Release Of Metals Research Articles

Electroactive nanofibrous membrane with antibacterial and deodorizing properties for air filtration

Water vapor from respiration can severely accelerate the charge dissipation of the face mask, reducing filtration efficiency. Moreover, the foul odor from prolonged mask wear tends to make people remove their masks, leading to the risk of infection. In this study, an electro-blown spinning electroactive nanofibrous membrane (Zn/CB@PAN) with antibacterial and deodorization properties was prepared by adding zinc (Zn) and carbon black (CB) nanoparticles to the polyacrylonitrile (PAN) nanofibers, respectively. The filtration efficiency of Zn/CB@PAN for PM0.3 was > 99% and could still maintain excellent durability within 4 h in a high-humidity environment (25 ℃ and RH = 95%). Moreover, the bacterial interception rate of the Zn/CB@PAN could reach 99.99%, and it can kill intercepted bacteria. In addition, the deodorization rate of Zn/CB@PAN in the moist state for acetic acid was 93.75% and ammonia was 95.23%, respectively. The excellent filtering, antibacterial, and deodorizing performance of Zn/CB@PAN can be attributed to the synergistic effect of breath-induced Zn/CB galvanic couples’ electroactivity, released metal ions, and generated reactive oxygen species. The developed Zn/CB@PAN could capture and kill airborne environmental pathogens under humid environments and deodorize odors from prolonged wear, holding promise for broad applications as personal protective masks.

Model-Assisted Optimization of Cobalt Biosorption on Macroalgae Padina pavonica for Wastewater Treatment

The release of heavy metals into the environment as a result of industrial and agricultural activities represents one of the century’s most significant issues. Cobalt is a hazardous metal that is employed in a variety of industries. In this study, response surface methodology (RSM) combined with Box–Behnken design (BBD) was utilized to optimize the Co(II) ion removal from synthetic wastewater by the brown macroalga Padina pavonica. The influence of three factors, namely algal inoculum size, pH, and initial metal concentration, was assessed in optimization studies. RSM proposed a second-order quadratic model with a p-value of <0.0001 and R2 of 0.984 for P. pavonica. According to the data related to RSM optimization, the maximum percentage of Co(II) removal of 84.3% was attained under the conditions of algal inoculum size of 5.98 g/L, pH of 6.73, and initial Co(II) concentration of 21.63 mg/L. The experimental data from the biosorption process were fitted well with the Langmuir, Freundlich, and Temkin isotherm models. The maximal Co(II) adsorption capacity was estimated using the Langmuir model to be 17.98 mg/g. Furthermore, the pseudo-second-order kinetic model was shown to have the best fit for Co biosorption by P. pavonica, showing that the mechanism of Co(II) biosorption was chemisorption controlled by surface biosorption and intra-particle diffusion. Thermodynamic parameters were also investigated to evaluate the Gibbs free energy for the Co(II) ion, which was positive, showing that the biosorption process is nonspontaneous and exothermic, and the cobalt biosorption rate decreases with increasing temperature. Algal biomass was characterized by Fourier transform infrared spectroscopy, scanning electron microscopy, and energy dispersive spectroscopy. These analyses revealed the biosorbent’s diverse functional groups and porous, rough appearance. Therefore, P. pavonica can be used to implement sustainable, eco-friendly, and acceptable solutions to water pollution problems.

Salinity-Driven Interface Self-Assembly of a Biological Amphiphilic Emulsifier to Form Stable Janus Core-Shell Emulsion for Enhancing Agrichemical Delivery.

Agrichemical losses are a severe threat to the ecological environment. Additionally, some agrichemical compounds contain abundant salt, which increases the instability of formulations, leading to a lower agrichemical utilization and soil hardening. Fortunately, the biological amphiphilic emulsifier sodium deoxycholate alleviates these problems by forming stable Janus core-shell emulsions through salinity-driven interfacial self-assembly. According to the interfacial behavior, dilational rheology, and molecular dynamics simulations, Janus-emulsion molecules are more closely arranged than traditional-emulsion molecules and generate an oil-water interfacial film that transforms into a gel film. In addition, at the same spray volume, the deposition area of the Janus emulsion increased by 37.70% compared with that of the traditional emulsion. Owing to the topology effect and deformation, the Janus emulsion adheres to rice micropapillae, achieving better flush resistance. Meanwhile, based on response of the Janus emulsion to stimulation by carbon dioxide (CO2), the emulsion lost to the soil can form a rigid shell for inhibiting the release of pesticides and metal ions from harming the soil. The pyraclostrobin release rate decreased by 50.89% at 4 h after the Janus emulsion was exposed to CO2. The Chao1 index of the Janus emulsion was increased by 12.49% as compared to coconut oil delivery in soil microbial community. The Janus emulsion ingested by harmful organisms can be effectively absorbed in the intestine to achieve better control effects. This study provides a simple and effective strategy, which turns waste into treasure, by combining metal ions in agrichemicals with natural amphiphilic molecules to prepare stable emulsions for enhancing agrichemical rainfastness and weakening environmental risk.

Research on the decomposition mechanisms of lithium silicate ores with different crystal structures by autotrophic and heterotrophic bacteria

Ores serve as energy and nutrient sources for microorganisms. Through complex biochemical processes, microorganisms disrupt the surface structure of ores and release metal elements. However, there is limited research on the mechanisms by which bacteria with different nutritional modes act during the leaching process of different crystal structure ores. This study evaluated the leaching efficiency of two types of bacteria with different nutritional modes, heterotrophic bacterium Bacillus mucilaginosus (BM) and autotrophic bacterium Acidithiobacillus ferrooxidans (AF), on different crystal structure lithium silicate ores (chain spodumene, layered lepidolite and ring elbaite). The aim was to understand the behavioral differences and decomposition mechanisms of bacteria with different nutritional modes in the process of breaking down distorted crystal lattices of ores. The results revealed that heterotrophic bacterium BM primarily relied on passive processes such as bacterial adsorption, organic acid corrosion, and the complexation of small organic acids and large molecular polymers with metal ions. Autotrophic bacterium AF, in addition to exhibiting stronger passive processes such as organic acid corrosion and complexation, also utilized an active transfer process on the cell surface to oxidize Fe2+ in the ores for energy maintenance and intensified the destruction of ore lattices. As a result, strain AF exhibited a greater leaching effect on the ores compared to strain BM. Regarding the three crystal structure ores, their different stacking modes and proportions of elements led to significant differences in structural stability, with the leaching effect being highest for layered structure, followed by chain structure, and then ring structure. These findings indicate that bacteria with different nutritional modes exhibit distinct physiological behaviors related to their nutritional and energy requirements, ultimately resulting in different sequences and mechanisms of metal ion release from ores after lattice damage.

Titanium Nitride Coatings on CoCrMo and Ti6Al4V Alloys: Effects on Wear and Ion Release

While titanium nitride (TiN) coatings are well known for their biocompatibility and excellent mechanical properties, their wear particle and debris release in orthopedic implants remains a matter of active investigation. This study addresses the efficacy of TiN coatings on CoCrMo and Ti6Al4V alloys to enhance wear resistance and reduce ion release from prosthetic implants. Three different coating variants were utilized: one variant deposited using arc evaporation (Arc) followed by post-treatment, and two variants deposited using high-power impulse magnetron sputtering (HiPIMS) with or without post-treatment. The coatings’ performance was assessed through standard wear testing against ultra-high-molecular-weight polyethylene (UHMWPE) in bovine serum lubricant, and in the presence of abrasive PMMA bone cement particles in the lubricant. The results indicated that Arc and HiPIMS with post-treatment significantly reduced wear and eliminated detectable metal ion release, suggesting that these coatings could extend implant longevity and minimize adverse biological responses. Further long-term simulator and in vivo studies are recommended to validate these promising findings.

Risk control of heavy metal in waste incinerator ash by available solidification scenarios in cement production based on waste flow analysis

Incineration is a common method in municipal solid waste management, which has several advantages such as reducing the volume of waste, but with concerns about exhaust gas and ash management. In this study, heavy metals in bottom ash, secondary furnace ash and fly ash of two waste incinerators in Tehran and Nowshahr were analyzed and its control in cement production was investigated. For this purpose, twelve monthly samples of three types of incinerator ash were analyzed. By combining the studied ashes in the raw materials, the quantity of metals in the cement was analyzed. Finally, by investigating four scenarios based on quantitative variations in the routes of municipal solid waste, ash quantity and the related risk caused by its heavy metals were studied. The results showed that the concentration of heavy metals in the three ash samples of the studied incinerators was 19,513–23,972 µg/g and the composition of the metals included Hg (less than 0.01%), Pb (2.93%), Cd (0.59%), Cu (21.51%), Zn (58.7%), As (less than 0.01%), Cr (15.88%), and Ni (0.91%). The best quality of produced cement included 20% ash and 10% zeolite, which was the basis of the next calculations. It was estimated that the reduction of the release of metals into the environment includes 37 gr/day in best scenario equal to 10.6 tons/year. Ash solidification can be considered as a complementary solution in waste incinerator management.

The impact of microbial community structure changes on the migration and release of typical heavy metal (loid)s during the revegetation process of mercury-thallium mining waste slag

The effect of changes in microbial community structure on the migration and release of toxic heavy metal (loid)s is often ignored in ecological restoration. Here, we investigated a multi-metal (mercury and thallium, Tl) mine waste slag. With particular focus on its strong acidity, poor nutrition, and high toxicity pollution characteristics, we added fish manure and carbonate to the slag as environmental-friendly amendments. On this basis, ryegrass, which is suitable for the remediation of metal waste dumps, was then planted for ecological restoration. We finally explored the influence of changes in microbial community structure on the release of Tl and As in the waste slag during vegetation reconstruction. The results show that the combination of fish manure and carbonate temporarily halted the release of Tl, but subsequently promoted the release of Tl and arsenic (As), which was closely related to changes in the microbial community structure in the waste slag after fish manure and carbonate addition. The main reason for these patterns was that in the early stage of the experiment, Bacillaceae inhibited the release of Tl by secreting extracellular polymeric substances; with increasing time, Actinobacteriota became the dominant bacterium, which promoted the migration and release of Tl by mycelial disintegration of minerals. In addition, the exogenously added organic matter acted as an electron transport medium for reducing microorganisms and thus helped to reduce nitrate or As (Ⅴ) in the substrate, which reduced the redox potential of the waste slag and promoted As release. At the same time, the phylum Firmicutes, including specific dissimilatory As-reducing bacteria that are capable of converting As into a more soluble form, further promoted the release of As. Our findings provide a theoretical basis for guiding the ecological restoration of relevant heavy-metal (loid) mine waste dumps.

Environmental performance of unfired bricks produced from co-disposal of mine tailings and municipal solid waste incineration fly ash based on comprehensive leaching tests

The potential leaching of heavy metals is a crucial concern for construction materials produced from solidification/stabilization (S/S) treatment of wastes. This study comprehensively evaluated the leaching characteristics of heavy metals from the unfired bricks produced from co-disposal of Pb–Zn mine tailings and municipal solid waste incineration fly ash using batch, sequential, and semi-dynamic leaching tests. The results show that S/S treatment drastically reduced the leachability of heavy metals from the unfired bricks through lowering their distribution in the acid-soluble fraction. The effective diffusion coefficients of heavy metals within unfired bricks were all below 1.55 × 10−13 cm2/s, which is indicative of low mobility in the environment. The release of heavy metals from the unfired bricks was primarily governed by diffusion and dissolution. Slaking treatment of fly ash significantly reduced the leaching of heavy metals from the unfired bricks due to their improved structural integrity and compactness, which minimizes the surface area in the solid matrix accessible by the leaching medium. The leachability indices of heavy metals within the unfired bricks ranged from 13.12 to 18.10, suggesting that they are suitable for “controlled utilization” in specific scenarios. Compared to untreated mine tailings, converting them into unfired bricks could reduce the releases of heavy metals by several to hundreds of folds. These findings demonstrate that S/S can be an effective and sustainable strategy for co-disposal of mining tailings and incineration fly ash to produce construction materials with sound long-term environmental performance.

Influence of environmental factors on changes in the speciation of Pb and Cr in sediments of Wuliangsuhai Lake, during the ice-covered period.

Ecological pollution caused by heavy metals released from sediments is a worldwide concern. However, the effect of changes in sediment speciation on their release of heavy metals has not been adequately reported. In this study, the research focused on Pb and Cr in the ice period of Wuliangsuhai. This study analyzed changes in the sediment speciation of Pb and Cr before and after a release experiment using four risk assessment methods while varying the temperature, pH, and salinity of the water column. The results indicated that the total concentration of Pb ranged from 11.17 to 24.25mg/kg, while for Cr it ranged from 42.26 to 69.68mg/kg. Both elements exhibited mild contamination. The release of Pb and Cr from sediments increases with increasing water temperature, mainly due to the conversion of the residual fraction of Pb to the Fe-Mn oxide fraction and Cr converting more residual fraction to the organic matter and sulfide fraction. The release of sediment Pb and Cr decreased with increasing pH, with Pb converting more acid extractable fraction to the residual fraction and Cr converting more organic matter and sulfide fraction to the residual fraction. In contrast, the release of Pb and Cr increased and then decreased with increasing salinity. For Pb, the acid extractable fraction was more susceptible to conversion to the residual fraction by environmental influences, whereas for Cr, the organic matter and sulfide fraction were susceptible to conversion to the residual fraction.

Machine learning-based models to predict aquatic ecological risk for engineered nanoparticles: using hazard concentration for 5% of species as an endpoint.

Assessment and prediction for the ecotoxicity of engineered nanoparticles (ENPs) at the community or ecosystem levels represents a critical step toward a comprehensive understanding of the ecological risks of ENPs. Current studies on predicting the ecotoxicity of ENPs primarily focus on the cellular and individual levels, with limited exploration at the community or ecosystem levels. Herein, we present the first of the reports for the direct prediction of aquatic ecological risk for ENPs at the community level using machine learning (ML) approaches in the field of computational toxicology. Specifically, we extensively collected the threshold concentrations of twelve ENPs including metal- and carbon-based nanoparticles for aquatic species, i.e., hazardous concentrations at which 5% of species are harmed (HC5), established by a species sensitivity distribution. Afterwards, we used eight supervised ML methods including Adaboost, artificial neural network, C4.5 decision tree, K-nearest neighbor, logistic regression, Naive Bayes, random forest, and support vector machine to develop nine classification models and four regression models, respectively, for the qualitative and quantitative prediction of HC5. The evaluation of model performance yielded the internal validation accuracy of all classification models ranging from 71.4 to 100%, and the determination coefficient of regression models ranging from 0.702 to 0.999, indicating that the developed models showed good performance. By using a cross-validation method and an application domain characterization, the selected models were further validated to have powerful predictive ability. Furthermore, the incorporation of three nanostructural descriptors (metal oxide sublimation enthalpy, zeta potential, and specific surface area) linked to toxicity mechanisms (the release of metal ions, the stability of dispersions of particles in aqueous suspensions, and the surface properties of the material) effectively enhanced the prediction power and mechanistic interpretability of the selected models. These findings would not only be beneficial in the screening of ENPs with potential high ecological risks that need to be tested as a priority but also contribute to the development of environmental regulations and standards for ENPs.

Simulated gastric leachate of 3D printer metal-fill filaments induces cytotoxic effects in rat and human intestinal models

Metals are used in 3-dimensional (3D) printer filaments in the manufacture of 3D printed objects. Exposure to the filaments, printed objects and emissions from printing may pose health risks from release of toxic metals. This study investigated the cytotoxicity of extruded 3D printer filament leachates in rat and human intestinal cells. Copper-, bronze-, and steel-fill extruded filaments were incubated in acidic media for 2 h. Leachates were adjusted to pH 7 and cells exposed for 4 or 24 h. Concentration- and time-dependent decreases in rat and human cell viability were observed using a colorimetric assay and confirmed by microscopy. Copper- and bronze-fill leachates were more cytotoxic than steel. Copper-fill leachates had the highest copper concentrations by ICP-MS. Exposure to CuSO4 resulted in concentration-dependent cytotoxicity in rat cells. The copper chelator bathocuproine disulphonate alleviated cytotoxicity of CuSO4 and copper-fill leachate, suggesting that copper ions have a role in the cytotoxicity. Hydrogen peroxide increased and glutathione decreased in rat cells exposed to copper-fill leachate, suggesting the formation of reactive oxygen species. Overall, our data indicate that metals released from the acidic exposure of print objects using metal-fill filaments, especially copper, are toxic to rat and human intestinal cells and additional studies are needed.

Zeolite facilitates sequestration of heavy metals via lagged Fe(II) oxidation during sediment aeration

Aeration of sediments could induce the release of endogenous heavy metals (HMs) into overlying water. In this study, experiments involving FeS oxygenation and contaminated sediment aeration were conducted to explore the sequestering role of zeolite in the released HMs during sediment aeration. The results reveal that the dynamic processes of Fe(II) oxidation play a crucial role in regulating HMs migration during both FeS oxygenation and sediment aeration in the absence of zeolite. Based on the release of HMs, Fe(II) oxidation can be delineated into two stages: stage I, where HMs (Mn2+, Zn2+, Cd2+, Ni2+, Cu2+) are released from minerals or sediments into suspension, and stage II, released HMs are partially re-sequestered back to mineral phases or sediments due to the generation of Fe-(oxyhydr) oxide. In contrast, the addition of zeolite inhibits the increase of HMs concentration in suspension during stage I. Subsequently, the redistribution of HMs between zeolite and the newly formed Fe-(oxyhydr) oxide occurs during stage II. This redistribution of HMs generates new sorption sites in zeolite, making them available for resorbing a new load of HMs. The outcomes of this study provide potential solutions for sequestering HMs during the sediment aeration.

Soil Cd increased the leaf litter Cd remains of Solanum nigrum and Solanum lycopersicum

Plant litter decomposition is a natural pathway of heavy metal cycling in soil ecosystems, but the dynamics of heavy metal release during litter decomposition are relatively poorly understood. The purpose of this study was to investigate the effects of species, soil fauna and soil Cd addition on litter decomposition and Cd release dynamics. Therefore, we selected two plants, Solanum nigrum and S. lycopersicum with large differences in Cd accumulation capacity. First, they were enriched with Cd during the growing period and leaf litter was harvested after 6 months of pretreatment. Then, the decomposition of leaf litter was conducted with or without soil Cd and Eisenia fetida through lab pot tests. Our results showed that leaf litter Cd led to a significant decrease in litter decomposition rate (K value), with a maximum decrease of 32.1% in S. nigrum and 30.1% in S. lycopersicum. We observed that the presence of E. fetida significantly increased K value, but the effect was similar in the +leaf Cd treatment and the -leaf Cd treatment, both for S. nigrum and S. lycopersicum. Interestingly, the litter Cd concentration did not decrease during decomposition, but showed an increasing trend, especially for S. nigrum in the +soil Cd treatment. Moreover, the litter Cd remains was higher in the +soil Cd treatment compared to the -soil Cd treatment for both S. nigrum and S. lycopersicum, no matter whether with or without E. fetida. This result suggests that the Cd may be transferred from soil to litter, thus increasing the litter Cd remains. Overall, our study shows that leaf litter Cd slowed down the carbon cycling in ecosystems. In addition, the release of litter Cd has a lag, and the litter has a certain adsorption capacity for soil Cd, which intensifies the harm to the ecology during litter transfer.

The size of the femoral head does not influence metal ion levels after metal-on-polyethylene total hip arthroplasty: a five-year report from a randomized controlled trial.

In metal-on-polyethylene (MoP) total hip arthroplasty (THA), large metal femoral heads have been used to increase stability and reduce the risk of dislocation. The increased size of the femoral head can, however, lead to increased taper corrosion, with the release of metal ions and adverse reactions. The aim of this study was to investigate the relationship between the size of the femoral head and the levels of metal ions in the blood in these patients. A total of 96 patients were enrolled at two centres and randomized to undergo MoP THA using either a 32 mm metal head or a femoral head of between 36 mm and 44 mm in size, being the largest possible to fit the thinnest available polyethylene insert. The levels of metal ions and patient-reported outcome measures (Oxford Hip Score, University of California, Los Angeles Activity Scale) were recorded at two and five years postoperatively. At five years, the median levels of chromium, cobalt, and titanium were 0.5 μg/l (interquartile range (IQR) 0.50 to 0.62), 0.24 μg/l (IQR 0.18 to 0.30), and 1.16 μg/l (IQR 1.0 to 1.68) for the 32 mm group, and 0.5 μg/l (IQR 0.5 to 0.54), 0.23 μg/l (IQR 0.17 to 0.39), and 1.30 μg/l (IQR 1 to 2.05) for the 36 mm to 44 mm group, with no significant difference between the groups (p = 0.825, p = 1.000, p = 0.558). There were increased levels of metal ions at two years postoperatively in seven patients in the 32 mm group, compared with four in the 36 mm to 44 mm group, and at five years postoperatively in six patients in the 32 mm group, compared with seven in the 36 mm to 44 mm group. There was no significant difference in either the OHS (p = 0.665) or UCLA (p = 0.831) scores between patients with or without an increased level of metal ions. In patients who underwent MoP THA, we found no differences in the levels of metal ions five years postoperatively between those with a femoral head of 32 mm and those with a femoral head of between 36 mm and 44 mm, and no corrosion-related revisions. As taper corrosion can start after five years, there remains a need for longer-term studies investigating the relationship between the size of the femoral head size and corrosion in patients undergoing MoP THA.

Recent Progress of Novel Porous Materials in Wastewater Treatment

Unavoidably, the expansion of industry causes the release of numerous heavy metals, radionuclides, and organic pollutants into the environment. Due to these pollutants, the extremely toxic, highly carcinogenic chemicals provide a serious risk to people and aquatic life. Wastewater pollutants must be removed to safeguard the ecology. A huge specific surface area, multiple binding sites, a plethora of functional groups, variable pore size, and simplicity of surface modification are just a few advantages of porous materials. They are considered viable candidate materials for the efficient and selective removal of contaminants from aqueous solutions in a range of difficult circumstances due to their benefits. This work reviews the characteristics, methods of functionalization, and ways of modification of many novel porous materials in recent years. The use of these porous materials in the treatment of wastewater was examined. The development potential of porous materials is finally summed up.

Evaluation of Heavy Metals in Auto Mechanics in Aba Metropolis, South East, Nigeria Who Were Exposed to Petrol and Petroleum Products

Background: Every day, humans come into contact with heavy metals in the environment. These metals are widespread throughout the world and are known to affect and create specific biological changes that may be detrimental to the body. Auto mechanics are known to come in contact with these hazardous substances during vehicle maintenance and repair activities, which may lead to the release of heavy metals into the body as well as the environment. Aim: To evaluate the levels of heavy metals that auto mechanics are exposed to from petroleum and petroleum products in mechanic workshops in Aba Metropolis. Study Design: A cross sectional study with a total of 204 participants, 123 of whom were auto mechanics and 81 of whom were non auto mechanics (controls), had blood samples taken from them. Place and Duration of Study: The blood samples were taken from auto mechanic working in mechanic workshop spread around four locations of Aba Metropolis during the period of May 2022 to November, 2022. Samples were analyzed at Abia State University Teaching Hospital, Aba, Abia State and Laboratory Department, JAROS Inspection Services Limited, Port Harcourt, Rivers State, Methods: The levels of heavy metals (Pb, Hg, Cd, Cr, and As) in blood were measured using atomic absorption spectrophotometry. The Statistical Analysis System (SAS), STAT 15.1 was used to analyse the data from the study. Results: The serum concentration of heavy metals in reducing order, were Cr > Pb > As > Hg > Cd in the exposed individuals while in the control subjects, the order from the highest concentration was; Cr > Pb >As > Cd > Hg. The blood of auto mechanics had a significantly higher level of Pb and Hg than that of non-auto mechanics (p<0.05). Duration of exposure of the auto mechanics to petrol and its product showed an adverse effect from the results gotten in this study. Conclusion: Heavy metal contamination still poses a threat to health and well-being of the auto mechanics in Aba Metropolis.

Insights into processes and consequent metal(loid) behavior in dredged estuarine sediments upon electrokinetic treatment

The use and reuse of natural and waste materials after treatment has become increasingly crucial as a means of achieving sustainable and environmentally-friendly solutions, and is part of a broader trend towards embracing circular economy principles. This study aims to understand the behavior of different elements (metal(loid)s and non-metals) and minerals during and after electrokinetic remediation (EKR) and to develop an effective approach to monitor its progress and overcome unwanted occurrences. In this regard, estuarine sediments, collected from Tancarville (Seine River estuary, France), were electrokinetically treated using a 64 L laboratory reactor; treatment was done 8 h per day for 21 days. The physico-chemical properties (pH, electric conductivity, and oxido-reduction potential) and current were monitored during treatment. The spatial evolution of the physico-chemical, physical (grain size distribution), mineral (mainly carbonates), organic, and elemental (As, Ca, Cl, Mg, Na, Pb, Sr, Zn, and Zr) characteristics was studied to assess the treatment efficiency. The results showed that the acidic conditions in the anodic sediments caused the dissolution of carbonates (calcite, dolomite, and aragonite), resulting in a considerable reduction in As, Zn, and Pb. Additionally, Cl as well as electric conductivity were significantly reduced from most sediments, which is essential in agricultural practices. Furthermore, materials had precipitated and settled in the anolyte and catholyte chambers, which acted as sorbents for elements that were released from the sediments (mainly Zn and As). Finally, three distinct phases occurred during treatment and were mainly linked to the current intensity and electric conductivity on the one hand, and the dissolution of carbonates and metal(loid) release on the other. This approach can be used to treat sediments and other media to improve the overall efficiency of remediation processes and create an end product with desired characteristics.

Electrochemical and corrosion protection performance of Sr-HaP/PoPD coated LN stainless steel

BackgroundStainless steel is a common implant material used in orthopaedic surgeries. However, metallic ions are released from the implants when it placed inside the human body. Coating of biocompatible material such as strontium hydroxyapatite (Sr-HaP) is one of the methods to reduce the release of metallic ions into the body. MethodIn the present work, we have developed a bilayer coating namely poly-orthophenylenediamine (PoPD) on Sr-HaP deposited low nickel stainless steel (LNSS) via electrochemical deposition followed by electropolymerization methods. The Sr-HaP/PoPD coating was confirmed with Fourier transform infrared spectroscopy (FTIR) and high resolution scanning electron microscopy (HR-SEM). The corrosion protection performance of the coated LN SS specimens in Ringer's solution was investigated using potentiodynamic polarisation and electrochemical impedance spectroscopic techniques. The leach out characteristics of the coating was determined at the impressed potential. Significant findingsThe studies revealed that the passive film underneath the PoPD layer is acting like a shield and prevent the LN SS from corrosion. Furthermore, the potential bioactivity of LN SS is due to the presence of top porous Sr-HaP layer. Hence, the PoPD/Sr-HaP bilayer coating on LN SS substrate could be a promising material for orthopaedic implant applications.

Novel high-efficiency plasma nitriding process utilizing a high power impulse magnetron sputtering discharge

Lifetime and biocompatibility of orthopedic implants are crucial in meeting the new challenges brought about by the fall in the patient age and the aging population. The high-load surfaces in contact with the biological environment must display enhanced tribological properties, biocompatibility, and reduced metal ion release in long-term clinical performance. Surface modification techniques such as nitriding can significantly improve the in-service behavior of the medical-grade alloys in current use. We report on a novel approach for nitriding of CoCrMo alloys using high power impulse magnetron sputtering (HIPIMS) discharge. The new nitriding process has been successfully carried out at the National HIPIMS Technology Centre at Sheffield Hallam University, UK, in an industrial size Hauzer 1000-4 system enabled with HIPIMS technology. While the nitriding ion flux is controlled by the HIPIMS magnetron plasma source, the ion energy can be independently set via the substrate bias. Implementing the HIPIMS source allows reducing the operational pressure by one order of magnitude compared to conventional dc plasma nitriding (DCPN). Plasma analyses have identified significantly enhanced production of ions of molecular nitrogen (N2+), atomic nitrogen (N+), and N2H+ radicals in the HIPIMS discharge compared to DCPN. Because of the low pressure of operation of the HIPIMS process, the energy of ions is similar to the bias voltage, whereas the high pressures used in DCPN cause severe losses in ion energy due to scattering collisions within the sheath. The high flux and high ion energy are primarily responsible for achieving a fourfold increase in process productivity as compared to state-of-the-art plasma nitriding processes. The nitrided surface layers exhibit excellent mechanical and tribological properties, which bring about significant improvements in hardness, fracture toughness, and wear. The protective function of the nitrided layer against corrosion in the aggressive environments of simulated body fluid is remarkably augmented. The barrier properties of the nitrided layer have been demonstrated through a reduction in metal ion release by as much as a factor of 2, 4, and 10 for Co, Cr, and Mo, respectively.

Metalloproteomics: Unraveling the Metal Binding Proteins of Diverse Metal-Resistant Bacteria

The release of metals into the environment raises serious concerns about their harmful effects on both the wildlife and human health. The biosphere is experiencing with the pervasive presence of heavy metal pollutants such as arsenic (As), cadmium (Cd), mercury (Hg), lead (Pb), chromium (Cr), copper (Cu) and nickel (Ni), which pose significant environmental challenges. While certain metals are essential for regulating fundamental metabolic processes and upholding the overall physiology of microorganisms, excessive exposure to heavy metals can be detrimental to their survival and function. As a result of their remarkable adaptability, microorganisms, particularly bacteria such as Pseudomonas fluorescens, Escherichia coli, Serratia marcescens, Bacillus cereus and Alcaligenes sp., have evolved sophisticated defence mechanisms to combat the stress caused by heavy metals. One such process is the creation of metal-binding proteins (MBPs), which may bind and sequester metals, thus significantly lowering their toxicity in bacteria. Metalloproteomics, a subfield of metallomics, focuses on the discovery and characterization of such metal-binding proteins (MBPs) in metal-resistant bacteria, resulting in the opening of the doors for innovative bioremediation techniques and therapeutic treatments against bacterial diseases. This review explores the intriguing world of MBPs in metal-resistant bacteria and emphasizes their significant role in metal resistance, detoxification and homeostasis. Furthermore, metallochaperones in bacteria have been extensively studied using the metalloproteomic methodologies and techniques utilized in metal-binding proteins. This study also provides useful information on the interactions between these metallochaperones and different MBPs, which advances our understanding of how bacteria respond to exposure to such heavy metals.