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Evaporators 8.5-4 Soln
Evaporators 8.5-4 Soln
26 C
From Fig. 8.4-2 Duhring lines for aqueous solutions of NaOH
BPR3 = T3 Tsat
= (79 38.26) C
= 40.74 C
= 3 628.8
kg
h
= V1 = V2 = V3
F = L1 + V2
13 608 = L1 + 3 628.8
kg
L1 = 9 979.2 h
(E2) L1 = L2 + V2
9 979.2 = L2 + 3 628.8
kg
L2 = 6 350.4 h
(E3) L2 = L3 + V3
6 350.4 = L3 + 3628.8
L3 = 2721.6
kg
h
Tsat = 38.26 C
= (79 38.26) C :
(E2) x2 = 0.214 T3 = 79
BPR2 = T2 T3
BPR3 = 40.74 C
= (88.5 79) C :
BPR2 = 9.5 C
Tavailable
= (93.75 88.5) C
BPR1 = 5.25 C
Tavailable
= 19.48 C
T1
= T
=
T2
T1
19.48
1
U2
1
1
1
+
+
U1 U2 U3
19.48
1
3407
1
1
1
+
+
6246 3407 2271
19.48
1
2271
1
1
1
+
+
6246 3407 2271
6.40 C
= T
1
6246
1
1
1
+
+
6246 3407 2271
3. 49 C
= T
1
U1
1
1
1
+
+
U1 U2 U3
1
U3
1
1
1
+
+
U1 U2 U3
9.60 C
T2 = 6.02 C
T3 = 7.59
Calculating the actual boiling point of the solution and the condensing
temperature in each effect,
(E1) T1
= TS1 - T1
107.35 C
= (113.23 5.88) C
T1 =
TS1 =
113.23 C
(E1) T2
96.08 C
T2 =
TS2
102.1 C
= T1 - BPR1
TS2 =
= (107.35 5.25) C
(E1) T3
78.99 C
T3 =
TS3
86.58 C
= T2 BPR2
TS2 =
= (96.08 9.5) C
(E2)
(E3)
Condenser
TS1 = 113.23 C
TS4 = 38.26 C
TS2 = 102.1 C
TS2 = 86.58 C
T1 = 107.35 C
T2 = 96.08 C
T3 = 78.99 C
@TF = 37.8 C,
xF = 0.10
hF = 160.10
L1 :
hF = 438.50
kJ
kg
L2 :
hF = 367.00
kJ
kg
L3 :
hF = 295.75
kJ
kg
kJ
kg
= 2 679.33 + 1.884(5.25)
S1 = HS1 hS1
kJ
S1 = 2 221.37 kg
= 2696.35 474.98
= 2 654.49 + 1.884(9.5)
S2 = H1 hS2
kJ
S2 = 2 261.31 kg
= 2 689.22 427.91
= 2 571.17 + 1.884(40.74)
S3 = H2 hS3
kJ
S3 = 2 309.85 kg
= 2 672.39 362.54
eqn 1
eqnn 3
kJ
kg
L1 = 10 190.18
kJ
kg
L2 =
kJ
kg
6 521.66
Then,
V1 = 3 417.82
800.06
kJ
kg
V2 = 3 668.52
kJ
kg
V3 = 3
kJ
kg
1000
= 5 168.4(2221.37)( 3600 ) =
3.189 x 106 W
q2 = V1S2
1000
= 3 417.82(2261.31)( 3600 )=
2.147 x 106 W
q3 = V2S3
1000
= 3 668.52(2309.85)( 3600 )=
2.354 x 106 W
A1 =
q1
U 1 T 1
A2 =
q2
U 2 T 2
A3 =
q3
U 3 T 3
3.189 x 10
6 247 (5.88)
= 86.83 m2
2.147 x 106
3 407(6.02)
= 104.68 m2
2.354 x 10
2 271(7.59)
= 136.57 m2
Am =
109.36 m2
Trial 2
kJ
kg
L2 = 6 521.66
kJ
kg
L3 = 2
kJ
kg
= (79 38.26) C :
BPR3 = 40.74 C
(E2) BPR2 = T2 T3
= (87.8 79) C :
BPR2 = 8.8 C
(E1) BPR1 = T1 T2
= (92.9 87.8) C
Tavailable
BPR1 = 5.1 C
Tavailable
= 20.33 C
T 1 A 1
Am
5.88 (86.83)
109.36
4.66 C
T2 =
T 2 A 2
Am
6.02(104.68)
109.36
5.76 C
T3 =
T 3 A 3
Am
7.59(136.57)
109.36
9.48 C
Adjusted temperature,
T1 = 4.98 C
T2 = 5.85 C
T3 = 9.50
Calculating the actual boiling point of the solution and the condensing
temperature in each effect,
(E1) T1
= TS1 - T1
108.25 C
= (113.23 4.98) C
:
TS1 =
113.23 C
T1 =
(E1) T2
97.3 C
TS2
= T1 - BPR1
103.15 C
(E1) T3
C
TS3
= (108.25 5.1) C
T2 =
TS2 =
T3 = 79.0
= T2 BPR2
TS2 = 88.5
= (97.3 8.8) C
@TF = 37.8 C,
xF = 0.10
hF = 160.10
L1 :
L2 :
@T2 = 97.3 C,
x2 = 0.209
hF = 375
kJ
kg
L3 :
@T3 = 79v C,
x3 = 0.500
hF = 300
kJ
kg
hF = 420.10
kJ
kg
kJ
kg
= 2 680.95 + 1.884(5.1)
S1 = HS1 hS1
kJ
S1 = 2 221.37 kg
= 2696.35 474.98
= 2 657.64 + 1.884(8.8)
S2 = H1 hS2
kJ
S2 = 2 258.22 kg
= 2 690.56 432.34
= 2 571.17 + 1.884(40.74)
S3 = H2 hS3
kJ
S3 = 2 303.61 kg
= 2 674.22 370.61
eqn 1
eqnn 3
kJ
kg
L1 = 10 116.24
kJ
kg
L2 =
kJ
kg
6 488.32
Then,
V1 = 3 491.76
766.72
kJ
kg
V2 = 3 627.92
kJ
kg
V3 = 3
kJ
kg
1000
= 5 161.67(2221.37)( 3600 )=
3.185 x 106 W
q2 = V1S2
1000
= 3 491.76(2258.22)( 3600 )=
2.190 x 106 W
q3 = V2S3
1000
= 3 627.92(2303.61)( 3600 )=
2.321 x 106 W
A1 =
q1
U 1 T 1
A2 =
q2
U 2 T 2
3.185 x 10
6 247 (4.98)
= 102.39 m2
2.190 x 106
3 407(5.85)
= 109.88 m2
A3 =
q3
U 3 T 3
2.321 x 10
2 271(9.50)
= 107.58 m2
Am =
106.62 m2
The new computed values of A, though not equal are quite near to each
other. Therefore, an Am of 106.62 m2 can be concluded at S of 5 161.67
for the process.
kJ
kg