Molecular Evidence of Aqueous‐Processed NOCs: From Mechanistic Insights to Environmental Impacts

Abstract Nitrogen‐containing organic compounds (NOCs), encompassing a complex suite of oxidized and reduced organic nitrogen species, exert significant impacts on atmospheric light absorption, oxidation capacity, and global nitrogen cycling. Despite the growing recognition of NOCs as key components of atmospheric organic matter, their formation through aqueous‐phase processes and potential environmental impacts have long been underestimated. This review begins by summarizing the major classes of NOC molecules, then synthesizes observational evidence on their formation in the aqueous‐phase, particularly highlighting its critical role in generating nitroaromatic and N‐heterocyclic compounds. Built on the observational evidence, we further discuss the related evaluation of the multi‐faceted environmental impacts arising from the aqueous‐phase NOC formation. The evidence demonstrates that aqueous‐phase NOC chemistry exerts significant influence on atmospheric compositions, contributes up to 90% of brown carbon's radiative effects, enhances oxidative capacity and secondary organic aerosol production, and influences nitrogen speciation in wet deposition. However, most current model assessments exhibit considerable limitations in quantifying these effects, stemming primarily from oversimplified parameterizations of aqueous‐phase chemistry that fail to adequately represent the full complexity of atmospheric multiphase systems. Furthermore, existing observational data sets remain insufficient, severely constraining efforts to optimize model parameters and validate simulation outputs. To address these critical knowledge gaps, we propose an integrated research framework that combines long‐term monitoring of key NOC and various precursors and advanced simulations of aqueous‐phase chemistry at the micrometer‐scale reaction environments, which would constrain the parameterization of future models for the aqueous‐phase chemistry and impacts of NOCs.

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Publication Details

Journal
Journal of Geophysical Research Atmospheres
Published
2025-12-26
DOI
https://doi.org/10.1029/2025jd045757
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
0.00

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article

Molecular Evidence of Aqueous‐Processed NOCs: From Mechanistic Insights to Environmental Impacts

Tengfei Li, X. Wang, Nan Ma, Guohua Zhang et al.
Journal of Geophysical Research Atmospheres
Atmospheric chemistry and aerosols
article

Molecular Evidence of Aqueous‐Processed NOCs: From Mechanistic Insights to Environmental Impacts

Tengfei Li, X. Wang, Nan Ma, Guohua Zhang, Weiwei Hu, Xinhui Bi, Zongbo Shi, Xin Huang, Ping'an Peng, Tao Wang, Xuan Wang, Wei Sun, Mingjin Tang
article en

Abstract

Abstract Nitrogen‐containing organic compounds (NOCs), encompassing a complex suite of oxidized and reduced organic nitrogen species, exert significant impacts on atmospheric light absorption, oxidation capacity, and global nitrogen cycling. Despite the growing recognition of NOCs as key components of atmospheric organic matter, their formation through aqueous‐phase processes and potential environmental impacts have long been underestimated. This review begins by summarizing the major classes of NOC molecules, then synthesizes observational evidence on their formation in the aqueous‐phase, particularly highlighting its critical role in generating nitroaromatic and N‐heterocyclic compounds. Built on the observational evidence, we further discuss the related evaluation of the multi‐faceted environmental impacts arising from the aqueous‐phase NOC formation. The evidence demonstrates that aqueous‐phase NOC chemistry exerts significant influence on atmospheric compositions, contributes up to 90% of brown carbon's radiative effects, enhances oxidative capacity and secondary organic aerosol production, and influences nitrogen speciation in wet deposition. However, most current model assessments exhibit considerable limitations in quantifying these effects, stemming primarily from oversimplified parameterizations of aqueous‐phase chemistry that fail to adequately represent the full complexity of atmospheric multiphase systems. Furthermore, existing observational data sets remain insufficient, severely constraining efforts to optimize model parameters and validate simulation outputs. To address these critical knowledge gaps, we propose an integrated research framework that combines long‐term monitoring of key NOC and various precursors and advanced simulations of aqueous‐phase chemistry at the micrometer‐scale reaction environments, which would constrain the parameterization of future models for the aqueous‐phase chemistry and impacts of NOCs.

Journal of Geophysical Research AtmospheresVol. 131(1)
City University of Hong Kong (HK), Guangzhou Institute of Geochemistry (CN), Guangdong Academy of Sciences (CN), Guangdong-Hongkong-Macau Joint Laboratory of Collaborative Innovation for Environmental Quality (CN), University of Chinese Academy of Sciences (CN), University of Birmingham (GB)
National Natural Science Foundation of China, Guangdong Provincial Applied Science and Technology Research and Development Program, National Key Research and Development Program of China
Openalex Percentile: Top 32%
Atmospheric chemistry and aerosols
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