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dc.creatorMaluckov, Biljana S.
dc.creatorMitrić, Miodrag
dc.date.accessioned2018-06-29T10:31:32Z
dc.date.available2018-06-29T10:31:32Z
dc.date.issued2018
dc.identifier.issn1567-5394
dc.identifier.urihttp://linkinghub.elsevier.com/retrieve/pii/S1567539417305881
dc.identifier.urihttps://vinar.vin.bg.ac.rs/handle/123456789/7692
dc.description.abstractThe impact of different concentrations of three amino acids (cysteine, histidine and methionine) which are part of the amino acid sequence of rusticyanin on dissolution of pyrite is investigated by the application of electrochemical techniques. Cyclic voltammetric studies conducted in the anodic direction from corrosion potential have shown that in the vicinity of corrosion potential, histidine and methionine do not influence dissolution of pyrite independently on their concentrations. On the other hand, cysteine and solutions of these amino acids in the molar ratios Cys:His:Met/1:1:1 and Cys:His:Met/1:2:1 accelerate dissolution at concentrations 10−2mol L−1and 10−3mol L−1. Potentiodynamic polarization measurements showed that methionine does not affect the anodic and cathodic dissolution at all concentrations, while histidine does not affect significantly on the anodic dissolution at all concentrations. Cysteine and solutions of three amino acids in the molar ratio Cys:His:Met/1:1:1 and Cys:His:Met/1:2:1 cause intensive cathodic inhibition and anodic activation at concentrations 10−2mol L−1and 10−3mol L−1respectively.en
dc.relationinfo:eu-repo/grantAgreement/MESTD/Integrated and Interdisciplinary Research (IIR or III)/45015/RS//
dc.rightsrestrictedAccess
dc.sourceBioelectrochemistry
dc.subjectcysteineen
dc.subjectelectrochemistryen
dc.subjecthistidineen
dc.subjectmethionineen
dc.subjectpyriteen
dc.subjectrusticyaninen
dc.titleElectrochemical behavior of pyrite in sulfuric acid in presence of amino acids belonging to the amino acid sequence of rusticyaninen
dc.typearticleen
dc.rights.licenseARR
dcterms.abstractМалуцков, Биљана С.; Митрић, Миодраг;
dc.rights.holder© 2018 Published by Elsevier B.V.
dc.citation.volume123
dc.citation.spage112
dc.citation.epage118
dc.identifier.wos000440770200013
dc.identifier.doi10.1016/j.bioelechem.2018.04.021
dc.citation.rankM21
dc.type.versionpublishedVersion
dc.identifier.scopus2-s2.0-85046789177


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