Improved sensitivity gas chromatography-mass spectrometry determination of parabens in waters using ionic liquids

被引:20
|
作者
Ignacio Cacho, Juan [1 ]
Campillo, Natalia [1 ]
Vinas, Pilar [1 ]
Hernandez-Cordoba, Manuel [1 ]
机构
[1] Univ Murcia, Fac Chem, Dept Analyt Chem, E-30100 Murcia, Spain
关键词
Parabens; Waters; Ionic liquid (IL); Dispersive liquid-liquid microextraction (DLLME); Direct microvial insert thermal desorption; Gas chromatography-mass spectrometry (GC-MS); BAR SORPTIVE EXTRACTION; SOLID-PHASE MICROEXTRACTION; ENDOCRINE DISRUPTING CHEMICALS; SINGLE-DROP MICROEXTRACTION; IN-SITU DERIVATIZATION; THERMAL-DESORPTION; ORGANIC-COMPOUNDS; METHYL TRICLOSAN; TRACE ANALYSIS; SAMPLES;
D O I
10.1016/j.talanta.2015.09.022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new procedure for the introduction of ionic liquid samples in gas chromatography (GC) is proposed. This procedure, based on microvial insert thermal desorption, allows the direct analysis of the compounds preconcentrated by ionic liquid based liquid-liquid microextraction (IL-LLME) using the combination of a thermal desorption unit (TDU) and a programmed temperature vaporization injector (PTV). Two different IL-LLME methodologies, one based on the formation of a microdroplet emulsion by dispersive liquid-liquid microextraction (DLLME) and other through ultrasound-assisted emulsification microextraction (USAEME) were studied and evaluated. IL-DLLME proved advantageous and consequently, it was adopted for preconcentration purposes. This easy to apply approach was used for the determination of five parabens (methyl-, ethyl-, propyl-, butyl- and isobutyl paraben) in swimming pool waters, after in situ acetylation. The optimized conditions of TDU/PTV allowed the analytes contained in 20 mu L of the enriched IL to be transferred to the capillary column. Quantification of the samples was carried out against aqueous standards, and quantification limits of between 43 and 8.1 ng L-1 were obtained, depending on the compound. Concentrations of between 9 and 47 ng L-1 for some analytes were obtained in the analysis of ten samples. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:568 / 574
页数:7
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