Determination of Fe, Cu, and Pb in edible oils using choline chloride:ethylene glycol deep eutectic solvent-based dispersive liquid-liquid microextraction associated with microwave-induced plasma optical emission spectrometry

Please use this identifier to cite or link to this item: http://hdl.handle.net/10045/141904
Información del item - Informació de l'item - Item information
Title: Determination of Fe, Cu, and Pb in edible oils using choline chloride:ethylene glycol deep eutectic solvent-based dispersive liquid-liquid microextraction associated with microwave-induced plasma optical emission spectrometry
Authors: Zapater, Cristina | Aguirre Pastor, Miguel Ángel | González-Gallardo, Nerea | Ramón, Diego J. | Vidal, Lorena | Canals, Antonio
Research Group/s: Espectroscopía Atómica-Masas y Química Analítica en Condiciones Extremas | Alternative Methodologies In Chemistry (AMIC)
Center, Department or Service: Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología | Universidad de Alicante. Departamento de Química Orgánica | Universidad de Alicante. Instituto Universitario de Materiales | Universidad de Alicante. Instituto Universitario de Síntesis Orgánica
Keywords: Elemental analysis | Vegetable oils | Deep eutectic solvents | Miniaturized liquid-liquid extraction techniques | Greenness assessment | AGREEprep method
Issue Date: 26-Mar-2024
Publisher: Elsevier
Citation: Talanta. 2024, 274: 125939. https://doi.org/10.1016/j.talanta.2024.125939
Abstract: A new simple, fast and environmentally friendly deep eutectic solvent based dispersive liquid-liquid microextraction (DES-based DLLME) methodology assisted by vortex is presented for the separation and preconcentration of three elements (i.e., Fe, Cu and Pb) from edible oil samples (i.e., soybean, sunflower, rapeseed, sesame, and olive oil) prior to the determination by microwave-induced plasma optical emission spectrometry (MIP-OES). The deep eutectic solvent selected as extractant (i.e., choline chloride and ethylene glycol, 1:2) is synthesized and characterized by Fourier transform infrared spectroscopy (FT-IR), proton nuclear magnetic resonance spectroscopy (1H NMR) and differential scanning calorimetry (DSC), and the extraction conditions are optimized by a two steps experimental design. Under the optimum extraction conditions (i.e., diluted sample weight: 8.6 g; DES volume: 100 μL; extraction time: 1 min; centrifugation time and speed: 3 min and 3000 rpm; and dispersion system: vortex) the analytical method presents excellent linearity (i.e., R2 values higher than 0.99) in the range 10–500 μg kg−1, repeatability (i.e., CV values lower than 9.2%), and limits of detection (LOD) values of 3, 2 and 0.7 μg kg−1 for Pb, Fe and Cu, respectively. None of the analytes displayed amounts over the upper limit permitted by law, and recovery values of all analytes evaluated in the different samples using external standard calibration were close to 100%, which excludes significant matrix effects. Finally, AGREEprep metric has been used to evaluate the method greenness (final score of 0.47) and it has been compared successfully with previous publications for the same type of analytes and matrices.
Sponsor: This work was supported by the Spanish Ministry (PID2021-1262155OB-I00, PID2021-127332NB-I00); the Regional Government of Valencia (Spain) (CIPROM/2021/062, AICO/2021/013); and the University of Alicante (VIGROB-316FI).
URI: http://hdl.handle.net/10045/141904
ISSN: 0039-9140 (Print) | 1873-3573 (Online)
DOI: 10.1016/j.talanta.2024.125939
Language: eng
Type: info:eu-repo/semantics/article
Rights: © 2024 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Peer Review: si
Publisher version: https://doi.org/10.1016/j.talanta.2024.125939
Appears in Collections:INV - AMIC - Artículos de Revistas
INV - SP-BG - Artículos de Revistas

Files in This Item:
Files in This Item:
File Description SizeFormat 
ThumbnailZapater_etal_2024_Talanta.pdf3 MBAdobe PDFOpen Preview


Items in RUA are protected by copyright, with all rights reserved, unless otherwise indicated.