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Journal ArticleDOI

Solute‐Solute Interactions in Aqueous Solutions

John J. Kozak, +2 more
- 15 Jan 1968 - 
- Vol. 48, Iss: 2, pp 675-690
TLDR
In this article, the authors interpreted solvent-solute interactions in aqueous solutions of nonelectrolytes using both lattice and distribution function theories of the dissolved state.
Abstract
Solute‐solute interactions in aqueous solutions of nonelectrolytes are interpreted using both lattice and distribution function theories of the dissolved state. Experimental activity data of high precision can be obtained from the literature for aqueous solutions of many nonelectrolytes. If the logarithm of the solvent activity coefficient (γ1) is expressed as a power series in the mole fraction of the solute (x2), lnγ1 = Bx22 + Cx23 + ···, then the coefficients B and C can be determined analytically from the experimental measurements. Values of B were obtained for 52 aqueous mixtures; values of C were obtained for 39 of these mixtures. The solutes considered include aliphatic alcohols, amines, amides, ketones, fatty acids, amino acids, and sugars. In some cases, experimental data were available from which the temperature dependence of the quantities B and C could also be determined. The effect of solute size on the coefficients B and C was investigated using the lattice theories of Flory, Huggins, and Gu...

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Citations
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Journal ArticleDOI

Correlation between apparent molal volume and osmotic coefficient in aqueous nonelectrolyte solutions

TL;DR: In this article, a linear correlation between apparent molal volume and osmotic coefficient in aqueous solution is derived for the multiple association process of solute molecules (purine-like compounds).
Journal ArticleDOI

The enthalpy of dilution of aqueous cellobiose solutions at 298.15 K

TL;DR: In this paper, the free energy and enthalpic pairwise interaction coefficients obtained from the experimental results have been transposed to the McMillan-Mayer (MM) state to reflect better molecular events.
Journal Article

Hydrophobicity Varying with Temperature, Pressure, and Salt Concentration B

TL;DR: In this article, the authors investigated the relationship between the solvation free energy and the solvent-induced pair potential at a contact distance in temperature, pressure, and salt concentration variations, and showed that the slope of the linear relation is dependent on the mode of variation.
Journal ArticleDOI

Phase Diagram of Na2S2O3)+t‐Butanol+Water at Ambient Pressure and Temperature

TL;DR: In this article, the authors report the studies concerning liquid-liquid-solid equilibria for the ternary system Na2S2O3+t-butanol+water at ambient pressure and at room temperature (303±2 K).
Journal ArticleDOI

Thermochemistry of the dissolution of DL-α-alanyl-DL-norleucine in aqueous solutions of amides at 298.15 K

TL;DR: In this paper, enthalpies of dissolution of DL-α-alanyl-DL-norleucine were determined by calorimetry in aqueous solutions of formamide (FA), N-methylformamide (MFA), and N,N-dimethylformamide(DMF), at a concentration of amides of x2 = 0.0.4 molar parts and T = 298.15 K.
References
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Book

Molecular theory of gases and liquids

TL;DR: Molecular theory of gases and liquids as mentioned in this paper, molecular theory of gas and liquids, Molecular theory of liquid and gas, molecular theories of gases, and liquid theory of liquids, مرکز
Book ChapterDOI

Some factors in the interpretation of protein denaturation.

TL;DR: The chapter reviews that the denaturation is a process in which the spatial arrangement of the polypeptide chains within the molecule is changed from that typical of the native protein to a more disordered arrangement.
Journal ArticleDOI

Thermodynamics of High Polymer Solutions

TL;DR: In this paper, a statistical treatment of high polymer solutions has been carried out on the basis of an idealized model, originally proposed by Meyer, which is analogous to the one ordinarily assumed in the derivation of the ''ideal'' solution laws for molecules of equal size.
Journal ArticleDOI

Free Volume and Entropy in Condensed Systems III. Entropy in Binary Liquid Mixtures; Partial Molal Entropy in Dilute Solutions; Structure and Thermodynamics in Aqueous Electrolytes

TL;DR: The first and second papers in this series, which make it possible to interpret entropy data in terms of a physical picture, are applied to binary solutions, and equations are derived relating energy and volume changes when a solution is formed to the entropy change for the process as discussed by the authors.
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