CH 10
CH 10
CH 10
By: S K Mondal
Chapter 10
2.
Tds = du + pdv
Tds = dh vdp
2
=1 +
N
For mono-atomic gas N = 3
For di -atomic gas N = 5
For Tri-atomic gas N = 6
3.
4.
[N = degrees of freedom]
T
p
pv = C ; 2 = 2
T1 p1
5.
v1
v
2
RT1
u2 u1 =
1
(i)
1
1
p
p
(RT1 )
1
1 ; h 2 h1 =
p1
p1
1
2
p v p v
1 pd v = 1 1 12 2
6.
(p1 v1 p2 v 2 )
1
1
Isobaric process (p = C), n = 0, pv = C
Isothermal process (T = C), n = 1, pv1 = RT
Isentropic process (s = C), n = , pv = C
Isometric or isobaric process (V = C), n =
7.
v dp
p2 p3
=
p1 p2
(ii) Equal discharge temperature (T2 = T3 )
(i)
p1 p3
By: S K Mondal
Chapter 10
p3
p2
p1
T
1
S
1
8.
9.
p n
Volumetric Efficiency ( vol ) = 1 + C C 2
p1
Clearance volume
Where, C =
Piston displacement volume
RT
a
or
p=
v b v2
or
(ii)
pr + v 2 (3 v r 1) = 8Tr
r
RT (1 e)
A
(v + B) 2
2
v
v
a
b
C
A = A 0 1 ; B = B0 1 ; e =
v
vT3
v
p=
Where
(iii)
Virial Expansions:
pv
= 1 + Bp + Cp2 + Dp3 +
RT
pv
B C
D
Or
= 1 + + 2 + 3 + .......
v v
v
RT
Page 146 of 265
By: S K Mondal
a = 3 pc v 2c ; b =
10.
Chapter 10
vc
8 pc v c
; values of Z at critical point 0.375 for Van der Waal
; R=
3
3 Tc
gas.
a
bR
= x1 1 + x 2 2 + ....... + x c c
11.
12.
m1R1 + m2 R 2 + ....... mc R c
m1 + m2 + ........... mc
m u + m2 u2 + ....... m c uc
um = 1 1
;
m1 + m2 + ........... m c
Rm =
c pm
hm =
m1h1 + m2 h 2 + ....... m c h c
m1 + m 2 + ........... m c
c vm
p
p
p
sf si = m1R1 ln 1 + m2 R 2 ln 2 + ...... + m c R c ln c
p
p
p
Gibbs function G = RT n x ( k + ln p + ln x k )
13.
Q.10.2
(c)
Solution:
m=
pV
RT
101.325 216
kg = 255.9 kg
0.287 298
Given diameter
Height
(D) = 25 cm = 0.25 m
(H) = 80 cm = 0.8 m
D2
By: S K Mondal
Chapter 10
Temperature
(a)
(T) = 27 C = 300 K
pV
R 8.3143
=
kJ/kg K = 0.51964
Here R = Gas constant =
RT
M
16
= 3.023 kg
m=
(b)
(c)
Q.10.3
T=
pV
15000 0.03927
=
= 375 K = 102 C
mR
3.023 0.51964
A certain gas has cP = 0.913 and cV = 0.653 kJ/kg K. Find the molecular
weight and the gas constant R of the gas.
Solution:
Q.10.4
Solution:
R
8.3143
=
kJ/kg K = 0.3198 kJ/kg K
M
26
cp =
R = 1.55 kJ/kg K
1
R
cv =
= 1.23 kJ/kg K
and
1
Q.10.5
Solution:
Mono-atomic: c p =
R = 20.79 kJ/kg mole K;
1
R
= 12.47 kJ/kg mole K
1
cp =
R = 29.1 kJ/kg mole K;
1
cv =
Di-atomic:
cv =
R
= 20.79 kJ/kg mole K
1
By: S K Mondal
cp =
Polyatomic:
Chapter 10
Solution:
T3 = 288 K
(V 3 ) = 1000 m3/m =
Flow rate
Gas constant (R) =
5 3
m /s
18
R
= 0.51964 kJ/kg K
16
p3 V3 = m RT3
p V3
m =
= 0.22273 kg/s
RT3
dW
Pump work
= 15 kW
dt
m(h1 + 0 + gZ1 ) +
= m( h3 + 0 + g Z3 ) +
dt
dt
(Z
Z
)
dW
dQ
1
= m (h3 h1 ) + g 3
+
dt
1000
dt
Z dW
= m c P (T3 T1 ) + g
+
1000
dt
9.75 800
+ ( 15)
= 63.7 kJ/s = 63.7 kW (heat given to the system)
Q.10.7
cp =
R = 2.0943 kJ/kg
1
800m
P
1
By: S K Mondal
Solution:
Chapter 10
T2 = 100C = 373 K
p
p2 = 1 T2 = 357 kPa
T1
Mass (m) = 1 kg
T1 = 5 C = 278 K
mRT1
= 265.95 kPa
V
Work done = pdV = 0
p1 =
du + dW = dW = m c dT = m c
Change in internal Energy = du = 68.21 kJ
Change in Enthalpy = dh = m c (T T ) = 95.475 kJ
Heat transferred Q =
Change in Entropy =
d s = s2
(T2 T1 ) = 68.21 kJ
s1 = m c p ln
V2
p
+ m c v ln 2
V1
p1
p2
357
= 1 0.718 ln
265.95
p1
= 0.2114 kJ/kg K
= m c v ln
Q.10.8
Solution:
T1 = 278 K
V1 = 0.3 m3
m = 1 kg
p1 = 265.95 kPa
T2 = 100 C = 373 K
p2 = 265.95 kPa
mRT2
V2 =
= 0.40252 m3
p2
(a) Work during the process
2
(W12) =
p dV
= p(V2 V1 ) = 27.266 kJ
By: S K Mondal
Solution:
Chapter 10
V1 = 0.1 m3
p1 = 1.2 MPa = 1200 kPa
T1 = 473 K
1
1
2
S
R
8.3143
=
kJ/kg K = 4.157 kJ/kg K
M
2
p V
m = 1 1 = 0.06103 kg
RT1
Reversible isothermal expansion
So
T2 = T1 = 473 K
Enthalpy change (h) = m c p (T2 T1 ) = 0
R=
And
p2 = 0.1 MPa = 100 kPa
Heat transferred (Q) = u + W
mRT2
3
V2 =
= 1.2 m
p2
= u2 u1 + p dV
1
dV
= 0 + RT
V
V
= RT ln 2
V1
pV = RT
p=
RT
V
1.2
= 4.157 473 ln
0.1
= 4886 kJ
2
p dV
= 4886 kJ
Entropy change, s2 s1 = mc p ln
V2
p
+ mc v ln 2
V1
p1
1.2
100
= 0.06103 14.55 ln
+ 10.4 ln
0.1
1200
= 0.6294 kJ/kg K
For H2 diatomic gas ( = 1.4)
R
= 10.4 kJ/kg K
cp =
R = 14.55 kJ/kg K; cv =
1
1
Q.10.10
By: S K Mondal
Solution:
Chapter 10
v1 = 1 R T1 = 0.1653 m3/kg
p1
p2 = 0.2 MPa = 200 kPa
p1 v1 = p2 v 2 :
p
v2 = v1 1 = 0.31809 m3/kg
p2
1
T1
p
p
T2 = T1 2
= 1
T2
p2
p1
= 222 K
Change of Enthalpy
(H) = mc p (T2 T1 ) = 66.33 kJ/kg
2
S
Solution:
If the above process occurs in an open steady flow system, find the final
temperature, and per kg of air, the change in internal energy, the heat
transferred, and the shaft work. Neglect velocity and elevation changes.
T
p
Final temperature will be same because then also 2 = 2
T1
p1
i.e. T2 = 222 K
Change in internal energy = u = mc v (T2 T1 ) = 47.4 kJ/kg
2
(W) = v dp =
Shaft work
valid.
Heat transferred:
h1 + 0 + 0 +
Q.10.12
dQ
dW
= h2 + 0 + 0 +
dm
dm
dQ
dW
= (h 2 h1 ) +
= 66.33 + 66.33 = 0
dm
dm
[As it is reversible adiabatic so dQ = 0]
The indicator diagram for a certain water-cooled cylinder and piston air
compressor shows that during compression pv1.3 = constant. The
compression starts at 100 kPa, 25C and ends at 600 kPa. If the process is
reversible, how much heat is transferred per kg of air?
By: S K Mondal
Solution:
Chapter 10
p1 = 100 kPa
T1 = 298 K
RT1
= 0.8553 m3/kg
v1 =
p1
p2 = 600 kPa
1
n
p
v 2 = v1 1 = 0.21554 m3/kg
p2
2
pV
1.3
= constant
p
1
n 1
n
p
= 451 K
T2 = T1 2
p1
dQ
dW
h1 + 0 + 0 +
= h2 + 0 + 0 +
dm
dm
dQ
dW
= (h 2 h1 ) +
dm
dm
n[p1 v1 p2 v 2 ]
dW
=
n 1
dm
= 189.774 kJ/kg
= Cp(T2 T1) -189.774
= 153.765 189.774
= 36 kJ/kg
[Heat have to be rejected]
Q.10.13
Solution:
R
= 0.27714 kJ/kg K
30
= 1.3; n = 1.25
R
= 0.9238 kJ/kg K
cv =
1
R
cP =
= 1.2 kJ/kg K
1
p1 = 100 kPa; V1 = 1.5 m3; T1 = 350 K
p2 = 3 MPa = 3000 kPa
R=
2
p
p n
V2 = V1 1 = 0.09872 m3
p2
pV
m = 1 1 = 1.5464 kg
RT1
pV
T2 = 2 2 = 691 K
mR
1
V
By: S K Mondal
Chapter 10
2
p1 V
n
1
pdV
1
n
2
= p V = p2 V
= p1 V1n
p1 V1n
dV
=
1 V n n + 1
1
1
Vn 1 Vn 1
1
2
p2 V2 p1 V1
p V p2 V2
= 1 1
1n
n 1
100 1.5 3000 0.09872
kJ = 584.64 kJ
=
1.25 1
Heat transfer Q = u2 u1 + W1 2
= mc v (T2 T1 ) + W1 2
= [1.5464 0.9238 (691 350) 584.64] kJ
= 97.5 kJ
p
V
S = S2 S1 = mc v ln 2 + mc P ln 2
p1
V1
= 0.19 kJ/K
Q.10.14
Solution:
Try please.
Q.10.15
Solution:
Try please.
Q.10.16
An ideal gas cycle of three processes uses Argon (Mol. wt. 40) as a
working substance. Process 1-2 is a reversible adiabatic expansion from
0.014 m 3 , 700 kPa, 280C to 0.056 m 3 . Process 2-3 is a reversible
isothermal process. Process 3-1 is a constant pressure process in which
heat transfer is zero. Sketch the cycle in the p-v and T-s planes, and find
(a) the work transfer in process 1-2, (b) the work transfer in process 2-3,
and (c) the net work of the cycle. Take = 1.67.
Solution:
Try please.
Q.10.17
A gas occupies 0.024 m 3 at 700 kPa and 95C. It is expanded in the nonflow process according to the law pv1.2 = constant to a pressure of 70 kPa
Page 154 of 265
By: S K Mondal
Chapter 10
Try please.
Q.10.18
Solution:
Q.10.19
0.5 kg of helium and 0.5 kg of nitrogen are mixed at 20C and at a total
pressure of 100 kPa. Find (a) the volume of the mixture, (b) the partial
volumes of the components, (c) the partial pressures of the components,
(d) the mole fractions of the components, (e) the specific heats cP and cV
of the mixture, and (f) the gas constant of the mixture.
Solution:
Try please.
Q.10.20
Solution:
Try please.
Q.10.21
Solution:
Try please.
Q.10.22
A vessel is divided into three compartments (a), (b), and (c) by two
partitions. Part (a) contains oxygen and has a volume of 0.1 m 3 , (b) has a
volume of 0.2 m 3 and contains nitrogen, while (c) is 0.05 m 3 and holds
C O2 . All three parts are at a pressure of 2 bar and a temperature of 13C.
When the partitions are removed and the gases mix, determine the
change of entropy of each constituent, the final pressure in the vessel
and the partial pressure of each gas. The vessel may be taken as being
completely isolated from its surroundings.
(Ans. 0.0875, 0.0783,
0.0680
kJ/K; 2 bar; 0.5714, 1.1429, 0.2857 bar.)
Page 155
of 265
By: S K Mondal
Chapter 10
Solution:
0.1 m 3
0.2 m 3
0.05 m 3
N2
O2
W2
kg = 0.26915 kg
8.3143
Ra T
286
32
pVa
200 0.2
mb =
=
kg = 0.471 kg
8.3143
RbT
286
28
pVc
200 0.05
mc =
=
kg = 0.18504 kg
8.319
Rc T
286
44
v
T
p
p
S = S2 S1 = mc P ln 2 mR ln 2
Here T2 = T1 so 2 = 1
T1
p1
p1 v 2
(S2 S1 )O2 = mO2 R O2 ln
Vo
8.3143
9.35
ln
= 0.26915
VO2
32
0.1
= 0.087604 kJ/K
8.3143
V
0.35
= 0.471
ln
(S2 S1 )N2 = mN2 R N2 ln
= 0.078267 kJ/K
32
0.2
Vn2
8.3143
V
0.35
= 0.18504
ln
(S2 S1 )CO2 = mCO2 RCO2 ln
= 0.06804 kJ/K
44
0.05
VCO2
Partial pressure after mixing
0.1
Mole fraction of
O2 (x O2 ) =
0.35
0.2
Mole fraction of
N 2 (x N2 ) =
0.35
0.05
Mole fraction of
CO2, x O2 =
0.35
[ At same temperature and pressure same mole of gas has same]
0.1
200 = 57.143 kPa
O2 ; (pO2 ) = x O2 p =
Partial pressure of
0.35
0.2
200 = 114.29 kPa
Partial pressure of
N 2 ; (pN2 ) = x N 2 p =
0.35
0.05
Partial pressure of
200 = 28.514 kPa
CO2 ; (pCO2 ) = x CO2 p =
0.35
( )
By: S K Mondal
Chapter 10
Q.10.23
A Carnot cycle uses 1 kg of air as the working fluid. The maximum and
minimum temperatures of the cycle are 600 K and 300 K. The maximum
pressure of the cycle is 1 MPa and the volume of the gas doubles during
the isothermal heating process. Show by calculation of net work and
heat supplied that the efficiency is the maximum possible for the given
maximum and minimum temperatures.
Solution:
Try please.
Q.10.24
Solution:
= mc v T = mc v (T2 T1 )
2
2
T
1
1
V
S
Q2 3 = 0 as isentropic expansion.
Q3 1 = mc P T = mc P (T3 T1 )
Efficiency = 1
heat rejection
heat addition
T3
mc p (T3 T1 )
T
= 1 1
= 1
mc v (T2 T1 )
T2
T 1
1
p1 v1
p2 v 2
T2
p
=
as V1 = V2
= 2 = r
Here
T1
T2
T1
p1
And p2 v 2 = p3 v 3
And
or
p3 v 3
pv
= 2 2
T1
T3
Page 157 of 265
p2
v
= 3 = r
p3
v2
p2
= r
p1
as p3 = p1 then
By: S K Mondal
or
If
Chapter 10
T3
v
v
= 3 = 3 =r
T1
v1
v2
=
= 1
( 1)
r 1 (r 1)
Proved
=
r 1
r 1
4
and r = 8 then
3
cycle =
r 1 (r 1)
r 1
4
(8 1)
3
= 1 4
= 0.37778
3
(8 1)
Q.10.25
Solution :
RT
a
P=
.exp
vb
RTv
(a) Show that
a
a
pc = 2 2 , v c = 2b, Tc =
4Rb
4e b
(b) Expand in the form
B C
pv = RT 1 + + 2 + ....
v v
Q.10.26
Solution :
Try please.
Q.10.27
Calculate the volume of 2.5 kg moles of steam at 236.4 atm. and 776.76 K
with the help of compressibility factor versus reduced pressure graph.
At this volume and the given pressure, what would the temperature be
in K, if steam behaved like a van der Waals gas?
The critical pressure, volume, and temperature of steam are 218.2 atm.,
57 cm 3 /g mole, and 647.3 K respectively.
Solution :
Try please.
Q.10.28
By: S K Mondal
Solution:
Chapter 10
contains air at 3.5 bar, 205C. Find the change of entropy when A is
connected to B. Assume the mixing to be complete and adiabatic.
(Ans. 0.975 kJ/kg K)
VA = VB = 3m3
pA = 7 bar = 700 kPa
TA = 95C = 368 K
pB = 3.5 bar = 350 kPa
TB = 205C = 478 K
mA =
pA VA
= 19.883 kg
RTA
mB =
UA + UB = U
m A c v . TA + m B c v . TB = (m A + m B ) c v T
or
m A TA + mB TB
= 398.6 K
m A + mB
After mixing partial for of A
Total pressure
m RT
= 379.1 kPa
pAf = A
V
m RT
pBf = B
= 145.93 kPa
V
p
T
SA = SAf SA = m A c p ln
m A R ln Af
TA
pA
= 5.0957 kJ/K
p
T
m B R ln Bf
sBf sB = m B c P ln
TB
pB
= 0.52435 kJ/kg
Q.10.29
T=
pB VB
= 7.6538 kg
RTB
3m 3
3m 3
pA = 7 bar
TA = 95C
pB = 3.5 bar
TB = 205C
and
2
Ans. n =
+ 1
By: S K Mondal
Solution:
Chapter 10
2
p
T2
T
1
T1
1
T2
2
3 (T1 )
3
S
Then
v2
p
T
T
p
T
R
ln 2
+ c v ln 2 = c p ln 2 R ln 2 = c p ln 2 =
T1
v1
p1
T1
p1
T1
1
T
p
= c p ln 3 R ln 3
T2
p2
s2 s1 = 1 c P ln
or
s3 s 2
n 1
n 1
T
p T n
p n
Hence T3 = T1 and 3 = 3
3 = 3
T2
p2 T2
p2
T
T1
nR
n
T
T2 n
R
= cP ln 1 R
ln 1 =
ln T = R ln T n 1 1
4
n
1
T2
n 1 T2
1
As s2 s1 = s3 s2
or
or
or
or
T
R
T n
ln 2 = R ln 2
T1
1
T1 n 1 1
n
2
=
1
n 1
2n 2 = n n
n (n) = 2
2
n=
proved
+1
Q.10.30
Solution:
pV
2310 0.142
= 8.6768 kg
=
8.3143
R SO2 T
291
64
By: S K Mondal
m2 =
Chapter 10
910 0.142
= 3.4181 kg
RSO2 291
or
or
Q.10.31
Solution :
T2
p
= 2
T1
p1
220.65
6.9
or
=
291
23.1
220.65
ln
299 = 0.22903
1
6.9
ln
23.1
1
= 1 0.22903 = 0.77097
= 1.297
Rmix =
= 100 kg
= 1276 kg
RN2 =
R H2 =
m N2 R N2 + m H2 R H2 + mCO2 R CO2
m N2 + m H2 + mCO2
28
R
R
, RCO2 =
2
44
21 R + 50 R + 29 R
21 28 + 50 2 + 29 44
= 0.42334 kJ/kg K
=
c p Mix =
m N2 C pN + m H2 C pH + mCO2 C pCO
2
m N2 + m H2 + mCO2
Page 161 of 265
By: S K Mondal
=
Chapter 10
21 28 1.039 + 100 14.235 + 0.828 1276
= 1.5738 kJ/kg K
588 + 100 + 1276
R
= 0.74206
28
R
c VH2 = 14.235
= 10.078
2
R
c VCO2 = 0.828
= 0.63904
44
c VN2 = 1.039
cv
Mix
c p mix
mix =
= 1.368
cv mix
Given
p1 = 1 bar = 100 kPa
V2 = 0.085 m3
T1 = 10 C = 283 K
n
p2
v
= 1 = 51.2
p1
v2
p2 = 100 51.2 kPa
2
p
n 1
T2
p n
= 2
T1
p1
p V p2 V2
W= 1 1
n 1
T2 = 390.5 K
1
V
dV
W = pdV = C 4
1
1 V
Q = u2 u1 + W
m=
p1 V1
= 0.070948 kg
RT1
= mc v (T2 T1 ) + W
= (8.7748 16.15) kJ
= 7.3752 kJ
[i.e. Heat flow through system]
Page 162 of 265
By: S K Mondal
Chapter 10
Charge of entropy
T
p
S = S2 S1 = mc P ln 2 m R ln 2
T1
p1
390.5
690
= m 1.5738 ln
0.42334 ln
kJ/K
283
100
Q.10.32
Solution:
+
R ln
ln
4 1 27
Provided that the gases are different and that the ratio of specific heat
is the same for both gases and remains constant.
What would the entropy change be if the mixing gases were of the same
Species?
nRT
2 RT
nR 2 T
2 RT
VA =
=
VB =
=
p
p
p
p
2 mole
T
p
1 mole
2T
p
nRTf
=
pf =
Vf
and
9
Tp
3
4 RT
3R
Volume = VA + VB =
2
p
3
1
p
3
T
p
(S)A = n A c pA ln f R ln fA
TA
pA
4
2
= 2R
ln ln
3
3
1
Page 163 of 265
c PA =
R
1
4 RT
p
By: S K Mondal
Chapter 10
T
p
(S)B = n B c PB ln f R ln fB
TB
pB
2
1
= R
ln ln
3
3
1
= R ln + ln 3 +
+ ln
ln
9
3
1
4
32
27
= R ln
+
ln
Proved.
4
1
27
Q.10.33
Solution:
Try please.
Q.10.34
Solution:
Try please.
Q.10.35
Try please.
Q.10.36
By: S K Mondal
Chapter 10
Using S.F.E.E.
V2
Q W + 2 + g Z = h2 h1
2
or
Q W = mc p (T2 T1 )
=
mR(T2 T1 )
1
p1 v1 = mRT1
p2 v 2 = mRT2
p1 v1 p2 v 2
1 p1 v1
n 1
p n
=
1
p1 v1 2
p1
1
=
Q 0 and as
So
n 1
n
p
p1 v1 1
W=
p1
5
p
2
W = 3.5 p1 v1 1 proved
p1
Q.10.37
Solution:
p1 v1
200 0.5
=
= 0.33333 kJ/kg K
300
T1
Page 165 of 265
By: S K Mondal
Chapter 10
1.4
R =
0.33333 = 1.1667 kJ/kg K
cp =
1.4 1
1
c V = c p R = 0.83333 kJ/kg K
(b) Given p2 = 100 kPa
1
s2
p 1.3
v 2 = v1 1 = 0.85218 m3/kg
p2
V
p
s1 = c p ln 2 + cV ln 2
V1
p1
0.85218
100
= 1.1667 ln
+ 0.83333 ln
kJ/kg K
0.5
200
= 0.044453 kJ/kg K = 44.453 J/kg K
p
2
V
p 1.5
v2 = v1 1 = 0.7937 m3/kg
p2
0.7937
150
s2 s1 = 1.1667 ln
+ 0.83333 ln
kJ/kg K
0.5
200
= 0.03849 kJ/kg K
(d) n > is possible if cooling arrangement is used and S will be ve
Q.10.38
Solution:
p n
T2 = T1 2
= 457.9 K
p1
p V p2 V2
mR(T1 T2 )
=
W1 2 = 1 1
n 1
n 1
2 0.287(550 457.9)
=
= 211.46 kJ
1.25 1
Reversible polytropic process
Heat transfer
Q1 2 = u2 u1 + W1 2
= mc v (T2 T1 ) + W1 2
Page 166 of 265
2
V
By: S K Mondal
Chapter 10
Q.10.39
Solution:
V1 =
V2 = 0.010511 m3
P1
= 0.084091 m3
1.25
V
2
p2 = p1 1 = 100 81.25
V
2
p
n 1
p2 n
T2 = T1
1
p1
p1 V1 p2 V2
n 1
100 0.084091 1345.4 0.010511
=
1.25 1
= 22.93 kJ
Q1 2 = u2 u1 + W1 2
W1 2 =
= mc v (T2 T1 ) + W1 2
= 0.2 0.718 (492.77 293) 22.93
= 8.5865 kJ
Q.10.40
Solution:
By: S K Mondal
Chapter 10
p1 V1
= 0.89189 kg
RT1
p2 = 6 bar = 600 kPa
T2 = 120 C = 393 K
m=
T
p
2 = 2
T1
p1
n 1
n
1
V
T
ln 2
1
T1 = 0.2118
or 1 =
n
P
ln 2
P1
n = 1.2687
(a) The polytropic index, n = 1.2687
mRT2
0.189 0.287 393 3
m = 0.16766 m3
(b) Final volume of air (V1) =
=
600
p2
2
(c)
W1 2
pdV
1
p1 V1 p2 V2
n 1
Q1 2 = u2 u1 + W1 2
= mc v (T2 T1 ) + W1 2
= 0.89189 0.718(393 293) + W1 2
= 31.225 kJ
(d)
Q.10.41
Solution:
p
V
s = s2 s1 = m c v ln 2 + c P ln 2
p1
V1
600
0.16766
= 0.89189 0.718 ln
+ 1.005 ln
= 0.091663 kJ/K
150
0.5
m c
dT
By: S K Mondal
=
=
Chapter 10
m(c R) dT
mc dT mR dT
P
2000
= 1
T
(0.9169 + 2.577 10 4 T 3.974
298
2000
10 8 T 2 ) dT 1 0.287
dT kJ / kg
298
Tds = dh vdp
or
Tds = mc PdT v dp
2
2000
dT
T
1
298
2000
+ 2.577 10 4 (2000 298)
s2 s1 = 0.9169 ln
298
dS = m
cP
20002 2982
3.974 10 8
= 2.1065 kJ/kg K
Q.10.42
Solution:
p1
p
2
V
m=
p2
p1 v1
= 0.563 kg = 0.5643 kg
RT1
Page 169 of 265
By: S K Mondal
Chapter 10
8.3143
= 0.29694 kJ/kg
28
n
v1
p2 = p1 = 58.633 kPa
v2
RN2 =
V2 = 0.75 m3
n 1
p n
= 262.4 K
T2 = T1 2
p1
p V p2 V2
250 0.25 58.633 0.75
=
W= 1 1
= 57.891 kJ
n 1
(1.32 1)
Q = u2 u1 + W = mc v (T2 T1 ) + W
= 0.5643 0.7423 (262.4 373) + W
R
cv =
= 0.7423
1
= 1+
= 11.56 kJ
cp =
Q.10.43
Solution:
1.4
R =
0.29694 = 1.04 kJ/kg K
1.4 1
1
2
= 1.4
5
V
p
s = s2 s1 = m cP ln 2 + cV ln 2
V1
p1
0.75
58.633
= 0.5643 1.04 ln
+ 0.7423 ln
kJ/K
0.25
250
= 0.0373 kJ/kg K
V1 =
V2 = 1.5385
p1
T2 = 500C = 773 K
= 1.5385 m3 = V2
V=C
mRT2
(i) Find pressure (p2 ) =
V2
T
= 261 kPa 2.577 atm
(ii) Heat transfer Q =
mc
dT
= m [c P R]dT
S
Page 170 of 265
By: S K Mondal
Chapter 10
773
= 1
(1.1038 + 3.8675 10
0.51964) dT
300
(7732 3002 )
2
17.66 0.06188
+
T kJ/kg K
16
16
= 1.1038 + 3.8675 103 T = 1257.7 kJ/kg
cP =
(iii)
Work done =
pdV = 0
1
Tds = du = mc v dT
dT
dT
= m(c p R)
T
T
2
773
1 0.58411 + 3.8675 10 3 T
dS
=
dT
1
T
300
773
s2 s1 = 0.58411 ln
+ 3.8675 10 3 (773 300) = 2.3822 kJ/kg K
300
ds = mc v
Q.10.44
Solution:
= 1.66 bar
p2 = p1
V2
2
T
1
V
V
p
s = s2 s1 = c p ln 2 + cv ln 2
V1
p1
0.6
1.66
= 1.005 ln
kJ/kg K
+ 0.718 ln
1
0.9
= 0.043587 kJ/kg K
Q.10.45
By: S K Mondal
Chapter 10
its original state. Draw the cycle on p-v and T'-s coordinates. Show that
the cycle efficiency can be expressed in the following form
=1
Solution:
( 1) lnr
r 1/ 1
Where r is the pressure ratio, p2 /p1 . Determine the pressure ratio and
the cycle efficiency if the initial temperature is 27C and the maximum
temperature is 327C.
( Ans. 13.4, 32.4%)
Heat addition (Q1) = Q2 3 = mc p (T3 T2 )
p2
p1
T
2
1
1
S
p
Heat rejection (Q2) = mRT1 ln 2
p1
p
RT1 ln 2
Q
p1
= 1 2 = 1
C p (T3 T2 )
Q1
p
ln 2
1
p1
= 1
T3
T 1
1
Here,
p2
=r
p1
T3
p
= 3
T1
p1
cp =
= 1
And
(r
Proved
1)
ln r
1
1.4
T 1
600 1.4 1
r= 3
=
= 11.314
300
T1
(1.4 1)
ln (11.314)
= 1
1.4 1
(1.4)
[ (11.314) 1.4 1
= 0.30686
R
1
= r
By: S K Mondal
Q.10.46
Solution:
Chapter 10
2
8.3143
8.3143
5
300 ln (5) + 0.0224
300 ln
= 0.0064
32
28
4
= 1.248 kJ = 1248 J
A closed adiabatic cylinder of volume 1 m 3 is divided by a partition into
two compartments 1 and 2. Compartment 1 has a volume of 0.6 m 3 and
contains methane at 0.4 MPa, 40C, while compartment 2 has a volume of
0.4 m 3 and contains propane at 0.4 MPa, 40C. The partition is removed
and the gases are allowed to mix.
(a) When the equilibrium state is reached, find the entropy change of
the universe.
(b) What are the molecular weight and the specific heat ratio of the
mixture?
The mixture is now compressed reversibly and adiabatically to 1.2
MPa. Compute
(c) the final temperature of the mixture,
(d) The work required per unit mass, and
(e) The specific entropy change for each gas. Take c p of methane and
Q.10.47
Solution:
0.6
400 = 240 kPa
1
V1 = 0.6 m3
p1 = 400 kPa
T1 = 313 K
CH4
2
V2 = 0.4 m3
p2 = 400 kPa
T2 = 313 K
C3 H8
By: S K Mondal
Chapter 10
T
p
( S)CH4 = mCH4 c PCH ln 2 R ln 2
4
T1
p1
p
= mCH4 RCH4 ln i
pf
(a)
p
p1 V1
RCH4 ln i
RCH4 T1
pf
p
p1 V1
RCH4 ln i
pf
T1
1
p2 V2
pi
=
ln
T2
pf2
=
( S)C3H8
(b)
Molecular weight
xM = x1M1 + x2M2
x
x
Q.10.48
mix
c P mix
=
c v mix
51.256
= 1.1936
42.9417
1/
1 a 1
rk 1 a 1
=1
Solution:
Q2 3 = u3 u2 + pdV = mc v (T3 T2 )
Page 174 of 265
By: S K Mondal
Chapter 10
Q1 4 = mc p (T4 T1 )
= 1
m c p (T4 T1 )
m c v (T3 T2 )
T T1
= 1 4
T3 T2
1
v
T2
= 1
= rk 1
T1
v
2
T2 = T1 rk 1
1
p
T3
= 3
T4
p4
p3
=9
p2
p v
p2 v 2
= 3 3
T2
T3
T
3 = (a r)
T4
p
= 3
p1
V=C
3
Q1
W
V 1
= 2
V1 a
= (rk a 1 )
T4 = rk1 . a
1
k
1
= r
.a
p
p
= 1 2
p2 p3
= 1
Q1
2
. a T1 . rk 1
Q2
S
(a T1 T1 )
(aT1rk 1 T1rk 1 )
1
[ (a 1)]
= 1 1
Proved.
rk (a 1)
Given p1 = 1 bar = 100 kPa
T1 = 300K,
a = 2.5,
Q2
= a . T1
. T3
1
1
r1
r
p
T
3 = 3 = a,
p2
T2
p
= 1
p3
p=C
v
p2
= 1 = a
p1
v2
T3 = aT2 = aT1rk 1
p
T4
= 4
T3
p3
rk = 6,
= 1.4
By: S K Mondal
Chapter 10
1
1.4(2.51.4 1)
= 1 1.4 1
= 0.57876
6
(2.5 1)
Q1 = mc v (T3 T2 )
= m c v (aT1rk 1 T1rk 1 )
= m c v T1rk 1 (a 1)
= m 0.718 300 60.4 (2.5 1)
= 661.6 m kJ
W = Q1 = 382.9 m kJ
1
V4 V1 = 0.7957 m3
Let m.e.p. is pm then
pm ( V4 V1 ) = W
382.9 m
kPa
pm =
0.7957 m
= 481.21 kPa = 4.8121 bar
Q10.49
Solution:
Q10.50
Solution:
Q10.51
The relation between u, p and v for many gases is of the form u = a + bpv
where a and b are constants. Show that for a reversible adiabatic
process pv y = constant, where
= (b + 1)/b.
Try please.
(a) Show that the slope of a reversible adiabatic process on p-v
coordinates is
dp
1 cp
1 v
=
wherek =
dv kv c v
v p T
(b) Hence, show that for an ideal gas, pv = constant, for a reversible
adiabatic process.
Try please.
A certain gas obeys the Clausius equation of state p (v b) = RT and has
its internal energy given by u = c v T. Show that the equation for a
reversible adiabatic process is p ( v b ) = constant, where = c p / c v .
Solution:
Try please.
By: S K Mondal
Q10.52
Solution:
Q10.53
Chapter 10
Solution:
Q10.54
Solution:
Q10.55
Solution:
(d) 21 kPa for O2 ' (e) 0.84 m3 /kg, (f) 1.47 kg)
O2: N2 = 23: 77
23 77
:
32 28
= 0.71875: 2.75
(100)
2.75 100
:
(0.71875 2.75)
2.75
= 20.72: 79.28
Page 177 of 265
= 0.71875
By: S K Mondal
(b)
Chapter 10
O2 = 23 kg, N2= 77 kg
R=
23 R O2 + 77 R N2
23 + 77
8.3143
8.3143
+ 77
32
28
=
23 + 77
= 0.2884 kJ/kg K
23
(c)
(d)
Partial pressure of O2 = x O2 p
= 0.2072 101.325 kPa = 20.995 kPa
Partial pressure of N2 = x N 2 p = 0.7928 101.325 kPa = 80.33 kPa
(e)
RT
0.2884 288 3
=
m / kg = 0.81973 m3/kg
101.325
= 1 + 2
pN 2
pO2
1
1
1
+
=
+
=
v
v1 v 2
R O2 288 R N2 288
Sp. volume, v =
Density
(f)