39.5. Test methods and procedures. -- The following methods shall be used as reference methods to demonstrate compliance with subsection 39.3. 39.5.1. The following equation shall be used to calculate the TRE index for a given vent stream: TRE = (1/E) * [ a+b(FL)0.88 + c(FL) + d(FL)HT +e(FL)0.88(HT)0.88 + f(FL)0]
Where:
TRE = the total resource effectiveness index value.
E = the measured hourly emissions in units of kilograms/hour (kg/h).
FL = the vent stream flow rate in scm/min, at a standard temperature of 20°C. For a Category E stream (see Table 45-21F), the factor f(FL)0.5 shall be replaced with:
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HT = vent stream net heating value in units of MJ/scm, where the net enthalpy per mole of offgas is based on combustion at 25°C (68°F) and 760 millimeters of Mercury (mm Hg), but the standard temperature for determining the volume corresponding to one mole is 20°C, as in the definition of FL.
a, b, c, d, e, and f = specific coefficients for six different general categories of process vent streams. The set of coefficients that apply to a given air oxidation process vent stream are specified in Table 45-21F at the end of this rule.
39.5.2. Each owner or operator of an air oxidation facility seeking to comply with subdivision 39.1.2. or 39.3.3. shall recalculate the TRE index value for that air oxidation facility whenever process changes are made. Some examples of process changes are changes in production capacity, feedstock type, or catalyst type, or whenever there is replacement, removal, or addition of recovery equipment. The TRE index value shall be recalculated based on test data, or on best engineering estimates of the effects of the change to the recovery system.39.5.3. Method 1 or 1A of 40 CFR Part 60, Appendix A, as appropriate, for selection of the sampling sites. The control device inlet sampling site for determination of vent stream molar composition or VOC reduction efficiency shall be prior to the inlet of the control device and after the recovery system.39.5.4. Method 2, 2A, 2C, or 2D of 40 CFR Part 60, Appendix A, as appropriate, for determination of the volumetric flow rates.39.5.5. The emission rate correction factor, integrated sampling and analysis procedure of Method 3 of 40 CFR Part 60, Appendix A shall be used to determine the oxygen concentration (%O2d) for the purposes of determining compliance with the 20 ppmv limit. The sampling site shall be the same as that of the VOC samples and the samples shall be taken during the same time that the VOC samples are taken. The VOC concentration corrected to 3 percent O2 (Cc) shall be computed using the following equation: Cc = CVOC * ((17.9/(20.9 - %O2d))
Where:
Cc = Concentration of VOC corrected to 3 percent O2, dry basis, ppm by volume.
CVOC = Concentration of VOC, dry basis, ppm by volume.
%O2d = Concentration of O2, dry basis, percent by volume.
39.5.6. Method 18 of 40 CFR Part 60, Appendix A to determine concentration of VOC in the control device outlet and the concentration of VOC in the inlet when the reduction efficiency of the control device is to be determined.39.5.6.a. The sampling time for each run shall be 1 hour in which either an integrated sample or four grab samples shall be taken. If grab sampling is used, then the samples shall be taken at 15-minute intervals.39.5.6.b. The emission reduction (R) of VOC shall be determined using the following equation: R = ((Ei - Eo) / Ei) * 100
Where:
R = Emission reduction, percent by weight.
Ei = Mass rate of VOC entering the control device, kg VOC/hr.
Eo = Mass rate of VOC discharged to the atmosphere, kg VOC/hr.
39.5.6.c. The mass rates of VOC (E1, E0) shall be computed using the following equations: Click Here To View Image
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Where:
Cij, Coj = Concentration of sample component "j" of the gas stream at the inlet and outlet of the control device, respectively.
Mij, Moj = Molecular weight of sample component "j" of the gas stream at the inlet and outlet of the control device, respectively, g/g-mole (lb/lb-mole).
Qi, Qo = Flow rate of gas stream at the inlet and outlet of the control device, respectively, dscm/min (dscf/hr).
K2 = Constant, 2.494 x 10-6 (1/ppm) (g-mole/scm) (kg/g) (min/hr), where standard temperature for (g-mole/scm) is 20°C.
39.5.6.d. The VOC concentration (CVOC) is the sum of the individual components and shall be computed for each run using the following equation: Click Here To View Image
Where:
CVOC = Concentration of VOC, dry basis, ppm by volume,
Cj = Concentration of sample components in the sample.
n = Number of components in the sample.
39.5.7. When a flare is used to seek to comply with subdivision 39.3.2., the flare shall comply with the requirements of 40 CFR 60.18.39.5.8. The following test methods in Appendix A to 40 CFR Part 60, except as provided under 40 CFR 60.18, shall be used for determining the net heating value of the gas combusted to determine compliance under subdivision 39.3.2., and for determining the process vent stream TRE index value to determine compliance under subdivision 39.3.3.39.5.9. Method 1 or 1A, as appropriate, for selection of the sampling site. The sampling site for the vent stream flow rate and molar composition determination prescribed in subdivisions 39.5.10. and 39.5.11. shall be, except for the situations outlined in paragraph 39.5.9.a., prior to the inlet of any control device, prior to any post-reactor dilution of the stream with air, and prior to any post-reactor introduction of halogenated compounds into the vent stream. No transverse site selection method is needed for vents smaller than 4 inches in diameter. 39.5.9.a. If any gas stream other than the air oxidation vent stream is normally conducted through the final recovery device:39.5.9.a.1. The sampling site for vent stream flow rate and molar composition shall be prior to the final recovery device and prior to the point at which the nonair oxidation stream is introduced.39.5.9.a.2. The efficiency of the final recovery device is determined by measuring the VOC concentration using Method 18 at the inlet to the final recovery device after the introduction of any nonair oxidation vent stream and at the outlet of the final recovery device.39.5.9.a.3. This efficiency is applied to the VOC concentration measured prior to the final recovery device and prior to the introduction of the nonair oxidation stream to determine the concentration of VOC in the air oxidation stream from the final recovery device. This concentration of VOC is then used to perform the calculations outlined in subdivisions 39.5.12. and 39.5.13.39.5.10. The molar composition of the process vent stream shall be determined as follows: 39.5.10.a. Method 18 to measure the concentration of VOC including those containing halogens.39.5.10.b. ASTM D1946-77 to measure the concentration of carbon monoxide and hydrogen.39.5.10.c. Method 4 to measure the content of water vapor.39.5.11. The volumetric flow rate shall be determined using Method 2, 2A, 2C, or 2D, as appropriate.39.5.12. The net heating value of the vent stream shall be calculated using the following equation: Click Here To View Image
Where:
HT = Net heating value of the sample, MJ/scm, where the net enthalpy per mole of offgas is based on combustion at 25°C and 760 mm Hg, but the standard temperature for determining the volume corresponding to one mole is 20°C, as in the definition of Qs (offgas flow rate).
K1 = Constant, 1.740 x 10-7 (1)/ppm)((g-mole)/scm))(MJ/kcal) where standard temperature for (g-mole)/(scm) is 20°C.
Cj = Concentration of compound j in ppm, as measured for organics by Method 18 and measured for hydrogen and carbon monoxide by ASTM D1946-77 as indicated in subdivision 39.5.10.
Hj = Net heat of combustion of compound j, kcal/g-mole, based on combustion at 25°C and 760 mm Hg. The heats of combustion of vent stream components would be required to be determined using ASTM D2382-76 if published values are not available or cannot be calculated.
39.5.13. The emission rate of VOC in the process vent stream shall be calculated using the following equation: Click Here To View Image
Where:
EVOC = Emission rate of VOC in the sample, kg/hr
K2 = Constant, 2.494 x 10-6 (1/ppm) (g-mole/scm) (kg/g) (min/hr), where standard temperature for (g-mole/scm) is 20°C.
Cj = Concentration on a dry basis of compound j in ppm as measured by Method 18 as indicated in subdivision 39.5.10.
Mj = Molecular weight of sample j, g/g-mole
Qs = Vent stream flow rate (scm/min) at a standard temperature of 20°C.