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4.1 Objectives
On successful completion of this module you should be able to:
Polytropic processes:
● When the behaviour of closed systems was studied closely, it was observed that, for some
of them, the relationship between pressure and volume followed a trend: PVn = const.
Any process which followed this trend is called a “polytropic process” and the index n is
called the “polytropic constant”.
● If a process is adiabatic and reversible (i.e. isentropic), then the polytropic constant equals
the ratio of specific heats (i.e. n = k). This is the ideal situation. For a general polytropic
process (i.e. n < k), there is heat transfer across the boundary, and so the change in
internal energy is due to the combination of both work and heat transfer. The polytropic
constant is a short-cut method of determining the work in these cases.
● For a particular value of n, the percentage change in P is bigger than the percentage
change in V (by the power n). For a constant change in volume, when the volume is
smaller, then the pressure change is bigger, so it is harder to compress a fluid the more it
is compressed.1
● For higher values of n, more effort is required to change the volume (i.e. the pressure
needs to change by more to achieve the same volume change). This is because more of
the effort is being converted to (useful) work instead of being lost as heat. This means
that when trying to compress a fluid, it is harder but more efficient; when a fluid expands,
it more effectively transfers the energy into work and produces more power.
● There are other processes for which some other model (besides PVn = const) is
appropriate (e.g. constant pressure or constant temperature).
2
wb Pdv
1
The specific formulae for various processes are: Constant pressure (isobaric):
wb P v2 v1
v2
wb P1v1 ln
v1
v2
RT ln
v1
n 1 n
P2 v2 Pv R T2 T1 RT1 P2
wb 1 1
1
1 n 1 n 1 n P1
k 1
R T2 T1 RT1 P2
k
P2 v2 Pv
wb 1 1
1
1 k 1 k 1 k P1
Note
The formulae for boundary work here are slightly different to those for steady-
flow work in Module 7.2.9: be careful to use the correct one.
1
Thanks to Gerard A. for the discussion that resulted in this description
Exercise 4.1
Textbook problem 4.11 (7th Ed.):
Exercise 4.2
Textbook problem 4.10 (7th Ed.):
Exercise 4.3
Textbook problem 4.13 (5th Ed.):
Nitrogen at an initial state of 300 K, 150 kPa, and 0.2 m3 is compressed slowly
in an isothermal process to a final pressure of 800 kPa. Determine the work done
during this process.
Exercise 4.4
Textbook problem 4.14 (7th Ed.):
Exercise 4.5
Textbook problem 4.18 (7th Ed.):
Provides details of the first law as applied to closed systems (where no mass
crosses the boundary).
The major terms are: Heat transfer, Work and Internal energy (enthalpy is not
commonly used).
Exercise 4.6
Textbook problem 4.69 (7th Ed.):
● Answer: 58.2oC
Exercise 4.7
Textbook problem 4.71 (5th Ed.):
Exercise 4.8
Textbook problem 4.91 (7th Ed.):
The constant pressure and constant volume specific heats are important. You
need to remember that cv is used with internal energy and cp is used with
enthalpy. Note that there is only one specific heat for both liquids and solids
because they are incompressible, so you only use cv and cp for gasses.
Specific heats are functions of temperature, so the correct definition of changes in internal
energy or enthalpy involves integration: Eqs. (4-25) and (4-26). This process is normally used
to perform accurate calculations when using computers, where polynomial expressions
similar to Table A-2(c) are implemented. (It is also common when conducting simulations to
know the enthalpy and use numerical methods, such as those learned in ENG3103, to find the
temperature based on polynomial expressions for the specific heat.)
You can see in Table A-2 some values of specific heat as functions of temperature, while
Tables A-17–A-25 list values of internal energy and enthalpy as functions of temperature. For
hand calculations, you can use “representative” (average) values of specific heats, as shown
in Eqs. (4-27) and (4-28). This average can be calculated by taking the average of the specific
heats at the extreme temperatures:
c T1 c T2
cave
2
alternatively, the specific heat at the average temperature returns a similar value.
T T2
cave c 1
2
If the temperature does not vary much from room temperature, then the value at 300K in
Table A-2(a) can be used.
The other important quantity in this section is the ratio of specific heats, represented here
using the symbol k, but also commonly using the symbol . Many ideal gas properties relate
to the value of k, especially isentropic behaviour, which is described in Module 7 and used in
Module 8.
Exercise 4.9
Textbook problem 4.49 (5th Ed.) (parts b and c only):
Exercise 1
Text problem 4.60 (7th Ed.) (parts b and c only):
4.2.5 Internal energy, enthalpy, and specific heats of solids and liquids
Reading activity 1
Section 4.5
As noted previously, because solids and liquids are incompressible, there is only
a single specific heat that describes all changes in energy.
Modules 9 and 10 will use the second point after Eq. (4-37), that the change in
enthalpy in a pump can be calculated based on the change in pressure
(v2 = v1 = v by definition):
h v P2 P1