Search Results (48)

High-performance polyethersulfone (PES) ultrafiltration membranes integrating antibacterial activity and antifouling performance were fabricated via the in situ construction of bimetallic polyphenol networks (BMPNs) throughout the membrane architecture. Tannic acid (TA) functioned as a multifunctional molecular bridge, functionalizing silver metal–organic frameworks (Ag-MOFs) to yield hydrophilic T-Ag-MOFs and chelating Fe³⁺ ions from the coagulation bath to form a polyphenol network during phase inversion. T-Ag-MOF incorporation generated asymmetric morphologies featuring highly porous surfaces and sponge-like cross-sections, improving pure water permeability, mechanical integrity, and bovine serum albumin (BSA) rejection. TA-mediated functionalization increased hydrophilicity, imparted a negative surface charge, suppressed nonspecific protein adhesion, and enhanced flux recovery with low irreversible fouling. At an optimal loading of 0.4 wt%, the resultant T-Ag-MOF/Fe³⁺/PES composite membrane achieved a pure water permeability of 593.4 L m⁻² h⁻¹ bar⁻¹—1.77-fold higher than that of the pristine PES control—while sustaining a BSA rejection of 96.5%. Notably, interfacial compatibility between the T-Ag-MOFs and PES matrix was enhanced, facilitating strong, covalent-like filler–matrix adhesion. Moreover, the composite membrane delivered synergistic multifunctionality, including exceptional long-term aqueous stability, precisely tuned Ag⁺ release kinetics, and potent antibacterial activity, as evidenced by negligible uncontrolled ion leaching and a lack of structural degradation under prolonged hydration. Full article

Owing to its inherent electrical conductivity, reversible redox activity, and structural versatility, polypyrrole (PPy) has become an important material for advanced functional coatings. This review summarizes recent advances in PPy-based coatings, systematically exploring the correlation between fundamental material design and macroscopic multifunctional applications. First, the core structural characteristics of PPy and its primary fabrication strategies, including electrochemical deposition, chemical oxidative polymerization, solution processing, and hybrid composite engineering, are delineated. Subsequently, the role of PPy in surface protection is analyzed, with an emphasis on the synergistic mechanisms underlying corrosion mitigation, mechanical durability, and environmental barriers (e.g., anti-fouling and solar-driven desalination). In addition, the application expansion of PPy in emerging fields, such as electromagnetic interference (EMI) shielding, highly sensitive smart sensing, electroactive energy interfaces, and advanced biomedical electrodes, is summarized. Finally, current challenges—particularly the physicochemical trade-offs among conductivity, interfacial adhesion, and long-term stability—are discussed, and future development directions are prospected. By integrating green processing technologies and data-driven smart system integration, next-generation PPy coatings are expected to meet the demands of flexible electronics, sustainable energy, and precision medicine. Full article

Biomarker detection demands low cost, rapid turnaround, interference resistance, and wide dynamic range. However, traditional immunoassays and nucleic acid amplification methods remain constrained by complex matrices, batch stability, and portability limitations. Molecularly imprinted polymers (MIPs) exhibit “artificial antibody”-like specific recognition and high stability, while nanomaterials (NMs), depending on their composition, structure, and interfacial organization, can provide conductive pathways, catalytic activity, high-density loading sites, or mass-transfer-favorable architectures. Electrochemical biosensors synergistically constructed from these two components achieve complementary functions in recognition, mass transfer, and signal transduction. This paper systematically reviews key strategies and mechanisms for NM–MIP synergistic construction, focusing on six synergistic strategies that target key bottlenecks in mass transfer, signal generation, and interfacial stability: dynamic response regulation, hierarchical structural engineering, anti-fouling interfaces, multi-signal cross-validation, catalytic–recognition integration, and interfacial binding regulation. Representative biomarker cases are analyzed to illustrate how functional modules can coordinate across sample processing, signal generation, and recognition confirmation to improve analytical reliability and overall sensing performance. Finally, the review discusses challenges in clinical translation, including consistent manufacturing, matrix interference, long-term stability, and standardized validation, while outlining future directions toward mechanism-guided imprint design, intelligent data-assisted optimization, and integration with microfluidic and wearable platforms for multiplexed biomarker detection. 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

Clean water remains a pressing global challenge and developing membranes that are both efficient and durable is critical. This study combined two polymers, polyethersulfone (PES) and sulfone-modified polysulfone (SPSf), with NiFe-layered double hydroxides (LDHs) to create a new class of multifunctional membranes. The membranes were characterized using FTIR, SEM, water contact angle, and zeta potential. The addition of NiFe-LDH fillers improved the hydrophilicity and surface structure of the membranes and enhanced the separation performance of the resulting membranes. The best-performing membrane (M3, with 2 wt.% NiFe-LDH) delivered pure water flux of about 218 L.m⁻²h⁻¹, which was nearly three times higher than that of the pristine PES/SPSf membrane. Furthermore, M3 removed approximately 92.4% of bovine serum albumin (BSA), attributed to the synergistic combination of size exclusion, electrostatic repulsion, and hydrophilicity. The membrane also showed excellent antifouling properties, maintaining over 65.9% and 71.2% flux recovery after three fouling–cleaning cycles for BSA solution and surface water, respectively. Importantly, the M3 membrane achieved high removal efficiencies for heavy metals, rejecting 91% of Cd²⁺, 93% of Pb²⁺, and 88% of Cu²⁺. These results highlight how the synergy between PES/SPSf and NiFe-LDH can overcome the common challenges of fouling and low metal ion rejection, offering a promising route toward practical and sustainable water treatment solutions. Full article

In this study, we aimed to develop a high-performance, anti-fouling ultrafiltration membrane by integrating photocatalytic and Fenton-like functions into a polymer matrix, in order to address the critical challenge of membrane fouling and achieve simultaneous separation and degradation of organic pollutants. To this end, a novel Fe-V_O-TiO₂-embedded polyethersulfone (PES) composite membrane was designed and fabricated using a facile phase inversion method. The key innovation lies in the incorporation of Fe-V_O-TiO₂ nanoparticles containing abundant bulk-phase single-electron-trapped oxygen vacancies, which not only modulate membrane morphology and hydrophilicity but also enable sustained generation of reactive oxygen species for the pollutant degradation under light irradiation and H₂O₂. The optimized Fe-V_O-TiO₂-PES-0.04 membrane exhibited a significantly enhanced pure water flux of 222.6 L·m⁻²·h⁻¹ (2.2 times higher than the pure PES membrane) while maintaining a high bovine serum albumin (BSA) retention of 93% and an improved hydrophilic surface. More importantly, the membrane demonstrated efficient and stable synergistic Photocatalytic-Fenton activity, achieving 82% degradation of norfloxacin (NOR) and retaining 75% efficiency after eight consecutive cycles. A key finding is the membrane’s Photocatalytic-Fenton-assisted self-cleaning capability, with an 80% flux recovery after methylene blue (MB) fouling, which was attributed to in situ reactive oxygen species (·OH) generation (verified by ESR). This work provides a feasible strategy for designing multifunctional membranes with enhanced antifouling performance and extended service life through built-in catalytic self-cleaning. Full article

Microplastics (MPs) and Antifouling Paint Particles (APPs) are pervasive anthropogenic pollutants that threaten global ecosystems, with distinct yet overlapping environmental behaviors and toxic impacts. MPs disperse widely in aquatic systems via runoff and wastewater; their toxicity stems from physical, chemical, and synergistic effects. APPs are concentrated in coastal zones, estuaries, and shipyard areas, and are acutely toxic due to their high metal and biocide content. This study systematically characterized the composition, concentration, and size distribution of common MPs and APPs in ship-hull derusting wastewater produced by ultra-high-pressure water jetting, using pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS) coupled with particle size analysis. The wastewater exhibited a total suspended solids (TSS) concentration of 20.04 g·L⁻¹, within which six types of MPs were identified at 3.29 mg·L⁻¹ in total and APPs were quantified at 330.25 mg·L⁻¹, representing 1.65% of TSS. The residual fraction primarily consisted of algae, biological debris, and inorganic particles. Particle size distribution ranged from 3.55 to 111.47 μm, with a median size (D50) of 31 μm, while APPs were mainly 5–100 μm, with 81.4% < 50 μm. Extrapolation to the annual treated ship-hull surface area in 2024 indicated the generation of ~57,440 m³ wastewater containing ~0.2 tons of MPs and ~19 tons of APPs. These findings highlight the magnitude of pollutant release from ship maintenance activities and underscore the urgent need for targeted treatment technologies and regulatory policies to mitigate microplastic pollution in marine environments. Full article

Scaling and thermal loss on the surfaces of industrial equipment and pipelines usually lead to increased energy consumption and reduced operational efficiency. To solve these severe problems, developing advanced coatings with the dual functions of scale resistance and thermal insulation is an effective approach. Inspired by the antifouling agents released from corals and the thermal insulation of goose down, we herein have developed a bioinspired hollow silica microsphere-based (BHSM) coating, exhibiting the synergistic effect of anti-scaling and thermal insulation properties. The BHSM coating is composed of aluminum phosphate (AP) as an inorganic adhesive and scale inhibitor, and hollow silica microspheres (HSMs) as a thermal insulator. In brief, the effective anti-scaling capability comes from released phosphate ions of AP adhesive for chelating with mineral ions, while the high thermal insulation results from the internal air of the HSMs. Compared to the stainless steel (SS 304), the BHSM coating exhibited ~86% scale reduction. Furthermore, the extremely low thermal conductivity of the HSMs endows the BHSM coating with excellent thermal insulation, resulting in a 20% reduction in heat loss relative to the SS 304 surface. Thus, this work presents a promising strategy for anti-scaling and thermal insulation in industrial equipment and pipelines. 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

Marine biofouling presents a persistent challenge for maritime industries, necessitating the development of eco-friendly and intelligent antifouling strategies. In this work, an ATP-responsive nanocontainer was developed by encapsulating a natural organic compound (CS106-10), isolated from Talaromyces trachyspermus in cold seep sediments, together with D-phenylalanine (D-Phe) into ZIF-90 nanoparticles (D-Phe/CS106-10@ZIF-90). These nanoparticles were incorporated into zinc acrylate resin to fabricate a novel self-polishing antifouling coating. CS106-10, as a natural antifoulant, provided efficient and environmentally sustainable bactericidal activity, while D-Phe acted as a synergistic adjuvant to inhibit and disrupt biofilm formation. More importantly, the ATP-responsive ZIF-90 framework enabled controlled, on-demand release of antifouling agents in response to local metabolic signals associated with biofilm growth. Laboratory and real-sea evaluations confirmed that the composite coating effectively suppressed biofilm formation and significantly reduced the required dosage of conventional toxic antifoulants. This study integrates a natural antifoulant with an ATP-responsive metal–organic framework, providing new insight for developing antifouling coatings. Full article

In recent years, polymer-mediated signal amplification has drawn wide attention in bioelectronic sensing. With the rapid progress of biosensing and flexible electronics, polymers with excellent electron–ion transport properties, tunable molecular structures, and good biocompatibility have become essential materials for enhancing detection sensitivity and interfacial stability. However, current sensing systems still face challenges such as signal attenuation, surface fouling, and multi-component interference in complex biological environments, limiting their use in medical diagnosis and environmental monitoring. This review summarizes the progress of conductive polymers, molecularly imprinted polymers, hydrogels, and composite polymers in medical diagnosis, food safety, and environmental monitoring, focusing on their signal amplification mechanisms and structural optimization strategies in electronic transport regulation, molecular recognition enhancement, and antifouling interface design. Overall, polymers improve detection performance through interfacial electronic reconstruction and multidimensional synergistic amplification, offering new ideas for developing highly sensitive, stable, and intelligent biosensors. In the future, polymer-based amplification systems are expected to expand in multi-parameter integrated detection, long-term wearable monitoring, and in situ analysis of complex samples, providing new approaches to precision medicine and sustainable environmental health monitoring. 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

Architectural exterior wall coatings require a balance of elasticity, stain resistance, and durability. Although nano-SiO₂ enhances fracture resistance in elastic coatings, its limited hydrophobicity allows pollutant adhesion. Nano-TiO₂ can photocatalytically degrade organics but is often encapsulated by the polymer matrix, reducing its effectiveness. This study introduces a SiO₂-TiO₂ composite topcoat applied via aqueous dispersion to overcome these limitations. Experimental results demonstrate that the composite coating significantly outperforms single-component modifications, improving stain resistance by 21.3% after 12 months of outdoor exposure. The surface remains brighter with markedly reduced pollutant accumulation. Mechanistically, SiO₂ serves as an inert mesoporous carrier that improves the dispersion and photostability of TiO₂, minimizing agglomeration and photocorrosion. Its inherent hardness and hydrophobicity reduce physical adsorption sites. Together, SiO₂ and TiO₂ create a nanoscale rough surface that enhances hydrophobicity through a lotus-like effect. Under UV irradiation, TiO₂ generates radicals that decompose organic pollutants and inhibit microbial growth, enabling efficient self-cleaning with rainwater. This synergistic mechanism addresses the limitations of individual nanoparticles, successfully integrating elasticity with long-term anti-fouling and durability. This composite demonstrates a significant advancement in stain resistance and overall durability, offering potential applications in energy-efficient and environmentally sustainable building technologies. Full article

Chitosan biopolymer membranes reinforced with channel-selective ZIF-8 nanofillers were developed and thoroughly characterized as separators for bioelectrochemical systems. This study explores the synergistic effect of incorporating ZIF-8 into a chitosan matrix to enhance membrane performance. Key properties including water retention, chemical and thermal stability, surface resistance, antifouling capacity, and ionic conductivity were evaluated and benchmarked against commercial Nafion-117 and nanofiltration (NF) membranes. The ZIF-8/chitosan composite membranes (ZIF-8/CS) demonstrated excellent water retention and structural stability under harsh conditions, along with significantly reduced surface resistance and effective rejection of organic contaminants and salts (NaCl, Na₂SO₄). Notably, the composite ZIF-8/CS membranes achieved an ionic conductivity of 0.099 S/cm, approaching the value of Nafion-117 (0.13 S/cm) and substantially surpassing that of the NF membrane (0.013 S/cm). These results indicate that ZIF-8-reinforced chitosan membranes present a promising, sustainable, and cost-effective alternative to traditional separators in bioelectrochemical applications. Full article

The inherent hydrophobicity of poly(vinylidene fluoride) (PVDF) ultrafiltration membranes leads to severe membrane fouling when processing proteinaceous solutions and organic contaminants, significantly limiting their practical applications. This study presents a novel metal-ion mediated co-deposition strategy for fabricating high-performance antifouling poly(vinylidene fluoride) (PVDF) hollow fiber ultrafiltration membranes. Through Zn²⁺ coordination-driven self-assembly, a uniform and stable composite coating of dopamine (DA), tannic acid (TA), and ZIF-8 nanoparticles was successfully constructed on the membrane surface under mild conditions. The modified membrane exhibited significantly enhanced hydrophilicity, with a water contact angle of 21° and zeta potential of −29.68 mV, facilitating the formation of a dense hydration layer that effectively prevented protein adhesion. The membrane demonstrated exceptional separation performance, achieving a pure water permeability of 771 L/(m²∙h∙bar) and bovine serum albumin (BSA) rejection of 97.7%. Furthermore, it showed outstanding antifouling capability with flux recovery rates exceeding 83.6%, 74.7%, and 71.5% after fouling by BSA, lysozyme, and ovalbumin, respectively. xDLVO analysis revealed substantially increased interfacial free energy and stronger repulsive interactions between the modified surface and protein foulants. The antifouling mechanism was attributed to the synergistic effects of hydration layer formation, optimized pore structure, additional water transport pathways from ZIF-8 incorporation, and electrostatic repulsion from negatively charged surface groups. This work provides valuable insights into the rational design of high-performance antifouling membranes for sustainable water treatment and protein separation applications. Full article