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利用被动空气采样器对土耳其布尔萨城市和半城市地区持久性有机污染物的大气浓度、空间变化及来源进行识别

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

作者信息

Sari Mehmet Ferhat, Esen Fatma

机构信息

Department of Environmental Engineering, Faculty of Engineering, Bursa Uludag University, 16059, Nilüfer/Bursa, Turkey.

出版信息

Environ Sci Pollut Res Int. 2022 May;29(21):32082-32092. doi: 10.1007/s11356-021-17987-1. Epub 2022 Jan 11.

DOI:10.1007/s11356-021-17987-1
PMID:35013944
Abstract

In 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 (∑PAH) concentrations measured in urban and semi-urban areas were found to be 54.4 ± 22.6 ng/m and 51.7 ± 34.3 ng/m, 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. ∑PCB concentrations measured in the urban and semi-urban areas were found to be 522.5 ± 196.9 pg/m and 439.5 ± 166.6 pg/m, 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. ∑OCP concentrations measured in urban and semi-urban areas were found as 242.5 ± 104.6 pg/m and 275.9 ± 130.9 pg/m, 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.

摘要

在本研究中,使用被动空气采样器在城市和半城市地区对多环芳烃(PAHs)、多氯联苯(PCBs)和有机氯农药(OCPs)等环境持久性有机污染物(POPs)的浓度进行了为期12个月的测量。在采样期间,城市和半城市地区测得的14种PAH(∑PAH)浓度分别为54.4±22.6 ng/m³和51.7±34.3 ng/m³。分子诊断比值(MDRs)用于确定PAH的来源。根据MDR值,燃烧源是两个采样区域中最重要的PAH来源。然而,由于城市地区靠近工业区,燃烧源发生在高温(>800°C)条件下,而半城市地区的来源通常包括成岩燃料燃烧。城市和半城市地区测得的∑PCB浓度分别为522.5±196.9 pg/m³和439.5±166.6 pg/m³。同系物组分布用于确定PCBs的来源。根据同系物组分布,三氯、四氯和五氯PCBs在两个采样区域中占主导地位。城市和半城市地区测得的∑OCP浓度分别为242.5±104.6 pg/m³和275.9±130.9 pg/m³。此外,α-六氯环己烷/γ-六氯环己烷和β-/(α+γ)-六氯环己烷比值用于确定OCPs的来源。林丹是两个采样区域中主要的OCP。

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