An analysis of the thermodynamics of transfer of polar non-electrolytes from water to aqueous concentrated salt solutions

1977 ◽  
Vol 30 (12) ◽  
pp. 2597 ◽  
Author(s):  
RF Cross ◽  
PT McTigue

A calorimeter has been constructed and used to determine the limiting enthalpies of solution (ΔHS) of a series of alkyl acetates (methyl, ethyl, propyl, butyl and t-butyl) in water and aqueous solutions of some of the following salts: LiCl, NaCl, KCl, CsCl, KF, KBr, NaNO3 and NaClO4. These measurements are combined with previous activity coefficient determinations to obtain the thermodynamics of transfer for the esters. In the case of transfer to NaCl solutions, scaled-particle theory calculations are used to determine the thermodynamics of cavity transfer, which, when combined with the experimental total-transfer quantities, give rise to a set of quantities that we have called the interaction transfer quantities. These quantities indicate that the predominant factors in the transfer of neutral molecules containing both polar and non-polar segments from water to NaCl solutions are the transfer of the cavity and of the interactions of the polar group. The interactions of the alkyl side chains are shown to be similar to those of alkane molecules.


1985 ◽  
Vol 63 (12) ◽  
pp. 3403-3410 ◽  
Author(s):  
Peeter Kruus ◽  
Catherine A. Hayes

The solubility of carbon dioxide has been determined in tertiary butanol – water mixtures over the temperature range 1–25 °C. The solubility exhibits a sharp, temperature-dependent minimum in water-rich solutions corresponding to a maximum in the activity coefficient of t-butanol, which has also been determined. The activity coefficient of t-butanol has a prominent temperature-dependent maximum (γ > 7.0) at a solution composition of about 0.06 mole fraction alcohol. Application of the scaled particle theory indicates that volume effects are a governing factor in the gas solubility, but are insufficient to explain the total effect. The pH of t-butanol–water and t-butanol–water–CO2 mixtures reveals no major anomalous solvation effect.



1979 ◽  
Vol 57 (1) ◽  
pp. 71-76 ◽  
Author(s):  
Michael H. Abraham ◽  
Asadollah Nasehzadeh

A novel method for the assessment of the Ph4As+/Ph4B− assumption for free energies of transfer of single ions has recently been suggested by Treiner, and used by him to deduce that the assumption is not valid for transfers between water, propylene carbonate, sulpholane, dimethylsulphoxide, N-methyl-2-pyrrolidone, and perhaps also dimethylformamide. The basis of the method is the estimation of the free energy of cavity formation by scaled-particle theory, together with the hypothesis that the free energy of interaction of Ph4As+ (or Ph4B−) with solvent molecules is the same in all solvents, ΔGt0(int) = 0. It is shown in the present paper that (a) whether or not the Ph4As+/Ph4B− assumption applies to transfer to a given solvent depends on which other solvent is taken as the reference solvent in Treiner's method, (b) the calculation of the cavity free energy term by scaled-particle theory and by the theory of Sinanoglu – Reisse – Moura Ramos (SRMR) yields values so different that the method cannot be considered reliable, (c) the calculation of cavity enthalpies and entropies for Ph4As+ or Ph4B− by scaled-particle theory yields results that are chemically not reasonable, (d) the hypothesis that ΔGt0(int) = 0 conflicts with SRMR theory, and (e) the conclusions reached by Treiner are not in accord with recent work that in general supports the Ph4As+/Ph4B− assumption for solvents that are rejected by Treiner.





1976 ◽  
Vol 32 (1) ◽  
pp. 237-256 ◽  
Author(s):  
Erich Bergmann




2006 ◽  
Vol 125 (20) ◽  
pp. 204505 ◽  
Author(s):  
Swaroop Chatterjee ◽  
Pablo G. Debenedetti ◽  
Frank H. Stillinger


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