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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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Vapour Pressure Of Water
The vapor 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 vapor pressure is the pressure at which water vapor is in thermodynamic equilibrium with its condensed state. At pressures higher than saturation vapor pressure, water will condense, while at lower pressures it will evaporate or sublimate. The saturation vapor 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 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 temperature-vapor pressure relation inversely describes the relation between the boilin ...
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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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World Meteorological Organization
The World Meteorological Organization (WMO) is a List of specialized agencies of the United Nations, specialized agency of the United Nations responsible for promoting international cooperation on atmospheric science, climatology, hydrology and geophysics. The WMO originated from the International Meteorological Organization (IMO), a nongovernmental organization founded in 1873 as a forum for exchanging weather data and research. Proposals to reform the status and structure of the IMO culminated in the World Meteorological Convention of 1947, which formally established the World Meteorological Organization. The Convention entered into force on 23 March 1950, and the following year the WMO began operations as an intergovernmental organization within the UN system. The WMO is made up of 193 countries and territories, and facilitates the "free and unrestricted" exchange of data, information, and research between the respective meteorological and hydrological institutions of its m ...
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Pascal (unit)
The pascal (symbol: Pa) is the unit of pressure in the International System of Units (SI). It is also used to quantify internal pressure, stress, Young's modulus, and ultimate tensile strength. The unit, named after Blaise Pascal, is an SI coherent derived unit defined as one newton per square metre (N/m2). It is also equivalent to 10 barye (10 Ba) in the CGS system. 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. The unit of measurement called '' standard atmosphere (atm)'' is defined as . 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 Cana ...
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Absolute Temperature
Thermodynamic temperature, also known as absolute temperature, is a physical quantity which measures temperature starting from absolute zero, the point at which particles have minimal thermal motion. Thermodynamic temperature is typically expressed using the Kelvin scale, where the unit of measurement is the ''kelvin'' (unit symbol: K). The Kelvin scale uses the same degree interval as the Celsius scale but is offset so that 0 K corresponds to absolute zero. For comparison, a temperature of 295 K corresponds to 21.85 °C and 71.33 °F. Another absolute scale of temperature is the Rankine scale, which is based on the Fahrenheit degree interval. Historically, thermodynamic temperature was defined by Lord Kelvin in terms of a macroscopic relation between Work (thermodynamics), thermodynamic work and Heat, heat transfer as defined in thermodynamics, but the kelvin was redefined by international agreement in 2019 in terms of phenomena that are now understood as man ...
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Kelvin
The kelvin (symbol: K) is the base unit for temperature in the International System of Units (SI). The Kelvin scale is an absolute temperature scale that starts at the lowest possible temperature (absolute zero), taken to be 0 K. By definition, the Celsius scale (symbol °C) and the Kelvin scale have the exact same magnitude; that is, a rise of 1 K is equal to a rise of 1 °C and vice versa, and any temperature in degrees Celsius can be converted to kelvin by adding 273.15. The 19th century British scientist Lord Kelvin first developed and proposed the scale. It was often called the "absolute Celsius" scale in the early 20th century. The kelvin was formally added to the International System of Units in 1954, defining 273.16 K to be the triple point of water. The Celsius, Fahrenheit, and Rankine scales were redefined in terms of the Kelvin scale using this definition. The 2019 revision of the SI now defines the kelvin in terms of energy by setting the Bo ...
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Boiling Point
The boiling point of a substance is the temperature at which the vapor pressure of a liquid equals the pressure surrounding the liquid and the liquid changes into a vapor. The boiling point of a liquid varies depending upon the surrounding environmental pressure. A liquid in a partial vacuum, i.e., under a lower pressure, has a lower boiling point than when that liquid is at atmospheric pressure. Because of this, water boils at 100°C (or with scientific precision: ) under standard pressure at sea level, but at at altitude. For a given pressure, different liquids will boiling, boil at different temperatures. The normal boiling point (also called the atmospheric boiling point or the atmospheric pressure boiling point) of a liquid is the special case in which the vapor pressure of the liquid equals the defined atmospheric pressure at sea level, one Atmosphere (unit), atmosphere. At that temperature, the vapor pressure of the liquid becomes sufficient to overcome atmospheric pre ...
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Triple Point
In thermodynamics, the triple point of a substance is the temperature and pressure at which the three Phase (matter), phases (gas, liquid, and solid) of that substance coexist in thermodynamic equilibrium.. It is that temperature and pressure at which the sublimation (phase transition), sublimation, Melting, fusion, and vaporisation curves meet. For example, the triple point of Mercury (element), mercury occurs at a temperature of and a pressure of 0.165 Milli, mPascal (unit), Pa. In addition to the triple point for solid, liquid, and gas phases, a triple point may involve more than one solid phase, for substances with multiple polymorphism (materials science), polymorphs. Helium-4 is unusual in that it has no sublimation/deposition curve and therefore no triple points where its solid phase meets its gas phase. Instead, it has a vapor-liquid-superfluid point, a solid-liquid-superfluid point, a solid-solid-liquid point, and a solid-solid-superfluid point. None of these should be ...
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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 is the vapor pressure, is temperature (in °C or in K according to the value of ), 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 tran ...
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Tetens Equation
Tetens may refer to: People * Alfred Tetens (1835-1903), German explorer * Axel Tetens (1892–1961), Danish Olympic wrestler * Johannes Nikolaus Tetens (1736–1807), German-Danish philosopher and scientist * Otto Tetens (1865–1945), German scientist * T.H. Tetens (1899-1976), Jewish German journalist Other uses * Tetens equation, calculates the saturation vapor pressure of water over liquid and ice See also * Teten {{surname ...
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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'' = 0.2120 Dortmund Data Bank the following calculati ...
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