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  • carbonato complex formation  (1)
  • methanol tetramer  (1)
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 29 (2000), S. 505-520 
    ISSN: 1572-8927
    Schlagwort(e): Cyclohexane ; methanol ; thermodynamic modeling ; virial coefficient formalism ; methanol tetramer ; phase diagram ; high temperature
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The phase diagram of cyclohexane-methanol was thermodynamically modeledin the range of 150 ≤ T/K ≤ 360 and at a pressure of 1 bar on the basis ofavailable experimental data. The Gibbs energy functions of four pure solid andtwo mixture phases were taken into consideration. The liquid phase was describedby a model based on mole fraction statistics and the simplified assumption ofmethanol tetramers mixed with cyclohexane monomers. The gas phase was treatedas a nonideal mixture with a Gibbs energy modeled on the basis of the virialcoefficient formalism considering only monomers. The Gibbs energies of the twosolid modifications of pure methanol, as well as pure cyclohexane, were fixedusing literature data. The pressure dependence of the Gibbs energies of the liquidand solid phases were neglected. The complete T-x phase diagram includinggas/liquid equilibria as well as p-x phase diagrams in the range of 20 and 55°C werecalculated. Experimental and calculated data were found to agree reasonably well.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    ISSN: 1572-8927
    Schlagwort(e): Phase equilibrium: solubility ; carbonates ; magnesium ; eitelite ; Pitzer model ; carbonic acid ; carbonato complex formation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The stoichiometric solubility constant of eitelite (NaMg 0.5 CO 3 +2H+ ⇄ Na++0.5Mg 2+ +CO 2 (g)+H 2 O, log*K pso I =14.67±0.03 was determined at I=3 m (mol kg−1) (NaClO 4 ) and 25°C. The stability of magnesium (hydrogen-)carbonato complexes in this ionic medium was explicitely taken into account. Consequently, trace activity coefficients of free ionic species, calculated from the Pitzer model with ion-interaction parameters from the literature, were sufficient for an evaluation of the thermodynamic solubility constants and Gibbs energies of formation for eitelite (−1039.88±0.60), magnesite (−1033.60±0.40), hydromagnesite (−1174.30±0.50), nesquehonite (−1724.67±0.40), and brucite (−835.90±0.80 kJ-mol −1 ). The increasing solubilities of nesquehonite and eitelite at higher sodium carbonate molalities were explained by invoking a magnesium dicarbonato complex (Mg2++2CO 3 2− ⇄ Mg(CO3) 2 2− , log βz = 3.90 ± 0.08). A set of ion-interaction parameters was obtained from solubility and dissociation constants for carbonic acid in 1 to 3.5 m NaClO 4 media $$(\theta _{HCO_3^ - ,ClO_4^ - } = 0.081, \theta _{CO_3^{2 - } ,ClO_4^ - } = 0.071, \psi _{{\rm N}a^ + , HCO_3^ - , ClO_4^ - } = - 0.019,\psi _{{\rm N}a^ + , CO_3^{2 - } , ClO_4^ - } = - 0.006,\lambda _{ClO_4^ - ,CO_2 } = - 0.076)$$ which reproduce these constants to 0.02 units in log K. The following Pitzer parameters are consistent with the previously studied formation of magnesium (hydrogen-)carbonato complexes in 3m NaClO 4 $$(\psi _{Mg^{2 + } , HCO_3^ - , ClO_4^ - } = - 0.36, \lambda _{ClO_4^ - ,MgCO_3 } = 0.081)$$ . The model and Gibbs functions of solid phases derived here reproduce original solubility data (−log [H+], [Mg 2+ ] tot ) measured in perchlorate medium within experimental uncertainty.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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