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Thermodynamics I
Lecture 10: Closed and steady-state open system
Jan 25, 2016
(1)
When simplified,
0
0
v
g
7
*0
>+ dW
d U + + z =
dQ
s + dWEC
2gc gc
(2)
dU = P dV
(3)
2
Since the pressure (P ) depends on temperature (T ), we need to combine the ideal gas
equation with the first law equation,
Cv dT = RT
Cv
R
dV
dT = dV
V
T
V
(4)
T
Ti
(Cv /R)
Ti P
= i
P T
(6)
T
Ti
(Cv /R)
T
=
Ti
T
Ti
(Cv /R)+1
=
P
Pi
(7)
which becomes
T
Ti
(Cp /R)
=
P
Pi
(8)
We may also insert the ideal gas law into eqn. (5.) to convert to a formula relating P
and V, using PV/R,
(Cp /R)
PV
Vi
=
(9)
P iV i
V
i (R/Cv ) i i (R/Cv )+1 i (Cp /Cv )
P
V
V
V
V
=
=
=
(10)
i
P
V
V
V
V
In general,
P V (Cp /Cv ) = const
2
(11)
(12)
= 0, W
EC = 0),
Considering all assumptions (i.e. KE = 0, PE = 0, Q
in
0
v 2 g
7
0 = H + + z min H +
2gc gc
out
0
0
v 2 g
*0
7
out
W
+
z
Q
+
m
+
EC + W s
2gc gc
0
(13)
when simplify,
s = H m
s
0 = (H in H out )m
+W
+W
(14)
(15)
Recall the equation of shaft work and combine with the ideal gas equation,
dWs = dH = V dP
Cp dT = RT
dP
Cp
R
dT = dP
P
T
P
(16)
(17)
P2
P1
(R/Cp )
(18)
Steady-state adiabatic, reversible processing of an ideal gas results in the same relations
as Example 2.11. (i.e. eqn. (18.) is equal to eqn. (8.))
Note that this equation (8.) or (18.) are usually used as an approximation for both
open and closed systems.
T2 = (298 K)
25 bar
5 bar
27
= 472 K
(19)
Adapting the adiabatic energy balance equation (18.) and assuming the heat capacity
at constant pressure (Cp ig ) = constant,
"
#
(R/Cpig )
P
2
Wsig = H ig = Cpig T = Cpig T1
1
(20)
P1
7
Wsig = Cpig T = RT = (3.5)(8.314)(472 298) = 5063 J/mol
2
(21)
J
mole
1hr
= 5063
1000
mole
hr
3600sec
1hp
745.7 Js
!
= 1.9 hp
(22)
Z
P dV =
V2
RT
)dV = RT ln( )
V
V1
(23)
For an isothermal, ideal gas, V2 /V1 = P1 /P2 . Noting the reciprocal and negative
logarithm,
V2
P2
WEC = RT ln( ) = RT ln( )
(24)
V1
P1
The flow work performed on an ideal gas packet of unit mass is
Wf low = P Vout P Vin = RTout RTin = 0
(25)
The total requirement for isothermally compressing an ideal gas packet of unit mass is
P2
Ws = RT ln
= (8.314)(298)ln(5) = 3987 J/mol
(26)
P1
4
1hp
745.7 Js
!
= 1.5 hp
(27)
(29)
(225 201.4)
(2919.9 2792.8) = 2854.5 kJ/kg
(250 201.4)
(30)
(1.5
1.4)
H(1.5 M P a, 225o C) = (2865.5) +
(2854.5 2865.5) = 2860 kJ/kg
(1.6 1.4)
(31)
(120 100)
(2776.6 2675.8) = 2716.1 kJ/kg
(150 100)
(32)
(33)
of the turbine:
Step 4: Focus on system A, estimate the heat loss (Q)
Assumptions: Steady state flow; KE and PE are negligible
in
g
v2
+ z min
0=
H+
2g
gc
c
inlets
out
X
v2
g
+ W s
H+
+ z
mout + Q
2g
g
c
c
outlets
X
(34)
(35)
(36)
(37)
At Psat = 0.79 MPa, from the saturation pressure table, HL = 718.5 kJ/kg and H vap =
2049 kJ/kg. (Interpolation!)
q=
2716.1 718.5
H3 H L
=
= 0.975
vap
H
2049
(38)
(39)
H Lm
L + HV m
V
m
3
(40)
H L (m
3m
V ) + HV m
V
m
3
(41)
H Lm
3 H Lm
V + HV m
V
m
3
(42)
H3 =
H Lm
3m
V (H L H V )
m
3
(43)
H3 =
H Lm
3+m
V (H V H L )
m
3
(44)
H3 =
H3 =
H3 =
H3 = H L +
m
V
(H V H L )
m
3
H3 = H L + q(H vap )
(45)
(46)
where q is the vapor mass fraction of stream 3 and H vap is the difference of the
enthalpy of vapor and the enthalpy of liquid in stream 3.