Author:
Perron Gérald,Desrosiers Nicole,Desnoyers Jacques E.
Abstract
The densities and heat capacities per unit volume of the symmetrical tetraalkylammonium bromides (R4NBr) were measured in H2O, D2O, and 3 m aqueous urea from 0.01 to 1 mol kg−1 and from 5 to 55 °C with a flow digital densimeter and a flow microcalorimeter. Expansibilities were also measured at 25 °C for the same electrolytes in H2O and urea–water mixtures with a dilatometer. Apparent molal volumes [Formula: see text] heat capacities [Formula: see text] and expansibilities [Formula: see text] were derived. The [Formula: see text] of R4NCl and R4NI were also measured in H2O at 25 °C. The effect of urea concentration was investigated at 25 °C in the case of Bu4NBr.Once allowance is made for the anion, the properties of the larger R4N+ behave essentially as hydrophobic nonelectrolytes in water. The transfer functions from H2O to D2O have the same sign as the hydration functions and the transfer functions from H2O to urea–water mixtures the opposite sign. Whatever is the origin of the interactions giving rise to the peculiar behavior of hydrophobic R4N+ in water, these interactions are larger in D2O and smaller in the presence of urea.The excess volumes, heat capacities, and expansibilities of Bu4NBr and Pen4NBr, once corrected for the long-range Debye–Hückel interactions, all have the same sign as the hydration functions at infinite dilution, in contrast with excess free energies and enthalpies. This suggests some kind of cooperative effect as two hydrophobic solutes interact with each other without the formation of a hydrophobic bond. No conclusions can be drawn from the difference in excess functions in the various aqueous solvents.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
134 articles.
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