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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/25325
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dc.contributor.authorBevilaqua, Denise-
dc.contributor.authorAcciari, Heloisa Andréa-
dc.contributor.authorArena, Fabiana A.-
dc.contributor.authorBenedetti, Assis Vicente-
dc.contributor.authorFugivara, Cecilio Sadao-
dc.contributor.authorTremiliosi Filho, Germano-
dc.contributor.authorGarcia Júnior, Oswaldo-
dc.date.accessioned2014-05-20T14:17:45Z-
dc.date.accessioned2016-10-25T17:40:08Z-
dc.date.available2014-05-20T14:17:45Z-
dc.date.available2016-10-25T17:40:08Z-
dc.date.issued2009-02-01-
dc.identifierhttp://dx.doi.org/10.1016/j.mineng.2008.07.010-
dc.identifier.citationMinerals Engineering. Oxford: Pergamon-Elsevier B.V. Ltd, v. 22, n. 3, p. 254-262, 2009.-
dc.identifier.issn0892-6875-
dc.identifier.urihttp://hdl.handle.net/11449/25325-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/25325-
dc.description.abstractIn this work, the monitoring of the bacterial and chemical dissolution of bornite was evaluated using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS); the mineral surface was examined using scanning electron microscopy (SEM) and atomic force microscopy (AFM). The analysis of CV results allowed attributing the different peaks observed in both direct and reverse potential scanning to the oxidation of bornite to a secondary covellite and its reduction via different non stoichiometric copper sulphides intermediaries. EIS data for bornite were obtained in control medium up to 78 h of immersion, when a cellular suspension of A. ferrooxidans was added and the experiments continued up to a 192 h of test. The EIS response was different when bacteria were added in the beginning of the test or after some hours of immersion in acid solution. The experiments were performed in different cell configurations and a model of the electrode/electrolyte interface. The correspondent equivalent electrical circuit was used to fit impedance spectra for all studied conditions. A common equivalent circuit used for corrosion processes where anodic (degradation of the mineral) and cathodic (oxygen reduction) reactions occur in parallel, together film and biofilm formation was proposed. (C) 2008 Elsevier Ltd. All rights reserved.en
dc.description.sponsorshipCompanhia VALE, Brazil-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent254-262-
dc.language.isoeng-
dc.publisherPergamon-Elsevier B.V. Ltd-
dc.sourceWeb of Science-
dc.subjectBornite (Cu5FeS4)en
dc.subjectAcidithiobacillus ferrooxidansen
dc.subjectElectrochemical impedance spectroscopy (EIS)en
dc.subjectBioleachingen
dc.titleUtilization of electrochemical impedance spectroscopy for monitoring bornite (CU5FeS4) oxidation by Acidithiobacillus ferrooxidansen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUNESP, Inst Quim Araraquara, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUSP, Inst Quim São Carlos, BR-13560970 São Carlos, SP, Brazil-
dc.description.affiliationUnespUNESP, Inst Quim Araraquara, BR-14801970 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/j.mineng.2008.07.010-
dc.identifier.wosWOS:000263694700006-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofMinerals Engineering-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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