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The correct result would be P = 101.325 kPa, the normal (atmospheric) pressure. The deviation is −1.63 kPa or −1.61 %. It is important to use the same absolute units for T and T c as well as for P and P c. The unit system used (K or R for T) is irrelevant because of the usage of the reduced values T r and P r.
This is illustrated in the vapor pressure chart (see right) that shows graphs of the vapor pressures versus temperatures for a variety of liquids. [7] At the normal boiling point of a liquid, the vapor pressure is equal to the standard atmospheric pressure defined as 1 atmosphere, [ 1 ] 760 Torr, 101.325 kPa, or 14.69595 psi.
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.
where temperature T is in degrees Celsius (°C) and saturation vapor pressure P is in kilopascals (kPa). According to Monteith and Unsworth, "Values of saturation vapour pressure from Tetens' formula are within 1 Pa of exact values up to 35 °C." Murray (1967) provides Tetens' equation for temperatures below 0 °C: [3]
One way to write the van der Waals equation is: [8] [9] [10] = where is pressure, is temperature, and = / is molar volume. In addition is the Avogadro constant, is the volume, and is the number of molecules (the ratio / is a physical quantity with base unit mole (symbol mol) in the SI).
A saturation dome uses the projection of a P–v–T diagram (pressure, specific volume, and temperature) onto the P–v plane. The points that create the left-hand side of the dome represent the saturated liquid states, while the points on the right-hand side represent the saturated vapor states (commonly referred to as the “dry” region).
The van der Waals equation of state may be written as (+) =where is the absolute temperature, is the pressure, is the molar volume and is the universal gas constant.Note that = /, where is the volume, and = /, where is the number of moles, is the number of particles, and is the Avogadro constant.
The Antoine equation is a class of semi-empirical correlations describing the relation between vapor pressure and temperature for pure substances. The Antoine equation is derived from the Clausius–Clapeyron relation. The equation was presented in 1888 by the French engineer Louis Charles Antoine (1825–1897). [1]