Apparent Molal Volumes and Heat Capacities of Tetrabutylammonium Bromide in Aqueous Electrolyte Solutions

1975 ◽  
Vol 53 (21) ◽  
pp. 3206-3210 ◽  
Author(s):  
Nicole Desrosiers ◽  
Jacques E. Desnoyers

The apparent molal volumes and heat capacities of Bu4NBr were measured in aqueous solutions of NaF, NaCl, NaBr, KBr, NaAc, and NH4Ac at 25 °C with a flow densimeter and a flow microcalorimeter. The derived transfer functions of Bu4NBr from water to the electrolyte solutions, after correction for the long-range coulombic forces, are all negative. This suggests that the noncoulombic interactions between hydrophobic and hydrophilic ions result in negative contributions to volumes and heat capacities.




1978 ◽  
Vol 56 (1) ◽  
pp. 24-28 ◽  
Author(s):  
Alain Roux ◽  
Goolam M. Musbally ◽  
Gérald Perron ◽  
Jacques E. Desnoyers ◽  
Prem Paul Singh ◽  
...  

Measurements at 25 °C with flow calorimeters and densimeters have led to heat capacities and densities of aqueous solutions of 11 1:1 electrolytes: NaClO3, NaBrO3, NaIO3, NaNO3, NaClO4, NH4NO3, KClO3, KBrO3, KIO3, NH4Cl, and NH4ClO4. The first 6 salts were studied up to near saturation. We have used results of these measurements to obtain apparent molal heat capacities and apparent molal volumes of the various solutes. Extrapolation to infinite dilution on the basis of the Debye–Hückel theory bas led to [Formula: see text]and [Formula: see text] values for each solute. We have compared these standard values with results of earlier investigations.



1975 ◽  
Vol 53 (17) ◽  
pp. 2591-2597 ◽  
Author(s):  
Osamu Klyohara ◽  
Gérald Perron ◽  
Jacques E. Desnoyers

The densities and volumetric specific heats of p-dioxane, tetrahydropyran, morpholine, piperidine, and piperazine were measured in water at 25 °C with a flow densimeter and a flow microcalorimeter. The same properties were also determined for LiCl, NaCl, Me4NBr, and Bu4NBr at 0.1 m in dioxane–water, morpholine–water, and piperidine–water mixtures. The derived apparent molal volumes and heat capacities of the nonelectrolytes in water and the transfer functions of the electrolytes from water to the mixed solvent suggest that all the present cyclic amines and ethers are hydrophobic; the overall structural influence is very small with dioxane and large with piperidine.



1977 ◽  
Vol 55 (19) ◽  
pp. 3364-3367 ◽  
Author(s):  
JagDish C. Ahluwalia ◽  
Claude Ostiguy ◽  
Gerald Perron ◽  
Jacques E. Desnoyers

The apparent molal volumes and heat capacities of nine amino acids were measured in water at 25 °C with a flow densimeter and a flow microcalorimeter. It is shown that the poor additivity of the standard partial molal quantities of amino acids in water are attributable to the ionization of the two groups NH2 and COOH. The hydration of these ionic groups interfere with each other when they are separated by less than three carbon atoms.



1973 ◽  
Vol 51 (17) ◽  
pp. 2993-2998 ◽  
Author(s):  
Paul-André Leduc ◽  
Jacques E. Desnoyers

The apparent molal volumes and heat capacities were measured in water at 25 °C with a flow digital densimeter and a flow microcalorimeter for the following salts: tetrabutylammonium octanoate, tetrabutylammonium butanoate, tetrabutylammonium bromide, ammonium acetate, ammonium chloride, ammonium bromide, sodium octanoate, and sodium acetate. The tetrabutylammonium octanoate and butanoate and sodium octanoate form micelles at 0.13, 0.6, and 0.35 M, respectively. The concentration dependence of the apparent molal volumes of the carboxylate salts is similar to that of typical hydrophobic or hydrophilic electrolytes. On the other hand, in the submicellar region, the concentration dependence of their apparent molal heat capacities is abnormal when compared with model electrolytes. It seems that the heat capacities may be reflecting interactions involving a hydrogen bonding of the carboxylate group with water.



1973 ◽  
Vol 51 (2) ◽  
pp. 187-191 ◽  
Author(s):  
P. R. Philip ◽  
J. E. Desnoyers ◽  
A. Hade

The apparent molal volumes and heat capacities of tetraalkylammonium bromides were measured in urea–water mixtures at 25 °C. The volumes and heat capacities of transfer from water to urea-water mixtures indicate that structural hydration effects are smaller in urea–water mixtures than in water. Also a comparison with the corresponding transfer functions from H2O to D2O suggests that urea–water mixtures are less structured than pure water.



1978 ◽  
Vol 56 (13) ◽  
pp. 1827-1831 ◽  
Author(s):  
Giuseppa DiPaola ◽  
Bernard Belleau

Densities (24 °C) and volumetric specific beats (25 °C) were measured for amino acids (0.05–0.5 m) containing apolar side chains in water, and in aqueous solutions of glycerol, mannitol, sorbitol, NaCl, urea, and Gu•HCl, with a flow densimeter and flow microcalorimeter respectively.The derived apparent molal quantifies and transfer functions of the amino acids in aqueous polyol solutions reveal no specificities which might explain the origin of the unique behavior of polyols in protein systems. However, the study did reveal a regular increase in the structure-making ability of the amino acid as the hydrophobicity of the side chains increased. This structure-making tendency was reduced significantly in dilute solutions of the higher polyols.



1974 ◽  
Vol 52 (22) ◽  
pp. 3738-3741 ◽  
Author(s):  
Gérald Perron ◽  
Jacques E. Desnoyers ◽  
Frank J. Millero

The densities and volumetric specific heats of the alkaline earth chlorides have been measured in water at 25 °C in the concentration range 0.01 to 0.4 M with a flow densimeter and a flow microcalorimeter. Apparent molal volumes and heat capacities have been derived.



1976 ◽  
Vol 80 (5) ◽  
pp. 466-470 ◽  
Author(s):  
Wen-Yang Wen ◽  
Antonio LoSurdo ◽  
Carmel Jolicoeur ◽  
Jeanine Boileau


1972 ◽  
Vol 50 (19) ◽  
pp. 3167-3178 ◽  
Author(s):  
C. Jolicoeur ◽  
P. R. Philip ◽  
G. Perron ◽  
P. A. Leduc ◽  
J. E. Desnoyers

The apparent molal volumes [Formula: see text] and heat capacities [Formula: see text] of Bu4NBr, NaBPh4, Ph4PCl, and Ph4AsCl have been measured in water and methanol at 25 °C in the concentration range 0.01–0.2 M. The viscosity of aqueous NaBPh4 and Ph4AsCl have also been measured at 25 °C and in the same concentration range. Individual ionic values have been estimated for most of these properties. A comparison of these values for the quaternary ions BU4N+, [Formula: see text], Ph4P+, Ph4As+ illustrates sizable differences in the solute–solvent interactions of alkyl and aryl substituted ions. Some specificity is also suggested in the solvation of the tetraphenyl ions, as shown by a comparison of the properties which should reflect directly the size of the ions [Formula: see text]and also in (H2O → CH3OH) transfer functions.



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