-------
Table 3-4. INCREMENTAL COSTS OF SOLVENT EMISSION CONTROL OPTIONS FOR CONVEYORIZED SINGLE-COAT OPERATION,
DIP-COAT APPLICATION
(Mid-1977 thousand dollars)
Cost item
° Capital investment
0 Annual costs (credits )d
Material
Electricity
Fuel
Maintenance
Capital charges
0 Total annual ized cost (credit)
0 Solvent emissions controlled,
Mg/yr
0 Emission reduction, %
° Cost effectiveness (credit),
$/Mg of solvent controlled
Applicable control option
Haterborne coatings
source size3
small
12
2
0
0
1
2
5
6
80
833
mediuit
20
11
0
(2)
1
4
14
35
80
400
large
28
22
1
(3)
1
5
26
69
80
377
Electrodeposition (EDP)
source size
small
65
W
2
0
3
12
8
7
90
1143
medium
178
(46)
9
(1)
8
33
3
39
90
77
large
270
(93)
18
(2)
12
50
(15)
78
90
(192)
Carbon adsorption and
thermal Incineration
with 351 primary heat
recovery*1
source size
small
209
0
1
8
9
42
60
7
85
8571
medium
296
0
1
8
13
59
81
37
85
2189
large
357
0
2
9
16
71
98
73
85
1343
Carbon adsorption and
catalytic incineration
with 351 primary heat
recovery0
source size
small
188
0
1
2
9
38
50
7
85
7143
medium
276
0
1
2
13
55
71
37
85
1919
large
337
0
2
2
15
68
87
73
85
1192
Thermal incineration
with 90% primary heat
recovery1
source size
small
64
0
0
5
3
13
21
7
90
3000
medium
126
0
1
10
6
25
42
39
90
1077
large
201
0
1
16
9
40
66
78
90
846
OJ
See Table 3-2 for source sizes.
Carbon adsorption on dip-coat booth and incineration with 35 percent primary heat recovery on drying oven.
Thermal Incineration with 90 percent primary heat recovery on dip-coat booth and drying oven.
Increments of waste disposal costs, labor costs, and labor overhead are insignificant; these are not included in the annual costs.
-------
Table 3-5. INCREMENTAL COSTS OF SOLVENT EMISSION CONTROL OPTIONS FOR CONVEYORIZED SINGLE-COAT OPERATION,
SPRAY-COAT APPLICATION
(Mid-1977 thousand dollars)
Cost Hew
* Capital Investment
• Annual costs (credits)
Material
Electricity
Fuel
Maintenance
Capital charges
* Total annuallzed tfost
(credit)
° Solvent emissions con-
trolled, Ng/yr
" Emission reduction, %
° Cost effectiveness
(credit), $/Mg of
solvent controlled
Applicable control option
Waterborne coatings
source size*
small
12
2
0
0
1
2
5
8
80
625
medium
20
9
0
(2)
1
4
12
41
80
293
Urge
28
19
1
(3)
1
5
23
82
80
280
High solids coatings
sourct size
small
30
3
0
0
1
6
10
7
70
1429
medium
43
16
0
(1)
2
8
25
36
70
695
large
59
32
0
(3)
3
11
41
72
70
597
Powder deposition
source size
small
S6
13
0
0
3
10
26
9
90
2889
medium
76
71
0
(2)
3
14
86
46
90
1870
large
101
142
0
(3)
5
19
163
93
90
1753
Carbon adsorption and
thermal Incineration
with 351 primary heat
recovery'1
source size
snail
380
0
2
8
17
76
103
8
79
12875
medium
698
0
9
10
31
140
190
41
79
4634
large
971
0
17
12
44
195
268
81
79
3309
Carbon adsorption and
catalytic Incineration
with 35* primary heat
recovery'1
source size
small
369
0
2
2
16
72
92
8
79
11 500
medium
648
0
9
4
31
136
ISO
41
79
4390
large
957
0
17
6
43
190
256
81
79
3161
Thermal Incineration
with 90S primary heat
recovery1
source size
small
220
0
1
16
10
44
71
8
85
8875
medium
918
0
6
70
41
184
301
44
85
6841
large
1713
0
12
130
77
343
562
88
85
6386
UJ
I
See Table 3-2 for source sizes.
Carbon adsorption on spray-coat booth and incineration with 35 percent primary heat recovery on drying oven.
Thermal incineration with 90 percent primary heat recovery on spray-coat booth and drying oven.
Increments of waste disposal costs, labor costs, and labor overhead are insignificant; these are not Included 1n the annual costs.
-------
Table 3-6. INCREMENTAL COSTS OF SOLVENT EMISSION CONTROL OPTIONS FOR GONVEYORIZED TWO-COAT OPERATION,
FLOW- AND SPRAY-COAT APPLICATION
(Mid-1977 thousand dollars)
Cost Item
0 Capital Investment
0 Annual costs (credits) d
Material
Electricity
Fuel
Maintenance
Capital charges
0 Total annualized cost (credit)
0 Solvent emissions controlled,
Mg/yr
• Emission reduction, t
• Cost effectiveness (credit),
$/Mg of solvent controlled
Applicable control option
Waterborne coatings
source s zea
small
24
8
0
(1)
1
4
12
14
80
857
medium
40
43
1
(3)
2
7
50
76
80
658
large
56
86
1
(6)
3
10
94
152
80
618
Powder deposition
source s ze
small
56
(4)
0
(1)
3
10
8
16
90
500
medium
76
(21)
(2)
(6)
3
14
(12)
85
90
(141)
large
101
(42)
(3)
(13)
5
19
(34)
171
90
(199)
Carbon adsorption and
thermal Incineration
with 35S primary heat
recovery"
source size
small
580
0
3
16
26
116
161
15
82
10734
medium
974
0
10
18
44
195
267
78
82
3423
large
1299
0
19
20
58
260
357
155
82
2303
Carbon adsorption and
catalytic Incineration
with 351 primary heat
recovery"
source size
small
539
0
3
4
25
108
140
15
82
9333
medium
903
0
10
6
42
187
245
78
82
3141
large
1259
0
19
8
57
252
336
155
82
2167
Thermal incineration
with 90% primary heat
recovery^
source size
small
279
0
2
20
13
56
91
15
87
6067
medium
1002
0
7
78
46
204
335
82
87
4085
large
1869
0
13
149
54
374
590
165
87
3578
a See Table 3-2 for source sizes.
b Carbon adsorption on coating booth and incineration with 35 percent primary heat recovery on drying oven.
c Thermal incineration with 90 percent primary heat recovery on coating booth and drying oven.
d Increments of waste disposal costs, labor costs, and labor overhead are Insignificant; these are not included In the annual costs.
-------
Table 3-7. INCREMENTAL COSTS OF SOLVENT EMISSION CONTROL OPTIONS FOR CONVEYORIZED TWO-COAT OPERATION,
DIP- AND SPRAY-COAT APPLICATION
(Mid-1977 thousand dollars)
to
I
ro
Cost Hem
° Capital Investment
° Annual costs (credits)11
Material
Electricity
Fuel
Maintenance
Capital charges
0 Total annuallzed cost (credit)
° Solvent emissions controlled,
Mg/yr
0 Emission reduction, %
° Cost effectiveness (credit),
$/Mg of solvent controlled
Applicable control option
Waterborne coatings
source size8
small
24
8
0
(1)
1
4
12
14
80
857
medium
40
43
1
(3)
2
7
50
76
80
658
large
56
86
1
(6)
3
10
94
152
80
618
Powder deposition
source size
small
56
(4)
0
(1)
3
10
8
16
90
DOO
medium
76
(21)
(2)
(6)
3
14
(12)
85
90
(141)
large
101
(42)
(3)
(13)
5
19
(34)
171
90
(199)
Carbon adsorption and
thermal incineration
with 35X primary heat
recovery^
source size
small
589
0
3
16
26
118
163
15
82
10867
medium
994
0
10
18
45
199
272
78
82
3487
large
1328
0
19
21
60
266
366
155
82
2361
Carbon adsorption and
catalytic Incineration
with 35* primary heat
recovery"
source size
small
548
0
3
4
25
110
142
15
82
9460
medium
924
0
10
6
43
191
250
78
82
3205
Jarge
1288
0
19
9
58
258
344
155
82
2219
Thermal incineration
with 90* prlnary heat
recovery0
source size
small
285
0
2
21
13
57
93
15
87
6200
medium
1044
0
7
80
47
209
343
82
87
4183
large
1914
0
13
152
86
383
634
165
87
3842
See Table 3-2 for source sizes.
Carbon adsorption on coating booth and incineration with 35 percent primary heat recovery on drying oven.
Thermal incineration with 90 percent primary heat recovery on coating booth and drying oven.
Increments of waste disposal costs, labor co*ts, and labor overhead are Insignificant; these are not Included In the annual costs.
-------
Table 3-8. COSTS OF SOLVENT EMISSION CONTROL OPTIONS FOR CONVEYORIZED TWO-COAT OPERATION,
SPRAY-COAT APPLICATION
(Mid-1977 thousand dollars)
Cost item
° Capital investment
0 Annual costs(credits)
Material
Electricity
Fuel
Maintenance
Capital charges
0 Total annualized cost
(credit)
0 Solvent emissions con-
trolled, Mg/yr
° Emission reduction, %
0 Cost effectiveness
(credit), $/Mg of
solvent controlled
Applicable control option
Waterborne coatings
source size3
small
24
8
0
(1)
1
4
12
15
80
800
medium
40
43
1
(3)
2
7
50
82
80
610
large
56
86
1
(6)
3
10
94
165
80
570
High solids solvents
source size
small
60
11
0
0
3
12
26
14
70
1857
medium
86
56
0
(3)
4
16
73
72
70
1014
large
118
112
1
(5)
5
22
135
144
70
938
Powder
deposition process
source size
small
56
(7)
0
(1)
3
10
5
17
90
294
medium
76
(36)
(2)
(6)
3
14
(27)
93
90
(290)
large
101
(71)
(3)
(13)
5
19
(63)
186
90
(339)
Carbon adsorption and
thermal incineration
with 35t primary heat
recoveryb
source size
small
761
0
4
16
34
152
206
15
79
13733
medium
1397
0
17
20
63
279
379
81
79
4679
large
1943
0
34
24
87
389
534
163
79
3276
Carbon adsorption and
catalytic Incineration
"1th 35* primary heat
recovery**
source size
small
720
0
4
4
33
144
185
15
79
12233
medium
1296
0
17
8
61
271
357
81
79
4407
large
1902
0
34
12
86
380
512
163
79
3740
Thermal incineration
with 90i primary heat
recovery0
source size
small
439
0
3
32
20
88
143
16
85
8938
medium
1837
0
12
140
83
367
602
88
85
6841
large
3425
0
23
273
154
685
1135
175
85
6486
CO
I
See Table 3-2 for source sizes.
Carbon adsorption on spray-coat booth and incineration with 35 percent primary heat recovery on drying oven.
c Thermal incineration with 90 percent primary heat recovery on spray-coat booth and drying oven.
Increments of waste disposal costs, labor costs, and labor overhead are insignificant; these are not Included In the annual costs.
-------
Table 3-9. COSTS OF SOLVENT EMISSION CONTROL OPTIONS FOR MANUAL TWO-COAT OPERATION
(Mid-1977 thousand dollars)
Applicable control option
Cost item
° Capital investment
" Annual costs (credits)15
Material
Electricity
Fuel
Maintenance
Capiital charges
° Total annual ized cost (credit)
0 Solvent emissions controlled,
Mg/yr
0 Emission reduction, °i
° Cost effectiveness (credit),
$/Mg of solvent controlled
Waterborne coatings
source size*
small
34
24
0
(2)
2
6
30
12
80
2500
medium
37
35
0
(3)
2
7
41
18
80
2278
large
41
46
1
(3)
2
8
54
24
80
2250
High solids coatings
source s ze
small
72
50
0
(1)
3
14
66
10
70
6600
medium
78
66
0
(2)
4
15
83
15
70
5533
large
86
91
0
(3)
4
16
108
20
70
5400
Carbon adsorption
source size
small
1740
0
15
4
78
174
232
13
80
17841
medium
2226
0
21
5
100
223
299
18
80
16611
large
2596
0
27
7
117
260
353
24
80
14708
Thermal Incineration
with 90t primary heat
recovery
source size
small
1619
0
5
59
73
162
262
13
85
20154
medium
2216
0
7
85
100
222
364
19
85
19158
large
2758
0
10
110
124
276
458
25
85
18320
See Table3-2 for source sizes.
Increments of waste disposal costs, labor costs, and labor overheads are insignificant; these are not included in the annual
costs.
-------
savings are estimated for powder coating conversions (1, 2); however, a
higher coating thickness of 50 um (2 mils) assumed for powder coating
diminishes possible savings.
For electrodeposition, lower applied film thickness helps override
some of the associated increased electrical costs (1).
Annualized costs of incineration of oven emissions primarily
represent fuel required to raise the temperature of the exhaust gases
from 160°C (320°F) to 760°C (1400°F).
3.3 COST EFFECTIVENESS
Figures 3-1 through 3-7 present cost-effectiveness curves for the
options analyzed: Figures 3-1, 3-2, and 3-3 for conveyorized single-
coat operation; Figures 3-4, 3-5, and 3-6 for conveyorized two-coat
operation; and Figure 3-7 for manual two-coat operation. These curves
represent the effect of line size on the cost per unit weight of solvent
controlled. The cost per unit weight of solvent controlled decreases
with the increasing line size in all cases.
The two most cost-effective options evaluated for conveyorized
single flow-coat and single dip-coat operations appear to be conversion
to waterborne coatings and conversion to the electrodeposition process.
The most costly options appear to be add-on control devices. Conversion
to waterborne coatings seems to be a cost-effective option for spray
coating in a conveyorized single-coat operation; carbon adsorption
combined with thermal incineration with 35 percent primary heat recovery
is the most costly.
3-15
-------
10,000
S 8000 h
o
6000
o 4000
en
p 2000
*•••*
o
LLJ
tt
CJ
o
o
(2000)
• WATERBORNE COATINGS
O ELECTRODEPOSITION (EDP)
A CARBON ADSORPTION AND THERMAL INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
A CARBON ADSORPTION AND CATALYTIC INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
* THERMAL INCINERATION WITH 90%
PRIMARY HEAT RECOVERY
5 10
COATING RATE, TO5 m2/year
15
FIGURE 3-1. Cost-Effectiveness Comparison of Solvent
Emission Control Options
Conveyorized Single-Coat Operation
Flow-Coat Application
3-16
-------
^WATERBORNE COATINGS
O ELECTRODEPOSITION (EDP)
& CARBON ADSORPTION AND THERMAL INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
* CARBON ADSORPTION AND CATALYTIC INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
W THERMAL INCINERATION WITH 90%
PRIMARY HEAT RECOVERY
10,000
8000
o
CC
H-
O
o
to
o
6000
4000
§ 2000
UJ
QC
<"
o 0
o
(2000)
0
5 10
COATING RATE, ID5 m2/year
15
FIGURE 3-2. Cost-Effectiveness Comparison of Solvent
Emission Control Options
Conveyorized Single-Coat Operation
Dip-Coat Application
3-17
-------
18,000
15,000
s
£ 12,000
UJ
>
o
o 9000
«v.
•*%
*
£ 6000
en
CJ
to
3000
WATERBORNE COATINGS
CARBON ADSORPTION AND THERMAL INCINERATION
WITH 302 PRIMARY HEAT RECOVERY
CARBON ADSORPTION AND CATALYTIC INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
THERMAL INCINERATION WITH 90%
PRIMARY HEAT RECOVERY
POWDER DEPOSITION
HIGH SOLIDS COATINGS
I
5 10
COATING RATE, 105 m2/year
15
FIGURE 3-3. Cost-Effectiveness Comparison of Solvent
Emission Control Options
Conveyorized Single-Coat Operation
Spray-Coat Application
3-18
-------
o
o
o
to
15,000
12,000
9000
6000
3000
o
o
(3000)
• WATERBORNE COATINGS
A CARBON ADSORPTION AND THERMAL INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
A CARBON ADSORPTION AND CATALYTIC INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
* THERMAL INCINERATION WITH 90%
PRIMARY HEAT RECOVERY
S? POWDER DEPOSITION
\
5 10
COATING RATE, 105 m2/year
15
FIGURE 3-4. Cost-Effectiveness Comparison of Solvent
Emission Control Options
Conveyorized Two-Coat Operation
Flow- and Spray-Coat Application
3-19
-------
WATERBORNE COATINGS
CARBON ADSORPTION AND THERMAL INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
CARBON ADSORPTION AND CATALYTIC INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
THERMAL INCINERATION WITH 90%
PRIMARY HEAT RECOVERY
POWDER DEPOSITION
CJ
15,000
12,000
9000
o
en
vo
o
o
6000
3000
(3000)
0
5 10
COATING RATE, 105 m2/year
15
FIGURE 3-5. Cost-Effectiveness Comparison of Solvent
Emission Control Options
Conveyorized Two-Coat Operation
Dip- and Spray-Coat Application
3-20
-------
«^WATERBQRNE COATINGS
A CARBON ADSORPTION AND THERMAL INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
A CARBON ADSORPTION AND CATALYTIC INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
V THERMAL INCINERATION WITH 90%
PRIMARY HEAT RECOVERY
S7 POWDER DEPOSITION
• HIGH SOLIDS COATINGS
o
at
15,000
12,000
9000
O
01
o
o
6000
3000
(3000)
I
JQL-
5 10
COATING RATE, 105 m2/year
15
FIGURE 3-6. Cost-Effectiveness Comparison of Solvent
Emission Control Options
Conveyorized Two-Coat Operation
Spray-Coat Application
3-21
-------
p
I—
z
V)
U-
o
o
24,000
20,000
16,000
12,000
8000
4000
WATERBORNE COATINGS
CARBON ADSORPTION AND THERMAL INCINERATION
WITH 30% PRIMARY HEAT RECOVERY
THERMAL INCINERATION WITH 90%
PRIMARY HEAT RECOVERY
HISH SOLIDS COATINGS
I
10
COATING RATE, 105 m2/year
FIGURE 3-7. Cost-Effectiveness Comparison of Solvent
Emission Control Options
Manual Two-Coat Operation
3-22
-------
Conversion to a powder-coating process is the most cost-effec-
tive control option evaluated for conveyorized two-coat operations.
Add-on control systems appear to be considerably more expensive than
process modification options.
Conversion to waterborne coatings is the least costly option
evaluated for manual two-coat operations. Again, add-on control systems
cost much more than process changes.
In flow and dip coating in conveyorized single-coat operations,
thermal incineration with 90 percent primary heat recovery* appears to
be a more cost-effective add-on control than carbon adsorption with
either thermal or catalytic incineration-! with 30 percent primary heat
recovery. This system also appears to be the most cost-effective for
small size lines only in all other operations (spray-coating in con-
veyorized single-coat operations and all coatings in conveyorized two-
coat operations); however, it is the least cost-effective for medium
size and large size lines. For these applications, carbon adsorption
with thermal incineration at 30 percent primary heat recovery seems to
be more cost-effective than carbon adsorption with catalytic incinera-
tion at 30 percent primary heat recovery.
The carbon adsorption system appears to be more cost-effective than
thermal incineration, with 90 percent primary heat recovery on manual
two-coat operations.
* Thermal incineration with 90 percent primary heat recovery is applied
on coating booth and drying oven.
t Carbon adsorption on booth and thermal/catalytic incineration on drying
oven.
3-23
-------
3.4 SUMMARY
Cost analyses of the model lines indicate that modification of the
coating process to a low-solvent coating usually appears to be more
cost-effective for control of VOC than add-on control. However, because
annualized costs for alternative coating systems are greatly affected by
assumptions implicit in the calculation of coating costs, comparisons
between alternative coating systems can exhibit significant case by case
variations.
3-24
-------
3.5 REFERENCES
1. Second Interim Report on Air Pollution Control Engineering and Cost
Study of the General Surface Coating Industry. Prepared by Spring-
born Laboratories, Inc., under EPA Contract No. 68-02-2075. August
23, 1977.
2. Second Interim Report on Air Pollution Control Engineering and Cost
Study of the General Surface Coating Industry - Appendixes A & B.
Prepared by Springborn Laboratories, Inc., under EPA Contract No.
68-02-2075. August 23, 1977.
3. Study of Systems for Heat Recovery from Afterburners. Industrial
Gas Cleaning Institute, Stamford, Connecticut. EPA Contract No.
68-02-1473, Task No, 23. October 1977.
4. REECo Newsletters 1 through 4. REECo Regenerative Environmental
Equipment Co., Inc., Muncy, Pennsylvania. 1973.
5. Information supplied to U.S. EPA by Regenerative Environmental
Equipment Co., Inc. (REECo), March 31, 1978.
6. High Solids Coatings Volume 2, No. 2. Technology Marketing Corpora-
tion, Stamford, Connecticut. April 1977.
3.6 BIBLIOGRAPHY
Control of Volatile Organic Emissions from Existing Stationary
Sources, Volume I: Control Methods for Surface-Coating Operations.
EPA-450/2-76-Q28, Research Triangle Park, North Carolina. November
1976 (OAQPS No. 1.2-067).
Control of Volatile Organic Emissions from Existing Stationary
Sources, Volume II: Surface Coating of Cans, Coils, Paper, Fab-
rics, Automobiles, and Light-Duty Trucks. EPA-450/2-77-008,
Research Triangle Park, North Carolina. May 1977 (OAQPS No. 1.2-073),
Report of Fuel Requirements, Capital Cost and Operating Expense for
Catalytic and Thermal Afterburners. CE Air Preheater, Industrial
Gas Cleaning Institute, Stamford, Connecticut. EPA-450/3-76-031.
September 1976.
Capital and Operating Costs of Selected Air Pollution Control
Systems. SARD, Inc., Niles, Illinois. EPA Contract No. 68-02-
2072. May 1976.
3-25
-------
4.0 DETERMINATION OF APPLICABLE EMISSION LIMITATIONS
This chapter shows how an agency may use the logic diagram presented
as Figure 4.1 to develop a standard appropriate for almost any coating
process which applies surface coatings on a metal substrate.
The procedure for determining emission limits which represent
the presumptive norm achievable by various processes. It requires some
knowledge of the industry, the coating process and the requirements
demanded of the coating. The procedure is to start at the top of
Figure 4.1 and at each decision node (Indicated by a circle) choose
the appropriate option. Until reaching a block that presents the
level of control that is presumed to be achievable through the application
of RACT by the manufacturer.
As an example, to find the recommended emission limit for a
continuous operation that coats phosphate treated machine brackets with
a black oven cured dipcoat at 0.7 mils film thickness, the procedure
is as follows:
' Beginning at the top, proceed to node B.
' The item is not clear-coated, does not contain any heat sensitive
materials and is baked in an oven when coated, so proceed to node C.
11 The brackets are marketed in one color, so proceed to node D.
Because powder coatings are not applicable in this case, the
recommended emission limit for this process is 0.36 kg/liter
(3.0 Ibs/gal) minus water.
This would then be the level of control presumed to represent RACT
for this process. It may be achieved through the use of either water-
borne dip or electrodeposited water-borne coatings. Higher solids and
powder coatings can also be used but may result in thicker films than
4-1
-------
the 0.7 mil obtained from low solids coatings.
Current technology does not provide low-polluting coatings which
can successfully replace conventional coatings for all the specialty
items coated by the many industrial categories covered by these
emission limits. Some low-polluting coatings are being used on production
lines while others are in various stages of research. There will be,
however, situtations where low-polluting coatings may never be applicable
and even the use of add-on control technology may not be feasible
either technically or economically.
4-2
-------
Manufacture of Metal Parts and Products
Air or forced air-dried items:
Parts too large or too heavy for
practical size ovens and/or sensi-
tive heat requirements. Parts to
which heat sensitive materials are
attached. Equipment assembled
prior to too coating for specific
performance or quality standards.
0.42 kg/liter (3.5 Ibs/gal) (5)
No or infrequent color chance,
or small number of colors
applied.
Clear Coat
0.52 kg/liter
(4.3 Ibs/gal)
(6)
owder
J.05 kg/liter
P. 4 Ibs/gal)
Outdoor or harsh
exposure or extreme
performance
characteristics ,c>
0.42 kg/liter (i>'
(3.5 Ibs/gal)
Frequent color chanqe and/
or large number of colors
applied, or first coat on
untreated ferrous substrate
0.36 kg/liter
(3.0 Ibs/qal) (7)
Figure 4.1 Logic diagram for derivation of emission
limits for coatina of miscellaneous metal parts and
products.
4-3
-------
4.1 REFERENCES
1. The recommended emission limitations for this category are given in
"Control of Volatile Organic Emissions from Existing Stationary
Sources - Volume II: Surface Coating of Cans, Coils, Paper, Fabric,
Automobiles and Light Duty Trucks," EPA-450/2-77-008, May, 1977.
2. The recommended emission limitations for this category are given in
"Control of Volatile Organic Emissions from Existing Stationary Sources -
Volume III Surface Coating of Metal Furniture," EPA-450/2-77-032,
December, 1977.
3. The recommended emission limitations for this category are given in
"Control of Volatile Organic Emissions from Existing Stationary
Sources - Volume IV: Surface Coating for Insulation of Magnet
Wire," EPA-450/2-77-033, December, 1977.
4. The recommended emission limitations for this category are given in
"Control of Volatile Organic Emissions from Existing Stationary
Sources - Volume V: Surface Coating of Large Appliances," EPA-450/
2-77-034, December, 1977.
5. This emission limit is achievable by use of about 52 volume percent solids
organic solvent-borne coating. Units for this and other limitations
are kilograms of solvent emitted per liter of coating applied (minus
water).
6. This limit is achievable by use of a 41 volume percent solids organic
solvent-borne or a water-borne equivalent coating.
7. This emission limit is acheivable by use of a 59 volume percent higher
solids or a water-borne equivalent coating, or powder or electrodeposited
water-borne coatings. DuPont Comments to the First Draft of Control of
Volatile Organic Emissions from Existing Stationary Sources - Volume VI:
Surface Coating of Miscellaneous Metal Parts and Products, Letter Dated
April 20, 1978.
8. There are some products for which a coating thickness greater than 2 mils
is required out other coating quality or performance requirements preclude
the use of powder coatings. Comments from Deere and Company on the First
Draft of Control of Volatile Organic Emissions from Existing Stationary
Sources - Volume VI: Surface Coating of Miscellaneous Metal Parts and
Products, Letter dated March 29, 1978.
4-4
-------
5.0 ADVERSE AND BENEFICIAL EFFECTS OF APPLYING TECHNOLOGY
This chapter reviews the adverse and beneficial effects of each technique
which reduces VOC emissions. This includes not only environmental aspects but
also energy and cost. It also highlights any limitations of low organic
solvent technology as compared to conventional high organic solvent coatings.
5.1 WATER-BORNE (SPRAY, DIP, OR FLOW COAT)
There are several advantages to converting to water-borne coatings.
" Conversion to water-borne coatings will likely be the first option
considered by many facilities because of the possibility that these
coatings can be applied with minimal modification of existing equipment.
* Converting to water-borne coatings provides a potential decrease
in toxicity and flammability.
" Water-borne coatings may be thinned with water.
" Coating equipment can be cleaned or flushed with water rather
than organic solvent. (If water-borne coatings are allowed to dry, however,
they are then no longer soluble in water and must be cleaned with solvent.
' Use of water-borne coatings may allow a decrease in oven temperature.
" Use of water-borne coatings will permit some reduction in air flow
since the amount of organics which must be evaporated in the oven is
reduced. (The permissible reduction may be limited, however, by high humidity
within the oven which will result in condensation on the oven walls and possibly
cause improper curing of the film.
In some cases the dry-off oven may no longer be necessary.^
There are some potential disadvantages to water-borne coatings when compared
with conventional organic-borne coatings.
5-1
-------
• Spraying with water-borne coatings may require closer attention
to detail than with organic-borne coatings because temperature, humidity,
gun-to-metal-part distance, and flashoff time may affect the appearance
and performance of the coating.
' On many large electrostatic spray lines, use of water-borne coatings
may be impractical because of the difficulties involved in electrically
insulatina the entire system.
' Water-borne coatings applied by dip and flow coating application
equipment will need to be monitored more closely due to their more sensitive
chemistry.
" An additional rinse may be needed. Cleansing and pretreatment of the
substrate are more critical because of possible coating contamination and pH
3
changes within the dip or flow coating tank.
" Some equipment may have to be replaced or adjusted (due to different
surface tension of water than that of organic solvent) or protected from
corrosion. (In one converted flow coating operation, the only change was
that the number of nozzles had to be doubled to obtain the same coverage as
c
with conventional coatings.)
" The coating bath, flashoff time, temperature, air circulation, and
humidity may have to be controlled and frequently monitored, because changes
in weather conditions may affect the application of water-borne coatings.
5.2 ELECTRODEPOSITION
Several other advantages, in addition to reduced VOC emissions, accrue
from converting to electrodeposition.
' The major one is improved quality control, a consequence of the fully
automated process.
5-2
-------
It provides excellent and uniform coating coverage and corrosion
protection because the paint particles are able to get into small recesses
of parts.
" Fire hazards and potential toxicity are decreased in electrodeposition
due to the minimal organic solvent content.
If electrodeposition replaced a spray coating operation, the solid
and liquid wastes associated with spraying operations will be reduced
drastically.
* The lower organic content permits lower ventilation rates, resulting
in reduced energy consumption.
There are some disadvantages to the electrodeposition process.
" Electrodeposition may increase electrical consumption. The anaount
will depend on the original application system, the size of the electro-
deposition bath, and the thickness of the coating applied. Electrical energy
is required for the coating system, the refrigeration to overcome the
temperature rise from the electrical process, for good paint circulation
in the bath, and to operate the ultrafilter. Electrodeposition may consume
three times as much energy in the application area as water-borne flow or dip
coating operations. It does not, however, appear as energy inefficient
when compared to a spraying operation because the high air volumes are no
longer required. Energy consumption will also be less in the baking process.
The air flow in the oven may be reduced and the flashoff tunnel may be
omitted.
' A poor electrical connection will result in a poor coating (for
example, if the hooks which hold the metal parts are not properly cleaned or
hung and inadvertently provide an electrical insulation, the quality of the
coating will suffer.)
5-3
-------
" The coverage is so uniform that electrodeposited coatings will not
hide imperfections in the substrate.
" Conversion to electrodeposition will require a change of equipment
at significant capital cost and can be relatively expensive on small
scale production lines.
5.3 HIGHER SOLIDS COATINGS
One of the greatest advantages of converting to higher solids coatings
as a means of reducing emissions of VOC is that they may be applied with
little change to existing equipment. Some application equipment (i.e.,
spray guns) may have to be replaced or a paint heater may have to be
installed to reduce the viscosity of the higher solids coatings but these
are relatively inexpensive changes. Conversion to high solids coatings can
reduce a plant's energy consumption. Air flow in the spray booth can be
decreased because less organic solvent must be evaporated from a high solids
coating when applying the same volume of coating. Since the energy required
by the oven is largely dependent on the air flow (and it, in turn, is
heavily influenced by the organic concentration limitations imposed for
Q
safety reasons) , the use of higher solids coatings will reduce energy
requirements. Solid and liquid wastes may also decrease since less coating
is applied per dry mil. However, the tackiness of high solid coatings may
g
make cleanup more difficult.
Some two-component high solids coatings may contain isocyanate compounds
which are potentially toxic and must be handled and applied with caution.
These also require installation of special application equipment.
5.4 POWDER COATINGS
There are several advantages obtained after a facility is converted to
powder coatings.
5-4
-------
* VOC emissions are almost completely eliminated.
• There are no solid or liquid wastes to be disposed of as compared
to solvent-borne coatings.
' Powder does not require the purchase, or use of solvents to
control the viscosity of the coating or to clean the equipment.
' Powders can mask imperfections and weld marks.
* Conversion to powder coatings may reduce the energy requirements
in a spray booth because the large volumes of fresh air required for
application of solvent-borne coatings may not be required. Energy require-
ments for the ovens may also be reduced because little organics are being
evaporated requiring less dilution. (It has been estimated that a 35-70
percent overall reduction in energy requirements will result when a conven-
tional single coat spray application is replaced with powder and 55-70
percent reduction will occur for a two-coat spray application.)
" The exhaust air from the spray booth can be filtered and returned
to the working area.
" Up to 98 percent transfer efficiency of powder coatings can be
realized since the overspray can be reclaimed. Not all overspray is always
reusable, however, because a buildup of powder fines may have to be discarded,
and the larger and heavier granules may have to be reprocessed again before
they are suitable for reuse.
There are several disadvantages to converting to the use of powder
coatings.
" The conversion is non-reversible since all application equipment,
spray booths, and associated equipment (and often ovens) used for liquid
systems must be replaced. This will then limit the flexibility of the
facility to apply other coatings.
5-5
-------
" Coating film thicknesses of less than 0.9 mils have not been
successfully obtained with powders on a production line basis.
' Metallic powder coatings are not as esthetically pleasing as con-
ventional metallics.
" Color matching of a powder coating is difficult because its color
cannot be changed by the applicator. Solvent borne coatings can be.
" Powder films have appearance limitations for some applications.
" Uncured powder coatings must be kept dry since their subsequent
performance can be affected.
' Powder coatings are subject to explosions (as are many particulate
dusts).12
" Color changes for powder require about half an hour downtime if
powder is recovered for reuse. This may greatly curtail production
capacities. Color changes may be shortened if powders are not reclaimed
in their respective colors, but this results in a coating usage efficiency
of only 50 to 60 percent.
5.5 CARBON ADSORPTION
Although the technology is well documented and considered technically
feasible, there are not miscellaneous metal part or product facilities
known to be using carbon adsorption systems to reduce organic emissions
from coating application of flashoff areas. The energy required to operate
a carbon adsorption system is a potential disadvantage. The actual quantity
will depend on the size of adsorber(s) and the concentration of the solvents
entering the carbon bed. Any reduction which can be made in the amount of
air flow from the coating application and flashoff areas will permit
purchase of a smaller adsorber with an attendant reduction in energy requirements.
5-6
-------
The amount of solid and liquid waste generated by the use of a carbon
adsorber will depend on the type of coating application system. For
example, emissions from flow and dip coating operations do not require
filtration or scrubbing. Emissions from spray booths, however, may require
pretreatment by filtration or scrubbing since the overspray may foul the
adsorber bed. Water miscible solvents may produce a water pollution problem
if the adsorber is regenerated with steam. This, however, can be avoided by
incinerating the regeneration stream, by stripping the organics from the
condensate or using nitrogen gas as a stripping medium. Each will increase
the cost and energy consumption of a carbon adsorption unit. Since there
is little possibility that the recovered solvents may be reused in the
miscellaneous metal part and product industries, any recovery or solvents
would be for fuel value only.
An important factor when considering installation of a carbon adsorption
system is plant space. Large facilities may require many dual-bed carbon
adsorption units in parallel which will need a relatively large area within
the plant.
5.6 INCINERATION
The most common and widely applicable technique for the reduction of
organic emissions is incineration. Incinerators (or afterburners) have
been used for many years for reducing organic emissions. One disadvantage
is the quantity of additional fuel required unless heat recovery is used.
The use of primary heat recovery to preheat the inlet gas stream to near
incineration temperature will minimize and can even eliminate fuel require-
ments. If secondary heat recovery can be used for other energy-using
processes, fuel requirements can be reduced even further. If there are
enough areas where secondary heat may be utilized, an incineration system
5-7
-------
may even reduce the plant's overall fuel consumption. Table 5-1 shows the
potential decreases in energy usage when using incinerators followed by
tube and shell heat exchangers with heat recovery efficiencies of 38 percent
to 55 percent. Some examples where secondary heat from the incinerator
exhaust may be used are: oven makeup air, boiler, cleaning processes, dryoff
ovens, and plant room heating. Greater primary heat recovery efficiencies
(80 to 95 percent) are shown in Table 5-2 using other types of heat exchangers
such as ceramic wheel stone packed beds. These are reportedly very attractive
even for low organic concentration streams because of their low fuel requirements.
5-8
-------
TABLE 5-1
BURNER REQUIREMENTS FOR INCINERATORS
IN 106 BTU/HRa'b'13
NON-CATALYTIC INCINERATORS 5 percent LEL 15 percent LEL
No Heat Recovery
5000 scfm 5.82 4.05
15,000 scfm 17.48 12.16
30,000 scfm 34.95 24.31
38% Efficient Primary Heat Recovery
5000 scfm 3.32 1.56
15,000 scfm 10.09 4.73
30,000 scfm 19.97 9.38
Primary and 55% Efficient Secondary
Heat Recovery
5000 scfm 1.42 -0.34
15,000 scfm 4.40 -0.66
30,000 scfm 8.67 -1.82
CATALYTIC INCINERATORS
No Heat Recovery
5000 scfm 1.69 1.69
15,000 scfm 5.07 5.07
30,000 scfm 10.14 10.14
38% Efficient Primary Heat Recovery
5000 scfm 0,79 0.26
15,000 scfm 2.38 0.77
30,000 scfm 4.76 1.54
Primary and 55% Efficient Secondary
Heat Recovery
5000 scfm -0.21 -1.07
15,000 scfm -0.62 -3.22
30,000 scfm -1.24 -6.46
a) Based on 300°F oven outlet temperature; 1400°F outlet temperature for non-catalytic
and 600°F inlet temperature for catalytic incinerators.
b) (-) indicates net overall fuel savings.
c) These heat recovery efficiencies are based on sensible heat,
5-9
-------
TABLE 5-2
BURNER REQUIREMENTS FOR NONCATALYTIC INCINERATORS
WITH STONE PACKED BED HEAT EXCHANGERS
in 106 BTU/HRa'b'c>14
85% EFFICIENCY PRIMARYHEAT RECOVERY^
5,000 scfm
15,000 scfm
30,000 scfm
5 percent LEL 15 percent LEI
0.29
0.87
1.75
- 0.91
- 2.73
- 5.45
90% EFFICIENCY PRIMARY HEAT RECOVERY
5,000 scfm
15,000 scfm
30,000 scfm
5percent LEL
- 0.01
- 0.02
- 0.04
15 percent LEL
- 1.21
- 3.62
- 7.24
' These heat recovery efficiencies include sensible heat and the heat of
combustion of the VOC.
b' Energy value of VOC used is 1.2 MM/BTU/HR per 10,000 scfm.
' {-) indicates overall fuel savings
5-10
-------
5.7 REFERENCES
1. McCormick, Donald, "Converting a Flowcoater to Water-Borne Paint,"
Whirlpool Corporation. Presented at the NPCA Chemical Coatings
Conference, Cincinnati, Ohio, April 23, 1976.
2. Ibid.
3. Water-Borne Flow coating and Dip, Products Finishing, pages 73-76,
February, 1977.
4. Products Finishing, Op. Cit.
5. McCormick, Op, Cit.
6. Products Finishing, Op. Cit.
7. Kennedy, W. D., "Major Appliance Electrocoat," Whirlpool Corporation.
Presented at the NPCA Chemical Coatings Conference, Cincinnati, Ohio,
April 22, 1976.
8. DeVittorio, J. M., Ransburg Corporation, "Application Equipment for
High-Solids and Plural Component Coatings," Volume I, No. 2, April, 1976.
9. "Question Corner," High-Solids Coatings, Volume I, No. 3, July, 1976.
10. "Economic Justification of Powder Coating," Powder Finishing World,
pages 18-22, 4th Quarter, 1976.
11. LeBras, Louis, Technical Director, PPG Industries, Inc., Pittsburgh,
Pennsylvania. Letter to V. N. Gallagher in comment of the metal furniture
draft document. Letter dated August 31, 1977.
12. Ibid.
13. Combustion Engineering Air Preheater, Wellsvilie. New York. Report of
Fuel Requirements, Capital Cost, and Operating Expenses for Catalytic
and Thermal Afterburners, EPA Contract Report No. EPA-450/3-76-031,
September, 1976.
14. Mueller, James H., Regenerative Environmental Equipment Co., Inc., Morris
Plains, New Jersey. Letter to V. N. Gallagher in comment of this draft
document. Letter dated March 31, 1978.
5-11
-------
6.0 MONITORING TECHNIQUES AND ENFORCEMENT ASPECTS
This chapter discusses the recommended emission limits, the monitoring
techniques and enforcement aspects for both coatings which are low in organic
solvents and add-on control equipment.
Limitations in VOC may be expressed in terms of mass or volume and
may be based on the entire coating (including organic solvent) or only on
paint solids. In this guideline, limitations are expressed as the allow-
able mass of organic solvent per unit volume of coating (kgs per liter of
coating or Ibs per gallon of coating - minus water) as it is delivered to the coating
applicator. The water content of the coating is not included in the ratio.
The principal advantage of this format is that enforcement is relatively
simple. Field personnel can draw samples and have them analyzed quickly.
A disadvantage is that the relationship between the solvent fraction and
organic emissions is not linear. If the organic solvent content is expressed
in terms of mass of organic solvent per unit volume of paint solids (kgs per
liter or Ibs per gallon of solids), the disparity disappears. This relationship
is linear and more readily understood, e.g., a coating containing 2 Ibs of
organic solvent per gallon of solids releases twice as much organic solvent
as one with one pound per gallon. The disadvantage of this format, however,
is that the analytical methods are more complex. Appendix A of Volume II
of this series, "Control of Volatile Organic Emissions from Existing Stationary
Sources - Volume II: Surface Coating of Cans, Coils, Paper, Fabrics,
Automobiles,, and Light-Duty Trucks," presents ASTM test methods that permit
determination of the organic solvent per gallon of coating (minus water).
6-1
-------
For miscellaneous metal part and product coating facilities, it is
recommended that, if possible, emission limitations should be expressed
in terms of the organic solvent content of the coating since these values
can be determined with relatively simple analytical techniques. Alternative
compliance procedures should permit operators to use add-on control equip-
ment if they so choose. (Sample calculations to verify compliance with
this type of emission limit are shown in Appendix A of this document.)
Other options such as mass or volume of organic solvent per mass
of coating are generally less desirable although they may be entirely
appropriate for a given industry. Basing limitations on the mass of
coating or paint solids is not generally recommended because the specific
gravity of a coating solids tends to vary widely with the degree and type of
pigment employed. Highly pigmented paints have much greater density than
unpigmented clear coats or varnishes.
The recommended limitations assume the miscellaneous metal part and
product facilities merely convert an organic-borne coating to a coating
low in organic solvent. They do not consider the reduction in VOC emissions
which would result from a decrease in film thickness or an increase in the
transfer efficiency of a coating. For example, assume a facility applying
conventional coating at 1.2 mils film thickness, converts to a coating
which, although it contains less organic solvent, does not quite meet the
recommended emission limit. If the new coating is serviceable when applied
in a thinner coat, it may result in a reduction in VOC emissions comparable
to or even greater than a coating which meets the recommended emission limit,
Another example would be the emission reductions that accrue from
improved coating techniques. A facility that converts from a conventional
manual spray application (at a transfer efficiency of 40-70 percent) to an
6-2
-------
automated electrostatic spray system (at a transfer efficiency of 70-90
percent), or from any spray system to a flow or dip coat system (at a
transfer efficiency of at least 90 percent) would realize a significant
reduction in VOC emissions. All of these possibilities should be considered
in any evaluation of the overall reduction achieved by the operator.
In those few facilities where add-on control equipment is a more
likely option, it may be more appropriate to state emission limits in terms
of control efficiency across the incinerator, adsorber, etc. Otherwise,
where limitations are expressed only in terms of the solvent content of the
coating, it would be necessary to determine the mass emission rate from the
control system and relate it to the quantity of coating applied during
the test period. This is a more complicated procedure since it may not be
easy to determine the amount of coating consumed during the test period and
an analysis by mass of the organic solvent directed to the control device
would be even more difficult. Chapter 5 of "Control of Volatile Organic
Emissions from Existing Stationary Sources - Volume I: Control Methods
for Surface Coating Operations" presents approaches which may be used.
When add-on type devices are selected as the compliance method, the air
pollution control agency should require that the coating lines be equipped
with an approved capture device to assure effective containment. The capture
system will likely have to be custom designed to accommodate the individual
plant variables which affect performance. When reviewing the design of such
a system, however, the air pollution control official must also consider
requirements imposed by the Occupational Safety and Health Administration
and the National Fire Prevention Association.
It is recognized that some coatings will emit more VOC than merely its
solvent content. This incremental VOC may come from three possible sources.
6-3
-------
The first is the possibility that some of the monomer may evaporate. Also,
if the film forms by condensation polymerization, the evolution of by-products
may be a compounding factor. Finally, it has been reported that the industry
is using increasing quantities of "blocking agents" which are released from
the polymer matrix during the curing process.
There are now no approved analytical methods certified by the agency
for determining the quantity of VOC emitted by such reactions although
certainly the organic mass emission rate could be determined by expensive
and sophisticated analytical techniques. The more practical means of
quantifying the contribution of the polymerization reaction to the overall
emission problem would be by contacting the manufacturer of the coating.
Certainly, his knowledge of the fundamental chemical mechanisms involved
would allow calculation of an emission rate based on the chemical reaction.
This emission will occur during the cure (if at all) which is usually
temperature initiated by the oven. If the oven is controlled by an incinerator,
then verification of the efficiency of the device should be sufficient to
assure compliance with the coating regulations.
6-4
-------
APPENDIX A
SAMPLE CALCULATIONS OF CONTROL OPTIONS
This appendix will aid the local agency in determining if a coating
proposed for use by a miscellaneous metal part or product facility will
meet a recommended emission limit. It also explains how to compare the
actual VOC emissions from a facility regardless of the type of low-polluting
coating or add-on control device used.
The purpose of all coating operations is to cover a substrate with a
film that provides both corrosion resistance to the substrate and
esthetic appeal. Therefore, the rational basis for specifying an allowable
VOC emission limit would be in units of coating volume (e.g., grams of
VOC per square meter (Ibs/sq. ft) per unit thickness of film). However,
the complexity of any analytical method which would provide a measurement
of the volume of a cured coating precludes this approach. As a compromise,
the limitations were developed in terms of mass of VOC per unit volume of
uncured solids and organic solvent. Mathematically, then, the emission
factor (ef) for a coating would be expressed as:
m ef = (^urne ^action organic sol vent) (average organic solvent density)
* ' volume fraction of solids + volume fraction of organic solvent
(2} ef (volume fraction organic solvent) (average organic solvent density)
^ ' " 1- volume fraction of water
The following examples show the use of these equations to determine
the emission factor for both organic solvent-borne and water-borne coatings.
We will assume the applicable emission limitation is 0.34 kg/liter. This
represents a low solvent coating with 0.62 v/v solids content.
A-l
-------
CASE 1: Determine the emission factor for an organic solvent-borne coating
which contains 35 volume percent organic solvent.
Therefore: ef = (.35)(0.88_kg/liter*)
= 0.31 kgs/liter (2.6 Ibs/gal)
Since the emission factor is less than the recommended limit of
0.34 kg/liter (2.8 Ibs/gal), this coating is in compliance.
CASE 2: Determine the emission factor for a water-borne coating containing
25 volume percent solids. Of the 75 percent solvent, 80 volume percent
is water and 20 percent is organic solvent.
Since 80 percent of the solvent is water, the respective volumes of
water and organic solvent may be calculated as shown:
Volume water = .80 x .75 liter = .6 liter
Volume organic solvent = 0.75 liter - .6 liter = .15 liter
Therefore: ef = (0.15H0.88 kg/liter)*
I - u.o
= 0.32 kg/liter (2.64 Ibs/gal)
This coating also has an emission factor less than the recommended limit
and would comply.
The level of control represented by 0.34 kg/liter of coating
(2.8 Ibs/gal) less water can also be achieved with a conventional high
organic solvent coating if suitable add-on control equipment is installed.
However, this method of determining the equivalent emission limit factor
is not as straightforward as the previous two cases and must also consider
the volume of solids in the coating.
CASE 3: Determine the emission factor for a conventional organic-borne
coating containing 75 volume percent organic solvent.
*This density is considered typical and is equal to 7.36 Ibs/gal.
A-2
-------
TU * (.75H.88 kg/liter)
Therefore: ef = N M-] _ A* L
= 0.66 kg/liter (5.5 Ibs/gal)
However, this liter of coating contains only 0.25 liter of solids
whereas the low-solvent coating which the recommended emission limit of
0.34 kg/liter (2.8 gal) represented would contain 0.62 liter of solids.
(The fraction of solids in the low solvent coating can be back calcu-
lated from the recommended emission limit in the following manner.)
IP n ™ - (*)(0.88 kg/liter)
I * C • 9 U • OH" j-uj ---^_
x = 0.38, volume percent organic solvent
Therefore, fraction of solids = 1 - x = 0.62.
On a unit volume of solids basis, the conventional coating contains:
0.66 kg organic solvent _ 2.64 kg organic solvent or 22 Ibs VOC
0.25 Titer solidsliter solidsgal solids
And the recommended limit reference coating contains only:
0.34 kg organic solvent _ 0.55 kg organic solvent or 4.6 Ibs VOC
0.62 liter solidsliter solidsgal solids
Consequently, in order for a facility to use the conventional coating
yet emit no more VOC than the reference coating, the add-on control device
must capture and destroy (or collect) 2,09 kg of solvent per liter of solids
applied (2.64 - 0.55). This will require a control system that is at least
79 percent efficient. Since the add-on control devices can often operate
at 90 percent efficiency or greater, the agency must insure that at least
88 percent of the VOC emitted by the coating is captured and delivered to
the add-on control device. Since it will often not be practical to
attempt the complex analytical program essential to develop a material
A-3
-------
balance around the coating application and flashoff areas and ovens,
the agency may certify an acceptable capture system based on good
engineering practice.
APPENDIX A REFERENCE
1. Young, Dexter E., Environmental Protection Agency, memorandum
concerning requirements for ventilation of spray booths and
ovens. Dated March 10, 1977.
A-4
-------
TECHNICAL REPORT DATA
{Please read Instructions on the reverse before completing)
1. REPORT NO,
EPA-450/2-78-015
3. RECIPIENT'S ACCESSIOWNO,
4, TITLE AND SUBTITLE
Control of Volatile Organic Emissions from Existing
Stationary Sources - Volume VI: Surface Coating of
Miscellaneous Metal Parts and Products
5. REPORT DATE
June. 1978
6. PERFORMING ORGANIZATION CODE
7, AUTHORIS!
Vera Gallagher, John Pratapas
8. PERFORMING ORGANIZATION REPORT NO.
OAQPS No. 1.2-101
9. PERFORMING ORGANIZATION NAME AND ADDRESS
U.S. Environmental Protection Agency
Office of Air and Waste Management
Office of Air Quality Planning and Standards
Research Triangle Park, No'rth Carolina 27711
10. PROGRAM ELEMENT NO.
11, CONTRACT/GRANT NO.
12. SPONSORING AGENCY NAME AND ADDRESS
13. TYPE OF REPORT AND PERIOD COVERED
14. SPONSORING AGENCY CODE
15. SUPPLEMENTARY NOTES
16, ABSTRACT
This document provides the necessary guidance for development of
regulations to limit emissions of volatile organic compounds (VOC) from
the coating operations of miscellaneous metal parts and products. This
guidance includes emission limits which represent Reasonably Available
Control Technology (RACT) for the miscellaneous metal part and product
Industries, describes the industries, shows the methods by which VOC
emissions can be reduced in these industries and describes the monitoring
and enforcement aspects.
17,
KEY WORDS AND DOCUMENT ANALYSIS
DESCRIPTORS
b.IDENTIFIERS/OPEN ENDED TERMS
c. COSATI Field/Group
Air Pollution
Miscellaneous Metal Part and Product
Industries
Volatile Organic Compound Emission
Limits
Regulatory Guidance
Air Pollution Control
Stationary Sources
Organic Vapors
18. DISTRIBUTION STATEMENT
Unlimited
19. SECURITY CLASS (This Report)
Unclassified
21. NO. OF PAGES
20. SECURITY CLASS t
ii T « ** • t
Unclassified
22. PRICE
EPA Form 2220-1 (9-73)
-------
United States Office of Air, Noise, and Radiation
Environmental Protection Office of Air Quality Planning and Standards
Agency Research Triangle Park NC 27711
Official Business Publication No EPA-450/2-78-015 Postage and
Penalty for Private Use Fees Paid
4300 Environmental
Protection
Agency
EPA 335
If your address is incorrect, please change on the above label;
tear off; and return to the above address.
If you do not desire to continue receiving this technical report
series, CHECK HERE D ; tear off label; and return it to the
above address.
-------