;
D O I
10.1016/j.aca.2007.12.025
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A novel method, dispersive liquid-liquid microextraction (DLLME) coupled with high-performance liquid chromatography-variable wavelength detector (HPLC-VWD), has been developed for the determination of three phthalate esters (dimethyl phthalate (DMP), diethyl phthalate (DEP), and di-n-butyl phthalate (DnBP)) in water samples. A mixture of extraction solvent (41 mu L carbon tetrachloride) and dispersive solvent (0.75 mL acetonitrile) were rapidly injected into 5.0 mL aqueous sample for the formation of cloudy solution, the analytes in the sample were extracted into the fine droplets of CCl4. After extraction, phase separation was performed by centrifugation and the enriched analytes in the sedimented phase were determined by HPLC-VWD. Some important parameters, such as the kind and volume of extraction solvent and dispersive solvent, extraction time and salt effect were investigated and optimized. Under the optimum extraction condition, the method yields a linear calibration curve in the concentration range from 5 to 5000 ng mL(-1) for target analytes. The enrichment factors for DMP, DEP and DnBP were 45, 92 and 196, respectively, and the limits of detection were 1.8, 0.88 and 0.64 ng mL(-1), respectively. The relative standard deviations (R.S.D.) for the extraction of 10 ng mL(-1) of phthalate esters were in the range of 4.3-5.9% (n = 7). Lake water, tap water and bottled mineral water samples were successfully analyzed using the proposed method. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 58
页数:6
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