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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
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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

Kirkwood−Buff Integrals in Aqueous Alcohol Systems: Comparison between Thermodynamic Calculations and X-Ray Scattering Experiments

TL;DR: In this article, the Kirkwood−Buff integrals for the aqueous solutions of methanol, ethanol, propanols, and butanols were calculated using a large-angle X-ray scattering (SAXS) experiment.
Journal ArticleDOI

Thermodynamic study of solvation of some amino acids, diglycine and lysozyme in aqueous and mixed aqueous solutions

TL;DR: In this article, the partial molar adiabatic compressibilities of transfer at infinite dilution ΔtrK°2,S for all the studied model compounds are positive and increase with the concentration of n-propanol.
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Enthalpies of dilution of aqueous solutions of formamide, acetamide, propionamide, andN,N-dimethylformamide

TL;DR: In this paper, the enthalpies of dilution of aqueous solutions of formamide, acetamide, propionamide, N, N-dimethylformamide, and sucrose have been measured from about 0.15 to 2.0 moles-kg−1 at 25.0°C.
Journal ArticleDOI

Studies on volumetric properties of some saccharides in aqueous potassium chloride solutions over temperature range (288.15 to 318.15) K

TL;DR: In this article, the standard partial molar volumes, V 2 ∞ at infinite dilution of monosaccharides, have been determined in water and in aqueous solutions of potassium chloride (0.5, 1.0, 2.0 and 3.0) using a vibrating tube densimeter.
Journal ArticleDOI

Heat capacities and volumes of interaction between mixtures of alcohols in water at 298.15 k

TL;DR: In this paper, the heat capacities and densities of mixtures of aqueous solutions of normal alcohols (methanol to n-butanol) and t -butanol were measured at 298.15 K at low molalities.
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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