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dc.contributor.authorSouza, Danilo R. de-
dc.contributor.authorTrovó, Alam Gustavo-
dc.contributor.authorAntoniosi Filho, Nelson Roberto-
dc.contributor.authorSilva, Marcos A. A.-
dc.contributor.authorMachado, Antonio E. H.-
dc.creatorSouza, Danilo R. de-
dc.creatorTrovó, Alam Gustavo-
dc.creatorAntoniosi Filho, Nelson Roberto-
dc.creatorSilva, Marcos A. A.-
dc.creatorMachado, Antonio E. H.-
dc.date.accessioned2014-09-09T14:20:34Z-
dc.date.available2014-09-09T14:20:34Z-
dc.date.issued2013-
dc.identifier.issn0103-5053-
dc.identifier.urihttp://repositorio.ufba.br/ri/handle/ri/15862-
dc.descriptionp. 1451-1460pt_BR
dc.description.abstractParameters that influence the efficiency of the degradation of glyphosate (addition of Fe2+, simultaneous addition of Fe2+ and Fe3+ at a 1:1 (Fe2+/Fe3+) molar ratio, addition of oxalate and of H2O2) were evaluated at lab-scale. Synergic effects on its degradation and release of phosphate were observed using Fe2+/Fe3+, as well as adding oxalate. On the other hand, the concentration increase of Fe2+/Fe3+, oxalate and H2O2 did not promote a linear increase of glyphosate mineralization and release of phosphate. Using high concentrations of these species, the efficiency of glyphosate mineralization and release of phosphate was constant or even decreased. Under optimized conditions (0.27 mmol L-1 of Fe2+/Fe3+; 1.13 mmol L-1 of oxalate and 10.3 mmol L-1 of H2O2), close results for mineralization and release of phosphate were obtained in lab-scale and using a solar pilot plant. A direct ratio between reducing the toxicity and glyphosate concentration was also observed.pt_BR
dc.language.isoenpt_BR
dc.rightsAcesso Abertopt_BR
dc.sourcehttp://dx.doi.org/10.5935/0103-5053.20130185pt_BR
dc.subjectHerbicidept_BR
dc.subjectSunlightpt_BR
dc.subjectAgricultural effluentpt_BR
dc.subjectMineralizationpt_BR
dc.subjectDetoxificationpt_BR
dc.titleDegradation of the commercial herbicide glyphosate by photo-fenton process: evaluation of kinetic parameters and toxicitypt_BR
dc.title.alternativeJournal of the Brazilian Chemical Societypt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 24, n. 9pt_BR
dc.publisher.countryBrasilpt_BR
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