Search Results (603)

A retrospective ozone simulation was conducted with the Microscale Forward and Adjoint Chemical Transport (MicroFACT) model for an industrialized area of Detroit, Michigan, USA, using a 24 km × 24 km horizontal × 1.5 km vertical grid. The domain encompassed a regulatory monitoring station at East 7 Mile Rd at the northern edge of the grid. The episode day was 30 June 2022, when the station-measured 8 h ozone reached 76 ppb during predominantly southwesterly wind. The ozone impacts of mobile, point, nonpoint, and biogenic emissions were simulated at 400 m horizontal resolution. Simulation results were compared against station measurements of ozone, nitrogen oxides, and total reactive nitrogen. Local nitrogen oxide sources were found to titrate ozone, while ozone turbulently entrained to the surface from ~500 m aloft enhanced surface Ozone Production Efficiency and led to extended periods of high ozone concentrations very similar to observations. Volatile Organic Compound emission reductions produced only weak decreases in maximum 8 h ozone, suggesting that radicals were enhanced mostly by photolysis of subsiding ozone. Entrainment of ozone layers aloft may thus be critical in explaining historical ozone exceedances of the United States National Ambient Air Quality Standard at the East 7 Mile Rd station. Full article

Rainfall is an essential component of boreal forest ecosystems. Aerotechnogenic pollution significantly affects the composition of rainfall. To predict the dynamics of biogeochemical cycles and develop strategies to enhance forest resilience in the Arctic zone, it is necessary to study the composition and characteristics of rainfall. The objective of this study is to evaluate the variation in the chemical composition of stemflow in the most typical pine and spruce forests of Fennoscandia under conditions of aerotechnogenic pollution based on long-term monitoring data from 1999 to 2022. The research was carried out in forests exposed to atmospheric industrial pollution from the largest copper–nickel smelter in northern Europe (Murmansk Region, Russia). The study of rainwater composition was conducted in four microsites: open areas (OA), between crowns (BWC), below crowns (BC) and stemflow (SF). A significant influence of the tree canopy on the rainfall composition was noted. Stemflow was found to have the highest concentration of pollutants, indicating a significant biochemical role of this type of precipitation. The results showed an increase in the concentrations of heavy metals and sulfates in rainwater as we moved closer to the pollution source. Below crowns and in the stemflow of spruce forests, element concentrations are higher compared to pine forests. The highest concentrations of major pollutants in stemflow (Ni, Cu and SO₄²⁻) are observed in June—at the beginning of the growing season. Long-term dynamics reveal a decrease in the concentrations of Cu, Cd and Cr in defoliated forests and technogenic sparse forests. Stemflow volume rises from background to technogenic sparse forests due to deteriorating tree-crown conditions. This is associated with the deteriorating condition of tree stands, as manifested by reductions in tree height, diameter and needle cover. It has been established that under pollution conditions, trees’ assimilating organs actively accumulate heavy metals, thereby altering the composition of precipitation passing through the canopy. Full article

The interaction between moisture and textile materials plays a critical role in transient thermal comfort, particularly through the exothermic heat released during wetting. While the heat of wetting has been extensively characterized at the fiber level, its behavior in finished fabrics, where structure, porosity, and air gaps influence moisture uptake, remains poorly understood. This study quantifies the heat of wetting of clothing fabrics using a TAM Air isothermal microcalorimeter under controlled isothermal conditions (23 °C). Five fabric types representing different fiber chemistries (Merino wool, cotton, viscose, and polyester) were evaluated in both folded and dissected forms to assess the influence of sampling methods. Wool fabrics exhibited the highest heat release, followed by viscose and cotton, whereas polyester showed negligible exothermic response due to its non-hygroscopic nature. Overall, fabric-level heat of wetting values were lower and more variable than the corresponding fiber-level values reported in the literature, reflecting the combined effects of fabric structure, air permeability, surface hydrophilicity, and sampling uniformity. These findings demonstrate the feasibility and limitations of isothermal microcalorimetry for characterizing moisture–fabric interactions and highlight the need for improved sampling and measurement protocols to more accurately capture fabric-level sorption heat relevant to clothing comfort. Full article

To investigate the seasonal characteristics, sources, and regional transport patterns of precipitation components in the high-elevation mountainous regions, field sampling was conducted at Mt. Heng (Hunan, South China) from June 2021 to May 2022. In total, 114 precipitation samples were collected and subjected to chemical analysis, including pH, major inorganic ions, and heavy metals. During the study period, the precipitation at Mt. Heng was generally weakly acidic. The concentrations of metals and acidic anions (NO₃⁻ and SO₄²⁻) were higher in the winter and lower in the summer, whereas the concentration of the primary neutralizing cation, NH₄⁺, peaked during the summer. An association was observed between precipitation pH and metal concentrations, whereby acidic precipitation samples exhibited marginally elevated metal concentrations overall. An additional analysis of winter precipitation chemistry at Mt. Heng revealed an increasing trend of ions from 2015 to 2018, followed by a decrease from 2019 to 2021. This trend coincided with the concentrations of NO₂ and SO₂ in the surrounding cities, reflecting the results of clean air actions. The results of the source analysis revealed five major sources: secondary sources (41.5%), coal combustion (24.7%), a mixed source of biomass burning and aged sea salt (11.6%), dust (10.8%), and industrial emissions (11.4%). Backward trajectory cluster analysis revealed that air masses originating from the northern regions were generally more polluted than those from the southern regions. This study provides fundamental data and scientific support for regional atmospheric pollution control and ecological protection in South China. Full article

Valorizing coconut shell waste as a renewable lignocellulosic precursor offers a sustainable route to produce high-performance activated carbons for wastewater treatment. In this study, coconut shells were transformed into activated carbons through physical activation (air, CO₂, steam) and chemical activation (H₃PO₄, ZnCl₂, KOH), allowing direct comparison of how each method influences porosity and surface chemistry. Among the physically activated samples, steam activation produced the best material, A-ST, with S_BET = 738 m² g⁻¹, V_mi = 0.38 cm³ g⁻¹ and V_me = 0.07 cm³ g⁻¹. KOH activation yielded the top-performing carbon, A-KOH, achieving S_BET = 1600 m² g⁻¹, V_mi = 0.74 cm³ g⁻¹, and V_me = 0.22 cm³ g⁻¹. Adsorption tests with methylene blue, methyl orange, and orange G showed a clear link between physicochemical features and dye uptake. A-ST and A-KOH exhibited the highest capacities due to their wide micro–mesoporosity and favorable surface charge at the adsorption pH. In both cases, methylene blue was most strongly retained, confirming that large aromatic cations benefit from π–π interactions with graphene-like layers and easy micropore access. Overall, the results demonstrate that coconut-shell valorization is maximized when activation enhances both porosity and surface chemistry, enabling the production of tailored sorbents for the efficient removal of organic contaminants. Full article

Air pollution is a major but often under-integrated driver of forest dynamics at the global scale. This review combines a bibliometric analysis of 258 peer-reviewed studies with a synthesis of ecological, physiological, and biogeochemical evidence to clarify how multiple air pollutants influence forest structure, function, and regeneration. Research output is dominated by Europe, East Asia, and North America, with ozone, nitrogen deposition, particulate matter, and acidic precipitation receiving the greatest attention. Across forest biomes, air pollution affects growth, wood anatomy, nutrient cycling, photosynthesis, species composition, litter decomposition, and soil chemistry through interacting pathways. Regional patterns reveal strong context dependency, with heightened sensitivity in mountain and boreal forests, pronounced ozone exposure in Mediterranean and peri-urban systems, episodic oxidative stress in tropical forests, and long-term heavy-metal accumulation in industrial regions. Beyond being impacted, forests actively modify atmospheric chemistry through pollutant filtration, aerosol interactions, and deposition processes. The novelty of this review lies in explicitly framing air pollution as a dynamic driver of forest change, with direct implications for afforestation and restoration on degraded lands. Key knowledge gaps remain regarding combined pollution–climate effects, understudied forest biomes, and the scaling of physiological responses to ecosystem and regional levels, which must be addressed to support effective forest management under global change. Full article

The behavior of the carbon cycle within the Land-Ocean Aquatic Continuum (LOAC) is shaped not only by aquatic processes but also by chemical interactions occurring at the atmosphere–water interface. In particular, the transport of acid rain precursors such as SO₂ and NO_x to surface waters via deposition can alter the water’s pH balance, thereby affecting Dissolved Inorganic Carbon (DIC) fractions and CO₂ emission potential. In this study, air quality measurements from three monitoring stations (Bosna, Karatay, and Meram) in Konya province of Türkiye, along with precipitation and temperature data from a representative meteorological station for the period 2021–2023, were analyzed using the Mann–Kendall Trend Test. Additionally, seasonal pH values of groundwater were examined, and their trends were compared with those of the other variables. The findings reveal striking differences on a station basis. At the Bosna station, while NO (Z = 10.80), NO₂ (Z = 9.47), and NO_x (Z = 10.04) showed strong increasing trends, O₃ decreased significantly (Z = −15.14). At the Karatay station, significant increasing trends were detected for CO (Z = 10.01), PM₁₀ (Z = 8.59), SO₂ (Z = 5.55), and NO_x (Z = 2.44), whereas O₃ exhibited a negative trend (Z = −6.54). At the Meram station, a significant decrease was observed in CO (Z = −11.63), while NO₂ showed an increasing trend (Z = 3.03). Analysis of meteorological series indicated no significant trend in precipitation (Z = −0.04), but a distinct increase in temperature (Z = 2.90, p < 0.01). These findings suggest that the increasing NO_x load in the Konya atmosphere accelerates O₃ consumption and, combined with rising temperatures, creates a potential for change in the carbon chemistry of aquatic systems. The results demonstrate that atmospheric pollutant trends constitute an indirect but significant pressure factor on the aquatic carbon cycle in semi-arid regions and highlight the necessity of integrating atmospheric processes into carbon budget analyses within the scope of LOAC. Full article

ANSYS-Fluent was applied to simulate diffusion combustion flame in a two-dimensional (2D) industrial burner to determine the contours of the mass fraction of gas emissions, velocity, and combustion temperature. The effects of the boundary conditions, including momentum, thermal, and species (inlet air, inlet fuel, and outlet pressure) on combustion temperature and mass fraction (gas emissions) were analyzed in the designed burner. The present study focused on using and analyzing the volumetric reaction and the turbulence-chemistry interaction of the eddy dissipation model for the diffusion flame model. The simulation used the discrete ordinate model and p1 for radiation and the k-ε model for turbulence with enhanced wall treatment. Based on the results, the magnitude velocities of air and fuel, inlet temperature, and mass fractions of oxygen and inert gas can influence the parameters of flame temperature and gas emissions in the industrial burner. The flame shape for all the cases of inlet velocity was predominantly symmetric about the x = 0 mm for all the axial distances towards the outlet. The radial velocity contour at 0.01 m/s (300 K) gave better results with an area of 1.31 m/s to 4.08 m/s, which was wider than that of the case at 0.01 m/s (700 K). By varying the inlet temperature and oxygen mass fraction, the flame configurations on temperature, CO₂, and H₂O formed a symmetric flame structure. The temperature distribution resulted in the centerline being hotter than other radial positions for all of the inlet temperatures. The emissions of CO₂ and H₂O generally increased with the addition of the oxygen mass fraction. Full article

This review explores the pervasive role of water in generating, storing, and mediating electric charge across natural and artificial systems. Far from being a passive medium, water actively participates in electrostatic and electrochemical processes through its intrinsic ionization, interfacial polarization, and charge separation mechanisms. The Maxwell–Wagner–Sillars (MWS) effect is presented as a unifying framework explaining charge accumulation at air–water, water–ice, and water–solid interfaces, forming dynamic “electric mosaics” across Earth’s environments. The authors integrate diverse phenomena—triboelectricity, hygroelectricity, hydrovoltaic effects, elastoelectricity, and electric-field-driven phase transitions—showing that ambient water continually shapes the planet’s electrical landscape. Electrostatic shielding by humid air and hydrated materials is described, as well as the spontaneous electrification of sliding or dripping water droplets, revealing new pathways for clean energy generation. In addition, the review highlights how electric fields and interfacial charges alter condensation, freezing, and chemical reactivity, underpinning discoveries such as microdroplet chemistry, “on-water” reactions, and spontaneous redox processes producing hydrogen and hydrogen peroxide. Altogether, the paper frames water as a universal electrochemical medium whose interfacial electric imprint influences atmospheric, geological, and biological phenomena while offering novel routes for sustainable technologies based on ambient charge dynamics and water-mediated electrification. Full article

Copper is a promising alternative to conventional plasmonic materials, though its practical use is hindered by a strong tendency to oxidize. Through systematic analysis of its vibrational, optical, morphological, structural, and surface potential properties, we confirmed the stability of copper (Cu) particles and highlighted the role of functional groups in modulating their oxidation susceptibility. Oxidation kinetics at 150 °C, in the presence of antioxidants and capping agents, as well as long-term colloidal stability, appear closely tied to the degradation of these stabilizers, which correlates with particle aggregation. Notably, precursor chemistry significantly affects oxidation behavior. Varying concentrations of polyvinylpyrrolidone (PVP) demonstrate a positive correlation with particle size control and thermal stability, indicating that PVP enhances oxidation resistance under the tested conditions. Our findings underscore most importantly the metallic phase’s stability after exposure to air at a temperature of 150 °C, drawing attention to a possible precursor and capping agent combination that can result in oxidation-stable Cu particles, positioning them as cost-effective candidates for replacing more expensive plasmonic metals across diverse applications. Full article

Nitric acid (HNO₃) is predominantly produced in large production plants using the Ostwald process. In view of its widespread application as synthetic fertilizer, small- scale and local production has become of interest. The chemical precursor of nitric acid is NO_x gas, which can be produced from air at percentage-level concentrations using small-scale, electrically powered warm plasma reactors. Using gas-phase plasma, the downstream conversion of NO_x into fertilizer is a crucial, but as yet understudied step. This work aims to help close this gap and support the further development of plasma-driven nitrogen fixation and subsequent NO_x scrubbing. The chemistry of NO_x absorption through gas scrubbing is investigated at a 1% NO_x concentration using a synthetic mimic of a plasma-produced NO_x stream in order to maintain maximal controllability. pH values of the scrubber solution were kept in the range of 1 to 5 and it was recirculated for up to 30 h. The kinetics of NO_x absorption were found to be strongly pH-dependent, requiring several hours of recirculation to reach steady state conditions. Once at steady state, the NO_x removal efficiency turned out to be rather pH independent and reached around 84% for experiments at pH 1–4. The formation of nitrous acid (HNO₂) byproduct reached a constant value of around 3.43 mM based on a dynamic equilibrium of its formation and decomposition. Approaches to minimize undesired nitrite and nitrous acid byproduct formation are discussed. Full article

The increasing amount of carbon dioxide (CO₂) in the atmosphere is the main factor contributing to climate change. Recent studies have determined that simply reducing emissions is insufficient to restore the Earth’s atmospheric system—negative emissions are therefore necessary. Current carbon (i.e., CO₂) capture technologies use thermal or pressure swings. These approaches suffer from low energy efficiency, high cost, and geographic constraints. Electro-swing chemistry-based carbon capture has emerged as a promising potential solution to these challenges. However, strong CO₂-binding sorbents, not susceptible to oxygen interference, remain elusive. In this study, three electron-deficient quinones were designed and tested as CO₂ capture molecular sorbents. Cyclic voltammetry (CV) on these novel quinones reveals that 2,3-dicyano-1,4-benzoquinone (DBQ) has a second reduction potential positive of that of oxygen reduction. Moreover, this sorbent binds to CO₂ with a free energy ΔG_bind of −5.39 kcal/mol when activated by electrochemical reduction. These results suggest that DBQ may be a sorbent candidate that can capture >70% of CO₂ in the current atmosphere using electro-swing chemistry without the interference of oxygen in the air. This novel sorbent can be further developed for large-scale carbon capture and combating global warming and its associated impacts. Full article

High-resolution air quality data are critical for exposure assessment, regulatory compliance, and urban planning. In this study, we present modelled annual mean concentrations of NO₂, PM_2.5, PM₁₀, Black Carbon (BC), and particle number concentration (PNC) for all ~2.5 million Danish addresses in 2019 using the Air Quality at Your Street 2.0 system. The modelling framework combines coupled chemistry–transport models (DEHM/UBM/OSPM) with input from the Green Mobility Model and GPS-based vehicle speed data. Model outputs were evaluated against observations from the Danish Air Quality Monitoring Programme, showing strong agreement for NO₂, PM_2.5, PM₁₀, and BC, but notable overestimation of PNC background levels and underestimation of street contributions. Indicative exceedances of NO₂ EU limit values decreased markedly from 2012 to 2019, while exceedances of updated EU and WHO guidelines persist, especially for particulate matter. This work identifies key sources of model uncertainty and supports high-resolution national-scale assessment and citizen access via an interactive map. Full article

Volatile organosulfur compounds (VSCs) play significant roles in atmospheric chemistry and malodorous pollution. Accurate measurement of VSCs is challenging due to their high reactivity and adsorption tendencies, which are strongly influenced by sampling materials. This study comprehensively evaluates the performance of six types of sampling bags and passivated canisters for measuring nine VSCs. The results indicate that passivated canisters provide stable storage for all target VSCs for up to 7 days under dry conditions. Among the bags, polyvinyl fluoride (PVF) bags exhibited the lowest blank levels and preserved most VSCs (except disulfides) stably for 8 h. Field comparisons in a power battery recycling plant showed good agreement between PVF bag and canister measurements under dry conditions. However, in high-humidity stack gases, canisters showed severe losses of methanethiol and ethanethiol, likely due to humidity-driven conversion on metal surfaces, underscoring the necessity of drying humid-air samples. The application of these methods revealed significant VSCs emissions and distinct compositional profiles from power battery recycling processes, particularly pyrolysis drying, lithium leaching, and nickel–cobalt leaching processes, with concentrations of total VSCs reaching up to 1046.86 ppb. This work provides crucial guidance for selecting appropriate sampling methods for reliable VSCs measurement and offers the first emissions characteristics of VSCs from the power battery recycling industry, supporting future environmental monitoring and pollution control. Full article