Gu Ai-Jun, Liu Jia-Shu, Luo Shi-Peng, Bi Cheng-Lu, Su Ya-Lan, Ye Zhao-Lian, Gai Xin-Lei
School of Chemical and Environmental Engineering, Jiangsu University of Technology, Changzhou 213001, China.
Jiangsu Key Laboratory of Atmospheric Environment Monitoring and Pollution Control, School of Environmental Science and Engineering, Nanjing University of Information Science & Technology, Nanjing 210044, China.
Huan Jing Ke Xue. 2017 Aug 8;38(8):3110-3119. doi: 10.13227/j.hjkx.201701065.
A total of 55 ambient fine particle (PM) samples were collected in Changzhou City from January to August 2016. The concentrations of 17 PM-bound PAHs in the samples were analyzed by GC-MS. Results showed that seasonal average mass concentrations of PAHs in winter, spring, and summer were 140.24, 41.42, and 2.96 ng·m, respectively, which indicating that the pollution of PAHs in winter appeared more serious than in the other two seasons, and 4-6-ring high molecular weight PAHs were predominant in all three seasons. The average daily level of BaP was 3.64 ng·m and the days it exceeded the permitted standard accounted for 41% of total days. PAH concentration had significant negative correlations with temperature (correlation coefficient: -0.643) and visibility (correlation coefficient: -0.466), whereas it had good positive correlations with atmospheric pressure (correlation coefficient: 0.544) and poor correlations with wind speed and relative humidity. PAH concentrations were higher at nighttime than at daytime, because of the influences of temperature difference, atmospheric stratification, as well as pollution sources. The results from the air backward trajectory model indicated that PM-bound PAHs in Changzhou were mainly affected by local emission sources and short-distance transportation, whereas the contribution of long-distance transmission was small (only 11%). Based on analysis of characteristic ratios, PAHs were mainly sourced from coal burning, vehicle emissions, and biomass burning. An incremental lifetime cancer risk (ILCR) model was used to evaluate the health impact of PAHs via breathing exposure pathways. Results revealed that the ILCR of adults was higher than that of children. The ILCRs of the group for winter and spring were slightly higher than the risk threshold, but a difference was not obvious for summer.
2016年1月至8月期间,在常州市共采集了55个环境细颗粒物(PM)样本。通过气相色谱 - 质谱联用仪分析了样本中17种与PM结合的多环芳烃的浓度。结果表明,冬季、春季和夏季多环芳烃的季节性平均质量浓度分别为140.24、41.42和2.96 ng·m,这表明冬季多环芳烃污染比其他两个季节更严重,并且在所有三个季节中4 - 6环高分子量多环芳烃占主导地位。苯并[a]芘的日均浓度为3.64 ng·m,超标天数占总天数的41%。多环芳烃浓度与温度(相关系数:-0.643)和能见度(相关系数:-0.466)呈显著负相关,而与大气压力呈良好正相关(相关系数:0.544),与风速和相对湿度相关性较差。由于温差、大气分层以及污染源的影响,多环芳烃浓度夜间高于白天。空气后向轨迹模型结果表明,常州市与PM结合的多环芳烃主要受本地排放源和短距离传输影响,而长距离传输的贡献较小(仅11%)。基于特征比值分析,多环芳烃主要来源于燃煤、车辆排放和生物质燃烧。采用增量终生癌症风险(ILCR)模型评估多环芳烃通过呼吸暴露途径对健康的影响。结果显示,成年人的ILCR高于儿童。冬季和春季组的ILCR略高于风险阈值,但夏季差异不明显。