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典型沿海城市采暖期细颗粒物组分特征及来源解析
摘要点击 2367  全文点击 833  投稿时间:2019-07-04  修订日期:2019-11-22
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中文关键词  PM2.5  组分特征  源解析  正定矩阵因子分析法(PMF)  威海市
英文关键词  PM2.5  composition characteristic  source apportionment  positive matrix factorization(PMF)  Weihai
作者单位E-mail
李明燕 山东师范大学地理与环境学院, 济南 250014 limingyan0321@126.com 
杨文 威海市环境保护监测站, 威海 264200  
魏敏 山东师范大学地理与环境学院, 济南 250014  
朱红晓 山东师范大学地理与环境学院, 济南 250014  
刘厚凤 山东师范大学地理与环境学院, 济南 250014 110027@sdnu.edu.cn 
中文摘要
      为明确威海市采暖期细颗粒物的组分及来源,于2018年1~3月在威海市3个空气质量例行监测点采集了环境空气PM2.5样品,分析OC、EC、水溶性离子及元素组分特征,利用PMF模型解析PM2.5的来源.结果表明,采样期间威海市PM2.5日均质量浓度为(33.80±22.45)μg·m-3,NO3-、NH4+、SO42-、OC和EC是其主要组分.作为沿海城市其Cl-占比相对较高,同时PM2.5组分特征体现出颗粒物成分受本地工业特征污染物排放的影响.NO3-/SO42-和OC/EC比值均表明威海市采暖期移动源对PM2.5贡献大;水溶性离子中酸碱离子比例分析表明,威海市采暖期PM2.5呈弱碱性,NH4+过量,主要以NH4NO3和(NH42SO4等形式存在.污染时段威海市二次污染物浓度上升明显,主要组分NH4+、NO3-、SO42-、OC和EC质量浓度是清洁时段的4.21、5.27、3.23、2.02和1.81倍.源解析结果表明,二次气溶胶占PM2.5的32.4%~36.0%,移动源(15.6%~18.9%)、燃煤源(12.1%~17.8%)、生物质燃烧源(9.0%~10.4%)和扬尘(8.6%~11.3%)是威海市环境空气PM2.5的主要来源,而工艺过程源(2.1%~8.3%)、非道路移动源(2.4%~3.7%)和海盐(3.5%~5.6%)贡献比例较小.
英文摘要
      To clarify the pollution characteristics and sources of PM2.5 in Weihai during the heating period, PM2.5 samples from ambient air were collected at three routine air quality monitoring sites from January to March 2018. The OC, EC, water-soluble ions, and elements in PM2.5 were analyzed, and the sources of PM2.5 were identified using the PMF model. The results showed that the average daily mass concentration of PM2.5 was (33.80±22.45) μg·m-3, and the NO3-, NH4+, SO42-, OC, and EC were the main components of PM2.5. As a coastal city, the Cl- ratio was relatively high in PM2.5. Meanwhile, the compositions of PM2.5 were affected by the emission of pollutants with local industrial characteristics. Both NO3-/SO42- and OC/EC showed that mobile sources had a high contribution during the heating period. The acid-base ions in water-soluble ions showed that PM2.5 is weakly alkaline, and NH4+ is excessive. NH4+ mainly existed in the form of NH4NO3 and (NH4)2SO4. During the polluted period, the concentration of secondary pollutants significantly increased, and the mass concentrations of NH4+, NO3-, SO42-, OC, and EC were 4.21, 5.27, 3.23, 2.02, and 1.81 times that of the cleaning period, respectively. The PMF model showed that secondary aerosols were the major source of PM2.5, accounting for 32.4%-36.0% of PM2.5. The contributions of vehicle exhaust, coal combustion, biomass burning, and dust were 15.6%-18.9%, 12.1%-17.8%, 9.0%-10.4%, and 8.6%-11.3%, respectively, while the contributions of process emission (2.1%-8.3%), non-road mobile sources (2.4%-3.7%), and sea salt (3.5%-5.6%) were less.

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