Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe

Bibliographic Details
Main Author: Ferreira, Dennis S.
Publication Date: 2024
Other Authors: Pereira, Fabiola M.V. [UNESP], Olivieri, Alejandro C., Pereira-Filho, Edenir R.
Format: Article
Language: eng
Source: Repositório Institucional da UNESP
Download full: http://dx.doi.org/10.1016/j.aca.2024.342522
https://hdl.handle.net/11449/304530
Summary: Background: Electronic waste (e-waste) proliferation and its implications underscore the imperative for advanced analytical methods to mitigate its environmental impact. It is estimated that e-waste production stands at a staggering 20–50 million tons yearly, of which merely 20–25% undergo formal recycling. The e-waste samples evaluated contain computers, laptops, smartphones, and tablets. Results: Forty-one samples were processed, involving the disassembly and separation of components. Subsequently, two analytical techniques, laser-induced breakdown spectroscopy (LIBS) and energy dispersive X-ray fluorescence (ED-XRF), were applied to quantify aluminum (Al), copper (Cu), and iron (Fe) in the e-waste samples. The samples were then analyzed after acid mineralization with 50% v v−1 aqua regia in a digester block and finally by ICP OES. A solid residue composed of Si and Ti was observed after the digestion of the samples. Multivariate calibration strategies such as partial least-squares regression (PLS), principal component regression (PCR), maximum likelihood principal component regression (MLPCR), and error covariance penalized regression (ECPR) were used for calibration. Finally, the figures of merit were calculated to verify the most suitable models. The results revealed robust models with notable sensitivity, varying from 8.98 to 35.04 Signal (a.u.)(% w w−1) −1, low Limits of Detection (LoD) within the range of 0.001–0.2 % w w−1, and remarkable relative errors ranging from 2% to 33%, particularly for Cu and Fe. Significance: Notably, the models for Al faced inherent challenges, thus highlighting the complexities associated with its quantification in e-waste samples. In conclusion, this research represents an important step toward a more sustainable and efficient future for electronic waste recycling, signifying its relevance to global environmental welfare and resource conservation.
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spelling Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and FeData fusionE-wasteFigure of meritLIBSMultivariate calibrationBackground: Electronic waste (e-waste) proliferation and its implications underscore the imperative for advanced analytical methods to mitigate its environmental impact. It is estimated that e-waste production stands at a staggering 20–50 million tons yearly, of which merely 20–25% undergo formal recycling. The e-waste samples evaluated contain computers, laptops, smartphones, and tablets. Results: Forty-one samples were processed, involving the disassembly and separation of components. Subsequently, two analytical techniques, laser-induced breakdown spectroscopy (LIBS) and energy dispersive X-ray fluorescence (ED-XRF), were applied to quantify aluminum (Al), copper (Cu), and iron (Fe) in the e-waste samples. The samples were then analyzed after acid mineralization with 50% v v−1 aqua regia in a digester block and finally by ICP OES. A solid residue composed of Si and Ti was observed after the digestion of the samples. Multivariate calibration strategies such as partial least-squares regression (PLS), principal component regression (PCR), maximum likelihood principal component regression (MLPCR), and error covariance penalized regression (ECPR) were used for calibration. Finally, the figures of merit were calculated to verify the most suitable models. The results revealed robust models with notable sensitivity, varying from 8.98 to 35.04 Signal (a.u.)(% w w−1) −1, low Limits of Detection (LoD) within the range of 0.001–0.2 % w w−1, and remarkable relative errors ranging from 2% to 33%, particularly for Cu and Fe. Significance: Notably, the models for Al faced inherent challenges, thus highlighting the complexities associated with its quantification in e-waste samples. In conclusion, this research represents an important step toward a more sustainable and efficient future for electronic waste recycling, signifying its relevance to global environmental welfare and resource conservation.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Consejo Nacional de Investigaciones Científicas y TécnicasUniversidad Nacional de RosarioAgencia Nacional de Promoción Científica y TecnológicaGroup of Applied Instrumental Analysis (GAIA) Department of Chemistry Federal University of São Carlos (UFSCar), P.O. Box 676Group of Alternative Analytical Approaches (GAAA) Bioenergy Research Institute (IPBEN) Institute of Chemistry São Paulo State University (UNESP), São PauloDepartamento de Química Analítica Facultad de Ciencias Bioquímicas y Farmacéuticas Universidad Nacional de Rosario, Suipacha 531Instituto de Química Rosario (CONICET-UNR), 27 de Febrero 210 BisGroup of Alternative Analytical Approaches (GAAA) Bioenergy Research Institute (IPBEN) Institute of Chemistry São Paulo State University (UNESP), São PauloCNPq: 140867/2021–0CNPq: 302085/2022–0CNPq: 302719/2020–2CNPq: 307328/2019–8Agencia Nacional de Promoción Científica y Tecnológica: PICT 2020–00179Universidade Federal de São Carlos (UFSCar)Universidade Estadual Paulista (UNESP)Universidad Nacional de RosarioInstituto de Química Rosario (CONICET-UNR)Ferreira, Dennis S.Pereira, Fabiola M.V. [UNESP]Olivieri, Alejandro C.Pereira-Filho, Edenir R.2025-04-29T19:35:12Z2024-05-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1016/j.aca.2024.342522Analytica Chimica Acta, v. 1303.1873-43240003-2670https://hdl.handle.net/11449/30453010.1016/j.aca.2024.3425222-s2.0-85188961195Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengAnalytica Chimica Actainfo:eu-repo/semantics/openAccess2025-05-28T05:22:54Zoai:repositorio.unesp.br:11449/304530Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462025-05-28T05:22:54Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
title Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
spellingShingle Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
Ferreira, Dennis S.
Data fusion
E-waste
Figure of merit
LIBS
Multivariate calibration
title_short Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
title_full Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
title_fullStr Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
title_full_unstemmed Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
title_sort Electronic waste analysis using laser-induced breakdown spectroscopy (LIBS) and X-ray fluorescence (XRF): Critical evaluation of data fusion for the determination of Al, Cu and Fe
author Ferreira, Dennis S.
author_facet Ferreira, Dennis S.
Pereira, Fabiola M.V. [UNESP]
Olivieri, Alejandro C.
Pereira-Filho, Edenir R.
author_role author
author2 Pereira, Fabiola M.V. [UNESP]
Olivieri, Alejandro C.
Pereira-Filho, Edenir R.
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Federal de São Carlos (UFSCar)
Universidade Estadual Paulista (UNESP)
Universidad Nacional de Rosario
Instituto de Química Rosario (CONICET-UNR)
dc.contributor.author.fl_str_mv Ferreira, Dennis S.
Pereira, Fabiola M.V. [UNESP]
Olivieri, Alejandro C.
Pereira-Filho, Edenir R.
dc.subject.por.fl_str_mv Data fusion
E-waste
Figure of merit
LIBS
Multivariate calibration
topic Data fusion
E-waste
Figure of merit
LIBS
Multivariate calibration
description Background: Electronic waste (e-waste) proliferation and its implications underscore the imperative for advanced analytical methods to mitigate its environmental impact. It is estimated that e-waste production stands at a staggering 20–50 million tons yearly, of which merely 20–25% undergo formal recycling. The e-waste samples evaluated contain computers, laptops, smartphones, and tablets. Results: Forty-one samples were processed, involving the disassembly and separation of components. Subsequently, two analytical techniques, laser-induced breakdown spectroscopy (LIBS) and energy dispersive X-ray fluorescence (ED-XRF), were applied to quantify aluminum (Al), copper (Cu), and iron (Fe) in the e-waste samples. The samples were then analyzed after acid mineralization with 50% v v−1 aqua regia in a digester block and finally by ICP OES. A solid residue composed of Si and Ti was observed after the digestion of the samples. Multivariate calibration strategies such as partial least-squares regression (PLS), principal component regression (PCR), maximum likelihood principal component regression (MLPCR), and error covariance penalized regression (ECPR) were used for calibration. Finally, the figures of merit were calculated to verify the most suitable models. The results revealed robust models with notable sensitivity, varying from 8.98 to 35.04 Signal (a.u.)(% w w−1) −1, low Limits of Detection (LoD) within the range of 0.001–0.2 % w w−1, and remarkable relative errors ranging from 2% to 33%, particularly for Cu and Fe. Significance: Notably, the models for Al faced inherent challenges, thus highlighting the complexities associated with its quantification in e-waste samples. In conclusion, this research represents an important step toward a more sustainable and efficient future for electronic waste recycling, signifying its relevance to global environmental welfare and resource conservation.
publishDate 2024
dc.date.none.fl_str_mv 2024-05-15
2025-04-29T19:35:12Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1016/j.aca.2024.342522
Analytica Chimica Acta, v. 1303.
1873-4324
0003-2670
https://hdl.handle.net/11449/304530
10.1016/j.aca.2024.342522
2-s2.0-85188961195
url http://dx.doi.org/10.1016/j.aca.2024.342522
https://hdl.handle.net/11449/304530
identifier_str_mv Analytica Chimica Acta, v. 1303.
1873-4324
0003-2670
10.1016/j.aca.2024.342522
2-s2.0-85188961195
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Analytica Chimica Acta
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv repositoriounesp@unesp.br
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