Wear metals determination in lubricating oils by reversed-phase dispersive liquid-liquid microextraction and microwave induced plasma optical emission spectrometry

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Título: Wear metals determination in lubricating oils by reversed-phase dispersive liquid-liquid microextraction and microwave induced plasma optical emission spectrometry
Autor/es: Sáez, Carmen | Stoitsov, Dimitar | Aguirre Pastor, Miguel Ángel | Kmetov, Veselin Y. | Coscollà, Clara | Canals, Antonio
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: Wear metals determination | Lubricating oils | Liquid-liquid microextraction | Microwave induced plasma optical emission spectrometry
Fecha de publicación: 15-dic-2023
Editor: Royal Society of Chemistry
Cita bibliográfica: Journal of Analytical Atomic Spectrometry. 2024, 39: 370-377. https://doi.org/10.1039/D3JA00319A
Resumen: A periodic study of the engine oil can allow to anticipate possible breakdowns that the vehicle could have. Due to the complexity of the matrix of this type of samples, a sample treatment prior to analysis is necessary. Analytical chemistry is constantly searching for simpler, more sensitive and environmentally friendly methods. The reverse phase dispersive liquid-liquid microextraction fulfills all the characteristics for the analysis in this type of sample by microwave plasma atomic emission spectrometry (MIP OES). In this work, the extractant solvent used for the microextraction procedure is a diluted acid solution (i.e., 3 M HCl), which is a less-hazardous solvent, in comparison with other solvent used in microextraction procedures. Besides, it is perfectly compatible with MIP OES. The main experimental factors affecting the extraction of Cr, Cu, Mn, Mo, and Ni (i.e., amount of sample, extractant type, acid concentration, extractant volume, extractant time, and centrifugation time and speed) are optimized using a multivariate analysis consisting in two steps: a Plackett-Burman design followed by a circumscribed central composite design. Under optimum conditions (i.e., amount of sample: 5.9 g; extractant volume: 60 µL; extractant type: HCl; acid concentration: 3 M; extraction time: 3 min; centrifugation time: 3 min; centrifugation speed: 2000 rpm), the proposed analytical method is validated and employed to analyze different samples (i.e., used and unused engine oils). Two calibration methods have been evaluated since matrix effects have been observed in the used engine oil sample. These effects have been eliminated using standard addition calibration obtaining RSD and recovery values in the range of 4-12 % and 94-106 % respectively, for samples spiked with 1 µg g-1 of Cr, Cu, Mn, Mo and Ni. Finally, the greenness of this method has been assessed by the Eco-Scale metrics.
Patrocinador/es: The authors would like to thank the Spanish Ministry of Science and Innovation (PID2021-126155OB-I00), the Regional Government of Valencia (Spain) (CIPROM/2021/062), and University of Alicante (UAIND21-03C) for the financial support. 15% of this study is financed by the European Union-NextGenerationEU, through the National Recovery and Resilience Plan of the Republic of Bulgaria, project number BG-RRP-2.004-0001-C01. This article is based upon work from the Sample Preparation Study Group and Network, supported by the Division of Analytical Chemistry of the European Chemical Society. Finally, the authors would also like to thank Agilent Technologies Inc. for the loan of the MIP OES spectrometer and Ingeniatrics for the OneNeb® Series 2 provided. This work is part of the PhD. Degree of C. S.
URI: http://hdl.handle.net/10045/139304
ISSN: 0267-9477 (Print) | 1364-5544 (Online)
DOI: 10.1039/D3JA00319A
Idioma: eng
Tipo: info:eu-repo/semantics/article
Derechos: This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Revisión científica: si
Versión del editor: https://doi.org/10.1039/D3JA00319A
Aparece en las colecciones:INV - SP-BG - Artículos de Revistas

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