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Literature data on the apparent molar volumes φ of alanine in water and aqueous urea solutions at 298 K are analyzed. It is shown that the slope of the φ dependence on the alanine concentration is not dependent on the urea concentration. The standard partial volume of alanine increases linearly with the increase in the urea concentration (wt.%). The structural characteristics of hydrated complexes of alanine (hydration number, molar volume of water inside and outside the hydration sphere, and proper volume of alanine in solution) are given. The hydration number of alanine decreases by a factor of two in passing from water to a saturated (20m) urea solution. The effects of urea additions on the hydration numbers of alanine and glycine are compared.The thermodynamic characteristics of aqueous solutions are of fundamental importance for gaining new knowledge about such a phenomenon as hydration of substances and studying interparticle interactions and the structure of solutions. Thus, partial molar volumes "keep track" of the changes that occur with the unique structure of liquid water after dissolution of hydrophilic or hydrophobic substances as well as changes in the concentration of the solution and system parameters. They contain information about the state of water in a hydrate complex and allow one to calculate, within the current approaches, their structural characteristics such as the hydration number.Of particular interest, including in the structural aspect, are ternary systems, in which there is a wide range of particle-particle interactions. The purpose of this study is to analyze the data on apparent volumes of α-alanine in water and aqueous urea solutions, obtain an analytical expression for the dependence of the partial volume of alanine on the urea concentration, and calculate the hydration numbers of alanine. This paper continues the study of hydration numbers of substances in aqueous urea solutions [1,2].It should be mentioned that the properties and structure of aqueous urea solutions continue to be in focus of researchers [3][4][5][6][7][8][9]. Urea is most often referred to as a destroyer of water structure, but there are other points of view (see [10,11] and references therein). The analysis in [12] based on the criterion [13] allowed us to characterize both urea and amino acids studied in [12] (including α-alanine) as destroyers of water structure.The standard partial molar volumes of alanine in an aqueous urea solution at the molality m of 12.6 mol/kg water or less were determined in [14][15][16][17]. These characteristics are derived by extrapolating the apparent volumes φ to a zero
Literature data on the apparent molar volumes φ of alanine in water and aqueous urea solutions at 298 K are analyzed. It is shown that the slope of the φ dependence on the alanine concentration is not dependent on the urea concentration. The standard partial volume of alanine increases linearly with the increase in the urea concentration (wt.%). The structural characteristics of hydrated complexes of alanine (hydration number, molar volume of water inside and outside the hydration sphere, and proper volume of alanine in solution) are given. The hydration number of alanine decreases by a factor of two in passing from water to a saturated (20m) urea solution. The effects of urea additions on the hydration numbers of alanine and glycine are compared.The thermodynamic characteristics of aqueous solutions are of fundamental importance for gaining new knowledge about such a phenomenon as hydration of substances and studying interparticle interactions and the structure of solutions. Thus, partial molar volumes "keep track" of the changes that occur with the unique structure of liquid water after dissolution of hydrophilic or hydrophobic substances as well as changes in the concentration of the solution and system parameters. They contain information about the state of water in a hydrate complex and allow one to calculate, within the current approaches, their structural characteristics such as the hydration number.Of particular interest, including in the structural aspect, are ternary systems, in which there is a wide range of particle-particle interactions. The purpose of this study is to analyze the data on apparent volumes of α-alanine in water and aqueous urea solutions, obtain an analytical expression for the dependence of the partial volume of alanine on the urea concentration, and calculate the hydration numbers of alanine. This paper continues the study of hydration numbers of substances in aqueous urea solutions [1,2].It should be mentioned that the properties and structure of aqueous urea solutions continue to be in focus of researchers [3][4][5][6][7][8][9]. Urea is most often referred to as a destroyer of water structure, but there are other points of view (see [10,11] and references therein). The analysis in [12] based on the criterion [13] allowed us to characterize both urea and amino acids studied in [12] (including α-alanine) as destroyers of water structure.The standard partial molar volumes of alanine in an aqueous urea solution at the molality m of 12.6 mol/kg water or less were determined in [14][15][16][17]. These characteristics are derived by extrapolating the apparent volumes φ to a zero
Captopril is an angiotensin-converting enzyme (ACE) inhibitor that is used for the treatment of hypertension and congestive heart failure. This article addresses the accurate measurements of densities and refractive indices of solutions containing captopril in pure solvents such as water, methanol, ethanol and 1-propanol and aqueous mixtures of methanol, ethanol and propan-1-ol of 30%, 50% and 70% by volume in a wide range of drug concentration at 26 • C. This article also includes the evaluation of apparent molar volume, partial molar volume at infinite dilution and transfer volumes. The concentration dependence of the refractive indices studied and respective fitting parameters have been reported. Different properties are interpreted in terms of intermolecular interactions, effect of drug on structure of solvent/solvent mixture and overall structural fittings in solutions.
The analysis of changes in the partial volume of glycine 0 V 'in solutions of substances that have a different effect on water structure is presented. For glycine in mixtures of water with glycerol and ethylene glycol, we derive a single equation for the 0 V ' dependence on the volume fraction of alcohol. The addition of tert-butyl alcohol, ethylene glycol, glycerol, and urea to water leads to a decrease in the hydration number of the amino acid (glycine dehydrates). In 1m solutions the losses of hydration water are 3.2%, 4.5%, 5.7%, and 7.6% respectively. In a 4m solution of tert-butyl alcohol, glycine loses 44% of hydration water, the same as in a 15m urea solution and a 20m glycerol solution. A contribution of the structural dehydration of glycine is observed in dilute aqueous solutions of t-BuOH. In more concentrated solutions, intermolecular interactions in the binary mixed solvent counteract dehydration. These interactions compensate for 15-22% of water lost by glycine in a 20m solution of urea, glycerol, and ethylene glycol and a 4m solution of t-BuOH. The partial volumes are also discussed within preferential solvation concepts.Hydration numbers of substances are the important characteristics of aqueous solutions [1-9]. They can be regarded as a link between the elements of the triad: thermodynamic property, hydration of the solute, and solution structure. In this context, the hydration number is essentially "a thermodynamic hydration number" [10]*.The aim of this paper is to study the hydration numbers of glycine in solutions of substances that have a different effect on the water structure. Glycine itself is known to disrupt the structure of water [11]. One of the ways to find the desired characteristics is to use partial molar volumes. The standard partial volume of an amino acid in an aqueous solution 0 W V can be written as [1-3]where V in is the intrinsic (effective) volume of a particle in the solution; n W is the hydration number of the amino acid in water; V h is the molar volume of water in the hydration shell of a particle; and V W is the molar volume of water in bulk. We rewrite (1) with respect to the partial volume of an amino acid in a mixed solvent [12]where n is the hydration number of a particle in a mixed solvent; W V can be taken equal to the partial volume of water in a *In our opinion, the value obtained from thermodynamic characteristics is best defined by the term "aquation (aquatic) number."
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