{"title":"Atmospheric Imidazole Formation: Unraveling the Roles of Precursors, Humidity, and Aerosol Acidity","authors":"Huifeng Xu, Tong Sun, Yunyun Wang, Lingjia Wang, Linghong Chen, Xiang Gao, Kefa Cen","doi":"10.1016/j.envpol.2025.127214","DOIUrl":null,"url":null,"abstract":"To analyze the physicochemical properties and formation mechanisms of atmospheric imidazole-containing particles, a single-particle aerosol mass spectrometer (SPAMS) was employed to sample particulate matter in a major city in eastern China from December 19, 2018, to January 19, 2019. Throughout the monitoring period, particles containing carbonyls (183,952), amines and carbonyls (64,019), and imidazole (120,429) were collected. Four pollution episodes (E1-E4) and three clean periods (C1-C3) were identified based on increases in dominant precursor carbonyl particle concentrations. During pollution episodes, carbonyl-containing, amine-carbonyl mixed and imidazole-containing particles increased by 79.4%, 43.3%, and 61.9% on average, respectively. Relative humidity between 50%-70% and aerosol acidity in the range of 20-30 facilitated the conversion of carbonyl and amine/ammonium precursors into imidazole. Notably, glyoxal and methylglyoxal exhibited higher uptake rates under RH < 70%. Precursor particles peaked during the daytime. Imidazole particle concentrations were elevated at night, reflecting reduced photolysis and contributions from secondary formation processes. Principal component analysis (PCA) identified four factors, explaining 81.0% of the total variance. PC1 (41.0%) revealed C<sub>2</sub>HO<sub>3</sub><sup>-</sup>, NH<sub>4</sub>HSO<sub>4</sub>, and DEA as key precursors. Factor loading analysis across different periods revealed that imidazole formation is a multi-factor process influenced by precursor composition and environmental parameters.","PeriodicalId":311,"journal":{"name":"Environmental Pollution","volume":"158 1","pages":""},"PeriodicalIF":7.3000,"publicationDate":"2025-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Pollution","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1016/j.envpol.2025.127214","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENVIRONMENTAL SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
To analyze the physicochemical properties and formation mechanisms of atmospheric imidazole-containing particles, a single-particle aerosol mass spectrometer (SPAMS) was employed to sample particulate matter in a major city in eastern China from December 19, 2018, to January 19, 2019. Throughout the monitoring period, particles containing carbonyls (183,952), amines and carbonyls (64,019), and imidazole (120,429) were collected. Four pollution episodes (E1-E4) and three clean periods (C1-C3) were identified based on increases in dominant precursor carbonyl particle concentrations. During pollution episodes, carbonyl-containing, amine-carbonyl mixed and imidazole-containing particles increased by 79.4%, 43.3%, and 61.9% on average, respectively. Relative humidity between 50%-70% and aerosol acidity in the range of 20-30 facilitated the conversion of carbonyl and amine/ammonium precursors into imidazole. Notably, glyoxal and methylglyoxal exhibited higher uptake rates under RH < 70%. Precursor particles peaked during the daytime. Imidazole particle concentrations were elevated at night, reflecting reduced photolysis and contributions from secondary formation processes. Principal component analysis (PCA) identified four factors, explaining 81.0% of the total variance. PC1 (41.0%) revealed C2HO3-, NH4HSO4, and DEA as key precursors. Factor loading analysis across different periods revealed that imidazole formation is a multi-factor process influenced by precursor composition and environmental parameters.
期刊介绍:
Environmental Pollution is an international peer-reviewed journal that publishes high-quality research papers and review articles covering all aspects of environmental pollution and its impacts on ecosystems and human health.
Subject areas include, but are not limited to:
• Sources and occurrences of pollutants that are clearly defined and measured in environmental compartments, food and food-related items, and human bodies;
• Interlinks between contaminant exposure and biological, ecological, and human health effects, including those of climate change;
• Contaminants of emerging concerns (including but not limited to antibiotic resistant microorganisms or genes, microplastics/nanoplastics, electronic wastes, light, and noise) and/or their biological, ecological, or human health effects;
• Laboratory and field studies on the remediation/mitigation of environmental pollution via new techniques and with clear links to biological, ecological, or human health effects;
• Modeling of pollution processes, patterns, or trends that is of clear environmental and/or human health interest;
• New techniques that measure and examine environmental occurrences, transport, behavior, and effects of pollutants within the environment or the laboratory, provided that they can be clearly used to address problems within regional or global environmental compartments.