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  2. Antoine equation - Wikipedia

    en.wikipedia.org/wiki/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 Louis Charles Antoine (1825–1897). [1]

  3. Tetens equation - Wikipedia

    en.wikipedia.org/wiki/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. It is named after its creator, O. Tetens who was an early German meteorologist.

  4. Methanol (data page) - Wikipedia

    en.wikipedia.org/wiki/Methanol_(data_page)

    Here is a similar formula from the 67th edition of the CRC handbook. Note that the form of this formula as given is a fit to the Clausius–Clapeyron equation, which is a good theoretical starting point for calculating saturation vapor pressures: log 10 (P) = −(0.05223)a/T + b, where P is in mmHg, T is in kelvins, a = 38324, and b = 8.8017.

  5. Raoult's law - Wikipedia

    en.wikipedia.org/wiki/Raoult's_law

    Raoult's law (/ ˈ r ɑː uː l z / law) is a relation of physical chemistry, with implications in thermodynamics.Proposed by French chemist François-Marie Raoult in 1887, [1] [2] it states that the partial pressure of each component of an ideal mixture of liquids is equal to the vapor pressure of the pure component (liquid or solid) multiplied by its mole fraction in the mixture.

  6. Osmotic coefficient - Wikipedia

    en.wikipedia.org/wiki/Osmotic_coefficient

    where is the chemical potential of the pure solvent and is the chemical potential of the solvent in a solution, M A is its molar mass, x A its mole fraction, R the gas constant and T the temperature in Kelvin. [1] The latter osmotic coefficient is sometimes called the rational osmotic coefficient. The values for the two definitions are ...

  7. Goff–Gratch equation - Wikipedia

    en.wikipedia.org/wiki/Goff–Gratch_equation

    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 ...

  8. Vapor pressure - Wikipedia

    en.wikipedia.org/wiki/Vapor_pressure

    According to the American Meteorological Society Glossary of Meteorology, saturation vapor pressure properly refers to the equilibrium vapor pressure of water above a flat surface of liquid water or solid ice, and is a function only of temperature and whether the condensed phase is liquid or solid. [17]

  9. Lee–Kesler method - Wikipedia

    en.wikipedia.org/wiki/Lee–Kesler_method

    The correct result would be P = 101.325 kPa, the normal (atmospheric) pressure. The deviation is −1.63 kPa or −1.61 %. 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 .