Electromigration Research Articles

Treatment of landfill leachate by black soldier fly (Hermetia illucens L.) larvae and the changes of intestinal microbial community

Black soldier fly larvae (BSFL) (Hermetia illucens) are commonly used to treat organic waste. This work aims to evaluate the transformation effect, heavy metal migration, and alterations in the gut microbiota of BSFL in addition to treating landfill leachate (LL) with BSFL. We found that BSFL may grow in various landfill leachate concentrations without obvious toxicity and growth inhibition. In addition, the results indicated a significant increase in the content of ammonia nitrogen and the activity of urease and β-glucosidase (β-GC) in LL, increased from 2570.17 mg/L to 5853.67 mg/L, 1859.17 mg/(g·d) to 517,177.98 mg/(g·d), 313.73 μg/(g·h) to 441.91 μg/(g·h) respectively. Conversely, the content of total nitrogen (TN) and total organic carbon (TOC) decreased in LL, decreasing by 31.24% and 29.45% respectively. Heavy metals are accumulated in the leachate by the BSFL to differing degrees, the descending sequence of accumulation is Cd > As > Cu > Cr. As dropped by 26.0%, Cd increased by 22.6%, Cu reduced by 5.23%, and Cr increased by 317.1% in the remaining matrix. The concentration of heavy metals satisfies the organic fertilizers' limit index (NY/T1978). The diversity of intestinal microorganisms in BSFL decreased, from 2819 OTUs to 2338 OTUs, with Providencia and Morganella emerging as the core flora. The gene abundance of nitrogen metabolism in the microbiota increased significantly. The TOC, β-GC, and Copper (Cu) content in BSFL correlated significantly with the gut microbiota. In Summary, this study revealed the treatment effect of BSFL on LL, the migration of heavy metals, and changes in the intestinal microorganisms of BSFL. The content of heavy metals in BSFL was found to be much lower than the upper limit of feed protein raw materials, demonstrating that BSFL is a sustainable method to treat LL.

Local electronic structure constructing of layer‐structured oxide cathode material for high‐voltage sodium‐ion batteries

AbstractAs the cyclable sodium ions' primary suppliers, O3‐type layer‐structured manganese‐based oxides are recognized as one of the most competitive cathode candidates for sodium‐ion batteries. Suffering from complex structural transformations and transition metal migration during the sodium intercalation/deintercalation process, particularly at high voltage, the energy density and lifespan cannot satisfy the increasing demand. The orbital and electronic structure of the octahedral center metal element plays an important role in maintaining the octahedral structural integrity and improving the Na+ diffusivity by the introduced heterogeneous [Me–O] (Me: transition metals) chemical bonding. Herein, inspired by the 4f and 5d orbital bonding possibility from the abundant configuration of extranuclear electrons and large ion radius, O3‐type Na[La0.01Ni0.3Mn0.54Cu0.1Ti0.05]O2 was synthesized with a nearly single crystal structure. Based on the experimental and computational results, the introduced heterogeneous [La–O] chemical bond with larger bond strength can not only ensure the stability of the lattice oxygen framework and the reversibility of oxygen redox but also optimize the oxygen local electronic structure resulting from La 5d and O 2p orbital mixing due to O 2p → La 5d charge transfer. It delivers an optimal electrochemical performance with a high energy density and cycling lifespan.

Effect of aluminosilicates on the release and form transformation of semi-volatile heavy metals during the combustion of hyperaccumulator plants

With the development of phytoremediation of heavy metals contaminated soils, the harmless disposal of hyperaccumulator plants has been imminent. In this study, the effects of typical aluminosilicates on the heavy metal migration during the combustion of ryegrass were compared. The addition of kaolin, montmorillonite, and γ-Al2O3 were all effective in solidifying Pb and Zn. As the combustion temperature increased, the toxicity of remaining Pb and Zn decreased. Compared to montmorillonite, kaolin was more effective in capturing Pb and Zn at 600–825 °C, and the remaining Pb and Zn were mainly in acid-soluble form. The large amount of alkali/alkaline earth metals will react with the Si/Al components to form various potassium feldspars and calcium silicates, thus inhibiting the solidification of heavy/alkali metals. However, the Si in montmorillonite was more effective in converting Pb and Zn into residual form than kaolin when faced with the competition solidification of alkali/alkaline earth metals, at which time the percentage of Pb and Zn in the residual form increased from 13.27% and 6.00% to 39.21% and 9.84%, respectively. This work provided a research perspective based on the solidification of heavy metals by Si component, which enables a more comprehensive analysis of the differences in heavy metals solidification by Si/Al-based minerals.

Study of Characteristics and Heavy Metals Migration During Co-Combustion of Coal and Sludge

Study of Characteristics and Heavy Metals Migration During Co-Combustion of Coal and Sludge

Electropulsing of low-density duplex steel for strengthening and ductilization by microstructural refinement

The present investigation finds the effect of electropulsing treatment on the mechanisms of refining and reprecipitation of ordered L20 structure (B2) and its impact on tensile properties of low-density duplex steel of Fe-18Mn-10.5Al-1 C-6Ni composition. The selected composition without manganese is melted at 1600°C by induction heating in a vacuum but Mn is added into the melt at 1560°C, in the argon atmosphere to reduce the loss. The melt is cast into a plate form in a copper mold. The cast steel is homogenized, hot rolled, and annealed (PD1-A sample) to get elongated bands, spheroids, and platelets of B2 phase with an austenitic matrix which results in a yield strength of 1015 MPa, and tensile strength of 1285 MPa with a plastic elongation of 16.3%. Electropulsing partially dissolves the B2 phase at a temperature much lower than the equilibrium solvus by reducing barrier energy because of electron wind. As a result, the sizes of bands and spheroids are reduced, and platelets are disintegrated. Electron wind force deforms coarse precipitates, and fragments as well as spheroidized it. Electropulsing of annealed steel (PD1-AE) mobilizes dislocations, and recovers it in B2, but induces localized recrystallization of austenite. At a later time of the signal, the temperature rapidly falls and the matrix becomes supersaturated but electropulsing accelerates low-temperature precipitation of the B2 phase. Therefore, electropulsing can be adopted as a fast manufacturing process to dissolve, deform, fragment, spheroidize and reprecipitate high temperature phase at much lower temperature by dominant athermal effect of electron wind energy over thermal effect. Electropulsing also induces recovery and recrystallization at a relatively low temperature and reduces defect density. Reduction in the overall size of B2 and its distribution towards better uniformity provided an increased yield strength of 1077 MPa, tensile strength of 1355 MPa, and a plastic elongation of 21.6%. The selected duplex low-density steel follows two-stage work hardening of Ludwigson model with an additional stage of dynamic recovery. Fractography analysis confirms that both samples show mixed modes of ductile and brittle fracture, with an increase in size and area percentage of dimples.

Nanoplastics enhance the stability of kaolinite and affect the sorption of Pb2+ in aquatic environments

The heteroaggregation of nanoplastics with minerals has been widely investigated. However, few studies have focused on the interaction between similar negatively charged clay minerals and nanoplastics, especially how their interactions affect the migration of heavy metals. This study investigated heteroaggregation of kaolinite (a model of natural mineral) with polystyrene nanoplastics (PSNPs) and the effect of heteroaggregates on lead (Pb2+) sorption. Dynamic light scattering (DLS) measurement highlighted that PSNPs owned higher colloidal stability than kaolinite in aquatic environments. Due to the surface charge heterogeneity of kaolinite, the heteroaggregation behavior between kaolinite and PSNPs was highly pH-dependent. At pH 3.0 and 6.0, kaolinite particles with positively charged edge surfaces favored the association of PSNPs. PSNPs were found to be primarily attached on the kaolinite edge (010) surface, followed by Al-terminated (001) and Si-terminated (001¯) surfaces based on density functional theory (DFT) calculations. At pH 10.0, they had negligible interaction due to the strong electrostatic repulsion. Interestingly, kaolinite carried more negative charges after heteroaggregation with PSNPs, resulting in slower edge-to-face homoaggregation and higher dispersibility, and thus increasing the sorption capacity for Pb2+. This investigation provided a new understanding of nanoplastics interactions with negatively charged minerals and highlighted the vital role of nanoplastics in mineral stability and contaminant migration.

Temporal and spatial evolution of different heavy metal fractions and correlation with environmental factors after prolonged acid mine drainage irrigation: A column experiment

Acid mine drainage (AMD) has global significance due to its low pH and elevated heavy metal content, which have received widespread attention. After AMD irrigation in mining areas, heavy metals are distributed among soil layers, but the influencing factors and mechanisms remain unclear. AMD contamination of surrounding soil is primarily attributed to surface runoff and irrigation and causes significant environmental degradation. A laboratory soil column experiment was conducted to investigate the temporal and spatial distribution of the heavy metals Cd and Cu, as well as the impact of key environmental factors on the migration and transformation of these heavy metals following long-term soil pollution by AMD. After AMD addition, the soil exhibited a significant increase in acidity, accompanied by notable alterations in various environmental parameters, including soil pH, Eh, Fe(II) content, and iron oxide content. Over time, Cd and Cu in the soil mainly existed in the exchangeable and carbonate-bound fractions. In spatial terms, exchangeable Cu increased with increasing depth. Pearson correlation analysis indicated significant negative correlations between pH and Cu, Cd, and Eh in pore water, as well as negative correlations between pH and the exchangeable fraction of Cd (F1), carbonate-bound fraction of Cd (F2), and exchangeable fraction of Cu (F1) in the solid phase. Additionally, a positive correlation was observed between pH and the residual fraction of Cu (F5). Furthermore, the soil total Cd content exhibited a positive correlation with pyrophosphate-Fe (Fep) and dithionite-Fe (Fed), while CdF1, CdF2, total Cu, and CuF1 displayed positive correlations with Fep. Our findings indicate that the presence of AMD in soil leads to alterations in the chemical fractions of Cd and Cu, resulting in enhanced bioavailability. These results offer valuable insights for developing effective remediation strategies for soils near mining sites.

Modeling risk assessment of soil heavy metal pollution using partial least squares and fuzzy logic: A case study of a gully type coal-based solid waste dumpsite

Continuous release and migration of heavy metals from coal-based solid waste (CSW) dumpsites often results in significant encroachment on ecological lands and pollution of natural environments. As a result, there is an urgent need for long-term and rapid monitoring, analysis, and assessment to control environmental risks associated with large CSW dumpsites. We constructed a new composite model (PLS-FL) that uses partial least squares regression (PLSR) and fuzzy logic inference (FLI) to accurately predict heavy metal concentrations in soils and assess pollution risk levels. The potential application of the PLS-FL was tested through a gully type CSW case study. We compared 20 modeling strategies using the PLS-FL: five types heavy metals (Cd, Zn, Pb, Cr and As) * four spectral transformation methods (first derivative (FD), second derivative (SD), reverse logarithm (RL), and continuum removal (CR)) * one variable selection method (competitive adaptive reweighted sampling (CARS)). The results showed that the combination of derivative transformation and CARS was recommended for estimation, with R2C > 0.80 and R2P > 0.50. When comparing the PLSR model with four traditional machine learning methods (Support Vector Machines (SVM), Random Forests (RF), Extreme Learning Machines (ELM), and KNN), the PLSR model demonstrated the highest average prediction accuracy. Additionally, the FLI process no longer relies on human perception and expert opinion, enhancing the model's objectivity and reliability. The evaluation results revealed that the heavy metal contamination areas of the CSW dumpsite are concentrated at the bottom of the gully, with more severe contamination in the north. Furthermore, a high-risk zone exists in the interim storage area for CSW to the east of the dump. These findings align with the initial detections at the sampling sites and highlight the need for targeted monitoring and control in these areas. The application of the model will empower regulators to quickly assess the overall situation of large-scale heavy metal pollution and provide scientific program and data support for continuous large-scale pollution risk monitoring and sustainable risk management.

The Influence of the Soil Profile on the Formation of the Elemental Image of Grapes and Wine of the Cabernet Sauvignon Variety.

The features for assessing the authenticity of wines by region of origin are studied, based on the relationship between the mineral composition of the wine, the grapes, and the soil profile (0 to 160 cm) from the place of growth of Cabernet Sauvignon grapes. Soil, grape, and wine samples were taken from the territories of six vineyards in the Anapa district of Krasnodar Territory, Russia. Using the methods of ICP-OES, thermal, and X-ray phase analysis, the soils were differentiated into three groups, differing in mineralogical and mineral compositions. The soil samples of the first group contained up to 31% quartz, the second group up to 25% quartz and 19% mixed calcite, and the third group up to 32% calcite and 15% quartz. The formation of the elemental image of the grapes was studied, taking into account the total content and mobile forms of metals in the soil. The territorial proximity of the vineyards did not affect the extraction of elements from the soil into the grape berry, and the migration of metals for each territory was selective. According to the values of the biological absorption coefficient, the degree of transition of metals from the soil to a berry was estimated. For K, Ti, Zn, Rb, Cu, and Fe in all berries, the coefficient was higher than 1.00, which means that the berry extracts contained not only mobile-form, but also difficult-to-dissolve metal compounds. The migration of macro-components from the soil to the berry was low, and amounted to 6-7% for Ca, 0.8-3.0% for Na, and 25-70% for Mg of the concentration of their mobile forms. For all territories, the maximum correlation between metal concentrations in grapes and soil was observed for samples from a depth of 0-40 cm. The discriminant model based on concentrations of Rb, Al, K, Sr, Co, Na, Pb, Ca, and Ni showed the formation of clusters in the territories of vineyard cultivation. The developed model allow the problems of identifying wines by region to be solved with high accuracy, using their elemental image.

Facilitating an Ultrastable O3-Type Cathode for 4.5 V Sodium-Ion Batteries via a Dual-Reductive Coupling Mechanism.

O3-type layered oxides for sodium-ion batteries (SIBs) have attracted extensive attention due to their inherently sufficient Na content, which have been considered as one of the most promising candidates for practical applications. However, influenced by the irreversible oxygen loss and the phase transition of O3-P3, the O3-type cathodes are always limited by low cutoff voltages (typically <4.2 V), restraining the full release of the capacity. In this study, we originally propose a dual-reductive coupling mechanism in a novel O3-type Na0.8Li0.2Fe0.2Ru0.6O2 cathode with the suppressed O3-P3 phase transition, aiming at improving the reversibility of oxygen redox at high voltage regions. Consequently, thanks to the formation of the strong covalent Fe/Ru-(O-O) bonding and inhibited slab gliding from the O to P phase, the cathode delivers the preeminent cyclic stability among the numerous O3-type cathodes within a high voltage of 4.5 V (a capacity retention of 95.4% after 100 cycles within 1.5-4.5 V). More importantly, HAADF-STEM and 7Li solid-state NMR results reveal the absence of transition metal migration and the presence of reversible Li migration during cycling, which further contributes to the improved structural robustness of the cathode. This study proposes an innovative strategy to boost the reversibility of anionic redox and to achieve stable high-voltage O3-type layered oxides, promoting the further development of SIBs.

Applying Red Mud in Cadmium Contamination Remediation: A Scoping Review.

Red mud is an industrial solid waste rarely utilized and often disposed of in landfills, resulting in resource waste and environmental pollution. However, due to its high pH and abundance of iron and aluminum oxides and hydroxides, red mud has excellent adsorption properties which can effectively remove heavy metals through ion exchange, adsorption, and precipitation. Therefore, red mud is a valuable resource rather than a waste byproduct. In recent years, red mud has been increasingly studied for its potential in wastewater treatment and soil improvement. Red mud can effectively reduce the migration and impact of heavy metals in soils and water bodies. This paper reviews the research results from using red mud to mitigate cadmium pollution in water bodies and soils, discusses the environmental risks of red mud, and proposes key research directions for the future management of red mud in cadmium-contaminated environments.

Ultrafast bimetallic interface reinforcement in additively manufactured multi-material via electropulsing

The bimetallic interface in additively manufactured multi-material was subjected to intense thermal cycling, and thus forming sizable heat affected zone and drastic mutation of chemical component, which led to weak metallurgical bonding. In this investigation, the pulsed current (1255 Hz; 64 μs; 35.4 V; 191 A; 1000 ℃; 20 min) was used to rapidly broaden the compositional mutation zone from 16 μm to 45 μm, and the heat affected zone was completely eliminated. However, the roles of equivalent heat treatment (1000 ℃; 20 min) were opposite with the pulsed one. The width of compositional mutation zone became narrower and the morphology heat affected zone did not change after equivalent heat treatment. Furthermore, the hot compression experiment proved the better bimetallic interface quality of pulsed sample. The rapid regulation of microstructure and composition gradient is caused by increasing interfacial diffusion flux and the promotion of electron wind force to the solute atom.

Lattice-Boltzmann-Method-Based Numerical Simulation for Heavy Metal Migration Process during Deep-Sea Mining

During deep-sea mining, heavy metal pollutants can cause contamination in the marine environment. In this paper, the multiphasic coupling model is established to describe the heavy metal migration process during deep-sea mining, which takes the effects of the convection–diffusion, adsorption–desorption, and sedimentation–resuspension of heavy metals in the aquatic environment into full consideration. Due to the advantages of the Lattice Boltzmann method, it is adopted to numerically solve the multiphasic coupling model and achieve the simulation of the heavy metal migration process during deep-sea mining. In addition, taking cadmium as an example, the concentration variations are discussed and analyzed in detail. Based on the established model and Lattice Boltzmann method, the concentration distribution of heavy metals can be accurately described to provide the reasonable bases for the evaluation of marine environmental protection.

Synergistic strategy of surface-induced spinel structure and F doping to improve the electrochemical performance of Li-rich cathodes

Li-rich Mn-based materials provide higher capacity than commercial NCM layered materials due to the synergistic redox effect of cations and anions. However, lattice straining and structural collapse caused by the irreversible oxygen release at high voltage range during cycling, which results in severe capacity and voltage decay. Herein, a synergistic strategy of surface-induced spinel structure and F doping is provided to improve the structural stability. The surface spinel structure helps to reduce the structural collapse caused by electrolyte corrosion on the cathode and effectively inhibits voltage decay resulted from structural evolution. The stronger Mn-F bonds are formed by F doping to inhibit migration of transition metal (TM) and induce the uniform deposition of LiF to form the thinner and more stable CEI on the cathode. Accordingly, the designed cathode (LMNO-NF) shows remarkable cycling performance with the capacity retention of 86.68 ​% and voltage retention of 96.6 ​% for 200 cycles at 1C, higher than pristine material (68.76 ​% and 85.75 ​%). Therefore, this simple dual-modification strategy of one-step synthesis is promising for solving the structural evolution and voltage decay of Li-rich Mn-based cathode materials effectively, achieving further commercialization.

Numerical simulation of heavy metal migration in stabilized soils under multi-field coupling

Heavy metal contamination of soils has become a global issue. In pursuit of a reference for the management of heavy metal pollution, numerical simulations were used here to investigate the migration pattern of heavy metals in soil under multi-field coupling of rainfall, temperature, and hydraulic conductivity. Models were built using TOUGHREACT, and measured and simulated values were compared with those of existing studies to verify the accuracy of the software in simulating coupled water vapor-thermal transport and rainfall infiltration. Taking Nanjing rainfall data as an example, the transport pattern of zinc in soil under multi-field coupling was explored. Although evaporation and rainwater infiltration were found to increase with the temperature, the effects of evaporation and temperature counteracted each other, resulting in a weak influence of temperature on heavy metal transport. The hydraulic conductivity of stabilized soil was the main factor controlling zinc migration, with the saturation and heavy metal concentration clouds of soil columns tending to stabilize when the hydraulic conductivity of solidified soil was under 1 × 10-11 m/s.

Phytostabilization of Heavy Metals and Fungal Community Response in Manganese Slag under the Mediation of Soil Amendments and Plants.

The addition of soil amendments and plants in heavy metal-contaminated soil can result in a significant impact on physicochemical properties, microbial communities and heavy metal distribution, but the specific mechanisms remain to be explored. In this study, Koelreuteria paniculata was used as a test plant, spent mushroom compost (SMC) and attapulgite (ATP) were used as amendments, and manganese slag was used as a substrate. CK (100% slag), M0 (90% slag + 5% SMC + 5% ATP) and M1 (90% slag + 5% SMC + 5% ATP, planting K. paniculata) groups were assessed in a pilot-scale experiment to explore their different impacts on phytoremediation. The results indicated that adding the amendments significantly improved the pH of the manganese slag, enhancing and maintaining its fertility and water retention. Adding the amendments and planting K. paniculata (M1) significantly reduced the bioavailability and migration of heavy metals (HMs). The loss of Mn, Pb and Zn via runoff decreased by 15.7%, 8.4% and 10.2%, respectively, compared to CK. K. paniculata recruited and enriched beneficial fungi, inhibited pathogenic fungi, and a more stable fungal community was built. This significantly improved the soil quality, promoted plant growth and mitigated heavy metal toxicity. In conclusion, this study demonstrated that the addition of SMC-ATP and planting K. paniculata showed a good phytostabilization effect in the manganese slag and further revealed the response process of the fungal community in phytoremediation.

Effect of organic matter on the environmental behavior of sulfur and heavy metals in mariculture sediments during the aging process

Organic matter (OM) significantly impacts the environmental behavior of sulfur and heavy metals. In this study, the effects of OM on the migration and transformation of sulfur and heavy metals in mariculture sediments were investigated. The results indicated that baiting had a strong impact on the accumulation of acid volatile sulfur (AVS) (P < 0.05) and increased the environmental risk of sulfide in sediments. The addition of bait promoted the generation of chromium (II)-reducible sulfur (CRS); however, the resistance of AVS to CRS conversion increased with increasing bait addition. The addition of bait considerably influenced Cd accumulation. The acid-soluble fractions of Cr and Cu and the oxidizable fraction of Cd were primarily affected by the bait addition (coefficient of variation>15 %). An increase in the reducible fraction promoted the conversion of AVS to CRS, which reduced the degree of sediment aging. Higher OM levels reduced the diversity and abundance of the bacterial communities. The sulfate respiration functional microbiota was particularly affected by OM.

Combination Mechanism of Soil Dissolved Organic Matter and Cu2+ in Vegetable Fields, Forests and Dry Farmland in Lujiang County

Dissolved organic matter (DOM) serves as a critical link in the migration and transformation of heavy metals at the soil–solid interface, influencing the migration behaviour and transformation processes of Cu2+ in soil. There have been studies on the combination mechanisms between DOM and Cu2+ in paddy soils. However, the adsorption/complexation and redox processes between DOM and Cu2+ in other agricultural soil types (such as dry farmland and vegetable fields) are unclear. In order to reveal the combination process of DOM with Cu in different agricultural soil types and the dynamic changes in chemical behaviour that occur, this study analysed the variability of DOM components and structure in three soils using three-dimensional fluorescence spectroscopy and X-ray photoelectron spectroscopy. In addition, the priority order of different DOM compounds in combination with Cu and the change process in relation to the Cu valence state in the soil of Lujiang County, Anhui Province, was revealed based on laboratory experiments. The results showed that the composition of soil DOM was mainly composed of humic-like and fulvic-like substances with a clear terrestrial origin and that the organic matter showed a high degree of decomposition characteristics. The results indicated that the composition of soil DOM is mainly composed of humic and fulvic acid-like substances, and they have obvious characteristics of terrestrial origin. In addition, the soil organic matter showed high decomposition characteristics. The complex stability constants (lgKM) of humic acid-like substances with Cu2+ follow the order of forest land (lgKM = 5.21), vegetable land (lgKM = 4.90), and dry farmland (lgKM = 4.88). The lgKM of fulvic acid-like substances with Cu2+ is in the order of dry farmland (lgKM = 4.51) and vegetable land (lgKM = 4.39). Humic acid-like substances in soil DOM combine preferentially with Cu2+, showing a stronger chelating affinity than fulvic acid-like substances. Cu2+ complexes mainly include hydroxyl, phenolic hydroxyl and amino functional groups are included in soil DOM, accompanied by redox reactions. In comparison to dry farmland, the soil DOM in forest and vegetable fields undergoes more intense redox reactions simultaneously with the chelation of Cu2+. Therefore, the application of organic fertilisers to vegetable and forest soils may lead to uncertainties concerning the fate of heavy metals with variable chemical valence. These results contribute to a deeper understanding of the interaction mechanisms between DOM and Cu2+ in agricultural soils.

Regulation of surface structure to suppress voltage decay for high-stable Li-rich oxide cathodes

Layered lithium-rich manganese oxides (LMO) are promising cathode materials for high-energy density lithium-ion batteries due to their high specific capacity and working potential. However, serious voltage decay and undesirable cycle stability are big obstacles that hinder their industrialization and application. Herein, an innovative and industrially valuable strategy of constructing composite coatings and oxygen vacancies on the LMO surface is put forward to suppress voltage decay and enhance the cycling stability of LMO by precisely modulating NaBH4 treatment. The synergistic effect of surface spinel coating, NaBO2coating, and oxygen vacancies effectively inhibits the release of oxygen, impedes the occurrence of side reactions at the interface, inhibits the migration and dissolution of transition metals, suppresses the irreversible structure transformation and improves the reversibility of redox reaction. The capacity retention of the NaBH4-treated LMO material maintains 100 % after 200 cycles at 0.5C, as well as stable cycling at 2C with a discharge capacity of 180 mAh g−1 harvested. Moreover, the voltage decay is significantly suppressed by NaBH4 modification, especially the NaBH4-0.5 % sample exhibits a mere voltage decay of 1.73 mV per cycle in the 200 cycles. This study provides significant insights into the development of LMO cathodes with long-cycle performance.

Driving factors for distribution and transformation of heavy metals speciation in a zinc smelting site

Heavy metal pollution at an abandoned smelter pose a significant risk to environmental health. However, remediation strategies are constrained by inadequate knowledge of the polymetallic distribution, speciation patterns, and transformation factors at these sites. This study investigates the influence of soil minerals, heavy metal occurrence forms, and environmental factors on heavy metal migration behaviors and speciation transformations. X-ray diffraction analysis revealed that the minerals associated with heavy metals are mainly hematite, franklinite, sphalerite, and galena. Sequential extraction results suggest that lead and zinc are primarily present in the organic-sulfide fractions (F4) and residual form (F5) in the soil, accounting for over 70% of the total heavy metal content. Zinc displayed greater instability in carbonate-bound (16%) and exchangeable (2%) forms. The migration and diffusion patterns of heavy metals in the subsurface environment were visualized through the simulation of labile state heavy metals, demonstrating high congruence with groundwater pollution distribution patterns. The key environmental factors influencing heavy metal stable states (F4 and F5) were assessed by integrating random forest models and redundancy analysis. Primary factors facilitating Pb transformation into stable states were available phosphorus, clay content, depth, and soil organic matter. For Zn, the principal drivers were Mn oxides, soil organic matter, clay content, and inorganic sulfur ions. These findings enhance understanding of the distribution and transformation of heavy metal speciation and can provide valuable insights into controlling heavy metal pollution at non-ferrous smelting sites.