Greenhouse gas (GHG) emissions from agricultural production operations are recognized as an important air quality issue. A new technique following the U.S.
View Article and Find Full Text PDFAlmond harvest accounts for substantial particulate matter less than 10 microm in aerodynamic diameter (PM10) emissions in California each harvest season. This paper addresses the reduction of harvester ground speed from a standard 8 km/hr (5 mph) to 4 km/hr (2.5 mph) as a possible mitigation measure for reducing PM10 emissions.
View Article and Find Full Text PDFJ Air Waste Manag Assoc
May 2009
Studies show that agricultural and animal feeding operations (AFOs) contribute a considerable amount of ammonia (NH3) to the atmosphere. Agricultural NH3 emissions are recognized as an important air quality issue. Biological decomposition of manure from dairy operations results in emissions of NH3 and other gases.
View Article and Find Full Text PDFJ Air Waste Manag Assoc
March 2008
There is a need for a robust and accurate technique to measure ammonia (NH3) emissions from animal feeding operations (AFOs) to obtain emission inventories and to develop abatement strategies. Two consecutive seasonal studies were conducted to measure NH3 emissions from an open-lot dairy in central Texas in July and December of 2005. Data including NH3 concentrations were collected and NH3 emission fluxes (EFls), emission rates (ERs), and emission factors (EFs) were calculated for the open-lot dairy.
View Article and Find Full Text PDFThe particle size distributions (PSDs) of particulate matter (PM) in the downwind plume from simulated sources of a cotton gin were analyzed to determine the impact of PM settling on PM monitoring. The PSD of PM in a plume varies as a function of gravitational settling. Gravitational settling has a greater impact on the downwind PSD from sources with PSDs having larger mass median diameters (MMDs).
View Article and Find Full Text PDFControlled bench-scale laboratory experiments were conducted to evaluate the recovery of ammonia (NH3) and hydrogen sulfide (H2S) from dynamic isolation flux chambers. H2S (80-4000 ppb) and NH3 (5000-40,000 ppb) samples were diffused through the flux chamber to simulate ground level area source emissions while measuring the inlet and outlet flux chamber concentrations simultaneously. Results showed that the recovery of H2S during a 30-min sampling time was almost complete for concentrations >2000 ppb.
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