Composition Of PM2 Research Articles

Temporal Variations in Health Risk Indices and Combustion-Derived Components of PM1.0: Focus on Terephthalate and Levoglucosan

This study evaluated the health risks and chemical composition of PM1.0 and PM2.5 in Incheon, South Korea, emphasizing the critical role of particle size in public health impacts. The average concentrations were 10.89 μg/m³ for PM2.5 and 8.11 μg/m³ for PM1.0. PM1.0 displayed higher proportions of carbonaceous components and water-soluble ions, predominantly formed through photochemical reactions and atmospheric chemistry processes. Health risk assessments, using the Benzo[a]pyrene toxic equivalency factor, mutagenic and carcinogenic potential, risk index, and oxidative potential (DTT-OP), indicated that PM1.0 poses significantly higher health risks per unit mass compared to PM2.5. Key components in PM1.0, such as levoglucosan and terephthalic acid (TPA), indicate significant contributions from combustion sources like biomass burning and plastic incineration, particularly at night. PM1.0 showed higher carcinogenic and mutagenic risks than PM2.5. The correlation between levoglucosan, PAHs, and TPA supports common combustion origins. Effective management of combustion-related emissions is crucial for reducing health risks associated with PM1.0. The overall average risk index for PM1.0 is 1.30 times higher than PM2.5, implying that, on average, PM1.0 poses a 30% higher health risk across the measured indices compared to PM2.5. This study emphasizes the need for targeted management of combustion emissions, particularly those from plastic and fuel combustion, to mitigate the health risks posed by PM1.0. Effective control of the precursors contributing to PM1.0 formation is crucial for reducing the adverse health impacts of air pollution.

Elemental composition and health risk assessment of PM10, PM2.5, at different microenvironments: Addis Ababa, Ethiopia.

This study was designed to evaluate the health risks faced by inhabitants living in the slum areas of Addis Ababa, Ethiopia. The levels of PM2.5 and PM10 and elemental composition of the PM10 were measured in indoors (in the kitchen and living room) and outdoors (at the roadside). A total of 75 sampling locations (45 indoor and 30 outdoor) were selected for the study. The levels of PM2.5 and PM10 were determined using an AROCET531S instrument, while an universal air pump was used for the sampling of PM10 for the determination of trace elements by inductively coupled plasma-optical emission spectroscopy (ICP‒OES). The health impacts of PMs on the inhabitants of twelve microenvironments (MEs), where they spend much of their daily time, were estimated. The total amounts of PM2.5 and PM10, and trace metals in PM10 found in the nine or twelve MEs ranged from 10.6-119, 128-185, and 0.007-0.197 μg m-3, respectively. According to the United States Environment Protection Agency (USEPA) guidelines, ten of the twelve MEs can cause significant health problems for inhabitants (HI > 1) due to PM2.5 and PM10. Thus, special attention should be given by stakeholders/inhabitants to minimize the health impacts on long-term exposure. This study assessed the risk of levels of trace elements on the inhabitants who spend most of their daily lives. The study revealed that the lifetime cancer risk values for the individual and cumulative trace elements were within the tolerable range set by the USEPA guidelines.

Emission Factors, Chemical Composition and Ecotoxicity of PM10 from Road Dust Resuspension in a Small Inland City

Road dust resuspension in urban environments can contribute to high human exposure to metal(loid)s, polycyclic aromatic hydrocarbons, and other potentially toxic organic compounds. However, for many regions, information on loadings, emission factors and chemical profiles is lacking to accurately apply emission inventories and source apportionment models. In the present study, PM10 samples were collected with an in situ road dust sampler from eleven representative streets of Bragança, an inland city of the Iberian Peninsula, and were analysed for organic and elemental carbon by a thermal-optical technique, elemental composition by ICP-MS and ICP-OES, and ecotoxicity by a luminescence inhibition bioassay with Allivibrio fischeri. A global emission factor of 5.36 ± 2.35 mg veh−1 km−1 was obtained but in suburban areas the values reached twice the average. Total carbon accounted for 14.9 ± 6.8% of the PM10 mass, while element oxides represented the largest share (28.6 ± 18.7%). Very high enrichments were found for typical traffic-related elements such as Cu, Zn, S, Pb and Ni. The geochemical index Igeo further confirmed that road dust of the study region is extremely contaminated by elements mainly originated from tyre and brake wear. Although the total non-carcinogenic and carcinogenic risks associated with metal exposure were found to be low for both children and adults, the bioluminescence inhibition assay showed (eco)toxic responses for all samples, indicating that road dust resuspension may pose a significant human health and ecological threat.

Causes of the unremitting high ambient levels of PM10 in a suburban background site in NE Spain

Atmospheric PM10 and benzo(a)pyrene (BaP) concentrations in Manlleu (NE Spain) have remained high from 2008 to 2023, frequently exceeding EU limit/target values, and reaching BaP levels up to six times higher than urban averages in Spain. Furthermore, PM speciation campaigns were carried out in 2013, 2014–2015, 2016–2017 and 2021–2022. Chemical mass closure for autumn-winter showed a consistent PM10 composition for the different PM speciation campaigns, comprising 46–53% organic matter (OM), 18–26% secondary inorganic aerosol (SIA), 13–23% mineral matter (MM), and 5–9% elemental carbon (EC). Trend analysis revealed very light decrease and constant concentrations for PM10 and BaP, respectively over the study period, emphasizing the need for compliance with current and forthcoming EU air quality directives, the last aiming to halve PM10 limit values. Source apportionment of samples of the sporadic campaigns identified biomass burning (BB, 17.5 μg m−3, 48%) and MM and industry (16.3 μg m−3, 44%) as the main autumn-winter PM10 contributors, with high SIA concentrations attributed to several factors, including high ammonia (NH3) emissions. Local topography and meteorological conditions contribute to aggravate PM10 pollution. While metal concentrations have decreased since 2013, suggesting reduced industrial emissions, persistently high OM and EC concentrations indicate ongoing issues with BB emissions from domestic, commercial, and agricultural sources. Online analysis of black carbon (BC) and non-refractory PM1 components during winter 2016–2017 confirmed domestic and commercial BB as the primary sources of the BB contributions. These findings highlight the need of the implementation of more effective measures in reducing BB and agricultural/farming NH3 emissions. This study highlights the relevance of these issues for similar towns, the probable unremitting problem over the last decade, and the necessity of enhanced monitoring in small cities and policy actions to meet air quality standards under the new EU directive.

Overlooked Trace Molecules in Organic Aerosol Revealed by Gas Chromatography-Orbitrap Mass Spectrometry.

Molecular characterization of organic aerosol (OA) is crucial for understanding its sources and atmospheric processes. However, the chemical components of OA remain not well constrained. This study used gas chromatography-Orbitrap mass spectrometry (GC-Orbitrap MS) and GC-Quadrupole MS (GC-qMS) to investigate the organic composition in PM2.5 from Xi'an, Northwest China. GC-Orbitrap MS identified 335 organic tracers, including overlooked isomers and low-concentration molecules, approximately 1.6 times more than GC-qMS. The "molecular corridor" assessment shows the superior capability of GC-Orbitrap MS in identifying an expansive range of compounds with higher volatility and oxidation states, such as furanoses/pyranoses, di/hydroxy/ketonic acids, di/poly alcohols, aldehydes/ketones, and amines/amides. Seasonal variations in OA composition reflect diverse sources: increased di/poly alcohols in winter are derived from indoor emissions, furanoses/pyranoses and heterocyclics in spring and summer might be from biogenic emissions and secondary formation, and amides in autumn are probably from biomass burning. Integrating partial least squares discriminant analysis (PLS-DA) and potential source contribution function (PSCF) models, the source similarities and differences are further elucidated, highlighting the role of local emissions and transport from southern cities. This study offers new insights into the OA composition aided by the high mass resolution and sensitivity of GC-Orbitrap MS.

Seasonal and spatial variations of arsenic and its species in particulate matter in an urban environment of Brno, Czech Republic

The present paper deals with an analysis of total arsenic concentration using ICP-MS/MS and an analysis of concentration of several arsenic species, arsenite (AsIII), arsenate (AsV), monomethylarsonate (MMA), dimethylarsenite (DMA), and trimethylarsine oxide (TMAO), using HPLC-ICP-MS/MS in the PM10 fraction of airborne urban aerosol. The samples were collected during two campaigns, in the autumn of 2022 and in the winter of 2023, at three locations within the central European city of Brno, with the aim to evaluate the seasonal and spatial variations in the PM10 composition. The results confirmed only the seasonal variability in the content of the methylated arsenic species in PM10 influenced by biomethylation processes. To gain better understanding of the possible arsenic origin, a supplementary analysis of the total arsenic concentrations was performed in samples of different size fractions of particulate matter collected using ELPI + . Local emissions, including industrial activities and heating during the winter season, were suggested as the most likely predominant source contributing to the total As content in PM10.Graphical abstract

An analysis of the PM10 chemical composition and its spatial and seasonal variation in Piedmont (Italy) using Raman spectroscopy

Particulate Matter (PM) dramatically affects the well-being of a growing global population, particularly in urban areas. While air quality control is an important and pressing issue, particulate matter analysis typically focuses on size distribution and concentration, offering limited insights into chemical composition and pollutant sources.This study analyzes PM10 samples collected from five air quality monitoring stations across the Piedmont region. Specifically, the two of the stations are located in the urban environment of Turin, a city known as one of Europe's most polluted cities. The analysis has been carried out using primarily Raman Spectroscopy (RS) to identify the main PM components, investigate the different PM compositions, and evaluate the chemical and seasonal variations. Scanning Electron Microscopy (SEM) equipped with an Energy Dispersion X-ray spectrophotometer (EDX) has also been used to obtain further information about the elemental composition and the size distribution.Amorphous carbon, nitrate salt, sulfate salt, iron oxides, and quartz are the main compounds found. The results of our study highlight significant differences in the chemical composition of PM10, indicating variations in the sources and characteristics of PM. Notably, higher levels of nitrate and sulfate particles are linked respectively to cold and warm seasons. Whereas, amorphous carbon and iron oxides are associated with distinct geographic features at the sampling sites, such as traffic conditions. These findings emphasize the importance of understanding the different sources and characteristics of PM10 to develop effective air pollution mitigation strategies in the Piedmont region.

Chemical Composition of PM10 in a Classroom near the Copper Smelter in Bor, Serbia

Chemical Composition of PM10 in a Classroom near the Copper Smelter in Bor, Serbia

Dual-isotope ratios of carbonaceous aerosols for seasonal observation and their assessment as source indicators

Carbonaceous aerosols exhibit seasonal variations due to a complex interplay of emission sources, meteorological conditions, and chemical processes. This study presents the first year-round dual‑carbon isotopic analysis of carbonaceous aerosols in Northeastern Europe (Lithuania). The emphasis was placed on the processes affecting carbonaceous submicron particle (PM1) concentrations and their isotopic composition (δ13CTC, fc) during different seasons. Aerosol particles were collected in the two distinct sites: at an urban background site (Vilnius) and a coastal site (Preila). The concentrations of total carbon (TC) and black carbon (BC) varied both spatially and temporally. The annual average concentrations were 4 μg/m3 for TC and 2.3 μg/m3 for BC at the urban background site. They were considerably lower at the coastal site with 2.9 μg/m3 for TC and 0.74 μg/m3 for BC. The peak concentrations of TC and BC that occur during the cold season indicate a significant impact from residential heating. The δ13C in aerosols exhibited a distinct seasonal cycle with depleted δ13CTC values during the warm season (April–October). Through the integration of isotopic composition, contemporary carbon (fc), and BC source apportionment, we achieved precise predictions of isotopic parameter changes, encompassing pollution sources and the influence of meteorological parameters. To better understand the respective contributions of local and regional sources, air mass trajectories, wind patterns (speed and direction), and the polar conditional probability function (CPF) were studied in parallel. The study indicates that the isotopic composition of PM1 at both sites is primarily controlled by emission sources (local and regional), while meteorological conditions (temperature and mixing layer height) have less influence. These variations have important implications for regional air quality, climate dynamics, and public health, which are persistently subject to continuous research and monitoring.

Evaluating The Impact of Increased Heavy Oil Consumption on Urban Pollution Levels through Isotope (δ13C, δ34S, 14C) Composition

The impact of heavy fuel oil (HFO) on the chemical and isotopic composition of submicron particulate matter (PM1) was investigated. For this purpose, we conducted an analysis of water-soluble inorganic ions (WSIIs) and multiple isotopes (δ34S, δ13C, 14C) of PM1 and SO2 collected during two heating periods: before (2021–2022) and during the use of HFO (2022–2023) in Vilnius, Lithuania. The results showed that the combustion of HFO increased the concentrations of SO₂ (by 94%) and PM1-related sulfate (by 30%). It also altered the chemical composition of PM1, with sulfate becoming the predominant component (~40%) of WSIIs. The stable sulfur isotope ratios of SO2 (δ34SSO2) and sulfate (δ34SPM1) shifted significantly to more negative values (δ34SSO2 = 0.4‰, δ34SPM1 = −0.3‰) compared to the previous heating period. Anticorrelation between δ¹³C and δ³⁴S values indicated increased contributions of ¹³C-enriched fossil fuel sources (coal and HFO) in EC, although the share of fossil fuels in elemental carbon (EC) slightly decreased during the HFO period. The combustion of HFO affected the concentrations of PM1 chemical components and substantially impacted the isotopic composition and source contributions of sulfate and EC.

Laboratory study on the characteristics of fresh and aged PM1 emitted from typical forest vegetation combustion in Southwest China

The frequency and intensity of forest fires are amplified by climate change. Substantial quantities of PM1 emitted from forest fires can undergo gradual atmospheric dispersion and long-range transport, thus impacting air quality far from the source. However, the chemical composition and physical properties of PM emitted from forest fires and its changes during atmospheric transport remain uncertain. In this study, the evolution of organic carbon (OC), elemental carbon (EC), water-soluble ions, and water-soluble metals in the particulate phase of smoke emitted from the typical forest vegetation combustion in Southwest China before and after photo-oxidation was investigated in the laboratory. Two aging periods of 5 and 9 days were selected. The OC and TC mass concentrations tended to decrease after 9-days aged compared to fresh emissions. OP, OC2, and OC3 in PM1 are expected to be potential indicators of fresh smoke, while OC3 and OC4 may serve as suitable markers for identifying aged carbon sources from the typical forest vegetation combustion in Southwest China. K+ exhibited the highest abundant water-soluble ion in fresh PM1, whereas NO3− became the most abundant water-soluble ion in aged PM1. NH4NO3 emerged as the primary secondary inorganic aerosol emitted from typical forest vegetation combustion in Southwest China. Notably, a 5-day aging period proved insufficient for the complete formation of the secondary inorganic aerosols NH4NO3 and (NH4)2SO4. After aging, the mass concentration of the water-soluble metal Ni in PM1 from typical forest vegetation combustion in Southwest China decreased, while the mean mass concentrations of all other water-soluble metals increased in varying degrees. These findings provide valuable data support and theoretical guidance for studying the atmospheric evolution of forest fire aerosols, as well as contribute to policy formulation and management of atmospheric environment safety and human health.

The seasonal variation of Asian dust, anthropogenic PM, and their sources in Dushanbe, Tajikistan

Central Asia's arid climate and growing population make it susceptible to air pollution from mineral dust and anthropogenic sources. To assess the impact of these pollution sources on local air quality, the chemical composition of PM10 aerosol particles was collected within a year at Dushanbe, Tajikistan. Primary sources of the pollutants, their impact on PM10 composition, and their seasonal trends were assessed. The measurement approach employed analysis of trace metals, ions, organic compounds, laboratory investigations, diagnostic ratio calculations, all complemented by positive matrix factor analysis. The results reveal that for about 70% of the year, PM10 levels (80 ± 55 μg m−3 as the annual average) in Dushanbe were higher than the WHO limits, with varying levels during the seasons. Summer concentrations peaked up to 434 μg m−3 due to a combined mineral and road dust influence. Interestingly, winter concentrations reached 152 μg m−3 due to strong contributions (about 64%) from residential heating and fossil fuel combustion, often triggered during sub-10 °C temperatures. Mineral dust events were associated with elevated concentrations of trace metals, including Zn and Pb, alongside organic carbon and high-chain n - alkanes. During such events, Ca/Fe, Ca/Al ratios exceeded those of Saharan dust, suggesting a high salt content in Asian dust, potentially influenced by dried-off lake emissions. It was striking to observe that winter periods exhibited concerning levels of carcinogenic PAHs, such as benzo(b)fluoranthene (<25 ng m−3) and benzo[a]pyrene (<12 ng m−3, BaP), with average values of 4.1 ± 5.9 ng m−3 (BaP) that significantly exceed WHO recommendations. The high PM10 and PAH exposure could pose severe health risks, necessitating collective attention from the local authorities in developing new mitigation strategies concerning the reduction of emissions from residential heating of coal and wood in winter to curb combustion emissions and reduce exposure.

Pollution characteristics, source apportionment, and health risk assessment of PM10 and PM2.5 in rooftop and kerbside environment of Lanzhou, NW China.

To investigate air pollution in the kerbside environment and its associated human health risks, a study was conducted in Lanzhou during December 2018, as well as in April, June, and September 2019. The research aimed to characterize the composition of PM10 and PM2.5, including elements, ions, and carbonaceous components, at both rooftop and kerbside locations. Additionally, source apportionment and health risk assessment were conducted. The results showed that the average mass concentrations of PM10 on the rooftop were 176.01 ± 83.23μg/m3, and for PM2.5, it was 94.07 ± 64.89μg/m3. The PM10 and PM2.5 levels at the kerbside are 2.21 times and 1.79 times, respectively, greater than those on the rooftop. Moreover, the concentrations of elements, ions, and carbonaceous components in kerbside PM were higher than those at the rooftop location. Chemical mass closure analysis identified various sources, including organic matter, mineral dust, secondary ions, other ions, elements, and other components. In comparison to rooftop particulate matter (PM), mineral dust makes a more substantial contribution to kerbside PM. Secondary ions show an opposite trend, making a greater contribution to rooftop PM. The contribution of organic components within PM of the same particle size remains relatively consistent. The outcome of the health risk assessment indicates that Co, Cd, and As in PM within the kerbside and rooftop environments do not pose a notable carcinogenic risk. However, Al and Mn do present specific non-carcinogenic risks, particularly in the kerbside environment. Furthermore, children experience elevated non-carcinogenic risk compared to adults. These findings can serve as a scientific foundation for formulating policies within the local health department.

Never Walk Alone: Clathrin-coated Vesicle (CCV) Components in Plant Immunity

The plasma's protein makeup at the host-pathogen interaction membrane (PM) has significant effects on a plant cell's perception of and reacts to microbiological infections that invade. The capacity of a plant to adjust Its PM composition is essential for controlling the intensity, length, and immunological response integration. One method by which plant cells reconfigure the vesicular trafficking on their cell surface, encompassing secretion and endocytosis. During these trafficking procedures, cargo proteins (such as transporters, receptors for pattern recognition, and other proteins with immunological activities) by tiny, membrane-bound vesicles to or from the PM. Vesicles covered with clathrin (CCVs) that develop at the PM and trans-Golgi membranes Early endosomes and networks have become the most common vesicle form in the control of plant defense mechanisms.

Evaluating coarse PM composition and sources based on bulk and molecular speciation of PM2.5 and PM10 in Nanjing, East China

To understand the differences in the composition and sources of PM2.5 and PM10 caused by coarse particles, integrated PM2.5 and PM10 samples were synchronously collected in Nanjing, East China, in summer 2020 and winter 2020/2021. Bulk and molecular speciation and light absorption measurements of aerosol extracts were performed, followed by positive matrix factorization (PMF) based on the PM2.5 and PM10 data sets, respectively. The difference in average concentrations of total bulk species between PM2.5 and PM10 was mainly caused by the distribution of considerable NO3–, SO42–, Ca2+, and organic carbon (OC) in coarse particles. Coarse PM influenced by abrasion products from tire wear and leaves contributed about half of the low-volatility n-alkanes in summer. The contribution of coarse PM to biomass burning tracers and water-soluble OC increased in winter when biomass combustion was excessively active. More than 70% of sugar polyols were attributable to coarse PM in summer, and biomass burning could be an important source in winter. The light-absorbing organic chromophores were almost entirely associated with PM2.5, but water-soluble organic carbon (WSOC) exhibited stronger light absorption in PM10 extracts than in PM2.5 extracts possibly due to the influence of coarse PM on pH. PMF analysis indicated that biomass burning, aqueous-phase reactions, and processed dust were the main contributors of organic matter and its light absorption in winter. Biogenic primary and secondary sources made discernable contributions only in summer. The differences between PM2.5 and PM10 were likely attributed to mixing of crustal dust, combustion particles, and surface reactions.

Environmentally persistent free radicals from residential raw coal combustion and association with chemical components

Emerging environmental persistent free radicals (EPFRs), can generate reactive oxygen species (ROS), posing potential exposure risks to human health. Incomplete coal combustion is a major source of EPFRs. Organic carbonaceous fractions are essential and important players in the formation of EPFRs during coal combustion. However, relationship between individual organic carbonaceous and non-carbon fractions with EPFRs in such emissions are not well known. This paper investigated the characteristics of EPFRs discharged from simulated coal combustion. Our results showed that the concentration of EPFRs was major concentrated on PM1.1 (51.66–81.85 %), and more easily oxidized by oxygen resulting in producing more oxygen-centered radicals (semiquinone-type) in PM1.1. The mean of line width (ΔHp-p) was 5.87 ± 0.41G higher than that of biomass combustion, indicating more free radical species were emitted from coal combustion. Humic-like substances-carbon (HULIS-C) was the major contributor of the formation of EPFRs and facilitate the generated of EPFRs. Secondary processes have also contributed to the formation of EPFRs during the coal combustion. Our result also noted that there was no relationship between transition metals and EPFRs, may be due to the variability and complexity of the chemical properties and composition of PM. This is critical for the prediction of geochemical behavior and risk assessment of EPFRs, which can provide basic data to support policy development to address rural air pollutant emissions.

Composition, sources and potential source regions of aerosols under contrasting environment conditions of Lanzhou, a valley city of western China: Observations by means of topographic relief

Chemical composition in PM2.5 (particulate matter with a diameter less than 2.5 μm) is essential information for evaluating their climate, environment and health effects. Concentrations of carbonaceous components and water-soluble ions in PM2.5 and the differences under varying environmental conditions in western China are poorly understood. During the period from July 2021 to July 2022, we conducted synchronous offline sampling of PM2.5 by deploying four identical sampling devices at altitudes ranging from 1500 m to 3600 m along the unique topography of the Lanzhou River Valley in western China. The major chemical components in PM2.5 are carbonaceous aerosols, NO3− and SO42− with the average concentrations of 28.07, 8.66 and 6.01 μg m−3 for the urban and surrounding rural areas, and 9.94, 2.45 and 3.11 μg m−3 for background site of Lanzhou. The concentrations of OC (organic carbon) and EC (elemental carbon) gradually decrease from urban area to suburban sites with increasing elevation. Coal combustion, vehicle emissions, secondary formation, salted aerosols and surface dust resuspension are found to be the primary sources of PM2.5 in both urban and rural areas of Lanzhou. The contribution of vehicle emissions decreases from urban areas to mountainous rural areas, contrary to the coal combustion and biomass burning. The study is significant for taking targeted measures to solve air pollution problem at different environmental conditions (urban, rural and background) over complex terrain.

Risk of heavy metal(loid) compositions in fine particulate matter on acute cardiovascular mortality: a poisson analysis in Anyang, China.

Fine particulate matter (PM2.5) is a risk factor of cardiovascular disease. Associations between PM2.5 compositions and cardiovascular disease are a point of special interest but inconsistent. This study aimed to explore the cardiovascular effects of heavy metal(loid) compositions in PM2.5. Data for mortality, air pollutants and meteorological factors in Anyang, China from 2017 to 2021 were collected. Heavy metal(loid) in PM2.5 were monitored and examined monthly. A Case-crossover design was applied to the estimated data set. The interquartile range increase in cadmium (Cd), antimony (Sb) and arsenic (As) at lag 1 was associated with increment of 8.1% (95% CI: 3.3, 13.2), 4.8% (95% CI: 0.2, 9.5) and 3.5% (95% CI: 1.1, 6.0) cardiovascular mortality. Selenium in lag 2 was inversely associated with cerebrovascular mortality (RR = 0.920 95% CI: 0.862, 0.983). Current-day exposure of aluminum was positively associated with mortality from ischemic heart disease (RR = 1.083 95% CI: 1.001, 1.172). Stratified analysis indicated sex, age and season modified the cardiovascular effects of As (P < 0.05). Our study reveals that heavy metal(loid) play key roles in adverse effects of PM2.5. Cd, Sb and As were significant risk factors of cardiovascular mortality. These findings have potential implications for accurate air pollutants control and management to improve public health benefits.

Source apportionment and health risk assessment of PM10 bound carbonaceous and elemental species in the central Himalayas

In this extensive investigation, the sources and health risk assessment of carbonaceous aerosols, as well as the elemental compositions (Ca, Al, Fe, S, K, Mg, Pd, B, Mo, Zn, Ag, Nb, Ga, Cl, Ti, Zr, Na, Cr, Cu, Mn, Cs, P, Y, Sb, Ni, Sn, F, Sr, Br, Pm, U, Pb, Th, Br, Rb, and V) of PM10, were conducted throughout January-December 2021 in Nainital, a central Himalayan region of India. The average annual mass concentration of PM10 was determined to be 64±6 µg m-3. Carbonaceous aerosols (CAs), comprising OC, EC, WSOC, and SOC, exhibited annual averages of 9.3±0.8 µg m-3, 4.9±0.5 µg m-3, 1.5±0.2 µg m-3, 2.7±0.2 µg m-3, and 2.97±0.45 µg m-3, respectively. The elemental composition featured major contributors such as Ca, Al, Fe, S, and K, alongside trace levels of various elements (Mg, Pd, B, Mo, Zn, Ag, Nb, Ga, Cl, Ti, Zr, Na, and Cr). Positive Matrix Factorization (PMF) identified six primary contributors to PM10, each with varying percentage contributions: crustal/soil/road dust, soil re-suspension, combustion, vehicular emissions, industrial emissions, and biomass burning. The health risk assessment revealed elevated Hazard Quotient (HQ) values for Cr and Mn in children, indicating a non-carcinogenic health risk. Adults exposed to high Cr levels may face potential carcinogenic risks, while elements like Al, Pb, Cu, Zn, and Ni pose no health hazards, aligning with USEPA guidelines.

Measurement report: Hygroscopicity of size-selected aerosol particles in the heavily polluted urban atmosphere of Delhi: impacts of chloride aerosol

Abstract. Recent research has revealed the crucial role of wintertime, episodic high chloride (H-Cl) emissions in the Delhi region, which significantly impact aerosol hygroscopicity and aerosol-bound liquid water, thus contributing to the initiation of Delhi fog episodes. However, these findings have primarily relied on modeled aerosol hygroscopicity, necessitating validation through direct hygroscopicity measurements. This study presents the measurements of non-refractory bulk aerosol composition of PM1 from an Aerodyne aerosol chemical speciation monitor and for first-time size-resolved hygroscopic growth factors (nucleation, Aitken, and accumulated mode particles) along with their associated hygroscopicity parameters at 90 % relative humidity using a hygroscopic tandem differential mobility analyzer at the Delhi Aerosol Supersite. Our observations demonstrate that the hygroscopicity parameter for aerosol particles varies from 0.00 to 0.11 (with an average of 0.03 ± 0.02) for 20 nm particles, 0.05 to 0.22 (0.11 ± 0.03) for 50 nm particles, 0.05 to 0.30 (0.14 ± 0.04) for 100 nm particles, 0.05 to 0.41 (0.18 ± 0.06) for 150 nm particles, and 0.05 to 0.56 (0.22 ± 0.07) for 200 nm particles. Surprisingly, our findings demonstrate that the period with H-Cl emissions displays notably greater hygroscopicity (0.35 ± 0.06) in comparison to spans marked by high biomass burning (0.18 ± 0.04) and high hydrocarbon-like organic aerosol (0.17 ± 0.05) and relatively cleaner periods (0.27 ± 0.07). This research presents initial observational proof that ammonium chloride is the main factor behind aerosol hygroscopic growth and aerosol-bound liquid water content in Delhi. The finding emphasizes ammonium chloride's role in aerosol–water interaction and related haze/fog development. Moreover, the high chloride levels in aerosols seem to prevent the adverse impact of high organic aerosol concentrations on cloud condensation nuclei activity.