GSTDTAP  > 地球科学
DOI10.5194/acp-18-5549-2018
Novel pathway of SO2 oxidation in the atmosphere: reactions with monoterpene ozonolysis intermediates and secondary organic aerosol
Ye, Jianhuai1; Abbatt, Jonathan P. D.2; Chan, Arthur W. H.1
2018-04-24
发表期刊ATMOSPHERIC CHEMISTRY AND PHYSICS
ISSN1680-7316
EISSN1680-7324
出版年2018
卷号18期号:8页码:5549-5565
文章类型Article
语种英语
国家Canada
英文摘要

Ozonolysis of monoterpenes is an important source of atmospheric biogenic secondary organic aerosol (BSOA). While enhanced BSOA formation has been associated with sulfate-rich conditions, the underlying mechanisms remain poorly understood. In this work, the interactions between SO2 and reactive intermediates from monoterpene ozonolysis were investigated under different humidity conditions (10% vs. 50 %). Chamber experiments were conducted with ozonolysis of alpha-pinene or limonene in the presence of SO2. Limonene SOA formation was enhanced in the presence of SO2, while no significant changes in SOA yields were observed during alpha-pinene ozonolysis. Under dry conditions, SO2 primarily reacted with stabilized Criegee intermediates (sCIs) produced from ozonolysis, but at 50% RH heterogeneous uptake of SO2 onto organic aerosol was found to be the dominant sink of SO2, likely owing to reactions between SO2 and organic peroxides. This SO2 loss mechanism to organic peroxides in SOA has not previously been identified in experimental chamber studies. Organosulfates were detected and identified using an electrospray ionization-ion mobility spectrometry-high-resolution time-of-flight mass spectrometer (ESI-IMS-TOF) when SO2 was present in the experiments. Our results demonstrate the synergistic effects between BSOA formation and SO2 oxidation through sCI chemistry and SO2 uptake onto organic aerosol and illustrate the importance of considering the chemistry of organic and sulfur-containing compounds holistically to properly account for their reactive sinks.


领域地球科学
收录类别SCI-E
WOS记录号WOS:000430729000001
WOS关键词VAPOR WALL LOSS ; SULFUR-DIOXIDE ; CRIEGEE INTERMEDIATE ; ORGANOSULFATE FORMATION ; HETEROGENEOUS REACTION ; CHEMICAL-COMPOSITION ; RELATIVE-HUMIDITY ; SULFATE FORMATION ; MINERAL DUST ; GAS
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:93[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/20582
专题地球科学
作者单位1.Univ Toronto, Dept Chem Engn & Appl Chem, Toronto, ON, Canada;
2.Univ Toronto, Dept Chem, Toronto, ON, Canada
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GB/T 7714
Ye, Jianhuai,Abbatt, Jonathan P. D.,Chan, Arthur W. H.. Novel pathway of SO2 oxidation in the atmosphere: reactions with monoterpene ozonolysis intermediates and secondary organic aerosol[J]. ATMOSPHERIC CHEMISTRY AND PHYSICS,2018,18(8):5549-5565.
APA Ye, Jianhuai,Abbatt, Jonathan P. D.,&Chan, Arthur W. H..(2018).Novel pathway of SO2 oxidation in the atmosphere: reactions with monoterpene ozonolysis intermediates and secondary organic aerosol.ATMOSPHERIC CHEMISTRY AND PHYSICS,18(8),5549-5565.
MLA Ye, Jianhuai,et al."Novel pathway of SO2 oxidation in the atmosphere: reactions with monoterpene ozonolysis intermediates and secondary organic aerosol".ATMOSPHERIC CHEMISTRY AND PHYSICS 18.8(2018):5549-5565.
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