-------
TABLE 18. ANALYSES OF RESIDUES FROM THE FLUIDIZED-BED INCINERATION
OF PAINT MANUFACTURING WASTES
Run Number
Component
Mercury, ppm
Total carbon, %
Loss on Ignition, 7,
Calcium, %
Aluminum, %
Titanium, %
Iron, %
Silica, %
Magnesium, %
Lead, %
Manganese, %
Barium, %
Antimony, %
Chromium, %
Nickel, %
Molybdenum, %
Tin, %
Copper, %
Zinc, %
Sodium, %
Zirconium, %
Cobalt, %
Strontium, %
Vanadium, %
Potassium, %
17
0.12
0.71
: 7.38
10-20
2-4
0.2
2.0
10-20
3.0
2.0
0.04
0.02
<0.03
0.4
0.07
0.03
<0.01
0.02
0.3
0.5
0.05
<0.01
0.5
N.D.
N.D.
18
0.26
0.41
4.32
5-10
2-4
5-10
3-6
5-15
1.0
5-10
0.1
0.03
<0.03
2.0
0.2
0.03
<0.01
0.04
0.3
0.3
0.2
0.02
0.2
N.D.
N.D.
21
0.05
0.05
1.18
5-10
1.0
10-20
3.0
5-10
3.0
0.3
0.01
0.1
0.3
0.2
0.03
<0.01
0.01
0.08
1.0
<0.1
0.02
<0.01
0.01
N.D.
N.D.
22
0.07
0.04
0.87
5-10
1.0
10-20
3.0
5-10
3.0
0.3
0.01
0.1
0.3
0.2
0.03
<0.01
0.01
0.01
1.0
<0.1
0.02
<0.01
0.02
N.D.
N.D.
26
0.05
0.37
1.5
5-15
0.5
0.4
0.4
10-20
0.3
0.03
N.D.
N.D.
N.D.
15-30
0.02
<0.005
N.D.
0.01
N.D.
0.1
N.D.
0.02
N.D.
0.01
N.D.
27
0.08
0.18
1.3
5-15
0.5
0.3
0.3
10-20
0.3
0.03
N.D.
N.D.
N.D.
15-30
0.01
<0.005
N.D.
0.01
N.D.
0.1
N.D.
0.02
N.D.
0.01
N.D.
28
0.36
0.91
1.97
5-10
2.0
10-20
3.0
10-20
2.0
0.3
0.1
0.03
N.D.
2.0
0.04
0.01
0.01
0.01
0.2
0.3
0.05
0.01
0.2
N.D.
0.4
29
0.15
0.61
1.95
5-10
2.0
10-20
5.0
5-10
2.0
0.4
0.2
0.1
N.D.
0.3
0.05
0.01
<0.01
0.02
0.3
1.0
0.1
0.02
0.1
N.D.
0.6
29-A
0.03
0.06
0.65
5-10
2.0
10-20
5.0
5-10
1.0
0.4
0.2
0.1
N.D.
0.3
0.05
0.01
<0.01
0.02
0.3
1.0
0.1
0.02
0.1
N.D.
0.4
30
0.06
1.6
9.34
10-20
0.3
1.0
0.2
10-20
0.2
0.01
O.01
<0.01
N.D.
10-20
<0.01
<0.005
<0.01
0.03
<0.1
0.1
<0.01
0.02
<0.01
N.D.
0.1
33
0.03
0.14
1.85
3-6
0.4
3-6
2.0
20-40
0.5
0.6
0.3
0.02
N.D.
1.0
0.02
0.02
0.03
0.01
<0.1
<0.1
0.01
0.1
0.03
N.D.
0.1
N.D. = None detected.
-------
The spectrographic analyses show that the major elements present in the
residue from incineration of these paint wastes were calcium, silica,
titanium, iron, lead and magnesium. The residue from the incineration
of wash-out water from latex paint production (Runs 26 and 27) contained
large quantities (15-30 percent) of chromium.
The effluent from the exhaust gas scrubber was analyzed for mercury,
COD and total organic carbon. The results of these analyses are shown
in Table 19. In all runs except 17 and 18 the mercury level was found
TABLE 19. ANALYSES OF EXHAUST GAS SCRUBBER EFFLUENT FROM
THE FLUIDIZED-BED INCINERATION OF PAINT
MANUFACTURING WASTES
Run Number
17
18
21
22
26
27
28
29
29-A
30
33
Mercury ,
mg/1
6.9
1.1
<0.1
0.6
< 0.005
< 0.005
0.010
0.002
< 0.001
< 0.001
< 0.001
COD,
mg/1
24
29
25
28
18
24
N.A.
N.A.
N.A.
N.A.
N.A.
Total Organic
Carbon, mg/1
10
10
8
9
N.A.
N.A.
N.A.
N.A.
N.A.
N.A.
N.A.
N.A. = Not analyzed
to be less than 1 milligram per liter, COD less than 30 milligrams per
liter and the total organic carbon less than 10 milligrams per liter.
The influent water used for scrubbing the gases was also analyzed and
found to contain less than 0.001 milligram per liter of mercury and
8 milligrams per liter total organic carbon
Samples were taken of the exhaust gases and analyzed by mass spectro-
graphic techniques. The results of these analyses are shown in Table 20.
The most important noxious or toxic compounds found were hydrogen cyanide,
and nitrous oxides. It is expected that hydrogen cyanide comes from the
phthalocyanine that is used as a pigment in some blue and green paints.
37
-------
TABLE 20. MASS SPECTROGRAPHIC ANALYSIS OF EXHAUST GASES FROM FLUIDIZED-
BED INCINERATION OF PAINT MANUFACTURING WASTES
00
Components
Carbon dioxide, vol %
Argon, vol %
Oxygen, vol %
Nitrogen, vol %
Hydrogen, vol %
Carbon monoxide, vol %
Methane, vol %
Sulfur dioxide, ppm
Hydrogen sulfide, ppm
Carbonyl sulfide, ppm
Ethane, ppm
Hydrogen cyanide, ppm
Benzene, ppm
Nitrous oxide, ppm
Acetone, ppm
Ethane, ppm
Ethylene, ppm
Acetylene, ppm
Run
17
10. /
1.0
7.41
80.8
0.08
0.21
O.001
<2
<2
<2
37
50
13
28
26
N.D.
N.D.
N.D.
Run
18
12.4
1.0
5.47
'80.9
0.03
0.02
O.001
<2
<2
<2
9
39
3
45
3
N.D.
N.D.
N.D.
Run
21
10.6
0.95
7.13
81.1
0.04
0.06
<0.001
N.D.
N.D.
N.D .
N.D.
46
130
21
N.D.
N.D.'
<2
<2
Run
22
8.09
0.96
10.06
80.1
0.03
0.02
O.001
N.D.
N.D.
N.D.
N.D.
103
<2
57
N.D.
N.D.
<2
<2
Run
26
10.5
1.05
2.5'9
85.8
0.08
0.02
0.003
<2
<2
N.D.
25
N.D.
N.D.
53
N.D.
N.D.
N.D.
N.D.
Run
27
10.5
1.05
2.49
85.7
0.16
0.08
0.05
<2
<2
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
65
Run
28
7.64
0.95
11.6
79.8
0.05
0.03
<0.002
<1
<2
N.D.
N.D.
51
N.D.
63
26
N.D.
N.D.
N.D.
Run
29
11.6
0.97
6.96
80.4
0.03
0.002
<0.002
<2
<2
N.D.
N.D.
12
N.D.
34
18
N.D.
N.D.
N.D.
Run
30
8.9
1.0
5.83
84.1
0.01
<2
<2
<2
N.D.
N.D.
N.D.
<10
NvD.
N.D.
N.D.
N.D.
Run
33
12.0
1.0
5.75
81.1
0.05
<0.001
<0.001
.N.D.
-fc.D.
N,0.
N.D.
20
N.D.
185
N.Dv
N.D.
N.D.
N.D.
N.D. = None detected.
-------
During Runs 17 and 21, samples of exhaust gas were taken using a steel
bulb that could be heated during analysis. This was done in an effort
to determine the mercury content of thQ gases by means of mass spectro-
graphy. In the sample from Run 17, no mercury was detected at a limit
of 5 ppm. However, by concentrating the sample from Run 21, a detection
limit of 0.1 ppm was achieved. No mercury was found at this level either.
Experiments on Plastic Wastes
Experimental incineration was carried out on two types of waste from the
plastic manufacturing industry. Both were sludges from the primary treat-
ment of process wastes. One sludge was from styrene production (Runs 15,
16, 19, 20, and 31), and the other from production of polyvinyl chloride
(Runs 24, 25, and 32). Table 21 shows the operating conditions used for
the incineration of these sludges. The sludges were fed ;directly into
the bed via a feed gun mounted in the side of the unit.
Following the procedure for paint wastes, the residue after incineration
was analyzed. The results of these analyses are given in Table 22. The
analyses show that the residue contains very little (0.13 ppm or less)
mercury and the total carbon content is also quite low (1.54 percent or
less). The major elements found in the residue are silica, calcium,
aluminum and magnesium, which probably come from the lime, and aluminum,
iron, and magnesium salts used for coagulation in the primary treatment
process.
Exhaust gas scrubber effluent was analyzed for mercury content and found
to contain less than the detection limits of 0.001 ppm. The COD of the
effluent was quite low except from the runs in which the PVC waste
were incinerated. This could be due, in part, to the chloride content
of the effluent. These analyses are presented in Table 23.
Analyses of the exhaust gases from the incineration of plastic waste
is shown in Table 24. The gases are quite clean except in Run 25 which
contained benzene, ethylene, toluene, and acetylene. The reason for this
is not known, and it is assumed that complete combustion was not occurring
at the time the sample was taken.
An attempt was made to blend several types of wastes (liquids and solids)
from the production of laminated plastics. Even after dilution with large
quantities of water this blend could not be fed to the incinerator. The
mixture was not homogeneous and therefore could not be pumped with the
equipment customarily used for this purpose. The wastes involved were
(1) sanding dust, (2) resin production water of reaction, (3) waste
solvents, and (4) waste treaters and resins. It is felt that these
wastes could be incinerated if a suitable feeding system were to be
developed.
39
-------
TABLE 21. EXPERIMENTAL CONDITIONS EMPLOYED DURING
INCINERATION OF PLASTIC MANUFACTURING WASTES
Run
Number
15
16
S 19
20
24
25
31
32
Incineration
Description of Wastes Temperature,
Fed to Incinerator F
Primary
Primary
Primary
Primary
Primary
Primary
Primary
Primary
treatment
treatment
treatment
treatment
treatment
treatment
treatment
treatment
sludge
sludge
sludge
sludge
sludge (PVC)
sludge (PVC)
sludge
sludge (PVC)
1330
1580
1350
1720
1325
1800
1750
1350
Fluldizing
Velocity,
ft/sec
1
1
1
1
1
2
1
2
.5
.5
.5
.5
.8
.2
.8
.1
Exhaust
Gas, 0 ,
percent
6.
3.
5.
4.
3.
2.
4.0-5
3.0-4
0
6
5
8
3
8
.0
.0
Fuel
Required,
cfm
1.1
1.1
0.8
0.3
1.0
2.0
1.0
1.0
Feed
Rate,
g/min
95.5
84.7
78.5
92.7
101.5
98.6
60.0
68.0
Total,
Ibs
50.5
27.4
41.2
50.0
43.0
42.0
298
360
-------
TABLE 22. ANALYSES OF RESIDUE FROM FLUIDIZED-BED INCINERATION OF PLASTIC MANUFACTURING WASTES
Component
Mercury, ppm
Total carbon, %
Loss on Ignition, %
Chromium, %
Silica, %
Calcium, %
Aluminum, %
Lead, %
Magnesium, %
Iron , %
Vanadium, %
Nickel, %
Molybdenum, %
Copper , %
Sodium, %
Titanium, %
Cobalt, %
Zinc, %
Barium, %
Boron, %
Manganese, %
Tin, %
Potassium, %
Phosphorus , %
Zirconium, %
Strontium, %
Antimony, %
Run
15
0.13
1.54
4.49
0.03
10-20
10-20
3-5
0.08
2.0
3.0
N.D.
0.03
0.03
0.02
0.5
0.5
<0.01
0.1
0.02
N.D.
0.04
<0.01
N.D.
N.D,
0.02
0.02
0.03
Run
16
0.10
0.91
2.35
0.03
10-20
10-20
3-5
0.08
2.0
3.0
N.D.
0.07
0.03
0.02
0.5
0.5
<0.01
0.1
0.02
N.D.
0.04
<0.01
N.D.
N.D.
0.05
0.02
<0.03
Run
19
0.08
1.33
4.75
0.1
10-20
10-20
2-4
0.7
2.0
1.0
N.D.
0.03
0.01
0.02
0.3
0.3
<0.01
0.1
0.01
N.D.
0.03
<0.01
N.D.
N.D.
0.02
0.03
<0.03
Run
20
0.06
0.32
1.27
0.03
10-20
10-20
2-4
0.2
2.0
1.0
N.D.
0.01
0.01
0.02
0.3
0.1
<0.01
-<0.1
0.01
N.D.
0.03
<0.01
N.D.
N.D.
0.01
0.01
<0.03
Run
24
0.10
0.04
0.49
0.1
20-40
5.0
0.2
0.1
0.5
2.0
N.D.
0.03
<0.01
0.02
N.D.
1-2
N.D.
0.2
0.02
0.01
0.02
0.02
0.2
1.3
0.01
N.D.
N'.'D.
Run
25
0.06
0.02
0.71
0.1
20-40
2.0
0.7
0.03
0.2
1.0
N.D.
0.03
<0.01
0.02
N.D.
0.5
N.D.
0.1
0.01
<0.01
0.01
0.01
0.1
0.5
0.01
N.D.
N.D.
Run
31
0.06
3.0
16.9
1.0
5.10
15.30
3-5
0.01
3.0
2.0
N.D.
0.01
<0.01
0.03
1.0
0.2
<0.01
<0.1
0.01
N.D.
0.03
<0.01
0.4
N.D.
<0.01
0.01
N.D.
Run
32
0.04
0.19
2.38
1.0
20.40
5-10
2.0
0.01
0.5
1.0
N.D.
0.01
<0.01
0.005
0.2
2.0
<0.01
<0.1
0.01
N.D.
0.02
0.03
0.2
N.D.
0.01
0.01
N.D.
N.D. = None detected.
-------
TABLE 23. ANALYSES OF EXHAUST GAS SCRUBBER EFFLUENT FROM FLUIDIZED-
BED INCINERATION OF PLASTIC MANUFACTURING WASTES
Run Number
15
16
19
20
24
25
31
32
Total Solids,
mg/1
493
510
463
451
N.A.
N.A.
N.A.
N.A.
Total Organic
Carbon, mg/1
8.0
8.0
6.0
6.0
8.0
30.0
N.A.
N.A.
Mercury
mg/1
<0.0001
<0.0001
<0.0001
<0.0001
<0.0001
<0.0001
<0.0001
<0.0001
COD
mg/1
10
16
7
2
156
127
N.A.
N.A.
N. A. = Not analyzed.
-------
TABLE 24. MASS SPECTROGRAPHIC ANALYSES OF EXHAUST GASES FROM THE FLUIDIZED-
BED INCINERATION OF PLASTIC MANUFACTURING WASTES
-P-
u>
Component
Carbon dioxide, vol %
Argon, vol %
Oxygen, vol %
Nitrogen, vol %
Hydrogen, vol %
Carbon monoxide, vol %
Methane, vol %
Ethane, ppm
Benzene , ppm
Ethylene, ppm
Acetylene, ppm
Toluene , ppm
Nitrous oxide, ppm
Hydrogen cyanide , ppm
Sulfur dioxide, ppm
Carbonyl sulfide, ppm
Hydrogen sulfide, ppm
Run
15
8.67
1.01
6.56
83.6
0.14
<0.01
<0.01
18
N.D.
N.D.
N.D.
N.D.
15
N.D.
<2
<2
<2
Run
16
11.5
1.01
1.74
85.5
0.29
0.07
0.02
38
3
N.D.
N.D.
N.D.
980
N.D.
<2
<2
f2
Run
19
10.1
0.99
3.24
85.5
0.09
0.03
<0.01
N.D.
<2
8
8
N.D.
5
<2
N.D.
N.D.
N.D.
Run
20
9.7
0.99
4.65
84.1
0.09
<0.01
<0.01
N.D.
10
<2
<2
N.D.
37
<2
N.D.
N.D.
N.D.
Run
24
10.9
1.06
2.91
85.0
0.09
0.015
<.01
N.D.
N.D.
11
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
Run
25
9.68
0.93
0.33
75.6
4.39
2.59
5.99
N.D.
200
1100
2900
50
N.D.
N.D.
N.D.
N.D.
N.D.
Run
31
11.2
1.03
4.11
83.6
0.05
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
Run
32
10.3
1.02
4.28
83.5
<0.01
<0.01
<0.01
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
N.D.
Note: N.D. = None detected.
-------
TABLE 25. EXPERIMENTAL CONDITIONS EMPLOYED DURING INCINERATION OF RUBBER
MANUFACTURING WASTES
Incinerator
Run
Number
35
36
37(a)
38
Description of Wastes Temperature,
Fed to Incinerator
Primary treatment sludge
ditto
n
lr
F
1250
1450
1400
1450
Fluidizing
Velocity ,
ft/sec
1.7
1.9
2.0
2.0
Exhaust
Gas, 02 ,
percent
6.0
4.8
5.1
4.7
Fuel
Required
cfm
2.0
2.6
2.0
2.4
Feed
, Rate,
g/min
70
22
63
63
Total,
Ib
14.0
6.5
44
48
(a) During this run secondary sewage effluent was used as scrubbing media in the exhaust gas
scrubber.
-------
Experiments on Rubber Wastes
Two wastes from the rubber industry were selected for experimental in-
cineration; however, one of them, a sample of concentrated digestor
waste from a rubber reclaiming operation was never received. Four
separate runs were made on the sludge from the primary treatment of
synthetic rubber manufacturing wastes. The primary treatment involves
coagulation and flotation; therefore, the waste is actually a flotation
product. Table 25 summarizes the conditions used for incineration of
this waste. In all of these runs the sludges were introduced into the
bed through a feed gun mounted in the side of the unit. During Run Number
37 secondary sewage effluent was used as the scrubbing media. This was
done to see if the sewage effluent would scrub the gases as well as
water. The analysis of the exhaust gases show very little, if any,
difference in gas quality.
The analyses of the scrubber effluent as well as the secondary effluent
used are shown in Table 26. It can be seen that the mercury content in
Run 37 was not significantly higher than in Run 38 even though the
scrubbing media used (secondary sewage effluent) contained 0.002 ppm.
However, the COD of the run (Number 37) using sewage effluent was con-
siderably higher. The high COD content of the scrubber effluent from
Run 35 was probably due to the low (1250 F) incineration temperature.
TABLE 26. ANALYSES OF EXHAUST GAS SCRUBBER EFFLUENT FROM
FLUIDIZED-BED INCINERATION OF RUBBER MANUFACTURING
WASTES
Run Number Mercury, mg/1 COD, mg/1
35
36
37
38
0.0008
0.0034
0.012
0.011
1480
190
211
37
Secondary sewage 0.002 36
effluent
The results of the analyses of the residue from incineration of rubber
wastes, shown in Table 27, indicate a high mercury content (3 and 5 ppm)
for Runs 37 and 38. However, the total carbon content was low (less
than 0.43 percent) in both cases, which indicated that almost complete
combustion had occurred. As was the case with the residue from plastic
processing waste, the major elements present were silica, calcium,
aluminum, iron, and magnesium.
45
-------
TABLE 27. ANALYSES OF RESIDUE FROM FLUIDIZED-BED
INCINERATION OF RUBBER MANUFACTURING WASTES
Component
Mercury, ppm
Total carbon, %
Loss on Ignition, %
Aluminum, %
Silica, %
Magnesium, %
Calcium, %
Iron, %
Lead, %
Chromium, %
Boron, %
Barium, %
Manganese, %
Nickel, %
Molybdenum, %
Vanadium, %
Copper, %
Sodium, %
Titanium, %
Zirconium, %
Cobalt, %
Potassium, %
Run
35
0.40
2.65
20.2
10-20
3-5
2-4
3-5
1-2
0.2
0.5
0.05
0.01
0.02
0.01
<0.005
0.01
0.01
<0.1
0.7
0.01
0.01
0.3
Run
36
0.30
0.95
18.1
10-20
4-8
2-4
3-5
1-2
0.2
0.5
0.05
0.01
0.02
0.01
0.01
0.01
0.01
<0.1
0.7
0.01
0.01
0.3
Run
37
5
0.43
7.3
10-20
10-20
0.7
2.0
1-2
0.3
0.4
<0.01
0.01
0.01
0.02
0.005
0.02
0.01
<0.1
0.7
<0.01
0.01
0.3
Run
38
3
0.39
1.7
15-30
5-15
1.0
2.0
1-2
0.2
0.8
<0.01
0.01
0.01
0.02
<0.005
0.03
0.02
<0.1
0.4
<0.01
0.005
0.3
46
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Analyses of the exhaust gases from incineration of rubber manufacturing
wastes indicated that very little, if any, noxious or toxic gases were
produced. These data are presented in Table 28. The only components
of any significance were hydrogen cyanide (Run 37) and nitrous oxide
(Runs 35 and 36) .
Experiments on Textile Wastes
Due to the small amount of textile manufacturing in the State of Ohio,
only one waste was incinerated. This is a waste from a viscose process.
Table 29 gives the experimental operating conditions used for incineration
of this material. This waste was introduced into the bed via a feed gun
mounted in the side of the unit. Due to the presence of caustic in this
waste, attempts to operate at bed temperatures above 1250 F caused the
bed material to become sticky and defluidize. Therefore, combustion was
not complete as is witnessed by the high total carbon and loss on ignition
analyses shown in Table 30. It should also be noted in these data that
this residue contained from 30 to 60 percent sodium.
Analyses of the scrubber effluent indicate that very little pollutional
contaminants are present in this stream. The mercury content of less
than 0.001 milligram per liter and the COD of 1 milligram per liter point
this out. These analyses are shown in Table 31.
Table 32 presents the results of mass spectrographic analysis of the
exhaust gases from the fluidized-bed incineration of the viscose process
wastes. The nitrogen oxide content of these gases of 16 ppm probably
was due to the low incineration temperature. However, even at the low
temperature of combustion employed, the amount of sulfur compounds and
hydrocarbons are quite low.
47
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TABLE 28. MASS SPECTROGRAPHIC ANALYSIS OF EXHAUST
GASES FROM THE FLUIDIZED-BED INCINERA-
TION OF RUBBER MANUFACTURING WASTES
Component
Carbon dioxide, vol %
Argon, vol %
Oxygen, vol %
Nitrogen, vol %
Hydrogen, vol %
Carbon monoxide, vol %
Sulfur dioxide, ppm
Hydrogen sulfide, ppm
Methane, ppm
Hydrogen chloride, ppm
Hydrogen cyanide, ppm
Carbonyl sulfide, ppm
Nitrous oxide, ppm
Carbon disulfide, ppm
Ethylene, ppm
Run
35
8.87
0.97
6.86
82.4
0.01
0.9
<3
<3
<3
<3
N.D.
<3
10
3
100
Run
36
10.5
1.0
5.55
82.9
<0.01
0.03
<3
<3
<3
<3
N.D.
<3
10
<3
<100
Run
37
9.46
1.0
5.96
83.5
0.07
0.007
<3
N.D.
N.D.
<1
11
<1
<3
<1
N.D.
Run
38
8.05
0.99
8.3
81.4
0.04
0.016
<3
N.D.
N.D.
<1
<3
<1
<3
<1
N.D.
N.D. = None detected.
48
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TABLE 29 . EXPERIMENTAL CONDITIONS EMPLOYED DURING INCINERATION OF TEXTILE
MANUFACTURING WASTES
Incinerator Fluidizing Exhaust Fuel _ Feed _
Run Description of Wastes Temperature, Velocity, Gas, 02, Required} Rate, Total
Number Fed to Incinerator F ft/sec percent cfm g/min Ib
34 Viscose rayon wastes 1250 2.0-2.3 8.0-10.0 2.0 14 31
-------
TABLE 30. ANALYSES OF RESIDUE FROM FLUIDIZED-BED
INCINERATION OF TEXTILE MANUFACTURING WASTES
Run 34—Viscose Waste
Mercury, ppm 0.07
Total Carbon, % 9.0
Loss on Ignition, % 21.3
Calcium, % 0.2
Silica, % 2.0
Chromium, % 0.03
Aluminum, % 0.05
Titanium, % 0.2
Iron, % 0.05
Magnesium, % 0.01
Lead, % 0.2
Barium, % <0.01
Manganese, % O.01
Tin, % 0.01
Nickel, % <0.01
Molybdenum, % <0.005
Copper, % <0.005
Zirconium, % <0.01
Cobalt, % 0.01
Sodium, % 30-60
Zinc, % <0.1
Potassium, % 1.0
Strontium, % <0.01
50
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TABLE 31. ANALYSES OF EXHAUST GAS SCRUBBER EFFLUENT FROM
FLUIDIZED-BED INCINERATION OF TEXTILE WASTES
Run 34
Mercury,
mg/1
COD,
mg/1
Total Organic Carbon,
mg/1
Viscose Waste
<0.001
N.A.
N.A.
N. A. = Not analyzed.
TABLE 32. MASS SPECTROGRAPHIC ANALYSIS OF EXHAUST GASES FROM
FLUIDIZED-BED INCINERATION OF TEXTILE WASTES
Component
Run 34—Viscose Wastes
Carbon dioxide, vol %
Argon, vol %
Oxygen, vol %
Nitrogen, vol %
Hydrogen, vol %
Methane, vol %
Carbon monoxide, vol %
Nitrous oxide, ppm
Sulfur compounds, ppm
Hydrocarbons, ppm
5.26
1.02
11.6
82.1
0.02
<0.001
0.03
16
<3
<3
51
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SECTION VI
DISCUSSION OF EXPERIMENTAL RESULTS
Paint
The results of the experimental work conducted on the fluidized-bed in-
cineration of wastes from the manufacture of paint indicate that this
type of incineration is technically feasible. The physical operation
of the incineration system was quite good and very few operational
problems were encountered. Early in the program, it was found that
introduction of wastes into the incinerator under the bed rather than
as an overhead spray gave improved results. This was due to the high
volatile organic content of the wastes. Introduction of these wastes
as an overhead spray did not afford sufficient retention time for
complete combustion of the volatiles and organics.
During the incineration of the sludges from solvent recovery operations,
it was necessary to use cooling water in the freeboard of the incinera-
tor to prevent excessively high temperatures in this zone. This is
due, primarily, to the high heating value of these wastes. In one
of the experimental runs water of reaction from resin production was
used as cooling water. This appears to be quite attractive, since
two wastes are treated in one operation.
The incineration of the sludges from solvent recovery can be carried
out autogenously, that is, without the ^se of auxiliary fuel, because
of the high heating value of these wastes. In the incineration of the
wash-out water from latex paint production fuel is required to elevate
the temperature to a point where combustion will occur. The economics
of this type of incineration is discussed in another section of this
report.
Plastics
The experimentation on the fluidized-bed incineration of wastes from
plastic production indicated that this too is technically feasible.
The wastes incinerated experimentally, sludges from primary treatment
of styrene and polyvinyl chloride process wastes, are amenable to
fluidized-bed incineration. Even though these materials require
auxiliary fuel for combustion, this method of incineration remains
quite attractive since little or no noxious or toxic gases are produced.
The residue from the incineration of these wastes is a finely divided
dust that could be disposed of in a landfill. They contain no organic
53
-------
compounds that could be leached out and cause stream pollution problems.
There also is the possibility of recovering the calcium, iron, aluminum,
or magnesium from this residue prior to disposal.
The only effluent stream from this type of incineration that might
cause stream pollution is the scrubber effluent. However, in a com-
mercial installation of this type the scrubbing water could be recycled
to the scrubber to alleviate this problem.
Rubber
The results obtained from the experimentation on fluidized-bed inciner-
ation of wastes from rubber manufacturing indicate the technical feasi-
bility of the technique for treating the wastes under consideration.
However, the only waste incinerated from this area was the flotation
sludge from the primary treatment of synthetic rubber production wastes.
The concentrated digestor waste from rubber reclaiming that was selected
for experimentation was not received.
The sludge from synthetic rubber production was incinerated under con-
ditions which did not produce toxic or noxious gases. The effluent
from the exhaust gas scrubber contained only trace contaminants. During
Run Number 37 when secondary sewage effluent was used as scrubbing
media, the COD level increased from 36 to 211 milligrams per liter.
The mercury level increased during the run from 0.002 to 0.012 ppm.
The physical operation of the incineration system was quite good during
these experimental runs.
Textiles
The only waste which could be procured from the textile industry that
appeared suitable for incineration was the waste from a viscose
process. From the data collected during the experimentation it would
appear that complete combustion of the organics present in this waste
is not possible by this technique. It is, however, possible to inciner-
ate this particularly difficult waste material and achieve about 80
percent combustion. This would alleviate the potential pollution
problem that now exists from disposal of this material in a landfill.
Complete combustion could not be attained because of the low melting
point of this material requiring that the incinerator be operated at
low temperatures. The low melting point is due to the high caustic
content of this waste. Attempts to operate the incinerator at
temperatures above this point caused the bed material (sand) to become
sticky and defluidize. However, even though complete combustion was
not achieved, partial incineration does not produce toxic or noxious
gases.
54
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SECTION VII
POTENTIAL IMPACT ON WATER POLLUTION
This section discusses the potential of the various wastes for pollution
of streams and the reduction of same by incineration. The waste loads
and their possible contribution to pollution is discussed separately
in the following sections.
Paint
The plants involved in paint manufacture and related type operations in
Ohio that were visited during this program generate about 110,000,000
gallons of various wastes annually. Of these wastes only 640,000 gallons
are incinerated at the present time. The remaining wastes go either
directly to city sewerage systems or landfill operations. The amount
that is disposed of in landfill operations is only 470,000 gallons. This
means that the various city sewage treatment plants must process over
98 percent of the wastes generated by this industry. Of course, a
majority of these wastes are dilute process waters, such as cooling
tower water, that presents no problems, except the tremendous volumes
involved at the sewage treatment plants.
The results of the experimental program indicate that in the case of
solvent-bearing wastes from the paint industry, the total waste load can
be reduced considerably by fluidized-bed incineration. The average
total waste remaining for disposal after incineration of solvent recovery
sludges is about 3.5 percent of the original weight. The average chemical
oxygen demand of this type waste is reduced from 547,250 mg/liter to
essentially zero. However, the effluent from the scrubber used for
cleaning the exhaust gases from the incinerator contains an average of
about 24 mg/liter COD. This effluent could be recycled to the scrubber
continuously and incinerated concurrently with the solvent-bearing wastes.
On the basis of a typical plant which generates about 125,000 gallons per
year of solvent recovery sludge, the use of incineration would reduce COD
loading to the environment by about 525,000 pounds per year for this
plant. Assuming the plant to be representative of the national picture
(see Figure A-l), a total reduction of 360,000,000 pounds of COD per year
could be achieved in the United States.
Plastic
The plants visited that are involved in the manufacture of plastics
generate approximately 900,000 gallons of liquid waste, 9,500,000
55
-------
pounds of sludge from waste treatment facilities, and 35,000,000 pounds
of solid waste annually. These wastes are all currently disposed of
in landfill operations, and therefore create the possibility of stream
pollution by leaching. The COD level of the solid wastes from these
plants varies from 530,000 to 1,300,000 ppm. The liquid waste contained
about 120,000 mg per liter COD and the waste treatment sludge from 250,000
to 590,000 mg per liter.
Incineration of the primary treatment sludges reduces the waste to be
disposed oi to less than 5 percent of the original weight. The residue
from the liquid wastes would amount to only about 75 mg per liter and
the residue from the solid waste would amount to only about 2 percent or
less i' they were incinerated. As was the case with incineration of the
wastes from paint manufacture, the only COD in the products occurs in the
scrubber effluent, which amounts to only about 8 mg per liter and this
could be recycled and incinerated also.
Using as a basis a typical plant which generates 6,000,000 pounds per
year of primary treatment sludge, the possible reduction in COD by
incineration is about 3,500,000 pounds per year. Assuming this plant to
be representative of the entire plastics industry nationally which con-
sists of 340 plants (see Figure A-2), the total COD reduction for the
United States would be about 1,200,000,000 pounds per year.
Rubber
Very little information was obtained on rubber manufacturing wastes in
Ohio, although it was determined that the wastes vary considerably with
COD values, ranging from 21,000 to 540,000 mg per liter for various
sludges from primary treatment operations. The annual quantities of
waste generated in this industry also was exceedingly difficult to assess,
On the basis of one large synthetic rubber manufacturing plant which
provided quantities of flotation sludge for experimental studies, a
possible reduction in COD by incineration was calculated at about
1,000,000 pounds annually. Projecting this to a national level which
consists of only 28 plants (see Figure A-3), the total COD reduction
would be about 88,000,000 pounds.
Textile
Since the textile industry in Ohio is relatively small, little data were
obtained from this industry. Of the plants visited the major waste load
appears to be dye wastes and process waters. These wastes are quite
dilute (less than 1 percent solids) and are disposed of in city sewerage
systems. The COD level varies from 355 to 751 mg per liter. By contrast,
56
-------
another waste from the textile industry is viscose process waste which
contained about 121,000 mg per liter COD.
Incineration of the dilute dye wastes would not be economically feasible
because of the large quantities of water involved. Incineration of the
viscose process waste should be considered because of the high COD con-
tent of this material. However, additional research is needed for the
incineration of this particular waste to develop the proper operating
parameters. No information was obtained on the quantities of viscose
waste generated, but the amount probably is low since there are only
20 plants producing viscose in the United States (see Figure A-4).
57
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SECTION VIII
PRELIMINARY ECONOMIC EVALUATION
To assess the economic feasibility of incineration for disposal of wastes
in the paint, plastics, rubber, and textile industries, a preliminary
evaluation was made of the process requirements and costs for three specific
incineration systems. These systems were selected on the basis of experi-
mental results and conclusions which indicated
(1) The technical feasibility of incineration of waste solvents and
sludges from the paint industry using the heating value of these wastes
as a prime source of energy. The envisaged process also would permit
the incineration of certain other paint wastes such as reaction water
and latex wash-out concurrently with the solvent bearing wastes. Flows would
be adjusted so that autogenous operation could be achieved.
(2) The technical feasibility of incineration of sludges from plastic
primary treatment operations. These sludges could contain either styrene or
PVC polymers. On the basis of experimental results, it was determined
that additional energy input would be needed for incineration of these sludges.
This could be supplied by burning methane and/or fuel oil in a combustion
zone or by using solid plastic wastes as a source of energy.
(3) The incineration of rubber manufacturing waste sludges with additional
energy being supplied by combustion of methane and/or fuel oil.
The following sections discuss the design aspects of an incinerator which
would be required for each of these three example systems.
Example_I; Paint_Waste Incineration Process
The envisaged process for the incineration of solvent recovery sludges,
reaction waters, and latex wastes is illustrated in Figure 2. Capacity
was based on the production of 125,000 gallons annually of solvent
recovery sludge which had an average heating value of 120,000 Btu per
gallon. Operating conditions were selected on the basis of experimental
runs made during the study, (i.e., bed temperature 1750 F, superficial
velocity 2.0 fps) . The calculations made to determine material and energy
balances shown in the Appendix indicate that an incinerator of about 6 feet in
diameter would be required for this system. The results also indicate that
approximately 54 gallons per hour of latex wastes and/or reaction water
could be disposed of by incineration concurrently with the waste sludge.
59
-------
Latex washout ^— - ^
or f ^\
54 gal/hr \ S
Solvent Recovery \
Sludge, 25 gall(hr ^
Fln-M-tzing Air, . v
750 scfm
,.
Fluid-Bed
Incinerator
1750 F
2.0 fps
D - 5.75ft
\ Cyr
\
Bed DJ
L Gases to Stack
Ions'
Cyclone
Dust . Solids to Disposal
.scharge = 10 Ib/hr
r
Methane
(Start-up)
FIGURE 2. SIMPLIFIED FLOWSHEET OF INCINERATOR FOR PAINT WASTES
-------
Example II; Plastic Waste Incineration Process
The envisaged process for the incineration of primary treatment sludge
from plastic manufacture is illustrated in Figure 3. Capacity was based
on the production of 30,000,000 pounds annually of sludge containing
an average of 10 percent solids. The heating value of these solids was
estimated at 15,000 Btu per pound. Operating conditions were selected
on the basis of experimental runs which indicated a bed temperature of
1325 F and superficial velocity of 1.8 fps were required. The calcula-
tions made to determine material and energy requirements are shown in
Appendix B. The results indicate that an incinerator of about 12 feet
in diameter would be required for incineration of this waste sludge.
Added fuel must be supplied (i.e., 156 scfm of methane or 625 pounds
per hour of waste polymers).
Example III: Rubber Waste Incineration Process
A simplified flowsheet for incineration of a flotation sludge containing
rubber wastes is shown in Figure 4. In this example system, no informa-
tion was obtainable for a typical quantity of wastes generated by plants
in Ohio. Thus, capacity was arbitrarily selected at 10,000,000 pounds
annually. A typical sludge, however, is known to contain 15.4 percent
solids which have a heating value of about 15,000 Btu per pound of dry
solids. Operating conditions from experimental runs with this sludge
would be bed temperature of 1400 F and superficial velocity of 2.0 fps.
The results of design calculations (Appendix B) indicate this incinerator
would be about 7.5 feet in diameter with provision for burning about
32 scfm of methane in a combustion chamber.
Estimated Capital and Operating Costs
The essential capital and operating costs for the three systems selected
above are itemized in Table 33. Basically, the capital costs were esti-
mated for conventional fluidized-bed units currently being manufactured
by a number of companies. Operating costs were selected for the major
items that were believed to be significant based on experience with these
types of systems.
Generally, the cost data indicate that fluidized-bed incineration could
be used for disposal of these wastes at an operating cost of between 140
to 180 dollars per day for plants generating between 3,000,000 and
30,000,000 pounds of waste annually. This reduces to a cost of between
0.1 to 1.0 cent per pound of waste being disposed of by incineration.
The higher cost, for paint waste incineration, results from the use of
a small diameter fluidized-bed unit and from the use of low feed rates
necessary for the high heating value of these wastes.
61
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Primary Treatment Sludge
(Styrene Production)
6000 Ib/hr @ 10% solids
r-'
Waste polymers (alternate)
625 Ib/hr f"
L--
I
Fluidizing Air
2,250 scfin
Fluid-Bed
Incinerator
1325 F
1.8 fps
D - 12.3 ft
Combustion
Chamber
Methane Burner
(alternate) Air
156 scfm 1560 scfin
Gases to stack
Solids to disposal
= 50-100 Ib/hr
FIGURE 3. SIMPLIFIED FLOWSHEET OF INCINERATOR FOR PLASTIC WASTES
-------
Flotation Waste Sludge
(Rubber Production)
2000 Ib/hr @ 15.4% soli
Fluidizing Air
1,150 scfm
Fluid-Bed
Incinerator
1400 F
2.0 fps
D - 7.4 ft
Combustion
Chamber
Gases to Stack
Solids to Disposal
27 Ib/hr
Methane Burner
31.7 scfm Air
317 scfm
FIGURE 4. SIMPLIFIED FLOWSHEET OF INCINERATOR FOR RUBBER WASTES
-------
TABLE 33. ESTIMATED CAPITAL AND OPERATING COST
FOR EXAMPLE INCINERATION SYSTEMS
Example I Example II Example II
Essential Plant Cost, $ $200,000 $350,000 $250,000
Essential Operating Costs, $/day
1. Fuel @ $,25 per 10 Btu 0 0 4.10
2. Electric Power @ $.007/KWH 8.40 8.40 8.40
3. Supplies and Maintenance @ 6.00 10.50 7.50
0.003% of Plant Cost
4. Operating Labor @ 24 Man- 84.00 84.00 84.00
hr per day, $3.50 per
Man-hr
5. Amortization @ 0.0224% 44.80 78.50 56.00
of Plant Cost
Total Operating Costs 143.20 181.40 160.00
Cost per Pound of Waste l.lc 0.14 0.40
64
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SECTION IX
ACKNOWLEDGMENTS
This research program was conducted during the period of July, 1970, through
September, 1971. Battelle personnel participating in the program were
R. G. Brown, J. G. Price, M. F. Nichols, H. K. Nuzum, A. K. Reed, T. L.
Tewksbury, H. Nack and G. R. Smithson, Jr.
The cooperation and assistance of the following people is gratefully
acknowledged:
David Papier (Ohio Department of Natural Resources)
James F. Shea (Ohio Department of Health)
Eugene Harris (Environmental Protection Agency).
We also gratefully acknowledge the assistance of all company representatives
from each industry that cooperated in this survey.
65
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SECTION X
BIBLIOGRAPHY
Paint Industry
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505, (1960).
(2) "Disposal of Industrial Waste Materials", Society of Chemical Industry,
London, 164 pp. (1957).
(3) "A Process for Treating the Effluent from Plants for the Electro-
Deposition of Paint", Pressed Steel Fisher Limited and Guy, V. H.,
B.P. 1,071,458.
(4) Haschke, J., and Tetsch, B., "The Problem of Sanitation. Sewerage
Problems of a Large Town with Much Industrial Waste Water", Stadtehygiene,
9, 61-68 (1958) .
(5) Falkenhain, H. S., "Solving the Waste Water Problem", Kommunalwirtschaft,
No. 17/18, 365-371 (1954).
(6) Grunwald, A., Mach, M., Pavlik, M. and Sztraka, A., "Treatment of
Waste Waters from the Production of Pigmented Lacquer Materials",
Sb. vys. Sk. chemtechnol. Praz, Technol. Vod., 8, pt. 2, 41-111 (1968).
(7) Kolsch-Folzer-Werke Aktiengesellschaft, "Method of and Apparatus for
Separating Paint from Waste or Circulating Water Containing Paint",
B.P. 1,016,673.
(8) Kepinski, J., Glabisz, U., Blasykiewicz, G., Szyroki, Z., and Tilly, J.,
"Purification of Effluent from the Szczecin Paint and Lacquer Works",
Zesz. Nauk. Politech. szczecin., Ser. Chem., No. 5, 33-44 (1964);
Chem. Abstr., 64, 1808 (1966).
(9) Glavis, Frank J., Keighley, William, J., and Haag, Thomas, H., "Paint
Dispersions", Rohm & Haas Co., Fr. 1,391,326 (Cl. C 09d), March 5, 1965;
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(10) Eckenfelder, W. Wesley, Jr., and O'Connor, Donald J., "Chemical Treatment
of Paint and Pigment Wastes", (Manhattan Coll., New York, N. Y.). Proc. Ind.
Waste Conf., 1955, 17-27 (Pub. 1956).
(11) Sakharnov, A. V., and Zege, I. P., "Methods for Purifying Industrial
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12(6), 667-71 (1967) Russ).
67
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(12) Koelsch-Folzer-Werke, "Separating Paint from Waste or Circulating Water
Containing Paint", A.-G. Brit. 1,016,673 (Cl. C 0.2b), Jan. 12, 1966;
Ger. Appl. July 15, 1961, 4 pp.
(13) "Laboratory-Scale Treatment of Effluent From Synthetic Resin
Manufacture", J. Proc. Inst. Sew. Purif., Pt. 3, pp 277-291 and
Pt. 4, pp 377-391 (1964).
(14) Pesin, L. M., Derkovskaya, I. L., Golodnaya, S. L., Pukhovitskaya,
A. N., and Akopdzhanyan, E. A., "The Purification of Urea Resin
Waste Waters From Formaldehyde", Plast. Massy, No. 8, pp 58-60
(1964); Chem. Abstr., 61, pp 11743 (1964).
(15) Singleton, K. G., "The Treatment of Contaminated Waste Water From
Synthetic Resin Manufacture", J. Proc. Inst. Sew. Purif., pp
498-506 (1965); Wat. Pollut. Abstr., 25, Abstr. No. 1841 (1952)
and Abstr. No. 375 (1957).
(16) Jacobs, H. L., "Waste Treatment Methods—Recovery and Disposal",
Chem. Engng, 62, No. 4, pp 184-188 (1955).
(17) Sokolov, V. P., and Lobashov, K. A., "Composition and Purification
of Waste Waters From Production of Suspended Poly(Vinyl Chloride)",
Trudy Khim. khim. Tekhnol., No. 3, pp 199-209 (1965); Chem. Abstr.
67, pp 529 (1967).
(18) Hadfield, W. B., "Experiments on the Treatment of Effluent From
the Manufacture of Plastics", J. Inst. Sew. Purif., Pt. 2, pp
211-213 (1959).
(19) Sercu, C., "Burning Industrial Wastes Slurries", Wastes Engng, 30,
pp 18-20 (1959).
(20) "Symposium on Trade Wastes", Institute of Sewage Purification, pp
112 (1957).
(21) Fukuoka, S., Eto, H., Mikami, E., and Ono, H., "Microbial Purification
of Some Specific Industrial Wastes. VI. The Treatment of Industrial
Phenolic Resin Waste Water", Hakko Kogaku Zasshi, 45, pp 159-167
(1967).
(22) Clarke, D. G., "Resin Emulsion Wastes No Longer a Sticky Problem",
Wat. Wastes Engng, 5, No. 11, pp 46-48 (1968).
(23) Mills, R. E., "Industrial Waste Control at an Organic Chemical
Plant", Pap. 5th Ontario Industr. Waste Conf., pp 147-165 (1958).
(24) Kwie, W. W., "Ozone Treats Waste Streams From Polymer Plants",
Wat. Sewage Wks, 116, pp 74-78 (1969).
68
-------
(25) Rogovskaya, T. I., and Lazareva, M. F., "A Microbiological
Characterization of the Biological Film Purifying Effluents of
the Plastics Industry", Mikrobiologiya, 33, pp 148-151 (1964;
Microbiology, 33, pp 127-129 (1964); Wat. Pollut. Abstr., 38,
Abstr. No. 1354 (1965).
(26) Rogovskaya, T. I., and Lazareva, M. F., "A Microbiological
Characterization of Activated Sludge Purifying Effluents of the
Plastics Industry", Mikrobiologiya, 32, pp 1047-1051 (1963);
Microbiology, 32, pp 888-892 (1964).
(27) International Union of Pure and Applied Chemistry, "Water Economy
and Recirculation in the Struggle Against Pollution", Bull. mens.
Inform. Ass. franc. Et. Eaux, No. 59, (1957).
(28) Hessen, R. , "Phenol Removal From and Utilization of Waste Waters
From the Preparation of Phenol-Formaldehyde Resins", Plaste u.
Kautschuk, 4, pp 51-53 (1957); Chem. Zbl., 129, pp 3753-3754 (1958).
(29) U.S. Water Pollution Control Federation',' "A Review of the Literature
of 1963 on Waste Water and Water Pollution Control", J. Wat. Pollut.
Control Fed., 36, pp 535-573, 659-711, and 791-863 (1964).
(30) Askew, M. W. , "Plastics in Waste Treatment", 1, pp 483-486 and 492
(1966); 2, pp 31-35 (1967).
(31) "1955 Industrial Wastes Forum. Prevention of Stream Pollution
by the Treatment or Elimination of Wastes at Their Source", Sewage
industr. Wastes, 28, pp 651-677 (1956).
(32) "Industry Report: Chemical and Rubber", v. 6, No. 5-11 (1959).
(33) Landa, S., "The Recovery and Importance of Substances of Value
From Phenolic Waste Waters", Wasserw.-WassTechn., 6, pp 73-76 (1956);
LitBer. Wass Abwass. Luft u. Boden, 5, pp 165 (1956); Wat. Pollut.
Abstr., 29, Abstr. No. 1138 (1956).
(34) Pettet, A. E. , "Recent Developments in the Biological Treatment of
Trade Waste Waters in Great Britain", J. Bull. Centre, beige Et.
Document. Eaux, No. 36, pp 90-98 (1957).
(35) Ott, R., "The Waste Water Treatment Plant of the 01- und Chemiewerk
A. G. in Hausen", Ber. No. 62/2, Verbd. Schweizer Abwasserfachleute;
Gesundheitsing, 81, pp 90 (I960).
(36) Dixon, C. M. , "Industrial Wastes I Have Known", Wastes Engng, 31,
315 and 350, (1960).
(37) Bisterfeld & Stolting, and Dannenbaum, H., "Recovery of Phenol
and Formaldehyde", G.P- 933,892, Chem. Zbl., 129, pp 10792-10793
(1958).
69
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(38) Clarke, Duane Grookett, "Resin Emulsion Wastes No Longer a Sticky
Problem", (Pollut. Abatement Lab., Rohm and Haas Co., Bristol, Pa.)
Water Wastes Eng. 1968, 5 (11), 46-8 (Eng).
(39) Singleton, K. G., "Biological Treatment of Waste Water from Synthetic
Resin Manufacture", (CIBA(A.R.L.) Ltd., Duxford-Cambridge, Engl.)-
Purdue Univ., Eng. Bull., Ext. Ser. No. 121, 62-70, Appendix 70-1
(1966) (Eng.).
(40) Bruenger, Karl, Koch, Fritz, "Shredded Foam Coatings", (Continental
Summi-Werke A.-G.) Ger. 1,284,090 (C1.C08J, B 32b, B65d, E04b) ,
28 Nov. 1968, Appl. 05 Aug 1961; 2 pp.
(41) Plasticizers and Resins from Waste Rubber or Plastics (Englebert &
Co. G. m. b. H. (Erwin Hoss and Siegfried Bostrom, inventors). Ger.
953,014, Nov. 22, 1956 (Cl. 39c, 30).
(42) Schneider, Edward, "Utilization of Wastes from Synthetic Plastics",
Chemik (Gliwiee) 12, 61-5 (1959).
(43) Rueb, F., "Purification of Waste Gases in the Preparation and
Processing of Plastic Materials", Kunststoff Gummi 3(10), 420-2
(1964) (Ger).
(44) Raus, J. E., and Fralish, H. J., "How One Major Molder Handles Scrap
and Regrind", Plast Technol. 12(11), 51-3 (1966) Eng.
(45) Stepniak, Henryk, "Utilization of Scrap Plastics, Rubber, and
Artificial Fibers", Polimery 11(5), 197—9 (1966) (Pol).
(46) Tetuo, Ide, "Waste Water Treatment in the Polymer Industry", Kobunshi
1968, 17 (193), 326-32 (Japan).
(47) Frantisek, Mikula, Petru, Kamil and Hajas, Milan, "Polycaprolactam
Waste Depolymerization", Czech. 120-715 (Cl. C 08f), Nov. 15, 1966,
Appl. May 15, 1965; 3pp.
(48) Hadfield, W. B., "Treatment of Effluent from the Manufacture of
Plastics", J. Inst. Sewage Purification 1959, 211-13.
(49) Gottfried, Kalich, Schubert, Joachim, Gothe, Rudolf, and Gerathewohl,
Herbert, "Processing and Use of Thermosetting-Plastic Waste", Ger.
(East) 47,801 (Cl. C08g) May 20, 1966, Appl. Sept. 2, 1964, 2 pp.
70
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(50) Shurygin, A. P., and Bernadiner, M. N., "Thermal Detoxication of
Waste Waters in an Enlarged Experimental Cyclone-Type Combustion
Chamber", (Energetics Inst., Moscow). Khim. Prom. 42(5), 360-2
(1966) (Russ).
(51) Koehler, Reinold, "Bacterial Treatment of Chemical Effluents Polluted
by Organic Matter", Wasser, Luft Betrich 10(8), 512-16 (1966) (Germ).
(52) Masck, Vaclay, "Polycyclic Aromatic Hydrocarbons Occurring in Water",
Gaz, Woda Tech. Sanit. 39(8), 270-2 (1965) (Pol).
(53) Harkness, N., and Jenkins S. H., "Laboratory-Scale Treatment of
Effluent from Synthetic Resin Manufacture. III. Treatment, After
Dephenolation, by the Activated-Sludge Process", Inst. Sewage
Purif., J. Proc. 1964 (4), 377-82; cf. CA 61, 8051h.
(54) Jenkins, S. H., Slim, J. A., and Harkness, N., "Laboratory-Scale
Treatment of Effluent from Synthetic Resin Manufacture. I. Treatment
by Biological Filtration", (Birmingham Tame Rea Dist. Drainage
Board, Engl.). Inst. Sewage Purif., J. Proc. 1964, Pt. 3, 277-9.
(55) "Treatment to Make Thermoplastic Resin Scrap Reusable", Toyo
Rayon Co., Ltd. Brit. I.015j750
(56) Billingsley, G. S., "Resin Waste Regeneration" (E. I. du Pont de
Nemours & Co.), Belg. 635,637, Jan. 31, 1964, U. S. Appl. Aug. 1, 1962,
13 pp.
(57) Tschonhens, Boni, "Water Economics of the Bavarian Industries,
Especially Effluent Problems of the Large Chemical Industries",
(Munich, Ger.). Gas- u. Wasserfach 92, No. 10 (water), 125-31 (1951).
(58) Chemikalienhandelsges, Malex, "Working Up Synthetic Resin Wastes",
m. b. H. Austrian 216,489, July 25, 1961.
(59) Bueno, Jean, A. L., "Recovery of Synthetic Polymer Wastes", Fr.
1,345,753 (Cl. C 08f, C OBg), Dec. 13, 1963, Appl. Nov. 2, 1962, 6 pp.
71
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Plastic Industry
(1) U.S. Water Pollution Control Federation, "A Review of the Literature
of 1962 on Waste Water and Water Pollution Control", J. Wat. Pollut.
Contr. Fed., 35, pp 553-586, 687-727, and 819-876.
(2) Bringmann, G., and Schroder, W., "Large-Scale Biological Removal
of Phenol From Waste Waters of a Synthetic Resin Factory by the
Nocardia Process", Gesundheitsing., 81, pp 205-207 (1960).
(3) "Treatment of Trade Wastes Containing Formaldehyde", Effl. & Wat.
Treatm. J., 3, pp 88-89 (1963).
(4) Holland, G. A., Lasater, J. E., Neumann, E. D., and Eldridge, W. E.,
"Toxic Effects of Organic and Inorganic Pollutants on Young Salmon
and Trout", Res. Bull. Wash. Dep. Fish., No. 5, pp 278 (1960);
Wat. Pollut. Abstr., 28, Abstr. No. 1653 (1955).
(5) Svetljakova, M. N., "Removal of the Unpleasant Odour From Disinfected
(Chlorinated) Water", Hyg. & Sanit., Moscow, No. 3, pp 14-16 (1953);
LitBer. Wass Abwass. Luft u. Boden, 3, pp 39 (1954/55).
(6) Society of Chemical Industry, "Reports on the Progress of Applied
Chemistry", Vol. XXXVIII, pp 990 (1953).
^ "**J
(7) Sapotnitskii, S. A., Myasnikova, R. M., and Volynskii, V. E.,
"Resins Based on Lignosulphonate-Phenol Complex", Sb. Tr., Gos.
Nauch.-Issled. Inst. Gidroliz. Sulf.-Spirt. Prom., 9, pp 236-242
(1961); Abstr. Bull. Inst. Pap. Chem., 33, pp 747-748 (1963).
(8) "Plastics Materials and Resins", Publication I.W.P.-10; contract
14-12-104 (October 12, 1967).
(9) Rayet, R., "Some Reflections^on the Treatment of Trade Waste
Waters", Bull. Centre beige Et. Document. Eaux, No. 26, pp 261-
268 (1954).
(10) Buxton, R., Pollman, D., "Development of Improved Processes for
Filament Wound Reinforced Plastic Structures", Report No. 0714 01 02
(April, 1963).
(11) Rice (Cyrus Wm.) and Co., Pittsburgh, Pa., "Projected Wastewater
Treatment Costs in the Organic Chemicals Industry", pp 191 (January,
1969).
(12) Heller, A. N. , and Wenger, M. E., "Process Engineering in Stream
Pollution Abatement", Sewage industr. Wastes, 26, pp 171-181 (1953).
72
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(13) Balden, A. R., "The Disposal of Solid Wastes", Ind. Water Eng.
4(8), 25-7 (1967) (Eng).
(14) Gruenwald, A., Mach, M., Pavlik, M., and Sztraka, A., Purification
of Waste Waters from the Production of Painting Materials", Sb.
Vysoke Skoly Chem.-Techno1, Praze, Technol. Vody 8(2), 41-111 (1965)
(Russ).
(15) Grunwald, A., Pavlik, M., Mach, M., and Sztraka, A., "Treatment of
Waste Water from the Manufacture of Paint Coating Material", Vodni
Hospodarstvi 15(3), 123-4 (1965).
(16) Kepiuski, Jozef, Glabisz, Urszula, Blasykiewicz, Genowefa, Szyroki,
Zbigniew, and Tilly, Jadwiga, "Purification of Effluent from the
Szczecin Paint and Lacquer Works", (Katedra Chem. Politech. Szczecin,
Warsaw). Zeszyty Nauk, Politech. Szczecin, Chem. No. 5, 33-44 (1964)
(Pol) .
(17) Ballnus, Willi; Leiss, "Procedures for Treating Waste Water of the
Varnish Industry, (W. Ger.), Wasser, Luft, Betr., 1968, 12(5), 289,
292-3 (Ger).
(18) Ludwig, Harvey, F., and Ludwig, Russell, G., "How to Flocculate
Greases So They Won't Clog Sewers", (Univ. of California, Berkeley).
Eng. News-Record 147, No. 1, 40 (1951).
(19) Bednyagin, P., "Use of Enamel Waste Products", Za Progress Proizvodstva
Sovet. Narod. Khoz. Litovsk. S.S.R. 1958, No. 3, 40-2.
(20) Societe Continentale Parker, "Precipitation of Water-Diluted Paints"
Fr. 1,425,207, (Cl. C 09d), Jan. 14, 1966; Brit. Appl. Feb. 28, 1964,
3 PP
(21) Powers, Thomas J., "Waste-Disposal Problems and Solutions", (Dow
Chem. Co., Midland, Mich.). Paint Ind. Mag. 69, No. 12, 46-7, 48 (1954).
73
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Rubber Industry
(1) Klimkina, N. V., "Hygienie Standards for Harmful Waste Products of
the Synthetic Isoprene Rubber Industry Contained in Water Basins",
Hyg. & Sanit., Moscow, 1959, 24, No. 6, 8-16 (English Summary).
(2) Ivanov, V. A., and Gabrilevskaya, L. N., "The Bottom Deposits of
Autopolymers and their Influence on the Sanitary Condition of
Water Reservoirs", Hyg. & Sanit, Moscow, 1957, No. 4, 15-18
(English Summary).
(3) Morzycki, J., Zawapzki, J., and Kielar, K. , "Purification of Sewage
Contaminated with Latex", Pr. Inst. Wlok., 1963, 13, 149-162; Chem.
Abstr., 1966, 64, 3192.
(4) Mills, R. E., "Process Waste Burner Destroys Liquid Organic Chemical
Wastes Safely", Wat. Sewage Wks, 1964, 111, 337-340.
(5) Taradin, Ya. I., Batkova, A. A., Makeeva, E. N., and Stepanova, N. M. ,
"Final Biological Purification of Waste Waters from SNK-40 Rubber
Finishing Shops and Sanitation Conditions for their Discharge", Okhr.
Vod. Resursov Och. Stochn. Vod Sb., 1964, 88-96; Chem. Abstr., 1965,
62, 11522.
(6) Sinaiskii, G. M., Kurolap, N. S., and Voinova, V. K., "Combined
Method of Ion Exchange and Adsorption for Removing Nekal from
Waste Waters", Okhr. Vodn. Resursov Och. Stochn. Vod, 1964, 128-133;
Chem. Abstr., 1965, 62, 12889-12890.
(7) Schulmann, J., "Waste Waters from Synthetic Rubber Works", Voda, 1958,
37, 29-30; Chem. Zbl., 1960, 131, 16554.
(8) Wolfson, D. E., Beckman, J. A., Walters, J. G., and Bennett, D. J.,
"Destructive Distillation of Scrap Tires", Report of Investigations,
Bureau of Mines, Washington, D. C., Sept 69, pp 23, RI-7302.
(9) Jennings, A., "Pre-treatment of Latex Rubber Waste", J. Inst. Sew. Purif.,
1955, Pt. 1, 85.
(10) Zelinka, M., "Toxicity of Waste Waters from the Manufacture of
Synthetic Rubber", Voda, 1957, 36, 242-244; Chem. Zbl., 1958, 129, 6064-
6065.
(11) Nicolai, A. L., Eckenfelder, W. W., and Gardner, D. G., "Effluent
Treatment Study for a Rubber research Laboratory", Industr. Wastes,
1956, 1, 136-139; Publ. Hlth Engng Abstr., 1956, 36, No. 8, 23
74
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(12) Molesworth, T. V., "The Treatment of Aqueous Effluent from Rubber
Production using a Trickling Filter", Proc. nat. Rubber Res. Conf.,
Kuala Lumpur, 1960, 944-959.
(13) Truelle, M. A., "The Effect on Fish of Waste Waters from the Manu-
facture of Synthetic Rubber", Ann. Acad. tchecosl. Agric., 1958,
3(31), 333-340; Chem. Zbl., 1961, 132, 9936.
(14) Munteanu, A., Cute, E., Godeanu, S., Eminovici, A., and Murgoci, C.,
"Treatment of Waste Waters from the Manufacture of Synthetic Rubber",
Studii Prot. Epur. Apel., Buc., 1967, 9, 123-163 (English Summary).
(15) Montgomery, D. R., "Integrated System for Plant Wastes Combats
Stream Pollution", Chem. Engng, Albany, 1967, 74, No. 5, 108-110.
(16) Truelle, M. A., "Damage Caused by Waste Waters from the Manufacture
of Synthetic Rubber", Cslke Ryb., 1959, 14, 36-37; Sci. Pap. Inst.
Chem. Technol., Prague, Technol. Wat., 1962, 6 Pt. 2, 547.
(17) Duke, J. B., "Flotation of Metallic Soap" (to Minerals & Chemicals
Philipp Corp.) U.S.P. 3,158,570; Chem. Abstr., 1965, 62, 10213.
(18) Ivanov, V. I., "Clarification of Waste Waters from the Production of
Polysulphide Rubbers", Vestn. Tekh. Ekon, Inform, nauch-issled. Inst.
Tekh. Ekon, Issled. Cos. Kom. Khim. Gosplane SSSR, 1963, No. 2,
26-27; Chem. Abstr., 1964, 61, 14345.
(19) Vaicum. L., and Wlezek, M., "Biological Treatment of Waste Waters
from the Polyamide Synthetic Fibre Industry by the Activated-Sludge
Process", Studii Prot. Epur. Apel., Buc., 1967, 9, 95-112 (English
Summary).
(20) Taras, M. J., "Interference by Industrial Wastes in the Mohr Test
for Chlorides", Wat. & Sewage Wks, 1955, 102, 442-446.
(21) Khitrov, V. A., Zadorozhnii, V. P., "Utilizing Wastes of the Synthetic
Rubber Industry in the Role of Acid Corrosion Decelerators", Foreign
Technology Division—Wright-Patterson Air Force Base, Ohio, Rept. No.
FTD-TT-65-1626, Mar. 66, pp 12.
(22) Harkness, N., and Jenkins, S. H., "Chemical and Biological Oxidation
of Styrene and Isoprene", J. Inst. Sew. Purif., 1958, Pt. 2, 216-220.
(23) USSR Industrial Development: Joint Publications Research Service
Washington, D. C. , Soviet Chemical Industry No. 82., Report No. 19863,
Jun 63, pp 54.
75
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(24) Orestova, N. N., "Local Purification and Use of Waste Waters from the
Polymerization Shop in the Voronezh Synthetic Rubber Plant", Okhrana
Vodn. Resursov i Ochistka Stochn. Vod (Voronezh: Voronezhsk. Univ.)
Sb. 1964, 134-7 (Russ).
(25) Tobola, Stanislaw, "Problems of Technological Wastes in Chemical
Industry", Chemik (Gliwice) 18, 121-4 (1965) (Pol).
(26) Collier, James Tyhurst, "Combustible Gas from Resinous Waste", Brit.
888,745, Feb. 7, 1962, Appl. May 28, 1959.
(27) Berry, A. E., "Survey of Industrial Wastes in the Lake Huron-Lake
Erie Section of the International Boundary Waters", I. Introduction
and Canadian Section. (Ontario Dept. Health, Toronto). Sewage and
Ind. Wastes 23, 508-17 (1951); cf. C.A. 45, 2612h.
(28) Sharp, D. H., "Treatment of Special Industrial Wastes", Civ. Engng.
Lond., 1961, 56, 801-804.
76
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Textile industry
(1) U.S. Department of Health, Education, and Welfare, Public Health
Service, "Municipal and Industrial Waste Facilities", U.S. Publ.
Hlth. Serv. Publ. No. 622, Vols. 1-9, pp 2032 (1958).
(2) Economic Commission for Europe, "Sewage Treatment in Viscose
Fibre Production, Water Poll/Econ/Working Paper 25, pp 7 (1966).
(3) Lebedev, M. , and Agalova, V., "Experiences with Plants Treating
Waste Waters from the Wool Industry", Vodosnab. sanit. Tekh.,
No. 4, pp 34-37 (1967).
(4) Zekeova, Z. N., "Application of the Basic Principles of Biological
Activated-Sludge Treatment to the Treatment of Waste Waters from
"Chemlon" Manufacture", Pr. vysk. Ust. vodohospod., Bratislava,
No. 40, pp 78 (1966).
(5) Bode, H. E. , "Process for Sizing Textiles and the Disposition
of Sizing Wastes Therefrom, U.S.P. 3,093,504.
(6) Little, A. H., "The Treatment and Control of Bleaching and Dyeing
Wastes", Wat. Pollut. Control, Lond., 68, pp 178-189 (1969).
(7) Offhaus, K. Z. , "The Zinc Content in Waste Waters from the
Synthetic Fibre Industry and Its Toxicity", Wass. Abwass. Forsch.,
No. 1, pp 7-21 (1968).
(8) Ogawa, H., Horikawa, K., Yasuda, M., and Kagami, T, , "Chemical and
Biological Treatment of Wool Scouring Waste", Kanagawa-Ken Kogyo
Shikensho Kenkyo Hokoku, No. 21, pp 35-45; Chem. Abstr., 70, No. 16,
pp 210 (1969).
(9) Public Health Service, Cincinnati, Ohio, Bureau of Disease
Prevention and Environmental Control, "Control and Disposal of
Cotton-Ginning Wastes", PHS-Pub-999-AP-31, pp 104 (1967).
(10) Hoare, J. L. , Stewart, R. G., and Sweetman, B. J., "New Zealand
Wool Scouring Liquors—Treatment and Potassium Recovery", N. Z.
Jl Sci., 12, pp 237-251 (1969).
(11) U.S. Water Pollution Control Federation, "A Review of the Literature
of 1959 on Waste Water and Water Pollution Control", J. Wat. Pollut.
Contr. Fed., 32, pp 443-481, 545-593, and 681-720 (1960).
(12) Bhakuni, T. S., and Bopardikar, M. V., "Recovery of Zinc from
Spinning Bath Waste of a Viscose Rayon Factory by Ion-Exchange
Process", Envir. Hlth, India, 9, pp 327-338 (1967).
77
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(13) U.S. Federation of Sewage and Industrial Wastes Associations,
"A Critical Review of the Literature of 1954 on Sewage, Waste
Treatment, and Water Pollution",. Sewage industr. Wastes, 27,
pp 515-571 and 633-688 (1955).
(14) Holder, Shelby H., Jr., "Marketing and Utilization of Cotton
Mill Waste",
(15) National Center for Air Pollution Control, Public Health Service,
Department of Health, Education, and Welfare and Agricultural
Engineering Research Division, Agricultural Research Service,
Department of Agriculture, "Control and Disposal of Cotton-
Ginning Wastes", (May 3 and 4, 1966).
(16) Munteanu, A., "An Experimental Station for the Treatment of Waste
Waters from the Manufacture of Cellulose and Viscose Artificial
Fibres", Inst. hydrotech. Res., sci. Sess., Bucharest, Sect. 4,
pp 51-54 (1964).
(17) "Mersey and Weaver River Authority", First annual report, pp 88
(1965-1966).
(18) U.S. Federation of Sewage and Industrial Wastes Associations,
"A Critical Review of the Literature of 1953 on Sewage, Waste
Treatment, and Water Pollution", Sewage industr. Wastes, 26,
pp 573-615 and 695-744 (1954).
(19) Kossakowski, J., and Kotulski, B., "Purification of Industrial
Waste Waters from Poly(vinyl chloride) (PVC) Production", Przem.
chem., 43, pp 336-339 (1964); Chem. Abstr. , 61, p 14345 (1964).
(20) Klust, G. , and Mann, H., "Investigations on the Decomposition of
Cellulose as an Aid in the Evaluation of Waters", Wasserwirtschaf,
Stuttg., 53, pp 320-323 (1963).
(21) Peyron, E., "Effluents from Dyeing and Finishing Baths", Teintex,
32, pp 419-425 (1967); Chem. Abstr., 69, pp 490 (1968).
(22) Sluchocka, Z. , and Terpilowska, W., "Purification of Retting Waste
Waters by Biological Oxidation Ditches", Pr. Inst. Przem. Wlok,
lykow., 14, pp 119-141 (1967); Chem. Abstr., 68, pp 10424 (1968).
(23) Sluchocka, Z. , and Terpilowska, W., "Purification of Retting Waste
Waters in Biological Oxidation Ditches", Pr. Inst. Przem. Wlok,
lykow., 13, pp 89-106 (1965); Chem. Abstr., 68, pp 10424 (1968).
(24) Sharda, C. P., and Manivannan, K., "Viscose Rayon Factory Wastes
and Their Treatment", Technology, Sindri, 3, No. 4, pp 58-60 (1966),
78
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(25) Saxena, K. L., and Chakrabarty, R. N., "Viscose Rayon Wastes and
Recovery of Zinc Therefrom", Technology, Sindri, 3, No. 4,
PP 29-33 (1966).
(26) Biggs, A. I., "Biological Treatment of Textile Effluents",
Chemy Ind., pp 1536-1538 (1967).
(27) Little, A. H. , "Treatment of Textile Waste Liquors", J. Soc.
Dyers Colour., 83, pp 268-273 (1967); Text. Abstr., 58, pp 647
(1967).
(28) Lur'e, Yu. Yu., and Antipova, P. S., "Removal of Anionic Surfactants
from Waste Waters", Trudy vses. nauchno-issled. Inst. vodosn.,
Kanaliz, Gidrotekh. Soor, Inzh. Gidrogeol., No. 14, pp 43-49 (1966).
(29) Petru, A., "Biological Treatment of Waste Water from Wool-Washing
Plants without Chemical Pre-Treatment", Vod. Hospod., 17, pp 108-
109 (1967).
(30) Summers, T. H. , "Effluent Problems and Their Treatment in the
Textile Industry", J. Soc, Dyers Colour, 83, pp 373-379 (1967).
(31) Moore, T. L., and Turcotte, J. A., "Handling Industrial Wastes:
Four Engineering Decisions", Wastes Engng, 34, pp 238-239 and
256 (1963).
(32) Jarnefelt, H. , "The Effect of Supreme Waste Lyes on the Plankton
Community", Verh. int. Ver. Limnol, 14, pp 1057-1062 (1959, 1961).
(33) Moore, T. L. , "Cutting Wastes Treatment Costs by Reclamation and
Utilization", Wastes Engng, 33, pp 76-77 (1962).
(34) Eldib., I. A., "Foam Fractionation for Removal of Soluble Organics
from Waste Water", J. Wat. Pollut. Contr. Fed., 33, pp 914-931
(1961).
(35) Kaeding, "The Purification of Waste Water in the Production of
Polyamide Fibre", J. Fortschr. WassChem. Grenzged., No. 5, pp 258-
283,'(1967); Chem. Abstr., 67, pp 8846 (1967).
(36) Summers, T. H. , "Effluent Problems and Their Treatment in the
Textile Industry", J. Soc. Dyers Colour., 83, pp 373-379 (1967).
(37) The Cotton and Man-Made Fibres Research Association, "Textile
Effluent Treatment and Disposal", Shirley Inst. Pamph., No. 92.
pp 92 (1966).
79
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(38) Georgia Inst. of Tech., Atlanta, Environmental Resources Center,
"Determination of Degraded Dyes and Auxiliary Chemicals in
Effluents From Textile Dyeing Processes", pp 51 (March, 1970).
(39) U.S. Federation of Sewage and Industrial Wastes Associations,
"A Critical Review of the Literature of 1955 on Sewage, Waste
Treatment, and Water Pollution", Sewage industr. Wastes, 28,
pp 595-636 and 707-764 (1956).
(40) Meinck, F., Stoof, H., and Kohlschutter, H., "Industrial Waste
Waters", Gustav Fischer Verlag, Stuttgart, 2nd edit, pp 48 (1956);
Wat. Pollut. Abstr, 25, Abstr. No. 973 (1952) and 27, 2288 (1954).
(41) Gramley, Dale I. and Heath, Milton S., Jr., "A Study of Water
Pollution Control in the Textile Industry of North Carolina",
Rept. No. 21 W70-05124, pp 108 (January, 1970).
(42) U.S. Federation of Sewage and Industrial Wastes Associations,
"A Review of the Literature of 1958 on Sewage, Waste Treatment,
and Water Pollution", Sewage industr. Wastes, 31, pp 501-541,
615-661, and 763-803 (1959).
(43) Oldenbourg, R., "Disposal and Treatment of Industrial Waste Waters",
Internationale Fachausstellung Uber Wasser- Und Abwasserreinigung,
pp 348 (1959).
(44) Chakrabarty, R. N. , Saxena, K. L., and Chattopadhya, S. N. ,
"Studies on Recovery of Zinc From Viscose Rayon Waste", Envir.
Hlth, India, 9, pp 296-305 (1967).
(45) Taylor, E. F., Gross, G. C., Jones, C. E., and Rocheleau, R. F. ,
"Biochemical Oxidation of Wastes From the New Plant for Manufacturing
'Orion' at Waynesboro, Virginia", Proc. 15th industr. Waste Conf.,
Purdue University Engng Extn Ser. No. 106, pp 508-514 (1960).
(46) Sadow, R. D., "The Treatment of Zefran Fibre Wastes", Proc. 15th
industr. Waste Conf., Purdue University Engng Extn Ser. No. 106,
pp 359-372 (1960).
(47) Heinze, Johannes, P-aimn, Fellmad, and Richardt, Hans, "Recovery of
Dialkyl Terephthalates by Decomposing Wastes of Linear and Mixed
Polyesters", Ger. (East) 41,855, Oct. 15, 1965, Appl. Feb. 10, 1964;
5 pp.
80
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SECTION XI
APPENDICES
Page No.
A. Distribution of Paint, Plastics, Rubber, and Viscose
Rayon Plants in the United States (information from
1967 Census of Manufacturers for plants with 20 or
more employees) 82
Figure A-l. Number and Distribution of Paint
Manufacturing Plants in United States 82
Figure A-2. Number and Distribution of Plastics
Manufacturing Plants in United States 83
Figure A-3. Number and Distribution of Synthetic
Rubber Manufacturing Plants in United States 84
Figure A-4. Number and Distribution of Viscose Rayon
Plants in United States 85
B. Material and Energy Balance Calculations for Example
Incineration Systems 86
81
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CD
NJ
NEW ENGLAN
(30)
MIDDLE..
...ATL'ANTIC....
(165) !
WEST NORTH CENTRAL
6
FIGURE A-l. NUMBER AND DISTRIBUTION OF PAINT MANUFACTURING PLANTS IN UNITED STATES
-------
00
MIDDLED 987" 7>J"5
'
EAST SOUTH _.-„-,,.. .,, A.1T,
CENTRAL ^SOUTH^TLANTI
WEST SOUTH'-CENTRAL (18)
14
FIGURE A-2. NUMBER AND DISTRIBUTION OF PLASTICS MANUFACTURING PLANTS IN UNITED STATES
-------
00
WEST NORTH CENTRAL
(0) ,
WEST SOUTHTCENTRAL
(14)
FIGURE A-3. NUMBER AND DISTRIBUTION OF SYNTHETIC RUBBER MANUFACTURING PLANTS IN UNITED STATES
-------
oo
Ln
FIGURE A-4. NUMBER AND DISTRIBUTION OF VISCOSE RAYON PLANTS IN^UNITED STATES
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APPENDIX B
MATERIAL AND ENERGY BALANCE CALCULATIONS
FOR EXAMPLE INCINERATION SYSTEMS
Example I: Paint Waste lacineration
Basis: 125,000 gallons annually, solvent recovery sludge
Operating Schedule: 100 hours/week, 50 weeks/year
Conditions: Bed Temperature = 1750 F
Superficial Velocity =2.0 fps
(1) Heat Input (steady-state operation)
Q = 25 gal/hr x 120,000 Btu/gal = 3,000,000 Btu/hr
(2) Fluidizing Air (assume volume in cu ft = .. „„ — , also
assume 50% excess)
_ 3,000,000 x 1.5 x -i- = 750 scfm
V " 100
(3) Heat loss to gases (Q = n CpAt)
Q = 750 x 0.02 x 1680 x 60 = 1,500,000 Btu/hr
(4) Heat loss to reactor walls (assume 20% of heat input)
Q = 0.20 x 3,000,000 = 600,000 Btu/hr
(5) Reaction water or Latex feed (W x AH = excess heat input)
_ 3,000.000 - 2,100,000 1
W -- 2000 x
(6) Fluid bed diameter (area = gas flow/superficial velocity)
A = 750 x 175°530460 + 2.0 x 60 = 26.1 ft2 D = 5.75 ft.
86
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Example II: Plastic Waste Incineration
Basis: 30,000,000 pounds annually styrene primary treatment sludge
'' @ 10% solids
Operating Schedule: 100 hours/week, 50 weeks/year
Conditions: Bed Temperature = 1325 F
Superficial Velocity = 1.8 fps
(1) Heat input from solids
Q = 6,000 Ib/hr x . 10 x 15,000 Btu/lb = 9,000,000 Btu/hr
(2) Fluidizing air (assume volume in cu ft = r, also assume 50%
cess)
, 9,000 000
excess)
>
J-UU bU
(3) Heat requirements
Water = 6,000 Ib/hr x .90 x 1660 Btu/lb = 8,960,000 Btu/hr
Fluid Air = 2250 x .02 x 1255 x 60 = 3,390,000 Btu/hr
Total (except loss to walls) 12,350,000 Btu/hr
(4) Auxiliary fuel needed (assume 20% heat loss to walls)
0.8 [VnTT x 1000 Btu/cf + 9,000,000] = 12,350,000 + 0.2 x 1255 x 10V
CH4
5,150,000 1
VCH4 * 549 X 60 =
V (waste polymers) = 625 Ib/hr (alternate auxiliary fuel)
(5) Fluid bed diameter
A = (2250 + 1560) x 46° . 2.0 x 60 = 119 ft2
D = 12.3 ft
Example III: Rubber Waste Incineration
Basis: 10,000,000 pounds annually (15. 4% solids, 1.35% ash)
Operating Schedule: 100 hours/week, 50 weeks/year
Conditions: Bed Temperature = 1400 F
Superficial Velocity = 2.0 fps
(1) Heat input from solids
Q = 2,000 Ib/hr x . 154 x 15,000 Btu/lb = 4,620,000 Btu/hr
87
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(2) Fluidizing air (assume volume in cu ft = — , also assume 50%
excess)
T7 4,620,000 . _ 1 . ._. ,
V = -^- - x 1.5 x — = 1,150 scfm
(3) Heat requirements:
Water = 2,000 Ib/hr x .846 x 1700 Btu/lb = 2,870,000 Btu/hr
Fluid air = 1150 scfm x .02 x 1330 x 60 = 1,840,000 Btu/hr
Totals (except loss to walls) 4,710,000 Btu/hr
(4) Methane needed (assume 207» heat input loss to walls)
0.8 [Vrtl x 1000 Btu/cf + 4,620,000] = 4,710,000 + .02 x 1330 x 10V
• CH4
= 1,014.000 1_ = 31.7 scfm
CH. 534 X 60
4
(4) Fluid bed diameter:
A = (1150 + 317) x 14°° 46° 4 2.0 x 60 = 43 ft2
D = 7.4 ft
<>U,S. GOVERNMENT PRINTING OFFICE W72
1-3 OO
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1 | Ace c fat ion Number
J
w
2 1 Subject FlQld & Group
SELECTED WATER RESOURCES ABSTRACTS
INPUT TRANSACTION FORM
Columbus Laboratories -- Battelle
Title
Fluidized-bed Incineration of Selected Carbonaceous Industrial Wastes
10
Autliotfa)
T. L. Tewksbury
A. K. Reed
H. Nack
G. R. Smithson, Jr.
j£ I
- 1
Project Designation
Project No. 12120 FYF
21]
Note
22 Citation
23
Descriptors (Starred First)
Industrial wastes, *Incineration, Fluidized bed, Waste treatment
25
Identifiers (Starred First)
27 Abstract
This report describes a program that was conducted on the feasibility of fluidized-
bed incineration for selected carbonaceous industrial wastes. The program con-
sisted of an initial phase in which wastes from the paint, plastics, rubber, and
textile industries in Ohio were characterized. In the second phase, samples of
various wastes were obtained and analyzed, and based on their characteristics,
selected wastes were experimentally incinerated in a 10-inch-diameter fluidized-
bed system.
Results of the program indicate that sludges from solvent recovery operations
in the paint industry, sludges from primary treatment of process wastes from
plastic manufacturing, flotation sludges from primary treatment of synthetic
rubber manufacture, and the waste from the viscose process of the textile industry
can be incinerated in a fluidized-bed system without the production of noxious or
toxic exhaust gases. The program also indicates that incineration of the various
wastes significantly reduces their potential impact on stream pollution. It is
recommended that a demonstration plant be constructed and operated at a site
close to the source of several types of industrial wastes.
Tewksbury
Inxtitution
Battelle, Columbus Laboratories
WR:I02 (REV. JUUY U19)
WRSIC
SEND WITH COPY OF DOCUMENT. TOI WATER RESOURCES SCIENTIFIC INFORMATION CENTER
U.S. DEPARTMENT OF THE INTERIOR
WASHINGTON, D. C. 20240
CPO: 1970 - 407 -891
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