Faculty Publications

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  • Item
    Ultrasonic velocities, densities, and viscosities of glycylglycine and CoCl2 in aqueous and aqueous ethanol systems at different temperatures
    (2010) Santosh, M.S.; Bhat, D.K.; Bhatt, A.S.
    Ultrasonic velocity (u), density (?), and viscosity (?) have been measured for glycylglycine and CoCl2 in aqueous and aqueous ethanol systems at T = (288.15 to 318.15) K. Using the experimental values, the adiabatic compressibility (?s), molar hydration number (nH), apparent molar compressibility (KS?), apparent molar volume (V?), limiting apparent molar compressibility (KS ?{symbol}0), limiting apparent molar volume (V?{symbol}0), their constants (SK, SV), viscosity coefficients of A and B parameters of Jones-Dole equation, relative viscosity (?r), and excess Gibbs free energy of activation (? G* E) were calculated and the results of all these parameters have been discussed in terms of solute-solvent and solute-solute interactions. © 2010 Elsevier Ltd. All rights reserved.
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    Acoustical and compressibility parameters of glycylglycine-FeCl3 in aqueous ethanol mixture at T = (293.15, 303.15, and 313.15) K
    (2010) Santosh, M.S.; Bhat, D.K.
    Ultrasonic velocity measurement is a reliable procedure that allows quick and easy determination of solvent concentrations in mixtures. This paper presents data of ultrasonic velocities and isentropic compressibilities of (glycylglcyine-FeCl3) in aqueous ethanol mixture at T = (293.15, 303.15, and 313.15) K. Various acoustical parameters were calculated, because of their importance in the study of specific molecular interactions. A less-compressible phase of the fluid and a closer packing of molecules is observed with changes in the intermolecular free length. Quantitative investigation suggests that the mixing of ethanol with an aqueous glycylglycine-FeCl3 solution causes the rupture of hydrogen bonds, with increasing S and Lf values (where the former represents the change in isentropic compressibility and the latter represents the intermolecular free length). Theoretically computed values of isentropic compressibility in the studied mixture using different models indicate the superiority of the very complex procedure. © 2010 American Chemical Society.
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    Molar volume, compressibility and excess properties of glycylglycine in aqueous NiCl2 solutions
    (2010) Santosh, M.S.; Bhat, D.K.
    Volumetric and acoustical parameters are reported for glycylglycine in aqueous NiCl2 solution at T=(288.15-318.15)K. The apparent molar volumes and isentropic compressibilities were calculated from the experimental data of ultrasonic velocity and density. Together with these, excess isentropic compressibility (?SE), excess free volume (VfE), excess intermolecular free length (LfE) and deviations of ultrasonic velocity (?u) were obtained. The results are interpreted in terms of molecular interactions. The results show that the cation and anion play a significant role in influencing the behavior of glycylglycine in aqueous solutions. These effects were also attributed to the doubly charged behavior of glycylglycine and to the formation of physically bonded ion-pairs between charged groups of glycylglycine and cation and anion of the electrolyte. © 2010 Elsevier B.V.
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    Application of Prigogine-Flory-Patterson theory to volumetric, ultrasonic, and compressibility parameters of (glycylglycine + CuCl2) in aqueous ethanol mixtures
    (2011) Santosh, M.S.; Bhat, D.K.
    The molar volume and compressibility of (glycylglycine + CuCl2) in aqueous ethanol mixtures have been obtained at four different temperatures T = (288.15 to 318.15) K from ultrasonic velocity and density measurements. Excess molar volumes were found to be negative throughout the composition range indicating notable changes in hydrogen bonding and electrostatic interactions. Using the Prigogine-Flory-Patterson theory, quantitative estimation of different contributions, i.e. interactional, free volume, and P effect to VE have been obtained. The molar isentropic compressibility has been computed using the ultrasonic velocity and excess volume data. The trends in ?SE are affected by the size of the molecule leading to negative contributions. In order to compare the theoretical values of ultrasonic velocity, the equations of Nomoto and Junjie were used and found to predict the experimental data very well. © 2011 Elsevier Ltd. All rights reserved.