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== Vapor pressure of solids ==
== Vapor pressure of solids ==
[[Image:Vapor Pressure of Liquid and Solid Benzene.png|thumb|300px|Vapor Pressure of Liquid and Solid Benzene]]
[[Image:Vapor Pressure of Liquid and Solid Benzene.png|thumb|325px|Vapor Pressure of Liquid and Solid Benzene]]
Equilibrium vapor pressure can be defined as the pressure reached when a condensed phase is in equilibrium with its own vapor. In the case of an equilibrium solid, such as a [[crystal]], this can be defined as the pressure when the rate of [[sublimation (physics)|sublimation]] of a solid matches the rate of deposition of its vapor phase. For most solids this pressure is very low, but some notable exceptions are [[naphthalene]], [[dry ice]] (the vapor pressure of dry ice is 5.73 MPa (831 psi, 56.5 atm) at 20 degrees Celsius, meaning it will cause most sealed containers to explode), and ice.  All solid materials have a vapor pressure. However, due to their often extremely low values, measurement can be rather difficult. Typical techniques include the use of [[thermogravimetry]] and [[gas transpiration]].


The sublimation pressure can be calculated<ref>Moller B., Rarey J., Ramjugernath D., "Estimation of the vapour pressure of non-electrolyte organic compounds via group contributions and group interactions ", J.Mol.Liq., 143(1), 52-63, 2008
All solid materials have a vapor pressure which, for most solids, is very low. Some notable exceptions are [[naphthalene]], [[ice]] and  [[dry ice]] ([[carbon dioxide]]). The vapor pressure of dry ice is 5.73 MPa (56.5 atm) at 20 °C which would cause most sealed containers to rupture.
</ref> from extrapolated liquid vapor pressures (of the supercooled liquid) if the [[Enthalpy of fusion|heat of fusion]] is known. The heat of fusion has to be added in addition to the heat of vaporization to evaporize a solid. Assuming that the heat of fusion is temperature-independent and ignoring additional transition temperatures between different solid phases the equation  
 
Due to their often extremely low values, measurement of the vapor pressure of solids can be rather difficult. Typical techniques include the use of [[thermogravimetry]] and [[gas transpiration]].
 
The vapor pressure of a solid can be defined as the pressure at which the rate of [[sublimation (physics)|sublimation]] of a solid matches the rate of deposition of its vapor phase. The sublimation pressure can be calculated <ref>{{cite journal |author=B. Moller, J.Rarey and D.Ramjugernath |title=Estimation of the vapour pressure of non-electrolyte organic compounds via group contributions and group interactions|journal=J.Mol.Liq.|volume=143 |issue=1|pages=52-63|date=2008|id=|url=}}</ref> from extrapolated liquid vapor pressures (of the supercooled liquid) if the [[Enthalpy of fusion|heat of fusion]] is known. The heat of fusion has to be added in addition to the heat of vaporization to evaporize a solid. Assuming that the heat of fusion is temperature-independent and ignoring additional transition temperatures between different solid phases the equation  


<math>ln\,P^S_{solid} = ln\,P^S_{liquid} - \frac{\Delta H_m}{R} \left( \frac{1}{T} - \frac{1}{T_m} \right)</math>
<math>ln\,P^S_{solid} = ln\,P^S_{liquid} - \frac{\Delta H_m}{R} \left( \frac{1}{T} - \frac{1}{T_m} \right)</math>
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gives a fair estimation for temperatures not too far from the melting point. This equation also shows that the sublimation pressure is lower than the extrapolated liquid vapor pressure (ΔH<sub>m</sub> is positive) and the difference grows with increased distance from the melting point.
gives a fair estimation for temperatures not too far from the melting point. This equation also shows that the sublimation pressure is lower than the extrapolated liquid vapor pressure (ΔH<sub>m</sub> is positive) and the difference increases with increased distance from the melting point.
 
{{reflist}}

Revision as of 18:18, 9 December 2008

Vapor pressure of solids

Vapor Pressure of Liquid and Solid Benzene

All solid materials have a vapor pressure which, for most solids, is very low. Some notable exceptions are naphthalene, ice and dry ice (carbon dioxide). The vapor pressure of dry ice is 5.73 MPa (56.5 atm) at 20 °C which would cause most sealed containers to rupture.

Due to their often extremely low values, measurement of the vapor pressure of solids can be rather difficult. Typical techniques include the use of thermogravimetry and gas transpiration.

The vapor pressure of a solid can be defined as the pressure at which the rate of sublimation of a solid matches the rate of deposition of its vapor phase. The sublimation pressure can be calculated [1] from extrapolated liquid vapor pressures (of the supercooled liquid) if the heat of fusion is known. The heat of fusion has to be added in addition to the heat of vaporization to evaporize a solid. Assuming that the heat of fusion is temperature-independent and ignoring additional transition temperatures between different solid phases the equation

with:

= Sublimation pressure of the solid component at the temperature
= Extrapolated vapor pressure of the liquid component at the temperature
= Heat of fusion
= Gas constant
= Sublimation temperature
= Melting point temperature

gives a fair estimation for temperatures not too far from the melting point. This equation also shows that the sublimation pressure is lower than the extrapolated liquid vapor pressure (ΔHm is positive) and the difference increases with increased distance from the melting point.

  1. B. Moller, J.Rarey and D.Ramjugernath (2008). "Estimation of the vapour pressure of non-electrolyte organic compounds via group contributions and group interactions". J.Mol.Liq. 143 (1): 52-63.