Ariz. Admin. Code § R18-2-728 - Standards of Performance for Existing Ammonium Sulfide Manufacturing Plants
A. The provisions
of this Section are applicable to the following affected facilities in ammonium
sulfide manufacturing plants: sulfide unloading facilities, reactor-absorbers,
bubble cap scrubbers, and fume incinerators.
B. No person shall cause, allow or permit to
be emitted into the atmosphere, from any type of incinerator or other outlet
smoke, fumes, gases, particulate matter or other gas-borne material, the
opacity of which exceeds 20%.
C. No
person shall cause, allow or permit to be emitted into the atmosphere from any
emission point from any incinerator, or to pass a convenient measuring point
near such emission point, particulate matter of concentrations in excess of 0.1
grain per cubic foot, based on dry flue gas at standard conditions, corrected
to 12% carbon dioxide.
D. No person
shall allow hydrogen sulfide to be emitted from any location in such manner and
amount that the concentration of such emissions into the ambient air at any
occupied place beyond the premises on which the source is located exceeds 0.03
parts per million by volume for any averaging period of 30 minutes or
more.
E. Where a stack, vent or
other outlet is at such a level that fumes, gas mist, odor, smoke, vapor or any
combination thereof constituting air pollution are discharged to adjoining
property, the Director may require the installation of abatement equipment or
the alteration of such stack, vent, or other outlet by the owner or operator
thereof to a degree that will adequately dilute, reduce or eliminate the
discharge of air pollution to adjoining property.
F. The owner or operator of any ammonium
sulfide tailgas incinerator subject to the provisions of this Section shall do
both of the following:
1. Install, calibrate,
maintain, and operate a flow measuring device which can be used to determine
either the mass or volume of tailgas charged to the incinerator. The flow
measuring device shall have an accuracy of ± 5% over its operating
range.
2. Provide access to the
tailgas charged so that a well-mixed representative grab sample can be
obtained.
G. The test
methods and procedures required by this Section are as follows:
1. The reference methods in 40 CFR 60,
Appendix A shall be used to determine compliance with the standards prescribed
in this Section as follows:
a. Method 5 for
the concentration of particulate matter and the associated moisture
content;
b. Method 1 for sample and
velocity traverse;
c. Method 2 for
velocity and volumetric flow rate;
d. Method 3 for gas analysis and calculation
of excess air, using the integrated sample technique;
e. Method 11 shall be used to determine the
concentration of H2 S and Method 6 shall be used to
determine the concentration of SO2.
2. For Method 5, the sampling time for each
run shall be at least 60 minutes and the minimum sample volume shall be 0.85
dscm (30.0 dscf) except that shorter sampling times and smaller sample volumes,
when necessitated by process variables or other factors, may be approved by the
Director.
3. Particulate matter
emissions, expressed in g/dscm, shall be corrected to 12%
CO2 by using the following formula:
C12 = 12c
%CO2
where:
C12 = the concentration of particulate matter corrected to 12% CO2 ,
c = the concentration of particulate matter as measured by Method 5, and
%CO2 = the percentage of CO2 as measured by Method 3, or, when applicable, the adjusted outlet CO2 percentage.
4. If Method 11 is used, the gases sampled
shall be introduced into the sampling train at approximately atmospheric
pressure. Where fuel gas lines are operating at pressures substantially above
atmosphere, this may be accomplished with a flow control valve. If the line
pressure is high enough to operate the sampling train without a vacuum pump,
the pump may be eliminated from the sampling train. The sample shall be drawn
from a point near the centroid of the fuel gas line. The minimum sampling time
shall be 10 minutes and the minimum sampling volume 0.01 dscm (0.35 dscf) for
each sample. The arithmetic average of two samples of equal sampling time shall
constitute one run. Samples shall be taken at approximately one-hour intervals.
For most fuel gases, sample times exceeding 20 minutes may result in depletion
of the collecting solution, although fuel gases containing low concentrations
of hydrogen sulfide may necessitate sampling for longer periods of
time.
5. If Method 5 is used,
Method 1 shall be used for velocity traverses and Method 2 for determining
velocity and volumetric flow rate. The sampling site for determining
CO2 concentration by Method 3 shall be the same as for
determining volumetric flow rate by Method 2. The sampling point in the duct
for determining SO2 concentration by Method 3 shall be
at the centroid of the cross section if the cross sectional area is less than 5
m2 (54 ft2) or at a point
no closer to the walls than 1 m (3.28 feet) if the cross sectional area is 5
m2 or more and the centroid is more than 1 meter
from the wall. The sample shall be extracted at a rate proportional to the gas
velocity at the sampling point. The minimum sampling time shall be 10 minutes
and the minimum sampling volume 0.01 dscm (0.36 dscf) for each sample. The
arithmetic average of two samples of equal sampling time shall constitute one
run. Samples shall be taken at approximately one-hour intervals.
Notes
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