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dc.creatorde la Fourniere, Emmanuel
dc.creatorMeichtry, Jorge Martín
dc.creatorGautier, Eduardo Amilcar
dc.creatorCusto, Graciela
dc.creatorLitter, Marta Irene
dc.date.accessioned2024-03-19T20:27:34Z
dc.date.available2024-03-19T20:27:34Z
dc.date.issued2021-06-28
dc.identifier.urihttp://hdl.handle.net/20.500.12272/9935
dc.description.abstractAbstract: Background: Thiomersal (TM), a complex between 2-mercaptobenzoic acid (2-MBA) and ethylmercury (C2H5Hg+), is an antimicrobial preservative used in immunological, ophthalmic, cosmetic products, and vaccines. Objective: TM has been treated by UV/TiO2 photocatalysis in the presence or absence of oxygen at acidic pH. C2H5Hg+, 2-MBA, and 2-sulfobenzoic acid (2-SBA) were found as products. A 2-SBA photocatalytic treatment was undertaken to study sulfur evolution. Methods: Photocatalytic runs were performed using a UVA lamp (λmax = 352 nm), open to air or under N2. A suspension of the corresponding TM or 2-SBA salt and TiO2 was prepared, and pH was adjusted. Suspensions were stirred in the dark for 30 min and then irradiated. TM, 2-MBA, 2-SBA, and C2H5Hg+ were quantified by HPLC, sulfur by TXRF, and the deposits on the photocatalyst were analyzed by chemical reactions. The mineralization degree was followed by TOC. Sulfate was determined using BaCl2 at 580 nm. Results: Photocatalytic destruction of TM and total C2H5Hg+ was complete under N2 and air, but TM degradation was much faster in air. The evolution of TM and the products followed a pseudo-first order kinetics. Conclusion: TiO2-photocatalytic degradation is a suitable technique for the treatment of TM and its degradation products. In contrast to other organomercurial compounds, TM degradation is faster in the presence of O2, indicating that the oxidative mechanism is the preferred pathway. A significant TM mineralization (> 60%, NPOC and total S) was obtained. TM was more easily degraded than 2-SBA. Sulfate was the final productes_ES
dc.description.sponsorshipAgencia Nacional de Promocion Científica y Tecnologica (ANPCyT), Argentina, PICT-2011-0463 y PICT-2015-0208es_ES
dc.formatpdfes_ES
dc.language.isoenges_ES
dc.rightsembargoedAccesses_ES
dc.subjectHeterogeneous photocatalysis, thimerosal, ethylmercury 2-mercaptobenzoic acid, 2-sulfobenzoic acid, titanium dioxide, 2-sulfobenzoic acides_ES
dc.titleNew insights on the UV/TiO2 photocatalytic treatment of thiomersal and its 2-sulfobenzoic acid productes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderBentham Science Publisherses_ES
dc.description.affiliationde la Fourniere, Emmanuel. Comisión Nacional de Energía Atómica, Av. Gral. Paz 1499, 1650 San Martín, Prov. de Buenos Aires, Argentina. Meichtry, Jorge Martín. Comisión Nacional de Energía Atómica, Av. Gral. Paz 1499, 1650 San Martín, Prov. de Buenos Aires, Argentina. Centro de Tecnologías Químicas, Facultad Regional Buenos Aires, Universidad Tecnológica Nacional, Medrano 951, 1425 Buenos Aires, Argentina. Custo, Graciela. Comisión Nacional de Energía Atómica, Av. Gral. Paz 1499, 1650 San Martín, Prov. de Buenos Aires, Argentina. Gautier, Eduardo. Comisión Nacional de Energía Atómica, Av. Gral. Paz 1499, 1650 San Martín, Prov. de Buenos Aires, Argentina. Litter, Marta I. Comisión Nacional de Energía Atómica, Av. Gral. Paz 1499, 1650 San Martín, Prov. de Buenos Aires, Argentina. Instituto de Investigación e Ingeniería Ambiental –IIIA, UNSAM, CONICET, 3iA, Universidad de San Martín, Campus Miguelete, 25 de Mayo y Francia, 1650, San Martín, Prov. de Buenos Aires, Argentinaes_ES
dc.description.peerreviewedPeer Reviewedes_ES
dc.type.versionpublisherVersiones_ES
dc.rights.usePublished under the subscription model, copyrights transferred to Bentham Science Publishers.es_ES
dc.identifier.doi10.2174/2665976X02666210629104521
dc.creator.orcid0000-0002-5648-5372es_ES
dc.creator.orcid0000-0002-4832-7956es_ES
dc.creator.orcid0000-0002-0312-0177es_ES


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