Binary systems of trichloroethylene with benzene, toluene, p-xylene, carbon tetrachloride, and chloroform. 2. Viscosities at 303.15 K

1981 ◽  
Vol 85 (7) ◽  
pp. 886-889 ◽  
Author(s):  
Jagan Nath ◽  
S. N. Dubey
Keyword(s):  
Carbon Tetrachloride ◽  
Binary Systems ◽  
Benzene Toluene

Liquid-liquid equilibrium in binary glycols-toluene and glycols-xylene systems

1982 ◽  
Vol 47 (6) ◽  
pp. 1686-1694 ◽  
Author(s):  
Lumír Mandík ◽  
František Lešek
Keyword(s):  
Atmospheric Pressure ◽  
Binary Systems ◽  
Liquid Equilibrium ◽  
Benzene Toluene

Liquid-liquid equilibria were determined in the following binary systems: 1,2-ethandiol/toluene, 1,2-ethandiol/xylene, 1,2-propandiol/toluene, 1,2-propandiol/xylene, 1,4-butandiol/toluene, 1,4-butandiol/xylene, 1,3-butandiol/toluene, 1,3-butandiol/xylene, 1,3-butandiol/p-xylene, 2,2'-dioxydiethanol/toluene, 2,2'-dioxydiethanol/xylene. The solubility of 2,2-dimethyl-1,3-propandiol in benzene, toluene and xylene was also measured. Critical solubility temperatures at atmospheric pressure were determined for systems containing 1,2-propandiol and 1,3-butandiol.

COMPLEXES OF STANNIC IODIDE WITH AROMATIC HYDROCARBONS

1965 ◽  
Vol 43 (5) ◽  
pp. 1272-1278 ◽  
Author(s):  
J. F. Murphy ◽  
D. E. Baker
Keyword(s):  
Carbon Tetrachloride ◽  
Complex Formation ◽  
Aromatic Hydrocarbon ◽  
Aromatic Hydrocarbons ◽  
Extinction Coefficient ◽  
Regular Solutions ◽  
Benzene Toluene ◽  
Yield Values ◽  
Complex Stabilities ◽  
Iodide Complex

Spectrophotometric measurements on solutions of stannic iodide were found to provide evidence for complex formation with aromatic hydrocarbons. Calculations, based on spectra for mixed solutions of benzene and stannic iodide in carbon tetrachloride, yield values of 0.26 for the equilibrium constant (mole fraction), 28 400 1/mole cm for the molar extinction coefficient of the benzene – stannic iodide complex. Kinetic evidence indicates that the order of decreasing complex stabilities is from xylene to toluene to benzene. The formation of stannic iodide – aromatic hydrocarbon complexes provides an explanation for the discrepancy between measured solubilities of stannic iodide in benzene, toluene, and xylene, and the solubilities predicted by the Hildebrand theory of regular solutions.

Excess properties of binary systems formed by carbon tetrachloride with isopropanol and n-butanol

1997 ◽  
Vol 136 (1-2) ◽  
pp. 307-314 ◽  
Author(s):  
L Simoiu ◽  
I Trandafir ◽  
M Pleniceanu ◽  
M Baniceru
Keyword(s):  
Carbon Tetrachloride ◽  
Binary Systems ◽  
Excess Properties
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