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  • Articles  (2)
  • Activity coefficient  (1)
  • 5'-O-demethyl-8-O-methyl-dioncophylline A
  • enthalpy
  • 1990-1994  (1)
  • 1985-1989  (1)
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  • Articles  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 21 (1992), S. 311-321 
    ISSN: 1572-8927
    Keywords: Activity coefficient ; amino acid ; EMF ; first dissociation constant ; HEPES ; glycine ; MOPSO ; ionic interaction ; hydrochloric acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Ionic interaction in the three systems Hcl-HEPES (N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid), HCl-MOPSO (3-(N-Morpholino)-2-hydroxypropanesulfonic acid), and HCl-glycine have been studied in terms of their mutual influence on the respective activity coefficients of each component. Activity coefficients for each component of the three systems are calculated from emf measurements of solutions containing HCl and the amino acid in a H2/solution/AgCl,Ag cell at 25°C. The first dissociation constant of HEPES at 25°C has also been determined using emf and pH titration measurements.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 15 (1986), S. 675-692 
    ISSN: 1572-8927
    Keywords: Deuterium chloride ; deuterium oxide ; electrochemical cell ; emf ; enthalpy ; entropy ; free energy ; heat capacity ; isotope effect ; standard potential ; thermodynamics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The themodynamic properties of solutions of deuterium chloride (DCl) in deuterium oxide (D2O) have been determined from emf measurements of the electrochemical cell without transference from 5 to 50°C, and from 0.002 to 1.0 mol-kg−1. The standard potential of the silver/silver chloride electrode relative to the platinum/deuterium electrode has been determined. An equation for the Gibbs energy as a function of temperature has been derived from which the enthalpy, entropy, and heat capacity have been computed. Equations for the activity coefficient and the osmotic coefficient of DCl in D2O have been developed. The excess Gibbs energy of the solution and the excess partial molar free energy as a function of temperature have been calculated, from which the other excess thermodynamic properties have been computed. The values for the heat capacity and the apparent molar heat capacity have been compared with calorimetric data in the literature. The relative partial molar enthalpy has been calculated. The solvent isotope effect on the excess thermodynamic functions is discussed.
    Type of Medium: Electronic Resource
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