Development and application of a new analytical method to estimate the condensable vapor concentration in the atmosphere

被引:6
作者
Korhonen, H
Kerminen, VM
Kulmala, M
机构
[1] Finnish Meteorol Inst, Climate & Global Change, FIN-00880 Helsinki, Finland
[2] Univ Helsinki, Dept Phys Sci, Div Atmospher Sci, FIN-00014 Helsinki, Finland
关键词
D O I
10.1029/2004JD005458
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
A novel analytical method is presented to estimate the total condensable vapor concentration in the ambient atmosphere. The method requires the aerosol size distribution as its only input and is thus straightforward enough to apply to atmospheric data. In order to estimate the condensable vapor concentrations over boreal forest regions, the method was applied to four years of new particle formation days at SMEAR II site in southern Finland. The growth rate of newly formed particles provided additional information of the concentration of low-volatile vapors. Hence the contribution of low-volatile and semivolatile vapors to particle growth can be separated. The analysis indicated that the median of the condensable vapor concentrations during the nucleation events was approximately 7.6 x 10(7) cm(-3), with values varying between 2.0 x 10(7) and 1.8 x 10(8) cm(-3). Of the total concentration, the contribution of low- volatile compounds was 70% on average but ranged from 22% to over 100%. Sensitivity tests indicated that the obtained percentage of low volatiles is only slightly sensitive to chosen model parameters. When applying the method to ambient aerosol distribution measurements, the largest uncertainty is related to visually undetectable inhomogeneities in air mass and the boundary layer dynamics. These uncertainty factors together with the use of measured dry aerosol sizes instead of ambient sizes can lead the analysis to somewhat overestimate the importance of the low- volatile compounds to total aerosol growth. Even so, our results suggest that identification of submicron aerosol composition during new particle formation can provide information on the compounds that grow nucleation mode particles to larger sizes.
引用
收藏
页码:1 / 9
页数:9
相关论文
共 28 条
[1]   Modelling the formation of organic particles in the atmosphere [J].
Anttila, T ;
Kerminen, VM ;
Kulmala, M ;
Laaksonen, A ;
O'Dowd, CD .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2004, 4 :1071-1083
[2]   The Hohenpeissenberg aerosol formation experiment (HAFEX):: a long-term study including size-resolved aerosol, H2SO4, OH, and monoterpenes measurements [J].
Birmili, W ;
Berresheim, H ;
Plass-Dülmer, C ;
Elste, T ;
Gilge, S ;
Wiedensohler, A ;
Uhrner, U .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2003, 3 :361-376
[3]  
BOY M, 2004, ATMOS CHEM PHYS DISC, V4, P6341
[4]   Formation of secondary organic aerosols from isoprene and its gas-phase oxidation products through reaction with hydrogen peroxide [J].
Claeys, M ;
Wang, W ;
Ion, AC ;
Kourtchev, I ;
Gelencsér, A ;
Maenhaut, W .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (25) :4093-4098
[5]   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)
[6]   The global distribution of secondary particulate matter in a 3-D Lagrangian chemistry transport model [J].
Derwent, RG ;
Jenkin, ME ;
Johnson, CE ;
Stevenson, DS .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2003, 44 (01) :57-95
[7]  
Fuchs N.A., 1971, TOPICS CURRENT AEROS, P1, DOI [DOI 10.1016/B978-0-08-016674-2.50006-6, 10.1016/B978-0-08-016674-2.50006-6]
[8]  
Hämeri K, 2001, TELLUS B, V53, P359, DOI 10.1034/j.1600-0889.2001.d01-26.x
[9]   The NH3 mass accommodation coefficient for uptake onto sulfuric acid solutions [J].
Hanson, D ;
Kosciuch, E .
JOURNAL OF PHYSICAL CHEMISTRY A, 2003, 107 (13) :2199-2208
[10]   Closed-loop arrangement with critical orifice for DMA sheath excess flow system [J].
Jokinen, V ;
Makela, JM .
JOURNAL OF AEROSOL SCIENCE, 1997, 28 (04) :643-648