Search Results (754)

Nickel-based metal–organic frameworks (Ni-MOFs) have received enormous amounts of attention from the scientific community due to their excellent porosity, larger specific surface area, tunable structure, and intrinsic redox properties. In previous years, Ni-MOFs and their hybrid composite materials have been extensively explored for electrochemical sensing applications. As per the reported literature, Ni-MOF-based hybrid materials have been used in the fabrication of electrochemical sensors for the monitoring of ascorbic acid, glucose, L-tryptophan, bisphenol A, carbendazim, catechol, hydroquinone, 4-chlorophenol, uric acid, kaempferol, adenine, _L-cysteine, etc. The presence of synergistic effects in Ni-MOF-based hybrid materials plays a crucial role in the development of highly selective electrochemical sensors. Thus, Ni-MOF-based materials exhibited enhanced sensitivity and selectivity with reasonable real sample recovery, which suggested their potential for practical applications. In addition, Ni-MOF-based hybrid composites were also adopted as electrode modifiers for the development of supercapacitors. The Ni-MOF-based materials demonstrated excellent specific capacitance at low current densities with reasonable cyclic stability. This review article provides an overview of recent advancements in the utilization of Ni-MOF-based electrode modifiers with metal oxides, carbon-based materials, MXenes, polymers, and LDH, etc., for the electrochemical detection of environmental pollutants and biomolecules and for supercapacitor applications. In addition, Ni-based bimetallic and trimetallic catalysts and their composites have been reviewed for electrochemical sensing and supercapacitor applications. The key challenges, limitations, and future perspectives of Ni-MOF-based materials are discussed. We believe that the present review article may be beneficial for the scientific community working on the development of Ni-MOF-based materials for electrochemical sensing and supercapacitor applications. Full article

Understanding surface charge behavior is essential for improving ion separation during lithium brine treatment. This paper investigates the performance of a three-compartment electrodialysis system designed for the selective removal of divalent cations (Mg²⁺ and Ca²⁺). The relationship between zeta potential and the recovery of Li⁺, Na⁺, and K⁺ is analyzed. Zeta potential measurements at various pH values showed that Mg(OH)₂ particles maintained a positive charge. The system facilitated the precipitation of Mg(OH)₂ and Ca(OH)₂ via electrochemically generated OH⁻ ions. The specific electrical energy consumption was evaluated for each operating condition. The results showed that the zeta potential of the precipitates was affected by both the current density and temperature. This influenced lithium losses due to brine entrapment within the precipitated solids. At 600 A/m² and 50 °C, more than 99% of Mg²⁺ and Ca²⁺ were removed, and more than 90% of lithium was recovered, with a specific electric energy consumption of 2.58 kWh per kilogram of Li recovered. The system also generates HCl as a valuable by-product, which improves the sustainability of the process. This study provides a new framework for improving the energy efficiency of lithium purification from brines and lithium recovery. Full article

Solid Oxide Fuel Cells (SOFCs) offer high-efficiency electrochemical conversion of fuels like natural gas, yet detailed modeling is crucial for optimization. This paper presents a simulation study of a natural gas-fueled SOFC system, developed using Aspen Plus with Fortran integration. Distinct from prevalent paradigms assuming rated power output, this work adopts rated current density as the primary input, enabling a more direct investigation of the cell’s electrochemical behavior. We conducted a comprehensive sensitivity analysis of key parameters, including fuel utilization, water-carbon ratio, and current density, and further investigated the impact of different interconnection configurations on overall module performance. Results demonstrate that a single unit operating at a current density of 180 mA/cm², a fuel utilization of 0.75, and a water-carbon ratio of 1.5 can achieve a maximum net stack-level electrical efficiency of 54%. Furthermore, optimizing the interconnection of a 400 kW module by combining series and parallel units boosts the overall net system-level electrical efficiency to 59%, a 5-percentage-point increase over traditional parallel setups. This is achieved by utilizing a bottoming cycle for exhaust heat recovery. This research validates the rated current density approach for SOFC modeling, offering novel insights into performance optimization and modular design for integrated energy systems. Full article

This paper analyses the role of electronic waste (E-waste) as a secondary source of critical and precious minerals, addressing the challenges and opportunities in transitioning towards a circular economy (CE) for electronics. The surging global demand for these essential materials, driven by technological advancements and renewable energy infrastructure, necessitates alternative supply strategies due to the depletion of natural reserves and the environmental degradation associated with primary mining. E-waste contains a rich concentration of valuable metals, such as gold, silver, and platinum, making its recovery a promising solution aligned with CE principles, which can mitigate environmental impacts and ensure long-term material availability. This paper examines the environmental, economic, and technological aspects of E-waste recovery, focusing on core processes such as physical and mechanical separation, pyrometallurgical, hydrometallurgical, bio-metallurgical, and electrochemical techniques. It explores innovative strategies to improve material recovery efficiency and sustainability, with consideration of evolving regulatory frameworks, technological advancements, and stakeholder engagement. The analysis highlights that e-waste, particularly printed circuit boards, can contain 40–800 times more gold than mined ore, with 1000–3000 g of gold per tonne compared to 5–10 g per tonne in traditional ores. Recovery costs using advanced E-waste recycling technologies range between $10,000–$20,000 USD per kilogram of gold, significantly lower than the $30,000–$50,000 USD per kilogram in primary mining. Globally, over 50 million tonnes of E-waste are generated annually, yet less than 20% is formally recycled. Efficient recycling methods can recover up to 95% of base and precious metals under optimized conditions. The paper argues that E-waste recycling presents a viable pathway to conserve critical raw materials, reduce environmental degradation, and enhance circular economic resilience. However, it also emphasizes persistent challenges—including high initial investment, technological limitations in developing regions, and regulatory fragmentation—that must be addressed for scalable adoption. Full article

This study investigates the effectiveness of an environmentally friendly coating in mitigating corrosion and preserving the mechanical properties of carbon steel, copper, and aluminium. The coated and uncoated samples were subjected to a 20-day immersion in 5% NaCl solution. Corrosion behaviour was assessed using Linear Sweep Voltammetry (LSV), Open Circuit Potential (OCP), and Electrochemical Impedance Spectroscopy (EIS), while mechanical performance was evaluated through tensile testing. The coating’s thickness, surface roughness, water contact angle, and composition were characterised to understand its protective behaviour. The results show that the coating significantly reduced corrosion rates, with carbon steel exhibiting a 99.99% inhibition efficiency and aluminium showing the lowest corrosion rate due to a synergistic effect between the coating and native oxide layer. Mechanical testing revealed that coated carbon steel retained higher tensile strength and stiffness compared to its uncoated counterpart, while aluminium showed notable recovery in elastic modulus. Copper displayed minimal mechanical changes due to its inherent corrosion resistance. This work highlights the potential of eco-friendly coatings in enhancing both the corrosion resistance and mechanical durability of metallic materials in aggressive environments. Full article

The advancement of high-performance sodium-ion batteries (SIBs) necessitates cathode materials that exhibit both structural robustness and long-term electrochemical stability. Na₃V₂(PO₄)₃ (NVP), with its NASICON-type framework, is a promising candidate; however, its inherently low electronic conductivity restricts full capacity utilization. In this study, carbon-coated and Cu-substituted Na₃V₂(PO₄)₃ (NVCP) composites were synthesized via a solid-state reaction using agarose as a carbon source. Structural and morphological analyses confirmed the successful incorporation of Cu²⁺ ions into the rhombohedral lattice without disrupting the crystal structure and the formation of uniform conductive carbon layers. The substitution of Cu²⁺ induced increased carbon disorder and partial oxidation of V³⁺ to V⁴⁺, contributing to enhanced electronic conductivity. Consequently, NVCP exhibited excellent long-term cycling performance, maintaining over 99% of its initial capacity after 500 cycles at 0.5 C. Furthermore, the electrode demonstrated outstanding high-rate capabilities, with a capacity recovery of 97.98% after cycling at 20 C and returning to lower current densities. These findings demonstrate that Cu substitution combined with carbon coating synergistically enhances structural integrity and Na⁺ transport, offering an effective approach to engineer high-performance cathodes for next-generation SIBs. Full article

This study investigates the behavior of phosphate ion transport through two structurally distinct anion-exchange membranes—AMV (homogeneous) and HC-A (heterogeneous)—in an electrodialysis system under both static and stirred conditions at varying pH levels. Chronopotentiometric and current–voltage analyses were used to investigate the influence of pH and hydrodynamics on ion transport. Under underlimiting (ohmic) conditions, the AMV membrane exhibited simultaneous transport of H₂PO₄⁻ and HPO₄²⁻ ions at neutral and mildly alkaline pH, while such behavior was not verified at acidic pH and in all cases for the HC-A membrane. Under overlimiting current conditions, AMV favored electroconvection at low pH and exhibited significant water dissociation at high pH, leading to local pH shifts and chemical equilibrium displacement at the membrane–solution interface. In contrast, the HC-A membrane operated predominantly under strong electroconvective regimes, regardless of the pH value, without evidence of water dissociation or equilibrium change phenomena. Stirring significantly impacted the electrochemical responses: it altered the chronopotentiogram profiles through the emergence of intense oscillations in membrane potential drop at overlimiting currents and modified the current–voltage behavior by increasing the limiting current density, reducing electrical resistance, and compressing the plateau region that separates ohmic and overlimiting regimes. Additionally, both membranes showed signs of NH₃ formation at the anodic-side interface under pH 7–8, associated with increased electrical resistance. These findings reveal distinct ionic transport characteristics and hydrodynamic sensitivities of the membranes, thus providing valuable insights for optimizing phosphate recovery via electrodialysis. Full article

This review article compiled previous reports in the fabrication of hydroquinone (HQ) electrochemical sensors using differently modified electrodes. The electrode materials, which are also called electrocatalysts, play a crucial role in electrochemical detection of biomolecules and toxic substances. Metal oxides, MXenes, carbon-based materials such as reduced graphene oxide (rGO), carbon nanotubes (CNTs), layered double hydroxides (LDH), metal sulfides, and hybrid composites were extensively utilized in the fabrication of HQ sensors. The electrochemical performance, including limit of detection, linearity, sensitivity, selectivity, stability, reproducibility, repeatability, and recovery for real-time sensing of the HQ sensors have been discussed. The limitations, challenges, and future directions are also discussed in the conclusion section. It is believed that the present review article may benefit researchers who are involved in the development of HQ sensors and catalyst preparation for electrochemical sensing of other toxic substances. Full article

The contamination of drinking water sources with selenium (Se) oxyanions, including selenite (Se(IV)) and selenate (Se(VI)), contains serious health hazards with an oral intake exceeding 400 µg/day and therefore requires urgent attention. Various natural and anthropogenic sources are responsible for high Se concentrations in aquatic environments. In addition, the chemical behavior and speciation of selenium can vary noticeably depending on the origin of the source water. The Se(VI) oxyanion is more soluble and therefore more abundant in surface water. Se levels in contaminated waters often exceed 50 µg/L and may reach several hundred µg/L, well above drinking water limits set by the World Health Organization (40 µg/L) and Germany (10 µg/L), as well as typical industrial discharge limits (5–10 µg/L). Overall, Se is difficult to remove using conventionally available physical, chemical, and biological treatment technologies. The recent literature has therefore highlighted promising advancements in Se removal using emerging technologies. These include advanced physical separation methods such as membrane-based treatment systems and engineered nanomaterials for selective Se decontamination. Additionally, other integrated approaches incorporating photocatalysis coupled adsorption processes, and bio-electrochemical systems have also demonstrated high efficiency in redox transformation and capturing of Se from contaminated water bodies. These innovative strategies may offer enhanced selectivity, removal, and recovery potential for Se-containing species. Here, a current review outlines the sources, distribution, and chemical behavior of Se in natural waters, along with its toxicity and associated health risks. It also provides a broad and multi-perspective assessment of conventional as well as emerging physical, chemical, and biological approaches for Se removal and/or recovery with further prospects for integrated and sustainable strategies. Full article

7,12-Dimethylbenzo[a]anthracene (DMBA-7,12), a highly toxic and environmentally persistent polycyclic aromatic hydrocarbon (PAH), poses significant threats to marine biodiversity and human health due to its bioaccumulation through the food chain. Conventional chromatographic methods, while achieving comparable detection limits, are hindered by the need for expensive instrumentation and prolonged analysis times, rendering them unsuitable for rapid on-site monitoring of DMBA-7,12 in marine environments. Therefore, the development of novel, efficient detection techniques is imperative. In this study, we have successfully developed an electrochemical immunosensor based on a polydopamine (PDA)–chitosan (CTs) composite interface to overcome existing technical limitations. PDA provides a robust scaffold for antibody immobilization due to its strong adhesive properties, while CTs enhances signal amplification and biocompatibility. The synergistic integration of these materials combines the high efficiency of electrochemical detection with the specificity of antigen–antibody recognition, enabling precise qualitative and quantitative analysis of the target analyte through monitoring changes in the electrochemical properties at the electrode surface. By systematically optimizing key experimental parameters, including buffer pH, probe concentration, and antibody loading, we have constructed the first electrochemical immunosensor for detecting DMBA-7,12 in seawater. The sensor achieved a detection limit as low as 0.42 ng/mL. In spiked seawater samples, the recovery rates ranged from 95.53% to 99.44%, with relative standard deviations (RSDs) ≤ 4.6%, demonstrating excellent accuracy and reliability. This innovative approach offers a cost-effective and efficient solution for the in situ rapid monitoring of trace carcinogens in marine environments, potentially advancing the field of marine pollutant detection technologies. Full article

This work represents the first use of a phosphonium salt-functionalized β-Cyclodextrin polymer (β-CDP) as a highly selective sensing membrane for monitoring the safety of drinking water against perchlorate ions (ClO₄⁻) using electrochemical impedance spectroscopy (EIS). Structural confirmation via ¹H NMR, ¹³C NMR, ³¹P NMR, and FT-IR spectroscopies combined with AFM and contact angle measurements demonstrate how the enhanced solubility of modified cyclodextrin improves thin film quality. The innovation lies in the synergistic combination of two detection mechanisms: the “Host-Guest” inclusion in the cyclodextrin cavity and anionic exchange between the bromide ions of the phosphonium groups and perchlorate anions. Under optimized functionalization conditions, EIS reveals high sensitivity and selectivity, achieving a record-low detection limit (LOD) of ~10⁻¹² M and a wide linear range of detection (10⁻¹¹ M–10⁻⁴ M). Sensing mechanisms at the functionalized transducer interfaces are examined through numerical fitting of Cole-Cole impedance spectra via a single relaxation equivalent circuit. Real water sample analysis confirms the sensor’s practical applicability, with recoveries between 96.9% and 109.8% and RSDs of 2.4–4.8%. Finally, a comparative study with reported membrane sensors shows that β-CDP offers superior performance, wider range, higher sensitivity, lower LOD, and simpler synthesis. Full article

Microbial fuel cells (MFCs) are bio-electrochemical systems that harness microorganisms to convert organic pollutants in wastewater directly into electricity, offering a dual solution for sustainable wastewater treatment and renewable energy generation. This paper presents a holistic techno-economic and environmental feasibility assessment of large-scale MFC deployment in Dhaka’s industrial zone, Bangladesh, as a relevant case study. Here, treating 100,000 cubic meters of wastewater daily would require a capital investment of approximately USD 500 million, with a total project cost ranging between USD 307.38 million and 1.711 billion, depending on system configurations. This setup has an estimated theoretical energy recovery of 478.4 MWh/day and a realistic output of 382 MWh/day, translating to a per-unit energy cost of USD 0.2–1/kWh. MFCs show great potential for treating wastewater and addressing energy challenges. However, this paper explores remaining challenges, including high capital costs, electrode and membrane inefficiencies, and scalability issues. Full article

Dopamine (DA) is a neurotransmitter responsible for important functions in mammals’ bodies, including mood, movement and motivation. High or low dopamine levels are associated mainly with mental illnesses such as schizophrenia and depression. Therefore, contributing to the development of electrochemical devices to precisely determine the DA levels in urine samples, a simple and low-cost sensor is proposed in this work. The proposed sensor design is based on crosslinked chitosan films combining carbon black (CB) and deep eutectic solvents (DESs), incorporated onto the surface of a glassy carbon electrode (GCE). Fourier Transform Infrared Spectroscopy (FT-IR) was applied to characterize the produced DESs and their precursors, while the films were characterized by scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The sensor modified with CB and DES–ethaline (DES (ETHA)-CB/GCE) showed a significantly enhanced analytical signal for DA using differential pulse voltammetry under the optimized working conditions. Moreover, a better heterogeneous electron transfer rate constant (k⁰) was obtained, about 45 times higher than that of the bare GCE. The proposed sensor achieved a linear response range of 0.498 to 26.8 µmol L⁻¹ and limits of detection and quantification of 80.7 and 269 nmol L⁻¹, respectively. Moreover, the sensor was successfully applied in the quantification of DA in the synthetic urine samples, with recovery results close to 100%. Furthermore, the sensor presented good precision, as shown from the repeatability tests. The presented method to electrochemically detect DA has proven to be efficient and simple compared to the conventional methods commonly reported. Full article

Excessive levels of Pb²⁺ and Cd²⁺ in seawater pose significant combined toxicity to marine organisms, resulting in harmful effects and further threatening human health through biomagnification in the food chain. Traditional methods for detecting marine Pb²⁺ and Cd²⁺ rely on laboratory analyses, which are hindered by limitations such as sample degradation during transport and complex operational procedures. In this study, we present an electrochemical sensor based on intelligent mobile detection devices. By combining G-COOH-MWCNTs/ZnO with differential pulse voltammetry, the sensor enables the efficient, simultaneous detection of Pb²⁺ and Cd²⁺ in seawater. The G-COOH-MWCNTs/ZnO composite film is prepared via drop-coating and is applied to a glassy carbon electrode. The film is characterized using cyclic voltammetry, electrochemical impedance spectroscopy, and scanning electron microscopy, while Pb²⁺ and Cd²⁺ are quantified using differential pulse voltammetry. Using a 0.1 mol/L sodium acetate buffer (pH 5.5), a deposition potential of −1.1 V, and an accumulation time of 300 s, a strong linear correlation was observed between the peak response currents of Pb²⁺ and Cd²⁺ and their concentrations in the range of 25–450 µg/L. The detection limits were 0.535 µg/L for Pb²⁺ and 0.354 µg/L for Cd²⁺. The sensor was applied for the analysis of seawater samples from Maowei Sea, achieving recovery rates for Pb²⁺ ranging from 97.7% to 103%, and for Cd²⁺ from 97% to 106.1%. These results demonstrate that the sensor exhibits high sensitivity and stability, offering a reliable solution for the on-site monitoring of heavy metal contamination in marine environments. Full article

Electrolytic manganese residue (EMR) is a byproduct of electrolytic manganese production, rich in soluble pollutants such as manganese and ammonia nitrogen. Traditional stockpiling methods result in contaminant leaching and water pollution, threatening ecosystems. Meanwhile, EMR has significant resource-recovery potential. This paper systematically reviews the harmless process and resource technology of EMR, efficiency bottlenecks, and the current status of industrial applications. The mechanisms of chemical leaching, precipitation, solidification, roasting, electrochemistry, and microorganisms were analyzed. Among these, electrochemical purification stands out for its efficiency and environmental benefits, positioning it as a promising option for broad industrial use. The mechanisms of chemical leaching, precipitation, solidification, roasting, electrochemistry, and microorganisms were analyzed, revealing the complementarity between building materials and chemical materials (microcrystalline glass) in scale and high-value-added production. But the lack of impurity separation accuracy and market standards restricts its promotion. Finally, it proposes future directions for EMR resource utilization based on practical and economic considerations. Full article