Thermodynamics of liquid mixtures consisting of a very polar and a non-polar aromatic: (benzonitrile plus benzene, or toluene)

Citation
E. Wilhelm et al., Thermodynamics of liquid mixtures consisting of a very polar and a non-polar aromatic: (benzonitrile plus benzene, or toluene), J CHEM THER, 30(12), 1998, pp. 1509-1532
Citations number
52
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF CHEMICAL THERMODYNAMICS
ISSN journal
00219614 → ACNP
Volume
30
Issue
12
Year of publication
1998
Pages
1509 - 1532
Database
ISI
SICI code
0021-9614(199812)30:12<1509:TOLMCO>2.0.ZU;2-F
Abstract
For the two binary liquid systems {xC(6)H(5)CN + (1 - x)C6H6} and {xC(6)H(5 )CN + (1 - x) C6H5CH3}, excess molar volumes V-m(E), excess molar enthalpie s H-m(E), and excess molar heat capacities C-p, m(E) at constant pressure h ave been measured as a function of mole fraction x. Values of V-m(E) were d etermined at T = (298.15, 308.15, and 318.15) K, H-m(E) was determined at T = (293.15, 298.15, and 303.15) K, and C-p, m(E) was determined at T = 298. 15 K (all at atmospheric pressure). The instruments used were, respectively , a vibrating-tube densimeter (from Sodev), an LKB differential flow microc alorimeter equipped with two computer-controlled h.p.l.c. piston pumps (fro m Gilson), and a Picker flow microcalorimeter (from Setaram). In addition, isobaric heat capacities divided by volume C-p,C- m/V-m of the pure liquids , as well as several selected mixtures, were measured with a programmable d ifferential scanning calorimeter of the Calvet type (micro-d.s.c., from Set aram) between approximately T = 280 K and T = 350 K. Both systems show rela tively small negative excess molar volumes, which become more negative with increasing temperature. The excess molar enthalpies are highly unusual in that for both systems an M-shaped composition dependence is observed (two m axima and one minimum). The M-shape is much more prenounced for(benzonitril e + toluene) than for (benzonitrile + benzene), and appears to vanish for t he latter system below T = 298.15 K. The results can be understood in terms of a simple theory of complex formation (Guggenheim-McGlashan). The excess molar heat capacity at constant pressure at T = 29815 K of (benzonitrile toluene) is positive at all compositions, while that of (benzonitrile + be nzene) is positive only for 0 < x < 0.071, and negative otherwise (sigmoida l shape). Combining the heat capacities obtained with the Picker calorimete r at T = 298.15 K with our results for C-p,C- m/V-m obtained with the micro -d.s.c. in conjunction with our density data, excess molar heat capacities have also been derived for (benzonitrile + toluene) at T = (288.15, 308.15, 318.15, and 328.15) K. For this system, the maximum of the curve C-p, m(E) against x becomes somewhat smaller with increasing temperature and is shif ted towards larger values of x, i.e. the curves become more symmetric. (C) 1998 Academic Press.