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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 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. The basic form of the equation is:
This page provides supplementary chemical data on toluene. MSDS sheets. Structure and properties. Structure and properties Index of refraction, n D: 1.4969 at 20 °C ...
[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 .
The following table lists the Van der Waals constants (from the Van der Waals equation) for a number of common gases and volatile liquids. [ 1 ] To convert from L 2 b a r / m o l 2 {\displaystyle \mathrm {L^{2}bar/mol^{2}} } to L 2 k P a / m o l 2 {\displaystyle \mathrm {L^{2}kPa/mol^{2}} } , multiply by 100.
A 2023 study published in the International Journal of Environmental Research and Public Health found that simply engaging in walking after a carbohydrate-dense meal can help decrease blood sugar ...
In the case of degenerate energy levels, we can write the partition function in terms of the contribution from energy levels (indexed by j) as follows: =, where g j is the degeneracy factor, or number of quantum states s that have the same energy level defined by E j = E s.