The apparent molar heat capacity of aqueous hydrochloric acid from 10 to 140�C

1986 ◽  
Vol 15 (1) ◽  
pp. 1-22 ◽  
Author(s):  
Peter R. Tremaine ◽  
Kim Sway ◽  
Jos� A. Barbero
Keyword(s):  
Heat Capacity ◽  
Hydrochloric Acid ◽  
Molar Heat Capacity ◽  
Apparent Molar Heat Capacity ◽  
Aqueous Hydrochloric Acid

Capacité calorifique de polyélectrolytes en solution

1985 ◽  
Vol 63 (7) ◽  
pp. 1568-1571 ◽  
Author(s):  
Hubert Daoust ◽  
Hoa Le Thanh ◽  
Pierre Ferland ◽  
Daniel St-Cyr
Keyword(s):  
Heat Capacity ◽  
Sodium Salt ◽  
Polyacrylic Acid ◽  
Molar Heat Capacity ◽  
Conformational Transformation ◽  
Polymethacrylic Acid ◽  
High Dilution ◽  
Constant Concentration ◽  
Apparent Molar Heat Capacity ◽  
Low Concentrations

Heat capacities of polyelectrolytes in aqueous solutions have been measured at 25 °C using a Picker-type dynamic micro-calorimeter. The precision of the apparatus is such that it is possible to calculate the apparent molar heat capacity [Formula: see text] of the solute, even at high dilution. The polymers that were studied include polymethacrylic acid (PMAH) and polyacrylic acid (PAH), as well as its sodium salt and the sodium salt of the polystyrènesulfonate. For the salts, the results show that the value of [Formula: see text] decreases rapidly with dilution to low concentrations; this result is in perfect concordance with a relation derived from the theory of Lifson and Katchalsky. A study of the variation of [Formula: see text] at a constant concentration, with the extent of the neutralization of the acids PMAH and PAH has also been conducted. As has been shown previously, the chain of the PMAH undergoes a conformational transformation when the level of neutralization gets close to 25%. This transformation implies an increase of the value of [Formula: see text] [Journal translation]

Apparent molar heat capacity and relative enthalpy of aqueous NaOH between 323 and 523K

1988 ◽  
Vol 17 (5) ◽  
pp. 481-497 ◽  
Author(s):  
G. Conti ◽  
P. Gianni ◽  
A. Papini ◽  
E. Matteoli
Keyword(s):  
Heat Capacity ◽  
Molar Heat Capacity ◽  
Apparent Molar Heat Capacity ◽  
Relative Enthalpy

Approximation of adsorption heats of carbon monoxide on transition metals by means of an empirical model

1983 ◽  
Vol 48 (10) ◽  
pp. 2735-2739
Author(s):  
Jiří Fusek ◽  
Oldřich Štrouf ◽  
Karel Kuchynka
Keyword(s):  
Carbon Monoxide ◽  
Heat Capacity ◽  
Transition Metals ◽  
Molar Heat Capacity ◽  
Metal Adsorption ◽  
Heat Of Fusion ◽  
Class Structure ◽  
Fundamental Parameters ◽  
Adsorption Heats ◽  
Pauling Electronegativity

The class structure of transition metals chemisorbing carbon monoxide was determined by expressing the following fundamental parameters in the form of functions: The molar heat capacity, the 1st and 2nd ionization energy, the heat of fusion, Pauling electronegativity, the electric conductivity, Debye temperature, the atomic volume of metal. Adsorption heats have been predicted for twelve transition metals.

Heat capacities and enthalpies of fusion and transformation for solvates of some salts with dimethyl sulfoxide and dimethylformamide

1988 ◽  
Vol 53 (12) ◽  
pp. 3072-3079
Author(s):  
Mojmír Skokánek ◽  
Ivo Sláma
Keyword(s):  
Heat Capacity ◽  
Phase Transformation ◽  
Phase Transformations ◽  
Dimethyl Sulfoxide ◽  
Liquidus Temperature ◽  
Molar Heat Capacity ◽  
Solid Phase ◽  
Zinc Nitrate ◽  
Heat Capacities ◽  
Liquid Phases

Molar heat capacities and molar enthalpies of fusion of the solvates Zn(NO3)2 . 2·24 DMSO, Zn(NO3)2 . 8·11 DMSO, Zn(NO3)2 . 6 DMSO, NaNO3 . 2·85 DMSO, and AgNO3 . DMF, where DMSO is dimethyl sulfoxide and DMF is dimethylformamide, have been determined over the temperature range 240 to 400 K. Endothermic peaks found for the zinc nitrate solvates below the liquidus temperature have been ascribed to solid phase transformations. The molar enthalpies of the solid phase transformations are close to 5 kJ mol-1 for all zinc nitrate solvates investigated. The dependence of the molar heat capacity on the temperature outside the phase transformation region can be described by a linear equation for both the solid and liquid phases.

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