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Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation
Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation
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Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation
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Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation
Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation

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Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation
Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation
Journal Article

Temporal and Machine Learning-Based Principal Component and Clustering Analysis of VOCs and Their Role in Urban Air Pollution and Ozone Formation

2025
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Overview
This study investigates the temporal dynamics, sources, and photochemical behaviour of key volatile organic compounds (VOCs) along Marylebone Road, London (1 January 2015–1 January 2023), a heavily trafficked urban area. Hourly measurements of benzene, toluene, ethylbenzene, ethene, propene, isoprene, propane, and ethyne, alongside ozone (O3) and meteorological data, were analysed using correlation matrices, regression, cross-correlation, diurnal/seasonal analysis, wind-sector analysis, PCA (Principal Component Analysis), and clustering. Strong inter-VOC correlations (e.g., benzene–ethylbenzene: r = 0.86, R2 = 0.75; ethene–propene: r = 0.68, R2 = 0.53) highlighted dominant vehicular sources. Diurnal peaks of benzene, toluene, and ethylbenzene aligned with rush hours, while O3 minima occurred in early mornings due to NO titration. VOCs peaked in winter under low mixing heights, whereas O3 was highest in summer. Wind-sector analysis revealed dominant VOC emissions from SSW (south-southwest)–WSW (west-southwest) directions; ethyne peaked from the E (east)/ENE (east-northeast). O3 concentrations were highest under SE (southeast)–SSE (south-southeast) flows. PCA showed 39.8% of variance linked to traffic-related VOCs (PC1) and 14.8% to biogenic/temperature-driven sources (PC2). K-means clustering (k = 3) identified three regimes: high VOCs/low O3 in stagnant, cool air; mixed conditions; and low VOCs/high O3 in warmer, aged air masses. Findings highlight complex VOC–O3 interactions and stress the need for source-specific mitigation strategies in urban air quality management.