dc.creatorNETO, S. Aquino
dc.creatorANDRADE, A. R. de
dc.date.accessioned2012-10-19T14:14:12Z
dc.date.accessioned2018-07-04T15:00:32Z
dc.date.available2012-10-19T14:14:12Z
dc.date.available2018-07-04T15:00:32Z
dc.date.created2012-10-19T14:14:12Z
dc.date.issued2009
dc.identifierELECTROCHIMICA ACTA, v.54, n.7, p.2039-2045, 2009
dc.identifier0013-4686
dc.identifierhttp://producao.usp.br/handle/BDPI/20713
dc.identifier10.1016/j.electacta.2008.07.019
dc.identifierhttp://dx.doi.org/10.1016/j.electacta.2008.07.019
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1617492
dc.description.abstractThis paper has investigated the electrochemical oxidation of glyphosate herbicide (GH) on RuO(2) and IrO(2) dimensionally stable anode (DSA (R)) electrodes. Electrolysis was achieved under galvanostatic control as a function of pH, GH concentration, supporting electrolyte, and current density. The influence of the oxide composition on GH degradation seems to be significant in the absence of chloride; Ti/Ir(0.30)Sn(0.70)O(2) is the best electrode material to oxidize GH. GH oxidation is favored at low pH values. The use of chloride medium increases the oxidizing power and the influence of the oxide composition is meaningless. At 30 mA cm(-2) and 4 h of electrolysis, complete GH removal from the electrolyzed solution has been obtained. In chloride medium, application of 50 mA cm(-2) leads to virtually total mineralization ( release of phosphate ions = 91%) for all the evaluated oxide materials. (C) 2008 Elsevier Ltd. All rights reserved.
dc.languageeng
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD
dc.relationElectrochimica Acta
dc.rightsCopyright PERGAMON-ELSEVIER SCIENCE LTD
dc.rightsrestrictedAccess
dc.subjectGlyphosate herbicide
dc.subjectElectrochemical oxidation
dc.subjectDSA (R) electrodes
dc.subjectElectrolysis
dc.subjectWastewater
dc.titleElectrooxidation of glyphosate herbicide at different DSA (R) compositions: pH, concentration and supporting electrolyte effect
dc.typeArtículos de revistas


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