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Inorganofunctionalization of Ti(IV) and Zr(IV) on the MCM-41 Surface and its Interaction with a Mixed Valence Complex to use as Isoniazid Sensing

dc.contributor.authorde Souza Magossi, Maiara [UNESP]
dc.contributor.authorFernandes, Daniela Silvestrini [UNESP]
dc.contributor.authordos Santos Franco, Fernanda [UNESP]
dc.contributor.authordos Santos Felipe, Alexsandro [UNESP]
dc.contributor.authorde Vicente, Fábio Simões [UNESP]
dc.contributor.authordo Carmo, Devaney Ribeiro [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2021-06-25T11:00:43Z
dc.date.available2021-06-25T11:00:43Z
dc.date.issued2021-01-01
dc.description.abstractIn this work, it describes the preparation of Titanium and Zirconium functionalized MCM-41 and subsequent chemical modification with nickel hexacyanoferrate. The obtained materials (MTiNiH and MZrNiH) were characterized by Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy (SEM), X-ray Dispersive Energy Spectroscopy (EDS), Porosity and Surface Area and Voltammetry Cyclic (VC). The cyclic voltammogram of MTiNiH and MZrNiH modified graphite paste were sensitive to isoniazid concentrations. The MTiNiH modified graphite pulp electrode showed an analytical curve with a linear response of 2.0 × 10–5 to 5.0 × 10–4 mol L−1 and detection limit of 6.12 × 10–6 mol L−1 and MZrNiH modified electrode showed an analytical curve with a linear response of 3.0 × 10–5 to 3.0 × 10–4 mol L−1 and detection limit of 1.66 × 10–5 mol L−1. After catalytic electro-oxidation of isoniazid, a study of the main interferents was performed and the recovery of isoniazid in a synthetic urine sample was also evaluated. The MTiNiH and MZrNiH materials stand out for presenting good detection limit and recovery efficiency in real samples. Therefore, these materials can be considered is a strong candidate for the construction of electrochemical sensors for quick and easy detection of isoniazid.en
dc.description.affiliationDepartment of Physics and Chemistry Faculty of Engineering of Ilha Solteira São Paulo State University “Júlio de Mesquita Filho”–UNESP, Av. Brasil, 56
dc.description.affiliationDepartment of Chemistry Faculty of Philosophy Sciences and Letters of Ribeirão Preto University of São Paulo Ribeirão Preto–USP, Av. Bandeirantes
dc.description.affiliationDepartment of Physics Institute of Geosciences and Exact Sciences São Paulo State University “Júlio de Mesquita Filho”–UNESP, Av. 24-A
dc.description.affiliationUnespDepartment of Physics and Chemistry Faculty of Engineering of Ilha Solteira São Paulo State University “Júlio de Mesquita Filho”–UNESP, Av. Brasil, 56
dc.description.affiliationUnespDepartment of Physics Institute of Geosciences and Exact Sciences São Paulo State University “Júlio de Mesquita Filho”–UNESP, Av. 24-A
dc.identifierhttp://dx.doi.org/10.1007/s10904-021-02025-x
dc.identifier.citationJournal of Inorganic and Organometallic Polymers and Materials.
dc.identifier.doi10.1007/s10904-021-02025-x
dc.identifier.issn1574-1451
dc.identifier.issn1574-1443
dc.identifier.scopus2-s2.0-85106408682
dc.identifier.urihttp://hdl.handle.net/11449/207767
dc.language.isoeng
dc.relation.ispartofJournal of Inorganic and Organometallic Polymers and Materials
dc.sourceScopus
dc.subjectCyclic voltammetry
dc.subjectIsoniazid
dc.subjectMesoporous silica
dc.subjectNickel hexacyanoferrate
dc.titleInorganofunctionalization of Ti(IV) and Zr(IV) on the MCM-41 Surface and its Interaction with a Mixed Valence Complex to use as Isoniazid Sensingen
dc.typeArtigo
dspace.entity.typePublication
unesp.author.orcid0000-0002-0949-6941[6]
unesp.departmentFísica e Química - FEISpt

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