4.8 Article

Phase Behavior of Hydrocarbon-like Primary Organic Aerosol and Secondary Organic Aerosol Proxies Based on Their Elemental Oxygen-to-Carbon Ratio

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 55, 期 18, 页码 12202-12214

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.1c02697

关键词

atmospheric aerosol particles; air pollution; phase behavior; organic aerosol particles; secondary organic aerosol; primary organic aerosol; microscopy

资金

  1. Work Learn International Undergraduate Research Award [10045]
  2. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN/04441-2016]
  3. European Union's Horizon 2020 research and innovation program under the Marie Sklodowska-Curie grant [890200]
  4. Marie Curie Actions (MSCA) [890200] Funding Source: Marie Curie Actions (MSCA)

向作者/读者索取更多资源

The research found that internal mixtures of POA and SOA in the atmosphere almost always formed two phases when the O/C ratio of the POA was less than 0.11. When the O/C ratio of the POA was between 0.11 and 0.29, the mixtures mostly resulted in particles with one liquid phase. However, depending on the types of SOA and POA surrogates, two liquid phases were also observed in some cases, and an increase in phase-separated particles was observed when increasing the relative humidity within this O/C range.
A large fraction of atmospheric aerosols can be characterized as primary organic aerosol (POA) and secondary organic aerosol (SOA). Knowledge of the phase behavior, that is, the number and type of phases within internal POA + SOA mixtures, is crucial to predict their effect on climate and air quality. For example, if POA and SOA form a single phase, POA will enhance the formation of SOA by providing organic mass to absorb SOA precursors. Using microscopy, we studied the phase behavior of mixtures of SOA proxies and hydrocarbon-like POA proxies at relative humidity (RH) values of 90%, 45%, and below 5%. Internal mixtures of POA and SOA almost always formed two phases if the elemental oxygen-to-carbon ratio (O/C) of the POA was less than 0.11, which encompasses a large fraction of atmospheric hydrocarbon-like POA from fossil fuel combustion. SOA proxies mixed with POA proxies having 0.11 <= O/C <= 0.29 mostly resulted in particles with one liquid phase. However, two liquid phases were also observed, depending on the type of SOA and POA surrogates, and an increase in phase-separated particles was observed when increasing the RH in this O/C range. The results have implications for predicting atmospheric SOA formation and policy strategies to reduce SOA in urban environments.

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