Vapour pressure study of the deuterium exchange reaction in methanol-ethanol systems: equilibrium constant determination

1980 ◽  
Vol 33 (9) ◽  
pp. 1943 ◽  
Author(s):  
ZS Kooner ◽  
DV Fenby

The equilibrium constant of the reaction ���������������������� CH3OH(1)+C2H5OD(1) → CH3OD(1)+C2H5OH(1) is obtained from vapour pressure measurements on methanol+ethanol systems. The value obtained, 1.03�0.01 at 298 K, is in good agreement with that calculated independently from previously reported vapour pressure studies of water+methanol and water+ethanol systems. Vapour pressures at 298.15 K are reported for the systems CH3OH+C2H5OH, CH3OH+C2H5OD, CH3OD+C2H5OH and CH3OD+C2H5OD. Molar excess Gibbs functions are obtained from these vapour pressures.

1979 ◽  
Vol 32 (11) ◽  
pp. 2353 ◽  
Author(s):  
RC Phutela ◽  
ZS Kooner ◽  
DV Fenby

A method is proposed for the determination of the equilibrium constants of liquid-phase deuterium exchange reactions from vapour pressure measurements. It is applied to water-ethanol systems to give the equilibrium constant of the reaction 2C2H5OH(l) + D2(l) → 2C2H5OD(l) + H2O(l) The value obtained, 1.05+0.02 at 298 K, is significantly greater than the 'random' value and is more precise and reasonable than a recent calorimetric estimate. Vapour pressures at 298.14 K are reported for the systems H2O+C2H5OH, H2O+C2H5OD, D2O + C2H5OH and D2O + C2H5OD. Molar excess Gibbs functions are obtained from these vapour pressure measurements.


1980 ◽  
Vol 33 (1) ◽  
pp. 9 ◽  
Author(s):  
ZS Koner ◽  
RC Phutela ◽  
DV Fenby

The equilibrium constant of the reaction2CH3OH(l) + D2O(l) → 2CH3OD(l) + H2O(l) is obtained from vapour pressure measurements. The value, 1.09k0.02 at 298 K, is in satisfactory agreement with calculated values and with calorimetric estimates. Vapour pressures at 298.14 K are reported for the systems H2O + CH3OH, H2O+CH3OD, D2O + CH3OH and D2O+ CH3OD. Molar excess Gibbs functions are obtained from these vapour pressures.


1981 ◽  
Vol 34 (9) ◽  
pp. 1801
Author(s):  
ZS Kooner ◽  
DV Fenby

Vapour pressures and molar excess enthalpies at 298.15 K are reported for the systems H2O+(C2H5)2NH and D2O+(C2H5)2NH. They are analysed to give the equilibrium constant and enthalpy of the reaction ����������������� 2(C2H5)2NH(1)+D2O(1)→2(C2H5)2ND(1)+H2O(1) Molar excess enthalpies at 298.15 K of the systems CH3OH+(C2H5)2NH, CH3OD+(C2H5)2NH, C2H5OH+(C2H5)2NH and C2H5OD+(C2H5)2NH are used to obtain enthalpies of the reactions ���������� (C2H5)2NH(1)+ROD(1)→(C2H5)2ND(1)+ROH(1)� (R = CH3, C2H5)Thermodynamic properties of various NH/OD exchange reactions are calculated from statistical mechanical equations by use of harmonic frequencies.


1988 ◽  
Vol 92 (911) ◽  
pp. 36-53 ◽  
Author(s):  
P. R. Ashill ◽  
R. F. A. Keating

Summary A method is described for calculating wall interference in solid-wall wind tunnels from measurements of static pressures at the walls. Since it does not require a simulation of the model flow, the technique is particularly suited to determining wall interference for complex flows such as those over VSTOL aircraft, helicopters and bluff shapes (e.g. cars and trucks). An experimental evaluation shows that the method gives wall-induced velocities which are in good agreement with those of existing methods in cases where these techniques are valid, and illustrates its effectiveness for inclined jets which are not readily modelled.


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