Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol

A multivariate version of the classical univariate standard addition method is tested as a proof of concept for the voltammetric analysis of complex samples generating overlapped signals in the presence of significant matrix effects. The proposed strategy applies a multivariate calibration method su...

Descripción completa

Detalles Bibliográficos
Autores: Martínez, Kassandra, Ariño Blasco, Cristina, Díaz Cruz, José Manuel, Serrano i Plana, Núria, Esteban i Cortada, Miquel
Tipo de recurso: artículo
Estado:Versión aceptada para publicación
Fecha de publicación:2018
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2445/122531
Acceso en línea:https://hdl.handle.net/2445/122531
Access Level:acceso abierto
Palabra clave:Quimiometria
Voltametria
Chemometrics
Voltammetry
id ES_aeb002ff038f4e728ee83424910de4a1
oai_identifier_str oai:recercat.cat:2445/122531
network_acronym_str ES
network_name_str España
repository_id_str
spelling Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catecholMartínez, KassandraAriño Blasco, CristinaDíaz Cruz, José ManuelSerrano i Plana, NúriaEsteban i Cortada, MiquelQuimiometriaVoltametriaChemometricsVoltammetryA multivariate version of the classical univariate standard addition method is tested as a proof of concept for the voltammetric analysis of complex samples generating overlapped signals in the presence of significant matrix effects. The proposed strategy applies a multivariate calibration method such as partial least squares (PLS) to the full voltammograms measured for the sample alone and after combined additions of a series of standard solutions (one for every analyte). Then, a calibration model is built and further applied to the prediction of the concentration added to a blank, i.e., a full voltammetric signal measured in the absence of analytes. The absolute value of such predicted concentration is taken as the concentration of the analyte in the sample. The method has been successfully tested in different natural water samples spiked with hydroquinone and catechol and appears to be a promising tool for the analysis of overlapped signals in complex matrices.Elsevier B.V.2018202020182018info:eu-repo/semantics/articleinfo:eu-repo/semantics/acceptedVersion7 p.application/pdfhttps://hdl.handle.net/2445/122531Articles publicats en revistes (Enginyeria Química i Química Analítica)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésVersió postprint del document publicat a: https://doi.org/10.1016/j.chemolab.2018.05.002Chemometrics and Intelligent Laboratory Systems, 2018, vol. 178, p. 32-38https://doi.org/10.1016/j.chemolab.2018.05.002cc-by-nc-nd (c) Elsevier B.V., 2018http://creativecommons.org/licenses/by-nc-nd/3.0/esinfo:eu-repo/semantics/openAccessoai:recercat.cat:2445/1225312026-05-29T05:05:01Z
dc.title.none.fl_str_mv Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
title Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
spellingShingle Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
Martínez, Kassandra
Quimiometria
Voltametria
Chemometrics
Voltammetry
title_short Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
title_full Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
title_fullStr Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
title_full_unstemmed Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
title_sort Multivariate standard addition for the analysis of overlapping voltammetric signals in the presence of matrix effects: Application to the simultaneous determination of hydroquinone and catechol
dc.creator.none.fl_str_mv Martínez, Kassandra
Ariño Blasco, Cristina
Díaz Cruz, José Manuel
Serrano i Plana, Núria
Esteban i Cortada, Miquel
author Martínez, Kassandra
author_facet Martínez, Kassandra
Ariño Blasco, Cristina
Díaz Cruz, José Manuel
Serrano i Plana, Núria
Esteban i Cortada, Miquel
author_role author
author2 Ariño Blasco, Cristina
Díaz Cruz, José Manuel
Serrano i Plana, Núria
Esteban i Cortada, Miquel
author2_role author
author
author
author
dc.subject.none.fl_str_mv Quimiometria
Voltametria
Chemometrics
Voltammetry
topic Quimiometria
Voltametria
Chemometrics
Voltammetry
description A multivariate version of the classical univariate standard addition method is tested as a proof of concept for the voltammetric analysis of complex samples generating overlapped signals in the presence of significant matrix effects. The proposed strategy applies a multivariate calibration method such as partial least squares (PLS) to the full voltammograms measured for the sample alone and after combined additions of a series of standard solutions (one for every analyte). Then, a calibration model is built and further applied to the prediction of the concentration added to a blank, i.e., a full voltammetric signal measured in the absence of analytes. The absolute value of such predicted concentration is taken as the concentration of the analyte in the sample. The method has been successfully tested in different natural water samples spiked with hydroquinone and catechol and appears to be a promising tool for the analysis of overlapped signals in complex matrices.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018
2018
2020
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/acceptedVersion
format article
status_str acceptedVersion
dc.identifier.none.fl_str_mv https://hdl.handle.net/2445/122531
url https://hdl.handle.net/2445/122531
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv Versió postprint del document publicat a: https://doi.org/10.1016/j.chemolab.2018.05.002
Chemometrics and Intelligent Laboratory Systems, 2018, vol. 178, p. 32-38
https://doi.org/10.1016/j.chemolab.2018.05.002
dc.rights.none.fl_str_mv cc-by-nc-nd (c) Elsevier B.V., 2018
http://creativecommons.org/licenses/by-nc-nd/3.0/es
info:eu-repo/semantics/openAccess
rights_invalid_str_mv cc-by-nc-nd (c) Elsevier B.V., 2018
http://creativecommons.org/licenses/by-nc-nd/3.0/es
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 7 p.
application/pdf
dc.publisher.none.fl_str_mv Elsevier B.V.
publisher.none.fl_str_mv Elsevier B.V.
dc.source.none.fl_str_mv Articles publicats en revistes (Enginyeria Química i Química Analítica)
reponame:Recercat. Dipósit de la Recerca de Catalunya
instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
reponame_str Recercat. Dipósit de la Recerca de Catalunya
collection Recercat. Dipósit de la Recerca de Catalunya
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1869416602056785920
score 15,812429