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  • heat capacity changes  (3)
  • 8-hydroxyquinoline side arm  (1)
  • 1995-1999  (4)
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  • 1995-1999  (4)
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  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 26 (1997), S. 47-61 
    ISSN: 1572-8927
    Schlagwort(e): Dilution enthalpies ; activity coefficient ; alkali metal chlorides ; equilibrium constants ; enthalpy changes ; entropy changes ; heat capacity changes ; high temperature ; aqueous solution
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Dilution enthalpies, measured using isothermal flow calorimetry, are reported for aqueous solutions of LiCl, KCl, and CsCl at 300°C and 11.0 MPa, 325°C and 14.8 MPa, and 350°C and 17.6 MPa. The concentration range of the chloride solutions was 0.5 to 0.02m. Parameters for the Pitzer excess Gibbs ion-interaction equation were determined from the fits of the experimental heat data. Equilibrium constants, enthalpy changes, entropy changes, and heat capacity changes for ion association of the chloride salts were estimated from the heat data. For all systems, the enthalpy and entropy changes were positive and had accelerating increases with temperature. The resulting equilibrium constants show significant, but smaller, increases with temperature.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 26 (1997), S. 47-61 
    ISSN: 1572-8927
    Schlagwort(e): Dilution enthalpies ; activity coefficient ; alkali metal chlorides ; equilibrium constants ; enthalpy changes ; entropy changes ; heat capacity changes ; high temperature ; aqueous solution
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Dilution enthalpies, measured using isothermal flow calorimetry, are reported for aqueous solutions of LiCl, KCl, and CsCl at 300°C and 11.0 MPa, 325°C and 14.8 MPa, and 350°C and 17.6 MPa. The concentration range of the chloride solutions was 0.5 to 0.02 m. Parameters for the Pitzer excess Gibbs ion-interaction equation were determined from the fits of the experimental heat data. Equilibrium constants, enthalpy changes, entropy changes, and heat capacity changes for ion association of the chloride salts were estimated from the heat data. For all systems, the enthalpy and entropy changes were positive and had accelerating increases with temperature. The resulting equilibrium constants show significant, but smaller, increases with temperature.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 27 (1998), S. 183-194 
    ISSN: 1572-8927
    Schlagwort(e): Dilution enthalpies ; activity coefficients ; alkali metal hydroxides ; equilibrium constants ; enthalpy changes ; entropy changes ; heat capacity changes ; high temperature ; aqueous solution
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Dilution enthalpies, measured using isothermal flow calorimetry, are reported for aqueous solutions of KOH and CsOH at 300°C and 11.0 MPa, 325°C and 14.8 MPa, and for aqueous solutions of NaOH, KOH, and CsOH at 350°C and 17.6 MPa. Previously collected dilution enthalpies for aqueous solutions of NaOH at 300°C and 9.3 MPa and at 325°C and 12.4 MPa were included when fitting the Pitzer parameters. The concentration range of the hydroxide solutions was 0.5–0.02 molal. Parameters for the Pitzer excess Gibbs ion-interaction equation were determined from the fits of the experimental heat data. Equilibrium constants, enthalpy changes, entropy changes, and heat capacity changes for alkali metal ion association with hydroxide ion were estimated from the heat data. For all systems, the enthalpy changes and entropy changes were positive and had accelerating increases with temperature. The resulting equilibrium constants show significant, but smaller, increases with temperature.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 29 (1997), S. 259-268 
    ISSN: 1573-1111
    Schlagwort(e): Crown ether ; metal ion selectivity ; equilibrium constant ; enthalpy change ; entropy change ; 8-hydroxyquinoline side arm
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Thermodynamic quantities (log, K, ΔH, and TΔS) for theinteractions of six azacrown ethers each bearing an 8-hydroxyquinoline (CHQ)side arm (1-6) with Na+, K+, Ba2+, and Cu2+ were determined by calorimetrictitration in methanol solution at 25°C. The results indicate that theseligands form stable complexes with the cations studied. Ligands 1 and 3 thathave CHQ attached through position 7 (next to the OH group) show highselectivity for Cu2+ (log K values of 8.12 and 9.44, respectively) over Na+,K+, and Ba2+ by more than four orders of magnitude. On the other hand,ligands 2 and 4 that have CHQ attached through position 2 (next to thequinoline nitrogen group) form more stable complexes with Na+, K+, and Ba2+,but less stable complexes with Cu2+, than ligands 1 and 3. All ligandsinteract more strongly with K+ than with Na+. The K+/Na+ selectivity forligands 4 and 5 is about 1.5 log K units. All complexation reactions displaynegative enthalpy changes. In most cases the entropy changes are alsonegative, indicating that formation of the complexes is enthalpy driven. 1HNMR spectral experiments demonstrate coordination of the cations by alldonor atoms of the ligands including those of the CHQ arm. In all cases, theOH signal is observed in the 1H NMR spectra, suggesting that thecomplexation with the cations does not involve deprotonation of the CHQgroups in the ligands.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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