|
|
(8.1)
|
Here
the slash on the derivative is to remind us that this is not an exact differential.From
conservation of energy, we have
or
|
|
(8.2)
|
So
we see that if ds
= 0, then we get pure work.Similarly,
if dU = tds,
we get pure heat.An immediate consequence
of this is that cyclic processes cannot produce as much energy as was put
into them.To see this, recall that
since work is a form of energy, any form of work can be converted into
mechanical work.Similarly, we can
convert work completely into heat since work does not involve entropy.However,
we cannot convert heat completely into work, since heat enters the system
with a certain amount of entropy, which the work does not take away.Thus
entropy builds up in the process.This
cannot be allowed to continue indefinitely; rather the entropy must eventually
be removed from the system.The only
way to do this is to remove it as heat, but by conservation of energy that
requires us to put in an equal amount of extra heat at the start.
![]() |
(8.3)
|
Now,
recall that the total energy change is zero.This
means that the total work done must equal the difference between the heat
inputted and the heat extracted

or,
dividing by the heat input,
![]() |
(8.4)
|
This
is called the Carnot efficiency (or energy conversion efficiency)
for a reversible process.In a real
situation, the processes going on in a heat engine are not actually reversible,
so the true efficiency is always less than the Carnot efficiency.Notice
that even in the case of a reversible process, we can attain complete conversion
of heat into energy only in the case that
.

we
get
![]() |
(8.5)
|
We
can draw a Carnot engineschematically
as

To
show that the Carnot engine is an ideal engine, "make" the "device"

where
X is our device and C is a Carnot engine.Assume
efficiency hX
> hc.Then
![]()
From
this, we have that Qh' - Qh = Ql'
- Ql which means that we are transferring heat from the
lower to the higher temperature without doing any work, which violates
the second law of thermodynamics.

We
can easily see that the work done by the gas during one cycle is the area
contained within the enclosed region on the p-V diagram. It
should be stressed that it is not meaningful to speak of the heat content
or of the work content of a system. Using
the p-V diagram, we see that when we go around a closed loop in
the p-V diagram, a net amount of work is generated by the system,
and a net amount of heat is consumed by energy conservation. But
after going around the p-V diagram, the system has returned to its
original conditions. This means
that there cannot exist two functions Q(s,V)
and W(s,V)
such that the heat and the work required to take the system from a state
(sa,Va)
to (sb,Vb)
are given by the differences in Q and W. If
such functions existed, the net transfer of heat and work around the loop
would have to be zero, and we have already seen that this is not true. Thus,
the transfer of heat and work between to states depends on the path taken
in transitioning between the two states. This
path dependence is expressed when we denote heat and work transferred as
and
.
What
are the heat and work transferred for various paths? Let's
first consider an isothermal process. In
this case we have that the work done is
![]() |
(8.6)
|
Thus,
for an isothermal process, the Helmholtz function is a more appropriate
choice for the energy function than the system energy U. Also,
since F is a minimum in equilibrium, we see that the effect of work
performed on a system has the effect of increasing the Helmholtz free energy.

where
we have defined a new energy function, the enthalpy, H, as
|
|
(8.7)
|
The
enthalpy plays the same role in isobaric processes as the normal energy
U
does in processes at constant volume. There
are two types of constant pressure processes which are especially important. The
first one are those in which there is no effective work done.In
these processes, the heat transfer,
,
is equal to the change in the enthalpy, dH. An
example of this is the evaporation of a liquid from an open vessel.Thus
the heat of vaporization is just the enthalpy difference between the two
phases. The other processes
are those at constant pressure and temperature.In
this case, the heat transferred is
![]()
and
so

where
G
is another new energy function, called the Gibbs free energy. In
terms of the normal energy, it is defined as
|
|
(8.8)
|
Finally,
what happens if we are transferring particles to the system? Recall
|
|
(8.9)
|
wherem
is defined to be the chemical potential of the system. We
will discuss the chemical potential more later in the semester. The
work done on the system is given

We
call the term mdN
the chemical work.