Table 6.1
(continued)
Compounds
Formula Abbrev.
M
(g mol
À1
)
d
(20
C)
Melting
point
(
C)
Boiling
point
(
C)
s
(20
C)
(mg L
À1
)
Log
(K
ow )
H
(20
C)
(Pa m
3
mol
À1
)
D
air
(m
2
s
À1
)
D
water
(m
2
s
À1
)
IP
(eV)
Trichloroethylene
C
2 HCl
3
TCE
131.4
1.46
À86.4
87.2
1280
2.42 765
7.90
 10
À6
9.10
 10
À10
9.94
1,1Dichloroethylene
C
2 H
2 Cl
2 1,1DCE
96.9
1.22
À122.1 31.56
2420
2.13 2376
9.00
 10
À6
1.04
 10
À9
9.81
cis-1,2Dichloroethylene
C
2 H
2 Cl
2 cis-1,2DCE
96.9
1.28
À80
60.1
6410
1.86 341
7.36
 10
À6
1.13
 10
À9
–
trans-1,2Dichloroethylene
C
2 H
2 Cl
1,2DCE
96.9
1.26
À50
47.5
4520
2.09 875
7.07
 10
À6
1.19
 10
À9
9.64
Vinyl chloride
C
2 H
3 Cl VC
62.5
0.91
À153.8 À13.4
2763
0.60 2172
1.06
 10
À5
1.23
 10
À10
9.99
Hexachlorobenzene C
6 Cl
6
HCB
284.8
2.05
230
323–326 0.005
5.44 35.1
5.42
 10
À6
5.91
 10
À10
9.00
Pentachlorobenzene C
6 HCl
5
PeCB
250.3
1.83
86
277
0.419
5.17 52.6
–
–
9.11
1,2,3,4Tetrachlorobenzene
C
6 H
2 Cl
4 1,2,3,4TeCB
215.9
–
47.5
254
3.44
4.63 58.5
–
–
9.11
1,2,3,5Tetrachlorobenzene
C
6 H
2 Cl
4 1,2,3,5TeCB
215.9
–
54.5
246
3.44
4.63
–
–
–
9.16
1,2,4,5Tetrachlorobenzene
C
6 H
2 Cl
4 1,2,4,5TeCB
215.9
1.86
140
243–246 0.528
4.63
–
–
–
9.00
1,2,3Trichlorobenzene
C
6 H
3 Cl
3 1,2,3TCB
181.4
1.69
53–54
218–219 19.31
4.05
–
–
–
9.18
1,2,4Trichlorobenzene
C
6 H
3 Cl
3 1,2,4TCB
181.4
1.45
17
213.5
36.5
4.02 172
3.00
 10
À6
8.23
 10
À10
9.04
1,2,5Trichlorobenzene
C
6 H
3 Cl
3 1,2,5TCB
181.4
1.39
63–64
208
8.46
4.15
–
–
–
9.30
C
6 H
4 Cl
2
147.0
1.30
À45.6
180.5
147
3.38 133
3.00
 10
À6
7.90
 10
À10
9.06
288
R. Rodrigues et al.
(continued)
Compounds
Formula Abbrev.
M
(g mol
À1
)
d
(20
C)
Melting
point
(
C)
Boiling
point
(
C)
s
(20
C)
(mg L
À1
)
Log
(K
ow )
H
(20
C)
(Pa m
3
mol
À1
)
D
air
(m
2
s
À1
)
D
water
(m
2
s
À1
)
IP
(eV)
Trichloroethylene
C
2 HCl
3
TCE
131.4
1.46
À86.4
87.2
1280
2.42 765
7.90
 10
À6
9.10
 10
À10
9.94
1,1Dichloroethylene
C
2 H
2 Cl
2 1,1DCE
96.9
1.22
À122.1 31.56
2420
2.13 2376
9.00
 10
À6
1.04
 10
À9
9.81
cis-1,2Dichloroethylene
C
2 H
2 Cl
2 cis-1,2DCE
96.9
1.28
À80
60.1
6410
1.86 341
7.36
 10
À6
1.13
 10
À9
–
trans-1,2Dichloroethylene
C
2 H
2 Cl
1,2DCE
96.9
1.26
À50
47.5
4520
2.09 875
7.07
 10
À6
1.19
 10
À9
9.64
Vinyl chloride
C
2 H
3 Cl VC
62.5
0.91
À153.8 À13.4
2763
0.60 2172
1.06
 10
À5
1.23
 10
À10
9.99
Hexachlorobenzene C
6 Cl
6
HCB
284.8
2.05
230
323–326 0.005
5.44 35.1
5.42
 10
À6
5.91
 10
À10
9.00
Pentachlorobenzene C
6 HCl
5
PeCB
250.3
1.83
86
277
0.419
5.17 52.6
–
–
9.11
1,2,3,4Tetrachlorobenzene
C
6 H
2 Cl
4 1,2,3,4TeCB
215.9
–
47.5
254
3.44
4.63 58.5
–
–
9.11
1,2,3,5Tetrachlorobenzene
C
6 H
2 Cl
4 1,2,3,5TeCB
215.9
–
54.5
246
3.44
4.63
–
–
–
9.16
1,2,4,5Tetrachlorobenzene
C
6 H
2 Cl
4 1,2,4,5TeCB
215.9
1.86
140
243–246 0.528
4.63
–
–
–
9.00
1,2,3Trichlorobenzene
C
6 H
3 Cl
3 1,2,3TCB
181.4
1.69
53–54
218–219 19.31
4.05
–
–
–
9.18
1,2,4Trichlorobenzene
C
6 H
3 Cl
3 1,2,4TCB
181.4
1.45
17
213.5
36.5
4.02 172
3.00
 10
À6
8.23
 10
À10
9.04
1,2,5Trichlorobenzene
C
6 H
3 Cl
3 1,2,5TCB
181.4
1.39
63–64
208
8.46
4.15
–
–
–
9.30
C
6 H
4 Cl
2
147.0
1.30
À45.6
180.5
147
3.38 133
3.00
 10
À6
7.90
 10
À10
9.06
288
R. Rodrigues et al.