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Effect of thiourea during nickel electrodeposition from acidic sulfate solutions

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dc.contributor.author Mohanty, U.S.
dc.contributor.author Tripathy, B.C.
dc.contributor.author Das, S.C.
dc.contributor.author Misra, V.N.
dc.date.accessioned 2018-10-01T12:22:20Z
dc.date.available 2018-10-01T12:22:20Z
dc.date.issued 2005
dc.identifier.citation Metallurgical And Materials Transactions B-Process Metallurgy And Materials Processing Science, 36(6), 2005: 737-741
dc.identifier.issn 1073-5615
dc.identifier.uri http://ore.immt.res.in/handle/2018/1177
dc.description.abstract The effect of thiourea on the cathodic current efficiency (CE), deposit quality, crystallographic orientations, surface morphology, and polarization behavior of the cathode was investigated during nickel electrodeposition from acidic sulfate solutions for 2 hours at 60 degrees C. A slight decrease of 3 to 4 pet in the CE was observed, when the concentration of thiourea was increased from 2 to 40 mg dm(-3). The nickel deposit quality deteriorated significantly at higher thiourea concentrations; the surface morphology deteriorated and the contamination of the nickel deposits increased. The presence of thiourea affected the peak intensities of the crystal planes. Cyclic voltammetric studies on nickel deposition at 25 degrees C revealed depolarization behavior of the cathode at lower thiourea concentrations. <= 10 mg, dm(-3) ever, a mixed behavior is observed at higher thiourea concentrations. These changes were also observed Z, C in the exchange current density (i(0)) values.
dc.language en
dc.publisher Minerals, Metals & Materials Society
dc.relation.isreferencedby SCI
dc.rights Copyright [2005]. 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 Materials Sciences
dc.subject Materials Sciences
dc.subject Materials Sciences
dc.title Effect of thiourea during nickel electrodeposition from acidic sulfate solutions
dc.type Journal Article
dc.affiliation.author Natl Cheng Kung Univ, Dept Mat Sci & Engn, Tainan 701, Taiwan


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