Research output: Contribution to journal › Article › peer-review
A rotating disk sorptive extraction based on hydrophilic deep eutectic solvent formation. / Shishov, Andrey; Volodina, Natalia; Gagarionova, Svetlana; Shilovskikh, Vladimir; Bulatov, Andrey.
In: Analytica Chimica Acta, Vol. 1141, 02.01.2021, p. 163-172.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - A rotating disk sorptive extraction based on hydrophilic deep eutectic solvent formation
AU - Shishov, Andrey
AU - Volodina, Natalia
AU - Gagarionova, Svetlana
AU - Shilovskikh, Vladimir
AU - Bulatov, Andrey
N1 - Funding Information: The study was supported by a grant from the President of the Russian Federation MK-1154.2020.3. Scientific research was partially performed at Chemical Analysis and Materials Research Centre of Saint Petersburg State University. Publisher Copyright: © 2020 Elsevier B.V. Copyright: Copyright 2020 Elsevier B.V., All rights reserved.
PY - 2021/1/2
Y1 - 2021/1/2
N2 - An elegant preconcentration method assumed sorption of polar analytes from complex non-polar matrices on a rotating disk based on hydrophilic deep eutectic solvent formation is presented for the first time. The surface of poly(vinylidene fluoride-co-tetrafluoroethylene) rotating disk was coated with choline chloride acted as a precursor of deep eutectic solvent (hydrogen bond acceptor). The rotating disk was immersed in vegetable oil sample and phenolic compounds (hydrogen bond donors) were efficient separated on the disk during its rotation due to deep eutectic solvent formation. Ability of hydrophilic deep eutectic solvent decomposition in aqueous phase was used for fast analytes elution from the disk surface (2 min). Finally, the obtained aqueous solution of phenolic compounds and choline chloride was analyzed by high-performance liquid chromatography with fluorescence detection. Under optimal conditions, the limits of detection for gallic acid, protocatechuic acid, tyrosol, vanillic acid, p-coumarinic acid, syringaldehyde and thymol were in the range of 10–60 μg L−1. The developed approach allowed to significantly reduce sorption and elution time in comparison with previously reported rotating disk sorptive extraction approaches. The extraction mechanism based on deep eutectic solvent formation provided selective separation of target analytes with absolute extraction recovery in the range of 66–87%.
AB - An elegant preconcentration method assumed sorption of polar analytes from complex non-polar matrices on a rotating disk based on hydrophilic deep eutectic solvent formation is presented for the first time. The surface of poly(vinylidene fluoride-co-tetrafluoroethylene) rotating disk was coated with choline chloride acted as a precursor of deep eutectic solvent (hydrogen bond acceptor). The rotating disk was immersed in vegetable oil sample and phenolic compounds (hydrogen bond donors) were efficient separated on the disk during its rotation due to deep eutectic solvent formation. Ability of hydrophilic deep eutectic solvent decomposition in aqueous phase was used for fast analytes elution from the disk surface (2 min). Finally, the obtained aqueous solution of phenolic compounds and choline chloride was analyzed by high-performance liquid chromatography with fluorescence detection. Under optimal conditions, the limits of detection for gallic acid, protocatechuic acid, tyrosol, vanillic acid, p-coumarinic acid, syringaldehyde and thymol were in the range of 10–60 μg L−1. The developed approach allowed to significantly reduce sorption and elution time in comparison with previously reported rotating disk sorptive extraction approaches. The extraction mechanism based on deep eutectic solvent formation provided selective separation of target analytes with absolute extraction recovery in the range of 66–87%.
KW - Deep eutectic solvent
KW - HPLC-FLD
KW - Phenolic compounds
KW - Rotating disk
KW - Rotating disk sorptive extraction
KW - Sorption
KW - Vegetable oil
KW - GRAPHENE
KW - SILICA
KW - SOLID-PHASE EXTRACTION
KW - WATER
UR - http://www.scopus.com/inward/record.url?scp=85094317842&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/1d8becbb-6297-3d1e-83d1-87059ee4d9a3/
U2 - 10.1016/j.aca.2020.10.020
DO - 10.1016/j.aca.2020.10.020
M3 - Article
AN - SCOPUS:85094317842
VL - 1141
SP - 163
EP - 172
JO - Analytica Chimica Acta
JF - Analytica Chimica Acta
SN - 0003-2670
ER -
ID: 70790871