Characteristics, sources and reconstruction of primary & secondary components of PM2.5 in Delhi, India

IF 1.8 4区 地球科学 Q2 ENVIRONMENTAL SCIENCES
Sudhir Kumar Sharma, Sakshi Gupta, Preeti Tiwari, Rubiya Banoo, Akansha Rai, Narayanasamy Vijayan
{"title":"Characteristics, sources and reconstruction of primary & secondary components of PM2.5 in Delhi, India","authors":"Sudhir Kumar Sharma,&nbsp;Sakshi Gupta,&nbsp;Preeti Tiwari,&nbsp;Rubiya Banoo,&nbsp;Akansha Rai,&nbsp;Narayanasamy Vijayan","doi":"10.1007/s10874-025-09479-0","DOIUrl":null,"url":null,"abstract":"<div><p>Atmospheric fine particulate matter (PM<sub>2.5</sub>) constitutes a major component of organics, inorganic and heavy &amp; toxic elements which is increasingly recognized as a significant factor of the tropospheric chemistry of planet Earth due to its ability to influence the planet’s radiative balance. In recent years, PM<sub>2.5</sub> have been associated with declining air quality, negatively impacting both human health and the climate. Understanding the sources and behaviour of aerosols, both primary and secondary, as well as their spatial and temporal distribution, it is essential to evaluate their impact on air quality and climate. In the present study, a total 798 PM<sub>2.5</sub> samples were collected and examined for their chemical speciation [carbon contents (OC and EC), inorganic ionic species (NH<sub>4</sub><sup>+</sup>, Cl<sup>-</sup>, NO<sub>3</sub><sup>-</sup> and SO<sub>4</sub><sup>2-</sup>) and elemental contents (Si, Ti, al, Fe, Zn, Cu, Mn, Pb, As, Br, Cr, Mo and P)] at metropolitan site of Delhi over the period of January 2013 to December 2021. On the basis of long-term analysis, the mean concentrations of total carbon contents (OC:15.5 ± 8.5 µg m<sup>-3</sup> and EC: 7.0 ± 3.9 µg m<sup>-3</sup>), ionic species (Σ ionic species: 35.6 ± 25.6 µg m<sup>-3</sup>) and elements (Σ elements:17.2 ± 8.2 µg m<sup>-3</sup>) were estimated to be 18%, 28.5% and 13.7%, respectively of PM<sub>2.5</sub> (126 ± 77 µg m<sup>-3</sup>) mass concentrations. Since, oxygen and hydrogen are excluded from the present chemical monitoring process, to estimate the reconstructed gravimetric mass of PM<sub>2.5</sub> and to achieve mass closure, the IMPROVE weighting equations were applied. The IMPROVE equation/model resolved the highest mean contribution of PM<sub>2.5</sub> which comes from particulate organic matter (19.3%), followed by soil/crustal matter (17.2%), aged sea salt (13.9%), ammonium sulphate (12.5%), ammonium nitrate (9.4%) and light absorbing carbon (5.6%) with unidentified mass (22.1%). The seasonal variation in reconstructed PM<sub>2.5</sub> mass was also exercised for winter, summer, monsoon and post-monsoon seasons. In the present analysis, the highest contribution of primary organic aerosol (POA) was estimated to be 18% in winter and lowest in monsoon (13%). Whereas the highest contribution of secondary organic aerosols (SOA) was recorded as 10.4% in post-monsoon and lowest in summer (5.7%). The secondary inorganic components were estimated to be 27% in winter, 21% in summer, 23% in monsoon, and 18% in post-monsoon. Notably, the secondary aerosol formation (inorganic 22% and organic 8%) accounted for significant fractions of PM<sub>2.5</sub> mass (up to 30%) than the primary aerosol formation (16%) (total up to 46% of PM<sub>2.5</sub>). Positive Matrix Factorization (PMF) extracted six dominant sources [soil dust (SD: 19%), secondary aerosols (SA: 18%), vehicular emissions (VE: 19%), industrial emissions (IE: 16%), mixed sources (9%), combustion (BB + FFC: 19%)] of PM<sub>2.5</sub> in Delhi, India.</p></div>","PeriodicalId":611,"journal":{"name":"Journal of Atmospheric Chemistry","volume":"82 2","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-08-23","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/s10874-025-09479-0","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

Atmospheric fine particulate matter (PM2.5) constitutes a major component of organics, inorganic and heavy & toxic elements which is increasingly recognized as a significant factor of the tropospheric chemistry of planet Earth due to its ability to influence the planet’s radiative balance. In recent years, PM2.5 have been associated with declining air quality, negatively impacting both human health and the climate. Understanding the sources and behaviour of aerosols, both primary and secondary, as well as their spatial and temporal distribution, it is essential to evaluate their impact on air quality and climate. In the present study, a total 798 PM2.5 samples were collected and examined for their chemical speciation [carbon contents (OC and EC), inorganic ionic species (NH4+, Cl-, NO3- and SO42-) and elemental contents (Si, Ti, al, Fe, Zn, Cu, Mn, Pb, As, Br, Cr, Mo and P)] at metropolitan site of Delhi over the period of January 2013 to December 2021. On the basis of long-term analysis, the mean concentrations of total carbon contents (OC:15.5 ± 8.5 µg m-3 and EC: 7.0 ± 3.9 µg m-3), ionic species (Σ ionic species: 35.6 ± 25.6 µg m-3) and elements (Σ elements:17.2 ± 8.2 µg m-3) were estimated to be 18%, 28.5% and 13.7%, respectively of PM2.5 (126 ± 77 µg m-3) mass concentrations. Since, oxygen and hydrogen are excluded from the present chemical monitoring process, to estimate the reconstructed gravimetric mass of PM2.5 and to achieve mass closure, the IMPROVE weighting equations were applied. The IMPROVE equation/model resolved the highest mean contribution of PM2.5 which comes from particulate organic matter (19.3%), followed by soil/crustal matter (17.2%), aged sea salt (13.9%), ammonium sulphate (12.5%), ammonium nitrate (9.4%) and light absorbing carbon (5.6%) with unidentified mass (22.1%). The seasonal variation in reconstructed PM2.5 mass was also exercised for winter, summer, monsoon and post-monsoon seasons. In the present analysis, the highest contribution of primary organic aerosol (POA) was estimated to be 18% in winter and lowest in monsoon (13%). Whereas the highest contribution of secondary organic aerosols (SOA) was recorded as 10.4% in post-monsoon and lowest in summer (5.7%). The secondary inorganic components were estimated to be 27% in winter, 21% in summer, 23% in monsoon, and 18% in post-monsoon. Notably, the secondary aerosol formation (inorganic 22% and organic 8%) accounted for significant fractions of PM2.5 mass (up to 30%) than the primary aerosol formation (16%) (total up to 46% of PM2.5). Positive Matrix Factorization (PMF) extracted six dominant sources [soil dust (SD: 19%), secondary aerosols (SA: 18%), vehicular emissions (VE: 19%), industrial emissions (IE: 16%), mixed sources (9%), combustion (BB + FFC: 19%)] of PM2.5 in Delhi, India.

印度德里地区PM2.5一、二次分量特征、来源及重建
大气细颗粒物(PM2.5)是有机、无机和重毒性元素的主要组成部分,由于其影响地球辐射平衡的能力,越来越被认为是地球对流层化学的重要因素。近年来,PM2.5与空气质量下降有关,对人类健康和气候都有负面影响。了解初级和次级气溶胶的来源和行为,以及它们的时空分布,对于评估它们对空气质量和气候的影响至关重要。本研究在2013年1月至2021年12月期间,在德里市区共收集了798个PM2.5样本,并对其化学形态[碳含量(OC和EC),无机离子种类(NH4+, Cl-, NO3-和SO42-)和元素含量(Si, Ti, al, Fe, Zn, Cu, Mn, Pb, As, Br, Cr, Mo和P)]进行了检测。根据长期分析,总碳含量(OC:15.5±8.5µg m-3, EC: 7.0±3.9µg m-3)、离子种类(Σ: 35.6±25.6µg m-3)和元素(Σ:17.2±8.2µg m-3)的平均浓度分别为PM2.5(126±77µg m-3)质量浓度的18%、28.5%和13.7%。由于目前的化学监测过程中不包括氧和氢,为了估计PM2.5的重建重量质量并实现质量闭合,我们采用了改进加权方程。根据改进方程/模型,PM2.5的平均贡献最高,来自颗粒物有机质(19.3%),其次是土壤/地壳物质(17.2%)、陈年海盐(13.9%)、硫酸铵(12.5%)、硝酸铵(9.4%)和质量不明的吸光碳(5.6%)(22.1%)。对重建PM2.5质量进行了冬季、夏季、季风和季风后季节的季节变化分析。在目前的分析中,估计冬季一次有机气溶胶(POA)的贡献最高为18%,季风最低(13%)。次生有机气溶胶(SOA)的贡献率在季风后最高,为10.4%,夏季最低,为5.7%。次生无机组分冬季占27%,夏季占21%,季风期占23%,后季风期占18%。值得注意的是,二次气溶胶形成(无机22%和有机8%)占PM2.5质量的比例(高达30%)显著高于一次气溶胶形成(16%)(总计高达PM2.5的46%)。正矩阵分解(PMF)提取了印度德里PM2.5的6个主要来源[土壤粉尘(SD: 19%)、二次气溶胶(SA: 18%)、车辆排放(VE: 19%)、工业排放(IE: 16%)、混合源(9%)、燃烧(BB + FFC: 19%)]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Atmospheric Chemistry
Journal of Atmospheric Chemistry 地学-环境科学
CiteScore
4.60
自引率
5.00%
发文量
16
审稿时长
7.5 months
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信