Simultaneous derivatization and air-assisted liquid-liquid microextraction of some parabens in personal care products and their determination by GC with flame ionization detection

被引:36
作者
Farajzadeh, Mir Ali [1 ]
Khosrowshahi, Elnaz Marzi [1 ]
Khorram, Parisa [1 ]
机构
[1] Univ Tabriz, Fac Chem, Dept Analyt Chem, Tabriz 5166614766, Iran
关键词
Derivatization; Microextraction; Parabens; Personal care products; PHASE MICROEXTRACTION; COSMETIC PRODUCTS; MASS-SPECTROMETRY; EXTRACTION; CHROMATOGRAPHY; WATER; PRESERVATIVES; OPTIMIZATION; TRICLOSAN; SAMPLES;
D O I
10.1002/jssc.201300436
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simultaneous derivatization/air-assisted liquid-liquid microextraction technique has been developed for the sample pretreatment of some parabens in aqueous samples. The analytes were derivatized and extracted simultaneously by a fast reaction/extraction with butylchloroformate (derivatization agent/extraction solvent) from the aqueous samples and then analyzed by GC with flame ionization detection. The effect of catalyst type and volume, derivatization agent/extraction solvent volume, ionic strength of aqueous solution, pH, numbers of extraction, aqueous sample volume, etc. on the method efficiency was investigated. Calibration graphs were linear in the range of 2-5000g/L with squared correlation coefficients >0.990. Enhancement factors and enrichment factors ranged from 1535 to 1941 and 268 to 343, respectively. Detection limits were obtained in the range of 0.41-0.62g/L. The RSDs for the extraction and determination of 250g/L of each paraben were <4.9% (n = 6). In this method, the derivatization agent and extraction solvent were the same and there is no need for a dispersive solvent, which is common in a traditional dispersive liquid-liquid microextraction technique. Furthermore, the sample preparation time is very short.
引用
收藏
页码:3571 / 3578
页数:8
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