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An improved thermodynamic model for the complexation of trivalent actinides and lanthanide with oxalic acid valid to high ionic strength

Chemical Geology

Thakur, Punam; Xiong, Yongliang X.; Borkowski, Marian

The dissociation constants of oxalic acid (Ox), and the stability constants of Am3+, Cm3+ and Eu3+ with Ox2- have been determined at 25°C, over a range of concentration varying from 0.1 to 6.60m NaClO4 using potentiometric titration and extraction techniques, respectively. The experimental data support the formation of complexes, M(Ox)n3-2n, where (M=Am3+, Cm3+ and Eu3+ and n=1 and 2). The dissociation constant and the stability constant values measured as a function of NaClO4 concentration were used to estimate the Pitzer parameters for the respective interactions of Am3+, Cm3+ and Eu3+ with Ox. Furthermore, the stability constants data of Am3+-Ox measured in NaClO4 and in NaCl solutions from the literature were simultaneously fitted in order to refine the existing actinide-oxalate complexation model that can be used universally in the safety assessment of radioactive waste disposal. The thermodynamic stability constant: log β0101=6.30±0.06 and log β0102=10.84±0.06 for Am3+ was obtained by simultaneously fitting data in NaCl and NaClO4 media. Additionally, log β0101=6.72±0.08 and log β0102=11.05±0.09 for the Cm3+ and log β0101=6.67±0.08 and log β0102=11.15±0.09 for the Eu3+ were calculated by extrapolation of data to zero ionic strength in NaClO4 medium only. For all stability constants, the Pitzer model gives an excellent representation of the data using interaction parameters β(0), β(1), and Cϕ determined in this work. The thermodynamic model developed in this work will be useful in accurately modeling the potential solubility of trivalent actinides and early lanthanides to ionic strength of 6.60m in low temperature environments in the presence of Ox. The work is also applicable to the accurate modeling transport of rare earth elements in various environments under the surface conditions.

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TYPE Journal Article YEAR 2015
ScopusOSTIDOI

Experimental determination of lead carbonate solubility at high ionic strengths: a Pitzer model description

Monatshefte fur Chemie

Xiong, Yongliang X.

Abstract In this study, solubility measurements of lead carbonate, PbCO3(cr), cerussite, as a function of total ionic strengths are conducted in the mixtures of NaCl and NaHCO3 up to I = 1.2 mol kg-1 and in the mixtures of NaHCO3 and Na2CO3 up to I = 5.2 mol kg-1, at room temperature (22.5 ± 0.5 °C). The solubility constant (log Kos) for cerussite was determined as -13.76 ± 0.15 (2σ) with a set of Pitzer parameters describing the specific interactions of PbCO3(aq), Pb(CO3)2-2, and Pb(CO3)Cl- with the bulk-supporting electrolytes, based on the Pitzer model. The model developed in this work can reproduce the experimental results including model-independent solubility values from the literature over a wide range of ionic strengths with satisfactory accuracy. The model is expected to find applications in numerous fields, including the accurate description of chemical behavior of lead in geological repositories, the modeling of formation of oxidized Pb-Zn ore deposits, and the environmental remediation of lead contamination.

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TYPE Journal Article YEAR 2015
ScopusOSTIDOI
Results 51–75 of 109
Results 51–75 of 109