Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region

In this study, the processes behind observed new particle formation (NPF) events and subsequent organic-dominated particle growth at the Pallas Atmosphere–Ecosystem Supersite in Northern Finland are explored with the one-dimensional column trajectory model ADCHEM. The modeled sub-micron particle...

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Main Authors: E. Öström, Z. Putian, G. Schurgers, M. Mishurov, N. Kivekäs, H. Lihavainen, M. Ehn, M. P. Rissanen, T. Kurtén, M. Boy, E. Swietlicki, P. Roldin
Format: Article
Language:English
Published: Copernicus Publications 2017-07-01
Series:Atmospheric Chemistry and Physics
Online Access:https://www.atmos-chem-phys.net/17/8887/2017/acp-17-8887-2017.pdf
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spelling doaj-371acf226d1e4d8c871bc26c35a107a32020-11-24T22:37:15ZengCopernicus PublicationsAtmospheric Chemistry and Physics1680-73161680-73242017-07-01178887890110.5194/acp-17-8887-2017Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest regionE. Öström0E. Öström1Z. Putian2G. Schurgers3M. Mishurov4N. Kivekäs5H. Lihavainen6M. Ehn7M. P. Rissanen8T. Kurtén9M. Boy10E. Swietlicki11P. Roldin12P. Roldin13Division of Nuclear Physics, Lund University, Lund, P.O. Box 118, 221 00, SwedenCentre for Environmental and Climate Research, Lund University, Lund, P.O. Box 118, 221 00, SwedenDepartment of Physics, University of Helsinki, Helsinki, P.O. Box 64, 00014, FinlandDepartment of Geosciences and Natural Resource Management, University of Copenhagen, Copenhagen, 1350, DenmarkDepartment of Physical Geography and Ecosystem Science, Lund University, Lund, 223 62, SwedenFinnish Meteorological Institute, Helsinki, P.O. Box 503, 00101, FinlandFinnish Meteorological Institute, Helsinki, P.O. Box 503, 00101, FinlandDepartment of Physics, University of Helsinki, Helsinki, P.O. Box 64, 00014, FinlandDepartment of Physics, University of Helsinki, Helsinki, P.O. Box 64, 00014, FinlandDepartment of Chemistry, University of Helsinki, Helsinki, P.O. Box 55, 00014, FinlandDepartment of Physics, University of Helsinki, Helsinki, P.O. Box 64, 00014, FinlandDivision of Nuclear Physics, Lund University, Lund, P.O. Box 118, 221 00, SwedenDivision of Nuclear Physics, Lund University, Lund, P.O. Box 118, 221 00, SwedenDepartment of Physics, University of Helsinki, Helsinki, P.O. Box 64, 00014, FinlandIn this study, the processes behind observed new particle formation (NPF) events and subsequent organic-dominated particle growth at the Pallas Atmosphere–Ecosystem Supersite in Northern Finland are explored with the one-dimensional column trajectory model ADCHEM. The modeled sub-micron particle mass is up to  ∼  75 % composed of SOA formed from highly oxidized multifunctional organic molecules (HOMs) with low or extremely low volatility. In the model the newly formed particles with an initial diameter of 1.5 nm reach a diameter of 7 nm about 2 h earlier than what is typically observed at the station. This is an indication that the model tends to overestimate the initial particle growth. In contrast, the modeled particle growth to CCN size ranges ( >  50 nm in diameter) seems to be underestimated because the increase in the concentration of particles above 50 nm in diameter typically occurs several hours later compared to the observations. Due to the high fraction of HOMs in the modeled particles, the oxygen-to-carbon (O  :  C) atomic ratio of the SOA is nearly 1. This unusually high O  :  C and the discrepancy between the modeled and observed particle growth might be explained by the fact that the model does not consider any particle-phase reactions involving semi-volatile organic compounds with relatively low O  :  C. In the model simulations where condensation of low-volatility and extremely low-volatility HOMs explain most of the SOA formation, the phase state of the SOA (assumed either liquid or amorphous solid) has an insignificant impact on the evolution of the particle number size distributions. However, the modeled particle growth rates are sensitive to the method used to estimate the vapor pressures of the HOMs. Future studies should evaluate how heterogeneous reactions involving semi-volatility HOMs and other less-oxidized organic compounds can influence the SOA composition- and size-dependent particle growth.https://www.atmos-chem-phys.net/17/8887/2017/acp-17-8887-2017.pdf
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language English
format Article
sources DOAJ
author E. Öström
E. Öström
Z. Putian
G. Schurgers
M. Mishurov
N. Kivekäs
H. Lihavainen
M. Ehn
M. P. Rissanen
T. Kurtén
M. Boy
E. Swietlicki
P. Roldin
P. Roldin
spellingShingle E. Öström
E. Öström
Z. Putian
G. Schurgers
M. Mishurov
N. Kivekäs
H. Lihavainen
M. Ehn
M. P. Rissanen
T. Kurtén
M. Boy
E. Swietlicki
P. Roldin
P. Roldin
Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region
Atmospheric Chemistry and Physics
author_facet E. Öström
E. Öström
Z. Putian
G. Schurgers
M. Mishurov
N. Kivekäs
H. Lihavainen
M. Ehn
M. P. Rissanen
T. Kurtén
M. Boy
E. Swietlicki
P. Roldin
P. Roldin
author_sort E. Öström
title Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region
title_short Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region
title_full Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region
title_fullStr Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region
title_full_unstemmed Modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region
title_sort modeling the role of highly oxidized multifunctional organic molecules for the growth of new particles over the boreal forest region
publisher Copernicus Publications
series Atmospheric Chemistry and Physics
issn 1680-7316
1680-7324
publishDate 2017-07-01
description In this study, the processes behind observed new particle formation (NPF) events and subsequent organic-dominated particle growth at the Pallas Atmosphere–Ecosystem Supersite in Northern Finland are explored with the one-dimensional column trajectory model ADCHEM. The modeled sub-micron particle mass is up to  ∼  75 % composed of SOA formed from highly oxidized multifunctional organic molecules (HOMs) with low or extremely low volatility. In the model the newly formed particles with an initial diameter of 1.5 nm reach a diameter of 7 nm about 2 h earlier than what is typically observed at the station. This is an indication that the model tends to overestimate the initial particle growth. In contrast, the modeled particle growth to CCN size ranges ( >  50 nm in diameter) seems to be underestimated because the increase in the concentration of particles above 50 nm in diameter typically occurs several hours later compared to the observations. Due to the high fraction of HOMs in the modeled particles, the oxygen-to-carbon (O  :  C) atomic ratio of the SOA is nearly 1. This unusually high O  :  C and the discrepancy between the modeled and observed particle growth might be explained by the fact that the model does not consider any particle-phase reactions involving semi-volatile organic compounds with relatively low O  :  C. In the model simulations where condensation of low-volatility and extremely low-volatility HOMs explain most of the SOA formation, the phase state of the SOA (assumed either liquid or amorphous solid) has an insignificant impact on the evolution of the particle number size distributions. However, the modeled particle growth rates are sensitive to the method used to estimate the vapor pressures of the HOMs. Future studies should evaluate how heterogeneous reactions involving semi-volatility HOMs and other less-oxidized organic compounds can influence the SOA composition- and size-dependent particle growth.
url https://www.atmos-chem-phys.net/17/8887/2017/acp-17-8887-2017.pdf
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