Enhancing Trace Metal Extraction from Wastewater: Magnetic Activated Carbon as a High-Performance Sorbent for Inductively Coupled Plasma Optical Emission Spectrometry Analysis

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Títol: Enhancing Trace Metal Extraction from Wastewater: Magnetic Activated Carbon as a High-Performance Sorbent for Inductively Coupled Plasma Optical Emission Spectrometry Analysis
Autors: Abellán-Martín, Sergio J. | Villalgordo-Hernández, David | Aguirre Pastor, Miguel Ángel | Ramos-Fernández, Enrique V. | Narciso, Javier | Canals, Antonio
Grups d'investigació o GITE: Espectroscopía Atómica-Masas y Química Analítica en Condiciones Extremas | Materiales Avanzados
Centre, Departament o Servei: Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología | Universidad de Alicante. Departamento de Química Inorgánica | Universidad de Alicante. Instituto Universitario de Materiales
Paraules clau: Magnetic dispersive solid-phase extraction (MDSPE) | Magnetic activated carbon | Trace metal analysis | Multivariate optimization | Wastewater samples | Inductively coupled plasma optical emission spectrometry (ICP OES)
Data de publicació: 10-de novembre-2023
Editor: MDPI
Citació bibliogràfica: Abellán-Martín SJ, Villalgordo-Hernández D, Aguirre MÁ, Ramos-Fernández EV, Narciso J, Canals A. Enhancing Trace Metal Extraction from Wastewater: Magnetic Activated Carbon as a High-Performance Sorbent for Inductively Coupled Plasma Optical Emission Spectrometry Analysis. Separations. 2023; 10(11):563. https://doi.org/10.3390/separations10110563
Resum: A new fast, sensitive, and environmentally friendly analytical method has been developed for the simultaneous determination of Ba, Be, Cd, Cr, Cu, Fe, Hg, Mn, Ni, Pb, and Zn in wastewater samples using inductively coupled plasma optical emission spectroscopy (ICP OES). A preconcentration step using a magnetic dispersive solid-phase extraction (MDSPE) technique with a new magnetic sorbent was performed. The new sorbent material was a carbon containing magnetic cobalt and nitrogen groups. This material was synthetized using controlled pyrolysis of a zeolitic imidazolate framework (i.e., ZIF-67). In order to optimize the experimental parameters that affect the MDSPE procedure, a multivariate optimization strategy, using Plackett–Burman and circumscribed central composite designs (CCD), was used. The method has been evaluated employing optimized experimental conditions (i.e., sample weight, 10 g; sample pH, 7.6; amount of sorbent, 10 mg; dispersive agent, vortex; complexing agent concentration, 0.5%; ionic concentration, 0%; eluent, HCl; eluent concentration, 0.5 M; eluent volume, 300 μL; elution time, 3 min and extraction time, 3 min) using external calibration. Limits of detection (LODs) in a range from 0.073 to 1.3 μg L−1 were obtained, and the repeatability was evaluated at two different levels, resulting in relative standard deviations below 8% for both levels (n = 5). An increase in the sensitivity was observed due to the high enrichment factors (i.e., 3.2 to 13) obtained compared with direct ICP OES analysis. The method was also validated through carrying out recovery studies that employed a real wastewater sample and through the analysis of a certified reference material (ERM®-CA713). The recovery values obtained with the real wastewater were between 94 and 108% and between 90 and 109% for the analysis of ERM®-CA713, showing negligible matrix effects.
Patrocinadors: This research was funded by the Ministry of Spain grant number (PID2021-126155OB-I00, and PID2020-116998RB-I00) and by the Regional Government of Valencia (Spain) grant number (CIPROM/2021/062, CIPROM/2021/022, INVEST/2022/70, and PRTR-C17.I1).
URI: http://hdl.handle.net/10045/138580
ISSN: 2297-8739
DOI: 10.3390/separations10110563
Idioma: eng
Tipus: info:eu-repo/semantics/article
Drets: © 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Revisió científica: si
Versió de l'editor: https://doi.org/10.3390/separations10110563
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