Thermodynamic data for modelling actinide speciation in environmental waters
| Autor: | Hélène Capdevila, Pierre Vitorge |
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| Rok vydání: | 2003 |
| Předmět: | |
| Zdroj: | Radiochimica Acta. 91:623-632 |
| ISSN: | 2193-3405 0033-8230 |
| DOI: | 10.1524/ract.91.11.623.23466 |
| Popis: | An operational TDB is generated from the validated NEA-TDB by adding formation constants (eventually those of chemical analogues, and typically logβ°Pu(CO₃)₅⁶⁻ = 35.6, 4 pH1/2 = -37.5 for Np(VII) hydrolysis, possible maximum values for formation constants of several Pu(CO3)i(OH)j (4-2 i - j )+ complexes, and solubility products for compounds of tentative stoichiometries MO2+ x for M = U, Np, Pu and Am), and by estimating new numerical values (typically E°(AmO₂²⁺/AmO₂⁺) = 1.50, E°(AmO₂⁺/Am³⁺) = 1.48, E°(Am⁴⁺/Am³⁺)=2.49V/SHE). Beside checking the consistency of published experimental data, and performing sensitivity analysis of their interpretation as for any critical review work, activity coefficients and pH calibration also appeared to be critical. Dramatic decrease in aqueous Np(V) solubility is expected, when it is coprecipitated at trace concentration: solubility controlled by the hypothetical ideal solid solution Na2 x -1NpO2(CO3) x (s) (2≥ x ≥ 1), is calculated by solving the set of two thermodynamic equations [Na+]2 x -1 [NpO2 +][CO3 2-] x = K s x , together with (2x-1)[NpO2 +]/[Na+] = D, where K s x = K 2- x s1 (16K s2/27) x -1(2-1/x)2 x -1/x, K s1 and K s2 are the solubility products of the end-member compounds, and D = 27K s1 2/(16K s2) is the equilibrium constant for Ionic Exchange NpO2 +/Na+. Conversely, equilibrium constant, D, of any ionic exchange equilibrium can be interpreted as ratio of solubility products of end-member compounds (eventually surface compounds). |
| Databáze: | OpenAIRE |
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