Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms

We have investigated the formation and early growth of atmospheric secondary aerosol particles building on atmospheric measurements. The measurements were part of the QUEST 2 campaign which took place in spring 2003 in Hyytiälä (Finland). During the campaign numerous aerosol particle formation event...

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Main Authors: S.-L. Sihto, M. Kulmala, V.-M. Kerminen, M. Dal Maso, T. Petäjä, I. Riipinen, H. Korhonen, F. Arnold, R. Janson, M. Boy, A. Laaksonen, K. E. J. Lehtinen
Format: Article
Language:English
Published: Copernicus Publications 2006-01-01
Series:Atmospheric Chemistry and Physics
Online Access:http://www.atmos-chem-phys.net/6/4079/2006/acp-6-4079-2006.pdf
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author S.-L. Sihto
M. Kulmala
V.-M. Kerminen
M. Dal Maso
T. Petäjä
I. Riipinen
H. Korhonen
F. Arnold
R. Janson
M. Boy
A. Laaksonen
K. E. J. Lehtinen
author_facet S.-L. Sihto
M. Kulmala
V.-M. Kerminen
M. Dal Maso
T. Petäjä
I. Riipinen
H. Korhonen
F. Arnold
R. Janson
M. Boy
A. Laaksonen
K. E. J. Lehtinen
author_sort S.-L. Sihto
collection DOAJ
description We have investigated the formation and early growth of atmospheric secondary aerosol particles building on atmospheric measurements. The measurements were part of the QUEST 2 campaign which took place in spring 2003 in Hyytiälä (Finland). During the campaign numerous aerosol particle formation events occurred of which 15 were accompanied by gaseous sulphuric acid measurements. Our detailed analysis of these 15 events is focussed on nucleation and early growth (to a diameter of 3 nm) of fresh particles. It revealed that new particle formation seems to be a function of the gaseous sulphuric acid concentration to the power from one to two when the time delay between the sulphuric acid and particle number concentration is taken into account. From the time delay the growth rates of freshly nucleated particles from 1 nm to 3 nm were determined. The mean growth rate was 1.2 nm/h and it was clearly correlated with the gaseous sulphuric acid concentration. We tested two nucleation mechanisms – recently proposed cluster activation and kinetic type nucleation – as possible candidates to explain the observed dependences, and determined experimental nucleation coefficients. We found that some events are dominated by the activation mechanism and some by the kinetic mechanism. Inferred coefficients for the two nucleation mechanisms are the same order of magnitude as chemical reaction coefficients in the gas phase and they correlate with the product of gaseous sulphuric acid and ammonia concentrations. This indicates that besides gaseous sulphuric acid also ammonia has a role in nucleation.
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spelling doaj.art-1dd2e4259ad54f93ad35ed00b62cced32022-12-21T19:17:08ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242006-01-0161240794091Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanismsS.-L. SihtoM. KulmalaV.-M. KerminenM. Dal MasoT. PetäjäI. RiipinenH. KorhonenF. ArnoldR. JansonM. BoyA. LaaksonenK. E. J. LehtinenWe have investigated the formation and early growth of atmospheric secondary aerosol particles building on atmospheric measurements. The measurements were part of the QUEST 2 campaign which took place in spring 2003 in Hyytiälä (Finland). During the campaign numerous aerosol particle formation events occurred of which 15 were accompanied by gaseous sulphuric acid measurements. Our detailed analysis of these 15 events is focussed on nucleation and early growth (to a diameter of 3 nm) of fresh particles. It revealed that new particle formation seems to be a function of the gaseous sulphuric acid concentration to the power from one to two when the time delay between the sulphuric acid and particle number concentration is taken into account. From the time delay the growth rates of freshly nucleated particles from 1 nm to 3 nm were determined. The mean growth rate was 1.2 nm/h and it was clearly correlated with the gaseous sulphuric acid concentration. We tested two nucleation mechanisms – recently proposed cluster activation and kinetic type nucleation – as possible candidates to explain the observed dependences, and determined experimental nucleation coefficients. We found that some events are dominated by the activation mechanism and some by the kinetic mechanism. Inferred coefficients for the two nucleation mechanisms are the same order of magnitude as chemical reaction coefficients in the gas phase and they correlate with the product of gaseous sulphuric acid and ammonia concentrations. This indicates that besides gaseous sulphuric acid also ammonia has a role in nucleation.http://www.atmos-chem-phys.net/6/4079/2006/acp-6-4079-2006.pdf
spellingShingle S.-L. Sihto
M. Kulmala
V.-M. Kerminen
M. Dal Maso
T. Petäjä
I. Riipinen
H. Korhonen
F. Arnold
R. Janson
M. Boy
A. Laaksonen
K. E. J. Lehtinen
Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms
Atmospheric Chemistry and Physics
title Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms
title_full Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms
title_fullStr Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms
title_full_unstemmed Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms
title_short Atmospheric sulphuric acid and aerosol formation: implications from atmospheric measurements for nucleation and early growth mechanisms
title_sort atmospheric sulphuric acid and aerosol formation implications from atmospheric measurements for nucleation and early growth mechanisms
url http://www.atmos-chem-phys.net/6/4079/2006/acp-6-4079-2006.pdf
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