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Search Results (6,073)

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Keywords = High-Performance Polymers

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20 pages, 1981 KB  
Article
Development and Performance Evaluation of a High-Temperature-Resistant Salt-Responsive Micro-Crosslinked Polymer Gel Filtration Loss Reducer
by Fengfeng Xiao, Yuhao Xia, Wushuo Liu, Jingping Liu and Yuanwei Sun
Gels 2026, 12(7), 564; https://doi.org/10.3390/gels12070564 - 25 Jun 2026
Abstract
To address the difficulty in controlling the filtration performance of water-based drilling fluids under high-temperature and high-salinity conditions during the drilling of deep and ultra-deep wells, a salt-responsive micro-crosslinked polymer gel filtration loss reducer, designated LZX, was developed. The synthesis employed 2-acrylamido-2-methylpropane sulfonic [...] Read more.
To address the difficulty in controlling the filtration performance of water-based drilling fluids under high-temperature and high-salinity conditions during the drilling of deep and ultra-deep wells, a salt-responsive micro-crosslinked polymer gel filtration loss reducer, designated LZX, was developed. The synthesis employed 2-acrylamido-2-methylpropane sulfonic acid (AMPS), N,N-dimethylacrylamide (DMAA), dimethyldiallylammonium chloride (DMDAAC), and a betaine monomer containing an unsaturated double bond as monomers, with polyethylene glycol diacrylate (PEGDA) introduced as a crosslinker. Experimental results showed that the product structure matched the design expectations, and the thermal decomposition temperature of the main molecular chain exceeded 290 °C, indicating good thermal stability. At 220 °C under saturated salt conditions, a dosage of 2.5 wt% LZX maintained the API filtration loss at 5.8 mL and the HPHT filtration loss at 28.6 mL. Comparative experiments at different temperatures demonstrated that LZX exhibited superior filtration control performance compared to the commercial high-temperature filtration reducer Driscal Temp and Driscal D. The micro-crosslinked structure of LZX enhanced the rigidity of the molecular chains, raising the upper limit of its thermal resistance. Rheological and viscosity-average molecular weight measurements revealed that LZX exhibited typical antipolyelectrolyte behavior in high-salinity environments—the molecular chains tended to extend and the filtration reduction capability was accordingly maintained—preliminarily achieving a functional transition from passive salt tolerance to active salt responsiveness. LZX is expected to support the construction of high-performance water-based drilling fluids with high temperature and high salt resistance for future deep-earth drilling. Full article
(This article belongs to the Topic Polymer Gels for Oil Drilling and Enhanced Recovery)
20 pages, 3342 KB  
Review
Sustainable Development and Polymer-Based Functional Innovation in the Lacquer Industry: Resources, Technologies, and Industrialization Pathways
by Yihua Qian, Xiaoyu Wu, Yujia Liu, Xinhao Feng and Xinyou Liu
Polymers 2026, 18(13), 1578; https://doi.org/10.3390/polym18131578 - 25 Jun 2026
Abstract
Natural lacquer, a bio-based polymer derived from Toxicodendron vernicifluum, has attracted renewed scientific interest as a sustainable coating material with exceptional mechanical durability, chemical resistance, and aesthetic qualities. This review synthesizes current knowledge on the chemical composition, enzymatic curing mechanisms, and structure–property relationships [...] Read more.
Natural lacquer, a bio-based polymer derived from Toxicodendron vernicifluum, has attracted renewed scientific interest as a sustainable coating material with exceptional mechanical durability, chemical resistance, and aesthetic qualities. This review synthesizes current knowledge on the chemical composition, enzymatic curing mechanisms, and structure–property relationships of lacquer-based polymer systems, with particular focus on recent advances in functional modification and processing technology. Key findings indicate that laccase-catalyzed oxidative polymerization, operating optimally at pH 6.0–7.5 and 20–30 °C, governs the formation of a highly cross-linked urushiol network whose properties are fundamentally determined by side-chain unsaturation and emulsion stability. Mechanistic analysis reveals that polyurethane hybridization improves weathering resistance by introducing flexible aliphatic segments and additional hydrogen-bonding cross-links, while graphene oxide incorporation enhances anticorrosion performance through a physical barrier mechanism that prolongs ionic diffusion pathways. UV-curable LPEA derivatives achieve an 83% reduction in curing time relative to ambient-cured lacquer, enabling integration with industrial spray-coating lines. Despite these advances, several critical limitations remain inadequately resolved. Allergen reduction strategies have not yet achieved sufficient quantitative efficiency for large-scale commercial deployment, and the long-term stability of nanocomposite lacquer films under sustained UV exposure and hydrothermal conditions is not well established. Furthermore, most high-performance modification systems reported in the literature are demonstrated only on laboratory scale, with scalability, substrate compatibility, and lifecycle performance remaining largely unvalidated. The review identifies the absence of standardized performance evaluation protocols and the fragmentation of structure–property data across studies as key barriers to systematic progress, and proposes that future work prioritize the development of integrated processing–modification–performance frameworks to guide the rational design of next-generation lacquer-based functional materials. Full article
(This article belongs to the Section Biobased and Biodegradable Polymers)
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16 pages, 2978 KB  
Article
Rheological and Mechanical Characterization of Asphalt Binder Modified with Plastic Waste Polymers
by Yerzhan Imanbayev, Yerdos Ongarbayev, Ainur Zhambolova, Yernar Kanzharkan, Aliya Kenzhegaliyeva, Zhannur Myltykbayeva, Uzilkhan Yensegenova, Akkenzhe Bussurmanova and Anar Akkenzheyeva
Polymers 2026, 18(13), 1574; https://doi.org/10.3390/polym18131574 - 24 Jun 2026
Viewed by 96
Abstract
Asphalt concrete pavements in many regions suffer from premature deterioration caused by low-temperature cracking and rutting resistance under heavy traffic loads and high summer temperatures. While polymer-modified bitumen is widely used to improve pavement performance, the high cost of commercial polymers restricts its [...] Read more.
Asphalt concrete pavements in many regions suffer from premature deterioration caused by low-temperature cracking and rutting resistance under heavy traffic loads and high summer temperatures. While polymer-modified bitumen is widely used to improve pavement performance, the high cost of commercial polymers restricts its extensive application. This study evaluates the potential of polymer waste as an alternative modifier for asphalt binders to enhance mechanical performance while reducing economic and environmental costs. Experimental results demonstrate that an optimal plastic waste content of 1.0–1.5% significantly improves rutting resistance and increases binder rigidity. The incorporation of 1.5% low-density polyethylene (LDPE) and high-density polyethylene (HDPE) enhances deformation resistance, elastic modulus, and temperature stability. LDPE exhibits better compatibility with bitumen and dissolves more readily, contributing to improved binder homogeneity, whereas HDPE provides higher stiffness and thermal stability. The combined use of polymer waste with styrene–butadiene–styrene (SBS) produces a pronounced synergistic effect, leading to improvements in physical and mechanical properties exceeding 25% compared to Kazakhstan regulatory standards. Increasing polymer waste content further enhances the rigidity of both the binder and asphalt concrete, thereby improving rutting resistance and plastic deformation at elevated temperatures. The proposed approach offers a cost-effective and sustainable solution for road construction, promoting plastic waste recycling, reducing reliance on virgin polymers, and improving pavement durability, particularly under the climatic and traffic conditions of Kazakhstan. Full article
(This article belongs to the Section Polymer Processing and Engineering)
18 pages, 5453 KB  
Article
An Innovative Approach for Direct Identification of Microplastics in Freshwater Samples Using SWIR Hyperspectral Imaging
by Paola Cucuzza, Silvia Serranti, Giuseppe Capobianco and Eleonora Gorga
Sustainability 2026, 18(13), 6450; https://doi.org/10.3390/su18136450 - 24 Jun 2026
Viewed by 179
Abstract
Microplastics (MPs) are widely recognized as emerging contaminants in freshwater environments. Their identification often relies on extensive sample preparation and chemical treatments, which increase analysis time, reagent use, and overall resource consumption. Consequently, there is a growing need for sustainable analytical approaches enabling [...] Read more.
Microplastics (MPs) are widely recognized as emerging contaminants in freshwater environments. Their identification often relies on extensive sample preparation and chemical treatments, which increase analysis time, reagent use, and overall resource consumption. Consequently, there is a growing need for sustainable analytical approaches enabling reliable MP detection while minimizing sample handling. This study proposes an analytical workflow based on hyperspectral imaging (HSI) as a proof-of-concept approach for direct identification of MPs in freshwater samples. Water samples collected from three different rivers, containing heterogeneous natural materials, were spiked with MPs (250–1000 μm) of three common polymers, namely high-density polyethylene (HDPE), polystyrene (PS), and polypropylene (PP), to simulate realistic contamination scenarios. HSI acquisitions were performed in the short-wave infrared range (SWIR: 1000–2500 nm). Spectral preprocessing and principal component analysis (PCA) were applied for data exploration, while a hierarchical partial least squares-discriminant analysis (Hi-PLS-DA) model was developed to classify five target classes: natural materials, water, HDPE, PS, and PP. Despite sample complexity, the proposed workflow achieved satisfactory classification results, as demonstrated by the predicted class map and the corresponding statistical metrics (sensitivity, specificity, precision, and F1-score: 0.900–0.999). These results highlight the potential of the SWIR-HSI-based approach as a rapid and sustainable method for direct MP identification in freshwater samples and provide methodological insights for rapid MP screening strategies requiring minimal sample preparation. Full article
(This article belongs to the Special Issue Microplastics, Sustainable Water and Soil Environments)
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16 pages, 5489 KB  
Article
Valorization of Expanded Polystyrene by Embedding of High GFRP Loading Through Cold-Mixing Solvent-Assisted Process
by Federico Olivieri, Stefano Scognamiglio, Roberto Avolio, Rachele Castaldo, Mariacristina Cocca, Gennaro Gentile, Silvia Olivotto and Maria Emanuela Errico
Polymers 2026, 18(13), 1567; https://doi.org/10.3390/polym18131567 (registering DOI) - 24 Jun 2026
Viewed by 125
Abstract
The increasing accumulation of glass-fiber-reinforced polymer (GFRP) waste poses significant environmental challenges, calling for effective and scalable recycling strategies. In this work, a solvent-assisted cold mixing process was employed to incorporate very high amounts of GFRP (up to 75 wt%) into recycled expanded [...] Read more.
The increasing accumulation of glass-fiber-reinforced polymer (GFRP) waste poses significant environmental challenges, calling for effective and scalable recycling strategies. In this work, a solvent-assisted cold mixing process was employed to incorporate very high amounts of GFRP (up to 75 wt%) into recycled expanded polystyrene (ePS). The composites were deeply characterized, with particular attention to the role of particle size distribution and filler content. The results demonstrated that GFRP granulometry played a key role in determining composite performance. Intermediate particle sizes (0.25 mm) provided the best balance between dispersion, interfacial interaction, and mechanical properties, whereas excessively fine fractions introduced defects and reduced impact resistance (from 0.7 to 2.0 kJ/m2 going from dust to 0.25 mm at 75 wt%). Notably, the solvent-assisted approach has been widely recognized as an effective strategy to ensure homogeneous dispersion even at high filler contents, allowing subsequent melt processing without re-agglomeration. Recycled composites retained most of their chemical and mechanical properties after reprocessing, with only moderate performance losses mainly related to fiber fragmentation. Overall, this study demonstrates an effective and sustainable route for the simultaneous valorization of ePS and GFRP waste, enabling the production of highly loaded composites with preserved functionality and improved resource efficiency. Full article
(This article belongs to the Special Issue Functional Polymer Composites: Synthesis and Application)
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26 pages, 2833 KB  
Review
Recent Advances in Cellulose Depolymerization: Mechanistic Insights, Catalytic Innovations, and Scalable Pathways for Biomass Valorization
by Marián Lehocký
Polymers 2026, 18(13), 1565; https://doi.org/10.3390/polym18131565 - 23 Jun 2026
Viewed by 264
Abstract
Cellulose is the most promising abundant renewable polymer material with the highest potential for the future low-carbon biorefineries. However, its utilization in industry is limited by the structural recalcitrance as a result of organization of crystalline domains, fibrillar architecture hierarchy and intramolecular and [...] Read more.
Cellulose is the most promising abundant renewable polymer material with the highest potential for the future low-carbon biorefineries. However, its utilization in industry is limited by the structural recalcitrance as a result of organization of crystalline domains, fibrillar architecture hierarchy and intramolecular and intermolecular hydrogen bonding which is responsible for access restriction for the catalysts and consequent cleavage of the glycosidic bonds. Therefore, efficient depolymerization of cellulose is of paramount importance as a step in biomass conversion into the low molecular products. In this review, the recent advances in cellulose depolymerization are discussed. The chemical, enzymatic, thermal, thermochemical, mechanochemical, oxidative and hybrid catalytic method is thoroughly discussed. Attention is paid to the mechanism of the depolymerization reaction steps as glycosidic bond activation as hydrolytic, radical mediated, and energy assisted pathways. Selectivity and conversion efficiency based on substrate morphology, solvent system and catalyst design are also discussed. Further, there is a comparison of key performance metrics which are relevant for the industrial process as product yield, carbon efficiency, energy demand, stability of the catalyst, solvent recyclability and impact to the environmental lifecycle. The pros and cons of the various methods are also represented. Processes based on mineral acids enable rapid conversion. However, they suffer from corrosion, waste handling issues and degradation by-products. On the other hand, enzymatic depolymerization processes offer relatively high selectivity but they are limited in terms of feedstock sensitivity and slow reaction kinetics. The downstream valorization mechanisms are also described with the result being that no single available technology is capable of satisfying all industrial requirements. Thus, future progress expects integrated circular processes where advanced catalysis, process intensification and digital optimization strategies take place. Full article
(This article belongs to the Section Biobased and Biodegradable Polymers)
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39 pages, 18280 KB  
Article
Quantifying Impact Damage Severity in Conventional, Hybrid and Natural-Based Composite Structures: An Acousto–Ultrasonics Approach
by Kumar Shantanu Prasad, Gbanaibolou Jombo, Sikiru O. Ismail, Yong K. Chen and Hom Nath Dhakal
Appl. Sci. 2026, 16(13), 6313; https://doi.org/10.3390/app16136313 (registering DOI) - 23 Jun 2026
Viewed by 93
Abstract
This study presents an approach to quantifying impact-induced damage severity in composites, focusing on synthetic carbon fibre-reinforced polymer (CFRP), natural flax fibre-reinforced polymer (FFRP) and hybrid fibre reinforced polymer (HFRP) composite of carbon and flax. The investigation aims to quantitatively characterise impact damage [...] Read more.
This study presents an approach to quantifying impact-induced damage severity in composites, focusing on synthetic carbon fibre-reinforced polymer (CFRP), natural flax fibre-reinforced polymer (FFRP) and hybrid fibre reinforced polymer (HFRP) composite of carbon and flax. The investigation aims to quantitatively characterise impact damage under energies ranging from 10 to 70 J through acousto–ultrasonics (AU) testing, proposing an efficient technique for evaluating the integrity of various FRP composites under in-service conditions. AU testing was performed at azimuthal angles of 0°, 30°, 45°, 60° and 90°, utilising acousto–ultrasonic waveform indices (AUWIs), such as wave velocity, peak amplitude, energy content, centroid frequency and skewness factor. The damage severity index is correlated with the damage mode. The findings establish that wave velocity is a reliable parameter for quantifying damage severity across all composite material types considered, with high adjusted R2 values of 0.92 for CFRP, 0.89 for FFRP and 0.90 for HFRP. Peak amplitude also shows considerable sensitivity. Finally, this research highlights the limitations of traditional non-destructive evaluation (NDE) techniques and demonstrates the potential of combining multi-damage metrics with advanced imaging methods, such as X-ray micro-computed tomography (X-ray µCT) and scanning electron microscopy (SEM), to provide a comprehensive assessment of damage in various composite materials. The proposed methodology offers a promising approach for quantifying the impact damage severity in composite structures, as applicable to wind turbine blades, amongst other structural components. Full article
(This article belongs to the Special Issue Application of Acoustics as a Structural Health Monitoring Technology)
17 pages, 2596 KB  
Article
Intelligent Injection Molding: Machine Learning-Driven Optimization of Processing Parameters for Enhanced Mechanical Properties in Short-Fiber-Reinforced Thermoplastics
by Rafael Aguirre Flores, Francisco J. González, Felipe Avalos Belmontes and Jesús Francisco Lara Sánchez
Processes 2026, 14(13), 2037; https://doi.org/10.3390/pr14132037 - 23 Jun 2026
Viewed by 153
Abstract
Optimizing the injection molding of short-fiber-reinforced thermoplastics (SFRTs) is a persistent challenge due to the complex interplay between processing parameters and final mechanical performance. To address this, we developed and validated a machine learning (ML) pipeline to maximize both the tensile strength and [...] Read more.
Optimizing the injection molding of short-fiber-reinforced thermoplastics (SFRTs) is a persistent challenge due to the complex interplay between processing parameters and final mechanical performance. To address this, we developed and validated a machine learning (ML) pipeline to maximize both the tensile strength and Charpy impact resistance in polyamide 6 with 30% glass fiber (PA6-GF30). Through a designed experimental campaign, we systematically varied four key process parameters—melt temperature (260–300 °C), injection pressure (600–1000 bar), packing pressure (400–800 bar), and cooling time (15–35 s). The resulting dataset was used to train and compare three different regression models: Random Forest (RF), Gradient Boosting (GB), and Support Vector Regression (SVR). Our findings indicate that the Gradient Boosting (GB) algorithm yielded the most reliable predictions, significantly outperforming the other evaluated models. Further analysis using SHAP (Shapley Additive exPlanations) identified packing pressure as the dominant factor influencing tensile strength (contributing approximately 40% to the prediction), while melt temperature emerged as the key driver for impact resistance (around 35% contribution). By integrating our best-performing GB model with a multi-objective genetic algorithm, we identified an optimal set of parameters that simultaneously enhances both mechanical properties. Among the evaluated models (Random Forest, Support Vector Regression, and Gradient Boosting), the Gradient Boosting algorithm achieved the highest predictive accuracy. Compared to the baseline condition (280 °C melt temperature, 800 bar injection pressure, 600 bar packing pressure, 25 s cooling time), experimental validation of these optimized settings demonstrated substantial improvement: tensile strength increased from 145 MPa to 171 MPa (an 18% enhancement), and impact resistance rose from 45 kJ/m2 to 55 kJ/m2 (a 22% gain). This work establishes that an integrated ML and optimization framework can serve as a transformative approach for high-precision manufacturing of advanced engineering polymers. The primary novelty of this work lies in the development of a fully integrated, bias-free methodological framework that explicitly couples physical interpretability with multi-objective optimization, bridging the critical gap between black-box predictions and actionable industrial insights. Full article
(This article belongs to the Special Issue Processing and Applications of Polymer Composite Materials)
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25 pages, 4952 KB  
Article
Synergistic Enhancement of Freeze–Thaw Durability and Structural Integrity in Silty Clay Through Combined Microbial Carbonate Precipitation and Anionic Polyacrylamide Modification
by Hongfeng Li, Zijie Wei, Yanfang Tong, Dahong Yang and Guang-Zhu Zhang
Materials 2026, 19(13), 2702; https://doi.org/10.3390/ma19132702 - 23 Jun 2026
Viewed by 96
Abstract
Seasonal freeze–thaw cycling progressively rearranges pores and propagates microcracks in silty clay, reducing the reliability of cold-region earthworks. This study evaluated a bio–polymer stabilization strategy combining microbially induced carbonate precipitation (MICP) with anionic polyacrylamide (APAM) to improve mechanical performance and freeze–thaw durability. Six [...] Read more.
Seasonal freeze–thaw cycling progressively rearranges pores and propagates microcracks in silty clay, reducing the reliability of cold-region earthworks. This study evaluated a bio–polymer stabilization strategy combining microbially induced carbonate precipitation (MICP) with anionic polyacrylamide (APAM) to improve mechanical performance and freeze–thaw durability. Six groups were prepared at identical moisture and compaction conditions: water, APAM, and four MICP–APAM groups with bacterial optical densities (OD600) of 0.8, 1.0, 1.2, and 1.4. Unconfined compressive strength, unconsolidated-undrained triaxial compression, ultrasonic pulse velocity, and SEM, TG/DTG, XRD, and FTIR analyses were conducted before and after freeze–thaw cycling. The M1.0-APAM group showed the best overall performance, with UCS values of 1.35 MPa before cycling and 0.89 MPa after nine cycles, together with high shear resistance and ultrasonic velocity. Lower bacterial concentration provided insufficient cementation, whereas higher concentrations promoted non-uniform carbonate deposition, pore heterogeneity, and local stress concentration. Microstructural evidence indicated that OD600 ≈ 1.0 produced a relatively homogeneous network of fine carbonate clusters and polymer-associated films, with calcite formation supported by TG/DTG and XRD. The results show that MICP–APAM treatment enhances silty clay primarily through coordinated mineralization uniformity, pore refinement, and polymer bridging, providing a sustainable stabilization option for seasonally frozen soils. Full article
(This article belongs to the Section Construction and Building Materials)
36 pages, 5697 KB  
Article
Machine Learning Prediction of Thermal Properties of PHB/PHBV-Based Materials: A Quantitative Structure–Property Relationship Approach Using an Integrated Polymer Database
by Nikolaos P. Sotiropoulos, Leonidas Mindrinos, Jean-David Peltier, Konstantina V. Filippou, Marianna I. Kotzabasaki, Nikolaos Tsigkas and Chrysanthos Maraveas
Polymers 2026, 18(13), 1559; https://doi.org/10.3390/polym18131559 - 23 Jun 2026
Viewed by 286
Abstract
Bio-based and biodegradable polymers such as short-chain-length (scl) poly(3-hydroxybutyrate) (PHB) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) are widely adopted in diverse areas such as healthcare, manufacturing, and packaging. However, high production costs and the complexity of tailoring their thermal properties, such as glass transition temperature (Tg), [...] Read more.
Bio-based and biodegradable polymers such as short-chain-length (scl) poly(3-hydroxybutyrate) (PHB) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) are widely adopted in diverse areas such as healthcare, manufacturing, and packaging. However, high production costs and the complexity of tailoring their thermal properties, such as glass transition temperature (Tg), melting temperature (Tm), and crystallization temperature (Tc), hinder further adoption. The current study reported on the development of a raw dataset of PHB and PHBV materials compiled from 572 instances collected from the literature (558 instances) and in-house experiments (14 instances). The dataset encompassed compositional physicochemical parameters, molecular features, and corresponding thermal characteristics. After assessing data quality and filtering for completeness and available features, curated datasets were created for machine learning (ML) analysis. Two ML models, Random Forest (RF) and eXtreme Gradient Boosting (XGBoost), were utilized to predict values of Tg, Tc, and Tm using feature engineering methods that integrated chemistry-based descriptors with polymer-specific and experimental variables. The predictive performance of the models was systematically investigated using different combinations of input features to identify the most informative descriptor sets for each target property. The best-performing models were obtained using 118 data points for Tg and Tm and 201 data points for Tc, achieving R2 values of 0.77, 0.76, and 0.82 for Tg, Tc, and Tm, respectively. Despite the reliable prediction of the thermal properties of scl-PHAs, the main limitations of the study were the relatively small dataset size for certain targets and incomplete or missing reporting of experimental conditions in the literature sources, which may introduce variability in the compiled data. The findings implied that curated polymer datasets and interpretable ML models can support the rational design of sustainable polymers with tailored properties for specific applications. Full article
(This article belongs to the Special Issue Computational Modeling of Polymer Composites and Nanocomposites)
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13 pages, 7111 KB  
Article
Effect of Polymer Concentration and Surface Charge on Controllable Nanopesticides Delivery
by Ran Cao, Yue Wu, Nuo Xu, Yutao Zhang, Zhiqian Guo and Yisheng Xu
Polymers 2026, 18(13), 1557; https://doi.org/10.3390/polym18131557 - 23 Jun 2026
Viewed by 182
Abstract
The efficacy of polymer-based nanopesticides (NPs) is strongly governed by carrier concentration and surface charge, which affect shell thickness, drug release kinetics, and photostability. However, the influence of these two factors in pesticide release and delivery performance remains unclear. This study introduces a [...] Read more.
The efficacy of polymer-based nanopesticides (NPs) is strongly governed by carrier concentration and surface charge, which affect shell thickness, drug release kinetics, and photostability. However, the influence of these two factors in pesticide release and delivery performance remains unclear. This study introduces a NIR-II fluorescence dye-tracing strategy to enable high-resolution monitoring of NP behavior in model plants. By systematically varying polymer concentration and copolymer blocks, we investigate their impact on release behavior, photostability, and stem uptake. As the polymer concentration increased, NPs demonstrated a controlled slow release and better photostability, yet a lower pesticide loading capability. In model plants, PISNPs transport quickly and can accumulate at wound sites, effectively offering antifungal properties. This work provides experimental evidence for optimizing polymer carrier design to achieve efficient, controlled release while minimizing photodegradation risks, offering practical guidelines for developing high-performance, low-risk nanopesticide formulations. Full article
(This article belongs to the Section Polymer Applications)
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30 pages, 5293 KB  
Article
High-Performance Metal-Free Nitrogen-Doped Carbon Catalyst Derived from Polyurea–Polyimine Copolymer for Anion Exchange Membrane Fuel Cells
by Fu-Lung Lin, Che-Ju Tseng and Ko-Shan Ho
Catalysts 2026, 16(6), 573; https://doi.org/10.3390/catal16060573 - 22 Jun 2026
Viewed by 86
Abstract
Developing cost-effective alternatives to platinum-based catalysts remains paramount for commercializing anion exchange membrane fuel cells (AEMFCs). We report a metal-free nitrogen-doped carbon catalyst derived from a rationally designed polyurea–polyimine copolymer that outperforms commercial 20 wt% Pt/C in superior relative durability and methanol tolerance. [...] Read more.
Developing cost-effective alternatives to platinum-based catalysts remains paramount for commercializing anion exchange membrane fuel cells (AEMFCs). We report a metal-free nitrogen-doped carbon catalyst derived from a rationally designed polyurea–polyimine copolymer that outperforms commercial 20 wt% Pt/C in superior relative durability and methanol tolerance. Strategic integration of polyurea’s pore-forming capability with polyimine’s thermal stability enabled the synthesis of a catalyst (NC-1000N) featuring ultrahigh surface area (1276.5 m2 g−1), optimal nitrogen speciation (20.5% pyridinic-N, 45.3% graphitic-N), and enhanced graphitization, which improves the electrical conductivity of catalysts. NC-1000N exhibited exceptional oxygen reduction performance with an onset potential of 0.96 V, almost four-electron selectivity (n = 3.87), a medium Tafel slope (105 mV dec−1), and minimal charge transfer resistance (46.74 Ω). When evaluated in single-cell AEMFCs, NC-1000N delivered a peak power density of 372.1 mW cm−2, which is 26% higher than Pt/C at equivalent loading, while demonstrating superior stability (94.8% retention after 7 h) and complete methanol tolerance. Systematic pyrolysis temperature optimization (800–1000 °C) revealed critical structure–property relationships governing catalyst evolution from disordered precursor to highly graphitic, nitrogen-enriched carbon with precisely engineered active sites. This work establishes polymer-derived carbons and provides design principles for scalable synthesis of high-performance metal-free electrocatalysts for sustainable energy conversion technologies. Full article
(This article belongs to the Special Issue Catalytic Materials in Electrochemical and Fuel Cells)
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31 pages, 4805 KB  
Review
Ti3C2Tx-Based Materials and Coatings for De-Icing and Defogging of Wind Turbine Blades: Materials Basis, Structural Design, Engineering Integration, and Future Opportunities
by Weiwei Wu, Kening Peng, Kunqi Zhang, Zhifang Liu and Nana Yao
Nanomaterials 2026, 16(12), 784; https://doi.org/10.3390/nano16120784 - 22 Jun 2026
Viewed by 309
Abstract
In cold, humid environments, even a small amount of ice accumulation on the blade surface can degrade aerodynamic performance, increase drag, induce premature stall and vibration, and raise the risks of shutdown, fatigue, and ice throw. Existing blade anti-icing and de-icing strategies (such [...] Read more.
In cold, humid environments, even a small amount of ice accumulation on the blade surface can degrade aerodynamic performance, increase drag, induce premature stall and vibration, and raise the risks of shutdown, fatigue, and ice throw. Existing blade anti-icing and de-icing strategies (such as passive coatings, electrothermal heating, hot-air systems, and hybrid designs) struggle to simultaneously meet the requirements of lightweight construction, low-voltage rapid heating, conformability to curved surfaces, erosion resistance, long-term durability, and scalable manufacturing. MXenes, particularly Ti3C2Tx, have attracted attention due to their high electrical conductivity, broadband optical absorption, solution processability, tunable interfacial chemistry, and good compatibility with polymer matrices. However, their oxidation issue and blade-scale deployment challenges (coating chemistry, scalable fabrication, real-world testing) remain obstacles. Based on this, this review discusses Ti3C2Tx-based anti-icing, de-icing, and defogging strategies for wind turbine blades, with emphasis on material properties, functional mechanisms, coating architectures, fabrication routes, durability, and scalability, and highlights their potential for lightweight and energy-efficient all-weather blade protection. Finally, future research directions for Ti3C2Tx-based blade anti-icing and de-icing are prospected. This review not only aims to identify key knowledge gaps in current research but also strives to provide a theoretical reference for the application of Ti3C2Tx in the complex service environment of real wind turbine blades, thereby moving beyond idealized laboratory conditions. Full article
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29 pages, 4857 KB  
Review
Progress in (Photo)electrochemical Biosensors for the Detection of Amyloid-Beta Oligomer
by Yaliang Huang, Ning Wang, Xinyao Yi and Ning Xia
Biosensors 2026, 16(6), 349; https://doi.org/10.3390/bios16060349 - 22 Jun 2026
Viewed by 253
Abstract
Alzheimer’s disease (AD) has become a neurodegenerative disease with an increasing incidence rate and a large economic and social burden worldwide. Amyloid-beta oligomer (AβO) has been confirmed as a key neurotoxic species and a core diagnostic biomarker in AD. Traditional methods for AβO [...] Read more.
Alzheimer’s disease (AD) has become a neurodegenerative disease with an increasing incidence rate and a large economic and social burden worldwide. Amyloid-beta oligomer (AβO) has been confirmed as a key neurotoxic species and a core diagnostic biomarker in AD. Traditional methods for AβO detection have drawbacks, such as cumbersome operation, high cost, and dependence on sophisticated instruments, hindering their transformation into fast and real-time detection techniques. (Photo)electrochemical biosensors have attracted much attention due to their inherent advantages, such as high sensitivity, low cost, portability, and ease of miniaturization. This review systematically summarizes the latest progress of (photo)electrochemical biosensors for AβO detection, mainly based on two sensing modes: direct detection and sandwich-type detection. We comprehensively elaborated on the sensing performances and recognition elements, such as antibodies, aptamers, peptides, and molecularly imprinted polymers. The integration of functional nanomaterials and signal amplification strategies was emphasized to improve the sensitivity, selectivity, and stability of biosensors. In addition, we discussed the existing challenges and looked forward to the future development direction for the early diagnosis of AD. This article aims to provide a systematic reference for the rational design and practical application of advanced biosensors in biomarker detection and AD-related precision medicine. Full article
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21 pages, 2551 KB  
Article
Sulfonation-Time-Dependent Structure–Property Relationships of Electrospun Polyketone Nanofiber Membranes for PEMFC Applications
by Hongsik Byun, Geon-Hyeong Lee, Yeol-Lim Lee and Sang-Hun Lee
Polymers 2026, 18(12), 1542; https://doi.org/10.3390/polym18121542 - 21 Jun 2026
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Abstract
Electrospun sulfonated polyketone (PK) nanofiber membranes were prepared to investigate the sulfonation-time-dependent structure–property relationships of hydrocarbon-based polymer electrolyte membranes for PEMFC (Polymer Electrolyte Membrane Fuel Cell) applications. NaCl addition to the electrospinning solution increased solution conductivity and enabled the formation of uniform PK [...] Read more.
Electrospun sulfonated polyketone (PK) nanofiber membranes were prepared to investigate the sulfonation-time-dependent structure–property relationships of hydrocarbon-based polymer electrolyte membranes for PEMFC (Polymer Electrolyte Membrane Fuel Cell) applications. NaCl addition to the electrospinning solution increased solution conductivity and enabled the formation of uniform PK nanofibers with an average diameter of approximately 270 nm. Subsequent sulfonation introduced sulfonic-acid-related groups into the PK nanofiber framework, and the resulting membrane properties were strongly governed by sulfonation time. Among the tested membranes, PK-NC16 exhibited the highest proton conductivity of 0.107 ± 0.031 S cm−1 and an ion exchange capacity of 2.82 meq g−1, exceeding or comparable to those of Nafion 115 under the tested conditions. FTIR-based analysis indicated that the relative sulfonation index increased up to 16 h, whereas extended sulfonation for 24 h generated additional sulfone/sulfonate-related bands, suggesting possible side reactions or structural changes under prolonged acid treatment. The high water uptake of PK-NC16 enhanced proton transport but also revealed a hydration-sensitive polymer network, as reflected by a voltage degradation rate of approximately −590 μV h−1 during a 100 h short-term stability constant-current test. These results demonstrate that sulfonation time is a key parameter controlling the balance among ionic functionality, hydration, mechanical response, proton conductivity, and PEMFC-relevant single-cell performance in electrospun PK nanofiber membranes. Full article
(This article belongs to the Special Issue Multifunctional Application of Electrospun Fiber: 2nd Edition)
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