Search Results (165)

Glyphosate (GLY) is a systemic herbicide used in agriculture and has a carcinogenic effect after long-term usage. Herein, a molecularly imprinted electrochemical sensor based on palladium@yttrium oxide@boron nitride nanosheets (Pd/Y₂O₃@BN) nanocomposite was developed for the detection of GLY in drinking water. After the preparation of Pd/Y₂O₃@BN nanocomposite by using sonication and NaBH₄ reduction methods, Pd/Y₂O₃@BN nanocomposite as electrode material was applied on glassy carbon electrode by infrared lamp. Then, a molecularly imprinted glassy carbon electrode based on Pd/Y₂O₃@BN (MIP) was designed with cyclic voltammetry (CV) in presence of pyrrole monomer and GLY molecule. After the spectroscopic and microscopic characterizations, the linearity in the range of 1.0 × 10⁻⁹–1.0 × 10⁻⁸ M with a detection limit (LOD) of 3.3 × 10⁻¹⁰ M was obtained for GLY molecule. After MIP electrode was applied to drinking water samples with high recovery, the selectivity, stability, repeatability, and reproducibility features were studied. These promising results suggested that the as-fabricated MIP electrode presented a novel and highly effective approach for GLY assay. Full article

Thick (900–1500 µm), crack-free lithium manganese oxide (LMO) electrodes with a polyvinylidene fluoride (PVDF)-based polymer electrolyte were prepared using an innovated slurry casting method. The selectivity and intercalation capacity of the thick electrodes of 900–1500 μm were evaluated in aqueous chloride solutions containing main cations in synthetic Salar de Atacama brine using cyclic voltammetry (CV) measurements. The CV data indicated that a high Li⁺ selectivity of Li/Na = 152.7 could be achieved under potentiostatic conditions. With the thickest electrode, while the mass specific intercalation capacity was 6.234 mg per gram of LMO, the area specific capacity was increased by 3–11 folds compared to that for conventional thin electrodes to 0.282 mg per square centimeter. In addition, 82% of capacity was retained over 30 intercalation/dis-intercalation cycles. XRD and electrochemical analyses revealed that both Faradaic diffusion-controlled or battery-like intercalation and Faradaic non-diffusion controlled or pseudocapacitive intercalation contributed to the capacity and selectivity. This work demonstrates a practical technology for thick electrode fabrication that promises to result in a significant reduction in manufacturing and operational costs for lithium extraction from brines. Full article

Simultaneous detection of multiple neurochemicals and toxic metal ions in real time remains a major analytical challenge in neurochemistry and environmental sensing. In this study, we present a novel, biocompatible, laser-trimmed four-bore carbon fiber microelectrode (CFM) platform capable of ultra-fast, multi-analyte detection using fast-scan cyclic voltammetry (FSCV). Each of the four carbon fibers, spaced nanometers apart within a glass housing, was independently functionalized and addressed with a distinct waveform, allowing the selective and concurrent detection of four analytes without electrical crosstalk. To validate the system, we developed two electrochemical detection paradigms: (1) selective electrodeposition of gold nanoparticles (AuNPs) on one fiber for enhanced detection of cadmium (Cd²⁺), alongside dopamine (DA), arsenic (As³⁺), and copper (Cu²⁺); and (2) Nafion-modification of two diagonally opposing fibers for discriminating DA and serotonin (5-HT) from their interferents, ascorbic acid (AA) and 5-hydroxyindoleacetic acid (5-HIAA), respectively. Scanning electron microscopy and energy-dispersive X-ray spectroscopy analysis confirmed surface modifications and the spatial localization of electrodeposited materials. Electrochemical characterization in tris buffer, which mimics artificial cerebrospinal fluid, demonstrated enhanced analytical performance. Compared to single-bore CFMs, the four-bore design yielded a 28% increase in sensitivity for Cd²⁺ (147.62 to 190.02 nA µM⁻¹), 12% increase for DA (10.785 to 12.767 nA µM⁻¹), and enabled detection of As³⁺ with a sensitivity of 0.844 nA µM⁻¹, which was not possible with single-bore electrodes within the mixture of analytes. Limits of detection improved twofold for both DA (0.025 µM) and Cd²⁺ (0.005 µM), while As³⁺ was detectable down to 0.1 µM. In neurotransmitter-interference studies, sensitivity increased by 39% for DA and 33% for 5-HT with four-bore CFMs compared to single-bore CFMs, despite modest Nafion diffusion onto adjacent fibers. Overall, our four-bore CFM system enables rapid, selective, and multiplexed detection of chemically diverse analytes in a single scan, providing a highly promising platform for real-time neurochemical monitoring, environmental toxicology, and future integration with AI-based in vivo calibration models. Full article

This study investigates all-solid-state batteries employing multifunctional metallic current collectors/electrodes that remain electrochemically inert toward an alkali-based Na ion solid electrolyte. Inconel 625 was evaluated as the positive current collector in combination with aluminum as the negative electrode and the ferroelectric electrolyte Na2.99Ba0.005OCl. The inertness of both electrodes enabled the construction of a robust device architecture that behaved as a true battery, exhibiting a two-phase equilibrium discharge plateau at ~1.1 V despite the absence of traditional Faradaic reactions. After a one-month rest period, the cell was sequentially discharged through external resistors and retained full functionality for one year. Cyclic voltammetry confirmed a stable electrochemical response over repeated cycling. The final long-term discharge under a 9.47 kΩ load produced a steady ~0.92 V plateau and delivered a total capacity of 35 mAh (~2.3 mAh·cm⁻²). Post-mortem analyses revealed excellent chemical and mechanical stability of Inconel 625 after extended operation, while aluminum showed superficial surface degradation attributed to residual moisture, with X-ray diffraction indicating the formation of aluminum hydroxide. Scanning Kelvin probe measurements guided electrode selection and provided insight into interfacial energetics, whereas scanning electron microscopy confirmed interface integrity. Complementary density functional theory simulations optimized the crystalline bulk and surfaces of Inconel, demonstrating interfacial stability at the atomic scale. Overall, this work elucidates the fundamental driving forces underlying traditional battery operation by studying a “capacity-less” system, highlighting the central role of interfacial electrostatics in sustaining battery-like discharge behavior in the absence of redox-active electrodes. Full article

This study presents the design and application of an electrochemical sensor for selective detection of lead ions (Pb²⁺) based on ionophore-modified raspberry-like Fe₃O₄–Au nanostructures. The material was engineered with a magnetic Fe₃O₄ core, coated with polyethyleneimine (PEI) to facilitate nucleation, and subsequently decorated with Au nanoparticles, providing a raspberry-like (Fe₃O₄@PEI@AuNPs) nanostructure with high surface area and excellent electrochemical conductivity. Surface functionalization with Lead Ionophore IV (ionophore thiol) introduced Pb²⁺-selective binding sites, whose presence and structural evolution were verified by TEM and Raman spectroscopy. The Fe₃O₄ core endowed strong magnetic properties, enabling facile manipulation and immobilization onto screen-printed carbon electrodes (SPCEs) via physical adsorption, while the Au nanoparticles enhanced electron transfer, supplied thiol-binding sites for stable ionophore anchoring, and increased the effective electroactive surface area. Operational conditions were systematically optimized, with acetate buffer (HAc/NaAc, pH 5.7) and chronoamperometric preconcentration (CA) at −1.0 V for 175 s identified as optimal for differential pulse voltammetry (DPV) measurements. Under these conditions, the sensor exhibited a linear response toward Pb²⁺ from 0.025 mM to 2.00 mM with superior sensitivity and reproducibility compared to conventional AuNP-modified SPCEs. Furthermore, the ionophore-modified Fe₃O₄–Au nanostructure-based sensor demonstrated outstanding selectivity for Pb²⁺ over competing heavy metal ions (Cd²⁺, Hg²⁺, Cr³⁺), owing to the specific coordination interaction of Lead Ionophore IV with target ions. These findings highlight the potential of raspberry-like Fe₃O₄@PEI@AuNP nanostructures as a robust and efficient electrochemical platform for the sensitive and selective detection of toxic heavy metal ions. Full article

The discharge of dye-laden effluents remains an environmental challenge since conventional treatments remove color but not the organic load. This study systematically compared anodic oxidation (AO), electro-Fenton (EF), and photoelectro-Fenton (PEF) processes for three representative industrial dyes, such as Coriasol Red CB, Brown RBH, and Blue VT, and their ternary mixture, using boron-doped diamond (BDD) and Ti/IrO₂–SnO₂–Sb₂O₅ (MMO) anodes. Experiments were conducted in a batch reactor with 50 mM Na₂SO₄ at pH = 3.0 and current densities of 20–60 mA cm⁻². Kinetic analysis showed that AO-BDD was most effective at low pollutant loads, EF-BDD became superior at medium loads due to efficient H₂O₂ electrogeneration, and PEF-MMO dominated at higher loads by fast UVA photolysis of surface Fe(OH)²⁺ complexes. In a ternary mixture of 120 mg L⁻¹ of dyes, EF-BDD and PEF-MMO achieved >98% decolorization in 22–23 min with pseudo-first-order rate constants of 0.111–0.136 min⁻¹, whereas AO processes remained slower. COD assays revealed partial mineralization of 60–80%, with EF-BDD providing the most consistent reduction and PEF-MMO minimizing treatment time. These findings confirm that decolorization overestimates efficiency, and electrode selection must be tailored to dye structure and effluent composition. Process selection rules allow us to conclude that EF-BDD is the best robust dark option, and PEF-MMO, when UVA is available, offers practical guidelines for cost-effective electrochemical treatment of textile wastewater. Full article

This work introduces a novel approach to enhancing the performance of zinc anodes in zinc–air batteries through a photopolymerizable organic–inorganic hybrid coating. Electrochemical tests were conducted in a neutral NaCl electrolyte, selected to minimize electrolyte carbonation, anode corrosion, and zinc dendrite formation. The behavior of bare and coated zinc electrodes was investigated using linear sweep voltammetry, electrochemical impedance spectroscopy (EIS), potentiostatic measurements, galvanostatic discharge tests, and charge-discharge tests, while morphological and structural characterizations were carried out by Atomic Force Microscopy (AFM), Raman spectroscopy, and X-ray Diffraction (XRD). The results confirmed that the hybrid coating acts as a corrosion-resistant barrier, enhancing the reversibility and stability of zinc electrodes through a barrier mechanism. Charge–discharge tests further confirmed the improved performance of the coated electrode, obtaining at a current density of 1 mA/cm², a coulombic efficiency of 92.61% and a capacity retention of 90.18%, respectively, after 16 cycles. These findings highlight the effectiveness of the photopolymerizable hybrid coating in improving the durability and rechargeability of zinc–air batteries. Full article

Background/Objectives: Sodium (Na) concentration and the sodium-to-potassium (Na/K) ratio in human milk reflect epithelial tight junction integrity and have been proposed as non-invasive biomarkers of lactational dysfunction, including subclinical mastitis and ductal obstruction. However, their discriminative performance across varied mammary duct conditions, as well as their relevance to milk quality and nutritional integrity, remain underexplored. This study aimed to evaluate the ability of Na, K and the Na/K ratio to discriminate ductal obstruction from non-obstructed lactation—including normal, mixed, and donor milk—and to assess their applicability as nutritional and clinical screening biomarkers. Methods: The study analyzed 635 human milk samples from four groups: obstructed ducts (n = 94), mixed ducts (n = 39), normal ducts (n = 102), and donor milk (n = 400). Na and K concentrations were measured using validated handheld ion-selective electrode analyzers. Statistical analyses included Quade’s ANCOVA and receiver operating characteristic curve analysis, adjusting for infant age, gestational age, birth body weight, maternal age and storage duration. Results: Na concentrations were highest in obstructed ducts (Group A: median 810 ppm, IQR 368–1725) compared with normal ducts (Group C: 220 ppm, IQR 140–283) and donor milk (Group D: 98 ppm, IQR 80–130) (p < 0.001). A similar pattern was observed for the Na/K ratio (Group A: 1.5, IQR 0.6–3.1 vs. Group C: 0.3, IQR 0.2–0.5; Group D: 0.3, IQR 0.2–0.3). After adjusting, both Na and the Na/K ratio remained significantly elevated in milk from obstructed ducts compared to non-obstructed samples (p < 0.001). Donor milk exhibited the lowest and most stable electrolyte levels. Na demonstrated excellent discriminative performance (area under the curve = 0.96), slightly outperforming the Na/K ratio (area under the curve = 0.92). Conclusions: Na concentration and the Na/K ratio in human milk are sensitive and practical biomarkers of mammary gland integrity. Given that Na alone can be measured without additional calculations, its simplicity and strong performance support its application as a potential biomarker for ductal obstruction, with implications for both lactation support and nutritional science. Full article

Herein, we propose an ultrasensitive electrochemical immunosensor based on glucose oxidase labeling and enzyme-catalyzed Au staining. In brief, the primary antibody (Ab₁), bovine serum albumin, an antigen and then a bionanocomposite that contains a second antibody (Ab₂), poly(3-anilineboronic acid) (PABA), Au nanoparticles (AuNPs) and glucose oxidase (GOx) are modified on a glassy carbon electrode coated with multiwalled carbon nanotubes, yielding a corresponding sandwich-type immunoelectrode. In the presence of glucose, a chemical reduction of NaAuCl₄ by enzymatically generated H₂O₂ can precipitate a lot of gold on the Ab₂-PABA-AuNPs-GOx immobilized immunoelectrode. In situ anodic stripping voltammetry (ASV) detection of gold in 8 μL 1.0 M aqueous HBr-Br₂ is conducted for the antigen assay, and the ASV detection process takes approximately 6 min. This method is employed for the assay of human immunoglobulin G (IgG) and human carbohydrate antigen 125 (CA125), which demonstrates exceptional sensitivity, high selectivity and fewer required reagents/samples. The achieved limits of detection (S/N = 3) by the method are 0.25 fg mL⁻¹ for IgG (approximately equivalent to containing 1 IgG molecule in the 1 microlitre of the analytical solution) and 0.1 nU mL⁻¹ for CA125, which outperforms many previously reported results. Full article

Recent literature reports have shown that individual HEAs, especially those of the AlCoCrFeNi composition system alloyed with appropriately selected elements, exhibit excellent mechanical properties and corrosion resistance, making them promising candidates for replacing conventional materials such as austenitic steels in corrosive environments. Therefore, in the present study, the high-entropy alloy AlCoCrFeNiMo_0.25 was examined and compared with AISI 304L steel and the reference alloy AlCoCrFeNi. The HEA was produced by arc melting in vacuum. The effect of molybdenum addition (5% at.) on the structure, mechanical properties, and corrosion resistance was evaluated. Potentiodynamic polarization and electrochemical impedance spectroscopy tests were carried out in a 3.5% NaCl solution in a three-electrode electrochemical system. The addition of molybdenum to AlCoCrFeNiMo_x alloy additionally caused, along with the BCC phase, the formation of σ phase and FCC phase (less than 1%), as well as changes in the microstructure, leading to the fragmentation of grains and the formation of a mosaic structure. On the basis of nanoindentation tests, it was established that the addition of Mo increases hardness and elastic modulus and improves nanoindentation coefficients H/E and H³/E², as well as an increase in the elastic recovery index while decreasing plasticity index (vs. the reference equiatomic HEA). This indicates the improvement of anti-wear properties with impact loading resistance. In turn, electrochemical tests have shown that the addition of Mo improves corrosion resistance. Corrosion pitting develops in Al- and Ni-rich areas of HEA alloys, as a result of galvanic microcorrosion related to Cr chemical segregation. In general, the addition of 5% Mo results in a fine-grained mosaic structure, which primarily translates into favorable nanoindentation and corrosion properties of the AlCoCrFeNiMo_0.25 alloy. Full article

Effective control of calcium carbonate (CaCO₃) scale formation is crucial to improve the performance and economic efficiency of water systems. This study investigates the impact of various scale inhibitors on the nucleation and crystallization processes of CaCO₃. Calcium carbonate particles were synthesized by mixing CaCl₂·2H₂O and NaHCO₃ solutions, in the presence of various scale inhibitors that had not previously been investigated using the experimental techniques employed in this study. Particle size distribution and zeta potential were analyzed using dynamic light scattering (DLS), while Ca⁺² consumption and pH changes were monitored with ion-selective electrodes. Crystal morphology was evaluated using scanning electron microscopy (SEM) and cryo-transmission electron microscopy (cryo-TEM). We demonstrated that, in all samples, approximately 98% of the CaCO₃ particles (sized between 400 and 840 nm) are formed within the first 30 min of synthesis, and these particles then aggregate to form larger particles (840–1100 nm in size). Due to the solution’s high supersaturation, the inhibitors influence calcium consumption only after 5 min of synthesis. All inhibitors, especially DTPMP, decrease calcium consumption and particle size during synthesis. The zeta potential and morphology of the particles in the samples containing inhibitors differed from those in the control group. Cryo-TEM observations revealed distinct nanometric precursor phases in the calcite crystallization process without inhibitors and different nanostructures when scale inhibitors were used. Moreover, conchoidal fractures were observed in the nanoparticles formed in the presence of DTPMP. This study demonstrates the effectiveness of various inhibitors in reducing calcium consumption in solution and altering the morphology of CaCO₃ crystals, thereby preventing calcium carbonate (CaCO₃) scale formation. Full article

Current seawater desalination systems on ships face several limitations including outdated concentration detection methods, low detection accuracy, and insufficient real-time monitoring capabilities. This study addresses these issues by developing a concentration measurement device based on two-electrode conductivity measurement principles. The key innovation involves transforming conventional parallel plates into curved electrode plates that can be embedded directly into pipelines, enabling real-time concentration monitoring in shipboard seawater desalination systems. We established an equivalent circuit model and conducted simulation analysis of amplitude–frequency and phase–frequency response characteristics to guide excitation signal frequency selection. Using 3D printing technology, we fabricated pipeline components and manually processed curved electrode plates, then assembled experimental devices and determined optimal working parameters through systematic measurements of solution conductivity versus frequency and concentration. Laboratory testing with known concentration saline solutions demonstrated high measurement accuracy, with the device achieving a relative error of only 1.457% for 3.5% NaCl solution (simulated seawater) and 3.000% for commercial saline (0.9% NaCl) after calibration. Finally, we integrated a PLC control system for automated concentration measurement and display. Compared to traditional devices that require sampling in static water environments, this system can be distributed throughout shipboard desalination systems, providing more convenient, accurate, and efficient monitoring capabilities. Full article

This study focused on the development of Na⁺ ion sensing devices on a flexible substrate and investigated the impact of various additive materials on its sensing performance. For the Na⁺ ion sensing aspect, the film on the carbon working electrode used tert-butyl calix[4]arene tetraethyl acetate as the ion carrier. The main component of the film was polyvinyl chloride (PVC), with a plasticizer added to enhance its flexibility, ensuring better adaptation to the flexible substrate. In this base formulation, graphene oxide (GO) or multi-walled carbon nanotubes (MWCNTs) were incorporated into the sensing electrode to explore their effects on Na⁺ ion sensing capabilities. The results demonstrated that adding MWCNTs significantly improved the sensor’s sensitivity to Na⁺ ions. In addition, the study used the response slope to Na⁺ ions as a comparative reference for selectivity by calculating the ratio of the Na⁺ ion response slope to the response slopes of other ions (such as K⁺ and Ca²⁺). The findings showed that the sensors with MWCNTs exhibited better selectivity than the others with GO, and therefore, further analysis was performed on the response time of the sensors with MWCNTs. The results indicated that incorporating MWCNTs reduced the sensors’ response time and enhanced their overall sensitivity. However, excessive addition of MWCNTs would lead to a decrease in the selectivity of the fabricated sensors. This suggests that while MWCNTs offer promising improvements in performance, their concentration must be carefully optimized to maintain the sensors’ selectivity. Full article

This study aimed to evaluate the influence of different fluoride-containing toothpastes on fluoride uptake, surface roughness, and microhardness of six ion-releasing restorative dental materials, including glass hybrids (EQUIA Forte HT with and without coating), glass ionomer cements (Fuji IX), resin-modified GICs (Fuji II LC), alkasites (Cention Forte), and ion-releasing composites (Luminos UN and Activa). Specimens were prepared and subjected to a four-day brushing protocol using six toothpastes with varying fluoride formulations (NaF, SnF2, SMFP) and concentrations. Fluoride uptake was assessed by measuring fluoride release using an ion-selective electrode, while surface roughness and microhardness were assessed before and after brushing. Results revealed significant variations in fluoride uptake, with Fuji IX and EQUIA Forte HT showing the highest release, particularly when brushed with NaF-based toothpastes (Duraphat 5000 and 2800). Surface roughness increased post-brushing, with the greatest changes observed in Activa, while microhardness decreased across most materials, except for coated EQUIA Forte HT, which exhibited improved compactness. Resin-based composites, such as Luminos UN and Activa, demonstrated lower fluoride uptake and minimal changes in microhardness compared to GICs. The findings underscore the importance of material composition and toothpaste formulation in influencing fluoride dynamics, surface properties, and mechanical performance of restorative materials. Full article

Zeolite Battery Research Africa (ZEBRA) batteries (Na-NiCl₂ solid electrolyte batteries, SEBs) have commercial applications in energy storage due to their low costs and recyclability, long lifetime, and high safety. In commercial ZEBRA batteries, Ni electrode and beta’’-alumina solid electrolyte (BASE) have a more than 70% share of the overall cell material costs. Na-ZnCl₂ all-liquid batteries (ALBs), which replace Ni with abundant and low-cost Zn and BASE electrolyte with molten salt electrolyte, could reduce costs and provide a longer lifetime and higher safety, making their application in grid storage promising. However, compared to SEBs, ALBs are in an early development stage, particularly for their molten salt electrolytes, which have a significant effect on the battery performance. Physical and chemical properties of the salt electrolyte like melting temperatures and solubilities of electrode materials (i.e., Na and Zn metal) are vital for the molten salt electrolyte selection and battery cell design and optimization. In this work, the binary and ternary phase diagrams of salt mixtures containing NaCl, CaCl₂, BaCl₂, SrCl₂, and KCl, obtained via FactSage simulation and DSC measurements, as well as the solubilities of electrode materials (Na and Zn metals), are presented and used for the selection of the molten salt electrolyte. Moreover, various criteria, considered for the selection of the molten salt electrolyte, include high electromotive force (EMF) for suitable electrochemical properties, low melting temperature for large charge/discharge range, low solubilities of electrode materials for low self-discharge, low material costs, and high material abundance for easy scale-up. Based on these criteria, the NaCl-CaCl₂-BaCl₂ and NaCl-SrCl₂-KCl salt mixtures are selected as the two most promising ALB molten salt electrolytes and suggested to be tested in the ALB demonstrators currently under development. Full article