TY - JOUR
T1 - Atmospheric Photosensitization
T2 - A New Pathway for Sulfate Formation
AU - Wang, Xinke
AU - Gemayel, Rachel
AU - Hayeck, Nathalie
AU - Perrier, Sebastien
AU - Charbonnel, Nicolas
AU - Xu, Caihong
AU - Chen, Hui
AU - Zhu, Chao
AU - Zhang, Liwu
AU - Wang, Lin
AU - Nizkorodov, Sergey A.
AU - Wang, Xinming
AU - Wang, Zhe
AU - Wang, Tao
AU - Mellouki, Abdelwahid
AU - Riva, Matthieu
AU - Chen, Jianmin
AU - George, Christian
PY - 2020/3/17
Y1 - 2020/3/17
N2 - Northern China is regularly subjected to intense wintertime "haze events", with high levels of fine particles that threaten millions of inhabitants. While sulfate is a known major component of these fine haze particles, its formation mechanism remains unclear especially under highly polluted conditions, with state-of-the-art air quality models unable to reproduce or predict field observations. These haze conditions are generally characterized by simultaneous high emissions of SO2 and photosensitizing materials. In this study, we find that the excited triplet states of photosensitizers could induce a direct photosensitized oxidation of hydrated SO2 and bisulfite into sulfate S(VI) through energy transfer, electron transfer, or hydrogen atom abstraction. This photosensitized pathway appears to be a new and ubiquitous chemical route for atmospheric sulfate production. Compared to other aqueous-phase sulfate formation pathways with ozone, hydrogen peroxide, nitrogen dioxide, or transition-metal ions, the results also show that this photosensitized oxidation of S(IV) could make an important contribution to aerosol sulfate formation in Asian countries, particularly in China.
AB - Northern China is regularly subjected to intense wintertime "haze events", with high levels of fine particles that threaten millions of inhabitants. While sulfate is a known major component of these fine haze particles, its formation mechanism remains unclear especially under highly polluted conditions, with state-of-the-art air quality models unable to reproduce or predict field observations. These haze conditions are generally characterized by simultaneous high emissions of SO2 and photosensitizing materials. In this study, we find that the excited triplet states of photosensitizers could induce a direct photosensitized oxidation of hydrated SO2 and bisulfite into sulfate S(VI) through energy transfer, electron transfer, or hydrogen atom abstraction. This photosensitized pathway appears to be a new and ubiquitous chemical route for atmospheric sulfate production. Compared to other aqueous-phase sulfate formation pathways with ozone, hydrogen peroxide, nitrogen dioxide, or transition-metal ions, the results also show that this photosensitized oxidation of S(IV) could make an important contribution to aerosol sulfate formation in Asian countries, particularly in China.
UR - http://www.scopus.com/inward/record.url?scp=85082145803&partnerID=8YFLogxK
U2 - 10.1021/acs.est.9b06347
DO - 10.1021/acs.est.9b06347
M3 - Journal article
C2 - 32022545
AN - SCOPUS:85082145803
SN - 0013-936X
VL - 54
SP - 3114
EP - 3120
JO - Environmental Science and Technology
JF - Environmental Science and Technology
IS - 6
ER -