Thermodynamic properties of organic oxygen compounds XXXIII. The vapour pressure of acetone

1974 ◽  
Vol 6 (7) ◽  
pp. 693-700 ◽  
Author(s):  
D. Ambrose ◽  
C.H.S. Sprake ◽  
R. Townsend
2016 ◽  
Author(s):  
Georgios Tsagkogeorgas ◽  
Pontus Roldin ◽  
Jonathan Duplissy ◽  
Linda Rondo ◽  
Jasmin Tröstl ◽  
...  

Abstract. Here we explore the vapour pressure of sulphuric acid at very low relative humidity, where evaporation of sulphuric acid from particles can be important in the atmospheres of Earth and Venus. We performed experiments in the CLOUD chamber at CERN forming sulphuric acid particles via nucleation and then measuring evaporation versus temperature and relative humidity. We modelled the experiments with the ADCHAM model to constrain the thermodynamic properties governing the evaporation of sulphuric acid. ADCHAM includes a thermodynamics module coupled to an aerosol dynamics module. We derived the mole fractions and activity coefficients of H2SO4, HSO4−, SO42− and SO3 in the particles and then simulated the condensation and evaporation of H2SO4 and SO3. We constrained the equilibrium constants for the dissociation of H2SO4 to HSO4− (KH2SO4) and the dehydration of H2SO4 to SO3 (xKSO3). Our results suggest that particle shrinkage is mainly governed by H2SO4 evaporation, however, we cannot dismiss a contribution from SO3 evaporation. We conclude that KH2SO4 = 2–4 ∙ 109 mol ∙ kg−1 at 288.8 ± 5 K and xKSO3 ≥ 1.4 ∙ 1010.


1967 ◽  
Vol 9 (1) ◽  
pp. 24-35 ◽  
Author(s):  
M. R. Gibson ◽  
E. A. Bruges

Equations in the form of Chebyshev polynomials are presented which enable the thermodynamic properties of saturated water in its liquid and vapour phases to be calculated in a systematic manner. In the equations defining the pressure-temperature relationship the authors have made allowance for certain unpublished observations of the National Bureau of Standards and these are considered in the section relating to vapour pressure. It is believed that the assembly of equations specify for the first time the saturated liquid and vapour boundaries whose properties have previously only been available in tabular form.


2002 ◽  
Vol 38 (3-4) ◽  
pp. 237-247 ◽  
Author(s):  
W. Gierlotka ◽  
K. Fitzner ◽  
M. Sukiennik

The partial vapour pressure of mercury over liquid Hg-Tl liquid solutions were determined in the temperature range from 450 to 700 K by direct vapour pressure measurements carried out with the quartz gauge. From the measured ln pHg vs. T relationships activities of mercury were determined. Using Redlich-Kister formulas logarithms of the activity coefficients were described with the following equations: From which all thermodynamic functions in the solutions can be derived.


1978 ◽  
Vol 56 (19) ◽  
pp. 2538-2545 ◽  
Author(s):  
Donald R. Sadoway ◽  
S. N. Flengas

The vapour pressures for the decomposition of the solid and liquid compounds AMCl6 where A = Na, K, Rb, or Cs, and M = Nb or Ta, were measured by a fused quartz Bourdon spiral pressure gauge. The hexachlorotantalates were found to be more stable thermally than the hexachloroniobates. Enthalpies of decomposition were calculated. The dissociation temperatures of each sequence of compounds increase with increasing size of the radius of the alkali-metal cation. Partial pressures of NbCl5 or TaCl5 vapour in equilibrium with solutions representing the binary Systems KCl–KNbCl6 and KCl–KTaCl6, respectively, are also reported.


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