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夏季上海市区站点与中国东部沿海某海岛背景站点之间的颗粒物碳质污染物比较:浓度、组成及来源

Comparison of PM carbonaceous pollutants between an urban site in Shanghai and a background site in a coastal East China Sea island in summer: concentration, composition and sources.

作者信息

Wang Fengwen, Lin Tian, Li Yuanyuan, Guo Zhigang, Rose Neil L

机构信息

State Key Laboratory of Coal Mine Disaster Dynamics and Control, Chongqing University, Chongqing 400030, China.

出版信息

Environ Sci Process Impacts. 2017 Jun 21;19(6):833-842. doi: 10.1039/c7em00129k.

DOI:10.1039/c7em00129k
PMID:28513752
Abstract

Nine paired samples of atmospheric particulate matter with an aerodynamic diameter less than or equal to 2.5 μm (PM) were collected concurrently from an urban site in Shanghai, China and a background site in Huaniao Island (HNI) in the coastal East China Sea (ECS) between July 21 and 29, 2011. The samples were analyzed for 16 United States Environmental Protection Agency (USEPA) priority polycyclic aromatic hydrocarbons (PAHs), n-alkanes (20 species, C-C), hopanes (10 species, C-C), and steranes (12 species, C-C). These two sites, approximately 66 km apart, are both on the pathway of land-based pollutants as they are transported to the ECS by seasonal winds. As expected, concentrations in Shanghai were higher (average: 8.4 and 67.8 ng m for the 16 PAHs and n-alkanes, respectively) than those in HNI (average: 1.8 and 8.5 ng m, respectively). The dominant contributor to the 16 PAHs in Shanghai was 5-6-ring PAHs (60.0%), whereas 2-3-ring PAHs contributed the most (72.5%) in HNI. Plant waxes contributed 45.7% and 25.9% of the n-alkanes in Shanghai and HNI, respectively, implying a relatively greater contribution from petroleum residues to the n-alkanes in HNI. Principal component analysis (PCA) and the compositions of hopanes and steranes highlighted a prominent contribution from traffic emissions to carbonaceous PM aerosols. This study provides comprehensive details about the sources, formation, and transport of pollutants from eastern China to the coastal ECS.

摘要

2011年7月21日至29日期间,在中国上海的一个城市站点和东海(ECS)沿海花鸟岛(HNI)的一个背景站点同时采集了9对空气动力学直径小于或等于2.5μm的大气颗粒物(PM)样本。对样本进行了16种美国环境保护局(USEPA)优先多环芳烃(PAHs)、正构烷烃(20种,C-C)、藿烷(10种,C-C)和甾烷(12种,C-C)的分析。这两个站点相距约66公里,都位于陆源污染物通过季节性风输送到东海的路径上。不出所料,上海的浓度(16种PAHs和正构烷烃的平均浓度分别为8.4和67.8 ng/m)高于花鸟岛(平均浓度分别为1.8和8.5 ng/m)。上海16种PAHs的主要贡献者是5-6环PAHs(60.0%),而在花鸟岛,2-3环PAHs的贡献最大(72.5%)。植物蜡分别占上海和花鸟岛正构烷烃的45.7%和25.9%,这意味着石油残留物对花鸟岛正构烷烃的贡献相对更大。主成分分析(PCA)以及藿烷和甾烷的组成突出了交通排放对含碳PM气溶胶的显著贡献。本研究提供了有关中国东部污染物向沿海东海的来源、形成和传输的全面详细信息。

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