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  • NaCl  (10)
  • emf  (3)
  • Springer  (13)
  • American Association for the Advancement of Science
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  • Springer  (13)
  • American Association for the Advancement of Science
  • 1
    ISSN: 1572-8927
    Keywords: sound speeds ; compressibilities ; partial molar compressibilities ; NaCl ; Na2SO4 ; MgCl2 ; MgSO4 ; equations of state
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The relative sound velocities (U-U°) of aqueous NaCl, Na2SO4, MgCl2, and MgSO4 solutions were measured from 0.05m to saturation and from 0 to 45°C. The sound speeds were combined with our earlier work and fitted to a function of molality and temperature to standard deviations within 0.3 m-sec−1. The adiabatic compressibilities, βs, were determined from the sound speeds and used to calculate adiabatic apparent molar compressibilities, Kϕ,s, isothermal compressibilities, β, and apparent molar compressibilities, Kϕ, were determined from the adiabatic values using literature data for expansibilities and heat capacities. The values of Kϕ have been extrapolated to infinite dilution using an extended limiting law. The resulting K0 at various temperatures are in reasonable agreement with literature values. The results of this study have been combined with our earlier results to derive a secant bulk modulus equation of state for NaCl, Na2SO4, MgCl2, and MgSO4 solutions valid from 0 to 50°C and 0 to 1000 bar.
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  • 2
    ISSN: 1572-8927
    Keywords: samarium chloride: activity coefficients ; Nernst equation ; Harned's rule ; emf ; Pitzer equations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A comprehensive array of electrochemical cell measurements for the system HCl +SmCl3 + H2O was made from 5 to 55°C using a cell without liquid junction ofthe type:Pt; H2(g, 1 atm)|HCl (m A) + SmCl3 (m B)|AgCl, Ag (A)The present study, unlike previous studies of trivalent ions, are not complicatedby hydrolysis reactions. Measurements of the emf were performed for solutionsat constant total ionic strengths of 0.025, 0.05, 0.1, 0.25, 0.5, 1.0, 1.5, 2.0, 2.5,and 3.0 mol-kg−1. The mean activity coefficients of HCl (γHCl) in the mixtureswere calculated using the Nernst equation. All the experimental emf measurements(about 850) were first treated in terms of the simpler Harned's rule. Harnedinteraction coefficients (αAB and βAB) were calculated. The linear form of Harned'srule is valid for most ionic strengths, but quadratic terms are needed at I = 1.5and 3 mol-kg−1. The Pitzer model was used to evaluate the activity coefficientsusing literature values, β(0), β(1), and C φ, for HCl from 0 to 50°C and 25°C forSmCl3. The effect of temperature on the parameters for SmCl3 has been estimatedusing enthalpy and heat-capacity data. The mixing parameter ΘH,Sm wasdetermined at 25°C. The addition of the ΨH,Sm,Cl coefficient did not improve the fitsignificantly and no temperature dependence was found to be significant. Thevalue of ΘH,Sm = 0.2 ± 0.01 represented the values of γHCl with a standarddeviation of σ = 0.009 over the entire range of temperatures and ionic strength.The use of higher-order electrostatic effects (EΘH,Sm, EΘH,Sm) was included as itgave a better fit of the activity coefficients of HCl.
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  • 3
    ISSN: 1572-8927
    Keywords: Hydrochloric acid ; gadolinium chloride ; emf ; Harned's rule ; Pitzer equations ; activity coefficients ; mixtures of electrolytes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The emf of the cell $${\text{Pt, H}}_{\text{2}} ({\text{g, 1 atm}})|{\text{HCI(}}m_{\text{A}} {\text{),GdCl}}_{\text{3}} (m_B )|{\text{AgCl, Ag}}$$ without a liquid junction was used to investigate the HCl + GdCl3 + H2O mixedelectrolyte system. The emf of the cell was measured for HCl + GdCl3 + H2Osolutions at ionic strengths of 0.025, 0.05, 0.1, 0.5, 1.0, 1.5, and 2.0 mol-kg−1and at eleven temperatures ranging from 5 to 55°C at 5°C intervals. The meanactivity coefficients for HCl in the mixtures were determined using the Nernstequation. About 793 experimental emf data points were treated by the Harnedequations. Results show that hydrochloric acid follows Harned's rule at all ionicstrengths, but the quadratic term is needed for I = 1.5 mol-kg−1. Theion-interaction treatment of Pitzer was used to evaluate the results. The binary andternary mixing parameters at 25°C were found to be ΘH,Gd = 0.07 ± 0.03 andΨH,Gd,Cl = 0.14 ± 0.03. These values were determined using literature values ofβ(0), β(1), and C ψ for GdCl3 at 25°C and estimates of the effect of temperaturefrom 5 to 55°C using enthalpy and heat capacity data.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 16 (1987), S. 827-834 
    ISSN: 1572-8927
    Keywords: Acid dissociation constants ; emf ; TRISH ; TRIS buffers ; Pitzer coefficients
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The stoichiometric dissociation constant, pK*, of TRISH+ has been determined from emf measurements in NaClO4 solutions to 6.0m at 25°C. The results have been used to derive Pitzer coefficients for the interaction of TRISH+ with ClO 4 − . The coefficients have been compared to the values in NaCl solutions. The values of pK* for TRISH+ can be used to calibrate pH electrodes in NaClO4 solutions using TRIS buffers.
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  • 5
    ISSN: 1572-8927
    Keywords: Sound speeds ; compressibilities ; partial molal compressibilities ; NaCl ; Na2SO4 ; MgCl2 ; MgSO4 ; Pitzer theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The sound velocities of aqueous NaCl, Na2SO4, MgCl2, and MgSO4 solutions were measured from 25 to 95°C in 10o intervals from dilute to saturated solutions. The results were combined with our earlier data and fitted to functions of molality and temperature to within ±0.4 m-sec−1. The adiabatic compressibilities βS were calculated from sound speeds and used to calculate the adiabatic apparent molal compressibilities ξφ. Isothermal compressibilities β and isothermal apparent molal compressibilities χφ were calculated from βS using literature values for the expansibilities and heat capacities. The values of χφ were extrapolated to infinite dilution using the Debye-Huckel limiting law to determine partial molal compressibilities. The apparent molal compressibilities were fitted to Pitzer's equations. The Pitzer parameters for the concentration dependence of χφ were determined as a function of temperature. Correlations of χφ and Vφ at various temperatures were found for the electrolytes.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 18 (1989), S. 585-599 
    ISSN: 1572-8927
    Keywords: Fe(II) ; oxidation ; ionic strength ; NaCl ; NaClO4
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The rates of oxidation of Fe(II) in NaCl and NaClO 4 solutions were studied as a function of pH (6 to 9), temperature (5 to 25°C), and ionic strength (0 to 6m). The rates are second order with respect to [H+] or [OH−] and independent of ionic strength and temperature. The overall rate of the oxidation is given by $$d[Fe(II)]/dt = - k[Fe(II)][OH^ - ]^2 [O_2 ]$$ where [OH−]=K W * /[H+](K W * is the stoichiometric dissociation constant for water) and [O 2 ] is the molal concentration of the oxygen. The experimental results were fitted to equations of the form $$log{\text{ }}k = log{\text{ }}k_0 + {\rm A}\sqrt {\rm I} + {\rm A}\sqrt {\rm I} /T + CI$$ where log k0=21.56−1545/T, A=0.470, B=−646, and C=0.723 (σ=0.07) for NaCl; A=−1.638, B=0, and C=0.836 (σ=0.11) for NaClO 4 . The lower results in NaCl at higher ionic strengths are attributed to the formation of FeCl+ that has a slower rate of oxidation. The kinetic results giveβ FeCl = 1.2 ± 0.5, which is in reasonable agreement with literature data. Measurements of the effect of various ions on the rates were studied at constant ionic strength. The results were in the order HCO 3 − 〉Br−〉ClO 4 − 〉Cl−〉NO 3 − 〉SO 4 2− 〉B(OH) 4 − and were attributed to the relative strength of the interactions of Fe 2+ with these anions. The strong interactions of Fe 2+ with SO 4 2− and B(OH) 4 − were used to estimate the stability constants, logβ FeSO 4 = 1.8 ± 0.1 and logβ FeB(OH) 4 = 3.2 ± 0.1, which are in reasonable agreement with literature data.
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  • 7
    ISSN: 1572-8927
    Keywords: Sea salts ; NaCl ; Na2SO4 ; MgSO4 ; MgCl2 ; volumes of mixing ; densities
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The densities of mixtures of the six possible combinatons of the major sea salts (NaCl, Na2SO4, MgSO4, and MgCl2) were determined at constant ionic strengths of I=1.0 and I=3.0 at 25°C. The results are used to determine the volume changes for mixing (ΔV m ) the major sea salts. The values of ΔV m were fit to equations of the form ΔV m where y i is the molal ionic strength fraction of solute i, and υ0 and υ1 are parameters related to the interaction of like-charged ions. The cross-square rule was found to hold at both ionic strengths. Density estimates were made without and with the addition of volume of mixing terms to Young's Rule and compared to the experimental values. The densities calculated with the addition of volume of mixing terms gave better estimates, demonstrating that the densities of concentrated brines can be more accurately estimated using ΔV m terms. The equations of Reilly and Wood which include the cross-square rule were used to estimate the densities of the cross mixtures (NaCl−MgSO4 and MgCl2−Na2SO4). The estimated densities agree with the measured values to within ±30 ppm at I=1.0 and ±125 ppm at I=3.0.
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  • 8
    ISSN: 1572-8927
    Keywords: Speed of sound ; aqueous electrolytes ; compressibility ; sea salts ; NaCl ; Na2SO4 ; MgCl2 ; MgSO4
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The speed of sound of mixtures of the six possible combinations of the major sea salt ions (Na+, Mg2+, Cl−, and SO 4 2− ) have been determined at I=3.0 and at 25°C. The results have been used to determine the changes in the adiabatic compressibility of mixing ΔKm the major sea salts. The values of ΔKm have been fit to the equation ΔKm=y2y3I2[k0+k1(1-2y3)] where yi is the ionic strength fraction of solute i, k0 and k1 are parameters related to the interactions of like-charged ions. The Young cross-square rule is obeyed to within ±0.04×10−6 cm3-kg−1-bar−1. A linear correlation was found between the compressibility k0 and volume v0 interaction parameters (104k0=−0.24+3.999 v0, s=0.15) in agreement with out earlier findings. Estimates of the sound speeds for the cross square mixtures (NaCl+MgSO4 and MgCl2+Na2SO4) were made using the equations of Reilly and Wood. The estimated sound speeds were found to agree on the average with the measured values to ±0.36 m-sec−1.
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  • 9
    ISSN: 1572-8927
    Keywords: Densities ; partial molal volumes ; NaCl ; Na2SO4 ; MgCl2 ; MgSO4 ; Pitzer theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The densities of the major sea salts (NaCl, Na2SO4, MgCl2, and MgSO4) have been measured from 25 to 95°C and to saturation. These results have been combined with literature data and fitted to equations of the form $$\Delta d = Am{\text{ }} + {\text{ }}Bm^{3/2} {\text{ }} + {\text{ }}Cm^2 {\text{ }} + {\text{ }}Dm^{5/2} $$ where Δd=d−do (do is the density of water) and A, B, and C, etc., are polynomial functions of temperature. The standard deviations of the fits were better than ±50×10−6 g-cm−3 for all the salts from 0 to 95°C and to saturation. The apparent molal volumes Vϕ of the salts have been fitted to the equations of Pitzer. The infinite dilution values of Vϕ were in good agreement with literature data, provided the results were not overfit. The large deviations of Vϕ for MgSO4 from additivity as a function of concentration were attributed to the formation of MgSO4 ion pairs.
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  • 10
    ISSN: 1572-8927
    Keywords: Specific and apparent molar heat capacities ; multicomponent aqueous solutions ; mixed solutions ; NaCl ; KCl ; MgCl2 ; CaCl2 ; Young's rule ; flow calorimetry ; artificial Dead Sea waters ; brines
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The specific heat capacities of the aqueous multicomponent system NaCl +KCl+MgCl2+CaCl2 with ionic strength between 8.3 and 9.6 (resembling Dead Sea waters) were measured between 15°C and 45°C. The obtained data were fitted to an empirical equation as a function of concentration and temperature. The thermodynamic functions of the studied multicomponent system were found to be strongly influenced by changes in MgCl2 concentrations. The application of Young's rule to such concentrated systems was checked at 25°C. The calculated (by Young's rule) specific heat capacitiesC p and apparent molar heat capacities Cp,ϕ of these multicomponent electrolyte solutions were in reasonable agreement with the measured values (−0.008 J-g−1-K−1 and −2.6 J-mol−1-K−1, respectively).
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