Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/27540
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dc.contributor.authorAli, M Rostom-
dc.contributor.authorRahman, Md Ziaur-
dc.contributor.authorSaha, S Sankar-
dc.date.accessioned2014-03-31T11:31:16Z-
dc.date.available2014-03-31T11:31:16Z-
dc.date.issued2014-03-
dc.identifier.issn0975-0991 (Online); 0971-457X (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/27540-
dc.description127-133en_US
dc.description.abstractThe electroless and electrolytic deposition of nickel from a solution containing nickel chloride in either an ethylene glycol (EG)-choline chloride based or a urea-choline chloride based ionic liquids has been carried out onto copper and steel cathodes under different conditions. It is found that electroless nickel deposits of up to several microns has been obtained by dip coating from only EG based ionic liquids at temperature above 70°C without the use of catalysts. The influences of various experimental conditions on electrodeposition and the morphology of the deposited layers have been investigated by scanning electron microscopy and X-ray diffraction. It is shown that very smooth, shiny and dense with good adherence and bright metallic coloured nickel coatings can be obtained from both EG and urea-based ionic liquids at applied deposition potential of up to -0.50 V and applied deposition current density of up to -5.0 A m-2 between 50°C and 100°C. The cathodic current efficiency for the deposition of Ni is about 97%. en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJCT Vol.21(2) [March 2014]en_US
dc.subjectCyclic voltammetryen_US
dc.subjectElectrodepositionen_US
dc.subjectElectroless depositionen_US
dc.subjectEthalineen_US
dc.subjectNickelen_US
dc.subjectRelineen_US
dc.titleElectroless and electrolytic deposition of nickel from deep eutectic solvents based on choline chloridea en_US
dc.typeArticleen_US
Appears in Collections:IJCT Vol.21(2) [March 2014]

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