Electromigration Research Articles

Applications of Ni and Ag metallizations at the solder/Cu interfaces in advanced high-power automobile interconnects: An electromigration study

An advanced Pb-free solder interconnect, Cu line/Cu pillar/Ni/Sn1.8Ag/Ag/Cu lead frame/Sn3Ag0.5Cu/Au/Ni(P)/Cu trace, using the flip-chip quad flat no‑lead (FCQFN) packaging technology was designed for high-power automobile applications. An electromigration study revealing the Ni and Ag metallization effects on the interfacial reaction was investigated. Current stressing was conducted at a 2 A direct current at 160 °C until the defined 200 %-electrical-resistance-rise failure occurrence. Electromigration induced a two-stage electrical resistance increase mode in the advanced automobile test vehicle with a mechanism transition time of 585 h, as evidenced by the in situ resistance monitoring. Phase transformation from the constituent phases into the predominant (Cu,Ni)6Sn5 and Cu3Sn intermetallic compounds (IMCs) at the interfaces was proposed to explain the rapid resistance rise in the early-stage electromigration. Void formation and coalescence due to the Kirkendall effect and volume shrinkage during the phase transformation were proposed to explain the following steady resistance increase after the critical current stressing time. Furthermore, the phase transformation and growth of the IMCs behaved divergently at different interfaces and electron flow directions. The rapid phase transformation occurred in the downstream Sn1.8Ag solder interconnect due to the accelerated Ni metallization dissolution and formed a complete IMC joint. The anisotropic diffusion driven by the competitive or synergetic effect between the electron wind force and chemical potential gradient was proposed to explain the asymmetric microstructures after the electromigration experiment. The application of Ag metallization benefited the flip-chip soldering process, and the layer-type Ag3Sn IMC served as a diffusion barrier against Sn/Cu interdiffusion at the solder/Cu lead frame interface during the solid-state electromigration. In contrast, the Ni metallization was designed as a diffusion barrier to hinder interdiffusion and the undesirable Cu3Sn growth at the solder/Cu interface. The findings presented in this study could benefit the solder interconnect design with an appropriate metallization combination against undesirable electromigration failure.

Anomalous enhancing effects of electric pulse treatment on strength and ductility of TC17 linear friction welding joints

Mechanical properties of TC17 titanium alloy undergo a significant reduction after linear friction welding (LFW), of which the strength and ductility are hard to be improved simultaneously by traditional aging heat treatment (AHT), seriously limiting the application of LFW in the manufacturing of TC17 titanium alloy blisks. To this end, the present work proposes to use electric pulse treatment (EPT) to enhance the strength and ductility of TC17 LFW joints simultaneously by improving its microstructure. The results show that, in comparison to the uneven distribution of α phases in the welding zone (WZ), heat-affected zone (HAZ), and base metal (BM) zone after AHT, EPT can selectively homogenize the α phase distribution of WZ and HAZ without impacting the BM. The selective effect of EPT is reflected as the synergistic influence of the local Joule heating effect and the electron wind effect, which promotes the diffusion of β phase stabilizing element Mo and leads to a competitive precipitation of β phase and α phase in the α phase transition temperature range. The ratio of α phase to β phase in the WZ and HAZ finally approaches an equilibrium point which is similar to that of BM, leading to a uniform distribution of α phase and realizing the synergy of strength-ductility of LFW joint: the maximum strength increase observed is 12.9 %, accompanied by a corresponding elongation increase of 122 % (by AHT & EPT), and the maximum plasticity improvement is 185 %, accompanied by a corresponding strength increase of 4.3 % (by EPT for 1 h). This study provides essential insights for improving the strength and ductility of LFW TC17 titanium alloy blisks and enhancing the applications of LFW in aeroengine components.

Fluoroethylene Carbonate: Bis(2,2,2,) Trifluoroethyl Carbonate as High Performance Electrolyte Solvent Blend for High Voltage Application in NMC811|| Silicon Oxide‐Graphite Lithium Ion Cells

LiNixMnyCozO2 cathode materials combined with Si‐based anode materials are current state‐of‐the‐art high energy density chemistries for lithium ion batteries. Increasing the upper cut‐off voltage is an intriguing approach to achieve even higher energy density in lithium ion batteries. However, poor oxidation stability of the state‐of‐the‐art electrolytes leads to transition metal dissolution (TMD), migration, and deposition (TMDMD) on the negative electrode, followed by sudden and rapid capacity fade. Furthermore, the chemical instability of the lithium hexafluorophosphate causes hydro‐fluoric acid to develop, which targets the native SiOx layers on silicon anodes and breaks the chemical bond to the carboxymethylcellulose sodium salt binder. Herein, a fluorine‐rich electrolyte formulation consisting of lithium‐bis(fluorsulfonyl)imide with fluoroethylene carbonate (FEC): bis(2,2,2,) trifluoroethyl carbonate (BFEC) was applied in NMC811||10%SiOx‐90%graphite cells to achieve high oxidation stability and prevent TMD and deposition. Up‐to‐date, this is the premier electrochemical performance reported in literature with a capacity retention of 94.5% and 92.2% with 0.5 °C and 4.5 V upper cut‐off voltage cycling at 20 and 40 °C after 100 cycles, respectively. The post mortem analysis showed that stabilization is achieved by forming inorganic‐ and salt‐rich interphases that protect the electrolyte versus decomposition at the electrode.

Preparation and characterization of quercetin@ZIF-L/GO@AgNPs nanocomposite film for room-temperature strawberry preservation

Fresh strawberries are easily contaminated by microorganisms after picking. Therefore, how to effectively store and keep fresh strawberries has been a hot topic for scientists to study. In this study, we prepared a leaf shaped metal organic framework nanomaterial loaded with quercetin (Quercetin@ZIF-L) at first, which can achieve effective loading of quercetin (96%) within 45 min and has a controlled release effect under acidic conditions. In addition, by cleverly combining satellite graphene oxide @ silver nanoparticles (GO@AgNPs) with slow precipitation performance, Quercetin@ZIF-L/GO@AgNPs nanocomposite film with larger pore size and larger specific surface area was prepared by scraping method. The characterization data of water flux, retention rate, flux recovery rate and water vapor permeability show that the composite film has good physical properties. The experiment of film packaging showed that the fresh life of strawberry could be extended from 3 to 8 days, which significantly improved the storage and freshness cycle of strawberry. At the same time, the metal migration test proved that the residual amount of silver ion in strawberry met the EU standard and zinc ions are beneficial to the health, enriching the types of high-performance fresh-keeping materials and broadening the application.

The role of topography feedbacks in enrichment of heavy metal elements in terrace type region

Minerals, metallurgy, and other production activities will cause a large number of heavy metal elements to leak into the natural environment. A large number of heavy metal elements have been found in the farmland soil, where the adsorption of plants enhances the enrichment. Here, we have selected a region with three terraces to conduct a whole-area soil sample collection and satellite hyperspectral data processing study to explore the role of terrain in this enrichment process. Five spectral transformation methods and four feature enhancement algorithms were designed, and the content extraction model was established to quantitatively retrieve eight heavy metal elements. The results indicates that the three terraces are the source state, transition state, and stable state of heavy metals respectively with the decrease of elevation; The correlation coefficient of various heavy metal elements exceeds 0.92, and the enrichment pattern is consistent although slope and aspect have no significant correlation with the enrichment of heavy metal elements; Local Cd exceeds 30.00%, Hg exceeds 10 times, and As exceeds 48.30% according to the indicator provisions of Chinese national standard (GB 15618-2018). Such knowledge extends our understanding of the abundance, migration, and enrichment of heavy metals from the perspective of topography, which is crucial for pollution assessment and soil remediation.

Role of phosphate in microalgal-bacterial symbiosis system treating wastewater containing heavy metals

Phosphorus is one of the important factors to successfully establish the microalgal-bacterial symbiosis (MABS) system. The migration and transformation of phosphorus can occur in various ways, and the effects of phosphate on the MABS system facing environmental impacts like heavy metal stress are often ignored. This study investigated the roles of phosphate on the response of the MABS system to zinc ion (Zn2+). The results showed that the pollutant removal effect in the MABS system was significantly reduced, and microbial growth and activity were inhibited with the presence of Zn2+. When phosphate and Zn2+ coexisted, the inhibition effects of pollutants removal and microbial growth rate were mitigated compared to that of only with the presence of Zn2+, with the increasing rates of 28.3% for total nitrogen removal, 48.9% for chemical oxygen demand removal, 78.3% for chlorophyll-a concentration, and 13.3% for volatile suspended solids concentration. When phosphate was subsequently supplemented in the MABS system after adding Zn2+, both pollutants removal efficiency and microbial growth and activity were not recovered. Thus, the inhibition effect of Zn2+ on the MABS system was irreversible. Further analysis showed that Zn2+ preferentially combined with phosphate could form chemical precipitate, which reduced the fixation of MABS system for Zn2+ through extracellular adsorption and intracellular uptake. Under Zn2+ stress, the succession of microbial communities occurred, and Parachlorella was more tolerant to Zn2+. This study revealed the comprehensive response mechanism of the co-effects of phosphate and Zn2+ on the MABS system, and provided some insights for the MABS system treating wastewater containing heavy metals, as well as migration and transformation of heavy metals in aquatic ecosystems.

Red mud modified phosphogypsum based self-leveling mortar: Hydration mechanism, heavy metal migration law and spatial distribution characteristics

In the production processes of phosphoric acid and alumina, chemical enterprises generate solid waste such as red mud (RM), phosphogypsum (PG), and fly ash (FA). The environmentally friendly utilization of these waste materials is of crucial significance. Therefore, this study focuses on investigating the impact of collaborative modification using diverse solid wastes on the macroscopic properties and internal microstructure of self-leveling mortar. Through a careful selection process, the optimal ratio for red mud and phosphogypsum self-leveling mortar(RPSM) has been identified during the research. This study not only provides substantial support for the effective utilization of solid waste but also contributes to the improvement of overall performance and structural characteristics of the mortar. Based on this, the hydration characteristics, leaching patterns, and spatial distribution characteristics of heavy metals in RPSM were evaluated. The research revealed that the optimal ratios of RM, PG, FA, PC, river sand, and heavy calcium carbonate powder in RPSM were 20.7%, 13.8%, 17.1%, 13.8%, 17.3%, and 17.3%, respectively. Under a water-binder ratio of 0.18, the flexural and compressive strength of the mortar specimens after 14 d of curing can reach 4.3 and 31.6 MPa. Through comprehensive analysis and discussion of the performance, microstructure, and dynamics of the hydration process of RPSM, the main processes of mortar hydration were elucidated. Environmental risk assessments indicated no environmental risks from heavy metals in RPSM. Human health risk assessment suggested carcinogenic risks from Cr and Cd in RPSM through oral exposure, leading to restrictions on the content of characteristic heavy metals in different application scenarios. Furthermore, fitting results of the release kinetics of heavy metals indicated that the leaching of heavy metals in RPSM can be well fitted with kinetic models, allowing the determination of the optimal safe age of RPSM containing harmful heavy metals. Finally, using interpolation and vertical distribution simulation by software such as ArcGIS, the spatial distribution characteristics of heavy metals in RPSM during use were analyzed. The research can supply fundamental academic support for the recycling of solid wastes like RM and the control of environmental risks associated with heavy metal leaching in building materials.

Effects of drip and flood irrigation on soil heavy metal migration and associated risks in China

BackgroundDifferent irrigation methods have variable effects on the physiochemical properties of soils. The predicted widespread replacement of flood irrigation with drip irrigation will alter the micro-environment of the associated soils in terms of migration, transformation, morphology, and toxicology of heavy metals and pesticides. The dynamics of heavy metals in soil under drip irrigation have only been investigated with regard to the use of sewage and reclaimed water; studies comparing these patterns across different irrigation methods are scarce. PurposeHere, we aimed to investigate the effects of drip and flood irrigation on heavy metal distribution in soil and the related risks in three typical agricultural systems in China. MethodsWe used fixed-point sampling, digestion analytical methods, descriptive analyses, one-way analysis of variance (ANOVA), Nemerow pollution index analyses, and correlation analyses to investigate the different effects of drip and flood irrigation on heavy metals (Cd, Cr, Cu, Pb, and Zn) in soils from Hebei, Xinjiang, and Ningxia Provinces, China. Results and DiscussionAnalyses of soil samples collected from drip-irrigated fields revealed significant differences in the concentrations of soil heavy metals at depths of 0–60 cm. Drip irrigation had a greater effect on heavy metal content in the soil surface than flood irrigation. In addition, heavy metals likely accumulated at the edges of the wetting fronts following prolonged irrigation. In comparison to drip irrigation, flood irrigation elevated pollution levels in the soil. The amount of fertiliser affected the leaching and migration of heavy metals in the soils by altering the physiochemical characteristics of the drip irrigation solution. ConclusionDrip irrigation alters the dynamics of heavy metals in soil by influencing their migration and accumulation patterns. This effect can be attributed to the methods of adding water and fertilisers to the soil under drip irrigation. Altering these variables can impact the level of heavy metals that bioaccumulate in crops. This study provides a scientific basis for reducing heavy metal pollution under drip irrigation.

Fractionation of metals in soil for strawberry cultivation: Effect on metal migration in food chain and application in risk assessment

Although trace metals in strawberry production system have attracted growing attention, little is known about metal fractionation in soil for strawberry cultivation. We hypothesized that the metal fractions in soil influenced by strawberry production had significant effect on food chain transport of metals and their risk in soil. Here, samples of strawberries and soil were gathered in the Yangtze River Delta, China to verify the hypothesis. Results showed that the acid-soluble Cr, Cd, and Ni in soil for strawberry cultivation were 21.5%–88.3% higher than those in open field soil, which enhanced uptake and bioaccessible levels of these metals in strawberries. Overall, the ecological, mobility, and health risks of Pb, Zn, Ni, and Cu in soil were at a low level. However, the ecological risk of bioavailable Cd, mobility risk of Cd, and cancer risk of bioavailable Cr in over 70% of the soil samples were at moderate, high, and acceptable levels, respectively. Since the increased acid-soluble Cr and Ni in soil were related to soil acidification induced by strawberry production, nitrogen fertilizer application should be optimized to prevent soil acidification and reduce transfer of Cr and Ni. Additionally, as Cd and organic matter accumulated in soil, the acid-soluble Cd and the ecological and mobility risks of Cd in soil were enhanced. To decrease transfer and risk of Cd in soil, organic fertilizer application should be optimized to mitigate Cd accumulation, alter organic matter composition, and subsequently promote the transformation of bioavailable Cd into residual Cd in soil.

Adsorption mechanism and influencing factors of selenium under the coexistence of nanoparticles and microplastics

Microplastics (MPs), as a common “vector” of pollutants in the aquatic environment, have a significant impact on the migration and transformation of heavy metals. In order to explore the mechanism and the influencing factors of the adsorption behavior of microplastics (MPs) on selenium (Se) in aqueous solution under the coexistence of nanoparticles, polystyrene microplastics (PS), nano-titanium dioxide particles (TiO2) and their coexisting compounds (PS+TiO2) were used as adsorbents to investigate the adsorption kinetics, isotherms and thermodynamic processes of Se. The effects of pH, humic acid concentration and coexisting ions on the adsorption behavior of Se(VI) were also analyzed. The results showed that the adsorption process of Se(VI) by PS and PS+TiO2 could be well fitted by pseudo-second-order kinetic model and Freundlich isotherm model, and it was an endothermic reaction with increased entropy. The adsorption capacity of Se(VI) by PS, TiO2, and PS+TiO2 were decreased with the increase of solution pH. Humic acid and Ca2+ promoted the adsorption of Se(VI), while PO43- significantly inhibited the adsorption of Se(VI) in the above three systems. The main adsorption mechanism of PS on Se(VI) was electrostatic adsorption and hydrogen bonding. The TiO2 adsorbed on the surface of PS mainly affected the adsorption behavior of PS on Se(VI) through hydrogen bonding.

Health and ecological risk of heavy metals in agricultural soils related to Tungsten mining in Southern Jiangxi Province, China.

Dayu County, a major tungsten producer in China, experiences severe heavy metal pollution. This study evaluated the pollution status, the accumulation characteristics in paddy rice, and the potential ecological risks of heavy metals in agricutural soils near tungsten mining areas of Dayu County. Furthermore, the impacts of soil properties on the accumulation of heavy metals in soil were explored. The geo-accumulation index (Igeo), the contamination factor (CF), and the pollution load index (PLI) were used to evaluate the pollution status of metals (As, Cd, Cu, Cr, Pb, Mo, W, and Zn) in soils. The ecological risk factor (RI) was used to assess the potential ecological risks of heavy metals in soil. The health risks and accumulation of heavy metals in paddy rice were evaluated using the health risk index and the translocation factor (TF), respectively. Pearson's correlation coefficient was used to discuss the influence of soil factors on heavy metal contents in soil. The concentrations of metals exceeded the respective average background values for soils (As: 10.4, Cd: 0.10, Cu: 20.8, Cr: 48.0, Pb: 32.1, Mo: 0.30, W: 4.93, Zn: 69.0, mg/kg). The levels of As, Cd, Mo, and tungsten(W) exceeded the risk screening values for Chinese agricultural soil contamination and the Dutch standard. The mean concentrations of the eight tested heavy metals followed the order FJ-S > QL > FJ-N > HL > CJ-E > CJ-W, with a significant distribution throughout the Zhangjiang River basin. Heavy metals, especially Cd, were enriched in paddy rice. The Igeo and CF assessment indicated that the soil was moderately to heavily polluted by Mo, W and Cd, and the PLI assessment indicated the the sites of FJ-S and QL were extremely severely polluted due to the contribution of Cd, Mo and W. The RI results indicated that Cd posed the highest risk near tungsten mining areas. The non-carcinogenic and total carcinogenic risks were above the threshold values (non-carcinogenic risk by HQ > 1, carcinogenic risks by CR > 1 × 10-4 a-1) for As and Cd. Correlation analysis indicated that K2O, Na2O, and CaO are main factors affecting the accumulation and migration of heavy metals in soils and plants. Our findings reveal significant contamination of soils and crops with heavy metals, especially Cd, Mo, and W, near mining areas, highlighting serious health risks. This emphasizes the need for immediate remedial actions and the implementation of stringent environmental policies to safeguard health and the environment.

Rejuvenation of degraded Zener diodes with the electron wind force

In this study, we explore the rejuvenation of a Zener diode degraded by high electrical stress, leading to a leftward shift, and broadening of the Zener breakdown voltage knee, alongside a 57% reduction in forward current. We employed a non-thermal annealing method involving high-density electric pulses with short pulse width and low frequency. The annealing process took <30 s at near-ambient temperature. Raman spectroscopy supports the electrical characterization, showing enhancement in crystallinity to explain the restoration of the breakdown knee followed by improvement in forward current by ∼85%.

Design of high-entropy P2/O3 hybrid layered oxide cathode material for high-capacity and high-rate sodium-ion batteries

High-entropy layered cathode materials have garnered significant attention due to their exceptional structural stability and capacity retention. However, the complex composition of these materials has posed challenges for performance optimization. Herein, an innovative high-entropy P2/O3 hybrid layered oxide cathode material with impressive reversible capacity and high-rate capabilities is designed according to the configurational entropy adjustment strategy. Specifically, the unique structure of Na0.85Li0.05Ni0.3Fe0.1Mn0.5Ti0.05O2 (LNFMT) exhibits not only enhanced anionic activity but also mitigated migration of transition metals at high voltage. The high-entropy effect facilitates the migration of Li+ to Na layer, forming a pseudo-tetrahedral structure that hinders the movement of Fe3+. Additionally, the robust Ti-O bond ensures the internal cohesion of transition metal layers, enhancing the structural stability during de-/intercalation processes. As a result, the undesirable P2-O2 phase transformation is effectively suppressed in 1.5–4.5 V, leading to a remarkable capacity retention of over 70% after 100 cycles at 0.2 C. Moreover, LNFMT shows a high discharge capacity of 116 mAh/g at 10 C with excellent capacity retention of 94.23% after 150 cycles in 2.0–4.2 V, demonstrating its superior rate capability. This research showcases the significant impact of the high-entropy effect and provides a novel perspective for the design of sodium-ion cathode materials.

Changes in coal waste DOM chemodiversity and Fe/Al oxides during weathering drive the fraction conversion of heavy metals

The long-term accumulation of coal waste on the surface during natural weathering leads to the inevitable migration of heavy metals contained in the coal waste, which increases the likelihood of environmental contamination and health risks. Dissolved organic matter (DOM) and Fe/Al oxides play crucial roles in the transformation and bioavailability of heavy metals. Thus, we analyzed the Fe/Al oxide content and DOM molecular composition in coal waste with different degrees of weathering and explored the influence of DOM chemical diversity and Fe/Al oxides on the potential mobility of heavy metals. Results showed that weathering-driven decrease in Fe oxides (Fed, FeO, and Fep decreased from 82.4, 37.5, and 3.6 mg∙L−1 to 41.3, 24.7, and 2.3 mg∙L−1, respectively) led to decreases in the reducible fractions of V and Cr. The potential environmental risks of more toxic metals of Cd and As, also increased as a result of the residual fractions decreased to 32.6 % and 41.3 %, respectively. Weathering caused an increase in oxygen-to‑carbon ratio, double-bond equivalent, modified aromaticity index, nominal oxidation state of carbon, and molecular diversity and a decrease in (m/z)w and (H/C)w, suggesting that the DOM of highly weathered coal waste possessed high unsaturation, aromatic structures, hydrophilicity, and strong oxidative characteristics. Additionally, although VMF and CrMF showed significant negative correlations with O/C ratio, polyphenolic, carbohydrates, and condensed aromatics, pH remained a key environmental factor determining the potential environmental risks of V and Cr by changing the residual fractions. The mobilities of Cd and As were significantly negatively correlated with those of Fe/Al oxides, particularly Fed, FeO, Fep, and Alp. Our findings contribute to the understanding of the impact of weathering on the geochemical cycling of different coal waste components, providing priority options for environmental risk prevention and control in coal mining areas.

Native Mass Spectrometry Dissects the Structural Dynamics of an Allosteric Heterodimer of SARS-CoV-2 Nonstructural Proteins.

Structure-based drug design, which relies on precise understanding of the target protein and its interaction with the drug candidate, is dramatically expedited by advances in computational methods for candidate prediction. Yet, the accuracy needs to be improved with more structural data from high throughput experiments, which are challenging to generate, especially for dynamic and weak associations. Herein, we applied native mass spectrometry (native MS) to rapidly characterize ligand binding of an allosteric heterodimeric complex of SARS-CoV-2 nonstructural proteins (nsp) nsp10 and nsp16 (nsp10/16), a complex essential for virus survival in the host and thus a desirable drug target. Native MS showed that the dimer is in equilibrium with monomeric states in solution. Consistent with the literature, well characterized small cosubstrate, RNA substrate, and product bind with high specificity and affinity to the dimer but not the free monomers. Unsuccessfully designed ligands bind indiscriminately to all forms. Using neutral gas collision, the nsp16 monomer with bound cosubstrate can be released from the holo dimer complex, confirming the binding to nsp16 as revealed by the crystal structure. However, we observed an unusual migration of the endogenous zinc ions bound to nsp10 to nsp16 after collisional dissociation. The metal migration can be suppressed by using surface collision with reduced precursor charge states, which presumably resulted in minimal gas-phase structural rearrangement and highlighted the importance of complementary techniques. With minimal sample input (∼μg), native MS can rapidly detect ligand binding affinities and locations in dynamic multisubunit protein complexes, demonstrating the potential of an "all-in-one" native MS assay for rapid structural profiling of protein-to-AI-based compound systems to expedite drug discovery.

Research on long-term migration behaviors of heavy metals after close-distance coal seam backfill mining

The backfill mining of coal-based solid waste in goaf poses a potential risk of heavy metal pollution to the groundwater environment, and the migration behavior of heavy metals differs significantly under the disturbance of backfill mining in close-distance multi-layer coal seams and single-layer coal seams. In this study, a migration model of heavy metals after solid backfilling in the goaf of shallow-buried close-distance thick coal seams was established, and the impact of the overburden damage and the layered distribution of the filling body on the long-term migration behavior of heavy metals were analyzed. The results show that the migration of heavy metals after close-distance coal seam backfill mining exhibits a higher risk of heavy metal pollution. The peak permeability of overburden after close-distance coal seam backfill mining is about 600 × 10−19 m2 higher than that after single-layer coal seam backfill mining. The migration distance of heavy metals in the floor after backfill mining of close-distance coal seams is 7.41 m farther than that of single-layer coal seam backfill mining, and its migration time of heavy metals to the surface is 27 a earlier than that of single-layer coal seam. This research provides theoretical and empirical support for the ecological risk assessment and heavy metal pollution control in close-distance coal seam backfill mining. Environmental ImplicationThe main filling material of close-distance coal seams backfill mining is coal gangue. Heavy metal elements such as Mn and Cr will be released in the underground environment for a long time, and the migration behavior of heavy metal elements will have an impact on the groundwater environment for more than 1000 years. This research provides theoretical and empirical support for the ecological risk assessment of close-distance coal seam backfill mining and the mitigation of heavy metal pollution.

Migration of transition metals and potential for carbon mineralization during acid leaching of processed kimberlite from Venetia diamond mine, South Africa

Carbonation of mafic and ultramafic rocks and mineral wastes provides a permanent way to sequester excess atmospheric CO2. Recent research has shown that this method also offers the potential for enhanced recovery of critical metals from mine tailings. In this study, processed kimberlite from the Venetia diamond mine (South Africa) was used in column acid leaching experiments to assess both its carbonation potential and whether critical metals such as nickel could be recovered during mineral carbonation. Processed kimberlite was treated daily with one pore volume of either deionized water or dilute hydrochloric acid (0.04 M, 0.08 M, 0.12 M and 0.16 M) for 28 days. Iron-rich yellow precipitates consistent with yellow ground formed during the experiments both at the top of the residue columns (corresponding to the inlets of the columns) and within the leachates collected from the bases of columns. The carbonation potential and mobility of transition metals were investigated using a combination of quantitative X-ray diffraction (XRD) using Rietveld refinements, inductively coupled plasma mass spectrometry (ICP-MS), scanning electron microscopy (SEM) coupled with energy-dispersive X-ray spectroscopy (EDXS), transmission electron microscopy (TEM) coupled with EDXS, and synchrotron-based X-ray fluorescence microscopy (XFM). Our results show that the high proportion of clay minerals (e.g., lizardite, smectite, talc, chlorite) in the processed kimberlite act as the primary source for Mg and transition metals such as Ni; however, calcite dissolution is the main source for Ca. The amount of Mg and Ca extracted from processed kimberlite increases with HCl concentration. If acid leaching of processed kimberlite were used at Venetia, the amount of Mg leached from clay minerals would provide an estimated CO2 offset potential ranging from 2.1 to 15.8 % of the mine's total annual emissions. The leached Ca from silicate dissolution could also provide an estimated CO2 offset potential ranging from 2.1 to 8.1 % of the mine's total annual emissions. However, the amount of CO2 released by calcite dissolution during this process is equivalent to 2.1–14.3 % of total annual CO2 emissions at Venetia., thus resulting in a net estimated CO2 offset potential of 2.1–9.6 % if the Ca released from calcite could not be recarbonated. If all of the Ca could be reprecipitated as calcite, the acid leaching techniques employed in this study could offset 4.2–23.9 % of the Venetia mine's CO2 emissions. Ultimately, greater concentrations and/or amounts of acid may be used to access more of the offset potential of Mg phyllosilicates in kimberlite, but the CO2 released by calcite dissolution must also be won back by recarbonation.

Soil Contamination by Heavy Metals and Radionuclides and Related Bioremediation Techniques: A Review

The migration of heavy metals and radionuclides is interrelated, and this study focusses on the interaction and complex influence of various toxicants. The rehabilitation of radioactively contaminated territories has a complex character and is based on scientifically supported measures to restore industrial, economic, and sociopsychological relations. We aim for the achievement of pre-emergency levels of hygienic norms of radioactive contamination of output products. This, in its sum, allows for further economic activity in these territories without restrictions on the basis of natural actions of autoremediation. Biosorption technologies based on bacterial biomass remain a promising direction for the remediation of soils contaminated with radionuclides and heavy metals that help immobilise and consolidate contaminants. A comprehensive understanding of the biosorption capacity of various preparations allows for the selection of more effective techniques for the elimination of contaminants, as well as the overcoming of differences between laboratory results and industrial use. Observation and monitoring make it possible to evaluate the migration process of heavy metals and radionuclides and identify regions with a disturbed balance of harmful substances. The promising direction of the soil application of phosphogypsum, a by-product of the chemical industry, in bioremediation processes is considered.

Interface Engineering via Constructing Enhanced Ligand Enables Highly Stable Li‐Rich Layered Oxide Cathode

AbstractHigh‐energy‐density and cost‐effective lithium‐rich oxides (LRO) are considered as the promising cathode materials for the next‐generation lithium‐ion batteries . Nevertheless, the elevated cut‐off voltage and the complex interface interactions have presented significant challenges that can lead to material degradation. Specifically, the inevitable release of lattice oxygen and the highly reactive interface‐driven irreversible migration of transition metal (TM) ions in LRO make the construction of a robust interface extremely important. Herein, an effective and efficient coating approach is applied to stabilize the interface structure of LRO by introducing a coordination bond between the strong ligand of polyurethane (PU) and the surface of LRO particles. This functional coating stabilizes the crystal field stabilization energies of LRO by acting as a strong ligand in spectrochemistry to form a coordination bond with Mn4+ in Li2MnO3 at high voltage. Consequently, irreversible oxygen release and TM ions migration are greatly inhibited. Overall, the LRO‐PU cathode exhibits superior electrochemical cyclability with a retention of 80.0% at 1C after 300 cycles and enhanced rate capability with a retention of 80.9% at 0.1C after rate cycles, marking a significant step toward commercial implementation.

Mechanism of Electropulsing Treatment Technology for Flow Stress of Metal Material: A Review

Residual stress is caused by non–uniform deformation caused by non–uniform force, heat and composition, which is of great significance in engineering applications. It is assumed that the residual stress is always the upper limit of the elastic limit, so the reduction of the flow stress will reduce the residual elastic stress. It is particularly important to control the flow stress in metal materials. Compared with traditional methods, the use of electropulsing treatment (EPT) technology stands out due to its energy–efficient, highly effective, straightforward and pollution–free characteristics. However, there are different opinions about the mechanism of reducing flow stress through EPT due to the conflation of the effects from pulsed currents. Herein, a clear correlation is identified between induced stress levels and the application of pulsed electrical current. It was found that the decrease in flow stress is positively correlated with the current density and the duration of electrical contact and current action time. We first systematically and comprehensively summarize the influence mechanisms of EPT on dislocations, phase, textures and recrystallization. An analysis of Joule heating, electron wind effect, and thermal–induced stress within metal frameworks under the influence of pulsed currents was conducted. And the distribution of electric, thermal and stress fields under EPT are discussed in detail based on a finite element simulation (FES). Finally, some new insights into the issues and challenges of flow stress drops caused by EPT are proposed, which is critically important for advancing related mechanism research and the revision of theories and models.