Appendix A.3. Physical Properties of Inorganic and Organic Compounds
A.3-1. Standard Heats of Formation at 298.15 K (25°C) and 101.325 kPa (1 Atm Abs), (c) = crystalline, (g) = gas, (l) = liquid
Compound
(kJ/kg mol)10−3
kcal/g mol
Compound
(kJ/kg mol)10−3
kcal/g mol
NH3(g)
−46.19
−11.04
CaCO3(c)
−1206.87
−288.45
NO(g)
+90.374
+21.600
CaO(c)
−635.5
−151.9
H2O(l)
−285.840
−68.3174
CO(g)
−110.523
−26.4157
H2O(g)
−241.826
−57.7979
CO2(g)
−393.513
−94.0518
HCN(g)
+130.1
+31.1
CH4(g)
−74.848
−17.889
HCl(g)
−92.312
−22.063
C2H6(g)
−84.667
−20.236
H2SO4(l)
−811.32
−193.91
C3H8(g)
−103.847
−24.820
H3PO4(c)
−1281.1
−306.2
CH3OH(l)
−238.66
−57.04
NaCl(c)
−411.003
−98.232
CH3CH3OH(l)
−277.61
−66.35
NH4Cl(c)
−315.39
−75.38
Source: J. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973; and O. A. Hougen, K. M. Watson, and R. A. Ragatz, Chemical Process Principles, Part I, 2nd ed. New York: John Wiley & Sons, Inc., 1954.
A.3-2. Standard Heats of Combustion at 298.15 K (25°C) and 101.325 kPa (1 Atm Abs) (g) = gas, (l) = liquid, (s) = solid
Compound
Combustion Reaction
kcal/g mol
(kJ/kg mol)10−3
C(s)
−26.4157
−110.523
CO(g)
−67.6361
−282.989
C(s)
C(s) + O2(g) → CO2(g)
−94.0518
−393.513
H2(g)
−68.3174
−285.840
H2(g)
−57.7979
−241.826
CH4(g)
CH4(g) + 2O2(g) → CO2(g) + 2H2O(l)
−212.798
−890.346
C2H6(g)
−372.820
−1559.879
C3H8(g)
C3H8(g) + 5O2(g) → 3CO2(g) + 4H2O(l)
−530.605
−2220.051
d-Glucose (dextrose) C6H12O6(s)
C6H12O6(s) + 6O2(g) → 6CO2(g) + 6H2O(l)
−673
−2816
Lactose (anhydrous) C12H22O11(s)
C12H22O11(s) + 12O2(g) → 12CO2(g) + 11H2O(l)
−1350.1
−5648.8
Sucrose C12H22O11(s)
C12H22O11(s) + 12O2(g) → 12CO2(g) + 11H2O(l)
−1348.9
−5643.8
Source: R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973; and O. A. Hougen, K. M. Watson, and R. A. Ragatz, Chemical Process Principles, Part I, 2nd ed. New York: John Wiley & Sons, Inc., 1954.
Figure A.3-1. Mean molar heat capacities from 77°F (25°C) to t°F at constant pressure of 101.325 kPa (1 atm abs). (From O. A. Hougen, K. M. Watson, and R. A. Ragatz, Chemical Process Principles, Part I, 2nd ed. New York: John Wiley & Sons, Inc., 1954. With permission.)
A.3-3. Physical Properties of Air at 101.325 kPa (1 Atm Abs), SI Units
T (°C)
T (K)
ρ (kg/m3)
cp (kJ/kg·K)
μ × 105 (Pa · s, or kg/m · s)
k (W/m · K)
NPr
β × 103 (1/K)
gβρ2/μ2 (1/K · m3)
−17.8
255.4
1.379
1.0048
1.62
0.02250
0.720
3.92
2.79 × 108
0
273.2
1.293
1.0048
1.72
0.02423
0.715
3.65
2.04 × 108
10.0
283.2
1.246
1.0048
1.78
0.02492
0.713
3.53
1.72 × 108
37.8
311.0
1.137
1.0048
1.90
0.02700
0.705
3.22
1.12 × 108
65.6
338.8
1.043
1.0090
2.03
0.02925
0.702
2.95
0.775 × 108
93.3
366.5
0.964
1.0090
2.15
0.03115
0.694
2.74
0.534 × 108
121.1
394.3
0.895
1.0132
2.27
0.03323
0.692
2.54
0.386 × 108
148.9
422.1
0.838
1.0174
2.37
0.03531
0.689
2.38
0.289 × 108
176.7
449.9
0.785
1.0216
2.50
0.03721
0.687
2.21
0.214 × 108
204.4
477.6
0.740
1.0258
2.60
0.03894
0.686
2.09
0.168 × 108
232.2
505.4
0.700
1.0300
2.71
0.04084
0.684
1.98
0.130 × 108
260.0
533.2
0.662
1.0341
2.80
0.04258
0.680
1.87
0.104 × 108
A.3-3. Physical Properties of Air at 101.325 kPa (1 Atm Abs), English Units
T (°F)
μ (centipoise)
NPr
β × 103 (1/°R)
gβρ2/μ2 (1/° R · ft3)
0
0.0861
0.240
0.0162
0.0130
0.720
2.18
4.39 × 106
32
0.0807
0.240
0.0172
0.0140
0.715
2.03
3.21 × 106
50
0.0778
0.240
0.0178
0.0144
0.713
1.96
2.70 × 106
100
0.0710
0.240
0.0190
0.0156
0.705
1.79
1.76 × 106
150
0.0651
0.241
0.0203
0.0169
0.702
1.64
1.22 × 106
200
0.0602
0.241
0.0215
0.0180
0.694
1.52
0.840 × 106
250
0.0559
0.242
0.0227
0.0192
0.692
1.41
0.607 × 106
300
0.0523
0.243
0.0237
0.0204
0.689
1.32
0.454 × 106
350
0.0490
0.244
0.0250
0.0215
0.687
1.23
0.336 × 106
400
0.0462
0.245
0.0260
0.0225
0.686
1.16
0.264 × 106
450
0.0437
0.246
0.0271
0.0236
0.674
1.10
0.204 × 106
500
0.0413
0.247
0.0280
0.0246
0.680
1.04
0.163 × 106
Source: National Bureau of Standards, Circular461C, 1947; 564, 1955; NBS–NACA, Tables of Thermal Properties of Gases, 1949; F. G. Keyes, Trans. A.S.M.E., 73, 590, 597 (1951); 74, 1303 (1952); D. D. Wagman, Selected Values of Chemical Thermodynamic Properties. Washington, D.C.: National Bureau of Standards, 1953.
A.3-4. Viscosity of Gases at 101.325 kPa (1 Atm Abs) [Viscosity in (Pas) 103, (kg/ms) 103, or cp]
Temperature
K
°F
°C
H2
O2
N2
CO
CO2
255.4
0
−17.8
0.00800
0.0181
0.0158
0.0156
0.0128
273.2
32
0
0.00840
0.0192
0.0166
0.0165
0.0137
283.2
50
10.0
0.00862
0.0197
0.0171
0.0169
0.0141
311.0
100
37.8
0.00915
0.0213
0.0183
0.0183
0.0154
338.8
150
65.6
0.00960
0.0228
0.0196
0.0195
0.0167
366.5
200
93.3
0.0101
0.0241
0.0208
0.0208
0.0179
394.3
250
121.1
0.0106
0.0256
0.0220
0.0220
0.0191
422.1
300
148.9
0.0111
0.0267
0.0230
0.0231
0.0203
449.9
350
176.7
0.0115
0.0282
0.0240
0.0242
0.0215
477.6
400
204.4
0.0119
0.0293
0.0250
0.0251
0.0225
505.4
450
232.2
0.0124
0.0307
0.0260
0.0264
0.0236
533.2
500
260.0
0.0128
0.0315
0.0273
0.0276
0.0247
Source: National Bureau of Standards, Circular461C, 1947; 564, 1955; NBS–NACA, Tables of Thermal Properties of Gases, 1949; F. G. Keyes, Trans. A.S.M.E., 73, 590, 597 (1951); 74, 1303 (1952); D. D. Wagman, Selected Values of Chemical Thermodynamic Properties. Washington, D.C.: National Bureau of Standards, 1953.
A.3-5. Thermal Conductivity of Gases at 101.325 kPa (1 Atm Abs)
Temperature
H2
O2
N2
CO
CO2
btu/ h·ft·°F
btu/ h·ft·°F
btu/ h·ft·°F
btu/ h·ft·°F
btu/ h·ft·°F
K
°C
°F
W/m·K
W/m·K
W/m·K
W/m·K
W/m·K
255.4
−17.8
0
0.1592
0.0920
0.0228
0.0132
0.0228
0.0132
0.0222
0.0128
0.0132
0.0076
273.2
0
32
0.1667
0.0963
0.0246
0.0142
0.0239
0.0138
0.0233
0.0135
0.0145
0.0084
283.2
10.0
50
0.1720
0.0994
0.0253
0.0146
0.0248
0.0143
0.0239
0.0138
0.0152
0.0088
311.0
37.8
100
0.1852
0.107
0.0277
0.0160
0.0267
0.0154
0.0260
0.0150
0.0173
0.0100
338.8
65.6
150
0.1990
0.115
0.0299
0.0173
0.0287
0.0166
0.0279
0.0161
0.0190
0.0110
366.5
93.3
200
0.2111
0.122
0.0320
0.0185
0.0303
0.0175
0.0296
0.0171
0.0216
0.0125
394.3
121.1
250
0.2233
0.129
0.0343
0.0198
0.0329
0.0190
0.0318
0.0184
0.0239
0.0138
422.1
148.9
300
0.2353
0.136
0.0363
0.0210
0.0348
0.0201
0.0338
0.0195
0.0260
0.0150
449.9
176.7
350
0.2458
0.142
0.0382
0.0221
0.0365
0.0211
0.0355
0.0205
0.0286
0.0165
477.6
204.4
400
0.2579
0.149
0.0398
0.0230
0.0382
0.0221
0.0369
0.0213
0.0308
0.0178
505.4
232.2
450
0.2683
0.155
0.0422
0.0244
0.0400
0.0231
0.0384
0.0222
0.0334
0.0193
533.2
260.0
500
0.2786
0.161
0.0438
0.0253
0.0419
0.0242
0.0407
0.0235
0.0355
0.0205
Source: National Bureau of Standards, Circular461C, 1947; 564, 1955; NBS–NACA, Table of Thermal Properties of Gases, 1949; F. G. Keyes, Trans. A.S.M.E., 73, 590, 597 (1951); 74, 1303 (1952); D. D. Wagman, Selected Values of Chemical Thermodynamic Properties. Washington, D.C.: National Bureau of Standards, 1953.
A.3-6. Heat Capacity of Gases at Constant Pressure at 101.325 kPa (1 Atm Abs)
Temperature
H2
O2
N2
CO
CO2
kJ/kgK
btu/lbm°F
kJ/kgK
btu/lbm°F
kJ/kgK
btu/lbm°F
kJ/kgK
btu/lbm°F
kJ/kgK
btu/lbm°F
K
°C
°F
255.4
−17.8
0
14.07
3.36
0.909
0.217
1.034
0.247
1.034
0.247
0.800
0.191
273.2
0
32
14.19
3.39
0.913
0.218
1.038
0.248
1.038
0.248
0.816
0.195
283.2
10.0
50
14.19
3.39
0.917
0.219
1.038
0.248
1.038
0.248
0.825
0.197
311.0
37.8
100
14.32
3.42
0.921
0.220
1.038
0.248
1.043
0.249
0.854
0.204
338.8
65.6
150
14.36
3.43
0.925
0.221
1.038
0.248
1.043
0.249
0.883
0.211
366.5
93.3
200
14.40
3.44
0.929
0.222
1.043
0.249
1.047
0.250
0.904
0.216
394.3
121.1
250
14.44
3.45
0.938
0.224
1.043
0.249
1.047
0.250
0.929
0.222
422.1
148.9
300
14.49
3.46
0.946
0.226
1.047
0.250
1.051
0.251
0.950
0.227
449.9
176.7
350
14.49
3.46
0.955
0.228
1.047
0.250
1.055
0.252
0.976
0.233
477.6
204.4
400
14.49
3.46
0.963
0.230
1.051
0.251
1.059
0.253
0.996
0.238
505.4
232.2
450
14.52
3.47
0.971
0.232
1.055
0.252
1.063
0.254
1.017
0.243
533.2
260.0
500
14.52
3.47
0.976
0.233
1.059
0.253
1.068
0.255
1.030
0.246
Source: National Bureau of Standards, Circular461C, 1947; 564, 1955; NBS–NACA, Tables of Thermal Properties of Gases, 1949; F. G. Keyes, Trans. A.S.M.E., 73, 590, 597 (1951); 74, 1303 (1952); D. D. Wagman, Selected Values of Chemical Thermodynamic Properties. Washington, D.C.: National Bureau of Standards, 1953.
A.3-7. Prandtl Number of Gases at 101.325 kPa (1 Atm Abs)
Temperature
°C
°F
K
H2
O2
N2
CO
CO2
−17.8
0
255.4
0.720
0.720
0.720
0.740
0.775
0
32
273.2
0.715
0.711
0.720
0.738
0.770
10.0
50
283.2
0.710
0.710
0.717
0.735
0.769
37.8
100
311.0
0.700
0.707
0.710
0.731
0.764
65.6
150
338.8
0.700
0.706
0.700
0.727
0.755
93.3
200
366.5
0.694
0.703
0.700
0.724
0.752
121.1
250
394.3
0.688
0.703
0.696
0.720
0.746
148.9
300
422.1
0.683
0.703
0.690
0.720
0.738
176.6
350
449.9
0.677
0.704
0.689
0.720
0.734
204.4
400
477.6
0.670
0.706
0.688
0.720
0.725
232.2
450
505.4
0.668
0.702
0.688
0.720
0.716
260.0
500
533.2
0.666
0.700
0.688
0.720
0.702
Source: National Bureau of Standards, Circular461C, 1947; 564, 1955; NBS–NACA, Tables of Thermal Properties of Gases, 1949; F. G. Keyes, Trans. A.S.M.E., 73, 590, 597 (1951); 74, 1303 (1952); D. D. Wagman, Selected Values of Chemical Thermodynamic Properties. Washington, D.C.: National Bureau of Standards, 1953.
Figure A.3-2. Viscosities of gases at 101.325 kPa (1 atm abs). (From R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973. With permission.) SeeTable A.3-8 for coordinates for use with Fig. A.3-2.
A.3-8. Viscosities of Gases (Coordinates for Use with Fig. A.3-2)
No.
Gas
X
Y
No.
Gas
X
Y
1
Acetic acid
7.7
14.3
29
Freon-113
11.3
14.0
2
Acetone
8.9
13.0
30
Helium
10.9
20.5
3
Acetylene
9.8
14.9
31
Hexane
8.6
11.8
4
Air
11.0
20.0
32
Hydrogen
11.2
12.4
5
Ammonia
8.4
16.0
33
3H2 + 1N2
11.2
17.2
6
Argon
10.5
22.4
34
Hydrogen bromide
8.8
20.9
7
Benzene
8.5
13.2
35
Hydrogen chloride
8.8
18.7
8
Bromine
8.9
19.2
36
Hydrogen cyanide
9.8
14.9
9
Butene
9.2
13.7
37
Hydrogen iodide
9.0
21.3
10
Butylene
8.9
13.0
38
Hydrogen sulfide
8.6
18.0
11
Carbon dioxide
9.5
18.7
39
Iodine
9.0
18.4
12
Carbon disulfide
8.0
16.0
40
Mercury
5.3
22.9
13
Carbon monoxide
11.0
20.0
41
Methane
9.9
15.5
14
Chlorine
9.0
18.4
42
Methyl alcohol
8.5
15.6
15
Chloroform
8.9
15.7
43
Nitric oxide
10.9
20.5
16
Cyanogen
9.2
15.2
44
Nitrogen
10.6
20.0
17
Cyclohexane
9.2
12.0
45
Nitrosyl chloride
8.0
17.6
18
Ethane
9.1
14.5
46
Nitrous oxide
8.8
19.0
19
Ethyl acetate
8.5
13.2
47
Oxygen
11.0
21.3
20
Ethyl alcohol
9.2
14.2
48
Pentane
7.0
12.8
21
Ethyl chloride
8.5
15.6
49
Propane
9.7
12.9
22
Ethyl ether
8.9
13.0
50
Propyl alcohol
8.4
13.4
23
Ethylene
9.5
15.1
51
Propylene
9.0
13.8
24
Fluorine
7.3
23.8
52
Sulfur dioxide
9.6
17.0
25
Freon-11
10.6
15.1
53
Toluene
8.6
12.4
26
Freon-12
11.1
16.0
54
2,3,3-Trimethylbutane
9.5
10.5
27
Freon-21
10.8
15.3
55
Water
8.0
16.0
28
Freon-22
10.1
17.0
56
Xenon
9.3
23.0
Figure A.3-3. Heat capacity of gases at constant pressure at 101.325 kPa (1 atm abs). (From R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973. With permission.) SeeTable A.3-9 for use with Fig. A.3-3.
[2] F. G. Keyes, Tech. Rept. 37, Project Squid, Apr. 1, 1952;
[3] W. B. Mann and B. G. Dickens, Proc. Roy. Soc. (London). A134, 77 (1931);
[4]International Critical Tables. New York: McGraw-Hill Book Company, 1929;
[7] B. G. Dickens, Proc. Roy. Soc. (London), A143, 517 (1934).
A.3-11. Heat Capacities of Liquids (cp kJ/kgK)
Liquid
K
cp
Liquid
K
cp
Acetic acid
273
1.959
Hydrochloric acid (20 mol %)
273
2.43
311
2.240
293
2.474
Acetone
273
2.119
Mercury
293
0.01390
293
2.210
Methyl alcohol
293
2.512
Aniline
273
2.001
313
2.583
323
2.181
Nitrobenzene
283
1.499
Benzene
293
1.700
303
1.419
333
1.859
363
1.436
Butane
273
2.300
Sodium chloride (9.1 mol %)
293
3.39
i-Butyl alcohol
303
2.525
330
3.43
Ethyl alcohol
273
2.240
Sulfuric acid (100%)
293
1.403
298
2.433
Toluene
273
1.616
Formic acid
273
1.825
323
1.763
289
2.131
o-Xylene
303
1.721
Glycerol
288
2.324
305
2.412
Source: N. A. Lange, Handbook of Chemistry, 10th ed. New York: McGraw-Hill Book Company, 1967; National Research Council, International Critical Tables, Vol. V. New York: McGraw-Hill Book Company, 1929; R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973.
Figure A.3-4. Viscosities of liquids. (From R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973. With permission.) SeeTable A.3-12 for use with Fig. A.3-4.
A.3-12. Viscosities of Liquids (Coordinates for Use with Fig. A.3-4)
Liquid
X
Y
Liquid
X
Y
Acetaldehyde
15.2
4.8
Dibromomethane
12.7
15.8
Acetic acid, 100%
12.1
14.2
Dichloroethane
13.2
12.2
Acetic acid, 70%
9.5
17.0
Dichloromethane
14.6
8.9
Acetic anhydride
12.7
12.8
Diethyl ketone
13.5
9.2
Acetone, 100%
14.5
7.2
Diethyl oxalate
11.0
16.4
Acetone, 35%
7.9
15.0
Diethylene glycol
5.0
24.7
Acetonitrile
14.4
7.4
Diphenyl
12.0
18.3
Acrylic acid
12.3
13.9
Dipropyl ether
13.2
8.6
Allyl alcohol
10.2
14.3
Dipropyl oxalate
10.3
17.7
Allyl bromide
14.4
9.6
Ethyl acetate
13.7
9.1
Allyl iodide
14.0
11.7
Ethyl acrylate
12.7
10.4
Ammonia, 100%
12.6
2.0
Ethyl alcohol, 100%
10.5
13.8
Ammonia, 26%
10.1
13.9
Ethyl alcohol, 95%
9.8
14.3
Amyl acetate
11.8
12.5
Ethyl alcohol, 40%
6.5
16.6
Amyl alcohol
7.5
18.4
Ethyl benzene
13.2
11.5
Aniline
8.1
18.7
Ethyl bromide
14.5
8.1
Anisole
12.3
13.5
2-Ethyl butyl acrylate
11.2
14.0
Arsenic trichloride
13.9
14.5
Ethyl chloride
14.8
6.0
Benzene
12.5
10.9
Ethyl ether
14.5
5.3
Brine, CaCl2, 25%
6.6
15.9
Ethyl formate
14.2
8.4
Brine, NaCl, 25%
10.2
16.6
2-Ethyl hexyl acrylate
9.0
15.0
Bromine
14.2
13.2
Ethyl iodide
14.7
10.3
Bromotoluene
20.0
15.9
Ethyl propionate
13.2
9.9
Butyl acetate
12.3
11.0
Ethyl propyl ether
14.0
7.0
Butyl acrylate
11.5
12.6
Ethyl sulfide
13.8
8.9
Butyl alcohol
8.6
17.2
Ethylene bromide
11.9
15.7
Butyric acid
12.1
15.3
Ethylene chloride
12.7
12.2
Carbon dioxide
11.6
0.3
Ethylene glycol
6.0
23.6
Carbon disulfide
16.1
7.5
Ethylidene chloride
14.1
8.7
Carbon tetrachloride
12.7
13.1
Fluorobenzene
13.7
10.4
Chlorobenzene
12.3
12.4
Formic acid
10.7
15.8
Chloroform
14.4
10.2
Freon-11
14.4
9.0
Chlorosulfonic acid
11.2
18.1
Freon-12
16.8
15.6
Chlorotoluene, ortho
13.0
13.3
Freon-21
15.7
7.5
Chlorotoluene, meta
13.3
12.5
Freon-22
17.2
4.7
Chlorotoluene, para
13.3
12.5
Freon-113
12.5
11.4
Cresol, meta
2.5
20.8
Glycerol, 100%
2.0
30.0
Cyclohexanol
2.9
24.3
Glycerol, 50%
6.9
19.6
Cyclohexane
9.8
12.9
Heptane
14.1
8.4
Hexane
14.7
7.0
Pentane
14.9
5.2
Hydrochloric acid, 31.5%
13.0
16.6
Phenol
6.9
20.8
Iodobenzene
12.8
15.9
Phosphorus tribromide
13.8
16.7
Isobutyl alcohol
7.1
18.0
Phosphorus trichloride
16.2
10.9
Isobutyric acid
12.2
14.4
Propionic acid
12.8
13.8
Isopropyl alcohol
8.2
16.0
Propyl acetate
13.1
10.3
Isopropyl bromide
14.1
9.2
Propyl alcohol
9.1
16.5
Isopropyl chloride
13.9
7.1
Propyl bromide
14.5
9.6
Isopropyl iodide
13.7
11.2
Propyl chloride
14.4
7.5
Kerosene
10.2
16.9
Propyl formate
13.1
9.7
Linseed oil, raw
7.5
27.2
Propyl iodide
14.1
11.6
Mercury
18.4
16.4
Sodium
16.4
13.9
Methanol, 100%
12.4
10.5
Sodium hydroxide, 50%
3.2
25.8
Methanol, 90%
12.3
11.8
Stannic chloride
13.5
12.8
Methanol, 40%
7.8
15.5
Succinonitrile
10.1
20.8
Methyl acetate
14.2
8.2
Sulfur dioxide
15.2
7.1
Methyl acrylate
13.0
9.5
Sulfuric acid, 110%
7.2
27.4
Methyl i-butyrate
12.3
9.7
Sulfuric acid, 100%
8.0
25.1
Methyl n-butyrate
13.2
10.3
Sulfuric acid, 98%
7.0
24.8
Methyl chloride
15.0
3.8
Sulfuric acid, 60%
10.2
21.3
Methyl ethyl ketone
13.9
8.6
Sulfuryl chloride
15.2
12.4
Methyl formate
14.2
7.5
Tetrachloroethane
11.9
15.7
Methyl iodide
14.3
9.3
Thiophene
13.2
11.0
Methyl propionate
13.5
9.0
Titanium tetrachloride
14.4
12.3
Methyl propyl ketone
14.3
9.5
Toluene
13.7
10.4
Methyl sulfide
15.3
6.4
Trichloroethylene
14.8
10.5
Naphthalene
7.9
18.1
Triethylene glycol
4.7
24.8
Nitric acid, 95%
12.8
13.8
Turpentine
11.5
14.9
Nitric acid, 60%
10.8
17.0
Vinyl acetate
14.0
8.8
Nitrobenzene
10.6
16.2
Vinyl toluene
13.4
12.0
Nitrogen dioxide
12.9
8.6
Water
10.2
13.0
Nitrotoluene
11.0
17.0
Xylene, ortho
13.5
12.1
Octane
13.7
10.0
Xylene, meta
13.9
10.6
Octyl alcohol
6.6
21.1
Xylene, para
13.9
10.9
Pentachloroethane
10.9
17.3
Figure A.3-5. Heat capacity of liquids. (From R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973. With permission.)
A.3-13. Thermal Conductivities of Liquids (k = βW/m · K)[*]
Liquid
K
k
Liquid
K
k
Acetic acid
Ethylene glycol
273
0.265
100%
293
0.171
Glycerol, 100%
293
0.284
50%
293
0.346
n-Hexane
303
0.138
Ammonia
243–258
0.502
333
0.135
n-Amyl alcohol
303
0.163
Kerosene
293
0.149
373
0.154
348
0.140
Benzene
303
0.159
Methyl alcohol
333
0.151
100%
293
0.215
Carbon tetrachloride
273
0.185
60%
293
0.329
341
0.163
20%
293
0.492
n-Decane
303
0.147
100%
323
0.197
333
0.144
n-Octane
303
0.144
Ethyl acetate
293
0.175
333
0.140
Ethyl alcohol
NaCl brine
100%
293
0.182
25%
303
0.571
60%
293
0.305
12.5%
303
0.589
20%
293
0.486
Sulfuric acid
100%
323
0.151
90%
303
0.364
60%
303
0.433
Vaseline
332
0.183
Source: R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973. With permission.
[*] A linear variation with temperature may be assumed between the temperature limits given.
A.3-14. Heat Capacities of Solids (cp = βkJ/kg · K)
Solid
K
cp
Solid
K
cp
Alumina
373
0.84
Benzoic acid
293
1.243
1773
1.147
Camphene
308
1.591
Asbestos
1.05
Caprylic acid
271
2.629
Asphalt
0.92
Dextrin
273
1.218
Brick, fireclay
373
0.829
Formic acid
273
1.800
1773
1.248
Glycerol
273
1.382
Cement, portland
0.779
Lactose
293
1.202
Clay
0.938
Oxalic acid
323
1.612
Concrete
0.63
Tartaric acid
309
1.202
Corkboard
303
0.167
Urea
293
1.340
Glass
0.84
Magnesia
373
0.980
1773
0.787
Oak
2.39
Pine, yellow
298
2.81
Porcelain
293–373
0.775
Rubber, vulcanized
2.01
Steel
0.50
Wool
1.361
Source: R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973; National Research Council, International Critical Tables, Vol. V. New York: McGraw-Hill Book Company, 1929; L. S. Marks, Mechanical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1951; F. Kreith, Principles of Heat Transfer, 2nd ed. Scranton, Pa.: International Textbook Co., 1965.
A.3-15. Thermal Conductivities of Building and Insulating Materials
Source: L. S. Marks, Mechanical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1951; W. H. McAdams, Heat Transmission, 3rd ed. New York: McGraw-Hill Book Company, 1954; F. H. Norton, Refractories. New York: McGraw-Hill Book Company, 1949; National Research Council, International Critical Tables. New York: McGraw-Hill Book Company, 1929; M. S. Kersten, Univ. Minn. Eng. Ex. Sta., Bull. 28, June 1949; R. H. Heilman, Ind. Eng. Chem., 28, 782 (1936).
A.3-16. Thermal Conductivities, Densities, and Heat Capacities of Metals
Material
t(°C)
k(W/m·K)
Aluminum
20
2707
0.896
202 (0°C)
206 (100°C)
215 (200°C)
230 (300°C)
Brass (70–30)
20
8522
0.385
97 (0°C)
104 (100°C)
109 (200°C)
Cast iron
20
7593
0.465
55 (0°C)
52 (100°C)
48 (200°C)
Copper
20
8954
0.383
388 (0°C)
377 (100°C)
372 (200°C)
Lead
20
11 370
0.130
35 (0°C)
33 (100°C)
31 (200°C)
Steel 1%C
20
7801
0.473
45.3 (18°C)
45 (100°C)
45 (200°C)
43 (300°C)
308 stainless
20
7849
0.461
15.2 (100°C)
21.6 (500°C)
304 stainless
0
7817
0.461
13.8 (0°C)
16.3 (100°C)
18.9 (300°C)
Tin
20
7304
0.227
62 (0°C)
59 (100°C)
57 (200°C)
Source: L. S. Marks, Mechanical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1951; E. R. G. Eckert and R. M. Drake, Heat and Mass Transfer, 2nd ed. New York: McGraw-Hill Book Company, 1959; R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973; National Research Council, International Critical Tables. New York: McGraw-Hill Book Company, 1929.
A.3-17. Normal Total Emmissivities of Surfaces
Surface
K
ε
Surface
K
ε
Aluminum
Lead, unoxidized
400
0.057
highly oxidized
366
0.20
Nickel, polished
373
0.072
highly polished
500
0.039
Nickel oxide
922
0.59
850
0.057
Oak, planed
294
0.90
Aluminum oxide
550
0.63
Paint
Asbestos board
296
0.96
aluminum
373
0.52
Brass, highly
520
0.028
oil (16 different, all colors)
373
0.92–0.96
polished
630
0.031
Paper
292
0.924
Chromium, polished
373
0.075
Roofing paper
294
0.91
Copper
Rubber (hard, glossy)
296
0.94
oxidized
298
0.78
Steel
polished
390
0.023
oxidized at 867 K
472
0.79
Glass, smooth
295
0.94
polished stainless
373
0.074
Iron
304 stainless
489
0.44
oxidized
373
0.74
Water
273
0.95
Tin-plated
373
0.07
373
0.963
Iron oxide
772
0.85
Source: R. H. Perry and C. H. Chilton, Chemical Engineers' Handbook, 5th ed. New York: McGraw-Hill Book Company, 1973; W. H. McAdams, Heat Transmission, 3rd ed. New York: McGraw-Hill Book Company, 1954; E. Schmidt, Gesundh.-Ing. Beiheft, 20, Reihe 1, 1 (1927).
A.3-18. Henry's Law Constants for Gases in Water (H × 10−4)[*]
T
K
°C
CO2
CO
C2H6
C2H4
He
H2
H2S
CH4
N2
O2
273.2
0
0.0728
3.52
1.26
0.552
12.9
5.79
0.0268
2.24
5.29
2.55
283.2
10
0.104
4.42
1.89
0.768
12.6
6.36
0.0367
2.97
6.68
3.27
293.2
20
0.142
5.36
2.63
1.02
12.5
6.83
0.0483
3.76
8.04
4.01
303.2
30
0.186
6.20
3.42
1.27
12.4
7.29
0.0609
4.49
9.24
4.75
313.2
40
0.233
6.96
4.23
12.1
7.51
0.0745
5.20
10.4
5.35
Source: National Research Council, International Critical Tables, Vol. III. New York: McGraw-Hill Book Company, 1929.
[*]pA = HxA,pA = partial pressure of A in gas in atm, xA = mole fraction of A in liquid, H = Henry's law constant in atm/mole frac.
A.3-19. Equilibrium Data for SO2–Water System
Mole Fraction SO2in Liquid, xA
Partial Pressure of SO2in Vapor, pA (mm Hg)
Mole Fraction SO2in Vapor, yA; P =1 Atm
20°C (293 K)
30°C (303 K)
20°C
30°C
0
0
0
0
0
0.0000562
0.5
0.6
0.000658
0.000790
0.0001403
1.2
1.7
0.00158
0.00223
0.000280
3.2
4.7
0.00421
0.00619
0.000422
5.8
8.1
0.00763
0.01065
0.000564
8.5
11.8
0.01120
0.0155
0.000842
14.1
19.7
0.01855
0.0259
0.001403
26.0
36
0.0342
0.0473
0.001965
39.0
52
0.0513
0.0685
0.00279
59
79
0.0775
0.1040
0.00420
92
125
0.121
0.1645
0.00698
161
216
0.212
0.284
0.01385
336
452
0.443
0.594
0.0206
517
688
0.682
0.905
0.0273
698
0.917
Source: T. K. Sherwood, Ind. Eng. Chem., 17, 745 (1925).
A.3-20. Equilibrium Data for Methanol–Water System
Mole Fraction Methanol in Liquid, xA
Partial Pressure of Methanol in Vapor, pA (mm Hg)
39.9°C
(313.1 K)
59.4°C
(332.6 K)
0
0
0
0.05
25.0
50
0.10
46.0
102
0.15
66.5
151
Source: National Research Council, International Critical Tables, Vol. III. New York: McGraw-Hill Book Company, 1929.
A.3-21. Equilibrium Data for Acetone–Water System at 20°C (293 K)
Mole Fraction Acetone in Liquid, xA
Partial Pressure of Acetone in Vapor, pA (mm Hg)
0
0
0.0333
30.0
0.0720
62.8
0.117
85.4
0.171
103
Source: T. K. Sherwood, Absorption and Extraction. New York: McGraw-Hill Book Company, 1937. With permission.
A.3-22. Equilibrium Data for Ammonia–Water System
Mole Fraction NH3 in Liquid, xA
Partial Pressure of NH3in Vapor, pA (mm Hg)
Mole Fraction NH3in Vapor, yA; P =1 Atm
20°C (293 K)
30°C (303 K)
20°C
30°C
0
0
0
0
0
0.0126
11.5
0.0151
0.0167
15.3
0.0201
0.0208
12
19.3
0.0158
0.0254
0.0258
15
24.4
0.0197
0.0321
0.0309
18.2
29.6
0.0239
0.0390
0.0405
24.9
40.1
0.0328
0.0527
0.0503
31.7
51.0
0.0416
0.0671
0.0737
50.0
79.7
0.0657
0.105
0.0960
69.6
110
0.0915
0.145
0.137
114
179
0.150
0.235
0.175
166
260
0.218
0.342
0.210
227
352
0.298
0.463
0.241
298
454
0.392
0.597
0.297
470
719
0.618
0.945
Source: J. H. Perry, Chemical Engineers' Handbook, 4th ed. New York: McGraw-Hill Book Company, 1963. With permission.
A.3-23. Equilibrium Data for Ethanol–Water System at 101.325 kPa (1 Atm)[*]
Temperature
Vapor–Liquid Equilibria, Mass Fraction Ethanol
Temperature
Vapor–Liquid Equilibria, Mass Fraction Ethanol
Temperature
Mass Fraction
Enthalpy (btu/lbmof mixture)
Enthalpy (kJ/kg of mixture)
°C
°F
xA
yA
°C
°F
xA
yA
°C
°F
Liquid
Vapor
Liquid
Vapor
100.0
212
0
0
81.0
177.8
0.600
0.794
100.0
212
0
180.1
1150
418.9
2675
98.1
208.5
0.020
0.192
80.1
176.2
0.700
0.822
91.8
197.2
0.1
159.8
1082
371.7
2517
95.2
203.4
0.050
0.377
79.1
174.3
0.800
0.858
84.7
184.5
0.3
135.0
943
314.0
2193
91.8
197.2
0.100
0.527
78.3
173.0
0.900
0.912
82.0
179.6
0.5
122.9
804
285.9
1870
87.3
189.2
0.200
0.656
78.2
172.8
0.940
0.942
80.1
176.2
0.7
111.1
664
258.4
1544
84.7
184.5
0.300
0.713
78.1
172.7
0.960
0.959
78.3
173.0
0.9
96.6
526
224.7
1223
83.2
181.7
0.400
0.746
78.2
172.8
0.980
0.978
78.3
173.0
1.0
89.0
457.5
207.0
1064
82.0
179.6
0.500
0.771
78.3
173.0
1.00
1.00
Source: Data from L. W. Cornell and R. E. Montonna, Ind. Eng. Chem., 25, 1331 (1933); and W. A. Noyes and R. R. Warfel, J. Am. Chem. Soc., 23, 463 (1901), as given by G. G. Brown, Unit Operations. New York: John Wiley & Sons, Inc., 1950. With permission.
[*] Reference state for enthalpy is pure liquid at 273 K or 0°C.
A.3-24. Acetic Acid–Water–Isopropyl Ether System, Liquid–Liquid Equilibria at 293 K or 20°C
Water Layer (wt %)
Isopropyl Ether Layer (wt %)
Acetic Acid
Water
Isopropyl Ether
Acetic Acid
Water
Isopropyl Ether
0
98.8
1.2
0
0.6
99.4
0.69
98.1
1.2
0.18
0.5
99.3
1.41
97.1
1.5
0.37
0.7
98.9
2.89
95.5
1.6
0.79
0.8
98.4
6.42
91.7
1.9
1.93
1.0
97.1
13.30
84.4
2.3
4.82
1.9
93.3
25.50
71.1
3.4
11.40
3.9
84.7
36.70
58.9
4.4
21.60
6.9
71.5
44.30
45.1
10.6
31.10
10.8
58.1
46.40
37.1
16.5
36.20
15.1
48.7
Source: Trans. A.I.Ch.E., 36, 601, 628 (1940). With permission.
A.3-25. Liquid–Liquid Equilibrium Data for Acetone–Water–Methyl Isobutyl Ketone (MIK) System at 298–299 K or 25–26°C
Composition Data (wt %)
Acetone Distribution Data (wt %)
MIK
Acetone
Water
Water Phase
MIKPhase
98.0
0
2.00
2.5
4.5
93.2
4.6
2.33
5.5
10.0
77.3
18.95
3.86
7.5
13.5
71.0
24.4
4.66
10.0
17.5
65.5
28.9
5.53
12.5
21.3
54.7
37.6
7.82
15.5
25.5
46.2
43.2
10.7
17.5
28.2
12.4
42.7
45.0
20.0
31.2
5.01
30.9
64.2
22.5
34.0
3.23
20.9
75.8
25.0
36.5
2.12
3.73
94.2
26.0
37.5
2.20
0
97.8
Source: Reprinted with permission from D. F. Othmer, R. E. White, and E. Trueger, Ind. Eng. Chem., 33, 1240 (1941). Copyright by the American Chemical Society.