Size-segregated Particulate Matter Research Articles

Seasonal distribution and deposition patterns of size-segregated particulate matter in human respiratory system in Central Delhi, India

Seasonal distribution and deposition patterns of size-segregated particulate matter in human respiratory system in Central Delhi, India

Seasonal variation and size distribution of aromatic acids in urban aerosols in Beijing, China

Aromatic acids are an integral component of organic acids in the atmosphere, contributing to the formation of climate-altering brown carbon (BrC). To better understand the sources and formation processes of aromatic acids, we collected size-segregated particulate matter samples in urban Beijing from April 2017 to January 2018, which were analyzed using solvent-extraction followed by gas chromatography/mass spectrometry. Phthalic acid (o-PhA) had the greatest average annual concentration, followed by terephthalic acid (p-PhA), 4-hydroxybenzoic acid (4-OHBA), dehydroabietic acid (DA), syringic acid (SA), 3-hydroxybenzoic acid (3-OHBA), isophthalic acid (m-PhA), and vanillic acid (VA). We identified distinct seasonal variations in aromatic acids, with o-PhA peaking in summer due to photochemical activity, while p-PhA and 4-OHBA elevated in autumn and summer, respectively, influenced by open waste and biomass burning. Wintertime variations in all aromatic acids were driven by complex meteorology and increased anthropogenic emissions, including rural biomass burning for cooking and heating. Particle size distribution of aromatic acids was affected by seasonal agricultural activities and dust storms, multiple emission sources, and formation mechanisms. The o-PhA has predominantly bimodal distribution, with diverse sources and complex formation mechanisms including gas- and aqueous-phase chemistry. The applicability of o-PhA as a tracer for specific secondary organic aerosols has been questioned due to its potential primary sources. The 3-OHBA, 4-OHBA, VA, SA, and DA exhibited bimodal or trimodal patterns during haze and non-haze periods across different particle size ranges. The seasonal variation in VA/SA and VA/4-OHBA ratios demonstrated the complexity of biomass burning types, influenced by season, particle size, meteorological conditions, and combustion sources.

More evidence on primary sulfate emission from residential coal combustion in northern China: Insights from the size-segregated chemical profile, morphology, and sulfur isotope

This study addresses the ongoing debate concerning the origin of ambient sulfate in northern China, and provides more evidence for primary sulfate from the perspective of source emission. An extensive field experiment was conducted, involving the collection of size-segregated particulate matter emitted under various coal types and combustion conditions for subsequent analysis. Our findings reveal that residential coal combustion (RCC) emits significant amounts of primary sulfate, constituting approximately 26.48 ± 15.43% of the particulate mass. Moreover, these emissions exhibit a strong association with NH4+, leading to the formation of stable ammonium sulfate compounds. The emission of sulfate is intricately linked to both coal quality and combustion conditions. Notably, the oversight of δ34S isotope enrichment in RCC particulate matter, which distinctly differs from the raw coal, introduces uncertainties in the quantitative assessment of sulfate sources and formation pathways. Therefore, more in-depth explorations are necessary to elucidate the precise processes involved in RCC sulfate transformation and to accurately determine its environmental impact.

Particulate matter from a tropical city in southeast Brazil: Impact of biomass burning on polycyclic aromatic compounds levels, health risks, and in vitro toxicity

In the context of a rising global temperature, biomass burning represents an increasing risk to human health, due to emissions of highly toxic substances such as polycyclic aromatic hydrocarbon (PAHs). Size-segregated particulate matter (PM) was collected in a region within the sugarcane belt of São Paulo state (Brazil), where biomass burning is still frequent, despite the phasing out of manual harvesting preceded by fire. The median of the total concentration of the 15 PAHs determined was 2.3 ± 1.8 ng m−3 (n = 19), where 63% of this content was in PM1.0. Concentrations of OPAHs and NPAHs were about an order of magnitude lower. PM2.5 collected in the dry season, when most of the fires occur, presented PAHs and OPAHs total concentrations three times higher than in the wet season, showing positive correlations with fire foci number and levoglucosan (a biomass burning marker). These results, added to the fact that biomass burning explained 65% of the data variance (PCA analysis), evidenced the importance of this practice as a source of PAHs and OPAHs to the regional atmosphere. Conversely, NPAHs appeared to be mainly derived from diesel-powered vehicles. The B[a]P equivalent concentration was estimated to be 4 times higher in the dry season than in the wet season, and was greatly increased during a local fire event. Cytotoxicity and genotoxicity of PM1.0 organic extracts were assessed using in vitro tests with human liver HepG2 cells. For both types of tests, significant toxicity was only observed for samples collected during the dry season. Persistent DNA damage that may have impaired the DNA repair system was also observed. The results indicated that there was a health risk associated with the air particulate mixture, mainly related to biomass burning, demonstrating the urgent need for better remediation actions to prevent the occurrence of burning events.

Size-segregated characteristics of water-soluble oxidative potential in urban Xiamen: Potential driving factors and implications for human health

Oxidative potential (OP), defined as the ability of particulate matter (PM) to generate reactive oxygen species (ROS), has been considered as a potential health-related metric for PM. Particles with different sizes have different OP and deposition efficiencies in the respiratory tract and pose different health risks. In this study, size-segregated PM samples were collected at a coastal urban site in Xiamen, a port city in southeastern China, between August 2020 and September 2021. The water-soluble constituents, including inorganic ions, elements and organic carbon, were determined. Total volume-normalized OP based on the dithiothreitol assay was highest in spring (0.241 ± 0.033 nmol min−1 m−3) and lowest in summer (0.073 ± 0.006 nmol min−1 m−3). OP had a biomodal distribution with peaks at 0.25–0.44 μm and 1.0–1.4 μm in spring, summer, and winter and a unimodal pattern with peak at 0.25–0.44 μm in fall, which were different from the patterns of redox-active species. Variations in the seasonality of fine and coarse mode OP and their correlations with water-soluble constituents showed that the size distribution patterns of OP could be attributed to the combined effects of the size distributions of transition metals and redox-active organics and the interactions between them which varied with emissions, meteorological conditions and atmospheric processes. Respiratory tract deposition model indicated that the deposited OP and the toxic elements accounted for 47.9 % and 36.8 % of their measured concentrations, respectively. The highest OP doses and the excess lifetime carcinogenic risk (ELCR) were found in the head airway (>70 %). However, the size distributions of OP deposition and ELCR in the respiratory tract were different, with 63.9 % and 49.4 % of deposited ELCR and OP, respectively, coming from PM2.5. Therefore, attention must be paid to coarse particles from non-exhaust emissions and road dust resuspension.

Size distribution and elemental composition of airborne particulate matter on four plant species in vertical greenery systems

Vertical greenery systems (VGSs) have been proven to greatly improve the urban thermal environment. However, their effect on the retention of airborne particulate matter (PM) in the road environment remains unclear. This study aimed to assess the quantity of size-segregated PMs on both the upper (adaxial) and lower (abaxial) leaf surfaces, the mass of size-segregated PMs on the leaf surface and within the leaf wax, as well as the elemental composition of PMs retained in leaf stomata of four plant species in VGSs in Guangzhou. The findings revealed that VGSs exhibited greater retention of fine (<2.5 μm) PMs when compared to coarse (2.5–10 μm) and large (>10 μm) PMs. Among the four species studied, Tradescantia spathacea exhibited the highest PM retention in VGSs. The number density of accumulated PMs on the upper and lower leaf surfaces of the four plant species of VGSs at three heights varied significantly with species, heights, and their interaction (P < 0.05). The greatest stomatal block rate by PM occurred at a height of 0.6 m, the range was 91.1%–98.0%. The composition of PMs retained by the leaves primarily consisted of common element of C, O, Ca, K, Mg, and Si, which likely originated from natural sources. Heavy metals (HMs) such as Cr and Cd may have originated from brakes, while Zn and Cu might be attributed to tire wear and exhaust emissions. Therefore, VGSs effectively retained a substantial quantity of airborne PM and contributed to the mitigation of urban air pollution issues.

Size-fractionated ambient particulate matter induce toxicity: Oxidative potential, cytotoxic effect and inflammatory potential

Present study highlighted the importance of examining the toxicological profile of size-segregated particulate matter (PM) bound metals (Fe, Mn, Ni, Pb, Zn, Cu, Cr, Co, Cd) at urban site of Pune city, India. The total aerosol mass was composed of 61.2% and 38% fine and coarse particles, respectively with maximum distribution observed in 4.7–2.1 μm size mode. Elemental size distributions indicated the prime association of Fe, Mn and Zn with coarse sized PM, while remaining metals were predominantly associated with fine PM. Seasonal mass and elemental distribution profile of size-resolved PM was characterized with maximum concentration found in winter season. Enrichment factor analysis revealed the contribution of anthropogenic emissions to Co and Ni in fine mode while less enriched metals, Fe and Mn were allied with crustal and natural sources. Oxidative potential of particles in terms of Dithiothreitol (DTT) loss was found to be maximum in the size range of 4.7–1.1 μm with dominant contribution of PM bound metals (Fe, Cu, Cr, Mn, Ni, Pb, and Zn). On exposure to PM samples, prominent enhancement in the expression of cytokines (especially TNFα) as compared to the control has confirmed their inflammatory nature. Incubation of A549 cells with PM suspension (75 mg/ml) caused pronounced reduction (p < 0.01) in cell viability with significant morphological changes, associated with cell death. Respiratory deposition doses of PM in head region were found to be more impacted by coarse sized particles while contribution of fine PM was dominant in alveolar and tracheobronchial region, signifying serious health risks to the exposed population. In addition to the basic knowledge of toxicity mechanisms associated with size fractionated PM, these results together with the analysis of correlation between PM bound metals and biological assays will be relevant to better characterize the potential health risks and possible future mitigation strategies.

Significant changes in size distribution of aerosols in Beijing after clean air actions

Over the past few years, the physicochemical characteristics and sources of aerosols have changed following the implementation of strict clean air policies in Beijing. In this study, size-segregated particulate matters (PM) were collected using a micro-orifice uniform deposit impactor (MOUDI) in Beijing from July 2021 to June 2022 to understand the responses of particle size distribution and chemical composition to the implemented emission reduction measures. The results showed that although particulate pollution greatly improved, it is still severe in Beijing, especially in autumn and winter, with the annual average PM1.8 (aerosol particle with aerodynamic diameter less than 1.8 μm) concentration reaching 46.7 ± 37.4 μg/m3. NO3− was the most abundant ion in the particles throughout all seasons, and its proportion to water-soluble inorganic ions increased significantly with the aggravation of pollution. This highlights the importance and urgency of controlling mobile sources in future control measures. The highest concentration of SO42− occurring during summer demonstrates the effectiveness of fossil fuel combustion control in winter. The measured size distributions of PM and secondary inorganic ions were trimodal, which significantly differed from the observations conducted in Beijing using MOUDI before 2017, in which the measured size distributions of PM and secondary inorganic ions were bimodal. The enhancement of atmospheric oxidation and reduction of gaseous precursors can affect the formation path of aerosols, and thus, their particle size distribution. Aerosol aqueous-phase reactions play a vital role in pollution development, with the droplet mode further growing hygroscopically into a coarse mode during pollution maintenance.

Emission and optical characteristics of brown carbon in size-segregated particles from three types of Chinese ships

Brown carbon (BrC) is one of the important light absorption substances that have high light absorption ability under short wavelength light. However, limit studies have focused on the BrC emission from ships. In this study, size-segregated particulate matters (PM) were collected from three different types of ships, light absorption characteristics and size distribution of methanol-soluble BrC and water-soluble BrC in PM from ship exhausts were investigated. Results showed that four-stroke low-power diesel fishing boat (4-LDF) had the highest mass concentrations of methanol-soluble organic carbon (MSOC) and water-soluble organic carbon (WSOC), followed by 2-stroke high-power heavy-fuel-oil vessel (2-HHV), and four-stroke high-power marine-diesel vessel (4-HMV). While 2-HHV had obviously higher light absorption coefficients of methanol-soluble BrC (Abs365,M) and water-soluble BrC (Abs365,W) in unit weight of PM than the other two types of ships. The tested ships presented comparable or higher absorption efficiency of BrC in water extracts (MAE365,W) compared with other BrC emission sources. Majority of BrC was concentrated in fine particles, and the particle size distributions of both Abs365,M and Abs365,W showed bimodal patterns, peaking at 0.43–0.65 µm and 4.7–5.8 µm, respectively. However, different particle size distributions were found for MAE365,M between diesel and heavy fuel oil ships. Besides, different wavelength dependence in particles with different size were also detected. Ship exhaust could be confirmed as a non-ignorable BrC emission source, and complex influencing factor could affect the light absorption characteristics of ship emissions. Particle size should also be considered when light absorption ability of BrC was evaluated.

SARS-CoV2 in public spaces in West London, UK during COVID-19 pandemic

BackgroundSpread of SARS-CoV2 by aerosol is considered an important mode of transmission over distances >2 m, particularly indoors.ObjectivesWe determined whether SARS-CoV2 could be detected in the air of enclosed/semi-enclosed public...

Seasonal Variations, Size Distributions, and Sources of Chemical Components of Submicron Particulate Matter in Nanjing

Size-segregated particulate matter (PM) samples were collected in different seasons from 2016 to 2017 at the Xianlin Campus of Nanjing University. Mass concentrations of water-soluble inorganic ions, carbonaceous components, and elements were analyzed for PM with an aerodynamic diameter ≤ 1.1 μm (PM1.1; <0.4 μm, 0.4-0.7 μm, and 0.7-1.1 μm). The results showed that PM1.1, OC, NO3-, SO42-, and NH4+ exhibited higher ambient levels in fall-winter than those in spring-summer, which was attributed to the changes in local diffusion conditions, evaporation, and decomposition of non-refractory components. Elemental carbon (EC) reached its maximum concentration[(1.87±0.98) μg·m-3]in spring due to the increase in industrial and road dust resuspension. According to the characteristic ratio between bulk components, the anions in PM1.1 were dominated by NO3-, SO42-, and Cl- in Nanjing, and the carbonaceous components were mainly from fossil fuel combustions and associated aging processes. As the ambient temperature increased, the size distributions of thermo-unstable components including NH4+, NO3-, and OC shifted towards finer particles, whereas EC became more enriched in coarse particles, possibly due to the increase in emission intensity of motor vehicles and fugitive dust contributions. Since high relative humidity (>70%) is often accompanied by high temperature (>20℃) and improved diffusion conditions, a relative humidity of 60%-70% was more conducive to the formation of secondary inorganic ions in PM1.1. Source apportionment results based on the speciation data of PM1.1 showed that secondary formation processes[(66.6±18.3)%]and dust resuspension[(16.8±14.8)%]were the main contributors to PM1.1 in Nanjing, and further control of the emissions of gaseous precursors and dust is necessary.

Environmental exposure to manganese and health risk assessment from personal sampling near an industrial source of airborne manganese

Manganese (Mn), despite being a trace element necessary in small quantities for the correct functioning of the organism, at higher concentrations can induce health disorders, mainly in motor and cognitive functions, even at levels found in non-occupational environments. For this reason, US EPA guidelines define safe reference doses/concentrations (RfD/RfC) for health.In this study, the individualised health risk of exposure to Mn through different media (air, diet, soil) and routes of entry into the organism (inhalation, ingestion and dermal absorption) was assessed according to the procedure defined by the US EPA. Calculations related to Mn present in ambient air were made on the basis of data obtained from size-segregated particulate matter (PM) personal samplers carried by volunteers recruited in a cross-sectional study conducted in the Santander Bay (northern Spain), where an industrial source of airborne Mn is located.Individuals residing in the vicinity of the main Mn source (within 1.5 km) were found to have a hazard index (HI) higher than 1, indicating that there is a potential risk for these subjects to develop health alterations. Also, people living in Santander, the capital of the region, located 7–10 km from the Mn source, may have some risk (HI > 1) under some wind conditions (SW). In addition, a preliminary study of media and routes of entry into the body confirmed that inhalation of PM2.5-bound Mn is the most important route contributing to the overall non-carcinogenic health risk related to environmental Mn.

Distribution of environmentally persistent free radicals in size-segregated PMs emitted from residential biomass fuel combustion

Environmentally persistent free radicals (EPFRs) are considered as an emerging pollutant due to their potential environmental risks, but the distribution characteristics of particulate matters (PMs)-EPFRs from residential combustion source are poorly understood. In this study, biomass (corn straw, rice straw, pine and jujube wood) combustion was studied in lab-controlled experiments. More than 80% of PM-EPFRs were distributed in PMs with aerodynamic diameter (dae) ≤ 2.1 µm, and their concentration in fine PMs was about 10 times that in coarse PM (2.1 µm ≤ dae ≤ 10 µm). The detected EPFRs were carbon-centered free radicals adjacent to oxygen atoms or a mixture of oxygen- and carbon-centered radicals. The concentrations of EPFRs in coarse and fine PMs were positively correlated with char-EC, but the EPFRs in fine PMs exhibited a negative correlation with soot-EC (p < 0.05). The increase of PM-EPFRs signals with the increased dilution ratio during pine wood combustion was more significant than that from rice straw, which may be resulted from the interactions between the condensable volatiles and the transition metals. Our study provides useful information for better understanding the formation of combustion-derived PM-EPFRs, and will be instructive for its purposeful emissions control.

Status of particulate matter in the indoor air of residential units of Sunderbani area of Rajouri district (J&amp;K), India

Air pollution is currently the greatest environmental threat to human health and one of the fastest growing issues on the global health agenda. The extremely fine particulate matter (aerodynamic diameter &lt; 2.5 microns) is of greatest concern because the particles can penetrate deep into human lungs and enter the bloodstream. The elderly, asthmatics and immune-deficient population are the most vulnerable with the increasing levels of particulate matter. The present study was conducted to assess the concentration of size-segregated Indoor Particulate Matter (PM2.5, PM1.0, PM0.50, PM0.25) in Sunderbani, Rajouri, J&amp;K. The average values of PM2.5, PM1.0, PM0.50, and PM0.25 were reported as 110.36µg/m3, 180.50µg/m3, 276.99µg/m3 and 445.93µg/m3 respectively in the sampled households of the study area. The average value of PM2.5 in the study area was found to be above the permissible limits of 60µg/m3 given by central pollution control board (CPCB). This was the first study on concentration of size-segregated particulate matter in the indoor environment of study area and the data obtained from the study will serve as baseline data for future studies in the area.

Sources, chemical components, and toxicological responses of size segregated urban air PM samples in high air pollution season in Guangzhou, China

The sources, sizes, components, and toxicological responses of particulate matter (PM) have demonstrated remarkable spatiotemporal variability. However, associations between components, sources, and toxicological effects in different-sized PM remain unclear. The purposes of this study were to 1) determine the sources of PM chemical components, 2) investigate the associations between components and toxicology of PM from Guangzhou high air pollution season. We collected size-segregated PM samples (PM10–2.5, PM2.5–1, PM1–0.2, PM0.2) from December 2017 to March 2018 in Guangzhou. PM sources and components were analyzed. RAW264.7 mouse macrophages were treated with PM samples for 24 h followed by measurements of toxicological responses. The concentrations of PM10–2.5 and PM1–0.2 were relatively high in all samples. Water-soluble ions and PAHs were more abundant in smaller-diameter PM, while metallic elements were more enriched in larger-diameter PM. Traffic exhaust, soil dust, and biomass burning/petrochemical were the most important sources of PAHs, metals and ions, respectively. The main contributions to PM were soil dust, coal combustion, and biomass burning/petrochemical. Exposure to PM10–2.5 induced the most significant reduction of cell mitochondrial activity, oxidative stress and inflammatory response, whereas DNA damage, an increase of Sub G1/G0 population, and impaired cell membrane integrity were most evident with PM1–0.2 exposure. There were moderate or strong correlations between most single chemicals and almost all toxicological endpoints as well as between various toxicological outcomes. Our findings highlight those various size-segregated PM-induced toxicological effects in cells, and identify chemical components and sources of PM that play the key role in adverse intracellular responses. Although fine and ultrafine PM have attracted much attention, the inflammatory damage caused by coarse PM cannot be ignored.

Possible influence of shipping emissions on metals in size-segregated particulate matter in Guanabara Bay (Rio de Janeiro, Brazil).

In the world of growing maritime fleets, ships powered by fossil fuels are being widely used that are responsible for atmospheric emissions such as particulate matter (PM). When inhaled, these can cause serious injury to the body and affect internal organs, because the particle size is on a tiny scale. The International Convention for the Prevention of Pollution from Ships (MARPOL) regulates the standards for emissions from marine diesel engines. However, although they pose risks to human health and the environment, the metals present in PM are not covered by Brazilian national current legislation. This study is based on the results of sampling of PM in the atmosphere of Guanabara Bay, Rio de Janeiro, Brazil, by means of the MOUDI cascade impactor, followed by acid opening of the collected PM and subsequent chemical analysis by ICP-MS for the determination of Ba, Ca, Cd, Co, Cu, Cr, Fe, Mg, Mn, Ni, Pb, V, and Zn. In coarse particles, the mean values ranged from 0.11 ng m−3 for Ba to 24.9 ng m−3 for Fe; in fine particles, from 0.07 ng m−3 for Co to 25.0 ng m−3 for Fe; and in ultrafine particles, from 0.11 ng m−3 for Ba to 9.71 ng m−3 for Fe. Finally, the nanoparticles (Ba and Ca) were not detected and the maximum value obtained was 5.32 ng m−3 for Mn.

Pollution levels and health risk assessment of potentially toxic metals of size-segregated particulate matter in rural residential areas of high lung cancer incidence in Fuyuan, China.

The highest incidence and mortality rate of lung cancer in rural area of Fuyuan has been a research hotspot, and the pathogenesis is still unclear. Therefore, atmospheric particulate matters (APMs) samples were collected between 18 February and 01 March 2017, exploring water-soluble potentially toxic metals (WSPTMs) and water-soluble inorganic ionic species (WSIIs) levels, size distribution, sources, acidity and alkalinity, and potential carcinogenic and non-carcinogenic risks, hoping to provide scientific basic data to solve this problem.In our study, the average ratio of nitrate ion (NO3-)/sulfate ion (SO42-) within PM1.1, PM1.1-2.0, PM2.0-3.3, PM3.3-7.0, and PM>7.0 were 0.22, 0.18, 0.15, 0.34 and 0.36, respectively, that revealed that combustion sources contributed to PM were more significant. The anions in equilibrium (ANE) / cations in equilibrium (CAE) < 1 for all samples within PM1.1, PM2.0-3.3, PM3.3-7.0 indicate that the APMs were alkaline, but PM1.1-2.0 particulate matter shows weak acidity. SO42-prefers to combine with NH4+to form (NH4)2SO4, which hinders the formation ofNH4NO3, the remainingSO42-and NO3- to neutralize the K+,KNO3was formed at all particulate, however, K2SO4 can only be formed in PM<3.3. Arsenic (As) and Selenium (Se) were identified as the most enriched WSPTMs in all PM sizes, predominantly from anthropogenic emissions, were suggested that coal combustion is a significant source of PM-bound WSPTMs. Total WSPTMs exhibited high total carcinogenic risks (TCR) values (9.98 × 10-6, 1.06 × 10-5, and 1.19 × 10-5 for girls, boys and adults, respectively) in the smaller particles (< 1.1μm). Se was considered as the major contributor (63.60%) to carcinogenic risk (CR) in PM2.0 and had an inverse relationship with PM size that should be of prime concern.

Per- and polyfluoroalkyl substances in the atmosphere of waste management infrastructures: Uncovering secondary fluorotelomer alcohols, particle size distribution, and human inhalation exposure.

Per- and polyfluoroalkyl substances (PFAS) have been applied in numerous industrial and consumer products, the majority of which flow into waste management infrastructures (WMIs) at the end of their life cycles, but little is known about atmospheric releases of PFAS from these facilities. In this study, we addressed this key issue by investigating 49 PFAS, including 23 ionic and 26 neutral and precursor PFAS, in the potential sources (n=4; within or adjacent to WMIs) and reference sites (n=2; coastal and natural reserve sites) in urban and rural areas of Hong Kong, China. Duplicate samples of air and size-segregated particulate matter were collected for 48h continuously using a 11-stage Micro-Orifice Uniform Deposit Impactor (MOUDI). In general, fluorotelomer alcohols (FTOHs) and perfluoroalkane sulfonamides were the predominant PFAS classes found across sampling sites. We also demonstrated the release of several less frequently observed semivolatile intermediate products (e.g., secondary FTOHs) during waste treatment. Except for perfluorooctane sulfonate, the size-segregated distributions of particulate PFAS exhibited heterogeneity across sampling sites, particularly in the WMIs, implying combined effects of sorption affinity and emission sources. A preliminary daily air emission estimation revealed that landfill was a relatively important source of PFAS relative to the wastewater treatment plant. A simplified International Commission on Radiological Protection model was used to estimate lung depositional fluxes, and the results showed that inhaled particulate PFAS were mainly deposited in the head airway while fine and ultrafine particles carried PFAS deeper into the lung alveoli. The cumulative daily inhalation dose of gaseous and particulate PFAS ranged from 81.9 to 265pg/kg/d. In-depth research is required to understand the health effect of airborne PFAS on workers at WMIs.

Particulate matter exposure analysis in 12 critical urban zones of Chennai, India.

This research paper examines the exposure to particulate matter (PM) and its deposition on the human respiratory tract (HRT) in 12 critical urban zones - institutional zone, commercial zone, construction zone, hospital zone, landfill zone, industrial zone, residential zone, high-traffic zone, main roads, medium-traffic zone secondary roads, low-traffic zone, coastal zone, and environmentally sensitive zone. This study measured the size-segregated PM concentrations using a Grimm aerosol spectrometer. The multiple-path particle dosimetry model assesses particles' total and regional deposition mass rates for different urban zones. A stochastic model of the 60th percentile is used to illustrate the deposition of PM in the human lung. The deposition rate of PM in the HRT is examined for the different urban zones from different emission sources. The analysis shows that the PM concentration in zone V (dumpsite zone) is at an elevated level (i.e., PM10 = 570.4µg/m3, PM2.5 = 128.3µg/m3, and PM1 = 28.1µg/m3) and lowest at zone XII (eco-sensitive zone) (i.e., PM10 = 25.1µg/m3, PM2.5 = 1 6.9µg/m3, and PM1 = 14.8µg/m3). Further, dumpsite, commercial, and eco-sensitive zones are identified to be critical zones that influence higher deposition in the tracheobronchial and pulmonary regions. The investigation concludes that local turbulence and emission source significantly impacts air quality and deposition of PM at HRT. In addition, as the PM diameter decreases, the acidity of PM increases, and it can penetrate deep into the lower airways. Since this can have profound consequences, it is imperative to better understand the deposition of PM across various urban zones.

Ambient concentrations and dosimetry of inhaled size-segregated particulate matter during periods of low urban mobility in Bragança, Portugal

The restrictive measures in place during the COVID-19 pandemic provided a timely scenario to investigate the effects of human activities on air quality, and the extent to which mobility reduction strategies can impact atmospheric pollutant levels. Real-time concentrations of PM1, PM2.5 and PM10 were measured using a mobile platform in a small city of Portugal, during morning and afternoon rush hours, in two distinct phases of the pandemic: emergency phase (cold period, lockdown) and calamity phase (warm period, less restricted). The Multiple-Path Particle Dosimetry Model (MPPD) was used to calculate the PM deposition for adults. Large spatio-temporal variabilities and pronounced changes in mean PM concentrations were observed, with lower concentrations in the calamity phase: PM1 = 2.33 ± 1.61 μg m−3; PM2.5 = 5.15 ± 2.77 μg m−3; PM10 = 23.30 ± 21.53 μg m−3 than in the emergency phase: PM1 = 16.85 ± 31.80 μg m−3; PM2.5 = 30.92 ± 31.93 μg m−3; PM10 = 111.27 ± 104.53 μg m−3. These changes are explained by a combination of meteorological factors and local emissions, mainly residential firewood burning. Regarding regional deposition, PM1 was the main contributor to deposition in the tracheobronchial (5%) and pulmonary (12%) regions, and PM10 in the head region (92%). In general, total deposition doses were higher for males than for females. This work quantitatively demonstrated that even with a 38% reduction in urban mobility during the lockdown, the use of firewood for residential heating is the main contributor to the high concentrations of PM and the respective inhaled dose.