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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]
The fugacity of a condensed phase (liquid or solid) is defined the same way as for a gas: = and = It is difficult to measure fugacity in a condensed phase directly; but if the condensed phase is saturated (in equilibrium with the vapor phase), the chemical potentials of the two phases are equal (μ c = μ g).
The Arden Buck equations are a group of empirical correlations that relate the saturation vapor pressure to temperature for moist air.The curve fits have been optimized for more accuracy than the Goff–Gratch equation in the range −80 to 50 °C (−112 to 122 °F).
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. [1] 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 ...
The saturation with respect to water cannot be measured much below –50 °C, so manufacturers should use one of the following expressions for calculating saturation vapour pressure relative to water at the lowest temperatures – Wexler (1976, 1977), [1] [2] reported by Flatau et al. (1992)., [3] Hyland and Wexler (1983) or Sonntag (1994 ...
Such VLE diagrams are square with a diagonal line running from the (x 1 = 0, y 1 = 0) corner to the (x 1 = 1, y 1 = 1) corner for reference. These types of VLE diagrams are used in the McCabe–Thiele method to determine the number of equilibrium stages (or theoretical plates ) needed to distill a given composition binary feed mixture into one ...
where: k 1 is the rate coefficient for the reaction that consumes A and B; k −1 is the rate coefficient for the backwards reaction, which consumes P and Q and produces A and B. The constants k 1 and k −1 are related to the equilibrium coefficient for the reaction (K) by the following relationship (set v=0 in balance):
The Köhler curve is the visual representation of the Köhler equation. It shows the saturation ratio – or the supersaturation = % – at which the droplet is in equilibrium with the environment over a range of droplet diameters. The exact shape of the curve is dependent upon the amount and composition of the solutes present in the atmosphere.