Secondary organic aerosol formation from toluene in an atmospheric hydrocarbon mixture: Water and particle seed effects

被引:79
作者
Kamens, Richard M. [1 ]
Zhang, Haofei [1 ]
Chen, Eric H. [1 ]
Zhou, Yang [1 ,2 ]
Parikh, Harshal M. [1 ]
Wilson, Rebecca L. [1 ]
Galloway, Katherine E. [1 ]
Rosen, Elias P. [1 ]
机构
[1] Univ N Carolina, Dept Environm Sci & Engn, Chapel Hill, NC 27599 USA
[2] Shandong Univ, Environm Res Inst, Jinan 250100, Shandong, Peoples R China
关键词
Toluene SOA; Secondary organic aerosol modeling; SOA yields; Glyoxal; Water phase; M-XYLENE; AROMATIC-HYDROCARBONS; ALPHA-PINENE; PHOTOOXIDATION; MECHANISM; GLYOXAL; MODEL; DEGRADATION; OXIDATION; PRODUCTS;
D O I
10.1016/j.atmosenv.2010.11.007
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Atmospherically relevant secondary organic aerosol (SOA) concentrations from toluene, in an urban hydrocarbon environment, with oxides of nitrogen in natural sunlight, were studied in a large outdoor chamber with different initial humidity and types of initial seed aerosols. Ammonium sulfate particles (38 mu g m(-3)) in the presence of an atmospheric hydrocarbon mixture and NOx in sunlight under a dry atmosphere (%RH = 6 to 10%) show reduced SOA formation when compared to similar gas phase conditions with lower ammonium sulfate (7 mu g m(-3)) and higher relative humidities (%RH 40 to 90%). No post particle nucleation (particles in the 6 to 10 nm range) was observed in either seeded system. When initial background particles levels were below 0.5 mu g m(-3) particle nucleation was observed. A new condensed aromatic kinetic chemical mechanism was developed to simulate experimental data. A particle water phase was highly related to SOA formation. Reasonable fits to the gas and total SOA concentrations emphasize the important impact of different initial particle seed levels and particle phase water when simulating SOA formation from aromatic compounds like toluene. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2324 / 2334
页数:11
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