Molar excess volumes of binary liquid mixtures: 2-pyrrolidinone with C6–C10n-alkanols

1996 ◽  
Vol 74 (1) ◽  
pp. 121-127 ◽  
Author(s):  
Begoña García ◽  
Francisco J. Hoyuelos ◽  
Rafael Alcalde ◽  
José M. Leal

The excess volumes VE of the binary mixtures 2-pyrrolidinone–(C6–C10) n-alkanols have been calculated from density measurements over the whole composition range and the 298.15–318.15 K temperature range. The excess volumes were independent of temperature, but changed noticeably with the chain length of the alkanol. The VE values were only positive starting from heptanol, with the maximum value, 0.239 cm3 mol−1, for equimolar decanol. The observed changeover VE < 0 to VE > 0 suggests that the steric effect is primarily responsible for the positive contributions to VE. The thermal expansion coefficients α were evaluated from the variation of densities with temperature. Key words: excess volumes, 2-pyrrolidinone, n-alkanols, liquid mixtures, hydrogen bonding.


1988 ◽  
Vol 66 (4) ◽  
pp. 713-717 ◽  
Author(s):  
Tsukasa Okano ◽  
Hideo Ogawa ◽  
Sachio Murakami

Molar excess volumes, molar excess isentropic compressions, and molar excess isobaric heat capacities for binary liquid mixtures of methanol with 2-methylpropanol, 2-butanol, and 2-methyl-2-propanol have been determined at 298.15 K. The concentration dependence and magnitude of these thermodynamic functions are quite different from those of the methanol – 1-butanol system, which had been previously determined. Molar excess volumes for two of the present systems are positive over the whole concentration range, except for the 2-methyl-2-propanol system. For the latter system they are negative in the butanol-rich range. Molar excess isentropic compressions of these systems show slightly different concentration dependence from that of the excess volumes, but the order in magnitude resembles that of the excess volumes. Molar excess isobaric heat capacities for all systems are negative and show simple concentration dependence. The minimum values of excess heat capacities are correlated with the magnitude of molar isobaric heat capacities of the pure isomeric butanols. The behavior of these excess functions is discussed with reference to the differences in numbers and strength of hydrogen bonding between the pure liquid and the solution.





2019 ◽  
Vol 134 ◽  
pp. 20-30 ◽  
Author(s):  
L.M. Follegatti–Romero ◽  
F.H.B. Sosa ◽  
M.C. Costa ◽  
D.T. Tavares ◽  
L.H. de Oliveira ◽  
...  


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