Week 4 (1) Compressed
Week 4 (1) Compressed
Bath at 100oC
P
(MPa)
C
22
37
4
oC
L
o
M 100 C N
0.1 T=c
onsta
nt
30oC
0.00317
O
0oC
0.0006
A B
v
T (oC)
a
MP
C
22
374
stant
P = con
100 kPa
100
3.17 kPa
30
0.6 kPa
0
A B
v
From the pressure table, Tsat (200 kPa) = 127.4◦ C. Since the given T
(=200◦ C) is greater than this value, the state is superheated.
P P
(kPa) (kPa)
A 1555 A
250 250
T=200oC
T=127.4oC
v
Prof. V. Babu, IIT Madras Engineering Thermodynamics 107 / 395
Pure Substances Properties of two-phase mixtures
Alternatively, from the temperature table, Psat (200◦ C) = 1555 kPa. Since
the given P (=250 kPa) is less than this value, the state is superheated.
P
(kPa)
A 1555 A
250
T=200oC T=200oC
T=127.4oC
v v
Prof. V. Babu, IIT Madras Engineering Thermodynamics 107 / 395
Pure Substances Properties of two-phase mixtures
From the pressure table, Tsat (1000 kPa) = 179.9◦ C. Since the given T
(=140◦ C) is less than this value, the state is compressed/sub-cooled liquid.
P P
(kPa) (kPa)
1000 1000
B B
361.2
T=179.9oC
T=140oC
v
Prof. V. Babu, IIT Madras Engineering Thermodynamics 108 / 395
Pure Substances Properties of two-phase mixtures
1000
B
361.2
T=179.9oC
T=140oC T=140oC
v v
Prof. V. Babu, IIT Madras Engineering Thermodynamics 108 / 395
Pure Substances Properties of two-phase mixtures
T=200◦ C and v=0.1 m3 /kg : From the temperature table, for T=200◦ C,
the specific volume of the saturated liquid state is vf =
0.0011564 m3 /kg and that of the saturated vapor state is vg
= 0.1273 m3 /kg. Since the given value for the specific
volume, 0.1 m3 /kg lies in between these two values, the
state falls in the two phase mixture region.
T=250◦ C and v=0.2 m3 /kg : From the temperature table, for T=250◦ C,
the specific volume of the saturated liquid state is vf =
0.0012515 m3 /kg and that of the saturated vapor state is vg
= 0.0501 m3 /kg. Since the given value for the specific
volume, 0.2 m3 /kg is greater than vg , the state is
superheated.
T=200◦ C and v=0.1 m3 /kg : From the temperature table, for T=200◦ C,
the specific volume of the saturated liquid state is vf =
0.0011564 m3 /kg and that of the saturated vapor state is vg
= 0.1273 m3 /kg. Since the given value for the specific
volume, 0.1 m3 /kg lies in between these two values, the
state falls in the two phase mixture region.
T=250◦ C and v=0.2 m3 /kg : From the temperature table, for T=250◦ C,
the specific volume of the saturated liquid state is vf =
0.0012515 m3 /kg and that of the saturated vapor state is vg
= 0.0501 m3 /kg. Since the given value for the specific
volume, 0.2 m3 /kg is greater than vg , the state is
superheated.
where the subscripts f and g refer to the liquid and vapor phase
respectively and m denotes the mass of the mixture. The specific volume
of the mixture (v) is given as
V
v =
m
mf vf + mg vg
=
m
= (1 − x)vf + xvg
= vf + x(vg − vf )
Any specific property of the mixture (ϕ) in the two phase region may be
written in the same manner as
ϕ = ϕf + x(ϕg − ϕf )
For a liquid (a) specific volume changes very little with pressure as it is
incompressible and (b) internal energy changes very little with pressure.
Consequently, for a compressed/sub-cooled liquid state,
v(T, P ) ≈ vf (T )
u(T, P ) ≈ uf (T )
h(T, P ) ≈ uf (T ) + P vf (T )
It should be noted that the approximation given above for the specific
enthalpy is not equal to hf (T ), since the latter is equal to
uf (T ) + Psat (T ) vf (T ) by definition.
Ideal gases
T
C
Pv
1− < 0.1
RT
Ideal Gas
Ideal gases
1.1
1 2.5
2.0
0.9
1.5 Pv
0.8 1− < 0.1
RT
0.7
Pv / RT
Ideal Gas
0.6
0.5
0.4
0.3 T/Tcritical = 1.0
0.2
0.1
0 1 2 3 4 5 6 7
P/Pcritical
Worked example
Solution
The system for this problem is comprised of the ice and the liquid water.
Since it is not known whether any of the water evaporates, let us
determine the heat required for the final state to be water at 100◦ C. To
this end, we apply first law to the system under consideration to get
0
∆E = ∆U = Q − > ⇒ ∆Uice + ∆U = Q
W liq
where L denotes the latent heat of melting and c denotes the specific heat
capacity. The change in internal energy for the water to go from 20◦ C to
100◦ C is ∆Uliq = mliq cliq (100 − 20).
Prof. V. Babu, IIT Madras Engineering Thermodynamics 119 / 395
First Law Analysis of Systems
Solution (cont’d)
Thus,
Since the heat added is higher than this value by 312 kJ (= 3500-3188),
some amount of water will definitely vaporize. Heat required to vaporize
all of the water at 100◦ C is given as (mice + mliq ) L′ = 15820 kJ, where
L′ denotes the latent heat of vaporization. It is thus clear that the heat
supplied is not sufficient to evaporate all the water. Hence, the final
temperature is 100◦ C and the mass of water evaporated is equal to
312 kJ ÷ L′ = 0.1381 kg.
Worked example
Polytropic process
P n=∞
1
n=0
n=1
1<n<γ
n=γ
V
Polytropic processes for an ideal gas corresponding to various polytropic
indices. Starting from the initial state denoted 1, final states in the second
quadrant are attained as a result of compression and those in the fourth
quadrant are attained after expansion.
Prof. V. Babu, IIT Madras Engineering Thermodynamics 122 / 395
First Law Analysis of Systems
Solution
(a) Taking the air as the system, the work interaction for such a process
may be evaluated as
Z 2
P2 V2 − P1 V1 m R (T2 − T1 )
W = P dV = =
1 1−n 1−n
Here, we have used the fact that P V n = P1 V1n = P1 V2n and also used
the equation of state.
Solution (cont’d)
∆E = ∆U = Q − W ⇒ Q = m Cv (T2 − T1 ) + W
Upon substituting the numerical values, we get Q = -116.06 kJ. The sign
indicates that heat is lost by the system to the surroundings.
Solution
Solution (cont’d)
(c) Taking the air as the system, the work interaction for such a process
may be evaluated as
Z 2
P2 V2 − P1 V1 m R (T2 − T1 )
W = P dV = = = 2.258 kJ [3]
1 1−n 1−n
∆E = ∆U = Q − W [1]
⇒ Q = m Cv (T2 − T1 ) + W [2]
= −565.07 J [2]
Worked example
B A
Solution
Solution (cont’d)
(b) We take the entire vessel to be the system. Applying first law for
process 1-2, we get
0, insulated 0
∆E = ∆U = 7− W1−2 = −
Q > − Wstirrer
Wdisp
Displacement work, Wdisp is also zero since the system boundary does not
deform during the process. Therefore,
Solution (cont’d)
(c) Let the final state be denoted 3. Applying first law for process 2-3, we
get
0 0
∆E = ∆U = Q7−
W>2−3 = 0
⇒ m Cv (T3 − T2 ) = 0
⇒ T3 = T2 = 433 K
For process 2-3, there is no work interaction, since the stirrer is stopped
once the membrane ruptures. The final temperature is 433 K. The final
pressure may be calculated as
mRT3 2 × 288.68 × 433
P3 = = = 333.33 kPa
V3 0.25 + 0.5
Solution
(a) Mass of air in cylinder A is given as
(b) At any instant during the process, a force balance on the piston
assembly gives
(P − Patm ) Ap |A + Mp g = (P − Patm ) Ap |B
Upon substituting the known values into the right hand side, we get P1,B
= 325.45 kPa [3].
Prof. V. Babu, IIT Madras Engineering Thermodynamics 133 / 395
First Law Analysis of Systems
Solution (cont’d)
(c) Mass of air in cylinder B is given as
P1,B V1,B 325.45 × 103 × 0.0398
mB = = = 0.15 kg [1]
RT1,B 288.68 × 300
(d) The work interaction for the atmosphere may be evaluated as
Watm = Patm (∆Vatm,A + ∆Vatm,B )
Given that the piston assembly moves down by 2 m, ∆Vatm,A = −2 × Ap,A
and ∆Vatm,B = 2 × Ap,B . Therefore, Watm = -786 J [2].
(f) At any instant, considering the air in cylinder B as the system, we may
write,
0, insulated
dE = dU = δ Q − δW = −P dV
7
Prof. V. Babu, IIT Madras Engineering Thermodynamics 134 / 395
First Law Analysis of Systems
Solution (cont’d)
This expression may be written as
m Cv dT = −m P dv
RT
Cv dT = − dv
v
dT dv
= −(γ − 1)
T v
Upon integrating, we get T v γ−1 = constant. This is the equation that
describes the adiabatic, fully resisted process undergone by the air in
cylinder B. The final pressure in B may now be calculated using
V1,B γ
P2,B = P1,B
V2,B
Solution (cont’d)
(g) Final temperature in B is given as
P2,B V2,B 442.84 × 103 × 0.03194
T2,B = = = 327 K [2]
mB R 0.15 × 288.68
(h) If we apply first law to the air in cylinder B, we get
0, insulated
∆E = ∆U = 7− W ⇒ WB = −mB Cv (T2,B − T1,B )
Q
Therefore, WB = -(0.15)(721.7)(327-300) = -2923 J [3].
(i) From the expression given in part (b) for the force balance on the
piston assembly, we may write
Ap,B Ap,B Mp g
P2,A = Patm 1 − + P2,B −
Ap,A Ap,A Ap,A
Hence, the final pressure in A, P2,A = 258.7 kPa [2].
Prof. V. Babu, IIT Madras Engineering Thermodynamics 136 / 395
First Law Analysis of Systems
Solution (cont’d)
(j) Final volume of the air in cylinder A, V2,A = V1,A + 2 Ap,A = 0.10212
m3 . Final temperature in A may now be calculated as
∆E = ∆U = Q−W
⇒ QA = ∆UA + WA [1]
= ∆UA − (WB + Wpiston + Watm ) [1]
= mA Cv (T2,A − T1,A ) − (WB + Wpiston + Watm ) [1]
Worked example
Solution
For N2 , M = 28 kg/kmol and γ = 7/5. Therefore, R = 8314÷28 =
296.93 J/kg.K and Cv = R ÷ (γ − 1) = 742.32 J/kg.K.
The mass of air and N2 may be determined from the respective equations
of state using the given information. Since the partition in the middle is
perfectly thermally conducting, the air and N2 are always in thermal
equilibrium. Thus
and
P1 V 1 1000 × 103 × 0.015
mN2 = = = 0.107 kg
RT1 N2 296.93 × 473
N2 undergoes a constant volume process. Since the final pressure is
known, the final temperature may be evaluated from
Prof. V. Babu, IIT Madras Engineering Thermodynamics 139 / 395
First Law Analysis of Systems
Solution (cont’d)
The work interaction for air is -5479.61 J, since the work interaction for
N2 is zero.
Prof. V. Babu, IIT Madras Engineering Thermodynamics 140 / 395
First Law Analysis of Systems
Solution (cont’d)
If we apply first law to a system that contains the air alone, we get
∆Eair = ∆Uair = Qair − Wair
mair Cv,air (T2 − T1 ) = Qair − Wair
Note that the Q that appears in this expression is the heat interaction
between the air and N2 across the thermally conducting partition. Hence
Qair = Wair + mair Cv,air (T2 − T1 ) = −3653.71 J
Alternatively, if we apply first law to a system that contains the N2 alone,
we get
0, V = const
∆EN2 = ∆UN2 = QN2 − W *
N2
⇒ mN2 Cv,N2 (T2 − T1 ) = QN2
⇒ QN2 = (0.107)(742.32)(519 − 473) = 3653.71 kJ
Since, Qair = −QN2 , we get the same value for Qair as before.
Prof. V. Babu, IIT Madras Engineering Thermodynamics 141 / 395
First Law Analysis of Systems
Worked example
Solution
(a) A system appropriate for this problem was shown before. If we apply
first law to this system at an intermediate instant, we get
0
dE = dU = δ7− δW = −P dV
Q
where we have set δQ = 0, since the system and the surrounding air are
always at the same temperature and the vessel is insulated. This
expression may be written as
m Cv dT = −m P dv
RT
Cv dT = − dv
v
dT dv
= −(γ − 1)
T v
Upon integrating, we get T v γ−1 = constant.
Prof. V. Babu, IIT Madras Engineering Thermodynamics 143 / 395
First Law Analysis of Systems
Solution (cont’d)
Note that the mass of the system itself is not required for this analysis.
Worked example
Consider the frictionless piston-cylinder arrangement
shown in the figure in which the piston is spring
loaded. The top surface of the piston is exposed to the
atmosphere at 100 kPa. Initially, the cylinder contains
a certain quantity of N2 at 200 kPa, 27◦ C and
occupies 0.1 m3 . At this position, the spring just
touches the piston but does not exert any force. The
cross-sectional area of the frictionless piston is 0.05 m2 N2
and the spring constant is 15000 N/m. The valve is
800 kPa, 27oC
now opened and the N2 from the line at 800 kPa,
27◦ C flows into the cylinder until the pressure inside
the cylinder reaches the line pressure at which point,
the valve is closed. Determine (a) the mass of N2
initially present in the cylinder, (b) the final volume
occupied by N2 (c) the amount of N2 that enters the
cylinder and (d) the final temperature of N2 .
Prof. V. Babu, IIT Madras Engineering Thermodynamics 145 / 395
First Law Analysis of Systems
Solution
N2 N2
800 kPa, 27oC
Initial Final
Solution (cont’d)
The mass of N2 initially in the cylinder may be evaluated as
A2p
V2 = V1 + (800 − 200) × 103 × = 0.2 m3
k
Solution (cont’d)
The thermodynamic system appropriate for this problem is shown in the
figure using a dashed line. With respect to this system, let the mass of N2
initially in the line be mline kg. This is also the mass that enters the
cylinder. At the final state,
Solution (cont’d)
Z 2
W = Pline (0 − V1,line ) + P dV
1
Z 2
k
= −mline R Tline + 200 × 103 + 2 (V − V1 ) dV
1 Ap
15000 0.12 − 0
= −mline R Tline + 200 × 103 × (0.2 − 0.1) +
0.052 2
= −R Tline mline + 50000
Therefore,
m1 Cv (T2 − T1 ) + mline Cv (T2 − Tline ) = −50000 + R Tline mline
This may be rearranged to give
m1 Cv T2 + mline Cv [T2 − Tline − (γ − 1) Tline ] = m1 Cv T1 − 50000
Prof. V. Babu, IIT Madras Engineering Thermodynamics 149 / 395
First Law Analysis of Systems
Solution (cont’d)
Or
1
R T2 (m1 + mline ) −γ mline Cv Tline = m1 Cv T1 − 50000
γ−1 | {z }
=P2 V2
P2 V2
γ mline Cv Tline = −m1 Cv T1 + 50000 +
γ−1
Upon substituting the known values, we get mline = 1.283 kg. From Eqn.
(1), we may get T2 = 357 K.
Worked example
Air contains 79% nitrogen and 21% oxygen by volume. A rigid vessel
initially contains 0.01 m3 of air and 0.001 m3 of methane at 101325 Pa
and 25◦ C.
(a) Calculate the masses of nitrogen, oxygen and methane present in this
mixture.
(b) What is the mixture molecular weight after the addition of hydrogen?
Solution
Solution (cont’d)
1
M W mix = 0.673 0.204 0.049 0.074 = 14.19 kg/kmol
28 + 32 + 16 + 2
Worked example
A 17.3 liter tank contains a mixture of argon, helium and nitrogen at 298
K. The argon and helium mole fractions are 0.12 and 0.35 respectively. If
the partial pressure of the nitrogen is 0.8 atm, determine the pressure, the
total number of moles and the mass of the mixture in the tank. Also,
determine the amount of heat required to raise the temperature of the
mixture to 500 K.
Solution
Since yAr = 0.12 and yHe = 0.35, we can calculate yN2 to be 1 - yAr -
yHe = 0.53.
PN2
PN2 = yN2 P ⇒ P = = 1.509 atm
yN2
PV
PV = nRT ⇒ n= = 1.0676 moles
RT
Solution (cont’d)
!
1 1 1
C̄v,mix = R 0.12 5 + 0.35 5 + 0.53 7
3 −1 3 −1 5 −1
J
= 16.877
mol.K
Worked example
Worked example
A saturated mixture of R134a initially at 100 kPa is contained in a rigid
vessel of volume 0.02 m3 . The mixture is heated until it attains the critical
state. Determine the mass of the mixture and the heat transferred.
P
(kPa)
2
1
100
0.0019685 v (m3/kg)
Solution
The mixture undergoes a constant volume process. Since the final state is
the critical state, the property values are known. From the pressure table,
we can retrieve v2 = 0.00197 m3 /kg and u2 = 233.9 kJ/kg.
Here, we have set W = 0 since the vessel is rigid and hence the
displacement work is zero.
Solution (cont’d)
Thus,
Q = ∆U = m (u2 − u1 )
The initial state is a saturated mixture at 100 kPa and we may retrieve the
following property values from the pressure table: vf = 0.726 × 10−3
m3 /kg, vg = 0.19255 m3 /kg, uf = 17.19 kJ/kg and ug = 215.21 kJ/kg.
The dryness fraction at the initial state, x1 , can now be evaluated.
v1 − vf
x1 = = 0.0065
vg − vf
2 1
25 oC
0.0103 v (m3/kg)
Prof. V. Babu, IIT Madras Engineering Thermodynamics 160 / 395
First Law Analysis of Systems
Solution
Solution (cont’d)
The dryness fraction at the final state may be evaluated as
v2 − vf
x2 = = 0.3148
vg − vf
Since the pressure remains constant during the process, the displacement
work may be calculated as
Solution (cont’d)
∆E = ∆U = Q − W
⇒ Q = ∆U + W = m(u2 − u1 ) + W
Worked example
Worked example
A frictionless piston-cylinder device contains 2.6 kg of saturated R134a
mixture initially at 500 kPa and occupying 0.1 m3 . The mixture expands
according to the relation P V = constant until it becomes a saturated
vapor. Determine the final pressure, work done and heat transferred.
P
(kPa)
1
500
0.0385 v (m3/kg)
Solution
where uf = 72.92 kJ/kg and ug = 238.77 kJ/kg, from the pressure table.
Solution (cont’d)
The specific volume at the final state is then v2 = 0.19255 m3 /kg and the
specific internal energy is u2 = 215.21 kJ/kg.
Solution (cont’d)
∆E = ∆U = Q − W ⇒ Q = m(u2 − u1 ) + W
Worked example
Worked example
A vertical frictionless piston-cylinder arrangement contains 2 kg of water
initially at 1 bar. The piston initially rests on stops and will move when
the pressure reaches 3 bar. The enclosed volume when the piston is on the
stops is 250 L. An amount of heat equal to 4500 kJ is now transferred to
the water. Determine the final state and the work done.
P
(kPa)
2 3
300
100
1
0.125 v (m3/kg)
Q
Prof. V. Babu, IIT Madras Engineering Thermodynamics 168 / 395
First Law Analysis of Systems
Solution
The specific volume at the initial state, v1 = V1 ÷ m = 0.125 m3 /kg.
From the pressure table, corresponding to 1 bar, we can retrieve,
vf = 1.0431 × 10−3 m3 /kg and vg = 1.6958 m3 /kg, uf = 417.3 kJ/kg
and ug = 2505.5 kJ/kg. Since vf < v1 < vg , the water is initially a
saturated mixture.
Solution (cont’d)
0
∆E = ∆U = Q1−2 −
W
>1−2
⇒ Q1−2 = m (u2 − u1 )
where the displacement work has been set to zero since the pressure
increase occurs at a constant volume. Hence, at state 2, P = 3 bar and v
= 0.125 m3 /kg. From the pressure table, corresponding to 3 bar, we can
retrieve, vf = 1.0731 × 10−3 m3 /kg and vg = 0.6063 m3 /kg, uf = 561.19
kJ/kg and ug = 2543.4 kJ/kg. Since vf < v2 < vg , state 2 is also a
saturated mixture state.
Solution (cont’d)
Therefore, Q1−2 = 794.238 kJ. It thus becomes clear that the remainder,
namely, 4500-794.2384 = 3705.762 kJ of heat is further added to the
system. Note that the pressure remains constant during this process (2-3),
since the pressure is entirely due to atmospheric pressure and the weight of
the piston, both of which do not change during the process.
∆E = ∆U = Q2−3 − W2−3
m (u3 − u2 ) = Q2−3 − m P2 (v3 − v2 )
Solution (cont’d)
Determine
(a) the initial pressure in compartment B
(b) the dryness fraction of the mixture initially in compartment B
(c) the mass contained in compartment A and
(d) the final pressure and temperature.
(e) Calculate the heat transferred.
Solution
Solution (cont’d)
(b) The initial dryness fraction may be calculated as
v1,B − vf
x1,B = = 0.513 [2]
vg − vf
Solution (cont’d)
Further, it is given that the final pressure is the same in both the
compartments. Hence, P2,A = P2,B = 10.02 bar.
1,B 2
180 o
C
500
1,A
0.1 v (m3/kg)
Solution (cont’d)
The final pressure and specific volume in compartment A are known and
hence the final state in compartment A is known. From the superheated
table, it can be determined that the final state in A is superheated. The
final temperature in compartment A, T2,A = 607◦ C [1], from the
superheated table.
Solution (cont’d)
Solution (cont’d)
The specific internal energy at the final state is, u2,B = u2,A = 3309.8
kJ/kg [1]. Hence, ∆U = 3576.87 kJ [1]. Therefore, heat transferred,
Q = ∆U + W = 4187.088 kJ [1].
Worked example
Solution
(a) The appropriate system for this problem was shown before. If we apply
first law to this system, we get
0
∆E = ∆U = 7− W
Q
m(u2 − u1 ) = −Pline (V2 − V1 )line
= −Pline mline (0 − vline )
Here, m is the mass in the system and for the system under consideration,
m = mline . Also u1 = uline . Therefore,
Solution (cont’d)