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Quantifying Uncontrolled Landfill Gas Emissions from Two Florida ...

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The two scanning ORS instruments were deployed on top of each measurement area, in opposite<br />

corners of the landfill cells. Each instrument was used to scan to two five-mirror VRPM<br />

configurations. Path-integrated concentration data were collected along each beam path in the<br />

configuration. These data were input into the VRPM algorithm with wind data (collected<br />

concurrently) to produce an emissions plume map and downwind emissions flux value. More<br />

information on the VRPM algorithm can be found in Appendix A of this document.<br />

1.4 Total NMOC Measurements<br />

Concentrations of NMOC were determined <strong>from</strong> samples of landfill gas collected <strong>from</strong> the gas<br />

header pipe at each site. The samples were collected using an adapted version of EPA Method<br />

0040 – Sampling of Principal Organic Hazardous Constituents <strong>from</strong> Combustion Sources Using<br />

Tedlar Bags. This modified Method 0040 used the same analytical technique detailed in the<br />

method, but used the samples collected in a Summa canister. Analysis of VOC concentrations<br />

was done by Research Triangle Park Laboratories, Inc. using EPA Method TO-15,<br />

Determination of Volatile Organic Compounds (VOCs) in Air Collected in Specially-Prepared<br />

Canisters and Analyzed by <strong>Gas</strong> Chromatography/Mass Spectrometry (GC/MS) as seen in the<br />

Compendium of Methods for the Determination of Toxic Organic Compounds in Ambient Air,<br />

Second Edition (EPA 625/R-96/010b), and EPA Method 25-C, Determination of Nonmethane<br />

Organic Compounds in <strong>Landfill</strong> <strong>Gas</strong>. <strong>Landfill</strong> gases were also measured using a landfill gas<br />

monitor for the measurement of methane, carbon dioxide, oxygen, nitrogen, and hydrogen<br />

sulfide. Table 1-1 presents a list of target compounds for the GC/MS analysis. The list includes<br />

compounds identified as landfill gas constituents in Compilation of Air Pollutant Emission<br />

Factors, AP-42 (U.S. EPA, 1997).<br />

1.5 Total and Organo-Mercury Measurements<br />

Total and organo- mercury samples were collected at a location in the vicinity of a gas header<br />

pipe at each site. The total mercury samples were collected using an iodated charcoal trap as a<br />

sorbent. A backup tube was also present to assess any breakthrough. Additional samples were<br />

collected to analyze concentrations of organo-mercury (monomethyl and dimethyl). The<br />

methods, developed by Frontier Geosciences, involve drawing a measured volume of sample gas<br />

through different adsorbers, at a draw rate of approximately 400 L/min. The method used to<br />

collect samples for monomethylmercury (MMM) used a condenser train consisting of several<br />

water impingers in an ice bath. Dimethylmercury (DMM) is collected on a carbotrap cartridge.<br />

Samples were recovered, digested, and analyzed for mercury by cold-vapor atomic fluorescence<br />

spectroscopy (CVAFS).<br />

Total mercury sorbent tubes were also collected <strong>from</strong> the landfills and analyzed by a modified<br />

SW-846 Method 7473, “Mercury in Solids and Solutions by Thermal Decomposition, Mercury<br />

Amalgamation, and Atomic Adsorption Spectroscopy” and CFR Part 60 Method 30B,<br />

“Determination of Total Vapor Phase Mercury <strong>Emissions</strong> <strong>from</strong> Coal-Fired Combustion Sources<br />

Using Carbon Sorbent Tubes.” Samples were analyzed using the Lumex RA-915+ Zeeman<br />

spectrometer with a RP-M324 decomposition furnace attachment cell. No mercury<br />

amalgamation was necessary due to the sensitivity of the instrument. The iodated carbon samples<br />

were loaded into a quartz combustion boat and inserted into a decomposition furnace at 775 deg<br />

C. The mercury species are converted to elemental mercury and detected by the Zeeman atomic<br />

1-7

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