Dipartimento di Scienze Ambientali, Informatica e Statistica, Università Ca' Foscari, Via Torino 155, 30172, Venezia-Mestre, Italy.
Center for Air Resources Engineering and Science, Clarkson University, Potsdam, NY, 13699, USA.
Environ Sci Pollut Res Int. 2018 Nov;25(32):31987-32000. doi: 10.1007/s11356-018-2841-1. Epub 2018 Aug 20.
A yearlong sampling campaign (2012-2013) was conducted in six major cities of the Veneto region to investigate the spatial-temporal trends and the factors affecting the polycyclic aromatic hydrocarbon (PAHs) variations and identify the local sources. Sixty samples per city were collected for analyses in every alternate month (April, June, August, October, December, and February): 10 samples per sampling site in 10 consecutive days of the months selected. Samples were ultrasonically extracted with acetonitrile and processed through high-performance liquid chromatography. Total Σ-PAH concentrations ranged from 0.19 to 70.4 ng m with a mean concentration of 11.5 ng m. The mean benzo[a]pyrene (BaP) concentration reached 2.0 ng m, which is two-times higher than the limit set by the European Union. BaP contributed for 17.4% to the total concentration of PAHs, which showed the same pattern across the region with maxima during cold months and minima in the warm period. In this study, PAHs showed an inverse relationship with temperature, solar radiation, wind speed, and ozone. According to this study, biomass burning for household heating and cooking, followed by gaseous PAHs absorption on particles due to low atmospheric temperature, were the main reasons for increasing PAHs concentration in winter. Health risk, evaluated as lifetime lung cancer risk (LCR), showed a potential carcinogenic risk from the airborne BaP six-fold higher in the cold season than in the warm one. Diagnostic ratios and conditional probability functions were used to locate the sources, and results confirmed that local emission, overall domestic heating, and road transport exhausts were responsible for higher concentration rates of PAHs as well as of PM.
一项为期一年的采样活动(2012-2013 年)在威尼托地区的六个主要城市进行,旨在调查多环芳烃(PAHs)变化的时空趋势和影响因素,并确定当地污染源。每个城市每月采集两次样本,每次采集 60 个样本,分别在所选月份的 10 天内采集 10 个样本。样品用乙腈超声提取,用高效液相色谱法处理。Σ-PAH 浓度范围为 0.19 至 70.4ng/m,平均浓度为 11.5ng/m。苯并[a]芘(BaP)的平均浓度达到 2.0ng/m,是欧盟设定限值的两倍。BaP 对 PAHs 总浓度的贡献率为 17.4%,在整个地区呈现出相同的模式,即在寒冷月份达到最大值,在温暖时期达到最小值。在这项研究中,PAHs 与温度、太阳辐射、风速和臭氧呈反比关系。根据这项研究,冬季 PAHs 浓度增加的主要原因是家庭取暖和烹饪用生物质燃烧,以及由于大气温度低而导致气态 PAHs 被颗粒物吸收。健康风险,以终生肺癌风险(LCR)来评估,表明在寒冷季节,空气中 BaP 的致癌风险比温暖季节高出六倍。比值诊断和条件概率函数被用来定位污染源,结果证实,当地排放、整体家庭供暖和道路交通废气是造成 PAHs 以及 PM 浓度较高的原因。