(1) WHAT GENERAL
REQUIREMENTS MUST I MEET TO COMPLY WITH THE STANDARDS? You shall comply with
the applicable general provisions of ch. NR 460 as specified in ch. NR 460
Appendix JJJJ.
(2) IF I USE A
CONTROL DEVICE TO COMPLY WITH THE EMISSION STANDARDS, WHAT MONITORING MUST I
DO?
(a) Summary. A summary of monitoring you
shall do follows:
Monitoring Summary
If you operate a web coating line, and you
have the following:
|
Then you shall:
|
1. Intermittently-controlled work stations
|
Record parameters related to possible exhaust
flow bypass of control device and to coating use (par. (c))
|
2. Solvent recovery unit
|
Operate continuous emission monitoring system and
perform quarterly audits or determine volatile matter recovered and conduct a
liquid-liquid material balance (par. (d))
|
3. Control device
|
Operate continuous parameter monitoring system
(par. (e))
|
4. Capture system
|
Monitor capture system operating parameter (par.
(f))
|
(b) Capture system and control device
monitoring. Following the date on which the initial performance test of a
control device is completed to demonstrate continuing compliance with the
standards, you shall monitor and inspect each capture system and each control
device used to comply with s.
NR 466.23(1). You shall install and
operate the monitoring equipment as specified in pars. (c) and (f).
(c) Bypass and coating use monitoring. If you
own or operate web coating lines with intermittently-controlled work stations,
you shall monitor bypasses of the control device and the mass of each coating
material applied at the work station during any bypass. If using a control
device for complying with the requirements of this subchapter, you shall
demonstrate that any coating material applied on a never-controlled work
station or an intermittently-controlled work station operated in bypass mode is
allowed in your compliance demonstration according to s.
NR 466.25(14)
and (15). The bypass monitoring shall be
conducted using at least one of the procedures in subds. 1. to 4. for each work
station and associated dryer.
1. `Flow
control position indicator.' Install, calibrate, maintain and operate according
to the manufacturer's specifications a flow control position indicator that
provides a record indicating whether the exhaust stream from the dryer was
directed to the control device or was diverted from the control device. The
time and flow control position shall be recorded at least once per hour as well
as every time the flow direction is changed. A flow control position indicator
shall be installed at the entrance to any bypass line that could divert the
exhaust stream away from the control device to the atmosphere.
2. `Car-seal or lock-and-key valve closures.'
Secure any bypass line valve in the closed position with a car-seal or a
lock-and-key type configuration. A visual inspection of the seal or closure
mechanism shall be performed at least once every month to ensure that the valve
or damper is maintained in the closed position, and the exhaust stream is not
diverted through the bypass line.
3. `Valve closure continuous monitoring.'
Ensure that any bypass line valve or damper is in the closed position through
continuous monitoring of valve position when the emission source is in
operation and is using a control device for compliance with the requirements of
this subchapter. The monitoring system shall be inspected at least once every
month to verify that the monitor will indicate valve position.
4. `Automatic shutdown system.' Use an
automatic shutdown system in which the web coating line is stopped when flow is
diverted away from the control device to any bypass line when the control
device is in operation. The automatic system shall be inspected at least once
every month to verify that it will detect diversions of flow and would shut
down operations in the event of such a diversion.
(d) Solvent recovery unit. If you own or
operate a solvent recovery unit to comply with s.
NR 466.23(1), you shall meet the
requirements in either subd. 1. or 2., depending on how control efficiency is
determined.
1. `Continuous emission
monitoring system (CEMS).' If you are demonstrating compliance with the
emission standards in s.
NR 466.23(1) through continuous emission
monitoring of a control device, you shall install, calibrate, operate and
maintain the CEMS according to subd. 1. a. to c.
a. Measure the total organic volatile matter
mass flow rate at both the control device inlet and the outlet such that the
reduction efficiency can be determined. Each continuous emission monitor shall
comply with performance specification 6, 8 or 9, as appropriate, of 40 CFR part
60, Appendix B, incorporated by reference in s.
NR 484.04(21).
b. You shall follow the quality assurance
procedures in procedure 1, of 40 CFR part 60, Appendix F, incorporated by
reference in s.
NR 484.04(21m). In conducting the
quarterly audits of the monitors as required by procedure 1, Appendix F, you
shall use compounds representative of the gaseous emission stream being
controlled.
c. You shall have valid
data from at least 90% of the hours during which the process is
operated.
2.
`Liquid-liquid material balance.' If you are demonstrating compliance with the
emission standards in s.
NR 466.23(1) through liquid-liquid
material balance, you shall install, calibrate, maintain and operate according
to the manufacturer's specifications a device that indicates the cumulative
amount of volatile matter recovered by the solvent recovery device on a monthly
basis. The device shall be certified by the manufacturer to be accurate to
within ±2.0% by mass.
(e) Continuous parameter monitoring system
(CPMS). If you are using a control device to comply with the emission standards
in s.
NR 466.23(1), you shall install, operate
and maintain each CPMS specified in subds. 9. and 10. and par. (f) according to
the requirements in subds. 1. to 8. You shall install, operate and maintain
each CPMS specified in par. (c) according to subds. 5. to 7.
1. Each CPMS shall complete a minimum of one
cycle of operation for each successive 15-minute period. You shall have a
minimum of 4 equally spaced successive cycles of CPMS operation to have a valid
hour of data.
2. You shall have
valid data from at least 90% of the hours during which the process
operated.
3. You shall determine
the hourly average of all recorded readings according to subd. 3. a. and b.
a. To calculate a valid hourly value, you
shall have at least 3 of 4 equally spaced data values from that hour from a
continuous monitoring system (CMS) that is not out-of-control.
b. Provided all of the readings recorded in
accordance with this subdivision clearly demonstrate continuous compliance with
the standard that applies to you, then you are not required to determine the
hourly average of all recorded readings.
4. You shall determine the rolling 3-hour
average of all recorded readings for each operating period. To calculate the
average for each 3-hour averaging period, you shall have at least 2 of 3 of the
hourly averages for that period using only average values that are based on
valid data not from out-of-control periods.
5. You shall record the results of each
inspection, calibration and validation check of the CPMS.
6. At all times, you shall maintain the
monitoring system in proper working order, including maintaining necessary
parts for routine repairs of the monitoring equipment.
7. Except for monitoring malfunctions,
associated repairs or required quality assurance or control activities,
including calibration checks or required zero and span adjustments, you shall
conduct all monitoring at all times that the unit is operating. Data recorded
during monitoring malfunctions, associated repairs, out-of-control periods or
required quality assurance or control activities may not be used for purposes
of calculating the emissions concentrations and percent reductions specified in
s.
NR 466.25(1). You shall use all the
valid data collected during all other periods in assessing compliance of the
control device and associated control system. A monitoring malfunction is any
sudden, infrequent, not reasonably preventable failure of the monitoring system
to provide valid data. Monitoring failures that are caused in part by poor
maintenance or careless operation are not malfunctions.
8. Any averaging period for which you do not
have valid monitoring data, and the data are required, constitutes a deviation,
and you shall notify the department in accordance with s.
NR 466.26(1)
(c).
9. If you are using an oxidizer to comply
with the emission standards, you shall comply with subd. 9. a. to c.
a. Install, calibrate, maintain and operate
temperature monitoring equipment according to the manufacturer's
specifications. The calibration of the chart recorder, data logger or
temperature indicator shall be verified every 3 months or the chart recorder,
data logger or temperature indicator shall be replaced. You shall replace the
equipment whether you choose not to perform the calibration or the equipment
cannot be calibrated properly.
b.
For an oxidizer other than a catalytic oxidizer, install, calibrate, operate
and maintain a temperature monitoring device equipped with a continuous
recorder. The device shall have an accuracy of ±1% of the temperature
being monitored in degrees Celsius, or ±1° Celsius, whichever is
greater. The thermocouple or temperature sensor shall be installed in the
combustion chamber at a location in the combustion zone.
c. For a catalytic oxidizer, install,
calibrate, operate and maintain a temperature monitoring device equipped with a
continuous recorder. The device shall be capable of monitoring temperature with
an accuracy of ±1% of the temperature being monitored in degrees Celsius
or ±1° Celsius, whichever is greater. The thermocouple or
temperature sensor shall be installed in the vent stream at the nearest
feasible point to the inlet and outlet of the catalyst bed. Calculate the
temperature rise across the catalyst.
10. If you use a control device other than an
oxidizer or wish to monitor an alternative parameter and comply with a
different operating limit, you shall apply to the department for approval of an
alternative monitoring method under s.
NR 460.07(6).
(f) Capture system monitoring. If you are
complying with the emission standards in s.
NR 466.23(1) through the use of a
capture system and control device for one or more web coating lines, you shall
develop a site-specific monitoring plan containing the information specified in
subds. 1. and 2. for the capture systems. You shall monitor the capture system
in accordance with subd. 3. You shall make the monitoring plan available for
inspection by the department upon request.
1.
The monitoring plan shall do all of the following:
a. Identify the operating parameter to be
monitored to ensure that the capture efficiency determined during the initial
compliance test is maintained.
b.
Explain why the operating parameter is appropriate for demonstrating ongoing
compliance.
c. Identify the
specific monitoring procedures.
2. The monitoring plan shall specify the
operating parameter value or range of values that demonstrate compliance with
the emission standards in s.
NR 466.23(1). The specified operating
parameter value or range of values shall represent the conditions present when
the capture system is being properly operated and maintained.
3. You shall conduct all capture system
monitoring in accordance with the plan.
4. Any deviation from the operating parameter
value or range of values which are monitored according to the plan will be
considered a deviation from the operating limit.
5. You shall review and update the capture
system monitoring plan at least annually.
(3) WHAT PERFORMANCE TESTS SHALL I CONDUCT?
(a) Performance test methods. The performance
test methods you shall use are as follows:
Performance Test Methods
If you control organic HAP on any
individual web coating line or any group of web coating lines by:
|
You shall:
|
1. Limiting organic HAP or volatile matter
content of coatings
|
Determine the organic HAP or volatile matter and
coating solids content of coating materials according to procedures in pars.
(c) and (d). If applicable, determine the mass of volatile matter retained in
the coated web or otherwise not emitted to the atmosphere according to par.
(g).
|
2. Using a capture and control system
|
Conduct a performance test for each capture and
control system to determine the destruction or removal efficiency of each
control device other than solvent recovery according to par. (e) and the
capture efficiency of each capture system according to par. (f). If applicable,
determine the mass of volatile matter retained in the coated web or otherwise
not emitted to the atmosphere according to par. (g).
|
(b) Exceptions. If you are using a control
device to comply with the emission standards in s.
NR 466.23(1), you are not required to
conduct a performance test to demonstrate compliance if one or more of the
criteria in subds. 1. to 3. are met.
1. The
control device is equipped with continuous emission monitors for determining
inlet and outlet total organic volatile matter concentration and capture
efficiency has been determined in accordance with the requirements of this
subchapter such that an overall organic HAP control efficiency can be
calculated, and the continuous emission monitors are used to demonstrate
continuous compliance in accordance with sub. (2).
2. You have met the requirements of s.
NR 460.06(7) for waiver of performance
testing.
3. The control device is a
solvent recovery system and you comply by means of a monthly liquid-liquid
material balance.
(c)
Organic HAP content. If you determine compliance with the emission standards in
s.
NR 466.23(1) by means other than
determining the overall organic HAP control efficiency of a control device, you
shall determine the organic HAP mass fraction of each coating material
as-purchased by following one of the procedures in subds. 1. to 3., and
determine the organic HAP mass fraction of each coating material as-applied by
following the procedures in subd. 4. If the organic HAP content values are not
determined using the procedures in subds. 1. to 3., you shall submit an
alternative test method for determining their values for approval by the
administrator in accordance with
40 CFR
63.7(f). The recovery
efficiency of the test method shall be determined for all of the target organic
HAP and a correction factor, if necessary, shall be determined and applied.
1. `Method 311.' You may test the coating
material in accordance with Method 311 of 40 CFR part 63, Appendix A,
incorporated by reference in s.
NR 484.04(25). The Method 311
determination may be performed by the manufacturer of the coating material and
the results provided to the owner or operator. The organic HAP content shall be
calculated according to the criteria and procedures in subd. 1. a. to c.
a. Include each organic HAP determined to be
present at greater than or equal to 0.1% by mass for the United States
occupational safety and health administration-defined (OSHA-defined)
carcinogens as specified in
29 CFR 1910.1200(d)
(4) and greater than or equal to 1.0% by mass
for other organic HAP compounds.
b.
Express the mass fraction of each organic HAP you include according to subd. 1.
a. as a value truncated to 4 places after the decimal point, e.g., 0.3791.
c. Calculate the total mass
fraction of organic HAP in the tested material by summing the counted
individual organic HAP mass fractions and truncating the result to 3 places
after the decimal point, e.g., 0.763.
2. `Method 24.' For coatings, determine the
volatile organic content as mass fraction of non-aqueous volatile matter and
use it as a substitute for organic HAP using Method 24 of 40 CFR part 60,
Appendix A, incorporated by reference in s.
NR 484.04(13). The Method 24
determination may be performed by the manufacturer of the coating and the
results provided to you.
3.
`Formulation data.' You may use formulation data to determine the organic HAP
mass fraction of a coating material. Formulation data may be provided to you by
the manufacturer of the material. In the event of an inconsistency between
Method 311 of 40 CFR part 63, Appendix A, incorporated by reference in s.
NR 484.04(25), test data and a
facility's formulation data, and the Method 311 test value is higher, the
Method 311 data will govern. Formulation data may be used provided that the
information represents all organic HAP present at a level equal to or greater
than 0.1 % for OSHA-defined carcinogens as specified in
29 CFR 1910.1200(d)
(4) and equal to or greater than 1.0 % for
other organic HAP compounds in any raw material used.
4. `As-applied organic HAP mass fraction.' If
the as-purchased coating material is applied to the web without any solvent or
other material added, the as-applied organic HAP mass fraction is equal to the
as-purchased organic HAP mass fraction. Otherwise, the as-applied organic HAP
mass fraction shall be calculated using Equation 1a of s.
NR 466.25.
(d) Volatile organic and coating solids
content. If you determine compliance with the emission standards in s.
NR 466.23(1) by means other than
determining the overall organic HAP control efficiency of a control device and
you choose to use the volatile organic content as a surrogate for the organic
HAP content of coatings, you shall determine the as-purchased volatile organic
content and coating solids content of each coating material applied by
following the procedures in subd. 1. or 2. and the as-applied volatile organic
content and coating solids content of each coating material by following the
procedures in subd. 3.
1. `Method 24.' You
may determine the volatile organic and coating solids mass fraction of each
coating applied using Method 24 in 40 CFR part 60, Appendix A, incorporated by
reference in s.
NR 484.04(13). The Method 24
determination may be performed by the manufacturer of the material and the
results provided to you. If these values cannot be determined using Method 24,
you shall submit an alternative technique for determining their values for
approval by the administrator.
2.
`Formulation data.' You may determine the volatile organic content and coating
solids content of a coating material based on formulation data and may rely on
volatile organic content data provided by the manufacturer of the material. In
the event of any inconsistency between the formulation data and the results of
Method 24 in 40 CFR part 60, Appendix A, incorporated by reference in s.
NR 484.04(13), and the Method 24 results
are higher, the results of Method 24 will govern.
3. `As-applied volatile organic content and
coating solids content.' If the as-purchased coating material is applied to the
web without any solvent or other material added, the as-applied volatile
organic content is equal to the as-purchased volatile content and the
as-applied coating solids content is equal to the as-purchased coating solids
content. Otherwise, the as-applied volatile organic content shall be calculated
using Equation 1b of s.
NR 466.25 and the as-applied coating solids content shall
be calculated using Equation 2 of s.
NR 466.25.
(e) Control device efficiency. If you are
using an add-on control device other than solvent recovery, such as an
oxidizer, to comply with the emission standards in s.
NR 466.23(1), you shall conduct a
performance test to establish the destruction or removal efficiency of the
control device according to the methods and procedures in subds. 1. and 2.
During the performance test, you shall establish the operating limits required
by s.
NR 466.23(2) according to subd. 3.
1. An initial performance test to establish
the destruction or removal efficiency of the control device shall be conducted
such that control device inlet and outlet testing is conducted simultaneously
and the data are reduced in accordance with the test methods and procedures in
subd. 1. a. to i. You shall conduct 3 test runs as specified in s.
NR 460.06(4)
(c), and each test run shall last at least
one hour.
a. Method 1 or 1A of 40 CFR part
60, Appendix A, incorporated by reference in s.
NR 484.04(13), shall be used for sample
and velocity traverses to determine sampling locations.
b. Method 2, 2A, 2C, 2D, 2F or 2G of 40 CFR
part 60, Appendix A, incorporated by reference in s.
NR 484.04(13), shall be used to
determine gas volumetric flow rate.
c. Method 3, 3A or 3B of 40 CFR part 60,
Appendix A, incorporated by reference in s.
NR 484.04(13), shall be used for gas
analysis to determine dry molecular weight. You may also use as an alternative
to Method 3B the manual method for measuring the oxygen, carbon dioxide and
carbon monoxide content of exhaust gas in ANSI/ASME PTC 19.10-1981, "Flue and
Exhaust Gas Analyses, Part 10, Instruments and Apparatus", incorporated by
reference in s.
NR 484.11(6)
(b).
d. Method 4 of 40 CFR part 60, Appendix A,
incorporated by reference in s.
NR 484.04(13), shall be used to
determine stack gas moisture.
e.
The gas volumetric flow rate, dry molecular weight and stack gas moisture shall
be determined during each test run specified in subd. 1. g.
f. Method 25 or 25A of 40 CFR part 60,
Appendix A, incorporated by reference in s.
NR 484.04(13), shall be used to
determine total gaseous non-methane organic matter concentration. Use the same
test method for both the inlet and outlet measurements which shall be conducted
simultaneously. You shall submit notice of the intended test method to the
department for approval along with notification of the performance test
required under s.
NR 460.06(2). You shall use Method 25A
if any of the following 4 conditions apply to the control device:
1) The control device is not an
oxidizer.
2) The control device is
an oxidizer but an exhaust gas volatile organic matter concentration of 50 ppmv
or less is required to comply with the emission standards in s.
NR 466.23(1).
3) The control device is an oxidizer but the
volatile organic matter concentration at the inlet to the control system and
the required level of control are such that they result in exhaust gas volatile
organic matter concentrations of 50 ppmv or less.
4) The control device is an oxidizer but,
because of the high efficiency of the control device, the anticipated volatile
organic matter concentration at the control device exhaust is 50 ppmv or less,
regardless of inlet concentration.
g. Except as provided in s.
NR 460.06(4)
(c), each performance test shall consist of 3
separate runs with each run conducted for at least one hour under the
conditions that exist when the affected source is operating under normal
operating conditions. For the purpose of determining volatile organic compound
concentrations and mass flow rates, the average of the results of all the runs
shall apply.
h. Volatile organic
matter mass flow rates shall be determined for each run specified in subd. 1.
g. using Equation 1:
See
Image
where:
Mf is the total organic volatile matter mass flow rate in
kilograms (kg)/hour (h)
Qsd is the volumetric flow rate of gases entering or
exiting the control device, as determined according to par. (e) 1. b., dry
standard cubic meters (dscm)/h
Cc is the concentration of organic compounds as carbon,
ppmv
12.0 is the molecular weight of carbon
0.0416 is a conversion factor for molar volume, kg-moles
per cubic meter (mol/m3) at 293 Kelvin (K) and 760 millimeters of mercury
(mmHg)
i. For each run,
emission control device destruction or removal efficiency shall be determined
using Equation 2:
See
Image
where:
E is the organic volatile matter control efficiency of the
control device, percent
Mfi is the organic volatile matter mass flow rate at the
inlet to the control device, kg/h
Mfo is the organic volatile matter mass flow rate at the
outlet of the control device, kg/h
j. The control device destruction or removal
efficiency is determined as the average of the efficiencies determined in the
test runs and calculated in Equation 2 of this section.
2. You shall record process information as
may be necessary to determine the conditions in existence at the time of the
performance test. Operations during periods of startup, shutdown and
malfunction will not constitute representative conditions for the purpose of a
performance test.
3. If you are
using one or more add-on control devices other than a solvent recovery system
for which you conduct a liquid-liquid material balance to comply with the
emission standards in s.
NR 466.23(1), you shall establish the
applicable operating limits required by s.
NR 466.23(2). The operating limits apply
to each add-on emission control device, and you shall establish the operating
limits during the performance test required by this paragraph according to the
requirements in subd. 3. a. or b.
a. If your
add-on control device is a thermal oxidizer, establish the operating limits
according to the following 2 requirements:
1)
During the performance test, you shall monitor and record the combustion
temperature at least once every 15 minutes during each of the 3 test runs. You
shall monitor the temperature in the firebox of the thermal oxidizer or
immediately downstream of the firebox before any substantial heat exchange
occurs.
2) Use the data collected
during the performance test to calculate and record the average combustion
temperature maintained during the performance test. This average combustion
temperature is the minimum operating limit for your thermal oxidizer.
b. If your add-on control device
is a catalytic oxidizer, establish the operating limits according to subd. 3.
b. 1) and 2) or 3. b. 3) and 4):
1) During
the performance test, you shall monitor and record the temperature just before
the catalyst bed and the temperature difference across the catalyst bed at
least once every 15 minutes during each of the 3 test runs.
2) Use the data collected during the
performance test to calculate and record the average temperature just before
the catalyst bed and the average temperature difference across the catalyst bed
maintained during the performance test. These are the minimum operating limits
for your catalytic oxidizer.
3) As
an alternative to monitoring the temperature difference across the catalyst
bed, you may monitor the temperature at the inlet to the catalyst bed and
implement a site-specific inspection and maintenance plan for your catalytic
oxidizer as specified in subd. 3. b. 4). During the performance test, you shall
monitor and record the temperature just before the catalyst bed at least once
every 15 minutes during each of the 3 test runs. Use the data collected during
the performance test to calculate and record the average temperature just
before the catalyst bed during the performance test. This is the minimum
operating limit for your catalytic oxidizer.
4) You shall develop and implement an
inspection and maintenance plan for the catalytic oxidizers which you elect to
monitor according to subd. 3. b. 3). The plan shall address, at a minimum, all
of the following elements:
a) Annual sampling
and analysis of the catalyst activity, i.e., conversion efficiency, following
the manufacturer's or catalyst supplier's recommended procedures.
b) Monthly inspection of the oxidizer system
including the burner assembly and fuel supply lines for problems.
c) Annual internal and monthly external
visual inspection of the catalyst bed to check for channeling, abrasion and
settling. If problems are found, you shall take corrective action consistent
with the manufacturer's recommendations and conduct a new performance test to
determine destruction efficiency in accordance with this section.
(f) Capture efficiency. If you demonstrate
compliance by meeting the requirements of s.
NR 466.25(5),
(6), (7), (11), (14) (b) or (c) or (16), you
shall determine capture efficiency using the procedures in subd. 1., 2. or 3.,
as applicable.
1. You may assume your capture
efficiency equals 100% if your capture system is a permanent total enclosure
(PTE). You shall confirm that your capture system is a PTE by demonstrating
that it meets the requirements of section 6 of Method 204 of 40 CFR part 51, Appendix M, incorporated by reference in s.
NR 484.04(9), and that all exhaust gases
from the enclosure are delivered to a control device.
2. You may determine capture efficiency
according to the protocols for testing with temporary total enclosures that are
specified in Methods 204 and 204A through F of 40 CFR part 51, Appendix M,
incorporated by reference in s.
NR 484.04(9). You may exclude
never-controlled work stations from such capture efficiency
determinations.
3. You may use any
capture efficiency protocol and test methods that satisfy the criteria of
either the data quality objective or the lower confidence limit approach as
described in 40 CFR part 63, Subpart KK, Appendix A, incorporated by reference
in s.
NR 484.04(24). You may exclude
never-controlled work stations from capture efficiency determinations made
under this subdivision.
(g) Volatile matter retained in the coated
web or otherwise not emitted to the atmosphere. You may choose to take into
account the mass of volatile matter retained in the coated web after curing or
drying or otherwise not emitted to the atmosphere when determining compliance
with the emission standards in s.
NR 466.23(1). If you choose this option,
you shall develop a testing protocol to determine the mass of volatile matter
retained in the coated web or otherwise not emitted to the atmosphere and
submit this protocol to the department for approval. You shall submit this
protocol with your site-specific test plan under s.
NR 460.06(5). If you intend to take into
account the mass of volatile matter retained in the coated web after curing or
drying or otherwise not emitted to the atmosphere and demonstrate compliance
according to s.
NR 466.25(3)
(c), (d), (e) or (4), the test protocol you
submit shall determine the mass of organic HAP retained in the coated web or
otherwise not emitted to the atmosphere. Otherwise, compliance shall be shown
using the volatile organic matter content as a surrogate for the HAP content of
the coatings.
(h) Control devices
in series. If you use multiple control devices in series to comply with the
emission standards in s.
NR 466.23(1), the performance test shall
include, at a minimum, the inlet to the first control device in the series, the
outlet of the last control device in the series, and all intermediate streams,
such as gaseous exhaust to the atmosphere or a liquid stream from a recovery
device, that are not subsequently treated by any of the control devices in the
series.