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The Elementary Thermodynamics of LSE

Equation 11.1, which we applied to LLE, applies to any phase equilibrium, so it must apply to LSE, with phase 1 being the liquid and phase 2 being the solid. Substituting the definition of the fugacity in terms of the standard state fugacity and solving for the mol fraction of dissolved solid, we find [Pg.200]

If we make that guess, we can also assert that for the pure 1, so Eq. 11.9 becomes [Pg.200]

At the triple pointpi oUd phase = Pi, liquid- If we then assume that we are dealing with low pressures (the vapor pressures of most substances at the triple point are quite low) we may [Pg.200]

A soiid to vapor replaced by Muquid to vapor- We then subtract [Pg.201]

Melting-point data are much more widely available than triple-point data, and for most substances the 1-atm melting-point temperature the triple-point temperature, so it is common to substitute Tmeiting for Tp-ipie point in Eq- H-13, and also to multiply both sides by minus 1, finding [Pg.201]


See other pages where The Elementary Thermodynamics of LSE is mentioned: [Pg.200]    [Pg.201]   


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