4.6 Article

New low viscous hydrophobic deep eutectic solvents for the ultrasound-assisted dispersive liquid-liquid microextraction of endocrine-disrupting phenols in water, milk and beverage

期刊

JOURNAL OF CHROMATOGRAPHY A
卷 1662, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.chroma.2021.462728

关键词

Low viscous hydrophobic deep eutectic; solvent; Dispersive liquid-liquid microextraction; Endocrine-disrupting phenols

资金

  1. Fundamental Research Funds for the Central Universities [DUT18RC (4) 058]

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In this study, several new hydrophobic deep eutectic solvents (HDESs) were prepared and utilized in an ultrasound-assisted dispersive liquid-liquid microextraction method for the determination of endocrine-disrupting phenols (EDPs). The results showed that the obtained HDES exhibited good extraction efficiency.
In the present work, several new hydrophobic deep eutectic solvents (HDESs) were prepared with quaternary ammonium salts as hydrogen bond acceptors (HBAs) and salicylate esters as hydrogen bond donors (HBDs). Then, the obtained HDESs were used as extraction solvents to establish an ultrasound-assisted dispersive liquid-liquid microextraction method combined with high-performance liquid chromatographyultraviolet detection technique for the determination of four endocrine-disrupting phenols (EDPs) compounds. One of the obtained HDESs composed of tetrabutylammonium chloride (N 4 4 4 4 Cl) and methyl salicylate possessed a viscosity of 89.28 mPa center dot s lower than most reported ionic HDESs ( > 200 mPa center dot s), and the low viscous HDES was selected as the optimal extraction solvent. Several key parameters affecting the extraction efficiency were investigated, including the type and volume of HDES, ultrasound time, sample solution pH and salt addition. Under the optimized experimental conditions, the proposed method had good coefficients of determination ( R 2 > 0.9976) in the linear range of 0.5-400 mu g center dot L -1 , the limits of quantification and limits of detection respectively were 0.5-2.5 mu g center dot L -1 and 0.25-1 mu g center dot L -1 , and the recoveries were in the range of 81.79-109.82%. Finally, the method was used for the preconcentration and determination of EDPs in different samples, including bottled water, tea beverage and milk. (c) 2021 Elsevier B.V. All rights reserved.

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