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T0 R 0
2 0
3 0 TT
0
T
CP
dT ICPH (T0 ,T , A, B,C, D )
T0 R
Q = H = n × R × ICPH
(a) If 10 mol of SO2 is heated from 200 to 1100C, the heat requirement will be 10*R*ICPH, where ICPH
is the heat capacity integral. Using our spreadsheet to evaluate ICPH, we get
T 1 (K) T 2 (K) A B (1/K) C (1/K2) D (K2) ICPH (K)
473.15 1373.15 5.699 8.01E-04 0 -1.02E+05 5.65E+03
-1 -1
So, the heat requirement is 10 mol*8.314 J mol K *5650 K = 469700 J = 470 kJ
(b) Similarly, if we heat 12 moles of propane from 250 to 1200 C, the heat requirement is 12*R*ICPH.
Putting the heat capacity parameters for propane and these temperatures into the ICPH spreadsheet
gives
T 1 (K) T 2 (K) A B (1/K) C (1/K2) D (K2) ICPH (K)
523.15 1473.15 1.213 2.88E-02 -8.82E-06 0.00E+00 1.95E+04
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SVNAS 8th Edition Annotated Solutions Chapter 4
So, the total heat requirement is 12 mol*8.314 J mol-1 K-1*19500 K = 1.95106 J = 1950 kJ
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SVNAS 8th Edition Annotated Solutions Chapter 4
(b) Similarly, if we add 2500 kJ to 15 mol of 1-butene, we have H/R = 2500000 J / (15 mol *8.314 J mol-
1
K-1 )= 20045 K. Putting the heat capacity coefficients for 1-butene into the spreadsheet and trying
final temperatures until we get this value, we get
2 2
T 1 (K) T 2 (K) A B (1/K) C (1/K ) D (K ) ICPH (K)
533 1414 1.967 3.16E-02 -9.87E-06 0.00E+00 2.005E+04
So, the final temperature is 1414 K.
(c) This is the same, but in English units, in which we can use R = 1.986 Btu lbmol-1 R-1, so H/R = 106
Btu / (40 lbmol *1.986 Btu lbmol-1 R-1) = 12588 R = 6993 K. The initial temperature of 500 F is 533
K. So, we get
T 1 (K) T 2 (K) A B (1/K) C (1/K2) D (K2) ICPH (K)
533 1202.7 1.424 1.44E-02 -4.39E-06 0.00E+00 6.994E+03
And the final temperature is 1203 K = 1705 F.
4.3 (New)
To compute the outlet temperature, use
But first the heat capacity at 373.15 K must be determine for each compound using the Table C.1 and Eqn
4.5.
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SVNAS 8th Edition Annotated Solutions Chapter 4
Q=
122 F
nC p dT
The ideal gas heat capacity for air is given in table C.1 as
(
C p = R A + BT + DT −2 )
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SVNAS 8th Edition Annotated Solutions Chapter 4
T must be in Kelvins for use in this expression, so we convert 122F to 323.15 K and 932 F to 773.15 K.
We then have
773 K
Q = nR
323 K
A + BT + DT −2 dT
773 K
B D
Q = nR AT + T 2 −
2 T 323 K
Putting in n = 0.59 lbmol s , R = 1.986 Btu lbmol-1 R-1, A = 3.355, B = 0.57510-3 K-1, D = -1600 K2 gives
-1
Note that because the heat capacity integral comes out with units of K, while we are using R with units of
R, we have to multiply by 1.8 R/K.
4.5 (7th edition Prob. 4.4) How much heat is required when 10,000 kg of CaCO3 is heated at atmospheric
The number of moles of CaCO3 is 107 g/ 100.09 g mol-1 = 99910.08 mol CaCO 3. Evaluating the heat
(
(C ) = A + B T ( + 1) + C T 2 2 + +1 )
p 1
2 1 3
where T2/T1. DefineCPam as the value of CP evaluated at the arithmetic mean temperature Tam.
Then:
Where
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SVNAS 8th Edition Annotated Solutions Chapter 4
Whence,
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SVNAS 8th Edition Annotated Solutions Chapter 4
th
4.7. (7 edition prob. 4.6)
where τ ≡ T2/ T1. Define CPam as the value of CP evaluated at the arithmetic mean
temperature Tam.
Whence,
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SVNAS 8th Edition Annotated Solutions Chapter 4
𝑇1
�
�
1
th
4.8. (7 edition prob. 4.7)
Let step 12 represent the initial reversible adiabatic expansion, and step 23
the final constant-volume heating.
Given
R/C p
P
T =T 2
2 3
P3
Solve for Cp
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SVNAS 8th Edition Annotated Solutions Chapter 4
B) is 469.7 K. So, 25C corresponds to a reduced temperature of Tr1 = 298.15/469.7 = 0.6348. The normal
boiling point for n-pentane (also from appendix B) is 309.2 K, which corresponds to a reduced temperature
Tr2 = 309.2/469.7 = 0.6583. So, using equation 4.14, we have
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SVNAS 8th Edition Annotated Solutions Chapter 4
0.38
1 − Tr 2 1 −0.6583
0.38
H = H = 366.3 = 357.1 J g -1
2 1 1− 0.6348
1− Tr1
This is essentially exact agreement with the handbook value (it differs by 0.03%).
(b) In this part, we estimate the heat of vaporization at the normal boiling point without using the
information on the heat of vaporization at 25C, using equation 4.13
also use the critical pressure, Pc = 33.70 bar for n-pentane. Then, using equation 4.13:
1.092 ( ln Pc −1.013) 1.092 ( ln 33.7 −1.013)
H = RT = 8.314*309.2 = 25876 J mol-1
0.930 − T 0.930 − 0.6583
n n
rn
-1
Dividing by the molecular weight of n-pentane (72.15 g/mol) gives Hn = 358.6 J g . This is just 0.4%
higher than the handbook value, and it only required knowledge of the critical properties and the normal
boiling point temperature.
4.11. (Like 7th edition 4.10, but in different units, solutions below are for 7th edition version and
We want to evaluate the latent heat of vaporization using the Clapeyron equation:
dP sat
H = T V
dT
3 -1 3 -
(a) At -16C, we see that the vapor volume is 0.12551 m kg and the liquid volume is 0.000743 m kg
, so V = 0.124767 m kg . Now, we can estimate the slope of the vapor pressure curve from the
1 3 -1
values at -18, -16, and -14 C, which are 1.446,1.573, and 1.708 bar, respectively. So, we could
estimate the slope as
dP sat P 1.708bar − 1.446
bar
= = 00.0655bar.K-1 = 0.0655*102 kPa.K −1
dT T (273.15 + (−14))K − (273.15 + (−18))K
So, we have
H = (273.15 + (−16))K * 0.124767m3 .kg −1 * 0.0655 *102 kPa.K −1 = 210.4kPa.m3 .kg −1 = 210.4kJ.kg −1
3 -1 3 -
(b) At 0C, we see that the vapor volume is 0.069309 m kg and the liquid volume is 0.000722 m kg
1
, so V = 0.068587 m3kg-1. Now, we can estimate the slope of the vapor pressure curve from the
values at -2, 0, and 2 C, which are 2.722,2.928, and 3.146 bar, respectively. So, we could estimate
the slope as
UpdateddP 18/01/2017
sat
P − 10
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SVNAS 8th Edition Annotated Solutions3.146bar 2.722bar Chapter 4
= = 0.106bar.K-1 = 0.106 *102 kPa.K −1
dT T (273.15 + (2))K − (273.15 + (−2))K
So, we have
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SVNAS 8th Edition Annotated Solutions Chapter 4
H = (273.15 + (0))K * 0.068587m3 .kg −1 * 0.106 *102 kPa.K −1 =198.59kPa.m3 .kg −1 = 198.59kJ.kg−1
(c) At 12C, we see that the vapor volume is 0.046332 m3kg-1 and the liquid volume is 0.000797 m3kg-
1
, so V = 0.045535 m3kg-1. Now, we can estimate the slope of the vapor pressure curve from the
values at 10, 12, and 14 C, which are 4.146,4.43, and 4.732 bar, respectively. So, we could
estimate the slope as
dP sat P 4.732bar − 4.146bar
= = 0.1465bar.K-1 = 0.1465*102 kPa.K −1
dT T (273.15 + (14))K − (273.15 + (10))K
So, we have
H = (273.15 + (12))K * 0.045535m3 .kg −1 * 0.1465 *102 kPa.K −1 = 190.22kPa.m3 .kg −1 =190.22kJ.kg−1
(d) At 26C, we see that the vapor volume is 0.029998 m3kg-1 and the liquid volume is 0.000831 m3kg-
, so V = 0.029167 m kg . Now, we can estimate the slope of the vapor pressure curve from the
1 3 -1
values at 24, 26, and 28 C, which are 6.458,6.854, and 7.269 bar, respectively. So, we could
estimate the slope as
dP sat P 7.269bar − 6.458bar
= = 0.20275bar.K-1 = 0.20275*102 kPa.K −1
dT T (273.15 + (28))K − (273.15 + (24))K
So, we have
H = (273.15 + (26)K * 0.029167m3 .kg −1 * 0.20275 *102 kPa.K −1 = 176.91kPa.m3 .kg −1 =176.91kJ.kg−1
3 -1 3 -
(e) At 40C, we see that the vapor volume is 0.019966 m kg and the liquid volume is 0.000872 m kg
1
, so V = 0.019094 m3kg-1. Now, we can estimate the slope of the vapor pressure curve from the
values at 35, 40, and 45 C, which are 8.87, 10.166 and 11.599 bar, respectively. So, we could
estimate the slope as
dP sat P 11.599bar − 8.87bar
= = 0.2729bar.K-1 = 0.2729 *102 kPa.K −1
dT T (273.15 + (45))K − (273.15 + (35))K
So, we have
H = (273.15 + (40)K * 0.019094m3 .kg −1 * 0.2729 *102 kPa.K −1 = 163.17kPa.m3 .kg −1 = 163.17kJ.kg−1
Updated 18/01/2017 12
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SVNAS 8th Edition Annotated Solutions Chapter 4
4.12 (7th edition Prob. 4.11)
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SVNAS 8th Edition Annotated Solutions Chapter 4
(a) Equation 4.14 is used to estimate the latent heat at a temperature of interest from the (known) latent
heat at some other temperature, and may be written as:
0.38
1 −Tr 2
H = H
2 1
1− Tr1
For chloroform, the critical temperature is 536.4 K and the normal boiling point is 334.3 K. At 273 K, Tr1
= 0.5089 and at 334.3 K, Tr2 = 0.6232. So,
0.38
1 −0.6232
H 2 = 270.9 J g -1 = 245.0 J g -1
1− 0.5089
Similarly for tetrachloromethane (also known as carbon tetrachloride!), Tr1 = 0.4909 and Tr2 = 0.6287, so
0.38
1 −0.6287
H 2 = 217.8 J g -1 = 193.2 J g -1
1− 0.4909
(b) Equation 4.13 is used to estimate the heat of vaporization at the normal boiling point without knowing
the heat of vaporization at any temperature. It can be written as
1.092 ( ln Pc −1.013)
H n = RTn
0.930 − T
rn
where Pc, the critical pressure, must be given in bar. For chloroform, we get
1.092 ( ln ( 54.72 )−1.013 ) -1
-1 -1
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