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Factors controlling the evaporation of secondary organic aerosol from α-pinene ozonolysis
被引:79
|作者:
Yli-Juuti, Taina
[1
]
Pajunoja, Aki
[1
]
Tikkanen, Olli-Pekka
[1
]
Buchholz, Angela
[1
]
Faiola, Celia
[1
]
Vaisanen, Olli
[1
]
Hao, Liqing
[1
]
Kari, Eetu
[1
]
Perakyla, Otso
[2
]
Garmash, Olga
[2
]
Shiraiwa, Manabu
[3
]
Ehn, Mikael
[2
]
Lehtinen, Kari
[1
,4
]
Virtanen, Annele
[1
]
机构:
[1] Univ Eastern Finland, Dept Appl Phys, Kuopio, Finland
[2] Univ Helsinki, Dept Phys, Helsinki, Finland
[3] Univ Calif Irvine, Dept Chem, Irvine, CA 92717 USA
[4] Finnish Meteorol Inst, Kuopio, Finland
基金:
欧洲研究理事会;
芬兰科学院;
关键词:
KINETIC MULTILAYER MODEL;
PARTICLE-PHASE CHEMISTRY;
HIGH-RESOLUTION;
EVOLUTION;
GROWTH;
STATE;
DYNAMICS;
WATER;
D O I:
10.1002/2016GL072364
中图分类号:
P [天文学、地球科学];
学科分类号:
07 ;
摘要:
Secondary organic aerosols (SOA) forms a major fraction of organic aerosols in the atmosphere. Knowledge of SOA properties that affect their dynamics in the atmosphere is needed for improving climate models. By combining experimental and modeling techniques, we investigated the factors controlling SOA evaporation under different humidity conditions. Our experiments support the conclusion of particle phase diffusivity limiting the evaporation under dry conditions. Viscosity of particles at dry conditions was estimated to increase several orders of magnitude during evaporation, up to 10(9)Pas. However, at atmospherically relevant relative humidity and time scales, our results show that diffusion limitations may have a minor effect on evaporation of the studied -pinene SOA particles. Based on previous studies and our model simulations, we suggest that, in warm environments dominated by biogenic emissions, the major uncertainty in models describing the SOA particle evaporation is related to the volatility of SOA constituents.
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页码:2562 / 2570
页数:9
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