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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]
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.
e * is the saturation water vapor pressure T is the absolute air temperature in kelvins T st is the steam-point (i.e. boiling point at 1 atm.) temperature (373.15 K) e * st is e * at the steam-point pressure (1 atm = 1013.25 hPa) Similarly, the correlation for the saturation water vapor pressure over ice is:
The saturation vapor density (SVD) is the maximum density of water vapor in air at a given temperature. [1] The concept is related to saturation vapor pressure (SVP). It can be used to calculate exact quantity of water vapor in the air from a relative humidity (RH = % local air humidity measured / local total air humidity possible ) Given an RH percentage, the density of water in the air is ...
The Köhler equation relates the saturation ratio over an aqueous solution droplet of fixed dry mass to its wet diameter as: [4] = (), with: S {\displaystyle S} = saturation ratio over the droplet surface defined as S = p w / p w 0 {\textstyle S=p_{w}/p_{w}^{0}} , where p w {\textstyle p_{w}} is the water vapor pressure of the solution ...
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]
P s (T) is the saturation vapor pressure in hPa; exp(x) is the exponential function; T is the air temperature in degrees Celsius; Buck (1981) also lists enhancement factors for a temperature range of −80 to 50 °C (−112 to 122 °F) at pressures of 1,000 mb, 500 mb, and 250 mb. These coefficients are listed in the table below.