Dilution-based emissions sampling from stationary sources: Part 2--Gas-fired combustors compared with other fuel-fired systems.

With the recent focus on fine particle matter (PM2.5), new, self-consistent data are needed to characterize emissions from combustion sources. Such data are necessary for health assessment and air quality modeling. To address this need, emissions data for gas-fired combustors are presented here, using dilution sampling as the reference. The dilution method allows for collection of emitted particles under conditions simulating cooling and dilution during entry from the stack into the air. The sampling and analysis of the collected particles in the presence of precursor gases, SO2 nitrogen oxide, volatile organic compound, and NH3 is discussed; the results include data from eight gas fired units, including a dual-fuel institutional boiler and a diesel engine powered electricity generator. These data are compared with results in the literature for heavy-duty diesel vehicles and stationary sources using coal or wood as fuels. The results show that the gas-fired combustors have very low PM2.5 mass emission rates in the range of approximately 10(-4) lb/million Btu (MMBTU) compared with the diesel backup generator with particle filter, with approximately 5 x 10(-3) lb/MMBTU. Even higher mass emission rates are found in coal-fired systems, with rates of approximately 0.07 lb/MMBTU for a bag-filter-controlled pilot unit burning eastern bituminous coal. The characterization of PM2.5 chemical composition from the gas-fired units indicates that much of the measured primary particle mass in PM2.5 samples is organic or elemental carbon and, to a much less extent, sulfate. Metal emissions are quite low compared with the diesel engines and the coal- or wood-fueled combustors. The metals found in the gas-fired combustor particles are low in concentration, similar in concentration to ambient particles. The interpretation of the particulate carbon emissions is complicated by the fact that an approximately equal amount of particulate carbon (mainly organic carbon) is found on the particle collector and a backup filter. It is likely that measurement artifacts, mostly adsorption of volatile organic compounds on quartz filters, are positively biasing "true" particulate carbon emission results.

Development and validation of a canister method for measuring ethylene oxide in ambient air.

A sampling and analytical method for measuring ethylene oxide (EO) in ambient air was developed and evaluated. The method is based on the use of evacuated canisters and gas chromatography-mass spectrometry (GC-MS). The objectives of this work were to characterize the performance of the method with respect to the following: (1) stability/recovery of ethylene oxide in a canister over a 15-day holding time; (2) detection capability; and (3) measurement of EO in an ambient air matrix. Both electropolished and silica-lined stainless steel canisters were evaluated in this study. The method evaluation involved both laboratory and field tests. The recovery of the EO was evaluated both on an absolute basis and relative to a spiked internal standard of toluene. EO spiked at levels of 2 ppbv and 20 ppbv was found to be stable for holding times of up to 15 days at 25 degrees C in both a humidified nitrogen matrix and in ambient air. The detection limit of the method was found to be 0.25 ppbv using EPA's traditional approach of seven replicate analyses of a low-level standard and 0.20 ppbv using a probability-based approach. EO recoveries in the laboratory stability study generally were 100 +/- 25%, and did not vary by canister type, nor did the EO recoveries decrease with holding time. Field studies demonstrated that the method is capable of detecting EO (as well as benzene and toluene) in an ambient air matrix.