Connections between atmospheric sulphuric acid and new particle formation during QUEST III-IV campaigns in Heidelberg and Hyyti

被引:236
作者
Riipinen, I.
Sihto, S.-L.
Kulmala, M.
Arnold, F.
Dal Maso, M.
Birmili, W.
Saarnio, K.
Teinila, K.
Kerminen, V. -M.
Laaksonen, A.
Lehtinen, K. E. J.
机构
[1] Univ Helsinki, Dept Phys Sci, FIN-00014 Helsinki, Finland
[2] Max Planck Inst Nucl Phys, MPIK, Inst Atmospher Phys, D-69029 Heidelberg, Germany
[3] Leibniz Inst Tropospher Res, D-04318 Leipzig, Germany
[4] Finnish Meteorol Inst, FIN-00101 Helsinki, Finland
[5] Univ Kuopio, Dept Appl Phys, FIN-70211 Kuopio, Finland
[6] Finnish Meteorol Inst, Kuopio 70211, Finland
[7] Univ Kuopio, Dept Appl Phys, FIN-70211 Kuopio, Finland
关键词
D O I
10.5194/acp-7-1899-2007
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study investigates the connections between atmospheric sulphuric acid and new particle formation during QUEST III and BACCI/QUEST IV campaigns. The campaigns have been conducted in Heidelberg ( 2004) and Hyytiala ( 2005), the first representing a polluted site surrounded by deciduous forest, and the second a rural site in a boreal forest environment. We have studied the role of sulphuric acid in particle formation and growth by determining 1) the power-law dependencies between sulphuric acid ([H(2)SO(4)]), and particle concentrations (N(3-6)) or formation rates at 1 nm and 3 nm (J(1) and J(3)); 2) the time delays between [H(2)SO(4)] and N(3-6) or J(3), and the growth rates for 1-3 nm particles; 3) the empirical nucleation coefficients A and K in relations J(1)= A[H(2)SO(4)] and J(1)= K[H(2)SO(4)](2), respectively; 4) theoretical predictions for J(1) and J(3) for the days when no significant particle formation is observed, based on the observed sulphuric acid concentrations and condensation sinks. In both environments, N(3-6) or J(3) and [H(2)SO(4)] were linked via a power-law relation with exponents typically ranging from 1 to 2. The result suggests that the cluster activation theory and kinetic nucleation have the potential to explain the observed particle formation. However, some differences between the sites existed: The nucleation coefficients were about an order of magnitude greater in Heidelberg than in Hyytiala conditions. The time lags between J(3) and [H(2)SO(4)] were consistently lower than the corresponding delays between N(3-6) and [H(2)SO(4)]. The exponents in the J(3) proportional to[H(2)SO(4)](nJ 3)-connection were consistently higher than or equal to the exponents in the relation N(3-6) proportional to[H(2)SO(4)](nN36). In the J(1) values, no significant differences were found between the observed rates on particle formation event days and the predictions on non-event days. The J(3) values predicted by the cluster activation or kinetic nucleation hypotheses, on the other hand, were considerably lower on non-event days than the rates observed on particle formation event days. This study provides clear evidence implying that the main process limiting the observable particle formation is the competition between the growth of the freshly formed particles and their loss by scavenging, rather than the initial particle production by nucleation of sulphuric acid. In general, it can be concluded that the simple models based on sulphuric acid concentrations and particle formation by cluster activation or kinetic nucleation can predict the occurence of atmospheric particle formation and growth well, if the particle scavenging is accurately accounted for.
引用
收藏
页码:1899 / 1914
页数:16
相关论文
共 35 条
[1]  
Anttila T, 2005, BOREAL ENVIRON RES, V10, P511
[2]   Rapid formation of sulfuric acid particles at near-atmospheric conditions [J].
Berndt, T ;
Böge, O ;
Stratmann, F ;
Heintzenberg, J ;
Kulmala, M .
SCIENCE, 2005, 307 (5710) :698-700
[3]   Light scattering by fine particles during the Pittsburgh Air Quality Study: measurements and modeling [J].
Cabada, JC ;
Khlystov, A ;
Wittig, AE ;
Pilinis, C ;
Pandis, SN .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2004, 109 (D16) :D16S031-13
[4]  
Dal Maso M, 2005, BOREAL ENVIRON RES, V10, P323
[5]   Ultrafine (nanometre) particle mediated lung injury [J].
Donaldson, K ;
Li, XY ;
MacNee, W .
JOURNAL OF AEROSOL SCIENCE, 1998, 29 (5-6) :553-560
[6]   The contribution of sulphuric acid to atmospheric particle formation and growth: a comparison between boundary layers in Northern and Central Europe [J].
Fiedler, V ;
Dal Maso, M ;
Boy, M ;
Aufmhoff, H ;
Hoffmann, J ;
Schuck, T ;
Birmili, W ;
Hanke, M ;
Uecker, J ;
Arnold, F ;
Kulmala, M .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2005, 5 :1773-1785
[7]   Atmospheric peroxy radicals:: ROXMAS, a new mass-spectrometric methodology for speciated measurements of HO2 and ΣRO2 and first results [J].
Hanke, M ;
Uecker, J ;
Reiner, T ;
Arnold, F .
INTERNATIONAL JOURNAL OF MASS SPECTROMETRY, 2002, 213 (2-3) :91-99
[8]  
Hari P, 2005, BOREAL ENVIRON RES, V10, P315
[9]  
Hirsikko A, 2005, BOREAL ENVIRON RES, V10, P357
[10]   Analytical formulae connecting the "real" and the "apparent" nucleation rate and the nuclei number concentration for atmospheric nucleation events [J].
Kerminen, VM ;
Kulmala, M .
JOURNAL OF AEROSOL SCIENCE, 2002, 33 (04) :609-622