Seasonal simulation and source apportionment of SO42− with integration of major highlighted chemical pathways in WRF-Chem model in the NCP

IF 3.9 3区 环境科学与生态学 Q2 ENVIRONMENTAL SCIENCES Atmospheric Pollution Research Pub Date : 2024-07-27 DOI:10.1016/j.apr.2024.102268
Xiaoxi Zhao , Xiujuan Zhao , Dan Chen , Jing Xu , Yujing Mu , Bo Hu
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Abstract

Particulate sulfate (SO42−) is the major component of fine particles in the North China Plain (NCP). It plays an essential role in the entire atmosphere and climate system. Accurately reproducing the SO42− levels is challenging for chemical transport model. Here, the major highlighted multiple phase SO42− formation pathways are integrated into the WRF-Chem model and seasonal model performance of SO42− are assessed by observed SO42− at multiple sampling sites located in the NCP. The results show that the integration of these SO42− formation pathways obviously narrow the gap between simulation and observation in autumn, winter, and summer at three sampling sites in the NCP, for high RH conditions facilitate the hygroscopic growth of PM2.5 and promote the multiple phase reaction to form SO42−. The underestimation in autumn, winter, and summer may ascribe to the missed SO42− source from photo-induced chemical route and missed hygroscopicity of organic aerosols. The obviously discrepancy between simulation and observation in spring may ascribe to the large underestimation of SO2 levels and lack consideration of dust scheme. Source apportionment results show that the gas phase reaction played a vital role in the formation of SO42− in each season. The contribution of aqueous phase SO2 oxidation by H2O2 is higher in autumn and summer due to simultaneously high RH levels and stronger photochemical reaction activity. The Mn(II) catalytic SO2 oxidation pathway at the particle interface is important in autumn and make greater contribution to SO42− formation during winter severe haze events under extremely high RH levels.

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在 NCP 的 WRF-Chem 模型中结合主要的突出化学途径进行 SO42- 的季节模拟和来源分配
颗粒硫酸盐(SO42-)是华北平原(NCP)细颗粒物的主要成分。它在整个大气和气候系统中起着至关重要的作用。准确再现 SO42- 的水平对化学传输模式来说是一项挑战。本文将主要的多相 SO42- 形成途径集成到 WRF-Chem 模式中,并通过在华北平原多个采样点观测到的 SO42- 来评估 SO42- 的季节性模式性能。结果表明,由于高相对湿度条件有利于PM2.5的吸湿增长,并促进多相反应形成SO42-,因此在秋季、冬季和夏季,这些SO42-形成途径的集成明显缩小了国家大气中心三个采样点模拟与观测之间的差距。秋季、冬季和夏季的低估可能是由于错过了光诱导化学途径的 SO42- 来源和错过了有机气溶胶的吸湿性。春季模拟结果与观测结果之间的明显差异可能是由于对 SO2 水平的大幅低估以及缺乏对粉尘方案的考虑。源分配结果表明,气相反应在每个季节 SO42- 的形成过程中都发挥了重要作用。秋季和夏季的相对湿度水平较高,光化学反应活性较强,因此水相 SO2 被 H2O2 氧化的贡献率较高。颗粒界面的 Mn(II)催化 SO2 氧化途径在秋季很重要,在相对湿度极高的冬季严重雾霾事件中对 SO42- 的形成贡献更大。
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来源期刊
Atmospheric Pollution Research
Atmospheric Pollution Research ENVIRONMENTAL SCIENCES-
CiteScore
8.30
自引率
6.70%
发文量
256
审稿时长
36 days
期刊介绍: Atmospheric Pollution Research (APR) is an international journal designed for the publication of articles on air pollution. Papers should present novel experimental results, theory and modeling of air pollution on local, regional, or global scales. Areas covered are research on inorganic, organic, and persistent organic air pollutants, air quality monitoring, air quality management, atmospheric dispersion and transport, air-surface (soil, water, and vegetation) exchange of pollutants, dry and wet deposition, indoor air quality, exposure assessment, health effects, satellite measurements, natural emissions, atmospheric chemistry, greenhouse gases, and effects on climate change.
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