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Helmholz free energy

Careri (Ref 7b) suggested a procedure for computing exactly the thermodynamic functions of a nonequilibrium system. The state of the system was then varied, at fixed volume and temperature, so as to give a minimum Helmholz free energy, consistent with such conditions as are imposed to permit the exact computation. The condition under which this method leads to self-consistent equations is discussed in detail. The method is then applied in a way that is very close to the Lennard-Jones and Devonshire cell method, bur with cells of variable size. The distribution within a cell is assumed to be Gaussian. Mayer Careri claimed that the method is easier to apply than the cell method, but it seems to be rather complicated... [Pg.289]

At absolute zero TS vanishes and the Helmholz free energy equals the internal energy. As a consequence, at absolute zero the most stable polymorphic modification should have the lowest internal energy. Above absolute zero the entropy term will... [Pg.31]

INTERNAL ENERGY HELMHOLZ FREE ENERGY HEAT CONTENT GIBBS FREE ENERGY... [Pg.171]

This equation is equivalent to the statement that the surface tension is exactly equal to the Helmholz free energy per unit area. Thus, we may make use of the thermodynamic equilibrium statement that isolated systems tend toward the condition of lowest free energy to show that the stable state of a system is the one with minimum free energy, including the contribution of the surface free energy. [Pg.491]

From the data shown in Fig. 17.2 calculate the surface Helmholz free energy per... [Pg.502]

The second derivative of the four measures of energy, i.e., internal energy, U, enthalpy, H, Gibbs free energy, G, and Helmholz free energy. A, can be obtained with respect to two independent variables from among temperatnre, pressnre, volnme, and entropy. The order of differentiation does not matter as long as the function is analytic. This property is used to derive the Maxwell relations as follows ... [Pg.316]

Obtain an explicit expression for the Helmholz free energy of an ideal gas as a function of T, V and N. [Pg.150]

See Chapter 7 for a brief thermodynamic description of Gibbs and Helmholz free energies. [Pg.341]

The basic formulation follows (5.15)-(5.21), with the presence of damage introduced by incorporating it within the Helmholz free energy j/, namely (Weitsman 1987b)... [Pg.82]

Pratt, L.R. and Chandler, D., 1977, Interaction site cluster series for the Helmholz free energy and variational principle for chemical equilibria and intramolecular structures, J. Chem. Phys., 66 147. [Pg.15]

Helmholz free energy force number of moles of filler... [Pg.395]


See other pages where Helmholz free energy is mentioned: [Pg.2282]    [Pg.68]    [Pg.166]    [Pg.700]    [Pg.2037]    [Pg.33]    [Pg.164]    [Pg.2570]    [Pg.359]    [Pg.2550]    [Pg.701]    [Pg.502]    [Pg.2286]    [Pg.29]    [Pg.78]    [Pg.130]    [Pg.325]   
See also in sourсe #XX -- [ Pg.359 ]




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