High-Pressure Densities and Derived Volumetric Properties (Excess, Apparent and Partial Molar Volumes) of Binary Mixtures of Methanol + [BMIM][PF6]

2008 ◽  
Vol 37 (6) ◽  
pp. 801-833 ◽  
Author(s):  
I. M. Abdulagatov ◽  
A. Tekin ◽  
J. Safarov ◽  
A. Shahverdiyev ◽  
E. Hassel
2008 ◽  
Vol 476 (1-2) ◽  
pp. 51-62 ◽  
Author(s):  
I.M. Abdulagatov ◽  
F.Sh. Aliyev ◽  
M.A. Talibov ◽  
J.T. Safarov ◽  
A.N. Shahverdiyev ◽  
...  

Author(s):  
Heghine H. Ghazoyan

Densities of binary mixture of acrylonitrile in ethanol have been measured over the full range of compositions at temperatures from 293.15K to 323.15 K at the ambient pressure (87.9 kPa). The volumetric properties such as excess molar volumes, apparent molar volumes, partial molar volumes, excess partial molar volumes, standard partial molar volumes for binary mixture were calculated. Excess molar volumes were described by the Redlich–Kister polynomial equation. The Redlich–Kister coefficients and the standard deviations were calculated as well. The excess molar volumes exhibit mainly negative deviations from the ideal behavior over the whole range of composition for acrylonitrile+ethanol binary mixtures at low temperatures and become less negative with increasing temperature from 293.15 to 323.15 K. The results are interpreted on the basis of strong interaction between group of acrylonitrile and OH group of ethanol by hydrogen bonding. However, the sigmoid shape of plots of excess molar volumes versus molar fraction of ethanol from positive to negative values indicates to the varying interactions depending upon the composition of binary mixtures. Moreover, it is also attributed to the self-associating effect of ethanol therefore the self-associates of acrylonitrile by dipole-dipole interactions and the self-associates of ethanol by hydrogen bonding between same molecules at low concentrations predominate too.


1998 ◽  
Vol 22 (2-3) ◽  
pp. 225-235 ◽  
Author(s):  
Juan F. Van der Maelen Urı́a ◽  
Carmen Alvarez-Rúa Alvarez

1996 ◽  
Vol 12 (09) ◽  
pp. 816-824
Author(s):  
Zhong Ming-Hong ◽  
◽  
Ke Jie ◽  
Han Bu-Xing ◽  
Yan Hai-Ke

2016 ◽  
Vol 93 ◽  
pp. 337-346 ◽  
Author(s):  
Connor E. Deering ◽  
Edward C. Cairns ◽  
Jay D. McIsaac ◽  
Andrew S. Read ◽  
Robert A. Marriott

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Omer El-Amin Ahmed Adam ◽  
Ammar Hani Al-Dujaili ◽  
Akl M. Awwad

Densities of aqueous solutions of Ethylene glycol (EG), diethylene glycol (DEG), and triethylene glycol (TEG) were measured at temperatures from 293.15 to 318.15 K and molalities ranging from 0.0488 to 0.5288 mol·kg−1. Volumes of all investigated solutions at a definite temperature were linearly dependent on the solute molality; from this dependence the partial molar volumes at infinite dilution were determined for all solutes. It was found that the partial molar volumes at infinite dilution V-2,0 were concentration independent and slightly increase with increasing temperature. The partial molar volumes at infinite dilution V-2,0 or the limiting apparent molar volumes of ethylene glycols were fitted to a linear equation with the number of oxyethylene groups (n) in the solute molecule. From this equation a constant contribution of the terminal (OH) and the (CH2CH2O) groups to the volumetric properties was obtained. The thermal expansion coefficient (α1,2) for all investigated solutions was calculated at temperatures from 293.15 to 318.15 K. The thermal expansion coefficients for all solutes increase with increasing temperature and molality. Values of (α1,2) were higher than the value of the thermal expansion coefficient of the pure water.


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