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...
| Autores: | , , , , |
|---|---|
| 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 |
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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 |
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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) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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