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DOI | 10.1016/j.atmosenv.2020.117910 |
Formation of secondary organic aerosol from nitrate radical oxidation of phenolic VOCs: Implications for nitration mechanisms and brown carbon formation | |
Mayorga R.J.; Zhao Z.; Zhang H. | |
发表日期 | 2021 |
ISSN | 13522310 |
卷号 | 244 |
英文摘要 | Volatile phenolic derivatives are substantially emitted from biomass burning and produced from photochemistry of atmospheric aromatic volatile organic compounds (VOCs). Oxidation of phenolic VOCs at night by nitrate radicals (NO3∙) may represent a significant source of secondary organic aerosols (SOA) and brown carbon (BrC) formation in the atmosphere. In this study, NO3∙ oxidation of five phenolic derivatives, including phenol, catechol, 3-methylcatechol, 4-methylcatechol and guaiacol are investigated in laboratory experiments. The SOA constituents from the NO3∙ oxidation were analyzed using electrospray ionization ion mobility spectrometry time-of-flight mass spectrometry, which allows for characterization and identification of isomers in the oxidation products. Through these analyses, several classes of nitro-containing products in addition to the well-known nitrophenol compounds were observed, including: (1) the nitrophenol type of products with additional hydroxyl functional groups; (2) non-aromatic/ring-opening nitro-products with lower double bond equivalence; (3) phenol and catechol products from the C7 phenolic VOCs with carbon-containing substitutions; and (4) nitrated diphenyl ether dimers. The present work indicates that new products from previously unrecognized pathways are formed during NO3∙ oxidation of phenolic VOCs and may contribute an important portion of the SOA. Some of these products were also observed in ambient aerosols during biomass burning. We suggest that the ubiquity of the nitrophenol type of products in the SOA derived from phenolic VOC + NO3∙ are responsible for the strong light absorption measured in this study. Therefore, elucidation of these pathways will be critical for understanding the nighttime oxidation and BrC formation mechanisms. © 2020 Elsevier Ltd |
英文关键词 | Biomass burning; Ion mobility spectrometry; Light absorption; Nighttime oxidation; Nitrophenols |
语种 | 英语 |
scopus关键词 | Aerosols; Bromine compounds; Carbon; Electrospray ionization; Equivalence classes; Isomers; Light absorption; Mass spectrometry; Nitrates; Nitration; Phenols; Volatile organic compounds; Formation mechanism; In-laboratory experiments; Ion mobility spectrometry; Nitration mechanism; Oxidation products; Phenolic derivative; Secondary organic aerosols; Time of flight mass spectrometry; Oxidation; carbon; catechol; dimer; nitrate; nitrophenol; phenol; phenol derivative; radical; volatile organic compound; absorption; aerosol formation; biomass burning; brown carbon; nitrate; oxidation; phenolic compound; radical; volatile organic compound; Article; biomass; collisionally activated dissociation; dimerization; electrospray; ion mobility spectrometry; isomer; light absorption; nitration; oxidation; priority journal; secondary organic aerosol; steady state; time of flight mass spectrometry; ultraviolet visible spectroscopy |
来源期刊 | Atmospheric Environment
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/144869 |
作者单位 | Department of Chemistry, University of California, Riverside, CA 92521, United States |
推荐引用方式 GB/T 7714 | Mayorga R.J.,Zhao Z.,Zhang H.. Formation of secondary organic aerosol from nitrate radical oxidation of phenolic VOCs: Implications for nitration mechanisms and brown carbon formation[J],2021,244. |
APA | Mayorga R.J.,Zhao Z.,&Zhang H..(2021).Formation of secondary organic aerosol from nitrate radical oxidation of phenolic VOCs: Implications for nitration mechanisms and brown carbon formation.Atmospheric Environment,244. |
MLA | Mayorga R.J.,et al."Formation of secondary organic aerosol from nitrate radical oxidation of phenolic VOCs: Implications for nitration mechanisms and brown carbon formation".Atmospheric Environment 244(2021). |
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