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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 24 (1995), S. 735-752 
    ISSN: 1572-8927
    Keywords: Solubility ; equilibrium constants ; solubility product ; Fe2(SeO3)3·6H2O(c) ; ferric selenite ; selenite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The aqueous solubility of Fe2(SeO3)3·6H2O(c) was studied in deionized water adjusted to a range in pH values from 0.77 to 5.1 and in Na2SeO3 solutions ranging in concentrations from 0.0002 to 0.02 mol-dm−3. The studies were conducted from both the undersaturation and oversaturation directions, with equilibration periods ranging from 7 to 1725 days. Stoichiometric dissolution of the solid was observed in solutions with pH values up to nearly 4. In general, concentrations of both Se and Fe decreased as pH increased from 1 to 4. Analyses of the equilibrated suspensions confirmed the equilibrium solid to be Fe2(SeO3)3·6H2O(c) and the aqueous Se to be selenite. Pitzer's ion-interaction model was used with selected ion pairs to interpret the solubility data. The logarithm of the solubility product of ferric selenite $$Fe_2 (SeO_3 )_3 .6H_2 O(c) \begin{array}{*{20}c} \to \\ \leftarrow \\ \end{array} 2Fe^{3 + } + 3SeO_3^{2 - } + 6H_2 O$$ was found to be −41.58±0.11. This value is less than any reported in the literature for a ferric selenite by more than 10 orders of magnitude. The solubility data and calculations show an extremely strong interaction between aqueous Fe3+ and SeO 3 2− ; interpretation of these data requires the inclusion of FeSeO 3 + i.e. $$Fe^{3 + } + SeO_3^{2 - } \begin{array}{*{20}c} \to \\ \leftarrow \\ \end{array} FeSeO_3^ + , log K = 11.15 \pm 0.11$$
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 24 (1995), S. 879-895 
    ISSN: 1572-8927
    Keywords: Solubility ; crystalline NdPO4 ; sulfate complexes ; Nd ; Am ; Pitzer parameters ; solubility product
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effects of Nd(III)/Am(III) complexation with sulfate were studied by 1) re-examining existing data for the Am−SO4 system using more, advanced aqueous electrolyte models valid to high concentration to obtain reliable thermodynamic data for SO 4 2− complexes or ion interactions with Nd3+ and Am3+ and 2) conducting experimental solubility studies of NdPO4(c), an analog phase of AmPO 4 (c), a possibly important phase in high level nuclear wastes, in the presence of SO 4 2− to test the newly developed thermodynamic model and show the possible influence of sulfate in a repository environment. The data showed that the increase in the solubility of NdPO 4 (c) resulted primarily from the increase in ionic strength. Slightly higher observed Nd concentrations in the presence of sulfate, as compared with concentrations predicted at the experimental ionic strengths, resulted from the weak complexes or ion interactions involving Nd 3+ −SO 4 2− . The Pitzer ion interaction parameters, applicable to 0.5m sulfate, were obtained for Am 3+ −SO 4 2− from a reinterpretation of known solvent extraction data. These parameters are also consistent with literature data for Am 3+ /Na+ exchange and solvent extraction in the presence of sulfate. When used for the analogous Nd 3+ −SO 4 2− system to predict NdPO 4 (c) solubility in the presence of sulfate, they provided excellent agreement between the predicted and the observed solubilities, indicating that they can be reliably used to determine Nd 3+ or Am 3+ ion interactions with SO 4 2− in all ground waters where SO 4 2− is less than 0.5m
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 27 (1998), S. 1109-1122 
    ISSN: 1572-8927
    Keywords: Isosaccharinic acid ; solubility product ; aqueous complexes ; Ca complexes ; thermodynamic data
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The solubility of calcium isosaccharinate Ca(ISA)2(c) was determined at 23°C as a function of pH (1–14) and calcium ion molality (0.03–0.52). The similarity of solubility from the over- and undersaturation directions for different equilibration periods indicated that equilibrium in these solutions was reached rapidly (〈 7 days) and that these data can be used to develop thermodynamic equilibrium constants. The solubility data were interpreted using the Pitzer ion–interaction model. The logarithms of the thermodynamic equilibrium constants determined from these data were 1.30 for the dominant reaction at pH 〈 4.5 [Ca(ISA)2(c) + 2H+ ⇌ Ca2+ + 2HISA(aq)], and −2.22 for the dominant reaction at 4.5 [Ca(ISA)2(c)+ ⇌ Ca(ISA)2(aq)]. In addition, the logarithm of the dissociation constant of HISA [HISA(aq) ⇌ ISA- + H+] was calculated to be −4.46.
    Type of Medium: Electronic Resource
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