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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]
VLE of the mixture of chloroform and methanol plus NRTL fit and extrapolation to different pressures. The non-random two-liquid model [1] (abbreviated NRTL model) is an activity coefficient model introduced by Renon and Prausnitz in 1968 that correlates the activity coefficients of a compound with its mole fractions in the liquid phase concerned.
The Dortmund Data Bank [1] (short DDB) is a factual data bank for thermodynamic and thermophysical data. Its main usage is the data supply for process simulation where experimental data are the basis for the design, analysis, synthesis, and optimization of chemical processes.
The Antoine equation [3] [4] is a pragmatic mathematical expression of the relation between the vapor pressure and the temperature of pure liquid or solid substances. It is obtained by curve-fitting and is adapted to the fact that vapor pressure is usually increasing and concave as a function of temperature.
[4]: 215 In other words, the temperature, pressure and molar Gibbs free energy are the same between the two phases when they are at equilibrium. An equivalent, more common way to express the vapor–liquid equilibrium condition in a pure system is by using the concept of fugacity .
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In the article, it is stated that the Antoine equation is derived from the Clausius–Clapeyron relation. However to my knowledge this is not possible, as the Antoine equation is semi empirical. The best one can do is derive the August equation, which holds when the specific volume in a substances initial phase is very small compared to its gas ...