Search Results (1,915)

Transition metal phosphate is the prospective electrode material for supercapacitors (SCs). It has an open frame construction with spacious cavities and wide aisles, resulting in excellent electric storage capacity. However, the inferior rate behavior and cycling stability of transition metal phosphate materials in alkaline environments pose significant barriers to their application in SCs. Herein, Ni₁₁(HPO₃)₈(OH)₆/Co₃(HPO₄)₂(OH)₂ heterostructured materials synthesized through a one-step hydrothermal process exhibiting remarkable rate capability coupled with exceptional cycling endurance. Ni₁₁(HPO₃)₈(OH)₆/Co₃(HPO₄)₂(OH)₂ samples exhibit a micron-scale structure composed of sheet-like compositions and unique pore structure. The multistage pore structure is favorable for promoting the diffusion of protons and ions, enhancing the sample’s electrochemical storage capacity. Upon conducting electrochemical tests, it was observed that Ni₁₁(HPO₃)₈(OH)₆/Co₃(HPO₄)₂(OH)₂ composite electrode surpassed both the standalone Ni₁₁(HPO₃)₈(OH)₆ and Co₃(HPO₄)₂(OH)₂ electrode, achieving a remarkable specific capacity of 163 mAh g⁻¹ with exceptional stability and efficiency at 1 A g⁻¹. Notably, this electrode also exhibits superior rate performance, maintaining 82.5% and 71% of its original full capacity even at 50 A g⁻¹ and 100 A g⁻¹, respectively. Furthermore, it demonstrates superior stability in cycling, retaining a capacity of 92.7% at 10 A g⁻¹ after 5000 cycles. Moreover, Ni₁₁(HPO₃)₈(OH)₆/Co₃(HPO₄)₂(OH)₂ and porous carbon (PC) were assembled into a hybrid supercapacitor (HSC). Electrochemical tests reveal an impressive power density of up to 36 kW kg⁻¹ and an exceptional energy density of up to 47.4 Wh kg⁻¹ for the HSC. Moreover, Ni₁₁(HPO₃)₈(OH)₆/Co₃(HPO₄)₂(OH)₂//PC HSC exhibits robust capacity retention stability of 92.9% after enduring 10,000 cycles at 3 A g⁻¹, demonstrating its remarkable durability. This work imparts viewpoints into the design of transition metal phosphate heterostructured materials. Full article

Microbial fuel cell (MFC) technology holds significant promise for the production of clean energy and treatment of pollutants. Nevertheless, challenges such as low power generation efficiency and the high cost of electrode materials have impeded its widespread adoption. The porous microstructure of biochar and the exceptional photocatalytic properties of rutile endow it with promising catalytic potential. In this investigation, we synthesized a novel Rutile–Biochar (Rut-Bio) composite material using biochar as a carrier and natural rutile, and explored its effectiveness as a cathode catalyst to enhance the power generation efficiency of MFCs, as well as its application in remediating heavy metal pollution. Furthermore, the impact of visible light conditions on its performance enhancement was explored. The X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) analysis validated the successful fabrication of rutile composites loaded with biochar. The maximum current density and power density achieved by the MFCs were 153.9 mA/m² and 10.44 mW/m², respectively, representing a substantial increase of 113.5% and 225% compared to the control group. In addition, biochar-supported rutile MFCs showed excellent degradation performance of heavy metal pollutants under light conditions. Within 7 h, the Cr⁶⁺ degradation rate reached 95%. In contrast to the blank control group, the removal efficiency of pollutants exhibited increases of 630.8%. The cyclic degradation experiments also showcased the remarkable stability of the system over multiple cycles. This study successfully integrated natural rutile and biochar to fabricate highly efficient cathode photocatalyst composites, which not only enhanced the power generation performance of MFCs but also presented an environmentally sustainable and economically viable method for addressing heavy metal pollution. Full article

This study explored the development of hierarchical graphitic carbon structures (HGCs) from harmful inedible seaweed waste harvested in the summer. Elevated sea temperatures during the summer increase the cellulose content of seaweeds, making them unsuitable for consumption. By utilizing seaweed biomass, this study addresses critical marine environmental issues and provides a sustainable solution for promising electrode materials for energy storage devices. The fabrication process involved impregnating seaweed with Ni ions, followed by annealing to create a highly crystalline carbon structure. Subsequent etching produced numerous nano-sized pores and a large surface area (806 m²/g), significantly enhancing the number of electrically active sites. The resulting HGCs exhibited a high capacitance and maintained their capacity even after 10,000 cycles in fast-current systems. This innovative approach not only mitigates the environmental burden of seaweed waste but also offers a sustainable method for converting it into efficient energy storage materials. Full article

This article reviews the research and development focus of metallic glasses in the field of biomedical applications. Metallic glasses exhibit a short-range ordered and long-range disordered glassy structure at the microscopic level, devoid of structural defects such as dislocations and grain boundaries. Therefore, they possess advantages such as high strength, toughness, and corrosion resistance, combining characteristics of both metals and glasses. This novel alloy system has found applications in the field of biomedical materials due to its excellent comprehensive performance. This review discusses the applications of Ti-based bulk metallic glasses in load-bearing implants such as bone plates and screws for long-term implantation. On the other hand, Mg-based metallic glasses, owing to their degradability, are primarily used in degradable bone nails, plates, and vascular stents. However, metallic glasses as biomaterials still face certain challenges. The Young’s modulus value of Ti-based metallic glasses is higher than that of human bones, leading to stress-shielding effects. Meanwhile, Mg-based metallic glasses degrade too quickly, resulting in the premature loss of mechanical properties and the formation of numerous bubbles, which hinder tissue healing. To address these issues, we propose the following development directions: (1) Introducing porous structures into titanium-based metallic glasses is an important research direction for reducing Young’s modulus; (2) To enhance the bioactivity of implant material surfaces, the surface modification of titanium-based metallic glasses is essential. (3) Developing antibacterial coatings and incorporating antibacterial metal elements into the alloys is essential to maintain the long-term effective antibacterial properties of metallic biomaterials. (4) Corrosion resistance must be further improved through the preparation of composite materials, while ensuring biocompatibility and safety, to achieve controllable degradation rates and degradation modes. Full article

The electrochemical performance of in-house developed, spark plasma-sintered, Aluminum metal–matrix composites (MMCs) was evaluated using different electrochemical techniques. X-ray diffraction (XRD) and Raman spectra were used to characterize the nanocomposites along with FE-SEM and EDS for morphological, structural, and elemental analysis, respectively. The highest charge transfer resistance (R_ct), lowest corrosion current density, lowest electrochemical potential noise (EPN), and electrochemical current noise (ECN) were observed for GO-reinforced Al-MMC. The addition of honeycomb-like structure in the Al matrix assisted in blocking the diffusion of Cl⁻ or SO₄⁻². However, poor wettability in between Al matrix and Al₂O₃ reinforcement resulted in the formation of porous interface regions, leading to a degradation in the corrosion resistance of the composite. Post-corrosion surface analysis by optical profilometer indicated that, unlike its counterparts, the lowest surface roughness (Ra) was provided by GO-reinforced MMC. Full article

Transition metal oxides have been widely used in microwave-absorbing materials, but how to improve impedance matching is still an urgent problem. Therefore, we introduced urea as a polymer carbon source into a three-dimensional porous structure modified by Co₃O₄ nanoparticles and explored the influence of different heat treatment temperatures on the wave absorption properties of the composite. The nanomaterials, when calcined at a temperature of 450 °C, exhibited excellent microwave absorption capabilities. Specifically, at an optimized thickness of 9 mm, they achieved a minimum reflection loss (RL_min) of −97.3 dB, accompanied by an effective absorption bandwidth (EAB) of 9.83 GHz that comprehensively covered both the S and Ku frequency bands. On the other hand, with a thickness of 3 mm, the RL_min was recorded as −17.9 dB, with an EAB of 5.53 GHz. This excellent performance is attributed to the multi-facial polarization and multiple reflections induced by the magnetic loss capability of Co₃O₄ nanoparticles, the electrical conductivity of C, and the unique three-dimensional structure of diatomite. For the future development of bio-based microwave absorption, this work provides a methodology and strategy. Full article

Tetracycline’s accumulation in the environment poses threats to human health and the ecological balance, necessitating efficient and rapid removal methods. Novel porous metal–organic framework (MOF) materials have garnered significant attention in academia due to their distinctive characteristics. This paper focuses on studying the adsorption and removal performance of amino-modified MIL-101(Fe) materials towards tetracycline, along with their adsorption mechanisms. The main research objectives and conclusions are as follows: (1) NH₂-MIL-101(Fe) MOF materials were successfully synthesized via the solvothermal method, confirmed through various characterization techniques including XRD, FT-IR, SEM, EDS, XPS, BET, and TGA. (2) NH₂-MIL-101(Fe) exhibited a 40% enhancement in tetracycline adsorption performance compared to MIL-101(Fe), primarily through chemical adsorption following pseudo-second-order kinetics. The adsorption process conformed well to Freundlich isotherm models, indicating multilayer and heterogeneous adsorption characteristics. Thermodynamic analysis revealed the adsorption process as a spontaneous endothermic reaction. (3) An increased adsorbent dosage and temperature correspondingly improved NH₂-MIL-101(Fe)’s adsorption efficiency, with optimal performance observed under neutral pH conditions. These findings provide new strategies for the effective removal of tetracycline from the environment, thus holding significant implications for environmental protection. Full article

This study evaluates the preparation of novel ternary functional adsorbents based on polyaniline, zinc oxide nanoparticles, and moringa oleifera gum to produce zinc oxide/Moringa oleifera gum-grafted L-methionine-functionalized polyaniline bionanocomposites (ZM-g-Pani) and employed to sequestrate divalent metal ions (Cd²⁺, Hg²⁺ and Pb²⁺) from wastewater samples. The morphological and structural properties of ZM-g-Pani were exploited using FT-IR, FE-SEM/EDS, TEM, and XRD. FT-IR and FE-SEM studies show that the as prepared nanocomposite has an abundant number of reactive groups and a porous structure, thus demonstrating outstanding divalent metal cation removal. FT-IR study confirms that the attachment of L-methionine to polyaniline is facilitated by the C-S linkage. Both TEM and FE-SEM techniques confirmed the clustered granules of ZnO over the surface of polyaniline, which ultimately provided more surface area to adsorb metal ions. The study demonstrated that Cd²⁺, Hg²⁺ and Pb²⁺ ions could undergo physical sorption and chemisorption simultaneously during the adsorption process. The maximum adsorption capacity was 840.33, 497.51, and 497.51 mg/g for Cd²⁺, Hg²⁺, and Pb²⁺, respectively. The impact of co-existing ions, including NO₃⁻, PO₄³⁻, SO₄²⁻, Cl⁻, Na⁺, Cu²⁺, and Al³⁺, showed that there were no notable alterations in the adsorption of the selected metal ions with ZM-g-Pani. ZM-g-Pani showed eight successive regeneration cycles for Cd²⁺, Hg²⁺, and Pb²⁺ with more than 85% removal efficiency. Full article

In recent years, the remediation of heavy metal-contaminated soils has attracted great attention worldwide. Previous research on the removal of toxic heavy metals from wastewater effluents through adsorption by typical solid wastes (e.g., fly ash and coal gangue) has mainly focused on the control of wastewater pollutants. In this study, a coal gangue (CG) by-product from Hancheng City was used as a raw material to prepare polymeric aluminum chloride-loaded coal gangue-based porous carbon (PAC-CGPC) by hydrothermal synthesis. This material was subsequently employed to assess its performance in mitigating Pb²⁺ in soils. In addition, the effects of the pore structure of the prepared material on the adsorption rates, adsorption mechanisms, and plant root uptakes of soil Pb²⁺ were investigated in this study. The raw CG and prepared PAC-CGPC materials exhibited specific surface areas of 1.8997 and 152.7892 m²/g, respectively. The results of adsorption kinetics and isotherms indicate that the adsorption of Pb²⁺ based on PAC-CGPC mainly follows a pseudo-second-order kinetic model, suggesting that chemisorption may be the dominant process. In addition, the adsorption isotherm results showed that the Freundlich model explained better the adsorption process of Pb²⁺, suggests that the adsorption sites of lead ions on APC-CGPC are not uniformly distributed and tend to be enriched in APC, and also shows the ion exchange between aluminum and lead ions. The thermodynamic model fitting results demonstrated the occurrence of spontaneous and exothermic PAC-CGPC-based adsorption of Pb²⁺, involving ion exchange and surface complexation. The effects of the PAC-CGPC addition on soybean plants were further explored through pot experiments. The results revealed substantial decreases in the Pb²⁺ contents in the soybean organs (roots, stems, and leaves) following the addition of the PAC-CGPC material at a dose of 3% compared with the control and raw CG groups. Furthermore, the addition of the PAC-CGPC material at a dose of 3% effectively reduced the bioavailable Pb²⁺ content in the soil by 82.11 and enhanced soybean growth by 15.3%. These findings demonstrated the inhibition effect of the PAC-CGPC material on the translocation of Pb²⁺ in the soybean seedlings. The modified CG adsorbent has highly pore structure and good hydrophilicity, making it prone to migration in unsaturated soils and, consequently, enhancing Pb²⁺ immobilization. This research provides theoretical support for the development of CG-based materials capable of immobilizing soil pollutants. Full article

The effects of process parameters on the electroless plating of ionic polymer–metal composites (IPMCs) were studied in this work. Specifically, the NaBH₄ reduction of platinum onto Nafion-117 was characterised. The effects of the concurrent variation of NaBH₄ concentration, stir time and temperature on surface resistance were studied through a full factorial design. The three-factor three-level factorial design resulted in 27 runs. Surface resistance was measured using a four-point probe. A regression model with an R² value of 97.45% was obtained. Surface resistance was found to decrease with increasing stir time (20 to 60 min) and temperature (20 to 60 °C). These responses were attributed to increased platinisation rates, resulting in more uniform electrode deposition, confirmed by scanning electron microscopy (SEM) and energy-dispersive X-ray (EDAX) analysis. Surface resistance decreased, going from 1% to 5% NaBH₄ concentration, but increased from 5% to 10% concentration. This behaviour was attributed to surface morphology: increased grain size inducing porous electrodes, in line with findings in the literature. The maximum tip displacement, measured through a computer vision system, as well as the maximum blocking force, measured through an analytical balance setup, were obtained for all 27 samples. The varying results were discussed with regards to surface and cross-sectional SEMs, alongside EDAX analysis. Full article

A one-dimensional computational model has been developed that can be used to identify operating conditions for the cathode side of a proton exchange membrane fuel cell such that both the inlet and outlet relative humidity is equal to 100%. By balancing the calculated pressure drop along the cathode side flow channel with the change in molar composition, inlet conditions for the cathode side can be identified with the goal of avoiding channel flooding. The channel length, height, width and the land-to-channel width ratio are input parameters for the model so that it might be used to dimension the cathode flow field. The model can be used to calculate the limiting current density, and we are presenting unprecedented high values as a result of the high pressure drop along the flow channels. Such high current densities can ultimately result in a fuel cell power density beyond the typical value of 1.0–2.0 W/cm² for automotive fuel cells. Full article

We present a review of current research on promising flame retardants using specific methods of applying metal–organic frameworks (MOFs) to the highly flammable fibrous surface of cotton fabric. In this review, we initially address the reasons why the search for new flame retardants has becomes critically important in textile finishing, the area responsible for adhering new functionalities to substrates. This addition of characteristics is closely linked to the nature of the fibers, so the reason for the improvement in cotton fabric in relation to flame retardancy is discussed. Furthermore, the development of highly porous nanomaterials that can generate composites with specific functions is described, as well as their application and methods of integration into textile surfaces. Finally, the main candidates for flame retardant functionality in cellulosic materials are identified. It is also hoped that this work will facilitate researchers to develop and formulate new methods of applying nanomaterials to textile substrates, with a view to becoming a reference for new research into the development of adhesion of emerging materials to traditional materials. Full article

The exploitation of high-performance membranes selective for propylene is important for developing energy-efficient propylene/propane (C₃H₆/C₃H₈) separation technologies. Although metal–organic frameworks with a molecular sieving property have been considered promising filler materials in mixed-matrix membranes (MMMs), their use in practical applications has been challenging due to a lack of interface compatibility. Herein, we adopted a surface coordination strategy that involved rationally utilizing carboxyl-functionalized PIM-1 (cPIM) and ZIF-8 to prepare a mixed-matrix membrane for efficient propylene/propane separation. The interfacial coordination between the polymer and the MOF improves their compatibility and eliminates the need for additional modification of the MOF, thereby maximizing the inherent screening performance of the MOF filler. Additionally, the utilization of porous PIM-1 guaranteed the high permeability of the MMMs. The obtained MMMs exhibited excellent separation performance. The 30 wt% ZIF-8/cPIM-1 membrane performed the best, exhibiting a high C₃H₆ permeability of 1023 Barrer with a moderate C₃H₆/C₃H₈ selectivity of 13.97 under 2 bars of pressure. This work presents a method that can feasibly be used for the preparation of defect-free MOF-based MMMs for specific gas separations. Full article

Biochar, an eco-friendly, porous carbon-rich material, is widely studied for immobilizing heavy metals in contaminated environments. This study prepared tobacco stalks, a typical agricultural waste, into biochar (TSB) modified by hydroxyapatite (HAP) at co-pyrolysis temperatures of 350 °C and 550 °C to explore its Cd(II) adsorption behavior and relevant mechanisms. XRD, SEM–EDS, FTIR, and BET analyses revealed that HAP successfully incorporated onto TSB, enriching the surface oxygen-containing functional groups (P–O and carboxyl), and contributing to the enhancement of the specific surface area from 2.52 (TSB350) and 3.63 m²/g (TSB550) to 14.07 (HAP–TSB350) and 18.36 m²/g (HAP–TSB550). The kinetics of Cd(II) adsorption onto TSB and HAP–TSB is well described by the pseudo-second-order model. Isotherm results revealed that the maximum adsorption capacities of Cd(II) on HAP–TSB350 and HAP–TSB550 were approximately 13.17 and 14.50 mg/g, 2.67 and 9.24 times those of TSB350 and TSB550, respectively. The Cd(II) adsorption amounts on TSBs and HAP–TSBs increased significantly with increasing pH, especially in HAP–TSB550. Ionic strength effects and XPS analysis showed that Cd(II) adsorption onto HAP–TSBs occurred mainly via electrostatic interaction, cation exchange with Ca²⁺, complexation with P–O and –COOH, and surface precipitation. These findings will provide a modification strategy for the reutilization of tobacco agricultural waste in the remediation of heavy metal contaminated areas. Full article

Hexavalent chromium (Cr(VI)) ions are among the most common hazardous metals that pose a serious risk to human health, causing human carcinogenesis and chronic kidney damage. In this study, a point-of-care testing (POCT) kit is proposed for Cr(VI) ions detection at room temperature. The kit contains a hydrophobic parafilm, a nylon membrane to resist outflow, and a hydrophilic Whatman filter paper suitable for coating the fluorescent graphitic carbon nitride sheet (g-C₃N₄). Crystalline, nano-porous, blue-emitting g-C₃N₄ was produced by pyrolysis utilizing carbohydrazide. The electrostatic interactions between the g-C₃N₄ and Cr(VI) ions inhibit the fluorescence behavior. The POCT kit can be used for on-site Cr(VI) ion detection dependent upon the blue emission value. The detection limit was attained at 4.64 nM of Cr(VI) ions. This analytical methodology was utilized on real samples from tap, pond, river, and industrial wastewater. This POCT kit can be a useful alternative for on-site detection of Cr(VI) ions. Full article