398

B
Physical and Chemical Property Data
Table B. 1 Atomic weights and numbers
Based on the atomic mass of 12C. Values for atomic weights apply to elements as they exist in nature.
9

Name

Symbol

Relative atomic mass

Atomic number

Actinium
Aluminium
Americium
Antimony
Argon
Arsenic
Astatine
Barium
Berkelium
Beryllium
Bismuth
Boron
Bromine
Cadmium
Caesium
Calcium
Californium
Carbon
Cerium
Chlorine
Chromium
Cobalt
Copper
Curium
Dysprosium
Einsteinium
Erbium
Europium
Fermium
Fluorine
Francium
Gadolinium
Gallium
Germanium
Gold
Hafnium
Helium
Holmium
Hydrogen
Indium
Iodine
Iridium
Iron
Krypton
Lanthanum

Ac
Al
Am
Sb
Ar
As
At
Ba
Bk
Be
Bi
B
Br
Cd
Cs
Ca
Cf
C
Ce
Cl
Cr
Co
Cu
Cm
Dy
Es
Er
Eu
Fm
F
Fr
Gd
Ga
Ge
Au
Hf
He
Ho
H
In
I
Ir
Fe
Kr
La

26.9815
121.75
39.948
74.9216
137.34
9.0122
208.98
10.811
79.904
112.40
132.905
40.08
12.011
140.12
35.453
51.996
58.9332
63.546
162.50
167.26
151.96
18.9984
157.25
69.72
72.59
196.967
178.49
4.0026
164.930
1.00797
114.82
126.9044
192.2
55.847
83.80
138.91

89
13
95
51
18
33
85
56
97
4
83
5
35
48
55
20
98
6
58
I7
24
27
29
96
66
99
68
63
100
9
87
64
31
32
79
72
2
67
1
49
53
77
26
36
57

Appendices

399

Name

Symbol

Lawrencium
Lead
Lithium
Lutetium
Magnesium
Manganese
Mendelevium
Mercury
Molybdenum
Neodymium
Neon
Neptunium
Nickel
Niobium
Nitrogen
Nobelium
Osmium
Oxygen
Palladium
Phosphorus
Platinum
Plutonium
Polonium
Potassium
Praseodymium
Promethium
Protactinium
Radium
Radon
Rhenium
Rhodium
Rubidium
Ruthenium
Samarium
Scandium
Selenium
Silicon
Silver
Sodium
Strontium
Sulphur
Tantalum
Technetium
Tellurium
Terbium
Thallium
Thorium
Thulium
Tin
Titanium
Tungsten
Uranium
Vanadium
Wolfram (Tungsten)
Xenon
Ytterbium
Yttrium
Zinc
Zirconium

Lr
Pb
Li
Lu
Mg
Mn
Md
Hg
Mo
Nd
Ne
Np
Ni
Nb
N
No
Os
O
Pd
P
Pt
Pu
Po
K
Pr
Pm
Pa
Ra
Rn
Re
Rh
Rb
Ru
Sm
Sc
Se
Si
Ag
Na
Sr
S
Ta
Tc
Te
Tb
Tl
Th
Tm
Sn
Ti
W
U
V
W
Xe
Yb
Y
Zn
Zr

Relative atomic mass

207.19
6.939
174.97
24.312
54.938
200.59
95.94
144.24
20.183
58.71
92.906
14.0067
190.2
15.9994
106.4
30.9738
195.09
39.102
140.907
186.2
102.905
85.47
101.07
150.35
44.956
78.96
28.086
107.868
22.9898
87.62
32.064
180.948
127.60
158.924
204.37
232.038
168.934
118.69
47.90
183.85
238.03
50.942
183.85
131.30
173.04
88.905
65.37
91.22

Atomic number
103
82
3
71
12
25
101
80
42
60
10
93
28
41
7
102
76
8
46
15
78
94
84
19
59
61
91
88
86
75
45
37
44
62
21
34
14
47
11
38
16
73
43
52
65
81
90
69
50
22
74
92
23
74
54
70
39
30
40

Appendices

400

Table B.2 Degree of reduction of biological materials

(Adapted from J.A. Rods, 1983, Energeticsand Kinetics in Biotechnology, ElsevierBiomedical Press, Amsterdam)
Compound

Formula

Degree of reduction y
relative to NH 3

Degree of reduction y
relative to N 2

Acetaldehyde
Acetic acid
Acetone
Adenine
Alanine
Ammonia
Arginine
Asparagine
Aspartic acid
n-Butanol
Butyraldehyde
Butyric acid
Carbon monoxide
Citric acid
Cytosine
Ethane
Ethanol
Ethene
Ethylene glycol
Ethyne
Formaldehyde
Formic acid
Fumaric acid
Glucitol
Gluconic acid
Glucose
Glutamic acid
Glutamine
Glycerol
Glycine
Graphite
Guanine
Histidine
Hydrogen
Isoleucine
Lactic acid
Leucine
Lysine
Malic acid
Methane
Methanol
Oxalic acid
Palmitic acid
Pentane
Phenylalanine
Proline
Propane

C2H40
C 2H402
C3H60
CsHsN 5
C3HyO2N
NH 3
C6Hi4O2N4
C4HsO3N2
C4H704N
C4HioO
C4HsO
C4H80 2
CO
C6H80 7
C4HsON 3
C2H6
C2H60
C2H4
C2H60 2
C2H 2
CH20
CH20 2
C4H40 4
C6HI406
C6Hi20 7
C6Hi20 6
CsHgO4N
C sHt003N2
C3HsO 3
C2HsO2N
C
CsHsON 5
C6H902 N3
H2
C6H 1302N
C3H60 3
C6Hi302N
C6HI402N 2
C4H605
CH 4
CH40
C2H20 4
C16H3202
C5H12
CgH l 102N
C5HgO2N
C3Hs
C 3HsO
C3H60 2
C3H403
C3H703N
C4H604

5.00
4.00
5.33
2.00
4.00
0
3.67
3.00
3.00
6.00
5.50
5.00
2.00
3.00
2.50
7.00
6.00
6.00
5.00
5.00
4.00
2.00
3.00
4.33
3.67
4.00
3.60
3.60
4.67
3.00
4.00
1.60
3.33
2.00
5.00
4.00
5.00
4.67
3.00
8.00
6.00
1.00
5.75
6.40
4.44
4.40
6.67
6.00
4.67
3.33
3.33
3.50

5.00
4.00
5.33
5.00
5.00
3.00
5.67
4.50
3.75
6.00
5.50
5.00
2.00
3.00
4.75
7.00
6.00
6.00
5.00
5.00
4.00
2.00
3.00
4.33
3.67
4.00
4.20
4.80
4.67
4.50
4.00
4.60
4.83
2.00
5.50
4.00
5.50
5.67
3.00
8.00
6.00

iso-Propanol
Propionic acid
Pyruvic acid
Serine
Succinic acid

1.00

5.75
6.40
4.78
5.00
6.67
6.00
4.67
3.33
4.33
3.50

Appendices

4oi

Compound

Formula

Degree of reduction y
relative to N H 3

Degree of reduction ?'

relative to N 2

Threonine
Thymine
Tryptophan
Tyrosine
Uracil
Valeric acid
Valine

C4H903N
C 5H 6~ 2N 2
Cl 1H 1202N2
CgH 1103N
C4H402N 2
C5H100 2
C5HI102N

4.00
3.20
4.18
4.22
2.50
5.20
4.80

4.75
4.40
4.73
4.56
4.00
5.20
5.40

Biomass

CH 1.8Oo.5No.2

4.20

4.80

Table B.3 Heat

capacities

(Adapted from R.M. Felder and ILW. Rousseau, 1978, ElementaryPrinciplesof ChemicalProcesses,John Wiley and Sons, New York)
Cp ( J gmol- 1 ~

1) = a + b T+ cT 2 + d T 3

Example. For acetone gas between 0~ and 1200"C:

Cp (J gmo1-1 *C-l) = 71.96 + (20.10 x 10 -2) T -

(12.78 x 10 -5) T 2 + (34.76 x 10 -9) T3, where Tisin *C.

Note that some equations require Tin K, as indicated.

State:g - gas; l - liquid; c - crystal.
Compound

State

Temperature unit

b. 102

c. 105

d. 109

Temperature range
(units of T)

Acetone
Air

g
g
g
g
c

~
oC
K
oC
K

71.96
28.94
28.09
35.15
89.5

20.10
0.4147
0.1965
2.954

- 12.78
0.3191
0.4799
0.4421

34.76
- 1.965
- 1.965
-6.686

0-1200
0-1500
273-1800
0-1200
276-373

g
l
l
g
g
g
g

~
oC
oC
oC
*C
oC
oC

36.11
103.1
158.8
61.34
34.28
28.84
29.13

4.233

-2.887

7.464

0-1500

15.72
4.268
0.00765
-0.1341

-8.749
0.000
0.3288
0.9715

19.83
-8.694
-0.8698
-4.335

100
0-1200
0-1200
0-1500
0-1200

33.51

1.547

0.3012

- 3.292

0-1500

g
g
l
l
g
1
g
g

*C
K
~
~
~
~
~
~

34.31
19.87
75.86
82.59
42.93
110.0
29.00
29.10

5.469
5.021

0.3661
1.268

-11.00
-11.00

8.301

-1.87

-8.03

0.2199
1.158

0.5723
-0.6076

-2.871
1.311

0-1200
273-1500
0
40
0-700
25
0-1500
0-1500

c
c
l
g
l
g

K
K
~
~
~
~

15.2
18.3
139.1
38.91
75.4
33.46

2.68
1.84
15.59
3.904

-3.104

8.606

0.6880

0.7604

-3.593

Ammonia
Calcium
hydroxide
Carbon dioxide
Ethanol

Formaldehyde
Hydrogen
Hydrogen
chloride
Hydrogen
sulphide
Methane
Methanol

Nitric acid
Nitrogen
Oxygen
Sulphur
(rhombic)
(monoclinic)
Sulphuric acid
Sulphur dioxide
Water

273-368
368-392
10-45
0-1500
0-100
0-1500

Appendices

402,
,,,

Table B.4 Mean heat capacities of gases

(Adapted from D.M. Himmelblau, 1974, Basic Principles and Calculations in ChemicalEngineering, 3rd edn, Prentice-Hall, New Jersey)

Reference state: Tref= 0~

Pref= 1 atm.

Cpm(J gmol- 1 o c - 1

T(~

0
18
25
100
200
300
400
500

Air

02

N2

H2

CO 2

H20

29.06
29.07
29.07
29.14
29.29
29.51
29.78
30.08

29.24
29.28
29.30
29.53
29.93
30.44
30.88
31.33

29.12
29.12
29.12
29.14
29.23
29.38
29.60
29.87

28.61
28.69
28.72
28.98
29.10
29.15
29.22
29.28

35.96
36.43
36.47
38.17
40.12
41.85
43.35
44.69

33.48
33.51
33.52
33.73
34.10
34.54
35.05
35.59

Table B.5 Specific heats of organic liquids

(From R.H. Perry, D.W. Green and J.O. Maloney, Eds, 1984, Chemical Engineers"Handbook, 6th edn, McGraw-Hill, New York)
Compound

Formula

Temperature (~

Cp (cal g - l ~

Acetic acid
Acetone

C2H40 2
C3H60

Acetonitrile
Benzaldehyde
Butyl alcohol (n-)

C2H3N
C7H60
C4Hl00

Butyric acid (n-)

C4H80 2

Carbon tetrachloride

CCI4

Chloroform

CHCI 3

26 to 95
3 to 22.6
0
24.2 to 49.4
21 to 76
22 to 172
2.3
19.2
21 to 115
30
0
40
20 to 100
0
20
30
0
15
30

0.522
0.514
0.506
0.538
0.541
0.428
0.526
0.563
0.687
0.582
0.444
0.501
0.515
0.198
0.201
0.200
0.232
0.226
0.234

Cresol
(o-)
(m-)

C7H80

Dichloroacetic acid

C2H2C120 2

Diethylamine
Diethyl malonate
Diethyl oxalate
Diethyl succinate
Dipropyl malonate
Dipropyl oxalate (n-)
Dipropyl succinate

C4H 1IN
C7H 1204
C6H100 4
CsH 14O4
C9H 1604
C8H140 4
C1oH 18O4

0 to 20
21 to 197
0 to 20
21 to 106
21 to 196
22.5
20
20
20
20
20
20

0.497
0.551
0.477
0.349
0.348
0.516
0.431
0.431
0.450
0.431
0.431
0.450

Appendices

4o3

Compound

Formula

Temperature (~

Cp(calg-1 ~

Ethanol
Ether

C2H60
C4HloO

Ethyl acetate

C4H802

Ethylene glycol

C2H602

Formic acid

CH202

Furfural

C5H402

Glycerol
Hexadecane (n-)
Isobutyl acetate
Isobutyl alcohol

C3H803
C16H34
C6H120 2
C4HIoO

Isobutyl succinate
Isobutyric acid
Lauric acid

C12H2204
C4H80 2
C12H2402

Methanol

CH40

Methyl butyl ketone

Methyl ethyl ketone
Methyl formate
Methyl propionate
Palmitic acid
Propionic acid

C6H120
C4H80
C2H402
C4H802
C16H3202
C3H602

Propyl acetate (n-)

Prowl butyrate
Propyl formate (n-)
Pyridine

C5H1002
C7H1402
C4H802
CsHsN

Quinoline
Salicylaldehyde
Stearic acid

C9H7N
C7H602
C18H3602

0 to 98
-5
0
3O
8O
120
140
180
20
20
-11.1
0
2.5
5.1
14.9
19.9
0
15.5
20 to 100
0
20 to 100
15 to 50
0 to 50
20
21 to 109
30
0
20
40 to 100
57
5 to I0
15 to 20
21 to 127
20 to 78
13 to 29
20
65to 104
0
20 to 137
20
20
20
20
21 to 108
0 to 20
0 to 20
18
75 to 137

O.680
O.525
0.521
O.545
0.687
0.800
0.819
1.037
0.457
0.476
0.535
0.542
0.550
0.554
0.569
0.573
0.436
0.509
0.524
0.367
0.416
0.576
0.496
0.459
0.716
0.603
0.442
0.450
0.572
0.515
0.590
0.601
0.553
0.549
0.516
0.459
0.653
0.444
0.560
0.459
0.459
0.459
0.405
0.431
0.395
0.352
0.382
0.550

Appendices

404

Table B.6 Specific heats of organic solids

(From R.H. Perry, D.W. Green and J.O. Maloney, Eds, 1984, ChemicalEngineers'Handbook, 6th edn, McGraw-Hill, New York)
Compound

Formula

Temperature (oc)
T

Cp(cal g- 1 oc-1 )

Acetic acid
Acetone
Aniline
Capric acid
Chloroacetic acid
Crotonic acid
Dextrin
Diphenylamine
Erythritol
Ethylene glycol
Formic acid

C2H40 2
C3H60
C6HTN
C10H2002
C 2H3CIO2
C4H60 2
(C6H 1005)x
Cl 2H i l N
C4HI004
C2H60 2
CH20 2

- 2 0 0 to 25
- 210 to - 80

Glucose

C 6H !20 6

Glutaric acid
Glycerol
Hexadecane
Lactose

C5H804
C3H80 3
C!6H34
Cl 2H22O 11
C12H22011.H20
Ci28240 2
C 6Hi0 O5
C6H!206
C3H40 4
C i 2H22011
C6H140 6
C2H204
C2H204.2H20

0.330 + 0.00080 T
0.540 + 0.0156 T
0.741
0.695
0.363
0.520 + 0.00020 T
0.291 + 0.00096 T
0.337
0.351
0.366 + 0.00110 T
0.387
0.430
0.277
0.300
0.299
0.330
0.495
0.287
0.299
0.430 + 0.000027 T
0.607
0.275
0.275
0.320
0.313 + 0.00025 T
0.259 + 0.00076 T
0.338
0.385
0.416
0.382
0.430
0.561
0.248 + 0.00153 T
0.299
0.301
0.287
0.308
0.366
0.320

Lauric acid
Levoglucosane
Levulose
Malonic acid
Maltose
Mannitol
Oxalic acid

Palmitic acid

C16H320 2

Phenol
Succinic acid
Sucrose
Sugar (cane)
Tartaric acid

C6H60
C4H60 4

Urea

CI 2H 22011
C12H22011
C4H60 6
C4H606.H20
CH4N20

8
60
38 to 70
0 to 90
26
60
- 190 to - 4 0
- 22
0
0
20
20
0
20
20
- 30 to 40
40
20
20
20
0 to 100
- 200 to 50
0
50
100
0
20
14 to 26
0 to 160
20
22 to 51
36
0
50
20

Appendices

405

Table B.7 Normal melting points and boiling points, and standard heats of phase change
(From R.M. Felder and R.W. Rousseau, 1978,

ElementaryPrinciplesof ChemicalProcesses,John Wiley, New York).

All thermodynamic data are at Iatm.

Compound

Molecular
weight

Melting
temperature
(~

Ahfat
melting point
(kJ gmol-1)

Acetaldehyde
Acetic acid
Acetone
Ammonia
Benzaldehyde
Carbon dioxide
Chloroform.
Ethanol
Formaldehyde
Formic acid
Glycerol
Hydrogen
Hydrogen chloride
Hydrogen sulphide
Methane
Methanol
Nitric acid
Nitrogen
Oxalic acid
Oxygen
Phenol
Phosphoric acid
Sodium chloride
Sodium hydroxide
Sulphur
(rhombic)
(monoclinic)
Sulphur dioxide
Sulphuric acid
Water

44.05
60.05
58.08
17.03
106.12
44.01
119.39
46.07
30.03
46.03
92.09
2.016
36.47
34.08
16.04
32.04
63.02
28.02
90.04
32.00
94.11
98.00
58.45
40.00

- 123.7
16.6
- 95.0
-77.8
- 26.0
- 56.6
-63.7
- 114.6
-92
8.30
18.20
- 259.19
- 114.2
- 85.5
- 182.5
- 97.9
-41.6
- 210.0

12.68
18.30
O. 12
1.99
2.38
0.94
3.167
10.47
0.720

- 218.75
42.5
42.3
808
319

0.444
11.43
10.54
28.5
8.34

256.53
256.53
64.07
98.08
18.016

113
119
- 75.48
10.35
0.00

10.04
14.17
7.402
9.87
6.0095

12.09
5.69
5.653
8.33
5.021

Normal
boiling
point (~

Ah v at
boiling point
(kJ gmol - l )

20.2
118.2
56.0
-33.43
179.0
(sublimates at - 78~
61.0
78.5
- 19.3
100.5
290.0
- 252.76
-85.0
-60.3
- 161.5
64.7
86
- 195.8
(decomposes at 186~
- 182.97
181.4

25.1
24.39
30.2
23.351
38.40

38.58
24.48
22.25
0.904
16.1
18.67
8.179
35.27
30.30
5.577
6.82

1465
1390

170.7

444.6
444.6
- 10.02
(decomposes at 340~
100.00

83.7
83.7
24.91
40.656

Table B.8 Heats of combustion

(From Handbook of Chemistry and Physics, 1992, 73rd edn, CRC Press, Boca Raton; Handbook of Chemistry and Physics, 1976, 57th edn, CRC Press, Boca
Raton; and R.M. Felder and R.W. Rousseau, 1978, ElementaryPrinciplesof ChemicalProcesses,John Wiley, New York)

Referenceconditions: 1 atm and 25~ or 20~ values marked with an asterisk refer to 20~
Products of combustion are taken to be CO 2 (gas), H 2 0 (liquid) and N 2 (gas); therefore, A h~ = 0 for CO 2 (g), H 2 0 (1) and N 2 (g).
State: g - gas; l - liquid; c - crystali s - solid.
Compound

Formula

Molecular
weight

State

Heat of combustion
A h e (kJ gmol- 1)

Acetaldehyde

C2H40

44.053

Acetic acid

C2H402

60.053

Acetone

C3H60

58.080

l
g
l
g
l
g

-1166.9
-1192.5
-874.2
-925.9
-1789.9
-1820.7

Appendices

406

Compound

Formula

Molecular
weight

Acetylene
Adenine

C2H 2
C5H5N 5

26.038
135.128

Alanine (D-)
Alanine (Lo)

C3H702N
C3H702N

89.094
89.094

Ammonia
Ammonium ion
Arginine (D-)
Asparagine (L-)
Aspartic acid (L-)
Benzaldehyde

NH 3
NH,~
C6HI402N4
C4H803N 2
C4H704N
C7H60

17.03

Butanoic acid

C4H80 2

88.106

1-Butanol

C4HI00

74.123

2-Butanol

C4Hl00

74.123

Butyric acid

C4H802

88.106

Caffeine
Carbon
Carbon monoxide
Citric acid
Codeine
Cytosine
Ethane
Ethanol

C8H1002N4
C
CO
C6H807
C18H2103N.H20
C4H5ON 3
C2H6
C2H60

111.103
30.070
46.069

Ethylene
Ethylene glycol

C2H 4
C2H602

28.054
62.068

Formaldehyde
Formic acid

CH20
CH20 2

30.026
46.026

Fructose (D-)
Fumaric acid
Galactose (D-)
Glucose (D-)
Glutamic acid (L-)
Glutamine (L-)
Glutaric acid
Glycerol

C6HI206
C4H40 4
C6H1206
C6H1206
C5H904N
C5HloO3N2
C5H804
C3H80 3

Glycine
Glycogen
Guanine
Hexadecane

C2H502N
(C6HloO5)xper kg
C5H5ON 5
C16H34

151.128
226.446

Hexadecanoic acid

C16H3202

256.429

Histidine (L-)
Hydrogen
Hydrogen sulphide
Inositol
Isoleucine (L-)
Isoquinoline

C6H902N 3
H2
H2S
C6H120 6
C6H1302N
C9HTN

155.157
2.016
34.08

174.203
132.119
133.104
106.124

12.011
28.010

116.073

147.131
146.146
132.116
92.095
75.067

131.175
129.161

State

Heat of combustion
Ah c (kJ gmo1-1)
-1301.1
-2778.1
-2886.9
-1619.7
-1576.9
-1715.0
-382.6
-383
-3738.4
-1928.0
-1601.1
-3525.1
-3575.4
-2183.6
-2241.6
-2675.9
-2728.2
-2660.6
-2710.3
-2183.6
-2241.6
-4246.5"
-393.5
-283.0
-1962.0
-9745.7"
-2067.3
-1560.7
-1366.8
-1409.4
-1411.2
-1189.2
-1257.0
-570.7
-254.6
-300.7
-2813.7
-1334.0
-2805.7
-2805.0
-2244.1
-2570.3
-2150.9
-1655.4
-1741.2
-973.1
-17530.1"
-2498.2
-10699.2
-10780.5
-9977.9
-10031.3
-10132.3
-3180.6
-285.8
-562.6
-2772.2*
-3581.1
-4686.5

Appendices

407

Compound

Formula

Molecular
weight

Lactic acid (D,L-)

Lactose
Leucine (D-)
Leucine (L-)
Lysine
Malic acid (L-)
Malonic acid
Maltose
Mannitol (D-)
Methane
Methanol

C3H603
C12H22Oll
C6H1302N
C6H1302N
C6H1402N2
C4H60 5
C3H404
C12H22Oll
C6H1406
CH 4
CH40

Morphine
Nicotine
Oleic acid
Oxalic acid
Papaverine
Pentane

C17H1903N.H20
CloH14N2
C18H3402
C2H204
C2oH2104N
C5H12

72.150

Phenylalanine(g-)
Phthalic acid
Proline (L-)
Propane
1-Propanol

C9HIIO2N
C8H604
C5H902N
C3H8
C3H80

165.192
166.133
115.132
44.097
60.096

2-Propanol

C3H80

60.096

Propionic acid

C3H602

74.079

1,2-Propyleneglycol

C3H802

76.095

1,3-Propyleneglycol

C3H802

76.095

Pyridine

C5H5N

79.101

Pyrimidine

C4H4N2

80.089

Salicylicacid

C7H60 3

138.123

Serine (L-)
Starch
Succinic acid
Sucrose
Thebaine
Threonine (L-)
Thymine
Tryptophan (L-)
Tyrosine (L-)
Uracil

C3H703N
(C6HloO5)xPerkg
C4H604
C12H22Oll
C19H2103N
C4H903N
C5H602N2
CllH1202N2
CgH1103N
C4H402N 2

105.094

119.120
126.115
204.229
181.191
112.088

Urea

CH4ON 2

60.056

Valine (L-)

C5HIIO2N

117.148

Xanthine

C5H402N 4
C5HloO 5

152.113

Xylose
Biomass

CH1.8Oo.5No.2

25.9

State

Heat of combustion
A hc (kJ gmol-1)
-1368.3
-5652.5
-3581.7
-3581.6
-3683.2
-1328.8
-861.8
-5649.5
-3046.5*
-890.8
-726.1
-763.7
-8986.6*
-5977.8*
-11126.5
-251.1
-10375.8*
-3509.0
-3535.6
-4646.8
-3223.6
-2741.6
-2219.2
-2021.3
-2068.8
-2005.8
-2051.1
-1527.3
-1584.5
-1838.2
-1902.6
-1859.0
-1931.8
-2782.3
-2822.5
-2291.6
-2341.6
-3022.2
-3117.3
-1448.2
-17496.6*
-1491.0
-5644.9
-10221.7*
-2053.1
-2362.2
-5628.3
-4428.6
-1716.3
-1842.8
-631.6
-719.4
-2921.7
-3084.5
-2159.6
-2340.5

131.175
131.175
146.189

16.043
32.O42

90.036

118.089

- 552