Open Access
Open access
Journal of Water and Climate Change, volume 16, issue 2, pages 563-587

Source identification and characterization of water-insoluble single particulate matter in rainfall sequences

Serpil Kilic 1
Murat Kilic 2
M Yunus Pamukoglu 3
1
 
a Central Research Laboratory Application and Research Center, Isparta University of Applied Sciences, Isparta, Turkey
2
 
b Vocational High School of Technical Sciences, Department of Chemistry and Chemical Processing Technologies, Isparta University of Applied Sciences, Isparta, Turkey
Publication typeJournal Article
Publication date2025-02-01
scimago Q2
SJR0.646
CiteScore4.8
Impact factor2.7
ISSN20402244, 24089354
Abstract
ABSTRACT

Analysis of atmospheric pollutants in rainwater provides valuable information on the environmental impacts of both natural and anthropogenic pollution sources. Air pollution studies often show that particulate matter (PM) collection on filters is used for subsequent analysis. However, this approach can result in significant particle accumulation on filters and complicate their characterization by semi-quantitative analytical techniques. In this study, insoluble PM in sequentially collected rainwater samples was analyzed for particle size, morphology, and chemical composition. Scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectrometry (EDS) and a particle size analyzer were used for these analyses. By combining SEM–EDS data with particle size distribution analyses, chemical composition findings, and upper atmosphere back-orbit modeling, specific sources of insoluble particles in rainwater were identified. In addition, rainwater samples were analyzed for pH, electrical conductivity, and major anions and cations. The pH values varied from 6.19 to 7.04, while the electrical conductivity values varied from 5.35 to 83.53 μS/cm. Among the major ions, relatively high concentrations of Ca2+, SO42−, and NO3− were detected, while F−, Mg2+, Na+, and Cl− were observed in lower concentrations. The contributions of sea salt were evidenced by the presence of Cl− and Na+ ions.

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