Photosensitized Formation of Secondary Organic Aerosols above the Air/Water Interface

被引:48
作者
Bernard, F. [1 ,2 ,3 ]
Ciuraru, R. [1 ,4 ]
Boreave, A. [1 ]
George, C. [1 ]
机构
[1] Univ Lyon 1, CNRS, IRCELYON, F-69626 Villeurbanne, France
[2] NOAA, Earth Syst Res Lab, Div Chem Sci, Boulder, CO USA
[3] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[4] Univ Paris Saclay, AgroParisTech, INRA, UMR ECOSYS, F-78850 Thiverval Grignon, France
基金
欧洲研究理事会;
关键词
SEA-SURFACE MICROLAYER; BOUNDARY-LAYER; WATER; CHEMISTRY; CHLOROPHYLL; SULFUR; OCEAN; NUCLEATION; PARTICLES; CARBON;
D O I
10.1021/acs.est.6b03520
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this study, we evaluated photosensitized chemistry at the air-sea interface as a source of secondary organic aerosols (SOA). Our results show that, in addition to biogenic emissions, abiotic processes could also be important in the marine boundary layer. Photosensitized production of marine secondary organic aerosol was studied in a custom-built multiphase atmospheric simulation chamber. The experimental chamber contained water, humic acid (1-10 mg L-1) as a proxy for dissolved organic matter, and nonanoic acid (0.1-10 mM), a fatty acid proxy which formed an organic film at the air-water interface. Dark secondary reaction with ozone after illumination resulted in SOA particle concentrations in excess of 1000 cm(-3), illustrating the production of unsaturated compounds by chemical reactions at the air-water interface. SOA numbers via photosensitization alone and in the absence of ozone did not exceed background levels. From these results, we derived a dependence of SOA numbers on nonanoic acid surface coverage and dissolved organic matter concentration. We present a discussion on the potential role of the air-sea interface in the production of atmospheric organic aerosol from photosensitized origins.
引用
收藏
页码:8678 / 8686
页数:9
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