For each process described below provide the temperature,
pressure, and specific volume at each state and the change in
enthalpy, internal energy, and entropy.
1. Water as saturated vapor at 65 psia goes isentropically to 25 psia.
Solution:
| State 1 | State 2 |
| T1 = 298F | T2 = 240F |
| P1 = 65 psia | P2 = 25 psia |
| v1 = 6.657 ft3/lbm | v2 = 15.33 ft3/lbm |
| h1 = 1179.6 Btu/lbm | h2 = 1104 Btu/lbm |
| u1 = 1099.5 Btu/lbm | u2 = 1033 Btu/lbm |
| s1 = 1.638 Btu/(lbmR) | s2 = 1.638 Btu/(lbmR) |
| phase: sat.vap. | phase: two phase
x2 = 0.94 |
At state 1 we know the pressure and that the substance is a saturated
vapor. This is sufficient information to fix the state. Then we
can go to Table A-5E and read the remaining properties for saturated
vapor at 65 psia. At state 2 we know the pressure, but we also
that we have an isentropic process, so that
s2 = s1 = 1.638 Btu/(lbmR)
So with the pressure and entropy known at State 2, it is fixed.
Next, we must determine the phase. We again go to Table A-5E and
find that at 25 psia
sf = 0.353 Btu/(lbmR) and sg = 1.714 Btu/(lbmR)
Since s2 lies between these values, so that we have
a two phase mixture with
Our temperature must be the saturation temperature at 25 psia
or 240F. With the quality known, we can determine our other properties
at state 2
Our changes are then given as
2. Air at 14 psia and 75F goes isotropically to 150F.
Solution:
| State 1 | State 2 |
| T1 = 75F = 535 R | T2 = 150F = 610 R |
| P1 = 14 psia | P2 = 15.96 psia |
| v1 = 14.14 ft3/lbm | v2 = 14.14 ft3/lbm |
| h1 = 127.7 Btu/lbm | h2 = 145.9 Btu/lbm |
| u1 = 91.2 Btu/lbm | u2 = 104.1 Btu/lbm |
| f1 = 0.599 Btu/(lbmR) | f2 = 0.630 Btu/(lbmR) |
For state 1 we know T and P, so the state is fixed. Using the
ideal gas equation
Then from the air tables, Table A-17E
At state 2, we know the temperature and that the process was isotropic,
then
which fixes our state. Then using the ideal gas law we solve for
the pressure
Then from the air tables, Table A-17E
Our changes are then given as
3. Helium at 200 kPa and 300 K goes isothermally to 100 kPa.
Solution:
| State 1 | State 2 |
| T1 = 300 K | T2 = 300 K |
| P1 = 200kPa | P2 = 100 kPa |
| v1 = 3.12 m3/kg | v2 = 6.24 m3/kg |
For state 1we know T and P, so the state is fixed. Using the ideal
gas equation
At state 2, we know the pressure and that the process was isothermal,
then
which fixes our state. Then using the ideal gas law we solve for
the specific volume
We note that since we have an ideal gas and an isothermal process,
our changes in enthalpy and internal energy will be zero. To calculate
our change in s we need the specific heat at constant pressure
which we take from Table A-2(a) as 5.198 kJ/(kgK). Then our changes
are then given as
4. Steam at 600C and 6 MPa goes isenthalpically to .01 MPa.
Solution:
| State 1 | State 2 |
| T1 = 600C | T2 = 240F |
| P1 = 6 MPa | P2 = 0.01 MPa = 10 kPa |
| v1 = 0.06525 m3/kg | v2 = 39.28 m3/kg |
| h1 = 3658 kJ/kg | h2 = 3658 kJ/kg |
| u1 = 3267 kJ/kg | u2 = 3265kJ/kg |
| s1 = 7.17 kJ/(kgK) | s2 = 10.11 kJ/(kgK) |
| phase: sup.vap. | phase: sup.vap. |
At state 1 we know the pressure and the temperature. This is sufficient
information to fix the state. To determine the fluid phase we
go to the saturation pressure table, Table A-5, and find the boiling
temperature at 6 MPa to be 275.64C which is less than 600C, so
that we have superheated vapor. We can then go to the superheat
vapor table, Table A-6, and read the remaining properties for
at 6 MPa and 600C.
At state 2 we know the pressure, but we also that we have an isenthalpic
process, so that
So with the pressure and enthalpy known at State 2, it is fixed.
Next, we must determine the phase. We again go to Table A-5 and
find that at 10 kPa
Since we must have a superheated vapor.
We go to the superheat vapor table, Table A-6, and find that at
10 kPa and h of 3658, we interpolate to obtain
Our changes are then given by
5. Air at 1.6 MPa and 500 K goes isobarically to 200 K.
Solution:
| State 1 | State 2 |
| T1 = 500K | T2 = 200 K |
| P1 = 1.6 MPa = 1600 kPa | P2 = 1600 kPa |
| v1 = 0.0897 m3/kg | v2 = 0.0359 m3/kg |
| h1 = 503 kJ/kg | h2 = 200 kJ/kg |
| u1 = 359.5 kJ/kg | u2 = 142.6 kJ/kg |
| f1 = 2.22 kJ/(kgK) | f2 = 1.30 kJ/(kgK) |
For state 1we know T and P, so the state is fixed. Using the ideal
gas equation
Then from the air tables, Table A-17
At state 2, we know the temperature and that the process was isobaric,
then
which fixes our state. Then using the ideal gas law we solve for
the specific volume
Then from the air tables, Table A-17
Our changes are then given as
6. Water at 10 psia and 190F goes isentropically to 100 psia.
Solution:
We note that at 10 psia the boiling temperature for water is 193.2F.
So we have a subcooled liquid. We also note that our compressed
liquid tables for water start at 500 psia. We will treat water
under these conditions as an incompressible substance.
| State 1 | State 2 |
| T1 = 190F | T2 = 190F |
| P1 = 10 psia | P2 = 100 psia |
| v1 = 0.0166 ft3/lbm | v2 = 0.0166 ft3/lbm |
For state 1 both T and P are given so the state is fixed. To obtain
a specific volume, we note that since specific volume only depends
on temperature for an incompressible liquid, we can read it from
the steam tables for saturated liquid at the given temperature.
Then from Table A-4E, we have
At state 2, we know the pressure and recall that for an isentropic
process for an incompressible liquid
Then looking up the specific volume
Finally we calculate our changes with
7. Refrigerant-134a at -25°C and 200 kPa goes isobarically to 10°C.
Solution:
| State 1 | State 2 |
| T1 = -25C | T2 = 10C |
| P1 = 200 kPa | P2 = 200 kPa |
| v1 = 0.0007281 m3/kg | v2 = 0.12207 m3/kg |
| h1 = 18.13 kJ/kg | h2 = 249.41 kJ/kg |
| u1 = 18.03 kJ/kg | u2 = 237.44 kJ/kg |
| s1 = 0.0749 kJ/(kgK) | s2 = 0.9998 kJ/(kgK) |
| phase: sub.liq. | phase: sup.vap. |
At state 1 we know the pressure and the temperature. This is sufficient information to fix the state. To determine the fluid phase we will go to the saturation pressure table for refrigerant-134a, Table A-12, and find a boiling temperature of -10.09C. Since this is greater than our given temperature (-25C) we must have a subcooled liquid. We go to the compressed liquid table and find that it does not exist. We will have to treat state 1 as an incompressible substance, but because of state 2 , we may still need to use compressible substance tables.
To begin in treating state 1 as a incompressible liquid, we note that none of v, s, or u depend on pressure, so that there values should be equal to those of saturated liquid at
-25C. Interpolating from Table A-11
To determine the enthalpy which does have a pressure dependence,
we consider a hypothetical process from saturation conditions
to the compressed conditions, then
At state 2 we know the temperature, but we also that we have an
isobaric process, so that
So with the pressure and temperature known at State 2, it is fixed.
Next, we must determine the phase. We again go to Table A-12 and
find that at 200 kPa the boiling temperature is -10.09C, which
means now we have superheated vapor. The remaining properties
are read from Table A-13
Our changes are then given by
8. Carbon dioxide at 2000°F and 1500 psia goes to 600F and 300 psia.
Solution:
| State 1 | State 2 |
| T1 = 2000F = 2460 R | T2 = 600F = 1060 R |
| P1 = 1500 psia | P2 =300 psia |
| v1 = 0.40 ft3/lbm | v2 = 0.862 ft3/lbm |
| h1 = 619 Btu/lbm | h2 = 212.5 Btu/lbm |
| u1 = 508 Btu/lbm | u2 = 164.7 Btu/lbm |
| f1 = 1.56 Btu/lbmR | f2 = 1.32 Btu/lbmR |
For state 1we know T and P, so the state is fixed. Using the ideal
gas equation
Our remaining properties can be read from the ideal gas tables,
Table A-20E.
At state 2, we know the pressure and the temperature which fixes
our state. Then using the ideal gas law we solve for the specific
volume
Our remaining properties can be read from the ideal gas tables,
Table A-20E.
Our changes are then given as
9. Refrigerant-134a goes from vapor to liquid at 70F.
Solution:
| State 1 | State 2 |
| T1 = 70°F | T2 = 70°F |
| P1 = 85.788 psia | P2 = 85.788 psia |
| v1 = 0.5538 ft3/lbm | v2 = 0.01311 ft3/lbm |
| h1 = 111.33 Btu/lbm | h2 = 33.89 Btu/lbm |
| u1 = 102.54 Btu/lbm | u2 = 33.68 Btu/lbm |
| s1 = 0.2173 Btu/(lbmR) | s2 = 0.0711 Btu/(lbmR) |
| phase: sat.vap. | phase: sat.liq. |
At state 1 we know the temperature and will assume we have saturated vapor. This is sufficient information to fix the state. We can then go to the saturation table,
Table A-11E and read the remaining properties for at 70F.
At state 2 we know the temperature and will assume we have saturated liquid. This is sufficient information to fix the state. We can then go to the saturation table,
Table A-11E and read the remaining properties for at 70F.
Our changes are then given by
10. A 1 m3 volume contains 0.2 kg of air at 250 K. Without changing the volume the pressure becomes 32 psia.
Solution:
| State 1 | State 2 |
| T1 = 250 K | T2 = 3833 K |
| P1 = 14.35 kPa | P2 = 32 psia = 220 kPa |
| v1 = 5.0 m3/kg | v2 = 5.0 m3/kg |
| h1 = 250 kJ/kg | h2 = |
| u1 = 178.3 kJ/kg | u2 = |
| f1 = 1.52 kJ/(kgK) | f2 = |
For state 1we know T and with the volume and mass information
we can calculate the specific volume
so the state is fixed. Using the ideal gas equation
Then from the air tables, Table A-17
At state 2, we know the temperature and that the process was isotropic,
then
which fixes our state. Then using the ideal gas law we solve for
the temperature
We go to the air tables, Table A-17, to look up the remaining
properties and note that our temperature is too high for the table.
Hence, we will need to use our constant specific heat approach.
Our average temperature is 2041 K, which is also off the table.
Let's just use the cP at the highest temperature or
1.2161 kJ/(kg K)
Our changes are then given as