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Nature of the anodic tellurate wave at the dropping mercury electrode

dc.contributor.authorJaselskis, Brunoen_US
dc.contributor.authorLanese, John G.en_US
dc.date.accessioned2006-04-13T14:55:31Z
dc.date.available2006-04-13T14:55:31Z
dc.date.issued1962-04en_US
dc.identifier.citationJaselskis, B., Lanese, J. G. (1962/04)."Nature of the anodic tellurate wave at the dropping mercury electrode." Journal of Inorganic and Nuclear Chemistry 24(4): 399-404. <http://hdl.handle.net/2027.42/32317>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B758S-48M3CYG-C6/2/d3bbd265fa913c7eefcf9411ea702955en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/32317
dc.description.abstractTellurate solutions at the dropping mercury electrode show an adsorption type anodic wave in the vicinity of zero volts vs. S.C.E. The presence of this anodic wave is attributed to depolarization of mercury electrode and the formation of an insoluble mercurous tellurate film given by the reaction 2 Hg[deg] + H6TeO6 --&gt; Hg2H4TeO6 + 2H+ + 2e. Under similar conditions an anodic wave is not observed with tellurite, selenate, selenite and arsenate.en_US
dc.format.extent271188 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleNature of the anodic tellurate wave at the dropping mercury electrodeen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, Michigan, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/32317/1/0000385.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0022-1902(62)80036-0en_US
dc.identifier.sourceJournal of Inorganic and Nuclear Chemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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