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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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Investigations to explore interactions in (polyhydroxy solute+l-ascorbic acid+H 2 O) solutions at different temperatures: Calorimetric and viscometric approach

TL;DR: In this article, the Jones-Dole viscosity B-coefficients for polyhydroxy solutes with cosolute ( l -ascorbic acid) were calculated and used to explore the nature of interactions of these solutes.
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Mixed micellar aggregates of nonionic and anionic surfactants with short hydrophobic tails: a microcalorimetric study.

TL;DR: It can be argued that the interactions among the hydrophilic heads in the C(6)E(5)-C( 6)SNa mixed micelles prevail on the contribution of the Hydrophobic tails in ruling the enthalpic properties of the system.
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Thermodynamics of tetramethylurea solutions in ethylene glycol: The evidence of pairwise solvophobic interaction

TL;DR: In this paper, the authors focus on the solute- solute interactions in dilute solutions of a typically hydrophobic solute tetramethylurea (TMU) in ethylene glycol (EG) which forms the three-dimensional hydrogen-bond network at the supramolecular level.
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Volume and compressibility changes on mixing solutions of alkali halides/sodium acetate with sodium salt of butyric acid at 298.15 K: Understanding like charge ionic (anion–anion) interactions in water

TL;DR: In this article, the authors measured density and sound velocity data for aqueous binary and ternary solution involving aqueously binary solutions of studied electrolytes at 29815-K and the data were utilized for the determinations of the apparent molar volume and apparent molastic compressibility values at finite concentrations.
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.
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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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