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Perfect Gases and Gaseous Mixtures

The activity of a perfect gas, as for any substance, is unitary, by definition, at standard state. Moreover, for a perfect gas, activity is (numerically) equivalent to pressure, at all pressures. Let us consider the relationship existing, with T held constant, between the chemical potential of component i in gaseous phase g at 1 bar (/a, 17 ) and at pressure P [Pg.612]

Because for a pure phase partial molar volume is equivalent to molar volume Vg, and since we have defined as standard state the condition of the pure component at P = 1 bar and T of interest  [Pg.612]

In the more general case of a standard state pressure of reference different from 1, we have [Pg.613]

Interaction forces among gaseous molecules are generally subdivided into [Pg.613]

The first term on the right in the sum of potentials in equation 9.12 is the electrostatic term (represented here as a simple dipole moment). Factor / is the angular function of dipole orientation  [Pg.614]


See other pages where Perfect Gases and Gaseous Mixtures is mentioned: [Pg.612]   


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