Chemical Composition Of PM2 Research Articles

Molecular composition of fresh and aged aerosols from residential wood combustion and gasoline car with modern emission mitigation technology.

Emissions from road traffic and residential heating contribute to urban air pollution. Advances in emission reduction technologies may alter the composition of emissions and affect their fate during atmospheric processing. Here, emissions of a gasoline car and a wood stove, both equipped with modern emission mitigation technology, were photochemically aged in an oxidation flow reactor to the equivalent of one to five days of photochemical aging. Fresh and aged exhausts were analyzed by ultrahigh resolution mass spectrometry. The gasoline car equipped with a three-way catalyst and a gasoline particle filter emitted minor primary fine particulate matter (PM2.5), but aging led to formation of particulate low-volatile, oxygenated and highly nitrogen-containing compounds, formed from volatile organic compounds (VOCs) and gases incl. NOx, SO2, and NH3. Reduction of the particle concentration was also observed for the application of an electrostatic precipitator with residential wood combustion but with no significant effect on the chemical composition of PM2.5. Comparing the effect of short and medium photochemical exposures on PM2.5 of both emission sources indicates a similar trend for formation of new organic compounds with increased carbon oxidation state and nitrogen content. The overall bulk compositions of the studied emission exhausts became more similar by aging, with many newly formed elemental compositions being shared. However, the presence of particulate matter in wood combustion results in differences in the molecular properties of secondary particles, as some compounds were preserved during aging.

The Cytotoxic Effects of Fine Particulate Matter (PM2.5) from Different Sources at the Air-Liquid Interface Exposure on A549 Cells.

The health of humans has been negatively impacted by PM2.5 exposure, but the chemical composition and toxicity of PM2.5 might vary depending on its source. To investigate the toxic effects of particulate matter from different sources on lung epithelial cells (A549), PM2.5 samples were collected from residential, industrial, and transportation areas in Nanjing, China. The chemical composition of PM2.5 was analyzed, and toxicological experiments were conducted. The A549 cells were exposed using an air-liquid interface (ALI) exposure system, and the cytotoxic indicators of the cells were detected. The research results indicated that acute exposure to different sources of particulate matter at the air-liquid interface caused damage to the cells, induced the production of ROS, caused apoptosis, inflammatory damage, and DNA damage, with a dose-effect relationship. The content of heavy metals and PAHs in PM2.5 from the traffic source was relatively high, and the toxic effect of the traffic-source samples on the cells was higher than that of the industrial- and residential-source samples. The cytotoxicity of particulate matter was mostly associated with water-soluble ions, carbon components, heavy metals, PAHs, and endotoxin, based on the analysis of the Pearson correlation. Oxidative stress played an important role in PM2.5-induced biological toxicity.

Key toxic components and sources affecting oxidative potential of atmospheric particulate matter using interpretable machine learning: Insights from fog episodes

Fog significantly affects the air quality and human health. To investigate the health effects and mechanisms of atmospheric fine particulate matter (PM2.5) during fog episodes, PM2.5 samples were collected from the coastal suburb of Qingdao during different seasons from 2021 to 2022, with the major chemical composition in PM2.5 analyzed. The oxidative potential (OP) of PM2.5 was determined using the dithiothreitol (DTT) method. A positive matrix factorization model was adopted for PM2.5. Interpretable machine learning (IML) was used to reveal and quantify the key components and sources affecting OP. PM2.5 exhibited higher oxidative toxicity during fog episodes. Water-soluble organic carbon (WSOC), NH4+, K+, and water-soluble Fe positively affected the enhancement of DTTV (volume-based DTT activity) during fog episodes. The IML analysis demonstrated that WSOC and K+ contributed significantly to DTTV, with values of 0.31 ± 0.34 and 0.27 ± 0.22 nmol min−1 m−3, respectively. Regarding the sources, coal combustion and biomass burning contributed significantly to DTTV (0.40 ± 0.38 and 0.39 ± 0.36 nmol min−1 m−3, respectively), indicating the significant influence of combustion-related sources on OP. This study provides new insights into the effects of PM2.5 compositions and sources on OP by applying IML models.

One-Year-Long, Comprehensive Analysis of PM Number and Mass Size Distributions in Warszawa (Poland)

Abstract The properties of particulate matter PM, including its impact on the environment and human health, depend mainly on the size (more precisely: size distribution) of the particles since the size is usually dependent on the processes/sources of the PM. This work presents the results of a one-year-long measurement campaign of PM. PALAS Fidas 200 from Airpointer air quality station was used. The PM was measured in Warsaw, Poland continuously from 1st May 2022 to 30th April 2023; size distribution was recorded with 120 s intervals and averaged in 3600 s periods. It was found, that the number and the mass size distribution varied depending on the averaging period (different hours of the day, different days of the week, and different months of the year). Additionally, the authors determined the periods of impact on selected sources (traffic emission, municipal emission, and industrial emission) on the number and mass size distributions of PM at the sampling site. Monitoring of number and mass size distributions of PM is a relatively easy and more cost-effective method than analysing the chemical composition of PM. Therefore, is crucial to develop a method of identifying sources of PM based on size distributions. It was found that such a method can be in the future as successful in source apportionment as in the analysis of chemical compositions.

A PM10 chemically characterized nation-wide dataset for Italy. Geographical influence on urban air pollution and source apportionment

Urban textures of the Italian cities are peculiarly shaped by the local geography generating similarities among cities placed in different regions but comparable topographical districts. This suggested the following scientific question: can different topographies generate significant differences on the PM10 chemical composition at Italian urban sites that share similar geography despite being in different regions? To investigate whether such communalities can be found and are applicable at Country-scale, we propose here a novel methodological approach. A dataset comprising season-averages of PM10 mass concentration and chemical composition data was built, covering the decade 2005–2016 and referring to urban sites only (21 cities). Statistical analyses, estimation of missing data, identification of latent clusters and source apportionment modeling by Positive Matrix Factorization (PMF) were performed on this unique dataset. The first original result is the demonstration that a dataset with atypical time resolution can be successfully exploited as an input matrix for PMF obtaining Country-scale representative chemical profiles, whose physical consistency has been assessed by different tests of modeling performance.Secondly, this dataset can be considered a reference repository of season averages of chemical species over the Italian territory and the chemical profiles obtained by PMF for urban Italian agglomerations could contribute to emission repositories.These findings indicate that our approach is powerful, and it could be further employed with datasets typically available in the air pollution monitoring networks.

Exploring the amplified role of HCHO in the formation of HMS and O3 during the co-occurring PM2.5 and O3 pollution in a coastal city of southeast China

Abstract. To develop effective strategies for controlling both PM2.5 and O3 levels, it is crucial to understand their synergistic mechanisms and key precursors and the atmospheric physiochemical processes involved. In this study, a wintertime co-occurring O3 and PM2.5 pollution event in a coastal city in southeast China was investigated based on high-time-resolution measurements of criteria air pollutants and chemical compositions of PM2.5, and O3 precursors, such as NOx, HCHO, and volatile organic compounds (VOCs). The results of this study revealed the characteristics of positively correlated PM2.5 and MDA8 O3 concentrations, and an increase in atmospheric oxidation capacity (AOC) during the cold seasons. Strong correlations (R2= 0.415–0.477) between HCHO, Fe, Mn, and sulfate concentrations were observed, suggesting the influence of catalyzed oxidation processes in the coastal city. Through an observation-based model (OBM) analysis coupled with the Regional Atmospheric Chemistry Mechanism, version 2 (RACM2) and the Chemical Aqueous-Phase Radical Mechanism, version 3.0 (CAPRAM 3.0), we found that high concentrations of precursors (SO2 and HCHO), high relative humidity, and moderately acidic pH conditions enhanced the heterogeneous formation of hydroxymethanesulfonate (HMS) in PM2.5. Furthermore, by employing an OBM coupled to the Master Chemical Mechanism (OBM-MCM), we verified that disabling the HCHO mechanism could decrease daytime net O3 production rates by reducing the production rates of HO2 + NO. These results were consistent with the daily values of AOC, OH, HO2, and RO2 concentrations. This study contributes to a better understanding of the significance of HCHO in photochemical reactions and the formation of HMS in a coastal city.

Variation of PM2.5 and PM10 in emissions and chemical compositions in different seasons from a manure-belt laying hen house

Particulate matter (PM) emissions from animal houses and the corresponding hazard have raised increasing attention during recent years. In this study, a large-scale manure-belt laying hen house located in Beijing, China was selected as the experimental site for the study of the emission rates (ER) and chemical compositions of PM2.5 and PM10 in 3 seasons, namely, summer, autumn, and winter, to investigate their possible influences on ambient air quality and human health. The results showed that the mean ER from the hen house in summer, autumn, and winter were 9.0 ± 1.7, 2.4 ± 0.7, and 1.9 ± 0.7 mg hen-1 d-1 for PM2.5 (P < 0.05), and 30.7 ± 1.1, 12.8 ± 1.5, and 10.9 ± 0.9 mg hen-1 d-1 for PM10 (P < 0.05), respectively. Moreover, large amounts of secondary inorganic aerosols (SIA) were observed inside the house in summer, accounting for 11.4 and 9.6% of indoor PM2.5 and PM10 mass, respectively, compared with the value of <1.4% in autumn and winter. Among the 31 detected elements in indoor PM, arsenic concentration exceeded the threshold set in legislation. Zn had a notably high concentration of 3,403 to 4,432 ng m-3 in indoor PM10, which was 28 to 71 times higher than that in ambient PM10. The findings suggest that the poultry-raising house emit PM2.5 and PM10 containing SIA and toxic heavy-metal elements such as As and Zn to the ambient with much more emissions in summer than in autumn and winter. Considering the increasing development of poultry-raising farming in China, the potential hazard derived from the exhaust of PM2.5 and PM10 should be focused on, especially during summer.

High-time-resolution chemical composition and source apportionment of PM2.5 in northern Chinese cities: implications for policy

Abstract. Fine particulate matter (PM2.5) pollution is still one of China's most important environmental issues, especially in northern cities during wintertime. In this study, intensive real-time measurement campaigns were conducted in Xi'an, Shijiazhuang, and Beijing to investigate the chemical characteristics and source contributions of PM2.5 and explore the formation of heavy pollution for policy implications. The chemical compositions of PM2.5 in the three cities were all dominated by organic aerosol (OA) and nitrate (NO3-). Results of source apportionment analyzed by a hybrid environmental receptor model (HERM) showed that the secondary formation source contributed more to PM2.5 compared to other primary sources. Biomass burning was the dominant primary source in the three pilot cities. The contribution of coal combustion to PM2.5 is non-negligible in Xi'an and Shijiazhuang but is no longer an important contributor in the capital city of Beijing due to the execution of a strict coal-banning policy. The potential formation mechanisms of secondary aerosol in the three cities were further explored by establishing the correlations between the secondary formation sources and aerosol liquid water content (ALWC) and Ox (O3+NO2), respectively. The results showed that photochemical oxidation and aqueous-phase reaction were two important pathways of secondary aerosol formation. According to source variations, air pollution events that occurred in campaigns were classified into three types: biomass-combustion-dominated, secondary-formation-source-dominated, and a combination of primary and secondary sources. Additionally, this study compares the changes in chemical composition and source contributions of PM2.5 in past decades. The results suggest that the clean-energy replacements for rural households should be urgently encouraged to reduce the primary source emissions in northern China, and collaborative control on ozone and particulate matter needs to be continuously promoted to weaken the atmosphere oxidation capacity for the sake of reducing secondary aerosol formation.

Characterizing the sources of ambient PM10 organic aerosol in urban and rural Catalonia, Spain

Organic aerosols (OA) have recently been shown to be the dominant contributor to the oxidative potential of airborne particulate matter in northeastern Spain. We collected PM10 filter samples every fourth day from January 2017 to March 2018 at two sampling stations located in Barcelona city and Montseny Natural Park, representing urban and rural areas, respectively. The chemical composition of PM10 was analyzed offline using a broad set of analytical instruments, including high-resolution time-of-flight mass spectrometry (HR-ToF-AMS), a total organic carbon analyzer (TCA), inductively coupled plasma atomic emission spectrometry (ICP-AES), inductively coupled plasma mass spectrometry (ICP-MS), ion chromatography (IC), and thermal-optical carbon analyzer. Source apportionment analysis of the water-soluble organic content of the samples measured via HR-ToF-AMS revealed two primary and two secondary sources of OA, which included biomass-burning OA (BBOA), sulfur-containing OA (SCOA), as well as summer- and winter‑oxygenated OA (SOOA and WOOA). The presence of hydrocarbon-like water-insoluble OA was also identified based on concentration trends in black carbon and nitrogen oxides. The results from the source apportionment analysis of the inorganic composition were correlated with different OA factors to assess potential source contributors. Barcelona showed significantly higher average water-soluble OA concentrations (5.63 ± 0.56 μg m-3) than Montseny (3.27 ± 0.37 μg m-3) over the sampling period. WOOA accounted for nearly 27 % of the averaged OA in Barcelona compared to only 7 % in Montseny. In contrast, SOOA had a greater contribution to OA in Montseny (47 %) than in Barcelona (24 %). SCOA and BBOA were responsible for 15–28 % of the OA at both sites. There were also seasonal variations in the relative contributions of different OA sources. Our overall results showed that local anthropogenic sources were primarily responsible for up to 70 % of ambient soluble OA in Barcelona, and regulating local-scale emissions could significantly improve air quality in urban Spain.

Evaluation of PM Chemical Composition in Thessaloniki, Greece Based on Air Quality Simulations

The average PM10 daily levels over the urban area of Thessaloniki, Greece, usually exceed the air quality limits and therefore the improved PM chemical composition and air quality modeling results that will facilitate the design of the most appropriate mitigation measures (e.g., limitations in wood combustion for heating purposes) are essential. The air quality modeling system WRF-CAMx was applied over a 2 × 2 km2 horizontal resolution grid covering the greater area of Thessaloniki for the year 2015, when Greece was still confronting the consequences of the financial crisis. The output hourly surface concentrations of twelve PM species at three sites of different environmental type characterization in the city of Thessaloniki were temporally and spatially analyzed. Carbonaceous aerosols (organic and elemental) are the major contributor to total PM10 levels during winter representing a 35–40% share. During summer, mineral aerosols (excluding dust) distribute by up to 48% to total PM10 levels, being the major contributor attributed to road traffic. PM species, during winter, increase in the morning and in the afternoon mainly due to road transport and residential heating, respectively, in addition with the unfavorable meteorological conditions. An underestimation of the primary organic carbon aerosol levels during winter is identified. The application of the modeling system using a different speciation profile for the fine particles emissions from residential heating based on observational data instead of the CAMS emissions profile revealed an improvement in the simulated OC/EC values for which a 50% increase was identified compared to the base run.

Emissions and meteorological impacts on PM2.5 species concentrations in Southern California using generalized additive modeling

The chemical composition of PM2.5 has a significant impact on human health and air quality, and its accurate knowledge can be used to identify contributing emission sources. Assessing and quantifying the impacts of various factors (e.g., emissions, meteorology, and large-scale climate patterns) on the main PM2.5 chemical components can give guidance for implementing effective regulations to improve air quality in the future. In this study, we developed generalized additive models (GAMs) to assess how emissions, meteorological factors, and large-scale climate indices affected ammonium, sulfate, nitrate, elemental carbon, and organic carbon from 2002 to 2019 in the South Coast Air Basin (SoCAB). Concentration trends from three sites in the SoCAB are studied. The statistical results showed that GAMs can capture the variability of these species' daily concentrations (R2 = 0.6 to 0.7) and annual concentrations (R2 = 0.93 to 0.99). Precursor emissions most significantly affect PM2.5 species production, though meteorological factors like maximum temperature, relative humidity, wind speed, and boundary layer height, also influence PM2.5 composition. In the future, these meteorological factors will become more significant in affecting PM2.5 speciation, although emissions will continue to strongly affect formation. Results show that the composition of most PM2.5 species will decrease in the future except for OC, which will become the largest contributor to PM2.5.

Chemical composition and potential sources of PM2.5 in Hanoi

The chemical composition of PM2.5 was monitored simultaneously at two sites, one in a general area of the city center and one at a roadside, in Hanoi, Vietnam, during August 2019–July 2020 using 220 daily (24 h) filter samples. PM mass, water soluble ions, trace elements, organic and elemental carbon and sugar anhydrides were measured. The annual average PM2.5 concentrations, 49 and 46 μg m−3 at the traffic and the general urban site, respectively, exceeded the national (25 μg m−3) and 2021 WHO limit values (5 μg m−3). Daily PM2.5 concentrations were the highest in winter when stagnant meteorological conditions prevailed. On average, half of the resolved mass was organic matter, of which about 40% was attributable to biomass burning, most likely rice straw field burning and domestic fuel combustion. One third of PM2.5 was secondary inorganic aerosol which was dominated by sulphate hence indicating a high contribution of stationary sources like coal combustion. The elemental carbon level was higher at the traffic site, except in April 2020 during the COVID-19 restrictions. Zinc was the most common trace element with high daily variations and large differences between the sites, and it often peaked with Cd, Cl− and Pb indicating contribution of industrial sources and/or coal combustion. The highest zinc concentrations appeared on a few days and likely originated from open burning of municipal solid waste. It appeared that scattered open waste and biomass burning, as well as coal combustion, are important sources causing spikes of PM2.5 pollution in Hanoi above the general levels caused by routine industrial and traffic sources, especially during stagnant winter days. Source contributions were further studied with positive matrix factorization producing six source factors: traffic (12%), local secondary inorganic aerosol (SIA, 18%), biomass burning (19%), industry (9%), long-range transported SIA (25%) and dust (17%).

Real-world emission for in-use non-road construction machinery in Wuhan, China.

Non-road construction machinery (NRCM) emissions pollutants significantly impact air quality. Six typical NRCM (2 excavators, 3 loaders, and 1 forklift) are analyzed based on a portable emission measurement system (PEMS) in Wuhan to estimate the real-world emission characteristics and chemical composition of PM2.5 of NRCM. The results show that the fuel-based average emission factors (EFs) of carbon monoxide (CO), hydrocarbon (HC), nitrogen oxides (NOx), and particulate matter (PM) are 19.4 ~ 35.7gkg-1 fuel, 2.9 ~ 7.9gkg-1 fuel, 57.5 ~ 95.3gkg-1 fuel, and 1.8 ~ 2.6gkg-1 fuel for the tested NRCM. The high NOx EF implies that the regulation of NOx emission in Wuhan should be strengthened. In addition, the PM2.5 chemical composition profiles for NRCM show that the PM2.5 emitted from NRCM is dominated by organic carbon and elemental carbon (56.11 ~ 73.85%), followed by water-soluble ions (WSIs, 1.47 ~ 3.46%), and elements (0.16 ~ 0.41%). The major WSIs species are Cl-, Na+ andNO3-, and the major elements are Ca, Na, and K, which are important markers for PM2.5 source analysis. The results of EFs and chemical composition emission characteristics of NRCM tailpipe pollutants obtained in the real-world can provide essential data support for accurately establish of emission inventory of non-road mobile sources in Wuhan.

Characteristics and Risk Assessment of Environmentally Persistent Free Radicals (EPFRs) of PM2.5 in Lahore, Pakistan.

Environmentally persistent free radicals (EPFRs) are an emerging pollutant and source of oxidative stress. Samples of PM2.5 were collected at the urban sites of Lahore in both winter and summertime of 2019. The chemical composition of PM2.5, EPRF concentration, OH radical generation, and risk assessment of EPFRs in PM2.5 were evaluated. The average concentration of PM2.5 in wintertime and summertime in Lahore is 15 and 4.6 times higher than the national environmental quality standards (NEQS) of Pakistan and WHO. The dominant components of PM2.5 are carbonaceous species. The concentration of EPFRs and reactive oxygen species (ROS), such as OH radicals, is higher in the winter than in the summertime. The secondary inorganic ions do not contribute to the generation of OH radicals, although the contribution of SO42+, NO3-, and NH4+ to the mass concentration of PM2.5 is greater in summertime. The atmospheric EPFRs are used to evaluate the exposure risk. The EPFRs in PM2.5 and cigarette smoke have shown similar toxicity to humans. In winter and summer, the residents of Lahore inhaled the amount of EPFRs equivalent to 4.0 and 0.6 cigarettes per person per day, respectively. Compared to Joaquin County, USA, the residents of Lahore are 1.8 to 14.5 times more exposed to EPFRs in summer and wintertime. The correlation analysis of atmospheric EPFRs (spin/m3) and carbonaceous species of PM2.5 indicates that coal combustion, biomass burning, and vehicle emissions are the possible sources of EPFRs in the winter and summertime. In both winter and summertime, metallic and carbonaceous species correlated well with OH radical generation, suggesting that vehicular emissions, coal combustion, and industrial emissions contributed to the OH radical generation. The study's findings provide valuable information and data for evaluating the potential health effects of EPFRs in South Asia and implementing effective air pollution control strategies.

Implications of the Improvement in Atmospheric Fine Particles: A Case Study of COVID-19 Pandemic in Northern Taiwan

The outbreak of COVID-19 pandemic in northern Taiwan led to the implementation of Level 3 alert measures during 2021 and thereby impacted the air quality significantly, which provided an unprecedented opportunity to better understand the control strategies on air pollutants in the future. This study investigated the variations in sources, chemical characteristics and human health risks of PM2.5 comprehensively. The PM2.5 mass concentrations decreased from pre-alert to Level 3 alert by 49.4%, and the inorganic ions, i.e., NH4+, NO3- and SO42-, dropped even more by 71%, 90% and 52%, respectively. Nonetheless, organic matter (OM) and elemental carbon (EC) simply decreased by 36% and 13%, which caused the chemical composition of PM2.5 to change so that the carbonaceous matter in PM2.5 dominated instead of the inorganic ions. Correlation-based hierarchical clustering analysis further showed that PM2.5 was clustered with carbonaceous matter during the Level 3 alert, while that clustered with inorganic ions during both pre-alert and post-alert periods. Moreover, 6 sources of PM2.5 were identified by positive matrix factorization (PMF), in which secondary nitrate (i.e., aging traffic aerosols) exhibited the most significant decrease and yet primary traffic-related emissions, dominated by carbonaceous matter, changed insignificantly. This implied that secondary traffic-related aerosols could be easily controlled when traffic volume declined, while primary traffic source needs more efforts in the future, especially for the reduction of carbonaceous matter. Therefore, cleaner energy for vehicles is still needed. Assessments of both carcinogenic risk and non-carcinogenic risk induced by the trace elements in PM2.5 showed insignificant decrease, which can be attributed to the factories that did not shut down during Level 3 alert. This study serves as a metric to underpin the mitigation strategies of air pollution in the future and highlights the importance of carbonaceous matter for the reduction in PM2.5.

Submicron Aerosol Composition and Source Contribution across the Kathmandu Valley, Nepal, in Winter.

The Kathmandu valley experiences an average wintertime PM1 concentration of ∼100 μg m-3 and daily peaks over 200 μg m-3. We present ambient nonrefractory PM1 chemical composition, and concentration measured by a mini aerosol mass spectrometer (mAMS) sequentially at Dhulikhel (on the valley exterior), then urban Ratnapark, and finally suburban Lalitpur in winter 2018. At all sites, organic aerosol (OA) was the largest contributor to combined PM1 (C-PM1) (49%) and black carbon (BC) was the second largest contributor (21%). The average background C-PM1 at Dhulikhel was 48 μg m-3; the urban enhancement was 120% (58 μg m-3). BC had an average of 6.1 μg m-3 at Dhulikhel, an urban enhancement of 17.4 μg m-3. Sulfate (SO4) was 3.6 μg m-3 at Dhulikhel, then 7.5 μg m-3 at Ratnapark, and 12.0 μg m-3 at Lalitpur in the brick kiln region. Chloride (Chl) increased by 330 and 250% from Dhulikhel to Ratnapark and Lalitpur on average. Positive matrix factorization (PMF) identified seven OA sources, four primary OA sources, hydrocarbon-like (HOA), biomass burning (BBOA), trash burning (TBOA), a sulfate-containing local OA source (sLOA), and three secondary oxygenated organic aerosols (OOA). OOA was the largest fraction of OA, over 50% outside the valley and 36% within. HOA (traffic) was the most prominent primary source, contributing 21% of all OA and 44% of BC. Brick kilns were the second largest contributor to C-PM1, 12% of OA, 33% of BC, and a primary emitter of aerosol sulfate. These results, though successive, indicate the importance of multisite measurements to understand ambient particulate matter concentration heterogeneity across urban regions.

Seasonal Variation of Mass Concentration and Chemical Composition of PM2.5 and PM10, Source Identification and Human Health Risk Assessment in Meknes City in Morocco

Seasonal Variation of Mass Concentration and Chemical Composition of PM2.5 and PM10, Source Identification and Human Health Risk Assessment in Meknes City in Morocco

Aerosols in Northern Morocco-2: Chemical Characterization and PMF Source Apportionment of Ambient PM2.5

Insufficient data on the chemical composition of PM2.5 and its emission sources in the southwestern (SW) Mediterranean area has been identified. Ambient PM2.5 samples were collected in an urban area of Tetouan city, northern Morocco. Chemical mass closure calculations and positive matrix factorization were performed for the comprehensive dataset of PM2.5 chemical analyses. Mass closure improved when multipliers (1.2 and 0.23, respectively) were used for the conversion of organic carbon (OC) and calcium ion (Ca2+) into particulate organic matter (POM) and mineral dust masses, respectively. The mass closure model performed well in this SW Mediterranean region, with a significant correlation (r2 = 0.97) obtained between gravimetrically measured and chemically determined PM2.5 mass. The one-year average concentration of PM2.5 was 17.96 μg/m3, and the major chemical components were POM (34%), secondary inorganic aerosol (SIA) (28%), and black carbon (18%), while unidentified mass was 4%. The mass concentration and most of the chemical components of PM2.5 showed clear seasonal variations, with a summer-high and winter-low pattern for SIA, dust, and BC. In the winter months, POM was the dominant component. Source apportionment analysis revealed that PM2.5 emission sources, regarding their typical tracers, were ammonium sulfate (SO42−, NH4+, K+, NO3−), road traffic and biomass burning emissions (OC, BC), fresh sea salt (Cl−, K+, NO3−), aged sea salt (Mg2+, Na+, Ca2+), and oxalate-rich (oxalate, NO3−) factors. Further, it is hoped that these findings help to improve the scientific understanding of SW Mediterranean aerosols.

Inter-annual variability of source contributions to PM10, PM2.5, and oxidative potential in an urban background site in the central mediterranean

Airborne particulate matter (PM) is studied because of its effects on human health and climate change. PM long-term characterisation allows identifying trends and evaluating the outcomes of environmental protection policies. This work is aimed to study the inter-annual variability of PM2.5 and PM10 concentrations and chemical composition in an urban background site (Italy). A dataset of daily PM2.5 and PM10 was collected in the period 2016–2017, including the content of OC, EC, major water-soluble ions, main metals, and compared to a similar dataset collected in the period 2013–2014. Oxidative potential using DTT assay (dithiothreitol) was evaluated and expressed in DTTV as 0.39 nmol/min·m3 in PM10 and 0.29 in PM2.5 nmol/min·m3. PM source apportionment was computed using the EPA PMF5.0 model and source contributions compared with those of a previous dataset collected between 2013 and 2014. Multi linear regression analysis identified which source contributed (p < 0.05) to the oxidative potential of each size fraction. Inter-annual trends were more evident on PM2.5 with reductions of biomass burning contribution and increases in traffic contribution in the 2016–2017 period. Crustal contributions were similar for the two periods, in both size fractions. Carbonates were comparable in PM10 with a slight increase in PM2.5. Sea spray decreased in PM10. The DTTV of PM2.5 peaked during cold periods, while, the DTTV of the PM10-2.5 fraction peaked in summer, suggesting that different sources, with different seasonality, influence OP in the PM2.5 and PM10-2.5 fractions. Analysis showed that sea spray, crustal, and carbonates sources contribute ∼13.6% to DTTV in PM2.5 and ∼62.4% to DTTV in PM10-2.5. Combustion sources (biomass burning and traffic) contribute to the majority of DTTV (50.6%) in PM2.5 and contribute for ∼26% to DTTV in PM10-2.5. Secondary nitrate contributes to DTTV in both fine and coarse fraction; secondary sulphate contribute to DTTV in PM2.5 with negligible contributions to DTTV in PM10-2.5.

Indoor-outdoor relationship of submicron particulate matter in mechanically ventilated building: Chemical composition, sources and infiltration factor

To evaluate the impact of outdoor particulate pollution on indoor air quality, the chemical composition and sources of submicron aerosol particles (PM1) were studied indoors and outdoors. Measurements were carried out during the heating season from October 15, 2020, to February 8, 2021, at the Center for Physical Sciences and Technologies in Vilnius, Lithuania. Online measurements of PM1 chemical composition were performed using an Aerosol Chemical Speciation Monitor (ACSM (organics, sulfate, and nitrate)) and an Aethalometer (equivalent black carbon, BC). In parallel with the online measurements, filter-based elemental composition and 14C analysis of PM1 were performed using a Particle-Induced broad-beam X-ray Emission (PIXE) and a Single Stage Accelerated Mass Spectrometer (SSAMS), respectively. The source apportionment results showed a dominant contribution of biomass burning to the total carbonaceous aerosol particles, including primary (30%) and secondary (40%) fractions. According to the enrichment factors, the main source of trace elements was road dust resuspension (30%), while anthropogenic emissions accounted for only 13% of trace elements. The infiltration factor (Finf) of all studied PM1 constituents was low (Finf∼0.03). This result indicates that the three-stage building filter system (G4-F7-F9) provides high protection against particle pollution of different origins and significantly reduces indoor exposure to PM1. The changed chemical composition of indoor PM1 can be attributed to species-specific evaporation and some minor indoor sources.