Exploring Surface‐Enhanced Heterogeneous Oxidation of Isoprene: Evidence for Atmospheric Haze Chemistry

Abstract Solid atmospheric particulates can act as heterogeneous drivers for gas loss and particle aging during haze episodes. Observational and experimental evidence reveals an unidentified competitive mechanism involving transition metal ions (TMIs) that catalyze the heterogeneous oxidation of isoprene. Hydroxyl radicals (OH) were generated through the reaction of singlet oxygen (O( 1 D)) with molecular water at the surface of earth‐abundant manganese (Mn) nanoparticles. The energy threshold for OH production was minimized to 213 kJ mol −1 in the presence of alkali K + ions, significantly lower than the 392 kJ mol −1 required for ozone photolysis. The rapid loss of isoprene (1.60 × 10 −2 s −1 ) for the particulate mixtures resulted in the formation of approximately 70% C 1 –C 4 carbonyl oligomers via interfacial binding modes, which promoted particle growth. This contrasts with the higher yields of C 5 products typically observed in gas‐phase reactions of isoprene with OH radicals. The findings could enhance the understanding of severe haze formation, particularly under complex air pollution conditions.

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Publication Details

Journal
Journal of Geophysical Research Atmospheres
Published
2024-12-30
DOI
https://doi.org/10.1029/2024jd042439
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
0.00

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article

Exploring Surface‐Enhanced Heterogeneous Oxidation of Isoprene: Evidence for Atmospheric Haze Chemistry

Junji Cao, Yuanchun Jiang, John G. Watson, Qingyan Fu et al.
Journal of Geophysical Research Atmospheres
Atmospheric chemistry and aerosols
article

Exploring Surface‐Enhanced Heterogeneous Oxidation of Isoprene: Evidence for Atmospheric Haze Chemistry

Junji Cao, Yuanchun Jiang, John G. Watson, Qingyan Fu, Junfeng Wang, Shuncheng Lee, Hong Liao, Cheng Huang, Long Cui, Mindong Chen, Haiwei Li, Judith C. Chow, Wingkei Ho, Hongli Wang, Jingyi Li, Ming Wang, Xinlei Ge, Yu Huang, Yunjiang Zhang
article en

Abstract

Abstract Solid atmospheric particulates can act as heterogeneous drivers for gas loss and particle aging during haze episodes. Observational and experimental evidence reveals an unidentified competitive mechanism involving transition metal ions (TMIs) that catalyze the heterogeneous oxidation of isoprene. Hydroxyl radicals (OH) were generated through the reaction of singlet oxygen (O( 1 D)) with molecular water at the surface of earth‐abundant manganese (Mn) nanoparticles. The energy threshold for OH production was minimized to 213 kJ mol −1 in the presence of alkali K + ions, significantly lower than the 392 kJ mol −1 required for ozone photolysis. The rapid loss of isoprene (1.60 × 10 −2 s −1 ) for the particulate mixtures resulted in the formation of approximately 70% C 1 –C 4 carbonyl oligomers via interfacial binding modes, which promoted particle growth. This contrasts with the higher yields of C 5 products typically observed in gas‐phase reactions of isoprene with OH radicals. The findings could enhance the understanding of severe haze formation, particularly under complex air pollution conditions.

Journal of Geophysical Research AtmospheresVol. 130(1)
Chinese Academy of Sciences (CN), Hong Kong University of Science and Technology (HK), Nanjing University of Information Science and Technology (CN), Ministry of Ecology and Environment (CN), Education University of Hong Kong (HK), Institute of Atmospheric Physics (CN), Institute of Earth Environment (CN), Desert Research Institute (US)
National Natural Science Foundation of China, Startup Foundation for Introducing Talent of Nanjing University of Information Science and Technology
Clean water and sanitation
Openalex Percentile: Top 73%
Atmospheric chemistry and aerosols
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