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 twenty percent.
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 0.08 grain per cubic foot, based on dry flue gas at standard conditions, corrected to twelve percent 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 thirty minutes or more.
E. 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 ±five percent over its operating range.
2. Provide access to the tailgas charged so that a well-mixed representative grab sample can be obtained.
F. 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. Methods 4 and 5 for the concentration of particulate matter and the associated moisture content;
b. Method 1 for sample and velocity traverses;
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 H 2 S and Method 6 shall be used to determine the concentration of SO 2 .
2. For Method 5, the sampling time for each run shall be at least sixty 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 control officer.
3. Particulate matter emissions, expressed in g/dscm, shall be corrected to twelve percent CO 2 by using the following formula:
where:
C 12 = the concentration of particulate matter corrected to twelve percent CO 2 ,
c = the concentration of particulate matter as measured by Method 5, and
%CO 2 = the percentage of CO 2 as measured by Method 3, or, when applicable, the adjusted outlet CO 2 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 ten 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 twenty 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 CO 2 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 SO 2 concentration by Method 3 shall be at the centroid of the cross section if the cross sectional area is less than five m 2 (fifty-four ft 2 ) or at a point no closer to the walls than one m (3.28 feet) if the cross sectional area is five m 2 or more and the centroid is more than one 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 ten 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.
(Ord. 1993-128 § 4 (part), 1993)