Documenti di Didattica
Documenti di Professioni
Documenti di Cultura
, (
V T U U =
V d
V
U
dT
T
U
U d
T V
|
|
.
|
\
|
c
c
+
|
|
.
|
\
|
c
c
=
( )
V
T U
/
c c
For all practical purpose in this text, the term is so small
that the second term on the righthand side of Equation (21.5) can
be neglected. Consequently, changes in the specified intenal energy
over a specified time interval can be computed by integrating
Equation (21.5) as follows:
(21.6)
For an ideal gas U is a function of temperature only. Equation
(21.6) alone is not valid if a phase change occurs during the
processs.
Note that you can only calculate differences in internal energy, or
calculate the internal energy relative to a reference state, but not
absolute values of internal energy.
( )
T
V U
/
c c
} }
= = = A
2
1
2
1
1 2
T
T
v
U
U
dT C U d U U U
The principles of the conservation of energy states that the total
energy of the system plus the surroundings can neither be created
nor destroyed*
*Can mass be converted into energy according to E=mc
2
? It is not
correct to say that E=mc
2
means mass is converted into energy. The
equal sign can mean that two quantities have the same value as in
measurements of two masses in an experiment, or it may mean (as
in general relativity) that the two variables are the same or are
equivalent things. It is in the latter sense that E=mc
2
applies, and
not in terns of converting a rest mass into energy. You might write
E=c
2
m. If m is negative, E is also negative. What this means is
as the inertia mass decreases, E decreases, and the reverse.
The Concept of the Conservation of Energy
Energy Balances for Closed Systems
System energy (U+PE+KE) = E
(E may change with time, AE)
Surroundings may do work
on the system, W
Heat, Q, may enter the
system
Unsteady state Systems
A(U+PE+KE)
inside
= AE = Q + W
Steady state Systems
0 = Q + W
All work done on a closed, steady state system must be transferred out as heat.
However, Heat added to a closed, steady state system Q does not always equal the
work done by the system (-W). (second law of thermodynamics).
Energy Balances for Open Systems
P
1
P
2
AE = ([U
1
+ P
1
V
1
] + E
k1
+ E
p1
) - ([U
2
+ P
2
V
2
] + E
k2
+ E
p2
) + Q - W
s
AE = (H
1
+ E
k1
+ E
p1
) (H
2
+ E
k2
+ E
p2
) + Q - W
s
Unsteady state Systems : AE = 0
Steady state Systems : AE = 0
The accumulation term (E) in the energy balance can be
nonzero because:
1. the mass in the system changes
2. the energy per unit mass in the system changes, and
3. both 1 and 2 occur.
Accumulation term (inside the system)
Type of energy in the system At time t
1
At time t
2
Internal
U
t1
U
t2
Kinetic KE
t1
E
t1
KE
t2
E
t2
Potential PE
t1
PE
t2
Mass of the system m
t1
m
t2
Energy accompanying mass transport (through the system boundary) during the interval
t
1
to t
2
Type of energy Transport in Transport out
Internal U
1
U
2
Kinetic KE
1
KE
2
Potential PE
1
PE
2
Mass of the flow m
1
m
2
Net heat exchange between the system
and the surroundings during the interval
t
1
to t
2
Q
Works terms (exchange with the
surroundings) during the interval t
1
to t
2
W
shaft
Net shaft, mechanical, and electrical work W W
mechanical
W
electrical
Flow work done on the system to introduce
material into the system
Flow work done on the surroundings to remove
material from the system
)
(
1 1 1
V p m
)
(
2 2 2
V p m
TABLE 22.1 Summary of the Symbols to be Used in the General Energy balance
The represent the so-called pV work, pressure
energy, flow work, or flow energy, that is, the
work done by the surroundings to put a mass of
matter into the system at boundary 1, and the work
done by the system on the surroundings as a unit
mass leaves th esystem at boundary 2, respectively.
Because the pressures at the entrance and exit to the
system are deemed to be constant for differential
displacement of mass, the work done per unit mass
by the surroundings on the system adds energy to the
system at boundary 1:
1 1 1 1
0
1 1
) 0
(
1
V p V p V d p W
V
= = =
}
Enthalpy
We will axpress the enthalpy in terms of the temperature and
pressure (a more convenient variable) than the specific volume).
(21.10)
By definition is the heat capacity at constant pressure, and
is given the special symbol Cp. For most practical purposes is
so small at modest pressure that the second term on the righthand
side of Equation (21.10) can be neglected.
However, in processes operating at high pressure, the second term on
the righthand side of Equation (21.10) cannot necessarily be
neglected, but must be evaluated from experimental data.
) , (
p T H H =
dp
p
H
dT
T
H
H d
T p
|
|
.
|
\
|
c
c
+
|
|
.
|
\
|
c
c
=
( )
p
T H c c /
( )
T
p H c c /