Thermodynamics of Mixtures of Aromatic Hydrocarbons with Alkanols Studied by Light Scattering

2001 ◽  
Vol 66 (7) ◽  
pp. 1011-1037 ◽  
Author(s):  
Petr Munk ◽  
Weizhuang Cheng ◽  
Anwei Qin ◽  
Julius Pouchlý

Measurement of light scattering of mixtures of aromatic hydrocarbons (benzene, toluene, ethylbenzene) and alkanols (methanol, ethanol, propan-1-ol, butan-1-ol, pentan-1-ol) having sufficiently different refractive indices, produced rather reliable thermodynamic data. From these data it was possible to deduce the composition dependence of the change in Gibbs energy of mixing ∆Gmix. These dependences were measured for eleven binary mixtures. A model of alcohol molecules forming linear aggregates which are in equilibrium was developed and used for interpretation of the data. All ∆Gmix data for the eleven mixtures as well as the ∆Hmix data obtained for these mixtures from literature could be interpreted using just two values that characterized the Gibbs energy and enthalpy of the formation of hydrogen bonds. The analysis also yielded plausible results concerning the contact interactions.

1996 ◽  
Vol 61 (6) ◽  
pp. 837-843
Author(s):  
Ladislav Kosa ◽  
Ivan Nerád ◽  
Katarína Adamkovičová ◽  
Jozef Strečko ◽  
Ivo Proks

Activities of the components, the Gibbs energy of mixing, and the excess entropy of mixing have been calculated for the Ca2MgSi2O7-CaSiO3 system. The mole fractions of the components were calculated assuming that in the point of the formal component Ca2MgSi2O7, the molar mass of the quasi-real particle in the melt corresponds to its formula molar mass, whereas in the point of the formal component CaSiO3 the molar mass of the quasi-real particle in the melt is 8.5 times higher than as corresponds to its formula. The fact that the enthalpy of mixing is zero whereas the excess entropy of mixing is non-zero suggests that Ca2MgSi2O7-CaSiO3 melts behave as athermal solutions.


1994 ◽  
Vol 23 (7) ◽  
pp. 795-812 ◽  
Author(s):  
Chr Christov ◽  
S. Petrenko ◽  
Chr Balarew ◽  
Vl. Valyashko

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