A SENSITIVE CRITERION OF THE PRECISION AND OF CONSTANT ERRORS IN THE CONDUCTANCE DATA OF WEAK ELECTROLYTES, THE DETERMINATION OF THE MOLAR CONDUCTANCE OF ORGANIC ELECTROLYTES AT ZERO CONCENTRATION AND A STUDY OF THE CORRECTION FOR THE SPECIFIC CONDUCTANCE OF THE CONDUCTIVITY OF WATER.

1914 ◽  
Vol 36 (11) ◽  
pp. 2268-2283 ◽  
Author(s):  
C. G. Derick
Keyword(s):  
Molar Conductance ◽  
Specific Conductance ◽  
Organic Electrolytes ◽  
Conductance Data ◽  
Weak Electrolytes

Study of the Comparative Solvation Behaviour of Na+ and Cu+ Cations in Acetonitrile + N,N-Dimethylformamide Mixtures at 298.15 K

2004 ◽  
Vol 59 (9) ◽  
pp. 615-620 ◽  
Author(s):  
Dip Singh Gill ◽  
Hardeep Anand ◽  
J. K. Puri
Keyword(s):  
Molar Conductance ◽  
Viscosity Data ◽  
Extended Form ◽  
Composition Region ◽  
Conductance Data ◽  
Reference Electrolyte ◽  
B Coefficients

Viscosity and molar conductance of Bu4NBPh4, Bu4NClO4, [Cu(CH3CN)4]ClO4, NaClO4 and NaBPh4 have been measured in the concentration ranges 0.02 - 0.5 mol dm−3 and 0.0005 - 0.0065 mol dm−3 at 298.15 K in AN + DMF mixtures containing 0, 10, 20, 40, 60, 75, 80, 90, and 100 mol % DMF. The viscosity data have been analyzed by the extended form of the Jones-Dole equation in the form: (η/η0) = 1+AC1/2+BC+DC2 to evaluate B and D parameters and the conductance data by the Shedlovsky equation to evaluate Λo and KA values of the salts. Ionic viscosity B-coefficients (B±) and ionic molar conductances (λ◦ i) have been calculated by using Bu4NBPh4 as a reference electrolyte. Solvated radii (ri) for Na+, Cu+ and ClO4 − have been estimated by using Gill’s modification of Stokes’ law. The variation of B± and ri as a function of mol % DMF shows that both Na+ and Cu+ are highly solvated in AN + DMF mixtures over the entire composition region. The solvation passes through a maximum between 40 to 80 mol % DMF. Both Na+ and Cu+ are more strongly solvated between 40 to 80 mol % DMF. Cu+ is relatively more strongly solvated than Na+ in AN + DMF mixtures. ClO4 − shows poor solvation in AN + DMF mixtures.

Solvation effects on the conductivity of concentrated electrolyte solutions

1976 ◽  
Vol 54 (18) ◽  
pp. 2953-2966 ◽  
Author(s):  
Douglas E. Goldsack ◽  
Raymond Franchetto ◽  
Arlene (Anttila) Franchetto
Keyword(s):  
Activity Coefficient ◽  
Alkali Halide ◽  
Infinite Dilution ◽  
Electrolyte Solutions ◽  
Molar Conductance ◽  
The Other ◽  
Solvation Number ◽  
Parameter Equation ◽  
Conductance Data ◽  
Halide Salts

The Falkenhagen–Leist–Kelbg equation for the conductivity of electrolyte solutions has been extended to include the effect of solvation on the concentration of the salt. Two equations have been derived, both of which have only two freely adjustable parameters at any temperature: Λ0 the molar conductance of the salt at infinite dilution and H0, a solvation number parameter for the salt. In one of these equations H0 is assumed to be independent of concentration. In the other, H0 is assumed to be dependent on concentration and an explicit concentration dependent formula is derived for H0. Conductance data for the alkali halide salts in the 0.5 to 10 m concentration range and 0 to 60 °C temperature range were found to be adequately reproduced by both these equations, but with the variable hydration parameter equation yielding better fits to the data. The H0 parameters from the fixed hydration parameter equation are found to be similar to those obtained from the analysis of activity coefficient and other data whereas the variable hydration parameter equation yields H0 parameters which are much larger.

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