Evaluation of electrosprayed graphene oxide coatings for elemental analysis by thin film microextraction followed by Laser-induced Breakdown Spectroscopy detection

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Título: Evaluation of electrosprayed graphene oxide coatings for elemental analysis by thin film microextraction followed by Laser-induced Breakdown Spectroscopy detection
Autor/es: Ripoll-Seguer, Laura | Legnaioli, Stefano | Palleschi, Vincenzo | Hidalgo, Montserrat
Grupo/s de investigación o GITE: Espectroscopía Atómica-Masas y Química Analítica en Condiciones Extremas
Centro, Departamento o Servicio: Universidad de Alicante. Departamento de Química Analítica, Nutrición y Bromatología | Universidad de Alicante. Instituto Universitario de Materiales
Palabras clave: LIBS | Electrospray deposition | Graphene oxide | Thin film microextraction | Liquid samples analysis
Área/s de conocimiento: Química Analítica
Fecha de publicación: sep-2021
Editor: Elsevier
Cita bibliográfica: Spectrochimica Acta Part B: Atomic Spectroscopy. 2021, 183: 106267. https://doi.org/10.1016/j.sab.2021.106267
Resumen: In this work, a solid phase microextraction procedure, denoted as Thin Film Microextraction (TFME), was combined with Laser-induced Breakdown Spectroscopy for the detection of several analytes in aqueous solutions (Cu, Cr, Ni and Pb). The adsorbent films, consisting of a thin layer of graphene oxide deposited on glass substrates, were generated by using the electrospray deposition technique (ESD). Several parameters affecting the quality and shape of the films resulting from the ESD process were studied, and the morphology and adsorption capacity of the films were evaluated. The generated films were used for extraction of the target analytes from aqueous solutions and, after extraction, the analytes-enriched adsorbents were analysed by LIBS without the need of any desorption or elution step. In order to assess the analytical capability of the TFME-LIBS procedure, different analytical figures of merit of the proposed TFME-LIBS methodology were evaluated. The obtained limits of detection were 14 μg kg−1 for Pb and 15 μg kg−1 for the rest of the tested analytes. Measurement repeatability was better than 4% RSD at low concentration level (20 μg kg−1) but deteriorated by increasing the concentration level at 100 μg kg−1, with %RSD ranging from 3.6% (Cr) to 24% (Pb). Method trueness, evaluated from the analysis of a real sample of bottled water, led to recovery values in the range 85%–106%.
Patrocinador/es: This work was supported by the Spanish Ministry of Economy and Competitiveness [CTQ2016-79991-R], the Regional Government of Valencia (Spain) [PROMETEO/2013/038 and PROMETEO/2018/087]; and the University of Alicante [UAUSTI17-04 and UAUSTI18-04]. L. Ripoll is grateful to the Ministry of Economy and Competitiveness for her PhD fellowship (FPI-MICINN (BES-2012-058759)).
URI: http://hdl.handle.net/10045/117294
ISSN: 0584-8547 (Print) | 1873-3565 (Online)
DOI: 10.1016/j.sab.2021.106267
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: © 2021 Published by Elsevier B.V.
Revisión científica: si
Versión del editor: https://doi.org/10.1016/j.sab.2021.106267
Aparece en las colecciones:INV - SP-BG - Artículos de Revistas

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