Erratum to “Isobaric thermal expansivity behaviour against temperature and pressure of associating fluids” [J. Chem. Thermodyn. 42(1) (2010) 23–27]

2010 ◽  
Vol 42 (7) ◽  
pp. 949
Author(s):  
Paloma Navia ◽  
Jacobo Troncoso ◽  
Luis Romaní
2015 ◽  
Vol 80 (11) ◽  
pp. 1423-1433 ◽  
Author(s):  
Gorica Ivanis ◽  
Aleksandar Tasic ◽  
Ivona Radovic ◽  
Bojan Djordjevic ◽  
Slobodan Serbanovic ◽  
...  

Densities data of n-hexane, toluene and dichloromethane at temperatures 288.15-413.15 K and at pressures 0.1-60 MPa, determined in our previous work, were fitted to the modified Tait equation of state. The fitted temperature-pressure dependent density data were used to calculate the derived properties: the isothermal compressibility, the isobaric thermal expansivity, the difference between specific heat capacity at constant pressure and at constant volume and the internal pressure, over the entire temperature and pressure intervals specified above. In order to assess the proposed modeling procedure, a comparison of the obtained values for the isothermal compressibility and the isobaric thermal expansivity with the corresponding literature data were performed. The average absolute percentage deviations for isothermal compressibility were: for n-hexane 2.01-3.64%, for toluene 0.64-2.48% and for dichloromethane 1.81-3.20%; for the isobaric thermal expansivity: for n-hexane 1.31-4.17%, for toluene 0.71-2.45% and for dichloromethane 1.16-1.61%. By comparing the obtained deviations values with those found in the literature it can be concluded that the presented results agree good with the literature data.


2021 ◽  
Vol 23 (4) ◽  
pp. 2964-2971
Author(s):  
Bernadeta Jasiok ◽  
Mirosław Chorążewski ◽  
Eugene B. Postnikov ◽  
Claude Millot

Thermophysical properties of liquid dibromomethane are investigated by molecular dynamics simulations between 268 and 328 K at pressures up to 3000 bar. Notably, the isotherms of the isobaric thermal expansivity cross around 800 bar.


2010 ◽  
Vol 55 (6) ◽  
pp. 2173-2179 ◽  
Author(s):  
Paloma Navia ◽  
Jacobo Troncoso ◽  
Luís Romaní

1935 ◽  
Vol 8 (3) ◽  
pp. 401-420 ◽  
Author(s):  
Arnold H. Scott

Abstract The specific volume, compressibility, and volume thermal expansivity of rubber-sulfur compounds containing from 3 to 31 per cent of sulfur have been measured at pressures from 1 to 800 bars and at temperatures from 10° to 85° C. The results are expressed in tables, curves, and equations, so that within the indicated limits the value of any of the above properties can be readily determined for a compound of specified composition under specified conditions of temperature and pressure. Specific volume, which is the reciprocal of the density, has been used throughout this paper, because this term is the one which is used directly in the definitions of compressibility and volume thermal expansivity. The work of Kimura and Namikawa indicated that the specific volume of rubber-sulfur compounds at atmospheric pressure was a linear function of the temperature. The use of the specific volume thus leads to equations which are simpler than if the density is used.


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