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  • Articles  (5)
  • molal volume  (3)
  • Activity coefficient  (2)
  • Springer  (5)
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  • Articles  (5)
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  • Springer  (5)
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  • 1
    ISSN: 1572-8927
    Keywords: Activity coefficient ; electromotive force ; Pitzer ; HCl ; Na2SO4 ; NaHSO4
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The electromotive force of HCl–Na2SO4 solutions has been determined from 5 to 50°C and ionic strengths from 0.5 to 6m with a Harned type cell $${\text{Pt; H}}_{\text{2}} ({\text{g, 1 atm}})|{\text{HCl(}}m_1 {\text{) + Na}}_{\text{2}} {\text{SO}}_{\text{4}} {\text{(}}m_2 {\text{)}}|{\text{AgCl, Ag}}$$ The results have been used to determine the activity coefficient of HCl in the mixtures. The activity coefficients have been analyzed with the Pitzer equations to account for the ionic interactions. The measurements were used to determine interaction coefficients (β0, β1) for NaHSO4 solutions from 5 to 50°C. The model represents the mean activity coefficients of HCl in the mixtures to ±0.005 over the entire temperature and concentration range of the measurements. The results have been combined with literature data to provide parameters that are valid from 0 to 250°C for NaHSO4 solutions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 1 (1972), S. 309-327 
    ISSN: 1572-8927
    Keywords: Effect of pressure ; ionization of water ; molal volume
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The apparent molal volumes of dilute (0.002 to 1.0m) aqueous HCl and NaOH solutions have been determined at 0, 25, and 50°C and NaCl solutions at 50°C. The partial molal volumes ( $$\bar V$$ ) of HCl, NaOH, and NaCl solutions have been determined from these apparent molal volumes and other reliable data from the literature. The partial-molal-volume changes ( $$\Delta \bar V_1 $$ ) for the ionization of water, H2O→H++OH−, have been determined from 0 to 50°C and 0 to 1m ionic strength from the partial molal volumes of HCl, NaOH, NaCl, and H2O. The partial molal compressibilities ( $$\bar K$$ for HCl, NaOH, NaCl, and H2O have been estimated from data in the literature and used to determine the partial molal compressibility changes ( $$\Delta \bar K_1 $$ ) for the ionization of water from 0 to 50°C and 0 to 1m ionic strength. The effect of pressure on the ionization constant of water has been estimated from partial-molal-volume and compressibility changes using the relation $$RTln(K^P /K) = - \Delta \bar V(P - 1) + \tfrac{1}{2}\Delta \bar K(P - 1)^2 $$ from 0 to 50°C and 0 to 2000 bars. The results agree very well with the directly measured values.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 3 (1974), S. 417-430 
    ISSN: 1572-8927
    Keywords: Ionization of boric acid ; molal volume ; effect of pressure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The apparent, φ v , and partial, $$\bar V_2 $$ molal volumes of dilute (0.02 to 0.7m) aqueous boric acid, B(OH)3, and sodium borate, NaB(OH)4, solutions have been determined from 0 to 50° C from precision density measurements. The φ v of boric acid is a linear function of the first power of concentration. For sodium borate, the Debye-Hückel theoretical limiting law slope for the φ v as a function of the square root of molar concentration is approached at all temperatures studied. The positive deviations at higher concentrations increase with decreasing temperature. The infinite-dilution volume properties of both B(OH)3 and NaB(OH)4 indicate that these solutes behave like “structure breakers” between 0 and 50°C (that is ∂2φ v ° /∂T2 is negative). The volume change for the ionization of boric acid in water $$\Delta \bar V^\circ $$ , is calculated from the volume data at various temperatures. This volume change has been used to estimate the effect of pressure on the ionization of boric acid solutions from 0 to 50°C and 0 to 1000 bars. The calculated effect of pressure on the ionization is in good agreement with direct measurements.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 3 (1974), S. 431-444 
    ISSN: 1572-8927
    Keywords: Boric acid ; molal volume ; nonelectrolyte-electrolyte mixture ; volumes of mixing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The apparent molal volume φ v of boric acid has been determined in various sodium chloride solutions at 0 and 25°C from precise density measurements. Similar to its behavior in pure water, the φ v of boric acid in NaCl solutions is a linear function of the concentration. The infinite dilution φ v ° and the slope S v * of B(OH)3 are larger in NaCl solutions than in pure water. NaCl appears to be able to dehydrate B(OH)3 and cause an increase in B(OH)3-B(OH)3 interactions. The mean apparent molal volumes Φ v of the B(OH)3−NaCl solutions are predicted from pure water data using a modification of Young's rule for electrolyte-nonelectrolyte mixtures and are compared to the directly measured values. A similar treatment was carried out on the density data of acetic acid-sodium chloride solutions. The modified Young's rule was found to give a good first approximation of the mean apparent molal volumes of nonelectrolyte-electrolyte systems. The deviations from the Young's rule approximation are studied as excess volumes of mixing boric acid and NaCl solutions.
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  • 5
    ISSN: 1572-8927
    Keywords: Activity coefficient ; electromitive force ; Pitzer, HCl ; Na2SO4 ; NaHSO4
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The electromotive force of HCl−Na2SO4 solutions has been determined from 5 to 50°C and ionic strengths from 0.5 to 6m with a Harned type cell $$Pt; H_2 (g, 1 atm)|HCl(m_1 ) + Na_2 SO_4 (m_2 )|AgCl, Ag$$ The results have been used to determine the activity coefficient of HCl in the mixtures. The activity coefficiencts have been analyzed with the Pitzer equations to account for the ionic interactions. The measurements were used to determine interaction coefficients (β0, β1) for NaHSO4 solutions from 5 to 50°C. The model represents the mean activity coefficients HCl in the mixtures to ±0.005 over the entire temperature and concentration range of the measurements. The results have been combined with literature data to provide parameters that are valid from 0 to 250°C for NaHSO4 solutions.
    Type of Medium: Electronic Resource
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