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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 cause the liquid to form vapor bubbles.
where P 1, P 2 are the vapor pressures at temperatures T 1, T 2 respectively, ΔH vap is the enthalpy of vaporization, and R is the universal gas constant. The rate of evaporation in an open system is related to the vapor pressure found in a closed system. If a liquid is heated, when the vapor pressure reaches the ambient pressure the liquid ...
The higher the vapor pressure of a liquid at a given temperature, the lower the normal boiling point (i.e., the boiling point at atmospheric pressure) of the liquid. The vapor pressure chart to the right has graphs of the vapor pressures versus temperatures for a variety of liquids. [11] As can be seen in the chart, the liquids with the highest ...
The boiling point of water is the temperature at which the saturated vapor pressure equals the ambient pressure. Water supercooled below its normal freezing point has a higher vapor pressure than that of ice at the same temperature and is, thus, unstable. Calculations of the (saturation) vapor pressure of water are commonly used in meteorology.
The Clausius–Clapeyron equation [8]: 509 applies to vaporization of liquids where vapor follows ideal gas law using the ideal gas constant and liquid volume is neglected as being much smaller than vapor volume V. It is often used to calculate vapor pressure of a liquid. [9]
The commonly known phases solid, liquid and vapor are separated by phase boundaries, i.e. pressure–temperature combinations where two phases can coexist. At the triple point, all three phases can coexist. However, the liquid–vapor boundary terminates in an endpoint at some critical temperature T c and critical pressure p c. This is the ...
[4]: 215 In other words, the temperature, pressure and molar Gibbs free energy are the same between the two phases when they are at equilibrium. An equivalent, more common way to express the vapor–liquid equilibrium condition in a pure system is by using the concept of fugacity. Under this view, equilibrium is described by the following equation:
This may be written in the following form, known as the Ostwald–Freundlich equation: =, where is the actual vapour pressure, is the saturated vapour pressure when the surface is flat, is the liquid/vapor surface tension, is the molar volume of the liquid, is the universal gas constant, is the radius of the droplet, and is temperature ...