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Oxidation of imidacloprid insecticide through PMS activation using CuFe2O4 nanoparticles: Role of process parameters and surface modifications

dc.contributor.authorNúñez-de la Rosa, Yeison
dc.contributor.authorBroterson, Yoisel B.
dc.contributor.authorBallesteros-Ballesteros, Vladimir A.
dc.contributor.authorDurango, Luis Guillermo Cuadrado
dc.contributor.authorToledo, Jorge Luis Nisperuza
dc.contributor.authorForim, Moacir Rossi
dc.contributor.authorde Souza, Fernanda Lourdes
dc.contributor.authorHammer, Peter [UNESP]
dc.contributor.authorAquino, José M.
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionFaculty of Engineering and Basic Sciences
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T19:14:48Z
dc.date.issued2024-08-01
dc.description.abstractThe contamination of water bodies by synthetic organic compounds coupled with climate change and the growing demand for water supply calls for new approaches to water management and treatment. To tackle the decontamination issue, the activation of peroxymonosulfate (PMS) using copper magnetic ferrite (CuMF) nanoparticles prepared under distinct synthesis conditions was assessed to oxidize imidacloprid (IMD) insecticide. After optimization of some operational variables, such as CuMF load (62.5–250 mg L−1), PMS concentration (250–1000 μM), and solution pH (3-10), IMD was completely oxidized in 2 h without interferences from leached metal ions. Such performance was also achieved when using tap water but was inhibited by a simulated municipal wastewater due to scavenging effects promoted by inorganic and organic species. Although there was evidence of the presence of sulfate radicals and singlet oxygen oxidizing species, only four intermediate compounds were detected by liquid chromatography coupled to mass spectrometry analysis, mainly due to hydroxyl addition reactions. Concerning the changes in surface properties of CuMF after use, no morphological or structural changes were observed except a small increase in the charge transfer resistance. Based on the changes of terminal surface groups, PMS activation occurred on Fe sites.en
dc.description.affiliationFederal University of São Carlos (UFSCar) Department of Chemistry, SP
dc.description.affiliationFundación Universitaria Los Libertadores Faculty of Engineering and Basic Sciences
dc.description.affiliationSão Paulo University Institute of Chemistry of São Carlos Department of Chemistry and Molecular Physics, Trabalhador São-Carlense Avenue, 400
dc.description.affiliationSão Paulo State University (UNESP) Institute of Chemistry Department of Physical Chemistry, SP
dc.description.affiliationUnespSão Paulo State University (UNESP) Institute of Chemistry Department of Physical Chemistry, SP
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFinanciadora de Estudos e Projetos
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFinanciadora de Estudos e Projetos: #01.22.0179.00
dc.description.sponsorshipIdFAPESP: #2014/50918-7
dc.description.sponsorshipIdFAPESP: #2019/07943-4
dc.description.sponsorshipIdFAPESP: #2021/13604-8
dc.description.sponsorshipIdCNPq: #305943/2020-0
dc.description.sponsorshipIdCNPq: #307800/2021-0
dc.description.sponsorshipIdCNPq: #310055/2023-7
dc.description.sponsorshipIdCNPq: #406537/2021-6
dc.description.sponsorshipIdCNPq: #465357/2014-8
dc.identifierhttp://dx.doi.org/10.1016/j.chemosphere.2024.142558
dc.identifier.citationChemosphere, v. 362.
dc.identifier.doi10.1016/j.chemosphere.2024.142558
dc.identifier.issn1879-1298
dc.identifier.issn0045-6535
dc.identifier.scopus2-s2.0-85195828443
dc.identifier.urihttps://hdl.handle.net/11449/302533
dc.language.isoeng
dc.relation.ispartofChemosphere
dc.sourceScopus
dc.subjectAdvanced oxidation process
dc.subjectEmerging contaminants
dc.subjectHeterogeneous catalysis
dc.subjectHydroxyl radicals
dc.subjectIn situ chemical activation
dc.titleOxidation of imidacloprid insecticide through PMS activation using CuFe2O4 nanoparticles: Role of process parameters and surface modificationsen
dc.typeArtigopt
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.orcid0000-0001-9564-8384 0000-0001-9564-8384[1]
unesp.author.orcid0000-0001-6099-9846[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt

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