{"title":"From clean air to severe haze: evolution of PM₂.₅ and water-soluble ions during a firework-influenced pollution episode","authors":"Zhendong Ke, Peipei Shao, Changlin Zhan, Chong Wei, Ziguo Liu, Ting Liu, Shan Liu","doi":"10.1007/s10874-026-09492-x","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>A severe air pollution episode occurred in Huangshi City, central China, during February 2024, coinciding with intensive Spring Festival fireworks. To investigate the chemical processes, PM₂.₅ mass and water-soluble inorganic ions (WSIIs) were analyzed in conjunction with ionic balance, correlation, and backward trajectory models. The episode exhibited three distinct phases. In the pre-pollution stage (February 5–8), PM₂.₅ remained stable around 60 µg/m³, with secondary inorganic aerosols (NO₃⁻, SO₄²⁻, NH₄⁺) as the major components under humid and stagnant conditions conducive to secondary aerosol formation. During the pollution peak (February 9–10), concentrations approached 800 µg/m³ due to firework emissions and stagnant conditions. Ion composition shifted markedly, with sharp increases in K⁺, Cl⁻, and Mg²⁺, concurrent decreases in NO₃⁻ and NH₄⁺, and a low neutralization ratio, indicating strongly acidic aerosols dominated by fireworks-derived sulfate. Ozone depletion further suppressed photochemistry and secondary aerosol production. In the post-pollution stage (February 11–14), improved dispersion and reduced emissions lowered PM₂.₅ to background levels, while NO₃⁻ and NH₄⁺ rebounded and dust-related ions (Ca²⁺, Mg²⁺) increased. Backward trajectory clustering revealed that northern transport contributed during the clean phase, local stagnation dominated the pollution peak, and mixed inflows supported atmospheric cleansing thereafter. These findings demonstrate that episodic fireworks can significantly reshape aerosol composition and acidity, with meteorological conditions determining the severity of pollution episodes.</p>\n </div>","PeriodicalId":611,"journal":{"name":"Journal of Atmospheric Chemistry","volume":"83 1","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2026-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Atmospheric Chemistry","FirstCategoryId":"89","ListUrlMain":"https://link.springer.com/article/10.1007/s10874-026-09492-x","RegionNum":4,"RegionCategory":"地球科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
A severe air pollution episode occurred in Huangshi City, central China, during February 2024, coinciding with intensive Spring Festival fireworks. To investigate the chemical processes, PM₂.₅ mass and water-soluble inorganic ions (WSIIs) were analyzed in conjunction with ionic balance, correlation, and backward trajectory models. The episode exhibited three distinct phases. In the pre-pollution stage (February 5–8), PM₂.₅ remained stable around 60 µg/m³, with secondary inorganic aerosols (NO₃⁻, SO₄²⁻, NH₄⁺) as the major components under humid and stagnant conditions conducive to secondary aerosol formation. During the pollution peak (February 9–10), concentrations approached 800 µg/m³ due to firework emissions and stagnant conditions. Ion composition shifted markedly, with sharp increases in K⁺, Cl⁻, and Mg²⁺, concurrent decreases in NO₃⁻ and NH₄⁺, and a low neutralization ratio, indicating strongly acidic aerosols dominated by fireworks-derived sulfate. Ozone depletion further suppressed photochemistry and secondary aerosol production. In the post-pollution stage (February 11–14), improved dispersion and reduced emissions lowered PM₂.₅ to background levels, while NO₃⁻ and NH₄⁺ rebounded and dust-related ions (Ca²⁺, Mg²⁺) increased. Backward trajectory clustering revealed that northern transport contributed during the clean phase, local stagnation dominated the pollution peak, and mixed inflows supported atmospheric cleansing thereafter. These findings demonstrate that episodic fireworks can significantly reshape aerosol composition and acidity, with meteorological conditions determining the severity of pollution episodes.
期刊介绍:
The Journal of Atmospheric Chemistry is devoted to the study of the chemistry of the Earth''s atmosphere, the emphasis being laid on the region below about 100 km. The strongly interdisciplinary nature of atmospheric chemistry means that it embraces a great variety of sciences, but the journal concentrates on the following topics:
Observational, interpretative and modelling studies of the composition of air and precipitation and the physiochemical processes in the Earth''s atmosphere, excluding air pollution problems of local importance only.
The role of the atmosphere in biogeochemical cycles; the chemical interaction of the oceans, land surface and biosphere with the atmosphere.
Laboratory studies of the mechanics in homogeneous and heterogeneous transformation processes in the atmosphere.
Descriptions of major advances in instrumentation developed for the measurement of atmospheric composition and chemical properties.