Beruflich Dokumente
Kultur Dokumente
Spring 2008
ME210/Advanced Thermodynamics
Final Exam, Tuesday, May 20, 2008
(19:45-22:00, 2 hours and 15 minutes, open book & notes)
U = Ui Uf =
1
1
1
1
m o v i2 m o v f2 = m o ( v i2 v f2 ) =
(0.8)( 200 2 0 2 )
2
2
2
2gc
= 497 lbf-ft
Solution:
(a)
Assuming constant cp
Q = mmix cp (Tf -Ti)
3
i =1
NiMi
kJ
c pi = 0.3077 x2.254 + 0.2692x1042
.
+ 0.423 x0.842 = 133
.
kg K
i=1 m mix
c p = mi cpi =
cv =
NiMi
kJ
c vi = 0.3077 x1735
.
+ 0.2692 x0.745 + 0.423 x0.653 = 1011
.
kg K
i =1 m mix
mi c vi =
i =1
Solution:
a)
G0<0, so the reaction is spontaneous at 298 K: a mixture of SO2(g), O2(g), and
SO3(g) in their standard state (1 atm) will spontaneously yield more SO3(g).
With S0<0, the term TS0>0 and becomes more positive at higher T.
Therefore, G0 will be less negative, and the reaction less spontaneous, with
increasing T.
b)
Calculating G0 at 9000C,
G0=H0-TS0= -198.4 kJ [(273+900)K](-187.9 J/K)(1 kJ/1000J) = 22 kJ
G0>0, so the reaction is nonspontaneous at the higher T.
Assuming the ideal-gas turbine and regenerator shown below, draw the p-v and
T-s diagrams and find Qin and the ratio of compressor to turbine work (i.e., back
work ratio).
4
1660oR
Solution:
rp =
P2
75
=
= 5.102
P1 14.7
k 1
= 1
T1 k
540
rp = 1
5.102
T4
1660
1.4 1
1.4
= 0.482
W
800 x0.70626
Btu
Q in = out =
= 1172.2
sec
0.482
Assuming isentropic compression and expansion:
o
P
T2 = T1 2
P1
T5 = T4 rp
1k
k
k 1
k
75
= 540
14.7
= 1660 x5.102
1.4 1
1.4
11.4
1.4
= 860.214 o R
= 1042 o R
kj
Btu
= 76.85
kg
lbm
kj
Btu
= c p ( T4 T5 ) = 1(1660 1042) = 618
= 148.304
kg
lbm
w comp
w turb
76.85
= 0.518
148.304
Solution:
v4
v
1
+ R air T1 ln 2 = R air T3 ln(r ) + R air T1 ln
v3
v1
r
4
wout = 53.34 (1460)ln(10)+53.34(660)ln(0.1) = 9.826x10 ft-lbf/lb
w out = w 3 4 + w 1 2 = R air T3 ln
= 1
qin =
TL
T
660
= 1 1 = 1
= 0.548
1460
TH
T3
0.548 x778
Exit temperature
Exit specific volume
The sign of the Joule-Thomson coefficient for this process and if it is
consistant with your answer in (a)
What should we do if we want the opposite of answer in (c) without
changing the upstream and exit pressures?
Solution:
(a) The inlet temperature and enthalpy of R-134a, from the refrigerant tables
(Tables A-11 through 13, pg. 902-905) is:
For P1=0.7 MPa === T1=Tsat=26.69 oC, h1=hf=88.82 kJ/kg
Assuming a throttling process, i.e.,
Q W = KE KE 0
At the final state, P2=160 kPa, the enthalpy is the same, i.e. h=88.82
kJ/kg. Again from the tables @ p=160 kPa:
Tsat= -15.60 oC, hf=31.21 kJ/kg, hg=241.11 kJ/kg
Note that hf <h< hg
Therefore, the refrigerant exists as a saturated mixture at the exit state at
T2 = Tsat = -15.60oC
T=T2-T1= -15.6 - 26.69= -42.3oC
(b)
The quality at this state is determined from
x2 =
h2 h f
h fg
88.82 31.21
= 0.2745
209.9
(c)
15.6 26.69
= 0.08
160 700
K/kPa