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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 29 (1990), S. 260-264 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 19 (1990), S. 175-185 
    ISSN: 1572-8927
    Keywords: Solubility ; barite ; celestite ; activity coefficient ; equilibrium constants
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The solubilities of barite [BaSO4(c)] and celestite [SrSO4(c)] in Na2SO4 were studied and found to be significantly lower than the experimental values reported in the literature. Our new solubility data are in excellent agreement with the predictions of ion interaction models, which have previously been parameterized primarily from solubility data obtained in chloride media. Our solubility data were analyzed both in terms of aqueous thermodynamic models that included ion association species and in terms of ion interaction models that did not require the explicit recognition of such species. In the case of SrSO4, although both ion association and ion interaction models can accurately model our solubility data, the ion interaction approach is preferred because it is easier to extend to higher concentrations. In the case of BaSO4, the aqueous ion interactions appear to be stronger than those for SrSO4, and so the explicit recognition of a BaSO4(aq) ion association species is preferred. The logarithms of the thermodynamic solubility products (log K sp ) for celestite and barite were −6.62±0.02 and −10.05±0.05, respectively. When the data were analyzed using models that include ion association species, the logarithms of the thermodynamic equilibrium constants for the SrSO4(aq) and BaSO4(aq) association reactions were 1.86±0.03 and 2.72±0.09, respectively.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-8927
    Keywords: Solubility ; equilibrium constants ; activity coefficient ; CdCO3(c) ; cadmium ; carbonato complexes ; ion interaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The aqueous solubility of CdCO3(c) was studied in 0.01M NaClO4, in solutions equilibrated with N2-CO2(g) mixtures that contained 0.0003, 0.001, or 0.138 atmospheres of CO2(g). The pH ranged from about 4.5 to 9, and the studies were conducted from both the oversaturation and the undersaturation directions, with the equilibration periods ranging from 6 to 57 d. To determine the carbonato complexes of Cd(II), the solubility of CdCO3(c) was also studied in 0.0016 to 1.00M Na2CO3 solutions at fixed hydroxide ion concentration, and in solutions with fixed aqueous C concentrations (0.1 and 0.01M C) over a range of OH− from 1×10−5 to 1.0M. The equilibrium Cd concentrations were reached in less than about 6 d. Pitzer's ion-interaction model was used to interpret these solubility data, as well as CdCO3(c) solubility data reported in the literature, which extended to 5.0M K2CO3 with an ionic strength of approximately 18.6 m. Our thermodynamic model required the introduction of two aqueous Cd2+-CO 3 2− complexes, CdCO3(aq) and Cd(CO3) 2 2− , as well as ion-interaction parameters for Cd(CO3) 2 2− with the bulk cations Na+ and K+. This model gave excellent agreement with all available experimental data extending to 5.0M K2CO3. The logarithms of the thermodynamic equilibrium constants for the reactions: $$\begin{gathered} CdCO_3 \left( c \right) \rightleftarrows Cd^{2 + } + CO_3^{2 - } \hfill \\ Cd^{2 + } + CO_3^{2 - } \rightleftarrows CdCO_3 \left( {aq} \right) \hfill \\ Cd^{2 + } + 2CO_3^{2 - } \rightleftarrows Cd\left( {CO_3 } \right)_2^{2 - } \hfill \\ \end{gathered} $$ were found to be −12.24±0.1, 4.71±0.1, and 6.49±0.1, respectively. The β0 ion-interaction parameters for Cd(CO3) 2 2− −Na+ and Cd(CO3) 2 2− −K+ were found to be −0.14 and −0.06, respectively.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-8927
    Keywords: Ion interaction ; hannebachite ; solubility ; aqueous thermodynamics ; CaSO3·1/2H2O(c) ; CaSO 3 0 ; suffite
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The solubility of CaSO3·1/2H2O(c) was studied under alkaline conditions (pH〉8.2), in deaerated and deoxygenated Na2SO3 solutions ranging in concentration from 0.0002 to 0.4M and in CaCl2 solutions ranging in concentration from 0.0002 to 0.01M, for equilibration periods ranging from 1 to 7 days. Equilibrium was approached from both the over- and the under-saturation directions. In all cases, equilibrium was reached in 〈1 days. The aqueous Ca2+−SO 3 2− ion interactions can be satisfactorily modeled using either ion-association or ion-interaction aqueous thermodynamic models. In the ion-association model, the log K°=2.62±0.07 for Ca2++SO 3 2− ⇆CaSO 3 0 . In the Pitzer ion-interaction model, the binary parameters β(0) and β(1) for Ca2+−SO 4 2− were used, and the value of β(2) was determined from the experimental data. As expected given the strong association constant, the value of β(0) was quite small (about −134). We feel a combination of the two models is most useful. The logarithm of the thermodynamic equilibrium constant (K°) of the CaSO3·1/2H2O(c) solubility reaction (CaSO3·1/2H2O(c)⇆Ca2++SO 3 2+ +0.5H2O) was found to be −6.64±0.07.
    Type of Medium: Electronic Resource
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