{"title":"Strong Impacts of Regional Atmospheric Transport on the Vertical Distribution of Aerosol Ammonium over Beijing","authors":"Ting Yang, Hongyi Li, Wenqing Xu, Yifan Song, Lei Xu, Haibo Wang, Futing Wang, Yele Sun, Zifa Wang* and Pingqing Fu*, ","doi":"10.1021/acs.estlett.3c00791","DOIUrl":null,"url":null,"abstract":"<p >Ammonium (NH<sub>4</sub><sup>+</sup>) is a significant component of fine aerosol particles (PM<sub>2.5</sub>), and its behavior in the atmosphere is crucial to air pollution. We present a novel study that analyzes the vertical distribution and temporal trends of NH<sub>4</sub><sup>+</sup> in the urban boundary layer of Beijing, tracking hourly concentrations throughout a complete haze episode. Our results unveil a surprising single-peak profile of NH<sub>4</sub><sup>+</sup> at heights of 300–700 m in the urban boundary layer with its hourly concentration reaching ∼50 μg m<sup>–3</sup>, which is 3 times higher than that at the ground level, in contrast to the conventional patterns of decreasing concentrations with height. The vertical structure is closely related to the observed escape of ammonia (NH<sub>3</sub>) or NH<sub>4</sub><sup>+</sup> from upwind industrial sources via elevated chimneys. The NH<sub>4</sub><sup>+</sup> plumes emitted through these sources are prone to transport at an altitude of 270–750 m for approximately 6 h, covering >250 km to Beijing. This study reveals that non-agricultural point emissions of NH<sub>4</sub><sup>+</sup> impact the vertical patterns of aerosol NH<sub>4</sub><sup>+</sup> in the urban boundary layer, demonstrating potential opportunities for limiting such emission sources to curb PM<sub>2.5</sub> pollution in the North China Plain.</p>","PeriodicalId":37,"journal":{"name":"Environmental Science & Technology Letters Environ.","volume":null,"pages":null},"PeriodicalIF":8.9000,"publicationDate":"2023-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Environmental Science & Technology Letters Environ.","FirstCategoryId":"1","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.estlett.3c00791","RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, ENVIRONMENTAL","Score":null,"Total":0}
引用次数: 0
Abstract
Ammonium (NH4+) is a significant component of fine aerosol particles (PM2.5), and its behavior in the atmosphere is crucial to air pollution. We present a novel study that analyzes the vertical distribution and temporal trends of NH4+ in the urban boundary layer of Beijing, tracking hourly concentrations throughout a complete haze episode. Our results unveil a surprising single-peak profile of NH4+ at heights of 300–700 m in the urban boundary layer with its hourly concentration reaching ∼50 μg m–3, which is 3 times higher than that at the ground level, in contrast to the conventional patterns of decreasing concentrations with height. The vertical structure is closely related to the observed escape of ammonia (NH3) or NH4+ from upwind industrial sources via elevated chimneys. The NH4+ plumes emitted through these sources are prone to transport at an altitude of 270–750 m for approximately 6 h, covering >250 km to Beijing. This study reveals that non-agricultural point emissions of NH4+ impact the vertical patterns of aerosol NH4+ in the urban boundary layer, demonstrating potential opportunities for limiting such emission sources to curb PM2.5 pollution in the North China Plain.
期刊介绍:
Environmental Science & Technology Letters serves as an international forum for brief communications on experimental or theoretical results of exceptional timeliness in all aspects of environmental science, both pure and applied. Published as soon as accepted, these communications are summarized in monthly issues. Additionally, the journal features short reviews on emerging topics in environmental science and technology.