Apparent molal heat capacities and volumes of aqueous electrolytes at 25 °C: NaClO3, NaClO4, NaNO3, NaBrO3, NaIO3, KClO3, KBrO3, KIO3, NH4NO3, NH4Cl, and NH4ClO4

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.

1976 ◽  
Vol 54 (21) ◽  
pp. 3315-3318 ◽  
Author(s):  
Prem Paul Singh ◽  
Earl M. Woolley ◽  
Keith G. McCurdy ◽  
Loren G. Hepler

We have made measurements with a flow calorimeter leading to apparent molal heat capacities of aqueous solutions of NaCl, HCl, KBr, KCl, KOH, NaBr, HBr, and NaOH at 298 K. Results have been used to derive apparent molal heat capacities of these electrolytes at infinite dilution and thence ΔCp0 = −215.2 ± 4 J K−1mol−1 for ionization of H2O(liq) at 298 K.


1981 ◽  
Vol 59 (17) ◽  
pp. 2599-2600 ◽  
Author(s):  
Gérald Perron ◽  
Jacques E. Desnoyers

The densities and heat capacities per unit volume of 1,3-dioxane and trioxane were measured in water at 25 °C in the concentration range 0.1 to 1 mol kg−1. Apparent molal volumes [Formula: see text] and [Formula: see text] heat capacities were derived. The infinite dilution [Formula: see text] shows excellent group additivity with other cyclic ethers in water but the additivity is less satisfactory for[Formula: see text]. No simple correlation can be made for the concentration dependence of these functions.


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.


1977 ◽  
Vol 55 (22) ◽  
pp. 3825-3830 ◽  
Author(s):  
Giuseppa DiPaola ◽  
Bernard Belleau

Volumetric specific heats (25 °C) and densities (24 °C) were measured with a flow microcalorimeter and flow densimeter for 12 polyols in water (0.05 to 2 m), and for NaCl and n-Bu4NBr in 1 m aqueous alditol solutions. The infinite dilution properties [Formula: see text] of the polyols show specificities in polyol−water interactions which are discussed in terms of the compatibility of the polyol stereochemistry and the existing water environment. The derived heat; capacities and volumes of transfer of hydrophobic and hydrophilic probes to aqueous solutions of homologous polyols suggest that structural interactions are reduced in these systems as compared to pure water.


1986 ◽  
Vol 64 (5) ◽  
pp. 996-1001 ◽  
Author(s):  
Jean-Pierre Morel ◽  
Claude Lhermet ◽  
Nicole Morel-Desrosiers

The thermodynamic parameters characterizing the interaction between Ca2+ and the suitably positioned sequences of hydroxyls of some sugar isomers have been determined. This was done by comparing the properties of D-ribose which bears such sequences of hydroxyls with the properties of D-arabinose chosen as an inactive reference. The enthalpies of solution and of dilution, the apparent molal heat capacities, and the apparent molal volumes of the two pentoses have been first measured in water at 25 °C. The measurement of these properties for the transfer of the sugars from water to CaCl2 solutions (and, conversely, for the transfer of CaCl2 from water to the sugar solutions) directly gives access to the Ca2+–hydroxyls pair interaction parameters. The thermodynamic properties of this reaction of association may then be estimated: [Formula: see text][Formula: see text] The analysis of these data shows that the weak association constant results from a large compensation between the favourable enthalpy and the unfavourable entropy of reaction.


1975 ◽  
Vol 53 (8) ◽  
pp. 1134-1138 ◽  
Author(s):  
Gérald Perron ◽  
Jacques E. Desnoyers ◽  
Frank J. Millero

The densities and volumetric specific heats of Na2SO4, K2SO4, MgSO4, Na2CO3, NaHCO3, and NaOH were measured up to an ionic strength of 1 in water at 25 °C with a flow densimeter and a flow microcalorimeter. From these data, the heat capacity for the formation of the ion pair MgSO40was evaluated as 84.9 J K−1 mol−1. There is an anomalous increase in the apparent molal heat capacities of Na2CO3 at low concentration but the apparent molal volumes are normal. This anomaly can be suppressed with NaOH. Attempts to account quantitatively for this behavior by an hydrolysis correction were not successful.


1979 ◽  
Vol 57 (21) ◽  
pp. 2798-2803 ◽  
Author(s):  
Jan J. Spitzer ◽  
Inger V. Olofsson ◽  
Prem Paul Singh ◽  
Loren G. Hepler

We have used a flow calorimeter and a flow densimeter for measurements at 25 °C of heat capacities and densities of aqueous solutions of four electrolytes of high charge type: LaCl3, Cr(NO3)3, K3Fe(CN)6, and K4Fe(CN)6. Results of these measurements have been used for calculating corresponding apparent molar heat capacities and apparent molar volumes, which have been extrapolated to infinite dilution to obtain the corresponding standard state apparent molar and partial molar properties. Uncertainties resulting from extrapolations of heat capacities are discussed. Results of our measurements are compared with those of earlier related investigations.


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