Metal Adsorption Capacity Research Articles

Facile Preparation of Poly(AA‐co‐NaAMPS) Hydrogels Toward Toxic Dyes and Heavy Metals Removal via Frontal Polymerization

ABSTRACTWastewater treatment contributes to the sustainable utilization of water resources for alleviating water scarcity. The application of polymeric materials as adsorbents for eliminating hazardous substances in water has garnered extensive attention owing to their remarkable adsorption efficiency, stability, and selectivity. Herein, a facile strategy is provided to rapidly synthesize poly(acrylic acid‐co‐sodium 2‐acrylamide‐2‐methylpropanesulfonate) (poly(AA‐co‐NaAMPS)) hydrogels with exceptional adsorptive capacity via frontal polymerization (FP). The FP processes are meticulously examined in terms of initiator dosage and monomer ratio. The as‐prepared hydrogels demonstrate pH‐responsive swelling ability and pH‐dependent adsorption capacity for various dyes and heavy metal ions. Compared with traditional batch polymerization (BP), the hydrogels prepared by FP exhibit superior swelling and adsorption abilities. Additionally, research on the adsorption mechanism for both dyes and heavy metal ions is conducted by fitting the adsorption kinetic data both with Langmuir and Freundlich equations. The maximum adsorption capacity (qm) of hydrogels derived from Langmuir model for dyes of methylene blue (MB) and rhodamine B (RB) is, respectively, 595.3 and 3078.5 mg g−1, while for heavy metal ions of Cr3+ and Cd2+ is, respectively, 1010.8 and 1191.3 mg g−1. This research exploits an alternative approach for the rapid preparation of high‐efficiency hydrogel adsorbents toward wastewater treatment.

Conservative mechanism through various rapeseed (Brassica napus L.) varieties respond to heavy metal (Cadmium, Lead, Arsenic) stress

IntroductionHeavy metal soil pollution is a global issue that can be efficiently tackled through the process of phytoremediation. The use of rapeseed in the phytoremediation of heavy metal-contaminated agricultural land shows great potential. Nevertheless, its ability to tolerate heavy metal stress at the molecular level remains unclear.MethodsHere, with 7-day seedlings as raw materials, we investigated physiological and biochemical indexes, analyzed the transcriptome sequencing for different treated materials (control, 50×, and 100×), combined with the results of transcriptome and proteome sequencing of the near-isogenic lines (F338 and F335) to reveal the response mechanism to heavy metal stress. Due to oxidative stress response caused by heavy metal stress, there are heavy effects on the emergence of rapeseeds and the growth of seedlings. Although rapeseed can alleviate oxidative stress by enhancing the enzyme activity, especially peroxidase in the oxidation system, this process has its limits. Rapeseed plants activate antioxidase, transport enzymes, and biological regulation to cope with heavy metal stress. Among these responses, peroxidase, ABC transporters, and abscisic acid are particularly significant in this process.Results and discussionBased on this study, we identified a breeding material with high adsorption capacity for heavy metals, which contributed to the research on resistance breeding in rapeseed. The results of this study may be useful to alleviate heavy metal soil pollution and tackle edible oil shortages in China.

Surface Modification of Starch by Isopropoxytris(ethylenediamino‐N‐ethoxy)Titanate with a Chelating Claw for Heavy Metal Removal

AbstractIsopropoxy tris(ethylenediamino‐N‐ethoxy) titanate‐modified starch (TIS) was prepared and characterized by XPS, FTIR, SEM, and TGA. It has been used for the removal of Cu2+, Co2+, Ni2+, and Mn2+ from aqueous solutions. At an optimal pH of 7, fast adsorption was observed within 10 min of contact, and 80% of the maximum capacity was achieved. Adsorption reached equilibrium after 30 min. This course followed a pseudo‐second‐order equation with the sequence Cu2+ > Mn2+ > Co2+ > Ni2+, which is related to the substitution rates of the hydrated metal ions. A linear relationship between the pseudo‐second‐order equation constant (logk2) and substitution rate constants (logkhs) of the hydrated metal ions was established. For the isotherm, the Langmuir equation fitted well with the adsorption data, suggesting monolayer coverage of the TIS surface. The maximum adsorption capacity for metal ions followed the order of Cu2+ > Co2+ > Ni2+ > Mn2+. FTIR and thermal studies indicated the chelation of metal ions with ethylenediamino groups, in agreement with the adsorption investigations.

Research progress in the adsorption of heavy metal ions from wastewater by modified biochar

The rapid development of modern industries is accompanied with the aggravating water heavy metal pollution, which poses a potential threat to the aquatic environment and the health of local populations. As an efficient and economical adsorbent, biochar demonstrates the adsorption capacity for heavy metal ions and its adsorption capacity is significantly enhanced after modification. Therefore, biochar can effectively mitigate environmental pollution. By reviewing the existing studies, we summarize the modification methods of biochar, compare the advantages and disadvantages of physical, biological, and chemical modification methods, analyze the effects of modification on the adsorption capacity of biochar for heavy metal ions, and expound the modification mechanism of biochar. On this basis, this article puts forward the future research directions of the application of biochar in treating coexisting pollutants, aiming to provide a reference for the application of biochar in the purification of heavy metal-containing wastewater.

Imperfections Immobilization and Regeneration in Perovskite with Redox-Active Supramolecular Assembly for Stable Solar Cells.

Imperfections in metal halide perovskites, such as those induced by light exposure or thermal stress, compromise device performance and stability. A key challenge is immobilizing volatile iodine produced by iodide oxidation and regenerating impurities like elemental lead and iodine. Here, we address this by integrating a redox-active supramolecular assembly of nickel octaethylporphyrin into perovskite film, functioning as both an immobilizer and redox shuttle. Decorated ethyl groups in porphyrin distorts the π ring, increasing the axial ligand adsorption capacity of central metal ion, while reducing intermolecular interactions and promoting iodine adsorption achieving a maximum uptake of 3.83 mg mg-1 to iodine. Adsorbed iodine transfers more electrons to Ni ions, leading to a weakened interaction within I-I bond and facilitating the production of iodide ions. Such a situation further enables selective oxidation of metallic lead defects to Pb2+. Porphyrin supramolecule facilitates hole transport across perovskite grain boundaries, leading to a champion device efficiency of 25.37% for a 0.10 cm2 active area, outperforms the value of control device being 23.96%. Modified devices without encapsulation exhibit significantly enhanced stability, maintaining over 90% of its initial performance after 1,000 hours of continuous 1-sun illumination at maximum power point at 65 oC.

Efficient Removal of Lead, Cadmium, and Zinc from Water and Soil by MgFe Layered Double Hydroxide: Adsorption Properties and Mechanisms

Both biochar and layered double hydroxide (LDH) have drawbacks in regard to the removal of heavy metals. The combined application of biochar and LDH not only solved the problem of the easy agglomeration of LDH but also effectively improved the heavy metal adsorption capacity of biochar. In this work, a MgFe–LDH banana straw biochar composite (MgFe–LDH@BB), with a regular hydrotalcite structure, was synthesized by employing a simple hydrothermal method. The composite showed an ultra-high adsorption capacity for lead (Pb), cadmium (Cd), and zinc (Zn) in water. A series of experiments were conducted to investigate the adsorption characteristics of MgFe–LDH@BB. At pH = 6.0, MgFe–LDH@BB demonstrated the effective adsorption of Pb, Cd, and Zn. In addition, the results showed that the adsorption of Pb, Cd, and Zn by MgFe–LDH@BB was rapid and conformed to pseudo-second-order kinetic and Langmuir models, indicating single-layer chemical adsorption. The maximum adsorption capacity of MgFe–LDH@BB for Pb, Cd, and Zn was 1112.6, 869.6, and 414.9 mg·g−1, respectively. Moreover, the adsorption mechanisms of MgFe–LDH@BB mainly included metal hydroxide/carbonate precipitation, complex formation with hydroxyl groups, and ion exchange. Meanwhile, MgFe–LDH@BB had the ability to immobilize heavy metals in soil. The surface-rich functional groups and cation exchange promoted the transformation of active heavy metal ions into a more stable form.

Enhancing Pb Adsorption on Crushed Microplastics: Insights into the Environmental Remediation

This study investigates the pollution characteristics and environmental risks of crushed microplastics (MPs) generated during plastic recycling, emphasizing their adsorption capacity for heavy metals, particularly lead (Pb). SEM-EDS analysis revealed that crushed MPs exhibit significantly higher adsorption capacity than primary MPs due to their larger surface area and more available adsorption sites, including oxygen-containing functional groups. The adsorption behavior of MPs was influenced by key factors such as MP size, MP quantity, pH, salinity, and biofilm formation. Smaller MPs demonstrated higher adsorption efficiency, while elevated pH enhanced Pb adsorption. Conversely, increased salinity reduced adsorption due to competition for adsorption sites. Increasing MP concentrations improved Pb removal efficiency, but higher MP quantities led to a decrease in maximum adsorption capacity, demonstrating a trade-off between removal efficiency and adsorption capacity. Isothermal adsorption experiments revealed that Pb adsorption on MPs follows a multi-layer mechanism, best characterized by the Freundlich model. The adsorption capacity increased nonlinearly with Pb concentration and stabilized as surface sites became saturated. The formation of biofilms on MPs further enhanced their adsorption capacity by providing additional functional groups and facilitating multi-layer adsorption, increasing ecological risks. Adsorption kinetics were best described by pseudo-second-order and intra-particle diffusion models, indicating chemical adsorption and boundary layer diffusion as dominant mechanisms. Magnetic Fe3O4 nanoparticles demonstrated a high recovery efficiency of 99.3% for MPs, highlighting their potential for environmental remediation. However, the presence of adsorbed Pb slightly reduced recovery performance, emphasizing the need to optimize recovery conditions for maximum efficiency. These findings underscore the dual threat posed by crushed MPs: their capacity to adsorb and concentrate harmful substances, increasing ecological toxicity, and the challenges associated with their recovery. This research provides critical insights into mitigating MP pollution and developing effective recovery strategies under realistic environmental conditions.

Chromium Isotope Fractionation During the Removal of Hexavalent Chromium by Oak-based Biochar

Chromium, especially in its hexavalent form (Cr(VI)), poses significant health risks due to its carcinogenic properties. Emerging research suggests that biochar, a carbon-rich material derived from biomass pyrolysis, holds promise as an effective and sustainable solution for Cr(VI) remediation. Biochar's unique physicochemical properties, such as its high surface area, porous structure, and functional groups, contribute to its exceptional adsorption capacity for metals. In a series of batch experiments with varying durations, an oak-based biochar was exposed to a 48 mg∙L⁻1 Cr(VI) solution. The results demonstrate that the biochar effectively removed 99% of the Cr(VI) after 100 hours, with a removal capacity greater than 5 mg∙g⁻1. Fourier transform infrared (FTIR) spectroscopy suggests that the removal of Cr(VI) involved aliphatic and aromatic C-H bonds. X-ray photoelectron spectroscopy (XPS) also indicated the role of aliphatic groups in the removal process and suggested the involvement of carbonyl groups. XPS analysis also detected both Cr(III) and Cr(VI) on the surface of the biochar, indicating the occurrence of reduction and sorption processes. The presence of Cr(III) and Cr(VI) was further confirmed at the Canadian Light Source (CLS) synchrotron facility using X-ray absorption near edge structure (XANES) spectroscopy. Cr isotope analysis showed an increase in δ⁵³Cr as the concentration of Cr in solution decreased, indicating Cr(VI) reduction. The isotope data followed a Rayleigh curve with a kinetic fractionation ε53Cr of -1.33 ‰, highlighting that Cr stable isotopes can effectively be used as an indicator of biochar-Cr reactions.

Effects of particle size and aging on heavy metal adsorption by polypropylene and polystyrene microplastics under varying environmental conditions

Microplastics have become a major environmental issue because of their widespread presence and tendency to adsorb heavy metals, which can have harmful effects on aquatic ecosystems and human health. The present study investigates the adsorption mechanisms of Pb2+ and Cu2+ ions on both pristine and artificially aged microplastics (MPs) made of polystyrene (PS) and polypropylene (PP). Furthermore, the influence of MP size on the adsorption capacity under different environmental conditions was evaluated. According to the characterization of MPs, aging leads to physical damage and an increase in the number of oxygen-containing functional groups on their surface. The experimental results highlight the significantly higher adsorption ability of smaller and aged MPs compared with that of pristine MPs for both the heavy metal ions. The pseudo-second-order equation provided a better fit for the adsorption kinetics study (R2 = 0.95), suggesting that chemisorption governs the rate-limiting phase in the adsorption mechanism on the MP surfaces. The concordance between the adsorption isotherm model and Freundlich model (R2 > 0.95) indicated a predominance of multilayer adsorption. The environmental factors such as pH, humic acid, temperature, and SO42- concentration significantly affected the adsorption of Pb2⁺ and Cu2⁺ onto PP and PS MPs. These variables play a crucial role in determining the nature of the interactions between heavy metal ions and the microplastic particles under diverse environmental conditions. Electrostatic interactions, surface complexation and van der Waals forces were identified as two factors that could either improve or diminish the metal ion adsorption capacity of MPs.

Potential engineering applications of volcanic scoria from Mount Cameroon area, Central Africa: evidence from petrography and geochemistry

This study was initiated to explore the suitability of volcanic scoria from Mount Cameroon along the Cameroon Volcanic Line (CVL) in engineering applications. The mineral composition has been obtained through thin sections observation and XRD method. The XRF analytical methods have been used to determine major element composition. The studied rocks are dark gray to reddish in color with a vacuolar structure and porphyritic microlithic texture recalling the Strombolian dynamism. They are mainly made up of pyroxene, olivine, plagioclase, opaque minerals, quartz, magnetite and iddingsite. The presence of phenocrysts of olivine and clinopyroxene is due to mantle contamination. The main chemical components of scoria of Mount Cameroon are silica, alumina, iron and calcium oxides. The abundant vitreous phases are responsible for the acidic character revealed by high SiO2 + Al2O3 contents. Fe2O3, MnO and MgO are hosted by ferromagnesian minerals while SiO2, Al2O3, K2O, NaO and P2O5 are found in acidic vitreous phases. The mineral and chemical composition of the scoria of Mount Cameroun is similar to those of scoria previously studied around the world. They can be used as absorbents for metals because of their high adsorption capacity and affinity for metals. The high SiO2 + Al2O3 + Fe2O3 contents and low LOI values show that the scoria from Mount Cameroon are suitable to the use in cement and concretes. They can improve the resistance to sulfate, and chlorite and alkali silica reaction. According to the chemical composition, the rocks are conforming to French standard NFP18310. Their high CaO contents are favorable to improve the quality of scoria blended cements.

The Effect of Different Aging Methods on the Heavy Metal Adsorption Capacity of Microplastics

The Effect of Different Aging Methods on the Heavy Metal Adsorption Capacity of Microplastics

Adsorption removal of copper(II) from water by zero valent iron loaded dendritic mesoporous silica

The object of research is synthesized dendritic mesoporous nanoscale silica (DMSN) modified with zero-valent iron (Fe0@DMSN). This material exhibits a high adsorption capacity for heavy metal ions, in particular copper, whose increased content in the aquatic environment poses a threat to living organisms. In this regard, the main physicochemical features of the removal of copper cations from the aqueous medium using the obtained sample were investigated. The morphology of the obtained dendritic silicas was studied by electron microscopy and the presence of a layer of zero-valent iron was confirmed by X-ray diffraction analysis and infrared spectroscopy. The parameters of the porous structure of the synthesized materials were determined. It was found that after modification of mesoporous silica with particles of zero-valent iron, the value of its specific surface area decreased from 504 m2/g to 312 m2/g. This may be due to the formation of a Fe0 layer not only on their surface but also in the channels of the inorganic matrix, which has a unique dendritic structure characteristic of this type of particles. At the same time, the number of active centers increases due to the enrichment of the silica surface with functional modifier groups that show a high affinity for metal cations. The adsorption capacity of Fe0@DMSN towards Cu2+ ions has been studied and it has been shown that the maximum adsorption value is 39.8 mg/g, which is significantly higher than that of the initial synthesized DMSN sample (0.7 mg/g). The experimental data obtained indicate that the obtained sorption material based on dendritic mesoporous silica nanoparticles with a layer of reactive zero-valent iron can be used for the purification of water contaminated with metal ions. In addition, the magnetic properties of such materials, known and proven by various scientists, will make it easy to separate the solid phase in the processes of sorption water purification using magnetic separation.

Optimization of extracellular polysaccharides (EPS) production by Stenotrophomonas rhizophila JC1 and its protective effect on alfalfa under Pb2+ stress

Stenotrophomonas rhizophila JC1 and its extracellular polysaccharides (EPS) have been shown to effectively adsorb heavy metals in previous studies. The fermentation conditions of EPS by S. rhizophila JC1 were optimized using the Box-Behnken design (BBD). The composition, structural characteristics, and heavy metal adsorption capacity of EPS were systematically evaluated. The alleviation mechanism of Pb2+ stress on alfalfa was investigated through EPS inoculation. The maximum EPS yield reached 0.313 %. EPS consisted of glucose, glucosamine, galactose, and mannose in a molar ratio of 12.20:1:22.29:1.68. EPS also contained four distinct polymers with molecular weights of 623,683.71 Da, 144,072.27 Da, 105,892.21 Da, and 51,094.79 Da. The adsorption processes conformed to the pseudo-second-order model and Langmuir isotherm model. High Pb2+ concentrations significantly reduced germination percentage, germinative force, root length, fresh weight, and soluble protein, inhibited photosynthesis, exacerbated oxidative stress, and caused damage to the antioxidant system, thereby inhibiting seedling growth. EPS at low concentrations can promote alfalfa seed germination and mitigate Pb2+ stress by reducing the aforementioned damage. This study highlights the potential of EPS in soil remediation and enhancing plant resistance to heavy metal stress.

Structural Characterization and Antioxidant Activity of Exopolysaccharide Produced from Beet Waste Residue by Leuconostoc pseudomesenteroides.

Lactic acid bacteria exopolysaccharide (EPS) is a large molecular polymer produced during the growth and metabolism of lactic acid bacteria. EPS has multiple biological functions and is widely used in fields such as food and medicine. However, the low yield and high production cost of EPS derived from lactic acid bacteria limit its widespread application. In this study, we used beet waste residue as a substrate to produce EPS by fermentation with Leuconostoc pseudomesenteroides to improve the utilization rate of agricultural waste and reduce the production cost of lactic acid bacterial EPS. After purification, the molecular weight (Mw) of EPS was determined to be 417 kDa using high-performance size exclusion chromatography (HPSEC). High-performance liquid chromatography (HPLC), Fourier transform infrared (FTIR) spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy revealed that the EPS was composed of glucose subunits with α-1,6 glycosidic linkages. The thermal analysis and heavy metal adsorption capacity revealed a relatively high degradation temperature of 315.54 °C and that the material could effectively adsorb Cu2+. Additionally, the findings indicated that the EPS exhibited a significant ability to neutralize free radicals, a property that was found to be concentration dependent. Furthermore, the results of the intracellular study showed the protective effect of freshly isolated EPS on tBHP-induced cellular oxidative stress at a concentration of 50 µg/mL. These results suggest that the EPS from L. pseudomesenteroides may be developed as antioxidant agents for functional food products and pharmaceutical applications due to its capacity to scavenge free radicals.

Surface water removal of Aluminum(III), Iron(III) and Manganese(II) using sustainable natural serpentinite mining tailings, proof of concept

To remediate surface water as the Doce River and spring waters from Minas Gerais, Brazil, this study examined the possibility of natural serpentinite mining tailings as a sustainable alternative for removing aluminum (III), iron (III), and manganese (II). The study used a Box-Behnken experimental design to examine how initial metal concentration, adsorbate dosage, and adsorption time affect metal removal effectiveness. Results demonstrated impressive performance, with removal rates exceeding 80 % for Al(III) and Fe(III) within the initial 5 min, and 60 % for Mn(II) within 30 min. This study delves deeper into the removal mechanisms, kinetics, adsorption isotherms and characterization identify physisorption and chemisorption pathways in which complex formation with released OH− groups and ion exchange with Mg(II) from serpentinite emerged as key contributors to the removal process. Furthermore, ion metal adsorption and regeneration cycles were assessed, exhibit sustained removal efficacy without notable capacity reduction. Each cycle shows an average metal adsorption capacity of 0.32 mg g−1 and an average Mg(II) release capacity of 0.98 mg g−1. Remarkably, the application of serpentinite successfully lowered the metals content of the Doce River and spring water to drinkable standards. A batch and continuous process is proposed for scaling-up serpentinite's metal adsorption. Overall, this study shows serpentinite's potential as a foundation for sustainable and cost-effective methods to treat surface water contamination with Al(III), Fe(III), and Mn(II).

Comparative study of silica-based porous materials in the purification of radioactive wastewater

A significant challenge in the treatment of low-level radioactive wastewater is the effective purification of low-concentration radionuclides. Silica-based adsorbents are advantageous for the deep-purification of low-concentration metal ions. This study investigates three primary types of silica-based adsorbents: functionalized mesoporous silica, various modified zeolites, and mesoporous calcium silicate hydrate (C-S-H). These adsorbents were synthesized and their deep-purification effects on heavy metals and radionuclides were compared. The results indicated that mesoporous silica showed relatively poor adsorption for most metal ions. Zeolites outperformed mesoporous silica, with Zn framework-modified zeolites showing enhanced adsorption for several metal ions. Notably, C-S-H displayed superior adsorption performance, achieving high adsorption capacities for various metal ions and radionuclides. Specifically, at a dose of 0.5 g/L, the adsorption efficiency of C-S-H for numerous radionuclides in nuclear power plant wastewater exceeded 92–99 %, highlighting its potential for practical applications. An in-depth analysis of the physical and chemical structure and the adsorption mechanisms of C-S-H revealed its large mesoporous structure and electrostatic attraction to cations across a wide pH range. Multivalent cations were removed through exchange with Ca2+ in C-S-H, whereas monovalent cations were removed through exchange with Na+ in C-S-H. The cyclic structure of silica-oxygen tetrahedra in C-S-H, which promotes large pore formation and provides abundant ion exchange sites, underpins its excellent adsorption properties. This study offers valuable insights for the selection and application of silica-based materials in radioactive wastewater treatment.

Manganese-modified biochar for sediment remediation: Effect, microbial community response, and mechanism

Heavy metal sediment pollution has become an increasingly serious problem associated with industrial development, so extensive studies have been conducted concerning their removal. Biochar has recently shown good potential for in-situ remediation of heavy metal-contaminated sediments. The heavy metal adsorption capacity of inexpensive biochar can be improved by loading it with metal oxides. In this study, manganese-modified biochar (MBC) was prepared by KMnO4-modified waste-activated sludge biochar and applied to immobilize Pb and Cd in sediments. Its effects on the sediment microbial community were also investigated. The Results showed that manganese modification of the biochar made it more conducive to the adsorption of heavy metals, owing to its higher specific surface area and graphitization structure, more active sites and oxygen-containing groups, and the presence of Mn2O3 crystal structure on the surface. The maximum adsorption capacities of this material for Pb2+ and Cd2+ in solution were 176.9 mg/g and 44.0 mg/g, respectively. The application of MBC to the remediation of heavy metal-contaminated sediments transformed Pb and Cd in the sediments from exchangeable to residual state. The F4 content of Pb in the sediments increased from 40.52%-42.36% to 49.11%–51.14% after application of 1% MBC, and to 63.94%–64.49% after application of 5% MBC. Correspondingly, the F1 content of Pb in the sediments decreased from 29.09%-30.68% to 17.43%–17.69% after the application of 5% MBC. Furthermore, MBC efficiently enriched the microbial biodiversity and affected the microbial population structure within 60 days. The relative abundance of uncultured f Symbiobacteraceae and Fonticella communities significantly increased after incubation. The results may provide empirical support for the combination of metal oxides and biochar for the remediation of heavy metal-contaminated sediments.

Amidoximated Bacterial Cellulose Film for Pb2+ Adsorption in Aqueous Environment

Abstract This study investigated the application of amidoximated bacterial cellulose (AMO-BC) film for lead (Pb) adsorption from aqueous solutions. In our previous study, bacterial cellulose has been successfully modified through amidoximation to enhance its metal adsorption capacity. In order to modify the bacterial cellulose (BC) film, acrylonitrile was grafted onto it initiated by an electron beam to create BC-grafted-polyacrylonitrile (BC-g-PAN). After that, amidoximated bacterial cellulose (AMO-BC) was generated when BC-g-PAN reacted with hydroxylamine hydrochloride to add amidoxime functional groups to the cellulose backbone. Then, AMO-BC before and after lead adsorption was characterized using Fourier-transform infrared spectroscopy (FTIR). The adsorption capacity of AMO-BC for lead ions was evaluated through batch adsorption experiments with the initial lead concentration of 200 mgL−1 and an adsorbent dose of 20 mg, on pH 6 for two hours of the adsorption process. The results showed that AMO-BC exhibited higher lead adsorption capacity than pristine bacterial cellulose i.e., 44.56 and 50.96 mg/gram for BC and AMO-BC films, respectively.

Multifunctional HxMoO3-y-MoO2/Carbon Composite Particles for Water Remediation.

Solving a scarcity of freshwater resources is an urgent global challenge by a safe and sustainable approach using renewable energy. We demonstrate the multifunctional catalyst of HxMoO3-y-MoO2/carbon composite particles toward highly efficient water remediation. A one-step mechanochemical reaction successfully upgraded the composites from commercially available MoO3-polypropylene (PP) powders without introducing hydrogen gas. The composite particles exhibited broad light absorption in the UV-visible (Vis)-near-infrared (NIR) region (200-2000 nm), with an optical band-gap narrowing to 1.03 eV. The plasmonic properties of HxMoO3-y-MoO2 allowed a fast water evaporation rate (3.29 kg m-2 h-1) with a photothermal conversion efficiency of 88.8%. In addition, the HxMoO3-y-MoO2 heterojunction dominated wide-spectrum activity under Vis and NIR light irradiation, up to 3 orders of magnitude higher than pristine MoO3 in the photocatalytic degradation of azo-dye pollutants. Furthermore, the byproduct carbon with abundant oxygen-containing groups efficiently eliminated water pollutants as a Brønsted acid catalyst and performed exceptional adsorption capacities of heavy metal ions in the dark.

Cost-Effective Synthesis of MXene Cadmium Sulfide (CdS) for Heavy Metal Removal.

Background Environmental contamination resulting from the release of untreated industrial wastewater has emerged as a critical worldwide issue. These effluents frequently have high levels of heavy metals and antibiotics, which are bad for aquatic ecosystems and human health. Oftentimes, conventional wastewater treatment techniques fall short of effectively eliminating these pollutants. Innovative materials that may efficiently absorb or break down contaminants from contaminated water sources are, therefore, desperately needed. Hydrothermally produced MXene cadmium sulfide (CdS) composites have shown great promise as an adsorbent material because of their special qualities, which include high surface area, chemical stability, and customizable surface functions that improve their adsorption capacity for heavy metals and antibiotics alike. Aim The aim of this study is to produce MXene-CdS nanoparticles in a cost-effective method for the simultaneous removal of heavy metals from aqueous contaminants for water pollution control. Methods and materials MXenes were synthesized by selectively etching Ti3AlC2 MAX-phase ceramics using aqueous HF. CdS nanoparticles were synthesized separately and integrated with MXenes via a hydrothermal process. The resulting MXene CdS nanocomposites were characterized using scanning electron microscopy (SEM) for morphology, energy dispersion spectrum (EDS) for elemental composition, X-ray diffraction(XRD) study for phase identification, and removal of heavy metals viaMXene CdS. Results Consistent distribution of CdS nanoparticles on the MXene surface and the creation of MXene CdS nanomembranes with a well-defined shape were observed by SEM analysis. Ti, C, Cd, and S elements, indiciaries of a successful composite formation, were confirmed to be present by EDS. The crystalline structure of both the MXene and CdS phases was confirmed by the distinctive peaks seen in the XRD patterns. MXene-CdS composites facilitate the effective removal of chromium ions from contaminated water. The excellent hydrophilicity of the produced nanomembrane allowed for effective interaction with watery contaminants. Conclusion This study showcases the successful synthesis and characterization of MXene-CdS nanocomposites for environmental remediation, particularly in removing toxic metals like chromium from industrial effluents. SEM analysis confirmed the uniform distribution of CdS nanoparticles on the MXene surface, while elemental composition validated their integration. XRD analysis confirmed the crystalline structures of both components. The nanocomposite exhibited excellent hydrophilicity, enhancing the efficient adsorption of heavy metals. Its large surface area and chemical stability contribute to high adsorption efficiency, making it ideal for wastewater treatment. The scalable synthesis process supports practical applications. This research highlights MXene-CdS nanocomposites as a cost-effective, sustainable solution for water pollution control.