Composition and secondary formation of fine particulate matter in the Salt Lake Valley: winter 2009.

Under the National Ambient Air Quality Standards (NAAQS), put in place as a result of the Clean Air Amendments of 1990, three regions in the state of Utah are in violation of the NAAQS for PM10 and PM2.5 (Salt Lake County, Ogden City, and Utah County). These regions are susceptible to strong inversions that can persist for days to weeks. This meteorology, coupled with the metropolitan nature of these regions, contributes to its violation of the NAAQS for PM during the winter. During January-February 2009, 1-hr averaged concentrations of PM10-2.5, PM2.5, NO(x), NO2, NO, O3, CO, and NH3 were measured. Particulate-phase nitrate, nitrite, and sulfate and gas-phase HONO, HNO3, and SO2 were also measured on a 1-hr average basis. The results indicate that ammonium nitrate averages 40% of the total PM2.5 mass in the absence of inversions and up to 69% during strong inversions. Also, the formation of ammonium nitrate is nitric acid limited. Overall, the lower boundary layer in the Salt Lake Valley appears to be oxidant and volatile organic carbon (VOC) limited with respect to ozone formation. The most effective way to reduce ammonium nitrate secondary particle formation during the inversions period is to reduce NO(x) emissions. However, a decrease in NO(x) will increase ozone concentrations. A better definition of the complete ozone isopleths would better inform this decision. Implications: Monitoring of air pollution constituents in Salt Lake City, UT, during periods in which PM2.5 concentrations exceeded the NAAQS, reveals that secondary aerosol formation for this region is NO(x) limited. Therefore, NO(x) emissions should be targeted in order to reduce secondary particle formation and PM2.5. Data also indicate that the highest concentrations of sulfur dioxide are associated with winds from the north-northwest, the location of several small refineries.

Receptor model source attributions for Utah's Salt Lake City airshed and the impacts of wintertime secondary ammonium nitrate and ammonium chloride aerosol.

UNLABELLED: Communities along Utah's Wasatch Front are currently developing strategies to reduce daily average PM2.5 levels to below National Ambient Air Quality Standards during wintertime persistent stable atmospheric conditions, or cold-air pools. Speciated PM2.5 data from the Wasatch Front airshed indicate that wintertime exceedances of the PM2.5 standard are mainly driven by high levels of ammonium nitrate. Stable wintertime conditions foster the formation of ammonium nitrate aerosol when sufficient sources of NO(x), ammonia, and oxidative capacity exist. However this work demonstrates that secondary ammonium chloride aerosol can also be a significant source of secondary wintertime PM2.5 if sufficient sources of atmospheric chlorine exist. Two factor analysis techniques, positive matrix factorization (PMF) and Unmix, were used to identify contributors to PM2.5 at three monitoring stations along Utah's Wasatch Front: Bountiful, Lindon, and Salt Lake City. The monitoring data included chemically speciated PM2.5 data for 227, 227, and 429 days at each location, respectively, during the period from May 2007 through May 2011. PMF identified 10-12 factors and Unmix identified 4-5 factors for each of the locations. The wintertime PMF and Unmix results showed large contributions from secondary PM2.5 when PM2.5 concentrations exceeded 20 microg/m3. PMF identified both ammonium nitrate and ammonium chloride aerosol as significant secondary contributors to PM2.5 (10-15% of total PM2.5 from ammonium chloride) during wintertime pollution episodes. Subsequent ion balance analysis of the monitoring data confirmed the presence of significant ammonium chloride aerosol on these highly polluted days at all three monitoring sites. The directly emitted primary PM2.5 portions of the source attribution results were further compared to county-level emissions inventories and showed generally good agreement for Salt Lake City and Lindon during wintertime except for wood smoke and fugitive dust, which have higher contributions in the receptor modeling results than in the emissions inventories. IMPLICATIONS: The study suggests that secondary ammonium chloride aerosol can be a significant source ofwintertime PM2.5 in an ammonia-rich environment, like the Wasatch Front airshed, if sufficient sources of atmospheric chlorine exist. During wintertime, cold-air-pool events, the source attribution results generally agree with the county emission inventories with the exception of wood smoke and cooking sources. At the Salt Lake City monitoring station, the estimated contributions from wood smoke and cooking are nearly double those of the corresponding inventory, suggesting that they are nearly as important as gasoline emissions.

Design and characterization of a two-stage human subject exposure chamber.

A human subject exposure chamber, designed to hold six to eight subjects, coupled to an approximately 30-m3 Teflon reaction bag was designed and built to provide exposures that mimic the production and photochemical oxidation of atmospheric pollutants resulting from the combustion of coal or wood from a stove. The combustion products are introduced into the Teflon bag under atmospheric conditions. Photochemical oxidation of this mixture is accomplished by exposure to tropospheric sun-like radiation from an array of ultraviolet and black lamps. The aerosol in the Teflon reaction bag is then transferred into the exposure room to maintain a constant, lower exposure level. Continuous and semicontinuous monitoring of the gas and particulate matter (PM) pollution in the exposure room and the reaction bag is accomplished using a suite of instruments. This suite of instruments allows for the measurement of the concentrations of total and nonvolatile PM, nitric oxide, nitrogen dioxide, carbon monoxide, carbon dioxide, and ozone. The concentration of the particles was monitored by an R&P tapered element oscillating microbalance monitor. The chemical composition of the PM and its morphological characterization is accomplished by collecting samples in filter packs and conducting ion chromatography, elemental X-ray fluorescence, and scanning electron microscopy analyses. The concentration and composition of emissions from combustion of wood and coal is described. The results of this study suggest that although the bulk compositions of particulate emissions from the combustion of coal or wood in a stove have many similarities, the wood smoke aerosol is photochemically reactive, whereas the coal smoke aerosol is not.

Vascular function and short-term exposure to fine particulate air pollution.

Exposure to fine particulate air pollution has been implicated as a risk factor for cardiopulmonary disease and mortality. Proposed biological pathways imply that particle-induced pulmonary and systemic inflammation play a role in activating the vascular endothelium and altering vascular function. Potential effects of fine particulate pollution on vascular function are explored using controlled chamber exposure and uncontrolled ambient exposure. Research subjects included four panels with a total of 26 healthy nonsmoking young adults. On two study visits, at least 7 days apart, subjects spent 3 hr in a controlled-exposure chamber exposed to 150-200 microg/m3 of fine particles generated from coal or wood combustion and 3 hr in a clean room, with exposure and nonexposure periods alternated between visits. Baseline, postexposure, and post-clean room reactive hyperemia-peripheral arterial tonometry (RH-PAT) was conducted. A microvascular responsiveness index, defined as the log of the RH-PAT ratio, was calculated. There was no contemporaneous vascular response to the few hours of controlled exposure. Declines in vascular response were associated with elevated ambient exposures for the previous 2 days, especially for female subjects. Cumulative exposure to real-life fine particulate pollution may affect vascular function. More research is needed to determine the roles of age and gender, the effect of pollution sources, the importance of cumulative exposure over a few days versus a few hours, and the lag time between exposure and response.

Semicontinuous PM2.5 and PM10 mass and composition measurements in Lindon, Utah, during winter 2007.

The U.S. Environmental Protection Agency is promoting the development and application of sampling methods for the semicontinuous determination of fine particulate matter (PM2.5, particles with an aerodynamic diameter <2.5 microm) mass and chemical composition. Data obtained with these methods will significantly improve the understanding of the primary sources, chemical conversion processes, and meteorological atmospheric processes that lead to observed PM2.5 concentrations and will aid in the understanding of the etiology of PM2.5-related health effects. During January and February 2007, several semicontinuous particulate matter (PM) monitoring systems were compared at the Utah State Lindon Air Quality Sampling site. Semicontinuous monitors included instruments to measure total PM2.5 mass (filter dynamic measurement system [FDMS] tapered element oscillating microbalance [TEOM], GRIMM), nonvolatile PM2.5 mass (TEOM), sulfate and nitrate (two PM2.5 and one PM10 [PM with an aerodynamic diameter <10 microm] ion-chromatographic-based samplers), and black carbon (aethalometer). PM10 semicontinuous mass measurements were made with GRIMM and TEOM instruments. These measurements were all made on a 1-hr average basis. Source apportionment analysis indicated that sources impacting the site were mainly urban sources and included mobile sources (gasoline and diesel) and residential burning of wood, with some elevated concentrations because of the effect of winter inversions. The FDMS TEOM and GRIMM instruments were in good agreement, but TEOM monitor measurements were low because of the presence of significant semi-volatile material. Semi-volatile mass was present dominantly in the PM2.5 mass.