Assignment FINAL
Assignment FINAL
Subject:
Chemical Engineering Thermodynamics-I
Topic:
Numerical Problems related to
Submitted To:
Prof.Dr.Mahmood Saleem
Submitted By:
Hamza Shafiq
Roll #:
CE-M10-41
Date of Issue:
10th Week (Wednesday)
Date of Submission:
Nozzles, Throttling, Expanders/Turbine,
Compressors/Pumps
Numerical 1:
Steam expands adiabatically in a nozzle from inlet conditions of 130(psia), 420 ℉ and a
velocity of 230(ft)( s−1 ¿ to a discharge pressure of 35(psia) where its velocity is 2,000(ft)( s−1 ¿.
What is the state of steam at the nozzle exit and what is SG for the process?
Solution:
u1=230 ft s−1
u2=2,000 ft s−1
P1=130 psia
P2=35 psia
T 1=420 ℉
H 1=1233.6 Btu/ lb
Btu
S1=1.6310
lb . R
As we know that
∆ u2
∆ H=
2
Therefore,
∆ H =(u¿¿ 22 −u21)/2 ¿
Thus,
Btu
∆ H =78.8
lb
As we know that
∆ H =H 2−H 1
Therefore,
H 2=∆ H + H 1
Btu
H 2=1154.8
lb
Btu
H liq =228.03
lb
Btu
H vap =1167.1
lb
Btu
Sliq =0.3809
lb . R
Btu
Svap =1.6872
lb . R
As we know that
Also
H 2−H vap
x=
H vap−H liq
x=0.987
Btu
S2=1.67
lb . R
For S g,
S g=1.67−1.631
Btu
S g=0.039
lb . R
Numerical 2:
Solution:
a)
P2=1.2 ¯¿
T 1=350 K
P1=80 ¯¿
T c =304.2 K
Pc =73.83 ¯
¿
ω=0.224
A=5.457
B=1.045 x 10−3
C=0
D=−1.157 x 105
T r=1.151
Pr =1.084
Ω=0.08664
ψ=0.42748
As we know that
Pr
β=Ω.
Tr
β=0.08159
Ψ
q=( )
Ω. T 1.5
r
q=3.9956
Guess z=1;
z−β
z=1+ β−qβ
z (z + β )
z=0.8047
For i=1
z+β
I i=ln ( )
z
I =2.3853
As we know that
H r =R .T 1 [ ( z−1 ) −1.5 qI ]
H r =−42169.92 kJ /mol
Also
Sr =R [ ln ( z ) −0.5 qI ]
9826 kJ
Sr =4.
mol . K
The most convenient way will be by guess the final downstream temperature initially and then
calculating it.
Assume, T 2=280 K
Z=0.721
H r =−2.681 kJ /mol
And
−5.177 kJ
Sr =
mol . K
As we know that
Hr
T 2= +T 1
Cp
T 2=349.39 K
And
P2
Δ S=C p ln (T ¿ ¿ 2/T 1)−Rln −S r ¿
P1
Therefore
Δ S=31.549 kJ /mol
b)
P2=1.2 ¯¿
T 1=350 K
P1=60 ¯¿
T c =282.3 K
Pc =50.40 ¯¿
ω=0.087
A=1.424
B=14.394 x 10−3
C=−4.392 x 10−3
D=0
T r=1.24
Pr =1.19
Ω=0.08664
ψ=0.42748
As we know that
Pr
β=Ω.
Tr
β=0.083
Ψ
q=( )
Ω. T 1.5
r
q=42.06
Guess z=1;
z−β
z=1+ β−qβ
z (z + β )
z=−1.872
For i=1
z+β
I i=ln ( )
z
I =3.070
As we know that
H r =R .T 1 [ ( z−1 ) −1.5 qI ]
H r =46134.7 kJ /mol
Also
Sr =R [ ln ( z ) −0.5 qI ]
kJ
Sr =−531.57
mol . K
The most convenient way will be by guess the final downstream temperature initially and then
calculating it.
Assume, T 2=302 K
Z=0.773
H r =−2.253 kJ /mol
And
kJ
Sr =−4.346
mol . K
As we know that
Hr
T 2= +T 1
Cp
T 2=302 K
And
P2
Δ S=C p ln (T ¿ ¿ 2/T 1)−Rln −S r ¿
P1
Therefore
Δ S=30 kJ /mol
c)
P2=1.2 ¯¿
T 1=250 K
P1=60 ¯¿
T c =162.2 K
Pc =34 ¯¿
ω=0.038
A=3.820
B=0.593 x 10−3
C=0
D=0.040 x 105
T r=1.981
Pr =1.765
Ω=0.08664
ψ=0.42748
As we know that
Pr
β=Ω.
Tr
β=0.077
Ψ
q=( )
Ω. T 1.5
r
q=1.7695
Guess z=1;
z−β
z=1+ β−qβ
z (z + β )
z=0.960
For i=1
z+β
I i=ln ( )
z
I =0.077
As we know that
H r =R .T 1 [ ( z−1 ) −1.5 qI ]
H r =−507.95 kJ /mol
Also
Sr =R [ ln ( z )−0.5 qI ]
Sr =−0.2255 kJ /molK
The most convenient way will be by guess the final downstream temperature initially and then
calculating it.
Assume, T 2=232 K
Z=0.956
H r =−0.521 kJ /mol
And
kJ
Sr =−1.396
mol . K
As we know that
Hr
T 2= +T 1
Cp
T 2=232.0 K
And
P2
Δ S=C p ln (T ¿ ¿ 2/T 1)−Rln −S r ¿
P1
Therefore
Δ S=32 kJ /mol
d)
P2=1.2 ¯¿
T 1=400 K
P1=20 ¯¿
T c =369.8 K
Pc =42.28 ¯¿
ω=0.152
A=1.213
B=28.785 x 10−3
C=−8.824 x 10−6
D=0
T r=1.081
Pr =0.471
Ω=0.08664
ψ=0.42748
As we know that
Pr
β=Ω.
Tr
β=0.0377
Ψ
q=( )
Ω. T 1.5
r
q=4.3899
Guess z=1;
z−β
z=1+ β−qβ
z (z + β )
z=0.88422
For i=1
z+β
I i=ln ( )
z
I =3.96
As we know that
H r =R .T 1 [ ( z−1 ) −1.5 qI ]
H r =871.03 kJ /mol
Also
Sr =R [ ln ( z ) −0.5 qI ]
kJ
Sr =−8.859
mol . K
The most convenient way will be by guess the final downstream temperature initially and then
calculating it.
Assume, T 2=380 K
H r =−1.39 kJ /mol
And
kJ
Sr =−2.33
mol . K
As we know that
Hr
T 2= +T 1
Cp
T 2=385.1 K
And
P2
Δ S=C p ln (T ¿ ¿ 2/T 1)−Rln −S r ¿
P1
Therefore
Δ S=22.163 kJ /mol
Numerical 3:
For a pressure-explicit equation of state, prove that the Joule/Thompson inversion curve is
the locus of states for which:
∂Z ∂Z
T( ) = p( )
∂T p ∂P T
Apply this equation to (a) the van der Waals equation; (b) the Redlich/Kwong equation.
∂Z
We know that the Joule Thompson inversion curve is locus of states for which ( ) =0 .
∂T ρ
∂x ∂ x ∂w
(∂ x /∂ y) z=( ) +( ) ( )
∂ y w ∂w y ∂ y z
∂Z ∂Z ∂Z ∂ρ
( ) =( ) +( ) ( )
∂ T P ∂T ρ ∂ ρ T ∂ T P
Therefore it become
∂Z ∂Z ∂Z ∂ρ
( ) =( ) +( ) ( )
∂ T ρ ∂T P ∂ ρ T ∂ T P
We know that
PV =ZRT
P=ZRT / V
P= ρZRT
Because ρ=1/V
Thus
P
ρ=
ZRT
∂ρ R −1 ∂Z
( ) = {
∂ T P T ( ZT ) 2 ( ( ))
Z +T
∂T P
}
∂ρ R
( ) = ¿
∂T P T
∂Z
Taking ( ) =0 , the preceding equations became
∂T ρ
∂Z ∂Z ∂ρ
( ) =−( ) ( )
∂T ρ ∂ ρ T ∂T P
And
∂ρ −P − ρ
( ) = =
∂ T P ZR T 2 T
∂Z −ρ ∂ Z
( )= ( )
∂T ρ T ∂ ρ T
Thus
∂Z ∂Z
T( ) =−ρ( )
∂T ρ ∂ρ T
a)
V a
P= −
V −b V 2
PV V a
= −
RT V −b VRT
1 aρ
Z= −
1−bρ RT
Then
1
Z= −qξ
1−ξ
On differentiating it
∂Z ∂Z −ξdq
( ) =( )=
∂ T ρ ∂T ξ dT
−1
2
dq Ψ T r
= .
( )
dT r
dT Ω dT
dq −Ψ
=
dT Ω T 2r T c
dq −Ψ −q
= =
dT Ω TT r T
Therefore
∂Z qξ
( )=
∂T ρ T
Also
∂Z
( ) =b ¿
∂ρ T
b)
RT a
P= −
V −b V (V +b)
1 qξ
Z= −
1−ξ 1+ξ
α =T −0.5
r
Ψ
Also q=
ΩT 1.5
r
This leads to
dq −1.5 q
=
dT T
And
∂Z 1.5 qξ
( )=
∂ T ρ T ( 1+ ξ)
Moreover
∂Z b bq
( ) = −
∂ ρ T (1−ξ ) ( 1+ξ )2
2
1+ ξ 2 1
q= ( ) (
1−ξ 2.5+1.5 ξ
)
Numerical 4:
Isobutene expands adiabatically in a turbine from 5,000kPa and 250℃ to 500kPa at the rate
of 0.7 kgmol s−1 . If the turbine efficiency is 0.80, what is the power output if the turbine and
what is the temperature of the isobutane leaving the turbine?
Solution:
P1=5000 kPa
T 1=250 ℃=523.13 K
T C =408.1 K
Pc =36.48 ¯¿
P2=500 kPa
For turbine
∆ S=0
A=1.677
B=37.853 x 10−3
C=−11.94 x 10−6
D=0
T r 1=1.282
Pr 1=1.3706
Pr 2=0.137
First we will have to calculate the final temperature assuming that the iso-butane is behaving ideal
As we know that
T2 P2
∆ S=C p ln ( ) T1
−Rln ( )
P1
We get
T 2=445.17 K
Therefore
T r 2=1.092
∆ H ig =∫ C p dT
T1
T2
Cp
∆ H ig =R ∫ dT
T1
R
T2
∆ H ig =R ∫ (A +BT +C T 2) dT
T1
Thus
−11.07 kJ
∆ H ig =
mol
In actual case
∆ H ' =∆ H ig + ∆ H R
For ∆ H R
∆ H R=H R 1−H R 2
H R1
=Pr 1 ¿
RTC
Where
0.422
Bo=0.083−
T 1.6
r1
0.172
B1=0.139−
T 4.2
r1
d B o 0.675
=
d T r 1 T 2.6
r1
d B 1 0.7 .22
= 5.2
d T r1 T r1
Also
H R2
=Pr 2 ¿
RTC
Where
0.422
Bo=0.083−
T 1.6
r2
0.172
B1=0.139−
T 4.2
r2
d B o 0.675
=
d T r 2 T 2.6
r2
d B 1 0.7 .22
= 5.2
d T r2 T r2
Thus on substituting the value in above mentioned equations for the determination of ∆ H R, we get
kJ
∆ H R=−8320.32
mol
Therefore we get
kJ
∆ H ' =−8331.4
mol
For η=0.8
Δ H =η Δ H '
kj
Δ H =−6665
mol
For η=0.7
We get
W =η . ΔH
W =−4666.1 kW
For the actual final temperature, we will use the following equation
T2
∆ H =C p ln ( )
T1
−∆ H R
Thus, we get
T 2=457.9 K
Numerical 5:
The steam rate to a turbine for variable output is controlled by a throttle valve in the inlet
line. Steam is supplied to the throttle valve at 1,700kPa and 225℃. During a test run, the
pressure at the turbine inlet is 1,000kPa, the exhaust steam at 10kPa has a quality of 0.95, the
steam flow rate is 0.5kg s−1 , and the power output of the turbine is 180kW
Solution:
P1=1700 kPa
T 1=225 ℃=498.13 K
kj
H 1=2851
kg
kJ
S1=6.513
kg
At 10 kPa
x 2=0.95
kJ
Sliq =0.6993
kg
kg
m . =0.5
s
W . =−180 kW
As we know that
kJ
H 2=2465
kg
Thus, as
Δ H =H 2−H 1
kJ
Δ H =−385.85
kg
As we know that
Q=m. . Δ H −W .
kJ
Q=−12.9
sec
x '2=0.78
kJ
H '2=2063
kg
As
W . =m . Δ H =m . (H ¿¿ 2' −H 1 )¿
W . =−392.4 kW
Numerical 6:
Turbine can be used to recover energy from high-pressure liquid streams. However they are
not used when the high-pressure stream is saturated liquid. Why? Illustrate by determining
the downstream state for isentropic expansion of saturated liquid water at 5 bar to a final
pressure of 1 bar.
Solution:
When a saturated liquid is expanded in a turbine some of the liquid vaporizes. A turbine properly
designed for expansion of liquids cannot handle the much larger volumes resulting from the formation
of vapor. Thus the expansion will be irreversible and the fraction of liquid vaporize will be greater
Numerical 7:
Solution:
P1=125 kPa
P2=700 kPa
m . =2.5 kg/ s
From steam table at 125 kPa
kj
H 1=2685.2
kg
kJ
S1=7.284
kgK
At 700 kPa
kJ
H '2=30513.3
kg
kJ
S2=7.458
kgK
η=78 %
As we know that
Δ H =η ¿
H '2 −H 1
ΔH=
η
kJ
Δ H =469.36
kg
Therefore
H 2= Δ H+ H 1
kj
H 2=3154.7
kg
Therefore using the final enthalpy value we can deduce the value of entropy
Thus
kJ
S2=7.46
molK
Also
W =m ΔH
Thus
W =1173.46 kW
Numerical 8:
Propylene is compressed adiabatically form 11.5 bar and 30℃ to 18 bars at the rate of
1kgmol s−1 . If the compressor efficiency is 0.8, what is the power requirement if the
compressor and what is the discharge temperature of the propylene?
Solution:
P1=11.5 ¯¿
T 1=30 ℃
T C =365.6 K
Pc =46.65 ¯¿
P2=18 ¯¿
For turbine
∆ S=0
A=1.67
B=22.706 x 10−3
C=−6.905 x 10−6
D=0
T r 1=0.8292
Pr 1=0.2465
Pr 2=0.386
First we will have to calculate the final temperature assuming that the propane is behaving ideal
As we know that
T2 P2
∆ S=C p ln ( )
T1
−Rln ( )
P1
Assuming that ∆ S=−3.11
We get
T 2=324.127 K
Therefore
T r 2=0.887
∆ H ig =∫ C p dT
T1
T2
Cp
∆ H ig =R ∫ dT
T1
R
T2
∆ H ig =R ∫ (A +BT +C T 2) dT
T1
Thus
1.409 kJ
∆ H ig =
mol
In actual case
∆ H ' =∆ H ig + ∆ H R
For ∆ H R
∆ H R=H R 1−H R 2
H R1
=Pr 1 ¿
RTC
Where
0.422
Bo=0.083−
T 1.6
r1
0.172
B1=0.139−
T 4.2
r1
d B o 0.675
=
d T r 1 T 2.6
r1
d B 1 0.7 .22
= 5.2
d T r1 T r1
Also
H R2
=Pr 2 ¿
RTC
Where
0.422
Bo=0.083−
T 1.6
r2
0.172
B1=0.139−
T 4.2
r2
d B o 0.67 5
= 2.6
d T r2 T r2
d B 1 0.7 .22
= 5.2
d T r2 T r2
Thus on substituting the value in above mentioned equations for the determination of ∆ H R, we get
kJ
∆ H R=−0.4449
mol
Therefore we get
kJ
∆ H ' =1.0241
mol
For η=0.8
Δ H =η Δ H '
kj
Δ H =0.81928
mol
W =m. ΔH
W =0.82 kW
For the actual final temperature, we will use the following equation
T2
∆ H =C p ln ( )
T1
−∆ H R
Thus, we get
T 2=327.1 K
Numerical 9:
Steam enters a nozzle at 800kPa and 280℃ at negligible velocity and discharges at a pressure
of 525kPa. Assuming isentropic expansion of the steam in the nozzle, what is the exit velocity
and what is the cross-sectional area at the nozzle exit for a flow rate of 0.75kg s−1 ?
Solution:
P1=800 kPa
T 1=280 ℃
H 1=3014.9 kJ /kg
S1=7.195 kJ /kgK
Similarly at
P2=52 kPa
S2=7.1595 kJ /kgK
H 2=2885.2 kJ /kg
V 2=531.2 c m3 / g
With heat, work potential energy and initial velocity equals to zero
u2=565.2 m s−1
m. V 2
A2=
u2
We get
2
A2=7.05 c m
Numerical 10:
P1=1 atm
T 1=35 ℃=308.13 K
P2=5 ¯¿
T 2=200 ℃=473.13 K
η=65 %
m3
V =0.5
s
C p=3.5 R
a)
As we know that
T '2 −T 1
T 2=T 1 +
η
T '2=415.46 K
T 2=T 1 ¿
For n step
T 2=T 1 ¿
P2
ln ()
R P1
n=
Cp T
ln ( 2 )
T1
n=3.74=4≈.
b)
W ideal
W=
η
R
P2
W=
C p T1[ ( )
P1
n cp
−1]
W . =111.15 kW
c)
Since the working gas is ideal and is entering and leaving the compressor and intercooler respectively at
the same temperature, therefore there is no change in the enthalpy.
Q . =W .
Therefore
Q . =−111.15 kW
d)
( 188.4−104.8 ) kJ
Δ HW =
kg
kJ
Δ H W =83.6
kg
m . =Q . / Δ H W
kg
m . =1.329
s
Numerical 11:
Liquid (identified below) at 25℃ are completely vaporized at 1 atm in a counter current heat
exchanger. Saturated steam is the heating medium, available at four pressures: 4.5,9,17 and
33 bars. Which variety of steam is most appropriate for each case? Assume a minimum
approach ∆ T of 10℃ for heat exxhange.
a) Benzene;
b) n-Decane;
c) Ethylene glycol;
d) o-Xylene
Solution:
For this we required the liquid with lowest saturated temperature to satisfy ΔT =0
For this benzene is the most appropriate for each case.
Numerical 12:
Solution:
The mass-flow rate m . is of course constant throughout the nozzle from entrance to exit.
The velocity u rises monotonically from nozzle entrance to nozzle exit as the pressure ratio decrease.
The area ratio decreases at the nozzle entrance to a minimum value at the throat and thereafter
increases to the nozzle exit.
Power cycles
Numerical 13:
A power plant operating on heat recovered from the exhaust gases of internal combustion
engine uses isobutane as the working medium in a modified Rankine Cycle in which the upper
pressure level is above the critical pressure of isobutane. Thus the isobutane doesn’t undergo
a change of phase as it absorbs heat prior to its entry into turbine. Isobutane vapor is heated
at 4,800kPa to 260℃, and enters the turbine as a supercritical fluid at these conditions:
Isentropic expansion in the turbine produces a superheated vapor at 450kPa, which is cooled
and condensed at constant pressure. The resulting saturated liquid enters the pump for
return to the heater. If the power output of the modified Rankine cycle is 1,000kW, what is
the isobutnae flow rate, the heat-transfer rates in the heater and condenser, and the thermal
efficiency of thee cycle? The vapor pressure of isobutnae is given in Table B.2 of App. B.
Solution:
P1=4800 kPa
T 1=533.13 K
T C =408.1 K
Pc =36.48 ¯¿
P2=450 kPa
For turbine
∆ S=0
A=1.677
B=37.853 x 10−3
C=−11.94 x 10−6
D=0
T r 1=1.3064
Pr 1=1.3158
Pr 2=0.123
Thus
T2
∆ H ig =∫ C p dT
T1
T2
Cp
∆ H ig =R ∫ dT
T1
R
T2
∆ H ig =R ∫ (A +BT +C T 2) dT
T1
Thus
−1.14 kJ
∆ H ig =
mol
In actual case
∆ H ' =∆ H ig + ∆ H R
For ∆ H R
∆ H R=H R 1−H R 2
H R1
=Pr 1 ¿
RTC
Where
0.422
Bo=0.083−
T 1.6
r1
0.172
B1=0.139−
T 4.2
r1
d B o 0.675
=
d T r 1 T 2.6
r1
d B 1 0.7 .22
= 5.2
d T r1 T r1
Also
H R2
=Pr 2 ¿
RTC
Where
0.422
Bo=0.083−
T 1.6
r2
0.172
B1=0.139−
T 4.2
r2
d B o 0.675
=
d T r 2 T 2.6
r2
d B 1 0.7 .22
= 5.2
d T r2 T r2
Thus on substituting the value in above mentioned equations for the determination of ∆ H R, we get
kJ
∆ H R=−8848.4
mol
Therefore
For calculating the work of pump we will have to find the volume of iso-butane as a saturated liquid 450
kPa. For this we will first have to calculate the saturation temperature, which can be calculated by the
following Antoine equation
As
B
ln Psat =A−
T +C
Therefore
B
T sat = −C
A−ln P sat
V c =262. c m3 /mol
Z c =0.282
T rsat =0.753
As we know that
2/7
1−T rsat )
V liq =V c Z (c
c m3
V liq =112.36
mol
W pump =V liq ( P1 −P 2 )
W pump =489 kW
For the mass rate
1000
m. =
W turbine+ W pump
kg
m. =0.12
s
For the heat-transfer rates we will first have to calculate the enthalpy changes in the cooler/condenser
with the saturated temperature as the initial temperature.
T2
∆ H ig =∫ C p dT
T sat
T2
Cp
∆ H ig =R ∫ dT
T sat
R
T2
∆ H ig =R ∫ ( A +BT +C T 2)dT
T sat
Thus
−1.746 kJ
∆ H ig =
mol
Therefore
∆ H a =∆ H ig +∆ H R
Implies that
808 kJ
∆ H a =−1.
mol
Also
T n=261.4 K
T rn=0.641
We know that
1.092 R T n ( ln Pc −1.013 )
∆ Hn=
0.93−T rn
kJ
∆ H n =21.18
mol
For the ∆ H b
0.38
1−T rsat
∆ H b =−∆ H n (
1−T rn )
Therefore
kJ
∆ H b =−18.37
mol
Q out =m. ( ∆ H a +∆ H b )
Qout =−4360 kW
Also
Q ¿ =5360 kW
As we know that
1000
η=
Q¿
η=0.18
%η=18 %
Numerical 14:
a) Show that the thermal efficiency of the air-standard Diesel cycle can be expressed as
1 γ−1
r cγ−1
η=1−
r () γ ( r c −1 )
where r is the compression ration and r c is the cutoff ratio, defined as r c =V A /V D . (See
fig.8.10)
b) Show that for the same compression ratio the thermal efficiency of the air-standard
Otto engine is greater than the thermal efficiency of the air standard Diesel cycle.
γ −1
1
()
Hint: show that the fraction which multiplies
r
in the equation for η is greater
than unity by expanding r γc in a Taylor series with the remainder taken to the first
derivative
c) If γ =1.4, how does the thermal efficiency of an air-standard Otto cycle with a
compression ratio 0f 8 compare with the thermal efficiency of an air-standard Diesel
cycle with the same compression ratio and cutoff ratio of 27 how the compression
changed if the cutoff ratio is 3?
Solution:
a)
As we know that
1 γ 1 γ
1 re
η=1− [
−
( ) ()
r
]
γ 1 1
−
re r
Where
r e =expansionratio=V B /V A
r =compression ratio=V c /V D
r c =cutoff ratio=V A /V D
Since V A =V B
r
=(V ¿ ¿ c /V D) /(V ¿ ¿ c /V A )=r c ¿ ¿
re
Or
1 rc
=
re r
Therefore
rc γ 1 γ
1 r
η=1− [
−
r( ) ()
]
γ rc 1
−
r r
1 γ−1
r γc −1
η=1− ()
r γ (r c −1)
b)
r γc −1
>1
γ (r c −1)
Taylor series with remainder, taken to the first derivative can be written as
1 γ −2
r γc =1+ γ ( r c −1 ) + γ ( γ −1 ) [ 1+θ ( r c −1 ) ] . ( r c −1 )2
2
1 γ −2
For a> 1 and r c >1 also γ ( γ −1 ) [ 1+θ ( r c −1 ) ] . ( r c −1 ) 2> 0
2
Therefore
r γc >1+γ ( r c −1 )
r γc −1> γ ( r c −1 )
r γc −1
>1
γ ( r c −1 )
Hence proved that with the same compression ratio the thermal efficiency of Otto engine is
greater than that of Diesel cycle.
c)
If γ =1.4 and r =8
ηotto =0.564
1 γ−1
r γc −1
η=1−
r () γ (r c −1)
Therefore
If r c =2
ηdiesel =0.49
And for r c =3
ηdiesel =0.43
Numerical 15:
An air-standard Diesel cycle absorbs 1,500Jmo l−1 of heat (step DA of fig.8.10, which simulates
combustion). The pressure and temperature at the beginning of the compression step are 1
bar and 20℃, and the pressure at the end of the compression step is 4 bar. Assuming air to
be an ideal gas for which C p= ( 72 ) R and C =( 52 ) R, what are the compression ratio and the
v
Solution:
7
C p= R
2
Pc =1 ¯¿
T C =293.13 K
P D=5 ¯¿
γ =1.4
As we know that
Pc V γc =PD V γD
1γ
Vc P
VD
=r= D
Pc ( )
r =3.1
Q DA=1,500 Jmol−1
Q DA=C p ( T A −T D )
Q DA
T A= +T D
CP
T D =515.8 K
VB
re=
VA
As we know that
V B =V c
Therefore
RT C
V B Vc PC
re= = =
V A V A RT A
PA
Since
P A =PD
Therefore
r e =2.8
Numerical 16:
Consider an air-standard cycle for the turbojet power plant shown in the figure 8.13. The
temperature and pressure of the air entering the compressor are 1 bar and 30℃. The
pressure ratio in the compressor is 6.5, and the temperature at the turbine inlet is 1,100℃. If
the expansion in the nozzle is isentropic and if the nozzle exhausts at 1 bar, what is the
pressure at the nozzle inlet(turbine exhaust) and what is the velocity if the air leaving the
nozzle?
Solution:
T A=303.15 K
T C =1373.15 K
7
CP= R
2
P A =PE =1 ¯¿
Pc =P B=6.5 ¯¿
g
Molecular Wt. of air = 29
mol
2
W AB =C P T A [r comp7 −1]
Also
R
PD
W CD =C P T C [ ( )
PC
CP
−1]
2
7
W CD =C P T C [r exp −1]
Therefore
2 2
[ ]
T C r exp 7 −1 =−T A [r comp 7 −1]
As we know that
r comp =6.5
Therefore
r exp =0.55
Also we know
PD
r exp =
PC
And
PB
r comp =
PA
Therefore
PD
=r r
P E exp comp
As we know that
γ −1
2 γ PD V D P
u2E−u 2D =
γ −1 ( )
[1− E
PD
γ
]
u D=0
γ −1 2
=
γ 7
P D V D =nR T D
We get
2
7 RTD 1
u E= 2
√ 2n
[1− (
r exp r comp)7
]
u E=843.33m s−1
Also
PD
=r r
P E exp comp
Thus
P D=3.56 ¯¿
Numerical 17:
Liquefied natural gas (LNG) is transported in very large tankers, stored as liquid in equilibrium
with its vapor at approximately atmospheric pressure. If LNG is essentially pure methane, the
storage temperature then is about 111.4K, the normal boiling point of methane. The
enormous amount of cold liquid can in principle serve as a heat sink for an on-board heat
engine. Energy discarded to the LNG serves for its vaporization. If the heat source is ambient
air at 300K, and if the efficiency of a heat engine is 60% of its Carnot value, estimate the
vaporization rate in moles vaporized per kJ of power output. For methane,
∆ H lvn =8.206 kjmo l −1.
Solution:
As
T C =111.4 K
T H =300 K
kJ
Δ H lvn =8.206
mol
As we know that
TC
ηcar not =1−
TH
ηcarnot =0.629
Also given
ηengine =0.377
Basis
W =1 kJ
W
ηengine =
Q heat
W
Q heat =
ηengine
Q heat =2.65 kJ
Also
Also as
Q cold
Δ H lvn mol
=0.20
W kJ
Numerical 18:
a) Carnot cycle;
b) Otto-cycle;
c) Diesel cycle;
d) Brayton cycle.
Why would a PT diagram not be helpful for depicting power cycles involving liquid/vapor
phase changes?
Solution:
a) Carnot Cycle
b) Otto-Cycle
c) Diesel Cycle
d) Brayton Cycle
Numerical 19:
Steam enters the turbine of a power plant operating on the Rankine cycle (fig.8.3) at
3,300kPa and exhausts at 50kPa. To show the effect of superheating on the performance of
the cycle, calculate the thermal efficiency of the cycle and the quality of the exhaust steam
form the turbine for turbine-inlet steam temperatures of 450, 550 and 650℃ .
Solution:
P1=50 kPa
P4 =3300 kPa
V 4 =1.030 c m3 / g
H 4 =340.564 kJ /kg
kJ
Sliq =1.09
molK
kJ
Svap =7.59
kgK
As we know that
W pump =V 4 ( P 4−P1 )
W pump =3.34 kW
Δ H =W pump
W pump =H 1 + H 4
H 1=W pump + H 4
kJ
H 1=343.91
kg
450
{
T = 550 ℃
650
3340.6
{
H 2= 3565.3 kJ /kg
3792.9
7.037 3
{
S2= 7.3282 kJ / kgK
7.5891
S'3=S 2
As
0.914
{
x '3= 0.959
0.999
2447.73
{
H '3= 2551.477 kJ /kg
2643.69
W turbine =H '3−H 2
−892.87
{
W turbine = −789.13 kW
−696.91
Q H =H 2−H 1
2996.68
{
Q H = 3221.389 kJ
3448.98
Also
W turbine +W pump
η=
QH
0.297
{
η= 0.314
0.332
Numerical 20:
Steam enters the turbine of a power plant operating on the Rankine cycle (fig.8.3) at 600 ℃
and exhaust at 30kPa. To show the effect of boiler pressure on the performance of the cycle,
calculate the thermal efficiency of the cycle and the quality if the exhaust steam from the
turbine for boiler pressures of 5,000, 7,500 and 10,000kPa.
Solution:
At30 kPa saturated liquid
V 4 =1.022 c m3
H 4 =89.302 kJ /kg
P1=30 kPa
5000
{
P4 = 7500 kPa
10000
3664.5
{
H 2= 3643.7 kJ /kg
3622.7
7.2578
{
S2= 7.0526 kJ /kgK
6.9013
As we know that
W pump =V 4 ( P 4−P1 )
5079.34
{
W pump = 7634.34 kW
10189.34
Also
W pump =H 1−H 4
H 1=H 4 + W pump
294.381
{
H 1= 296.936 kJ /kg
299.491
S'3=S 2
As
Thus
0.925
{
x '3= 0.895
0.873
2450.192
{
H '3= 2380.109 kJ /kg
2328.715
W turbine =H '3−H 2
−1214.308
{
W turbine = −1263.591 kW
−1293.985
Q H =H 2−H 1
3370.119
{
Q H = 3346.764 kJ
3323.209
Also
W turbine+ W pump
η=
QH
0.359
{
η= 0.375
0.386
Numerical 21:
A steam power plant operating on a regenerative cycle, illustrated in fig. 8.5 includes just one
feedwater heater. Steam enters the turbine at 650 psia and 900℉ and exhaust at 1 psia.
Steam for the feedwater heater is extracted from the turbine at 50 psia, and in condensing
raises the temperature at 50 psia. If the turbine and pump efficiencies are both 0.78, what is
the thermal efficiency of the cycle and what fraction of the steam entering the turbine is
extracted for the feedwater heater?
Solution:
At 4500 kPa∧500 ℃ from steam table
H 2=3439.3 kJ /kg
S2=7.3011 kJ /kg
S'3=S 2
H '3=2770.6 kJ /kg
η=0.78
As we know that
W 1=η ( H '3−H 2 )
W 1=−521.586 kW
Also
W 1= Δ H=H 3 −H 2
or
H 3=H 2 +W 1
Thus
H 3=2.98 x 10 3 kJ /kg
S'4 =S2
kJ
Sliq =0.8321
kgK
S '4−S liq
x '4 =
S vap−Sliq
x '4 =0.876
Also
Also
H 4 =H 2+ η ( H '4 −H 2 )
We know that
H 5=H liq
V 5=1.017 m3 / g
P5=20 kPa
P6=4500 kPa
V 5 ( P 6−P5 )
W pump =
η
W pump =5.841 kW
Also
or
H 6=H 5 +W pump
Thus
H 6=257.294 kJ /kg
H 7=584.270 kJ /kg
T 7=138.86 ℃
T 1=138.87−6=132.87 ℃
V satliq =1.073 c m3 /g
1 1083−1.063
β= ( )
V satliq 20
β=9.32 x 10−4
P1=P6
As we know that
H 1=561.305 kJ /kg
m=0.132 kg
Also
W 2 =( 1−m ) (H 4 −H 3)
W 2 =−307.567 kW
W net =−823.3 kW
Also
Q H =H 2−H 1
Q H =2878 kJ
W net
η=
QH
η=0.286
Refrigeration & Air Conditioning
Numerical 22:
Solution:
T 2=277.13 K
T 4=307.13 K
η=0.76
Q C =1200 kJ / s
H 2=2508.9 kJ /kg
kJ
S2=9.0529
kgK
H 4 =142.4 kJ / kg
As it is an isentropic expansion
S'2=S 2
Via interpolation
H '3=2814.7 kJ /kg
H '3−H 2
Δ H 23 =
η
Therefore
Δ H 23 =402.386 kJ /kg
Also we know
Δ H 23 =H 3 −H 2
H 3= Δ H 23+ H 2
Therefore
Thus
m=QC /Δ H 12
m=Q C / H 2−H 1
0.507 kg
m=
s
Also
Q H =m ( H 4−H 3 )
kJ
Q H =−1404
s
Similarly
W =m Δ H 23
W =204 kW
Qc
ω=
W
ω=5.881
Also
T2
ω carnot =
T 4 −T 2
Thus
ω carnot =9.238
Numerical 23:
Solution:
At 20 ℉∧33.110 psia
H 2=105.907 Btu/lb
S2=0.22325 Btu/lbR
At 80 ℉
H 4 =37.978 Btu /lb
H 1=H 4 −H 2 A + H 2
H 1=27.885 Btu/lb
As
Btu
Q c =2000
s
Therefore
Qc
m=
H 2−H 1
lb
m=25.634
s
Btu
H '3=127
lb
η=0.75
H '3 −H 2 A
Δ H comp=
η
Therefore
Btu
Δ H comp=14.667
lb
Thus
W =m Δ H comp
Therefore
W =390.66 kW
As
QC
m=
H 2−H 4
So
lb
m=29.443
s
As we know
H '3 −H 2
Δ H comp=
η
Therefore
Btu
Δ H comp=13.457
lb
Thus
W =m Δ H comp
Therefore
W =418.032 kW
Numerical 24:
A heat pump is used to heat a house in the winter and to cool it in the summer. During the
winter, the outside air serves as a low temperature heat source; during the summer, it acts as
a high-temperature heat sink. The heat transfer rate through the walls and inside and outside
of the house, summer and winter. The heat-pump motor is rated at 1.5kW. Determine the
minimum outside temperature for which the house can be maintained at 20℃ during the
winter and the maximum outside temperature for which the house can be maintained at 25
℃ during the summer.
Solution:
Winter
T H =293.13 K
W =1.5 kW
As
Q H =−0.75(T H −T C )
Guess T C =250 K
Therefore
Q H =−32.3475 kJ
As
T H −T c
W /Q H =
TH
Therefore
T c =268.94 K
Summer
T C =293.13 K
Guess T H =300 K
Therefore
Q C =0.75(T H −T C )
Thus
Q C =1.5975 kJ
As
W T −T c
= H
0.75(T H −T c ) TH
Therefore
T H =322.5 K
Numerical 25:
The contents of the freezer in a home refrigerator are maintained at -20℃. The kitchen
temperature is 20℃. If the heat leaks amount to 125,000kJ per day, and if the electricity
costs $0.08 per kWhr, estimate the yearly cost of running the refrigerator. Assume a
coefficient of performance equal to 60% of the Carnot value.
Solution:
T H =20 ℃ =293.13 K
T C =−20 ℃=253.13 K
QC =125000 kJ /day
As we know that
Tc
ω carnot =
T H −T c
Thus
ω carnot =6.328
As
ω=0.6 ω carnot
Therefore
ω=3.979
As
QC
W=
ω
Thus
W =0.381 kW
We know that
0.08 W
cost=
kWhr
Therefore
dolllars
co st=267.18
yr
Numerical 26:
The condenser of a home refrigerator is commonly underneath the appliance; thus the
condensing the refrigerant exchanges heat with household air, which has an average
temperature of about 70℉. It is proposed to reconfigure a refrigerator so that the condenser
is outside the home, where the average yearly temperature is about 50℉. Discuss the pros
and cons of this proposal. Assume a freezer temperature of 0℉ and an actual coefficient of
performance 60% that of a Carnot refrigerator.
Solution:
On average, the coefficient of performance will increase, thus providing savings on electric casts. On the
other hand, installation casts would be higher. The proposed arrangement would result in cooling of the
kitchen, as the refrigerator would act as an air conditioner. This would be detrimental in the winter, but
beneficial in the summer, at least in temperate climates.
Numerical 27:
Which is the more efficient way to increase the coefficient of performance of a Carnot
refrigerator to increase T c with T H constant, or to decrease T H with T c constant? For a real
refrigerator, does either of these strategies make sense?
Solution:
As we know that
Tc
ω=
T H −T c
On differentiating it
∂ω TH
( ) =
∂ T C T ( T H −T c )2
H
And
∂ω Tc
( ) =
∂ T H T ( T H −T c )2
c
For a real refrigeration system, increasing T cis hardly an option if refrigeration is required at a particular
value of T c. Decreasing T H is no more realistic, because for all practical purposes, T H is fixed by
environmental conditions, and not subject to control
Numerical 28:
Solution:
a)
Q c =4 kJ /s
W =1.5 kW
As we know that
ω=Qc /W
Therefore
ω=2.66
b)
As
W =QH −Qc
Or
Q H =W +Qc
Thus
kJ
Q H =5.5
s
c)
T H =40 ℃+ 273.13=313.13 K
As
Tc
ω=
T H −T c
Therefore
ω
T c =T H ( ω+1 )
Thus
T c =227.2 K