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Atmospheric concentration, spatial variations, and source identification of persistent organic pollutants in urban and semi-urban areas using passive air samplers in Bursa, Turkey

dc.contributor.authorSari, Mehmet Ferhat
dc.contributor.authorEsen, Fatma
dc.contributor.buuauthorSari, Mehmet Ferhat
dc.contributor.buuauthorESEN, FATMA
dc.contributor.departmentMühendislik Fakültesi
dc.contributor.departmentÇevre Mühendisliği Bölümü
dc.contributor.orcid0000-0001-7114-7286
dc.contributor.scopusid57208564588
dc.contributor.scopusid10340657500
dc.date.accessioned2025-05-13T06:36:27Z
dc.date.issued2022-05-01
dc.description.abstractIn this study, the concentration of ambient persistent organic pollutants (POPs) such as polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and organochlorine pesticides (OCPs) were measured for 12 months in urban and semi-urban areas using a passive air sampler. During the sampling period, a total of 14 PAH (∑14PAH) concentrations measured in urban and semi-urban areas were found to be 54.4 ± 22.6 ng/m3 and 51.7 ± 34.3 ng/m3, respectively. Molecular diagnostic ratios (MDRs) were used to determine PAH sources. According to the MDR values, combustion sources were the most important PAH sources in both sampling areas. However, since the urban area is close to the industrial zone, the combustion sources occurred at high temperatures (> 800 °C), while the sources in the semi-urban area generally consisted of petrogenic fuel combustion. ∑50PCB concentrations measured in the urban and semi-urban areas were found to be 522.5 ± 196.9 pg/m3 and 439.5 ± 166.6 pg/m3, respectively. Homologous group distributions were used to determine the source of PCBs. According to the homologous group distributions, tri-, tetra-, and penta-chlorinated PCBs were dominant in both sampling areas. ∑10OCP concentrations measured in urban and semi-urban areas were found as 242.5 ± 104.6 pg/m3 and 275.9 ± 130.9 pg/m3, respectively. Also, α-HCH/γ-HCH and β-/(α + γ)-HCH ratios were used to determine the source of OCPs. Lindane was the predominant OCP in both sampling areas.
dc.identifier.doi10.1007/s11356-021-17987-1
dc.identifier.endpage32092
dc.identifier.issn0944-1344
dc.identifier.issue21
dc.identifier.scopus2-s2.0-85122886534
dc.identifier.startpage32082
dc.identifier.urihttps://hdl.handle.net/11452/51691
dc.identifier.volume29
dc.indexed.scopusScopus
dc.language.isoen
dc.publisherSpringer
dc.relation.bapOUAP (MH)-2020/8
dc.relation.journalEnvironmental Science and Pollution Research
dc.relation.tubitak116Y208
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectSpatial variation
dc.subjectPCBs
dc.subjectPassive air samplers
dc.subjectPAHs
dc.subjectOCPs
dc.subject.scopusPolychlorinated Biphenyl; Persistent Organic Pollutant; Environmental Monitoring
dc.titleAtmospheric concentration, spatial variations, and source identification of persistent organic pollutants in urban and semi-urban areas using passive air samplers in Bursa, Turkey
dc.typeArticle
dspace.entity.typePublication
local.contributor.departmentMühendislik Fakültesi/Çevre Mühendisliği Bölümü
local.indexed.atScopus
relation.isAuthorOfPublication390ef9f4-c0c5-4ea8-bb8a-f92b80233fb8
relation.isAuthorOfPublication.latestForDiscovery390ef9f4-c0c5-4ea8-bb8a-f92b80233fb8

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