Degradação eletroquímica do cloranfenicol em reator de fluxo

dc.contributorUniversidade São Francisco
dc.contributorUniversidade Estadual de Campinas (UNICAMP)
dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T14:19:46Z
dc.date.accessioned2022-10-05T15:19:03Z
dc.date.available2014-05-20T14:19:46Z
dc.date.available2022-10-05T15:19:03Z
dc.date.created2014-05-20T14:19:46Z
dc.date.issued2010-01-01
dc.identifierQuímica Nova. Sociedade Brasileira de Química, v. 33, n. 5, p. 1088-1092, 2010.
dc.identifier0100-4042
dc.identifierhttp://hdl.handle.net/11449/25949
dc.identifier10.1590/S0100-40422010000500015
dc.identifierS0100-40422010000500015
dc.identifierWOS:000280479300015
dc.identifierS0100-40422010000500015.pdf
dc.identifier2933194342093387
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3898996
dc.description.abstractThis paper reports a study of electrochemical degradation of the chloramphenicol antibiotic in aqueous medium using a flow-by reactor with DSA® anode. The process efficiency was monitored by chloramphenicol concentration analysis with liquid chromatography (HPLC) during the experiments. Analysis of Total Organic Carbon (TOC) was performed to estimate the degradation degree and Ion Chromatography (IC) was performed to determinate inorganic ions formed during the eletrochemical degradation process. In electrochemical flow-by reactor, 52% of chloramphenicol was degraded, with 12% TOC reduction. IC analysis showed the production of chloride ions (25 mg L-1), nitrate ions (6 mg L-1) and nitrite ions (4.5 mg L-1).
dc.languagepor
dc.publisherSociedade Brasileira de Química
dc.relationQuímica Nova
dc.relation0.646
dc.relation0,255
dc.rightsAcesso aberto
dc.sourceSciELO
dc.subjectchloramphenicol
dc.subjectelectrochemical reactor
dc.subjectDSA® anodes
dc.titleDegradação eletroquímica do cloranfenicol em reator de fluxo
dc.typeArtigo


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