Journal
ENVIRONMENTAL SCIENCE & TECHNOLOGY
Volume 53, Issue 15, Pages 8553-8562Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.est.9b01609
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Funding
- Swiss National Science Foundation [200020_159809]
- SNSF Ambizione Grant [PZ00P2_179703]
- American National Science Foundation (NSF)
- NSF [AGS-1853639]
- Swiss National Science Foundation (SNF) [PZ00P2_179703, 200020_159809] Funding Source: Swiss National Science Foundation (SNF)
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Organic aerosols are subjected to atmospheric processes driven by sunlight, including the production of reactive oxygen species (ROS) capable of transforming their physicochemical properties. In this study, secondary organic aerosols (SOA) generated from aromatic precursors were found to sensitize singlet oxygen (O-1(2)), an arguably underappreciated atmospheric ROS. Specifically, we quantified O-1(2), OH radical, and H2O2 quantum yields within photoirradiated solutions of laboratory-generated SOA from toluene, biphenyl, naphthalene, and 1,8-dimethylnaphthalene. At 5 mg(C) L-1 of SOA extracts, the average steady-state concentrations of O-1(2) and of OH radicals in irradiated solutions were 3 +/- 1 X 10(-14) M and 3.6 +/- 0.9 x 10(-17) M, respectively. Furthermore, ROS quantum yields of irradiated ambient PM10 extracts were comparable to those from laboratory-generated SOA, suggesting a similarity in ROS production from both types of samples. Finally, by using our measured ROS concentrations, we predict that certain organic compounds found in aerosols, such as amino acids, organo- nitrogen compounds, and phenolic compounds have shortened lifetimes by more than a factor of 2 when O-1(2) is considered as an additional sink. Overall, our findings highlight the importance of SOA as a source of O-1(2) and its potential as a competitive ROS species in photooxidation processes.
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