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Rare earth metal as a dopant element: Cerium ion as an articulator in hexavalent chromium removal by magnetic iron oxides

dc.contributor.authorChagas, Pricila Maria Batista
dc.contributor.authorLima, Maísa M.M.
dc.contributor.authorCaetano, Aline Aparecida
dc.contributor.authorCarvalho, Lucas Bragança [UNESP]
dc.contributor.authorPiva, Nayra Maria de Abreu
dc.contributor.authorLuiz, Maria Eduarda Resende
dc.contributor.authorGuimarães, Iara do Rosário
dc.contributor.institutionUniversidade Federal de Lavras (UFLA)
dc.contributor.institutionUniversity of California
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T20:16:01Z
dc.date.issued2023-10-01
dc.description.abstractThis study highlights introducing the rare earth metal cerium (Ce(IV)) into the structure of magnetite (Fe3O4) to achieve enhanced adsorptive properties for the removal of chromium (Cr(VI)) from an aqueous medium. Different ratios of Ce(IV) were introduced into the iron oxide matrix, termed FeCe-5, FeCe-10, and FeCe-20. Their numerical values correspond to the nominal content of the dopant element added to the synthesis medium. The solid materials were characterized for morphology and chemical structure, and N2 physical adsorption/desorption measurements were performed. The solid materials doped with Ce(IV) have a high surface area compared to Fe3O4, and the solid material with the highest content of the dopant ion (Ce(IV)) has a 4-fold greater surface area. This increase in the dopant content in the iron oxide structure leads to a total chromium removal of 93.3%. Isotherms studies on the solid materials show that chromium adsorption follows the Langmuir model. The adsorption capacity to Fe3O4 is 12.59 mg/g and FeCe-10 is 22.49 mg/g at 35 °C. By fitting the kinetic and isothermal models, it is found that for the Fe3O4 and FeCe-10 materials Cr(VI) removal occurs in very different ways, attributed to the different surface areas and compositions of the oxide, with the formation of the goethite (α-FeOOH) phase. The FeCe-10 reuse process was performed and the removal capacity the Cr(VI) is reduced after the first cycle. This result is attributed to a strong and irreversible adsorption of Cr(VI) on the FeCe-10.en
dc.description.affiliationLaboratory of Environmental Catalysis and New Materials Department of Chemistry Federal University of Lavras, MG
dc.description.affiliationDepartment of Viticulture & Enology University of California
dc.description.affiliationInstitute of Science and Technology São Paulo State University
dc.description.affiliationUnespInstitute of Science and Technology São Paulo State University
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent1616-1626
dc.identifierhttp://dx.doi.org/10.1016/j.jre.2022.08.019
dc.identifier.citationJournal of Rare Earths, v. 41, n. 10, p. 1616-1626, 2023.
dc.identifier.doi10.1016/j.jre.2022.08.019
dc.identifier.issn1002-0721
dc.identifier.scopus2-s2.0-85165247829
dc.identifier.urihttps://hdl.handle.net/11449/309601
dc.language.isoeng
dc.relation.ispartofJournal of Rare Earths
dc.sourceScopus
dc.subjectAdsorption
dc.subjectBimetallic oxides
dc.subjectCr(VI)
dc.subjectFe–Ce interaction
dc.subjectOxygen vacancies
dc.subjectRare earths
dc.titleRare earth metal as a dopant element: Cerium ion as an articulator in hexavalent chromium removal by magnetic iron oxidesen
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0001-5198-3092[1]
unesp.author.orcid0000-0001-8070-5112 0000-0001-8070-5112[2]
unesp.author.orcid0000-0003-3849-9479[3]
unesp.author.orcid0000-0002-1956-0580[4]

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