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Enabling decentralized treatment of BPA through electrified photo-activated advanced oxidation

dc.contributor.authorGaber, Mohamed S.
dc.contributor.authorGarcia-Segura, Sergi
dc.contributor.authorLanza, Marcos R. V.
dc.contributor.authorSantos, Alexsandro J. dos [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)pt
dc.date.accessioned2025-12-10T16:11:59Z
dc.date.issued2026-02-25
dc.description.abstractThis study explores the integration of electrochemical hydrogen peroxide (H2O2) generation with UVC irradiation as a sustainable strategy for decentralized water treatment. H2O2 was produced in situ using a gas diffusion electrode (GDE) coupled with Ti/IrO2 or boron-doped diamond (BDD) anodes. The metal oxide Ti/IrO2 electrode enabled greater H2O2 accumulation with lower energy consumption due to a lower onset potential for water oxidation. The removal of bisphenol A (BPA) was evaluated under electrochemical oxidation (EO) and UVC-assisted conditions. Treatment with BDD outperformed Ti/IrO2 while achieving complete BPA degradation and up to 46.8% mineralization, the increased oxidation capacity was attributed to the higher generation of reactive radicals on BDD. Radical scavenging experiments revealed that BPA degradation was mainly driven by •OH (~67%), with contributions from SO4•⁻ (~16%). Electron paramagnetic resonance (EPR) experiments were also performed to provide direct evidence of free radical formation, supporting the scavenger results. The process remained effective at environmentally relevant BPA concentrations (<1.0 mg L-1), with energy consumption as low as 3.8 kWh m-3, significantly lower than conventional EO. Degradation pathways involved hydroxylated intermediates and short-chain carboxylic acids, with oxalic and acetic acids persisting after treatment. Matrix constituents markedly affected performance: chloride enhanced removal via active chlorine species, while bicarbonate and natural organic matter suppressed degradation through radical scavenging and light screening. Experiments with tap water confirmed process stability over multiple treatment cycles. These findings demonstrate that photo-assisted EO with in situ H2O2 generation is a highly effective and energy-efficient strategy for BPA removal, with the BDD/GDE/UVC system showing superior performance and scalability potential for advanced water treatment. The system operated without pH adjustment or added catalysts which are key advantages for low-cost and flexible deployment when considering decentralized water treatment systemsen
dc.description.sponsorshipOutra
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipId2022/12895-1
dc.description.sponsorshipId2023/16167-3
dc.description.sponsorshipId2025/05801-9
dc.description.versionPostprint
dc.identifier.citationGABER, Mohamed S.; GARCIA-SEGURA, Sergi; LANZA, Marcos R. V.; SANTOS, Alexsandro J. dos. Enabling decentralized treatment of BPA through electrified photo-activated advanced oxidation. Separation and Purification Technology, Oxford, v. 382, pt. 5, 136095, Feb. 2026. DOI: https://doi.org/10.1016/j.seppur.2025.136095. Disponível em: https://www.sciencedirect.com/science/article/pii/S1383586625046921/pdfft?md5=6eb17a51597e1e6e3cab784f6141dc7b&pid=1-s2.0-S1383586625046921-main.pdf. Acesso em: 5 dez. 2025.
dc.identifier.doihttps://doi.org/10.1016/j.seppur.2025.136095
dc.identifier.issn1383-5866
dc.identifier.issn1873-3794
dc.identifier.lattes4431449069339555
dc.identifier.orcidhttps://orcid.org/0000-0002-5408-2238
dc.identifier.urihttps://hdl.handle.net/11449/316667
dc.language.isoeng
dc.publisherElsevier
dc.relation.ispartofSeparation and Purification Technology
dc.rights.accessRightsAcesso restritopt
dc.subjectMicropollutant removalen
dc.subjectPhoto-assisted treatmenten
dc.subjectHydroxyl radicalsen
dc.subjectOff-grid systemsen
dc.subjectElectrochemical water treatmenten
dc.titleEnabling decentralized treatment of BPA through electrified photo-activated advanced oxidationen
dc.title.alternativeEnabling decentralized treatment of BPA through electrified photo-activated advanced oxidationen
dc.typeArtigopt
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Letras e Ciências Exatas, São José do Rio Pretopt
unesp.departmentQuímica e Ciências Ambientais - IBILCEpt
unesp.embargo24 meses após a data da defesapt

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