Pregled bibliografske jedinice broj: 2503
Redox and Adsorption Processes of Hydrolyzed Uranyl Species on a Mercury Electrode from Sodium Chloride Solutions
Redox and Adsorption Processes of Hydrolyzed Uranyl Species on a Mercury Electrode from Sodium Chloride Solutions // Electroanalysis, 9 (1997), 12; 936-940 (međunarodna recenzija, članak, znanstveni)
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Naslov
Redox and Adsorption Processes of Hydrolyzed Uranyl Species on a Mercury Electrode from Sodium Chloride Solutions
Autori
Djogić, Renata ; Krznarić, Damir ; Branica, Marko
Izvornik
Electroanalysis (1040-0397) 9
(1997), 12;
936-940
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
uranyl(VI)-ion; hydrolysis; adsorption
Sažetak
Reduction and adsorption processes of hydrolyzed uranyl species on the mercury drop electrode, from 0.55 mol L-1 NaCl, were studied by electrochemical cathodic stripping techniques: cyclic voltammetry, alternating current voltammetry, chronoamperometry and double potential step chronocoulometry. The only uranyl species adsorbed on the Hg electrode (between pH 5 and 7) was found to be uncharged uranyl dihydroxide, as well as its reduction product. At bulk concentrations between 3 and 5 mmol L-1, the reactant forms an adsorbed compact film as a result of surface polymerization, nucleation or other condensation process. The adsorption isotherm at pH 6.2 and -0.2 V was measured. It was fitted with Frumkin type isotherm. At the plateau, a reduction current corresponding to 6.7x10-9 mol cm-2 of uranyl ions was measured. This represents on the average 7 adsorbed layers of UO2(OH)2o, presuming an orthorhombic crystal cell structure. Multilayer adsorption is certain even if a polymeric form of uranyl dihyroxide was considered.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Institut "Ruđer Bošković", Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus