Heat capacities, volumes, and expansibilities of sodium phenyl carboxylates in water

1977 ◽  
Vol 55 (19) ◽  
pp. 3368-3370 ◽  
Author(s):  
Claude Ostiguy ◽  
Jagdish C. Ahluwalia ◽  
Gerald Perron ◽  
Jacques E. Desnoyers
Keyword(s):  
Unit Volume ◽  
Heat Capacities ◽  
Simple Explanation ◽  
Flow Microcalorimeter ◽  
Partial Molal Heat Capacities ◽  
Apparent Molal Heat Capacities

The heat capacities per unit volume at 25 °C and densities from 10 to 55 °C of sodium phenyl carboxylates were measured with a flow microcalorimeter and a flow densimeter. The apparent molal heat capacities and volumes were used to derive standard partial molal heat capacities [Formula: see text], volumes [Formula: see text], and expansibilities [Formula: see text]. The CH2 contribution to [Formula: see text] is the same as that usually observed for aliphatic solutes but the contribution to [Formula: see text] and [Formula: see text] is not constant and significantly different. No simple explanation can be offered for this anomaly.

Apparent molal heat capacities and volumes of amino acids in aqueous polyol solutions

1978 ◽  
Vol 56 (13) ◽  
pp. 1827-1831 ◽  
Author(s):  
Giuseppa DiPaola ◽  
Bernard Belleau
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Aqueous Solutions ◽  
Transfer Functions ◽  
Heat Capacities ◽  
Side Chains ◽  
Dilute Solutions ◽  
Flow Microcalorimeter ◽  
Regular Increase ◽  
Apparent Molal Heat Capacities

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.

Polyol–Water interactions. Apparent molal heat capacities and volumes of aqueous polyol solutions

1977 ◽  
Vol 55 (22) ◽  
pp. 3825-3830 ◽  
Author(s):  
Giuseppa DiPaola ◽  
Bernard Belleau
Keyword(s):  
Aqueous Solutions ◽  
Infinite Dilution ◽  
Pure Water ◽  
Water Environment ◽  
Heat Capacities ◽  
Flow Microcalorimeter ◽  
Specific Heats ◽  
Structural Interactions ◽  
Apparent Molal Heat Capacities

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.

Heat capacities and volumes of some non-electrolytes in N,N-dimethylformamide at 298.15 K

1987 ◽  
Vol 65 (12) ◽  
pp. 2810-2814 ◽  
Author(s):  
Henryk Piekarski
Keyword(s):  
Ethylene Glycol ◽  
Heat Capacities ◽  
Scaled Particle Theory ◽  
Partial Molal Volume ◽  
Cavity Formation ◽  
Particle Theory ◽  
Molal Volume ◽  
Analogous Data ◽  
Other Substances ◽  
Apparent Molal Heat Capacities

Heat capacities and densities of dilute solutions of formamide, acetone, tetrahydrofuran, ethylene glycol, 2-methoxyethanol, and 2-ethoxyethanol in N,N-dimethylformamide were determined at 298.15 K. Apparent molal heat capacities and volumes for these solutes in DMF were calculated and compared with the analogous data for other substances in DMF solution as well as with the data concerning solutions in methanol and water. Heat capacities of cavity formation (ΔCcav) in DMF were calculated on the basis of the Scaled Particle Theory. ΔCcav appeared to be linearly correlated with the standard partial molal volume of corresponding solutes in DMF. Similar dependences were also found for aqueous and methanolic solutions of the non-electrolytes.

Heat capacities of binary mixtures of n-octane with each of the hexane isomers at 298.15 K

1986 ◽  
Vol 64 (11) ◽  
pp. 2139-2141 ◽  
Author(s):  
George C. Benson ◽  
Patrick J. D'Arcy
Keyword(s):  
Binary Mixtures ◽  
Excess Molar Volumes ◽  
Heat Capacities ◽  
Flory Theory ◽  
Molar Volumes ◽  
Flow Microcalorimeter ◽  
Theory Of Mixtures

Volumetric heat capacities for binary mixtures of n-octane with n-hexane, 2-methylpentane, 3-methylpentane, 2,2-dimethylbutane, and 2,3-dimethylbutane were measured at 298.15 K in a Picker flow microcalorimeter. The results were combined with previously published excess molar volumes to obtain excess molar isobaric heat capacities. Interpretation of the results in terms of the Flory theory of mixtures is discussed.

The heat capacities and volumes of some low molecular weight amides, ketones, esters, and ethers in water over the whole solubility range

1978 ◽  
Vol 56 (22) ◽  
pp. 2808-2814 ◽  
Author(s):  
Geneviève Roux ◽  
Gérald Perron ◽  
Jacques E. Desnoyers
Keyword(s):  
Hydrophobic Interactions ◽  
Heat Capacities ◽  
Initial Slope ◽  
Pure Liquid ◽  
Factors Affecting ◽  
Solubility Range ◽  
Low Concentrations ◽  
Hydrophobic Solutes ◽  
Molal Volumes ◽  
Apparent Molal Heat Capacities

The densities and heat capacities per unit volume of aqueous solutions of propionamide, methylacetate, ethylacetate, methylethylketone and diethylketone, and bis(2-ethoxyethyl)ether were measured over the whole solubility range with a flow densimeter and a flow microcalorimeter. Most systems were studied at 10, 25, and 40 °C. Properties of the pure liquids were also measured whenever possible. The derived apparent molal volumes [Formula: see text] all decrease with concentration in the water-rich region, except with ethyl acetate which increases at high temperature. In general the more hydrophobic the solute the more negative the initial slope. All apparent molal heat capacities [Formula: see text] decrease as a function of concentration and the decrease is more important for more hydrophobic solutes. The apparent molal expansibilities [Formula: see text] are obtained from [Formula: see text]. They are positive for all solutes but, at low concentrations, they are smaller than the corresponding molar value of the pure liquid. Various factors affecting hydrophobic interactions are examined.

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 ◽  
...  
Keyword(s):  
Aqueous Solutions ◽  
Infinite Dilution ◽  
Heat Capacities ◽  
Aqueous Electrolytes ◽  
Apparent Molal Volumes ◽  
Hückel Theory ◽  
Standard Values ◽  
Molal Volumes ◽  
Apparent Molal Heat Capacities

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.

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