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  • 1970-1974  (7)
  • dissociation constant  (2)
  • hydrochloric acid  (2)
  • osmotic coefficients  (2)
  • ionization
Materialart
Erscheinungszeitraum
Jahr
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 3 (1974), S. 593-602 
    ISSN: 1572-8927
    Schlagwort(e): Activity coefficients ; iodic acid ; ionic equilibria ; isopiestic measurements ; osmotic coefficients
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Isopiestic vapor pressure measurements have been used to determine the osmotic coefficients of aqueous solutions of iodic acid at molalities from 0.1 to 17 mole-kg−1 at 25°C. The isopiestic standards were solutions of sodium chloride and solutions of sulfuric acid. Because of the corrosive nature of iodic acid, platinum cups were used. Stoichiometric activity cofficients of iodic acid were derived by a Gibbs-Duhem integration. The activity coefficients for solutions of molality greater than 0.5 mole-kg−1 cannot be accounted for in terms of the two equilibria, namely, the acidic dissociation of iodic acid and formation of the ion H(IO3) 2 − , shown by Pethybridge and Prue to explain adequately the behavior in dilute solutions. The activity coefficient is unexpectedly small in concentrated solutions, suggesting the formation of neutral aggregates of iodic acid. The presence of dimers and tetramers, or alternatively trimers and tetramers, can explain the observed results up to a molality of 7 mole-kg−1.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 1 (1972), S. 167-172 
    ISSN: 1572-8927
    Schlagwort(e): Excess free energy of mixing ; mixed salt solutions ; osmotic coefficients ; KCl ; K2SO4 ; NaCl ; Na2SO4
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Aqueous solutions of sodium chloride, potassium chloride, sodium sulfate, and potassium sulfate can be mixed in six ways to give ternary mixtures. Two of these have already been studied and results are now presented for the remaining four systems: H2O−NaCl−K2SO4, H2O−Na2SO4−K2SO4, H2O−KCl−Na2SO4, and H2O−KCl−K2SO4.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 1 (1972), S. 507-516 
    ISSN: 1572-8927
    Schlagwort(e): Acetic acid ; dissociation constant ; N methylpropionamide ; nonaqueous solvents ; solute-solvent interactions ; weak acids
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The dissociation constant of acetic acid in N-methylpropionamide (NMP) has been determined at 11 temperatures from 5 to 55°C by measurement of the electromotive force of cells without liquid junction containing hydrogen gas electrodes and silver-silver chloride electrodes. The pK at 25°C was found to be 7.995 (molal scale) as compared with 4.756 in water; thus, acetic acid is much weaker in NMP than in water despite the higher dielectric constant of the nonaqueous solvent (176 as compared with 78.3 at 25°C). The standard changes of enthalpy and entropy for the dissociation of acetic acid were calculated from the temperature coefficient of pK, and thermodynamic functions for the transfer dissociation process were obtained. The weakness of acetic acid in NMP is discussed in terms of electrostatic effects and solute-solvent interactions.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 1572-8927
    Schlagwort(e): Acidic dissociation ; dissociation constant ; emf measurements ; ionization processes ; N-methylpropionamide ; solvation ; tris-(hydroxymethyl)aminomethane
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The dissociation constant of protonated tris(hydroxymethyl)aminomethane (tris·H+) in the solvent N-methylpropionamide (NMP) has been determined at intervals of 5°C from 10 to 55°C by measurement of the emf of cells without liquid junction using hydrogen and silver-silver chloride electrodes. At 25°C, pK a was found to be 8.831, as compared with 8.075 in water. The standard changes in Gibbs energy, enthalpy, and entropy for the dissociation process have been evaluated from the dissociation constant and its change with temperature. By comparison with similar data for the dissociation of tris·H+ in water, thermodynamic functions for the transfer from water to NMP have been derived. The dissociation process is isoelectric, and the solvent dielectric constant is high (ε=176 at 25°C). Consequently, electrostatic charging effects are expected to be minimal, and the change in dissociation constant depends primarily on solute-solvent interactions. The results, combined with transfer energies for HCl, tris, and tris·HCl from emf and solubility measurements, demonstrate that the decreased acidic strength of tri·H+ in NMP is attributable in large part to the fact that NMP is less effective than water in stabilizing tris and its salts.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 2 (1973), S. 173-191 
    ISSN: 1572-8927
    Schlagwort(e): Calcium bromide ; calcium chloride ; hydration of ions ; hydrochloric acid ; lithium bromide ; lithium chloride ; osmotic coefficient ; perchloric acid ; potassium hydroxide ; sodium chloride ; sodium hydroxide ; solvation of ions
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract A stepwise hydration-equilibrium model for aqueous electrolytes is developed and shown to give a good quantitative account of osmotic coefficients of strong, highly soluble electrolytes up to concentrations of 20–30 m. The main parameters needed are two equilibrium constants describing the stepwise hydration and the number of hydration sites. Choice of ion-size parameter has only a minor effect.
    Materialart: Digitale Medien
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Journal of solution chemistry 3 (1974), S. 837-845 
    ISSN: 1572-8927
    Schlagwort(e): Activity coefficient ; ammonium chloride ; Harned's rule ; hydrochloric acid ; mixtures of electrolytes
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Electromotive-force measurements of cells containing hydrochloric acid and ammonium chloride at constant total molality have been used to determine the variation of the logarithm of the activity coefficient of hydrochloric acid with change in the amount of ammonium chloride in the solution. The results are interpreted in the light of the recent work of Pitzer, and it is found that Harned's rule holds for both electrolytes.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    ISSN: 1572-8927
    Schlagwort(e): Acidic dissociation ; ampholyte dissociation ; dissociation constants ; ionization ; methanol-water solvents ; solute-solvent effects ; N-Tris(hydroxymethyl)methylglycine (“tricine”) ; zwitterions
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The pK values for the two acidic dissociation steps of the ampholyte N-tris-(hydroxymethyl)methylglycine (“tricine”) in 50 mass % methanol-water solvent have been determined by emf measurements of cells of the type Pt|H2(g, 1 atm), tricine buffer, Br−, AgBr|Ag over the range 5 to 50°C (pK 1)and 5 to 60°C (pK 2).The standard thermodynamic quantities ΔHo, ΔSo, and ΔC p o for the two dissociation processes have been derived and are compared with the corresponding values for tricine and the parent glycine in water and with those for other acids in 50 mass % methanol-water solvent. Both tricine and protonated tricine become weaker acids when methanol is added to the aqueous solvent. It appears that a strong stabilization of the zwitterion in water is responsible for this behavior. This conclusion is supported by comparing the changes in entropy and heat capacity for the dissociation of tricine with the values of these quantities for the dissociation of “model” acids of simple structure, such as ammonium ion and acetic acid.
    Materialart: Digitale Medien
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