Organics in the Northeastern Pacific and their impacts on aerosol hygroscopicity in the subsaturated and supersaturated regimes

被引:23
作者
Kaku, K. C. [1 ]
Hegg, D. A.
Covert, D. S.
Santarpia, J. L.
Jonsson, H.
Buzorius, G.
Collins, D. R.
机构
[1] Univ Washington, Dept Atmospher Sci, Seattle, WA 98195 USA
[2] Edgewood Chem Biol Ctr, Aberdeen Proving Ground, MD USA
[3] NPS, Dept Res, CIRPAS, Marina, CA USA
[4] Texas A&M Univ, Dept Atmospher Sci, College Stn, TX USA
关键词
D O I
10.5194/acp-6-4101-2006
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Aerosol samples were collected by aircraft during the summer of 2004 in the Northeastern Pacific and compared to measurements of aerosol hygroscopicity. Chemical speciation analyses of the samples revealed that a significant portion of the marine aerosols was organic, and on average 8% of the total aerosol mass was insoluble organic material, tentatively attributed to natural marine emissions. Two chemical models were explored in an attempt to achieve closure between the marine aerosol chemical and physical properties through reproduction of the observed aerosol growth, both in the subsaturated and supersaturated regimes. Results suggest that at subsaturated relative humidities, the nonideal behavior of water activity with respect to aerosol chemistry has an important effect on aerosol growth. At supersaturations, the underprediction of critical supersaturations by all models suggests the hypothesis that formation of a complete monolayer by the insoluble organics may inhibit the activation of aerosols to form cloud droplets.
引用
收藏
页码:4101 / 4115
页数:15
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