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Coarse particulate matter (PM10-2.5) concentration data from residential outdoor sites were collected using portable samplers as part of an exposure assessment for the North Carolina Asthma and Children's Environment Studies (NC-ACES). PM10-2.5 values were estimated using the differential between independent PM10 and PM2.5 collocated MiniVol measurements. Repeated daily 24-h integrated PM10 and PM2.5 residential outdoor monitoring was performed at a total of 26 homes during September 2003–June 2004 in the Research Triangle Park, NC area. This effort resulted in the collection of 73 total daily measurements. This assessment was conducted to provide data needed to investigate the association of exposures to coarse particle PM mass concentrations with observed human health effects. Potential instrument bias between the differential MiniVol methodology and a dichotomous sampler were investigated. Results indicated that minimal bias of PM10-2.5 mass concentration estimates (slope = 0.8, intercept =0.36μg m-3) existed between the dichotomous and differential MiniVol procedures. Residential outdoor PM10-2.5 mass concentrations were observed to be highly variable across measurement days and ranged from 1.1 to 12.6μg m-3 (mean of 5.4μg m-3). An average correlation coefficient of r=0.75 existed between residential outdoor PM10-2.5 mass concentrations and those obtained from the central ambient monitoring site. Temporal and spatial variability of PM10-2.5 mass concentrations during the study were observed and are described in this report.  相似文献   

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Twenty-four-hour integrated gaseous NH3 and fine particulate (PM2.5)NH4+ were measured during 2004 at eight sites in the southeastern U.S. Mean NH3 concentrations for 2004 ranged from 2.44 ppbv at an urban-industrial site in North Birmingham, AL, to 0.23 ppbv at a rural-forested site near Centreville, AL. NH3 mixing ratios were found to be higher at urban sites than at nearby rural (or suburban sites) except for sites which were directly influenced by local sources. Only weak correlations with temperature were observed for NH3 at the sites; slightly greater correlations were observed for total ammonia (NHx=NH3+NH4+) vs. temperature. A weak seasonal variation was observed for NH3 mixing ratios at all sites, with all but one site exhibiting biannual maxima in spring and late summer/fall. Mean PM2.5 NH4+ concentrations ranged from 1.78μgm-3 in Atlanta, GA, to 1.02μgm-3 at Oak Grove, MS, and were more uniform across the network than NH3 mixing ratios, with only slightly larger values at urban sites as compared to nearby rural (or suburban) sites. All sites exhibited highest NHx between July and September and lowest NHx in November and December. The gaseous NH3 fraction (NH3/(NH3+NH4+)) was observed to decrease with increasing values of PM2.5 SO42- at all sites. At two rural-forested sites and two sites near the Gulf of Mexico, the NH3 gaseous fraction approached a relatively constant value of 5–10% as PM2.5SO42- increased beyond 5–7μgm-3, suggesting that NH3 availability at these locations limits aerosol neutralization.  相似文献   

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