Vapor pressure or equilibrium vapor pressure is the pressure exerted by a vapor in thermodynamic equilibrium with its condensed phases (solid or liquid) at a given temperature in a closed system. The equilibrium vapor pressure is an indication of a liquid's evaporation rate. It relates to the tendency of particles to escape from the liquid (or a solid). A substance with a high vapor pressure at normal temperatures is often referred to as volatile.
The vapor pressure of any substance increases non-linearly with temperature according to the Clausius–Clapeyron relation. The atmospheric pressure boiling point of a liquid (also known as the normal boiling point) is the temperature at which the vapor pressure equals the ambient atmospheric pressure. With any incremental increase in that temperature, the vapor pressure becomes sufficient to overcome atmospheric pressure and lift the liquid to form vapor bubbles inside the bulk of the substance. Bubble formation deeper in the liquid requires a higher pressure, and therefore higher temperature, because the fluid pressure increases above the atmospheric pressure as the depth increases.
The vapor pressure that a single component in a mixture contributes to the total pressure in the system is called partial pressure. For example, air at sea level, and saturated with water vapor at 20 °C, has partial pressures of about 23 mbar of water, 780 mbar of nitrogen, 210 mbar of oxygen and 9 mbar of argon.
Measurement and units 
Vapor pressure is measured in the standard units of pressure. The International System of Units (SI) recognizes pressure as a derived unit with the dimension of force per area and designates the pascal (Pa) as its standard unit. One pascal is one newton per square meter (N·m−2 or kg·m−1·s−2).
Experimental measurement of vapor pressure is a simple procedure for common pressures between 1 and 200 kPa. Most accurate results are obtained near the boiling point of substances and large errors result for measurements smaller than 1kPa. Procedures often consist of purifying the test substance, isolating it in a container, evacuating any foreign gas, then measuring the equilibrium pressure of the gaseous phase of the substance in the container at different temperatures. Better accuracy is achieved when care is taken to ensure that the entire substance and its vapor are at the prescribed temperature. This is often done, as with the use of an isoteniscope, by submerging the containment area in a liquid bath.
Estimating vapor pressures with Antoine equation 
and it can be transformed into this temperature-explicit form:
where: is the absolute vapor pressure of a substance
- is the temperature of the substance
- , and are substance-specific coefficients (i.e., constants or parameters)
- is typically either or 
A simpler form of the equation with only two coefficients is sometimes used:
which can be transformed to:
Sublimations and vaporizations of the same substance have separate sets of Antoine coefficients, as do components in mixtures. The Antoine equation is accurate to a few percent for most volatile substances (with vapor pressures over 10 Torr).
Relation to boiling point of liquids 
As a general trend, vapor pressures of liquids at ambient temperatures increase with decreasing boiling points. This is illustrated in the vapor pressure chart (see right) that shows graphs of the vapor pressures versus temperatures for a variety of liquids.
For example, at any given temperature, methyl chloride has the highest vapor pressure of any of the liquids in the chart. It also has the lowest normal boiling point (-24.2 °C), which is where the vapor pressure curve of methyl chloride (the blue line) intersects the horizontal pressure line of one atmosphere (atm) of absolute vapor pressure.
Although the relation between vapor pressure and temperature is non-linear, the chart uses a logarithmic vertical axis to produce slightly curved lines, so one chart can graph many liquids. A nearly straight line is obtained when the logarithm of the vapor pressure is plotted against 1/(T+230) where T is the temperature in degrees Celsius. The vapor pressure of a liquid at its boiling point equals the pressure of its surrounding environment.
Liquid mixtures 
Raoult's law gives an approximation to the vapor pressure of mixtures of liquids. It states that the activity (pressure or fugacity) of a single-phase mixture is equal to the mole-fraction-weighted sum of the components' vapor pressures:
where p tot is the mixture's vapor pressure, i is one of the components of the mixture and Χi is the mole fraction of that component in the liquid mixture. The term piΧi is the partial pressure of component i in the mixture. Raoult's Law is applicable only to non-electrolytes (uncharged species); it is most appropriate for non-polar molecules with only weak intermolecular attractions (such as London forces).
Systems that have vapor pressures higher than indicated by the above formula are said to have positive deviations. Such a deviation suggests weaker intermolecular attraction than in the pure components, so that the molecules can be thought of as being "held in" the liquid phase less strongly than in the pure liquid. An example is the azeotrope of approximately 95% ethanol and water. Because the azeotrope's vapor pressure is higher than predicted by Raoult's law, it boils at a temperature below that of either pure component.
There are also systems with negative deviations that have vapor pressures that are lower than expected. Such a deviation is evidence for stronger intermolecular attraction between the constituents of the mixture than exists in the pure components. Thus, the molecules are "held in" the liquid more strongly when a second molecule is present. An example is a mixture of trichloromethane (chloroform) and 2-propanone (acetone), which boils above the boiling point of either pure component.
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 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, which causes most sealed containers to rupture), 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.
There are a number of methods for calculating the sublimation pressure (i.e., the vapor pressure) of a solid. One method is to estimate the sublimation pressure from extrapolated liquid vapor pressures (of the supercooled liquid), if the heat of fusion is known, by using this particular form of the Clausius–Clapeyron relation:
|= 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|
This method assumes that the heat of fusion is temperature-independent, ignores additional transition temperatures between different solid phases, and it gives a fair estimation for temperatures not too far from the melting point. It also shows that the sublimation pressure is lower than the extrapolated liquid vapor pressure (ΔHm is positive) and the difference grows with increased distance from the melting point.
Boiling point of water in nature 
Like all liquids, water boils when its vapor pressure reaches its surrounding pressure. In nature, the atmospheric pressure is lower at higher elevations and water boils at a lower temperature. The boiling temperature of water for atmospheric pressures can be approximated by the Antoine equation:
or transformed into this temperature-explicit form:
Dühring's rule 
Dühring's rule states that a linear relationship exists between the temperatures at which two solutions exert the same vapor pressure.
The following table is a list of a variety of substances ordered by increasing vapor pressure.
|Tungsten||100 Pa||0.001||0.75||3203 °C|
|Ethylene glycol||500 Pa||0.005||3.75||20 °C|
|Xenon difluoride||600 Pa||0.006||4.50||25 °C|
|Water (H2O)||2.3 kPa||0.023||17.5||20 °C|
|Propanol||2.4 kPa||0.024||18.0||20 °C|
|Ethanol||5.83 kPa||0.0583||43.7||20 °C|
|Methyl isobutyl ketone||26.48 kPa||0.2648||198.62||25 °C|
|Freon 113||37.9 kPa||0.379||284||20 °C|
|Acetaldehyde||98.7 kPa||0.987||740||20 °C|
|Butane||220 kPa||2.2||1650||20 °C|
|Formaldehyde||435.7 kPa||4.357||3268||20 °C|
|Propane||1.013 MPa||10.133||7600||25.6 °C|
|Carbonyl sulfide||1.255 MPa||12.55||9412||25 °C|
|Carbon dioxide||5.7 MPa||57||42753||20 °C|
Estimating vapor pressure from molecular structure 
Meaning in meteorology 
In meteorology, the term vapor pressure is used to mean the partial pressure of water vapor in the atmosphere, even if it is not in equilibrium, and the equilibrium vapor pressure is specified otherwise. Meteorologists also use the term saturation vapor pressure to refer to the equilibrium vapor pressure of water or brine above a flat surface, to distinguish it from equilibrium vapor pressure, which takes into account the shape and size of water droplets and particulates in the atmosphere.
See also 
- Absolute humidity
- Clausius-Clapeyron relation
- Partial pressure
- Relative humidity
- Relative volatility
- Raoult's law
- Saturation vapor density
- Triple point
- Vapor-liquid equilibrium
- Vapor pressure of water
- Reid vapor pressure
- True vapor pressure
- Vapor pressures of the elements (data page)
- K. Růžička, M. Fulem, V. Růžička. "Vapor Pressure of Organic Compounds. Measurement and Correlation".
- What is the Antoine Equation? (Chemistry Department, Frostburg State University, Maryland)
- R.K.Sinnot (2005). Chemical Engineering Design (4th ed.). Butterworth-Heinemann. p. 331. ISBN 0-7506-6538-6.
- Perry, R.H. and Green, D.W. (Editors) (1997). Perry's Chemical Engineers' Handbook (7th ed.). McGraw-Hill. ISBN 0-07-049841-5.
- Dreisbach, R. R. and Spencer, R. S. (January 1949). "Infinite Points of Cox Chart Families and dt/dP Values at any Pressure". Industrial and Engineering Chemistry, 41 (1). p. 176.
- 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
- J. F. Pankow et al. (2008). "SIMPOL.1: a simple group contribution method for predicting vapor pressures and enthalpies of vaporization of multifunctional organic compounds". Atmos. Chem. Phys. 8: 2773–2796.
- "Vapour pressure of pure liquid compounds. Estimation by EVAPORATION"
- S. Compernolle et al. (2011). "EVAPORATION: a new vapour pressure estimation method for organic molecules including non-additivity and intramolecular interactions". Atmos. Chem. Phys. 11: 9431–9450.
- Glossary (Developed by the American Meteorological Society)
- A Brief Tutorial (An article about the definition of equilibrium vapor pressure)