Title: The Second Law: Machinery
1Chapter 5
2Internal Energy
U is a function of S and V
Purely thermodynamic definition of temperature
Generate relations between the properties of a
system and discover the power of thermodynamics
for establishing unexpected relationships.
3Maxwell Relations
4Gibbs Energy
5- Gibbs energy varies with temperature and
pressure. - As S gt 0, G decreases when the T is raised at
constant p and composition. - G decreases most sharply when the entropy of the
system is large - Therefore, the Gibbs energy of the gaseous phase
of a substance, which has a high molar entropy,
is more sensitive to temperature than its liquid
and solid phases. - V gt 0, G always increases when the pressure is
increased at constant T and composition. - As the molar volumes of gases are large, G is
more sensitive to pressure for the gas phase than
others.
6T dependence of G
- If the enthalpy of the system is know, then the
temperature dependence of G/T is known. - The equilibrium constant of a reaction is related
to G/T.
This equation is most useful when applied to
changes DG Gf - Gi
7p dependence of G
The Gibbs energy of solids and liquids are
supposed to be independent of pressure.
If we set pip
8Chemical Potential
For real gases, the true pressure, p, is replaced
by an effective pressure called fugacity,f.
9Fugacity and Pressure
Hypothetical kinetic energy only gas
Entire effect of all the intermolecular forces
All gases are perfect as p 0, so f p
as p 0, then f 1 as p 0
10- For most gases Z lt 1 up to moderate p and Z gt 1
for higher p. - If Z lt 1 throughout the integration, then f lt 1.
- This means f lt p, the molecules tend to stick
together. - Chemical potential of the gas is less than that
of a perfect gas. - At higher p, Z gt 1, f gt 1 and f gt p, repulsive
interactions are dominant and tend to drive the
particles apart. - Chemical potential of the gas is greater than
that of a perfect gas at the same T. - The fugacity of nitrogen at 273 K.