TY - JOUR
T1 - Organic solvent-free elevated temperature liquid–liquid extraction combined with a new switchable deep eutectic solvent-based dispersive liquid–liquid microextraction of three phenolic antioxidants from oil samples
AU - Afshar Mogaddam, Mohammad Reza
AU - Farajzadeh, Mir Ali
AU - Tuzen, Mustafa
AU - Jouyban, Abolghasem
AU - Khandaghi, Jalil
N1 - Publisher Copyright:
© 2021
PY - 2021/9
Y1 - 2021/9
N2 - An organic solvent-free extraction procedure using elevated temperature liquid–liquid extraction/ dispersive liquid–liquid microextraction based on deep eutectic solvent has been performed for the extraction of three synthetic phenolic antioxidants from oil samples. In the developed approach, firstly the antioxidants were extracted into an aqueous alkaline solution in an elevated temperature. Then, a few microliters of deep eutectic solvent formed from tetrabutylammonium chloride and hydroquinone was dissolved in the alkaline solution and a homogenous solution was obtained. In the following it was dispersed into an acidic solution. In this step, an acid–base reaction was occurred and the analytes were migrated into the fine droplets of the deep eutectic solvent. The extracted analytes were determined by gas chromatography-flame ionization detector. Validation data showed that low limits of detection (0.13–0.42 ng/mL) and quantification (0.36–1.41 ng/mL), high extraction recovery (74–89%) and enrichment factor (370–445), and good precision (relative standard deviation ≤ 7.4%) can be obtained by the developed method. Finally, the method was used for quantification of the antioxidants in several edible oil samples.
AB - An organic solvent-free extraction procedure using elevated temperature liquid–liquid extraction/ dispersive liquid–liquid microextraction based on deep eutectic solvent has been performed for the extraction of three synthetic phenolic antioxidants from oil samples. In the developed approach, firstly the antioxidants were extracted into an aqueous alkaline solution in an elevated temperature. Then, a few microliters of deep eutectic solvent formed from tetrabutylammonium chloride and hydroquinone was dissolved in the alkaline solution and a homogenous solution was obtained. In the following it was dispersed into an acidic solution. In this step, an acid–base reaction was occurred and the analytes were migrated into the fine droplets of the deep eutectic solvent. The extracted analytes were determined by gas chromatography-flame ionization detector. Validation data showed that low limits of detection (0.13–0.42 ng/mL) and quantification (0.36–1.41 ng/mL), high extraction recovery (74–89%) and enrichment factor (370–445), and good precision (relative standard deviation ≤ 7.4%) can be obtained by the developed method. Finally, the method was used for quantification of the antioxidants in several edible oil samples.
KW - Deep eutectic solvent
KW - Dispersive liquid–liquid extraction
KW - Edible oil
KW - Gas chromatography–flame ionization detection
KW - Liquid–liquid extraction
UR - https://www.scopus.com/pages/publications/85107799376
U2 - 10.1016/j.microc.2021.106433
DO - 10.1016/j.microc.2021.106433
M3 - Article
AN - SCOPUS:85107799376
SN - 0026-265X
VL - 168
JO - Microchemical Journal
JF - Microchemical Journal
M1 - 106433
ER -