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Ionic liquid-based miniaturized aqueous biphasic system to develop an environmental-friendly analytical preconcentration method. | LitMetric

Ionic liquid-based miniaturized aqueous biphasic system to develop an environmental-friendly analytical preconcentration method.

Talanta

Department of Chemistry (Analytical Division), Universidad de La Laguna (ULL), Tenerife, 38206, Spain; University Institute of Tropical Diseases and Public Health, Universidad de La Laguna (ULL), La Laguna, Tenerife, 38206, Spain. Electronic address:

Published: October 2019

Two ILs containing guanidinium cations (butylguanidinium chloride -CGu-Cl- and hexylguanidinium chloride -CGu-Cl-) were synthesized and characterized. Their cytotoxicity was also assessed, obtaining adequate CC values of 680 ± 99 mg·L for CGu-Cl and 135 ± 8 mg·L for CGu-Cl. Miniaturized aqueous biphasic systems (μ-ABSs) were developed using amounts lower than 1% (w/w) of these synthesized guanidinium-based ILs, KPO as salting-out agent, and ultrapure water. The phases diagrams of both systems were determined, and the CGu-Cl-based μ-ABS was selected for the development of a microextraction method in combination with high performance liquid chromatography (HPLC) with fluorescence detection (FD) for the determination of five polycyclic aromatic hydrocarbons (PAHs) as model analytes. A point of the biphasic region of the CGu-Cl-based μ-ABS corresponding to a mixture of 0.75% (w/w) of the IL, 37.7% (w/w) of KPO and 61.55% (w/w) of ultrapure water, and 30 min of equilibrium time, were selected as optimum conditions to obtain high enrichment factors and proper analytical microextraction performance. The CGu-Cl-based μ-ABS-HPLC-FD method exhibited low limits of detection, between 0.010 ng·L and 2.0 ng·L, average relative recoveries of 96.7%, high enrichment factors ranging from 44.1 to 60.4, average extraction efficiencies of 61.7%, and intermediate precision relative standard deviations lower than 17% for a concentration level of 12 ng·L. The developed method was applied successfully in the analysis of different tap water samples.

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http://dx.doi.org/10.1016/j.talanta.2019.05.083DOI Listing

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