Isothermal compressibility and isobaric thermal expansivity of linear and branched hexanols at 298.15 K

1994 ◽  
Vol 39 (2) ◽  
pp. 349-350 ◽  
Author(s):  
Gloria Tardajos ◽  
Elena Junquera ◽  
Emilio Aicart
Keyword(s):  
Isothermal Compressibility ◽  
Thermal Expansivity ◽  
Isobaric Thermal Expansivity

scholarly journals Modeling of density and calculations of derived volumetric properties for n-hexane, toluene and dichloromethane at pressures 0.1-60 MPa and temperatures 288.15-413.15 K

2015 ◽  
Vol 80 (11) ◽  
pp. 1423-1433 ◽  
Author(s):  
Gorica Ivanis ◽  
Aleksandar Tasic ◽  
Ivona Radovic ◽  
Bojan Djordjevic ◽  
Slobodan Serbanovic ◽  
...  
Keyword(s):  
Isothermal Compressibility ◽  
Constant Pressure ◽  
Thermal Expansivity ◽  
Volumetric Properties ◽  
Density Data ◽  
Tait Equation Of State ◽  
Derived Properties ◽  
Temperature And Pressure ◽  
The Difference ◽  
Isobaric Thermal Expansivity

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.

Liquid dibromomethane under pressure: a computational study

2021 ◽  
Vol 23 (4) ◽  
pp. 2964-2971
Author(s):  
Bernadeta Jasiok ◽  
Mirosław Chorążewski ◽  
Eugene B. Postnikov ◽  
Claude Millot
Keyword(s):  
Molecular Dynamics ◽  
Molecular Dynamics Simulations ◽  
Thermophysical Properties ◽  
Computational Study ◽  
Thermal Expansivity ◽  
Dynamics Simulations ◽  
Isobaric Thermal Expansivity

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.

Isobaric Thermal Expansivity for Nonpolar Compounds

2010 ◽  
Vol 55 (6) ◽  
pp. 2173-2179 ◽  
Author(s):  
Paloma Navia ◽  
Jacobo Troncoso ◽  
Luís Romaní
Keyword(s):  
Thermal Expansivity ◽  
Nonpolar Compounds ◽  
Isobaric Thermal Expansivity

Thermal Expansivity and Isothermal Compressibility Measurements on Rare Gas Solids by an Optical Method

1970 ◽  
Vol 41 (13) ◽  
pp. 5082-5084 ◽  
Author(s):  
H. J. Coufal ◽  
R. Veith ◽  
P. Korpiun ◽  
E. Lüscher
Keyword(s):  
Optical Method ◽  
Isothermal Compressibility ◽  
Thermal Expansivity ◽  
Rare Gas

Molar volume, thermal expansivity and isothermal compressibility of trans-decahydronaphthalene up to 200MPa and 446K

2005 ◽  
Vol 14 (12) ◽  
pp. 2433-2439 ◽  
Author(s):  
Zhu Hu-Gang ◽  
Liu Zhi-Hua ◽  
Tian Yi-Ling ◽  
Xue Yuan ◽  
Yin Liang
Keyword(s):  
Molar Volume ◽  
Isothermal Compressibility ◽  
Thermal Expansivity
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