期刊
ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 49, 期 1, 页码 243-249出版社
AMER CHEMICAL SOC
DOI: 10.1021/es505331d
关键词
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资金
- U.S. Department of Energy Office of Basic Energy Sciences, Chemical Sciences, Geosciences
- Bioscience Division and Office of Biological and Environmental Research (Atmospheric Research Program)
- Department of Energy's Office of Biological and Environmental Research at Pacific Northwest National Laboratory
Secondary organic aerosols (SOA) dominate atmospheric organic aerosols that affect climate, air quality, and health. Recent studies indicate that, contrary to previously held assumptions, at low relative humidity (RH) these particles are semisolid and evaporate orders of magnitude slower than expected. Elevated relative humidity has the potential to affect significantly formation, properties, and atmospheric evolution of SOA particles. Here we present a study of the effect of RH on the room-temperature evaporation kinetics of SOA particles formed by ozonolysis of a-pinene and limonene. Experiments were carried out on a-pinene SOA particles generated, evaporated, and aged at <5%, 50 and 90% RH, and on limonene SOA particles at <5% and 90% RH. We find that in all cases evaporation begins with a relatively fast phase, during which 30-70% of the particle mass evaporates in 2 h, followed by a much slower evaporation rate. Evaporation kinetics at <5% and 50% RH are nearly the same, while at 90% RH a slightly larger fraction evaporates. In all cases, aging the particles prior to inducing evaporation reduces the evaporative losses; with aging at elevated RH leading to a more significant effect. In all cases, the observed SOA evaporation is nearly size-independent.
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