Search Results (62)

Carbon-based materials, including graphene, carbon nanotubes, laser-induced graphene, and pyrolyzed glassy carbon, are widely used in sensing applications due to their high conductivity, large surface area, and tunable surface chemistry. Meanwhile, microfluidic systems enable precise fluid handling, reduced sample consumption, and enhanced analytical performance through improved mass transport and device miniaturization. The integration of carbon-based materials with microfluidic platforms has enabled the development of compact, portable, and highly sensitive devices for water monitoring. This review summarizes recent advances in carbon-based microfluidic sensors for water monitoring applications. Key carbon materials and their sensing mechanisms, particularly electrochemical transduction, are discussed. Various microfluidic integration strategies, including paper-based devices, polymer-based devices, MEMS-based systems, and flexible platforms, are highlighted, with emphasis on mass transport enhancement and overall system performance. Representative recent advances in carbon-based microfluidic sensors for water monitoring, including the detection of heavy metal ions, nutrients, and emerging contaminants, are reviewed. Finally, challenges related to scalable manufacturing, long-term operational stability, biofouling/surface fouling, and reproducible system integration are discussed, together with future perspectives on intelligent carbon-based microfluidic platforms featuring AI-assisted analytics, sense-response functionality, and self-healing and dynamic antifouling capabilities for water monitoring. These advances are expected to enable real-time, low-cost, and field-deployable water monitoring systems for environmental protection and public health management. Overall, this review highlights the critical role of integrating carbon-based sensing materials with microfluidic engineering in advancing next-generation water monitoring technologies. Full article

Next-generation wastewater treatment and recycling rely on membrane-based processes, but they face a trade-off among permeability, selectivity, and fouling resistance. In the present study, thin-film nanocomposite (TFN) membranes were fabricated by incorporating a ternary TiO₂-SiO₂-biochar nanofiller into a polysulfone (PSf) support using nonsolvent-induced phase separation, after which m-phenylenediamine and trimesoyl chloride were used via interfacial polymerization to produce a selective polyamide layer. The membrane compositions were M1 (22 wt.% PSf), M2 (22 wt.% PSf/0.5 wt.% TiO₂/0.5 wt.% SiO₂/0.5 wt.% biochar), and M3 (polyamide-coated M2). FTIR, XRD, SEM, contact-angle, porosity, and mechanical analyses supported successful membrane formation and changes in morphology, wettability, and structural strength after nanofiller incorporation and TFC coating. The addition of a nanofiller increased the hydrophilicity of the membranes by decreasing the water contact angle from 98.6 ± 0.8° for pristine PSf to 35.6 ± 1.5° for the nanocomposite membrane. Consequently, the pure-water permeability increased from 21 to 37 L m⁻² h⁻¹ bar⁻¹. After polyamide layer formation, the optimized TFN membrane maintained a contact angle of 55.4 ± 3.8° and achieved a high Congo red rejection of 98% with permeate flux of 7–9 L m⁻² h⁻¹ bar⁻¹. The membrane also showed good antifouling performance, with flux recovery ratios exceeding 90%. For heavy-metal-containing solutions, the optimized membrane showed apparent removal efficiencies of 78–98% for multivalent heavy metals (Pb²⁺, Hg²⁺, Cd²⁺, Mn²⁺, Zn²⁺, Cu²⁺, Ni²⁺, Fe³⁺, As³⁺, and Cr⁶⁺). Static adsorption tests showed the order M2 > M3 > M1, confirming that exposed TiO₂-SiO₂-biochar sites contribute to pollutant uptake, while the superior filtration performance of M3 is attributed to the combined effect of the polyamide selective layer and adsorption-assisted interactions. Overall, the TiO₂-SiO₂-biochar-based TFN membrane provides a promising platform for dye removal and preliminary heavy-metal attenuation from contaminated water. Full article

Electrochemical sensors have emerged as promising tools for rapid pesticide screening in food and environmental samples because they combine simple instrumentation, fast response, portability, and compatibility with disposable electrodes. This review organizes recent progress through a cross-system framework linking pesticide class, interfacial electrochemical process, and material design. Carbon materials, metal–organic frameworks and their derivatives, metal nanoparticles, metal compounds, conducting polymers, MXene-based composites, and selected emerging materials are compared in terms of enrichment capability, charge-transfer regulation, catalytic amplification, recognition-layer integration, and suitability for real-sample analysis. Emphasis is placed on issues that are often under-discussed in performance-centered surveys, including matrix interference, electrode fouling, batch-to-batch reproducibility, storage stability, scalability, and cost-effectiveness. Representative examples show that the most useful advances arise not simply from lowering the limit of detection but from improving structure–function understanding and translating interfacial design into robust analytical performance. Future work should prioritize standardized fabrication and benchmarking protocols, in situ and operando identification of active sites and interface evolution, matrix-specific antifouling validation, multiresidue and metabolite analysis, and hybrid portable devices coupled with intelligent readout. Full article

The coexistence of emulsified oil, dissolved organics, and heavy metal ions in industrial oily wastewater makes one-step treatment highly challenging. Herein, an organic-inorganic co-modified PVDF composite membrane (MTSP) was fabricated via nonsolvent-induced phase separation, with tea polyphenols, SiO₂, and fibrous MXene synergistically incorporated. The resulting membrane exhibited a superhydrophilic/underwater oleophobic surface, with a water contact angle of 1° and an underwater oil contact angle of ~136°, owing to the optimized surface chemistry and hierarchical pore structure. As a result, the MTSP membrane effectively suppressed oil fouling while enabling rapid water transport. At 0.1 bar, the optimized membrane delivered an oil/water separation efficiency of ~99.5% and a high flux of 2420–2670 L·m⁻²·h⁻¹, while maintaining >99% separation efficiency for various emulsified oils, including kerosene, edible oil, n-hexane, and 1,2-dichloroethane. It also showed excellent recyclability and chemical stability, retaining >98–99% efficiency after five cycles and after 24 h exposure to pH 1 and pH 12 conditions. Notably, for complex simulated wastewater containing emulsified kerosene, phenol, and Fe³⁺, Cu²⁺, Zn²⁺, and Cd²⁺, the membrane maintained ~99% oil/water separation efficiency and simultaneously removed ~79% of phenol and 70–86% of heavy metal ions in a single filtration process. The superior performance is attributed to the synergistic effects of the superhydrophilic/underwater-oleophobic membrane surface, hierarchical transport channels enabling rapid water permeation, and multifunctional sites that adsorb/coordinate dissolved pollutants. This work provides a simple, scalable design strategy for PVDF-based membranes that integrate high-flux separation, antifouling performance, and multi-pollutant remediation for the treatment of complex oily wastewater. Full article

In response to the significant challenges posed by ice accumulation and contamination from various fluids in complex operating conditions for metallic materials, this study utilises picosecond laser precision machining to develop a ‘slippery surface’ featuring a micro-channel network structure. The core innovation of this study lies in the use of laser-machined micrometre-scale array textures to overcome the limitations of traditional isolated pores. These globally interconnected micro-channels serve as highly efficient reservoirs and dynamic transport channels for lubricants, significantly enhancing the interfacial capillary locking force of the lubricant. Experimental results demonstrate that this unique network geometry endows the surface with exceptional fluid replenishment and self-healing properties, enabling it to exhibit outstanding broad-spectrum hydrophobicity towards various fluids—including water, crude oil and ethanol (surface tension range: 17.9–72.0 mN m⁻¹)—with sliding angles consistently below 12°, whilst effectively slowing the dehydration and solidification processes of biological fluids. At a low temperature of −15 °C, the surface achieved an ice formation delay of up to 286 s, with an ice adhesion strength of only 33.9 kPa, ensuring that accumulated ice could be spontaneously detached under minimal external force. Furthermore, the micro-channel network structure serves as a key protective mechanism against mechanical wear, maintaining robust slippery properties even after three hours of high-pressure water jet scouring (Weber number of 300). This reliable interface, achieved through structural management, provides an efficient and scalable platform for addressing the all-weather anti-icing and antifouling requirements of outdoor infrastructure. Full article

Activated sludge treatment is plagued by high secondary pollution risks, and ship antifouling paint particles (APPs) as hazardous heavy metal-rich solid wastes generated from hull derusting wastewater, pose severe environmental threats and intractable disposal dilemmas. This study developed a novel pilot-scale activated sludge reduction process coupling APPs-derived carbon-based catalysts with ultrasound-Fe²⁺/peroxydisulfate (PDS) advanced oxidation. Columnar catalysts were fabricated via direct carbonization-molding using waste APPs from an 82,000 deadweight bulk carrier were used as the sole raw material to prepare columnar catalysts via direct carbonization-molding; single-factor and orthogonal experiments optimized process parameters, Scanning Electron Microscopy (SEM), Energy Dispersive Spectroscopy (EDS) and X-ray Photoelectron Spectroscopy (XPS) characterized catalyst and sludge properties, free radical quenching experiments elucidated reaction mechanisms and a 90-day continuous pilot run assessed catalytic stability. The process achieved a 43.5% sludge removal rate under optimal conditions, accompanied by 100% toluene and 92.3% phenolic compound degradation, as well as efficient total phosphorus (TP) and total nitrogen (TN) removal. Mechanistic studies via characterization and quenching experiments confirmed the catalyst enhanced PDS activation through free/non-free radical synergy and accelerated Fe²⁺/Fe³⁺ redox cycling. A 90-day continuous pilot operation demonstrated excellent long-term catalytic stability, with sludge removal rate remaining above 38%. This “waste treating waste” technology realizes high-value APPs resource utilization, provides a low-carbon sludge disposal pathway, and offers a scalable solution for collaborative pollution control in the wastewater treatment and shipping industries. Full article

Acrylate-based self-polishing copolymer antifouling paint particles (SPC-APPs) are persistent micropollutants that act as carriers for biocidal heavy metals, posing significant ecological hazards to aquatic ecosystems. Despite their toxicity, the occurrence, characterization, and metal-leaching risks of SPC-APPs in estuarine environments remain largely understudied. This study investigated the contamination characteristics of SPC-APPs in surface sediments from the Yangtze River Estuary, a hotspot of shipping activity. A multi-technique analytical protocol was employed, combining density separation with scanning electron microscopy–energy-dispersive spectroscopy (SEM-EDS), inductively coupled plasma mass spectrometry (ICP-MS), and pyrolysis–gas chromatography/mass spectrometry (Py-GC/MS) to characterize the morphology, quantify particle abundance, and assess the correlation between SPC-APPs and sedimentary heavy metals. SPC-APPs were ubiquitously detected across all sampling sites, with abundances ranging from (0.82 ± 0.15) × 10³ to (3.65 ± 0.42) × 10³ particles g⁻¹ dry sediment. A distinct distribution property (South Branch > North Branch > offshore shoal) was identified, primarily driven by shipping density and hydrodynamic sorting. Morphologically, particles exhibited irregular, abraded surfaces, with EDS confirming Cu (1.76~5.63 wt%) and Zn (0.27~3.65 wt%) as major metallic components. Py-GC/MS analysis identified specific mass fragments (m/z 41, 69, 87) as diagnostic markers. Strong positive correlations were observed between SPC-APP abundance and sediment Cu (r = 0.82, p < 0.01) and Zn (r = 0.76, p < 0.01) concentrations, indicating that these particles are a primary source of metal contamination. Ecological risk assessment based on sediment quality benchmarks showed that Cu in the South Branch reached 82~91% of the probable effect concentration (PEC), highlighting potential risks to benthic organisms. This study provides critical baseline data on the distribution and speciation of SPC-APPs, underscoring their role as vectors for toxic metals and the need for targeted pollution control in high-shipping-intensity estuarine regions. Full article

Polysulfone (PSU) membranes are widely recognized for their thermal stability, mechanical strength, and chemical resistance, making them suitable for diverse separation applications. This review highlights recent advances in PSU membrane development, focusing on fabrication techniques, structural modifications, and emerging applications. Phase inversion remains the predominant method for membrane synthesis, allowing precise control over morphology and performance. Functional enhancements through blending, chemical grafting, and incorporation of nanomaterials—such as metal–organic frameworks (MOFs), carbon nanotubes, and zwitterionic polymers—have significantly improved gas separation, and water purification., In gas separation, PSU-based mixed matrix membranes demonstrate enhanced CO₂/CH₄ selectivity, particularly when integrated with MOFs like ZIF-7 and ZIF-8. In water treatment, PSU membranes effectively remove algal toxins and heavy metals, with surface modifications improving hydrophilicity and antifouling properties. Despite these advancements, challenges remain in optimizing cross-linking strategies and understanding structure–property relationships. This review provides a comprehensive overview of PSU membrane technologies and outlines future directions for their development in sustainable and high-performance separation systems. Full article

Industrial heat exchangers are widely used in industries such as petrochemicals, energy and power, and food processing, making them one of the most important pieces of heat and mass transfer equipment in industry. During operation, a layer of fouling often adheres to the heat transfer surfaces, which reduces the heat transfer coefficient of the equipment and increases the thermal resistance of the surfaces. Additionally, fouling can corrode the material of the heat transfer surfaces, compromise their integrity, and even lead to perforations and leaks, severely impacting equipment operation and safety while increasing energy consumption and costs for enterprises. The application of anti-fouling coatings on surfaces is a key technology to address fouling on heat transfer surfaces. This paper focuses on introducing major types of anti-fouling coatings, including polymer-based coatings, “metal material + X”-type coatings, “inorganic material + X”-type coatings, carbon-based material coatings, and other varieties. It analyzes and discusses the current research status and hotspots for these coatings, elaborates on their future development directions, and proposes ideas for developing new coating systems. On the other hand, this paper summarizes the current research on the main factors—surface roughness, surface free energy, surface wettability, and coating corrosion resistance—that affect the anti-fouling performance of coatings. It outlines the research hotspots and challenges in understanding the influence of these three factors and suggests that future research should consider the synergistic effects of multiple factors, providing valuable insights for further studies in the field of anti-fouling coatings. Full article

This work presents a detailed analysis of polysulfone (PSF) based mixed matrix membranes (MMMs) modified with NiMOF@MGO for water purification. Magnetic iron oxide nanoparticles were synthesized and incorporated into the NiMOF@GO framework, with successful formation confirmed by FT-IR, XRD, BET, TGA, and SEM analyses. Membranes were prepared via phase inversion and modified with varying NiMOF@MGO contents. SEM, AFM, and contact angle analyses demonstrated enhanced membrane hydrophilicity with increasing MOF concentration, reducing the contact angle from 59.74° (0.05 wt%) to 49.70° (0.2 wt%). The highest flux of 117.85 L/m²·h was observed for the PMM-0.2 membrane. Heavy metal removal was most efficient at pH 6, with the PMM-0.1 membrane achieving 95.97% and 95.92% rejection for Pb²⁺ and Cu²⁺, respectively. In oil-water separation, PMM-0.1 exhibited optimal performance, with a water flux of 45.84 L/m²·h. Antifouling tests showed the PMM-0.2 membrane had the highest flux recovery of 85.97%, indicating improved fouling resistance. Overall, incorporation of NiMOF@MGO significantly enhanced membrane hydrophilicity, flux, selectivity and antifouling performance, demonstrating its potential for advanced water purification applications. Full article

Background: Copper nanoparticles (CuNPs) are promising antibacterial agents, but instability and heterogeneity in ‘green’ routes limit translation. Methods: We developed a one-step synthesis in which pre-polymerized polycatechin acts as both reductant and capping agent to form copper–polycatechin core–shell nanoparticles (Cu@polycat). Physicochemical properties (TEM/DLS/XRD/FTIR/ζ), colloidal stability (pH, salt, serum), ion release, and antibacterial activity against planktonic and biofilm E. coli/S. aureus were evaluated. Results: Cu@polycat featured a ~21.5 nm metallic core and ~45 nm hydrodynamic diameter (shell ≈ 12 nm, estimated from TEM–DLS) with ζ ≈ −34 mV, conferring high stability across physiological conditions. Cu@polycat outperformed uncoated CuNPs, displaying 8-fold lower MICs and rapid bactericidal kinetics (>5-log10 in 6–8 h). Synergy between the copper core and polycatechin corona was confirmed (FICI ≈ 0.08). Cu@polycat inhibited biofilm formation by >80% and reduced viable counts in 24 h mature biofilms by ≥3-log10, whereas ampicillin was ineffective under the same biofilm conditions. Conclusions: A polycatechin-based green route furnishes a stable, synergistic nano-antibacterial platform with potent anti-biofilm activity, supporting development for wound-care and anti-fouling device coatings. Full article

Electro-Fenton (EF) technology holds significant promise for degrading recalcitrant organic pollutants. Still, it faces distinct challenges in high-pollutant-load wastewater, including insufficient radical generation, electrode passivation, and mass transfer limitations. This review systematically organizes recent advances in material design and operational strategies to address these issues. We highlight innovative cathode materials (e.g., graphene-based structures, carbon nanotubes, and metal–organic frameworks), stable anodes such as boron-doped diamond, and catalysts tailored for harsh conditions. Key operational improvements are discussed, including pH adaptability, current density optimization, and oxygen supply enhancement. The integration of hybrid systems, such as bio-electro-Fenton and photo-electro-Fenton, is also examined. Looking forward, future research for treating high-pollutant load wastewater should focus on: (1) Developing electrodes and catalysts with superior antifouling properties and long-term stability in high-strength, complex wastewaters; (2) Constructing intelligent control systems capable of real-time response to water quality fluctuations for adaptive parameter optimization; (3) Exploring energy-efficient, self-sustaining EF systems coupled with renewable energy sources or incorporating energy recovery units. This review aims to provide a comprehensive reference for subsequent research endeavors and practical applications related to the treatment technology of EF systems in high-pollutant-load wastewater contexts. Full article

Tryptophan (Trp) and tryptamine (Tryp), critical biomarkers in mood regulation, immune function, and metabolic homeostasis, are increasingly recognized for their roles in both oral and systemic pathologies, including neurodegenerative disorders, cancers, and inflammatory conditions. Their rapid, sensitive detection in biofluids such as saliva—a non-invasive, real-time diagnostic medium—offers transformative potential for early disease identification and personalized health monitoring. This review synthesizes advancements in electrochemical sensor technologies tailored for Trp and Tryp quantification, emphasizing their clinical relevance in diagnosing conditions like oral squamous cell carcinoma (OSCC), Alzheimer’s disease (AD), and breast cancer, where dysregulated Trp metabolism reflects immune dysfunction or tumor progression. Electrochemical platforms have overcome the limitations of conventional techniques (e.g., enzyme-linked immunosorbent assays (ELISA) and mass spectrometry) by integrating innovative nanomaterials and smart engineering strategies. Carbon-based architectures, such as graphene (Gr) and carbon nanotubes (CNTs) functionalized with metal nanoparticles (Ni and Co) or nitrogen dopants, amplify electron transfer kinetics and catalytic activity, achieving sub-nanomolar detection limits. Synergies between doping and advanced functionalization—via aptamers (Apt), molecularly imprinted polymers (MIPs), or metal-oxide hybrids—impart exceptional selectivity, enabling the precise discrimination of Trp and Tryp in complex matrices like saliva. Mechanistically, redox reactions at the indole ring are optimized through tailored electrode interfaces, which enhance reaction kinetics and stability over repeated cycles. Translational strides include 3D-printed microfluidics and wearable sensors for continuous intraoral health surveillance, demonstrating clinical utility in detecting elevated Trp levels in OSCC and breast cancer. These platforms align with point-of-care (POC) needs through rapid response times, minimal fouling, and compatibility with scalable fabrication. However, challenges persist in standardizing saliva collection, mitigating matrix interference, and validating biomarkers across diverse populations. Emerging solutions, such as AI-driven analytics and antifouling coatings, coupled with interdisciplinary efforts to refine device integration and manufacturing, are critical to bridging these gaps. By harmonizing material innovation with clinical insights, electrochemical sensors promise to revolutionize precision medicine, offering cost-effective, real-time diagnostics for both localized oral pathologies and systemic diseases. As the field advances, addressing stability and scalability barriers will unlock the full potential of these technologies, transforming them into indispensable tools for early intervention and tailored therapeutic monitoring in global healthcare. Full article

The efficient removal of emulsified oil and trace organic pollutants via forward osmosis (FO) technology remains challenging due to limited water flux and membrane fouling. In this study, a series of metal oxide-modified PES-based composite FO membranes were fabricated and systematically evaluated to compare the effects of ZnO, Al₂O₃, and CuO nanoparticles on membrane structure and separation performance. The results demonstrated that the membrane modified with 0.04 g of ZnO nanoparticles achieved optimal synergy in terms of hydrophilicity, surface charge, and pore structure. The pure water flux increased from 5.48 L·m⁻²·h⁻¹ for the pristine membrane to 18.5 L·m⁻²·h⁻¹ for the ZnO-modified membrane, exhibiting a 237.5% increase in pure water flux compared to the pristine PES membrane, an oil rejection rate exceeding 97%, and over 95% rejection of typical negatively charged trace organic pollutants such as ibuprofen and tetracycline. Moreover, the ZnO-modified membrane showed excellent antifouling performance and structural stability in various organic solvent systems. This study not only optimized the interfacial chemistry and microstructure of the FO membrane but also enhanced pollutant repellence and the self-cleaning capability through increased hydrophilicity and surface negative charge density. These findings highlight the significant potential of ZnO modification for enhancing the overall performance of FO membranes and provide an effective strategy for developing high-performance, broadly applicable FO membranes for complex water purification. Full article

Urushiol, the principal bioactive component of natural lacquer, has emerged as a promising candidate for developing eco-friendly antimicrobial coatings due to its unique catechol structure and long alkyl chains. This review systematically elucidates the molecular mechanisms underpinning urushiol’s broad-spectrum antimicrobial activity, including membrane disruption via hydrophobic interactions, oxidative stress induction through redox-active phenolic groups, and enzyme inhibition via hydrogen bonding. Recent advances in urushiol-based composite systems—such as metal coordination networks, organic–inorganic hybrids, and stimuli-responsive platforms—are critically analyzed, highlighting their enhanced antibacterial performance, environmental durability, and self-healing capabilities. Case studies demonstrate that urushiol derivatives achieve >99% inhibition against both Gram-positive and Gram-negative pathogens, outperforming conventional agents like silver ions and quaternary ammonium salts. Despite progress, challenges persist in balancing antimicrobial efficacy, mechanical stability, and biosafety for real-world applications. Future research directions emphasize precision molecular engineering, synergistic multi-target strategies, and lifecycle toxicity assessments to advance urushiol coatings in medical devices, marine antifouling, and antiviral surfaces. This work provides a comprehensive framework for harnessing natural phenolic compounds in next-generation sustainable antimicrobial materials. Full article