Reduction behavior of uranium in the presence of citric acid
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Yoshinori Suzuki
We examined the reduction behavior of UO22+ in citrate media at pH 2.0−7.0 by column electrodes. At pH 2.0, UO22+ was reduced to U(IV) through a one-step reduction process, while it was reduced to U(IV) through a two-step reduction process at pH 3.0−5.0. The reduction potential of UO22+ shifted to lower values with an increase in pH from 2.0 to 7.0. At pH 6.0 and 7.0, UO22+ was not reduced to U(IV) completely at the electrode potential above -0.8 V vs . silver/silver chloride electrode. Ultraviolet-visible spectroscopy and speciation calculation of UO22+ in citrate media indicated that uranium existed as a mixture of UO22+, [UO2Cit]- and [(UO2)2Cit2]2- at pH 2−3, and a predominant species at pH 3−5 was [(UO2)2Cit2]2- (H3Cit: citric acid). At pH 5−7, polymeric complexes, probably, [(UO2)3Cit3]3- and [(UO2)6Cit6(OH)10]16- were present. These findings suggest that the reduction of UO22+ is more difficult by polymerization of UO22+ with citric acid at higher pHs. Absorption spectra of the reduced complexes showed that U(IV) forms soluble complexes with citric acid at pH 2.0−5.0, and presence of U(V) species was not observed during the reduction of UO22+.
© Oldenbourg Wissenschaftsverlag
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Articles in the same Issue
- Preface Migration 2005
- Solubility measurement of zirconium(IV) hydrous oxide
- Solubility of ThO2·xH2O(am) and the formation of ternary Th(IV) hydroxide-carbonate complexes in NaHCO3-Na2CO3 solutions containing 0−4 M NaCl
- Ion interaction (SIT) coefficients for the Th4+ ion and trace activity coefficients in NaClO4, NaNO3 and NaCl solution determined by solvent extraction with TBP
- Leaching of neptunium from garnet- and murataite-based ceramics
- Coprecipitation of thorium and lanthanum with UO2+x(s) as host phase
- Rare Earth element (REE) incorporation in natural calcite: Upper limits for actinide uptake in a secondary phase
- Protonation of D-gluconate and its complexation with Np(V) in acidic to nearly neutral solutions
- Complexing properties of α-isosaccharinate: thorium
- Determination of the thermodynamic quantities of complexation between Eu(III) and carboxylic acids by microcalorimetry
- Potentiometric investigations on the interaction of humic acid with Cu(II) and Eu(III) ions
- Investigation of complexation of thorium by humic acid using chemically immobilized humic acid on silica gel
- Correlation between X-ray chemical shift and partial charge in Tc(IV) complexes: Determination of Tc partial charge in TcnOy(4n-2y)+
- Oxidation and dissolution rates of UO2(s) in carbonate-rich solutions under external alpha irradiation and initially reducing conditions
- On the stability of Pu(III) at different pH under non-inert conditions
- Reduction behavior of uranium in the presence of citric acid
- Leaching of zirconolite ceramics under H+ and He2+ irradiation
- Reduction of plutonium(VI) in brine under subsurface conditions
- Theoretical first step towards an understanding of the uranyl ion sorption on the rutile TiO2(110) face: A DFT periodic and cluster study
- Cm(III) sorption onto γ-Al2O3: New insight into sorption mechanisms by time-resolved laser fluorescence spectroscopy and extended X-ray absorption fine structure
- Modelling sorption data for the actinides Am(III), Np(V) and Pa(V) on montmorillonite
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- The uptake of radium by calcium silicate hydrates and hardened cement paste
- Np(V)O2+ sorption on hydroxyapatite-effect of calcium and phosphate anions
- Uranium(VI) interaction with pyrite (FeS2): Chemical and spectroscopic studies
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