GSTDTAP  > 地球科学
DOI10.5194/acp-20-515-2020
Multi-generation OH oxidation as a source for highly oxygenated organic molecules from aromatics
Garmash, Olga1; Rissanen, Matti P.1,2; Pullinen, Iida3,9; Schmitt, Sebastian3,10; Kausiala, Oskari1,11; Tillmann, Ralf3; Zhao, Defeng3,12,13; Percival, Carl4; Bannan, Thomas J.4; Priestley, Michael4,5; Hallquist, Asa M.6; Kleist, Einhard7; Kiendler-Scharr, Astrid3; Hallquist, Mattias5; Berndt, Torsten8; McFiggans, Gordon4; Wildt, Juergen3,7; Mentel, Thomas3; Ehn, Mikael1
2020-01-15
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2020
卷号20期号:1页码:515-537
文章类型Article
语种英语
国家Finland; Germany; England; Sweden; Peoples R China
英文摘要

Recent studies have recognised highly oxygenated organic molecules (HOMs) in the atmosphere as important in the formation of secondary organic aerosol (SOA). A large number of studies have focused on HOM formation from oxidation of biogenically emitted monoterpenes. However, HOM formation from anthropogenic vapours has so far received much less attention. Previous studies have identified the importance of aromatic volatile organic compounds (VOCs) for SOA formation. In this study, we investigated several aromatic compounds, benzene (C6H6), toluene (C7H8), and naphthalene (C10H8), for their potential to form HOMs upon reaction with hydroxyl radicals (OH). We performed flow tube experiments with all three VOCs and focused in detail on benzene HOM formation in the Julich Plant Atmosphere Chamber (JPAC). In JPAC, we also investigated the response of HOMs to NOx and seed aerosol. Using a nitrate-based chemical ionisation mass spectrometer (CI-APi-TOF), we observed the formation of HOMs in the flow reactor oxidation of benzene from the first OH attack. However, in the oxidation of toluene and naphthalene, which were injected at lower concentrations, multi-generation OH oxidation seemed to impact the HOM composition. We tested this in more detail for the benzene system in the JPAC, which allowed for studying longer residence times. The results showed that the apparent molar benzene HOM yield under our experimental conditions varied from 4.1% to 14.0%, with a strong dependence on the OH concentration, indicating that the majority of observed HOMs formed through multiple OH-oxidation steps. The composition of the identified HOMs in the mass spectrum also supported this hypothesis. By injecting only phenol into the chamber, we found that phenol oxidation cannot be solely responsible for the observed HOMs in benzene experiments. When NOx was added to the chamber, HOM composition changed and many oxygenated nitrogen-containing products were observed in CI-APi-TOF. Upon seed aerosol injection, the HOM loss rate was higher than predicted by irreversible condensation, suggesting that some undetected oxygenated intermediates also condensed onto seed aerosol, which is in line with the hypothesis that some of the HOMs were formed in multi-generation OH oxidation. Based on our results, we conclude that HOM yield and composition in aromatic systems strongly depend on OH and VOC concentration and more studies are needed to fully understand this effect on the formation of HOMs and, consequently, SOA. We also suggest that the dependence of HOM yield on chamber conditions may explain part of the variability in SOA yields reported in the literature and strongly advise monitoring HOMs in future SOA studies.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000507330900001
WOS关键词OXIDIZED MULTIFUNCTIONAL COMPOUNDS ; GAS-PHASE REACTIONS ; ATMOSPHERIC CHEMISTRY ; PEROXY-RADICALS ; OZONOLYSIS PRODUCTS ; CHEMICAL MECHANISM ; HIGH-RESOLUTION ; RO2 RADICALS ; AEROSOL ; AUTOXIDATION
WOS类目Environmental Sciences ; Meteorology & Atmospheric Sciences
WOS研究方向Environmental Sciences & Ecology ; Meteorology & Atmospheric Sciences
引用统计
被引频次:71[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://119.78.100.173/C666/handle/2XK7JSWQ/278557
专题地球科学
作者单位1.Univ Helsinki, Fac Sci, Inst Atmospher & Earth Syst Res Phys, Helsinki, Finland;
2.Tampere Univ, Fac Engn & Nat Sci, Phys Unit, Aerosol Phys Lab, Tampere, Finland;
3.Forschungszentrum Julich, Inst Energie & Klimaforsch, IEK Troposphere 8, Julich, Germany;
4.Univ Manchester, Sch Nat Sci, Dept Earth & Environm Sci, Manchester, Lancs, England;
5.Univ Gothenburg, Dept Chem & Mol Biol, Atmospher Sci, Gothenburg, Sweden;
6.IVL Swedish Environm Res Inst, Gothenburg, Sweden;
7.Forschungszentrum Julich, Inst Bio & Geowissensch, IBG Pflanzenwissensch 2, Julich, Germany;
8.Leibniz Inst Tropospharenforsch TROPOS, D-04318 Leipzig, Germany;
9.Univ Eastern Finland, Dept Appl Phys, Kuopio, Finland;
10.TSI GmbH, Aachen, Germany;
11.Karsa Oy, Helsinki, Finland;
12.Fudan Univ, Dept Atmospher & Ocean Sci, Shanghai, Peoples R China;
13.Fudan Univ, Inst Atmospher Sci, Shanghai, Peoples R China
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GB/T 7714
Garmash, Olga,Rissanen, Matti P.,Pullinen, Iida,et al. Multi-generation OH oxidation as a source for highly oxygenated organic molecules from aromatics[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2020,20(1):515-537.
APA Garmash, Olga.,Rissanen, Matti P..,Pullinen, Iida.,Schmitt, Sebastian.,Kausiala, Oskari.,...&Ehn, Mikael.(2020).Multi-generation OH oxidation as a source for highly oxygenated organic molecules from aromatics.ATMOSPHERIC CHEMISTRY AND PHYSICS,20(1),515-537.
MLA Garmash, Olga,et al."Multi-generation OH oxidation as a source for highly oxygenated organic molecules from aromatics".ATMOSPHERIC CHEMISTRY AND PHYSICS 20.1(2020):515-537.
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