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Characterization and Source Identification of PM10-bound Polycyclic Aromatic Hydrocarbons in Urban Air of Tianjin, China

机译:天津城市空气中与PM10结合的多环芳烃的表征和来源鉴定

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PM10 samples were collected at six sampling sites in city center of Tianjin from April 2008 to January 2009. The concentrations of 17 selected polycyclic aromatic hydrocarbons (PAHs) in PM10 were quantified. Spatial and seasonal variations of PAHs were characterized. The dominant PAHs in PM10 samples were fluoranthene, pyrene, benz[a]anthracene, phenanthrene, chrysene, benzo[b]fluoranthene, anthracene, indeno[1,2,3-cd]pyrene and benzo[a]pyrene, accounting for above 85% of total PAHs. The total PAHs concentrations of the six sampling sites ranged from 23.4 to 513 ng/m3. Spatial variations were predominantly due to the different strengths of source emission. The total PAHs concentrations at Dongli Monitoring Station (DL) site and Beichen Science and Technology Park (BC) site were higher than those at other four sites in heating period, while those at Meijiang community (MJ) site and Beichen Science and Technology Park (BC) site were higher in no-heating period. Higher PAHs concentrations during heating period and lower concentrations during no-heating period were observed at the six sampling sites, which may be caused by the stronger emissions from stationary combustion sources in heating period and the quicker air dispersion, washout effects, photo-degradation and higher percentage in the air in vapor phase in no-heating period. The PAHs concentrations in gaseous phase were predicted with gas/particle partition model, and the BaP and BaP equivalency results indicated that the health risk of gas and particle phase PAHs to human in Tianjin were higher than that in other cities. The contributions from potential sources to PAHs in PM10 were estimated by the diagnostic ratios between PAHs and principal component analysis (PCA). In whole sampling period, coal combustion was found to the predominant contributor of PM10-bound PAHs, followed by vehicles emission and wood combustion.
机译:从2008年4月至2009年1月在天津市中心的六个采样点采集了PM10样品。对PM10中17种选定的多环芳烃(PAHs)的浓度进行了定量。表征了PAHs的空间和季节变化。 PM10样品中主要的PAH是荧蒽,pyr,苯并[a]蒽,菲,蒽,苯并[b]荧蒽,蒽,茚并[1,2,3-cd] cd和苯并[a] py总PAH的85%。六个采样点的总PAHs浓度范围为23.4至513 ng / m3。空间变化主要是由于源发射强度的不同。东丽监测站站点和北辰科技园区站点的PAHs总浓度在供暖期间高于其他四个站点,而梅江社区站点和北辰科技园区的PAHs浓度较高( BC)站点在不加热期间较高。在六个采样点,观察到加热期间PAHs浓度较高,而在非加热期间PAHs浓度较低,这可能是由于加热期间固定燃烧源的排放量增加,以及空气扩散更快,冲洗效果,光降解和在不加热期间,气相中的空气百分比更高。用气体/颗粒分配模型预测了气相中PAHs的浓度,BaP和BaP的当量结果表明,天津市气相和颗粒相PAHs对人类的健康风险高于其他城市。通过PAHs和主成分分析(PCA)之间的诊断比率,估算了PM10中潜在来源对PAHs的贡献。在整个采样期间,发现煤燃烧是与PM10结合的PAH的主要贡献者,其次是车辆排放和木材燃烧。

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