Determination of Particulate Emissions from Stationary Sources
This method is for the determination of particulate matter (PM) from stationary sources. Particulate matter is defined as any material that condenses at or above the filtration temperature in the method.
Samples are collected isokinetically from a source on a pre-tared (to a constant weight) glass fiber filter containing no organic binders maintained at a temperature of 120 ± 14°C (248 ± 25°F). A Method 5 train consisting of a heated probe, heated filter, and series of impingers is used to collect the sample. The first two impingers are filled with 100mL of water, the third impinger is left empty, and the fourth impinger is filled with 200-300g of silica gel.
The filters used for sample collection must be dessicated for at least 24 hours at a contant temperature (20 +/- 5.6°C) and pressure to a constant weight (less than or equal to a 0.5mg weight change to the nearest 0.1mg) and pre-tared prior to use. The filter must have a 99.95% efficiency on 0.3 micron dioctyl phthalate smoke particles.
Once the sample has been collected, the filter is removed and placed in a petri dish. If it is necessary to fold the filter, make sure the PM is on the inside of the fold. This is container 1. Container 2 consists of the PM brushed from the probe, probe assembly and front half of the filter holder and the corresponding acetone rinse. The volume of the impinger contents is recorded and the silica gel is weighed to determine the moisture content of the stack gas. The impinger contents are typically not analyzed. At the laboratory, the filter is dessicated to a constant weight. The amount of PM on the filter is equal to the weight change from the pre-sampling weight and the final constant weight of the filter post-sampling. The volume of Container 2 is measured, evaporated to dryness at ambient temperature and pressue, and dessicated for 24 hours to a constant weight. The sum of the results of both containers is the total PM for the sample.
(EPA 40CFR Part 60 Appendix A)
* The analytes and detection limits listed for each method represent the typical detection limits and analytes reported for that particular method. Keep in mind that analyte lists may vary from laboratory to laboratory. Detection limits may also vary from lab to lab and are dependent upon the sample size, matrix, and any interferences that may be present in the sample.