Atmospheric nanoparticles formed from heterogeneous reactions of organics

被引:236
作者
Wang, Lin [1 ,2 ]
Khalizov, Alexei F. [1 ,2 ]
Zheng, Jun [1 ,2 ]
Xu, Wen [1 ,2 ]
Ma, Yan [1 ,2 ,3 ]
Lal, Vinita [1 ,2 ]
Zhang, Renyi [1 ,2 ]
机构
[1] Texas A&M Univ, Dept Atmospher Sci, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
[3] Nanjing Univ Informat Sci & Technol, Sch Environm Sci & Engn, Nanjing 210044, Peoples R China
基金
中国国家自然科学基金; 美国国家科学基金会;
关键词
PARTICLE FORMATION; AEROSOL; IONIZATION; METHYLGLYOXAL; NUCLEATION; CHEMISTRY; EVENTS; GROWTH;
D O I
10.1038/NGEO778
中图分类号
P [天文学、地球科学];
学科分类号
07 ;
摘要
Atmospheric aerosols directly and indirectly affect the radiative balance of the Earth's atmosphere(1). Nanoparticles are a key component of atmospheric aerosols, growing rapidly under ambient conditions(2-4). Organic species are thought to lead to the growth of nanoparticles smaller than 20 nm (refs 5, 6), but the identity of these species and the underlying chemical mechanisms remain elusive. Here we exposed nanoparticles to a range of organic vapours-2,4-hexadienal, glyoxal and trimethylamine-and monitored particle size to determine the contribution of organic vapours to nanoparticle growth. We show that organic species enhance the growth of nanoparticles, producing non-volatile oligomers, polymers and alkylaminium sulphates in the particle phase. Nanoparticle growth increased with relative humidity in the presence of glyoxal and trimethylamine, but decreased at higher relative humidities in the presence of 2,4-hexadienal, dependent on the reaction mechanism of the organic species involved. Oligomerization and polymerization were largely suppressed in particles smaller than 4 nm and nanoparticle growth increased with particle size. Our findings help to explain the presence of previously measured, but unidentified non-volatile compounds in atmospheric nanoparticles and to improve model simulations of new particle formation.
引用
收藏
页码:238 / 242
页数:5
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