dc.creatorMALPASS, G. R. P.
dc.creatorMIWA, D. W.
dc.creatorMIWA, A. C. P.
dc.creatorMACHADO, S. A. S.
dc.creatorMOTHEO, A. J.
dc.date.accessioned2012-10-20T05:30:58Z
dc.date.accessioned2018-07-04T15:51:30Z
dc.date.available2012-10-20T05:30:58Z
dc.date.available2018-07-04T15:51:30Z
dc.date.created2012-10-20T05:30:58Z
dc.date.issued2009
dc.identifierJOURNAL OF HAZARDOUS MATERIALS, v.167, n.1/Mar, p.224-229, 2009
dc.identifier0304-3894
dc.identifierhttp://producao.usp.br/handle/BDPI/31724
dc.identifier10.1016/j.jhazmat.2008.12.109
dc.identifierhttp://dx.doi.org/10.1016/j.jhazmat.2008.12.109
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1628362
dc.description.abstractThis paper presents the results concerning the degradation of the pesticide carbaryl comparing two methods: electrochemical (EC) and photo-assisted electrochemical (PAEC). The experimental variables of applied current density, electrolyte flow-rate and initial carbaryl concentration were investigated. The results demonstrate that the electrochemical degradation of carbaryl was greatly enhanced when simultaneous UV light was applied. The greatest difference between the PAEC and EC method was apparent when lower current densities were applied. The extent of COD removal was much enhanced for the combined method, independent of the applied current density. It should be noted that the complete removal of carbaryl was achieved with out the need to add NaCl to the reaction mixture, avoiding the risk of chlorinated organic species formation. (C) 2009 Elsevier B.V. All rights reserved.
dc.languageeng
dc.publisherELSEVIER SCIENCE BV
dc.relationJournal of Hazardous Materials
dc.rightsCopyright ELSEVIER SCIENCE BV
dc.rightsrestrictedAccess
dc.subjectCarbaryl
dc.subjectElectrochemical degradation
dc.subjectPesticides
dc.subjectPhoto-assisted electrochemical degradation
dc.titleStudy of photo-assisted electrochemical degradation of carbaryl at dimensionally stable anodes (DSA (R))
dc.typeArtículos de revistas


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