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Molecular characteristics, sources and environmental risk of aromatic compounds in particulate matter during COVID-2019: Nontarget screening by ultra-high resolution mass spectrometry and comprehensive two-dimensional gas chromatography

不饱和度 化学 烷基苯 环境化学 质谱法 芳香烃 气相色谱法 多环芳烃 微粒 有机化学 色谱法 碳氢化合物
作者
Xiaowei Chi,Lian Gao,Yibing Lyu,Lin Qiao,Di Huang,Yang Liu,Li Da,Minghui Zheng
出处
期刊:Environment International [Elsevier]
卷期号:167: 107421-107421 被引量:2
标识
DOI:10.1016/j.envint.2022.107421
摘要

Aromatic compounds, including many polycyclic aromatic hydrocarbons (PAHs), are suspected carcinogens and may originate from different sources. To investigate the impact of anthropogenic emission reductions on unknown aromatic compounds in particulate matter, we collected samples during the pre-COVID period in 2020, the COVID-19 lockdown period in 2020, and the same period as the lockdown in 2019. Besides the 16 PAHs, other aromatic compounds were analyzed by Fourier transform ion cyclotron resonance mass spectrometry and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry. Four main compound classes were identified: CH, CHO, CHNO, and CHOS. Hierarchical cluster analysis showed the aromatic compounds varied during the different periods. Compared with before the pandemic, the relative abundances of aromatic compounds with low degrees of unsaturation and long alkyl chains (e.g., alkylbenzenes) increased. These compounds probably mainly arose from fossil fuel combustion and petrochemical industry emissions. The CHO compounds, which were dominated by those with high degrees of oxidation, might originate from secondary organic aerosols. Aromatic aldehydes (e.g., cyclamen aldehyde) and benzoates (e.g., 2-ethylhexyl benzoate) probably with high toxicity deserve more attention. During lockdown, nitro derivatives of condensed PAHs were the main CHNO compounds, and the numbers of homologs decreased perhaps because of significant reductions in NOx and PAHs. CHOS compounds with long carbon chains and low degrees of unsaturation were predominant and the numbers of homologs increased. Five compounds (e.g. 1,3-dimethyl pyrene) were predicted to possibly exhibit persistent and bio-accumulated by EPI Suite model, which need further research. The results provide insight on aromatic compounds and their source appointment in atmospheric particulate matter.
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