DEVELOPMENT OF VOLTAMMETRIC METHOD FOR DETERMINATION OF TRACE OF Cu(II) IN THE PRESENCE OF Fe(III) IN WATER USING 5,5'-DIPHENYLIMIDAZOLIDINE-2,4-DIONE DERIVATIVE
creativework.keywords | copper, iron, method, surface water, voltammetry | |
creativework.publisher | University of Chemical Technology and Metallurgy | en |
dc.contributor.author | Georgieva S. | |
dc.contributor.author | Todorov P. | |
dc.contributor.author | Bezfamilnyi A. | |
dc.date.accessioned | 2024-07-16T11:16:50Z | |
dc.date.accessioned | 2024-07-16T11:19:22Z | |
dc.date.available | 2024-07-16T11:16:50Z | |
dc.date.available | 2024-07-16T11:19:22Z | |
dc.date.issued | 2021-01-01 | |
dc.description.abstract | A new cyclic voltammetric method has been developed for the determination of Cu(II) in the presence of Fe(III) in tap and surface water samples using complexing properties of 5,5'-diphenylimidazolidine-2,4-dione derivative. In acetate buffer solution (0.1 mol L-1; pH 5.25 ± 0.01) containing minimum ten-fold excess of imidazolidine derivative, copper metal ion was determined as complex compound following redox process into the working hanging mercury drop electrode (HMDE) versus Ag/AgCl, 3 mol L-1 KCl using as a reference electrode. Limits of detection as low as 0.0415 mg L-1 Cu(II) was achieved. The interfering effect of various cations as K(I), Na(I), Mg(II), Ca(II), Al(III), Zn(II), Fe(II), Fe(III) and anions: Cl-, NO3-, SO42-, PO43-, most common in surface and tap water samples, were also assessed. | |
dc.identifier.issn | 1314-7978 | |
dc.identifier.issn | 1314-7471 | |
dc.identifier.scopus | SCOPUS_ID:85111767275 | en |
dc.identifier.uri | https://rlib.uctm.edu/handle/123456789/1329 | |
dc.language.iso | en | |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85111767275&origin=inward | |
dc.title | DEVELOPMENT OF VOLTAMMETRIC METHOD FOR DETERMINATION OF TRACE OF Cu(II) IN THE PRESENCE OF Fe(III) IN WATER USING 5,5'-DIPHENYLIMIDAZOLIDINE-2,4-DIONE DERIVATIVE | |
dc.type | Article | |
oaire.citation.issue | 5 | |
oaire.citation.volume | 56 |