Search Results (149)

This study investigates the emission characteristics and environmental impacts of pollutants from bagasse-fired biomass boilers through the integrated field monitoring of two sugarcane processing plants in Guangxi, China. Comprehensive analyses of flue gas components, including PM_2.5, NOx, CO, heavy metals, VOCs, HCl, and HF, revealed distinct physicochemical and emission profiles. Bagasse exhibited lower C, H, and S content but higher moisture (47~53%) and O (24~30%) levels compared to coal, reducing the calorific values (8.93~11.89 MJ/kg). Particulate matter removal efficiency exceeded 98% (water film dust collector) and 95% (bag filter), while NOx removal varied (10~56%) due to water solubility differences. Heavy metals (Cu, Cr, Ni, Pb) in fuel migrated to fly ash and flue gas, with Hg and Mn showing notable volatility. VOC speciation identified oxygenated compounds (OVOCs, 87%) as dominant in small boilers, while aromatics (60%) and alkenes (34%) prevailed in larger systems. Ozone formation potential (OFP: 3.34~4.39 mg/m³) and secondary organic aerosol formation potential (SOAFP: 0.33~1.9 mg/m³) highlighted aromatic hydrocarbons (e.g., benzene, xylene) as critical contributors to secondary pollution. Despite compliance with current emission standards (e.g., PM < 20 mg/m³), elevated CO (>1000 mg/m³) in large boilers indicated incomplete combustion. This work underscores the necessity of tailored control strategies for OVOCs, aromatics, and heavy metals, advocating for stricter fuel quality and clear emission standards to align biomass energy utilization with environmental sustainability goals. Full article

The Baikal region, including areas with poor environmental conditions, has significant clean background zones. In the summer of 2023, we analyzed the physical and chemical parameters of aerosol particles with different size fractions at Irkutsk and Listvyanka monitoring stations. Reduced wildfires and minimal impact from fuel and energy industries allowed us to observe regional and transboundary pollution transport. A large data array indicated that, during the shift of cyclones from Mongolia to the south of the Baikal region, the concentrations of Na⁺, Ca²⁺, Mg²⁺, K⁺, and Cl⁻ ions increased at the Irkutsk station, dominated by NH₄⁺ and SO₄²⁻. The growth of the ionic concentrations at the Listvyanka station was observed in aerosol particles during the northwesterly transport. When air masses arrived from the southerly direction, the atmosphere was the cleanest. The analysis of 27 elements in aerosols revealed that Al, Fe, Mn, Cu, and Zn made the greatest contribution to air pollution at the Irkutsk station, while Fe, Al, Cu, Cr, Mn, and Ni made the greatest contribution to air pollution at the Listvyanka station. The dynamics of the investigated elements were mainly due to natural processes in the air under various synoptic situations and weather conditions in the region, although anthropogenic factors also affected the formation of aerosol composition wth certain directions of air mass transport. Full article

To elucidate the compositional characteristics and sources of heavy metals in aerosols at China’s Great Wall Station in Antarctica, high-volume aerosol sampling was conducted from 4 January to 26 December 2022, on Fildes Peninsula, King George Island. Ten heavy metals (V, Cr, Mn, Fe, Ni, Cu, Zn, As, Cd, and Pb) in total suspended particulates (TSPs) were quantified via inductively coupled plasma mass spectrometry (ICP-MS). Enrichment factor (EF) analysis, correlation metrics, and backward trajectory clustering were integrated to identify potential sources. The results revealed pronounced enrichment (EF > 10) for Cr, As, Zn, Cd, and Pb, indicating dominant non-crustal contributions. Source apportionment identified three pathways: (1) long-range transported anthropogenic emissions, including Southern Hemisphere marine traffic (e.g., V and Ni from ship fuel combustion) and industrial pollutants from South America (Pb and Cd); (2) local anthropogenic sources, primarily diesel generators and tourism-related gasoline combustion (Cu and Zn); and (3) crustal inputs via glacial melt and weathering (Fe and Mn). This study pioneers the quantification of direct anthropogenic impacts (e.g., power generation and tourism) on aerosol heavy metals in Antarctic research zones, offering critical insights into transboundary pollutant dynamics and regional mitigation strategies. Full article

Optical properties and chemical composition of atmospheric fine particles (PM_2.5) are critical to their environmental and health effects. In this study, we analyzed the organic aerosols (OA) in PM_2.5 samples in Nanjing, China, collected during the summer and winter of 2019 and 2023. Results show a decline in both concentrations and light-absorbing abilities of methanol—soluble organic carbon (MSOC) and water-soluble OC (WSOC) in OA from 2019 to 2023. Due to increased combustion activities, MSOC and WSOC concentrations, and their corresponding mass absorption efficiencies were all higher in winter than in summer. Furthermore, fluorescence indices suggest that OA in Nanjing was influenced by a mix of microbial/biogenic sources. Fluorescent properties of both WSOC and MSOC were dominated by humic-like components but the remaining contribution from protein-like components was more significant in MSOC. The molecular composition of OA did not show a remarkable difference between 2019 and 2023. Overall, CHON compounds were the most abundant species, followed by CHO and CHN compounds, and aliphatic compounds dominated all molecular types except for CHN (in positive mode) and CHON, CHOS (in negative mode). Regarding the OA sources, the numbers of molecules from fossil fuel combustion and biomass burning (BB) were a bit more in 2023 than in 2019, and signal intensities of BB-related molecules were also higher in winter than in summer; the presence of organosulfates indicate the contribution of aqueous-phase oxidation to OA, especially during high relative humidity conditions. At last, correlations between OA molecules and light absorption efficiencies indicate that the key light-absorbing species in winter and summer were likely quite different despite similar chemical compositions, and in summer, CH and CHN compounds were important to light absorption, whereas CHNS compounds became more important in winter. Full article

This study examines the seasonality of Black Carbon (BC) and Brown Carbon (BrC) spectral absorption characteristics at a continental background site (Kozani) in southern Balkans (NW Greece). It aims to assess the seasonality and impact of different sources on light absorption properties, BC concentrations, and the fraction of BrC absorption. Moderate-to-low BC concentrations were observed, ranging from 0.05 µg m⁻³ to 2.44 µg m⁻³ on an hourly basis (annual mean: 0.44 ± 0.27 µg m⁻³; median: 0.39 µg m⁻³) with higher levels during winter (0.53 ± 0.33), reflecting enhanced emissions from residential wood burning (RWB) for heating purposes. Atmospheric conditions are mostly clean during spring (MAM) (BC: 0.34 µg m⁻³), associated with increased rainfall. BC components associated with fossil fuel combustion (BC_ff) and biomass burning (BC_bb), maximize in summer (0.36 µg m⁻³) and winter (0.28 µg m⁻³), respectively, while the absorption Ångstrôm exponent (AAE_370–880) values ranged from 1.09 to 1.93 on daily basis. The annual mean total absorption coefficient (b_abs,520) inferred by aethalometer (AE33) was 4.09 ± 2.65 Mm⁻¹ (median: 3.51 Mm⁻¹), peaking in winter (5.30 ± 3.35 Mm⁻¹). Furthermore, the contribution of BrC absorption at 370 nm, was also high in winter (36.7%), and lower during the rest of the year (17.3–29.8%). The measuring station is located at a rural background site 4 km outside Kozani City and is not directly affected by traffic and urban heating emissions. Therefore, the regional background atmosphere is composed of a significant fraction of carbonaceous aerosols from RWB in nearby villages, a characteristic feature of the Balkan’s rural environment. Emissions from the lignin-fired power plants, still operating in the region, have decreased during the last years and moderately affect the atmospheric conditions. Full article

Nickel, as a toxic trace element in fine particulate matter (PM_2.5), has detrimental effects on both air quality and human health. Based on measurements from 2020 to 2021 using a single-particle aerosol mass spectrometer (SPAMS), this study investigates the properties of nickel-containing particles (NCPs) in Guangzhou. The composition, sources, and temporal trends of NCPs were evaluated and the impact of the clean ship fuel policy introduced in 2020 was also examined. The key findings include: (1) Nickel particles account for 0.08% number fraction of PM_2.5, which is consistent with previously reported mass fraction in PM_2.5. (2) Three distinct types of NCPs were identified, including Ni-fresh, Ni-aged, and Ni-ash. Each type exhibits unique characteristics in size distribution, wind direction dependence, sources, and temporal variations. Ni-fresh particles originate from shipping emissions in the Huangpu Port area 2 km away and are the major contributors to fine nickel particles in the region. (3) Ni-aged and Ni-ash particles, which carry secondary components, tend to be larger (>500 nm) and are representative of regional or background nickel particles. (4) The implementation of the clean ship fuel policy has effectively reduced the number concentrations of NCPs and is beneficial to regional and local air quality. Full article

This study presents the longest time series of aerosol optical properties and Precipitable Water Vapor (PW) from two AERONET sites in the Indo-Gangetic Plains (IGP). Analyzing 22 years of data (2001–2022) from Kanpur and 16 years (2007–2023) from Gandhi College, the study focuses on Aerosol Optical Depth (AOD), Ångström Exponent (α), Single Scattering Albedo (SSA), and Precipitable Water Vapor (PW). Significant variability in aerosol properties is observed across monthly, seasonal, and annual scales. The highest mean AOD₅₀₀ values, coupled with higher α_440–870 during post-monsoon and winter, indicate the dominance of fine-mode aerosols. A decrease in SSA with wavelength during these seasons further highlights the absorbing nature of these fine-mode aerosols, driven by fossil fuels and biomass burning. In contrast, summer and pre-monsoon have relatively lower mean AOD₅₀₀, lowest α_440–870, and increased SSA with wavelength, suggesting the dominance of coarse-mode scattering dust aerosols. PW exhibits a seasonal cycle, reaching its peak during the monsoon due to moisture transport from the Arabian Sea and Bay of Bengal, then decreasing post-monsoon as drier conditions prevail. Long-term annual trends reveal increasing aerosol concentrations, with AOD₅₀₀ rising by 18% at Kanpur and 29% at Gandhi College, suggesting faster aerosol loading at the latter. Sub-period analysis indicates a slowdown in AOD₅₀₀ increase during 2012–2023 at Kanpur, indicating potential stabilization post-industrialization, while Gandhi College’s more pronounced AOD₅₀₀ and α_440–870 increase underscores the growing impact of fine aerosols in rural IGP areas. Kanpur shows a sustained SSA increase, though at a slower rate in recent years, indicating dominant scattering aerosols. In contrast, Gandhi College has transitioned from moderate SSA increases to declines at longer wavelengths, suggesting enhanced fine-mode absorbing aerosols. At Gandhi College, the decline in PW reduces atmospheric moisture, limiting wet scavenging and likely contributing to the rise in fine-mode aerosols, especially during the monsoon and post-monsoon seasons. Our findings highlight the evolving aerosol sources in the IGP, with Kanpur stabilizing and rural areas like Gandhi College seeing continued increases in pollution. Full article

Black carbon (BC) aerosols emitted from biomass, fossil fuel, and waste combustion contribute to the radiation budget imbalance and are transported over extensive distances in the Earth’s atmosphere. These aerosols undergo physical and chemical modifications with co-existing aerosols (e.g., nitrate, sulfate, ammonium) through aging processes during long-range transport and are primarily removed from the troposphere by wet deposition. Using precipitation samples collected in North America between 26 October and 1 December 2020 by the National Atmospheric Deposition Program (NADP), we investigated the relationships between BC and both water-soluble ions and water-soluble organic carbon (WSOC) using Spearman’s rank coefficients. We then attempted to identify the sources of BC in the wet deposition using factor analysis (FA) and satellite data of fire smoke. BC showed a very strong correlation with nitrate (ρ = 0.83). Strong correlations were also found with WSOC, ammonium, calcium, and sulfate ions (ρ = 0.78, 0.74, 0.74, and 0.67, respectively). FA showed that BC was in the same factor as nitrate, ammonium, sulfate, and WSOC, indicating that BC could originate from secondary aerosol formation and biomass burning. Supported by satellite data of fire and smoke, BC and other correlated pollutants were believed to be associated with wildfire outbreaks in several states in the United States (US) during November 2020. Full article

Oak Ridge National Laboratory is collecting and characterizing aerosols released when spent nuclear fuel (SNF) rods are fractured in bending. An aerosol collection system was designed and tested to collect respirable sized (<10 μm aerodynamic diameter [AED]) particulates inside a hot cell facility. The setup is a modified version of the commercially available Sioutas cascade impactor, to which additional stages were added to expand the aerosol collection range from 2.5 to ~15 μm AED. To accommodate the additional stages and specific test conditions, the operating flow rate for aerosol collection was reduced, and testing was conducted by using pressure drop measurements, surrogate dust collection, and particle size characterization. The fluid flow distribution within the cascade and its stages was simulated in STAR-CCM+, and the stage-wise pressure drops obtained using the computational fluid dynamics model were then compared to experimental data. Lagrangian particle simulations were also performed, and stage-wise collection statistics were obtained from the simulation for comparison with the experimental data obtained using SNF-surrogate dust particles. The results provide valuable insights into the stage-wise particle collection characteristics of the modified cascade impactor and can also be used to improve the prediction accuracy of the manufacturer-determined analytical correlations. Full article

Diesel vehicles are recognized as significant mobile sources of particulate matter emissions. As a renewable and environmentally friendly alternative to conventional fossil diesel, biodiesel offers the benefit of reducing greenhouse gas emissions. However, existing research on biodiesel emissions primarily focuses on primary emissions, with a limited understanding of their impact on secondary organic aerosol (SOA) formation. In this study, a diesel engine test bench was employed under idle conditions using three commonly used biodiesel blends. Exhaust emissions were directly introduced into the HAP-SWFU chamber, a quartz glass smog chamber designed to characterize both primary emissions and SOA formation during the photochemical oxidation process. The black carbon and primary organic aerosol (POA) emission factors for the three biodiesel blends under idle conditions ranged from 0.31 to 0.58 g kg⁻¹ fuel and 0.99 to 1.06 g kg⁻¹ fuel, respectively. The particle size of exhaust particulates peaked between 20 and 30 nm, and nucleation-idle conditions were found to be the dominating mode. The SOA production factor was between 0.92 and 1.15 g kg⁻¹ fuel, and the SOA/POA ratio ranged from 1.35 to 2.37, with an average of 1.86. This study concludes that the POA emission factor for biodiesel under idle conditions is comparable to values reported in previous studies on pure diesel exhaust, with the maximum SOA production factor reduced by 38%. Full article

The chemistry of atmospheric precipitation serves as an important proxy for discriminating the source(s) of air contaminants in urban environments as well as to discuss the dynamic of atmospheric chemistry exchanges. This approach can be undertaken at time scales varying from single events to seasonal and yearly time frames. Here, we characterized the chemical composition of two single rain episodes (18 July 2018 and 21 February 2019) collected in Wrocław (SW Poland). Our results demonstrated inner variations and seasonality (within the rain event as well as between summer and winter), both in ion concentrations as well as in their potential relations with local air contaminants and scavenging processes. Coupling statistical analysis of chemical parameters with meteorological/synoptic conditions and HYSPLIT back trajectories allowed us to identify three main factors (i.e., principal components; PC) controlling the chemical composition of precipitation, and that these fluctuated during each event: (i) PC1 (40%) was interpreted as reflecting the long-range transport and/or anthropogenic influences of emission sources that included biomass burning, fossil fuel combustion, industrial processes, and inputs of crustal origin; (ii) PC2 (20%) represents the dissolution of atmospheric CO₂ and HF into ionic forms; and (iii) PC3 (20%) originates from agricultural activities and/or biomass burning. Time variations during the rain events showed that each factor was more important at the start of the event. The study of both SO₄²⁻ and Ca²⁺ concentrations showed that while sea spray inputs fluctuated during both rain events, their overall impact was relatively low. Finally, below-cloud particle scavenging processes were only observed for PM₁₀ at the start of the winter rain episode, which was probably explained by the corresponding low rain intensity and an overlap from local aerosol emissions. Our study demonstrates the importance of multi-time scale approaches to explain the chemical variability in rainwater and both its relation to emission sources and the atmosphere operating processes. Full article

A study of carbonaceous species, polycyclic aromatic hydrocarbons (PAHs), and nitro-PAHs associated with PM_2.5 was conducted to assess their carcinogenic potential and associated health risks in the two main cities of the State of Morelos: Cuernavaca and Cuautla. The annual median concentrations in Cuernavaca of organic carbon (OC) and elemental carbon (EC) were 6.2 µg m⁻³ and 0.6 µg m⁻³, respectively, whereas in Cuautla, OC concentrations averaged 4.8 µg m⁻³ and EC 0.6 µg m⁻³. OC/EC ratios, total carbonaceous aerosols (TCA), primary (POC) and secondary organic carbon (SOC), as well as elemental carbon reactive (ECR) were estimated, also showing prevalence of primary emissions such as biomass burning. The seventeen PAHs recommended by the EPA and twelve nitro-PAHs were measured using gas chromatography–mass spectrometry. The annual median sum of PAHs was 9.7 ng m⁻³ in Cuernavaca and 11.2 ng m⁻³ in Cuautla, where carcinogenic high-molecular-weight compounds were the most dominant; the annual median sums of nitro-PAHs were 287 pg m⁻³ and 432 pg m⁻³, respectively. Diagnostic ratios were applied to identify potential sources of PAH emissions, suggesting that fuel combustion is the major contributor in both sites, followed by coal biomass burning and agricultural activities. The annual carcinogenic potential as benzo(a)pyrene equivalent was 2.2 ng m⁻³ for both sites. The lifetime excess cancer risk from PAH inhalation was estimated to range from 1.8 × 10⁻⁴ to 2 × 10⁻⁴ in Cuernavaca and from 1.5 × 10⁻⁴ to 2.2 × 10⁻⁴ in Cuautla, similar to values observed in other urban regions globally. Full article

Air pollution can induce diseases and increase the risks of death, and it also has close links with climate change. Carbonaceous matter is an important component of aerosols, but studies quantifying the source apportionment of carbonaceous compositions in different-sized aerosols from a stable carbon isotopic perspective remain scarce. In this study, fine (particulate size < 2.5 μm) and coarse (particulate size 2.5~10 μm) particles were collected from December 2021 to February 2022 (winter) and from June to August 2022 (summer) in the tropical city of Haikou; the concentrations of water-soluble inorganic ions (WSIIs) and total carbonaceous matter (TC) and the stable carbon isotope of TC (δ¹³C-TC) values in both fine and coarse particles were analyzed. Higher concentrations of TC, SO₄²⁻, NO₃⁻, and NH₄⁺ but lower δ¹³C-TC values in fine particles than those in coarse particles in both winter and summer indicated that combustion-related emissions dominate fine particulate TC sources. The δ¹³C-TC values coupled with the stable isotope mixing model in R (SIAR) results showed that combustion-related emissions contributed 77.5% and 76.6% to the TC of fine particles in winter and summer, respectively. Additionally, the lowest δ¹³C-TC values were observed in summertime fine particles; plant physiological activity was identified as an important source of fine particulate TC in summer and contributed 12.4% to fine particulate TC. For coarse particles, higher δ¹³C-TC values and Ca²⁺ and Na⁺ concentrations but lower TC concentrations implied significant contributions from natural emissions (29.2% in winter and 44.3% in summer) to coarse particulate TC. This study underscores that instead of fossil fuels and biomass, clean energy can decrease 45–78% of aerosol TC at Haikou. In addition, our results also provide a dataset for making environmental policy and optimizing the energy structure, which further favors the sustainable development of air quality. Full article

Thousands of particle number (PN) counters have been introduced to the European market, following the implementation of PN tests during the periodic technical inspection (PTI) of diesel vehicles equipped with particulate filters. Expanding the PN-PTI test to gasoline vehicles may face several challenges due to the different exhaust aerosol characteristics. In this study, two PN-PTI instruments, type-examined for diesel vehicles, measured fifteen petrol passenger cars with different test protocols: low and high idling, with or without additional load, and sharp accelerations. The instruments, one based on diffusion charging and the other on condensation particle counting, demonstrated good linearity compared to the reference instrumentation with R-squared values of 0.93 and 0.92, respectively. However, in a considerable number of tests, they registered higher particle concentrations due to the presence of high concentrations below their theoretical 23 nm cut-off size. The evaluation of the different test protocols showed that gasoline direct injection engine vehicles without particulate filters (GPFs) generally emitted an order of magnitude or higher PN compared to those with GPFs. However, high variations in concentration levels were observed for each vehicle. Port-fuel injection vehicles without GPFs mostly emitted PN concentrations near the lower detection limit of the PN-PTI instruments. Full article

The South China Sea (SCS) is a crucial region for studying atmospheric aerosols, given its unique geographical location and the interaction of various natural and anthropogenic sources. In this study, we measured the isotopic characteristics of sulfate and nitrate in PM_2.5 and utilized a Bayesian isotope mixing model (SIAR) to analyze their sources and formation pathways. Sulfur isotopic values in sulfate (δ³⁴S-SO₄²⁻) were 8.7 ± 1.8‰, while nitrogen and oxygen isotopic values in nitrate (δ¹⁵N-NO₃⁻ and δ¹⁸O-NO₃⁻) were −0.9 ± 2.4‰ and 52.3 ± 7.3‰, respectively. The results revealed that sulfate was primarily influenced by marine biogenic sulfur emissions (mostly dimethyl sulfide, DMS), fossil fuel combustion, and biomass burning. Nitrate formation was dominated by the NO₂ + •OH pathway (accounting for 69.8–85.7%), with significant contributions from vehicle emissions, biomass burning, and lightning. These findings offer key insights into the complex interactions between natural and anthropogenic aerosol sources in the SCS, contributing to a broader understanding of marine aerosol chemistry. Full article