Search Results (2,969)

Hydraulic fracturing in ultra-deep reservoirs faces significant challenges, including high wellbore friction and inadequate thermal stability of conventional fracturing fluids. To address these issues, we developed a potassium formate-weighted fracturing fluid with delayed crosslinking, excellent friction reduction, and superior temperature resistance, using a hydrophobic associating polymer thickener and a multi-ligand organic zirconium crosslinker. The weighted fracturing fluid has a density of 1.4 g/cm³ and completes crosslinking within 300 s at 90 °C. It achieves a maximum friction reduction rate of 63.2%. Below 60 °C, the system relies on a supramolecular thickener network for low viscosity and friction reduction; above 60 °C, chemical crosslinking between the thickener and zirconium ions creates a dual-network structure that significantly enhances temperature and shear resistance. After 120 min of shearing at 200 °C and 170 s⁻¹, the retained viscosity reaches 75.3 mPa·s. Complete gel breaking is achieved by sodium bromate via an oxidation reaction. This dual-network delayed crosslinking system successfully reconciles the conflict between low wellbore friction and high-temperature proppant-carrying capacity. This work presents a superior weighted fracturing fluid for ultra-deep reservoirs, as well as an innovative technique for their development. Full article

Fiber-reinforced polymer (FRP) composites are widely used to strengthen reinforced concrete (RC) columns due to their high strength, durability, and ease of installation. Accurate prediction of the axial capacity of CFRP-strengthened concrete columns is essential for reliable structural design. Yet conventional empirical models often exhibit limited accuracy due to the complex interactions among structural parameters. This study develops a deep learning-based model to predict the axial capacity of CFRP-wrapped RC columns using a database of 469 experimental tests collected from published studies. A deep neural network (DNN) was optimized using the Optuna hyperparameter tuning framework and k-fold cross-validation to enhance model accuracy and robustness. Model performance was evaluated using statistical indicators, including R², RMSE, MAE, MAPE, and the a20-index. The results show excellent predictive performance with R² values approaching 0.99 and an a20-index of 0.98, demonstrating strong agreement between predicted and experimental results. Comparisons with the ACI 440.2R-17 and CSA S806-12 design codes indicate that the proposed DNN model provides significantly improved prediction accuracy, with lower errors. The developed approach offers a reliable and efficient tool for estimating the axial capacity of CFRP-strengthened concrete columns. Full article

Cellulose-derived gel films are promising matrices for the immobilization and delivery of beneficial microorganisms in sustainable plant protection. This study evaluated the effects of polymer molecular weight and chemical structure on the physicochemical properties and biocontrol performance of hydroxyethyl cellulose (HEC) films of low, medium, and high molecular weight, as well as sodium carboxymethyl cellulose (CMC-Na), loaded with Bacillus subtilis. The films were characterized in terms of morphology, swelling behavior, mechanical properties, microbial viability, and antifungal activity against Fusarium avenaceum and Alternaria solani. Increasing HEC molecular weight produced progressively denser and more homogeneous gel networks, resulting in improved structural integrity, whereas CMC-Na formed dense but less stable networks. Swelling studies at pH 4, 7, and 9 showed high water uptake for all HEC systems, with enhanced structural stability observed in high-molecular-weight films, whereas CMC-Na dissolved rapidly under all conditions. Mechanical testing further confirmed that increasing molecular weight enhanced stiffness and tensile strength but reduced flexibility. Immobilized in gel matrices, B. subtilis remained viable after 12 months of storage and rapidly reactivated after rehydration. All biohybrid films inhibited fungal growth, with stronger formulation-dependent responses against F. avenaceum than against A. solani. In general, polymer molecular weight and structure were identified as key parameters controlling network organization, hydration behavior, mechanical performance, and biological functionality. These findings highlight the potential of cellulose-derived gel matrices as tunable carriers for microbial biocontrol applications. Full article

Nanogrooves provide instructive cues to cells in culture. Several nanofabrication techniques have been developed to create biomimetic substrates, advancing our understanding of cell adhesion. Their integration into nervous system models highlights the critical role of the extracellular matrix (ECM) in developing functional tissue constructs for in vitro platforms such as Brain-on-Chip (BoC) and Nervous System-on-Chip (NoC). This study presents a nanofabrication approach that integrates photolithography and microtransfer molding (μTM) to pattern nanogrooves using photocurable polymer NOA81 onto microelectrode array (MEA) plates. The resulting nanogrooves exhibited a pattern periodicity of 976 nm and a ridge width of 232 nm, as confirmed by scanning electron microscopy and atomic force microscopy. We assessed the biocompatibility and functional impact of these modified substrates using human induced pluripotent stem cell (hiPSC)-derived neuronal cultures. Neurons cultured on nanogroove-modified MEAs exhibited aligned neural processes due to the anisotropic surface features and expressed vivid spiking behavior and higher burst frequency compared to randomly cultured neuronal networks. In conclusion, the proposed fabrication technique integrates nanogrooves with commercial MEAs using a combination of microtransfer molding and photolithography, resulting in modified culture substrates that enhance spike activity and network organization, aiding in the development of more in vivo-like neural models. Full article

Eucommia ulmoides gum (EUG), a sustainable plant-derived natural polymer, was functionalized via three distinct routes, including vulcanization, epoxidation, and hydroxylation to yield vulcanized (VEUG), epoxidized (EEUG), and hydroxylated EUG (HEUG), respectively. We systematically characterized the effects of modification route and degree on the chemical structure, crystallization behavior, thermal stability, hydrophilicity, and mechanical properties of functionalized EUG and further evaluated the high/low-temperature performance, microstructure, and mechanical properties of the corresponding modified asphalt binders (VEMA, EEMA, HEMA) as a function of modifier type and loading. For VEUG, C-S cross-linking networks formed during vulcanization suppress EUG crystallization, enabling a rigid-plastic to elastic transition, while high-temperature cleavage of C-S bonds reduces its initial thermal stability. For EEUG, epoxidation breaks C=C double bonds and introduces epoxy groups to strengthen intermolecular interactions; subsequent ring-opening grafting of hydroxyl groups onto EEUG yields HEUG, which forms additional cross-links via dynamic hydrogen bonds. Increasing modification degree for both EEUG and HEUG reduces their number- and weight-average molecular weights with narrower distribution, diminishes crystallinity, enhances thermal stability and hydrophilicity, and drives a rigid-plastic to elastic transition, characterized by decreased strength (0.65 MPa < σ_HEUG < σ_EEUG < 10.18 MPa) and markedly improved ductility (143.6% < ε_EEUG < 262.0%, 679.9% < ε_HEUG < 1360.3%). In asphalt binders, VEUG’s cross-linked network endows VEMA with refined more abundant bee-like microstructures, drastically boosting high- and low-temperature performance: relative to pristine EUG-modified asphalt (EUGMA), VEMA’s DMT modulus decreases by 94%, and adhesion increases by 87%. EEMA forms covalent bonds with polar asphalt components via epoxy groups, while HEMA constructs a hydrogen-bonded cross-linked network; both effectively inhibit asphaltene aggregation. With increasing modifier loading, EEMA and HEMA exhibit increased modulus, reduced adhesion, and gradually improved high- and low-temperature performance, except for the non-significant high-temperature enhancement of HEMA at higher loadings. Full article

Conductive hydrogels are attractive for flexible electronics, but their practical use is often limited by resistance drift during repeated deformation and performance degradation at low temperatures. Here, core–shell polyaniline-coated polyacrylonitrile (PANi@PAN) electrospun nanofibers were incorporated into a polyacrylamide/hydroxypropyl cellulose (PAM/HPC) hydrogel matrix to construct a hybrid conductive network. The PANi shell serves as an electronic pathway alongside ionic conduction in the hydrated polymer network, leading to markedly improved electromechanical stability. The resistance drift is about 11% after 2000 stretching–relaxation cycles at 0–100% strain, about 12 times lower than that of the nanofiber-free hydrogel. Stable electrical responses are maintained under large deformation, with a resistance drift as low as 3.3% over a strain range of 0–400%. The hydrogels show a conductivity of 0.32 S m⁻¹ while retaining high stretchability (>600%). An ethylene glycol/water binary solvent is used to suppress ice formation and improve moisture retention, allowing stable electromechanical performance at −15 °C over 500 cycles. The hydrogel also adheres reliably to human skin (about 10.25 kPa) and functions as a conformal strain sensor without extra fixation. Full article

Chronic skin inflammatory diseases including psoriasis and atopic dermatitis affect millions worldwide, imposing substantial physical, psychological, and economic burdens. Despite advances in topical therapies, conventional formulations suffer from poor skin penetration, rapid clearance, local and systemic side effects, and suboptimal patient adherence. Polymeric nanogels, internally crosslinked three-dimensional polymer networks with dimensions of 10–200 nm, emerged as promising platforms to overcome these limitations. Their unique properties including high water content, tunable porosity, biocompatibility, deformability, and stimulus-responsive behavior enhance skin penetration allowing for targeted therapeutic action. This review examines nanogel synthesis methods optimized for targeting skin inflammatory diseases, including biopolymer-based approaches utilizing chitosan and hyaluronic acid, offering insights into how different methods and advanced architecture provide multifunctional capacities and bioactivities. Translation challenges including manufacturing scalability, long-term safety assessment, and regulatory compliance are critically discussed alongside emerging opportunities in personalized medicine and smart microneedle integrated systems for adaptive therapy. Full article

Exopolysaccharides (EPSs) are emerging as sustainable polymers for biomedical hydrogels. Here, we report hydrogels from sulfated EPSs produced by Porphyridium cruentum and ionically crosslinked with Ca²⁺, Ce³⁺, or Cu²⁺ to generate tunable networks with bioactive potential. Rheological analysis showed viscoelastic behavior was primarily governed by cation nature and accessible binding site density, with diminishing gains above 2.5 wt% EPS and limited benefit beyond 10 wt% crosslinker. Ce³⁺ produced the most solid-like gel, Ca²⁺ yielded more thixotropic networks, and Cu²⁺ promoted rapid, heterogeneous crosslinking consistent with fast surface complexation. These network signatures showed distinct in vitro performances. Cation selection tuned antibacterial activity against Staphylococcus aureus and Escherichia coli, with Cu²⁺ achieving rapid bactericidal effects and Ce³⁺ enabling an 8-log reduction after 24 h. The ABTS assay showed that Ca²⁺- and Ce³⁺-crosslinked gels had antioxidant potential (≥40 µM Trolox eq.mg⁻¹); however, antioxidant capacity was assay dependent. Conditioned-medium assays showed ≥75% viability at day 3 for Ca²⁺- and Ce³⁺-crosslinked gels against human dermal fibroblasts (HDFs), while only Ce³⁺-crosslinked gels were cytocompatible against human keratinocytes (HaCaTs). Cu²⁺-crosslinked gels were highly cytotoxic across all tested conditions. Macrophage cytokine readouts (TNF-α and IL-6) indicated formulation-dependent immunobiological response. This work establishes microalgal EPSs as versatile polymers and links crosslinking chemistry to rheological modulation and multifunctional biomedical performance, while direct wound-healing efficacy remains to be demonstrated in future in vivo or wound repair functional models. Full article

Conductive core–shell superabsorbent polymers (SAPs) are emerging as multifunctional additives for cementitious materials, combining moisture management with electrical functionality. In cement-based systems, a swellable polymeric core enables internal curing and crack-sealing through controlled water uptake and release, while a conductive shell introduces ionic and/or electronic charge transport, addressing key limitations of conventional non-conductive SAPs. This dual functionality provides a pathway toward smart cementitious composites with enhanced durability, self-sensing capability, and moisture-responsive behavior. This review focuses on the physical chemistry mechanisms governing conductive core–shell SAPs in cementitious environments, with emphasis on swelling thermodynamics, water transport kinetics, interfacial phenomena, and charge transport mechanisms. The roles of osmotic pressure, elastic network constraints, ionic effects, and pore solution chemistry are critically discussed, together with their impact on conductivity, hydration processes, microstructure development, and long-term performance. The relative contributions of ionic and electronic conduction are examined in relation to hydration state, shell morphology, and percolation of conductive networks. In addition, the relevance of core–shell SAP architectures to sustainable packaging is briefly discussed as a secondary application, illustrating how similar physicochemical principles—such as moisture buffering and functional coatings—apply beyond construction materials. Finally, key knowledge gaps are identified, including long-term stability in highly alkaline environments, trade-offs between swelling capacity and conductivity, environmental impacts of conductive phases, and the need for integrated experimental and modeling approaches. Addressing these challenges is essential for the rational design and practical implementation of conductive core–shell SAPs in next-generation cementitious materials. Full article

Flunarizine is a calcium channel blocker widely used in neurological disorders; however, its low aqueous solubility may influence formulation stability and drug dispersion in polymer-based systems. The present study aimed to evaluate the compatibility of flunarizine with selected excipients and to investigate its incorporation into polymeric hydrogel matrices. Binary mixtures of flunarizine with excipients such as hydroxypropyl-β-cyclodextrin, polyethylene glycol (PEG 6000), Tween 20, gelatin, and citric acid were prepared and characterized using Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TG/DTG), and high-performance liquid chromatography (HPLC). The FTIR spectra of the analyzed samples do not reveal the appearance of new absorption bands that may indicate chemical interactions; instead, minor spectral variations were observed due to weak intermolecular interactions within the polymer network. Thermal analysis revealed decomposition patterns consistent with those of the individual components, suggesting the absence of significant incompatibilities. A validated RP-HPLC method enabled sensitive and reliable quantification of flunarizine in the analyzed systems, with a limit of detection (LOD) of 0.05 µg/mL and a limit of quantitation (LOQ) of 0.16 µg/mL. Accuracy testing showed average recovery rates of 100% across 80–120% spiking levels. Overall, the results support the compatibility of flunarizine with the investigated excipients and the suitability of the studied hydrogels as potential drug delivery matrices. Full article

As the most abundant natural polymer on Earth, cellulose offers distinct advantages including renewability, biocompatibility, and modifiability. Among its various morphologies, spherical cellulose hydrogels (SCHs) represent a particularly versatile form ranging from micrometer to millimeter scales. They possess a unique hydrophilic 3D network, excellent flowability, high specific surface area, and outstanding mechanical stability, demonstrating great potential for biomedical applications. This mini-review highlights the primary bottom-up fabrication strategies for SCHs, including dripping, spraying, emulsion, and microfluidics, and the mechanisms by which different fabrication processes regulate their size, morphology, and structure are elucidated. On this basis, the recent advancements in SCHs across key biomedical domains, specifically in chromatographic separation, controlled drug delivery, tissue engineering, and wound healing, are discussed. Finally, the current challenges and future directions in this field are summarized and predicted, aiming to provide a reference for the development and application of high-performance cellulose-based biomaterials. Full article

Polymer–metal hybrid composites (PMHCs) represent an emerging class of materials that combine the lightweight processability of polymers with the structural and functional advantages of metals. Recent advances in material design and manufacturing have shifted attention from traditional particulate or fibrous reinforcement toward metallic architectures—continuous, architected, or topologically optimized metallic networks intentionally embedded within polymer matrices. These metallic architectures play a key role in defining the composite’s global performance, influencing stiffness, energy absorption, failure mechanisms, and multifunctional properties such as electrical or thermal conductivity. This review examines how the geometry, connectivity, and topology of metallic reinforcements govern mechanical behavior and functional responses in PMHCs. Emphasis is placed on the interplay between architecture and interface design, including surface modification strategies and mechanical interlocking phenomena. Furthermore, the paper discusses the contribution of additive manufacturing technologies in enabling complex metallic architectures and hybrid processing routes. By integrating structural, interfacial, and manufacturing perspectives, this review develops a coherent framework for understanding how metallic architecture drives the evolution of PMHCs toward multifunctional and design-driven engineering applications. The analysis of the literature consistently indicates that architectural configuration—rather than material selection alone—represents the primary factor governing multifunctional performance. Full article

The separation of rare earth elements (REEs) is challenging due to their similar chemical properties. This study developed a series of novel polystyrene–ion-imprinted poly(hydroxamic acid) interpenetrating polymer networks (PS-IIPHAs) for the highly selective adsorption of La³⁺, Ce³⁺, and Y³⁺. The effects of the solution pH, contact time, initial concentrations, and temperature on the adsorption performance of the resins were systematically investigated. The results showed that adsorption equilibrium was reached within 4 h at a pH of 1.0, following the Langmuir isotherm, with maximum adsorption capacities of 2.425, 3.012, and 2.927 mmol/g for La³⁺, Ce³⁺, and Y³⁺, respectively. The resins exhibited excellent selectivity toward the template ions, with separation factors of 35.45 for Ce³⁺-La³⁺, 17.52 for Y³⁺-La³⁺, and 11.04 for Ce³⁺-Y³⁺. These results indicate PS-IIPHAs as promising adsorbents for the efficient, highly selective recovery of REEs. Full article

The clinical effectiveness of clear orthodontic aligners mainly depends on the thermomechanical stability of the polymers in this challenging hydrothermal environment. In this study, we compare the water-induced viscoelastic changes and glass transition temperature (Tg) stability of four polymers with different microarchitectures. Specifically, we examined directly printed photopolymer networks (Tera Harz TC-85 and LuxCreo 4D Aligner), a monolithic thermoplastic (Duran+), and a multilayer thermoplastic (ClearCorrect). Samples were immersed in physiological saline (0.9 wt.% NaCl) at 37 °C for 7 days, and Dynamic Mechanical Analysis (DMA) was performed in three conditions: dry, after immersion, and after a 2 h desorption step, mimicking a typical clinical 22:2 wear cycle. All polymers showed a decrease in Tg after immersion, with TC-85 exhibiting the greatest reduction relative to the dry baseline. Tg recovery after a 2 h ambient desorption step was incomplete and was significantly associated with the amount of water retained after 2 h drying (expressed as % of initial uptake; R² = 0.419), whereas total water absorption after 7 days was not associated with short-term thermal recovery. Full article

Landfills are complex repositories where macroplastics degrade into MPs. This review examines mechanical, chemical, and biological pathways of plastic fragmentation, as well as the occurrence, characteristics, and removal efficiency of MPs in landfill leachate. We also explore the landfill plastisphere from the perspective of this complex matrix, considering how plastic surfaces and microbial life may potentially converge to form a key biogeochemical interface that could influence carbon and nitrogen transformations. The plastisphere’s complex surface structure drives microbial differentiation. Given its established links to GHG production in soil and water, we propose it likely represents a key contributor to GHG emissions in the more complex landfill environment. To bridge this conceptual gap, we review a mathematical scaffolding encompassing biofilm growth, polymer degradation kinetics, and gas flux, which can as a theoretical baseline requiring future in situ parameterization to evaluate plastisphere-driven biogeochemical interactions. Building on recent advances in monitoring and remote sensing technologies, including IOT networks, UAV imagery, and AI analysis, we outline a low-carbon landfill framework designed to optimize operational controls. This framework is described to simultaneously mitigate MP release and reduce GHG emissions, lowering carbon footprints. Amid surging plastic pollutants, this review underscores the necessity of holistic, integrated mitigation strategies. Full article