Compositions and Sources of Organic Aerosol in PM2.5 in Nanjing in China

环境化学 气溶胶 空气质量指数 微粒 环境科学 薄雾 污染 左旋葡糖 化学 烟火 空气污染 生物质燃烧 气象学 生态学 有机化学 物理 生物
作者
Wenjing Li,Song Guo,Zhiqi Xu,Xinfeng Wang,A. N. Wang,Mindong Chen
出处
期刊:Atmosphere [Multidisciplinary Digital Publishing Institute]
卷期号:14 (6): 971-971
标识
DOI:10.3390/atmos14060971
摘要

Organic aerosols are harmful to the environment because of their impact on air quality and visibility. They have serious effects not only on living beings and ecosystems because of their biological toxicity, but they also have an indirect effect on regional climate change as cloud condensation nuclei and radiation force. Many measures have been applied to decrease air pollution. Although the air quality has greatly improved, the standard of the World Health Organization (WHO) is far from being met at present. In this study, fine particulates were collected in Nanjing throughout 2019, and high-performance liquid chromatography–electrospray ion–mass spectrometry/mass spectrometry (HPLC-ESI-MS/MS) was carried out to determine 14 organic acids, 10 nitrated phenols, 1 aldehyde, and 1 ketone in aerosol samples. In this study, we further determined the changes in the pollutants in Nanjing in recent years compared to previous studies and characterized more kinds of species in the air. We found that different kinds of nitrated phenols showed similar trends of being abundant in winter and substituted in spring, autumn, and summer. 4-Nitrophenol was the most abundant species (2.83 ng m−3) among the nitrated phenols. p-Coumaric acid presented the highest level in summer with an average concentration of 1.55 ng m−3, indicating that grass burning was significant in summer, possibly due to wheat stalk and perennial ryegrass burning. The positive matrix fraction (PMF) model was applied to identify the sources of aerosols in Nanjing, including coal burning, grass burning, softwood burning, hardwood burning, anthropogenic secondary organic aerosols (SOAs), and biogenic SOAs. Coal burning and softwood burning contributed much more to the total determined species with values of 20.3% and 18.2%, respectively. Anthropogenic SOAs contributed 17.1%, and hardwood burning contributed 16.7%. The contribution of biogenic SOAs was 15%, and the grass-burning source contribution was the lowest, with 12.6%. With consideration of the large contribution from anthropogenic combustion activities, more strict measures are required to reduce emission pollutants in the future.

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