US EPA Method 102 - Determination Of Particulate And Gaseous Mercury Emissions From Chlor-Alkali Plants (Hydrogen Streams)
NOTE: This method does not include all of the specifications (e.g., equipment and supplies) and procedures (e.g., sampling and analytical) essential to its performance. Some material is incorporated by reference from other methods in this part and in Appendix A to 40 CFR Part 60. Therefore, to obtain reliable results, persons using this method should have a thorough knowledge of at least the following additional test methods: Method 1, Method 2, Method 3, Method 5, and Method 101.
This method is applicable for the determination of Hg emissions, including both particulate and gaseous Hg, from chlor-alkali plants and other sources (as specified in the regulations) where the carrier-gas stream in the duct or stack is principally hydrogen.
Adherence to the requirements of this method will enhance the quality of the data obtained from air pollutant sampling methods.
2.1 Particulate and gaseous Hg emissions are withdrawn isokinetically from the source and collected in acidic iodine monochloride (ICl) solution. The Hg collected (in the mercuric form) is reduced to elemental Hg, which is then aerated from the solution into an optical cell and measured by atomic absorption spectrophotometry.
Same as Method 101, Section 4.2.
This method may involve hazardous materials, operations, and equipment. This test method may not address all of the safety problems associated with its use. It is the responsibility of the user of this test method to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to performing this test method.
Same as Method 101, Section 5.2.
The sampler must conduct the source test under conditions of utmost safety because hydrogen and air mixtures are explosive. Since the sampling train essentially is leakless, attention to safe operation can be concentrated at the inlet and outlet. If a leak does occur, however, remove the meter box cover to avoid a possible explosive mixture. The following specific precautions are recommended:
5.3.1 Operate only the vacuum pump during the test. The other electrical equipment, e.g., heaters, fans, and timers, normally are not essential to the success of a hydrogen stream test.
5.3.2 Seal the sample port to minimize leakage of hydrogen from the stack.
5.3.3 Vent sampled hydrogen at least 3 m (10 ft) away from the train. This can be accomplished by attaching a 13-mm (0.50-in.) ID Tygon tube to the exhaust from the orifice meter.
NOTE: A smaller ID tubing may cause the orifice meter calibration to be erroneous. Take care to ensure that the exhaust line is not bent or pinched.
Same as Method 101, Section 6.0, with the exception of the following:
6.1 Probe Heating System. Do not use, unless otherwise specified.
6.2 glass Fiber filter. Do not use, unless otherwise specified.
Same as Method 101, Section 7.0.
Same as Method 101, Section 8.0, with the exception of the following:
8.1.1 If a nomograph is used, take special care in the calculation of the molecular weight of the stack gas and in the setting of the nomograph to maintain isokinetic conditions during sampling (Sections 22.214.171.124 through 126.96.36.199 below).
188.8.131.52 Calibrate the meter box orifice. Use the techniques described in APTD-0576 (see Reference 9 in Section 17.0 of Method 5). calibration of the orifice meter at flow conditions that simulate the conditions at the source is suggested. calibration should either be done with hydrogen or with some other gas having similar Reynolds Number so that there is similarity between the Reynolds Numbers during calibration and during sampling.
184.108.40.206 The nomograph described in APTD-0576 cannot be used to calculate the C factor because the nomograph is designed for use when the stack gas dry molecular weight is 29 ± 4. Instead, the following calculation should be made to determine the proper C factor:
NOTE: This calculation is left in English units, and is not converted to metric units because nomographs are based on English units.
220.127.116.11 Set the calculated C factor on the operating nomograph, and select the proper probe nozzle diameter and K factor as specified in APTD-0576. If the C factor obtained in Section 18.104.22.168 exceeds the values specified on the existing operating nomograph, expand the C scale logarithmically so that the values can be properly located.
8.1.2 If a calculator is used to set isokinetic rates, it is suggested that the isokinetic equation presented in Reference 13 in Section 17.0 ofMethod 101 be consulted.
When the stack diameter (or equivalent diameter) is less than 12 inches, conventional pitot tube-Probe assemblies should not be used. For sampling guidelines, see Reference 14 in Section 17.0 of Method 101.
Same as Method 101, Section 9.0.
Same as Method 101, Section 10.0.
Same as Method 101, Section 11.0.
Same as Method 101, Section 12.0.
Same as Method 101, Section 13.0.
13.1 Analytical Range. After initial dilution, the range of this method is 0.5 to 120 g Hg/ml. The upper limit can be extended by further dilution of the sample.
Same as Method 101, Section 16.0.