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Role of Mo6+ during nickel electrodeposition from sulfate solutions

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dc.contributor.author Mohanty, U.S.
dc.contributor.author Tripathy, B.C.
dc.contributor.author Singh, P.
dc.contributor.author Das, S.C.
dc.contributor.author Misra, V.N.
dc.date.accessioned 2018-10-01T12:22:58Z
dc.date.available 2018-10-01T12:22:58Z
dc.date.issued 2008
dc.identifier.citation Journal Of Applied Electrochemistry, 38(2), 2008: 239-244
dc.identifier.issn 0021-891X
dc.identifier.uri http://ore.immt.res.in/handle/2018/1378
dc.description.abstract The effect of Mo6+ on the current efficiency, deposit quality, surface morphology, crystallographic orientations and polarisation behaviour of the cathode during electrodeposition of nickel from sulfate solutions was investigated. Mo6+ did not have a significant effect on current efficiency over the concentration range 2-100 mg dm(-3). However; a decrease in current efficiency by a magnitude of more than 20% was seen at 500 mg dm(-3). The quality of the nickel deposit with reference to the visual appearance and contamination level varied with varying concentration of Mo6+; this was also reflected in the morphology and crystallographic orientations of the deposits. Addition of Mo6+ to the electrolyte introduced two new crystal planes i.e., (220) and (311). Depolarisation of the cathode was noted at lower concentrations of Mo6+ (2-40 mg dm(-3) whereas polarisation of the cathode was observed at Mo6+ concentration > 40 mg dm(-3). The effect of Mo6+ on parameters such as Tafel slope (b), transfer coefficient (alpha) and exchange current density (i(0)) were also determined.
dc.language en
dc.publisher Springer
dc.relation.isreferencedby SCI
dc.rights Copyright [2008]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subject Chemical Sciences
dc.title Role of Mo6+ during nickel electrodeposition from sulfate solutions
dc.type Journal Article
dc.affiliation.author Natl Cheng Kung Univ, Ctr Micro Nano Sci & Technol, Tainan 701, Taiwan


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