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利用气溶胶化学形态监测驱动因子分析探索德里亚微米气溶胶的化学成分和过程。

Exploring the chemical composition and processes of submicron aerosols in Delhi using aerosol chemical speciation monitor driven factor analysis.

作者信息

Panda Upasana, Dey Supriya, Sharma Amit, Singh Aishwarya, Reyes-Villegas Ernesto, Darbyshire Eoghan, Carbone Samara, Das Trupti, Allan James, McFiggans Gordon, Ravikrishna R, Coe Hugh, Liu Pengfei, Gunthe Sachin S

机构信息

EE Division, Department of Civil Engineering, Indian Institute of Technology Madras, Chennai, India.

Department of Environment and Sustainability, CSIR-Institute of Minerals and Materials Technology, Bhubaneswar, India.

出版信息

Sci Rep. 2025 Apr 24;15(1):14383. doi: 10.1038/s41598-025-99245-9.

Abstract

Wintertime non-refractory submicron particulate matter (NR-PM) species were measured in Delhi with an Aerodyne Aerosol Chemical Speciation Monitor (ACSM) during February-March 2018. The average NR-PM mass concentration throughout the study was 58.0 ± 42.6 µg m, where the contribution of organic aerosol (OA) was 69% of the total NR-PM. In Delhi, chloride (10%) was the main inorganic contributor, followed by ammonium (8%), sulfate (7%), and nitrate (6%), contrasting with the prevalence of sulfate in most urban environments. Source apportionment analysis of the OA identified five major factors, including three primary contributors: hydrocarbon-like OA (HOA), biomass burning OA (BBOA), cooking-related OA (COA) and two secondary contributors: oxygenated primary OA (OPOA), and more-oxidized oxygenated OA (MO-OOA). A 19% rise in OPOA concentration was observed during high chloride episodes, suggesting the potential role of chloride in the atmospheric chemical transformation of OA. Traffic emissions significantly contribute to ambient OA, accounting for at least 41% of the total OA mass. Furthermore, the OA exhibited low oxidation levels regardless of its source. The f:f analysis revealed slower atmospheric oxidization of OA compared to other urban locations worldwide. Further investigations, including chamber experiments tailored to the Delhi atmosphere, are necessary to elucidate the atmospheric oxidants and the genesis of secondary OA alongside primary emissions.

摘要

2018年2月至3月期间,在德里使用Aerodyne气溶胶化学形态监测仪(ACSM)对冬季非难熔亚微米颗粒物(NR-PM)物种进行了测量。在整个研究过程中,NR-PM的平均质量浓度为58.0±42.6µg/m³,其中有机气溶胶(OA)占总NR-PM的69%。在德里,氯化物(10%)是主要的无机成分,其次是铵(8%)、硫酸盐(7%)和硝酸盐(6%),这与大多数城市环境中硫酸盐的普遍情况形成对比。对OA的源解析分析确定了五个主要因素,包括三个主要贡献者:类烃OA(HOA)、生物质燃烧OA(BBOA)、烹饪相关OA(COA)以及两个次要贡献者:氧化初级OA(OPOA)和更氧化的氧化OA(MO-OOA)。在高氯化物事件期间,观察到OPOA浓度上升了19%,这表明氯化物在OA的大气化学转化中可能发挥作用。交通排放对环境中的OA有显著贡献,至少占总OA质量的41%。此外,无论其来源如何,OA的氧化水平都较低。f:f分析表明,与全球其他城市地区相比,OA在大气中的氧化速度较慢。需要进一步的研究,包括针对德里大气的腔室实验,以阐明大气氧化剂以及与一次排放同时存在的二次OA的成因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ccb/12022066/930765cf2edd/41598_2025_99245_Fig1_HTML.jpg

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