Regl. 6302, art. 405(b)(9)-5
3, provided that it is calibrated Initially and recalibrated periodically as follows:
Length: 2,369 wordsOfficial source
Cite as Reglamento Núm. 6302, Art. 405(b)(9)-5
7.1.1 Standard Dry Gas Meter Calibration.
7.1.1.1 The dry gas meter to be calibrated
and used as a secondary reference meter
should be of high quality and have an appropriately sized capacity, e.g., 3 liters/rev (0.1
ft ³/rev). A spirometer (400 liters or more capacity). or equivalent, may be used for this
callbration, although a wet test meter is
usually more practical. The wet test meter
should have a capacity of 30 liters/rev
(1
ft 3/rev) and capable of measuring volume to
within +1.0 percent: wet test meters should
be checked against a spirometer or a liquid
displacement meter to ensure the accuracy
of the wet test meter. Spirometers or wet
test meters of other sizes may be used, provided that the specified accuracies of the
procedure are maintained.
7.1.1.2 Set up the components as shown in
Figure 5.7. A spirometer. or equivalent, may
Pt. 60, App. A, Meth. 5
be used in place of the wet test meter in the
system. Run the pump for at least 5 minutes
at a flow rate of about 10 liters/min (0.35 cfm)
to condition the interior surface of the wet
test meter. The pressure drop indicated by
the manometer at the inlet side of the dry
40 CFR Ch. I (7-1-99 Edition)
gas meter should be minimized [no greater
than 100 mm H₂O (4 In. H₂O) at a flow rate of
30 liters/min (1-cfm)]. This can be accomplished by using large diameter tubing connections and straight pipe fittings.
EC01JN92.109
7.1.1.3 Collect the data as shown in the example data sheet (see Figure 5-8). Make triplicate runs at each of the flow rates and at
no less than five different flow rates. The
range of flow rates should be between 10 and
34 liters/min (0.35 and 1.2 cfm) or over the expected operating range.
EC01JN92.110
7.1.1.4 Calculate flow rate, Q. for each run
using the wet test meter gas volume, Vw and
the run time. 8. Calculate the dry gas meter
coefficient. Yds. for each run. These calculations are as follows:
Pt. 60, App. A, Meth. 5
40 CFR Ch. I (7-1-99 Edition)
EC15NO91.130
Where:
K1=0.3858 for International system of units
(SI); 17.64 for English units.
Vw=Wet test meter volume, liters (ft 3).
Vds=Dry gas meter volume. liters (ft 3).
tds=Average dry gas meter temperature, . C
(°F).
tstd=273° C for SI units; 460° F for English
units.
tw=Average wet test meter temperature, o C
(°F).
Phar=Barometric pressure, mm Hg (in. Hg).
Ap=Dry gas meter inlet differential pressure,
mm H₂O (in. H₂O).
8=Run time, min.
7.1.1.5 Compare the three Yds values at
each of the flow rates and determine the
maximum and minimum values. The difference between the maximum and minimum
values at each flow rate should be no greater
than 0.030. Extra sets of triplicate runs may
be made in order to complete this requirement. In addition. the meter coefficients
should be between 0.95 and 1.05. If these specifications cannot be met in three sets of successive triplicate runs, the meter is not suitable as a calibration standard and should not
be used as such. If these specifications are
met, average the three Yds values at each
flow rate resulting in five average meter coefficients, Yds.
7.1.1.6 Prepare a curve of meter coefficient. Yds, versus flow rate, Q. for the dry gas
meter. This curve shall be used as a reference when the meter is used to callbrate
other dry gas meters and to determine
whether recalibration is required.
7.1.2 Standard Dry Gas Meter Recalibration.
7.1.2.1 Recalibrate the standard dry gas
meter against a wet test meter or spirometer
annually or after every 200 hours of operation, whichever comes first. This requirement is valid provided the standard dry gas
meter is kept in a laboratory and, If transported. cared for as any other laboratory instrument. Abuse to the standard meter may
cause a change in the callbration and will require more frequent recalibrations.
7.1.2.2 As an alternative to full recalibration, a two-point calibration check may be
made. Follow the same procedure and equipment arrangement as for a full recalibration,
but run the meter at only two flow rates
[suggested rates are 14 and 28 liters/min (0.5
and 1.0 cfm)]. Calculate the meter coefficients for these two points, and compare the
values with the meter calibration curve. If
the two coefficients are within ±1.5 percent
of the callbration curve values at the same
flow rates, the meter need not be recalibrated until the next date for a recalibration
check.
7.2 Critical Orifices As Calibration Standards. Critical orifices may be used as callbration standards in place of the wet test meter
specified in Section 5.3. provided that they
are selected, calibrated, and used as follows:
7.2.1 Section of Critical Orifices.
7.2.1.1 The procedure that follows describes the use of hypodermic needles or
stainless steel needle tubings which have
been found suitable for use as critical orifices. Other materials and critical orifice designs may be used provided the orifices act
as true critical orifices: i.e., a critical vacuum can be obtained, as described in Section
7.2.2.2.3. Select five critical orifices that are
appropriately sized to cover the range of flow
rates between 10 and 34 liters/min or the expected operating range. Two of the critical
orifices should bracket the expected operating range.
A minimum of three critical orifices will
be needed to calibrate a Method 5 dry gas
meter (DGM): the other two critical orifices
can serve as spares and provide better selection for bracketing the range of operating
flow rates. The needle sizes and tubing
lengths shown below give the following approximate flow rates:
Gauge/cm
Flow rate (li-
Flow rate (IIters/min)
Gauge/cm
ters/min)
12/7.6
32.56
14/2.5
19.54
12/10.2
30.02
14/5.1
17.27
13/2.5
25.77
14/7.6
16.14
13/5.1
23.50
15/3.2
14.16
13/7.6
22.37
15/7.6
11.61
13/10.2
20.67
15/10.2
10.48
7.2.1.2 These needles can be adapted to a
Method 5 type sampling train as follows: Insert a serum bottle stopper. 13- by 20-mm
sleeve type. into a 1/2-inch Swagelok quick
connect. Insert the needle into the stopper as
shown in Figure 5-9.
Environmental Protection Agency, EPA
EC01JN92.111
7.2.2 Critical Orifice Calibration. The procedure described In this section uses the
Method 5 meter box configuration with a
DGM as described in Section 2.1.8 to callbrate the critical orifices. Other schemes
may be used, subject to the approval of the
Administrator.
7.2.2.1 Calibration of Meter Box. The critical orifices must be calibrated in the same
configuration as they will be used; i.e., there
should be no connections to the inlet of the
orifice.
7.2.2.1.1 Before calibrating the meter box,
leak check the system as follows: Fully open
the coarse adjust valve, and completely close
the by-pass valve. Plug the inlet. Then trun
on the pump, and determine whether there is
any leakage. The leakage rate shall be zero;
Le., no detectable movement of the DGM
dial shall be seen for 1 minute.
7.2.2.1.2 Check also for leakages in that
portion of the sampling train between the
pump and the orifice meter. See Section 5.8
for the procedure: make any corrections, if
necessary. If leakage is detected, check for
cracked gaskets, loose fittings, worn O-rings,
etc., and make the necessary repairs.
7.2.2.1.3 After determining that the meter
box is leakless. calibrate the meter box according to the procedure given in Section 5.3.
Make sure that the wet test meter meets the
requirements stated in Section 7.1.1.1. Check
the water level in the wet test meter. Record
the DGM calibration factor, Y.
7.2.2.2 Calibration of Critical Orifices. Set
up the apparatus as shown in Figure 5-10.
EC01JN92.112
7.2.2.2.1 Allow a warm-up time of 15 minutes. This step is important to equilibrate
the temperature conditions through the
DGM.
7.2.2.2.2 Leak check the system as in Section 7.2.2.1.1. The leakage rate shall be zero.
7.2.2.2.3 Before calibrating the critical
orifice, determine its suitability and the appropriate operating vacuum as follows: Turn
on the pump, fully open the coarse adjust
valve, and adjust the by-pass valve to give a
vacuum reading corresponding to about half
of atmospheric pressure. Observe the meter
box orifice manometer reading, H. Slowly increase the vacuum reading until a stable
reading is obtained on the meter box orifice
manometer. Record the critical vacuum for
each orifice.
Orifices that do not reach a critical value
shall not be used.
7.2.2.2.4 Obtain the barometric pressure
using a barometer as described in Section
2.1.9. Record the barometric pressure. Phar, In
mm Hg (in. Hg).
7.2.2.2.5 Conduct duplicate runs at a vacuum of 25 to 50 mm Hg (1 to 2 in. Hg) above
the critical vacuum. The runs shall be at
least 5 minutes each. The DGM volume readings shall be in increments of 0.00283 m³ (0.1
ft3) or in Increments of complete revolutions
of the DGM. As a guideline, the times should
not differ by more than 3.0 seconds (this includes allowance for changes In the DGM
temperatures) to achieve ± 0.5 percent in K'.
Record the information listed in Figure 5-11.
7.2.2.2.6 Calculate K' using Equation 5-9.
EC16N091.131
Where:
EC16NO91.132
Temb=Absolute ambient temperature, °K (°R).
Average the K' values. The individual K'
values should not differ by more than ±0.5
percent from the average.
7.2.3 Using the Critical Orifices as Callbration Standards.
7.2.3.1 Record the barometric pressure.
Date
Train ID
DGM cal. factor
Critical orifice ID
Run number
Dry gas meter
1
2
Final reading
m³(ff)
Initial reading
m3(ft3)
Difference, Vm
m3 (ft')
Iniet/Outlet temperatures:
Initial
°C °F)
,
/
Final
°C °F)
/
/
Avg. Temperature,
°C °F)
L.
Time, e
min/sec
/
/
Run number
Dry gas meter
1
2
min
Orifice man. rdg., A H
mm (in.) H2O
Bar. pressure, Phar
mm (in.) Hg
Ambient temperature,
°C (°F)
Lamb.
Pump vacuum
mm (in.) Hg
K' factor
Average
Figure 5-11. Data sheet for determining K'
factor.
7.2.3.2 Calibrate the metering system according to the procedure outlined in Sections
7.2.2.2.1 to 7.2.2.2.5. Record the Information
listed in Figure 5.12.
7.2.3.3 Calculate the standard volumes of
air passed through the DGM and the critical
orifices, and calculate the DGM calibration
factor, Y. using the equations below:
EC16NO91.133
EC16NO91.249
EC16NO91.250
where:
Ver(sta)=Volume of gas sample passed through
the critical orifice, corrected to standard
conditions, dsm 3 (dsef).
K,=0.3858 "K/mm Hg for metric units
=17.64 R/in. Hg for English units.
7.2.3.4 Average the DGM calibration values for each of the flow rates. The calibration factor, Y, at each of the flow rates
should not differ by more than +2 percent
from the average.
7.2.3.5 To determine the need for recalibrating the critical orifices, compare the
DGM Y factors obtained from two adjacent
orifices each time a DGM is calibrated; for
example, when checking 13/2.5, use orifices
12/10.2 and 13/5.1. If any critical orifice yields
a DGM Y factor differing by more than 2 percent from the others. recalibrate the critical
orifice according to Section 7.2.2.2.
Date
Train ID
Critical orifice ID
Critical orifice K' factor
Pt. 60, App. A, Meth. 5
Run number
Dry gas meter
1
2
Final reading
nt (ft3)
Initial reading
ni (ft3)
Difference, Vₘ
m3 (ff3)
Iniet/outlet temperatures:
Initial
°C (°F)
/
/
Final
°C (°F)
/
/
Avg. Temperature, Ln
°C (°F)
Time, e
min/sec
/
1
min
Orifice man. rdg., A H
mm (in.)
H₂O.
Bar. pressure, Pher
mm (in.) Hg
Ambient temperature, Lamb
°C (°F)
Pump vacuum
mm (in.) Hg
Vm(mg)
m3 (ft')
Ver(mtd)
m3 (ft3)
DGM cal. factor, Y
Figure 5-12. Data sheet for determining
DGM Y factor.
8. Bibliography
1. Addendum to Specifications for Incinerator Testing at Federal Facilities. PHS,
NCAPC. Dec. 6, 1967.
2. Martin, Robert M. Construction Details
of Isokinetic Source-Sampling Equipment.
Environmental Protection Agency. Research
Triangle Park, NC. APTD-0581. April 1971.
3. Rom, Jerome J. Maintenance, Calibration, and Operation of Isokinetic Source
Sampling Equipment. Environmental Protection Agency. Research Triangle Park, NC.
APTD-0576. March, 1972.
4. Smith, W. S., R. T. Shigehara, and W.F.
Todd. A Method of Interpreting Stack Sampling Data. Paper Presented at the 63d Annual Meeting of the Air Pollution Control
Association, St. Louis, MO. June 14-19, 1970.
5. Smith, W. S., et al. Stack Gas Sampling
Improved and Simplified With New Equipment. APCA Paper No. 67-119. 1967.
6. Specifications for Incinerator Testing at
Federal Facilities. PHS. NCAPC. 1967.
7. Shigehara, R. T. Adjustments in the
EPA Nomograph for Different Pitot Tube Coefficients and Dry Molecular Weights. Stack
Sampling News 2:4-11, October. 1974.
8. Vollaro, R. F. A Survey of Commercially
Available Instrumentation For the Measurement of Low-Range Gas Velocities. U.S. Environmental Protection Agency, Emission
Measurement Branch. Research Triangle
Park, NC. November, 1976 (unpublished
paper).
9. Annual Book of ASTM Standards. Part
26. Gaseous Fuels: Coal and Coke; Atmospheric Analysis. American Society for Testing and Materials. Philadelphia. PA. 1974. pp.
617-622.
10. Felix. L. G., G. I. Clinard, G. E. Lacey.
and J. D. McCain. Inertial Cascade Impactor
Substrate Media for Flue Gas Sampling. U.S.
Environmental Protection Agency. Research
Triangle Park, NC 27711, Publication No.
EPA-6007-77-060. June 1977. 83 p.
11. Westlin, P. R. and R. T. Shigehara. Procedure for Calibrating and Using Dry Gas
Volume Meters as Calibration Standards.
Source Evaluation Society Newsletter.
3(1):17-30. February 1978.
12. Lodge, J.P., Jr., J.B. Pate, B.E.
Ammons, and G.A. Swanson. The Use of
Hypodermic Needles as Critical Orifices in
Air Sampling. J. Air Pollution Control Association. 16:197-200. 1966.
METHOD 5A-DETERMINATION OF PARTICULATE
EMISSIONS FROM THE ASPHALT PROCESSING
AND ASPHALT ROOFING INDUSTRY
1. Applicability and Principle
1.1 Applicability. This method applies to
the determination of particulate emissions
from asphalt roofing industry process saturators, blowing stills, and other sources as
specified in the regulations.
1.2 Principle. Particulate matter is withdrawn isokinetically from the source and
collected on a glass filter fiber maintained at
a temperature of °+10 °C (108°±18 °F). The
particulate mass. which includes any material that condenses at or above the filtration
temperature, is determined gravimetrically
after removal of uncombined water.
2. Apparatus
2.1 Sampling Train. The sampling train
conflguration is the same as shown in Figure
5-1 of Method 5. The sampling train consists
of the following components:
2.1.1 Probe Nozzle. Pitot Tube, Differential Pressure Gauge, Filter Holder, Condenser, Metering System. Barometer, and
Gas Density Determination Equipment.
Same as Method 5. Sections 2.1.1, 2.1.3 to
2.1.5, and 2.1.7 to 2.1.10, respectively.
2.1.2 Probe Liner. Same as in Method 5.