Journal
JOURNAL OF MOLECULAR LIQUIDS
Volume 352, Issue -, Pages -Publisher
ELSEVIER
DOI: 10.1016/j.molliq.2022.118744
Keywords
Ibuprofen; Ionic liquid; Apparent molar volume; Apparent molar isentropic compressibility
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The salt effect of sodium chloride, potassium chloride, choline acetate, choline lactate, and choline propionate on ibuprofen in aqueous solutions of 1-propanol was investigated using various methods. It was found that sodium chloride and potassium chloride have a salting-out effect, while choline acetate, choline lactate, and choline propionate have a salting-in effect.
In this study, salt effect of sodium chloride, potassium chloride, choline acetate (ChAce), choline lactate (ChLac) and choline propionate (ChPro) for ibuprofen in aqueous solutions of 1-propanol were investigated using volumetric, acoustic and viscometric methods. Density, speed of sound and viscosity of quaternary systems (ibuprofen + water + 1-propanol + NaCl/KCl/ChAce/ChLac/ChPro) were measured at temperatures T = 288.15, 298.15 and 308.15 K. Limiting apparent molar volume and limiting apparent molar isentropic compressibility at infinite dilution were calculated using experimental density and speed of sound. Limiting apparent molar volume of ibuprofen increased in the presence of NaCl and KCl; whereas limiting apparent molar volume decreased in the presence of ionic liquids. Therefor NaCl and KCl have salting-out effect; whereas ChAce, ChLac and ChPro have salting-in effect. Also, molar free energy activation of solvent and solute were evaluated using viscosity data. The molar free energy activation of solute was greater than solvent; therefore ibuprofen has a maker structure nature in solvents (water + 1-propanol + NaCl/KCl/ChAce/ChLac/ChPro). (C) 2022 Elsevier B.V. All rights reserved.
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