Search Results (1,042)

Previous studies indicate that the alkali-induced oxidation of quercetin (Que) or kaempferol (Kae) converts them into hydroxylated-benzoyl-benzofuranones (BZFs), a type of metabolite whose antioxidant potency is substantially higher. To explore whether the former conversion can take place under a more biologically relevant oxidizing setting, these flavonols were incubated in a nitrite-containing acidic medium. Under such condition, the concentrations of Que or Kae rapidly decayed, simultaneously generating their corresponding BZFs. When Que and Kae were co-incubated, the depletion of the parent flavonols accelerated without changes in BZF formation. Similar results were observed when either Que or Kae were incubated with some of their corresponding 3-O-glycosides. In turn, when Que was co-incubated with certain flavanols or phenolic acids, the latter compounds nearly doubled not only the oxidative disappearance of Que but also its BZF formation. Interestingly, the concentrations of Que-BZF and Kae-BZF reached under all former incubation scenarios are greater than those previously reported to be needed to protect intestinal epithelial cells against the oxidative and lytic damage induced by ROS. We suggest that, if these conversions also took place in vivo, the gastric fluid could be potentially seen as a chemical milieu where the antioxidant properties of Que and Kae could be enormously amplified. Full article

In this study, Cu-Fe bimetallic-supported adsorbents were prepared using alkali-activated coconut shell activated carbon (AC-OH) as a carrier by impregnation method. To optimize the adsorption effect, the effects of the second metal type, Fe loading amount, Cu/Fe ratio, and operating conditions on the adsorption effect of extremely low-concentration SO₂ (1 ppm) were systematically investigated. The results showed that when the Cu loading was 5% by mass and the Fe loading was 3% by mass, the adsorbent exhibited optimal adsorption performance, with a breakthrough time of up to 36.5 h and a corresponding breakthrough sulfur capacity of 14.424 mg/g. Further exploration of the conditions shows that the coexistence of O₂ and H₂O can significantly promote the adsorption of SO₂, while reducing the space velocity is beneficial for prolonging the breakthrough time. In terms of regeneration stability, after two adsorption–regeneration cycles, the adsorption activity of the adsorbent decreased to 72.7% of the fresh sample, and the deactivation was mainly attributed to the accumulation of sulfate species and the loss or aggregation of active components. By combining XRD, FT-IR, XPS, SEM and other characterization techniques, the structure–activity relationship and deactivation mechanism of the adsorbent were analyzed. This bimetallic-modified activated carbon has shown great potential for deep purification of extremely low concentrations of SO₂. Full article

The large-scale disposal of coal fly ash (CFA), coal bottom ash (CBA), and desulfurization gypsum (DG) from coal-fired power plants poses serious environmental challenges, driving the need for high-value utilization strategies. In this study, we propose a synergistic approach to prepare foam glass-ceramics from CFA, CBA, and DG via a sintering-foaming method. The effects of sintering temperature (1200–1230 °C) and DG content (0–5 wt.%) on phase composition, pore structure, and overall material properties were systematically investigated. The optimal sample, obtained at 1220 °C with 2 wt.% DG exhibits outstanding comprehensive performance: a bulk density of 1.0030 g/cm³, porosity of 62.09%, compressive strength of 9.66 MPa, and thermal conductivity of 0.6156 W/(m·K). Additionally, it demonstrates excellent chemical stability, with acid resistance exceeding 96% and alkali resistance over 98%, while the leaching concentrations of heavy metals (Pb, Cr, Cu, Zn) remain far below regulatory limits. Mechanistic analysis reveals a crystallization–foaming coupling effect. At an appropriate DG content (2 wt.%), a synergy is established: bubble formation provides heterogeneous nucleation sites that promote crystal precipitation, while moderate crystallization increases melt viscosity and stabilizes the pore structure. Conversely, excessive DG (3–5 wt.%) reduces melt viscosity, leading to bubble coalescence and rupture, suppressed crystallization, and consequently deteriorated material properties. This work provides a theoretical foundation for the synergistic utilization of multiple power plant wastes and the structure–property regulation of foam glass-ceramics. Full article

Achieving the co-combustion of biomass and coal in utility boilers while reducing carbon dioxide emissions poses significant challenges owing to the divergent physicochemical properties of the fuels. These differences can induce high-temperature corrosion and erosion of heating surfaces, threatening boiler safety. Despite this, integrated CFD-based assessments of sulfidic corrosion and particle erosion risks remain insufficiently addressed under realistic biomass–coal cofiring conditions. In this study, an integrated CFD-based risk assessment framework was established for biomass–coal cofiring boilers. The main novelty lies in the combined evaluation of high-temperature sulfidic corrosion and particle erosion risks under different biomass injection strategies. Specifically, user-defined functions were developed to classify high-temperature sulfidic corrosion risks based on local O₂, CO, and H₂S concentrations; the effects of biomass injection layers were quantitatively compared; the Oka erosion model was coupled with CFD particle tracking to predict wall wear; and an entropy-weighted multi-indicator method was used to rank the overall safety of different cofiring strategies. This study found that sufficiently high near-wall H₂S concentrations in the main combustion zone indicate an increased risk of sulfidic corrosion under reducing-atmosphere conditions. Compared with pure coal combustion, biomass injection through layer A exacerbates wall corrosion, whereas biomass injection through layer AB mitigates it. Erosion is primarily localized near burner nozzles. Notably, biomass cofiring reduces the average erosion rate by 7.9–30.2% but increases the local maximum erosion rate by 7.1–25.1%. The comprehensive evaluation indicates that the condition with 30% RS injected from layer AB, mixed with coal, yields the best overall performance. The corrosion assessment is limited to sulfidic corrosion risks associated with reducing atmospheres and does not explicitly model alkali- or chlorine-induced corrosion. This study provides a theoretical foundation for biomass cofiring optimization and offers practical guidance for boiler operational safety and maintenance. Full article

Melatonin, a potent endogenous antioxidant, holds promise for enhancing stress tolerance in woody plants, yet its molecular mechanism under saline–alkali stress remains poorly understood. This study systematically investigated the effects of exogenous melatonin on Ulmus pumila ‘Zhonghua Jinye’ by integrating physiological assays, transcriptomics, and metabolomics. Two-year-old cuttings were subjected to 150 mmol·L⁻¹ saline–alkali stress and treated with varying melatonin concentrations (0, 50, 100, 200, 400 μmol·L⁻¹; three replicates). Physiological evaluations identified 100 μmol·L⁻¹ melatonin (SMT100) as optimal, significantly enhancing antioxidant enzyme activities (SOD, CAT, APX, GR) by 28.7–41.5% and reducing reactive oxygen species (H₂O₂ by 31.5%; O₂⁻ by 38.2%) compared to untreated stressed controls. Integrated omics analysis (CK, S, SMT100 groups) revealed that saline–alkali stress suppressed the flavonoid biosynthesis pathway, down-regulating key genes such as UpANS1 (10.74-fold), UpANS2, UpHCT1, and UpDFR2, thereby reducing the accumulation of protective flavonoids like quercetin and kaempferol. Conversely, melatonin treatment reactivated this pathway, significantly up-regulating UpANS1 (17.36-fold induction), UpDFR2 (5.55-fold), UpCHS1, UpF3H6, and UpLAR2. This genetic reconfiguration promoted the synthesis of antioxidant flavonoids, enhancing the plant’s overall stress resilience, thus identifying UpANS1 as candidates associated with treatment response. The study provides a scientific basis for cultivating U. pumila ‘Zhonghua Jinye’ in saline–alkali soils and clarifies the molecular mechanism by which melatonin alleviates combined saline–alkali stress via flavonoid pathway regulation. Full article

Zinc processing generates large volumes of tailings enriched with potentially toxic elements such as zinc, lead, arsenic, and antimony, creating environmental challenges. Conventional disposal in tailings dams is associated with land occupation, contamination risks, and geotechnical concerns, reinforcing the need for more sustainable management strategies. This study presents a bibliometric and semi-systematic review of alkali-activated binders for the stabilization and solidification of zinc mine tailings, based on nine studies published between 2019 and 2026. The results indicate that this is a recent and expanding research field, with a marked concentration of studies in China. Current research mainly focuses on the links between microstructure, heavy metal immobilization, and mechanical performance. Alkali-activated systems, commonly based on blast furnace slag, fly ash, and coal gangue, can produce dense matrices with compressive strengths of up to 100.77 MPa and high immobilization efficiency. Their performance is largely governed by the type of reaction products formed, particularly calcium silicate hydrate, calcium aluminosilicate hydrate, and sodium aluminosilicate hydrate gels, which control microstructural development and stabilization mechanisms such as encapsulation, structural incorporation, and secondary phase formation. Overall, the reviewed studies suggest that alkali-activated binders have potential as alternative binders to Portland cement for the management and valorization of zinc mine tailings. Full article

Co-contamination of biphenyl and heavy metals is widespread in industrial environments, but systematic studies on the simultaneous treatment of both pollutants using a single microbial strategy remain limited. In this study, we characterized the biphenyl degradation performance, metabolic pathway, transcriptomic response, and Cr(VI) tolerance of Rhodococcus sp. TG-1, and developed an alkali-modified biochar immobilization system to enhance its degradation efficiency for biphenyl under Cr(VI) stress. Degradation experiments were carried out under optimal conditions (30 °C, pH 7.0), and it was found that strain TG-1 degraded 76.84% of 300 mg/L biphenyl within 3 days. Intermediate metabolites were identified by LC-MS, and five key intermediates were detected, confirming that TG-1 metabolizes biphenyl via the classical 2,3-dihydroxybiphenyl dioxygenase pathway, with subsequent entry into the tricarboxylic acid cycle. Transcriptomic analysis was performed to profile gene expression, revealing 845 differentially expressed genes under biphenyl stress, including 672 upregulated genes significantly enriched in aromatic degradation pathways. Seven complete bph gene clusters responsible for biphenyl catabolism were also identified. Strain TG-1 exhibited high tolerance to Cr(VI), with a minimum inhibitory concentration (MIC) of 500 mg/L. However, its biphenyl degradation efficiency dropped to 51.32% in the presence of 200 mg/L Cr(VI). After immobilization using alkali-modified straw biochar (JBC), heavy metal toxicity was alleviated, and the biphenyl removal rate increased to 99.30% under co-contamination conditions. Scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) analyses confirmed that TG-1 was stably loaded onto the biochar surface through hydrogen bonding and electrostatic interactions. Altogether, this study provides a promising bacterial strain and a green immobilization strategy for enhancing biphenyl removal in the presence of Cr(VI), offering a practical approach for the treatment of environments co-contaminated with aromatic compounds and heavy metals. Full article

The accumulation of polylactic acid nano-plastics (PLA-NPs) in saline–alkali soils poses a potential threat to crop growth; however, the underlying toxicological mechanisms remain poorly understood. We conducted a hydroponic experiment to investigate the effects of polylactic acid (PLA) NPs (100 and 500 mg L⁻¹) under conditions both in the presence (50 mmol L⁻¹ NaCl) and absence of salt stress on maize seed germination, seedling growth, physiological characteristics, and transcriptomic responses. The results showed that exposure to PLA-NPs, particularly at a high concentration (500 mg L⁻¹), significantly inhibited seed germination and seedling growth. Compared to the low concentration (100 mg L⁻¹) of PLA-NPs, the high concentrations (500 mg L⁻¹) reduced the germination percentage by 25.0% and fresh weight by 25.8% and increased root MDA (6.7%), SOD (30.0%), POD (6.3%), ASA (13.4%), and GSH (13.1%). Under the same concentration of the PLA, PLA + NaCl treatments exerted stronger inhibitory effects than PLA-NPs alone, with the seed germination percentage and fresh weight reduced by an average of 52.7% and 6.6%, respectively. Notably, the inhibitory effects and integrated biomarker response (IBR) index of the PLA 500 + NaCl treatment were the highest. The presence of PLA-NPs in roots was confirmed using confocal laser scanning microscopy. GO enrichment analysis showed that pathways related to nutrient reservoir activity, oxidoreductase activity, hydrogen peroxide catabolic process, and hydrogen peroxide metabolic process were enriched under PLA-NP and PLA + NaCl treatments. KEGG analysis further indicated enrichment in phenylpropanoid biosynthesis, ABC transporters, and alpha-linolenic acid metabolism. The PLA-NP and PLA + NaCl treatments upregulated genes associated with oxidoreductase activity (Zm00001eb238800, Zm00001eb128620, and Zm00001eb020790). These findings suggest that synergistic toxicity of PLA-NPs and salinity stress in maize is primarily driven by the internalization of PLA-NPs and Na⁺ within maize roots, which negatively impacts maize seed germination and seedling growth by disrupting redox homeostasis and metabolic balance, thereby forcing plants to reallocate resources from growth toward oxidative stress defense. This study provides critical insights into the environmental risks of biodegradable nano-plastics in saline–alkali soil environments. Full article

The increasing concentration of atmospheric CO₂ has intensified the urgent need for efficient and sustainable carbon capture technologies. Covalent organic frameworks (COFs) have emerged as a highly promising class of porous crystalline materials for CO₂ adsorption and separation owing to their structural tunability, high surface area, and precisely designable pore environments. This review summarizes recent advances in COF-based CO₂ capture systems, covering pristine COFs, functionalized frameworks, composite materials, and membrane-based architectures. In pristine COFs, CO₂ adsorption is mainly governed by micropore confinement and physisorption within well-defined channels, where surface area and pore size distribution play key roles. Functionalized COFs introduce additional active sites, including amine groups, heteroatoms, ionic functionalities, and alkali metal centers, which significantly enhance CO₂ affinity through stronger electrostatic and acid–base interactions, often leading to mixed physisorption–chemisorption behavior. Composite COFs and mixed-matrix membranes further improve performance through synergistic effects, interfacial engineering, and enhanced mass transport. Despite these advantages, challenges remain in achieving an optimal balance between capacity, selectivity, and regenerability under realistic conditions such as humidity, low CO₂ partial pressure, and multicomponent gas streams. Issues related to scalable synthesis, structural stability, and processability also limit practical applications. Overall, this review highlights key structure–property relationships and outlines future directions, including humid-stable COFs, direct air capture, computational design strategies, and advanced membrane technologies, for next-generation CO₂ capture materials. Full article

Waterlogged archaeological wood represents a unique cultural heritage but is highly susceptible to physical and chemical degradation, which complicates conservation and restoration. This study aimed to prepare artificial archaeological Cunninghamia lanceolata wood using NaOH vacuum impregnation and systematically evaluate the effects of NaOH concentration and treatment cycles as two treatment variables on wood degradation. Untreated heartwood specimens were treated with 5%, 10%, 20%, and 30% NaOH solutions for 2, 4, and 6 cycles. The NaOH treatment first induced chemical and structural deterioration, including selective degradation of hemicelluloses, changes in cellulose crystallinity, and progressive damage to the wood cell-wall structure. XRD analysis revealed a significant reduction in cellulose crystallinity from 35.96% to 10.11%, while FTIR confirmed the degradation of hemicelluloses and the relative enrichment of lignin-related structures. SEM observations further showed severe cell-wall erosion, lumen deformation, and local collapse, indicating that alkali treatment effectively reproduced typical microstructural features of degraded waterlogged wood. These chemical and microstructural changes subsequently led to marked changes in physical and mechanical properties. Mass loss increased with NaOH concentration and cycle number, while basic density decreased and maximum water content increased, indicating enhanced deterioration and water-holding capacity. Treated specimens also exhibited increased swelling and shrinkage rates and a substantial reduction in longitudinal compressive strength, with the most pronounced deterioration occurring under higher NaOH concentrations and repeated cycles. The study demonstrates that NaOH treatment can reproducibly simulate the physical, chemical, and microstructural characteristics of waterlogged archaeological wood, providing a reliable experimental model for studying wood degradation mechanisms and supporting conservation strategies. Full article

Groundwater contamination by redox-sensitive elements (RSEs) such as arsenic (As), chromium (Cr), vanadium (V), and selenium (Se) pose a critical challenge in alluvial aquifers, where seasonal hydrological forcing drives dynamic hydrogeochemical and redox conditions. This study investigates the seasonal evolution of groundwater hydrogeochemistry and multi-metal behavior in shallow aquifers of the Mid-Gangetic Plain, India, with particular emphasis on the role of seasonal redox decoupling. Monsoon conditions were dominated by strongly reducing environments (ORP: −150 to −70 mV), predominantly Ca–Mg–SO₄ and Na–Cl type facies. Under these conditions, significant correlations among RSEs in particular (As–V, As–Se) indicated coupled mobilization governed by the reductive dissolution of Fe–Mn (oxyhydr)oxides. Monsoon groundwater also exhibited strong associations between RSEs and agronomic indicators (NO₃⁻, SO₄²⁻), suggesting the influence of recharge-mediated agricultural inputs on redox-sensitive geochemical processes. In contrast, post-monsoon conditions showed a clear transition to sub-oxic states (ORP up to +121 mV) and were dominated by Ca–Mg–HCO₃ facies, accompanied by substantial increases in bicarbonate (~372%), electrical conductivity (~62%), and total dissolved solids (~21%). Despite the partial oxidation of the aquifer system, redox-sensitive metals did not respond uniformly. Instead, inter-element correlations weakened or disappeared, indicating a transition from coupled to decoupled contaminant behavior. Arsenic concentrations increased up to 20.8 µgL⁻¹, whereas Cr and V displayed variable enrichment controlled by alkali-induced desorption and carbonate-mediated surface interactions. This transition reflects seasonal redox decoupling, whereby seasonal redox shifts lead to metal-specific rather than coordinated multi-metal behavior. We propose a Seasonal Redox Decoupling Framework (SRDF) to explain the shift from coupled reductive release during monsoon conditions to selective mobilization pathways in the post-monsoon period. These findings demonstrate that seasonal redox shifts control not only metal concentrations but also inter-element relationships, leading to metal-specific risk profiles. This underscores the need for seasonally adaptive monitoring and management strategies in hydrologically dynamic alluvial aquifers. Full article

The increasing accumulation of mine waste and the associated release of toxic elements represent a major environmental challenge, particularly in regions impacted by Pb–Zn mining activities. In this context, this study aims to investigate the valorization of mine waste from Lakhouat, an abandoned Pb–Zn site in Northern Tunisia, as a sustainable additive in metakaolin-based geopolymers. This approach contributes to circular economy strategies by transforming hazardous waste into value-added materials for environmental and construction applications. Geopolymer formulations were synthesized by incorporating mine waste at different proportions (0, 5, 10, 20, and 30 wt.%) with metakaolin, while maintaining constant SiO₂/Al₂O₃ and Na₂O/Al₂O₃ molar ratios. The materials were prepared through alkali activation using sodium silicate and sodium hydroxide, followed by curing. Comprehensive characterization was carried out using X-ray fluorescence (XRF), X-ray diffraction (XRD), and scanning electron microscopy (SEM). In addition, adsorption experiments using methylene blue (MB) were conducted to evaluate the environmental performance of the synthesized geopolymers. The results revealed that the mine waste contains high concentrations of potentially toxic elements (up to 2.23 wt.% Pb and 8.2 wt.% Zn), highlighting the need for effective stabilization. Microstructural analysis confirmed the formation of predominantly amorphous geopolymer matrices with varying degrees of reaction depending on MW content. The highest compressive strengths (25–30 MPa) were achieved for formulations containing 5–10 wt.% MW after 28 days of curing. Furthermore, the geopolymers demonstrated efficient methylene blue removal, following pseudo-second-order kinetics and fitting the Langmuir isotherm model, with enhanced adsorption performance observed at higher MW contents. These findings indicate that MW-based geopolymers are promising materials for mine waste valorization and methylene blue removal. However, standardized leaching tests are required to confirm the long-term immobilization of Pb, Zn, Cd, As, and other potentially toxic elements within the geopolymer matrix. The study highlights their potential as sustainable, low-impact materials, supporting waste valorization and contributing to the development of environmentally resilient systems within a circular economy framework. Full article

Soil salinization severely constrains plant growth, yet the roles of ion composition and rhizosphere microbial communities in shaping plant performance remain poorly resolved. Here, we investigated multiple crop and wild plant species in saline–alkali soils and compared rhizosphere ion composition, microbial communities, and plant growth status. Restricted plant growth was consistently associated with elevated Na⁺ and Cl⁻ concentrations, while fungal diversity was significantly higher in well-growing plants. Ion composition (particularly Na⁺, Cl⁻, SO₄^2–, and Mg²⁺) was strongly correlated with microbial community structure, and a set of microbial taxa, including bacterial phyla such as Deinococcota and Gemmatimonadota and fungal phyla within Ascomycota and Basidiomycota, were repeatedly associated with plant growth status across species. Notably, plant species exhibited distinct apparent, threshold-like responses, and in several cases, plant growth differences were not fully explained by salinity levels alone, suggesting that rhizosphere microbial communities may buffer salt stress. Together, our results reveal that ion composition governs plant growth not only through direct ionic stress but also via microbially mediated pathways, highlighting an ion–microbe–plant interaction framework underlying growth variation in saline–alkali soils. Full article

Excessive chemical fertilization in maize production has reduced fertilizer-use efficiency and increased pressure on soil quality, whereas reducing fertilizer input without yield loss remains challenging. This challenge has shifted attention toward strategies that improve crop nutrient acquisition and utilization under lower fertilizer supply. Harpin protein-based enzyme complexes may provide a regulatory approach, but their field performance under reduced fertilization remains unclear. A two-year field experiment was conducted from 2023 to 2024 using two maize cultivars, Heyu236 and Fuyuan2. In 2023, the harpin protein-based enzyme complex was applied at 200-fold and 300-fold dilutions under conventional fertilization to identify effective spraying concentrations. In 2024, the same two concentrations were evaluated under conventional fertilization and 15%, 30%, and 45% fertilizer reductions. In the 2023 concentration screening trial under conventional fertilization, the enzyme complex increased kernels per ear by 5.6–9.7% and tended to increase the yield by 0.4–17.2% (not significant). In 2024, under reduced fertilization, enzyme application combined with 30% fertilizer reduction produced a stable yield response. In particular, the 300-fold dilution combined with 30% fertilizer reduction increased kernels per ear by 18.1% and 13.2% and grain yield by 16.9% and 9.5% in Fuyuan2 and Heyu 236, respectively. Soil analyses showed that the enzyme treatment mainly improved nutrient availability, as reflected by higher available P, available K, alkali-hydrolyzable N, organic matter, and available Cu, Zn, Fe, and Mn in the soil. These findings suggest that the harpin protein-based enzyme complex helped maintain maize yield under moderate fertilizer reduction by improving kernel formation and soil nutrient availability. Among the tested treatments, foliar application at 300-fold dilution combined with 30% fertilizer reduction showed the greatest potential for reducing fertilizer input while sustaining maize productivity. Full article

The successful realization of a circular economy in the cement industry, coupled with a substantial reduction in carbon emissions, relies on the development of sustainable alternative binder systems. This study investigated the physicomechanical performance and sulfate resistance of composites produced by alkali activation of natural perlite and blast furnace slag. The aim of the research was to improve mechanical properties under low- and medium-alkalinity conditions (5–10 M NaOH). The samples were cured at an ambient temperature of 20 °C and then treated with heat at 60 °C. These samples were then mechanically processed and subjected to five soak–dry cycles in 5% and 10% Na₂SO₄ solutions. The results showed that heat treatment resulted in the formation of a dense C-A-S-H gel, increasing compressive strength approximately eightfold, from 11.64 MPa to 92 MPa. However, perlite’s porous and brittle structure limits its flexural strength to 0.27 MPa; this value is insufficient for structural applications. Under severe sulfate attack (10% Na₂SO₄), samples cured at ambient temperature showed a 12% mass increase in the first cycle due to solution infiltration into capillary voids. As a consequence of extensive ettringite and gypsum formation, the specimens experienced severe deterioration, resulting in a complete loss of mechanical integrity and a residual compressive strength of 0 MPa. In contrast, heat-treated samples showed limited ion diffusion due to a denser matrix and an improved aggregate interface transition zone, resulting in a 2.6% mass increase and a residual compressive strength of 5.17 MPa. Consequently, the obtained findings indicate that thermally treated alkali-activated slag–perlite composites exhibit high resistance against sodium sulfate attack and may have potential for use in specific industrial environments with high sulfate concentrations. However, the performance of these materials under more complex aggressive conditions, such as mining environments involving magnesium sulfate exposure and acidic drainage waters, should be further validated through future studies. Full article