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Discrimination of Euro 5 gasoline vs. Diesel light-duty engine primary and secondary particle emissions using multivariate statistical analysis of high-resolution mass spectrometry (HRMS) fingerprint

汽油 指纹(计算) 多元统计 柴油 多元分析 环境科学 分辨率(逻辑) 小学(天文学) 粒子(生态学) 化学 分析化学(期刊) 汽车工程 色谱法 统计 计算机科学 数学 工程类 人工智能 物理 地质学 有机化学 海洋学 天文
作者
Camille Noblet,François Lestremau,Adrien Dermigny,Nicolas Karoski,Claudine Chatellier,Jérôme Beaumont,Yao Liu,Boris Vansevenant,Jean‐Luc Besombes,Alexandre Albinet
标识
DOI:10.5194/ar-2025-25
摘要

Abstract. Emissions from gasoline and diesel vehicles are predominant anthropogenic sources in ambient air, and their accurate source apportionment is a major concern for air quality policymakers aiming to implement effective strategies to reduce air pollution. Recent studies indicate that particulate matter (PM) emissions from modern cars equipped with the latest after-treatment technologies are mainly related to secondary organic aerosol (SOA) production, particularly in the case of gasoline vehicles. However, distinguishing in ambient air between emissions from gasoline and Diesel vehicles remains challenging and is rarely achieved. This study aimed to evaluate the potential of non–targeted screening (NTS) analyses for determining specific organic molecular markers of primary organic aerosols (POA) and SOA from gasoline and Diesel vehicles, which could enhance PM source apportionment efforts. Experiments were conducted using a chassis dynamometer with Euro 5 gasoline and Diesel vehicles under three different driving cycles. Exhaust emissions were diluted before being introduced into a potential aerosol mass oxidation flow reactor (PAM-OFR) to simulate atmospheric aging and SOA formation. Samples were collected both upstream and downstream of the PAM-OFR and analysed using NTS approaches with liquid- and gas-chromatography coupled to quadrupole time-of-flight mass spectrometry (LC- and GC-QToF-MS). The chemical fingerprints obtained were compared using multivariate statistical analyses, including principal component analysis (PCA), hierarchical clustering analysis (HCA), and partial least square discriminant analysis (PLS-DA). Results revealed specific fingerprints of POA and SOA for each type of vehicle tested and about 10 markers unique to each fraction of Diesel and gasoline vehicles. This study demonstrates the promise of combining high-resolution mass spectrometry based NTS with advanced multivariate statistical analyses to differentiate OA fingerprints and discover specific markers of Diesel and gasoline vehicular sources for further use in PM source apportionment studies.

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