Polycyclic Aromatic Hydrocarbons In PM2 Research Articles

A comprehensive examination of temporal-seasonal variations of PM1.0 and PM2.5 in taiwan before and during the COVID-19 lockdown

COVID-19 has been a significant global concern due to its contagious nature. In May 2021, Taiwan experienced a severe outbreak, leading the government to enforce strict Pandemic Alert Level 3 restrictions in order to curtail its spread. Although previous studies in Taiwan have examined the effects of these measures on air quality, further research is required to compare different time periods and assess the health implications of reducing particulate matter during the Level 3 lockdown. Herein, we analyzed the mass concentrations, chemical compositions, seasonal variations, sources, and potential health risks of PM1.0 and PM2.5 in Central Taiwan before and during the Level 3 lockdown. As a result, coal-fired boilers (47%) and traffic emissions (53%) were identified as the predominant sources of polycyclic aromatic hydrocarbons (PAHs) in PM1.0, while in PM2.5, the dominant sources of PAHs were coal-fired boilers (28%), traffic emissions (50%), and iron and steel sinter plants (22.1%). Before the pandemic, a greater value of 20.9 ± 6.92 μg/m3 was observed for PM2.5, which decreased to 15.3 ± 2.51 μg/m3 during the pandemic due to a reduction in industrial and anthropogenic emissions. Additionally, prior to the pandemic, PM1.0 had a contribution rate of 79% to PM2.5, which changed to 89% during the pandemic. Similarly, BaPeq values in PM2.5 exhibited a comparable trend, with PM1.0 contributing 86% and 65% respectively. In both periods, the OC/EC ratios for PM1.0 and PM2.5 were above 2, due to secondary organic compounds. The incremental lifetime cancer risk (ILCR) of PAHs in PM2.5 decreased by 4.03 × 10-5 during the pandemic, with PM1.0 contributing 73% due to reduced anthropogenic activities.

Coal and biomass combustion emissions increase the cancer and health risks of polycyclic aromatic hydrocarbons in PM2.5 from Nanchang, central China

This study collected 365 daily PM2.5 samples from Nanchang City and analysed the characteristics, sources, and risks of polycyclic aromatic hydrocarbons (PAHs). The findings indicated that the yearly average ΣPAH concentration (the sum of 15 PAHs) was 7.20 ± 4.52 ng m−3, with the highest concentration in winter (12.24 ± 4.95 ng m−3), followed by autumn (7.05 ± 3.1 ng m−3), spring (5.85 ± 2.47 ng m−3) and summer (3.76 ± 1.72 ng m−3). The molecular characteristics and diagnostic ratios analysis suggested that the PAHs originated from vehicle exhaust, combustion (coal and biomass), and petroleum volatilisation. The results of quantitative estimation showed that vehicle exhaust and combustion sources contributed the most (about 43% and 40%) to PAHs. The petroleum industry accounted for a smaller proportion, approximately 17%. Seasonally, combustion sources (coal and biomass) contributed more in winter (56%) and autumn (51%), whereas vehicle exhaust contributed more in summer (51%) and spring (54%). High atmospheric pressure inhibited the diffusion of PAHs but high temperatures may have promoted PAH decomposition. The results of the risk assessment showed that Nanchang residents exposed to PAHs face a potentially low carcinogenic risk but a definite non-carcinogenic health risk during autumn and winter. Furthermore, adults had greater cancer and health risks compared to children. During autumn and winter, it is probable that combustion emissions were the primary contributing factor to risks of PAHs.

Characteristics of Polycyclic Aromatic Hydrocarbons in Size-Resolved Particles in the Roadside Environment of Beijing: Seasonality, Source, and Toxicological Effects

The polycyclic aromatic hydrocarbons (PAHs) in size-resolved particles emitted from diverse sources are required for quantification to reduce the emissions in order to protect public health. Twenty-four PAHs in size-segregated particles in the roadside environment of Beijing were observed from 1 October 2021 to 30 September 2022. The size distributions of PAHs were bimodal, with peak concentrations ranging from size fractions of 0.43 to 0.65 μm and 4.7 to 5.8 μm in all four seasons, respectively. The highest concentration of PAHs in fine particles (PM2.1) was 35.3 ng m−3 in winter, followed by 16.0 ng m−3 in autumn, 15.3 ng m−3 in spring, and 6.5 ng m−3 in summer. Conversely, the concentration of PAHs in coarse particles (PM2.1–9) ranged from 6.8 ng m−3 (summer) to 20.5 ng m−3 (winter) from low to high. The size fractions of 0.43–2.1 μm PAHs increased most from clear to polluted days, which could be ascribed to the heterogeneous reactions. Source apportionment using positive matrix factorization showed that four sources, namely biomass combustion, coal combustion, diesel vehicles, and gasoline vehicles accounted for PAHs with the estimation of 17.4%, 22.1%, 26.4%, and 23.2% to PAHs in PM2.1; and 19.6%, 24.3%, 23.6%, and 20.1% in PM2.1–9, respectively. Furthermore, we used the human alveolar epithelial cell (BEAS-2B) to assess the toxicological effects of size-resolved atmospheric PAHs. The results showed that the cell survival rate caused by fine particles was lower than that of coarse particles with the same concentrations of PAHs, which is mainly related to the higher content of highly toxic PAHs in fine particles.

Emissions of polycyclic aromatic hydrocarbons in PM2.5 emitted from motor vehicles exhaust (PAHs-PM2.5-MVE) under the plateau with low oxygen content

Emissions of PAHs and their derivatives from motor vehicles exhaust are mainly due to inadequate combustion of fossil fuels, the combustion efficiency of engine is lower under the plateau with low oxygen content, which will exacerbate the emission of pollutants, especially organic substance. In order to investigate the emission of PAHs-PM2.5-MVE under the plateau with low oxygen content, tunnel experiments and bench tests were conducted in a typical plateau region in Yunnan Province. The study indicated the concentrations of PAHs-PM2.5-MVE in the tunnels of Caohai and Xidu reached 548.11 ± 307.12 and 1241.19 ± 197.54 ng/m3, respectively. The emission factor of PAHs-PM2.5-MVE in the Caohai Tunnel was estimated to be 438.61 ± 296.86 μg/veh/km, and that for gasoline and diesel vehicles in bench tests were 442.83 ± 82.57 and 4098.04 ± 551.21 μg/kg fuel. Meanwhile, the emission factors of carbonaceous component, CO and PAHs-PM2.5-MVE were at a high level that were higher than those in plain which due to the inadequate combustion of fuels in engine. A probabilistic risk assessment framework was integrated to quantitatively estimate the exposure risk for the population of the tunnels, the HPAHs-PM2.5-MVE had potential carcinogenic risk. The study can improve our understanding of the influence of organic substance from inadequate combustion of fuels on the environment and human.

Exploration and comparison of the relationship between PAHs and ROS in PM2.5 emitted from multiple anthropogenic sources in the Guanzhong Plain, China

Anthropogenic emissions have emerged as an important source of urban atmospheric PM2.5, exacerbating air pollution and the associated health implications. This study analyses PM2.5, originating from major anthropogenic sources (industries, motor vehicles, and solid-fuel combustion for domestic applications) in the Guanzhong Plain in China, along with the parent- (p-), alkylated- (a-), and oxygenated- (o-) polycyclic aromatic hydrocarbons (PAHs) and reactive oxygen species (ROS) levels in PM2.5. Industrial emissions are mainly characterised by high abundances of benzo[b]fluoranthene (BbF), benzo[k]fluoranthene (BkF), and benz[a]fluoranthene (BaF). The 4-ring p-PAHs, such as fluoranthene (FLA), pyrene (PYR), benzo[a]anthracene (BaA), and chrysene (CHR) proportions and the diagnostic ratios of indeno[1,2,3-cd]pyrene (IcdP)/[IcdP + benzo[ghi]perylene (BghiP)] and 1-acenaphthenone (1ACO)/[1ACO + 9-fluorenone (9FO)] in motor vehicle emission PM2.5 were higher than the other sources. Household solid fuel combustion features high proportions of methylnaphthalene (M-NAP), i.e., 2 M-NAP and 1 M-NAP and 3-ring p-PAHs. Acenaphthylene (ACY), acenaphthene (ACE), anthracene (ANT), 1,4-chrysenequinone (1,4CHRQ), and reactive oxygen species (ROS) were positively correlated among the three anthropogenic sources. Moreover, the correlations between other PAHs and ROS varied significantly among the three sources. As mixed and compound organic pollutants, 2- and 3-ring p-PAHs were more positively correlated with the ROS activity of household solid fuel combustion sources compared with industrial and motor vehicle sources. Based on the relative contribution of these three sources to PAHs in PM2.5, we estimated the cancer risks of males and females in the Guanzhong area to be 2.95 × 10−6 and 2.87 × 10−6, respectively, exceeding the safety threshold of 1 × 10−6. This study provides a basic dataset for conducting a refined source apportionment of PM2.5 and a scientific basis for further understanding the relationship between PM2.5, PAHs, and ROS in northern China.

Characterization and health risk assessment of PM2.5-bound polycyclic aromatic hydrocarbons in Yangon and Mandalay of Myanmar

To better understand the potential adverse health effects of atmospheric fine particles in the Southeast Asian developing countries, PM2.5 samples were collected at two urban sites in Yangon and Mandalay, representing coastal and inland cities in Myanmar, in winter and summer during 2016 and 2017. The concentrations of 21 polycyclic aromatic hydrocarbons (PAHs) in PM2.5 were determined using a gas chromatography–mass spectrometry (GC–MS). The concentrations of PAHs in PM2.5 in Yangon and Mandalay ranged from 7.6 to 180 ng m−3, with an average of 72 ng m−3. The PAHs were significantly higher in winter than in summer, and significantly higher in Mandalay than in Yangon. The health risk analysis of PAHs, based on the toxic equivalent quantity (TEQ) calculation, and the incremental lifetime cancer risk (ILCR) assessment indicated that PM2.5 in Myanmar has significant health risks with higher health risks in Mandalay compared to Yangon. Diagnostic ratios of PAHs, correlation of PAHs with other species in PM2.5 and the positive matrix factorization (PMF) analysis showed that TEQ is strongly affected by biomass burning and vehicular emissions in Myanmar. Additionally, it was found that the aging degree of aerosols and air mass trajectories had great influences on the concentration and composition of PAHs in PM2.5 in Myanmar, thereby affecting the toxicity of PM2.5.

Probing the occurrence, sources and cancer risk assessment of polycyclic aromatic hydrocarbons in PM2.5 in a humid metropolitan city in China.

Fifty-two consecutive PM2.5 samples from December 2021 to February 2022 (the whole winter) were collected in the center of Chongqing, a humid metropolitan city in China. These samples were analysed for the 16 USEPA priority polycyclic aromatic hydrocarbons (16 PAHs) to explore their composition and sources, and to assess their cancer risks to humans. The total concentrations of the 16 PAHs (ng m-3) ranged from 16.45 to 174.15, with an average of 59.35 ± 21.45. Positive matrix factorization (PMF) indicated that traffic emissions were the major source (42.4%), followed by coal combustion/industrial emission (31.3%) and petroleum leakage/evaporation (26.3%). The contribution from traffic emission to the 16 PAHs increased from 40.0% in the non-episode days to as high as 46.2% in the air quality episode during the sampling period. The population attributable fraction (PAF) indicates that when the unit relative risk (URR) is 4.49, the number of lung cancer cases per million individuals under PAH exposure is 27 for adults and 38 for seniors, respectively. It was 5 for adults and 7 for seniors, when the URR is 1.3. The average incremental lifetime cancer risk (ILCR) for children, adolescents, adults and seniors was 0.25 × 10-6, 0.23 × 10-6, 0.71 × 10-6, and 1.26 × 10-6, respectively. The results of these two models complemented each other well, and both implied acceptable PAH exposure levels. Individual genetic susceptibility and exposure time were identified as the most sensitive parameters. The selection and use of parameters in risk assessment should be further deepened in subsequent studies to enhance the reliability of the assessment results.

Characterisation of polycyclic aromatic hydrocarbons associated with indoor PM0.1 and PM2.5 in Hanoi and implications for health risks

Polycyclic aromatic hydrocarbons (PAHs) associated with indoor PM pose a high risk to human health because of their toxicity. A total of 160 daily samples of indoor PM2.5 and PM0.1 were collected in Hanoi and analysed for 15 PAHs. In general, the concentrations of carcinogenic PAHs (car-PAHs) accounted for 21% ± 2%, 19.1% ± 2%, and 26% ± 3% of the concentrations of 15 PAHs in PM2.5, PM0.1-2.5, and PM0.1, respectively. Higher percentages of car-PAHs were found in smaller fractions (PM0.1), which can be easily deposited deep in the pulmonary regions of the human respiratory tract. The concentrations of 15 PAHs were higher in winter than in summer. The most abundant PAH species were naphthalene and phenanthrene, accounting for 11%–21% and 19%–23%, respectively. The PAH content in PM0.1 was almost twice as high as those in PM2.5 and PM0.1-2.5. Principal component analysis found that vehicle emissions and the combustion of biomass and coal were the main outdoor sources of PAHs, whereas indoor sources included cooking activities, the combustion of incense, scented candles, and domestic uses in houses. According to the results, 60%–90% of the PM0.1-bound BaP(eq) was deposited in the alveoli region, whereas 63%–75% of the PM2.5-bound BaP(eq) was deposited in head airways (HA), implying that most of the particles deposited in the HA region were PM0.1-2.5. The contributions of dibenz[a,h]anthracene and benzo[a]pyrene were dominant and contributed from 36% to 51% and 31%–50%, respectively, to the carcinogenic potential, whereas benzo[a]pyrene contributed from 30% to 49% to the mutagenic potential for both size fractions. The incremental lifetime cancer risk, simulated by Monte Carlo simulation, was within the limits set by the US EPA, indicating an acceptable risk for the occupants. These results provide an additional scientific basis for protecting human health from exposure to indoor PAHs.

Characterization and Source Apportionment of Polycyclic Aromatic Hydrocarbons in PM2.5 in Lanzhou

To study the pollution characteristics and sources of 16 PAHs in PM2.5 in Lanzhou, PM2.5 samples were collected in four seasons. GC-MS was employed to analyze the concentration of PAHs. Positive matrix factorization(PMF), trajectory cluster, and potential source contribution function(PSCF) were used to identify the sources of PAHs. The results indicated that the average concentration of PAHs in PM2.5 in Lanzhou decreased in the order of winter[(118±16.2) ng·m-3]>autumn[(50.8±21.6) ng·m-3]>spring[(22.2±8.87) ng·m-3]>summer[(4.65±1.32) ng·m-3]. The results of correlation analysis showed that PM2.5 and TPAHs in Lanzhou had an extremely significant negative correlation with temperature; an extremely significant positive correlation with atmospheric pressure; and a poor correlation with wind direction, wind speed, and relative humidity. The proportion of PAHs with 4-5 rings was much higher than that of those with 6 rings and 2-3 rings, with similar results across the four seasons. Source apportionment results illustrated that the contribution of industrial emissions and biomass and natural gas combustion were dominant in spring and summer seasons. Industrial emissions and coal combustion were dominant in autumn and winter, respectively. The vehicle emissions had no significant change across the four seasons. Trajectory cluster and PSCF analyses showed that the airflow coming from Mongolia, northeast Xinjiang, and Qinghai had important effects on the ambient air quality in Lanzhou.

Insight into personal exposure characteristics and health effects of PM2.5 and PM0.25-bound PAHs and their derivatives with different heating ways in the Fenwei Plain, China

Personal exposure (PE) to polycyclic aromatic hydrocarbons (PAHs) and their derivatives in particulate matter with two aerodynamic sizes of 2.5 and 0.25 μm (PM2.5 and PM0.25) from rural housewives was studied in the Fenwei Plain, China. A total of 15 households were divided into five different groups based on the type of solid fuel and heating device used, including biomass briquette-furnace (BBF), biomass-elevated Kang (BEK), outdoor lump coal-boiler (OLC), indoor briquette coal-stove (IBC), and electricity (ELE). The PE concentrations of the PAHs and biomarkers in urine collected from the participants were determined. The results showed that the PE concentrations of total quantified PAHs in the biomass group (i.e., BBF and BEK) were 2.2 and 2.0 times higher than those in the coal groups (i.e., OLC and IBC) in PM2.5 and PM0.25, respectively. The housewives who used biomass as fuel suffered from higher potential health impacts than the coal fuel users. The incremental lifetime cancer risk for the PAHs in PM2.5 in the BBF and BEK groups exceeded the international safety threshold. Furthermore, the PE concentrations of oxygenated PAH (o-PAHs) in PM2.5 and PM0.25 in the biomass groups and the nitrated PAHs (n-PAHs) in PM0.25 in the coal groups showed strong correlations with the biomarkers. The results of this study proved the associations between exposure to the different classes of PAHs and health hazards. The findings could also serve as a guideline in establishing efficient measures for using solid fuels for cooking and household warming in northern China.

Temporal and spatial distributions, source identification, and health risk assessment of polycyclic aromatic hydrocarbons in PM2.5 from 2016 to 2021 in Shenzhen, China.

Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous contaminants in the atmosphere that have drawn intense attention due to their carcinogenicity and mutagenicity. In this work, 1424 air samples were collected between January 2016 and December 2021 in three areas of Shenzhen, China to determine the concentrations of PM2.5 and PAHs and their spatiotemporal variation. Human health risks due to the daily intake and uptake of PAHs and the resulting incremental lifetime cancer risk (ILCR) were also evaluated. PAHs were detected frequently in the samples at concentrations between 0.28 and 32.7ng/m3 (median: 1.04ng/m3). PM2.5 and PAH concentrations decreased from 2016 to 2021, and the Yantian area had lower median concentrations of PM2.5 (23.0μg/m3) and PAHs (0.02ng/m3) than the Longgang and Nanshan areas. The concentrations of PM2.5 and PAHs were significantly higher in winter than in summer. Analysis of diagnostic ratios indicated that petroleum combustion was the dominant source of airborne PAHs in Shenzhen. The estimated daily intake (EDI) and uptake (EDU) of PAHs by local residents decreased gradually with increasing age, indicating that infants are at particular risk of PAH exposure. However, the incremental lifetime cancer risks (ILCRs) were below the threshold value of 10-6, indicating that inhalation exposure to PAHs posed a negligible carcinogenic risk to Shenzhen residents. While promising, these results may underestimate actual PAH exposure levels, so further analysis of health risks due to PAHs in Shenzhen is needed.

Characterization of the sources and health risks of polycyclic aromatic hydrocarbons in PM2.5 and their relationship with black carbon: A case study in northern Taiwan

Polycyclic aromatic hydrocarbons (PAHs) and black carbon (BC) often coexist in PM2.5 because both form during the incomplete combustion of organic matter. These compounds are regarded as hazardous air pollutants with potential health effects, including respiratory and cardiovascular effects. In this study, to evaluate the health risks of PAHs and BC at an urban site in northern Taiwan, 16 priority PAHs and BC, identified by the United States Environmental Protection Agency, were analyzed and quantified in PM2.5 to determine their concentrations, their relationship with each other, and their likely sources. The results indicated that the mean concentrations of total PAHs and BC were 0.91 ng m−3 and 0.97 μg m−3, respectively, with a significant positive correlation between them, indicating the same emission sources. The results also indicated that fossil fuel combustion and traffic emissions were primary contributors to PAHs, with wood and biomass combustion playing a less prominent role. Among these 16 priority PAHs, benzo[a]pyrene, dibenz[a,h]anthracene, benzo[b]fluoranthene, and indeno[1,2,3-cd]pyrene served as major carcinogenic compounds, accounting for 89.0% of the total carcinogenic toxicity. Thus, the lifetime excess cancer risk resulting from PAH exposure was estimated as 8.03 × 10−6, indicating a potential carcinogenic risk to human health at the sampling site. Overall, this study highlights the need for future mitigation policies for traffic emissions and fossil fuel combustion for reducing the local emissions of BC and co-produced PAHs in northern Taiwan.

Characteristics, sources and health risk assessment of trace metals and polycyclic aromatic hydrocarbons in PM2.5 from Hefei, China.

Trace metals (TRs) and polycyclic aromatic hydrocarbons (PAHs) are major toxic components of fine particulate matter (PM2.5) and related to various health adverse outcomes. The study aims to get a better understanding of the contents, sources and risks of PM2.5-bounded TRs and PAHs in Hefei, China, during the period of 2019-2021. We collected 504 samples and measured twelve TRs and sixteen priority PAHs by inductively coupled plasma mass spectrometry and high-performance liquid chromatography. The annual mass concentrations of PM2.5 was fluctuated in the year of 2019-2021 at 50.95, 47.48 and 59.38μg/m3, with seasonal variations in rank order of winter > spring > autumn > summer. The median concentrations of PM2.5-bounded ƩTRs and ƩPAHs were also fluctuated, 132.85, 80.93 and 120.27ng/m3 for ƩTRs, 2.57, 5.85 and 2.97ng/m3 for ƩPAHs, in the year of 2019, 2020 and 2021, respectively. Seasonal variations of ƩTRs and ƩPAHs show the highest concentration in winter. Positive matrix factorization was used for identified pollution emission sources, and TRs mainly originated from coal combustion, traffic emission and fugitive dust, while PAHs stemmed from biomass, diesel, gasoline and coal combustion. Health risk assessment indicated that adults were more vulnerable than children, the carcinogenic risk assessment of As and Cr manifested a certain degree of cancer risk (1.0 × 10-6 < CR < 1.0 × 10-4) in adults group, and health risks of TRs were higher than PAHs in Hefei. These findings suggest that PM2.5-bounded TRs and PAHs should be considered when making emission control strategies for air pollution, and winter, combustion sources and adults should achieve more policy attention to decrease exposure risks in Hefei.

Health Impacts of Air Pollution in Tianjin

Ambient air pollution is a dominant determinant of health. The health effects and economic losses due to air pollution are very important for decision-making. Since the implementation of the "Air Pollution Prevention and Control Action Plan" and "blue sky defense war" policies, the air quality of Tianjin has changed significantly. Here, the health effects and economic losses attributable to ambient air pollution in Tianjin from 2013 to 2020 wereestimated. For the particulate matter which has complex components, we assessed the inhalation health risks of heavy metals and polycyclic aromatic hydrocarbons (PAHs) in PM2.5. The variation in the concentration of the main components of PM2.5 was also analyzed. The results showed that improved air quality had positive health benefits. The health benefits from SO2 were the highest among the six air pollutants, and 3786 deaths were avoided in 2020 compared to in 2013 due to lower SO2 concentration. The economic losses caused by air pollutants ranged from several billion to ten billion yuan. Among the six air pollutants, particulate matter and ozone had higher health losses in recent years. The health risks of heavy metals and PAHs in PM2.5 showed a decreasing trend. However, Cr(Ⅵ), As, Cd, and Ni in PM2.5in the winter of 2020 still had respiratorysystem carcinogenic risk, whereas there was no health risk of PAHs in PM2.5in 2019-2020. The concentrations of main components of PM2.5 have decreased significantly. In the future, the reduction of health loss caused by air pollution depends on synergy governance of particulate matter and ozone and further research on health effects.

Fine particulate matter (PM2.5) induces inhibitory memory alveolar macrophages through the AhR/IL-33 pathway.

Fine particulate matter (PM2.5) concentrations have decreased in the past decade. The adverse effects of acute PM2.5 exposure on respiratory diseases have been well recognized. To explore the long-term effects of PM2.5 exposure on chronic obstructive pulmonary disease (COPD), mice were exposed to PM2.5 for 7days and rest for 21days, followed by challenges with lipopolysaccharide (LPS) and porcine pancreatic elastase (PPE). Unexpectedly, PM2.5 exposure and rest alleviated the disease severity and airway inflammatory responses in COPD-like mice. Although acute PM2.5 exposure increased airway inflammation, rest for 21days reversed the airway inflammatory responses, which was associated with the induction of inhibitory memory alveolar macrophages (AMs). Similarly, polycyclic aromatic hydrocarbons (PAHs) in PM2.5 exposure and rest decreased pulmonary inflammation, accompanied by inhibitory memory AMs. Once AMs were depleted, pulmonary inflammation was aggravated. PAHs in PM2.5 promoted the secretion of IL-33 from airway epithelial cells via the aryl hydrocarbon receptor (AhR)/ARNT pathway. High-throughput mRNA sequencing revealed that PM2.5 exposure and rest drastically changed the mRNA profiles in AMs, which was largely rescued in IL-33-/- mice. Collectively, our results indicate that PM2.5 may mitigate pulmonary inflammation, which is mediated by inhibitory trained AMs via IL-33 production from epithelial cells through the AhR/ARNT pathway. We provide the rationale that PM2.5 plays complicated roles in respiratory disease.

The presence of polycyclic aromatic hydrocarbons (PAHs) in air particles and estimation of the respiratory deposition flux

Polycyclic aromatic hydrocarbons (PAHs) in the atmospheric particles constitute a topic of growing health concern. This study aims to calculate PAH concentrations, identify the source, assess the health risk from exposure to carcinogenic PAHs, and the respiratory deposition flux. PM10 and PM2.5 were collected in September 2019 in the urban, semi-urban, and semi-urban-industrial areas of Kuala Lumpur, Batu Pahat, and Bukit Rambai, respectively. A total of 18 PAHs from PM10 and 17 PAHs from PM2.5 were extracted using dichloromethane and determined using gas chromatography coupled with a flame ionization detector (GC-FID). The health risk assessment (HRA) calculated included B[a]P equivalent (B[a]Peq), lifetime lung cancer risk (LLCR), incremental lifetime cancer risk (ILCR), and respiratory deposition dose (RDD). The results show PAHs in PM10 recorded in Kuala Lumpur (DBKL), Batu Pahat (UTHM), and Bukit Rambai are 9.91, 8.45, and 9.57 ng/m3, respectively. The average PAHs in PM2.5 at the three sampling sites are 11.65, 9.68, and 9.37 ng/m3, respectively. The major source of PAHs obtained from the DRs indicates pyrogenic activities for both particle sizes. For PM10, the total B[a]Peq in DBKL, UTHM, and Bukit Rambai were 1.97, 1.82, and 2.32 ng/m3, respectively. For PM2.5 samples, the total B[a]Peq in DBKL, UTHM, and Bukit Rambai were 2.80, 2.33, and 2.57 ng/m3, respectively. The LLCR and ILCR show low to moderate risk for all age groups. The RDD of adults and adolescents is highest in both PM10 and PM2.5, followed by children, toddlers, and infants. Overall, we perceive that adults and adolescents living in the urban area of Kuala Lumpur are at the highest risk for respiratory health problems because of prolonged exposure to PAHs in PM10 and PM2.5, followed by children, toddlers, and infants.

Comparison of characteristics and sources of water-soluble inorganic ions, trace elements, and polycyclic aromatic hydrocarbons in PM2.5 on polluted and normal days in Ulsan, South Korea

Comparison of characteristics and sources of water-soluble inorganic ions, trace elements, and polycyclic aromatic hydrocarbons in PM2.5 on polluted and normal days in Ulsan, South Korea

Rapid determination of 16 polycyclic aromatic hydrocarbons in atmospheric fine particles by molecularly imprinted column-high performance liquid chromatography

A high performance liquid chromatographic method based on the purification of polycyclic aromatic hydrocarbon molecularly imprinted columns was developed, this method was used for the rapid quantitative determination of 16 polycyclic aromatic hydrocarbons(PAHs) in fine particulate matter(PM_(2.5)). The polycyclic aromatic hydrocarbons of the sample were extracted with acetonitrile ultrasonically, purified by molecular imprinting column(MIP-PAHs), and tested after being concentrated by nitrogen blowing. The 16 PAHs showed a good linear relationship in the range of 1-40 ng/mL, and the correlation coefficient r&gt;0.9996; the recoveries were 77.13%-107.67% at the three standard addition levels of 5.0, 10.0 and 20.0 ng/mL, the relative standard deviation was 0.15%-4.63%(n=7); the detection limit of the method was 0.004-0.078 ng/m~3, and the quantification limit was 0.016-0.336 ng/m~3. The detection of 16 PAHs in PM_(2.5) using this method is more accurate, more sensitive and less time consuming than the result of the simple ultrasonic extraction method and the Soxhlet extraction method in Determination of PAHs in ambient air and exhaust gases in gas phase and particulate matter by high performance liquid chromatography(HJ 647-2013).

Polycyclic aromatic hydrocarbons in PM2.5 from an e-waste source site and a receptor site in Southern China: Atmospheric transport and process implications

Polycyclic aromatic hydrocarbons (PAHs) are potential contaminants released from informal electronic waste (e-waste) recycling. PAHs in PM2.5 collected at a rural e-waste (source) site and a background (receptor) site in Southern China were measured. Seasonal variations and regional transport of PAHs were investigated, and their sources and atmospheric processes were implied. The median concentrations of ∑18PAHs at the e-waste site (13.7 ng/m3) were one order of magnitude higher than those at the background site (median = 1.54 ng/m3), indicating the informal e-waste dismantling was a significant source. The seasonal variations of PAH concentrations at the two sites were similar, exhibiting noticeably unimodal distributions in winter, predominantly associated with the strengthened e-waste dismantling activities. Three molecular diagnostic ratios (MDRs) can be collectively used as potential markers of field informal e-waste burning sources. The dispersion model revealed that regional atmospheric transport from this e-waste site was a source of PAHs in the background air. Some MDRs significantly changed at the background site compared to the source site but could not be explained by the lifetime and/or gas-particle partition of the isomers. The differences complied with recent theories about the multiphase reactivity and evaporation of PAHs on aerosols. It was proposed that in warm and humid climates, the losses of PAHs from PM2.5 were dominated by their phase separation or diffusion, which was n-octanol/water partition coefficient (KOW) dependent. This hypothesis was further supported by data in the literature.

Aryl hydrocarbon receptor activation-mediated vascular toxicity of ambient fine particulate matter: contribution of polycyclic aromatic hydrocarbons and osteopontin as a biomarker

BackgroundExposure to ambient fine particulate matter (PM2.5) is associated with vascular diseases. Polycyclic aromatic hydrocarbons (PAHs) in PM2.5 are highly hazardous; however, the contribution of PM2.5-bound PAHs to PM2.5-associated vascular diseases remains unclear. The ToxCast high-throughput in vitro screening database indicates that some PM2.5-bound PAHs activate the aryl hydrocarbon receptor (AhR). The present study investigated whether the AhR pathway is involved in the mechanism of PM2.5-induced vascular toxicity, identified the PAH in PM2.5 that was the major contributor of AhR activation, and identified a biomarker for vascular toxicity of PM2.5-bound PAHs.ResultsTreatment of vascular smooth muscle cells (VMSCs) with an AhR antagonist inhibited the PM2.5-induced increase in the cell migration ability; NF-κB activity; and expression of cytochrome P450 1A1 (CYP1A1), 1B1 (CYP1B1), interleukin-6 (IL-6), and osteopontin (OPN). Most PM2.5-bound PAHs were extracted into the organic fraction, which drastically enhanced VSMC migration and increased mRNA levels of CYP1A1, CYP1B1, IL-6, and OPN. However, the inorganic fraction of PM2.5 moderately enhanced VSMC migration and only increased IL-6 mRNA levels. PM2.5 increased IL-6 secretion through NF-κB activation; however, PM2.5 and its organic extract increased OPN secretion in a CYP1B1-dependent manner. Inhibiting CYP1B1 activity and silencing OPN expression prevented the increase in VSMC migration ability caused by PM2.5 and its organic extract. The AhR activation potencies of seven PM2.5-bound PAHs, reported in the ToxCast database, were strongly correlated with their capabilities of enhancing the migration ability of VSMCs. Benzo(k)fluoranthene (BkF) contributed the most to the AhR agonistic activity of ambient PM2.5-bound PAHs. The association between PM2.5-induced vascular toxicity, AhR activity, and OPN secretion was further verified in mice; PM2.5-induced intimal hyperplasia in pulmonary small arteries and OPN secretion were alleviated in mice with low AhR affinity. Finally, urinary concentrations of 1-hydroxypyrene, a major PAH metabolite, were positively correlated with plasma OPN levels in healthy humans.ConclusionsThe present study offers in vitro, animal, and human evidences supporting the importance of AhR activation for PM2.5-induced vascular toxicities and that BkF was the major contributor of AhR activation. OPN is an AhR-dependent biomarker of PM2.5-induced vascular toxicity. The AhR activation potency may be applied in the risk assessment of vascular toxicity in PAH mixtures.