Приказ основних података о документу

dc.creatorZečević, Strahinja K.
dc.creatorDražić, Dragutin M.
dc.creatorGojković, Snežana Lj.
dc.date.accessioned2021-02-08T09:45:09Z
dc.date.available2021-02-08T09:45:09Z
dc.date.issued1989
dc.identifier.issn0022-0728
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/4209
dc.description.abstractThe kinetics of oxygen reduction were studied on iron in borate and bicarbonate buffered solutions, pH 9.8, using the rotating disk-ring method. Under these conditions O2 reduction occurs both on the oxidized surface and on the oxide-free one, depending on potential. On the oxidized surface the series mechanism was found to be operative. On the oxide-free surface the four-electron reduction was observed, but, due to the very small rate of H2O2 formation with respect to the total reduction current, a reliable distinction between the parallel and series mechanism could not be made. All the rate constants of the O2 and H2O2 reactions on the Fe surface were determined. No catalytic decomposition of H2O2 was found. The kinetics of the O2 reduction reaction is slower on more oxidized surfaces.sr
dc.language.isoensr
dc.publisherElseviersr
dc.relationNational Science Foundation (U.S.A.), contract No. JFP 522/NSFsr
dc.relationResearch Fund of the S.R. Serbiasr
dc.rightsrestrictedAccesssr
dc.sourceJournal of Electroanalytical Chemistrysr
dc.subjectoxygen reductionsr
dc.subjectironsr
dc.subjectThe kinetics of oxygen reductionsr
dc.subjectrotating disk-ring methodsr
dc.titleOxygen reduction on iron. Part III. An analysis of the rotating disk-ring electrode measurements in near neutral solutionssr
dc.typearticlesr
dc.rights.licenseARRsr
dcterms.abstractГојковић, Снежана Љ.; Зечевић, Страхиња К.; Дражић, Драгутин М.;
dc.citation.volume265
dc.citation.issue1-2
dc.citation.spage179
dc.citation.epage193
dc.identifier.doi10.1016/0022-0728(89)80188-3
dc.identifier.scopus2-s2.0-0000380265
dc.type.versionpublishedVersionsr


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Приказ основних података о документу