Semiautomatic method for the ultra-trace arsenic speciation in environmental waters via magnetic solid phase extraction prior to HPLC-ICP-MS determination

dc.centroFacultad de Cienciases_ES
dc.contributor.authorMontoro-Leal, Pablo
dc.contributor.authorGarcía-Mesa, Juan Carlos
dc.contributor.authorLópez-Guerrero, María del Mar
dc.contributor.authorSiles-Cordero, María Teresa
dc.contributor.authorVereda-Alonso, Elisa Isabel
dc.date.accessioned2021-01-08T08:45:20Z
dc.date.available2021-01-08T08:45:20Z
dc.date.created2020
dc.date.issued2021-01-08
dc.departamentoQuímica Analítica
dc.descriptionSHOTGUN PRESENTATIONes_ES
dc.description.abstractA new magnetic functionalized material based on graphene oxide magnetic nanoparticles (MGO) was designed and characterized in order to develop a magnetic solid phase extraction method (MSPE) to enrich both inorganic and organic arsenic species in environmental waters. A FIA system is used to preconcentrate the arsenic species simultaneously, while the ultra-trace separation and determination of arsenobetaine (AsBet), cacodylate, As(III) and As(V) species have been achieved by high performance liquid chromatography coupled to inductively coupled plasma mass spectrometry (HPLC-ICP-MS) technique. The sample is introduced in the FIA system where the MSPE takes place, and 1 ml of eluent is collected in a chromatographic vial. After preconcentration, the vial is introduced in the autosampler of HPLC-ICP-MS. Therefore, preconcentration and separation/determination processes are automatic and conducted separately (Figure 1). The strategy of this work was focused on the compatibility between the MSPE eluent and the mobile phase of HPLC column system, resulting in an efficient and reliable semiautomatic preconcentration and detection of inorganic and organic arsenic speciation. To the best of our knowledge, this is the first method combining an online MSPE and HPLC-MS, and one of the first using a magnetic nanomaterial based on MGO for online MSPE. Under the optimized conditions, the preconcentration factors obtained for AsBet, cacodilate, As(III) and As(V) with 12 mL sample solution were 4, 12, 6 and 19, respectively. The LODs for the arsenic species were AsBet 7 ng L -1, cacodylate 0.4 ng L-1, As(III) 1.0 ng L-1 and As(V) 0.2 ng L-1 and RSDs < 5%. The developed method was validated by analyzing tap water, well water and seawater samples, and Certified Reference Materials; fortified lake water TMDA 64.3 and seawater Cass-6 NRC, promising for routine monitoring of arsenic species in environmental wateres_ES
dc.description.sponsorshipUniversidad de Málaga. Campus de Excelencia Internacional Andalucía Tech Fondos FEDER y Junta de Andalucía Proyecto UMA18-FEDERJA-060 Plan Propio, Proyecto Puente, Universidad de Málagaes_ES
dc.identifier.urihttps://hdl.handle.net/10630/20667
dc.language.isoenges_ES
dc.relation.eventdateDel 30/11/2020 al 03/12/2020es_ES
dc.relation.eventplaceCaparica (Portugal)es_ES
dc.relation.eventtitle4 th International Caparica Christmas Conference on Sample Treatment 2020es_ES
dc.rights.accessRightsopen accesses_ES
dc.subjectExtracción (Química)es_ES
dc.subjectArsénicoes_ES
dc.subjectNanopartículases_ES
dc.subject.otherSpeciationes_ES
dc.subject.otherArsenices_ES
dc.subject.otherMSPEes_ES
dc.subject.otherHPLC-ICP-MSes_ES
dc.titleSemiautomatic method for the ultra-trace arsenic speciation in environmental waters via magnetic solid phase extraction prior to HPLC-ICP-MS determinationes_ES
dc.typeconference outputes_ES
dspace.entity.typePublication
relation.isAuthorOfPublication79951f8b-a0de-4c85-9aa0-545906d745fe
relation.isAuthorOfPublication98eedf62-d065-420d-af2c-8094def4bcd4
relation.isAuthorOfPublicationa33d331d-0317-4e4d-8473-4155d01e910c
relation.isAuthorOfPublication.latestForDiscovery79951f8b-a0de-4c85-9aa0-545906d745fe

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