Diurnal and Seasonal Variations in the Phase State of Secondary Organic Aerosol Material over the Contiguous US Simulated in CMAQ

被引:18
作者
Li, Ying [1 ]
Carlton, Annmarie G. [1 ]
Shiraiwa, Manabu [1 ]
机构
[1] Univ Calif Irvine, Dept Chem, Irvine, CA 92697 USA
来源
ACS EARTH AND SPACE CHEMISTRY | 2021年 / 5卷 / 08期
基金
美国国家科学基金会;
关键词
glass transition teniperatisre; viscosity; organic molecular composition; GLASS-TRANSITION TEMPERATURE; MULTIPHASE CHEMICAL-KINETICS; SIZE DISTRIBUTION DYNAMICS; ATMOSPHERIC AEROSOLS; AIR-QUALITY; ICE NUCLEATION; LIQUID WATER; REACTIVE UPTAKE; GAS UPTAKE; VISCOSITY;
D O I
10.1021/acsearthspacechem.1c00094
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Secondary organic aerosol (SOA) accounts for a substantial portion of atmospheric particulate matter. Phase state plays an important role in the formation and evolution of SOA, while current air quality models usually assume that SOA particles are homogeneous and well -mixed liquids. In this study, we simulate glass transition temperature (Tg) and particle viscosity of SOA based on organic molecular composition over the contiguous US in 2016 using the Community Multiscale Air Quality (CMAQ) model. Simulations show that oligomers from anthropogenic and biogenic SOA and acid-catalyzed isoprene SOA are large contributors to Tg of dry SOA, and the dominant species that regulates the dry Tg variation is dependent on location and season. At the surface, the Tg of dry SOA is higher in the western than in the eastern US, which is due to higher mass fractions of accretion products in the 27 3,0estern US. Taking into account the tt 280.0water uptake by SOA, the estimated SOA K1. isimages cosity shows, a prominent geospatial gradient, which nearly a mirror of Centr. tSOASt relative humidity. SOA viscosity exhibits a strong diel cycle; and the phase state tends to be more viscous in daytime. The seasonal variations in SOA viscosity are substantially smaller than the diurnal variations. Simulations for four diverse field sites show that Tg and SOA viscosity exhibit significant vertical variations that increase with the altitude. SOA in winter undergoes glass transition at lower altitude (-3 km) than the other three seasons, and SOA occurs as a non liquid phase at lower altitude at night than during the daytime. This suggests that chemical transport models may need to consider the bulk diffusion limitations in partitioning into viscous SOA in dry western areas of US and aloft in the humid eastern US as well as dry periods during the day to accurately predict SOA formation, size distribution dynamics, and subsequent impacts.
引用
收藏
页码:1971 / 1982
页数:12
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