Density study of (D (+) mannose + water), (D (+) mannose + water + sodium cyclamate), (D (+) maltose monohydrate + water) and (D (+) maltose monohydrate + water + sodium cyclamate) systems at T = 298.15 K

Effect of different concentrations of aqueous solutions of sodium cyclamate on sugars (mono and disaccharides) are observed by measuring the densities of (sugar + water) and (sugar + water + sodium cyclamate) systems. Densities of aqueous solutions of D (+) mannose (monosaccharide) and D (+) maltose monohydrate (disaccharide) in (0.05, 0.15, 0.3) mol.kg-1 of sodium cyclamate (Na-Cyclamate) at T = 298.15 K have been measured. From experimental values of densities , Vɸ0( partial molar volumes) ΔtrsVɸ0 (partial molar volumes of transfer) ASV (apparent specific volumes) interaction parameters (𝑉𝐴𝐵) and (𝑉𝐴𝐵𝐵 ) have been determined. The calculated values of various parameters have been used to interpret the results in terms of (D (+) mannose – water), (D (+) mannose –water– Na-cyclamate), (D (+) maltose monohydrate – water) and (D (+) maltose monohydrate – water – Na-cyclamate) interactions in sugar– water – Na-cyclamate and quality of taste sense of solutions.

Revealing the Toxicity of Chlorate Through the Analysis of Molecular Interaction using Viscosity Measurements and Apparent Molar Volumes

While chlorate has the ability to induce flowering in longan, it also has adverse impacts on the crop. Revealing the toxicity of chlorate in the environment is more than just about the environment and about human health, as well.Because of the large introduction of this chemical into the environment from the paper processing industry, there is indeed a lot of concern about its toxicity. Chlorate toxicology in the longan plant has been thoroughly investigated in solutions using viscosities and apparent molar volumes. The hydration of molecules and volume changes are involved in various chemical and biological processes in plant tissues, and their complete understanding demands a good idea for volumetric and viscometric study. It offers good data acquisition techniques for solute, solvent and solvent-solvent interactions. Multi-component systems containing KClO3+ water + ionic solid (ionic solids = KCl, KNO3 ,NH4NO3 and KH2PO4, are currently being worked out to study the dependence of transport properties of potassium chlorate in aqueous electrolyte solutions, with concentrations and temperature of solutions. The assessed kd values are used to predict whether the solvolysis of KClO3 in the presence of other electrolytes is a quick or slow process.

Density and Viscosity of LiCl, LiBr, LiI and Kcl in Aqueous Methanol at 313.15K

The densities and viscosities of electrolytes are essential to understand many physicochemical processes that are taking place in the solution. In the present research, the densities and viscosities of lithium halides, LiX (X = Cl, Br, I ) and KCl in (0, 20, 40, 50, 60, 80 and 100) mass % of methanol + water at 313.15K were calculated employing experimental densities (ρ), the apparent molar volumes( ϕv) and limiting apparent molar volumes (0v) of the electrolytes. The (0v) of electrolyte offer insights into solute-solution interactions. In terms of the Jones-Dole equation for strong electrolyte solution, the experimental data of viscosity were explored. Viscosity coefficients A and B have been interpreted and discussed. The B-coefficient values in these systems increase with increase of methanol in the solvents mixtures. This implied that when the dielectric constant of the solvent decreases, so do the solvent-solvent interactions in these systems.

Density, Ultrasonic Velocity, Isentropic Compressibility, Molar Volumes and Related Excess Parameters Studies on Ethyl Acetate with 1-Ethanol at 303K, 308K, and 313K

A binary liquid mixture that consists of ethyl acetate and 1-ethanol has been prepared at various concentrations by the mole fraction method. The ultrasonic velocity and density have been determined at 303K, 308K and 313K. From the experimental data, the excess isentropic compressibility, excess molar volumes, excess internal pressures, and excess molar enthalpy have been computed. The variations were observed as polynomial and fitted to the Redlich-Kister polynomial functions. By using this function, adjustable parameters and the standard deviations have been calculated. The experimental and theoretical data reveal that the existence of the intermolecular interactions between the selected liquid system. The partial molar compressibility’s and partial molar volume also calculated at infinite dilution of the system. In general, the intermolecular forces have tended to the variations in the magnitude and sign of the excess parameters. The excess molar volume (Vme), excess isentropic compressibility (), excess internal pressure ( ) and the enthalpy ( ) show the negative magnitude at the entire range of concentrations and temperatures. The significant variations of these parameters with the mole fraction of ethyl acetate have been analysed. Furthermore, the strength of the intermolecular interactions decreased with increasing the experimental temperatures as 303K > 308K >313K.