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Theoretical treatment of ion transfers in two polarisable interface systems when the analyte has access to both interfaces.

dc.contributor.authorOlmos Martínez, José Manuel
dc.contributor.authorMolina Gómez, María de los Ángeles
dc.contributor.authorLaborda Ochando, Eduardo
dc.contributor.authorMillán-Barrios, Enrique
dc.contributor.authorOrtuño Sánchez-Pedreño, Joaquín Ángel
dc.contributor.departmentQuímica Analítica
dc.date.accessioned2024-02-10T18:25:43Z
dc.date.available2024-02-10T18:25:43Z
dc.date.created2017
dc.date.issued2018
dc.descriptionThis document is the Accepted Manuscript version of a Published Work that appeared in final form in Analytical Chemistry, copyright © 2017 American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acs.analchem.7b04321es
dc.descriptionItem en revisión, pendiente de cumplimentar metadatos.
dc.description.abstractA new theory is presented to tackle the study of transfer processes of hydrophilic ions in two polarisable interface systems when the analyte is initially present in both aqueous phases. The treatment is applied to macrointerfaces (linear diffusion) and microholes (highly convergent diffusion), obtaining analytical equations for the current response in any voltammetric technique. The novel equations predict two signals in the current-potential curves that are symmetric when the compositions of the aqueous phases are identical while asymmetries appear otherwise. The theoretical results show good agreement with the experimental behaviour of the “double transfer voltammograms” reported by Dryfe et al. in cyclic voltammetry (CV) (Anal. Chem. 2013, 86, 435-442) as well as with cyclic square wave voltammetry (cSWV) experiments here performed. The theoretical treatment is also extended to the situation where the target ion is lipophylic and it is initially present in the organic phase. The theory predicts an opposite effect of the lipophilicity of the ion on the shape of the voltammograms, which is validated experimentally via both CV and cSWV. For the above two cases, simple and manageable expressions and diagnosis criteria are derived for the qualitative and quantitative study of ions lipophilicity. The formal ion-transfer potentials can be easily quantified from the separation between the two signals making use of explicit analytical equations.es
dc.formatapplication/pdfes
dc.format.extent20es
dc.identifier.citationAnalytical Chemistry (2018), 90(3), 2088–2094
dc.identifier.doihttps://doi.org/10.1021/acs.analchem.7b04321
dc.identifier.issnElectronic: 1520-6882
dc.identifier.issnPrint: 0003-2700
dc.identifier.urihttp://hdl.handle.net/10201/139209
dc.languageenges
dc.publisherAmerican Chemical Society (ACS)es
dc.relationEsta publicación es resultante de 3 proyectos de investigación. Uno de ellos es de ámbito regional, está financiado por la Fundación Séneca de la Región de Murcia dentro de la convocatoria de “Ayudas a los Grupos y Unidades de Excelencia Científica de la Región de Murcia (2015)" y tiene por título "Advances in the study of charge transfer processes at static and dynamic micro- and nano-interfaces" (referencia 19887/GERM/15). Los otros dos proyectos son de ámbito nacional. El primero de ellos está financiado por el Ministerio de Economía y Competitividad dentro del Programa Estatal de Fomento de la Investigación Científica y Técnica de Excelencia, Subprograma Estatal de Generación de Conocimiento, convocatoria 2015, modalidad 1: Proyectos de I+D, y tiene por título "Electrocatálisis molecular en diferentes interfases: análisis de la respuesta electroquímica"(referencia CTQ2015-65243-P). El segundo de ellos está financiado por el Ministerio de Economía y Competitividad dentro de la Convocatoria 2015 de Acciones de dinamización "Redes de Excelencia" del Programa Estatal de Investigación Científica y Técnica de Excelencia, Subprograma Estatal de Generación de Conocimiento y tiene por título "Red de Excelencia Sensores y Biosensores" (referencia CTQ2015-71955-REDT)es
dc.relation.publisherversionhttps://pubs.acs.org/doi/10.1021/acs.analchem.7b04321es
dc.rightsinfo:eu-repo/semantics/openAccesses
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectTwo polarisable interfaceses
dc.subjectIon-transfer voltammetryes
dc.subjectAnalytical theoryes
dc.subjectStandard ion-transfer potentiales
dc.subjectSolvent polymeric membraneses
dc.subject.otherCDU::5 - Ciencias puras y naturaleses
dc.titleTheoretical treatment of ion transfers in two polarisable interface systems when the analyte has access to both interfaces.es
dc.typeinfo:eu-repo/semantics/articlees
dspace.entity.typePublicationes
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