Search Results (3,439)

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

As a green energy technology, triboelectric nanogenerators (TENGs) convert mechanical energy into electricity and have gained significant attention in response to growing global environmental concerns. However, the widespread use of petroleum-based polymers as triboelectric materials in high-performance TENGs raises concerns over plastic pollution. In this work, we report a high-performance biodegradable TENG utilizing chitosan/laser-induced graphene (LIG) composite films as triboelectric layers. Modified chitosan substrates were first converted into LIGs via a convenient one-step CO₂ laser engraving, subsequently incorporated into chitosan matrices to form homogeneous composite films. A TENG device was designed by pairing the LIG/chitosan composite film with the fluorinated ethylene propylene (FEP) film, and copper electrodes. The introduction of LIG effectively strengthens charge storage and dielectric properties of the chitosan matrix, thereby significantly boosting the triboelectric output performance. Experimental results demonstrate that the as-assembled TENG with an LIG concentration of 1 wt.% achieves a peak open-circuit voltage of 196 V and short-circuit current of 2.1 μA, with a maximum power density of 295 mW/m². It can drive LED lights and small low-power electronic devices. Furthermore, the designed TENG device exhibits good biodegradability, flexibility, and stability, serving as a self-powered sensor for monitoring human joint movements. This work provides a simple and scalable strategy for integrating laser-induced graphene with biomass-based polymers, offering new insights into the design of high-performance, biobased triboelectric materials. Full article

Constructing efficient conductive networks in flexible polymer matrices remains a central challenge in electromagnetic interference (EMI) shielding material design. In this work, a ‘point-line’ hybrid filler system combining conductive carbon black (CB) and multi-walled carbon nanotubes (MWCNTs) was incorporated into a silicone rubber matrix to systematically engineer the conductive network architecture. By optimising the CB/MWCNT blending ratio, a composite with a tensile strength of 8.5 MPa, elongation at break of 180%, and EMI shielding effectiveness of 50 dB was achieved at a 1:1 weight ratio. Further surface modification of the hybrid fillers using five surfactants, including sodium dodecylbenzene sulfonate (SDBS), cetyltrimethylammonium bromide (CTAB), polyvinylpyrrolidone (PVP), nonylphenol ethoxylate (NPEO), and octylphenol ethoxylate (OPEO), was systematically investigated. OPEO modification was proved the most effective, improving EMI shielding performance to 58 dB while enhancing tensile strength by 11.8% and elongation at break by 50%. These results demonstrate that rational filler hybridisation combined with targeted surfactant modification offers a practical and scalable route to high-performance flexible EMI shielding composites. Full article

Aramid fiber is a high-performance fiber with excellent mechanical properties, heat resistance, and corrosion resistance. Its exceptional shear and fatigue properties make it a promising material for civil engineering applications. This study summarizes the basic properties and current development of aramid fiber, as well as the applications of aramid fiber and its composites in civil engineering, including aramid fiber-reinforced composite (AFRP)-concrete/steel composite structures, AFRP rebars, and AFRP rock anchors. The results indicate that the poor interfacial bonding performance between aramid fibers and the resin matrix is the primary bottleneck restricting the application of AFRP composites in civil engineering. Consequently, developing a continuous surface treatment method suitable for industrial-scale production remains a key challenge for the widespread adoption of these composites. Furthermore, in certain specific working conditions and environments—such as seismic retrofitting of rectangular concrete columns, impact/explosion resistance reinforcement, and rock anchoring—AFRPs show the potential to replace traditional inorganic fiber-reinforced polymer composites. However, systematic investigation into the fundamental mechanical properties and long-term service performance of AFRP is still required prior to their practical application. Full article

Developing membranes with superior antifouling properties is crucial for efficient and sustainable water treatment. In this study, polysulfone (PSM) composite membranes were fabricated by incorporating hydroxylated titanium nanotubes (TNT@OH) via the non-solvent-induced phase separation method. The hydroxylation of TNTs enhanced their dispersion in the polymer matrix and promoted strong polymer–nanoparticle interactions. Comprehensive characterization using FTIR, XRD, TGA, FESEM, and AFM confirmed the successful integration of TNT@OH, resulting in membranes with improved hydrophilicity, porosity, and thermal stability. The contact angle decreased from ~88° for neat PSM to ~50° at 7 wt% TNT@OH, while surface free energy increased significantly. Mechanical strength and flexibility were also enhanced at optimal TNT@OH loadings (3–5 wt%), owing to uniform dispersion and strong interfacial bonding. Filtration experiments using humic acid (HA) and natural organic matter (NOM) demonstrated remarkable improvements in water flux, rejection efficiency, and fouling resistance. The composite membranes achieved HA rejection rates of up to 98%, with reduced irreversible fouling and higher flux recovery ratios across multiple filtration–cleaning cycles. The proposed antifouling mechanism is attributed to the formation of a stable hydration layer by surface hydroxyl groups, which prevents foulant adhesion and facilitates cleaning. These findings suggest that incorporating TNT@OH into polysulfone membranes is a promising approach for developing high-performance ultrafiltration membranes with enhanced permeability, mechanical robustness, and long-term antifouling stability, thereby making them suitable for advanced water purification applications. Full article

High-efficiency energy storage technologies have become particularly crucial with the ever-increasing demand for energy in recent years. Research on polymer nanocomposite dielectric materials has emerged as a prominent focus. Particularly, there is an urgent demand for the development of advanced dielectric film materials that exhibit superior energy storage performance over a wide temperature range. To this end, this study aims to investigate the effect of the molecular weight of reduced polyaniline (R-PANI) on the dielectric properties of all-organic composite films based on high-temperature-resistant polyetherimide (PEI). All-organic R-PANI/PEI composite films were fabricated by blending PEI matrix with R-PANI of varying molecular weights. Through combined density functional theory (DFT) calculations and experimental measurements, the blocking mechanism of R-PANI on charge carrier migration within the composite films was elucidated, showing a significant enhancement in the discharge energy density of PEI polymers while maintaining high charge–discharge efficiency. With charge–discharge efficiency maintained above 95%, R-PANI3/PEI achieved a discharge energy density of 2.36 J cm⁻³ at room temperature, nearly double that of pristine PEI (1.2 J cm⁻³). At 150 °C, the 1.0 wt% R-PANI3/PEI composite film retained a discharge energy density of 2.27 J cm⁻³ with a charge–discharge efficiency of 89.2%, outperforming pure PEI (1.1 J cm⁻³, 85.1%). These findings provide a new strategy for the design of all-organic composite dielectric films and demonstrate the potential of R-PANI in the application of high-performance capacitors and electrical energy storage. Full article

Due to the widespread use of microwave electromagnetic radiation, this study examines the microwave electromagnetic properties and compressive strength of composites made from inexpensive components such as Mg_0.5Zn_0.5Fe₂O₄, polystyrene, and activated carbon. Experimental samples were fabricated using thermopressing. The formation of the dielectric core/shell structure for Mg-Zn/polystyrene composites (1:1) and composites with activated carbon additives at weight concentrations of 3, 6.6, and 9.0% was determined using SEM image analysis. Microwave properties were investigated by analyzing the frequency dependences of complex permittivity and magnetic permeability in the frequency range of 100 MHz–5 GHz. As shown by the simulation and experimental measurements of scattering parameters obtained, the compost shows improved microwave absorption properties in the frequency range of 1–5 GHz. Reflection loss spectra showed peaks with values of −17.8 and −18 dB in the frequency range of 2.5–5 GHz for samples with 4.8 wt. % and 6.6 wt. % carbon loading, respectively. The absorption bandwidths of −10 dB in the range of 1.7–2.13 GHz were observed in the best samples. Studies have shown that samples containing 9.0 wt. % of carbon material with thicknesses of 6–10 mm can be considered as an electromagnetic shielding material in the microwave range 1–5 GHz. It was shown that, despite a decrease in porosity from 15.59 to 7.17%, with an increase in the concentration of carbon material in the composites, the compressive strength also decreases from 62.05 to 36.45 MPa. The developed composites are potentially suitable as microwave absorbers for civil applications. Full article

Superhydrophobic coatings are regarded as a promising passive anti-icing strategy; however, their practical engineering application, particularly in electrical insulation, is severely hindered by the performance deterioration caused by mechanical damage and a lack of theoretical understanding of microscopic ice adhesion mechanisms. In this study, a layered polymer composite coating was designed to resolve the trade-off between abrasion resistance and low ice adhesion. The chemistry of the coating relies on a synergistic “primer–topcoat” design: the primer consists of an epoxy resin matrix chemically modified by amino silicone oil to lower its surface energy and improve toughness, while the topcoat features hierarchical SiO₂ clusters functionalized with hexamethyldisilazane (HMDS) and silane coupling agents. This architecture was fabricated via a controllable layer-by-layer spraying method. Systematic investigations revealed that the hierarchical micro/nanostructure, composed of microscale protrusions and nanoscale SiO₂ clusters, provides excellent superhydrophobicity (contact angle of 155.2°, sliding angle of 2°). Crucially, the crosslinked polymer network and stable siloxane (Si-O-Si) covalent bonding ensure that the coating maintains its functionality after a cumulative sand impact of 3 kg, demonstrating superior mechanical durability. Furthermore, differentiated theoretical models for ice adhesion in Cassie–Baxter and Wenzel states were established based on intermolecular interactions, identifying that maintaining a stable Cassie–Baxter state is key to reducing adhesion. This study offers a robust approach to balancing functionality and durability in polymer composites through synergistic structural design, providing both a scalable fabrication strategy and a quantitative theoretical framework for understanding interfacial ice adhesion. Full article

Bone is a hierarchically organized composite material with unique mechanical properties and an intrinsic regenerative capacity that conventional repair strategies, including autografts, allografts, xenografts, and metallic or ceramic implants, fail to fully replicate due to donor scarcity, immunogenicity, mechanical mismatch, and poor long-term integration. Bone tissue engineering (TE) offers a biologically informed alternative by integrating osteoconductive scaffolds, osteogenic progenitor cells, and osteoinductive signaling molecules into a unified regenerative framework. Unlike existing reviews that evaluate these components in isolation, this review provides a mechanistically integrated analysis that repositions scaffold design as a biologically instructive platform whose topography, stiffness, porosity, and surface chemistry collectively govern cell adhesion, mechanotransduction, osteogenic differentiation, and extracellular matrix remodeling. Critically, it moves beyond cataloging materials and fabrication approaches to evaluate how specific scaffold features drive biological outcomes and to identify frequently understated limitations, including polymer-ceramic degradation kinetics and the inadequacy of small-animal models for clinical translation. By synthesizing advances in biomaterials, additive manufacturing, and smart scaffold technologies within this integrative framework, this review provides researchers and clinicians with a structured framework for evaluating emerging strategies and prioritizing future directions in functional bone regeneration. Full article

In this work, a composite solid polymer electrolyte was prepared for anodic bonding encapsulation. The effects of additives on the anodic bonding performance of the composites were investigated. Characterizations including AC impedance and X-ray diffraction show that CeO₂ and TiO₂ particles reduce the crystallinity of the (PEG)₁₂LiClO₄ matrix, thereby improving ionic conductivity and mechanical properties. The composite of (PEG)₁₂LiClO₄ with 5 wt.% CeO₂ and 5 wt.% TiO₂ achieves a room-temperature ionic conductivity of 1.01 × 10⁻⁵ S·cm⁻¹. Anodic bonding tests and interfacial characterization confirm its optimal bonding performance with aluminum. The interfacial tensile strength reaches 4.65 MPa at room temperature, and element migration is observed across the bonding interface. Full article

While carbon fiber-reinforced polymer (CFRP) composites are widely utilized in aerospace applications due to their exceptional specific strength and stiffness, they are inevitably subjected to impact loads during service, which can easily induce internal damage such as delamination. To mitigate these issues, this study investigates the low-velocity impact behavior of an SMA-reinforced CFRP U-shaped structure, emphasizing the critical role of curing-induced residual stresses. A numerical model incorporating the thermal-mechanical manufacturing history was developed and validated against experimental data. Results indicate that while embedded superelastic SMA wires effectively suppress crack propagation and enhance energy absorption, neglecting residual stresses leads to a significant overestimation of structural rigidity and peak loads. Due to the coefficient of thermal expansion mismatch between the SMA wires and the resin matrix, the SMA-CFRP system exhibits higher sensitivity to initial internal stresses than pure CFRP. By accounting for the residual stress field, the relative error in predicted peak force and absorbed energy for the SMA-CFRP model was reduced from 9.3% to 3.5% and 18.9% to 7.8%, respectively. These findings demonstrate that residual stress lowers the failure threshold and is essential for capturing the synergistic effects of SMA phase transformation and matrix damage, providing a more accurate reconstruction of the structural energy balance. Full article

Modern agriculture faces major challenges due to rapid population growth, climate change, and environmental constraints. Advanced polymeric systems for controlled-release fertilizers (CRFs) are essential to address these challenges. Urea is one of the most widely used nitrogen fertilizers; however, its agronomic efficiency is limited by volatilization and losses. In this study, we report a sustainable strategy to encapsulate urea using a matrix derived from industrial sulfur waste and vegetable oil, improving agronomic efficiency while valorizing industrial residues and renewable resources. Through inverse vulcanization, a sponge-like polymer (Bp-SF) was synthesized. Two urea-loaded bio-composites (Bp-SF25U and Bp-SF32U) were also prepared. FT-IR analysis confirmed urea encapsulation and the formation of polymeric structures from sunflower oil. SEM revealed a porous morphology, while contact angle measurements confirmed the hydrophobic nature of the polymer matrix. Release kinetics showed sustained nitrogen release for more than 77 days, reaching approximately 60% cumulative release, governed by diffusion, with a fraction of urea retained within the matrix, potentially enabling prolonged nutrient availability. Pot experiments with maize showed that a lower dose of encapsulated urea (79 mg) produced similar plant growth responses to a higher dose of free urea (92 mg), indicating improved nitrogen use efficiency. These sulfur cross-linked biopolymers represent a promising strategy to enhance urea efficiency while supporting greener fertilization strategies aligned with circular economy principles. Full article

The valorization of agri-food residues represents an attractive strategy within the circular economy for the development of bio-based materials. In this study, a PLA–cellulose biocomposite (PLACEL10) was developed using cellulose extracted from vine pruning residues (Vitis vinifera, Tintilla de Rota). Cellulose was isolated through sequential acid and alkaline treatments, and the extracted material was incorporated into PLA by melt blending to produce injection-molded specimens. FT-IR confirmed the progressive removal of non-cellulosic components during extraction, while SEM revealed a relatively homogeneous dispersion of cellulose within the polymer matrix. Mechanical characterization showed that PLACEL10 exhibited higher stiffness and tensile strength than the processed PLA and BCF10 controls, although with reduced elongation at break. Biocompatibility was evaluated using hFOB 1.19 osteoblasts by MTS assay, showing viability values above 95% and a proliferative response at 72 h. These results suggest that vine-pruning-derived cellulose can act as an effective reinforcement in PLA and support the potential of this agricultural residue as a feedstock for bio-based composites with possible biomedical and packaging applications. Although the current extraction route involves chemical treatments and cannot be considered fully green, the approach provides a promising route for agricultural waste valorization. Full article

In this study, a polyethylene glycol (PEG)-based solid electrolyte composite (PEG)₁₀LiClO₄/NaAlOSiO suitable for anodic bonding packaging was successfully fabricated via a combined ball milling and hot pressing process. The micromorphology, ion transport characteristics, and mechanical packaging properties of the composite were systematically investigated using characterization techniques including electrochemical impedance spectroscopy, X-ray diffraction, scanning electron microscopy, and anodic bonding performance tests. The results demonstrate that doping with NaAlOSiO molecular sieve can effectively reduce the crystallinity of the polymer matrix, construct more efficient carrier transport pathways, and simultaneously enhance the ionic conductivity and mechanical properties of the material. When the mass fraction of NaAlOSiO doping is 8 wt.%, the composite exhibits a room temperature ionic conductivity of up to 1.31 × 10⁻⁵ S·cm⁻¹. Under room temperature and a bonding voltage of 800 V, the sample with this doping ratio achieves the optimal anodic bonding with metallic Al, and the tensile strength of the bonding interface reaches 5.93 MPa, showing excellent application prospects in micro–nano-packaging. Full article

This study investigated the impact of incorporating calcined eggshell and carbon nanotube (CNT) on the properties of polyvinyl alcohol (PVOH) blends. Prior to solution casting, eggshell waste underwent a calcination process and then the samples were prepared via solution cast method. Mechanical properties study revealed a significant enhancement in tensile strength and elongation at break with increasing loads of calcined eggshell and CNT. Higher tensile strength was observed with increasing CNT loading for PVOH blends added with 1 phr and 3 phr calcined eggshell, owing to the reinforcing role of CNT in the composite matrix. In contrast, the tensile strength at 0.3 phr CNT is lower than at 0.2 phr CNT due to CNT agglomeration, which weakens the interfacial adhesion with the PVOH matrix and hinders effective stress transfer during deformation. SEM images depicted well-dispersion and interaction effect of calcined eggshell particles and CNT particles at low loading levels. The good interaction effect between calcined eggshell and PVOH matrix (which both exhibit hydrophilic behaviour) is mainly attributed to the presence of hydrogen bonding in the polymer matrix, as proven in FTIR analysis. XRD analysis revealed significant peaks in the 2θ range of 19° to 21°, suggesting that increased amounts of calcined eggshells influenced the crystallite size of the original PVOH matrix. In summary, the addition of calcined eggshell and CNT at low loading levels markedly enhanced the mechanical, physical, and thermal properties of the composite material. Full article