首页|期刊导航|南京大学学报(自然科学版)|中国芳香族二次有机气溶胶半显式氧化生成机制改进与模拟

中国芳香族二次有机气溶胶半显式氧化生成机制改进与模拟OA

Formation and evolution of aromatic secondary organic aerosol in China:Insights from a semi-explicit oxidation scheme implemented in CESM2.1

中文摘要英文摘要

芳香族二次有机气溶胶(Secondary Organic Aerosol,SOA)是中国城市地区大气中重要的细颗粒物组分,在地球系统模式的大气化学模块中引入半显式机制(简写为"SXP")表征人为源排放的芳香族挥发性有机物氧化过程,用于研究过氧自由基(RO2)自氧化与终止反应之间的竞争关系,评估了由自氧化反应生成的芳香族SOA.与中国地面观测数据的对比评估表明,相较于采用挥发性区间(Volatility Basis Set,VBS)的默认模式(简写为"BASE"),SXP对地表SOA浓度的模拟平均偏差降低了约5%;SXP与BASE模拟结果之间的SOA差值表现出明显的区域和季节依赖性,SXP模拟结果在夏季、南方更高.机理分析表明,SXP与BASE模拟结果的差异主要来源于地表芳香族SOA的生成受到一氧化氮(NO)的调控.在低浓度NO环境下(<15 ppbv),SXP模拟的芳香族SOA浓度相较于BASE高约20%~50%;在高浓度NO环境下(>25 ppbv),SXP模拟结果相较于BASE低约10%.主要原因是在SXP模拟过程中考虑了自氧化反应与NO终止反应对RO2 的竞争关系,高浓度NO环境下自氧化反应受到抑制,导致芳香族SOA的生成效率显著降低.最后,分析了中国减排情境下(2013-2019年)的芳香族SOA浓度的变化,为氮氧化物减排背景下中国人为源SOA浓度变化趋势的解释和预测提供了科学依据.

Aromatic secondary organic aerosol(SOA)is a key component of fine particulate matter in urban areas of China,contributing significantly to air pollution.In this study,a semi-explicit aromatic oxidation scheme(SXP)was implemented in the atmospheric chemistry module of the Earth System Model to better represent the oxidation processes of anthropogenic aromatic volatile organic compounds(VOCs).The SXP scheme explicitly simulates the competition between RO2 autoxidation and termination reactions and is used to evaluate the contribution of autoxidation to aromatic SOA formation.Compared with the default model(BASE)that uses the volatility basis set(VBS),the simulation results of the SXP scheme reduces the average bias in surface SOA concentrations by approximately 5%.The differences between the simulation results of SXP and BASE show distinct regional and seasonal patterns,with SXP simulating higher SOA levels in southern China and during the summer months.Mechanistic analysis indicates that the differences arise primarily from the influence of NOx on aromatic SOA formation.Under low-concentration NO conditions(<15 ppbv),SXP simulates 20%~50%higher aromatic SOA compared to BASE.In contrast,under high-concentration NO conditions(>25 ppbv),SXP simulates approximately 10%lower SOA levels than BASE.This is due to the inclusion of the competition between RO2 autoxidation and NO termination reactions,where high NO concentrations suppress autoxidation and reduce SOA formation efficiency.Finally,the study examines changes in aromatic SOA during 2013-2019,a period of significant emission reductions in China.The results provide insights into the trends of anthropogenic SOA under NOx reduction scenarios,helping to improve understanding of the impact of NO on aromatic SOA formation and its regional distribution.This work underscores the importance of accounting for the competition between autoxidation and NO termination reactions in accurately predicting SOA formation in response to emission controls.

王菁翊;董新奕;汪名怀

南京大学大气科学学院,南京,210023||南京大学-赫尔辛基大学大气与地球系统科学国际合作联合实验室,南京,210023南京大学大气科学学院,南京,210023||南京大学-赫尔辛基大学大气与地球系统科学国际合作联合实验室,南京,210023南京大学大气科学学院,南京,210023||南京大学-赫尔辛基大学大气与地球系统科学国际合作联合实验室,南京,210023

天文与地球科学

芳香族二次有机气溶胶含氧有机分子自氧化反应地球系统模式

aromatic secondary organic aerosoloxygenated organic moleculesautoxidation reactionCESM2.1

《南京大学学报(自然科学版)》 2026 (4)

505-522,18

国家自然科学基金(42575126)

10.13232/j.cnki.jnju.2026.04.001

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