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dc.contributor.authorOrtiz Suárez, David 
dc.contributor.authorMuñoz García, Macarena 
dc.contributor.authorGarcia, Jorge
dc.contributor.authorCires Gómez, Samuel 
dc.contributor.authorMartínez de Pedro, Zahara 
dc.contributor.authorQuesada del Corral, Antonio 
dc.contributor.authorCasas, Jose A.
dc.contributor.otherUAM. Departamento de Biologíaes_ES
dc.contributor.otherUAM. Departamento de Ingeniería Químicaes_ES
dc.date.accessioned2022-11-23T10:45:11Z
dc.date.available2022-11-23T10:45:11Z
dc.date.issued2022-10-22
dc.identifier.citationEnvironmental Science and Pollution Research (2022): 1-10en_US
dc.identifier.issn0944-1344 (print)en_US
dc.identifier.issn1614-7499 (online)en_US
dc.identifier.urihttp://hdl.handle.net/10486/705319
dc.description.abstractCylindrospermopsin (CYN) is a potent cyanobacterial toxin found in freshwaters worldwide. In this work, the feasibility of the photo-Fenton process under neutral pH using light emitting diodes as irradiation source for the removal of this hazardous cyanotoxin from freshwater was investigated. The impact of the kind of iron chelating agent (ethylenediamine-N, N′-disuccinic acid vs. ethylenedinitrilotetraacetic acid) as well as the effect of the main operating conditions viz. H2O2 dose, Fe(III) load, initial CYN concentration, and Fe(III):EDDS molar ratio on the performance of the process was systematically evaluated. EDDS was selected as the most appropriate iron chelating agent considering the kinetics of the process and the environmental impact (Vibrio fischeri and Artemia salina). Under optimized conditions ([H2O2] = 30 mg L−1; [Fe(III)] = 5 mg L−1; Fe(III):ligand = 1:0.5 (molar ratio)), complete removal of CYN was achieved in 15-min reaction time. Furthermore, the catalytic system showed to be effective in real water matrices (river and reservoir waters) spiked with CYN. Although the presence of inorganic ions (mainly HCO3−/CO32−) and dissolved organic carbon decreased the oxidation rate of CYN due to scavenging reactions and iron coordination, respectively, complete elimination of the cyanotoxin was achieved in all cases. The fate of EDDS along the process was also evaluated to demonstrate that the catalytic system investigated, apart from its effectiveness, warrants the complete absence of residues after reaction. Therefore, the proposed system constitutes a promising method for cyanotoxin treatment either as a drinking water treatment step in conventional plants or as a potential remediation strategy in the natural environmenten_US
dc.description.sponsorshipOpen Access funding provided thanks to the CRUE-CSIC agreement with Springer Nature. This research has been supported by the CYTED Ibero-American Science and Technology Program for Development (CYTED-2019) through the project TALGENTOX (PCI2020-112013) and by the Spanish Ministry for Science and Innovation (MICINN) through the project PID2019-105079RB-I00. D. Ortiz has received a FPU predoctoral grant (FPU19/04816) from the Spanish Ministry of Universities. M. Munoz has received a Ramón y Cajal postdoctoral contract (RYC-2016–20648) from the Spanish MINECOen_US
dc.format.extent10 pag.es_ES
dc.format.mimetypeapplication/pdfen_US
dc.language.isoengen
dc.publisherSpringeren_US
dc.relation.ispartofEnvironmental Science and Pollution Researches_ES
dc.rights© The Author(s) 2022en_US
dc.subject.otherCyanotoxinen_US
dc.subject.otherCylindrospermopsinen_US
dc.subject.otherDegradationen_US
dc.subject.otherEDDSen_US
dc.subject.otherLEDsen_US
dc.subject.otherPhoto-Fentonen_US
dc.titlePhoto-Fenton oxidation of cylindrospermopsin at neutral pH with LEDsen_US
dc.typearticleen_US
dc.subject.ecienciaBiología y Biomedicina / Biologíaes_ES
dc.subject.ecienciaQuímicaes_ES
dc.relation.publisherversionhttps://doi.org/10.1007/s11356-022-23681-7en_US
dc.identifier.doi10.1007/s11356-022-23681-7en_US
dc.identifier.publicationfirstpage1es_ES
dc.identifier.publicationlastpage10es_ES
dc.relation.projectIDGobierno de España. PID2019-105079RB-I00es_ES
dc.type.versioninfo:eu-repo/semantics/publishedVersionen_US
dc.rights.ccReconocimientoes_ES
dc.rights.accessRightsopenAccessen_US
dc.facultadUAMFacultad de Cienciases_ES


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