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Phase distribution, sources and risk assessment of PAHs, NPAHs and OPAHs in a rural site of Pearl River Delta region, China

机译:中国珠江三角洲农村地区PAH,NPAH和OPAH的相分布,来源和风险评估

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Gaseous and particulate samples were collected in the late autumn of 2010 from Wanqingsha (WQS), a rural site in the Pearl River Delta (PRD) region, China. Eighteen polycyclic aromatic hydrocarbons (PAHs), twenty–nine nitrated PAHs (NPAHs) and six oxygenated PAHs (OPAHs) were measured, and their gas–particle partitioning, sources and risks were discussed. The results showed that the atmospheric mass distribution was dominated by three and four rings compounds. Phenanthrene, 2–nitrofluoranthene and benzanthrone were the most abundant parent PAH, NPAH and OPAH, respectively. The partitioning of these compounds was strongly dependent on their molecular weights. The absorption model provides a better prediction of the particulate fraction of PAHs than the adsorption model, and might be applied for the discrimination of PAH derivatives sources. Molecular diagnostic ratios suggested that coal combustion or biomass burning, not vehicle emission, were the dominant sources in WQS. The ratios of 2–nitrofluoranthene/2– nitropyrene and 2–nirtofluoranthene/1–nitropyrene indicated that secondary formation by OH initiated reactions was the main formation pathway for NPAHs, with an average contribution of 92.6% during the sampling period, and the formation might be enhanced under hazy conditions. Most of OPAHs were under the impact of regional pollution. Risk assessment showed an overall lifetime excess inhalation cancer risk of 1.12 × 10–5 in which the six NPAHs taken into calculation contributed 3.5% although they only accounted for 0.7% of the 18 compound masses used in the assessment.
机译:气态和颗粒状样品于2010年深秋从中国珠江三角洲(PRD)地区的农村地盘万青沙(WQS)采集。测量了18种多环芳烃(PAH),29种硝化PAH(NPAH)和6种氧化PAH(OPAH),并讨论了它们的气体-颗粒分配,来源和风险。结果表明,大气质量分布主要由三环和四环化合物决定。菲,2-硝基荧蒽和苯并蒽酮分别是最丰富的母体PAH,NPAH和OPAH。这些化合物的分配强烈取决于它们的分子量。与吸附模型相比,吸收模型可以更好地预测PAHs的颗粒分数,并且可以用于PAH衍生物来源的判别。分子诊断率表明,煤炭燃烧或生物质燃烧而非车辆排放是WQS的主要来源。 2-硝基荧蒽/ 2-硝基py和2-硝基荧蒽/ 1-硝基py的比率表明,OH引发反应的二次形成是NPAH的主要形成途径,在采样期间的平均贡献率为92.6%。在朦胧的条件下被增强。大多数OPAH受到区域污染的影响。风险评估显示,一生中吸入性过度癌症的总体风险为1.12×10 –5 ,其中被计算的六个NPAH占3.5%,尽管它们仅占评估使用的18种化合物的0.7%

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