Modelling the formation of organic particles in the atmosphere

被引:37
作者
Anttila, T
Kerminen, VM
Kulmala, M
Laaksonen, A
O'Dowd, CD
机构
[1] Finnish Meteorol Inst, FIN-00880 Helsinki, Finland
[2] Univ Helsinki, Dept Phys Sci, FIN-00014 Helsinki, Finland
[3] Univ Kuopio, Dept Appl Phys, FIN-70211 Kuopio, Finland
[4] Natl Univ Ireland, Dept Expt Phys, Galway, Ireland
关键词
D O I
10.5194/acp-4-1071-2004
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Particle formation resulting from activation of inorganic stable clusters by a supersaturated organic vapour was investigated using a numerical model. The applied aerosol dynamic model included a detailed description of the activation process along with a treatment of the appropriate aerosol and gas-phase processes. The obtained results suggest that both gaseous sulphuric acid and organic vapours contribute to organic particle formation in continental background areas. The initial growth of freshly-nucleated clusters is driven mainly by condensation of gaseous sulphuric acid and by a lesser extent self-coagulation. After the clusters have reached sizes of around 2 nm in diameter, low-volatile organic vapours start to condense spontaneously into the clusters, thereby accelerating their growth to detectable sizes. A shortage of gaseous sulphuric acid or organic vapours limit, or suppress altogether, the particle formation, since freshly-nucleated clusters are rapidly coagulated away by pre-existing particles. The obtained modelling results were applied to explaining the observed seasonal cycle in the number of aerosol formation events in a continental forest site.
引用
收藏
页码:1071 / 1083
页数:13
相关论文
共 47 条
[1]   Surface tension of organic acids plus water binary mixtures from 20 degrees C to 50 degrees C [J].
Alvarez, E ;
Vazquez, G ;
SanchezVilas, M ;
Sanjurjo, B ;
Navaza, JM .
JOURNAL OF CHEMICAL AND ENGINEERING DATA, 1997, 42 (05) :957-960
[2]  
[Anonymous], 2001, CLIM CHANG 2001
[3]  
[Anonymous], 1970, HIGHLY DISPERSED AER
[4]   Condensational growth of atmospheric nuclei by organic vapours [J].
Anttila, T ;
Kerminen, VM .
JOURNAL OF AEROSOL SCIENCE, 2003, 34 (01) :41-61
[5]   Evolution of newly formed aerosol particles in the continental boundary layer:: A case study including OH and H2SO4 measurements [J].
Birmili, W ;
Wiedensohler, A ;
Plass-Dülmer, C ;
Berresheim, H .
GEOPHYSICAL RESEARCH LETTERS, 2000, 27 (15) :2205-2208
[6]   Sesquiterpene ozonolysis: Origin of atmospheric new particle formation from biogenic hydrocarbons [J].
Bonn, B ;
Moortgat, GK .
GEOPHYSICAL RESEARCH LETTERS, 2003, 30 (11) :39-1
[7]   Influence of water vapor on the process of new particle formation during monoterpene ozonolysis [J].
Bonn, B ;
Schuster, G ;
Moortgat, GK .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (12) :2869-2881
[8]   ATMOSPHERIC NUCLEI IN THE REMOTE FREE-TROPOSPHERE [J].
CLARKE, AD .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1992, 14 (1-4) :479-488
[9]   NEW PARTICLE FORMATION IN THE MARINE BOUNDARY-LAYER [J].
COVERT, DS ;
KAPUSTIN, VN ;
QUINN, PK ;
BATES, TS .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D18) :20581-20589
[10]   Condensation and coagulation sinks and formation of nucleation mode particles in coastal and boreal forest boundary layers -: art. no. 8097 [J].
Dal Maso, M ;
Kulmala, M ;
Lehtinen, KEJ ;
Mäkelä, JM ;
Aalto, P ;
O'Dowd, CD .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2002, 107 (D15)