Modeling the Role of Alkanes, Polycyclic Aromatic Hydrocarbons, and Their Oligomers in Secondary Organic Aerosol Formation

2012 ◽  
Vol 46 (11) ◽  
pp. 6041-6047 ◽  
Author(s):  
Havala O. T. Pye ◽  
George A. Pouliot
2009 ◽  
Vol 9 (1) ◽  
pp. 1873-1905
Author(s):  
A. W. H. Chan ◽  
K. E. Kautzman ◽  
P. S. Chhabra ◽  
J. D. Surratt ◽  
M. N. Chan ◽  
...  

Abstract. Current atmospheric models do not include secondary organic aerosol (SOA) production from gas-phase reactions of polycyclic aromatic hydrocarbons (PAHs). Recent studies have shown that primary semivolatile emissions, previously assumed to be inert, undergo oxidation in the gas phase, leading to SOA formation. This opens the possibility that low-volatility gas-phase precursors are a potentially large source of SOA. In this work, SOA formation from gas-phase photooxidation of naphthalene, 1-methylnaphthalene (1-MN), 2-methylnaphthalene (2-MN), and 1,2-dimethylnaphthalene (1,2-DMN) is studied in the Caltech dual 28-m3 chambers. Under high-NOx conditions and aerosol mass loadings between 10 and 40 μg m


2018 ◽  
Vol 52 (22) ◽  
pp. 13381-13390 ◽  
Author(s):  
Simone M. Pieber ◽  
Anastasios Kambolis ◽  
Davide Ferri ◽  
Deepika Bhattu ◽  
Emily A. Bruns ◽  
...  

2017 ◽  
Vol 200 ◽  
pp. 143-164 ◽  
Author(s):  
Alla Zelenyuk ◽  
Dan G. Imre ◽  
Jacqueline Wilson ◽  
David M. Bell ◽  
Kaitlyn J. Suski ◽  
...  

When secondary organic aerosol (SOA) particles are formed by ozonolysis in the presence of gas-phase polycyclic aromatic hydrocarbons (PAHs), their formation and properties are significantly different from SOA particles formed without PAHs. For all SOA precursors and all PAHs, discussed in this study, the presence of the gas-phase PAHs during SOA formation significantly affects particle mass loadings, composition, growth, evaporation kinetics, and viscosity. SOA particles formed in the presence of PAHs have, as part of their compositions, trapped unreacted PAHs and products of heterogeneous reactions between PAHs and ozone. Compared to ‘pure’ SOA particles, these particles exhibit slower evaporation kinetics, have higher fractions of non-volatile components, like oligomers, and higher viscosities, assuring their longer atmospheric lifetimes. In turn, the increased viscosity and decreased volatility provide a shield that protects PAHs from chemical degradation and evaporation, allowing for the long-range transport of these toxic pollutants. The magnitude of the effect of PAHs on SOA formation is surprisingly large. The presence of PAHs during SOA formation increases mass loadings by factors of two to five, and particle number concentrations, in some cases, by more than a factor of 100. Increases in SOA mass, particle number concentrations, and lifetime have important implications to many atmospheric processes related to climate, weather, visibility, and human health, all of which relate to the interactions between biogenic SOA and anthropogenic PAHs. The synergistic relationship between SOA and PAHs presented here are clearly complex and call for future research to elucidate further the underlying processes and their exact atmospheric implications.


2004 ◽  
Vol 38 (12) ◽  
pp. 3343-3350 ◽  
Author(s):  
M. D. Keywood ◽  
J. H. Kroll ◽  
V. Varutbangkul ◽  
R. Bahreini ◽  
R. C. Flagan ◽  
...  

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