Metal Ion Concentration Research Articles

One‐pot hydrothermal biochar obtained from malt bagasse waste as an electrode‐modifying material towards the stripping voltammetric sensing of lead

AbstractPb2+ ions are highly toxic to living beings because they tend to bioaccumulate in the body. For this reason, the development of simpler, low‐cost, and easy‐to‐operate techniques that can detect and quantify low concentrations of metal ions would help to identify contaminating media and improve public health. This work proposes a Pb2+ voltammetric sensor based on a carbon paste electrode modified with hydrothermal biochar (hydrochar, HC) obtained from malt bagasse waste (HC/CPE). The obtained hydrochar was characterized by zero‐charge point, FT‐IR, XRD and thermogravimetry. The differential pulse adsorptive anodic stripping voltammetry (DPAdASV) technique was used to perform the Pb2+ determination. After optimizing important parameters for detecting Pb2+ ions and the parameters of the voltammetric technique employed, a linear response range of 0.50 to 7.06 μmol L−1 with a limit of detection (LOD) and limit of quantification (LOQ) of 55.0 and 181.5 nmol L−1 were achieved, respectively. The developed voltammetric procedure was applied towards the Pb2+ determination at tap water and river water samples, with excellent recoveries (ranging of 91.19 to 109.22 %), proving that the HC‐based electrode has great potential for detecting Pb2+ ions. Hydrothermal carbonization allowed the biomass to be converted into functionalized hydrochar, eliminating the need for subsequent functionalization/activation steps for use as a Pb2+ adsorbing material on the electrodic surface. The proposed sensor also proved to be easy to assemble and environmentally friendly by using biomass waste as the carbon material. Thus, the proposed sensor adds to the literature the possibility of simple and easy detection of metal ions with a waste reuse bias.

Advancements in Starch‐Based Aerogels and Hydrogels for Treatment of Water Containing Heavy Metals – A Short Review

AbstractRapid industrialization and profligate use of resources in the present era has led to increase in the concentration of toxic heavy metal ions in water bodies and has become a serious environmental concern. Starch hydrogels and aerogels with engineered functionality, porosity, regeneration characteristics, and high surface to volume ratio have rendered them potential candidates for the adsorption of heavy metal ions from wastewater streams. However, grafting, crosslinking, and composting of the starch aerogels and hydrogels to tailor them in response to various stimuli such as ionic strength, pH, and temperature has added an advantage in the treatment of wastewater containing heavy metal ions. This review critically analyses the various synthesis routes for the production of starch‐based aerogels and hydrogels with physico‐chemical characteristics (amylose content, gelatinization temperature, surface area, density, and porosity) and their applicability to adsorb heavy metal (Cd, Cu, Co, Ni, Cr, Pb, Zn, Fe, and Co) ions from wastewater. Future prospects in the development of economical and robust starch‐based aerogels and hydrogels in terms of their stability and reusability have also been discussed.

Competitive Adsorption of Aqueous Cd(II) and Pb(II) Solutions onto Silicas Synthesized with Saponin as Template Agent

The aim of the research was to prepare silica adsorbents using an environmentally friendly pathway, a template synthesis with saponin biosurfactant as a structure-directing agent. The adsorbents prepared in this way exhibit improved adsorption properties while maintaining environmental innocuousness. For the preparation of porous silica, the biosurfactant template sol–gel method was used with tetraethoxysilane as a silica precursor. The silica adsorbents were analyzed by FTIR spectroscopy, nitrogen adsorption–desorption and SEM/EDX microscopy, TEM/HRTEM microscopy, and thermogravimetric analyses. Batch tests were carried out to remediate Pb(II)/Cd(II) ions in single/binary aqueous solutions, and the effect of the surfactant on the adsorption properties was assessed. The optimal adsorption parameters (pH, contact time, initial concentration of metal ions) have been determined. The adsorption was fitted using Langmuir and Freundlich adsorption isotherms and kinetic models. Mathematical modeling of the retention process of Pb(II) and Cd(II) ions from binary solutions indicated a competitive effect of each of the two adsorbed metal ions. The experimental results demonstrated that saponin has the effect of modifying the silica structure through the formation of pores, which are involved in the retention of metal ions from aqueous solutions and wastewater.

Novel High-Performance Functionalized and Grafted Bio-Based Chitosan Adsorbents for the Efficient and Selective Removal of Toxic Heavy Metals from Contaminated Water.

Novel functionalized and/or grafted crosslinked chitosan adsorbents were synthesized and used to remove several toxic heavy metal ions such as nickel, lead, chromium, and cadmium ions from contaminated water. The chitosan biopolymer was functionalized by maleic anhydride (CS_MA) acting also as a crosslinking agent. Glutaraldehyde-crosslinked chitosan (CS_GA) grafted with poly(methyl methacrylate) (CS_MMA) was also synthesized. The synthesized adsorbents were characterized using a variety of analytical techniques such as SEM, TGA, and FTIR, which confirmed their chemical structures and morphology. The adsorption capacity of the adsorbents was analyzed under various conditions of contact time, adsorbent dose, initial concertation, temperature, and pH and evaluated against those of pure chitosan (CS) and the crosslinked chitosan(CS_GA). The ultimate removal conditions were 0.5 g/100 mL adsorbent dose, an initial metal ion concentration of 50 ppm, a temperature of 45 °C, and pH 9. CS_MMA had the highest removal percentages for all metal ions, ranging from 92% to 94%. The adsorption was demonstrated to fit a pseudo-first-order model that followed a Langmuir adsorption isotherm. The results highlight the capacity of the synthesized polymers to efficiently remove major toxic contaminants at low cost from contaminated water, present especially in low-income areas, without harming the environment.

Co-removal and recycling of Ba2+ and Ca2+ in hypersaline wastewater based on the microbially induced carbonate precipitation technique: Overlooked Ba2+ in extracellular and intracellular vaterite

This study investigates the co-precipitation of calcium and barium ions in hypersaline wastewater under the action of Bacillus licheniformis using microbially induced carbonate precipitation (MICP) technology, as well as the bactericidal properties of the biomineralized product vaterite. The changes in carbonic anhydrase activity, pH, carbonate and bicarbonate concentrations in different biomineralization systems were negatively correlated with variations in metal ion concentrations, while the changes in polysaccharides and protein contents in bacterial extracellular polymers were positively correlated with variations in barium concentrations. In the mixed calcium and barium systems, the harvested minerals were vaterite containing barium. The increasing concentrations of calcium promoted the incorporation and adsorption of barium onto vaterite. The presence of barium significantly increased the contents of O-CO, N-CO, and Ba-O in vaterite. Calcium promoted barium precipitation, but barium inhibited calcium precipitation. After being treated by immobilized bacteria, the concentrations of calcium and barium ions decreased from 400 and 274 to 1.72 and 0 mg/L (GB/T15454–2009 and GB8978–1996). Intracellular minerals were also vaterite containing barium. Extracellular vaterite exhibited bactericidal properties. This research presents a promising technique for simultaneously removing and recycling hazardous heavy metals and calcium in hypersaline wastewater.

Nanoconfined polyethyleneimine in mesoporous MCM-41 silica for heavy metal ions removal

Water contamination resulting from the presence of the various coexistent pollutants is an urgent environmental challenge, and effective treatment is demanded to remove the toxic substances. The removal of pollutants by adsorption, as an effective, efficient and economic strategy, has been widely used in water treatment. In this work, PEI@MCM-41 was prepared by infiltrating polyethyleneimine (PEI) into the pores of mesoporous MCM-41, and applied for the removal of heavy metal ions. The adsorption kinetics of Cu2+, Ni2+ and Cd2+ by PEI@MCM-41 were supposed to be pseudo-second-ordered, and the adsorption capacities were as high as 39.30, 33.67 and 21.10 mg·g−1, respectively. The influence of temperature, pH, coexistent salt and heavy metal ions concentration on the adsorption performance was studied. Owing to the nanoconfinement effect and hydrogen bond, PEI remained stable during the adsorption and desorption process, and the adsorption capacity for Cu2+ maintained 84.15 % even after four consecutive adsorption–desorption cycles. This work demonstrates that the potential practical applicability of PEI@MCM-41 as promising adsorbent in the removal of heavy metal ions.

Polypyrrole-coated zinc/nickel oxide nanocomposites as adsorbents for enhanced removal of Pb(II) in aqueous solution and wastewater: An isothermal, kinetic, and thermodynamic study

One common heavy metal that is extremely harmful to the kidneys, reproductive system, and nervous system of humans is lead (Pb). This study aimed to investigate the effectiveness of a novel nanocomposite adsorbent, synthesised from polypyrrole, zinc oxide, and nickel (PPy/ZnO-NiO), in eliminating Pb(II) ions from a water-based solution. This adsorbent offers excellent metal selectivity, environmental stability, ease of manufacture, and reusability. Several techniques, namely XRD, FTIR, TGA, SEM, TEM, EDX, and BET, were employed to characterize the synthesised nanocomposite adsorbent. The study examined the impact of multiple factors influencing the adsorption process, including pH, temperature, contact period, metal ion concentration, and adsorbent dose, along with isotherms, kinetics, and thermodynamics processes. The adsorption of Pb ions was examined via various isotherm models, including the Temkin, Freundlich, and Langmuir, and thus various factors inherent to pseudo-first-order, pseudo-second-order, and Elovich kinetics were determined. The data revealed that both the Langmuir sorption model and pseudo-second-order kinetics match the adsorption data well. The highest adsorption capacities of the PPy/ZnO-NiO nanocomposite adsorbent for Pb(II) metal ions were 436.48, 450.48, and 469.56 mg/g at 298, 305, and 310 K, respectively, and the optimal pH was 5. An actual water sample that had been tainted with Pb(II) ions was used to test the applicability of the PPy/ZnO-NiO nanocomposite for the removal of Pb(II) ions. Based on the available data, the PPy/ZnO-NiO nanocomposite appears to be effective in terms of elimination of Pb(II) from five different raw water samples, such as tap water, surface water, groundwater, sewage plant wastewater, and domestic wastewater.

Self-Sustained-Release Strategy Realizes Colloid Oriented Assembly to Fabricate Prussian Blue with Hierarchical Structure.

The controlled self-assembly of nanomaterials has been a great challenge in nanosynthesis, especially for hierarchical architectures with high complexity. Particularly, the structural design of Prussian blue (PB) series materials with robustness and fast nucleation is even more difficult. Herein, a self-sustained-release strategy based on the slow release of metal ions from coordination ions is proposed to guide the assembly of PB crystals. The key to this strategy is the slow release by ligand, which can create ultra-low concentrations of metal ions so as to provide the possibility to realize the surface charge manipulation of PB primary colloids. By adding electrolyte or changing the polarity of the solution, the surface charge regulation of PB colloid is realized, and the PB hierarchical structures with branch fractal structure (PB-BS), octahedral fractal structure, and spherical fractal structure are effectively constructed. This work not only achieves the designability of the PB structure, but also synchronizes the functionalization during the PB assembly growth process by in situ encapsulation of the effective catalytic active component L-Ascorbic acid. As a result, the assembled PB-BS exhibits greatly enhanced catalytic activity and selectivity in styrene oxidation with the selectivity of oxidized styrene increasing from 35.6% (PB) to 80.5% (PB-BS).

Metal Ion Responsive Luminescent Bio-Templated Co-Assemblies: Label-Free Detection of Multi-Metal Ions in Aqueous Media.

Recently, anionic bio-templates have emerged as promising platforms for designing dynamic and stimuli-responsive chromophoric assemblies capable of light harvesting in aqueous media thereby mimicking natural photosynthesis. Here, we present multi-metal ion-responsive luminescent co-assemblies between cationic pyrene-imidazolium amphiphile and anionic bio-templates (ATP, heparin, and DNA) in aqueous media. The anionic bio-templates enhance Förster resonance energy transfer (FRET) in the co-assemblies, with pyrene serving as an excellent donor for generating tunable multi-luminescent materials with embedded acceptor dyes. However, a significant loss in energy transfer towards acceptor dyes was observed in the presence of various metal ions, attributed to excimeric emission quenching facilitated by electron transfer between the pyrene chromophore and metal ions. Interestingly, detailed studies revealed that only ATP-based co-assemblies exhibited quenching phenomena in the presence of metal ions, contrasting with heparin and ctDNA co-assemblies. Additionally, label-free detection of multi-metal ions in aqueous environments, such as Fe2+, Fe3+, and Cu2+ ions, was successfully achieved with lower detection limits of 0.01 μM (3 ppb), 0.12 μM (30 ppb), and 0.58 μM (150 ppb) respectively. These co-assemblies hold significant promise for practical applications in environmental and biomedical sensing, enabling sensitive monitoring of metal ion concentrations.

Ultrathin and Self-Supporting MOF/COF-Based Composite Membranes for Hydrogen Separation and Purification from Coke Oven Gas.

Coke oven gas (COG) is considered to be one of the most likely raw materials for large-scale H2 production in the near or medium term, with membrane separation technologies standing out from traditional technologies due to their less energy-intensive structures as well as simple operation and occupation. Based on the "MOF-in/on-COF" pore modification strategy, the COF membrane (named the PBD membrane) and ZIF-67 were used as assembly elements to design advanced molecular sieving membranes for hydrogen separation. The composition and microstructure of membranes before and after ZIF-67 loading as well as ZIF-67-in-PBD membranes under different preparation conditions (metal ion concentration, metal-ligand ratio, and reaction time) were investigated by various characterizations to reveal the synthesis regularity and microstructure regulation. Furthermore, H2/CH4 separation performances and separation mechanisms were also analyzed and compared. Finally, a dense, continuous, ultrathin, and self-supporting ZIF-67-in-PBD membrane with a Co2+ concentration of 0.02 mol/L, a metal-ligand ratio of 1:4, and a reaction time of 6 h exhibited the largest specific surface area, micropore proportion, and the best H2/CH4 separation selectivity (α = 33.48), which was significantly higher than the Robeson upper limit and was in a leading position among reported MOF membranes. The separation mechanism was mainly size screening, and adsorption selectivity also contributed a little.

An optimized framework for metal ion analysis in automobile industrial sewage

This research paper presents an optimized approach for analyzing metal ions in automobile industrial sewage by integrating Dove Swarm Optimization (DSO) and a Recurrent Neural Network (RNN), termed DSbRNM. The DSbRNM approach is designed to detect and predict the concentration of metal ions in sewage samples. DSO is utilized to select the most relevant features, optimizing the feature set for the RNN. This optimization allows the RNN to perform classification with high accuracy, predicting metal ion concentrations effectively. The effectiveness of the DSbRNM approach was validated by analyzing real industrial sewage samples and comparing the results with those obtained using machine learning (ML) based convolutional methods. The results demonstrate that DSbRNM provides more accurate and reliable predictions of metal ion ranges. Furthermore, DSbRNM outperformed convolutional methods in terms of accuracy, recall, precision, and F1 score. The DSbRNM approach offers a rapid and effective solution for analyzing metal ions in automobile industrial sewage, enhancing the efficiency and effectiveness of wastewater treatment processes.

Heavy Metal Detection and Removal by Composite Carbon Quantum Dots/Ionomer Membranes.

The combination of ion exchange membranes with carbon quantum dots (CQDs) is a promising field that could lead to significant advances in water treatment. Composite membranes formed by sulfonated poly(ether ether ketone) (SPEEK) with embedded CQDs were used for the detection and removal of heavy metal ions, such as lead and cadmium, from water. SPEEK is responsible for the capture of heavy metals based on the cation exchange mechanism, while CQDs detect their contamination by exhibiting changes in fluorescence. Water-insoluble "red" carbon quantum dots (rCQDs) were synthesized from p-phenylenediamine so that their photoluminescence was shifted from that of the polymer matrix. CQDs and the composites were characterized by several techniques: FTIR, Raman, UV/VIS, photoluminescence, XPS spectroscopies, and AFM microscopy. The heavy metal ion concentration was analyzed by inductively coupled plasma-optical emission spectroscopy (ICP-OES). The concentration ranges were 10.8-0.1 mM for Pb2+ and 10.0-0.27 mM for Cd2+. SPEEK/rCQDs showed a more pronounced turn-off effect for lead. The composite achieved 100% removal efficiency for lead and cadmium when the concentration was below a half of the ion exchange capacity of SPEEK. The regeneration of membranes in 1 M NaCl was also studied. A second order law was effective to describe the kinetics of the process.

Combined effect of zinc and cadmium ions on nitrification performance during the biological nitrogen removal of simulated livestock breeding wastewater.

Zinc and cadmium ions are usually found in livestock breeding wastewater, and the mixed ions will have an impact on the biological nitrogen removal. Nitrification performance plays an important role in biological nitrogen removal. In order to investigate the combined effect of zinc and cadmium ions on nitrification performance and to reveal the interactions between zinc and cadmium ions, three concentration ratios of zinc and cadmium ions, as well as 18 different concentration gradients were designed with the direct equipartition ray and the dilution factor method. The effect of pollutants on the nitrification performance of biological nitrogen removal was analyzed by the nonlinear regression equation, and the concentration-addition model was conducted to probe into the relationship between the mixed pollutants and the nitrification performance. The results showed that the effect on nitrification performance increased significantly with the increase of reaction duration and pollutant concentration, which indicated that the effects are concentration-dependent and time-dependent. The concentration-addition model suggested that the interactions between zinc and cadmium ions with different concentration ratios were mainly antagonistic, and as the percentage of cadmium ions in the mixtures increased, the antagonism between the mixtures became stronger. This study will provide a relevant theoretical basis for the regulation of the ratios and concentrations of heavy metal ions during the biological treatment of livestock breeding wastewater.

Cancer Incidence Relation to Heavy Metals in Soils of Kyzylorda Region of Kazakhstan.

The purpose of this study was to investigate the relationship of soil pollution factors such as heavy metal ions with the incidence of cancer in the Kyzylorda region of Kazakhstan. Concentrations of heavy metal ions in the soils of different sites of Kyzylorda region, Kazakhstan, were sampled and correlated with incidence of cancer in 2021. Chromium content in the soil exceeded maximum permissible concentration (MPC) in the samples for all sites except Kazaly and Shieli, and the highest excess of 2.8 MPC was found in Terenozek. Content of copper, lead, and cobalt ions was also increased and varied in the range 1.9-15.4, 1.2-4, and 1.2-2.44 MPC, respectively. In addition, lung cancer incidence was statistically significantly correlated with soil concentration to MPC ratio of copper, cobalt, and lead; colorectal cancer was correlated with soil concentration of chromium. Cases of invasive cancer and mutations were recorded Terenozek and Kyzylorda areas. The higher the soil concentration correlate with higher cancer incidence in Kyzylorda region, Kazakhstan.

Sorption Efficacy of Weathered Basalt Rock for Metal Ions of Nuclear Importance

Background:: A safe and long-term isolation of radionuclides is crucial for efficient waste management in the nuclear fuel cycle. Clay minerals of geological origin are considered candidate barrier materials for the sequestration of nuclear waste for geological disposal applications. Objective:: The present study encompasses a systematic characterization of weathered basalt rock and the influence of its constituent clay minerals (formed mainly due to the weathering process) in the uptake of metal ions of nuclear importance, such as cesium (Cs+) and strontium (Sr2+). Methods: The structural profile of the weathered basalt has been investigated using different analytical techniques, including polarizing microscope, XRD, FTIR and EDXRF. The sorption behaviour of the rock sample for Cs+ and Sr2+ has been investigated in a comprehensive batch mode by varying the experimental conditions. The analytical findings for structure and batch sorption performance of the material have been further correlated to understand the influence of different parameters on the uptake of metal ions and the underlying mechanism. Results:: Structural analyses confirmed the presence of clay minerals viz., kaolinite, illite and montmorillonite in the sample. A comprehensive sorption performance assessment carried out in batch mode at different experimental conditions revealed that the uptake of both the metal ions was rapid and dependent on initial metal ion concentration and solution pH. The uptake of Cs+ ions was found to be higher as compared to the Sr2+ ions. EDXRF analysis confirmed the loading of Cs+ and Sr2+ on the weathered basalt. Experimental batch sorption data presented a better agreement with the theoretical Freundlich isotherm pertaining to the heterogeneous nature of the sorbent. Conclusion:: The studies highlight that the clay minerals formed by structural alteration of basalt rock upon intense weathering could be very useful in fixing the nuclear fission waste components such as Cs+ and Sr2+.

Importance of Changes in the Copper Production Process through Mining and Metallurgical Activities on the Surface Water Quality in the Bor Area, Serbia

This paper considers the impact of copper mining-influenced water and metallurgical wastewater on the surface water in the Bor area, Serbia. Sampling, realized through the four campaigns (2020–2021), confirmed that both types of water, discharged without appropriate treatment in the Bor River, had a signific impact on the concentration of metal ions, pH and electrical conductivity on the watercourse in the Bor area. The highest concentrations of the following metal ions, Cu—271 mg/L, As—25,991 μg/L, Ni—13,856 μg/L, Cd—2627 μg/L, and Pb—2855 μg/L, were registered in the metallurgical wastewater samples. After changes occurred in the copper production process by stopping the discharge of untreated wastewater into the Bor River, the concentrations of monitored elements were drastically decreased. In the period 2022–2024, the concentration values for Cu, As and Pb ions were below the maximum allowable value, and the concentration values of Ni and Cd ions were also decreased. The values for pH and electrical conductivity were in the maximum allowable range. The return of wastewater to the copper production process would lead to both a reduction in the primary water consumption and reduction in the negative impact on the environment.

Synthesis and characterization of X (X = Ni or Fe) modified BaTiO3 for effective degradation of Reactive Red 120 dye under UV-A light and its biological activity

For the sustainable advancement of industrial expansion that is environmentally conscious, harmful dyes must be removed from wastewater. Untreated effluents containing colors have the potential to harm the ecosystem and pose major health risks to people, animals, and aquatic life. Here, we have fabricated Ni or Fe modified with BaTiO3 materials and effectively utilized them for Reactive Red 120 (RR 120) dye degradation under UV-A light. The synthesized materials were characterized, and their structural, and photo-physical properties were reported. Phase segregation was not present in the XRD pattern, as evidenced by the absence of secondary phase peaks linked to iron, nickel, or oxides. Low metal ion concentrations may be the cause of this, and the presence of those elements was confirmed by XPS measurements. The Raman spectra of the BaTiO3/Ni and BaTiO3/Fe samples show a widened peak at 500 cm−1, which suggests that Ni or Fe are efficiently loaded onto the BaTiO3. RR 120 dye photodegradation under UV light conditions was effectively catalyzed by BaTiO3/Fe, as evidenced by its superior performance in the UV irradiation technique over both BaTiO3 and BaTiO3/Ni. Compared to bare BaTiO3, both metal-modified materials efficiently degraded the RR 120 dye. Acidic pH facilitated the degradation process, which makes sense given that the heterogeneous photo-Fenton reaction was the mechanism of degradation along with BaTiO3 sensitization. High-acidity sewage can be dangerous and carcinogenic, and conventional biological treatment methods are not appropriate for managing it. In the current investigation, it may be used to treat color effluents with extremely low pH levels. Additionally, the ability of the produced nanocomposites to inhibit the growth of twenty pathogens was examined, along with two fungi, fifteen Gram-negative Bacilli (GNB), one Gram-positive Bacilli (GPB), and two Gram-positive Cocci (GBC).

Elimination of nickel and chromium(VI) ions from industerial wastewater by electrodialysis/characteristics/impact of parameters

<p>Healthy water is a concern for the world due to rapid population growth and technological advancement. The entry of heavy metals into water as a result of various activities causes water pollution that has persistent effects. In this study, a specially designed electrodialysis cell was used to remove chromium (VI) and nickel ions from wastewater. The chambers were partitioned by Ionac MC 3470 cation exchange and Ionac MA 3475 anion exchange membranes. The cathode and anode were made of carbon fiber and stainless steel, respectively. The effects of voltage, initial pH, time, Na2SO4 concentration, feed flow rate and metal ion concentration on metal removal efficiency, energy consumption, current efficiency, current density and flux were investigated. Optimum values for 98.5% removal of 80 mg/L Cr(VI) ion in 90 min voltage 30 V, pH=3, addition of Na2SO4 0.5 g and feed flow rate 52. 8 ml/min, as observed. At the end of this period, concentration 1 mg/L, energy consumption 40 W/L, flow efficiency 30% and flux 12 x 10.-5 mol/m2s were calculated. Optimum values of 25 V, pH=3, addition of Na2SO4 0.2 g and Qf = 42.6 mL/min were observed for 94.3% removal of 50 mg/L Ni2+ ions in 90 min. At the end of this period, the nickel ion concentration was 4 mg/L, the energy consumption was 34 Wh/L, the flow efficiency was 96.51%, and the flux was calculated as 40×10-5 mol/m2s. This study shows that the electrodialysis method can be effectively used to elimonation chromium (VI) and nickel (II) ions from dilute wastewaters.</p>

Effective fabrication and characterization of eco-friendly nano particles composite for adsorption Cd (II) and Cu (II) ions from aqueous solutions using modelling studies

The public health and environment are currently facing significant risks due to the discharge of industrial wastewater, which contains harmful heavy metals and other contaminants. Therefore, there is a pressing need for sustainable and innovative technologies to treat wastewater. The main objective of this research was to develop novel composites known as chitosan, Padina pavonica, Fe(III), and nano MgO incorporated onto pomegranate peel with the specific purpose of removing Cd (II) and Cu (II) ions from aqueous solutions. The characterization of these nanocomposites involved the utilization of several analytical methods, including Fourier-transform infrared spectroscopy, scanning electron microscopy, X-ray diffraction, thermal gravimetric analysis, and X-ray photoelectron spectroscopy. The efficiency of these nanocomposites was evaluated through batch mode experiments, investigating the impact of factors such as pH, initial concentration, contact time, and adsorbent dose on the adsorption of Cu(II) ions. The optimum conditions for the removal of ions were pH = 5 for Cu (II) and 6 for Cd (II), contact time: 120 min, adsorbent dosage: 0.2 g, initial metal ion concentration: 50 mg/L for each metal ion for the present study. The MgO@Pp demonstrated the highest removal efficiencies for Cu(II) and Cd(II) at 98.2% and 96.4%, respectively. In contrast, the CS@Fe-PA achieved removal efficiencies of 97.2% for Cu(II) and 89.2% for Cd(II). The modified MgO@Pp exhibited significantly higher total adsorption capacities for Cu(II) and Cd(II) at 333.3 and 200 mg/g, respectively, compared to CS@Fe-PA, which had capacities of 250 and 142 mg/g, respectively. The adsorption of Cd (II) and Cu (II) ions by MgO@Pp was found to be a spontaneous process. The R2 values obtained using the Freundlich and Redlich-Peterson models were the highest for the MgO@Pp composite, with values of 0.99, 0.988, 0.987, and 0.994, respectively, for Cu (II) and Cd (II). The pseudo-second-order equation was determined to be the best-fit kinetic model for this process. Reusability experiments confirmed that the adsorbents can be utilized for up to four regeneration cycles. Based on the findings of this study, MgO @ Pp is the most promising alternative and could be instrumental in developing strategies to address existing environmental pollution through adsorption.

Explosive Leidenfrost-Droplet-Mediated Synthesis of Monodispersed High-Entropy-Alloy Nanoparticles for Electrocatalysis.

High-entropy-alloy nanoparticles (HEA NPs) exhibit promising potential in various catalytic applications, yet a robust synthesis strategy has been elusive. Here, we introduce a straightforward and universal method, involving the microexplosion of Leidenfrost droplets housing carbon black and metal salt precursors, to fabricate PtRhPdIrRu HEA NPs with a size of ∼2.3 nm. The accumulated pressure within the Leidenfrost droplet triggers an intense explosion within milliseconds, propelling the carbon support and metal salt rapidly into the hot solvent through explosive force. The exceptionally quick temperature rise ensures the coreduction of metal salts, and the dilute local concentration of metal ions limits the final size of the HEA NPs. Additionally, the explosion process can be fine-tuned by selecting different solvents, enabling the harvesting of diverse HEA NPs with superior electrocatalytic activity for alcohol electrooxidation and hydrogen electrocatalysis compared to commercial Pt (Pd) unitary catalysts.