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Arden Buck Equation
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 .Buck 1981 A set of several equations were developed, each of which is applicable in a different situation. Formula The equations suggested by (which are modifications of the equations in ) are: : P_\left(T \right) = 6.1121 \exp \left(\left( 18.678 - \frac \right)\left( \frac \right)\right) , over liquid water, > 0 °C : P_\left(T \right) = 6.1115 \exp \left(\left( 23.036 - \frac \right)\left( \frac \right)\right) , over ice, < 0 °C where: * is the saturation vapor pressure in * is the

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Saturation Vapor Pressure
Vapor pressure (or vapour pressure in English-speaking countries other than the US; see spelling differences) or equilibrium vapor pressure is defined as 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 pressure exhibited by vapor present above a liquid surface is known as vapor pressure. As the temperature of a liquid increases, the kinetic energy of its molecules also increases. As the kinetic energy of the molecules increases, the number of molecules transitioning into a vapor also increases, thereby increasing the vapor pressure. The vapor pressure of any substance increases non-linearly with temperature according ...
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Vapour Pressure Of Water
The vapour pressure of water is the pressure exerted by molecules of water vapor in gaseous form (whether pure or in a mixture with other gases such as air). The saturation vapour pressure is the pressure at which water vapour is in thermodynamic equilibrium with its condensed state. At pressures higher than vapour pressure, water would condense, whilst at lower pressures it would evaporate or sublimate. The saturation vapour pressure of water increases with increasing temperature and can be determined with the Clausius–Clapeyron relation. The boiling point of water is the temperature at which the saturated vapour pressure equals the ambient pressure. Calculations of the (saturation) vapour pressure of water are commonly used in meteorology. The temperature-vapour pressure relation inversely describes the relation between the boiling point of water and the pressure. This is relevant to both pressure cooking and cooking at high altitude. An understanding of vapour pressure is ...
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Goff–Gratch Equation
The Goff–Gratch equation is one (arguably the first reliable in history) amongst many experimental correlation proposed to estimate the saturation water vapor pressure at a given temperature. Another similar equation based on more recent data is the Arden Buck equation. Historical note This equation is named after the authors of the original scientific article who described how to calculate the saturation water vapor pressure above a flat free water surface as a function of temperature (Goff and Gratch, 1946). Goff (1957) later revised his formula, and the latter was recommended for use by the World Meteorological Organization in 1988, with further corrections in 2000. The current 2015 edition of the WMO Technical Regulations (WMO-No. 49) however states in Volume 1, Part III, Section 1.2.1, that any formula or constant given in the Guide to Meteorological Instruments and Methods of Observation a.k.a. CIMO-Guide (WMO-No. 8) shall be used, and this document only contains the muc ...
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Pascal (unit)
The pascal (symbol: Pa) is the unit of pressure in the International System of Units (SI), and is also used to quantify internal pressure, stress, Young's modulus, and ultimate tensile strength. The unit, named after Blaise Pascal, is defined as one newton per square metre and is equivalent to 10 barye (Ba) in the CGS system. The unit of measurement called standard atmosphere (atm) is defined as 101,325 Pa. Common multiple units of the pascal are the hectopascal (1 hPa = 100 Pa), which is equal to one millibar, and the kilopascal (1 kPa = 1000 Pa), which is equal to one centibar. Meteorological observations typically report atmospheric pressure in hectopascals per the recommendation of the World Meteorological Organization, thus a standard atmosphere (atm) or typical sea-level air pressure is about 1013 hPa. Reports in the United States typically use inches of mercury or millibars (hectopascals). In Canada these reports are given in kilopascal ...
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Exponential Function
The exponential function is a mathematical function denoted by f(x)=\exp(x) or e^x (where the argument is written as an exponent). Unless otherwise specified, the term generally refers to the positive-valued function of a real variable, although it can be extended to the complex numbers or generalized to other mathematical objects like matrices or Lie algebras. The exponential function originated from the notion of exponentiation (repeated multiplication), but modern definitions (there are several equivalent characterizations) allow it to be rigorously extended to all real arguments, including irrational numbers. Its ubiquitous occurrence in pure and applied mathematics led mathematician Walter Rudin to opine that the exponential function is "the most important function in mathematics". The exponential function satisfies the exponentiation identity e^ = e^x e^y \text x,y\in\mathbb, which, along with the definition e = \exp(1), shows that e^n=\underbrace_ for positive i ...
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Antoine Equation
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 (1825–1897). Equation The Antoine equation is :\log_ p = A-\frac. where ''p'' is the vapor pressure, is temperature (in °C or in K according to the value of C) and , and are component-specific constants. The simplified form with set to zero: :\log_ p = A-\frac is the August equation, after the German physicist Ernst Ferdinand August (1795–1870). The August equation describes a linear relation between the logarithm of the pressure and the reciprocal temperature. This assumes a temperature-independent heat of vaporization. The Antoine equation allows an improved, but still inexact description of the change of the heat of vaporization with the temperature. The Antoine equation can also be transforme ...
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Tetens Equation
The Tetens equation is an equation to calculate the saturation vapour pressure of water over liquid and ice. It is named after its creator, O. Tetens who was an early German meteorologist. He published his equation in 1930,Tetens, O. 1930. Über einige meteorologische Begriffe. Z. Geophys 6: 297-309. and while the publication itself is rather obscure, the equation is widely known among meteorologists and climatologists because of its ease of use and relative accuracy at temperatures within the normal ranges of natural weather conditions. The equation is structurally identical to the August-Roche-Magnus equation, but the coefficients differ. Formula Monteith and Unsworth (2008) provide Tetens' formula for temperatures above 0 °C:Monteith, J.L., and Unsworth, M.H. 2008. ''Principles of Environmental Physics''. Third Ed. AP, Amsterdam. http://store.elsevier.com/Principles-of-Environmental-Physics/John-Monteith/isbn-9780080924793/ ::P = 0.61078 \exp\left(\frac\right), where tem ...
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Lee–Kesler Method
The Lee–Kesler method allows the estimation of the saturated vapor pressure at a given temperature for all components for which the critical pressure ''P''c, the critical temperature ''T''c, and the acentric factor ''ω'' are known. Equations \ln P_ = f^ + \omega \cdot f^ f^=5.92714 - \frac - 1.28862 \cdot \ln T_ + 0.169347 \cdot T_^6 f^=15.2518 - \frac-13.4721 \cdot \ln T_ + 0.43577 \cdot T_^6 with P_=\frac (reduced pressure) and T_=\frac (reduced temperature). Typical errors The prediction error can be up to 10% for polar components and small pressures and the calculated pressure is typically too low. For pressures above 1 bar, that means, above the normal boiling point, the typical errors are below 2%. Example calculation For benzene with * ''T''c = 562.12 KBrunner E., Thies M.C., Schneider G.M., J.Supercrit.Fluids, 39(2), 160-173, 2006 * ''P''c = 4898 kPa * ''T''b = 353.15 K * ''ω'' = 0.2120Dortmund Data Bank the following calculation for T=Tb resul ...
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Atmospheric Thermodynamics
Atmospheric thermodynamics is the study of heat-to-work transformations (and their reverse) that take place in the earth's atmosphere and manifest as weather or climate. Atmospheric thermodynamics use the laws of classical thermodynamics, to describe and explain such phenomena as the properties of moist air, the formation of clouds, atmospheric convection, boundary layer meteorology, and vertical instabilities in the atmosphere. Atmospheric thermodynamic diagrams are used as tools in the forecasting of storm development. Atmospheric thermodynamics forms a basis for cloud microphysics and convection parameterizations used in numerical weather models and is used in many climate considerations, including convective-equilibrium climate models. Overview The atmosphere is an example of a non-equilibrium system. Atmospheric thermodynamics describes the effect of buoyant forces that cause the rise of less dense (warmer) air, the descent of more dense air, and the transformation of water ...
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