Long-term characterization of ionic species in aerosols from urban and high-altitude sites in western India: Role of mineral dust and anthropogenic sources [An article from: Atmospheric Environment] Buy on Amazon

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Long-term characterization of ionic species in aerosols from urban and high-altitude sites in western India: Role of mineral dust and anthropogenic sources [An article from: Atmospheric Environment]

Book Details

PublisherElsevier
ISBN / ASINB000RR7W7U
ISBN-13978B000RR7W70
MarketplaceFrance  🇫🇷

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This digital document is a journal article from Atmospheric Environment, published by Elsevier in . 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.

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Concentrations of water-soluble-ionic-species (NH"4^+, Na^+, K^+, Mg^2^+, Ca^2^+, Cl^-, NO"3^-, SO"4^2^- and HCO"3^-) in the ambient aerosols and their temporal variability have been studied for a 3-year period (2000-2002) from an urban site (Ahmedabad, 23.0^oN, 72.6^oE, 49m asl) and a high-altitude station (Mt Abu, 24.6^oN, 72.7^oE, 1680m asl) located in a semi-arid region of western India. During the drier months (January-April, September-December), the average concentrations (@mgm^-^3) of water-soluble species in the aerosols over Ahmedabad are: HCO"3^-: 4.95, SO"4^2^-: 4.57, Ca^2^+: 2.96, NO"3^-: 2.07, Cl^-: 0.99, Na^+: 0.81, K^+: 0.76, NH"4^+: 0.48, Mg^2^+: 0.25. During the wet period of the SW-monsoon (May-August), the contribution of Na^+ (2.42@mgm^-^3) and Cl^- (3.96@mgm^-^3) are significantly enhanced. In spite of the geographic and altitude differences, the composition of aerosols from the two sites shows comparable ratios among the major species (Ca^2^+, HCO"3^- and SO"4^2^-). On average, during dry period, nss-SO"4^2^-/nss-Ca^2^+ and HCO"3^-/nss-Ca^2^+ ratios over Ahmedabad are 1.6 and 1.7; and those over Mt Abu are 1.9 and 2.0, respectively. During wet phase, the corresponding ratios are 1.3 and 1.7 over Ahmedabad and 1.2 and 1.8 over Mt Abu. Although the concentrations of several species are significantly different over the two sites and exhibit large seasonal variations, their inter-annual variability is nowhere pronounced. Unlike the chemical characteristics reported over other urban regions, aerosols sampled in this study are of alkaline nature with major neutralizing component as Ca^2^+ rather than NH"4^+. As a result, significant uptake of acidic species (NO"3^- and SO"4^2^- derived from pollution sources) by mineral aerosols (CaCO"3) is a dominant chemical transformation process over the study sites.

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