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Secondary aluminium-iron (III) chloride batteries with a low temperature molten salt electrolyte
dc.contributor.authorDonahue, Francis M.en_US
dc.contributor.authorMancini, S. E.en_US
dc.contributor.authorSimonsen, Leif R.en_US
dc.date.accessioned2006-09-08T20:54:46Z
dc.date.available2006-09-08T20:54:46Z
dc.date.issued1992-03en_US
dc.identifier.citationDonahue, F. M.; Mancini, S. E.; Simonsen, L.; (1992). "Secondary aluminium-iron (III) chloride batteries with a low temperature molten salt electrolyte." Journal of Applied Electrochemistry 22(3): 230-234. <http://hdl.handle.net/2027.42/42959>en_US
dc.identifier.issn0021-891Xen_US
dc.identifier.issn1572-8838en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/42959
dc.description.abstractSecondary aluminium-iron (III) chloride batteries using a low temperature molten salt electrolyte were constructed and tested. Discharge current densities were in the range 5 to 100 mA (∼ 1 to 20 mA cm −2 ; ∼ C /4 to 5 C ); charging currents were 5mA ( C /4 to C /2). Utilization of the positive electrode reactant was low due to the discharge rates and loading procedure. The mode for self discharge was dissolution of the positive electrode reactant and transport to the aluminium negative electrode where it reacted.en_US
dc.format.extent503741 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Chapman and Hall ; Springer Science+Business Mediaen_US
dc.subject.otherChemistryen_US
dc.subject.otherPhysical Chemistryen_US
dc.subject.otherElectrochemistryen_US
dc.subject.otherIndustrial Chemistry/Chemical Engineeringen_US
dc.titleSecondary aluminium-iron (III) chloride batteries with a low temperature molten salt electrolyteen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumMinotaur Technologies, 48103-4115, Ann Arbor, MI, USA; Department of Chemical Engineering, The University of Michigan, 48109-2136, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherMinotaur Technologies, 48103-4115, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherMinotaur Technologies, 48103-4115, Ann Arbor, MI, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/42959/1/10800_2005_Article_BF01030182.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1007/BF01030182en_US
dc.identifier.sourceJournal of Applied Electrochemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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