Particulate matter (PM) is a major factor contributing to air quality deterioration that enters the atmosphere as a consequence of various natural and anthropogenic activities. In PM, polycyclic aromatic hydrocarbons (PAHs) represent a class of organic chemicals with at least two aromatic rings that are mainly directly emitted via the incomplete combustion of various organic materials. Numerous toxicological and epidemiological studies have proven adverse links between exposure to particulate matter-bound (PM-bound) PAHs and human health due to their carcinogenicity and mutagenicity. Among human exposure routes, inhalation is the main pathway regarding PM-bound PAHs in the atmosphere. Moreover, the concentrations of PM-bound PAHs differ among people, microenvironments and areas. Hence, understanding the behaviour of PM-bound PAHs in the atmosphere is crucial. However, because current techniques hardly monitor PAHs in real-time, timely feedback on PAHs including the characteristics of their concentration and composition, is not obtained via real-time analysis methods. Therefore, in this review, we summarize personal exposure, and indoor and outdoor PM-bound PAH concentrations for different participants, spaces, and cities worldwide in recent years. The main aims are to clarify the characteristics of PM-bound PAHs under different exposure conditions, in addition to the health effects and assessment methods of PAHs.

Polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs (NPAHs) in PM_2.5 samples were collected at a roadside monitoring station in Kanazawa, Japan, in every season from 2017 to 2018. Nine PAHs and five NPAHs were determined using high-performance liquid chromatography with fluorescence detection and chemiluminescence detection, respectively. The mean concentrations of PAHs and NPAHs were highest in winter and lowest in summer. Fluoranthene and pyrene were the dominant PAHs and 1-nitropyrene was the dominant NPAH in all seasons, and these compounds were mainly emitted by diesel vehicles. The concentration ratio of benzo(a)pyrene (BaP) to benzo(ghi)perylene (BgPe) ((BaP)/(BgPe)) and of indeno(1,2,3-cd)pyrene (IDP) to the sum of IDP and benzo(ghi)perylene (BgPe) ((IDP)/((IDP)+(BgPe0) might still be useful indicators for identifying traffic emission sources today. Moreover, our results showed that the carcinogenic risk in all seasons was below the acceptable limit set by the WHO.

Polycyclic aromatic hydrocarbons (PAHs) are a class of important organic pollutants widely emitted from anthropogenic activities, with a general distribution in the gas and particulate phases. Some PAHs are carcinogenic, teratogenic, and mutagenic. Inhalation exposure to PAHs is correlated with adverse health outcomes in the respiratory and cardiovascular systems. Thus, it is significant to determine the exposure level of the general population. This study summarizes the evaluation methods for PAH exposure, focusing on different exposure parameters. External exposure can be determined via the collection of the environmental pollution concentration through active samplers or passive samplers during environmental monitoring or personal sampling. Time-activity patterns give critical exposure information that captures the exposure period, origin, and behaviors. Modeling is a labor-less approach for human exposure estimation, and microenvironmental exposure requires specific research. It is important to select appropriate methods to quantify the exposure level to provide accurate data to establish the exposure–risk relationship and make scientific suggestions for the protection of public health.

Particulate matter (PM) was collected in three different areas, SY-1, SY-2, and SY-3, in Shenyang, China, during the warm and cold seasons from 2012 to 2014. SY-1 was located beside a thermal power plant, far from the central area. SY-2 was near a coal heating boiler on the main road, close to the central area. SY-3 was on the main road, without fixed emission sources. Nine PM-bound polycyclic aromatic hydrocarbons (PAHs) were analyzed. The results showed that the mean concentration of total PAHs was higher in the cold season (92.6–316 ng m⁻³) than in the warm season (18.4–32.2 ng m⁻³). Five- and six-ring PAHs occupied a large percentage at all sites in the warm season, and four-ring PAHs were the dominant components in the cold season. Several diagnostic PAH ratios indicated that the main sources of PAHs in Shenyang in the warm and cold seasons were not only coal burning but also vehicle emission. In this study, we suggest that a benzo[a]pyrene/benzo[ghi]perylene ratio ([BaP]/[BgPe]) of 0.6 was a useful indicator to speculate the relative significance of coal burning and vehicle exhaust. Although the Shenyang government has undertaken actions to address air pollution, the PM and PAH concentrations did not decrease significantly compared to those in our previous studies. The cancer risk calculated from the BaP equivalent total concentration at all three sites in the warm and cold seasons exceeded the acceptable limit established by the US EPA.

Background: Background sites are mainly affected by long-range-transported air pollutants, resulting in potential adverse effects on local atmospheric environments. A 4–5 year observational study was conducted to illustrate the air pollution profile at the Kanazawa University Wajima air monitoring station (KUWAMS), an ideal remote background site in Japan. Methods: Nine polycyclic aromatic hydrocarbons (PAHs) in the particulate phase and various air pollutants were continuously monitored for 4–5 years. Diagnostic ratios of PAHs and back-trajectory analysis were applied to trace the possible sources of the air pollutants collected at the sampling site. Results: The atmospheric concentration of PAHs in the atmosphere at the site decreased from 2014 to 2019, benefit from the predominant air pollution control policy in China and Japan. Common air pollutants including sulfur dioxide (SO₂), nitrogen oxides (NO_x), ozone, methane (CH₄), and non-methane hydrocarbon (NMHC) were detected in low concentrations from 2016 to 2019, while ozone (O₃) and particulate matter (PM_2.5, PM with a diameter less than 2.5 μm) were present in high levels that exceeded the Japanese standards. Most air pollutants peaked in spring and showed evident diurnal variations in spring and summer. Conclusions: This is the first study to clarify the atmospheric behaviors of multiple air pollutants at a background site in Japan. Significant external air pollutant impact and unneglectable air pollution were demonstrated at KUWAMS, indicating the importance of studying atmospheric pollution at remote sites.

Daily PM_2.5 (particulate matter with aerodynamic diameter ≤2.5 μm) samples were simultaneously collected at two background sites (Wajima Air Monitoring Station (WAMS) and Fukue-Jima Atmosphere and Aerosol Monitoring Station (FAMS)) in Japan in the East Asian winter and summer monsoon periods of 2017 and 2019, to compare the characteristics of air pollutants among different regions and to determine the possible variation during the long-range transport process. Polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs (NPAHs), and water-soluble inorganic ions (WSIIs) were analyzed. Despite the PM_2.5 concentrations at FAMS (8.90–78.5 µg/m³) being higher than those at WAMS (2.33–21.2 µg/m³) in the winter monsoon period, the average concentrations of ∑PAHs, ∑NPAHs, and ∑WSIIs were similar between the two sites. Diagnostic ratios indicated PAHs mainly originated from traffic emissions and mostly aged, whereas NPAHs were mostly secondarily formed during long-range transport. WSIIs at WAMS were mainly formed via the combustion process and secondary reactions, whereas those at FAMS mainly originated from sea salt and dust. Backward trajectories revealed the air masses could not only come from Asian continental coastal regions but also distant landlocked areas in the winter monsoon period, whereas most came from the ocean in the summer monsoon period. These findings can provide basic data for the establishment of prediction models of transboundary air pollutants in East Asia.