High SO2 Research Articles

Sulfite Management during Vinification and Impact on the Flavor of Solaris Wine

Effective sulfur dioxide (SO2) management is crucial in winemaking to minimize oxidative changes in wine flavor during storage. This study explored the impact of various SO2 management techniques on Solaris white wine’s flavor components and sensory properties. Five treatments were administered: ‘SO2 in juice’ (50 mg/L SO2 added to juice pre-fermentation), ‘Control’ (60 mg/L SO2 added post-fermentation), ‘Low SO2’ (50 mg/L SO2 post-fermentation), ‘High SO2’ (100 mg/L SO2 post-fermentation), and ‘No SO2’ (no SO2 added). The ‘Control’ followed a standard procedure, in which the achieved level of free sulfite is measured and extra SO2 added to reach the recommended level of free sulfite for the pH of the wine. Here, 50 + 10 mg/L was added. Volatile compounds were analyzed using dynamic headspace sampling coupled with gas chromatography–mass spectrometry after 0, 3, 6, and 12 months of storage. Sensory evaluation by a trained panel after 12 months revealed stronger perceptions of ‘overall impression’, ‘chemical’, ‘bitter’, ‘overripe fruit’, and ‘honey’ notes in the ‘No SO2’ and ‘SO2 in juice’ wines. The data underscore the significant influence of SO2 management on the flavor stability of Solaris white wines, emphasizing the need for strategic SO2 interventions during winemaking to enhance sensory quality over time.

High-Performance Porous Organic Polymers for Environmental Remediation of Toxic Gases.

Sulfur dioxide (SO2) is a harmful acidic gas generated from power plants and fossil fuel combustion and represents a significant health risk and threat to the environment. Benzimidazole-linked polymers (BILPs) have emerged as a promising class of porous solid adsorbents for toxic gases because of their chemical and thermal stability as well as the chemical nature of the imidazole moiety. The performance of BILPs in SO2 capture was examined by synergistic experimental and theoretical studies. BILPs exhibit a significantly high SO2 uptake of up to 8.5 mmol g-1 at 298 K and 1.0 bar. The density functional theory (DFT) calculations predict that this high SO2 uptake is due to the dipole-dipole interactions between SO2 and the functionalized polymer frames through O2S(δ+)···N(δ-)-imine and O═S═O(δ-)···H(δ+)-aryl and intermolecular attraction between SO2 molecules (O═S═O(δ-)···S(δ+)O2). Moderate isosteric heats of adsorption (Qst ≈ 38 kJ mol-1) obtained from experimental SO2 uptake studies are well supported by the DFT calculations (≈40 kJ mol-1), which suggests physisorption processes enabling rapid adsorbent regeneration for reuse. Repeated adsorption experiments with almost identical SO2 uptake confirm the easy regeneration and robustness of BILPs. Moreover, BILPs possess very high SO2 adsorption selectivity at low concentration over carbon dioxide (CO2), methane (CH4), and nitrogen (N2): SO2/CO2, 19-24; SO2/CH4, 118-113; SO2/N2, 600-674. This study highlights the potential of BILPs in the desulfurization of flue gas or other gas mixtures through capturing trace levels of SO2.

Emission characteristics of condensable particulate matter during the production of solid waste-based sulfoaluminate cement: Compositions, heavy metals, and preparation impacts

Recycling solid waste for preparing sulfoaluminate cementitious materials (SACM) represents a promising approach for low-carbon development. There are drastic physical-chemical reactions during SACM calcination. However, there is a lack of research on the flue gas pollutants emissions from this process. Condensable particulate matter (CPM) has been found to constitute the majority of the primary PM emitted from various fuel combustion. In this study, the emission characteristics of CPM during the calcination of SACM were determined using tests in both a real-operated kiln and laboratory experiments. The mass concentration of CPM reached 96.6 mg/Nm3 and occupied 87% of total PM emission from the SACM kiln. Additionally, the mass proportion of SO42− in the CPM reached 93.8%, thus indicating that large quantities of sulfuric acid mist or SO3 were emitted. CaSO4 was one key component for the formation of main mineral ye'elimite (3CaO·3Al2O3·CaSO4), and its decomposition probably led to the high SO42− emission. Furthermore, the use of CaSO4 as a calcium source led to SO42− emission factor much higher than conventional calcium sources. Higher calcination temperature and more residence time also increased SO42− emission. The most abundant heavy metal in kiln flue gas and CPM was Zn. However, the total condensation ratio of heavy metals detected was only 40.5%. CPM particles with diameters below 2.5 μm and 4–20 μm were both clearly observed, and components such as Na2SO4 and NaCl were conformed. This work contributes to the understanding of CPM emissions and the establishment of pollutant reduction strategies for waste collaborative disposal in cement industry.

Interaction of intractable gaseous SO2 with new adsorbent—Metal organic frameworks: M-MOF-74 (M = Co, Ni, Zn)

The nature of adsorption between MOF absorbent and SO2 remains a challenging issue due to the difficulty in understanding their interaction force and dynamic behavior on molecular level. Herein, a new series of M-MOF-74 (M = Co, Ni, Zn) with high SO2 adsorption performance were synthesized through an improved solvothermal method. The interaction between M-MOF-74 (M = Co, Ni, Zn) and SO2 was revealed by combining in-situ infrared spectroscopy and density functional theory (DFT) calculations. It was found that Zn-MOF-74 shows excellent SO2 uptakes (8.16 mmol g−1), significantly higher than that of Co-MOF (6.11 mmol/g) and Ni-MOF (6.36 mmol/g). These results were consistent with SO2 binding energies calculated at optimal adsorption sites, which were −11.1 kcal/mol, −12.2 kcal/mol, −18.2 kcal/mol for M-MOF-74 (M = Co, Ni, Zn), respectively. The specific adsorption behavior of Zn-MOF-74 towards SO2 is attributed to its higher negative attraction of electrostatic potential(∼48.2 kcal/mol)and van der Waals pulling forces (∼−2.6 kcal/mol). The higher interaction force between Zn-MOF-74 and SO2 was elucidated not only by their strong dominant dispersion interactions, but also by the formation of hydrogen bonding between SO2 and benzene ring, as demonstrated by independent gradient model (IGM) and infrared analysis. What's more, a unique radial SO2 movement with high speed of 323 p.m.2/ps, which was much higher than that of traditional molecular sieve (∼240 p.m.2/ps) adsorbent, were observed towards Zn-MOF-74 framework wall. Then the pore size of MOF-74 and SO2 motion trajectory was analyzed by Molecular Dynamics. This work gives insight into mechanisms on SO2 adsorption in MOFs.

Kinetics of the Gas-Phase Reactions of syn- and anti-CH3CHOO Criegee Intermediate Conformers with SO2 as a Function of Temperature and Pressure.

Kinetics of reactions between SO2 and CH3CHOO Criegee intermediate conformers have been measured at temperatures between 242 and 353 K and pressures between 10 and 600 Torr using laser flash photolysis of CH3CHI2/O2/N2/SO2 gas mixtures coupled with time-resolved broadband UV absorption spectroscopy. The kinetics of syn-CH3CHOO + SO2 are pressure-dependent and exhibit a negative temperature dependence, with the observed pressure dependence reconciling apparent discrepancies between previous measurements performed at ∼298 K. Results indicate a rate coefficient of (4.80 ± 0.46) × 10-11 cm3 s-1 for the reaction of syn-CH3CHOO with SO2 at 298 K and 760 Torr. In contrast to the behavior of the syn-conformer, the kinetics of anti-CH3CHOO + SO2 display no significant dependence on temperature or pressure over the ranges investigated, with a mean rate coefficient of (1.18 ± 0.21) × 10-10 cm3 s-1 over all conditions studied in this work. Results indicate that the reaction of syn-CH3CHOO with SO2 competes with unimolecular decomposition and reaction with water vapor in areas with high SO2 concentration and low humidity, particularly at lower temperatures.

Heterogeneous variations in wintertime PM2.5 sources, compositions and exposure risks at urban/suburban rural/remote rural areas in the post COVID-19/Clean-Heating period

Inevitably, both unblocking of the COVID-19 (UNCOV) and uncertainty in the clean heating policy (2017–2021) in winter 2022 imposed complex impacts on PM2.5 variations. Together, the urban-rural and rural-rural disparities in these impacts remain unclear. To address this gap, we conducted a synchronous observation at urban (UA)/suburban rural (SRA)/remote rural (RRA) areas to probe PM2.5 evolutions in the post COVID-19/clean-heating (PCOV/PCH) period for further site-specific policy implications. Similar meteorological conditions among sites benefited examining the effects of emission variations. On average, PM2.5 presented a decline order as RRA > UA > SRA. Invoking the positive matrix factorization (PMF) results, specially, the primary emissions (PE) rebounded again after experiencing a continuous decline since the stringent emission-control polices initiated in 2013. PE contributions were up to 80.2 %–83.0 % for three points. SRA benefited most from coal-to-gas and coal combustion (CC) has become its minimum contributor (10.8 %). Concurrently, subsidy reduction and natural-gas (NG) shortage compelled biomass burning (BB) to be the largest origin (21.9 %) marked by the highest K+, Cl− and OC/EC. Regarding RRA, CC (26.5 %) and BB (19.6 %) have been the first and second largest origins despite that the coal-to-electricity policy, indicating the slowdown of policy enforcement. The highest SO42−, As, Sb, Tl, OC, EC and the lowest NO3−/SO42− further verified the dominant CC. Production recovery made industrial emissions (IE) become the largest source (26.8 %) at UA. The metal associated health risks peaked at RRA due to large impacts of CC, though the most of metals related to small-scale industries peaked at UA. This is the first work to highlight that more targeted site-specific strategies in prevention/control of dominant primary sources should be formulated in the PCOV/CH period.

Research on CeO2 Activated Carbon Electrode Capacitance Method for Sulfate Removal from Mine Water

Sulfate is a typical characteristic pollutant in mine water. Because of its high concentration and large discharge of mine water, it has become a difficult problem in mineral exploitation. Capacitive deionization (CDI) is an innovative and economical removal technology. There are few reports on the use of CDI to remove SO42− from mine water. In this study, a CeO2 activated carbon electrode with good wettability, excellent electrochemical performance, and suitable pore structure was prepared by the sol-gel method. The application of the CeO2 activated carbon electrode to the capacitive method for treating high SO42− mine water was investigated using simulated wastewater and actual mine water. The study structure shows that CeO2:activated carbon (AC) has the best wettability, the highest specific capacitance, and the lowest electrical conductivity when the mass ratio of CeO2 is 5%. At 100 mg/L, the electrode has the maximum SO42− ion specific adsorption capacity (SAC). At 1 V and 20 mL/min, this value is measured. The electrode has a SAC value of 9.36 mg/g, far higher than the AC electrode’s 4.1 mg/g. The effect of CDI process factors such the voltage, flow rate, and initial concentration was studied to find the best treatment method. SAC retention is 91% after 10 adsorption–desorption cycles, demonstrating outstanding electrode performance. Under the best CDI process (1.4 volts, 30 mL/min), mine water was treated. After 20 cycles of treatment, the concentration of SO42− in mine water decreased from 1170 mg/L to 276.46 mg/L, and the removal rate was 76.37%. This study proved that the CeO2 modified activated carbon electrode capacitance method can effectively remove sulfate ions and other ions from mine water.

Unraveling the multi-pollutant removal using M-MoWTi (M = Fe, Mn, Cr) catalyst: experiment and mechanistic study of competition for active sites.

Multi-pollutant removal (MPR) of NO and VOCs simultaneously is efficient of flue gas treatment in coal-fired power plants. But reducing the competition for active sites between NH3, NO, C6H6, and C7H8 remains challenging. Herein, Cr, Mn, and Fe were respectively doped to MoWTi catalyst via wet impregnation. The Fe3+ + Mo5+ ↔ Fe2+ + Mo6+ redox cycle led to an increased proportion of low valence ions (Mo5+ and W5+) and facilitated the creation of active oxygen vacancies with several active sites. It also possessed plentiful mild to strong acid sites with ideal ratio. These factors enhanced catalytic activity of Fe-MoWTi. Remarkable MPR efficiencies of NO, C6H6, and C7H8 were achieved under industrial SCR condition, characterized by low oxygen but high SO2 levels at 340 °C, with removal rates reaching 89.85%, 97.57%, and 86.30% respectively. Theory calculations further revealed that Fe-MoWTi favor NH3 and O2 adsorptions. NO elimination was found to follow both Eley-Rideal (E-R) and Langmuir-Hinshelwood (L-H) processes, supported by in situ DRIFTS analysis. The reactions involving NO/NO2/nitrite/nitrate occurred with NH3(ads)/ NH4+(ads)/NH2 (ads). C6H6 and C7H8 underwent gradual oxidation, formatting alcohols, aldehydes, acids, and maleic acids, before eventually being mineralized to gaseous CO2 and H2O. Findings hold significant potential for application, providing guidance for the development of catalysts with improved resistance against SO2 poisoning and enhanced MPR capabilities.

Insights into PM2.5 pollution of four small and medium-sized cities in Chinese representative regions: Chemical compositions, sources and health risks

Fine particles (PM2.5) pollution is still a severe issue in some cities in China, where the chemical characteristics of PM2.5 remain unclear due to limited studies there. Herein, we focused on PM2.5 pollution in small and medium-sized cities in key urban agglomerations and conducted a comprehensive study on the PM2.5 chemical characteristics, sources, and health risks. In the autumn and winter of 2019–2020, PM2.5 samples were collected simultaneously in four small and medium-sized cities in four key regions: Dingzhou (Beijing-Tianjin-Hebei region), Weinan (Fenwei Plain region), Fukang (Northern Slope of the Tianshan Mountain region), and Bozhou (Yangtze River Delta region). The results showed that secondary inorganic ions (43.1 %–67.0 %) and organic matter (OM, 8.6 %–36.4 %) were the main components of PM2.5 in all the cities. Specifically, Fukang with the most severe PM2.5 pollution had the highest proportion of SO42− (31.2 %), while the dominant components in other cities were NO3− and OM. The Multilinear Engine 2 (ME2) analysis identified five sources of PM2.5 in these cities. Coal combustion contributed most to PM2.5 in Fukang, but secondary sources in other cities. Combined with chemical characteristics and ME2 analysis, it was preliminarily determined that the primary emission of coal combustion had an important contribution to high SO42− in Fukang. Potential source contribution function (PSCF) analysis results showed that regional transport played an important role in PM2.5 in Dingzhou, Weinan and Bozhou, while PM2.5 in Fukang was mainly affected by short-range transport from surrounding areas. Finally, the health risk assessment indicated Mn was the dominant contributor to the total non-carcinogenic risks and Cr had higher carcinogenic risks in all cities. The findings provide a scientific basis for formulating more effective abatement strategies for PM2.5 pollution.

Important Role of Low Cloud and Fog in Sulfate Aerosol Formation During Winter Haze Over the North China Plain

AbstractSulfate aerosol greatly contributes to wintertime haze pollution in emission‐intensive regions like the North China Plain (NCP) in China. Fast sulfate increase and accumulation are usually recorded during winter haze; however, the multiphase oxidation of sulfur dioxide (SO2) and the physical processes affecting near‐surface sulfate are not fully understood. By combining in situ observations and numerical simulations, we found that high sulfur oxidation ratios (>0.6) under heavily polluted conditions are associated with low clouds and fog over NCP, induced by the moist southerly airflow. Thick low clouds and high SO2 levels in NCP provide a reaction environment for sulfate production. The sulfate production rate in cloud water can reach 0.5–1.3 μg m−3 h−1. The results demonstrate that the vertical mixing of sulfate generated within the cloud water to the surface plays a significant role in rapid sulfate production, highlighting the importance of understanding cloud‐water processes in haze pollution.

Role of the In-Situ-Formed Surface (Pt-S-O)-Ti Active Structure in SO2-Promoted C3H8 Combustion over a Pt/TiO2 Catalyst.

Typically, SO2 unavoidably deactivates catalysts in most heterogeneous catalytic oxidations. However, for Pt-based catalysts, SO2 exhibits an extraordinary boosting effect in propane catalytic oxidation, but the promotive mechanism remains contentious. In this study, an in situ-formed tactful (Pt-S-O)-Ti structure was concluded to be a key factor for Pt/TiO2 catalysts with a substantial SO2 tolerance ability. The experiments and theoretical calculations confirm that the high degree of hybridization and orbital coupling between Pt 5d and S 3p orbitals enable more charge transfer from Pt to S species, thus forming the (Pt-S-O)-Ti structure with the oxygen atom dissociated from the chemisorbed O2 adsorbed on oxygen vacancies. The active oxygen atom in the (Pt-S-O)-Ti active structure is a robust site for C3H8 adsorption, leading to a better C3H8 combustion performance. This work can provide insights into the rational design of chemical bonds for high SO2 tolerance catalysts, thereby improving economic and environmental benefits.

Assessment of Secondary Sulfate Aqueous-Phase Formation Pathways in the Tropical Island City of Haikou: A Chemical Kinetic Perspective.

Sulfate (SO42-) is an essential chemical species in atmospheric aerosols and plays an influential role in their physical-chemical characteristics. The mechanisms of secondary SO42- aerosol have been intensively studied in air-polluted cities. However, few studies have focused on cities with good air quality. One-year PM2.5 samples were collected in the tropical island city of Haikou, and water-soluble inorganic ions, as well as water-soluble Fe and Mn, were analyzed. The results showed that non-sea-salt SO42- (nss-SO42-) was the dominant species of water-soluble inorganic ions, accounting for 40-57% of the total water-soluble inorganic ions in PM2.5 in Haikou. The S(IV)+H2O2 pathway was the main formation pathway for secondary SO42- in wintertime in Haikou, contributing to 57% of secondary SO42- formation. By contrast, 54% of secondary SO42- was produced by the S(IV)+Fe×Mn pathway in summer. In spring and autumn, the S(IV)+H2O2, S(IV)+Fe×Mn, and S(IV)+NO2 pathways contributed equally to secondary SO42- formation. The ionic strength was the controlling parameter for the S(IV)+NO2 pathway, while pH was identified as a key factor that mediates the S(IV)+H2O2 and S(IV)+Fe×Mn pathways to produce secondary SO42-. This study contributes to our understanding of secondary SO42- production under low PM2.5 concentrations but high SO42- percentages.

Selenium–phosphorus modified biochar reduces mercury methylation and bioavailability in agricultural soil

Biochar is a frequently employed for solidifying and stabilizing mercury (Hg) contamination in soil. However, it often results in an elevated presence of soil methylmercury (MeHg), which introduces new environmental risks. Consequently, there is a necessity for developing a safer modified biochar for use in Hg-contaminated soil. This study employed sodium selenite (at a safe dosage for soil) and hydroxyapatite to modify straw biochar (BC) based on the interaction between selenium (Se) and phosphorus (P). This process led to the formation of Se-modified biochar (Se-BC), P-modified biochar (P-BC), and Se and P co-modified biochar (Se-P-BC). Additionally, solvent adsorption experiments and pot experiments (BC/soil mass ratio: 0.5 %) were conducted to investigate the impacts of these soil amendments on soil Hg methylation and bioavailability. Se and P co-modification substantially increased the surface area, pore volume, and Hg adsorption capacity of BC. BC treatment increased the simulated gastric acid-soluble Hg, organo-chelated Hg, and MeHg in the soil. Conversely, Se-P-BC significantly reduced these forms of Hg in the soil, indicating that Se-P-BC can transform soil Hg into less bioavailable states. Among the different biochar treatments, Se-P-BC exhibited the most pronounced reductions in soil MeHg, total Hg, and MeHg in water spinach, achieving reductions of 63 %, 71 %, and 70 %, respectively. The co-modification of Se and P displayed a synergistic reduction effect in managing soil Hg pollution, which is associated with the increase of available Se in the soil due to phosphorus addition. The significantly reduced dissolved organic carbon and the abnormally high SO42− concentration in the soil of Se-P-BC treatment also inhibited Hg methylation and bioavailability in the soil. In summary, Se-P-BC substantially increased reduction percentage in plant Hg content while mitigating the risk of secondary pollution arising from elevated soil MeHg.

Fluoride and acid enrichment in coal fire sponges in the Wuda coalfield, Inner Mongolia, Northern China

Coal fire sponges (CFSs) are a type of sponge-like contaminated soil bulge common in coal fire areas. However, the impacts of CFSs on the local environment are not yet understood. Thus, this study investigated soil samples from CFSs in the Wuda coalfield, Inner Mongolia, China, focusing on the acidity, sulfate, and fluorine content. The results showed that the CFSs were highly acidic, with an average pH of 0.76, and contained high levels of SO42− (257.29 × 103 μg/g), total fluorine (TF, 2011.6 μg/g), and water-soluble fluorine (WF, 118.94 μg/g), significantly exceeding those in the regional background soil and indicating that CFSs are a point source of heavy pollution. Soils in the 8000 m2 reclamation zone showed elevated acidity and high SO42− (129.6 × 103 μg/g), TF (1237.8 μg/g), and WF (43.05 μg/g) levels, which was likely the result of the weathering and dissemination of CFS. The CFS samples were rich in hydrogen fluoride, releasing 202.05 ppb of it when heated to 40 °C. Correlation analysis indicated that the acid sulfate soils in CFSs are likely caused by HSO4−/SO42−. Time-of-flight secondary ion mass spectrometry detected four characteristic ions (F−, H3O+, H2SO4+, and HSO4−) in all micro-domains of each sample, indicating that ionic fluorine compounds and sulfuric acid hydrate were found in the CFS samples. Sulfate minerals detected in CFSs included CaSO4, Fe2(SO4)3, CdSO4, NH4HSO4, and Na2SO4. Thus, the results identified CFSs as a transmission channel for contamination, with erosional surface soils as the carrier, for the first time. CFSs pose a serious threat of contamination, albeit over limited areas.

Long‐term atmospheric corrosion rates of Zn55Al‐coated steel

AbstractHot‐dip Zn55Al‐coated steel samples have been exposed for up to 6 years at 11 different weathering sites, including marine, marine‐industrial, acid‐rain and dry atmospheres. From the mass loss measurements, Zn55Al metallic coating showed globally long‐term good corrosion resistance in all weathering conditions compared with hot‐dip Zn‐0.2Al‐coated steel (Z). Yet, weaker performance was observed on Zn55Al in high SO2 polluted atmosphere, particularly when combined with seawater aerosols. This is explained by a more acidic surface condition linked to high SO2. Although the extent of corrosion in this phase was different at the different sites, the final corrosion products formed after 6 years were rather similar at all sites. This consists of hydrous aluminium sulphate or hydrous aluminium hydroxy sulphate and, probably also a smaller amount of sulphate‐containing zinc corrosion products or Al/Zn products.

Discovery of anion‐pillared metal–organic frameworks for efficient SO2/CO2 separation via computational screening

AbstractAdsorptive removal of SO2 from its low‐concentrated gas mixtures is significant to the health and environment. However, the on‐demand discovery of such adsorbents remains a great challenge. Herein, a high‐throughput computational screening for SO2/CO2 separation is performed in an anion‐pillared metal–organic framework (MOF) database. As a proof‐of‐concept, SIFSIX‐7‐Cu, one of the computationally top‐ranked MOFs, is identified and experimentally synthesized for the verification. The high SO2 uptake (14.7 mmol g−1), IAST selectivity (120 for a mixture of 0.2/99.8 molar ratio), and excellent balance between the regenerability (63.5%) and adsorbent performance score (36.3) make it superior to the performance of most reported adsorbents. This work not only provides an excellent candidate for SO2/CO2 separation, but also will facilitate the development of theoretical prediction‐experimental verification methodology in the discovery of novel materials.

Kinetic study of isoprene hydroxy hydroperoxide radicals reacting with sulphur dioxide and their global-scale impact on sulphate formation.

Isoprene is the most relevant volatile organic compound emitted during the biosynthesis of metabolism processes. The oxidation of isoprene by a hydroxy radical (OH) is one of the main consumption schemes that generate six isomers of isoprene hydroxy hydroperoxide radicals (ISOPOOs). In this study, the rate constants of ISOPOOs + sulphur dioxide (SO2) reactions that eventually generate sulphur trioxide (SO3), the precursor of sulphate aerosol (SO42-(p)), are determined using microcanonical kinetic theories coupled with molecular structures and energies estimated by quantum chemical calculations. The results show that the reaction rates range from 10-27 to 10-20 cm3 molecule-1 s-1, depending on the atmospheric temperature and structure of the six ISOPOO isomers. The effect of SO3 formation from SO2 oxidation by ISOPOOs on the atmosphere is evaluated by a global chemical transport model, along with the rate constants obtained from microcanonical kinetic theories. The results show that SO3 formation is enhanced in regions with high SO2 or low nitrogen oxide (NO), such as China, the Middle East, and Amazon rainforests. However, the production rates of SO3 formation by ISOPOOs + SO2 reactions are eight orders of magnitude lower than that from the OH + SO2 reaction. This is indicative of SO42-(p) formation from the direct oxidation of SO2 by ISOPOOs, which is almost negligible in the atmosphere. The results of this study entail a detailed analysis of SO3 formation from gas-phase reactions of isoprene-derived products.

Combustion characteristics of low-quality lignite for different bed material sphericities in a circulating fluidized bed boiler: A numerical study

This study delves into the combustion behavior of various lignite types within a circulating fluidized bed boiler (CFBB), with a primary focus on the impact of different bed material sphericity ratios (0.5, 0.7, and 0.9). Utilizing bed material with a sphericity ratio of 0.9 sourced from the Çan power plant and verified through experimentation, the research reveals several key findings. Notably, furnace temperatures tended to rise with higher sphericity ratios, albeit with variations between lignite types, particularly highlighting the complexity of this relationship in the case of GLI-Tunçbilek lignite. Pressure levels in the combustion chamber remained consistent across different sphericity ratios, indicating minimal influence on pressure dynamics. Improved combustion efficiency, especially at the bottom of the boiler, was observed at lower sphericity levels (0.5 and 0.7) for Çan lignite, as reflected in CO2 mole fractions. While NOx emissions generally decreased with lower sphericity, the sensitivity to sphericity varied by lignite type, with Ilgın lignite showcasing low NOx but high SO2 emissions, underscoring the intricate interplay between lignite properties, sphericity, and emissions. Overall, this study advances our understanding of CFBB combustion dynamics, offering insights valuable for optimizing performance and emissions control, particularly in lignite-based power.

Non-linear associations between meteorological factors, ambient air pollutants and major mosquito-borne diseases in Thailand.

Transmission intensity for mosquito-borne diseases are highly heterogenous and multi-factorial. Understanding risk factors associated to disease transmission allow the optimization of vector control. This study sets out to understand and compare the combined anthropogenic and environmental risk factors of four major mosquito-borne diseases, dengue, malaria, chikungunya and Japanese encephalitis in Thailand. An integrated analysis of mosquito-borne diseases, meteorological and ambient air pollutants of 76 provinces of Thailand was conducted over 2003-2021. We explored the use of generalized linear models and generalized additive models to consider both linear and non-linear associations between meteorological factors, ambient air pollutants and mosquito-borne disease incidence. Different assumptions on spatio-temporal dependence and nonlinearity were considered through province-specific and panel models, as well as different spline functions. Disease-specific model evidence was assessed to select best-fit models for epidemiological inference downstream. Analyses indicated several findings which can be generally applied to all diseases explored: (1) higher AH above mean values was positively associated with disease case counts (2) higher total precipitation above mean values was positively associated with disease case counts (3) extremely high temperatures were negatively associated with disease case counts (4) higher SO2 and PM2.5 surface concentrations were negatively associated with disease case counts. However, the relationships between disease and RH, non-extreme temperatures and CO surface concentration were more mixed, with directions of associations changing across the different diseases considered. This study found protective and enhancing effects of meteorological and ambient air pollutant factors on mosquito-borne diseases burdens in Thailand. Further studies should employ these factors to understand and predict risk factors associated with mosquito-borne disease transmission.

Copper/Nickel/Cobalt modified molybdenum-tungsten-titanium dioxide-based catalysts for multi-pollution control of nitrogen oxide, benzene, and toluene: Enhanced redox capacity and mechanism study

Previous studies have indicated the potential of monometallic-modified TiO2 catalysts in controlling nitrogen oxide (NOx) and volatile organic compounds (VOCs) in coal-fired flue gas. Unfortunately, increasing selective catalytic reduction (SCR) activity under complicated coal-fired flue gas status is tricky. In this study, modified Co-MoWTiO2 catalysts with multiple active sites were synthesized using the wet impregnation method, which exhibited excellent multi-pollution control ability of NO, benzene and toluene under low oxygen and high SO2 concentrations. The modification of Mo and Co achieved high dispersion and electron transfer. The interaction between W5+/W6+ and Co2+/Co3+ promoted gas-phase O2 adsorption on the catalyst surface, forming of reactive oxygen species (Oα). Density functional theory (DFT) calculations informed that the doping of Co effectively enhanced the NH3 and O2 adsorption capacity of the catalyst, and Co possessed the maximum adsorption energy for NH3 and O2. Possible pathways of multi-pollution control of NO, C6H6, and C7H8 were speculated. NH3/NH4+ on the Lewis/Bronsted acid site is reacted with intermediates of NO (e.g., NO2, nitrite, nitrate) via the Langmuir-Hinshelwood and Eley-Rideal mechanism. The introduction of NO and NH3 did not disrupt the oxidation pathways of benzene and toluene. Following the Mars-van Krevelen mechanism, C6H6 and C7H8 were progressively mineralized by Oα into CO2 and H2O.