Multi-class organic pollutants in atmospheric particulate matter (PM2.5) from a Southwestern Europe industrial area: Levels, sources and human health risk

Joel Sánchez-Piñero; Natalia Novo-Quiza; Jorge Moreda-Piñeiro; Isabel Turnes-Carou; Soledad Muniategui-Lorenzo; Purificación López-Mahía

doi:10.1016/j.envres.2022.114195

Multi-class organic pollutants in atmospheric particulate matter (PM_2.5) from a Southwestern Europe industrial area: Levels, sources and human health risk

Environ Res. 2022 Nov;214(Pt 4):114195. doi: 10.1016/j.envres.2022.114195. Epub 2022 Aug 27.

Authors

Joel Sánchez-Piñero¹, Natalia Novo-Quiza², Jorge Moreda-Piñeiro², Isabel Turnes-Carou², Soledad Muniategui-Lorenzo², Purificación López-Mahía²

Affiliations

¹ University of A Coruña. Grupo Química Analítica Aplicada (QANAP), Instituto Universitario de Medio Ambiente (IUMA), Department of Chemistry. Faculty of Sciences. Campus de A Coruña, s/n. 15071, A Coruña, Spain. Electronic address: joel.sanchez@udc.es.
² University of A Coruña. Grupo Química Analítica Aplicada (QANAP), Instituto Universitario de Medio Ambiente (IUMA), Department of Chemistry. Faculty of Sciences. Campus de A Coruña, s/n. 15071, A Coruña, Spain.

PMID: 36030919
DOI: 10.1016/j.envres.2022.114195

Abstract

The occurrence of 50 multi-class pollutants comprising 18 polycyclic aromatic hydrocarbons (PAHs), 12 phthalate esters (PAEs), 12 organophosphorus flame retardants (OPFRs), 6 synthetic musk compounds (SMCs) and 2 bisphenols was studied in atmospheric particulate matter (PM_2.5) samples collected at an industrial area focused on automotive manufacturing located at the Southwestern Atlantic European region (Vigo city, Spain) during 1-year period. Among all quantitated pollutants in PM_2.5 samples, bisphenol A (BPA) was the most predominant with an average concentration of 6180 pg m^-3, followed by PAHs comprising benzo(b+j)fluoranthene (BbF + BjF) and benzo(g,h,i)perylene (BghiP), accounting for 546 pg m^-3 and 413 pg m^-3 respectively. In addition, two OPFRs concerning tris(chloropropyl) phosphate (TCPP) and triphenyl phosphine oxide (TPPO) were the next following the concentration order, accounting for 411 pg m^-3 and 367 pg m^-3 respectively; being butyl benzyl phthalate (BBP) the most profuse PAE (56.1 pg m^-3 by average). High relative standard deviations (RSDs) were observed during the whole sampling period, while statistically significant differences were only observed for PAHs concentrations during cold and warm seasons. Furthermore, some water-soluble ions and metal(oid)s were analysed in PM_2.5 samples to be used as PM source tracers, whose concentrations were quite below the target levels set in the current legislation. Data obtained from principal component analysis (PCA) and PAHs molecular indices suggested a pyrogenic and petrogenic origin for PAHs, whereas occurrence of the remaining compounds seems to be attributed to resources used in the automotive industrial activity settled in the sampling area. Moreover, although a substantial anthropogenic source to PM_2.5 in the area was observed, marine and soil resuspension contributions were also accounted. Finally, carcinogenic and non-carcinogenic risks posed by PM_2.5-bound pollutants inhalation were assessed, being both averages within the safe level considering the whole period.

Keywords: Fine particulate matter; Health risk assessment; Industrial chemicals; Organic pollutants; PM source Apportionment; Seasonal trends.

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Air Pollutants* / analysis
China
Environmental Monitoring
Environmental Pollutants* / analysis
Humans
Particulate Matter / analysis
Polycyclic Aromatic Hydrocarbons* / analysis
Risk Assessment
Seasons

Substances

Air Pollutants
Environmental Pollutants
Particulate Matter
Polycyclic Aromatic Hydrocarbons