Source apportionment based on an atmospheric dispersion model and multiple linear regression analysis [An article from: Atmospheric Environment] Buy on Amazon

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Source apportionment based on an atmospheric dispersion model and multiple linear regression analysis [An article from: Atmospheric Environment]

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PublisherElsevier
ISBN / ASINB000RR4G5G
ISBN-13978B000RR4G55
AvailabilityAvailable for download now
Sales Rank99,999,999
MarketplaceUnited States  🇺🇸

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This digital document is a journal article from Atmospheric Environment, published by Elsevier in 2005. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
Understanding the contribution of each emission source of air pollutants to ambient concentrations is important to establish effective measures for risk reduction. We have developed a source apportionment method based on an atmospheric dispersion model and multiple linear regression analysis (MLR) in conjunction with ambient concentrations simultaneously measured at points in a grid network. We used a Gaussian plume dispersion model developed by the US Environmental Protection Agency called the Industrial Source Complex model (ISC) in the method. Our method does not require emission amounts or source profiles. The method was applied to the case of benzene in the vicinity of the Keiyo Central Coastal Industrial Complex (KCCIC), one of the biggest industrial complexes in Japan. Benzene concentrations were simultaneously measured from December 2001 to July 2002 at sites in a grid network established in the KCCIC and the surrounding residential area. The method was used to estimate benzene emissions from the factories in the KCCIC and from automobiles along a section of a road, and then the annual average contribution of the KCCIC to the ambient concentrations was estimated based on the estimated emissions. The estimated contributions of the KCCIC were 65% inside the complex, 49% at 0.5-km sites, 35% at 1.5-km sites, 20% at 3.3-km sites, and 9% at a 5.6-km site. The estimated concentrations agreed well with the measured values. The estimated emissions from the factories and the road were slightly larger than those reported in the first Pollutant Release and Transfer Register (PRTR). These results support the reliability of our method. This method can be applied to other chemicals or regions to achieve reasonable source apportionments.
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