Zhou Jiabin, Wang Tieguan, Huang Yunbi, Mao Ting, Zhong Ningning
College of Natural Resources and Information Technology, University of Petroleum, Beijing 102249, China.
Chemosphere. 2005 Nov;61(6):792-9. doi: 10.1016/j.chemosphere.2005.04.002. Epub 2005 May 31.
PAHs in five-stage size segregated aerosol particles were investigated in 2003 at urban and suburban sites of Beijing. The total concentration of 17 PAHs ranged between 0.84 and 152 ng m(-3), with an average of 116 ng m(-3), in urban area were 1.1-6.6 times higher than those measured in suburban area. It suggested a serious pollution level of PAHs in Beijing. PAHs concentrations increased with decreasing the ambient temperature. Approximately 68.4-84.7% of PAHs were adsorbed on particles having aerodynamic diameter 2.0 microm. Nearly bimodal distribution was found for PAHs with two and three rings, more than four rings PAHs, however, followed unimodal distribution. The overall mass median diameter (MMD) for PAHs decreased with increasing molecular weight. Diagnostic ratios and normalized distribution of PAHs indicated that the PAHs in aerosol particles were mainly derived from fossil fuel combustion. Coal combustion for domestic heating was probably major contributor to the higher PAHs loading in winter, whereas PAHs in other seasons displayed characteristic of mixed source of gasoline and diesel vehicle exhaust. Biomass burning and road dust are minor contributors to the PAHs composition of these aerosol particles. Except for source emission, other factors, such as meteorological condition, photochemical decay, and transportation from source to the receptor site, should to be involved in the generation of the observed patterns.
2003年,在北京的城区和郊区对五阶段粒径分级的气溶胶颗粒中的多环芳烃进行了研究。城区17种多环芳烃的总浓度在0.84至152纳克/立方米之间,平均为116纳克/立方米,比郊区测量值高1.1至6.6倍。这表明北京多环芳烃污染严重。多环芳烃浓度随环境温度降低而升高。约68.4%至84.7%的多环芳烃吸附在空气动力学直径为2.0微米的颗粒上。二环和三环多环芳烃呈现近似双峰分布,然而,四环及以上多环芳烃遵循单峰分布。多环芳烃的总体质量中值直径(MMD)随分子量增加而减小。多环芳烃的诊断比值和归一化分布表明,气溶胶颗粒中的多环芳烃主要来源于化石燃料燃烧。冬季家庭取暖用煤燃烧可能是多环芳烃负荷较高的主要原因,而其他季节的多环芳烃呈现汽油和柴油车辆尾气混合源的特征。生物质燃烧和道路扬尘对这些气溶胶颗粒的多环芳烃组成贡献较小。除源排放外,其他因素,如气象条件、光化学衰减以及从源到受体站点的传输,也应参与到观测模式的形成过程中。